Abstract is: The Journal of Evolutionary Biology is a peer-reviewed scientific journal published monthly covering the field of evolutionary biology. It is owned by the European Society for Evolutionary Biology. The founding editor-in-chief was Stephen C. Stearns. He was succeeded by Pierre-Henri Gouyon (1992–1995), Rolf Hoekstra (1996–1999), Peter van Tienderen (2000–2003), Juha Merilä (2004–2007), Allen Moore (2007–2010), Michael G. Ritchie (2011-2017), and Wolf U. Blanckenhorn (2017-2021). The current editor is Max Reuter (University College London).
academic journal | Q737498 |
society journal | Q73364223 |
delayed open access journal | Q5253501 |
scientific journal | Q5633421 |
P6981 | ACNP journal ID | 31022 |
2108658 | ||
P1159 | CODEN | JEBIEQ |
P8375 | Crossref journal ID | 1071 |
P1250 | Danish Bibliometric Research Indicator (BFI) SNO/CNO | 11805 |
P356 | DOI | 10.1111/(ISSN)1420-9101 |
P1058 | ERA Journal ID | 3273 |
P646 | Freebase ID | /m/0415kjg |
P1160 | ISO 4 abbreviation | J. Evol. Biol. |
P236 | ISSN | 1010-061X |
1420-9101 | ||
P7363 | ISSN-L | 1010-061X |
P1055 | NLM Unique ID | 8809954 |
P243 | OCLC control number | 474043725 |
P856 | official website | http://link.springer.de/link/service/journals/00036/index.htm |
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1420-9101 | ||
P10283 | OpenAlex ID | S138169916 |
P3181 | OpenCitations bibliographic resource ID | 55347 |
P7662 | Scilit journal ID | 52489 |
4319889 | ||
P1156 | Scopus source ID | 18920 |
P4616 | UniProt journal ID | 1041 |
P495 | country of origin | Switzerland | Q39 |
P1240 | Danish Bibliometric Research Indicator level | 2 | |
P571 | inception | 1988-01-01 | |
P8875 | indexed in bibliographic review | Scopus | Q371467 |
Science Citation Index Expanded | Q104047209 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | evolutionary biology | Q840400 |
P123 | publisher | Wiley-Blackwell | Q767319 |
P1476 | title | Journal of Evolutionary Biology |
Q59417330 | Q59417330 |
Q81145526 | 'Adaptive Dynamics' vs. 'adaptive dynamics' |
Q28273446 | 'Anti-bee' and 'pro-bird' changes during the evolution of hummingbird pollination in Penstemon flowers |
Q46897505 | 'Prudent habitat choice': a novel mechanism of size-assortative mating |
Q30569927 | 'Representative Genes', is it OK to use a small amount of data to obtain a phylogeny that is at least close to the true tree? |
Q80457270 | 'Social heterosis' as a process that maintains genetic variation--a comment |
Q36245822 | 20 questions on adaptive dynamics |
Q97547867 | 200 million years of anuran body size evolution in relation to geography, ecology, and life history |
Q125292223 | A Successful FailureA review by Gerdien de JongGregor Mendel, the First Geneticist. By Vitezslav Orel, transl. Stephen Finn, Oxford University Press, 1996. ISBN 0‐19‐854774‐9. Price: £29.50. |
Q126014387 | Body Size and Mammalian Paleobiology: Estimation and Biological Implications. Edited by John Damuth and Bruce J. MacFadden Cambridge University Press. 1990. |
Q30830866 | A Drosophila laboratory evolution experiment points to low evolutionary potential under increased temperatures likely to be experienced in the future |
Q46140315 | A G matrix analogue to capture the cumulative effects of nongenetic inheritance. |
Q49997319 | A biomechanical analysis of prognathous and orthognathous insect head capsules: Evidence for a many to one mapping of ridge strain to head strain. |
Q123014916 | A biomechanical perspective on the use of forelimb length as a measure of sexual selection in frogs |
Q51719745 | A broad-scale analysis of population differentiation for Zn tolerance in an emerging model species for tolerance study: Arabidopsis halleri (Brassicaceae). |
Q33980483 | A cancer-causing gene is positively correlated with male aggression in Xiphophorus cortezi |
Q30442551 | A cautionary tale of two matrices: the duality of multivariate abstraction |
Q33344076 | A change in climate causes rapid evolution of multiple life-history traits and their interactions in an annual plant |
Q47205972 | A change in competitive context reverses sexual selection on male size. |
Q54587435 | A change of expression in the conserved signaling gene MKK7 is associated with a selective sweep in the western house mouse Mus musculus domesticus. |
Q50304394 | A chemical level in the coevolutionary arms race between an ant social parasite and its hosts. |
Q45913137 | A clarification of Pouydebat et al., 2008, evolution of grasping among anthropoids. |
Q52680784 | A cline in the Drosophila melanogaster period gene in Australia: neither down nor under. |
Q48298522 | A comparative analysis of experimental selection on the stickleback pelvis. |
Q52655378 | A comparative analysis of predator-induced plasticity in larval Triturus newts. |
Q45211203 | A comparative analysis of senescence in adult damselflies and dragonflies (Odonata). |
Q51540247 | A comparative analysis of the mechanisms underlying speciation on Lord Howe Island. |
Q101334569 | A comparative analysis of the photoprotection hypothesis for the evolution of autumn colors |
Q91325817 | A comparative morphometric study of sensory capacity in geometrid moths |
Q41990326 | A comparative perspective on longevity: the effect of body size dominates over ecology in moths |
Q113181530 | A comparison between allozyme data and phenotypic distances from defensive secretion in Oreina leaf-beetles (Chrysomelinae) |
Q39435301 | A comparison between desert and Mediterranean antlion populations: differences in life history and morphology |
Q43905141 | A comparison of methods to estimate cross-environment genetic correlations |
Q121353916 | A comparison of methods to partition selection acting via components of fitness: Do larger male bullfrogs have greater hatching success? |
Q44659026 | A comparison of nuclear and cytoplasmic genetic effects on sperm competitiveness and female remating in a seed beetle |
Q57170991 | A competitive environment influences sperm production, but not testes tissue composition, in house mice |
Q39448542 | A comprehensive assessment of geographic variation in heat tolerance and hardening capacity in populations of Drosophila melanogaster from eastern Australia |
Q37960132 | A conceptual model for the origin of worker behaviour and adaptation of eusociality |
Q57266150 | A cost of maternal care in the dung beetle Onthophagus taurus? |
Q91279196 | A costly chemical trait: phenotypic condition dependence of cuticular hydrocarbons in a dung beetle |
Q50526350 | A cryptic heterogametic transition revealed by sex-linked DNA markers in Palearctic green toads. |
Q28248394 | A database of vertebrate longevity records and their relation to other life-history traits |
Q51828962 | A diffusion-based approach to stochastic individual growth and energy budget, with consequences to life-history optimization and population dynamics. |
Q52641779 | A direct experimental test of founder-flush effects on the evolutionary potential for assortative mating. |
Q57933270 | A dispatch from the multivariate frontier |
Q56920110 | A distinction between the origin and maintenance of sex |
Q46313330 | A dynamic framework for the study of optimal birth intervals reveals the importance of sibling competition and mortality risks |
Q51925563 | A fable of four functions. |
Q37106311 | A facultative endosymbiont in aphids can provide diverse ecological benefits. |
Q47839969 | A field reciprocal transplant experiment reveals asymmetric costs of migration between lake and river ecotypes of three-spined sticklebacks (Gasterosteus aculeatus). |
Q51801156 | A field test for host fruit odour discrimination and avoidance behaviour for Rhagoletis pomonella flies in the western United States. |
Q46849379 | A field test of a model for the stability of androdioecy in the freshwater shrimp, Eulimnadia texana |
Q51565715 | A formal theory of the selfish gene. |
Q84580924 | A framework for estimating the fixation time of an advantageous allele in stepping-stone models |
Q53029237 | A framework for power and sensitivity analyses for quantitative genetic studies of natural populations, and case studies in Soay sheep (Ovis aries). |
Q33342780 | A general model for the evolution of mutualisms. |
Q33990324 | A general model of the public goods dilemma. |
Q124847864 | A genetic analysis of some components of reproductive isolation between two closely related species, Spodoptera latifascia (Walker) and S. descoinsi (Lalanne‐Cassou and Silvain) (Lepidoptera: Noctuidae) |
Q45381935 | A genetic background with low mutational robustness is associated with increased adaptability to a novel host in an RNA virus |
Q57361037 | A genetic map of Cottus gobio (Pisces, Teleostei) based on microsatellites can be linked to the physical map of Tetraodon nigroviridis |
Q61659088 | A genetic metapopulation model for reef fishes in oceanic islands: the case of the surgeonfish, Acanthurus triostegus |
Q56986403 | A genic view of species integration |
Q52712348 | A geographic mosaic of trophic interactions and selection: trees, aphids and birds |
Q46406818 | A geographical mosaic of coevolution in a slave-making host-parasite system |
Q33306125 | A geometric morphometric appraisal of beak shape in Darwin's finches. |
Q51174954 | A history of phenotypic plasticity accelerates adaptation to a new environment. |
Q34009480 | A hybrid zone dominated by fertile F1s of two alpine shrub species, Phyllodoce caerulea and Phyllodoce aleutica, along a snowmelt gradient. |
Q51691800 | A hybrid zone with coincident clines for autosomal and sex-specific markers in the Sorex araneus group. |
Q59599281 | A linear dominance hierarchy among clones in chimeras of the social amoeba Dictyostelium discoideum |
Q90200341 | A male's seminal fluid increases later competitors' productivity |
Q51712487 | A measure of sexual selection in hermaphroditic animals: parentage skew and the opportunity for selection. |
Q52659284 | A measure of the within-chromosome synergistic epistasis for Drosophila viability. |
Q57020605 | A melanin-based trait is more strongly related to body size in the tropics than in temperate regions in the globally distributed barn owl family |
Q38246709 | A meta-analysis of the strength and nature of cytoplasmic genetic effects |
Q126098129 | A meta‐analysis on the heritability of vertebrate telomere length |
Q33521086 | A microsatellite linkage map for Drosophila montana shows large variation in recombination rates, and a courtship song trait maps to an area of low recombination. |
Q46174055 | A molecular phylogeny of enteric bacteria and implications for a bacterial species concept |
Q33283076 | A morphospace-based test for competitive exclusion among flying vertebrates: did birds, bats and pterosaurs get in each other's space? |
Q46615460 | A multigenerational effect of parental age on offspring size but not fitness in common duckweed (Lemna minor). |
Q52737631 | A multivariate test of evolutionary constraints for thermal tolerance in Drosophila melanogaster. |
Q51509979 | A multivariate view of the evolution of sexual dimorphism. |
Q60379694 | A narrow hybrid zone between two crayfish species from a Mexican cave |
Q100527481 | A need to consider the evolutionary genetics of host-symbiont mutualisms |
Q34346180 | A new African fossil caprin and a combined molecular and morphological Bayesian phylogenetic analysis of caprini (Mammalia: Bovidae). |
Q47207722 | A new route to the evolution of cooperation |
Q43641696 | A nonsemen copulatory fluid influences the outcome of sperm competition in Japanese quail |
Q100495718 | A novel method for using RNA-seq data to identify imprinted genes in social Hymenoptera with multiply mated queens |
Q60565325 | A novel method of behavioural thermoregulation in butterflies |
Q46577608 | A novel method of comparing mating success and survival reveals similar sexual and viability selection for mobility traits in female tree crickets. |
Q44098373 | A one-locus model of androdioecy with two homomorphic self-incompatibility groups: expected vs. observed male frequencies |
Q40547462 | A phallus for free? Quantitative genetics of sexual trade-offs in the snail Bulinus truncatus |
Q47260844 | A phantom extinction? New insights into extinction dynamics of the Don-hare Lepus tanaiticus |
Q43749555 | A phylogenetic approach to assessing the targets of microbial warfare |
Q45138349 | A phylogenomic approach to reconstructing the diversification of serine proteases in fungi |
Q45877908 | A phylogeny of frugivorous hornbills linked to the evolution of Indian plants within Asian rainforests |
Q40161189 | A possible link between parasite defence and residual reproduction. |
Q44702336 | A potential mechanism for cryptic female choice in a flour beetle |
Q33935325 | A quantitative genetic analysis of hibernation emergence date in a wild population of Columbian ground squirrels |
Q52021335 | A quantitative trait locus for recognition of foreign eggs in the host of a brood parasite. |
Q97566809 | A rapidly evolved shift in life history timing during ecological speciation is driven by the transition between developmental phases |
Q46638672 | A role for ecology in the evolution of colour variation and sexual dimorphism in Hawaiian damselflies |
Q50760362 | A role for habitat area in the geographic mosaic of coevolution between red crossbills and lodgepole pine. |
Q30884706 | A role for the mismatch repair system during incipient speciation in Saccharomyces. |
Q52679382 | A screen for immunity genes evolving under positive selection in Drosophila. |
Q39332102 | A sex-linked SCAR marker in Bryonia dioica (Cucurbitaceae), a dioecious species with XY sex-determination and homomorphic sex chromosomes |
Q57803669 | A shared coevolutionary history does not alter the outcome of coalescence in experimental populations of Pseudomonas fluorescens |
Q37832284 | A simple derivation and classification of common probability distributions based on information symmetry and measurement scale |
Q57912687 | A simulation study on the performance of differentiation-based methods to detect selected loci using linked neutral markers |
Q50462913 | A single mitochondrial haplotype and nuclear genetic differentiation in sympatric colour morphs of a riverine cichlid fish. |
Q36702186 | A tale of two matrices: multivariate approaches in evolutionary biology. |
Q60412731 | A tale of two methods: putting biology before statistics in the study of phenotypic evolution |
Q40210579 | A test for Y-linked additive and epistatic effects on surviving bacterial infections in Drosophila melanogaster. |
Q50480532 | A test of Darwin's 'lop-eared' rabbit hypothesis. |
Q51695702 | A test of fitness consequences of hybridization in sibling species of Lake Victoria cichlid fish. |
Q51968690 | A test of quantitative genetic theory using Drosophila- effects of inbreeding and rate of inbreeding on heritabilities and variance components. |
Q112796097 | A test of the photoprotection hypothesis for the evolution of autumn colours: Chlorophyll resorption, not anthocyanin production, is correlated with nitrogen translocation |
Q51799636 | A time-sequence functional analysis of mating behaviour and genital coupling in Drosophila: role of cryptic female choice and male sex-drive in the evolution of male genitalia. |
Q43466518 | A trade-off between sexual signalling and immune function in a natural population of the drumming wolf spider Hygrolycosa rubrofasciata |
Q63379952 | A wake-up call for studies of natural selection? |
Q46610446 | ADH enzyme activity and Adh gene expression in Drosophila melanogaster lines differentially selected for increased alcohol tolerance |
Q82548730 | Abiotic heterogeneity drives parasite local adaptation in coevolving bacteria and phages |
Q42018867 | Absence of population-level phenotype matching in an obligate pollination mutualism. |
Q52682425 | Abundant, diverse, and consequential P elements segregate in promoters of small heat-shock genes in Drosophila populations. |
Q51900250 | Acclimation of thermal physiology in natural populations of Drosophila melanogaster : a test of an optimality model. |
Q39284096 | Accounting for female space sharing in St. Kilda Soay sheep (Ovis aries) results in little change in heritability estimates. |
Q29039294 | Adaptation and Natural Selection revisited |
Q45350844 | Adaptation and constraint in a stickleback radiation |
Q111591392 | Adaptation and correlated fitness responses over two time scales in Drosophila suzukii populations evolving in different environments |
Q80831781 | Adaptation in a spider mite population after long-term evolution on a single host plant |
Q51147818 | Adaptation in temporally variable environments: Stickleback armor in periodically breaching bar-built estuaries. |
Q42484816 | Adaptation of Saccharomyces cerevisiae to saline stress through laboratory evolution |
Q42000252 | Adaptation of an outbreaking insect defoliator to chronic nutritional stress. |
Q47445804 | Adaptation of experimental yeast populations to stressful conditions in relation to population size |
Q39027446 | Adaptation or exaptation? An experimental test of hypotheses on the origin of salinity tolerance in Bufo calamita. |
Q53507852 | Adaptation to an extraordinary environment by evolution of phenotypic plasticity and genetic assimilation. |
Q91419325 | Adaptation to developmental diet influences the response to selection on age at reproduction in the fruit fly |
Q36201718 | Adaptation to environmental stress: a rare or frequent driver of speciation? |
Q52719983 | Adaptation to marginal habitats by evolution of increased phenotypic plasticity. |
Q62767476 | Adaptation to the laboratory environment in Drosophila subobscura |
Q81439929 | Adaptation to the most abundant host genotype in an agricultural plant-pathogen system--potato late blight |
Q79753851 | Adaptive allocation of stress-induced deformities on bird feathers |
Q47179025 | Adaptive brain size divergence in nine-spined sticklebacks (Pungitius pungitius)? |
Q42474111 | Adaptive contraction of diet breadth affects sexual maturation and specific nutrient consumption in an extreme generalist omnivore. |
Q87636465 | Adaptive cyanogenesis clines evolve recurrently through geographical sorting of existing gene deletions |
Q31095958 | Adaptive divergence in embryonic thermal plasticity among Atlantic salmon populations |
Q43541625 | Adaptive divergence within and between ecotypes of the terrestrial garter snake, Thamnophis elegans, assessed with F(ST)-Q(ST) comparisons |
Q33222656 | Adaptive dynamics and the paradigm of diversity. |
Q51191008 | Adaptive dynamics as a mathematical tool for studying the ecology of speciation processes. |
Q30275762 | Adaptive dynamics of cuticular hydrocarbons in Drosophila |
Q61693826 | Adaptive dynamics, game theory and evolutionary population genetics |
Q81145541 | Adaptive dynamics: the continuity argument |
Q28291417 | Adaptive eukaryote-to-eukaryote lateral gene transfer: stress-related genes of algal origin in the closest unicellular relatives of animals |
Q38327760 | Adaptive evolution in GroEL from distantly related endosymbiotic bacteria of insects. |
Q40279216 | Adaptive evolution of the Bordetella autotransporter pertactin |
Q38878788 | Adaptive landscape and functional diversity of Neotropical cichlids: implications for the ecology and evolution of Cichlinae (Cichlidae; Cichliformes). |
Q43891107 | Adaptive latitudinal cline of photoperiodic diapause induction in the parasitoid Nasonia vitripennis in Europe |
Q57430973 | Adaptive molecular evolution of a defence gene in sexual but not functionally asexual evening primroses |
Q42519256 | Adaptive morphological shifts to novel habitats in marine sculpin fishes |
Q128212095 | Adaptive phenotypic and genomic divergence in the common chaffinch (Fringilla coelebs) following niche expansion within a small oceanic island |
Q44167656 | Adaptive plasticity and genetic divergence in feeding efficiency during parallel adaptive radiation of whitefish (Coregonus spp.). |
Q48695519 | Adaptive radiation in African weakly electric fish (Teleostei: Mormyridae: Campylomormyrus): a combined molecular and morphological approach |
Q36325031 | Adaptive radiation in microbial microcosms |
Q29542536 | Adaptive radiation versus intraspecific differentiation: morphological variation in Caribbean Anolis lizards |
Q33877833 | Adaptive responses for seed and leaf phenology in natural populations of sessile oak along an altitudinal gradient |
Q79321095 | Adaptive seasonal trend in brood sex ratio: test in two sister species with contrasting breeding systems |
Q52641791 | Adaptive sex-specific life history plasticity to temperature and photoperiod in a damselfly. |
Q29306438 | Adaptive significance of environmental sex determination in an amphipod |
Q56836405 | Adaptive significance of environmental sex determination in an amphipod |
Q34007534 | Adaptive speciation and sexual dimorphism contribute to diversity in form and function in the adaptive radiation of Lake Matano's sympatric roundfin sailfin silversides |
Q51830605 | Adaptive speciation when assortative mating is based on female preference for male marker traits. |
Q52682424 | Adaptive switch from infanticide to parental care: how do beetles time their behaviour? |
Q53735341 | Adaptive topography of fluctuating selection in a Mendelian population. |
Q46716987 | Additive genetic variance and developmental plasticity in growth trajectories in a wild cooperative mammal |
Q50939035 | Additive genetic variance in polyandry enables its evolution, but polyandry is unlikely to evolve through sexy or good sperm processes. |
Q100738018 | Adjustment of sex allocation to co-foundress number and kinship under local mate competition: an inclusive-fitness analysis |
Q47297918 | Adjustment of sperm allocation under high risk of sperm competition across taxa: a meta-analysis. |
Q43788574 | Admixture and patterns of linkage disequilibrium in a free-living vertebrate population |
Q38848604 | Adult dietary protein has age- and context-dependent effects on male post-copulatory performance. |
Q34420913 | Adult sex ratio variation: implications for breeding system evolution |
Q39473847 | Advances in finding Alba: the locus affecting life history and color polymorphism in a Colias butterfly. |
Q87859941 | Advancing meta-analysis beyond simple parameter estimation |
Q44534632 | Age and sex affect quantitative genetic parameters for dominance rank and aggression in free-living greylag geese |
Q56094892 | Age-advertisement and the evolution of the peacock's train |
Q84712050 | Age-dependent mutational effects curtail the evolution of senescence by antagonistic pleiotropy |
Q38943534 | Age-dependent trajectories differ between within-pair and extra-pair paternity success. |
Q63975787 | Age-related decline in humoral immune function in Collared Flycatchers |
Q35574777 | Ageing and reproduction: antioxidant supplementation alleviates telomere loss in wild birds. |
Q105728249 | Alerstam, T. 1990. Bird Migration. Cambridge University Press, Cambridge, New York, Melbourne, 420 pp. US $105.00, f55.00. Translated by D. A. Christie from the Swedish Fågelflyttning (Alerstam 1982, Signum) |
Q35061745 | All eggs are made equal: meta-analysis of egg sexual size dimorphism in birds |
Q33724656 | Allen's rule revisited: quantitative genetics of extremity length in the common frog along a latitudinal gradient |
Q48687177 | Allocation of maternal- and ejaculate-derived proteins to reproduction in female crickets, Teleogryllus oceanicus |
Q47980281 | Allochronic differentiation among Daphnia species, hybrids and backcrosses: the importance of sexual reproduction for population dynamics and genetic architecture |
Q57738863 | Allochronic differentiation among Daphnia species, hybrids and backcrosses: the importance of sexual reproduction for population dynamics and genetic architecture |
Q46817830 | Allometry and performance: the evolution of skull form and function in felids |
Q34171792 | Allometry and sexually dimorphic traits in male anurans |
Q37001555 | Allometry of diving capacities: ectothermy vs. endothermy |
Q93141840 | Allopatric and sympatric diversification within roach (Rutilus rutilus) of large pre-alpine lakes |
Q85235880 | Alteration of pathogenicity‐linked life‐history traits by resistance of its host Solanum tuberosum impacts sexual reproduction of the plant pathogenic oomycete Phytophthora infestans |
Q43787787 | Alternative developmental pathways and the propensity to migrate: a case study in the Atlantic salmon |
Q89588159 | Alternative evolutionary outcomes following endosymbiont-mediated selection on male mating preference alleles |
Q46914688 | Alternative intrapopulation life-history strategies and their trade-offs in an African annual fish. |
Q52676927 | Alternative measures of response to Pseudomonas aeruginosa infection in Drosophila melanogaster. |
Q51901123 | Alternative parasite development in transmission strategies: how time flies! |
Q46467040 | Alternative reproductive tactics and reproductive success in male Carollia perspicillata (Seba's short-tailed bat). |
Q52699777 | Alternative reproductive tactics and the propensity of hybridization. |
Q52712350 | Altitudinal and seasonal variation in microsatellite allele frequencies of Drosophila buzzatii. |
Q46700769 | Altitudinal flower size variation correlates with local pollinator size in a bumblebee-pollinated herb, Prunella vulgaris L. (Lamiaceae). |
Q52666602 | Altitudinal patterns for latitudinally varying traits and polymorphic markers in Drosophila melanogaster from eastern Australia. |
Q52659265 | Altitudinal variation for stress resistance traits and thermal adaptation in adult Drosophila buzzatii from the New World. |
Q45995915 | Altitudinal variation in behavioural thermoregulation: local adaptation vs. plasticity in California grasshoppers. |
Q50792092 | Altitudinal variation in egg retention and rates of embryonic development in oviparous Zootoca vivipara fits predictions from the cold-climate model on the evolution of viviparity. |
Q43054858 | Altruistic self-removal of health-compromised honey bee workers from their hive |
Q80118051 | Alveolata histone-like proteins have different evolutionary origins |
Q126109889 | Among-population variation and correlations in sexually dimorphic traits of Silene latifolia |
Q33227986 | Amount of introgression in flycatcher hybrid zones reflects regional differences in pre and post-zygotic barriers to gene exchange |
Q52700768 | Ample genetic variation but no evidence for genotype specificity in an all-parthenogenetic host-parasitoid interaction. |
Q126209345 | An Alloparental Potpourri: The Need for Open Minds and Pluralism A review by M. Bekoff |
Q42942641 | An EST-based genome scan using 454 sequencing in the marine snail Littorina saxatilis |
Q49561451 | An analysis of G matrix variation in two closely related cricket species, Gryllus firmus and G. pennsylvanicus |
Q40509690 | An analysis of genetic differentiation among assortatively mating Drosophila melanogaster in Zimbabwe |
Q50472796 | An analysis of pre- and post-hatching maternal effects mediated by carotenoids in the blue tit. |
Q88492848 | An empirical test for a zone of canalization in thermal reaction norms |
Q113855132 | An empirical test of the `predictability' hypothesis for the evolution of viviparity in reptiles |
Q50576812 | An epidemiological model of host-parasite coevolution and sex. |
Q90776483 | An evaluation of the methods to estimate effective population size from measures of linkage disequilibrium |
Q51722507 | An evolutionary analysis of the relationship between spite and altruism. |
Q33943675 | An evolutionary modelling approach to understanding the factors behind plant invasiveness and community susceptibility to invasion |
Q80960942 | An experimental evaluation of self-interference in Narcissus assoanus: functional and evolutionary implications |
Q91137399 | An experimental evaluation of traits that influence the sexual behaviour of pollinators in sexually deceptive orchids |
Q45229158 | An experimental test for alternative reproductive strategies underlying a female-limited polymorphism. |
Q92836372 | An experimental test for body size-dependent effects of male harassment and an elevated copulation rate on female lifetime fecundity and offspring performance |
Q46744881 | An experimental test of density-dependent selection on temperament traits of activity, boldness and sociability. |
Q57062650 | An experimental test of the causes of small-scale phenotypic differentiation in a population of great tits |
Q51316455 | An experimental test of the role of predators in the maintenance of a genetically based polymorphism. |
Q87199148 | An experimental test of whether cheating is context dependent |
Q51662822 | An explicit test for the contribution of environmental maternal effects to rapid clinal differentiation in an invasive plant. |
Q81487188 | An inclusive fitness analysis of altruism on a cyclical network |
Q42037848 | An indirect approach to imply trade-off shapes: population level patterns in resistance suggest a decreasingly costly resistance mechanism in a model insect system |
Q87118945 | An interspecific comparison between morphology and swimming performance in cyprinids |
Q57164701 | An inversion supergene in Drosophila underpins latitudinal clines in survival traits |
Q43076586 | An offer you cannot refuse: down-regulation of immunity in response to a pathogen's retaliation threat |
Q44951222 | An unexpected influence of widely used significance thresholds on the distribution of reported P-values |
Q52728243 | An unusual barrier to gene flow: perpetually immature larvae from inter-population crosses in the flour beetle, Tribolium castaneum. |
Q31161520 | Analysing small insect glands with UV-LDI MS: high-resolution spatial analysis reveals the chemical composition and use of the osmeterium secretion in Themira superba (Sepsidae: Diptera). |
Q61968856 | Analysis of asymmetries in the African fruit bats Eidolon helvum and Rousettus egyptiacus (Mammalia: Megachiroptera) from the islands of the Gulf of Guinea. I. Variance and size components of bilateral variation |
Q61968857 | Analysis of asymmetries in the African fruit bats Eidolon helvum and Rousettus egyptiacus (Mammalia: Megachiroptera) from the islands of the Gulf of Guinea. II. Integration and levels of multivariate fluctuating asymmetry across a geographical range |
Q46260133 | Analysis of microsatellite variation in Pinus radiata reveals effects of genetic drift but no recent bottlenecks. |
Q51692109 | Analysis of range expansion in two species undergoing character displacement: why might invaders generally 'win' during character displacement? |
Q125390595 | Analysis of reticulate relationships within the Daphnia longispina species complex. Allozyme phenotype and morphology |
Q48970683 | Analysis of the effects of early nutritional environment on inbreeding depression in Drosophila melanogaster |
Q44796159 | Analysis of the importance of genotypic variation, metabolic rate, morphology, sex and development time on immune function in the cricket, Gryllus firmus |
Q33574080 | Ancestral polymorphism in exon 2 of bluethroat (Luscinia svecica) MHC class II B genes. |
Q39968077 | Ancestral state reconstruction analysis of hymenopteran sex determination mechanisms |
Q51149668 | Animal behaviour and algal camouflage jointly structure predation and selection. |
Q112796098 | Animal chromosome counts reveal a similar range of chromosome numbers but with less polyploidy in animals compared to flowering plants |
Q47334315 | Ant aggression and evolutionary stability in plant-ant and plant-pollinator mutualistic interactions |
Q54394001 | Antagonistic coevolution across productivity gradients: an experimental test of the effects of dispersal. |
Q99568252 | Antagonistic interactions subdue inter-species green-beard cooperation in bacteria |
Q46286020 | Antagonistic pleiotropy can maintain fitness variation in annual plants |
Q47269467 | Antagonistic selection between adult thorax and wing size in field released Drosophila melanogaster independent of thermal conditions. |
Q96158921 | Antagonistic species interaction drives selection for sex in a predator-prey system |
Q28186311 | Anthropogenic disturbance promotes hybridization between Banksia species by altering their biology |
Q52697944 | Aphid genotypes vary in their response to the presence of fungal endosymbionts in host plants. |
Q40384572 | Aphid specialization on different summer hosts is associated with strong genetic differentiation and unequal symbiont communities despite a common mating habitat |
Q80516102 | Apparent mutational hotspots and long distance linkage disequilibrium resulting from a bottleneck |
Q52696319 | Applying the genetic theories of ageing to the cytoplasm: cytoplasmic genetic covariation for fitness and lifespan. |
Q44634819 | Approximate Bayesian computation reveals the factors that influence genetic diversity and population structure of foxsnakes |
Q30837044 | Arcyptera fusca and Arcyptera tornosi repetitive DNA families: whole-comparative genomic hybridization (W-CGH) as a novel approach to the study of satellite DNA libraries |
Q39167976 | Are ant supercolonies crucibles of a new major transition in evolution? |
Q38529248 | Are aposematic signals honest? A review |
Q38976375 | Are hybrid species more fit than ancestral parent species in the current hybrid species habitats? |
Q60462432 | Are hybridogenetic complexes structured by habitat in water frogs? |
Q90823532 | Are offspring begging levels exaggerated beyond the parental optimum? Evidence from a bidirectional selection experiment |
Q51648367 | Are parental care trade-offs in shorebirds driven by parental investment or sexual selection? |
Q35011652 | Are plant pathogen populations adapted for encounter with their host? A case study of phenological synchrony between oak and an obligate fungal parasite along an altitudinal gradient |
Q53091486 | Are reptile and amphibian species younger in the Northern Hemisphere than in the Southern Hemisphere? |
Q110792385 | Are reward polymorphisms subject to frequency- and density-dependent selection? Evidence from a monoecious species pollinated by deceit |
Q36197546 | Are species differences in maternal effects arising from maternal care adaptive? |
Q40080690 | Are there interactive effects of mate availability and predation risk on life history and defence in a simultaneous hermaphrodite? |
Q43510474 | Are you my mother? Kin recognition in the ant Formica fusca |
Q91065378 | Artificial selection for increased dispersal results in lower fitness |
Q44598956 | Artificial selection on allometry: change in elevation but not slope. |
Q39176959 | Artificial selection on ant female caste ratio uncovers a link between female-biased sex ratios and infection by Wolbachia endosymbionts. |
Q45771869 | Artificial selection on larval growth curves in Tribolium: correlated responses and constraints |
Q34987650 | Assessing concurrent patterns of environmental niche and morphological evolution among species of horned lizards (Phrynosoma). |
Q36135014 | Assessing reproductive isolation using a contact zone between parapatric lake-stream stickleback ecotypes |
Q41161558 | Assessing the alignment of sexual and natural selection using radiomutagenized seed beetles |
Q46122780 | Assessing the extent of genome-wide intralocus sexual conflict via experimentally enforced gender-limited selection |
Q57203660 | Assessing the nucleotide diversity of three aphid species by RAPD |
Q92150575 | Assessing the potential for post-ejaculatory female choice in a polyandrous beach-spawning fish |
Q91845800 | Assessing the repeatability, robustness to disturbance, and parent-offspring colony resemblance of collective behavior |
Q46102195 | Assessing the speed and predictability of local adaptation in invasive California poppies (Eschscholzia californica). |
Q90557349 | Associated evolution of fruit size, fruit color and spines in Neotropical palms |
Q45006663 | Association between host's genetic diversity and parasite burden in damselflies |
Q48186236 | Association between inbreeding depression and floral traits in a generalist-pollinated plant |
Q33980519 | Association of Mc1r variants with ecologically relevant phenotypes in the European ocellated lizard, Lacerta lepida. |
Q54740456 | Association with host mitochondrial haplotypes suggests that feminizing microsporidia lack horizontal transmission. |
Q46250158 | Associations of Stream Geomorphic Conditions and Prevalence of Alternative Reproductive Tactics Among Sockeye Salmon Populations |
Q58042367 | Assortative mating across a hybrid zone in Chorthippus parallelus (Orthoptera: Acrididae) |
Q58042320 | Assortative mating and the genic view of speciation |
Q45228769 | Assortative mating based on cooperativeness and generosity |
Q40188373 | Assortative mating but no evidence of genetic divergence in a species characterized by a trophic polymorphism |
Q114080039 | Assortative mating for between‐patch dispersal status in a wild bird population: Exploring the role of direct and indirect underlying mechanisms |
Q52734029 | Assortative mating for relatedness in a large naturally occurring population of Drosophila melanogaster. |
Q34539144 | Assortative preferences and discrimination by females against hybrid male song in the grasshoppers Chorthippus brunneus and Chorthippus jacobsi (Orthoptera: Acrididae). |
Q51577671 | Asymmetric and differential gene introgression at a contact zone between two highly divergent lineages of field voles (Microtus agrestis). |
Q85305687 | Asymmetric conspecific sperm precedence in relation to spawning times in the Montastraea annularis species complex (Cnidaria: Scleractinia) |
Q43818439 | Asymmetric gene flow and constraints on adaptation caused by sex ratio distorters |
Q45974738 | Asymmetrical reproductive character displacement in the house mouse. |
Q45074475 | Asymmetry in thermal tolerance trade-offs between the B and Q sibling species of Bemisia tabaci (Hemiptera: Aleyrodidae). |
Q36667594 | Asymmetry within social groups: division of labour and intergroup competition |
Q38417250 | Asynchronous hatching in the burying beetle, Nicrophorus quadripunctatus, maxmizes parental fitness |
Q40275778 | Asynchronous hatching provides females with a means for increasing male care but incurs a cost by reducing offspring fitness |
Q90694719 | Attractive male sticklebacks carry more oxidative DNA damage in the soma and germline |
Q34315058 | Atypical panmixia in a European dolphin species (Delphinus delphis): implications for the evolution of diversity across oceanic boundaries |
Q114898692 | Auditory changes in noctuid moths endemic to a bat-free habitat |
Q28267196 | Automixis in Artemia: solving a century-old controversy |
Q92992557 | Autosomal suppression and fitness costs of an old driving X chromosome in Drosophila testacea |
Q34087479 | Avian colour perception predicts behavioural responses to experimental brood parasitism in chaffinches. |
Q50795758 | Avian growth and development rates and age-specific mortality: the roles of nest predation and adult mortality. |
Q110615194 | Axes of multivariate sexual signal divergence among incipient species: Concordance with selection, genetic variation and phenotypic plasticity |
Q35872241 | Axial allometry in a neutrally buoyant environment: effects of the terrestrial-aquatic transition on vertebral scaling |
Q52676936 | Back to one: consequences of derived monogyny in an ant with polygynous ancestors. |
Q46798436 | Background matching ability and the maintenance of a colour polymorphism in the red devil cichlid |
Q42277233 | Bacterial motility confers fitness advantage in the presence of phages. |
Q51245452 | Bacteriocins and the assembly of natural Pseudomonas fluorescens populations. |
Q80117962 | Balancing synthesis with pluralism in sociobiology |
Q37760563 | Bargaining in biology? |
Q60311507 | Barn swallow chicks beg more loudly when broodmates are unrelated |
Q46324328 | Barnacles, barrier loci and the systematic building of species |
Q46324324 | Barrier loci and progress towards evolutionary generalities |
Q33928057 | Basal cold but not heat tolerance constrains plasticity among Drosophila species (Diptera: Drosophilidae). |
Q84747350 | Basal metabolic rate and risk-taking behaviour in birds |
Q80831705 | Basal metabolic rate: heritability and genetic correlations with morphological traits in the zebra finch |
Q51467634 | Bateman's principle and immunity in a sex-role reversed pipefish. |
Q46757169 | Batesian mimics influence the evolution of conspicuousness in an aposematic salamander. |
Q37121897 | Bayesian approaches in evolutionary quantitative genetics |
Q99210936 | Becoming creatures of habit: among- and within-individual variation in nesting behavior shifts with age |
Q41343385 | Bees explain floral variation in a recent radiation of Linaria. |
Q83454805 | Begging at high level simultaneously impairs growth and immune response in southern shrike (Lanius meridionalis) nestlings |
Q52707295 | Behavioural and biomaterial coevolution in spider orb webs. |
Q46014220 | Behavioural differences between individuals and two populations of stickleback (Gasterosteus aculeatus). |
Q52649747 | Behavioural interactions, kin and disease susceptibility in the bumblebee Bombus terrestris. |
Q46953728 | Behavioural isolation may facilitate homoploid hybrid speciation in cichlid fish. |
Q63649344 | Behavioural mechanisms of sexual isolation involving multiple modalities and their inheritance |
Q31044195 | Behavioural response to combined insecticide and temperature stress in natural populations of Drosophila melanogaster |
Q108898650 | Behavioural response to songs between genetically diverged allopatric populations of Darwin's small tree finch in the Galápagos |
Q51180844 | Behavioural, ecological and genetic evidence confirm the occurrence of host-associated differentiation in goldenrod gall-midges. |
Q47426166 | Bergmann's Rule rules body size in an ectotherm: heat conservation in a lizard along a 2200-metre elevational gradient. |
Q125723634 | Berthold, P. 1993. Bird Migration: A General Survey. Oxford University Press. ISBN: 0‐19‐854692‐0 (H.b.) 0‐19‐854691‐2 (P.b.) |
Q125935046 | Bet-hedging via dispersal aids the evolution of plastic responses to unreliable cues |
Q52773621 | Between-sex genetic covariance constrains the evolution of sexual dimorphism in Drosophila melanogaster. |
Q53895197 | Between-year variation of MHC allele frequencies in great reed warblers: selection or drift? |
Q46566398 | Beyond animals and plants: dynamic maternal effects in the fungus Neurospora crassa. |
Q51540132 | Beyond hybridization: diversity of interactions with heterospecifics, direct fitness consequences and the effects on mate preferences. |
Q119627641 | Beyond morphs: Inter-individual colour variation despite strong genetic determinism of colour morphs in a wild bird |
Q46609309 | Beyond the wing planform: morphological differentiation between migratory and nonmigratory dragonfly species |
Q48195764 | Beyond topology: coevolution of structure and flux in metabolic networks |
Q90586046 | Biased predation could promote convergence yet maintain diversity within Müllerian mimicry rings of Oreina leaf beetles |
Q34803632 | Biased sex-ratio and sex-biased heterozygote disadvantage affect the maintenance of a genetic polymorphism and the properties of hybrid zones. |
Q35663823 | Big cat, small cat: reconstructing body size evolution in living and extinct Felidae. |
Q46257111 | Bigger testes increase paternity in a simultaneous hermaphrodite, independently of the sperm competition level. |
Q46770736 | Bird predation selects for wing shape and coloration in a damselfly. |
Q51615976 | Birth-death symmetry in the evolution of a social trait |
Q45190470 | Blending of heritable recognition cues among ant nestmates creates distinct colony gestalt odours but prevents within-colony nepotism. |
Q41932711 | Blood parasites mediate morph-specific maintenance costs in a colour polymorphic wild bird. |
Q49821901 | Bloody-minded parasites and sex: the effects of fluctuating virulence. |
Q60232248 | Body shape evolution among ploidy levels of theSqualius alburnoideshybrid complex (Teleostei, Cyprinidae) |
Q33283075 | Body shape vs. colour associated initial divergence in the Telmatherina radiation in Lake Matano, Sulawesi, Indonesia |
Q98472825 | Body size and climate as predictors of plumage colouration and sexual dichromatism in parrots |
Q41393760 | Body size and sexual size dimorphism in primates: influence of climate and net primary productivity |
Q90255049 | Body size and sperm quality in queen- And worker-produced ant males |
Q47174822 | Body size as a primary determinant of ecomorphological diversification and the evolution of mimicry in the lampropeltinine snakes (Serpentes: Colubridae). |
Q57006967 | Body size does not predict species richness among the metazoan phyla |
Q34735859 | Body size evolution in Mesozoic birds |
Q33358905 | Body size evolution in Mesozoic birds: little evidence for Cope's rule |
Q47273390 | Body size evolution in South American Liolaemus lizards of the boulengeri clade: a contrasting reassessment. |
Q46851135 | Body size evolution in Titanosauriformes (Sauropoda, Macronaria). |
Q36103460 | Body size evolution of a shell-brooding cichlid fish from Lake Tanganyika. |
Q33439205 | Bone microstructures and mode of skeletogenesis in osteoderms of three pareiasaur taxa from the Permian of South Africa |
Q39269583 | Bower-building behaviour is associated with increased sperm longevity in Tanganyikan cichlids. |
Q51599667 | Brain plasticity over the metamorphic boundary: carry-over effect of larval environment on froglet brain development. |
Q90694751 | Brain size affects responsiveness in mating behaviour to variation in predation pressure and sex ratio |
Q47390380 | Brain size and the expression of pheomelanin-based colour in birds |
Q39282858 | Brain size evolution in pipefishes and seahorses: the role of feeding ecology, life history and sexual selection. |
Q93363083 | Brain size predicts behavioural plasticity in guppies (Poecilia reticulata): An experiment |
Q47431292 | Brain size, head size and behaviour of a passerine bird |
Q104257741 | Breeding behavior predicts patterns of natural hybridization in North American minnows (Cyprinidae) |
Q38368025 | Breeding biology and the evolution of dynamic sexual dichromatism in frogs. |
Q51158639 | Brood sex ratio variation in a cooperatively breeding bird. |
Q51641702 | Budding dispersal and the sex ratio. |
Q35309256 | Bursts of transposable elements as an evolutionary driving force |
Q34309347 | By-product information can stabilize the reliability of communication |
Q126023652 | Byrne, Richard. 1995. The Thinking Ape: Evolutionary Origins of Intelligence. Oxford University Press. Price: £30.00 (H.b.) or £13.50 (P.b.). 264 pp. ISBN: 0‐19‐852188‐X (H.b.) or 0‐19‐852265‐7 (P.b.). |
Q56932954 | Calcium and salinity as selective factors in plate morph evolution of the three-spined stickleback (Gasterosteus aculeatus ) |
Q31143179 | Call divergence is correlated with geographic and genetic distance in greenish warblers (Phylloscopus trochiloides): a strong role for stochasticity in signal evolution? |
Q34286838 | Camouflage through an active choice of a resting spot and body orientation in moths |
Q84174622 | Can AFLP genome scans detect small islands of differentiation? The case of shell sculpture variation in the periwinkle Echinolittorina hawaiiensis |
Q47559543 | Can Ebola Virus evolve to be less virulent in humans? |
Q39174873 | Can alternative mating tactics facilitate introgression across a hybrid zone by circumventing female choice? |
Q45044652 | Can cytoplasmic incompatibility inducing Wolbachia promote the evolution of mate preferences? |
Q51358334 | Can evolution of sexual dimorphism be triggered by developmental temperatures? |
Q45886374 | Can maternally transmitted endosymbionts facilitate the evolution of haplodiploidy? |
Q34245414 | Can mechanism help explain insect host choice? |
Q51706665 | Can natural phenotypic variances be estimated reliably under homogeneous laboratory conditions? |
Q45836947 | Can natural selection favour altruism between species? |
Q35549473 | Can paternal leakage maintain sexually antagonistic polymorphism in the cytoplasm? |
Q83978168 | Can phosphorus limitation contribute to the maintenance of sex? A test of a key assumption |
Q51766216 | Can sexual selection drive female life histories? A comparative study on Galliform birds. |
Q39178193 | Can we continue to neglect genomic variation in introgression rates when inferring the history of speciation? A case study in a Mytilus hybrid zone. |
Q36442491 | Cannabinoid receptors in invertebrates. |
Q34630663 | Cannibalism as an interacting phenotype: precannibalistic aggression is influenced by social partners in the endangered Socorro Isopod (Thermosphaeroma thermophilum). |
Q60463494 | Cannibalizing Harmonia axyridis (Coleoptera: Coccinellidae) larvae use endogenous cues to avoid eating relatives |
Q22065681 | Capturing the superorganism: a formal theory of group adaptation |
Q51715446 | Carotenoid and protein supplementation have differential effects on pheasant ornamentation and immunity. |
Q46809569 | Carotenoid-based bill coloration functions as a social, not sexual, signal in songbirds (Aves: Passeriformes). |
Q60228118 | Carotenoid-based bill colour as an indicator of immunocompetence and sperm performance in male mallards |
Q31094014 | Carry-over effects of conditions at the wintering grounds on breeding plumage signals in a migratory bird: roles of phenotypic plasticity and selection |
Q35815748 | Cascading costs of reproduction in female house wrens induced to lay larger clutches |
Q52641728 | Caste fate conflict in swarm-founding social hymenoptera: an inclusive fitness analysis. |
Q46144274 | Caste ratios affect the reproductive output of social trematode colonies |
Q38460713 | Caste-biases in gene expression are specific to developmental stage in the ant Formica exsecta |
Q47553024 | Casual movement speed but not maximal locomotor capacity predicts mate searching success |
Q30422999 | Causes of male sexual trait divergence in introduced populations of guppies |
Q33479276 | Cell-mediated immunity and multi-locus heterozygosity in bluethroat nestlings. |
Q50483749 | Cell-mediated immunity predicts the probability of local recruitment in nestling blue tits. |
Q88887675 | Change in male coloration associated with artificial selection on foraging colour preference |
Q96828045 | Change in sexual signaling traits outruns morphological divergence across an ecological gradient in the postglacial radiation of the songbird genus Junco |
Q50709389 | Changed environmental conditions weaken sexual selection in sticklebacks. |
Q33928052 | Changes in behavioural trait integration following rapid ecotype divergence in an aquatic isopod. |
Q52029057 | Changes in genetic architecture during relaxation in Drosophila melanogaster selected on divergent virgin life span. |
Q52733337 | Changes in reciprocal herkogamy during the tristyly-distyly transition in Oxalis alpina increase efficiency in pollen transfer. |
Q51629254 | Changes in the selection differential exerted on a marine snail during the ontogeny of a predatory shore crab. |
Q47671005 | Changes in thermotolerance and Hsp70 expression with domestication in Drosophila melanogaster |
Q46566372 | Changing the habitat: the evolution of intercorrelated traits to escape from predators |
Q33274246 | Character displacement: in situ evolution of novel phenotypes or sorting of pre-existing variation? |
Q46747776 | Characterization and evolutionary analysis of tributyltin-binding protein and pufferfish saxitoxin and tetrodotoxin-binding protein genes in toxic and nontoxic pufferfishes |
Q51589855 | Characterization of a divergent chromosome region in the willow warbler Phylloscopus trochilus using avian genomic resources. |
Q46292129 | Characterizing selection in black-throated blue warblers using a sexual network approach. |
Q45917541 | Cheating is not always punished: killer female plants and pollination by deceit in the dwarf palm Chamaerops humilis. |
Q40235302 | Chemical communication of queen supergene status in an ant. |
Q22121953 | Chloroplast DNA indicates a single origin of the allotetraploid Arabidopsis suecica |
Q60557670 | Chloroplast DNA variation within and among five Plantago species |
Q45968209 | Chromosomal basis of viability differences in Tigriopus californicus interpopulation hybrids. |
Q51694074 | Chromosomal rearrangements and genetic structure at different evolutionary levels of the Sorex araneus group. |
Q43195660 | Chronic malaria infections increase family inequalities and reduce parental fitness: experimental evidence from a wild bird population |
Q47341621 | Chronic malnutrition favours smaller critical size for metamorphosis initiation in Drosophila melanogaster |
Q44568567 | Circannual variation in blood parasitism in a sub-Saharan migrant passerine bird, the garden warbler. |
Q52740795 | Cis- and trans-acting genetic factors contribute to heterogeneity in the rate of crossing over between the Drosophila simulans clade species. |
Q47412373 | Classic predictions about sex change do not hold under all types of size advantage |
Q92725052 | Climate change, sex reversal and lability of sex-determining systems |
Q89995204 | Climate-associated genetic variation in Fagus sylvatica and potential responses to climate change in the French Alps |
Q36069257 | Climate-mediated adaptation after mainland colonization of an ancestrally subtropical island lizard, Anolis carolinensis |
Q46335034 | Climate-related environmental variation in a visual signalling device: the male and female dewlap in Anolis sagrei lizards. |
Q58616956 | Climatic niche evolution in turtles is characterized by phylogenetic conservatism for both aquatic and terrestrial species |
Q60369901 | Climatic niche evolution in turtles is characterized by phylogenetic conservatism for both aquatic and terrestrial species |
Q47394322 | Clinal variation and laboratory adaptation in the rainforest species Drosophila birchii for stress resistance, wing size, wing shape and development time |
Q30655890 | Clinal variation in a brown lemur (Eulemur spp.) hybrid zone: combining morphological, genetic and climatic data to examine stability. |
Q39380069 | Clinal variation in post-winter male fertility retention; an adaptive overwintering strategy in Drosophila melanogaster |
Q45438359 | Clonal diversity driven by parasitism in a freshwater snail |
Q56983889 | Clonal diversity in high arctic ostracodes |
Q51634642 | Clonal erosion and genetic drift in cyclical parthenogens--the interplay between neutral and selective processes. |
Q57027237 | Clonal integration in Ranunculus reptans: by-product or adaptation? |
Q92522334 | Close-kin mating, but not inbred parents, reduces hatching rates and offspring quality in a threatened tortoise |
Q43614622 | Closing of the Tethys Sea and the phylogeny of Eurasian killifishes (Cyprinodontiformes: Cyprinodontidae). |
Q90047866 | Co-evolution of cerebral and cerebellar expansion in cetaceans |
Q34387958 | Co-evolution of male and female reproductive characters across the Scathophagidae (Diptera). |
Q51646408 | Co-evolution of plumage characteristics and winter sociality in New and Old World sparrows. |
Q45950566 | Co-evolutionary dynamics between public good producers and cheats in the bacterium Pseudomonas aeruginosa. |
Q29038718 | Co-evolutionary patterns and diversification of ant-fungus associations in the asexual fungus-farming ant Mycocepurus smithii in Panama |
Q93171320 | Co-foundress confinement elicits kinship effects in a naturally sub-social parasitoid |
Q91274739 | Co-inheritance of sea age at maturity and iteroparity in the Atlantic salmon vgll3 genomic region |
Q45273552 | Co-variation between the intensity of behavioural manipulation and parasite development time in an acanthocephalan-amphipod system. |
Q50656595 | Coevolution and the adaptive value of autumn tree colours: colour preference and growth rates of a southern beech aphid. |
Q51667285 | Coevolution between crossbills and black pine: the importance of competitors, forest area and resource stability. |
Q39031793 | Coevolution between flight morphology, vertical stratification and sexual dimorphism: what can we learn from tropical butterflies? |
Q79325919 | Coevolution between hosts and parasites with partially overlapping geographic ranges |
Q51811602 | Coevolution of male and female reproductive traits in a simultaneously hermaphroditic land snail. |
Q60367515 | Coevolution of virulence and immunosuppression in multiple infections |
Q52654821 | Coevolutionary arms races: increased host immune defense promotes specialization by avian fleas. |
Q42654468 | Coevolutionary relationship between helminth diversity and MHC class II polymorphism in rodents |
Q34461636 | Coexistence and origin of trophic ecotypes of pygmy whitefish, Prosopium coulterii, in a south-western Alaskan lake |
Q41651959 | Coinfection and the evolution of drug resistance |
Q62085694 | Collective action in an RNA virus |
Q92973606 | Collective aggressiveness limits colony persistence in high- but not low-elevation sites at Amazonian social spiders |
Q36066327 | Colonization and demographic expansion of freshwater fauna across the Hawaiian archipelago. |
Q51559939 | Colonizing the world in spite of reduced MHC variation. |
Q60325800 | Colony size, social complexity and reproductive conflict in social insects |
Q59118128 | Colony-level sex ratio selection in the eusocial Hymenoptera |
Q83981172 | Coloration signals the ability to cope with elevated stress hormones: effects of corticosterone on growth of barn owls are associated with melanism |
Q33247046 | Colour forms of Amazonian cichlid fish represent reproductively isolated species. |
Q57892745 | Colour pattern component phenotypic divergence can be predicted by the light environment |
Q41996916 | Colour pattern homology and evolution in Vanessa butterflies (Nymphalidae: Nymphalini): eyespot characters |
Q114589440 | Colour pattern variation forms local background matching camouflage in a leaf‐mimicking toad |
Q53852206 | Colour polymorphism in birds: causes and functions. |
Q51715454 | Colour variation and alternative reproductive strategies in females of the common lizard Lacerta vivipara. |
Q101632496 | Colour variation in female common lizards: why we should speak of morphs, a reply to Coteet al. |
Q51609321 | Colour, design and reward: phenotypic integration of fleshy fruit displays. |
Q43906971 | Colour-variable birds have broader ranges, wider niches and are less likely to be threatened |
Q51790801 | Colourful male guppies produce faster and more viable sperm. |
Q34136790 | Colourful stripes send mixed messages to safe and risky partners in a diffuse cleaning mutualism |
Q100723768 | Combined effects of rearing and testing temperatures on sperm traits |
Q28306134 | Combined influence of maternal and paternal quality on sex allocation in red-capped robins |
Q33665249 | Combining capture-recapture data and pedigree information to assess heritability of demographic parameters in the wild |
Q46911480 | Combining experimental evolution and field population assays to study the evolution of host range breadth |
Q30665739 | Combining fossil and molecular data to date the diversification of New World Primates |
Q57587021 | Combining mitochondrial DNA sequences and morphological data to infer species boundaries: phylogeography of lanceheaded pitvipers in the Brazilian Atlantic forest, and the status of Bothrops pradoi (Squamata: Serpentes: Viperidae) |
Q58034970 | Combining probability from independent tests: the weighted Z-method is superior to Fisher's approach |
Q48275494 | Come on feel the noise - from metaphors to null models |
Q24619323 | Coming to America: multiple origins of New World geckos |
Q60305184 | Comments on "Epigenetic inheritance in evolution" |
Q44957411 | Common garden experiment reveals pathogen isolate but no host genetic diversity effect on the dynamics of an emerging wildlife disease. |
Q59693187 | Common sex-linked deleterious alleles in a plant parasitic fungus alter infection success but show no pleiotropic advantage |
Q102385385 | Community lifespan, niche expansion and the evolution of interspecific cooperation |
Q80231874 | Compact genes are highly expressed in the moss Physcomitrella patens |
Q30085649 | Comparative analysis of encephalization in mammals reveals relaxed constraints on anthropoid primate and cetacean brain scaling |
Q46947042 | Comparative analysis reveals that polyploidy does not decelerate diversification in fish. |
Q28254874 | Comparative anatomy and phylogenetic distribution of the mammalian cecal appendix |
Q57212290 | Comparative evaluation of maximum parsimony and Bayesian phylogenetic reconstruction using empirical morphological data |
Q60198482 | Comparative evaluation of maximum parsimony and Bayesian phylogenetic reconstruction using empirical morphological data |
Q38275095 | Comparative genomic study of arachnid immune systems indicates loss of beta-1,3-glucanase-related proteins and the immune deficiency pathway. |
Q46322777 | Comparative rates of lower jaw diversification in cichlid adaptive radiations. |
Q37008984 | Comparative studies of quantitative trait and neutral marker divergence: a meta-analysis. |
Q29040834 | Comparative study in stingless bees (Meliponini) demonstrates that nest entrance size predicts traffic and defensivity |
Q126201219 | Comparative transcriptome analysis at the onset of speciation in a mimetic butterfly—The Ithomiini Melinaea marsaeus |
Q29027336 | Comparing artificial and natural selection in rate of adaptation to genetic stress in Aspergillus nidulans |
Q46845755 | Comparing measures of breeding inequality and opportunity for selection with sexual selection on a quantitative character in bighorn rams. |
Q57614954 | Comparing molecular measures for detecting inbreeding depression |
Q47410602 | Comparing phylogenetic signal in intraspecific and interspecific body size datasets |
Q57912694 | Comparing three different methods to detect selective loci using dominant markers |
Q57237103 | Comparison of genetic differentiation at marker loci and quantitative traits |
Q52976390 | Competing dwarf males: sexual selection in an orb-weaving spider. |
Q37611546 | Competition between relatives and the evolution of dispersal in a parasitoid wasp. |
Q44818560 | Competition, breeding success and ageing rates in female meerkats |
Q46569391 | Competitive environments induce shifts in host fidelity |
Q51700448 | Competitive speciation and costs of choosiness. |
Q52675730 | Complementary sex determination in the parasitoid wasp Cotesia vestalis (C. plutellae). |
Q51652954 | Complete lack of mitochondrial divergence between two species of NE Atlantic marine intertidal gastropods. |
Q45970745 | Complex evolution of orthologous and paralogous decarboxylase genes. |
Q43933774 | Complex genetic architecture of population differences in adult lifespan of a beetle: nonadditive inheritance, gender differences, body size and a large maternal effect |
Q51906455 | Complex genotype interactions influence social fitness during the developmental phase of the social amoeba Dictyostelium discoideum. |
Q40344092 | Complex mitonuclear interactions and metabolic costs of mating in male seed beetles |
Q52740227 | Complex patterns of local adaptation in heat tolerance in Drosophila simulans from eastern Australia. |
Q38878161 | Complex phenotype-environment associations revealed in an East African cyprinid |
Q33370376 | Complex population history of two Anopheles dirus mosquito species in Southeast Asia suggests the influence of Pleistocene climate change rather than human-mediated effects |
Q43519765 | Complex selection associated with Hox genes in a natural population of lizards |
Q52085992 | Complexity and integration in sexual ornamentation: an example with carotenoid and melanin plumage pigmentation. |
Q67195638 | Complexity for complexity's sake? |
Q113791767 | Composition of a chemical signalling trait varies with phylogeny and precipitation across an Australian lizard radiation |
Q101041576 | Compost spatial heterogeneity promotes evolutionary diversification of a Bacterium |
Q50948543 | Concurrent coevolution of intra-organismal cheaters and resisters. |
Q51104996 | Condition dependence and the maintenance of genetic variance in a sexually dimorphic black scavenger fly. |
Q34946146 | Condition dependence of developmental stability in the sexually dimorphic fly Telostylinus angusticollis (Diptera: Neriidae). |
Q51108690 | Condition dependence of female choosiness in a field cricket. |
Q40832732 | Condition dependence of male and female genital structures in the seed beetle Callosobruchus maculatus (Coleoptera: Bruchidae). |
Q51683524 | Condition dependence of sexually dimorphic colouration and longevity in the ambush bug Phymata americana. |
Q52698164 | Condition dependence varies with mating success in male Drosophila bunnanda. |
Q93234216 | Condition dependent mortality exacerbates male (but not female) reproductive senescence and the potential for sexual conflict |
Q50690631 | Condition-dependent expression of red colour differs between stickleback species. |
Q50457862 | Condition-dependent genetic benefits of extrapair fertilization in female blue tits Cyanistes caeruleus. |
Q83331058 | Condition-dependent mutation rates and sexual selection |
Q42044143 | Condition-dependent traits and the capture of genetic variance in male advertisement song |
Q30314475 | Conditions for the invasion of male-haploidy in diploid populations |
Q44687671 | Conditions when hybridization might predispose populations for adaptive radiation |
Q56688720 | Confidence of paternity and paternal care: covariation revealed through the experimental manipulation of the mating system in the beetle Onthophagus taurus |
Q52697532 | Conflicting selection on diaspore traits limits the evolutionary potential of seed dispersal by ants. |
Q45239254 | Conflicting selection on the timing of germination in a natural population of Arabidopsis thaliana |
Q47435858 | Conflicting selection pressures on seed size: evolutionary ecology of fruit size in a bird-dispersed tree, Olea europaea |
Q51650797 | Connecting behaviour and performance: the evolution of biting behaviour and bite performance in bats. |
Q38976937 | Connecting proximate mechanisms and evolutionary patterns: pituitary gland size and mammalian life history. |
Q52782601 | Connecting thermal performance curve variation to the genotype: a multivariate QTL approach. |
Q45269368 | Consequence of herbivory for the fitness cost of herbicide resistance: photosynthetic variation in the context of plant-herbivore interactions |
Q60540284 | Consequences of |
Q51897448 | Consequences of genetic erosion on fitness and phenotypic plasticity in European tree frog populations (Hyla arborea). |
Q52092616 | Consequences of inter-population crosses on developmental stability and canalization of floral traits in Dalechampia scandens (Euphorbiaceae). |
Q50587511 | Consequences of mating and predation risk for longevity in a freshwater snail: abstinence makes the heart beat longer. |
Q104466169 | Consequences of population structure for sex allocation and sexual conflict |
Q35557692 | Conservation of multivariate female preference functions and preference mechanisms in three species of trilling field crickets |
Q97540096 | Conserved ZZ/ZW sex chromosomes in Caribbean croaking geckos (Aristelliger: Sphaerodactylidae) |
Q47561445 | Conserved roles of Osiris genes in insect development, polymorphism and protection |
Q57269605 | Consistent individual differences in cooperative behaviour in meerkats (Suricata suricatta) |
Q92670698 | Consistent within-individual plasticity is sufficient to explain temperature responses in red deer reproductive traits |
Q44730354 | Conspicuous visual signals do not coevolve with increased body size in marine sea slugs. |
Q51692489 | Conspicuousness is correlated with toxicity in marine opisthobranchs. |
Q47436170 | Constant relative age and size at sex change for sequentially hermaphroditic fish |
Q39627392 | Constant, cycling, hot and cold thermal environments: strong effects on mean viability but not on genetic estimates. |
Q30361568 | Constrained evolution of the sex comb in Drosophila simulans. |
Q52649757 | Constrained sex allocation in a parasitoid due to variation in male quality. |
Q27021370 | Constraints imposed by pollinator behaviour on the ecology and evolution of plant mating systems |
Q51558922 | Constraints on adaptation: explaining deviation from optimal sex ratio using artificial neural networks. |
Q36012183 | Constraints on geographic variation in fiddler crabs (Ocypodidae: Uca) from the western Atlantic |
Q33294921 | Constraints on microbial metabolism drive evolutionary diversification in homogeneous environments. |
Q43457557 | Constraints on the evolution of function-valued traits: a study of growth in Tribolium castaneum |
Q57093833 | Constraints on the evolution of phenotypic plasticity in the clonal plant Hydrocotyle vulgaris |
Q60557314 | Constraints on the evolution of phenotypic plasticity in the clonal plant Hydrocotyle vulgaris |
Q114144505 | Contamination effects on sexual selection in wild dung beetles |
Q89874683 | Contemporary climate change hinders hybrid performance of ecologically dominant marine invertebrates |
Q35257268 | Contemporary ecotypic divergence during a recent range expansion was facilitated by adaptive introgression |
Q35884634 | Contemporary evolution of host plant range expansion in an introduced herbivorous beetle Ophraella communa |
Q30892983 | Contemporary evolution of plant reproductive strategies under global change is revealed by stored seeds |
Q51975639 | Contemporary gene flow and the spatio-temporal genetic structure of subdivided newt populations (Triturus cristatus, T. marmoratus). |
Q92670219 | Context is key: A comment on Herczeg et al. 2019 |
Q35873921 | Context-dependent alarm signalling in an insect |
Q40201557 | Context-dependent development of sexual ornamentation: implications for a trade-off between current and future breeding efforts |
Q50886092 | Context-dependent effects of Y chromosome and mitochondrial haplotype on male locomotive activity in Drosophila melanogaster. |
Q47546813 | Context-dependent effects of yolk androgens on nestling growth and immune function in a multibrooded passerine |
Q52097246 | Context-dependent sexual advertisement: plasticity in development of sexual ornamentation throughout the lifetime of a passerine bird. |
Q57197901 | Contrasted patterns of mitochondrial and nuclear structure among nursery colonies of the bat Myotis myotis |
Q56781988 | Contrasting effects of long distance seed dispersal on genetic diversity during range expansion |
Q33231360 | Contrasting genetic structures across two hybrid zones of a tropical reef fish, Acanthochromis polyacanthus (Bleeker 1855). |
Q38688627 | Contrasting patterns of X-chromosome divergence underlie multiple sex-ratio polymorphisms in stalk-eyed flies. |
Q51719756 | Contrasting patterns of body shape and neutral genetic divergence in marine and lake populations of threespine sticklebacks. |
Q52699838 | Contrasting patterns of phenotypic variation linked to chromosomal inversions in native and colonizing populations of Drosophila subobscura. |
Q44221226 | Contrasting patterns of selection acting on MHC class I and class II DRB genes in the Alpine marmot (Marmota marmota). |
Q47175565 | Contrasting patterns of selection on the size and coloration of a female plumage ornament in common yellowthroats. |
Q46812195 | Contrasting reproductive strategies of triploid hybrid males in vertebrate mating systems |
Q51692584 | Contrasting sexual selection on males and females in a role-reversed swarming dance fly, Rhamphomyia longicauda Loew (Diptera: Empididae). |
Q46983890 | Contribution of the X chromosome to a marked reduction in lifespan in interspecies female hybrids of Drosophila simulans and D. mauritiana |
Q59599286 | Control of male production in the swarm-founding wasp, Polybioides tabidus |
Q38951535 | Control of parental investment changes plastically over time with residual reproductive value |
Q101059338 | Convergence in sympatry: evolution of blue-banded wing pattern in Morpho butterflies |
Q51837844 | Convergence in trophic morphology and feeding performance among piscivorous natricine snakes. |
Q58556815 | Convergent Evolution Of Locomotor Morphology But Not Performance In Gymnotiform Swimmers |
Q40450666 | Convergent evolution across the Australian continent: ecotype diversification drives morphological convergence in two distantly related clades of Australian frogs. |
Q44172756 | Convergent evolution of eye ultrastructure and divergent evolution of vision-mediated predatory behaviour in jumping spiders |
Q42007574 | Convergent evolution of morphology and habitat use in the explosive Hawaiian fancy case caterpillar radiation |
Q83176748 | Convergent lifespan reaction norms in the yeast cultures exposed to different environmental stresses |
Q46320519 | Cool sperm: why some placental mammals have a scrotum |
Q52931151 | Cooperating for direct fitness benefits. |
Q48434926 | Cooperation and conflict during evolutionary transitions in individuality |
Q45951154 | Cooperation as a volunteer's dilemma and the strategy of conflict in public goods games. |
Q22065682 | Cooperation within and among species |
Q51151504 | Cooperative personalities and social niche specialization in female meerkats. |
Q47791244 | Cope's Rule in the Pterosauria, and differing perceptions of Cope's Rule at different taxonomic levels |
Q47333390 | Cope's rule in cryptodiran turtles: do the body sizes of extant species reflect a trend of phyletic size increase? |
Q51956108 | Cophylogenetic relationships between penguins and their chewing lice. |
Q57191467 | Coping with predator stress: interclonal differences in induction of heat-shock proteins in the water flea Daphnia magna |
Q33199143 | Copulation reduces male but not female longevity in Saltella sphondylli (Diptera: Sepsidae). |
Q42727407 | Copulatory plugs inhibit the reproductive success of rival males |
Q34045153 | Coral reefs as drivers of cladogenesis: expanding coral reefs, cryptic extinction events, and the development of biodiversity hotspots |
Q33514094 | Correction of a bootstrap approach to testing for evolution along lines of least resistance |
Q51695712 | Correlated evolution between male ejaculate allocation and female remating behaviour in seed beetles (Bruchidae). |
Q47435846 | Correlated evolution of colour pattern and body size in polymorphic pygmy grasshoppers, Tetrix undulata. |
Q123145259 | Correlated evolution of larval development, egg size and genome size across two genera of snapping shrimp |
Q46487118 | Correlated evolution of life history and host range in the nonphotosynthetic parasitic flowering plants Orobanche and Phelipanche (Orobanchaceae). |
Q51700335 | Correlated evolution of multivariate traits: detecting co-divergence across multiple dimensions. |
Q51564811 | Correlated evolution of phenotypic plasticity in metamorphic timing. |
Q51150022 | Correlated evolution of thermal niches and functional physiology in tropical freshwater fishes. |
Q88795818 | Correlated paternity measures mate monopolization and scales with the magnitude of sexual selection |
Q39721502 | Correlated response in plasticity to selection for early flowering in Arabidopsis thaliana |
Q33268527 | Correlated responses to artificial body size selection in growth, development, phenotypic plasticity and juvenile viability in yellow dung flies. |
Q52043771 | Correlated responses to selection for stress resistance and longevity in a laboratory population of Drosophila melanogaster. |
Q28743595 | Correlates of species richness in the largest Neotropical amphibian radiation |
Q45096263 | Correlational selection does not explain the evolution of a behavioural syndrome. |
Q40336043 | Correlations between heterozygosity and measures of genetic similarity: implications for understanding mate choice |
Q51699355 | Correlations between sex rate estimates and fitness across predominantly parthenogenetic flatworm populations. |
Q40547456 | Correlations between ultraviolet coloration, overwinter survival and offspring sex ratio in the blue tit. |
Q57269592 | Corrigendum |
Q57933171 | Corrigendum |
Q58088975 | Corrigendum |
Q60490479 | Corrigendum |
Q62557054 | Corrigendum |
Q95378589 | Corrigendum |
Q95499799 | Corrigendum |
Q88623073 | Corrigendum: A multigenerational effect of parental age on offspring size but not fitness in common duckweed (Lemna minor) |
Q46725841 | Corticosterone manipulation reveals differences in hierarchical organization of multidimensional reproductive trade-offs in r-strategist and K-strategist females |
Q46983882 | Corticosterone regulates multiple colour traits in Lacerta [Zootoca] vivipara males |
Q51577161 | Cost of cooperation rules selection for cheats in bacterial metapopulations. |
Q39795525 | Cost of resistance to parasites in digital organisms |
Q80404330 | Costly carotenoids: a trade-off between predation and infection risk? |
Q52715836 | Costs and benefits of defences induced by predators differing in dangerousness. |
Q35938618 | Costs and benefits of genetic heterogeneity within organisms |
Q92983509 | Costs and benefits of giant sperm and sperm storage organs in Drosophila melanogaster |
Q84916717 | Costs and benefits of polyandry in a placental poeciliid fish Heterandria formosa are in accordance with the parent-offspring conflict theory of placentation |
Q40235237 | Costs and benefits of sublethal Drosophila C virus infection. |
Q110615418 | Costs and limits of phenotypic plasticity: Tests with predator-induced morphology and life history in a freshwater snail |
Q110616049 | Costs and limits of phenotypic plasticity: Tests with predator-induced morphology and life history in a freshwater snail |
Q45856957 | Costs of growing up as a subordinate sibling are passed to the next generation in blue-footed boobies |
Q42045316 | Costs of resistance: genetic correlations and potential trade-offs in an insect immune system |
Q90584946 | Costs of walking: differences in egg size and starvation resistance of females between strains of the red flour beetle (Tribolium castaneum) artificially selected for walking ability |
Q93031577 | Costs of weaponry: Unarmed males sire more offspring than armed males in a male-dimorphic mite |
Q51691795 | Costs, benefits and the evolution of inducible defences: a case study with Daphnia pulex. |
Q42021080 | Countergradient vs. cogradient variation in growth and diapause in a lichen-feeding moth, Eilema depressum (Lepidoptera: Arctiidae). |
Q61659097 | Counterselection on sex chromosomes in the Mus musculus European hybrid zone |
Q50496919 | Covariance among premating, post-copulatory and viability fitness components in Drosophila melanogaster and their influence on paternity measurement. |
Q126028706 | Covariation among floral traits in Spergularia marina (Caryophyllaceae): geographic and temporal variation in phenotypic and among‐family correlations |
Q34387976 | Covariation between brain size and immunity in birds: implications for brain size evolution. |
Q79733614 | Cranial evolution in sakis (Pithecia, Platyrrhini). II: Evolutionary processes and morphological integration |
Q47655040 | Cranial shape and correlated characters in crocodilian evolution |
Q34195654 | Crest evolution in newts: implications for reconstruction methods, sexual selection, phenotypic plasticity and the origin of novelties |
Q29027832 | Crickets detect the genetic similarity of mating partners via cuticular hydrocarbons |
Q57453563 | Crickets increase sexual signalling and sperm protection but live shorter in the presence of rivals |
Q90366238 | Crocodylomorph cranial shape evolution and its relationship with body size and ecology |
Q92727540 | Cross-decades stability of an avian hybrid zone |
Q42006961 | Cross-generational effects of temperature on flight performance, and associated life-history traits in an insect |
Q47621843 | Crossing the taxonomic divide: conflict and its resolution in societies of reproductively totipotent individuals |
Q87413598 | Crossing the threshold: gene flow, dominance and the critical level of standing genetic variation required for adaptation to novel environments |
Q47916285 | Crowd control: sex ratio affects sexually selected cuticular hydrocarbons in male Drosophila serrata. |
Q38404722 | Cryptic differences in colour among Müllerian mimics: how can the visual capacities of predators and prey shape the evolution of wing colours? |
Q47729422 | Cryptic diversification in ancient asexuals: evidence from the bdelloid rotifer Philodina flaviceps |
Q51564705 | Cryptic female choice via sperm dumping favours male copulatory courtship in a spider. |
Q47250994 | Cryptic recombination in the ever-young sex chromosomes of Hylid frogs |
Q59591273 | Cryptic speciation among intestinal parasites (Trematoda: Digenea) infecting sympatric host fishes (Sparidae) |
Q64236734 | Crystal toxins and the volunteer's dilemma in bacteria |
Q30626612 | Cultural and climatic changes shape the evolutionary history of the Uralic languages. |
Q36161637 | Cultural isolation is greater than genetic isolation across an avian hybrid zone |
Q47645692 | Cultural niche construction and human evolution |
Q45256590 | Cultural transmission and the evolution of human behaviour: a general approach based on the Price equation |
Q47363160 | Cumulative cultural dynamics and the coevolution of cultural innovation and transmission: an ESS model for panmictic and structured populations |
Q60441300 | Cumulative effects of founding events during colonisation on genetic diversity and differentiation in an island and stepping-stone model |
Q50769698 | Curves as traits: genetic and environmental variation in mate preference functions. |
Q30427124 | Cuticular hydrocarbon divergence in the jewel wasp Nasonia: evolutionary shifts in chemical communication channels? |
Q80921048 | Cuticular hydrocarbons are heritable in the cricket Teleogryllus oceanicus |
Q51578960 | Cuticular hydrocarbons influence female attractiveness to males in the Australian field cricket, Teleogryllus oceanicus. |
Q97536131 | Cycles of trans-Arctic dispersal and vicariance, and diversification of the amphi-boreal marine fauna |
Q125257507 | Cyclical environmental changes as a factor maintaining genetic polymorphism. 1. Two‐locus haploid selection |
Q46100537 | Cytonuclear conflict in interpopulation hybrids: the role of RNA polymerase in mtDNA transcription and replication. |
Q91621470 | Cytonuclear incongruences hamper species delimitation in the socially polymorphic desert ants of the Cataglyphis albicans group in Israel |
Q45884518 | Cytoplasmic feminizing elements in a two‐population model: infection dynamics, gene flow modification, and the spread of autosomal suppressors |
Q63980012 | Cytoplasmic incompatibilities in the mosquito Culex pipiens: How to explain a cytotype polymorphism?* |
Q51473380 | DDT resistance, epistasis and male fitness in flies. |
Q48073607 | DNA sequence analysis and the phylogeographical history of the rodent Deltamys kempi (Sigmodontinae, Cricetidae) on the Atlantic Coastal Plain of south of Brazil |
Q35153483 | Darwin's finches and their diet niches: the sympatric coexistence of imperfect generalists |
Q83958066 | Darwinian transformation of a 'scarcely nutritious fluid' into milk |
Q31039482 | Data depth, data completeness, and their influence on quantitative genetic estimation in two contrasting bird populations |
Q125373565 | David M. Green and Stanley K. Sessions (eds.), 1991. Amphibian Cytogenetics and Evolution. Academic Press, pp. 456. $89.50. ISBN: 0‐12‐297880‐3 |
Q89110979 | Day-flying moths are smaller: evidence for ecological costs of being large |
Q95285287 | Death feigning as an adaptive anti-predator behavior: further evidence for its evolution from artificial selection and natural populations |
Q34725734 | Decay of unused characters by selection and drift |
Q51857647 | Decompositions of Price's formula in an inhomogeneous population structure. |
Q61697956 | Deconstructing a floral phenotype: do pollinators select for corolla integration in Lavandula latifolia? |
Q34735787 | Decoupling of taxonomic diversity and morphological disparity during decline of the Cambrian trilobite family Pterocephaliidae |
Q52641834 | Defence against multiple enemies. |
Q113855135 | Defensive role of leaf trichomes in resistance to herbivorous insects in Datura stramonium |
Q37060484 | Defining biological communication |
Q82208811 | Degeneration patterns of the olfactory receptor genes in sea snakes |
Q46294153 | Delayed dispersal and prolonged brood care in a family-living beetle. |
Q38467801 | Delayed effects of larval predation risk and food quality on anuran juvenile performance |
Q42044139 | Delaying evolution of insect resistance to transgenic crops by decreasing dominance and heritability |
Q34815194 | Deleterious effects of recombination and possible nonrecombinatorial advantages of sex in a fungal model |
Q92080034 | Delusions of grandeur: Seed count is not a good fitness proxy under individual variation in phenology |
Q39842198 | Demographic drivers of age-dependent sexual selection. |
Q52695791 | Demographic factors and genetic variation influence population persistence under environmental change. |
Q89690972 | Demographic fluctuations lead to rapid and cyclic shifts in genetic structure among populations of an alpine butterfly, Parnassius smintheus |
Q45960257 | Demographic history, geographical distribution and reproductive isolation of distinct lineages of blue rockfish (Sebastes mystinus), a marine fish with a high dispersal potential. |
Q33667975 | Demography and the tragedy of the commons. |
Q51935146 | Demography, altruism, and the benefits of budding. |
Q89111000 | Demography, life history and the evolution of age-dependent social behaviour |
Q35586692 | Dendritic connectivity shapes spatial patterns of genetic diversity: a simulation-based study. |
Q110792383 | Density limits and survival of local populations in 64 carabid species with different powers of dispersal |
Q39337806 | Describing mate preference functions and other function-valued traits. |
Q51595005 | Desiccation resistance and mating behaviour in laboratory populations of Drosophila simulans originating from the opposing slopes of Lower Nahal Oren (Israel). |
Q34300007 | Detecting cryptic speciation in the widespread and morphologically conservative carpet chameleon (Furcifer lateralis) of Madagascar |
Q62383059 | Detecting genetic variation in developmental instability by artificial selection on fluctuating asymmetry |
Q50776509 | Detecting local adaptation in a natural plant-pathogen metapopulation: a laboratory vs. field transplant approach. |
Q43698507 | Detecting positive selection in the budding yeast genome |
Q34302699 | Detecting small-scale genotype-environment interactions in apomictic dandelion (Taraxacum officinale) populations |
Q92992456 | Detecting the macroevolutionary signal of species interactions |
Q51526832 | Determinants of age-dependent change in a secondary sexual character. |
Q47984398 | Determinants of distribution and prevalence of avian malaria in blue tit populations across Europe: separating host and parasite effects |
Q30835445 | Determinants of male fitness: disentangling intra- and inter-sexual selection. |
Q48859633 | Determinants of mating and sperm-transfer success in a simultaneous hermaphrodite |
Q40546984 | Determinants of sperm transfer in the scorpionfly Panorpa cognate: male variation, female condition and copulation duration |
Q51635256 | Developmental acclimation affects clinal variation in stress resistance traits in Drosophila buzzatii. |
Q91865843 | Developmental diet irreversibly shapes male post-copulatory traits in the neriid fly Telostylinus angusticollis |
Q46473408 | Developmental effects of visual environment on species-assortative mating preferences in Lake Victoria cichlid fish |
Q51842459 | Developmental instability as phenodeviance in a secondary sexual trait increases sharply with thermal stress. |
Q34070802 | Developmental plasticity, morphological variation and evolvability: a multilevel analysis of morphometric integration in the shape of compound leaves. |
Q124850937 | Developmental stability in flowers of Clarkia tembloriensis (Onagraceae) |
Q92995550 | Developmental stress and telomere dynamics in a genetically polymorphic species |
Q44294377 | Developmental temperature affects the expression of ejaculatory traits and the outcome of sperm competition in Callosobruchus maculatus |
Q40673844 | Developmental thermal plasticity among Drosophila melanogaster populations |
Q53221984 | Devoted fathers or selfish lovers? Conflict between mating effort and parental care in a harem-defending arachnid. |
Q30689201 | Diapause termination of Rhagoletis cerasi pupae is regulated by local adaptation and phenotypic plasticity: escape in time through bet-hedging strategies |
Q57212084 | Diatoms do radiate: evidence for a freshwater species flock |
Q60229291 | Diatoms do radiate: evidence for a freshwater species flock |
Q42022816 | Did the introduction of maize into Europe provide enemy-free space to Ostrinia nubilalis? Parasitism differences between two sibling species of the genus Ostrinia |
Q48727973 | Diet and social conditions during sexual maturation have unpredictable influences on female life history trade-offs |
Q39457522 | Diet specialization in an extreme omnivore: nutritional regulation in glucose-averse German cockroaches. |
Q36089206 | Diet, bite force and skull morphology in the generalist rodent morphotype. |
Q51656354 | Diet-dependent female evolution influences male lifespan in a nuptial feeding insect. |
Q51630090 | Dietary flavonoids enhance conspicuousness of a melanin-based trait in male blackcaps but not of the female homologous trait or of sexually monochromatic traits. |
Q92799204 | Dietary polyunsaturated fatty acids affect volume and metabolism of Drosophila melanogaster sperm |
Q33801541 | Differences in bacterial diversity of host-associated populations of Phylloxera notabilis Pergande (Hemiptera: Phylloxeridae) in pecan and water hickory |
Q34253701 | Differences in caste dimorphism among three hornet species (Hymenoptera: Vespidae): forewing size, shape and allometry |
Q35835655 | Differences in developmental strategies between long-settled and invasion-front populations of the cane toad in Australia |
Q83378791 | Differences in parasite susceptibility and costs of resistance between naturally exposed and unexposed host populations |
Q91064650 | Differences in perceived predation risk associated with variation in relative size of extra-pair and within-pair offspring |
Q96350420 | Differences in the contributions of sex-linkage and androgen regulation to sex-biased gene expression in juvenile and adult sticklebacks |
Q34322350 | Differences in timing of migration and response to sexual signalling drive asymmetric hybridization across a migratory divide |
Q42985285 | Different transmission strategies of a parasite in male and female hosts |
Q48177468 | Differential correlates of diet and phylogeny on the shape of the premaxilla and anterior tooth in sparid fishes (Perciformes: Sparidae). |
Q38444255 | Differential effects of egg albumen content on barn swallow nestlings in relation to hatch order |
Q52574931 | Differential effects of offspring and maternal inbreeding on egg laying and offspring performance in the burying beetle Nicrophorus vespilloides. |
Q57064064 | Differential gene exchange between parapatric morphs of Littorina saxatilis detected using AFLP markers |
Q47236048 | Differential introgression from a sister species explains high F(ST) outlier loci within a mussel species |
Q47284973 | Differential investment in pre- vs. post-copulatory sexual selection reinforces a cross-continental reversal of sexual size dimorphism in Sepsis punctum (Diptera: Sepsidae). |
Q84999628 | Differential niche modification by males and females of a dioecious herb: extending the Jack Sprat effect |
Q90585055 | Differential predation alters pigmentation in threespine stickleback (Gasterosteus aculeatus) |
Q45256834 | Differential rates of morphological divergence in birds |
Q91202996 | Differential response to larval crowding of a long- and a short-lived medfly biotype |
Q57142519 | Differential selection of growth rate-related traits in wild barley, Hordeum spontaneum, in contrasting greenhouse nutrient environments |
Q60484812 | Differential selection of growth rate-related traits in wild barley, Hordeum spontaneum, in contrasting greenhouse nutrient environments |
Q34278774 | Differential strength of sex-biased hybrid inferiority in impeding gene flow may be a cause of Haldane's rule |
Q48237562 | Differential visual ornamentation between brood parasitic and parental cuckoos. |
Q43618111 | Differentiation of morphology, genetics and electric signals in a region of sympatry between sister species of African electric fish (Mormyridae). |
Q41442380 | Digging for gold nuggets: uncovering novel candidate genes for variation in gastrointestinal nematode burden in a wild bird species. |
Q50054159 | Digging their own macroevolutionary grave: Fossoriality as an evolutionary dead-end in snakes |
Q47251337 | Digging through model complexity: using hierarchical models to uncover evolutionary processes in the wild |
Q52650410 | Diminishing returns in social evolution: the not-so-tragic commons. |
Q35163063 | Dioecy is associated with higher diversification rates in flowering plants |
Q63508144 | Direct and correlated responses to artificial selection on male mating frequency in the stalk-eyed fly Cyrtodiopsis dalmanni |
Q47393720 | Direct and correlated responses to artificial selection on sexual size dimorphism in the flour beetle, Tribolium castaneum |
Q64032579 | Direct and correlated responses to selection for desiccation resistance: a comparison of Drosophila melanogaster and D. simulans |
Q60484815 | Direct and correlated responses to selection on iridoid glycosides in Plantago lanceolata L |
Q45965181 | Direct and indirect assortative mating: a multivariate approach to plant flowering schedules. |
Q93174868 | Direct and indirect effects of sexual signal loss on female reproduction in the Pacific field cricket (Teleogryllus oceanicus) |
Q91262332 | Direct and indirect genetic effects on reproductive investment in a grasshopper |
Q115033069 | Direct and indirect phenotypic effects on sociability indicate potential to evolve |
Q125563411 | Direct and indirect selection on mate choice during pollen competition: Effects of male and female sexual traits on offspring performance following two‐donor crosses |
Q51709771 | Direct benefits and costs for hybridizing Ficedula flycatchers. |
Q51568002 | Direct fitness for dynamic kin selection. |
Q51925559 | Direct fitness or inclusive fitness: how shall we model kin selection? |
Q51766194 | Direct vs. inclusive fitness in the evolution of aphid cornicle length. |
Q47436160 | Directional changes in sexual size dimorphism in shorebirds, gulls and alcids. |
Q39969286 | Directional mitochondrial introgression and character displacement due to reproductive interference in two closely related Pterostichus ground beetle species |
Q56005205 | Directional selection in the evolution of elongated upper canines in clouded leopards and sabre-toothed cats |
Q80118029 | Disassociation between weak sexual isolation and genetic divergence in a hermaphroditic land snail and implications about chirality |
Q52755966 | Discontinuous gas exchange exhibition is a heritable trait in speckled cockroaches Nauphoeta cinerea. |
Q47361991 | Discord in the family Sparidae (Teleostei): divergent phylogeographical patterns across the Atlantic-Mediterranean divide. |
Q91065383 | Discordant patterns of introgression across a narrow hybrid zone between two cryptic lineages of an Iberian endemic newt |
Q31062044 | Discovering phenotypic causal structure from nonexperimental data |
Q38970403 | Discrete and morphometric traits reveal contrasting patterns and processes in the macroevolutionary history of a clade of scorpions. |
Q51535252 | Discrete colour polymorphism in the tawny dragon lizard (Ctenophorus decresii) and differences in signal conspicuousness among morphs. |
Q42015117 | Disentangling determinants of egg size in the Geometridae (Lepidoptera) using an advanced phylogenetic comparative method. |
Q30831228 | Disentangling plastic and genetic changes in body mass of Siberian jays |
Q47570697 | Disentangling sex allocation in a viviparous reptile with temperature-dependent sex determination: a multifactorial approach. |
Q42038715 | Disjunct distributions during glacial and interglacial periods in mountain butterflies: Erebia epiphron as an example |
Q48335890 | Disparate patterns of thermal adaptation between life stages in temperate vs. tropical Drosophila melanogaster |
Q33387002 | Dispersal and population genetic structure of Telmatherina antoniae, an endemic freshwater Sailfin silverside from Sulawesi, Indonesia |
Q29999944 | Dispersal and population structure of a New World predator, the army antEciton burchellii |
Q56951002 | Dispersal and rapid evolution in brown trout colonizing virgin Subantarctic ecosystems |
Q114080045 | Dispersal reduces interspecific competitiveness by spreading locally harmful traits |
Q113348649 | Dispersal, kinship and inbreeding in an island population of the Great Tit |
Q46075386 | Displacement of flowering phenologies among plant species by competition for generalist pollinators |
Q39547176 | Disruptive selection as a driver of evolutionary branching and caste evolution in social insects. |
Q37105311 | Disruptive viability selection on a black plumage trait associated with dominance |
Q45053898 | Disruptive viability selection on adult exploratory behaviour in eastern chipmunks |
Q48275475 | Dissecting differentiation landscapes: a linked selection's perspective. |
Q60514229 | Distinct colonization waves underlie the diversification of the freshwater sculpin (Cottus gobio ) in the Central European Alpine region |
Q37052139 | Distinguishing four fundamental approaches to the evolution of helping |
Q83287062 | Distortion of symmetrical introgression in a hybrid zone: evidence for locus-specific selection and uni-directional range expansion |
Q48001427 | Distribution of genetic variability in populations of two chromosomal races of Dichroplus pratensis (Melanoplinae, Acrididae) and their hybrid zone. |
Q33403034 | Divergence along a steep ecological gradient in lake whitefish (Coregonus sp.). |
Q39095960 | Divergence in brain composition during the early stages of ecological specialization in Heliconius butterflies |
Q46333793 | Divergence in host use ability of a marine herbivore from two habitat types |
Q46644638 | Divergence in mating signals correlates with genetic distance and behavioural responses to playback. |
Q34013876 | Divergence in parental care, habitat selection and larval life history between two species of Peruvian poison frogs: an experimental analysis |
Q80960927 | Divergence in replicated phylogenies: the evolution of partial post-mating prezygotic isolation in bean weevils |
Q51729472 | Divergence in the calling songs between sympatric and allopatric populations of the southern wood cricket Gryllus fultoni (Orthoptera: Gryllidae). |
Q51281222 | Divergence of gastropod life history in contrasting thermal environments in a geothermal lake. |
Q34135959 | Divergence of ovipositor length and egg shape in a brood parasitic bitterling fish through the use of different mussel hosts |
Q97650418 | Divergence of seminal fluid gene expression and function among natural snail populations |
Q47980257 | Divergent genetic and epigenetic post-zygotic isolation mechanisms in Mus and Peromyscus. |
Q33890459 | Divergent host plant specialization as the critical driving force in speciation between populations of a phytophagous ladybird beetle |
Q89259607 | Divergent parasite infections in sympatric cichlid species in Lake Victoria |
Q34114459 | Divergent patterns of diversification in courtship and genitalic characters of Timema walking-sticks |
Q51674311 | Divergent selection and phenotypic plasticity during incipient speciation in Lake Victoria cichlid fish. |
Q43494744 | Divergent sexual selection via male competition: ecology is key. |
Q57808471 | Divergent subgenome evolution after allopolyploidization in African clawed frogs (Xenopus) |
Q42028198 | Divergent timing of egg-laying may maintain life history polymorphism in potentially multivoltine insects in seasonal environments. |
Q129674599 | Divergent warning patterns influence male and female mating behaviours in a tropical butterfly |
Q91075821 | Diverse genotypes of the amphibian-killing fungus produce distinct phenotypes through plastic responses to temperature |
Q121604957 | Diverse strategies that animals use to deter intraspecific predation |
Q60484610 | Diversification in temporally heterogeneous environments: effect of the grain in experimental bacterial populations |
Q34256249 | Diversification of egg-deposition behaviours and the evolution of male parental care in darters (Teleostei: Percidae: Etheostomatinae). |
Q28648503 | Diversity and disparity through time in the adaptive radiation of Antarctic notothenioid fishes |
Q50451839 | Diversity and the maintenance of sex by parasites. |
Q94561532 | Diversity in CRISPR-based immunity protects susceptible genotypes by restricting phage spread and evolution |
Q41066165 | Diversity in warning coloration is easily recognized by avian predators |
Q49561478 | Diversity of age-specific reproductive rates may result from ageing and optimal resource allocation |
Q33408316 | Diversity patterns amongst herbivorous dinosaurs and plants during the Cretaceous: implications for hypotheses of dinosaur/angiosperm co-evolution |
Q51664980 | Division of labour within flowers: heteranthery, a floral strategy to reconcile contrasting pollen fates. |
Q51143232 | Divorce in the barn owl: securing a compatible or better mate entails the cost of re-pairing with a less ornamented female mate. |
Q43951397 | Do aggressive signals evolve towards higher reliability or lower costs of assessment? |
Q80231871 | Do cuckoos choose nests of great reed warblers on the basis of host egg appearance? |
Q44384169 | Do different disparity proxies converge on a common signal? Insights from the cranial morphometrics and evolutionary history of Pterosauria (Diapsida: Archosauria). |
Q39353951 | Do evolutionary constraints on thermal performance manifest at different organizational scales? |
Q51749466 | Do female black field crickets Teleogryllus commodus benefit from polyandry? |
Q51339410 | Do female parasitoid wasps recognize and adjust sex ratios to build cooperative relationships? |
Q51688571 | Do flowers wave to attract pollinators? A case study with Silene maritima. |
Q31153203 | Do group dynamics affect colour morph clines during a range shift? |
Q46620723 | Do habitat shifts drive diversification in teleost fishes? An example from the pufferfishes (Tetraodontidae). |
Q55871158 | Do hairworms (Nematomorpha) manipulate the water seeking behaviour of their terrestrial hosts? |
Q51188981 | Do immunological, endocrine and metabolic traits fall on a single Pace-of-Life axis? Covariation and constraints among physiological systems. |
Q51592217 | Do individuals in better condition survive for longer? Field survival estimates according to male alternative reproductive tactics and sex. |
Q42875316 | Do insect pests perform better on highly defended plants? Costs and benefits of induced detoxification defences in the aphid Sitobion avenae. |
Q87414357 | Do mites evolving in alternating host plants adapt to host switch? |
Q42037845 | Do mothers producing large offspring have to sacrifice fecundity? |
Q56940741 | Do operational sex ratios influence sex allocation in viviparous lizards with temperature-dependent sex determination? |
Q51144925 | Do parasites and antioxidant availability affect begging behaviour, growth rate and resistance to oxidative stress? |
Q31027992 | Do precocial mammals develop at a faster rate? A comparison of rates of skull development in Sigmodon fulviventer and Mus musculus domesticus. |
Q100523329 | Do the ages of parents or helpers affect offspring fitness in a cooperatively breeding bird? |
Q51721074 | Do vertically transmitted symbionts co-existing in a single host compete or cooperate? A modelling approach. |
Q51699110 | Dobzhansky-Muller model of hybrid dysfunction supported by poor burst-speed performance in hybrid tiger salamanders. |
Q39835048 | Does a trade‐off between current reproductive success and survival affect the honesty of male signalling in species with male parental care? |
Q91480358 | Does adaptation to different diets result in assortative mating? Ambiguous results from experiments on Drosophila |
Q53162512 | Does attractiveness in men provide clues to semen quality? |
Q45333853 | Does character displacement initiate speciation? Evidence of reduced gene flow between populations experiencing divergent selection |
Q51321556 | Does competition drive character differences between species on a macroevolutionary scale? |
Q51944419 | Does competitive divergence occur if assortative mating is costly? |
Q51842586 | Does egg competition occur in marine broadcast-spawners? |
Q46497113 | Does foraging mode mould morphology in lacertid lizards? |
Q52664032 | Does genetic diversity hinder parasite evolution in social insect colonies? |
Q47955443 | Does high relatedness promote cheater-free multicellularity in synthetic lifecycles? |
Q85904810 | Does hybridization influence speciation? |
Q51790805 | Does inbreeding avoidance maintain gender dimorphism in Wurmbea dioica (Colchicaceae)? |
Q36339317 | Does increased heat resistance result in higher susceptibility to predation? A test using Drosophila melanogaster selection and hardening |
Q33925691 | Does maternal care evolve through egg recognition or directed territoriality? |
Q35691368 | Does multiple paternity affect seed mass in angiosperms? An experimental test in Dalechampia scandens. |
Q37105352 | Does multiple paternity influence offspring disease resistance? |
Q34982066 | Does nasal echolocation influence the modularity of the mammal skull? |
Q90251483 | Does operational sex ratio influence relative strength of purging selection in males versus females? |
Q35789777 | Does plasticity enhance or dampen phenotypic parallelism? A test with three lake-stream stickleback pairs |
Q44631212 | Does predation result in adult sex ratio skew in a sexually dimorphic insect genus? |
Q58089040 | Does predation select for or against avian coloniality? A comparative analysis |
Q46885054 | Does relaxed predation drive phenotypic divergence among insular populations? |
Q83113196 | Does selection by resistant hosts trigger local adaptation in plant-pathogen systems? |
Q34300070 | Does selection on increased cold tolerance in the adult stage confer resistance throughout development? |
Q117215099 | Does sexual conflict contribute to the evolution of novel warning patterns? |
Q91676645 | Does thermal plasticity align with local adaptation? An interspecific comparison of wing morphology in sepsid flies |
Q57742192 | Does time until mating affect progeny sex ratio? A manipulative experiment with the parasitoid wasp |
Q30010560 | Does vocal learning accelerate acoustic diversification? Evolution of contact calls in Neotropical parrots. |
Q33759635 | Domestic chickens defy Rensch's rule: sexual size dimorphism in chicken breeds |
Q92287224 | Dominance effects strengthen premating hybridization barriers between sympatric species of grasshoppers (Acrididae, Orthoptera) |
Q51146560 | Dose-dependent effects of an immune challenge at both ultimate and proximate levels in Drosophila melanogaster. |
Q40253459 | Dose-dependent schistosome-induced mortality and morbidity risk elevates host reproductive effort |
Q46556515 | Drift effects on the multivariate floral phenotype of Calceolaria polyrhiza during a post-glacial expansion in Patagonia |
Q51614036 | Drosophila melanogaster males respond differently at the behavioural and genome-wide levels to Drosophila melanogaster and Drosophila simulans females. |
Q96025942 | Dunnock social status correlates with sperm speed, but fast sperm does not always equal high fitness |
Q51663060 | Duplicate retention in signalling proteins and constraints from network dynamics. |
Q34244156 | Dynamic Wolbachia prevalence in Acromyrmex leaf-cutting ants: potential for a nutritional symbiosis. |
Q30451110 | Dynamic linkage relationships to the mating-type locus in automictic fungi of the genus Microbotryum |
Q90142021 | Dynamic phenotypic correlates of social status and mating effort in male and female red junglefowl, Gallus gallus |
Q47551909 | Dynamic sex chromosomes in Old World chameleons (Squamata: Chamaeleonidae). |
Q45052357 | Dynamic social behaviour in a bacterium: pseudomonas aeruginosa partially compensates for siderophore loss to cheats |
Q42037843 | Dynamics of host plant use and species diversity in Polygonia butterflies (Nymphalidae). |
Q38935389 | Dynamics of the evolution of Batesian mimicry: molecular phylogenetic analysis of ant-mimicking Myrmarachne (Araneae: Salticidae) species and their ant models |
Q46891715 | Dynamics of transcriptome evolution in the model eukaryote Neurospora |
Q46649995 | Early constraints in sexual dimorphism: survival benefits of feminized phenotypes |
Q35897084 | Early diversification of sperm size in the evolutionary history of the old world leaf warblers (Phylloscopidae). |
Q46835527 | Early diversification trend and Asian origin for extent bat lineages |
Q47262226 | Early evolutionary differentiation of morphological variation in the mandible of South American caviomorph rodents (Rodentia, Caviomorpha). |
Q37669368 | Early exposure to nonlethal predation risk by size-selective predators increases somatic growth and decreases size at adulthood in three-spined sticklebacks. |
Q92476976 | Early life of fathers affects offspring fitness in a wild rodent |
Q60311578 | Early maternal effects and antibacterial immune factors in the eggs, nestlings and adults of the barn swallow |
Q51806986 | Early maternal investment in mice: no evidence for compatible-genes sexual selection despite hybrid vigor. |
Q57749049 | Early maternal, genetic and environmental components of antioxidant protection, morphology and immunity of yellow-legged gull (Larus michahellis) chicks |
Q28651887 | Early reproductive investment, senescence and lifetime reproductive success in female Asian elephants |
Q100523336 | Early-life effects on body size in each sex interact to determine reproductive success in the burying beetle Nicrophorus vespilloides |
Q88428420 | Ecological and demographic correlates of cooperation from individual to budding dispersal |
Q46835483 | Ecological and evolutionary drivers of range size in Coenagrion damselflies |
Q42030922 | Ecological and genetic associations across a Heliconius hybrid zone |
Q42007021 | Ecological and genetic factors influencing the transition between host-use strategies in sympatric Heliconius butterflies |
Q59393795 | Ecological and morphological diversification within single species and character displacement in Mandarina, endemic land snails of the Bonin Islands |
Q51194791 | Ecological and morphological patterns in communities of land snails of the genus Mandarina from the Bonin Islands. |
Q38600582 | Ecological and phylogenetic variability in the spinalis muscle of snakes. |
Q51192331 | Ecological components and evolution of selfing in the freshwater snail Galba truncatula. |
Q51175473 | Ecological divergence and habitat isolation between two migratory forms of Japanese threespine stickleback (Gasterosteus aculeatus). |
Q46923528 | Ecological divergence and sexual selection drive sexual size dimorphism in New World pitvipers (Serpentes: Viperidae). |
Q34831661 | Ecological divergence and speciation between lemur (Eulemur) sister species in Madagascar |
Q91747020 | Ecological divergence and speciation in common bottlenose dolphins in the western South Atlantic |
Q36214835 | Ecological diversification associated with the benthic-to-pelagic transition by North American minnows |
Q33205139 | Ecological diversification in a group of Indomalayan pitvipers (Trimeresurus): convergence in taxonomically important traits has implications for species identification. |
Q38727742 | Ecological drivers of body size evolution and sexual size dimorphism in short-horned grasshoppers (Orthoptera: Acrididae). |
Q96954014 | Ecological fitting is the forerunner to diversification in a plant virus with broad host range |
Q60394147 | Ecological genetics of a cyclical parthenogen in temporary habitats |
Q30314317 | Ecological genetics of sediment browsing behaviour in a planktonic crustacean |
Q51177419 | Ecological niche modelling as an exploratory tool for identifying species limits: an example based on Mexican muroid rodents. |
Q33609183 | Ecological opportunity and the origin of adaptive radiations |
Q31046115 | Ecological radiation with limited morphological diversification in salamanders |
Q33299927 | Ecological selection against hybrids in natural populations of sympatric threespine sticklebacks |
Q57071205 | Ecological sorting and character displacement contribute to the structure of communities of Clarkia species |
Q50737915 | Ecological specialization correlates with genotypic differentiation in sympatric host-populations of the pea aphid. |
Q38932545 | Ecological speciation along an elevational gradient in a tropical passerine bird? |
Q39703099 | Ecological speciation in dynamic landscapes. |
Q36017454 | Ecological speciation in sympatric palms: 1. Gene expression, selection and pleiotropy. |
Q36067124 | Ecological speciation in sympatric palms: 2. Pre- and post-zygotic isolation |
Q51194783 | Ecological, morphological and phylogenetic correlates of interspecific variation in plasma carotenoid concentration in birds. |
Q50733955 | Ecology, life history and resource allocation in the ant, Leptothorax nylanderi. |
Q40062525 | Ecomorphological convergence in planktivorous surgeonfishes |
Q35394231 | Ecomorphological variation in male and female wall lizards and the macroevolution of sexual dimorphism in relation to habitat use. |
Q56503274 | Ecomorphology of plesiosaur flipper geometry |
Q44368855 | Ecomorphology of the African felid ensemble: the role of the skull and postcranium in determining species segregation and assembling history. |
Q58827502 | Ecomorphometric variation and sexual dimorphism in the common shrew (Sorex araneus) |
Q39134262 | Ectoparasite fitness in auxiliary hosts: phylogenetic distance from a principal host matters |
Q59117997 | Effect of habitat saturation on the number and turnover of queens in the polygynous ant, Myrmica sulcinodis |
Q52760123 | Effect of juvenile hormone on senescence in males with terminal investment. |
Q51603650 | Effect of male age on sperm traits and sperm competition success in the guppy (Poecilia reticulata). |
Q49038574 | Effect of metal stress on life history divergence and quantitative genetic architecture in a wolf spider |
Q89230463 | Effect of migration and environmental heterogeneity on the maintenance of quantitative genetic variation: a simulation study |
Q51598212 | Effect of parasitic sex-ratio distorters on host gene frequencies in a mainland-island context. |
Q55564831 | Effect of spatial connectivity on host resistance in a highly fragmented natural pathosystem. |
Q33205995 | Effect of vagility potential on dispersal and speciation in rainforest insects |
Q38440732 | Effective heritability of targets of sex-ratio selection under environmental sex determination |
Q47264585 | Effective population size associated with self-fertilization: lessons from temporal changes in allele frequencies in the selfing annual Medicago truncatula |
Q47222033 | Effective population size, reproductive success and sperm precedence in the butterfly, Bicyclus anynana, in captivity. |
Q46354199 | Effective size of density-dependent two-sex populations: the effect of mating systems |
Q79733597 | Effectiveness of sexual selection in preventing fitness deterioration in bulb mite populations under relaxed natural selection |
Q51771287 | Effects of B chromosomes and supernumerary segments on morphometric traits and adult fitness components in the grasshopper, Dichroplus elongatus (Acrididae). |
Q113097521 | Effects of CMS types and restorer alleles on plant performance in Plantago lanceolata L.: an indication for cost of restoration |
Q34179635 | Effects of among-offspring relatedness on the origins and evolution of parental care and filial cannibalism |
Q82720191 | Effects of antagonistic coevolution on parasite-mediated host coexistence |
Q34599299 | Effects of cytoplasmic genes on sperm viability and sperm morphology in a seed beetle: implications for sperm competition theory? |
Q57057381 | Effects of diet on cranial morphology and biting ability in musteloid mammals |
Q48396026 | Effects of early resource limitation and compensatory growth on lifetime fitness in the ladybird beetle (Harmonia axyridis). |
Q38478881 | Effects of egg yolk testosterone on growth and immunity in a precocial bird |
Q64032262 | Effects of exposure to short-term heat stress on fitness components in Drosophila melanogaster |
Q47361950 | Effects of food abundance on genetic and maternal variation in the growth rate of juvenile red squirrels |
Q47433878 | Effects of food restriction across stages of juvenile and early adult development on body weight, survival and adult life history |
Q79321086 | Effects of four generations of density-dependent selection on life history traits and their plasticity in a clonally propagated plant |
Q46520898 | Effects of gene flow on phenotype matching between two varieties of Joshua tree (Yucca brevifolia; Agavaceae) and their pollinators. |
Q42660916 | Effects of genetic similarity on the life-history strategy of co-infecting trematodes: are parasites capable of intrahost kin recognition? |
Q113270348 | Effects of genetic vs. environmental quality on condition‐dependent morphological and life history traits in a neriid fly |
Q48556546 | Effects of host condition on susceptibility to infection, parasite developmental rate, and parasite transmission in a snail-trematode interaction |
Q38994516 | Effects of immune challenge on the oviposition strategy of a noctuid moth |
Q52659258 | Effects of inbreeding and rate of inbreeding in Drosophila melanogaster- Hsp70 expression and fitness. |
Q34535735 | Effects of inbreeding and temperature stress on life history and immune function in a butterfly |
Q49049150 | Effects of inbreeding on aversive learning in Drosophila. |
Q94540633 | Effects of inbreeding on behavioural plasticity of parent-offspring interactions in a burying beetle |
Q47867375 | Effects of malaria double infection in birds: one plus one is not two. |
Q122234082 | Effects of male genetic contribution and paternal investment to egg and hatchling size in the cricket, |
Q122906484 | Effects of male genetic contribution and paternal investment to egg and hatchling size in the cricket, Gryllus firmus |
Q51183785 | Effects of metabolic rate and sperm competition on the fatty-acid composition of mammalian sperm. |
Q46888539 | Effects of nutrient availability on primary sexual traits and their response to selection in Spergularia marina (Caryophyllaceae). |
Q43917922 | Effects of ornamentation and phylogeny on the evolution of wing shape in stalk-eyed flies (Diopsidae). |
Q46388345 | Effects of ovarian fluid and genetic differences on sperm performance and fertilization success of alternative reproductive tactics in Chinook salmon. |
Q45884037 | Effects of parasitic sex-ratio distorters on host genetic structure in the Armadillidium vulgare-Wolbachia association |
Q37659652 | Effects of parental radiation exposure on developmental instability in grasshoppers |
Q36157192 | Effects of pathogen exposure on life-history variation in the gypsy moth (Lymantria dispar) |
Q43435648 | Effects of pollen availability and the mutation bias on the fixation of mutations disabling the male specificity of self-incompatibility. |
Q54432722 | Effects of polyandry on male phenotypic diversity |
Q47567998 | Effects of prior exposure to antibiotics on bacterial adaptation to phages |
Q110616053 | Effects of spatial autocorrelation, natal philopatry and phenotypic plasticity on the heritability of laying date |
Q46724064 | Effects of the [PSI+] prion on rates of adaptation in yeast |
Q89739469 | Effects of two seminal fluid transcripts on post-mating behaviour in the simultaneously hermaphroditic flatworm Macrostomum lignano |
Q57471490 | Effects of variation in resource acquisition during different stages of the life cycle on life-history traits and trade-offs in a burying beetle |
Q45866467 | Effects of within-colony competition on body size asymmetries and reproductive skew in a social spider |
Q43786345 | Egg and time limitation mediate an egg protection strategy |
Q51664606 | Egg jelly influences sperm motility in the externally fertilizing frog, Crinia georgiana. |
Q91354802 | Egg load is a cue for offspring sex ratio adjustment in a fig-pollinating wasp with male-eggs-first sex allocation |
Q83931693 | Egg phenotype differentiation in sympatric cuckoo Cuculus canorus gentes |
Q46308345 | Egg shape mimicry in parasitic cuckoos. |
Q47205985 | Egg size, embryonic development time and ovoviviparity in Drosophila species |
Q89995248 | Egg-induced changes to sperm phenotypes shape patterns of multivariate selection on ejaculates |
Q50421729 | Egg-laying environment modulates offspring responses to predation risk in an amphibian. |
Q92795753 | Egg-size plasticity in Apis mellifera: Honey bee queens alter egg size in response to both genetic and environmental factors |
Q51965184 | Eight personal rules for doing science. |
Q46670761 | Elevational speciation in action? Restricted gene flow associated with adaptive divergence across an altitudinal gradient |
Q51900246 | Enantiomorphs differ in shape in opposite directions between populations. |
Q44540680 | Endocrine phenotype, reproductive success and survival in the great tit, Parus major |
Q99206708 | Endosymbionts facilitate rapid evolution in a polyphagous herbivore |
Q52704993 | Energetic cost of calling: general constraints and species-specific differences. |
Q125912581 | Enforced specialization fosters mutual cheating and not division of labour in the bacterium Pseudomonas aeruginosa |
Q33321023 | Engines of speciation: a comparative study in birds of prey |
Q100960735 | Enhanced leaky sex expression in response to pollen limitation in the dioecious plant Mercurialis annua |
Q39188945 | Enhanced male coloration after immune challenge increases reproductive potential |
Q42034828 | Environment and pollinator-mediated selection on parapatric floral races of Mimulus aurantiacus |
Q60441133 | Environment-dependent inbreeding depression in a hermaphroditic freshwater snail |
Q43478926 | Environment-dependent reversal of a life history trade-off in the seed beetle Callosobruchus maculatus |
Q50051796 | Environmental and genetic control of cold tolerance in the Glanville fritillary butterfly. |
Q100527445 | Environmental and morphological constraints interact to drive the evolution of communication signals in frogs |
Q50445383 | Environmental and not maternal effects determine variation in offspring phenotypes in a passerine bird. |
Q30456377 | Environmental conditions during early life determine the consequences of inbreeding in Agrostemma githago (Caryophyllaceae). |
Q34823425 | Environmental determinants of population divergence in life-history traits for an invasive species: climate, seasonality and natural enemies |
Q85006628 | Environmental effects on the detection of adaptation |
Q47251896 | Environmental factors associated with genetic and phenotypic divergence among sympatric populations of Arctic charr (Salvelinus alpinus). |
Q51608245 | Environmental gradients structure Daphnia pulex × pulicaria clonal distribution. |
Q50524165 | Environmental heterogeneity influences the reliability of secondary sexual traits as condition indicators. |
Q52770698 | Environmental heterogeneity, multivariate sexual selection and genetic constraints on cuticular hydrocarbons in Drosophila simulans. |
Q46786900 | Environmental osmolality influences sperm motility activation in an anuran amphibian |
Q61927279 | Environmental stress and the costs of whole-organism phenotypic plasticity in tadpoles |
Q89441494 | Environmental stress does not increase the mean strength of selection |
Q64032223 | Environmental stress, adaptation and evolution: an overview |
Q53627596 | Environmental variation influences the magnitude of inbreeding depression in Cucurbita pepo ssp. texana (Cucurbitaceae). |
Q39526706 | Environmental variation, hybridization, and phenotypic diversification in Cuatro Ciénegas pupfishes. |
Q122861467 | Environmentally independent selection for hybrids between divergent freshwater stickleback lineages in semi‐natural ponds |
Q51705057 | Environmentally induced changes in carotenoid-based coloration of female lizards: a comment on Vercken et al. |
Q39417127 | Environmentally induced dispersal-related life-history syndrome in the tropical butterfly, Bicyclus anynana |
Q30420938 | Epidemiology in evolutionary time: the case of Wolbachia horizontal transmission between arthropod host species |
Q56083611 | Epigenetic inheritance and prions |
Q57883313 | Epigenetic inheritance and prions |
Q60305183 | Epigenetic inheritance in evolution |
Q36396596 | Epigenetics in natural animal populations |
Q60305709 | Epigenetics: Regulation not replication |
Q47419474 | Epistasis affecting litter size in mice. |
Q50716194 | Epistasis and maternal effects in experimental adaptation to chronic nutritional stress in Drosophila. |
Q84065505 | Epistasis and the evolutionary dynamics of measured genotypic values during simulated serial bottlenecks |
Q112246543 | Epistatic interactions of spontaneous mutations in haploid strains of the yeast Saccharomyces cerevisiae |
Q57159437 | Erratum |
Q95432508 | Erratum |
Q95531067 | Erratum |
Q95591372 | Erratum |
Q60533740 | Errors in meta-analyses of selection |
Q61656453 | Escape behaviour and ultimate causes of specific induced defences in an anuran tadpole |
Q51715481 | Escape from flatland. |
Q46308350 | Escape from predators and genetic variance in birds. |
Q52946960 | Escherichia coli populations adapt to complex, unpredictable fluctuations by minimizing trade-offs across environments. |
Q35599902 | Escherichia coli populations in unpredictably fluctuating environments evolve to face novel stresses through enhanced efflux activity |
Q39563769 | Establishing a perimeter position: speciation around the Indian Ocean Basin |
Q51351771 | Estimating fluctuating selection in age-structured populations. |
Q40830673 | Estimating sampling error of evolutionary statistics based on genetic covariance matrices using maximum likelihood. |
Q91533496 | Estimating selection on the act of inbreeding in a population with strong inbreeding depression |
Q46749967 | Estimating the heritability of female lifetime fecundity in a locally adapted Drosophila melanogaster population |
Q33546621 | Estimating the ratio of effective to actual size of an age-structured population from individual demographic data |
Q45367383 | Estimation of effective population size and detection of a recent population decline coinciding with habitat fragmentation in a ground beetle |
Q101045338 | Estimation of environmental, genetic and parental age at conception effects on telomere length in a wild mammal |
Q30909847 | Estimation of relative fitnesses from relative risk data and the predicted future of haemoglobin alleles S and C. |
Q51593468 | Eumelanin- and pheomelanin-based colour advertise resistance to oxidative stress in opposite ways. |
Q60379730 | European Society for Evolutionary Biology 2nd Congress Roma, Italy - September 3-7, 1989 |
Q60379735 | European Society for Evolutionary Biology 2nd Congress Roma, Italy - September 3-7, 1989 |
Q52697943 | Eusociality and the success of the termites: insights from a supertree of dictyopteran families. |
Q39175751 | Evaluating the contributions of change in investment and change in efficiency to age-related declines in male and female reproduction. |
Q104067086 | Evaluating the correlation between genome-wide diversity and the release of plastic phenotypic variation in experimental translocations to novel natural environments |
Q91853115 | Evaluating the existence and benefit of major histocompatibility complex-based mate choice in an isolated owl population |
Q35429819 | Evaluating the post-copulatory sexual selection hypothesis for genital evolution reveals evidence for pleiotropic harm exerted by the male genital spines of Drosophila ananassae |
Q47201119 | Evaluation of offspring size-number invariants in 12 species of lizard |
Q45701904 | Evaluation of pre- and post-zygotic mating barriers, hybrid fitness and phylogenetic relationship between Cyprinodon variegatus variegatus and Cyprinodon variegatus hubbsi (Cyprinodontiformes, Teleostei). |
Q52659262 | Evidence for a robust sex-specific trade-off between cold resistance and starvation resistance in Drosophila melanogaster. |
Q34341266 | Evidence for a single median fin-fold and tail in the Lower Cambrian vertebrate, Haikouichthys ercaicunensis |
Q35163544 | Evidence for adaptive divergence of thermal responses among Bemisia tabaci populations from tropical Colombia following a recent invasion. |
Q43415154 | Evidence for adaptive phenotypic differentiation in Baltic Sea sticklebacks |
Q125811710 | Evidence for an even sex allocation in haplodiploid cyclical parthenogens |
Q33504844 | Evidence for autotetraploidy associated with reproductive isolation in Saccharomyces cerevisiae: towards a new domesticated species |
Q79325890 | Evidence for bimodal hybrid zones between two species of char (Pisces: Salvelinus) in northwestern North America |
Q45832746 | Evidence for complex selection on four-fold degenerate sites in Drosophila melanogaster |
Q34511361 | Evidence for cryptic glacial refugia from North American mountain sheep mitochondrial DNA. |
Q57236956 | Evidence for genetic differentiation in timing of maturation among nine-spined stickleback populations |
Q89018514 | Evidence for lower plasticity in CTMAX at warmer developmental temperatures |
Q38880099 | Evidence for male-biased effective sex ratio and recent step-by-step colonization in the bivalve Pinctada mazatlanica |
Q92803061 | Evidence for rapid downward fecundity selection in an ectoparasite (Philornis downsi) with earlier host mortality in Darwin's finches |
Q34495420 | Evidence for rapid evolution of phenology in an invasive grass |
Q38859170 | Evidence for rapid evolutionary change in an invasive plant in response to biological control |
Q46884182 | Evidence for sex-specific selection in brain: a case study of the nine-spined stickleback |
Q47588331 | Evidence for small scale variation in the vertebrate brain: mating strategy and sex affect brain size and structure in wild brown trout (Salmo trutta). |
Q123140931 | Evidence for the Predator Attraction Hypothesis in an amphibian predator–prey system |
Q112796099 | Evidence of a rapid and adaptive response of hemipteran mouthparts to a physical barrier |
Q46278733 | Evidence of evolutionary optimization of fatty acid length and unsaturation |
Q46633767 | Evidence of gene orthology and trans-species polymorphism, but not of parallel evolution, despite high levels of concerted evolution in the major histocompatibility complex of flamingo species |
Q30822697 | Evidence of genetic change in the flowering phenology of sea beets along a latitudinal cline within two decades. |
Q44641502 | Evidence of multiple paternity and mate selection for inbreeding avoidance in wild eastern chipmunks |
Q47673350 | Evidence of opposing fitness effects of parental heterozygosity and relatedness in a critically endangered marine turtle? |
Q51125371 | Evidence of restoration cost in the annual gynodioecious Phacelia dubia. |
Q33887596 | Evidence of trade-offs shaping virulence evolution in an emerging wildlife pathogen |
Q41737196 | Evidence that microgynes of Myrmica rubra ants are social parasites that attack old host colonies |
Q101631256 | Evolution and biogeography of the genus Tarentola (Sauria: Gekkonidae) in the Canary Islands, inferred from mitochondrial DNA sequences |
Q92447606 | Evolution and diversity of the courtship repertoire in the Drosophila montium species group (Diptera: Drosophilidae) |
Q35665049 | Evolution and functional significance of derived sternal ossification patterns in ornithothoracine birds |
Q33877822 | Evolution and stability of the G-matrix during the colonization of a novel environment. |
Q50733996 | Evolution in stressful environments II: adaptive value and costs of plasticity in response to low light in Sinapis arvensis. |
Q30811056 | Evolution in the sabre-tooth cat, Smilodon fatalis, in response to Pleistocene climate change |
Q92522384 | Evolution of Escherichia coli in different carbon environments for 2,000 generations |
Q45708206 | Evolution of RNA virus in spatially structured heterogeneous environments |
Q52001784 | Evolution of a complex coevolved trait: active pollination in a genus of fig wasps. |
Q89679585 | Evolution of a conspicuous melanin-based ornament in gulls Laridae |
Q44925838 | Evolution of acoustic and visual signals in Asian barbets |
Q46880235 | Evolution of aging: individual life history trade-offs and population heterogeneity account for mortality patterns across species. |
Q35180392 | Evolution of alternative male morphotypes in oxyurid nematodes: a case of convergence? |
Q111263701 | Evolution of antagonistic and mutualistic traits in the yucca‐yucca moth obligate pollination mutualism |
Q40277680 | Evolution of antigenic diversity in the tick-transmitted bacterium Borrelia afzelii: a role for host specialization? |
Q46689181 | Evolution of anuran brains: disentangling ecological and phylogenetic sources of variation |
Q39033188 | Evolution of avian clutch size along latitudinal gradients: do seasonality, nest predation or breeding season length matter? |
Q40798971 | Evolution of behavioural and cellular defences against parasitoid wasps in the Drosophila melanogaster subgroup. |
Q58038293 | Evolution of bite force in Darwin's finches: a key role for head width |
Q56456676 | Evolution of bite performance in turtles |
Q49138141 | Evolution of body condition-dependent dispersal in metapopulations |
Q42647785 | Evolution of body shape in differently coloured sympatric congeners and allopatric populations of Lake Malawi's rock-dwelling cichlids |
Q33321925 | Evolution of bone microanatomy of the tetrapod tibia and its use in palaeobiological inference |
Q99420490 | Evolution of chemotactic hitchhiking |
Q56484059 | Evolution of colour patterns in East African cichlid fish |
Q38334187 | Evolution of complex life cycles in trophically transmitted helminths. I. Host incorporation and trophic ascent |
Q38341978 | Evolution of complex life cycles in trophically transmitted helminths. II. How do life-history stages adapt to their hosts? |
Q47367497 | Evolution of cultural communication systems: the coevolution of cultural signals and genes encoding learning preferences |
Q51887315 | Evolution of cuticular hydrocarbon diversity in ants. |
Q46486995 | Evolution of dark colour in toucans (Ramphastidae): a case of molecular adaptation? |
Q48244910 | Evolution of density-dependent movement during experimental range expansions. |
Q87391433 | Evolution of dispersal in metacommunities of interacting species |
Q52007557 | Evolution of dispersal in metapopulations with local density dependence and demographic stochasticity. |
Q46893293 | Evolution of egg dummies in Tanganyikan cichlid fishes: the roles of parental care and sexual selection |
Q52649752 | Evolution of eusociality and the soldier caste in termites: a validation of the intrinsic benefit hypothesis. |
Q46489649 | Evolution of extrafloral nectaries: adaptive process and selective regime changes from forest to savanna. |
Q59622875 | Evolution of grasping among anthropoids |
Q51811595 | Evolution of habitat-dependent sex allocation in plants: superficially similar to, but intrinsically different from animals. |
Q51956111 | Evolution of handling time can destroy the coexistence of cycling predators. |
Q35001276 | Evolution of host resistance and trade-offs between virulence and transmission potential in an obligately killing parasite. |
Q52838787 | Evolution of increased adult longevity in Drosophila melanogaster populations selected for adaptation to larval crowding. |
Q128364540 | Evolution of intermediate latency strategies in seasonal parasites |
Q125475593 | Evolution of intraspecific floral variation in a generalist–specialist pollination system |
Q48151670 | Evolution of larval competitiveness and associated life-history traits in response to host shifts in a seed beetle |
Q42036395 | Evolution of larval host plant associations and adaptive radiation in pierid butterflies |
Q44377612 | Evolution of late-life fecundity in Drosophila melanogaster |
Q115033096 | Evolution of life cycles and reproductive traits: Insights from the brown algae |
Q50939055 | Evolution of male age-specific reproduction under differential risks and causes of death: males pay the cost of high female fitness. |
Q84368972 | Evolution of maternal care in diploid and haplodiploid populations |
Q93074480 | Evolution of mating types in finite populations: The precarious advantage of being rare |
Q47415077 | Evolution of monogamous marriage by maximization of inclusive fitness |
Q48317035 | Evolution of morphology and locomotor performance in anurans: relationships with microhabitat diversification |
Q125924303 | Evolution of multiple prey defences: From predator cognition to community ecology |
Q90126659 | Evolution of multivariate wing allometry in schizophoran flies (Diptera: Schizophora) |
Q51091463 | Evolution of paternal care in diploid and haplodiploid populations. |
Q110616052 | Evolution of phenotypic plasticity a comparative approach in the phylogenetic neighbourhood of Arabidopsis thaliana |
Q50671017 | Evolution of phenotypic plasticity and environmental tolerance of a labile quantitative character in a fluctuating environment. |
Q90831375 | Evolution of phenotypic plasticity: Genetic differentiation and additive genetic variation for induced plant defence in wild arugula Eruca sativa |
Q115033072 | Evolution of physical linkage between loci controlling ecological traits and mating preferences |
Q46839587 | Evolution of pleiotropic costs in experimental populations |
Q47617628 | Evolution of precopulatory and post-copulatory strategies of inbreeding avoidance and associated polyandry |
Q48275505 | Evolution of recombination rates and the genomic landscape of speciation |
Q46665827 | Evolution of reduced post-copulatory molecular interactions in Drosophila populations lacking sperm competition |
Q51635852 | Evolution of reproductive effort in viscous populations: the importance of population dynamics. |
Q37664065 | Evolution of resistance to single and combined floral phytochemicals by a bumble bee parasite. |
Q109967545 | Evolution of resource allocation between growth and reproduction in animals with indeterminate growth |
Q112796095 | Evolution of seed mass associated with mating systems in multiple plant families |
Q39818475 | Evolution of sex chromosomes prior to speciation in the dioecious Phoenix species. |
Q46800729 | Evolution of sex-biased maternal effects in birds. IV. Intra-ovarian growth dynamics can link sex determination and sex-specific acquisition of resources |
Q40470657 | Evolution of sex-biased maternal effects in birds: I. Sex-specific resource allocation among simultaneously growing oocytes. |
Q40328216 | Evolution of sex-biased maternal effects in birds: II. Contrasting sex-specific oocyte clustering in native and recently established populations |
Q50647973 | Evolution of sex-biased maternal effects in birds: III. Adjustment of ovulation order can enable sex-specific allocation of hormones, carotenoids, and vitamins. |
Q49187088 | Evolution of sexual dichromatism in relation to nesting habits in European passerines: a test of Wallace's hypothesis |
Q112810466 | Evolution of sexual size dimorphism in birds: test of hypotheses using blue tits in contrasted Mediterranean habitats |
Q33493574 | Evolution of sexual size dimorphism in grouse and allies (Aves: Phasianidae) in relation to mating competition, fecundity demands and resource division |
Q34017777 | Evolution of sexual size monomorphism: the influence of passive mate guarding. |
Q38273506 | Evolution of spatially structured host-parasite interactions. |
Q51634637 | Evolution of specialization in a spatially continuous environment. |
Q92987916 | Evolution of specialized microbial cooperation in dynamic fluids |
Q51553358 | Evolution of sperm quality but not quantity in the internally fertilized fish Xiphophorus nigrensis. |
Q36298339 | Evolution of starvation resistance in Drosophila melanogaster: measurement of direct and correlated responses to artificial selection. |
Q45721086 | Evolution of stickleback feeding behaviour: genetics of population divergence at different ontogenetic stages |
Q58869812 | Evolution of the alternation of haploid and diploid phases in life cycles. II. Maintenance of the haplo-diplontic cycle |
Q79839433 | Evolution of the isochore structure in the scale of chromosome: insight from the mutation bias and fixation bias |
Q129355536 | Evolution of thermal performance curves: A meta‐analysis of selection experiments |
Q42000684 | Evolution of tolerance in an invasive weed after reassociation with its specialist herbivore |
Q31134058 | Evolution of total net fitness in thermal lines: Drosophila subobscura likes it 'warm'. |
Q62085695 | Evolution of trophic transmission in parasites: the need to reach a mating place? |
Q40265607 | Evolution of virulence under intensive farming: salmon lice increase skin lesions and reduce host growth in salmon farms |
Q63628678 | Evolution of viviparity in horned lizards (Phrynosoma): testing the cold-climate hypothesis |
Q33283073 | Evolution of viviparity in warm-climate lizards: an experimental test of the maternal manipulation hypothesis |
Q24671758 | Evolution of whole-body enantiomorphy in the tree snail genus Amphidromus |
Q35366469 | Evolution of wing shape in hornets: why is the wing venation efficient for species identification? |
Q56919296 | Evolution on Two Scales A review by M. J. Benton. Evolution and Ecology. The Pace of Life. By K. D. Bennett. Cambridge University Press, Cambridge, 1997. xviii + 241 pages. ISBN: 0-521-39028-1 (hardback), 0-52139921-1 (paperback). Price $69.95/f50.00 |
Q84456702 | Evolution towards self-compatibility when mates are limited |
Q29040228 | Evolution, development and complexity in Pere Alberch (1954-1998) |
Q46651464 | Evolution, plasticity and evolving plasticity of phenology in the tree species Alnus glutinosa |
Q33715739 | Evolutionarily accelerated invasions: the rate of dispersal evolves upwards during the range advance of cane toads |
Q28596166 | Evolutionarily advanced ant farmers rear polyploid fungal crops |
Q34666428 | Evolutionary acceleration in the most endangered mammal of Canada: speciation and divergence in the Vancouver Island marmot (Rodentia, Sciuridae). |
Q38681327 | Evolutionary allometry reveals a shift in selection pressure on male horn size. |
Q51725482 | Evolutionary aspects of population structure for molecular and quantitative traits in the freshwater snail Radix balthica. |
Q125853850 | Evolutionary aspects of the metapopulation dynamics of Biomphalaria pfeifferi, the intermediate host of Schistosoma mansoni |
Q38967197 | Evolutionary associations between host traits and parasite load: insights from Lake Tanganyika cichlids |
Q112796096 | Evolutionary biology and development model of medicines: A necessary ‘pas de deux’ for future successful bacteriophage therapy |
Q36917105 | Evolutionary biology of starvation resistance: what we have learned from Drosophila. |
Q38738829 | Evolutionary bottlenecks in brackish water habitats drive the colonization of fresh water by stingrays. |
Q51236264 | Evolutionary changes in plant tolerance against herbivory through a resurrection experiment. |
Q47304325 | Evolutionary divergence and possible incipient speciation in post-glacial populations of a cosmopolitan aquatic plant |
Q60379700 | Evolutionary divergence in Dolichopoda cave crickets: A comparison of single copy DNA hybridization data with allozymes and morphometric distances |
Q115033076 | Evolutionary divergence in phenotypic plasticity shapes brain size variation between coexisting sunfish ecotypes |
Q51152371 | Evolutionary divergence of reaction norms in ecological context: a commentary. |
Q33294919 | Evolutionary diversification of clades of squamate reptiles |
Q46403864 | Evolutionary diversification of the auditory organ sensilla in Neoconocephalus katydids (Orthoptera: Tettigoniidae) correlates with acoustic signal diversification over phylogenetic relatedness and life history. |
Q52676933 | Evolutionary domestication in Drosophila subobscura. |
Q50482157 | Evolutionary dynamics and population biology of a polymorphic insect. |
Q52648274 | Evolutionary dynamics of a B chromosome invasion in island populations of the grasshopper Eyprepocnemis plorans. |
Q51392298 | Evolutionary dynamics of interlinked public goods traits: an experimental study of siderophore production in Pseudomonas aeruginosa. |
Q85028568 | Evolutionary dynamics of mating system shifts in Arabidopsis lyrata |
Q114621941 | Evolutionary dynamics of sex‐biased genes expressed in cricket brains and gonads |
Q46294954 | Evolutionary dynamics of the leaf phenological cycle in an oak metapopulation along an elevation gradient. |
Q50734003 | Evolutionary ecology of Datura stramonium: equal plant fitness benefits of growth and resistance against herbivory. |
Q48244874 | Evolutionary emergence and maintenance of horizontally transmitted mutualism that do not rely on the supply of standing variation in symbiont quality |
Q38597929 | Evolutionary genetic consequences of facultative sex and outcrossing |
Q56814337 | Evolutionary genetics and ecology of sperm-dependent parthenogenesis |
Q56865557 | Evolutionary genetics and ecology of sperm-dependent parthenogenesis |
Q42044144 | Evolutionary genetics of dorsal wing colour in Colias butterflies |
Q62638489 | Evolutionary genetics of sex-limited traits under fluctuating selection |
Q115390689 | Evolutionary history and ecology shape the diversity and abundance of phytochemical arsenals across monkeyflowers |
Q47361940 | Evolutionary history of asexual hybrid loaches (Cobitis: Teleostei) inferred from phylogenetic analysis of mitochondrial DNA variation |
Q38901437 | Evolutionary history of the butterflyfishes (f: Chaetodontidae) and the rise of coral feeding fishes. |
Q35896911 | Evolutionary history of the little fire ant Wasmannia auropunctata before global invasion: inferring dispersal patterns, niche requirements and past and present distribution within its native range |
Q51657230 | Evolutionary history shapes the association between developmental instability and population-level genetic variation in three-spined sticklebacks. |
Q44991229 | Evolutionary impacts of hybridization and interspecific gene flow on an obligately estuarine fish |
Q47348627 | Evolutionary implications of mitochondrial genetic variation: mitochondrial genetic effects on OXPHOS respiration and mitochondrial quantity change with age and sex in fruit flies |
Q59442917 | Evolutionary implications of the mode of D quadrant specification in coelomates with spiral cleavage |
Q44792038 | Evolutionary mode, tempo, and phylogenetic association of continuous morphological traits in the aquatic moss genus Amblystegium |
Q84201894 | Evolutionary modularity of the mouse mandible: dissecting the effect of chromosomal reorganizations and isolation by distance in a Robertsonian system of Mus musculus domesticus |
Q43705760 | Evolutionary neutrality of mtDNA introgression: evidence from complete mitogenome analysis in roe deer. |
Q61762087 | Evolutionary patterns and mechanisms in consumer-resource interactions |
Q91743494 | Evolutionary potential of a widespread clonal grass under changing climate |
Q39078943 | Evolutionary potential of morphological traits across different life-history stages |
Q91634577 | Evolutionary potential of thermal preference and heat tolerance in Drosophila subobscura |
Q37164670 | Evolutionary problems in centrosome and centriole biology |
Q39150663 | Evolutionary reduction of developmental plasticity in desert spadefoot toads |
Q38369213 | Evolutionary relationships among pollinators and repeated pollinator sharing in sexually deceptive orchids. |
Q52744022 | Evolutionary relationships of flavobacterial and enterobacterial endosymbionts with their scale insect hosts (Hemiptera: Coccoidea). |
Q109351725 | Evolutionary rescue at different rates of environmental change is affected by trade‐offs between short‐term performance and long‐term survival |
Q110616054 | Evolutionary responses ofDrosophila melanogasterto selection at different larval densities: changes in genetic variation, specialization and phenotypic plasticity |
Q39909272 | Evolutionary routes to stable ownership. |
Q47776805 | Evolutionary specialization in mammalian cortical structure |
Q35592689 | Evolutionary stasis despite selection on a heritable trait in an invasive zooplankton |
Q34214085 | Evolutionary stasis in Euphorbiaceae pollen: selection and constraints |
Q33340891 | Evolutionary traction: the cost of adaptation and the evolution of sex. |
Q49561442 | Evolutionary trade-offs in locomotor capacities in lacertid lizards: are splendid sprinters clumsy climbers? |
Q90028729 | Evolutionary transition between bee pollination and hummingbird pollination in Salvia: Comparing means, variances and covariances of corolla traits |
Q84456695 | Evolutionary transitions among dioecy, androdioecy and hermaphroditism in limnadiid clam shrimp (Branchiopoda: Spinicaudata) |
Q79315697 | Evolvability and genetic constraint in Dalechampia blossoms: components of variance and measures of evolvability |
Q50440842 | Evolvability of an avian life history trait declines with father's age |
Q42003764 | Evolved variation in cold tolerance among populations of Eldana saccharina (Lepidoptera: Pyralidae) in South Africa. |
Q41060859 | Exaggerated male genitalia intensify interspecific reproductive interference by damaging heterospecific female genitalia. |
Q52641793 | Examining costs of induced and constitutive immune investment in Tenebrio molitor. |
Q30449370 | Examining the social landscapes of alternative reproductive strategies. |
Q59693129 | Existence of a pattern of reproductive character displacement in Homobasidiomycota but not in Ascomycota |
Q51087739 | Experimental adaptation to high and low quality environments under different scales of temporal variation. |
Q115555192 | Experimental analysis of an early life-history stage: avian predation selects for larger body size of hatchling turtles |
Q57205430 | Experimental analysis of the evolutionary potential of hybridization in leopard frogs (Anura: Ranidae) |
Q38962084 | Experimental and genetic analyses reveal that inbreeding depression declines with increased self-fertilization among populations of a coastal dune plant |
Q51598323 | Experimental coevolution leads to a decrease in parasite-induced host mortality. |
Q92116107 | Experimental evidence for accelerated adaptation to desiccation through sexual selection on males |
Q33826760 | Experimental evidence for the phenotypic impact of admixture between wild and biocontrol Asian ladybird (Harmonia axyridis) involved in the European invasion |
Q92670206 | Experimental evidence for the role of sexual selection in the evolution of cuticular hydrocarbons in the dung beetle, Onthophagus taurus |
Q44822273 | Experimental evidence for trait utility of gill raker number in adaptive radiation of a north temperate fish |
Q84002375 | Experimental evidence of early costs of reproduction in conspecific viviparous and oviparous lizards |
Q34914472 | Experimental evidence that competition and habitat use shape the individual fitness surface |
Q51646301 | Experimental evidence that high levels of inbreeding depress sperm competitiveness. |
Q90739997 | Experimental evolution demonstrates evolvability of preferential nutrient allocation to competing traits in response to chronic malnutrition |
Q44655394 | Experimental evolution for generalists and specialists reveals multivariate genetic constraints on thermal reaction norms |
Q35565310 | Experimental evolution in fluctuating environments: tolerance measurements at constant temperatures incorrectly predict the ability to tolerate fluctuating temperatures |
Q35170027 | Experimental evolution of external immune defences in the red flour beetle. |
Q34776715 | Experimental evolution of field populations of Daphnia magna in response to parasite treatment. |
Q48339086 | Experimental evolution of infectious behaviour in a facultative ectoparasite |
Q51632482 | Experimental evolution of local parasite maladaptation. |
Q51616716 | Experimental evolution of protozoan traits in response to interspecific competition |
Q38694430 | Experimental evolution reveals differences between phenotypic and evolutionary responses to population density. |
Q91544095 | Experimental evolution reveals divergence in female genital teeth morphology in response to sexual conflict intensity in a moth |
Q50063803 | Experimental infection magnifies inbreeding depression in house mice |
Q57027079 | Experimental life-history evolution: selection on growth form and its plasticity in a clonal plant |
Q47269061 | Experimental manipulation of population-level MHC diversity controls pathogen virulence evolution in Mus musculus. |
Q46256297 | Experimental manipulation reveals a trade-off between weapons and testes. |
Q51636693 | Experimental modifications imply a stimulatory function for male tsetse fly genitalia, supporting cryptic female choice theory. |
Q34335409 | Experimental reduction of codon bias in the Drosophila alcohol dehydrogenase gene results in decreased ethanol tolerance of adult flies |
Q115033084 | Experimental sexual selection affects the evolution of physiological and life‐history traits |
Q46447179 | Experimental sexual selection in Chlamydomonas |
Q60370394 | Experimental study of temperature effects on the sex ratio of broods in Terrestrial Crustacea Armadillidium vulgare Latr. Possible implications in natural populations |
Q39978399 | Experimental support for the role of nest predation in the evolution of brood parasitism |
Q85028579 | Experimental test of a trade‐off between moult and immune response in house sparrows Passer domesticus |
Q40366807 | Experimental tests of host-virus coevolution in natural killer yeast strains. |
Q48042486 | Experimentally evolved and phenotypically plastic responses to enforced monogamy in a hermaphroditic flatworm |
Q50222090 | Experimentally increased reproductive effort alters telomere length in the blue tit (Cyanistes caeruleus). |
Q40083292 | Experimentally induced host-shift changes life-history strategy in a seed beetle. |
Q99566750 | Experimentally induced intrasexual mating competition and sex-specific evolution in female and male nematodes |
Q30872292 | Explaining the sawtooth: latitudinal periodicity in a circadian gene correlates with shifts in generation number. |
Q44228881 | Exploring patterns of variation in clutch size-density reaction norms in a wild passerine bird. |
Q84146225 | Exploring the effect of the Cardinium endosymbiont on spiders |
Q28268428 | Exploring the evolution of environmental sex determination, especially in reptiles |
Q51225029 | Exposure to a novel male during late pregnancy influences subsequent growth of offspring during lactation. |
Q46747761 | Expression of sexual ornaments in a polymorphic species: phenotypic variation in response to environmental risk |
Q34833479 | Extensive hybridization and associated geographic trends between two rockfishes Sebastes vulpes and S. zonatus (Teleostei: Scorpaeniformes: Sebastidae). |
Q91529462 | Extensive hybridization and past introgression between divergent lineages in a quasi-clonal hermaphroditic fish: ramifications for species concepts and taxonomy |
Q89006357 | Extensive phenotypic diversification coexists with little genetic divergence and a lack of population structure in the White Wagtail subspecies complex (Motacilla alba) |
Q89174308 | Extent of adaptation is not limited by unpredictability of the environment in laboratory populations of Escherichia coli |
Q102145518 | Extinction and the temporal distribution of macroevolutionary bursts |
Q34335414 | Extinction of the acoustic startle response in moths endemic to a bat-free habitat |
Q46469466 | Extra-nuclear effects on growth and development in the sand cricket Gryllus firmus |
Q46122002 | Extra-pair fertilizations contribute to selection on secondary male ornamentation in a socially monogamous passerine |
Q89759661 | Extra-pair paternity as a strategy to reduce the costs of heterospecific reproduction? Insights from the crow hybrid zone |
Q40006717 | Extreme genetic diversity in asexual grass thrips populations |
Q47300872 | Extreme mtDNA divergences in a terrestrial slug (Gastropoda, Pulmonata, Arionidae): accelerated evolution, allopatric divergence and secondary contact |
Q91439986 | Extreme variation in testes size in an insect is linked to recent mating activity |
Q91450113 | Extrinsic and intrinsic constraints interact to drive extra-pair paternities in the Alpine marmot |
Q88887478 | Eyes Wide Shut: the impact of dim-light vision on neural investment in marine teleosts |
Q57649062 | Facing the facts |
Q33943687 | Factors influencing progress toward sympatric speciation. |
Q125376928 | Factors influencing the composition of mixed populations of a hemiclonal hybrid and its sexual host |
Q49561369 | Facultative sex allocation in snow skink lizards (Niveoscincus microlepidotus). |
Q51814367 | Facultative use of thelytokous parthenogenesis for queen production in the polyandrous ant Cataglyphis cursor. |
Q51294442 | Faithful females receive more help: the extent of male parental care during incubation in relation to extra-pair paternity in songbirds. |
Q46947018 | Faster clonal turnover in high-infection habitats provides evidence for parasite-mediated selection. |
Q39024050 | Faster evolution of highly conserved DNA in tropical plants |
Q47260490 | Feather mites and birds: an interaction mediated by uropygial gland size? |
Q37233254 | Fecundity compensation and tolerance to a sterilizing pathogen in Daphnia |
Q50277613 | Fecundity selection on ornamental plumage colour differs between ages and sexes and varies over small spatial scales. |
Q39780894 | Feeding with speed: prey capture evolution in cichilds |
Q51548296 | Female Cape sugarbirds (Promerops cafer) modify egg investment both for extra-pair mates and for male tail length. |
Q28249242 | Female ambrosia beetles adjust their offspring sex ratio according to outbreeding opportunities for their sons |
Q50266045 | Female behaviour and the interaction of male and female genital traits mediate sperm transfer during mating. |
Q46680238 | Female choice for male cuticular hydrocarbon profile in decorated crickets is not based on similarity to their own profile |
Q35592167 | Female choice of sexually antagonistic male adaptations: a critical review of some current research |
Q50462745 | Female coloration indicates female reproductive capacity in blue tits. |
Q51830625 | Female common lizards (Lacerta vivipara) do not adjust their sex-biased investment in relation to the adult sex ratio. |
Q28292212 | Female crickets assess relatedness during mate guarding and bias storage of sperm towards unrelated males |
Q46339087 | Female crickets trade offspring viability for fecundity |
Q40215863 | Female discrimination thresholds frequently exceed local male display variation: implications for mate choice dynamics and sexual selection |
Q46893402 | Female effects, but no intrinsic male effects on paternity outcome in crickets. |
Q47641281 | Female fecundity and offspring survival are not increased through sexual cannibalism in the spider Larinioides sclopetarius. |
Q35175421 | Female house mice avoid fertilization by t haplotype incompatible males in a mate choice experiment. |
Q51735107 | Female mate choice across mating stages and between sequential mates in flour beetles. |
Q46828783 | Female mate choice predicts paternity success in the absence of additive genetic variance for other female paternity bias mechanisms in Drosophila serrata |
Q51560118 | Female mate preferences in Drosophila simulans: evolution and costs. |
Q89018487 | Female mate preferences on high-dimensional shape variation for male species recognition traits |
Q101134384 | Female mating experience and genetic background independently influence male mating success in fruit flies |
Q51605293 | Female nutritional status determines the magnitude and sign of responses to a male ejaculate signal in Drosophila melanogaster. |
Q49561462 | Female polyandry affects their sons' reproductive success in the red flour beetle Tribolium castaneum |
Q46467034 | Female preference functions drive interpopulation divergence in male signalling: call diversity in the bushcricket Ephippiger diurnus. |
Q115033098 | Female reproductive mode shapes allometric scaling of male traits in live‐bearing fishes (family Poeciliidae) |
Q43976826 | Female resistance behaviour and progeny sex ratio in two Bradysia species (Diptera: Sciaridae) with paternal genome elimination |
Q92002455 | Female resistance to sexual coercion can evolve to preserve the indirect benefits of mate choice |
Q96964759 | Female sperm storage mediates postcopulatory costs and benefits of ejaculate anticipatory plasticity in the guppy |
Q91822337 | Female-driven intersexual coevolution in beetle genitalia |
Q52641775 | Females avoid manipulative males and live longer. |
Q43906713 | Females benefit from multiple mating but not multiple mates in the burying beetle Nicrophorus vespilloides |
Q38611883 | Females drive asymmetrical introgression from rare to common species in Darwin's tree finches |
Q43410490 | Females suffer a reduction in the viability of stored sperm following an immune challenge |
Q58039334 | Fertility interactions in Drosophila: Theoretical model and experimental tests |
Q34946985 | Fewer invited talks by women in evolutionary biology symposia. |
Q92391063 | Field estimates of fitness costs of the pace-of-life in an endangered damselfly |
Q37696526 | Fight or flight? - Flight increases immune gene expression but does not help to fight an infection |
Q57172674 | Finding the one: optimal choosiness under sequential mate choice |
Q40315241 | Fine scale spatial structuring of sex and mitochondria in Silene vulgaris |
Q51332334 | Fine-scale genetic analysis of species-specific female preference in Drosophila simulans. |
Q59293271 | Fine-scale genetic structure and gene dispersal in Centaurea corymbosa (Asteraceae) I. Pattern of pollen dispersal |
Q51767930 | Fisher's fundamental theorem of inclusive fitness and the change in fitness due to natural selection when conspecifics interact. |
Q39440381 | Fisher's sons' effect in sexual selection: absent, intermittent or just low experimental power? |
Q91972951 | Fitness advantages of the biased use of paired laterally symmetrical penises in an insect |
Q46906690 | Fitness and morphological outcomes of many generations of hybridization in the copepod Tigriopus californicus. |
Q28305989 | Fitness and the level of homozygosity in a social insect |
Q44635734 | Fitness conflicts and the costs of sociality in communal egg layers: a theoretical model and empirical tests |
Q30454665 | Fitness consequences of social network position in a wild population of forked fungus beetles (Bolitotherus cornutus). |
Q90665786 | Fitness consequences of the selfish supergene Segregation Distorter |
Q28290944 | Fitness consequences of variable maternal provisioning in quacking frogs (Crinia georgiana) |
Q83153121 | Fitness correlates with the extent of cheating in a bacterium |
Q30972910 | Fitness declines towards range limits and local adaptation to climate affect dispersal evolution during climate-induced range shifts. |
Q42027209 | Fitness differences associated with Pgi SNP genotypes in the Glanville fritillary butterfly (Melitaea cinxia). |
Q46618032 | Fitness differences between parapatric lake and stream stickleback revealed by a field transplant |
Q33724661 | Fitness disadvantages to disrupted embryogenesis impose selection against suboptimal nest-site choice by female grass snakes, Natrix natrix (Colubridae) |
Q51780602 | Fitness effects of X chromosome drive in the stalk-eyed fly, Cyrtodiopsis dalmanni. |
Q39669929 | Fitness effects of female mate choice: preferred males are detrimental for Drosophila melanogaster females. |
Q48305528 | Fitness effects of mutation: testing genetic redundancy in Arabidopsis thaliana. |
Q42110743 | Fitness effects of new mutations in Chlamydomonas reinhardtii across two stress gradients. |
Q51095192 | Fitness landscapes emerging from pharmacodynamic functions in the evolution of multidrug resistance. |
Q56838455 | Fitness measures in selection analyses: sensitivity to the overall number of offspring produced in a lifetime |
Q92372275 | Fitness of reciprocal F1 hybrids between Rhinanthus minor and Rhinanthus major under controlled conditions and in the field |
Q43854297 | Fitness trade-offs and the maintenance of alternative male morphs in the bulb mite (Rhizoglyphus robini). |
Q42239239 | Fitness valleys constrain HIV-1's adaptation to its secondary chemokine coreceptor. |
Q50123447 | Fitness variation among host species and the paradox of ineffective rhizobia |
Q79321153 | Fitness-associated recombination on rugged adaptive landscapes |
Q49561432 | Fitness-consequences of geitonogamous selfing in a clonal marine angiosperm (Zostera marina). |
Q46328071 | Fitness-dependent mutation rates in finite populations |
Q33398072 | Five questions on ecological speciation addressed with individual-based simulations |
Q47235839 | Fixed effect variance and the estimation of repeatabilities and heritabilities: Issues and solutions. |
Q48313495 | Flexible mate choice may contribute to ecotype assortative mating in pumpkinseed sunfish (Lepomis gibbosus). |
Q79325884 | Flexible mating: cross-pollination affects sex-expression in a marine clonal plant |
Q87845378 | Flexible parents: joint effects of handicapping and brood size manipulation on female parental care in Nicrophorus vespilloides |
Q48210095 | Flies who cannot take the heat: genome-wide gene expression analysis of temperature-sensitive lethality in an inbred line of Drosophila melanogaster. |
Q47200625 | Flight of Sharovipteryx mirabilis: the world's first delta-winged glider |
Q52646279 | Floral evolution and pollinator mate choice in a sexually deceptive orchid. |
Q61697949 | Floral integration, phenotypic covariance structure and pollinator variation in bumblebee-pollinated Helleborus foetidus |
Q46816372 | Floral isolation is the major reproductive barrier between a pair of rewarding orchid sister species |
Q46887377 | Floral odour and reproductive isolation in two species of Silene. |
Q96161745 | Floral trait differentiation in Anacamptis coriophora: phenotypic selection on scents, but not on colour |
Q52002132 | Flowering time plasticity in Arabidopsis thaliana: a reanalysis of Westerman & Lawrence (1970). |
Q36623195 | Fluctuating asymmetry and developmental instability in evolutionary biology: past, present and future |
Q50733999 | Fluctuating asymmetry in a secondary sexual trait: no associations with individual fitness, environmental stress or inbreeding, and no heritability. |
Q57228288 | Fluctuating asymmetry in red junglefowl |
Q104206900 | Fluctuating asymmetry of sexual and nonsexual traits in stalk-eyed flies: a poor indicator of developmental stress and genetic quality |
Q64032474 | Fluctuating asymmetry, fecundity and development time in Drosophila: is there an association under optimal and stress conditions? |
Q49586357 | Fluctuating selection and its (elusive) evolutionary consequences in a wild rodent population. |
Q47168395 | Fluctuating viability selection on morphology of cliff swallows is driven by climate |
Q79753828 | Flycatcher song in allopatry and sympatry--convergence, divergence and reinforcement |
Q42092601 | Fold or hold: experimental evolution in vitro. |
Q38441100 | Food availability affects the maternal transfer of androgens and antibodies into eggs of a colonial seabird |
Q43433768 | Food fight: sexual conflict over free amino acids in the nuptial gifts of male decorated crickets. |
Q35604819 | Foraging mode affects the evolution of egg size in generalist predators embedded in complex food webs |
Q79787821 | Foraging performance of diet-induced morphotypes in pumpkinseed sunfish (Lepomis gibbosus) favours resource polymorphism |
Q91558978 | Fork tails evolved differently in swallows and swifts |
Q56919343 | Form and Function and Phylogeny A review by M. J. Benton. Life's Splendid Drama. By P. J. Bowler. Chicago University Press. 1996. 533 pages. f30.25 (US $37.95). ISBN: 0-226-06921-4 (cloth), 0-226-06922-2 (paper) |
Q29541152 | Form follows function: morphological diversification and alternative trapping strategies in carnivorous Nepenthes pitcher plants |
Q52641782 | Forty years of solitude: life-history divergence and behavioural isolation between laboratory lines of Drosophila melanogaster. |
Q42036997 | Fossil-calibrated molecular phylogenies reveal that leaf-mining moths radiated millions of years after their host plants. |
Q45892960 | Fossils and phylogeny uncover the evolutionary history of a unique antipredator behaviour. |
Q52641830 | Foundress re-emergence and fig permeability in fig tree-wasp mutualisms. |
Q51866631 | Frequency and inheritance of non-male producing clones in Daphnia magna: evolution towards sex specialization in a cyclical parthenogen? |
Q79321116 | Frequency dependence in matings with water-borne sperm |
Q33352788 | Frequency of independent origins of viviparity among caecilians (Gymnophiona): evidence from the first 'live-bearing' Asian amphibian |
Q79238746 | Frequency-dependent predation and maintenance of prey polymorphism |
Q47779696 | Frequency-dependent selection acting on the widely fluctuating sex ratio of the aphid Prociphilus oriens |
Q113036738 | Frequency-dependent selection by pollinators: mechanisms and consequences with regard to behaviour of bumblebees Bombus terrestris (L.) (Hymenoptera: Apidae) |
Q44319643 | From kissing to belly stridulation: comparative analysis reveals surprising diversity, rapid evolution, and much homoplasy in the mating behaviour of 27 species of sepsid flies (Diptera: Sepsidae). |
Q45981293 | From nature to the laboratory: the impact of founder effects on adaptation. |
Q46942284 | Frugivores and cheap fruits make fruiting fruitful. |
Q33584086 | Functional adaptation of spiriferide brachiopod morphology |
Q92743609 | Functional consequences of phenotypic variation between locally adapted populations: Swimming performance and ventilation in extremophile fish |
Q35468696 | Functional constraints on the evolution of long butterfly proboscides: lessons from Neotropical skippers (Lepidoptera: Hesperiidae). |
Q46624535 | Functional decoupling between flowers and leaves in the Ameroglossum pernambucense complex can facilitate local adaptation across a pollinator and climatic heterogeneous landscape |
Q97079877 | Functional implications of the specialized staminal appendages in alpine ginger (Roscoea spp.: Zingiberaceae) |
Q47844569 | Functional rare males in diploid parthenogenetic Artemia. |
Q45924993 | Functional replacement of a primary metabolic pathway via multiple independent eukaryote-to-eukaryote gene transfers and selective retention. |
Q47366635 | Functional significance of seminal receptacle length in Drosophila melanogaster |
Q79321118 | Functional trade-offs in the limb muscles of dogs selected for running vs. fighting |
Q50890586 | Game theory and the evolution of fearfulness in wild birds. |
Q81543364 | Games among cannibals: competition to cannibalize and parent-offspring conflict lead to increased sibling cannibalism |
Q34432922 | Gateway to genetic exchange? DNA double-strand breaks in the bdelloid rotifer Adineta vaga submitted to desiccation |
Q51706650 | Gene expression profile analysis of Drosophila melanogaster selected for resistance to environmental stressors. |
Q48548656 | Gene flow across a hybrid zone maintained by a weak heterogametic incompatibility and positive selection of incompatible alleles |
Q113348647 | Gene flow and immigration rate in an island population of great tits |
Q60289789 | Gene flow and species cohesion following the spread of Schiedea globosa (Caryophyllaceae) across the Hawaiian Islands |
Q45884337 | Gene flow between sexual and asexual strains of parasitic wasps: a possible case of sympatric speciation caused by a parthenogenesis-inducing bacterium |
Q58776144 | Gene flow does not prevent personality and morphological differentiation between two blue tit populations |
Q58039315 | Gene flow rates in Yugoslavian populations of the smooth newt Triturus vulgaris |
Q34092536 | General quantitative genetic methods for comparative biology: phylogenies, taxonomies and multi-trait models for continuous and categorical characters |
Q41069138 | Generation of a neutral FST baseline for testing local adaptation on gill raker number within and between European whitefish ecotypes in the Baltic Sea basin |
Q46170942 | Generative models versus underlying symmetries to explain biological pattern |
Q110616051 | Genes affecting phenotypic plasticity in Arabidopsis : pleiotropic effects and reproductive fitness of photomorphogenic mutants |
Q54691706 | Genes under weaker stabilizing selection increase network evolvability and rapid regulatory adaptation to an environmental shift. |
Q38726538 | Genetic accommodation in the wild: evolution of gene expression plasticity during character displacement |
Q34470516 | Genetic admixture supports an ancient hybrid origin of the endangered Hawaiian duck |
Q33366833 | Genetic analysis of sympatric char populations in western Alaska: Arctic char (Salvelinus alpinus) and Dolly Varden (Salvelinus malma) are not two sides of the same coin |
Q44576013 | Genetic and environmental effects on a condition-dependent trait: feather growth in Siberian jays |
Q81317955 | Genetic and environmental effects on secondary sex traits in guppies (Poecilia reticulata) |
Q33890465 | Genetic and environmental sources of covariance among internal reproductive traits in the yellow dung fly. |
Q63975776 | Genetic and environmental variation in immune response of collared flycatcher nestlings |
Q50485124 | Genetic and environmental variation in the visual properties of bluefin killifish, Lucania goodei. |
Q30975411 | Genetic and morphological data supporting the hypothesis of adaptive radiation in the endemic fish of Lake Matano |
Q48001418 | Genetic and morphological differentiation in Tephritis bardanae (Diptera: Tephritidae): evidence for host-race formation |
Q99552745 | Genetic and morphological divergence between Littorina fabalis ecotypes in Northern Europe |
Q51574397 | Genetic and nutritional effects on male traits and reproductive performance in Tribolium flour beetles. |
Q57520009 | Genetic and phenotypic influences on clone-level success and host specialization in a generalist parasite |
Q42014106 | Genetic and phenotypic variation in juvenile development in relation to temperature and developmental pathway in a geometrid moth. |
Q52641787 | Genetic architecture for normal and novel host-plant use in two local populations of the herbivorous ladybird beetle, Epilachna pustulosa. |
Q43933771 | Genetic architecture of population differences in oviposition behaviour of the seed beetle Callosobruchus maculatus |
Q42006363 | Genetic architecture of sensory exploitation: QTL mapping of female and male receiver traits in an acoustic moth. |
Q52641827 | Genetic architecture of susceptibility to herbivores in hybrid willows. |
Q51725478 | Genetic architecture of traits associated with serpentine adaptation of Silene vulgaris. |
Q28277160 | Genetic assimilation can occur in the absence of selection for the assimilating phenotype, suggesting a role for the canalization heuristic |
Q30654206 | Genetic background, and not ontogenetic effects, affects avian seasonal timing of reproduction. |
Q45642546 | Genetic basis and fitness correlates of dynamic carotenoid-based ornamental coloration in male and female common kestrels Falco tinnunculus. |
Q46380435 | Genetic basis for soma is present in undifferentiated volvocine green algae |
Q42031257 | Genetic basis of adaptive evolution of a polyphenism by genetic accommodation |
Q46447449 | Genetic basis of between-individual and within-individual variance of docility |
Q34376835 | Genetic basis of differential opsin gene expression in cichlid fishes |
Q51729476 | Genetic caste determination in Pogonomyrmex harvester ants imposes costs during colony founding. |
Q38199217 | Genetic causes of transitions from sexual reproduction to asexuality in plants and animals |
Q114080035 | Genetic colour variation visible for predators and conspecifics is concealed from humans in a polymorphic moth |
Q52653092 | Genetic conflicts and intercellular heterogeneity. |
Q63379948 | Genetic correlation between resting metabolic rate and exploratory behaviour in deer mice (Peromyscus maniculatus) |
Q83140972 | Genetic correlation in relation to differences in dosage of a stressor |
Q34811159 | Genetic covariance between components of male reproductive success: within-pair vs. extra-pair paternity in song sparrows |
Q38962067 | Genetic determination of female castes in a hybridogenetic desert ant. |
Q35055675 | Genetic differences among populations in sexual dimorphism: evidence for selection on males in a dioecious plant |
Q46115528 | Genetic differences and phenotypic plasticity in body size between high- and low-altitude populations of the ground beetle Carabus tosanus |
Q36203328 | Genetic differentiation and adaptive evolution at reproductive loci in incipient Drosophila species |
Q125367052 | Genetic differentiation and habitat partition of Robertsonian house mouse populations (Mus musculus domesticus) of Tunisia |
Q33288435 | Genetic differentiation and natural hybridization between the Sardinian endemic Maniola nurag and the European Maniola jurtina |
Q57763906 | Genetic differentiation and phylogeny of beech on the Balkan peninsula |
Q39330043 | Genetic differentiation associated with host plants and geography among six widespread species of South American Blepharoneura fruit flies (Tephritidae). |
Q34056463 | Genetic differentiation in life-history traits of introduced and native common ragweed (Ambrosia artemisiifolia) populations |
Q40382574 | Genetic distinction between contiguous urban and rural multimammate mice in Tanzania despite gene flow. |
Q51288059 | Genetic divergence and isolation by thermal environment in geothermal populations of an aquatic invertebrate. |
Q33751640 | Genetic divergence in morphology-performance mapping between Misty Lake and inlet stickleback. |
Q28251114 | Genetic divergence is more tightly related to call variation than landscape features in the Amazonian frogs Physalaemus petersi and P. freibergi |
Q46975257 | Genetic divergence predicts reproductive isolation in damselflies |
Q38901313 | Genetic divergence with ongoing gene flow is maintained by the use of different hosts in phytophagous ladybird beetles genus Henosepilachna. |
Q56287853 | Genetic divergence without spatial isolation in polecatMustela putoriuspopulations |
Q46743168 | Genetic diversity does not explain variation in extra-pair paternity in multiple populations of a songbird. |
Q47267882 | Genetic diversity, population structure and sex-biased dispersal in three co-evolving species. |
Q41656671 | Genetic diversity, virulence and fitness evolution in an obligate fungal parasite of bees |
Q42598755 | Genetic drift or natural selection? Hybridization and asymmetric mitochondrial introgression in two Caribbean lizards (Anolis pulchellus and Anolis krugi). |
Q46767260 | Genetic factors affecting food-plant specialization of an oligophagous seed predator |
Q80960865 | Genetic heterogeneity within organisms and the evolution of individuality |
Q42028342 | Genetic independence of female signal form and male receiver design in the almond moth, Cadra cautella |
Q57026962 | Genetic isolation of fragmented populations is exacerbated by drift and selection |
Q79787780 | Genetic life history effects on juvenile survival in bluegill |
Q49049118 | Genetic load, inbreeding depression and heterosis in an age‐structured metapopulation |
Q80118033 | Genetic mating patterns studied in pools with manipulated nest site availability in two populations of Pomatoschistus minutus |
Q35673379 | Genetic panmixia within a narrow contact zone between chromosomally and ecologically distinct black fly sibling species (Diptera: Simuliidae). |
Q79321077 | Genetic polymorphism and trade-offs in the early life-history strategy of the Pacific oyster, Crassostrea gigas (Thunberg, 1795): a quantitative genetic study |
Q55869557 | Genetic polymorphism inCaulerpa taxifolia(Ulvophyceae) chloroplast DNA revealed by a PCR-based assay of the invasive Mediterranean strain |
Q38961522 | Genetic population structure in an equatorial sparrow: roles for culture and geography. |
Q52680776 | Genetic population structure, queen supersedure and social polymorphism in a social Hymenoptera. |
Q128160168 | Genetic response of a perennial grass to warm and wet environments interacts and is associated with trait means as well as plasticity |
Q83113119 | Genetic robustness and selection at the protein level for synonymous codons |
Q57170989 | Genetic signatures of lipid metabolism evolution in Cetacea since the divergence from terrestrial ancestor |
Q79897364 | Genetic similarity, breeding distribution range and sexual selection |
Q125944286 | Genetic structure of Polytrichum formosum in relation to the breeding system as revealed by microsatellites |
Q60379598 | Genetic structure of natural populations of Castanea sativa in Turkey: evidence of a hybrid zone |
Q41080721 | Genetic structure of phenotypic robustness in the collaborative cross mouse diallel panel. |
Q55845463 | Genetic variability and phylogeographical patterns of a nonindigenous species invasion: a comparison of exotic vs. native zebra and quagga mussel populations |
Q90741087 | Genetic variability and transgenerational regulation of investment in sex in the monogonont rotifer Brachionus plicatilis |
Q89545903 | Genetic variance for behavioural 'predictability' of stress response |
Q49561469 | Genetic variation and asexual reproduction in the facultatively parthenogenetic cockroach Nauphoeta cinerea: implications for the evolution of sex. |
Q34683934 | Genetic variation and co-variation for fitness between intra-population and inter-population backgrounds in the red flour beetle, Tribolium castaneum |
Q52848546 | Genetic variation but weak genetic covariation between pre- and post-copulatory episodes of sexual selection in Drosophila melanogaster. |
Q84781949 | Genetic variation for maternal effects on parasite susceptibility |
Q125391101 | Genetic variation for sexual dimorphism in flower size within and between populations of gynodioecious Thymus vulgaris |
Q39162664 | Genetic variation in carbon isotope discrimination in six European populations of Castanea sativa Mill. originating from contrasting localities. |
Q42022641 | Genetic variation in flowering phenology and avoidance of seed predation in native populations of Ulex europaeus |
Q42019954 | Genetic variation in herbivore resistance and tolerance: the role of plant life‐history stage and type of damage |
Q52646276 | Genetic variation in infestation with a directly transmitted ectoparasite. |
Q79321100 | Genetic variation in organisms with sexual and asexual reproduction |
Q51962944 | Genetic variation in pathogen-induced early hatching of toad embryos. |
Q47726089 | Genetic variation in the shape of cold survival curves in a single fly population suggests potential for selection from climate variability. |
Q60569509 | Genetic variation in tolerance of competition and neighbour suppression in Arabidopsis thaliana |
Q79321136 | Genetic variation of polygenic characters and the evolution of genetic degeneracy |
Q30663609 | Genetic variation underlies temperature tolerance of embryos in the sea urchin Heliocidaris erythrogramma armigera. |
Q83490270 | Genetic variation underlying the expression of a polyphenism |
Q79753853 | Genetic variation, disequilibrium and natural selection on reproductive traits in Allium vineale |
Q31066777 | Genetic, physiologic and ecogeographic factors contributing to variation in Homo sapiens: Homo floresiensis reconsidered |
Q51725460 | Genetically idiosyncratic responses of Drosophila melanogaster populations to selection for improved learning ability. |
Q51615794 | Genetics of body shape and armour variation in threespine sticklebacks. |
Q42035832 | Genetics of host plant use and life history in the comma butterfly across Europe: varying modes of inheritance as a potential reproductive barrier |
Q43942134 | Genetics of male nuptial colour divergence between sympatric sister species of a Lake Victoria cichlid fish |
Q42037837 | Genetics of sex pheromone blend differences between Heliothis virescens and Heliothis subflexa: a chromosome mapping approach. |
Q56984182 | Genetics of sexual Ostracoda from a low Arctic site |
Q51298901 | Genital divergence in sympatric sister snails. |
Q48275420 | Genome evolution, structural rearrangements and speciation |
Q47300690 | Genome size and recombination in angiosperms: a second look |
Q90769495 | Genome size variation and species diversity in salamanders |
Q46568960 | Genome-specific introgression between wheat and its wild relative Aegilops triuncialis |
Q30451329 | Genomic admixture increases fitness during a biological invasion |
Q101238209 | Genomic inference of complex domestication histories in three Solanaceae species |
Q101054565 | Genomic landscape of reproductive isolation in Lucania killifish: The role of sex loci and salinity |
Q35192827 | Genomic regions repeatedly involved in divergence among plant-specialized pea aphid biotypes |
Q46259145 | Genotype and diet affect resistance, survival, and fecundity but not fecundity tolerance. |
Q51728054 | Genotype by environment interactions in viability and developmental time in populations of cactophilic Drosophila. |
Q42037840 | Genotype x environment interaction for male attractiveness in an acoustic moth: evidence for plasticity and canalization. |
Q42014435 | Genotype × environment interaction, environmental heterogeneity and the lek paradox |
Q45003436 | Genotype-by-environment interactions due to antibiotic resistance and adaptation in Escherichia coli |
Q51295489 | Genotype-by-environment interactions for cuticular hydrocarbon expression in Drosophila simulans. |
Q91184171 | Genotype-by-environment interactions for seminal fluid expression and sperm competitive ability |
Q50795750 | Genotype-by-environment interactions leads to variable selection on life-history strategy in Common Evening Primrose (Oenothera biennis). |
Q46752243 | Genotype-by-environment interactions underlie the expression of pre- and post-copulatory sexually selected traits in guppies |
Q40542035 | Genotype-by-genotype interactions between an insect and its pathogen. |
Q43703653 | Genotype-by-genotype specificity remains robust to average temperature variation in an aphid/endosymbiont/parasitoid system |
Q91529733 | Genotype-environment interactions rule the response of a widespread butterfly to temperature variation |
Q91726022 | Genotypes and their interaction effects on reproduction and mating-induced immune activation in Drosophila melanogaster |
Q51538054 | Genotype‐by‐environment interactions for female preference |
Q110616050 | Genotype–environment interaction and the ontogeny of diet‐induced phenotypic plasticity in size and shape of Melanoplus femurrubrum (Orthoptera: Acrididae) |
Q56984188 | Genotypic diversity of asexual Ostracoda from a low arctic site |
Q63383866 | Genotypic selection in Daphnia populations consisting of inbred sibships |
Q64032265 | Genotypic variation for reproductive characters, and the influence of pollen-ovule ratio on selfing rate in rape seed (Brassica napus) |
Q50789091 | Genotypic vs. condition effects on parasite-driven rare advantage. |
Q46728572 | Geographic body size variation in the periodical cicadas Magicicada: implications for life cycle divergence and local adaptation. |
Q107968143 | Geographic patterns in colonial reproductive strategy in Myrmecina nipponica : Links between biogeography and a key polymorphism in ants |
Q31028235 | Geographic range size, life history and rates of diversification in Australian mammals |
Q51709741 | Geographic structure in a widespread plant-mycorrhizal interaction: pines and false truffles. |
Q111264612 | Geographic structure of lineage associations in a plant-bacterial mutualism |
Q111267229 | Geographic structure of lineage associations in a plant-bacterial mutualism |
Q51562879 | Geographic variation in corticosterone response to chronic predator stress in tadpoles. |
Q36351592 | Geographic variation in mimetic precision among different species of coral snake mimics. |
Q38871990 | Geographic variation in phenotypic plasticity in response to dissolved oxygen in an African cichlid fish |
Q51566612 | Geographic variation in sperm traits reflects predation risk and natural rates of multiple paternity in the guppy. |
Q46781516 | Geographic variation of life-history traits in the sand lizard, Lacerta agilis: testing Darwin's fecundity-advantage hypothesis. |
Q82232405 | Geographical patterns of adaptation within a species' range: interactions between drift and gene flow |
Q51583893 | Geographical variation in allometry in the guppy (Poecilia reticulata). |
Q59594798 | Geographical variation in calling song of the field cricket Teleogryllus oceanicus: the importance of spatial scale |
Q51193020 | Geographical variation in reproductive ageing patterns and life-history strategy of a short-lived passerine bird. |
Q45395434 | Geographically variable selection in Ambystoma tigrinum virus (Iridoviridae) throughout the western USA. |
Q34714320 | Getting a grip on the evolution of grasping in musteloid carnivorans: a three-dimensional analysis of forelimb shape. |
Q83867990 | Getting in shape: adaptation and phylogenetic inertia in morphology of Australian anuran larvae |
Q47296482 | Gis-based niche models reveal unifying climatic mechanisms that maintain the location of avian hybrid zones in a North American suture zone |
Q51635847 | Give 'til it hurts: trade-offs between immunity and male reproductive effort in the decorated cricket, Gryllodes sigillatus. |
Q51591773 | Giving offspring a head start in life: field and experimental evidence for selection on maternal basking behaviour in lizards. |
Q47296470 | Glacial refugia and the phylogeography of Steller's sea lion (Eumatopias jubatus) in the North Pacific |
Q48275466 | Glittering gold and the quest for Isla de Muerta |
Q36233945 | Global analysis reveals that cryptic diversity is linked with habitat but not mode of life |
Q99566747 | Glucocorticoid levels are linked to lifetime reproductive success and survival of adult barn owls |
Q33313501 | Go east: phylogeographies of Mauremys caspica and M. rivulata- discordance of morphology, mitochondrial and nuclear genomic markers and rare hybridization |
Q58042269 | Godfrey M. Hewitt (1940-2013), President of ESEB 1999-2001 |
Q51713128 | Good genes, genetic compatibility and the evolution of polyandry: use of the diallel cross to address competing hypotheses. |
Q90659424 | Good parenting may not increase reproductive success under environmental extremes |
Q90917774 | Grab my tail: evolution of dazzle stripes and colourful tails in lizards |
Q47436177 | Gradual and quantum genome size shifts in the hystricognath rodents |
Q51556338 | Grain of environment explains variation in the strength of genotype × environment interaction. |
Q30855720 | Grandparental effects in marine sticklebacks: transgenerational plasticity across multiple generations. |
Q51278931 | Graphic illustration of a potential problem: a commentary on Morrissey (2016). |
Q90376361 | Greater opportunities for sexual selection in male than in female obligate brood parasitic birds |
Q125558332 | Greater reproductive assurance of asexual plant compared with sexual relative in a low‐density sympatric population: Experimental evidence for pollen limitation |
Q51385075 | Group adaptation, formal darwinism and contextual analysis. |
Q51408271 | Group structure, kinship, inbreeding risk and habitual female dispersal in plural-breeding mammals. |
Q45945227 | Grow with the flow: a latitudinal cline in physiology is associated with more variable precipitation in Erythranthe cardinalis. |
Q50765993 | Growth form evolution and shifting habitat specialization in annual plants. |
Q110615414 | Growth temperature and phenotypic plasticity in two |
Q110615219 | Growth temperature and phenotypic plasticity in two Drosophila sibling species: probable adaptive changes in flight capacities |
Q115158979 | Guthrie, R. D. 1990. Frozen Fauna of the Mammoth Steppe: The story of Blue Babe. The University of Chicago Press, Chicago and London, 323 pp. $19.50 |
Q42026794 | HSP70 expression in the Copper butterfly Lycaena tityrus across altitudes and temperatures |
Q52043767 | Habitat dependent associations between parasitism and fluctuating asymmetry among endemic stickleback populations. |
Q129663159 | Habitat heterogeneity limits prey colour polymorphism maintained via negative frequency-dependent selection |
Q51281057 | Habitat preference and flowering-time variation contribute to reproductive isolation between diploid and autotetraploid Anacamptis pyramidalis. |
Q33466501 | Habitat saturation and the spatial evolutionary ecology of altruism |
Q81670514 | Habitat specialization and adaptive phenotypic divergence of anuran populations |
Q33885500 | Habitat use affects morphological diversification in dragon lizards |
Q44234021 | Habitat variation and wing coloration affect wing shape evolution in dragonflies |
Q80831693 | Habitat-dependent geographical variation in ontogenetic allometry of the shiner perch Cymatogaster aggregata Gibbons (Teleostei: Embiotocidae) |
Q51689155 | Habitat-dependent song divergence at subspecies level in the grey-breasted wood-wren. |
Q46391284 | Habitat-related variation in the plasticity of a UV-sensitive photoreceptor over a small spatial scale in the palmate newt |
Q51637797 | Habitat-specific population structure in native western flower thrips Frankliniella occidentalis (Insecta, Thysanoptera). |
Q60462371 | Haematological parameters do senesce in the wild: evidence from different populations of a long-lived mammal |
Q35167330 | Haldane's rule revisited: do hybrid females have a shorter lifespan? Survival of hybrids in a recent contact zone between two large gull species. |
Q81670530 | Hamilton's rule, imprinting and parent-offspring conflict over seed mass in partially selfing plants |
Q50251472 | Hamilton's rule, inclusive fitness maximization, and the goal of individual behaviour in symmetric two-player games |
Q33772117 | Haploids adapt faster than diploids across a range of environments |
Q58616954 | Harsh conditions during early development influence telomere length in an altricial passerine: links with oxidative stress and corticosteroids |
Q81145558 | Has adaptive dynamics contributed to the understanding of adaptive and sympatric speciation? |
Q33247047 | Has the evolution of complexity in the amphibian papilla influenced anuran speciation rates? |
Q121607319 | Hatching fraction and timing of resting stage production in seasonal environments: effects of density dependence and uncertain season length |
Q115158977 | Haynes, G. 1991. Mammoths, mastodants and elephants: biology, behavior and the fossil record. Cambridge University Press, Cambridge. 413 p. ISBN:0-521-38435-4 |
Q51587357 | Head shape evolution in Gymnophthalmidae: does habitat use constrain the evolution of cranial design in fossorial lizards? |
Q58038156 | Head shape evolution in Tropidurinae lizards: does locomotion constrain diet? |
Q46951667 | Head shape evolution in monitor lizards (Varanus): interactions between extreme size disparity, phylogeny and ecology. |
Q47374438 | Heat stress and age induced maternal effects on wing size and shape in parthenogenetic Drosophila mercatorum |
Q48515112 | Heightened condition dependence is not a general feature of male eyespan in stalk-eyed flies (Diptera: Diopsidae). |
Q33909067 | Helpers at the nest compensate for reduced maternal investment in egg size in carrion crows. |
Q47221517 | Hemiclonal analysis reveals significant genetic, environmental and genotype x environment effects on sperm size in Drosophila melanogaster |
Q51766210 | Hemiclonal reproduction slows down the speed of Muller's ratchet in the hybridogenetic frog Rana esculenta. |
Q58588475 | Herbivores and plant defenses affect selection on plant reproductive traits more strongly than pollinators |
Q57065547 | Herbivores and the evolution of the semelparous perennial life-history of plants |
Q113855137 | Herbivores and the evolution of the semelparous perennial life-history of plants |
Q92454949 | Heritabilities, social environment effects and genetic correlations of social behaviours in a cooperatively breeding vertebrate |
Q51722518 | Heritability and fitness-related consequences of squid personality traits. |
Q46527354 | Heritability and genetic correlations of personality traits in a wild population of yellow-bellied marmots (Marmota flaviventris). |
Q46281604 | Heritability and social brood effects on personality in juvenile and adult life-history stages in a wild passerine |
Q42024213 | Heritability of and strong single gene (Pgi) effects on life-history traits in the Glanville fritillary butterfly |
Q46302097 | Heritability of anti-predatory traits: vigilance and locomotor performance in marmots |
Q60430763 | Heritability of corticosterone response and changes in life history traits during selection in the zebra finch |
Q42003107 | Heritability of flight and resting metabolic rates in the Glanville fritillary butterfly |
Q35015536 | Heritability of gonad size varies across season in a wild songbird. |
Q47264612 | Heritability of life-history tactics and genetic correlation with body size in a natural population of brook charr (Salvelinus fontinalis). |
Q51544101 | Heritability of male attractiveness persists despite evidence for unreliable sexual signals in Drosophila simulans. |
Q39362044 | Heritability of resistance against ectoparasitism in the Drosophila-Macrocheles system |
Q82866707 | Heritability of resistance to oxidative stress in early life |
Q50450982 | Heritability of resting metabolic rate in a wild population of blue tits. |
Q84043447 | Heritability of short-scale natal dispersal in a large-scale foraging bird, the wandering albatross |
Q112177715 | Heritability of sperm competition success in the bulb mite, |
Q44877431 | Heritability, covariation and natural selection on 24 traits of common evening primrose (Oenothera biennis) from a field experiment. |
Q51300558 | Heritability, evolvability, phenotypic plasticity and temporal variation in sperm-competition success of Drosophila melanogaster. |
Q47260140 | Heritability, plasticity and canalization of Ural owl egg size in a cyclic environment |
Q46921297 | Heritable body size mediates apparent life-history trade-offs in a simultaneous hermaphrodite |
Q57131656 | Heritable variation and genetic correlation of quantitative traits within and between ecotypes of Avena barbata |
Q45362185 | Heritable variation in an extended phenotype: the case of a parasitoid manipulated by a virus |
Q48195717 | Heritable variation in circulating glucocorticoids and endocrine flexibility in a free-living songbird |
Q51686185 | Heritable variation in the timing of spermatophore removal, a mechanism of post-copulatory female choice in crickets. |
Q111896151 | Heritable variation of sex ratio in a polychaete worm |
Q31144157 | Heterochrony and post-natal growth in mammals--an examination of growth plates in limbs. |
Q36232277 | Heterogeneity and concordance in locus-specific differentiation and introgression between species of towhees |
Q48826234 | Heterosis and inbreeding depression in bottlenecked populations: a test in the hermaphroditic freshwater snail Lymnaea stagnalis |
Q46448570 | Heterosis in hybrids within and between yeast species |
Q92445917 | Heterosis is common and inbreeding depression absent in natural populations of Arabidopsis thaliana |
Q42009278 | Heterospecific courtship, minority effects and niche separation between cryptic butterfly species. |
Q46936685 | Heterospecific female mimicry in Ficedula flycatchers |
Q98228171 | Heterospecific mating interactions as an interface between ecology and evolution |
Q46960700 | Heterozygosity and orange coloration are associated in the guppy (Poecilia reticulata). |
Q48180992 | Heterozygosity at a single locus explains a large proportion of variation in two fitness-related traits in great tits: a general or a local effect? |
Q57614301 | Heterozygosity is unrelated to adult fitness measures in a large, noninbred population of great tits (Parus major) |
Q90379217 | Hibernation constrains brain size evolution in mammals |
Q45884820 | Hidden cytoplasmic incompatibility alters the dynamics of male-killer/host interactions. |
Q96224105 | Hidden genetic variance contributes to increase the short-term adaptive potential of selfing populations |
Q36984063 | Hidden genetic variation in the germline genome of Tetrahymena thermophila |
Q33458844 | Hidden support from unpromising data sets strongly unites snakes with anguimorph 'lizards'. |
Q40748686 | Hidden suppression of sex ratio distortion suggests Red queen dynamics between Wolbachia and its dwarf spider host |
Q29391560 | Hierarchical behaviour, habitat use and species size differences shape evolutionary outcomes of hybridization in a coral reef fish |
Q56834313 | High dose refuge strategies and genetically modified crops - reply to Tabashnik et al |
Q47819109 | High genetic divergences indicate ancient separation of parthenogenetic lineages of the oribatid mite Platynothrus peltifer (Acari, Oribatida). |
Q42012666 | High host-plant nitrogen content: a prerequisite for the evolution of ant-caterpillar mutualism? |
Q52671461 | High recombination frequency creates genotypic diversity in colonies of the leaf-cutting ant Acromyrmex echinatior. |
Q50979717 | High-density linkage maps fail to detect any genetic component to sex determination in a Rana temporaria family. |
Q39709874 | Higher in vitro resistance to oxidative stress in extra-pair offspring. |
Q51620675 | Higher parasite resistance in Daphnia populations with recent epidemics. |
Q46945459 | Higher rates of sex evolve under K-selection |
Q40918298 | Higher relatedness mitigates mortality in a nematode with lethal male fighting. |
Q46295177 | Higher temperatures during development reduce body size in the zebra finch in the laboratory and in the wild. |
Q48124043 | Hill-Robertson interference maintained by Red Queen dynamics favours the evolution of sex. |
Q91759877 | Hindered and constrained: limited potential for thermal adaptation in post-metamorphic and adult Rana temporaria along elevational gradients |
Q34666440 | Historic and contemporary levels of genetic variation in two New Zealand passerines with different histories of decline |
Q39850261 | Historical and contingent factors affect re-evolution of a complex feature lost during mass extinction in communities of digital organisms |
Q101477927 | Historical climatic instability predicts the inverse latitudinal pattern in net diversification of modern mammalian biota |
Q44175705 | Historical contingency and behavioural divergence in territorial Anolis lizards |
Q53065508 | Historical mutation rates predict susceptibility to radiation in Chernobyl birds. |
Q46541181 | Histories of host shifts and cospeciation among free-living parasitoids of Rhagoletis flies |
Q44875130 | History rather than hybridization determines population structure and adaptation in Populus balsamifera. |
Q59267564 | Hoffman, A. 1989. Arguments on evolution. A paleontologist's perspective. 274 pp. Oxford University Press, New York and Oxford. ISBN 0-19-504443-6. f22.50 |
Q57826086 | Homology, behaviour and spider webs: web construction behaviour of Linyphia hortensis and L. triangularis (Araneae: Linyphiidae) and its evolutionary significance |
Q47387831 | Honest olfactory ornamentation in a female-dominant primate |
Q52764111 | Honey bee hygienic behaviour does not incur a cost via removal of healthy brood. |
Q45825297 | Horizontally acquired DAP pathway as a unit of self-regulation |
Q44933971 | Hormones and honest signals: males with larger ornaments elevate testosterone more when challenged |
Q53017844 | Horn growth rate and longevity: implications for natural and artificial selection in thinhorn sheep (Ovis dalli). |
Q46818846 | Host alkaloids differentially affect developmental stability and wing vein canalization in cactophilic Drosophila buzzatii. |
Q88066919 | Host association influences variation at salivary protein genes in the bat ectoparasite Cimex adjunctus |
Q44847492 | Host behaviour manipulation as an evolutionary route towards attenuation of parasitoid virulence |
Q42046053 | Host choice promotes reproductive isolation between host races of the larch budmoth Zeiraphera diniana |
Q42014439 | Host conservatism, host shifts and diversification across three trophic levels in two Neotropical forests |
Q46691223 | Host control over infection and proliferation of a cheater symbiont |
Q33372572 | Host ecology and life-history traits associated with blood parasite species richness in birds |
Q42043895 | Host ecology determines the relative fitness of virus genotypes in mixed-genotype nucleopolyhedrovirus infections. |
Q50619420 | Host genetic architecture in single and multiple infections. |
Q52675722 | Host inbreeding increases susceptibility to ectoparasitism. |
Q40407028 | Host lifespan and the evolution of resistance to multiple parasites |
Q40504207 | Host nuclear genotype influences phenotype of a conditional mutualist symbiont |
Q51700351 | Host plant and latitude-related diapause variation in Rhagoletis pomonella: a test for multifaceted life history adaptation on different stages of diapause development. |
Q82232325 | Host ploidy, parasitism and immune defence in a coevolutionary snail-trematode system |
Q59827546 | Host resistance and parasite virulence in greenfinch coccidiosis |
Q51731459 | Host shift by the burying beetle, Nicrophorus pustulatus, a parasitoid of snake eggs. |
Q102061942 | Host shifting and host sharing in a genus of specialist flies diversifying alongside their sunflower hosts |
Q41995915 | Host specialization involving attraction, avoidance and performance, in two phytophagous moth species |
Q59652788 | Host specificity of a generalist parasite: genetic evidence of sympatric host races in the seabird tick Ixodes uriae |
Q41026638 | Host switching in cowbird brood parasites: how often does it occur? |
Q57138126 | Host use of a hemiparasitic plant: no trade-offs in performance on different hosts |
Q34811139 | Host-parasite coevolution and patterns of adaptation across time and space |
Q34833346 | Host-parasite coevolution favours parasite genetic diversity and horizontal gene transfer |
Q50504879 | Host-parasite coevolution induces selection for condition-dependent sex. |
Q45376119 | Host-parasite coevolution: genetic variation in a virus population and the interaction with a host gene |
Q48034270 | Host-parasite interactions for virulence and resistance in a malaria model system |
Q42034832 | Host-plant effects the expression of resistance to Bacillus thuringiensis kurstaki in Trichoplusia ni (Hubner): an important factor in resistance evolution |
Q52696321 | Host-race formation: promoted by phenology, constrained by heritability. |
Q60484807 | Host-related genetic differentiation in the anther smut fungus Microbotryum violaceum in sympatric, parapatric and allopatric populations of two host species Silene latifolia and S. dioica |
Q33390673 | Hot and not-so-hot females: reproductive state and thermal preferences of female Arizona Bark Scorpions (Centruroides sculpturatus). |
Q46469144 | Hot spots become cold spots: coevolution in variable temperature environments |
Q80404355 | How a complex life cycle can improve a parasite's sex life |
Q80117957 | How altruism evolves: assortment and synergy |
Q92476446 | How clonal are clones? A quest for loss of heterozygosity during asexual reproduction in Daphnia magna |
Q51672664 | How did the Great Auk raise its young? |
Q80960909 | How do natural and sexual selection contribute to sympatric speciation? |
Q100523351 | How do species barriers decay? Concordance and local introgression in mosaic hybrid zones of mussels |
Q44664667 | How ecology shapes caste evolution: linking resource use, morphology, performance and fitness in a superorganism |
Q51810492 | How effective is recognition of siblings on the basis of genotype? |
Q39964848 | How is sexual conflict over parental care resolved? A meta-analysis |
Q36068966 | How mechanisms of habitat preference evolve and promote divergence with gene flow. |
Q30872273 | How much can history constrain adaptive evolution? A real-time evolutionary approach of inversion polymorphisms in Drosophila subobscura. |
Q39068967 | How phylogeny and foraging ecology drive the level of chemosensory exploration in lizards and snakes. |
Q47235246 | How should parents adjust the size of their young in response to local environmental cues? |
Q92992405 | How stabilizing selection and nongenetic inheritance combine to shape the evolution of phenotypic plasticity |
Q59411549 | How stress selects for reversible phenotypic plasticity |
Q53124075 | How the European Society for Evolutionary Biology and the Journal of Evolutionary Biology were founded. |
Q46259116 | How the environment shapes animal signals: a test of the acoustic adaptation hypothesis in frogs. |
Q46257787 | How the length of genital parts affects copulation performance in a carabid beetle: implications for correlated genital evolution between the sexes |
Q39334513 | How to distinguish altruism from spite (and why we should bother). |
Q34196838 | How to infer reliable diploid genotypes from NGS or traditional sequence data: from basic probability to experimental optimization. |
Q42629681 | How to separate genetic and environmental causes of similarity between relatives |
Q38234467 | How traits shape trees: new approaches for detecting character state-dependent lineage diversification |
Q52733724 | Hsp70 protein levels and thermotolerance in Drosophila subobscura: a reassessment of the thermal co-adaptation hypothesis. |
Q44707467 | Human birthweight evolution across contrasting environments. |
Q38452369 | Human-induced changes in the reproductive traits of Lake Constance common whitefish (Coregonus lavaretus). |
Q52736138 | Humidity affects genetic architecture of heat resistance in Drosophila melanogaster. |
Q53910292 | Humoral immune response in relation to senescence, sex and sexual ornamentation in the barn swallow (Hirundo rustica). |
Q46828240 | Hybrid breakdown and mitochondrial dysfunction in hybrids of Nasonia parasitoid wasps |
Q38789976 | Hybrid crosses and the genetic basis of interspecific divergence in lifespan in Pristionchus nematodes |
Q39641210 | Hybrid dynamics in a species group of swallowtail butterflies |
Q30738229 | Hybrid female mate choice as a species isolating mechanism: environment matters |
Q34395101 | Hybrid incompatibility is consistent with a hybrid origin of Heliconius heurippa Hewitson from its close relatives, Heliconius cydno Doubleday and Heliconius melpomene Linnaeus. |
Q51667281 | Hybrid sterility and inviability in the parasitic fungal species complex Microbotryum. |
Q34549649 | Hybrid zones, barrier loci and the 'rare allele phenomenon'. |
Q51700339 | Hybridization and introgression in a mixed population of the intertidal seaweeds Fucus evanescens and F. serratus. |
Q56783543 | Hybridization and invasiveness in the freshwater snail Melanoides tuberculata: hybrid vigour is more important than increase in genetic variance |
Q44903779 | Hybridization and regional sex ratios in Nemophila menziesii |
Q51715468 | Hybridization and reproductive isolation among syntopic populations of the topminnows Fundulus notatus and F. olivaceus. |
Q38074482 | Hybridization and speciation |
Q85904807 | Hybridization and the build-up of genomic divergence during speciation |
Q44738331 | Hybridization and the origin of species |
Q91626117 | Hybridization and transgressive exploration of colour pattern and wing morphology in Heliconius butterflies |
Q63975814 | Hybridization between Pied and Collared Flycatchers-sexual selection and speciation theory |
Q52342283 | Hybridization could be a common phenomenon within the highly diverse lizard genus Liolaemus. |
Q81145570 | Hybridization dynamics between sympatric species of trout: loss of reproductive isolation |
Q51540135 | Hybridization is important in evolution, but is speciation? |
Q85904826 | Hybridization may rarely promote speciation |
Q42657407 | Hybridization occurs between Drosophila simulans and D. sechellia in the Seychelles archipelago |
Q57002515 | Hybridization without guilt: gene flow and the biological species concept |
Q34549657 | Hybridization, speciation and novelty |
Q39077700 | Hybridization: its varied forms and consequences |
Q121929359 | Identification of a cis‐sex chromosome transition in banded geckos (Coleonyx, Eublepharidae, Gekkota) |
Q93366107 | Identification of a novel sperm class and its role in fertilization in Drosophila |
Q83140977 | Identifying energy constraints to parasite resistance |
Q88715511 | Identifying the loci of speciation: the challenge beyond genome scans |
Q50598956 | Idiosyncratic evolution of maternal effects in response to juvenile malnutrition in Drosophila. |
Q96226529 | Illustrating the importance of meta-analysing variances alongside means in ecology and evolution |
Q34539130 | Imbalanced genomic imprinting in brain development: an evolutionary basis for the aetiology of autism |
Q51458673 | Immature performance linked with exaggeration of a sexually selected trait in an armed beetle. |
Q48195707 | Immediate and delayed life history effects caused by food deprivation early in life in a short-lived lizard. |
Q128162692 | Immigration delays but does not prevent adaptation following environmental change: experimental evidence |
Q89174280 | Immune deployment increases larval vulnerability to predators and inhibits adult life-history traits in a dragonfly |
Q101240429 | Immune priming depends on age, sex and Wolbachia in the interaction between Armadillidium vulgare and Salmonella |
Q52839954 | Immune-challenged house wren broods differ in the relative strengths of their responses among different axes of the immune system. |
Q46116793 | Immunogenic males: a genome-wide analysis of reproduction and the cost of mating in Drosophila melanogaster females |
Q47671018 | Immunoglobulin plasma concentration in relation to egg laying and mate ornamentation of female barn swallows (Hirundo rustica). |
Q22121954 | Impact of a population bottleneck on symmetry and genetic diversity in the northern elephant seal |
Q51575058 | Impact of plant flowering phenology on the cost/benefit balance in a nursery pollination mutualism, with honest males and cheating females. |
Q84384930 | Impact of selection on genes involved in regulatory network: a modelling study |
Q45009422 | Impacts of environmental variability on desiccation rate, plastic responses and population dynamics of Glossina pallidipes |
Q50904862 | Impaired sperm quality, delayed mating but no costs for offspring fitness in crickets winning a fight. |
Q112796092 | Implications of nitrogen translocation efficiency for hypotheses on the evolution of autumn colours— |
Q36442487 | Implications of the difference between true and predicted breeding values for the study of natural selection and micro-evolution |
Q52666606 | In search of clinal variation in the period and clock timing genes in Australian Drosophila melanogaster populations. |
Q38914495 | In situ marker-based assessment of leaf trait evolutionary potential in a marginal European beech population. |
Q53880731 | In vitro embryo survival and early viability of larvae in relation to male sexual ornaments and parasite resistance in roach, Rutilus rutilus L. |
Q54374796 | In vitro tests of natural allelic variation of innate immune genes (avian β-defensins) reveal functional differences in microbial inhibition. |
Q43527472 | Inbred women in a small and isolated Swiss village have fewer children |
Q93092175 | Inbreeding alters context-dependent reproductive effort and immunity in male crickets |
Q51615477 | Inbreeding and courtship calling in the cricket Teleogryllus commodus. |
Q51709729 | Inbreeding avoidance in spiders: evidence for rescue effect in fecundity of female spiders with outbreeding opportunity. |
Q48278949 | Inbreeding depresses short and long distance dispersal in three congeneric spiders |
Q57614375 | Inbreeding depression along a life-history continuum in the great tit |
Q54432829 | Inbreeding depression and genetic load of sexually selected traits: how the guppy lost its spots |
Q26810454 | Inbreeding depression and heterosis in populations of Schiedea viscosa, a highly selfing species |
Q64032266 | Inbreeding depression and mating-distance dependent offspring fitness in large and small populations of Lychnis flos-cuculi (Caryophyllaceae) |
Q57131664 | Inbreeding depression and outbreeding depression in Digitalis purpurea: optimal outcrossing distance in a tetraploid |
Q64032257 | Inbreeding depression in Lychnis flos-cuculi (Caryophyllaceae): effects of different levels of inbreeding |
Q39939158 | Inbreeding depression in an asexual population of Mimulus guttatus |
Q43439640 | Inbreeding depression in an insect with maternal care: influences of family interactions, life stage and offspring sex. |
Q26865124 | Inbreeding depression in male gametic performance |
Q48959531 | Inbreeding depression in the competitive fertilization success of male crickets |
Q114144510 | Inbreeding reduces fitness of seed beetles under thermal stress |
Q33420042 | Inbreeding variability and population structure in the invasive haplodiploid palm-seed borer (Coccotrypes dactyliperda). |
Q52696836 | Inbreeding, energy use and condition. |
Q42019309 | Incipient allochronic speciation in the pine processionary moth (Thaumetopoea pityocampa, Lepidoptera, Notodontidae). |
Q34487766 | Incipient habitat race formation in an amphibian |
Q43893004 | Incipient post-zygotic barrier in a model system of ecological speciation with gene flow. |
Q33195290 | Incongruent nuclear and mitochondrial phylogeographic patterns in the Timarcha goettingensis species complex (Coleoptera, Chrysomelidae). |
Q38645636 | Inconvenient truths in population and speciation genetics point towards a future beyond allele frequencies. |
Q47290493 | Increase in song frequency decreases spermatophore size: correlative evidence of a macroevolutionary trade-off in katydids (Orthoptera: Tettigoniidae). |
Q52722209 | Increased copulation duration before ejaculate transfer is associated with larger spermatophores, and male genital titillators, across bushcricket taxa. |
Q28246628 | Increased ecological amplitude through heterosis following wide outcrossing in Banksia ilicifolia R.Br. (Proteaceae) |
Q45886125 | Increased male mating rate in Drosophila is associated with Wolbachia infection |
Q51595712 | Increased opportunity for sexual conflict promotes harmful males with elevated courtship frequencies. |
Q51693581 | Increasing productivity accelerates host-parasite coevolution. |
Q43500117 | Independence among physiological traits suggests flexibility in the face of ecological demands on phenotypes |
Q89348686 | Independent and interactive effects of immune activation and larval diet on adult immune function, growth and development in the greater wax moth (Galleria mellonella) |
Q46493840 | Independent reversals to terrestriality in squirrels (Rodentia: Sciuridae) support ecologically mediated modes of adaptation |
Q57148263 | Independent sources of condition dependency and multiple pathways determine a composite trait: lessons from carotenoid-based plumage colouration |
Q115033088 | Indications for rapid evolution of trait means and thermal plasticity in range‐expanding populations of a butterfly |
Q50748487 | Indirect consequences of artificial selection on plasticity to light quality in Arabidopsis thaliana. |
Q84190376 | Indirect effects of FRIGIDA: floral trait (co)variances are altered by seasonally variable abiotic factors associated with flowering time |
Q60289830 | Indirect evidence from DNA sequence diversity for genetic degeneration of the Y-chromosome in dioecious species of the plant Silene: the SlY4/SlX4 and DD44-X/DD44-Y gene pairs |
Q34106874 | Indirect genetic effects in a sex-limited trait: the case of breeding time in red-billed gulls |
Q50546768 | Indirect genetics effects and evolutionary constraint: an analysis of social dominance in red deer, Cervus elaphus. |
Q46972640 | Indirect mate choice, direct mate choice and species recognition in a bower-building cichlid fish lek. |
Q51703553 | Individual MHC class I and MHC class IIB diversities are associated with male and female reproductive traits in the three-spined stickleback. |
Q90282146 | Individual and synergistic effects of male external genital traits in sexual selection |
Q92670189 | Individual asymmetry as a predictor of fitness in the bat Carollia perspicillata |
Q60164274 | Individual differences in developmental precision and fluctuating asymmetry: a model and its implications |
Q41723757 | Individual genetic diversity and probability of infection by avian malaria parasites in blue tits (Cyanistes caeruleus). |
Q46627104 | Individual inversions or their combinations: which is the main selective target in a natural population of Drosophila subobscura? |
Q85904795 | Individual mating decisions and hybridization |
Q46257867 | Individual vocal signatures in barn owl nestlings: does individual recognition have an adaptive role in sibling vocal competition? |
Q36263534 | Induced defences alter the strength and direction of natural selection on reproductive traits in common milkweed |
Q51564647 | Infection intensity and infectivity of the tick-borne pathogen Borrelia afzelii. |
Q40665179 | Infection risk dictates immunological divergence among populations in a Mediterranean lizard. |
Q44163643 | Infection with Wolbachia protects mosquitoes against Plasmodium-induced mortality in a natural system. |
Q53021683 | Inference of parasite local adaptation using two different fitness components. |
Q60330321 | Inferring local adaptation from QST?FSTcomparisons: neutral genetic and quantitative trait variation in European populations of great snipe |
Q46960628 | Inferring the mode of colonization of the rapid range expansion of a solitary bee from multilocus DNA sequence variation. |
Q91276185 | Inferring the potentially complex genetic architectures of adaptation, sexual dimorphism and genotype by environment interactions by partitioning of mean phenotypes |
Q51771281 | Influence of developmental environment on male- and female-mediated sperm precedence in Drosophila melanogaster. |
Q92530743 | Influence of gene position on the expression divergence of oxidative response genes in intraspecific yeast |
Q43756752 | Influence of genetic architecture on contemporary local evolution in the soapberry bug, Jadera haematoloma: artificial selection on beak length |
Q51740906 | Influence of genetic dissimilarity in the reproductive success and mate choice of brown trout - females fishing for optimal MHC dissimilarity. |
Q51830617 | Influence of genotype-temperature interaction on pollen performance. |
Q51604332 | Influence of host profitability and microenvironmental conditions on parasite specialization on a main and an alternative hosts. |
Q37426117 | Influence of learning on range expansion and adaptation to novel habitats |
Q40852793 | Influence of niche similarity on hybridization between Myriophyllum sibiricum and M. spicatum |
Q47300792 | Influence of number of pollinations and pollen load size on maternal fitness costs in Collinsia heterophylla: implications for existence of a sexual conflict over timing of stigma receptivity |
Q40747165 | Influence of oxidative homeostasis on bacterial density and cost of infection in Drosophila-Wolbachia symbioses |
Q44138310 | Influence of seasonal timing on thermal ecology and thermal reaction norm evolution in Wyeomyia smithii |
Q45907021 | Inheritance in tetraploid yeast revisited: segregation patterns and statistical power under different inheritance models. |
Q51771295 | Inheritance of progeny sex ratio in Urtica dioica. |
Q63975809 | Inheritance of size and shape in a natural population of collared flycatchers, Ficedula albicollis |
Q34412740 | Inheritance of song and stridulatory peg number divergence between Chorthippus brunneus and C. jacobsi, two naturally hybridizing grasshopper species (Orthoptera: Acrididae). |
Q119734456 | Insectivory leads to functional convergence in a group of Neotropical rodents |
Q46178963 | Insight into post-mating interactions between the sexes: relatedness suppresses productivity of singly mated female Drosophila melanogaster |
Q34125940 | Insights into the adaptive significance of vertical pupil shape in snakes |
Q55842533 | Insularity and adaptation in coupled victim-enemy associations |
Q47440323 | Insularity and the evolution of melanism, sexual dichromatism and body size in the worldwide-distributed barn owl. |
Q34191562 | Integrating candidate gene and quantitative genetic approaches to understand variation in timing of breeding in wild tit populations |
Q47262195 | Integration and dissociation of limb elements in flying vertebrates: a comparison of pterosaurs, birds and bats |
Q44692792 | Integration of the mammalian shoulder girdle within populations and over evolutionary time |
Q91959822 | Intensity of infection with intracellular Eimeria spp. and pinworms is reduced in hybrid mice compared to parental subspecies |
Q44581073 | Inter- and intrasexual genetic correlations of exaggerated traits and locomotor activity |
Q88868969 | Interacting effects of predation risk and resource level on escape speed of amphibian larvae along a latitudinal gradient |
Q50445388 | Interaction between female mating preferences and predation may explain the maintenance of rare males in the pentamorphic fish Poecilia parae. |
Q30425835 | Interaction between temperature and male pheromone in sexual isolation in Drosophila melanogaster |
Q40202827 | Interaction effects of cell diffusion, cell density and public goods properties on the evolution of cooperation in digital microbes. |
Q110030339 | Interaction of a host plant and its holoparasite: effects of previous selection by the parasite |
Q89694198 | Interactions between cytoplasmic and nuclear genomes confer sex-specific effects on lifespan in Drosophila melanogaster |
Q47559140 | Interactions between host sex and age of exposure modify the virulence-transmission trade-off. |
Q50471617 | Interactive effects of competition and social environment on the expression of sexual dimorphism. |
Q91948704 | Interactive effects of social environment, age and sex on immune responses in Drosophila melanogaster |
Q39461331 | Intergenerational effects of inbreeding in Nicrophorus vespilloides: offspring suffer fitness costs when either they or their parents are inbred |
Q38433875 | Intergenomic epistasis causes asynchronous hatch times in whitefish hybrids, but only when parental ecotypes differ |
Q35243420 | Intermediate number of major histocompatibility complex class IIB length variants relates to enlarged perivisceral fat deposits in the blunt-head cichlid Tropheus moorii |
Q58556822 | Interplay between age-based competitive asymmetries within the brood and direct competition between inbred and outbred offspring in a burying beetle |
Q35589233 | Interplay of robustness and plasticity of life-history traits drives ecotypic differentiation in thermally distinct habitats. |
Q51706658 | Interpopulation variation in predator foraging behaviour promotes the evolutionary divergence of prey. |
Q38635379 | Interpreting the genomic landscape of speciation: a road map for finding barriers to gene flow. |
Q98281934 | Intersexual differences in density-dependent dispersal and their evolutionary drivers |
Q56656968 | Intersexual ontogenetic conflict |
Q46959126 | Interspecies and intraspecies interactions in social amoebae. |
Q52649744 | Interspecific aggression and character displacement in the damselfly Calopteryx splendens. |
Q46359259 | Interspecific competition counteracts negative effects of dispersal on adaptation of an arthropod herbivore to a new host. |
Q51730348 | Interspecific competition promotes habitat and morphological divergence in a secondary contact zone between two hybridizing songbirds. |
Q51339413 | Interspecific genetics of speciation phenotypes: song and preference coevolution in Hawaiian crickets. |
Q46874712 | Interspecific patterns of phenotypic selection do not predict intraspecific patterns |
Q38995877 | Interspecific sexual attraction because of convergence in warning colouration: is there a conflict between natural and sexual selection in mimetic species? |
Q51987642 | Interspecific variation in egg testosterone levels: implications for the evolution of bird song. |
Q51695709 | Interspecific variation in ejaculate allocation and associated effects on female fitness in seed beetles. |
Q57159470 | Interspecific variation in plumage colour among birds: species recognition or light environment? |
Q50748482 | Interspecific variation in the use of carotenoid-based coloration in birds: diet, life history and phylogeny. |
Q41177204 | Intra- and trans-generational effects of larval diet on susceptibility to an entomopathogenic fungus, Beauveria bassiana, in the greater wax moth, Galleria mellonella. |
Q48064737 | Intra-isolate genome variation in arbuscular mycorrhizal fungi persists in the transcriptome |
Q34271073 | Intra-specific variation in the morphology and the benefit of large genital sclerites of males in the adzuki bean beetle (Callosobruchus chinensis). |
Q53181021 | Intralocus sexual conflict, adaptive sex allocation, and the heritability of fitness. |
Q41305716 | Intralocus tactical conflict: genetic correlations between fighters and sneakers of the dung beetle Onthophagus taurus. |
Q80960862 | Intraorganismal genetic heterogeneity: is it a useful concept? |
Q48259894 | Intrasexual selection favours an immune-correlated colour ornament in a dragonfly. |
Q60370311 | Intraspecific conflict over host manipulation between different larval stages of an acanthocephalan parasite |
Q39270964 | Intraspecific divergence and evolution of a life-history trade-off along a successional gradient in Hawaii's Metrosideros polymorpha |
Q51599953 | Intraspecific divergence in the lateral line system in the nine-spined stickleback (Pungitius pungitius). |
Q59060602 | Intraspecific ecomorphological variation: linear and geometric morphometrics reveal habitat-related patterns within Podarcis bocagei wall lizards |
Q91181755 | Intraspecific mating system evolution and its effect on complex male secondary sexual traits: Does male-male competition increase selection on size or shape? |
Q48114183 | Intraspecific variation in behaviour: effects of evolutionary history, ontogenetic experience and sex. |
Q92803018 | Intrinsic post-ejaculation sperm ageing does not affect offspring fitness in Atlantic salmon |
Q38965187 | Intrinsic reproductive isolating mechanisms in the maintenance of a hybrid zone between ecologically divergent subspecies. |
Q51799609 | Intrinsic reproductive isolation between Trinidadian populations of the guppy, Poecilia reticulata. |
Q40563449 | Intrinsic survival advantage of social insect queens depends on reproductive activation |
Q92474555 | Introducing the new JEB Forum section |
Q125358929 | Introgression between highly divergent fungal sister species |
Q62572746 | Introgressive hybridization between two Iberian endemic cyprinid fish: a comparison between two independent hybrid zones |
Q51709763 | Invasion and fixation of sex-reversal genes. |
Q110630218 | Invasion of rare mutants does not imply their evolutionary success: a counterexample from metapopulation theory |
Q110630260 | Invasion of rare mutants does not imply their evolutionary success: a counterexample from metapopulation theory |
Q34553963 | Invasive house mice facing a changing environment on the Sub-Antarctic Guillou Island (Kerguelen Archipelago). |
Q92225577 | Inverted meiosis and the evolution of sex by loss of complementation |
Q51994174 | Investigating Müllerian mimicry: predator learning and variation in prey defences. |
Q52693851 | Investigating latitudinal clines for life history and stress resistance traits in Drosophila simulans from eastern Australia. |
Q45238736 | Investigating the production of sexual resting structures in a plant pathogen reveals unexpected self-fertility and genotype-by-environment effects |
Q50228092 | Investment in attending to cues and the evolution of amplifiers. |
Q56673449 | Investment in survival and reproduction along a semelparity-iteroparity gradient in theBetaspecies complex |
Q45951206 | Investment in the public good through conditional phenotypes of large effect. |
Q38693388 | Is bigger better? The relationship between size and reproduction in female Asian elephants. |
Q91275711 | Is embryo abortion a post-zygotic barrier to gene flow between Littorina ecotypes? |
Q46714364 | Is geographic variation within species related to macroevolutionary patterns between species? |
Q47317542 | Is size-assortative mating important for rapid pigment differentiation in a freshwater isopod? |
Q51300169 | Is specialization an evolutionary dead end? Testing for differences in speciation, extinction and trait transition rates across diverse phylogenies of specialists and generalists. |
Q35954923 | Is the hook of muroid rodent's sperm related to sperm train formation? |
Q34981810 | Is the peacock's train an honest signal of genetic quality at the major histocompatibility complex? |
Q45160698 | Is the weighted z-test the best method for combining probabilities from independent tests? |
Q28307663 | Island hopping introduces Polynesian field crickets to novel environments, genetic bottlenecks and rapid evolution |
Q62556848 | Isolation by distance in a continuous population under stochastic demographic fluctuations |
Q51610477 | Isolation by time and habitat and coexistence of distinct host races of the common cuckoo. |
Q120686182 | Isotopic niches do not follow the expectations of niche conservatism in the bird genus Cinclodes |
Q35159343 | Isotopic variation across the Audubon's-myrtle warbler hybrid zone. |
Q81145566 | Issues of terminology, gradient dynamics and the ease of sympatric speciation in Adaptive Dynamics |
Q87423031 | JEB Editorial 2016 |
Q34056447 | Jack of all trades masters novel host plants: positive genetic correlations in specialist and generalist insect herbivores expanding their diets to novel hosts |
Q46871082 | Joint evolution of differential seed dispersal and self-fertilization |
Q88409691 | Juvenile divergence in adaptive traits among seven sympatric fish ecomorphs arises before moving to different lacustrine habitats |
Q52659273 | Juvenile immune status affects the expression of a sexually selected trait in field crickets. |
Q39448230 | Keeping the band together: evidence for false boundary disruptive coloration in a butterfly |
Q35047592 | Key innovations and island colonization as engines of evolutionary diversification: a comparative test with the Australasian diplodactyloid geckos |
Q52002179 | Kin discrimination and sex ratios in a parasitoid wasp. |
Q62925437 | Kin recognition and cannibalism in a subsocial spider |
Q92902066 | Kin recognition and co-operative foraging in Drosophila melanogaster larvae |
Q34302753 | Kin recognition: evidence that humans can perceive both positive and negative relatedness. |
Q48173485 | Kin selection and the evolution of sexual conflict |
Q57765882 | Kin structure and queen execution in the Argentine ant Linepithema humile |
Q80117943 | Kinds of kindness: classifying the causes of altruism and cooperation |
Q46680509 | Kinship reinforces cooperative predator inspection in a cichlid fish |
Q56235187 | Kleptoparasitism as an explanation for paradoxical oviposition decisions of the parasitoidAsobara tabida |
Q125352233 | Klump, G. M., Dooling, R. J., Fay, R. R., Stebbins, W. C. (editors). 1995. Methods in Comparative Psychoacoustics, Birkhäuser Verlag, Basel, 345 pp., (Hardcover). ISBN: 3‐7643‐5079‐2. |
Q29028531 | Laboratory environments are not conducive for allopatric speciation |
Q49990007 | Laboratory maintenance does not alter ecological and physiological patterns among species: a Drosophila case study. |
Q35808108 | Lack of adaptation from standing genetic variation despite the presence of putatively adaptive alleles in introduced sweet vernal grass (Anthoxanthum odoratum). |
Q113171472 | Lack of assortative mating might explain reduced phenotypic differentiation where two grasshopper species meet |
Q47226031 | Lack of parallel genetic patterns underlying the repeated ecological divergence of beach and stream-spawning kokanee salmon |
Q58039307 | Lack of seasonal changes in mitochondrial DNA variability of a Drosophila subobscura population |
Q33410371 | Lacustrine radiations in African Synodontis catfish. |
Q48275455 | Land ahoy? Navigating the genomic landscape of speciation while avoiding shipwreck |
Q33810596 | Land planarians (Platyhelminthes) as a model organism for fine-scale phylogeographic studies: understanding patterns of biodiversity in the Brazilian Atlantic Forest hotspot. |
Q46182782 | Large body size in an island-dwelling bird: a microevolutionary analysis |
Q48218942 | Large discrepancies in differentiation of allozymes, nuclear and mitochondrial DNA loci in recently founded Pacific populations of the pearl oyster Pinctada margaritifera |
Q47237878 | Large geographic range size reflects a patchwork of divergent lineages in the long-toed salamander (Ambystoma macrodactylum). |
Q47435882 | Large size in an island-dwelling bird: intraspecific competition and the Dominance Hypothesis |
Q36053603 | Large-brained birds suffer less oxidative damage |
Q48258255 | Large-brained mammals live longer |
Q35165010 | Larval and nurse worker control of developmental plasticity and the evolution of honey bee queen-worker dimorphism |
Q126306231 | Larval development and poor trophic resource availability: Local adaptations and plasticity in a widespread amphibian species |
Q41398387 | Late Quaternary climatic vegetational shifts in an ecological transition zone of northern Madagascar: insights from genetic analyses of two endemic rodent species |
Q38417628 | Late-life and intergenerational effects of larval exposure to microbial competitors in the burying beetle Nicrophorus vespilloides |
Q42010741 | Latitudinal clines in alternative life histories in a geometrid moth |
Q44487512 | Latitudinal clines in the grasshopper Dichroplus elongatus: coevolution of the A genome and B chromosomes? |
Q52097341 | Latitudinal countergradient variation in the common frog (Rana temporaria) development rates--evidence for local adaptation. |
Q97536176 | Latitudinal variation in norms of reaction of phenology in the greater duckweed Spirodela polyrhiza |
Q41536060 | Latitudinal variation in resistance and tolerance to herbivory in the perennial herb Lythrum salicaria is related to intensity of herbivory and plant phenology |
Q55888271 | Lawton, J. H. and May, R. M. (Eds.). Extinction Rates. 1995. Oxford University Press, Oxford. xii + 233 pp. ISBN: 0-19-854829. X. Price: f17.95 |
Q47620466 | Leader preference in Neoconocephalus ensiger katydids: a female preference for a nonheritable male trait. |
Q90798282 | Learning-induced host preference in male parasitoid wasps as a potential driver of ecological speciation |
Q101631253 | Lerista bougainvillii, a case study for the evolution of viviparity in reptiles |
Q34554461 | Lessons learned from microsatellite development for nonmodel organisms using 454 pyrosequencing |
Q48965848 | Levels of inbreeding depression over seven generations of selfing in the androdioecious clam shrimp, Eulimnadia texana |
Q43839651 | Levels of selection in positive-strand virus dynamics |
Q51987634 | Life cycle abbreviation in the trematode Coitocaecum parvum: can parasites adjust to variable conditions? |
Q51931855 | Life cycle abbreviation in trematode parasites and the developmental time hypothesis: is the clock ticking? |
Q126111944 | Life history adaptation along a latitudinal cline in the water strider Aquarius remigis (Heteroptera: Gerridae) |
Q63383852 | Life history and virulence are linked in the ectoparasitic salmon louse Lepeophtheirus salmonis |
Q60233919 | Life history evolution in |
Q38445200 | Life history evolution in cichlids 1: revisiting the evolution of life histories in relation to parental care |
Q47354029 | Life history evolution in cichlids 2: directional evolution of the trade-off between egg number and egg size |
Q112836576 | Life history plasticity in the satyrine butterfly |
Q46410485 | Life history, immunity, Peto's paradox and tumours in birds |
Q44257973 | Life history, predation and flight initiation distance in a migratory bird |
Q46311651 | Life in the unthinking depths: energetic constraints on encephalization in marine fishes |
Q39598896 | Life span variation in 13 Drosophila species: a comparative study on life span, environmental variables and stress resistance |
Q31021252 | Life-history invariants with bounded variables cannot be distinguish from data generated by random processes using standard analyses |
Q60557493 | Life-history trade-offs promote the evolution of dioecy |
Q46888497 | Lifetime fitness and age-related female ornament signalling: evidence for survival and fecundity selection in the pied flycatcher |
Q51130028 | Lifetime reproductive success and longevity of queens in an annual social insect. |
Q59313000 | Light quantity and quality induce shade-avoiding plasticity in a marine macroalga |
Q35696836 | Liking the good guys: amplifying local adaptation via the evolution of condition-dependent mate choice. |
Q34539153 | Limb disparity and wing shape in pterosaurs |
Q47361391 | Limb-bone histology of temnospondyls: implications for understanding the diversification of palaeoecologies and patterns of locomotion of Permo-Triassic tetrapods. |
Q92116393 | Limited female dispersal predicts the incidence of Wolbachia across ants (Hymenoptera: Formicidae) |
Q39366043 | Limited gene dispersal and spatial genetic structure as stabilizing factors in an ant-plant mutualism |
Q90058687 | Limited gene exchange between two sister species of leaf beetles within a hybrid zone in the Alps |
Q44419391 | Limited gene flow may enhance adaptation to local optima in isolated populations of the Roesel's bush cricket (Metrioptera roeselii). |
Q99559446 | Limited genetic parallels underlie convergent evolution of quantitative pattern variation in mimetic butterflies |
Q44552980 | Limited genomic consequences of mixed mating in the recently derived sister species pair, Collinsia concolor and Collinsia parryi |
Q92960762 | Limited mass-independent individual variation in resting metabolic rate in a wild population of snow voles (Chionomys nivalis) |
Q30439184 | Limited plasticity in the phenotypic variance-covariance matrix for male advertisement calls in the black field cricket, Teleogryllus commodus |
Q51935157 | Limits of Hamilton's rule. |
Q36201707 | Limits to adaptation in asexual populations |
Q92331661 | Limits to environmental masking of genetic quality in sexual signals |
Q51632487 | Linking divergent selection on vegetative traits to environmental variation and phenotypic diversification in the Iberian columbines (Aquilegia). |
Q48367758 | Linking genotype to phenotype in a changing ocean: inferring the genomic architecture of a blue mussel stress response with genome-wide association |
Q53147284 | Linking signal fidelity and the efficiency costs of communication. |
Q47375625 | Little evidence for Cope's rule from Bayesian phylogenetic analysis of extant mammals. |
Q35747342 | Little evidence for morphological change in a resilient endemic species following the introduction of a novel predator. |
Q102130467 | Little parallelism in genomic signatures of local adaptation in two sympatric, cryptic sister species |
Q92514998 | Little to no inbreeding depression in a tapeworm with mixed mating |
Q56609958 | Little, C. 1990. The Terrestrial Invasion: an Ecophysiological Approach to the Origins of Land Animals. Cambridge University Press, Cambridge. ix + 304 pp. f 40.00, $ 69.50 (pbk. f 13.95, $ 29.95) |
Q46403861 | Local adaptation along an environmental cline in a species with an inversion polymorphism. |
Q35350921 | Local adaptation and divergence in colour signal conspicuousness between monomorphic and polymorphic lineages in a lizard |
Q56864118 | Local adaptation and effect of host genotype on the rate of pathogen evolution: an experimental test in a plant pathosystem |
Q51391086 | Local adaptation and matching habitat choice in female barn owls with respect to melanic coloration. |
Q34470832 | Local adaptation and population structure at a micro-geographical scale of a fungal parasite on its host plant |
Q35706125 | Local adaptation at range edges: comparing elevation and latitudinal gradients. |
Q82290628 | Local adaptation at the range peripheries of Sitka spruce |
Q52705309 | Local adaptation does not always predict high mating success. |
Q39327469 | Local adaptation of Ruellia nudiflora (Acanthaceae) to biotic counterparts: complex scenarios revealed when two herbivore guilds are considered |
Q44303250 | Local adaptation of a Drosophila parasitoid: habitat-specific differences in thermal reaction norms. |
Q109967860 | Local adaptation of a holoparasitic plant, Cuscuta europaea: variation among populations |
Q31143245 | Local adaptation of reproductive performance during thermal stress. |
Q51662810 | Local adaptation of stress related traits in Drosophila buzzatii and Drosophila simulans in spite of high gene flow. |
Q50502032 | Local adaptation to developmental density does not lead to higher mating success in Drosophila melanogaster. |
Q51489376 | Local adaptation to salinity in the three-spined stickleback? |
Q115431565 | Local adaptation, evolutionary potential and host-parasite coevolution: interactions between migration, mutation, population size and generation time |
Q115390684 | Local adaptation, geographical distance and phylogenetic relatedness: Assessing the drivers of siderophore‐mediated social interactions in natural bacterial communities |
Q34928230 | Local climate determines intra- and interspecific variation in sexual size dimorphism in mountain grasshopper communities. |
Q50304509 | Local co-adaptation leading to a geographical mosaic of coevolution in a social parasite system. |
Q83978179 | Local host competition in the evolution of virulence |
Q46617075 | Local human pressures influence gene flow in a hybridizing Daphnia species complex |
Q52641722 | Local mate competition with lethal male combat: effects of competitive asymmetry and information availability on a sex ratio game. |
Q46477243 | Local population density and group composition influence the signal-preference relationship in Enchenopa treehoppers (Hemiptera: Membracidae). |
Q89360321 | Local prey community composition and genetic distance predict venom divergence among populations of the northern Pacific rattlesnake (Crotalus oreganus) |
Q92902048 | Local thermal adaptation detected during multiple life stages across populations of Drosophila melanogaster |
Q60380011 | Locally asymmetric introgressions between subspecies suggest circular range expansion at the Antirrhinum majus global scale |
Q81670538 | Locally differentiated cryptic pigmentation in the freshwater isopod Asellus aquaticus |
Q83606702 | Locomotor activity of mice divergently selected for basal metabolic rate: a test of hypotheses on the evolution of endothermy |
Q34314446 | Locomotory abilities and habitat of the Cretaceous bird Gansus yumenensis inferred from limb length proportions. |
Q39549849 | Long day plants and the response to global warming: rapid evolutionary change in day length sensitivity is possible in wild beet. |
Q82487350 | Long distance dispersal and the fate of a gene from the colonization front |
Q56920154 | Long-term experimental evolution in |
Q115729603 | Long-term experimental evolution in Escherichia coli. V. Effects of recombination with immigrant genotypes on the rate of bacterial evolution |
Q39077266 | Long-term panmixia in a cosmopolitan Indo-Pacific coral reef fish and a nebulous genetic boundary with its broadly sympatric sister species. |
Q92568979 | Longer life span is associated with elevated immune activity in a seasonally polyphenic butterfly |
Q64032233 | Longevity and resistance to cold stress in cold-stress selected lines and their controls in Drosophila melanogaster |
Q46324159 | Looks matter: changes in flower form affect pollination effectiveness in a sexually deceptive orchid. |
Q91239132 | Losing the trait without losing the signal: Evolutionary shifts in communicative colour signalling |
Q40707107 | Loss of adaptation following reversion suggests trade-offs in host use by a seed beetle |
Q80454456 | Loss of complementation and the logic of two-step meiosis |
Q56032148 | Loss of genetic diversity and fitness in Common Toad (Bufo bufo) populations isolated by inimical habitat |
Q24611833 | Loss of genetic variability in social spiders: genetic and phylogenetic consequences of population subdivision and inbreeding |
Q41564638 | Lotus hosts delimit the mutualism-parasitism continuum of Bradyrhizobium |
Q47587593 | Loudness of birdsong is related to the body size, syntax and phonology of passerine species |
Q51664127 | Lovesick: immunological costs of mating to male sagebrush crickets. |
Q54457668 | Low abundance of Escherichia coli microsatellites is associated with an extremely low mutation rate. |
Q44700538 | Low genetic diversity and strong but shallow population differentiation suggests genetic homogenization by metapopulation dynamics in a social spider |
Q44041400 | Low heritabilities, but genetic and maternal correlations between red squirrel behaviours. |
Q47551881 | Low levels of hybridization in two species of African driver ants. |
Q52693069 | Low migration decreases interference competition among parasites and increases virulence. |
Q42011050 | Low parasitism rates in parthenogenetic bagworm moths do not support the parasitoid hypothesis for sex. |
Q44252491 | Low rates of X-Y recombination, not turnovers, account for homomorphic sex chromosomes in several diploid species of Palearctic green toads (Bufo viridis subgroup). |
Q35766834 | Low reproductive isolation and highly variable levels of gene flow reveal limited progress towards speciation between European river and brook lampreys. |
Q39125800 | Lower fecundity in parthenogenetic geckos than sexual relatives in the Australian arid zone. |
Q30440757 | Lowering sample size in comparative analyses can indicate a correlation where there is none: example from Rensch's rule in primates |
Q51595009 | MC1R-dependent, melanin-based colour polymorphism is associated with cell-mediated response in the Eleonora's falcon. |
Q33260363 | MHC class I variation associates with parasite resistance and longevity in tropical pythons. |
Q51339398 | MHC genotype predicts mate choice in the ring-necked pheasant Phasianus colchicus. |
Q35592157 | MHC studies in nonmodel vertebrates: what have we learned about natural selection in 15 years? |
Q40863893 | MHC, parasites and antler development in red deer: no support for the Hamilton & Zuk hypothesis. |
Q58557397 | MHC-linked susceptibility to a bacterial infection, but no MHC-linked cryptic female choice in whitefish |
Q43860638 | Machine learning identifies specific habitats associated with genetic connectivity in Hyla squirella |
Q43509118 | Macro- and microgeographic genetic structure in an ant species with alternative reproductive tactics in sexuals. |
Q46056919 | Macroecological patterns of sexual size dimorphism in turtles of the world. |
Q57007001 | Macroevolution of hoverflies (Diptera: Syrphidae): the effect of using higher-level taxa in studies of biodiversity, and correlates of species richness |
Q100527458 | Macroevolutionary dynamics of parasite diversification: a reality check |
Q47431280 | Macroevolutionary pattern of sexual size dimorphism in geckos corresponds to intraspecific temperature-induced variation |
Q45746788 | Macroevolutionary patterns in the origin of mutualisms involving ants. |
Q34412734 | Macroevolutionary trends in the Dinosauria: Cope's rule |
Q44860805 | Macronutrient intake regulates sexual conflict in decorated crickets |
Q51687274 | Maintenance of clinal variation for shell colour phenotype in the flat periwinkle Littorina obtusata. |
Q61659000 | Maintenance of genetic differentiation across a transition zone in the sea: discordance between nuclear and cytoplasmic markers |
Q33364747 | Maintenance of polygenic sex determination in a fluctuating environment: an individual-based model. |
Q47809114 | Maize Sh2 gene is constrained by natural selection but escaped domestication. |
Q51657443 | Major disruption of gene expression in hybrids between young sympatric anadromous and resident populations of brook charr (Salvelinus fontinalis Mitchill). |
Q60542854 | Major gene effects on phenotype and fitness: the relative roles of Pgm-3 and Gp-9 in introduced populations of the fire ant Solenopsis invicta |
Q46527713 | Major histocompatibility complex diversity is positively associated with stream water temperatures in proximate populations of sockeye salmon |
Q89380990 | Major histocompatibility complex variation and blood parasites in resident and migratory populations of the common yellowthroat |
Q51780593 | Male Drosophila melanogaster have higher mating success when adapted to their thermal environment. |
Q90143159 | Male age and its association with reproductive traits in captive and wild house sparrows |
Q51542878 | Male and female secondary sexual traits show different patterns of quantitative genetic and environmental variation in the horned beetle Onthophagus sagittarius. |
Q44691517 | Male attractiveness, fertility and susceptibility to oxidative stress are influenced by inbreeding in Drosophila simulans. |
Q48245833 | Male behaviour drives assortative reproduction during the initial stage of secondary contact |
Q46813496 | Male body size and condition affects sperm number and production rates in mosquitofish, Gambusia holbrooki |
Q39076810 | Male burying beetles extend, not reduce, parental care duration when reproductive competition is high |
Q50146939 | Male choice generates stabilizing sexual selection on a female fecundity correlate |
Q30456200 | Male courtship preferences demonstrate discrimination against allopatric colour morphs in a cichlid fish |
Q47621182 | Male facial attractiveness and masculinity may provide sex- and culture-independent cues to semen quality |
Q52641789 | Male fitness of honeybee colonies (Apis mellifera L.). |
Q51402673 | Male inbreeding status affects female fitness in a seed-feeding beetle. |
Q42003621 | Male interference with pollination efficiency in a hermaphroditic orchid |
Q46906810 | Male mate choice relies on major histocompatibility complex class I in a sex-role-reversed pipefish. |
Q43946181 | Male mating preferences pre-date the origin of a female trait polymorphism in an incipient species complex of Lake Victoria cichlids. |
Q51163831 | Male mealworm beetles increase resting metabolic rate under terminal investment. |
Q52641771 | Male parentage does not vary with colony kin structure in a multiple-queen ant. |
Q51657240 | Male personality, life-history strategies and reproductive success in a promiscuous mammal. |
Q92028073 | Male phenotypes in a female framework: Evidence for degeneration in sperm produced by male snails from asexual lineages |
Q47756527 | Male quality, signal reliability and female choice: assessing the expectations of inter-sexual selection |
Q51687768 | Male sand crickets trade-off flight capability for reproductive potential. |
Q36201713 | Male sterility at extreme temperatures: a significant but neglected phenomenon for understanding Drosophila climatic adaptations |
Q51682177 | Male sterility, fitness gain curves and the evolution of gender specialization from distyly in Erythroxylum havanense. |
Q39402353 | Male territoriality and 'sex confusion' in recently adapted lizards at White Sands |
Q56171466 | Male-biased gene flow across an avian hybrid zone: evidence from mitochondrial and microsatellite DNA |
Q49977931 | Male-male aggression is unlikely to stabilize a poison frog polymorphism |
Q50471673 | Male-male competition and speciation: aggression bias towards differently coloured rivals varies between stages of speciation in a Lake Victoria cichlid species complex. |
Q37361615 | Male-male competition, female mate choice and their interaction: determining total sexual selection |
Q46612896 | Males adjust their signalling behaviour according to experience of male signals and male-female signal duets |
Q91966559 | Males from populations with higher competitive mating success produce sons with lower fitness |
Q51546536 | Male‐induced costs of mating for females compensated by offspring viability benefits in an insect |
Q58827513 | Mandible asymmetry and genetic diversity in island populations of the common shrew, Sorex araneus |
Q52698829 | Manifold aspects of specificity in a nematode-bacterium mutualism. |
Q47376668 | Manipulating developmental stress reveals sex-specific effects of egg size on offspring phenotype |
Q51766203 | Manipulation of oviposition choice of the parasitoid wasp, Encarsia pergandiella, by the endosymbiotic bacterium Cardinium. |
Q51145270 | Manipulation of parental nutritional condition reveals competition among family members. |
Q36235681 | Mapping of within-species segregation distortion in Drosophila persimilis and hybrid sterility between D. persimilis and D. pseudoobscura |
Q38963608 | Marine-freshwater transitions are associated with the evolution of dietary diversification in terapontid grunters (Teleostei: Terapontidae). |
Q51476766 | Marker-based estimates of relatedness and inbreeding coefficients: an assessment of current methods. |
Q125965574 | Martin Lockley: Tracking Dinosaurs. A New Look at an Ancient World. 238 pp. Cambridge University Press, Cambridge 1991. Paperback $14.95. ISBN: 0‐521‐42598‐0. |
Q57940316 | Mass-dependent reproductive strategies in wild bighorn ewes: a quantitative genetic approach |
Q112207623 | Matching field and laboratory environments: effects of neglecting daily temperature variation on insect reaction norms |
Q52697696 | Mate availability contributes to maintain the mixed-mating system in a scolytid beetle. |
Q49186289 | Mate choice among yeast gametes can purge deleterious mutations |
Q50664651 | Mate choice and the operational sex ratio: an experimental test with robotic crabs. |
Q50614799 | Mate choice based on a key ecological performance trait. |
Q51672618 | Mate choice for nonadditive genetic benefits and the maintenance of genetic diversity in song sparrows. |
Q39057668 | Mate choice opportunity leads to shorter offspring development time in a desert insect |
Q39268485 | Mate competition and resource competition are inter-related in sexual selection |
Q50489787 | Mate recognition in a freshwater fish: geographical distance, genetic differentiation, and variation in female preference for local over foreign males. |
Q45919045 | Mate-sampling costs and sexy sons. |
Q60311511 | Maternal allocation strategies and differential effects of yolk carotenoids on the phenotype and viability of yellow-legged gull (Larus michahellis) chicks in relation to sex and laying order |
Q34705672 | Maternal and paternal condition effects on offspring phenotype in Telostylinus angusticollis (Diptera: Neriidae). |
Q46347951 | Maternal antibodies but not carotenoids in barn swallow eggs covary with embryo sex. |
Q44888120 | Maternal care, mother-offspring aggregation and age-dependent coadaptation in the European earwig |
Q46630591 | Maternal control of offspring sex and male morphology in the Otitesella fig wasps |
Q44610912 | Maternal effects and heritability of annual productivity |
Q51140480 | Maternal effects are long-lasting and influence female offspring's reproductive strategy in the swordtail fish Xiphophorus multilineatus. |
Q125833336 | Maternal effects shape offspring physiological condition but do not senesce in a wild mammal |
Q38446342 | Maternal genetic effects on adaptive divergence between anadromous and resident brook charr during early life history |
Q60490513 | Maternal genetic effects set the potential for evolution in a free-living vertebrate population |
Q38419496 | Maternal investment increases with altitude in a frog on the Tibetan Plateau |
Q44921013 | Maternal sex and mate relatedness affect offspring quality in the gynodioecious Silene acaulis |
Q46318366 | Maternal sexual interactions affect offspring survival and ageing |
Q36236229 | Maternal source of variability in the embryo development of an annual killifish. |
Q51749455 | Maternal transmission of cytoplasmic DNA in interspecific hybrids of peat mosses, Sphagnum (Bryophyta). |
Q46772564 | Maternal-foetal genomic conflict and speciation: no evidence for hybrid placental dysplasia in crosses between two house mouse subspecies |
Q79787809 | Mating preferences, sexual selection and patterns of cladogenesis in ray-finned fishes |
Q45046189 | Mating stimulates female feeding: testing the implications for the evolution of nuptial gifts |
Q48474619 | Mating strategies in dominant meerkats: evidence for extra-pair paternity in relation to genetic relatedness between pair mates. |
Q30786784 | Mating systems and selection efficacy: a test using chloroplastic sequence data in Angiosperms |
Q50759658 | Mating triggers dynamic immune regulations in wood ant queens. |
Q30446786 | Maximized virulence in a sterilizing pathogen: the anther-smut fungus and its co-evolved hosts |
Q91669781 | May the (selective) force be with you: Spatial sorting and natural selection exert opposing forces on limb length in an invasive amphibian |
Q34803050 | Measurement scale in maximum entropy models of species abundance. |
Q60412810 | Measurements of selection on floral traits in black mustard, Brassica nigra |
Q51682641 | Measuring and comparing evolvability and constraint in multivariate characters. |
Q64080756 | Measuring morphological complexity of segmented animals: centipedes as model systems |
Q52664024 | Measuring natural and sexual selection on breeding values of male display traits in Drosophila serrata. |
Q51561803 | Measuring sexual selection on females in sex-role-reversed Mormon crickets (Anabrus simplex, Orthoptera: Tettigoniidae). |
Q115033074 | Measuring, comparing and interpreting phenotypic selection on floral scent |
Q91862559 | Mechanical and structural adaptations to migration in the flight feathers of a Palaearctic passerine |
Q50687026 | Mechanism of a plastic phenotypic response: predator-induced shell thickening in the intertidal gastropod Littorina obtusata. |
Q51568922 | Mechanisms and fitness effects of antibacterial defences in a carrion beetle. |
Q60412754 | Mechanisms of constraints: the contributions of selection and genetic variance to the maintenance of cotyledon number in wild radish |
Q37052144 | Mechanisms of pathogenesis and the evolution of parasite virulence |
Q33358021 | Mechanistic constraints and the unlikely evolution of reciprocal cooperation |
Q28283984 | Medicago-Sinorhizobium symbiotic specificity evolution and the geographic expansion of Medicago |
Q39013051 | Medullary bone in fossils: function, evolution and significance in growth curve reconstructions of extinct vertebrates |
Q52780431 | Meiotic drive influences the outcome of sexually antagonistic selection at a linked locus. |
Q43598412 | Melanic through nature or nurture: genetic polymorphism and phenotypic plasticity in Harmonia axyridis |
Q33693821 | Melanin coloration has temperature-dependent effects on breeding performance that may maintain phenotypic variation in a passerine bird. |
Q38977536 | Meta-analysis of magnitudes, differences and variation in evolutionary parameters |
Q51623708 | Metabolic rates, genetic constraints, and the evolution of endothermy. |
Q33397123 | Metapopulation persistence in fragmented landscapes: significant interactions between genetic and demographic processes. |
Q56986076 | Methodological challenges to realizing the potential of hybridization research |
Q42452327 | Mice divergently selected for high and low basal metabolic rates evolved different cell size and organ mass |
Q129964591 | Michener’s group-size paradox in cooperatively breeding birds |
Q35158598 | Microbiome investigation in the ecological speciation context of lake whitefish (Coregonus clupeaformis) using next-generation sequencing |
Q41932804 | Microcephaly genes and the evolution of sexual dimorphism in primate brain size |
Q101631245 | Microgeographic variation in Anolis oculatus, on the island of Dominica, West Indies |
Q34335396 | Microsatellite and single-nucleotide polymorphisms indicate recurrent transitions to asexuality in a microsporidian parasite. |
Q38971608 | Microsatellite evidence for obligate autogamy, but abundant genetic variation in the herbaceous monocarp Lobelia inflata (Campanulaceae). |
Q101631258 | Microsatellite mutations in litters of the Australian lizard Egernia stokesii |
Q39409826 | Microsatellite variation among diverging populations of Drosophila mojavensis |
Q35163637 | Migrate small, sound big: functional constraints on body size promote tracheal elongation in cranes |
Q51699351 | Migration load in plants: role of pollen and seed dispersal in heterogeneous landscapes. |
Q79325904 | Migratory costs and contemporary evolution of reproductive allocation in male chinook salmon |
Q47252767 | Migratory divides and their consequences for dispersal, population size and parasite-host interactions. |
Q39106994 | Mimicry and the evolution of premating isolation in Heliconius melpomene Linnaeus |
Q98720376 | Mimicry genes reduce pre-adult survival rate in Papilio polytes: A possible new mechanism for maintaining female-limited polymorphism in Batesian mimicry |
Q35548843 | Mismatch in the distribution of floral ecotypes and pollinators: insights into the evolution of sexually deceptive orchids |
Q46884168 | Misregulation of spermatogenesis genes in Drosophila hybrids is lineage-specific and driven by the combined effects of sterility and fast male regulatory divergence |
Q45369038 | Mitochondrial DNA as a tool for reconstructing past life-history traits in mammals |
Q88868925 | Mitochondrial complementation: a possible neglected factor behind early eukaryotic sex |
Q60503623 | Mitochondrial differentiation in a polymorphic land snail: evidence for Pleistocene survival within the boundaries of permafrost |
Q57614880 | Mitochondrial haplotype does not affect sperm velocity in the zebra finchTaeniopygia guttata |
Q47177449 | Mixed evidence for early bursts of morphological evolution in extant clades. |
Q46379310 | Mixed evidence for the erosion of intertactical genetic correlations through intralocus tactical conflict. |
Q46812590 | Mixed infections may promote diversification of mutualistic symbionts: why are there ineffective rhizobia? |
Q128160048 | Mixed support for an alignment between phenotypic plasticity and genetic differentiation in damselfly wing shape |
Q51619085 | Mobile DNA can drive lineage extinction in prokaryotic populations. |
Q91639990 | Model-based demographic inference of introgression history in European whitefish species pairs' |
Q51935156 | Modelling social evolution: the relative merits and limitations of a Hamilton's rule-based approach. |
Q60367795 | Modelling the establishment and spread of autotetraploid plants in a spatially heterogeneous environment |
Q46489826 | Modelling the evolution of common cuckoo host-races: speciation or genetic swamping? |
Q60567776 | Modelling the genetics and demography of step cline formation: gastropod populations preyed on by experimentally introduced crabs |
Q52374391 | Modelling the influence of parental effects on gene-network evolution. |
Q51569065 | Modelling the maintenance of egg polymorphism in avian brood parasites and their hosts. |
Q52641769 | Modelling the spatial configuration of refuges for a sustainable control of pests: a case study of Bt cotton. |
Q51722521 | Models of cooperation. |
Q93197015 | Moderate heritability and low evolvability of sperm morphology in a species with high risk of sperm competition, the collared flycatcher Ficedula albicollis |
Q98383691 | Modification of reproductive schedule in response to pathogen exposure in a wild insect: support for the terminal investment hypothesis |
Q37235688 | Modifying effects of phenotypic plasticity on interactions among natural selection, adaptation and gene flow |
Q51627925 | Modular genetic architecture of floral morphology in Nicotiana: quantitative genetic and comparative phenotypic approaches to floral integration. |
Q51811607 | Modulation of sexual signalling by immune challenged male mealworm beetles (Tenebrio molitor, L.): evidence for terminal investment and dishonesty. |
Q48497694 | Molecular and pedigree measures of relatedness provide similar estimates of inbreeding depression in a bottlenecked population |
Q30848043 | Molecular and quantitative genetic differentiation across Europe in yellow dung flies. |
Q60379665 | Molecular biogeography: using the Corsica-Sardinia microplate disjunction to calibrate mitochondrial rDNA evolutionary rates in mountain newts (Euproctus) |
Q60379670 | Molecular biogeography: using the Corsica-Sardinia microplate disjunction to calibrate mitochondrial rDNA evolutionary rates in mountain newts (Euproctus) |
Q112810467 | Molecular data suggest a hybrid origin for the invasive Caulerpa racemosa (Caulerpales, Chlorophyta) in the Mediterranean Sea |
Q38883629 | Molecular divergence in tropical tree populations occupying environmental mosaics |
Q63379783 | Molecular evidence for the paraphyly of Scolecophidia and its evolutionary implications |
Q51703563 | Molecular evidence of Pleistocene bidirectional faunal exchange between Europe and the Near East: the case of the bicoloured shrew (Crocidura leucodon, Soricidae). |
Q110530546 | Molecular evolution and convergence of the rhodopsin gene in Gymnogobius , a goby group having diverged into coastal to freshwater habitats |
Q34470823 | Molecular evolution of animal antimicrobial peptides: widespread moderate positive selection |
Q51068324 | Molecular evolution of candidate genes involved in post-mating-prezygotic reproductive isolation. |
Q48001451 | Molecular evolution of plant haemoglobin: two haemoglobin genes in Nymphaeaceae Euryale ferox |
Q83287130 | Molecular evolution of the avian growth hormone gene and comparison with its mammalian counterpart |
Q92996529 | Molecular evolution of the sex peptide network in Drosophila |
Q52705476 | Molecular evolutionary analysis of seminal receptacle sperm storage organ genes of Drosophila melanogaster. |
Q61772259 | Molecular information on bowerbird phylogeny and the evolution of exaggerated male characteristics |
Q90161079 | Molecular insights into post-mating immune response in a fish with internal fertilization |
Q30474952 | Molecular patterns of differentiation in canyon treefrogs (Hyla arenicolor): evidence for introgressive hybridization with the Arizona treefrog (H. wrightorum) and correlations with advertisement call differences |
Q38912130 | Molecular phylogenetics reveals a pattern of biome conservatism in New World anchovies (family Engraulidae). |
Q45353136 | Molecular phylogeny and divergence dates for Australasian elapids and sea snakes (hydrophiinae): evidence from seven genes for rapid evolutionary radiations. |
Q54520241 | Molecular phylogeny and plumage evolution in gulls (Larini) |
Q57273723 | Molecular phylogeny of araneomorph spiders |
Q56384989 | Molecular phylogeny of cuckoos supports a polyphyletic origin of brood parasitism |
Q101631249 | Molecular phylogeny of the Canary Island lacertids (Gallotia): mitochondrial DNA restriction fragment divergence in relation to sequence divergence and geological time |
Q55953747 | Molecular phylogeny of the tribe Bovini (Mammalia: Artiodactyla): alternative placement of the Anoa |
Q35769181 | Molecular species delimitation methods recover most song-delimited cicada species in the European Cicadetta montana complex |
Q30910817 | Molecular, morphological and behavioural data reveal the presence of a cryptic species in the widely studied Drosophila serrata species complex. |
Q56114887 | Monogamous pair bonds and mate switching in the Western Australian seahorse Hippocampus subelongatus |
Q50868468 | More on the genetical theory of multilevel selection. |
Q97079416 | Morph-dependent fitness and directional change of morph frequencies over time in a Dutch population of Common buzzards Buteo buteo |
Q47225301 | Morph-ratio variation, population size and female reproductive success in distylous Pulmonaria officinalis (Boraginaceae). |
Q57208014 | Morph-specific selection on floral traits in a polymorphic plant |
Q44342025 | Morphological and genetic divergence of intralacustrine stickleback morphs in Iceland: a case for selective differentiation? |
Q79321166 | Morphological and microsatellite differentiation in Melospiza melodia (Aves) at a microgeographic scale |
Q123128696 | Morphological asymmetry and interspecific hybridization: A case study using hylid frogs |
Q34999945 | Morphological change and phenotypic plasticity in native and non-native pumpkinseed sunfish in response to sustained water velocities |
Q36339368 | Morphological constraints on changing avian migration phenology. |
Q44226869 | Morphological convergence as a consequence of extreme functional demands: examples from the feeding system of natricine snakes. |
Q46305179 | Morphological determinants of signal carrier frequency in katydids (Orthoptera): a comparative analysis using biophysical evidence of wing vibration. |
Q51170324 | Morphological differentiation correlates with ecological but not with genetic divergence in a Gehyra gecko. |
Q81670533 | Morphological divergence and origin of sympatric populations of European whitefish (Coregonus lavaretus L.) in Lake Femund, Norway |
Q45934309 | Morphological evidence of correlational selection and ecological segregation between dextral and sinistral forms in a polymorphic flatfish, Platichthys stellatus. |
Q51177916 | Morphological evolution in Tropidurinae squamates: an integrated view along a continuum of ecological settings. |
Q33254008 | Morphological integration and adaptation in the snake feeding system: a comparative phylogenetic study |
Q53705443 | Mosaicism and chimerism as components of intraorganismal genetic heterogeneity. |
Q90935849 | Mother's curse and indirect genetic effects: Do males matter to mitochondrial genome evolution? |
Q50453629 | Moult speed affects structural feather ornaments in the blue tit. |
Q57699108 | Moult speed constrains the expression of a carotenoid-based sexual ornament |
Q33410379 | Mountain birch under multiple stressors--heavy metal-resistant populations co-resistant to biotic stress but maladapted to abiotic stress. |
Q92875411 | Movement of a Heliconius hybrid zone over 30 years: A Bayesian approach |
Q56698371 | Moving in two worlds: aquatic and terrestrial locomotion in sea snakes (Laticauda colubrina, Laticaudidae) |
Q45786524 | Moving to mate: the evolution of separate and combined sexes in multicellular organisms. |
Q80960871 | Much ado about nothing... so far? |
Q34175007 | Much ado about nothing: Nowak et al.'s charge against inclusive fitness theory |
Q113855133 | Much mathematics of many loci |
Q48793188 | Much more than a ratio: multivariate selection on female bodies. |
Q50237330 | Multicellular group formation in response to predators in the alga Chlorella vulgaris |
Q47690996 | Multicoloured greenbeards, bacteriocin diversity and the rock-paper-scissors game |
Q46864700 | Multigenerational response to artificial selection for biased clutch sex ratios in Tigriopus californicus populations |
Q50868455 | Multilevel selection theory and evidence: a critique of Gardner, 2015. |
Q52734023 | Multilocus analysis of nucleotide variation in Drosophila madeirensis, an endemic species of the Laurisilva forest in Madeira. |
Q41379340 | Multilocus phylogenetic and geospatial analyses illuminate diversification patterns and the biogeographic history of Malagasy endemic plated lizards (Gerrhosauridae: Zonosaurinae). |
Q46378385 | Multimodal signalling in estrildid finches: song, dance and colour are associated with different ecological and life-history traits |
Q37832760 | Multimodel inference in ecology and evolution: challenges and solutions. |
Q39709943 | Multiple cryptic species of sympatric generalists within the avian blood parasite Haemoproteus majoris |
Q57052362 | Multiple infection dynamics has pronounced effects on the fitness of RNA viruses |
Q44590458 | Multiple infections, kin selection and the evolutionary epidemiology of parasite traits |
Q59187070 | Multiple mating, sperm competition and meiotic drive |
Q56552601 | Multiple mating, sperm transfer and oviposition pattern in the giant sperm species, Drosophila bifurca |
Q125975520 | Multiple origins of self‐fertilization in tristylous Eichhornia paniculata (Pontederiaceae): Inferences from style morph and isozyme variation |
Q53910565 | Multiple parasites are driving major histocompatibility complex polymorphism in the wild. |
Q43413098 | Multiple parasites mediate balancing selection at two MHC class II genes in the fossorial water vole: insights from multivariate analyses and population genetics |
Q79325917 | Multiple paternity and population genetic structure in natural populations of the poeciliid fish, Heterandria formosa |
Q40428017 | Multiple paternity in a wild population of Armadillidium vulgare: influence of infection with Wolbachia? |
Q117378014 | Multiple paternity in superfetatious live‐bearing fishes |
Q44805981 | Multiple paternity or multiple queens: two routes to greater intracolonial genetic diversity in the eusocial Hymenoptera. |
Q51799606 | Multiple pathways of maternal effects in black-headed gull eggs: constraint and adaptive compensatory adjustment. |
Q52721734 | Multiple quantitative trait loci influence intra-specific variation in genital morphology between phylogenetically distinct lines of Drosophila montana. |
Q42021075 | Multiple sources of reproductive isolation in a bimodal butterfly hybrid zone |
Q44145119 | Multiplicative interaction between the two major mechanisms of permethrin resistance, kdr and cytochrome P450-monooxygenase detoxification, in mosquitoes |
Q82950284 | Multiplicity of infection does not accelerate infectivity evolution of viral parasites in laboratory microcosms |
Q60198480 | Multispecies coalescent analysis confirms standing phylogenetic instability in Hexapoda |
Q114080033 | Multispecies colour polymorphisms associated with contrasting microhabitats in two Mediterranean wrasse radiations |
Q52753589 | Multivariate analysis of adaptive capacity for upper thermal limits in Drosophila simulans. |
Q30252737 | Multivariate genetic architecture of the Anolis dewlap reveals both shared and sex-specific features of a sexually dimorphic ornament. |
Q34111080 | Multivariate phenotypes and the potential for alternative phenotypic optima in wall lizard (Podarcis muralis) ventral colour morphs. |
Q50883877 | Multivariate selection and intersexual genetic constraints in a wild bird population. |
Q58015758 | Multivariate selection for the rest of us |
Q46450407 | Multivariate sexual selection on male tegmina in wild populations of sagebrush crickets, Cyphoderris strepitans (Orthoptera: Haglidae). |
Q52577654 | Mutation accumulation in populations of varying size: large effect mutations cause most mutational decline in the rotifer B. calyciflorus under UV-C radiation. |
Q115033071 | Mutation and selection processes regulating short tandem repeats give rise to genetic and phenotypic diversity across species |
Q81317950 | Mutation and the experimental evolution of outcrossing in Caenorhabditis elegans |
Q85194170 | Mutation surfing and the evolution of dispersal during range expansions |
Q52648271 | Mutation-selection balance accounting for genetic variation for viability in Drosophila melanogaster as deduced from an inbreeding and artificial selection experiment. |
Q112207618 | Mutational collapse of fitness in marginal habitats and the evolution of ecological specialisation |
Q84999624 | Mutualism variation in the nodulation response to nitrate |
Q39196532 | Mutualism, hybrid inviability and speciation in a tropical ant-plant |
Q80801846 | Mutualism, market effects and partner control |
Q91274777 | N-glycoproteins exhibit a positive expression level-evolutionary rate correlation |
Q92294666 | Na+ /K+ -ATPase gene duplications in clitellate annelids are associated with freshwater colonization |
Q41925500 | Narrow hybrid zones in spite of very low population differentiation in neutral markers in an island bird species complex. |
Q96645846 | Narrow phenotypic and parasitic clines shape secondary contact zones of closely-related Erebia butterflies |
Q51691317 | Natal dispersal patterns are not associated with inbreeding avoidance in the Seychelles warbler. |
Q47268510 | Natural and sexual selection against immigrants maintains differentiation among micro-allopatric populations |
Q51612348 | Natural hybridization between extremely divergent chromosomal races of the common shrew (Sorex araneus, Soricidae, Soricomorpha): hybrid zone in European Russia. |
Q53252886 | Natural hybridization between extremely divergent chromosomal races of the common shrew (Sorex araneus, Soricidae, Soricomorpha): hybrid zone in Siberia. |
Q52656845 | Natural selection and genetic variation for female resistance to harm from males. |
Q42633330 | Natural selection and glucocorticoid physiology |
Q33358908 | Natural selection drives patterns of lake-stream divergence in stickleback foraging morphology. |
Q89370167 | Natural selection for body shape in resource polymorphic Icelandic Arctic charr |
Q51625321 | Natural selection hampers divergence of reproductive traits in a seed beetle. |
Q34253566 | Natural selection in the water: freshwater invasion and adaptation by water colour in the Amazonian pufferfish. |
Q34888419 | Natural selection maximizes Fisher information. |
Q44223949 | Natural selection on a measure of parasite resistance varies across ages and environmental conditions in a wild mammal |
Q30870040 | Natural selection on quantitative immune defence traits: a comparison between theory and data. |
Q57237107 | Natural selection on the genetical component of variance in body condition in a wild bird population |
Q50747652 | Natural selection, evolvability and bias due to environmental covariance in the field in an annual plant. |
Q37937060 | Natural selection. I. Variable environments and uncertain returns on investment |
Q37937057 | Natural selection. II. Developmental variability and evolutionary rate. |
Q28732824 | Natural selection. III. Selection versus transmission and the levels of selection |
Q27003368 | Natural selection. IV. The Price equation |
Q38060807 | Natural selection. V. How to read the fundamental equations of evolutionary change in terms of information theory |
Q38075188 | Natural selection. VI. Partitioning the information in fitness and characters by path analysis. |
Q26995429 | Natural selection. VII. History and interpretation of kin selection theory |
Q113855144 | Nature's experiment with in situ hybridization? A hypothesis for the mechanism of Rb fusion |
Q44582703 | Nectar sugar composition of European Caryophylloideae (Caryophyllaceae) in relation to flower length, pollination biology and phylogeny |
Q39006669 | Negative association between parental care and sibling cooperation in earwigs: a new perspective on the early evolution of family life? |
Q57266138 | Negatively condition dependent predation cost of a positively condition dependent sexual signalling |
Q34811121 | Neighbouring-group composition and within-group relatedness drive extra-group paternity rate in the European badger (Meles meles). |
Q46904913 | Neo-sex chromosome inheritance across species in Silene hybrids |
Q93340880 | Neotropical frogs and mating songs: The evolution of advertisement calls in glassfrogs |
Q46661297 | Nestling coloration is adjusted to parent visual performance in altricial birds irrespective of assumptions on vision system for Laniidae and owls, a reply to Renoult et al. |
Q83302862 | Nestling colouration is adjusted to parent visual performance in altricial birds |
Q63257203 | Nestling growth in the Great Tit I. Heritability estimates under different environmental conditions |
Q47566233 | Nestlings' carotenoid feather ornament affects parental allocation strategy and reduces maternal survival |
Q30538685 | Neural steroid sensitivity and aggression: comparing individuals of two songbird subspecies |
Q38756958 | Neutral processes forming large clones during colonization of new areas. |
Q22065683 | Neutral theory: a historical perspective |
Q82041924 | Nice natives and mean migrants: the evolution of dispersal-dependent social behaviour in viscous populations |
Q88887233 | Niche conservatism and phylogenetic clustering in a tribe of arid-adapted marsupial mice, the Sminthopsini |
Q58588481 | Niche differentiation among clones in asexual grass thrips |
Q45414342 | Niche differentiation and colonization of a novel environment by an asexual parasitic wasp |
Q51579088 | Niche divergence and lineage diversification among closely related Sistrurus rattlesnakes. |
Q44969418 | Niche evolution and thermal adaptation in the temperate species Drosophila americana. |
Q47342483 | Night and day: the comparative study of strepsirrhine primates reveals socioecological and phylogenetic patterns in olfactory signals |
Q91833393 | No Evidence for Divergence in Male Harmfulness or Female Resistance in Response to Changes in the Opportunity for Dispersal |
Q44367138 | No association between sperm competition and sperm length variation across dung flies (Scathophagidae). |
Q87315487 | No correlation between multi-locus heterozygosity and fitness in the common buzzard despite heterozygote advantage for plumage colour |
Q51907433 | No direct selection to increase offspring number of bet-hedging strategies in large populations: Simons' model revisited. |
Q43606376 | No effect of host-parasite co-evolution on host range expansion. |
Q41464656 | No evidence for MHC class I-based disassortative mating in a wild population of great tits. |
Q40581985 | No evidence for a trade-off between sperm length and male premating weaponry. |
Q91676656 | No evidence for an intragenomic arms race under paternal genome elimination in Planococcus mealybugs |
Q52755974 | No evidence for behavioural adaptations to nematode parasitism by the fly Drosophila putrida. |
Q43967555 | No evidence for condition-dependent expression of male genitalia in the dung beetle Onthophagus taurus. |
Q50283005 | No evidence for general condition-dependence of structural plumage colour in blue tits: an experiment. |
Q125261155 | No evidence for incipient speciation by selfing in North American Arabidopsis lyrata |
Q60455243 | No evidence for parallel sympatric speciation in cichlid species of the genus Pseudotropheus from north-western Lake Malawi |
Q51729463 | No evidence for survival selection on carotenoid-based nestling coloration in great tits (Parus major). |
Q34483350 | No evidence for the 'Meselson effect' in parthenogenetic oribatid mites (Oribatida, Acari). |
Q48565584 | No evidence for the 'expensive-tissue hypothesis' from an intraspecific study in a highly variable species. |
Q90079215 | No evidence of inbreeding depression in fast declining herds of migratory caribou |
Q51683174 | No evidence of mitochondrial genetic variation for sperm competition within a population of Drosophila melanogaster. |
Q57467426 | No evidence of quantitative signal honesty across species of aposematic burnet moths (Lepidoptera: Zygaenidae) |
Q47374008 | No evidence of trade-offs in the evolution of sperm numbers and sperm size in mammals |
Q91408583 | No evidence that Y-chromosome differentiation affects male fitness in a Swiss population of common frogs |
Q48443420 | No evidence that experimental manipulation of sexual conflict drives premating reproductive isolation in Drosophila melanogaster |
Q43552505 | No fecundity cost of female secondary sexual trait expression in the horned beetle Onthophagus sagittarius. |
Q92722693 | No gains for bigger brains: Functional and neuroanatomical consequences of relative brain size in a parasitic wasp |
Q51755235 | No genetic evidence of sex-biased dispersal in a lekking bird, the capercaillie (Tetrao urogallus). |
Q46317382 | No geographic variation in thermoregulatory colour plasticity and limited variation in heat-avoidance behaviour in Battus philenor caterpillars. |
Q51917919 | No heightened condition dependence of zebra finch ornaments--a quantitative genetic approach. |
Q90261790 | No mate preference associated with the supergene controlling social organization in Alpine silver ants |
Q64997769 | No measurable fitness cost to experimentally evolved host defence in the Caenorhabditis elegans-Serratia marcescens host-parasite system. |
Q104130171 | No obvious transcriptome-wide signature of indirect selection in termites |
Q35282470 | No patterns in thermal plasticity along a latitudinal gradient in Drosophila simulans from eastern Australia |
Q80960915 | No place like home: competition, dispersal and complex adaptation |
Q45885489 | No resistance to male-killing Wolbachia after thousands of years of infection |
Q51606600 | No reversion to single mating in a socially parasitic ant. |
Q109746378 | No room for males in caves: Female‐biased sex ratio in subterranean amphipods of the genus Niphargus |
Q93002747 | No selection for change in polyandry under experimental evolution |
Q31039479 | No sympatric speciation here: multiple data sources show that the ant Myrmica microrubra is not a separate species but an alternate reproductive morph of Myrmica rubra. |
Q51725446 | No trade-off between learning ability and parasitoid resistance in Drosophila melanogaster. |
Q56984125 | Non-equilibrium gene frequency divergence: persistent founder effects in natural populations |
Q80511452 | Nonadditive effects of group membership can lead to additive group phenotypes for anti-predator behaviour of guppies, Poecilia reticulata |
Q30776607 | Nonantagonistic interactions between the sexes revealed by the ecological consequences of reproductive traits |
Q47371136 | Noncoding plastid trnT-trnF sequences reveal a well resolved phylogeny of basal angiosperms |
Q51295499 | Nongenetic inheritance and the evolution of costly female preference. |
Q50694877 | Nonlinear effects of temperature on body form and developmental canalization in the threespine stickleback. |
Q46532000 | Nonlinear relationships and phylogenetically independent contrasts |
Q82359830 | Nonlinear selection and the evolution of variances and covariances for continuous characters in an anole |
Q112796091 | Non‐reproducible signals of adaptation to elevation between open and understorey microhabitats in snapdragon plants |
Q115431570 | Novel chloroplast DNA polymorphism in a sympatric region of two pines1 |
Q51194037 | Novel evolutionary pathways of sex-determining mechanisms. |
Q39028563 | Nowhere to run: the role of habitat openness and refuge use in defining patterns of morphological and performance evolution in tropical lizards |
Q50557364 | Nuptial coloration varies with ambient light environment in a freshwater fish. |
Q34712499 | Obligate asex in a rotifer and the role of sexual signals |
Q42727401 | Occasional recombination of a selfish X-chromosome may permit its persistence at high frequencies in the wild |
Q34308951 | Occurrence, costs and heritability of delayed selfing in a free-living flatworm |
Q51075294 | Oceanic barriers promote language diversification in the Japanese Islands. |
Q101329566 | Oceanic dispersal barriers in a holoplanktonic gastropod |
Q35419311 | Of mice and the 'Age of Discovery': the complex history of colonization of the Azorean archipelago by the house mouse (Mus musculus) as revealed by mitochondrial DNA variation. |
Q92957572 | Offspring phenotype is shaped by the nonsperm fraction of semen |
Q99209783 | Offspring sex ratios are stable across the life-course in Drosophila simulans |
Q60456548 | Offspring-driven local dispersal in female sand lizards (Lacerta agilis) |
Q46833070 | Oh sister, where art thou? Spatial population structure and the evolution of an altruistic defence trait. |
Q58038309 | Omnivory in lacertid lizards: adaptive evolution or constraint? |
Q87860284 | On bias and precision in meta-analysis: the error in the error |
Q40336048 | On hidden heterogeneity in directional asymmetry--can systematic bias be avoided? |
Q51026723 | On the effect of phenotypic dimensionality on adaptation and optimality. |
Q51519381 | On the evolution of heightened condition dependence of male sexual displays. |
Q46208500 | On the genetic parameter determining the efficiency of purging: an estimate for Drosophila egg-to-pupae viability. |
Q113348648 | On the genetical basis of the laying-date in an island population of blue tits |
Q50443682 | On the heritability of blue-green eggshell coloration. |
Q46569201 | On the limits of interpreting some plastic responses through a cooperator/cheater prism. A comment on Harrison |
Q47182098 | On the logical relationship between natural selection and self-organization |
Q41710554 | On the origin of Robertsonian fusions in nature: evidence of telomere shortening in wild house mice. |
Q47352342 | On the origin of termite workers: weighing up the phylogenetic evidence |
Q41328928 | On the potential strength and consequences for nonrandom gene flow caused by local adaptation in flowering time |
Q46789020 | On the track of the Red Queen: bark beetles, their nematodes, local climate and geographic parthenogenesis. |
Q60562589 | On the utility of meta-analyses in the study of natural selection |
Q44166626 | On the worldwide spread of an insecticide resistance gene: a role for local selection. |
Q80203462 | One big, and many small reasons that direct selection on offspring number is still open for discussion |
Q30665730 | One phase of the dormancy developmental pathway is critical for the evolution of insect seasonality |
Q39993660 | One size fits all? Determinants of sperm transfer in a highly dimorphic orb-web spider |
Q46748812 | One tool, many uses: precopulatory sexual selection on genital morphology in Aquarius remigis |
Q92443834 | Ongoing hybridization obscures phylogenetic relationships in the Drosophila subquinaria species complex |
Q52720443 | Only helpful when required: a longevity cost of harbouring defensive symbionts. |
Q47445792 | Ontogenetic and spatial variation in size-selective mortality of a marine fish |
Q50517507 | Ontogenetic thermal tolerance and performance of ectotherms at variable temperatures. |
Q40111863 | Ontogenetic trajectories in the ornithischian endocranium |
Q47338833 | Ontogenic sources of variation in sexual size dimorphism in a viviparous lizard |
Q114621935 | Ontogeny, phylogeny and mechanisms of adaptive changes in evaporative water loss in geckos |
Q60481861 | Opposing fitness consequences of colour pattern in male and female snakes |
Q101463637 | Opposing population trends of fork-tailed swallows and reddish-coloured swallows in our changing world |
Q91934279 | Opposite responses to selection and where to find them |
Q47429966 | Opposites attract: MHC-associated mate choice in a polygynous primate. |
Q52641730 | Opposites attract? Mate choice for parasite evasion and the evolutionary stability of sex. |
Q47194365 | Optimal climbing speed explains the evolution of extreme sexual size dimorphism in spiders. |
Q79321125 | Optimal growth strategies of larval helminths in their intermediate hosts |
Q39451033 | Optimal life-history schedule in a metapopulation with juvenile dispersal |
Q46787679 | Optimal numbers of matings: the conditional balance between benefits and costs of mating for females of a nuptial gift-giving spider |
Q34415262 | Optimality models in the age of experimental evolution and genomics |
Q35103333 | Optimally weighted Z-test is a powerful method for combining probabilities in meta-analysis. |
Q57057681 | Optimum body size: effects of food quality and temperature, when reproductive growth rate is restricted, with examples from aphids |
Q51540888 | Order-preserving principles underlying genotype-phenotype maps ensure high additive proportions of genetic variance. |
Q38973687 | Ordinary least squares regression is indicated for studies of allometry |
Q28754541 | Organism size promotes the evolution of specialized cells in multicellular digital organisms |
Q60555506 | Orientation behaviour and heterozygosity of sandhopper populations in relation to stability of beach environments |
Q34246590 | Origin and population history of a recent colonizer, the yellow warbler in Galápagos and Cocos Islands |
Q61659089 | Origin and radiation of the house mouse: clues from nuclear genes |
Q56340050 | Origin and radiation of the house mouse: mitochondrial DNA phylogeny |
Q60429862 | Origin of European rabbit (Oryctolagus cuniculus) in a Mediterranean island: Zooarchaeology and ancient DNA examination |
Q113855140 | Origin of the crustacean schizoramous limb: A re-analysis of the duplosegmentation hypothesis |
Q44577044 | Origins of cheating and loss of symbiosis in wild Bradyrhizobium |
Q54643205 | Origins of clonal diversity in the hypervariable asexual ostracode Cypridopsis vidua |
Q33342539 | Ornament evolution in dragon lizards: multiple gains and widespread losses reveal a complex history of evolutionary change |
Q38380150 | Ornament size and colour as alternative strategies for effective communication in gliding lizards. |
Q50737907 | Ornaments or offspring? Female sticklebacks (Gasterosteus aculeatus L.) trade off carotenoids between spines and eggs. |
Q125798559 | Osawa, S. and Honjo, T. (eds.) 1991. Evolution of Life. Fossils, Molecules, and Culture. Springer‐Verlag, Tokyo. 460 pp., with 125 illustrations. DM 248. ISBN: 0‐387‐70064‐1. |
Q39641121 | Otolith shape lends support to the sensory drive hypothesis in rockfishes |
Q42031935 | Out-of-Africa origin and dispersal-mediated diversification of the butterfly genus Junonia (Nymphalidae: Nymphalinae). |
Q44540201 | Outcrossing hermaphroditic polychaete worms adjust their sex allocation to social conditions. |
Q100505692 | Ovarian fluid proteome variation associates with sperm swimming speed in an externally fertilising fish |
Q58034939 | Overdominance interacts with linkage to determine the rate of adaptation to a new optimum |
Q83141864 | Overdominant maintenance of diversity in the sea star Pisaster ochraceus |
Q39070851 | Overwintering in Drosophila melanogaster: outdoor field cage experiments on clinal and laboratory selected populations help to elucidate traits under selection |
Q51555479 | Oxidative phosphorylation gene transcription in whitefish species pairs reveals patterns of parallel and nonparallel physiological divergence. |
Q42965969 | Oxidative stress and the effect of parasites on a carotenoid-based ornament. Corrigendum |
Q33751716 | Paleogenomic data suggest mammal-like genome size in the ancestral amniote and derived large genome size in amphibians. |
Q126083356 | Papi, F. (ed.), 1992. Animal homing. Chapman & Hall, London, 390pp. Price: £37.50. ISBN: 0‐412‐36390‐9 |
Q83931680 | Parallel amino acid replacements in the rhodopsins of the rockfishes (Sebastes spp.) associated with shifts in habitat depth |
Q35992018 | Parallel and nonparallel behavioural evolution in response to parasitism and predation in Trinidadian guppies |
Q43969268 | Parallel and nonparallel ecological, morphological and genetic divergence in lake-stream stickleback from a single catchment. |
Q35565405 | Parallel chemical switches underlying pollinator isolation in Asian Mitella |
Q51538059 | Parallel divergence in mate guarding behaviour following colonization of a novel habitat. |
Q36902145 | Parallel effects of the inversion In(3R)Payne on body size across the North American and Australian clines in Drosophila melanogaster |
Q34329877 | Parallel episodes of phyletic dwarfism in callitrichid and cheirogaleid primates |
Q33283072 | Parallel evolution of lake whitefish dwarf ecotypes in association with limnological features of their adaptive landscape |
Q52671458 | Parallel evolution of larval morphology and habitat in the snail-killing fly genus Tetanocera. |
Q33242266 | Parallel evolution of the sexes? Effects of predation and habitat features on the size and shape of wild guppies. |
Q52320739 | Parallel evolutionary forces influence the evolution of male and female songs in a tropical songbird. |
Q42006187 | Parallel invasions produce heterogenous patterns of life history adaptation: rapid divergence in an invasive insect |
Q93024441 | Parallel plumage colour evolution and introgressive hybridization in wheatears |
Q34264734 | Parallel reduction in expression of the eye development gene hedgehog in separately derived cave populations of the amphipod Gammarus minus. |
Q42609185 | Parallel speciation or long-distance dispersal? Lessons from seaweeds (Fucus) in the Baltic Sea. |
Q43410315 | Parallelism and historical contingency during rapid ecotype divergence in an isopod |
Q48275446 | Parallelism in genomic landscapes of differentiation, conserved genomic features and the role of linked selection. |
Q41329206 | Parallels between two geographically and ecologically disparate cave invasions by the same species, Asellus aquaticus (Isopoda, Crustacea). |
Q36363912 | Parasite escape through trophic specialization in a species flock |
Q41673926 | Parasite evolution in response to sex-based host heterogeneity in resistance and tolerance |
Q128905507 | Parasite evolution of host manipulation strategies with fluctuating ecological dynamics |
Q41103266 | Parasite host range and the evolution of host resistance |
Q33199141 | Parasite-induced surfacing in the cockle Austrovenus stuchburyi: adaptation or not? |
Q33751645 | Parasite-mediated evolution of the functional part of the MHC in primates |
Q38443794 | Parasite-mediated selection and the role of sex and diapause in Daphnia |
Q51634645 | Parasites and deleterious mutations: interactions influencing the evolutionary maintenance of sex. |
Q113855143 | Parasites and sexual selection: Current status of the Hamilton and Zuk hypothesis |
Q51574387 | Parasites as mediators of heterozygosity-fitness correlations in the Great Tit (Parus major). |
Q47175077 | Parasites favour intermediate nestling mass and brood size in cliff swallows. |
Q44822814 | Parasites make male pipefish careless |
Q38238098 | Parasitic success without sex – the nematode experience |
Q129355570 | Parasitism and host dispersal plasticity in an aquatic model system |
Q90297338 | Parasitism offers large rewards but carries high risks: Predicting parasitic strategies under different life history conditions in lampreys |
Q47588285 | Parasitism, host immune defence and dispersal. |
Q47172929 | Parent-offspring conflict and selection on egg size in turtles |
Q59652803 | Parent-offspring regression suggests heritable susceptibility to ectoparasites in a natural population of kittiwake Rissa tridactyla |
Q35896736 | Parental and hybrid Daphnia from the D. longispina complex: long-term dynamics in genetic structure and significance of overwintering modes. |
Q50700339 | Parental effects and the evolution of phenotypic memory. |
Q60484824 | Parental effects in Lychnis flos-cuculi. I: Seed size, germination and seedling performance in a controlled environment |
Q60484825 | Parental effects in Lychnis flos-cuculi. II: Selection on time of emergence and seedling performance in the field |
Q46971534 | Parental effects on the larval performance of a tapeworm in its copepod first host. |
Q60566051 | Parental effort and response to nestling begging in the house sparrow: repeatability, heritability and parent-offspring co-evolution |
Q51702450 | Parental investment with a superior alien in the brood. |
Q37156779 | Parental investment, sexual selection and sex ratios. |
Q59652804 | Parent–offspring regression suggests heritable susceptibility to ectoparasites in a natural population of kittiwake |
Q49561401 | Parthenogenetic flatworms have more symbionts than their coexisting, sexual conspecifics, but does this support the Red Queen? |
Q51740902 | Partial host fidelity in nest selection by the shiny cowbird (Molothrus bonariensis), a highly generalist avian brood parasite. |
Q29026720 | Partial local mate competition and the sex ratio: A study on non-pollinating fig wasps |
Q35769305 | Parting ways: parasite release in nature leads to sex-specific evolution of defence. |
Q47865213 | Partitioning of resources: the evolutionary genetics of sexual conflict over resource acquisition and allocation |
Q46862161 | Partner switching can favour cooperation in a biological market |
Q46458916 | Paternal effects on seed germination: a barrier to the genetic assimilation of an endemic plant taxon? |
Q81145586 | Paternal inheritance of the primary sex ratio in a copepod |
Q48070662 | Paternal-specific S-allele transmission in sweet cherry (Prunus avium L.): the potential for sexual selection. |
Q35766930 | Paternity analyses in wild-caught and laboratory-reared Caribbean cricket females reveal the influence of mating environment on post-copulatory sexual selection |
Q57125464 | Path analysis of natural selection via survival and fecundity across contrasting environments in Avena barbata |
Q46849507 | Path analysis of the genetic integration of traits in the sand cricket: a novel use of BLUPs |
Q50777022 | Pathogen fitness components and genotypes differ in their sensitivity to nutrient and temperature variation in a wild plant-pathogen association. |
Q48668287 | Pattern, process and geographic modes of speciation |
Q28655701 | Patterns and implications of extensive heterochrony in carnivoran cranial suture closure |
Q38904124 | Patterns and mechanisms in instances of endosymbiont-induced parthenogenesis |
Q113791781 | Patterns of bird song evolution on islands support the character release hypothesis in tropical but not in temperate latitudes |
Q51541260 | Patterns of cranial ontogeny in lacertid lizards: morphological and allometric disparity. |
Q43733351 | Patterns of cranial shape diversification during the phylogenetic branching process of New World monkeys (Primates: Platyrrhini). |
Q46347574 | Patterns of diversification of Afrotropical Otiteselline fig wasps: phylogenetic study reveals a double radiation across host figs and conservatism of host association |
Q35593849 | Patterns of epistasis in RNA viruses: a review of the evidence from vaccine design |
Q51373692 | Patterns of floral colour neighbourhood and their effects on female reproductive success in an Antirrhinum hybrid zone. |
Q96585295 | Patterns of genomic divergence and introgression between Japanese stickleback species with overlapping breeding habitats |
Q46269861 | Patterns of male fitness conform to predictions of evolutionary models of late life |
Q51527927 | Patterns of mammalian diversification in recent evolutionary times: global tendencies and methodological issues. |
Q81487178 | Patterns of mating call preferences in túngara frogs, Physalaemus pustulosus |
Q34315117 | Patterns of molecular evolution in dioecious and non-dioecious Silene |
Q38939509 | Patterns of parental care in Neotropical glassfrogs: fieldwork alters hypotheses of sex-role evolution. |
Q51145557 | Patterns of reproductive isolation in a haplodiploid - strong postmating, prezygotic barriers among three forms of a social spider mite. |
Q43587283 | Patterns of speciation in endemic Mexican Goodeid fish: sexual conflict or early radiation? |
Q51725454 | Patterns of variation in wing morphology in the cactophilic Drosophila buzzatii and its sibling D. koepferae. |
Q92960911 | Pedigree-free quantitative genetic approach provides evidence for heritability of movement tactics in wild roe deer |
Q51737750 | Pelvis morphology suggests that early Mesozoic birds were too heavy to contact incubate their eggs. |
Q41077972 | Persistence and resistance as complementary bacterial adaptations to antibiotics. |
Q33351757 | Persistence of an extreme male-biased adult sex ratio in a natural population of polyandrous bird |
Q83242070 | Persistence of costly novel genes in the absence of positive selection |
Q84134111 | Persistence of vigilance and flight response behaviour in wild reindeer with varying domestic ancestry |
Q50120268 | Pervasive, yet idiosyncratic, epistatic pleiotropy during adaptation in a behaviourally complex microbe |
Q51148799 | Phenological shifts in North American red squirrels: disentangling the roles of phenotypic plasticity and microevolution. |
Q33303603 | Phenoloxidase activity and pathogen resistance in yellow dung flies Scathophaga stercoraria |
Q40547201 | Phenotype-associated inbreeding biases estimates of inbreeding depression in a wild bird population |
Q51273069 | Phenotypes optimized for early-life reproduction exhibit faster somatic deterioration with age, revealing a latent cost of high condition. |
Q115527395 | Phenotypic and functional variation in venom and venom resistance of two sympatric rattlesnakes and their prey |
Q34149054 | Phenotypic and genetic divergence among harbour porpoise populations associated with habitat regions in the North Sea and adjacent seas |
Q51830623 | Phenotypic and genetic variation in emergence and development time of a trimorphic damselfly. |
Q80374151 | Phenotypic correlations among fitness and its components in a population of the housefly |
Q46500254 | Phenotypic differentiation is associated with divergent sexual selection among closely related barn swallow populations |
Q45831214 | Phenotypic divergence but not genetic distance predicts assortative mating among species of a cichlid fish radiation |
Q44969361 | Phenotypic integration and conserved covariance structure in calopterygid damselflies |
Q52369394 | Phenotypic integration in an extended phenotype: among-individual variation in nest-building traits of the alfalfa leafcutting bee (Megachile rotundata). |
Q44300773 | Phenotypic integration in flowers of neotropical lianas: diversification of form with stasis of underlying patterns |
Q87514812 | Phenotypic integration plasticity in Daphnia magna: an integral facet of G × E interactions |
Q39091399 | Phenotypic landscapes: phenological patterns in wild and cultivated barley |
Q110615412 | Phenotypic plasticity and selection in |
Q110616047 | Phenotypic plasticity and selection in Drosophila life history evolution. 2. Diet, mates and the cost of reproduction |
Q56774627 | Phenotypic plasticity and selection in Drosophila life-history evolution. I. Nutrition and the cost of reproduction |
Q46758216 | Phenotypic plasticity and the evolution of trade-offs: the quantitative genetics of resource allocation in the wing dimorphic cricket, Gryllus firmus |
Q110615193 | Phenotypic plasticity drives phenological changes in a Mediterranean blue tit population |
Q110616038 | Phenotypic plasticity for life history traits in Drosophila melanogaster. I. Effect on phenotypic and environmental correlations |
Q110616040 | Phenotypic plasticity for life history traits in Drosophila melanogaster. II. Epigenetic mechanisms and the scaling of variances |
Q110616035 | Phenotypic plasticity in Phlox. III. Variation among natural populations of P. drummondii |
Q110616044 | Phenotypic plasticity in age and size at maturity and its effects on the integrated phenotypic expressions of life history traits of Cardamine flexuosa (Cruciferae) |
Q110616046 | Phenotypic plasticity in morphological traits in two populations of Drosophila melanogaster |
Q48309445 | Phenotypic plasticity in response to environmental heterogeneity contributes to fluctuating asymmetry in plants: first empirical evidence. |
Q42018871 | Phenotypic plasticity in sexual communication signal of a noctuid moth. |
Q34573807 | Phenotypic plasticity in two marine snails: constraints superseding life history |
Q46680552 | Phenotypic plasticity is not affected by experimental evolution in constant, predictable or unpredictable fluctuating thermal environments |
Q83242088 | Phenotypic plasticity of a cooperative behaviour in bacteria |
Q51658430 | Phenotypic plasticity of desiccation resistance in Glossina puparia: are there ecotype constraints on acclimation responses? |
Q34435469 | Phenotypic plasticity of host-parasite interactions in response to the route of infection. |
Q46935485 | Phenotypic plasticity of immune defence linked with foraging activity in the ant Cataglyphis velox |
Q34186399 | Phenotypic plasticity, heterochrony and ontogenetic repatterning during juvenile development of divergent Arctic charr (Salvelinus alpinus). |
Q51875929 | Phenotypic robustness can increase phenotypic variability after nongenetic perturbations in gene regulatory circuits. |
Q52088100 | Phenotypic selection and regulation of reproduction in different environments in wild barley. |
Q113791776 | Phenotypic selection on an ornamental trait is not modulated by breeding density in a pied flycatcher population |
Q57164703 | Phenotypic selection on growth rhythm in whitebark pine under climatic conditions warmer than seed origins |
Q93074437 | Phenotypic variability can promote the evolution of adaptive plasticity by reducing the stringency of natural selection |
Q35680759 | Phenotypic variation and covariation indicate high evolvability of acoustic communication in crickets |
Q60582711 | Phenotypic variation in growth trajectories in the Arctic charr Salvelinus alpinus |
Q34674150 | Phenotypically plastic traits regulate caste formation and soldier function in polyembryonic wasps |
Q46745156 | Pheromonal dominance and the selection of a socially parasitic honeybee worker lineage (Apis mellifera capensis Esch.). |
Q47653515 | Pheromones do regulate sexual development in Dictyostelium discoideum |
Q113282445 | Phylogenetic analysis and the evolution of queen number in eusocial Hymenoptera |
Q52581397 | Phylogenetic analysis of floral integration in Schizanthus (Solanaceae): does pollination truly integrate corolla traits? |
Q80831748 | Phylogenetic analysis of interspecific variation in nectar of hummingbird-visited plants |
Q39546911 | Phylogenetic analysis of the ecological correlates of dioecy in angiosperms |
Q33493576 | Phylogenetic and biological species diversity within the Neurospora tetrasperma complex |
Q39734178 | Phylogenetic and size constrains on cranial ontogenetic allometry of spiny rats (Echimyidae, Rodentia). |
Q88615353 | Phylogenetic comparative analysis supports aposematic colouration-body size association in millipede assassins (Hemiptera: Reduviidae: Ectrichodiinae) |
Q37801983 | Phylogenetic comparative approaches for studying niche conservatism. |
Q52655372 | Phylogenetic congruence of mealybugs and their primary endosymbionts. |
Q38698990 | Phylogenetic convergence and multiple shell shape optima for gliding scallops (Bivalvia: Pectinidae). |
Q43729777 | Phylogenetic determinants of potential host shifts in fungal pathogens |
Q46286032 | Phylogenetic distribution of a male pheromone that may exploit a nonsexual preference in lampreys. |
Q50908264 | Phylogenetic eigenvectors and nonstationarity in the evolution of theropod dinosaur skulls. |
Q48323029 | Phylogenetic estimates of diversification rate are affected by molecular rate variation. |
Q29306033 | Phylogenetic evidence for the evolution of ecological specialization in Timema walking-sticks |
Q51534791 | Phylogenetic patterns of skeletal morphometrics and pelvic traits in relation to locomotor mode in frogs. |
Q38907476 | Phylogenetic relationships and divergence dates of softshell turtles (Testudines: Trionychidae) inferred from complete mitochondrial genomes |
Q56672309 | Phylogenetic relationships and evolution of cleaning behaviour in the family Labridae: importance of body colour pattern |
Q56644863 | Phylogenetic relationships in Monanthes (Crassulaceae) based on morphological, chloroplast and nuclear DNA variation |
Q41431465 | Phylogenetic relationships of the Cretaceous frog Beelzebufo from Madagascar and the placement of fossil constraints based on temporal and phylogenetic evidence. |
Q47781078 | Phylogenetic signal, feeding behaviour and brain volume in Neotropical bats |
Q47414714 | Phylogenetically structured variance in felid bite force: the role of phylogeny in the evolution of biting performance |
Q46281655 | Phylogenomics of pike cichlids (Cichlidae: Crenicichla): the rapid ecological speciation of an incipient species flock |
Q30048019 | Phylogeny and adaptive radiation in the Onychopoda (Crustacea, Cladocera): evidence from multiple gene sequences |
Q51618143 | Phylogeny and evolution of sexually selected tail ornamentation in widowbirds and bishops (Euplectes spp.). |
Q55871802 | Phylogeny of Medusozoa and the evolution of cnidarian life cycles |
Q92227920 | Phylogeographic and phenotypic outcomes of brown anole colonization across the Caribbean provide insight into the beginning stages of an adaptive radiation |
Q101631246 | Phylogeographic histories of representative herpetofauna of the southwestern U.S.: mitochondrial DNA variation in the desert iguana (Dipsosaurus dorsalis) and the chuckwalla (Sauromalus obesus) |
Q43520887 | Phylogeographic patterns and cryptic speciation across oceanographic barriers in South African intertidal fishes |
Q35229459 | Phylogeographic structure, demographic history and morph composition in a colour polymorphic lizard |
Q60230472 | Phylogeographical patterns in chloroplast DNA variation within the Acacia acuminata (Leguminosae: Mimosoideae) complex in Western Australia |
Q34567241 | Phylogeography and alpha taxonomy of the common dolphin (Delphinus sp.). |
Q125608784 | Phylogeography of Artemisia frigida (Anthemideae, Asteraceae) based on genotyping‐by‐sequencing and plastid DNA data: Migration through Beringia |
Q48020282 | Phylogeography of Caribbean lizard malaria: tracing the history of vector-borne parasites. |
Q34191566 | Phylogeography of the Cape velvet worm (Onychophora: Peripatopsis capensis) reveals the impact of Pliocene/Pleistocene climatic oscillations on Afromontane forest in the Western Cape, South Africa |
Q50142857 | Physical contact is essential for macrocyst formation in wild Dictyostelium discoideum: a response to O'Day |
Q51555578 | Physiological adaptation along environmental gradients and replicated hybrid zone structure in swordtails (Teleostei: Xiphophorus). |
Q51576434 | Physiological implications of genomic state in parthenogenetic lizards of reciprocal hybrid origin. |
Q43194566 | Physiological stress links parasites to carotenoid-based colour signals. |
Q102055210 | Pitfalls and virtues of population genetic summary statistics: detecting selective sweeps in recent divergences |
Q40451399 | Pitfalls in experiments testing predictions from sperm competition theory. |
Q38981685 | Pitfalls in understanding the functional significance of genital allometry |
Q48915092 | Placental invasiveness and brain-body allometry in eutherian mammals |
Q50674966 | Plant-like mating in an animal: sexual compatibility and allocation trade-offs in a simultaneous hermaphrodite with remote transfer of sperm. |
Q47393711 | Plastic and evolutionary responses of cell size and number to larval malnutrition in Drosophila melanogaster |
Q48255607 | Plastic and evolutionary responses to heat stress in a temperate dung fly: negative correlation between basal and induced heat tolerance? |
Q83412948 | Plastic responses to parents and predators lead to divergent shoaling behaviour in sticklebacks |
Q46272751 | Plasticity and cross-tolerance to heterogeneous environments: divergent stress responses co-evolved in an African fruit fly. |
Q51308451 | Plasticity and evolution in correlated suites of traits. |
Q125420426 | Plasticity and genetic effects contribute to different axes of neural divergence in a community of mimetic Heliconius butterflies |
Q43749084 | Plasticity and heritability of morphological variation within and between parapatric stickleback demes. |
Q39367127 | Plasticity in reproduction and growth among 52 range-wide populations of a Mediterranean conifer: adaptive responses to environmental stress |
Q52001783 | Plasticity in resource allocation based life history traits in the Pacific oyster, Crassostrea gigas. I. Spatial variation in food abundance. |
Q46864738 | Plasticity in sex allocation in the plant Mercurialis annua is greater for hermaphrodites sampled from dimorphic than from monomorphic populations. |
Q50669972 | Playing smart vs. playing safe: the joint expression of phenotypic plasticity and potential bet hedging across and within thermal environments. |
Q80511446 | Pleiotropy and GAL pathway degeneration in yeast |
Q51644612 | Pleistocene glaciations and contemporary genetic diversity in a Beringian fish, the broad whitefish, Coregonus nasus (Pallas): inferences from microsatellite DNA variation. |
Q49561414 | Ploidy evolution in the yeast Saccharomyces cerevisiae: a test of the nutrient limitation hypothesis |
Q44271757 | Plumage polymorphism and fitness in Swainson's hawks |
Q81145563 | Pluralism in evolutionary theory |
Q36019855 | Pollen and sperm heteromorphism: convergence across kingdoms? |
Q89506787 | Pollen colour morphs take different paths to fitness |
Q51652797 | Pollen competition as an asymmetric reproductive barrier between two closely related Silene species. |
Q50798696 | Pollen competition reduces inbreeding depression in Collinsia heterophylla (Plantaginaceae). |
Q34344020 | Pollen feeding, resource allocation and the evolution of chemical defence in passion vine butterflies |
Q46678918 | Pollen limitation and its influence on natural selection through seed set. |
Q51534888 | Pollen limitation of female reproductive success at fine spatial scale in a gynodioecious and wind-pollinated species, Beta vulgaris ssp. maritima. |
Q59185501 | Pollen transfer dynamics and the evolution of gametophytic self-incompatibility |
Q33222657 | Pollinating fig wasps: genetic consequences of island recolonization |
Q40830814 | Pollination by sexual deception promotes outcrossing and mate diversity in self-compatible clonal orchids. |
Q47592567 | Pollination context alters female advantage in gynodioecious Silene vulgaris. |
Q46545184 | Pollination, mating and reproductive fitness in a plant population with bimodal floral-tube length. |
Q36164804 | Pollinator adaptation and the evolution of floral nectar sugar composition |
Q60451096 | Pollinator behaviour and the evolution of Louisiana iris hybrid zones |
Q42021281 | Pollinator shifts and the loss of style polymorphism in Narcissus papyraceus (Amaryllidaceae). |
Q34974948 | Pollinator shifts between Ophrys sphegodes populations: might adaptation to different pollinators drive population divergence? |
Q46361794 | Pollinator-mediated assemblage processes in California wildflowers |
Q44472002 | Pollinator-mediated selection in a specialized hummingbird-Heliconia system in the Eastern Caribbean |
Q52708100 | Pollinator-mediated selection in a specialized pollination system: matches and mismatches across populations. |
Q52749629 | Pollinator-mediated selection on floral morphology: evidence for transgressive evolution in a derived hybrid lineage. |
Q63980009 | Pollinators entering female dioecious figs: why commit suicide? |
Q46087809 | Polyandrous females acquire indirect benefits in a nuptial feeding species |
Q44794072 | Polyandrous females found fitter populations |
Q51161713 | Polyandrous females produce sons that are successful at post-copulatory competition. |
Q29398992 | Polyandry and colony genetic structure in the primitive ant Nothomyrmecia macrops |
Q51709746 | Polyandry in coal tits Parus ater: fitness consequences of putting eggs into multiple genetic baskets. |
Q42010740 | Polyandry-fecundity relationship in insects: methodological and conceptual problems |
Q42041382 | Polymorphic mimicry, microhabitat use, and sex-specific behaviour |
Q40806590 | Polymorphisms in a desaturase 2 ortholog associate with cuticular hydrocarbon and male mating success variation in a natural population of Drosophila serrata. |
Q91842293 | Population biology of a selfish sex ratio distorting element in a booklouse (Psocodea: Liposcelis) |
Q42648766 | Population differences in behaviour are explained by shared within-population trait correlations |
Q60513397 | Population differences in early life-history traits in grayling |
Q85305634 | Population differences in response to hypoxic stress in Atlantic salmon |
Q30435744 | Population differentiation and hybrid success in Campanula americana: geography and genome size |
Q44232773 | Population differentiation and restricted gene flow in Spanish crossbills: not isolation-by-distance but isolation-by-ecology |
Q31063059 | Population differentiation in the context of Holocene climate change for a migratory marine species, the southern elephant seal. |
Q51548291 | Population differentiation in the swordtail characin (Corynopoma riisei ): a role for sensory drive? |
Q108065824 | Population divergence and morphometric integration in the greenfinch (Carduelis chloris) – evolution against the trajectory of least resistance? |
Q50787465 | Population divergence in chemical signals and the potential for premating isolation between islet- and mainland populations of the Skyros wall lizard (Podarcis gaigeae). |
Q123241530 | Population divergence of developmental thermal optima in Swedish common frogs, Rana temporaria |
Q57002651 | Population genetic analysis of microsatellite variation of guppies (Poecilia reticulata) in Trinidad and Tobago: evidence for a dynamic source-sink metapopulation structure, founder events and population bottlenecks |
Q40676254 | Population genomics of eusocial insects: the costs of a vertebrate-like effective population size. |
Q101222146 | Population genomics reveals repeated signals of adaptive divergence in northeastern European Atlantic salmon |
Q47338815 | Population size, female fecundity, and sex ratio variation in gynodioecious Plantago maritima |
Q30910786 | Population structure and speciation in the genus Tursiops based on microsatellite and mitochondrial DNA analyses |
Q42016582 | Population structure in relation to host-plant ecology and Wolbachia infestation in the comma butterfly |
Q57568197 | Population systematics of the snake genus Naja (Reptilia: Serpentes: Elapidae) in Indochina: Multivariate morphometrics and comparative mitochondrial DNA sequencing (cytochrome oxidase I) |
Q35165019 | Populations with elevated mutation load do not benefit from the operation of sexual selection |
Q46862176 | Positive effect of the yellow morph on female reproductive success in the flower colour polymorphic Iris lutescens (Iridaceae), a deceptive species |
Q37105538 | Positive genetic correlation between brain size and sexual traits in male guppies artificially selected for brain size. |
Q52654825 | Possible coevolution of male and female genital form and function in a calopterygid damselfly. |
Q47606051 | Possible glimpses into early speciation: the effect of ovarian fluid on sperm velocity accords with post-copulatory isolation between two guppy populations. |
Q91290925 | Post-glacial colonization routes coincide with a life-history breakpoint along a latitudinal gradient |
Q46460175 | Post-hatching parental care masks the effects of egg size on offspring fitness: a removal experiment on burying beetles. |
Q51387451 | Post-mating prezygotic barriers to gene exchange between hybridizing field crickets. |
Q82205199 | Post-mating reproductive barriers in two unidirectionally hybridizing sunfish (Centrarchidae: Lepomis) |
Q47256929 | Post-pleistocene demographic history of the North Atlantic endemic Irish moss Chondrus crispus: glacial survival, spatial expansion and gene flow |
Q50448688 | Post-weaning parental care increases fitness but is not heritable in North American red squirrels. |
Q28647892 | Post-zygotic isolation in cactophilic Drosophila: larval viability and adult life-history traits of D. mojavensis/D. arizonae hybrids |
Q34447402 | Postcopulatory inbreeding avoidance in guppies. |
Q96645645 | Postglacial establishment of locally adapted fish populations over a steep salinity gradient |
Q47287015 | Postglacial intra-lacustrine divergence of Icelandic threespine stickleback morphs in three neovolcanic lakes. |
Q39732645 | Postmating isolation and genetically variable host use in ecologically divergent host forms of Neochlamisus bebbianae leaf beetles |
Q51780607 | Postzygotic incompatibilities between the pupfishes, Cyprinodon elegans and Cyprinodon variegatus: hybrid male sterility and sex ratio bias. |
Q81317977 | Potential fitness benefits from mate selection in the Atlantic cod (Gadus morhua) |
Q58557835 | Potential genetic benefits of mate selection in whitefish |
Q46728567 | Potential rapid evolution of foot morphology in Italian plethodontid salamanders (Hydromantes strinatii) following the colonization of an artificial cave |
Q40421266 | Pre-adapting parasitic phages to a pathogen leads to increased pathogen clearance and lowered resistance evolution with Pseudomonas aeruginosa cystic fibrosis bacterial isolates |
Q103732868 | Pre-introduction introgression contributes to parallel differentiation and contrasting hybridisation outcomes between invasive and native marine mussels |
Q56774630 | Precise control of sex allocation in pseudo-arrhenotokous phytoseiid mites |
Q51740916 | Precision in sex allocation is influenced by mate choice in Drosophila melanogaster. |
Q80101013 | Predation and the persistence of melanic male mosquitofish (Gambusia holbrooki) |
Q34640364 | Predation by killer whales (Orcinus orca) and the evolution of whistle loss and narrow-band high frequency clicks in odontocetes |
Q47561679 | Predation drives morphological convergence in the Gambusia panuco species group among lotic and lentic habitats. |
Q44513150 | Predation drives stable coexistence ratios between red and green pea aphid morphs |
Q51667990 | Predation mediated population divergence in complex behaviour of nine-spined stickleback (Pungitius pungitius). |
Q114080040 | Predation risk and the evolution of a vertebrate stress response: Parallel evolution of stress reactivity and sexual dimorphism |
Q58279139 | Predation risk determines pigmentation phenotype in nuthatches by melanin-related gene expression effects |
Q51616722 | Predation- and competition-mediated brain plasticity in Rana temporaria tadpoles. |
Q44869503 | Predation-associated divergence of male genital morphology in a livebearing fish |
Q122053349 | Predator response to the coloured eyespots and defensive posture of Colombian four‐eyed frogs |
Q48451786 | Predator-induced phenotypic plasticity in tadpoles: extension or innovation? |
Q36151750 | Predator-prey interactions amongst Permo-Triassic terrestrial vertebrates as a deterministic factor influencing faunal collapse and turnover |
Q40922756 | Predator-prey interactions, flight initiation distance and brain size |
Q51416533 | Predictability rather than amplitude of temperature fluctuations determines stress resistance in a natural population of Drosophila simulans. |
Q51740922 | Predictable males and unpredictable females: sex difference in repeatability of parental care in a wild bird population. |
Q82490570 | Predicting epistasis: an experimental test of metabolic control theory with bacterial transcription and translation |
Q50782357 | Predicting evolution of floral traits associated with mating system in a natural plant population. |
Q46155821 | Predicting the pathway to wind pollination: heritabilities and genetic correlations of inflorescence traits associated with wind pollination in Schiedea salicaria (Caryophyllaceae). |
Q51709766 | Predominance of outcrossing in Lymnaea stagnalis despite low apparent fitness costs of self-fertilization. |
Q35147286 | Preferential host switching and codivergence shaped radiation of bark beetle symbionts, nematodes of Micoletzkya (Nematoda: Diplogastridae). |
Q50473177 | Preferential phenotypic association linked with cooperation in paper wasps. |
Q50704866 | Prehatching maternal investment and offspring immunity in the pied flycatcher (Ficedula hypoleuca). |
Q33198793 | Premating barriers to gene exchange and their implications for the structure of a mosaic hybrid zone between Chorthippus brunneus and C. jacobsi (Orthoptera: Acrididae). |
Q44572673 | Premating isolation is determined by larval rearing substrates in cactophilic Drosophila mojavensis. IX. Host plant and population specific epicuticular hydrocarbon expression influences mate choice and sexual selection |
Q46199262 | Premating isolation is determined by larval rearing substrates in cactophilic Drosophila mojavensis. VIII. Mating success mediated by epicuticular hydrocarbons within and between isolated populations |
Q42034824 | Presence of soldier larvae determines the outcome of competition in a polyembryonic wasp. |
Q51710891 | Processed pseudogenes are located preferentially in regions of low recombination rates in the human genome. |
Q111808066 | Propagule interactions and the evolution of virulence |
Q44158686 | Protection against a fungal pathogen conferred by the aphid facultative endosymbionts Rickettsia and Spiroplasma is expressed in multiple host genotypes and species and is not influenced by co-infection with another symbiont |
Q47863384 | Protein deprivation decreases male survival and the intensity of sexual antagonism in southern field crickets Gryllus bimaculatus. |
Q35772345 | Protein pheromone expression levels predict and respond to the formation of social dominance networks |
Q50079665 | Protein sequences of linked genes are highly conserved in two bacterial species |
Q39545310 | Proteomic evidence of a paedomorphic evolutionary process within a marine snail species: a strategy for adapting to extreme ecological conditions? |
Q47852765 | Protistan predation interferes with bacterial long-term adaptation to substrate restriction by selecting for defence morphotypes |
Q80404255 | Proximate causes of adaptive growth rates: growth efficiency variation among latitudinal populations of Rana temporaria |
Q87848166 | Proximate mechanisms of the differences in reproductive success of males bearing different alleles of Pgdh - a gene involved in a sexual conflict in bulb mite |
Q79321132 | Proximate mechanisms of variation in the carotenoid-based plumage coloration of nestling great tits (Parus major L.). |
Q84400528 | Pseudogene rescue: an adaptive mechanism of codon reassignment |
Q43629260 | Pulling together or pulling apart: hybridization in theory and practice |
Q84916720 | Pulsed-resource dynamics increase the asymmetry of antagonistic coevolution between a predatory protist and a prey bacterium |
Q34705660 | Punctuated genome size evolution in Liliaceae. |
Q124987000 | Punctuational ecological changes rather than global factors drive species diversification and the evolution of wing phenotypes inMorphobutterflies |
Q44168070 | Pupal period and adult size in Drosophila melanogaster: a cautionary tale of contrasting correlations between two sexually dimorphic traits |
Q101239469 | Putative chromosomal rearrangements are associated primarily with ecotype divergence rather than geographic separation in an intertidal, poorly-dispersing snail |
Q37690851 | Putting information back into biological communication. |
Q45950474 | Pyoverdin cheats fail to invade bacterial populations in stationary phase. |
Q51683530 | QTL mapping of inbreeding-related cold sensitivity and conditional lethality in Drosophila melanogaster. |
Q58886325 | Quality-quantity trade-off of human offspring under adverse environmental conditions |
Q91351751 | Quantifying individual variation in reaction norms: Mind the residual |
Q38103632 | Quantifying the effects of migration and mutation on adaptation and demography in spatially heterogeneous environments. |
Q82651406 | Quantitative genetic and translocation experiments reveal genotype-by-environment effects on juvenile life-history traits in two populations of Chinook salmon (Oncorhynchus tshawytscha) |
Q33925681 | Quantitative genetic inheritance of morphological divergence in a lake-stream stickleback ecotype pair: implications for reproductive isolation. |
Q51629248 | Quantitative genetic parameters for wild stream-living brown trout: heritability and parental effects. |
Q39161970 | Quantitative genetic variation for thermal performance curves within and among natural populations of Drosophila serrata. |
Q39665521 | Quantitative genetics of behavioural reaction norms: genetic correlations between personality and behavioural plasticity vary across stickleback populations. |
Q36284444 | Quantitative genetics of costly neonatal sexual size dimorphism in squirrel monkeys (Saimiri boliviensis). |
Q33943681 | Quantitative genetics of migration syndromes: a study of two barn swallow populations |
Q50782361 | Quantitative genetics of sexually dimorphic traits and capture of genetic variance by a sexually-selected condition-dependent ornament in red junglefowl (Gallus gallus). |
Q60211891 | Quantitative host resistance drives the evolution of increased virulence in an emerging pathogen |
Q37945355 | Questioning the cultural evolution of altruism |
Q35197263 | Quick divergence but slow convergence during ecotype formation in lake and stream stickleback pairs of variable age. |
Q60727597 | R0 or r: A matter of taste? |
Q51145276 | RAD-seq linkage mapping and patterns of segregation distortion in sedges: Meiosis as a driver of karyotypic evolution in organisms with holocentric chromosomes. |
Q36623200 | RNA world - the dark matter of evolutionary genomics |
Q31148229 | Radiation and divergence in the Rhagoletis pomonella species complex: inferences from DNA sequence data. |
Q40676260 | Radiation of the Drosophila nannoptera species group in Mexico |
Q40315247 | Rampant host switching and multiple female body colour transitions in Philotrypesis (Hymenoptera: Chalcidoidea: Agaonidae). |
Q44358738 | Rampant host- and defensive phenotype-associated diversification in a goldenrod gall midge. |
Q125470485 | Range expansions of sexual versus asexual organisms: Effects of reproductive assurance and migration load |
Q92847546 | Range-wide genetic structure of a cooperative mouse in a semi-arid zone: Evidence for panmixia |
Q30857671 | Rapid and convergent evolution of parental care in hydrobiid gastropods from New Zealand |
Q46984956 | Rapid and unpredictable changes of the G-matrix in a natural bird population over 25 years |
Q35795370 | Rapid changes in genetic architecture of behavioural syndromes following colonization of a novel environment. |
Q46642386 | Rapid changes in plasticity across generations within an expanding cedar forest. |
Q36226363 | Rapid differentiation and asynchronous coevolution of male and female genitalia in stink bugs. |
Q42677058 | Rapid diversification of Tragopogon and ecological associates in Eurasia |
Q44329586 | Rapid diversification of male genitalia and mating strategies in Ohomopterus ground beetles |
Q46795170 | Rapid diversification of sexual signals in Hawaiian Nesosydne planthoppers (Hemiptera: Delphacidae): the relative role of neutral and selective forces |
Q52845737 | Rapid evolution and gene expression: a rapidly evolving Mendelian trait that silences field crickets has widespread effects on mRNA and protein expression. |
Q99209831 | Rapid evolution and plasticity of genitalia |
Q50866314 | Rapid evolution of antioxidant defence in a natural population of Daphnia magna. |
Q56567116 | Rapid evolution of body fluid regulation following independent invasions into freshwater habitats |
Q58042344 | Rapid evolution of courtship song pattern in Drosophila willistoni sibling species |
Q46680494 | Rapid evolution of elaborate male coloration is driven by visual system in Australian fairy-wrens (Maluridae). |
Q44223888 | Rapid evolution of larval life history, adult immune function and flight muscles in a poleward-moving damselfly |
Q56948529 | Rapid evolution of parasitoids when faced with the symbiont-mediated resistance of their hosts |
Q85003758 | Rapid evolution of sex frequency and dormancy as hydroperiod adaptations |
Q51185972 | Rapid evolution of sexual signals in sympatric Calopteryx damselflies: reinforcement or 'noisy-neighbour' ecological character displacement? |
Q47446982 | Rapid evolution of social learning |
Q91119853 | Rapid evolution of testis size relative to sperm morphology suggests that post-copulatory selection targets sperm number in Anolis lizards |
Q51695950 | Rapid evolution towards heavy metal resistance by mountain birch around two subarctic copper-nickel smelters. |
Q39287205 | Rapid evolutionary change in a secondary sexual character linked to climatic change |
Q34573817 | Rapid increase in cuckoo egg matching in a recently parasitized reed warbler population |
Q46944099 | Rapid increase in dispersal during range expansion in the invasive ladybird Harmonia axyridis. |
Q45196155 | Rapid loss of MHC class II variation in a bottlenecked population is explained by drift and loss of copy number variation |
Q47291664 | Rapid miocene-pliocene dispersal and evolution of Mediterranean rajid fauna as inferred by mitochondrial gene variation. |
Q42033531 | Rapid population divergence in thermal reaction norms for an invading species: breaking the temperature-size rule |
Q46953711 | Rapid prey evolution can alter the structure of predator-prey communities |
Q50688789 | Rapid shifts in multiple life history traits in a population of threespine stickleback. |
Q42023226 | Rapid spread of male-killing Wolbachia in the butterfly Hypolimnas bolina. |
Q82232421 | Rapid temporal change in the expression and age-related information content of a sexually selected trait |
Q39238677 | Rate heterogeneity across Squamata, misleading ancestral state reconstruction and the importance of proper null model specification |
Q57052385 | Rate of deleterious mutation and the distribution of its effects on fitness in vesicular stomatitis virus |
Q28649359 | Rate of evolutionary change in cranial morphology of the marsupial genus Monodelphis is constrained by the availability of additive genetic variation |
Q79321147 | Rates of deleterious mutation and the evolution of sex in Caenorhabditis |
Q43940072 | Rates of phenotypic evolution of ecological characters and sexual traits during the Tanganyikan cichlid adaptive radiation |
Q51698898 | Re-establishment of clinal variation in flowering time among introduced populations of purple loosestrife (Lythrum salicaria, Lythraceae). |
Q36537393 | Re-mating across years and intralineage polygyny are associated with greater than expected levels of inbreeding in wild red deer |
Q110616043 | Reaction norms and the genetic basis of phenotypic plasticity in the wing pattern of the butterfly Bicyclus anynana |
Q109746377 | Realistic genetic architecture enables organismal adaptation as predicted under the folk definition of inclusive fitness |
Q30459742 | Recent admixture generates heterozygosity-fitness correlations during the range expansion of an invading species. |
Q31090595 | Recent invasion of the mountain birch Betula pubescens ssp. tortuosa above the treeline due to climate change: genetic and ecological study in northern Sweden |
Q56976346 | Recent northward range expansion promotes song evolution in a passerine bird, the Light-vented Bulbul |
Q43969480 | Receptive females mitigate costs of sexual conflict |
Q50280296 | Reciprocal preening and food sharing in colour-polymorphic nestling barn owls |
Q46208750 | Reciprocity: you have to think different |
Q50670985 | Recognizing odd smells and ejection of brood parasitic eggs. An experimental test in magpies of a novel defensive trait against brood parasitism. |
Q80454452 | Recombination and loss of complementation: a more than two-fold cost for parthenogenesis |
Q52710456 | Recombination and selection in the maintenance of the adaptive value of inversions. |
Q33303604 | Recombination diversifies chloroplast trnF pseudogenes in Arabidopsis lyrata. |
Q51709738 | Recombination is suppressed and variability reduced in a nascent Y chromosome. |
Q35083738 | Recombination, chromosome number and eusociality in the Hymenoptera. |
Q49561489 | Reconciling gene trees with organism history: the mtDNA phylogeography of three Nesotes species (Coleoptera: Tenebrionidae) on the western Canary Islands. |
Q46396284 | Reconstructing asymmetrical reproductive character displacement in a periodical cicada contact zone |
Q122983805 | Reconstruction of evolutionary changes in fat and toxin consumption reveals associations with gene losses in mammals: A case study for the lipase inhibitor PNLIPRP1 and the xenobiotic receptor NR1I3 |
Q38105623 | Recovering speciation and extinction dynamics based on phylogenies |
Q38699023 | Recovery and immune priming modulate the evolutionary trajectory of infection-induced reproductive strategies. |
Q53085187 | Recovery from hybrid breakdown in a marine invertebrate is faster, stronger and more repeatable under environmental stress. |
Q42045321 | Red & black or black & white? Phylogeny of the Araschnia butterflies (Lepidoptera: Nymphalidae) and evolution of seasonal polyphenism |
Q113282443 | Red Queen bees. Parasites in Social Insects. By Paul Schmid-Hempel. Princeton University Press, Princeton. 1998. xii + 410 pages. ISBN 0-691-05923. |
Q112796093 | Red and yellow pigments in autumn leaves are associated with higher nitrogen resorption |
Q50726720 | Reduced inbreeding depression due to historical inbreeding in Drosophila melanogaster: evidence for purging. |
Q39626892 | Reduced inbreeding depression in peripheral relative to central populations of a monocarpic herb |
Q79741012 | Reducing the cost of resistance; experimental evolution in the filamentous fungus Aspergillus nidulans |
Q34423746 | Refining the conditions for sympatric ecological speciation. |
Q47247416 | Regional divergence and mosaic spatial distribution of two closely related damselfly species (Enallagma hageni and Enallagma ebrium). |
Q46662482 | Regional variation in sex ratios and sex allocation in androdioecious Mercurialis annua. |
Q45018787 | Regional variation in the spatial scale of selection at MPI* and GPI* in the acorn barnacle Semibalanus balanoides (Crustacea). |
Q43117371 | Regulation of stress response is heritable and functionally linked to melanin-based coloration |
Q46635052 | Reinforced postmating reproductive isolation barriers in Neurospora, an Ascomycete microfungus |
Q38380224 | Reinforcement and a cline in mating behaviour evolve in response to secondary contact and hybridization in shield-back katydids (Orthoptera: Tettigoniidae). |
Q42034821 | Reinforcement of mate preference among hybridizing Heliconius butterflies |
Q88527691 | Rejoinder: Further considerations for meta-analysis of transformed quantities such as absolute values |
Q80374145 | Relatedness affects competitive performance of a parasitic plant (Cuscuta europaea) in multiple infections |
Q49150276 | Relationship between fluctuating asymmetry and fitness within and between stressed and unstressed populations of the wolf spider Pirata piraticus |
Q39917848 | Relationship between osteology and aquatic locomotion in birds: determining modes of locomotion in extinct Ornithurae |
Q51609316 | Relationships among morphology, clinging performance and habitat use in Liolaemini lizards. |
Q122600850 | Relationships of reproductive traits and body size with attainment of sexual maturity and age in Blanding's turtles (Emydoidea blandingi) |
Q46590792 | Relative fitness of a generalist parasite on two alternative hosts: a cross-infestation experiment to test host specialization of the hen flea Ceratophyllus gallinae (Schrank). |
Q51620458 | Relative fitness of females and hermaphrodites in a natural gynodioecious population of wild radish, Raphanus sativus L. (Brassicaceae): comparison based on molecular genotyping. |
Q49561392 | Relative fitness of two hermaphroditic mating types in the androdioecious clam shrimp, Eulimnadia texana |
Q51119418 | Relative longevity and field metabolic rate in birds. |
Q44168568 | Relative migration rates and local adaptation in a mosquito-protozoan interaction |
Q79238719 | Relative number of generations of hosts and parasites does not influence parasite local adaptation in coevolving populations of bacteria and phages |
Q38932148 | Relatively weak inbreeding depression in selfing but also in outcrossing populations of North American Arabidopsis lyrata. |
Q35640957 | Relaxed predation results in reduced phenotypic integration in a suite of dragonflies |
Q46960619 | Relaxed trait covariance in interspecific cichlid hybrids predicts morphological diversity in adaptive radiations. |
Q93263796 | Releasing small ejaculates slowly increases per-gamete fertilization success in an external fertilizer: Galeolaria caespitosa (Polychaeta: Serpulidae) |
Q52646380 | Remating and sperm displacement in a natural population of Drosophila buzzatii inferred from mother-offspring analysis of microsatellite loci. |
Q44600993 | Remating in Drosophila melanogaster: an examination of the trading-up and intrinsic male-quality hypotheses |
Q45155899 | Renewed diversification is associated with new ecological opportunity in the Neotropical turtle ants |
Q38922776 | Repeatability and heritability of reproductive traits in free-ranging snakes. |
Q99552779 | Repeatable social network node-based metrics across populations and contexts in a passerine |
Q35027191 | Repeated and predictable patterns of ecotypic differentiation during a biological invasion: lake-stream divergence in parapatric Swiss stickleback |
Q36354378 | Repeated evolution of digital adhesion in geckos: a reply to Harrington and Reeder |
Q40666174 | Repeated evolution of exaggerated dewlaps and other throat morphology in lizards |
Q90199293 | Repeated evolution of terrestrial lineages in a continental lizard radiation |
Q91645899 | Repeated switches from cooperative to selfish worker oviposition during stingless bee evolution |
Q51112800 | Replicated evolutionary divergence in the cuticular hydrocarbon profile of male crickets associated with the loss of song in the Hawaiian archipelago. |
Q50724828 | Replicated population divergence caused by localized coevolution? A test of three hypotheses in the red crossbill-lodgepole pine system. |
Q52705308 | Repression of competition favours cooperation: experimental evidence from bacteria. |
Q51570748 | Reproduction-longevity trade-offs reflect diet, not adaptation. |
Q47370055 | Reproductive ageing and sexual selection on male body size in a wild population of antler flies (Protopiophila litigata). |
Q46260724 | Reproductive and post-reproductive life history of wild-caught Drosophila melanogaster under laboratory conditions. |
Q43674670 | Reproductive barriers between two sympatric beetle species specialized on different host plants. |
Q79733626 | Reproductive character displacement is not the only possible outcome of reinforcement |
Q34787479 | Reproductive compensation |
Q51534621 | Reproductive division of labour and thelytoky result in sympatric barriers to gene flow in honeybees (Apis mellifera L.). |
Q123240916 | Reproductive energetics of the role reversing bushcricket, Kawanaphila nartee (Orthoptera: Tettigoniidae: Zaprochilinae) |
Q92712490 | Reproductive fitness consequences of progenesis: Sex-specific pay-offs in safe and risky environments |
Q46573361 | Reproductive isolation and hybrid pollen disadvantage in Ipomopsis. |
Q30412694 | Reproductive isolation and patterns of genetic differentiation in a cryptic butterfly species complex |
Q51695697 | Reproductive isolation between chromosomal races of the house mouse Mus musculus domesticus in a parapatric contact area revealed by an analysis of multiple unlinked loci. |
Q51935150 | Reproductive isolation in a threespine stickleback hybrid zone. |
Q126080278 | Reproductive isolation via divergent genital morphology due to cascade reinforcement inOhomopterusground beetles |
Q35388573 | Reproductive mode evolution in lizards revisited: updated analyses examining geographic, climatic and phylogenetic effects support the cold-climate hypothesis |
Q96647647 | Reproductive senescence and parental effects in an indeterminate grower |
Q51657291 | Reproductive strategies under multiparasitism in natural populations of the parasitoid wasp Nasonia (Hymenoptera). |
Q40305141 | Reproductive suppression follows threats to child survival |
Q38992124 | Reproductive trade-offs in a long-lived bird species: condition-dependent reproductive allocation maintains female survival and offspring quality. |
Q51780613 | Reproductive tradeoffs and yolk steroids in female leopard geckos, Eublepharis macularius. |
Q113345216 | Reproductive trade‐offs and phenotypic selection change with body condition, but not with predation regime, across island lizard populations |
Q44163706 | Reproductive value in a complex life cycle: heat tolerance of the pitcher-plant mosquito, Wyeomyia smithii |
Q51719732 | Resistance in introduced populations of a freshwater snail to native range parasites. |
Q48190768 | Resistance to environmental stress in Drosophila ananassae: latitudinal variation and adaptation among populations |
Q99619230 | Resistance to natural and synthetic gene drive systems |
Q51426752 | Resistance to oxidative stress shows low heritability and high common environmental variance in a wild bird. |
Q34014122 | Resolving current disagreements and ambiguities in the terminology of animal communication. |
Q37877775 | Resolving the iterated prisoner's dilemma: theory and reality. |
Q33268529 | Resolving the tragedy of the commons: the feedback between intraspecific conflict and population density |
Q40432014 | Resource abundance and the critical transition to cooperation |
Q98472832 | Resource allocation is determined by both parents and offspring in a burying beetle |
Q125799373 | Resource allocation to growth, reproduction and survival in Gladiolus : The cost of male function |
Q111264616 | Resource allocation: a conflict in the fig/fig wasp mutualism? |
Q88418646 | Resource availability, mating opportunity and sexual selection intensity influence the expression of male alternative reproductive tactics |
Q37371020 | Resource limitation and responses to rivals in males of the fruit fly Drosophila melanogaster |
Q42026326 | Resource specialization in a phytophagous insect: no evidence for genetically based performance trade-offs across hosts in the field or laboratory |
Q60393651 | Resource stability and geographic isolation are associated with genome divergence in western Palearctic crossbills |
Q51755223 | Resource-dependent sex-allocation in a simultaneous hermaphrodite. |
Q90737304 | Resources mediate selection on module longevity in the field |
Q52018856 | Response of fluctuating and directional asymmetry to selection on wing shape in Drosophila melanogaster. |
Q48255524 | Response of parasitoid egg load to host dynamics and implications for egg load evolution |
Q114080041 | Response to: A comment on The adaptive value of gluttony: Predators mediate the life history trade‐offs of satiation threshold by Pruitt and Krauel (2010) by Postma et al. (2021) |
Q80404347 | Responses to selection on male-phase duration in Chamerion angustifolium |
Q52659270 | Restricted gene flow between two social forms in the ant Formica truncorum. |
Q47176346 | Resurrecting the differential mortality model of sexual size dimorphism |
Q62767447 | Reverse evolution of fitness inDrosophila melanogaster |
Q46744857 | Revisiting Fisher: range size drives the correlation between variability and abundance of British bird eggs |
Q33283070 | Revisiting Jablonski (1993): cladogenesis and range expansion explain latitudinal variation in taxonomic richness |
Q39616788 | Revisiting the cost of carnivory in mammals. |
Q115431569 | Ricklefs, R. E. and Schluter, D. (eds.). 1993. Species Diversity in Ecological Communities: Historical and Geographical Perspectives. University of Chicago Press, paper $27.95. 414 pp. ISBN: 0-226-71823-9. |
Q126130815 | Ridley, Mark. Evolution. Blackwell Scientific Publications, Oxford, 1993. £19.50. viii + 670 pp., illus. ISBN: 0‐632‐03 481‐5. |
Q40082112 | Rise and fall of vector infectivity during sequential strain displacements by mosquito-borne dengue virus. |
Q44485229 | Risk-induced hatching timing shows low heritability and evolves independently of spontaneous hatching in red-eyed treefrogs. |
Q45353732 | Risk-taking and the evolution of mechanisms for rapid escape from predators |
Q46157468 | Ritual fights and male reproductive success in a human population. |
Q39207697 | Rivers, refuges and population divergence of fire-eye antbirds (Pyriglena) in the Amazon Basin. |
Q99627555 | Riverscape properties contribute to the origin and structure of a hybrid zone in a Neotropical freshwater fish |
Q52680787 | Robust clines and robust sampling: a reply to Kyriacou et al. |
Q49603552 | Robustness of the approximate likelihood of the protracted speciation model |
Q52736141 | Robustness of the outcome of adult bumblebee infection with a trypanosome parasite after varied parasite exposures during larval development. |
Q57057635 | Role of ageing and temperature in shaping reaction norms and fecundity functions in insects |
Q33735140 | Role of epibenthic resource opportunities in the parallel evolution of lake whitefish species pairs (Coregonus sp.) |
Q34750341 | Role of propagule pressure in colonization success: disentangling the relative importance of demographic, genetic and habitat effects |
Q33247044 | Role of sexual and natural selection in evolution of body size and shape: a phylogenetic study of morphological radiation in grouse. |
Q53061166 | Routes to indirect fitness in cooperatively breeding vertebrates: kin discrimination and limited dispersal. |
Q83395789 | SNP deserts of Asian cultivated rice: genomic regions under domestication |
Q46936690 | Salt tolerance evolves more frequently in C4 grass lineages |
Q56623283 | Sanctions and mutualism stability: when should less beneficial mutualists be tolerated? |
Q101410299 | Satyrization in Drosophila fruiflies |
Q39263806 | Scale effects and constraints for sound production in katydids (Orthoptera: Tettigoniidae): correlated evolution between morphology and signal parameters |
Q61770905 | Scary clowns: adaptive function of anemonefish coloration |
Q124881542 | Schierwater, B., Streit, B., Wagner, G. P. and DeSalle R. (Eds.). 1994. Molecular Ecology and Evolution: Approaches and Applications. Birkhäuser Verlag, 622 pp. ISBN: 3‐7643‐2942‐4. |
Q92868424 | Science policies: How should science funding be allocated? An evolutionary biologists' perspective |
Q39982287 | Seasonal dispersal of pests: one surge or two? |
Q46720725 | Seasonal polyphenism in wing coloration affects species recognition in rubyspot damselflies (Hetaerina spp.). |
Q42010734 | Seasonal selection and resource dynamics in a seasonally polyphenic butterfly. |
Q46272744 | Seasonal shifts along the oviparity-viviparity continuum in a cold-climate lizard population |
Q37385463 | Seasonal variation in life history traits in two Drosophila species |
Q39365950 | Seasonal variation in male alternative reproductive tactics. |
Q36350051 | Secondary compounds from exotic tree plantations change female mating preferences in the palmate newt (Lissotriton helveticus). |
Q33410374 | Secondary contact during adaptive radiation: a community matrix for Lake Malawi cichlids. |
Q46260624 | Segregation of male-sterility alleles across a species boundary. |
Q40018352 | Selection and constraints on offspring size-number trade-offs in sand lizards (Lacerta agilis). |
Q35595937 | Selection and evolutionary potential of spring arrival phenology in males and females of a migratory songbird. |
Q47198433 | Selection efficiency and effective population size in Drosophila species |
Q110616055 | Selection experiments and the study of phenotypic plasticity1 |
Q42028311 | Selection for cuticular melanism reveals immune function and life-history trade-offs in Spodoptera littoralis. |
Q57272349 | Selection for distinct gene expression properties favours the evolution of mutational robustness in gene regulatory networks |
Q38441697 | Selection for increased allocation to offspring number under environmental unpredictability |
Q51612343 | Selection for increased body length in Subantarctic fur seals on Amsterdam Island. |
Q44673444 | Selection for individual recognition and the evolution of polymorphic identity signals in Polistes paper wasps |
Q51458137 | Selection for sex in finite populations. |
Q35522632 | Selection for territory acquisition is modulated by social network structure in a wild songbird. |
Q45373152 | Selection for thermostability can lead to the emergence of mutational robustness in an RNA virus. |
Q46906791 | Selection from parasites favours immunogenetic diversity but not divergence among locally adapted host populations |
Q49186735 | Selection in a fluctuating environment and the evolution of sexual dimorphism in the seed beetle Callosobruchus maculatus |
Q45418203 | Selection in a fluctuating environment leads to decreased genetic variation and facilitates the evolution of phenotypic plasticity |
Q56961826 | Selection of evolutionary models for phylogenetic hypothesis testing using parametric methods |
Q51652961 | Selection of low investment in sex in a cyclically parthenogenetic rotifer. |
Q44026059 | Selection of trait combinations through bee and fly visitation to flowers of Polemonium foliosissimum. |
Q39411390 | Selection on a eumelanic ornament is stronger in the tropics than in temperate zones in the worldwide-distributed barn owl. |
Q47333397 | Selection on body size and sexual size dimorphism differs between host species in a seed-feeding beetle |
Q52818430 | Selection on bristle length has the ability to drive the evolution of male abdominal appendages in the sepsid fly Themira biloba. |
Q50458941 | Selection on female behaviour fluctuates with offspring environment. |
Q51682172 | Selection on floral and carbon uptake traits of Lobelia siphilitica is similar in females and hermaphrodites. |
Q42045317 | Selection on floral characters in natural Spanish populations of Silene latifolia |
Q51713127 | Selection on flowering time and floral display in an alpine and a lowland population of Arabidopsis lyrata. |
Q96163639 | Selection on fruit traits is mediated by the interplay between frugivorous birds, fruit flies, parasitoid wasps, and seed-dispersing ants |
Q40664984 | Selection on incremental variation of eye size in a wild population of Daphnia |
Q60394115 | Selection on life-history traits and genetic population divergence in rotifers |
Q45166620 | Selection on male longevity in a monogamous human population: late-life survival brings no additional grandchildren |
Q46808278 | Selection on outlier loci and their association with adaptive phenotypes in Littorina saxatilis contact zones. |
Q42007467 | Selection on phenotypic plasticity of morphological traits in response to flooding and competition in the clonal shore plant Ranunculus reptans. |
Q44153460 | Selection on quantitative colour variation in Centaurea cyanus: the role of the pollinator's visual system |
Q51894508 | Selection on signal–reward correlation: limits and opportunities to the evolution of deceit in Turnera ulmifolia L. |
Q44168594 | Selection pressures have caused genome-wide population differentiation of Anthoxanthum odoratum despite the potential for high gene flow |
Q56654681 | Selective Differentiation during the Colonization and Establishment of a Newly Invasive Species |
Q84822729 | Selective abortion and the evolution of genomic imprinting |
Q47371124 | Selective and genetic constraints on the evolution of body size in a stream-dwelling salmonid fish. |
Q35094686 | Selective maintenance of recombination between the sex chromosomes |
Q51660883 | Selective nectar robbing in a gynodioecious plant (Glechoma longituba) enhances female advantage. |
Q47980242 | Selective pressures on MHC class II genes in the guppy (Poecilia reticulata) as inferred by hierarchical analysis of population structure |
Q86849340 | Self-fertilization and inbreeding limit the scope for sexually antagonistic polymorphism |
Q52009782 | Self-serving punishment and the evolution of cooperation. |
Q46162941 | Selfing ability and dispersal are positively related, but not affected by range position: a multispecies study on southern African Asteraceae |
Q45196425 | Selfing and resource allocation in Schiedea salicaria (Caryophyllaceae), a gynodioecious species |
Q46923022 | Selfing, adaptation and background selection in finite populations |
Q114080036 | Selfish migrants: How a meiotic driver is selected to increase dispersal |
Q50955980 | Senescence in immune priming and attractiveness in a beetle. |
Q50798699 | Senescence in relation to latitude and migration in birds. |
Q39781486 | Senescent males carry premutagenic lesions in sperm |
Q46229578 | Senescent sperm performance in old male birds |
Q46960666 | Sensory evolution of hearing in tettigoniids with differing communication systems |
Q89374621 | Sensory trait variation contributes to biased dispersal of threespine stickleback in flowing water |
Q91865824 | Sequence, structure and evolutionary analysis of cold shock domain proteins, a member of OB fold family |
Q50773251 | Sequential mate choice and sexual isolation in threespine stickleback species. |
Q31028247 | Sequential radiation of unrelated organisms: the gall fly Eurosta solidaginis and the tumbling flower beetle Mordellistena convicta |
Q89252280 | Serotonin, behavior, and natural selection in New World monkeys |
Q51965185 | Seven answers from adaptive dynamics. |
Q39775323 | Severe extinction and rapid recovery of mammals across the Cretaceous-Palaeogene boundary, and the effects of rarity on patterns of extinction and recovery. |
Q46642270 | Severe outbreeding and inbreeding depression maintain mating system differentiation in Epipactis (Orchidaceae). |
Q46737299 | Sex allocation according to multiple sexually dimorphic traits of both parents in the barn swallow (Hirundo rustica). |
Q58869821 | Sex allocation in an hermaphroditic plant: the case of gynodioecy in Thymus vulgaris L |
Q39067490 | Sex allocation, juvenile mortality and the costs imposed by offspring on parents and siblings. |
Q51669855 | Sex and asymmetry in humans: what is the role of developmental instability? |
Q51740894 | Sex and differentiation: population genetic divergence and sexual dimorphism in Mexican goodeid fish. |
Q31147915 | Sex and immunity in the yellow dung fly Scathophaga stercoraria |
Q115033094 | Sex and morph differences in age‐dependent trait changes in a polymorphic songbird |
Q45736862 | Sex at the margins: parthenogenesis vs. facultative and obligate sex in a Neotropical ant. |
Q38208014 | Sex change in plants and animals: a unified perspective |
Q79325896 | Sex choice in plants: facultative adjustment of the sex ratio in the perennial herb Begonia gracilis |
Q83364548 | Sex chromosome evolution in the clam shrimp, Eulimnadia texana |
Q60299920 | Sex chromosome turnovers and genetic drift: a simulation study |
Q92443850 | Sex differences in nutrient intake can reduce the potential for sexual conflict over fitness maximization by female and male crickets |
Q39024177 | Sex differences in the effects of juvenile and adult diet on age-dependent reproductive effort. |
Q51723842 | Sex drives intracellular conflict in yeast. |
Q42214931 | Sex in an uncertain world: environmental stochasticity helps restore competitive balance between sexually and asexually reproducing populations |
Q92727755 | Sex increases the probability of evolutionary rescue in the presence of a competitor |
Q40665112 | Sex investment ratios in eusocial Hymenoptera support inclusive fitness theory |
Q39886184 | Sex ratio and gamete size across eastern North America in Dictyostelium discoideum, a social amoeba with three sexes |
Q51728058 | Sex ratio selection and multi-factorial sex determination in the housefly: a dynamic model. |
Q30442554 | Sex ratio variance and the maintenance of environmental sex determination |
Q47282722 | Sex ratio variation in gynodioecious Lobelia siphilitica: effects of population size and geographic location |
Q47282711 | Sex ratio, sex-specific chick mortality and sexual size dimorphism in birds. |
Q51432660 | Sex uncovered: the evolutionary biology of reproductive systems. |
Q40581893 | Sex without sex chromosomes: genetic architecture of multiple loci independently segregating to determine sex ratios in the copepod Tigriopus californicus |
Q52659278 | Sex, mutation and fitness: asymmetric costs and routes to recovery through compensatory evolution. |
Q38003708 | Sex, outcrossing and mating types: unsolved questions in fungi and beyond |
Q48335859 | Sex-antagonistic genes, XY recombination and feminized Y chromosomes. |
Q47630901 | Sex-biased dispersal, kin selection and the evolution of sexual conflict |
Q53095511 | Sex-biased genetic component distribution among populations: additive genetic and maternal contributions to phenotypic differences among populations of Chinook salmon. |
Q40201563 | Sex-biased preferential care in the cooperatively breeding Arabian babbler |
Q51534629 | Sex-differential effects of inbreeding on overwinter survival, birth date and mass of bighorn lambs. |
Q112207627 | Sex-linked altruism: A stepping-stone in the evolution of social behavior? |
Q41472626 | Sex-linked inheritance, genetic correlations and sexual dimorphism in three melanin-based colour traits in the barn owl. |
Q52649742 | Sex-ratio distorter of Drosophila simulans reduces male productivity and sperm competition ability. |
Q33934836 | Sex-ratio meiotic drive and interspecific competition |
Q51546541 | Sex-related variation in migration phenology in relation to sexual dimorphism: a test of competing hypotheses for the evolution of protandry. |
Q46371887 | Sex-specific associative learning cues and inclusive fitness benefits in the Seychelles warbler |
Q47677813 | Sex-specific compensatory growth in the larvae of the greater wax moth Galleria mellonella |
Q51755221 | Sex-specific ecomorphological variation and the evolution of sexual dimorphism in dwarf chameleons (Bradypodion spp.). |
Q102330220 | Sex-specific effects of experimental ectoparasite infestation on telomere length in great tit nestlings |
Q46558425 | Sex-specific effects of inbreeding in wild-caught Drosophila melanogaster under benign and stressful conditions |
Q51408289 | Sex-specific fitness variation in gynodioecious Beta vulgaris ssp. maritima: do empirical observations fit theoretical predictions? |
Q51317464 | Sex-specific genotype-by-environment interactions for cuticular hydrocarbon expression in decorated crickets, Gryllodes sigillatus: implications for the evolution of signal reliability. |
Q50445385 | Sex-specific heritability of cell-mediated immune response in the blue tit nestlings (Cyanistes caeruleus). |
Q50699664 | Sex-specific life history responses to nymphal diet quality and immune status in a field cricket. |
Q37404664 | Sex-specific plasticity and genotype × sex interactions for age and size of maturity in the sheepshead swordtail, Xiphophorus birchmanni. |
Q47273405 | Sex-specific plasticity of growth and maturation size in a spider: implications for sexual size dimorphism |
Q42981414 | Sex-specific reaction norms to intraspecific larval competition in the mosquito Aedes aegypti |
Q51200405 | Sex-specific recombination rates and allele frequencies affect the invasion of sexually antagonistic variation on autosomes. |
Q51623846 | Sex-specific selection on energy metabolism--selection coefficients for winter survival. |
Q39282789 | Sex-specific selection under environmental stress in seed beetles |
Q60299945 | Sex-specific selective pressures on body mass in the greater white-toothed shrew, Crocidura russula |
Q28828953 | Sexual Selection on male cuticular hydrocarbons via male-male competition and female choice |
Q97558823 | Sexual and ecological selection on a sexual conflict gene |
Q47375379 | Sexual and lifetime selection on body size in a marine fish: the importance of life-history trade-offs |
Q43349023 | Sexual and natural selection in the evolution of extended phenotypes: the use of green nesting material in starlings. |
Q87509893 | Sexual antagonism and meiotic drive cause stable linkage disequilibrium and favour reduced recombination on the X chromosome |
Q35642222 | Sexual antagonism in the pistil varies among populations of a hermaphroditic mixed-mating plant. |
Q56774633 | Sexual cannibalism in Nephila plumipes as a consequence of female life history strategies |
Q51566605 | Sexual coevolution in the traumatically inseminating plant bug genus Coridromius. |
Q38401472 | Sexual coloration and sperm performance in the Australian painted dragon lizard, Ctenophorus pictus |
Q52646385 | Sexual conflict and cooperation under naturally occurring male enforced monogamy. |
Q34470838 | Sexual conflict and female immune suppression in the cricket, Allonemobious socius |
Q60492186 | Sexual conflict and indirect benefits |
Q48387578 | Sexual conflict does not drive reproductive isolation in experimental populations of Drosophila pseudoobscura |
Q51467621 | Sexual conflict in Gerris gillettei (Insecta: Hemiptera): intraspecific intersexual correlated morphology and experimental assessment of behaviour and fitness. |
Q31028219 | Sexual conflict in Sepsis cynipsea: female reluctance, fertility and mate choice. |
Q47420109 | Sexual conflict in wing size and shape in Drosophila melanogaster. |
Q46463756 | Sexual conflict is not counterbalanced by good genes in the laboratory Drosophila melanogaster model system |
Q34666420 | Sexual conflict over care: antagonistic effects of clutch desertion on reproductive success of male and female penduline tits |
Q46549753 | Sexual dichromatism in wing pigmentation of New World dragonflies follows Rensch's rule. |
Q46132637 | Sexual dimorphism and the genetic potential for evolution of sex allocation in the gynodioecious plant, Schiedea salicaria. |
Q38611625 | Sexual dimorphism in epicuticular compounds despite similar sexual selection in sex role reversed seed beetles |
Q28749591 | Sexual dimorphism in primate aerobic capacity: a phylogenetic test |
Q93337608 | Sexual dimorphism modifies habitat-associated divergence: Evidence from beach and creek breeding sockeye salmon |
Q45886563 | Sexual functionality of Leptopilina clavipes (Hymenoptera: Figitidae) after reversing Wolbachia-induced parthenogenesis |
Q40570824 | Sexual healing: mating induces a protective immune response in bumblebees |
Q51693956 | Sexual imprinting on continuous variation: do female zebra finches prefer or avoid unfamiliar sons of their foster parents? |
Q29354003 | Sexual isolation and extreme morphological divergence in the Cumana guppy: a possible case of incipient speciation |
Q51248656 | Sexual isolation promotes divergence between parapatric lake and stream stickleback. |
Q90831760 | Sexual isolation with and without ecological isolation in marine isopods Jaera albifrons and J. praehirsuta |
Q51722494 | Sexual reproduction advances autumn leaf colours in mountain birch (Betula pubescens ssp. czerepanovii). |
Q52940850 | Sexual rest and post-meiotic sperm ageing in house mice. |
Q50920423 | Sexual selection and assortative mating: an experimental test. |
Q84814824 | Sexual selection and condition-dependence |
Q39526631 | Sexual selection and ecological generalism are correlated in antbirds. |
Q51310199 | Sexual selection and experimental evolution of chemical signals in Drosophila pseudoobscura. |
Q55881105 | Sexual selection and peripatric speciation: the Kaneshiro model revisited |
Q91853188 | Sexual selection and population divergence III. interspecific and intraspecific variation in mating signals |
Q51464031 | Sexual selection and temporal phenotypic variation in a damselfly population. |
Q52753145 | Sexual selection and the evolution of secondary sexual traits: sex comb evolution in Drosophila. |
Q93095513 | Sexual selection and the evolution of sperm morphology in sharks |
Q30457059 | Sexual selection in a hermaphroditic plant through female reproductive success |
Q60370353 | Sexual selection in an isopod with Wolbachia-induced sex reversal: males prefer real females |
Q38060808 | Sexual selection in fungi. |
Q56168837 | Sexual selection in the monogamous barn swallow (Hirundo rustica). II. Mechanisms of sexual selection |
Q104466197 | Sexual selection increased offspring production via evolution of male and female traits |
Q51173508 | Sexual selection is positively associated with ecological generalism among agamid lizards. |
Q24670505 | Sexual selection maintains whole-body chiral dimorphism in snails |
Q51140190 | Sexual selection on Drosophila serrata male pheromones does not vary with female age or mating status. |
Q47248507 | Sexual selection on brain size in shorebirds (Charadriiformes). |
Q46828462 | Sexual selection on female ornaments in the sex-role-reversed Gulf pipefish (Syngnathus scovelli). |
Q50193795 | Sexual selection on male development time in the parasitoid wasp Nasonia vitripennis |
Q33203005 | Sexual selection on morphological and physiological traits and fluctuating asymmetry in the black scavenger fly Sepsis cynipsea. |
Q33195292 | Sexual selection on morphological and physiological traits and fluctuating asymmetry in the yellow dung fly. |
Q104139523 | Sexual selection on performance traits in an Australian lizard with alternative reproductive tactics |
Q46474532 | Sexual selection predicts brain structure in dragon lizards. |
Q79315679 | Sexual selection promotes hybridization between Pecos pupfish, Cyprinodon pecosensis and sheepshead minnow, C. variegatus |
Q47313862 | Sexual selection uncouples the evolution of brain and body size in pinnipeds. |
Q79315692 | Sexual selection, antennae length and the mating advantage of large males in Asellus aquaticus |
Q79321092 | Sexual selection, antennae length and the mating advantage of large males in Asellus aquaticus |
Q47224990 | Sexual selection, sexual size dimorphism and Rensch's rule in Odonata |
Q34278781 | Sexual size dimorphism and timing of spring migration in birds |
Q33306979 | Sexual size dimorphism predicts the frequency of multiple mating in the sex-role reversed pipefish Syngnathus typhle |
Q60337426 | Sexual variation in heritability and genetic correlations of morphological traits in house sparrow (Passer domesticus) |
Q44417228 | Sexually antagonistic co-evolution: a model and an empirical test |
Q34521818 | Sexually antagonistic coevolution in insects is associated with only limited morphological diversity |
Q60362971 | Sexually antagonistic selection on primate size |
Q90320071 | Sexually dimorphic gene expression and transcriptome evolution provide mixed evidence for a fast-Z effect in Heliconius |
Q35889182 | Sexually selected dichromatism in the hihi Notiomystis cincta: multiple colours for multiple receivers |
Q53852134 | Sexually selected nest-building--Pomatoschistus minutus males build smaller nest-openings in the presence of sneaker males. |
Q91880850 | Sexually selected sexual selection: Can evolutionary retribution explain female ornamental colour? |
Q46078231 | Sexy sons from re-mating do not recoup the direct costs of harmful male interactions in the Drosophila melanogaster laboratory model system |
Q115033101 | Sex‐specific associations between life‐history traits and a novel reproductive polymorphism in the Pacific field cricket |
Q60152764 | Shape at the cross-roads: homoplasy and history in the evolution of the carnivoran skull towards herbivory |
Q51812211 | Shape, variance and integration during craniogenesis: contrasting marsupial and placental mammals. |
Q82487361 | Shared and unique features of morphological differentiation between predator regimes in Gambusia caymanensis |
Q30010539 | Sharp acoustic boundaries across an altitudinal avian hybrid zone despite asymmetric introgression. |
Q64032490 | Shifting clinal patterns and microsatellite variation in Drosophila serrata populations: a comparison of populations near the southern border of the species range |
Q80231867 | Short- and long-term benefits and detriments to recombination under antagonistic coevolution |
Q51941114 | Short- and long-term consequences of early developmental conditions: a case study on wild and domesticated zebra finches. |
Q51703570 | Short-term rates of parasite evolution predict the evolution of host diversity. |
Q51685730 | Should food-deceptive species flower before or after rewarding species? An experimental test of pollinator visitation behaviour under contrasting phenologies. |
Q51646260 | Sib-mating in the ant Plagiolepis pygmaea: adaptative inbreeding? |
Q40165762 | Sibling competition does not exacerbate inbreeding depression in the burying beetle Nicrophorus vespilloides |
Q39673174 | Sibship effects on dispersal behaviour in a pre-industrial human population |
Q34236347 | Sick ants become unsociable |
Q84266724 | Signal convergence in fruits: a result of selection by frugivores? |
Q58454501 | Signalling conflict between prey and predator attraction |
Q47978867 | Signalling of information that is neither cryptic nor private |
Q38852988 | Signals of selection in conditionally expressed genes in the diversification of three horned beetle species. |
Q47297172 | Signature of selection on the rhodopsin gene in the marine radiation of American seven-spined gobies (Gobiidae, Gobiosomatini). |
Q51589859 | Signatures of selection acting on the innate immunity gene Toll-like receptor 2 (TLR2) during the evolutionary history of rodents. |
Q59351706 | Significant differences in maternal carotenoid provisioning and effects on offspring fitness in Chinook salmon colour morphs |
Q30822530 | Silene tatarica microsatellites are frequently located in repetitive DNA. |
Q34893150 | Similar evolutionary potentials in an obligate ant parasite and its two host species |
Q46733855 | Similar patterns of frequency-dependent selection on animal personalities emerge in three species of social spiders |
Q51774694 | Similar preferences for ornamentation in opposite- and same-sex choice experiments. |
Q46691704 | Similar slow down in running speed progression in species under human pressure |
Q122915901 | Similarity, parsimony and conjectures of homology: The chelonian shoulder girdle revisited |
Q51013929 | Simultaneous hermaphrodites reproducing in pairs self-fertilize some of their eggs: an experimental test of predictions of mixed-mating and Hermaphrodite's Dilemma theory. |
Q51923435 | Single and multigenerational responses of body mass to atmospheric oxygen concentrations in Drosophila melanogaster : evidence for roles of plasticity and evolution. |
Q38917453 | Single and multiple mating reduces longevity of female dumpling squid (Euprymna tasmanica). |
Q34253246 | Single origin of human commensalism in the house sparrow. |
Q50491912 | Sire coloration influences offspring survival under predation risk in the moorfrog. |
Q44163727 | Size and asymmetry: are there costs to winning the royalty race? |
Q47354017 | Size asymmetry in intraspecific competition and the density-dependence of inbreeding depression in a natural plant population: a case study in cassava (Manihot esculenta Crantz, Euphorbiaceae). |
Q46927214 | Size differentiation in Finnish house sparrows follows Bergmann's rule with evidence of local adaptation. |
Q34248385 | Size scaling and stiffness of avian primary feathers: implications for the flight of Mesozoic birds |
Q92411336 | Size-dependent costs of migration: Migrant bird species are subordinate to residents, but only at small body sizes |
Q47222043 | Size-dependent sex allocation in a simultaneous hermaphrodite parasite |
Q48092179 | Sleep and vigilance linked to melanism in wild barn owls |
Q34738251 | Slow molecular evolution in 18S rDNA, rbcL and nad5 genes of mosses compared with higher plants |
Q29392199 | Small body size increases the regional differentiation of populations of tropical mantellid frogs (Anura: Mantellidae) |
Q81802131 | Small effective population sizes in two planktonic freshwater copepod species (Eudiaptomus) with apparently large census sizes |
Q47986354 | Social amoebae mating types do not invest unequally in sexual offspring |
Q50272631 | Social cohesion among kin, gene flow without dispersal and the evolution of population genetic structure in the killer whale (Orcinus orca). |
Q44667658 | Social competition, corticosterone and survival in female lizard morphs |
Q46030036 | Social context predicts recognition systems in ant queens. |
Q92290406 | Social effects of territorial neighbours on the timing of spring breeding in North American red squirrels |
Q51657923 | Social environment affects the life history tactic of a phoretic mite. |
Q47419486 | Social group size, potential sperm competition and reproductive investment in a hermaphroditic leech, Helobdella papillornata (Euhirudinea: Glossiphoniidae). |
Q46971485 | Social heterosis and the maintenance of genetic diversity |
Q43413714 | Social influence on age and reproduction: reduced lifespan and fecundity in multi-queen ant colonies |
Q43932131 | Social monogamy vs. polyandry: ecological factors associated with sex roles in two closely related birds within the same habitat |
Q113791787 | Social organization in ungulates: Revisiting Jarman’s hypotheses |
Q34575748 | Social semantics: altruism, cooperation, mutualism, strong reciprocity and group selection. |
Q56269052 | Social semantics: how useful has group selection been? |
Q38393026 | Social semantics: toward a genuine pluralism in the study of social behaviour |
Q58557943 | Social situation, sperm competition and sex allocation in a simultaneous hermaphrodite parasite, the cestodeSchistocephalus solidus |
Q47566981 | Social traits, social networks and evolutionary biology. |
Q87349959 | Social versus nonsocial cues and responses: a reply to Alizon |
Q47207727 | Sociality, age at first reproduction and senescence: comparative analyses of birds |
Q46960585 | Socially flexible female choice and premating isolation in field crickets (Teleogryllus spp.). |
Q91438768 | Soil microbes alter plant fitness under competition and drought |
Q43895342 | Song perception among incipient species as a mechanism for reproductive isolation. |
Q50773330 | Song similarity predicts hybridization in flycatchers. |
Q51987637 | Sounds different: inbreeding depression in sexually selected traits in the cricket Teleogryllus commodus. |
Q80374152 | Sources of stochasticity in models of sex allocation in spatially structured populations |
Q57212848 | Southwood's Kaleidoscope |
Q35001281 | Space, sympatry and speciation |
Q39283411 | Spatial and demographic population genetic structure in Catasetum viridiflavum across a human-disturbed habitat |
Q42025305 | Spatial and genetic structure of host-associated differentiation in the parasitoid Copidosoma gelechiae |
Q28304119 | Spatial and temporal patterns of parthenogenesis and parasitism in the freshwater snail Melanoides tuberculata |
Q59293312 | Spatial autocorrelation of allozyme and quantitative markers within a natural population of Centaurea jacea (Asteraceae) |
Q45985830 | Spatial distribution of nests constrains the strength of sexual selection in a warbler. |
Q31028240 | Spatial ecological and genetic structure of a mixed population of sexual diploid and apomictic triploid dandelions. |
Q53600065 | Spatial heterogeneity and the stability of host-parasite coexistence. |
Q41621103 | Spatial heterogeneity lowers rather than increases host-parasite specialization. |
Q59185503 | Spatial patterns of polygenic variation in Impatiens capensis, a species with an environmentally controlled mixed mating system |
Q33517802 | Spatial regression techniques for inter-population data: studying the relationships between morphological and environmental variation. |
Q50770845 | Spatial scale of local adaptation in a plant-pathogen metapopulation. |
Q33652877 | Spatial seed and pollen games: dispersal, sex allocation, and the evolution of dioecy |
Q44280468 | Spatial sorting may explain evolutionary dynamics of wing polymorphism in pygmy grasshoppers. |
Q58869797 | Spatial structure of nuclear factors involved in sex determination in the gynodioecious |
Q83646613 | Spatial variation in the fitness of divergent aposematic phenotypes of the poison frog, Dendrobates tinctorius |
Q33877827 | Spatial variation in the temporal change of male and female melanic ornamentation in the barn owl. |
Q51546636 | Spatially explicit models of divergence and genome hitchhiking. |
Q47630246 | Spatially heterogeneous stochasticity and the adaptive diversification of dormancy |
Q48218936 | Spatially structured genetic variation in a broadcast spawning bivalve: quantitative vs. molecular traits |
Q35514434 | Spatially varying selection shapes life history clines among populations of Drosophila melanogaster from sub-Saharan Africa |
Q46562441 | Spatiotemporal fluctuations in natural selection acting on the gall-parasitic aphid Tetraneura sorini |
Q41704701 | Specialized avian Haemosporida trade reduced host breadth for increased prevalence |
Q99356715 | Speciation and gene flow across an elevational gradient in New Guinea kingfishers |
Q36199138 | Speciation in a keystone plant genus is driven by elevation: a case study in New Guinean Ficus |
Q51703557 | Speciation in killifish and the role of salt tolerance. |
Q51530721 | Speciation in ninespine stickleback: reproductive isolation and phenotypic divergence among cryptic species of Japanese ninespine stickleback. |
Q46587642 | Speciation in peripheral populations: effects of drift load and mating systems |
Q46692131 | Speciation is not necessarily easier in species with sexually monomorphic mating signals |
Q46941938 | Speciation within genomic networks: a case study based on Steatocranus cichlids of the lower Congo rapids |
Q46324319 | Speciation, species persistence and the goals of studying genomic barriers to gene flow. |
Q101211893 | Speciation-by-depth on coral reefs: sympatric divergence with gene flow or cryptic transient isolation? |
Q47599530 | Species cohesion despite extreme inbreeding in a social spider. |
Q31028225 | Species concepts and species reality: salvaging a Linnaean rank |
Q30665746 | Species distribution models contribute to determine the effect of climate and interspecific interactions in moving hybrid zones |
Q82983509 | Species range expansion by beneficial mutations |
Q47436466 | Species richness in agamid lizards: chance, body size, sexual selection or ecology? |
Q56171426 | Species with a chemical defence, but not chemical offence, live longer |
Q33288437 | Species-level selection reduces selfishness through competitive exclusion |
Q115555186 | Specific induced responses to different predator species in anuran larvae |
Q91480416 | Specificity and seasonal prevalence of anther smut disease Microbotryum on sympatric Himalayan Silene species |
Q47450357 | Sperm competition and brain size evolution in mammals. |
Q80454442 | Sperm competition and diversity in rodent copulatory behaviour |
Q52057533 | Sperm competition and male ejaculate investment in Nauphoeta cinerea: effects of social environment during development. |
Q46494662 | Sperm competition and maternal effects differentially influence testis and sperm size in Callosobruchus maculatus |
Q61782051 | Sperm competition and small size advantage for males of the golden orb-web spider Nephila edulis |
Q34650464 | Sperm competition and the evolution of testes size in birds |
Q84822733 | Sperm competition and the evolution of the sperm hook in house mice |
Q34163524 | Sperm competition does not influence sperm hook morphology in selection lines of house mice |
Q51766197 | Sperm competition games: the risk model can generate higher sperm allocation to virgin females. |
Q51077076 | Sperm competition generates evolution of increased paternal investment in a sex role-reversed seed beetle. |
Q34573811 | Sperm competition in a fish with external fertilization: the contribution of sperm number, speed and length |
Q113345217 | Sperm competition risk affects ejaculate strategy in terms of sperm number but not sperm size in squid |
Q83930566 | Sperm competition roles and ejaculate investment in a promiscuous mammal |
Q57602454 | Sperm competition selects for increased testes mass in Australian frogs |
Q52692833 | Sperm competition within a dominance hierarchy: investment in social status vs. investment in ejaculates. |
Q47603231 | Sperm competition, but not major histocompatibility divergence, drives differential fertilization success between alternative reproductive tactics in Chinook salmon |
Q93174902 | Sperm competitive advantage of a rare mitochondrial haplogroup linked to differential expression of mitochondrial oxidative phosphorylation genes |
Q92841410 | Sperm head abnormalities are more frequent in songbirds with more helical sperm: A possible trade-off in sperm evolution |
Q56932853 | Sperm is a sexual ornament in rose bitterling |
Q93068923 | Sperm morphology and evidence for sperm competition among parrots |
Q51790797 | Spermicide, cryptic female choice and the evolution of sperm form and function. |
Q35938628 | Spite and the scale of competition |
Q42014666 | Spiteful interactions between sympatric natural isolates of Xenorhabdus bovienii benefit kin and reduce virulence. |
Q112667127 | Split sex ratios and virginity in a gall-inducing thrips |
Q22337214 | Sponge paraphyly and the origin of Metazoa |
Q41627474 | Squamate hatchling size and the evolutionary causes of negative offspring size allometry |
Q51180351 | Stability of floral specialization in Trollius europaeus in contrasting ecological environments. |
Q80454475 | Stabilizing natural selection on the early expression of a secondary sexual trait in a passerine bird |
Q51342367 | Stabilizing sexual selection for female ornaments in a dance fly. |
Q37118784 | Stabilizing survival selection on presenescent expression of a sexual ornament followed by a terminal decline. |
Q36387144 | Stable eusociality via maternal manipulation when resistance is costless. |
Q60563381 | Stable genetic polymorphism in heterogeneous environments: balance between asymmetrical dispersal and selection in the acorn barnacle |
Q81678072 | Stable public goods cooperation and dynamic social interactions in yeast |
Q92693099 | Stage- and thermal-specific genetic architecture for preadult viability in natural populations of Drosophila melanogaster |
Q47191757 | Stalk size and altruism investment within and among populations of the social amoeba |
Q92414291 | Starvation tolerance associated with prolonged sleep bouts upon starvation in a single natural population of Drosophila melanogaster |
Q40656893 | State-dependent cooperation in burying beetles: parents adjust their contribution towards care based on both their own and their partner's size. |
Q40362208 | Static allometry of unicellular green algae: scaling of cellular surface area and volume in the genus Micrasterias (Desmidiales). |
Q112177700 | Status‐dependence and morphological trade‐offs in the expression of a sexually selected character in the mite, Sancassania berlesei |
Q56553456 | Stearns, Stephen C., 1992. The Evolution of Life Histories. Oxford University Press, London xii + 249 pp., f16.95 |
Q51614224 | Strain filtering and transmission of a mixed infection in a social insect. |
Q48693742 | Strategic exploitation of fluctuating asymmetry in male Endler's guppy courtship displays is modulated by social environment |
Q60441198 | Strength, diversity and plasticity of postmating reproductive barriers between two hybridizing oak species (Quercus robur L. and Quercus petraea (Matt) Liebl.) |
Q36201702 | Stress and adaptation in conservation genetics |
Q46824320 | Stress avoidance in a common annual: reproductive timing is important for local adaptation and geographic distribution |
Q58556830 | Strikingly high levels of heterozygosity despite 20 years of inbreeding in a clonal honey bee |
Q46776796 | Strong and parallel salinity-induced phenotypic plasticity in one generation of threespine stickleback |
Q51703560 | Strong artificial selection in the wild results in predicted small evolutionary change. |
Q46636391 | Strong differences in chemical recognition cues between two closely related species of ants from the genus Lasius (Hymenoptera: Formicidae). |
Q39698207 | Strong dominance of functional alleles over gene deletions in both intensely growing and deeply starved yeast cells. |
Q83606699 | Strong effects of heterosis on the evolution of dispersal rates |
Q50478800 | Strong environmental determination of a carotenoid-based plumage trait is not mediated by carotenoid availability. |
Q111289025 | Strong genotype‐by‐genotype interactions between aphid‐defensive symbionts and parasitoids persist across different biotic environments |
Q34984216 | Strong inbreeding depression in male mating behaviour in a poeciliid fish |
Q51790310 | Strong morphological support for the molecular evolutionary tree of placental mammals. |
Q125054483 | Strong phenotypic trait correlations between mating partners do not result from assortative mating in wild great tits (Parus major) |
Q48001407 | Strong premating divergence in a unimodal hybrid zone between two subspecies of the house mouse |
Q46733833 | Strong selection on male plumage in a hybrid zone between a hybrid bird species and one of its parents |
Q39909037 | Strong sexual selection in males against a mutation load that reduces offspring production in seed beetles |
Q52744073 | Strong specificity in the interaction between parasitoids and symbiont-protected hosts. |
Q46254809 | Stronger selective constraint on downstream genes in the oxidative phosphorylation pathway of cetaceans |
Q42453266 | Structure and evolution of the horizontal septum in vertebrates |
Q51150885 | Structure versus time in the evolutionary diversification of avian carotenoid metabolic networks. |
Q52717966 | Studies of the species barrier between Drosophila subobscura and D. madeirensis V: the importance of sex-linked inversion in preserving species identity. |
Q90866689 | Sublethal larval exposure to imidacloprid impacts adult behaviour in Drosophila melanogaster |
Q79321107 | Suboptimal timing of reproduction in Lobelia inflata may be a conservative bet-hedging strategy |
Q51719751 | Substantial changes in the genetic basis of tadpole morphology of Rana lessonae in the presence of predators. |
Q36371762 | Subtle but ubiquitous selection on body size in a natural population of collared flycatchers over 33 years |
Q60370379 | Success and failure of horizontal transfers of feminizing Wolbachia endosymbionts in woodlice |
Q88914149 | Successful despite poor flight performance: range expansion is associated with enhanced exploratory behaviour and fast development |
Q41008474 | Superinfection and the coevolution of parasite virulence and host recovery |
Q50735575 | Supertree analyses of the roles of viviparity and habitat in the evolution of atherinomorph fishes. |
Q40641919 | Survival after pathogen exposure in group-living insects: don't forget the stress of social isolation! |
Q46302424 | Survival benefits select for group living in a social spider despite reproductive costs. |
Q51439773 | Survival costs of reproduction predict age-dependent variation in maternal investment. |
Q83395791 | Survival of the steepest: hypersensitivity to mutations as an adaptation to soft selection |
Q51663135 | Survival selection on escape performance and its underlying phenotypic traits: a case of many-to-one mapping. |
Q111344992 | Survivorship and fecundity of the radiate and non-radiate morphs of Groundsel, Senecio vulgaris L., raised in pure stand and mixture |
Q47412895 | Swift laboratory thermal evolution of wing shape (but not size) in Drosophila subobscura and its relationship with chromosomal inversion polymorphism. |
Q99610711 | Symbiont-mediated fly survival is independent of defensive symbiont genotype in the Drosophila melanogaster-Spiroplasma-wasp interaction |
Q52709452 | Symbiont-mediated phenotypic variation without co-evolution in an insect-fungus association. |
Q35430099 | Symbiotic bacteria enable olive flies (Bactrocera oleae) to exploit intractable sources of nitrogen. |
Q113855138 | Sympatric and allopatric combinations of hen fleas and great tits: a test of the local adaptation hypothesis |
Q35561640 | Sympatric divergence and clinal variation in multiple coloration traits of Ficedula flycatchers |
Q51698901 | Sympatric genetic differentiation of a generalist pathogenic fungus, Botrytis cinerea, on two different host plants, grapevine and bramble. |
Q42032266 | Sympatric host races of the European corn borer: adaptation to host plants and hybrid performance |
Q44958194 | Sympatric shift in a male sexual ornament in the damselfly Calopteryx splendens |
Q51648523 | Synergistic and antagonistic interaction between different branches of the immune system is related to melanin-based coloration in nestling tawny owls. |
Q60575286 | Synergistic epistasis and alternative hypotheses |
Q60542804 | Synergy, partner choice and frequency dependence: their integration into inclusive fitness theory and their interpretation in terms of direct and indirect fitness effects |
Q125484266 | Systematic approaches to assessing high-temperature limits to fertility in animals |
Q46400908 | Tadpole begging reveals high quality. |
Q92287177 | Tail colour signals performance in blue tit nestlings |
Q34312595 | Task specialization in two social spiders, Stegodyphus sarasinorum (Eresidae) and Anelosimus eximius (Theridiidae). |
Q50581789 | Teamwork, pleasure and bargaining in animal social behaviour. |
Q39317760 | Telomere attrition and growth: a life-history framework and case study in common terns. |
Q46710010 | Telomere dynamics in parasitic great spotted cuckoos and their magpie hosts |
Q29304042 | Temnospondyli bite club: ecomorphological patterns of the most diverse group of early tetrapods |
Q49561350 | Temperature and clinal variation in larval growth efficiency in Drosophila melanogaster |
Q91669908 | Temperature coupling of mate attraction signals and female mate preferences in four populations of Enchenopa treehopper (Hemiptera: Membracidae) |
Q126176081 | Temperature dependence of development rate and adult size in Drosophila species: biophysical parameters |
Q34463805 | Temperature dependence of evolutionary diversification: differences between two contrasting model taxa support the metabolic theory of ecology |
Q38912629 | Temperature dependent larval resource allocation shaping adult body size in Drosophila melanogaster |
Q47240696 | Temperature fluctuations during development reduce male fitness and may limit adaptive potential in tropical rainforest Drosophila |
Q33920143 | Temperature niche shift observed in a Lepidoptera population under allochronic divergence |
Q51578738 | Temperature stress increases hybrid incompatibilities in the parasitic wasp genus Nasonia. |
Q41996227 | Temperature- and sex-related effects of serine protease alleles on larval development in the Glanville fritillary butterfly |
Q63976315 | Temperature-dependent costs of parasitism and maintenance of polymorphism under genotype-by-environment interactions |
Q92647586 | Temperature-induced developmental plasticity in Plodia interpunctella: Reproductive behaviour and sperm length |
Q104482637 | Temperature-mediated plasticity in incubation schedules is unlikely to evolve to buffer embryos from climatic challenges in a seasonal songbird |
Q104206903 | Tempo and mode in evolution: phylogenetic inertia, adaptation and comparative methods |
Q47342863 | Tempo, mode and phylogenetic associations of relative embryo size evolution in angiosperms. |
Q48922376 | Temporal change in inbreeding depression in life-history traits in captive populations of guppy (Poecilia reticulata): evidence for purging? |
Q56621829 | Temporal change in mite abundance and its effect on barn swallow reproduction and sexual selection |
Q51728067 | Temporal differentiation and spatial coexistence of sexual and facultative asexual lineages of an aphid species at mating sites. |
Q50775523 | Temporal dynamics of genotypic diversity reveal strong clonal selection in the aphid Myzus persicae. |
Q33845333 | Temporal patterns of diversification in Andean Eois, a species-rich clade of moths (Lepidoptera, Geometridae). |
Q42907682 | Temporal variation in glucocorticoid levels during the resting phase is associated in opposite way with maternal and paternal melanic coloration |
Q45967467 | Temporal variation in the pollen:ovule ratios of Clarkia (Onagraceae) taxa with contrasting mating systems: field populations. |
Q51606158 | Temporal variation of heterozygosity-based assortative mating and related benefits in a lesser kestrel population. |
Q90264541 | Temporally consistent species differences in parasite infection but no evidence for rapid parasite-mediated speciation in Lake Victoria cichlid fish |
Q38982053 | Terminal investment in the gustatory appeal of nuptial food gifts in crickets |
Q91204741 | Terminal investment strategies following infection are dependent on diet |
Q92495247 | Terrestriality constrains salamander limb diversification: Implications for the evolution of pentadactyly |
Q39784789 | Testicular melanization has evolved in birds with high mtDNA mutation rates. |
Q47246374 | Testing Allsop and West's size at sex change invariant within a fish species: a spurious ratio or a useful group descriptor? |
Q51144930 | Testing Wallace's intuition: water type, reproductive isolation, and divergence in an Amazonian fish. |
Q45990377 | Testing alternative mechanisms of evolutionary divergence in an African rain forest passerine bird. |
Q51194753 | Testing alternative models for sexual isolation in natural populations of Littorina saxatilis: indirect support for by-product ecological speciation? |
Q125778425 | Testing drivers of acoustic divergence in cicadas (Cicadidae: Tettigettalna) |
Q46176658 | Testing evolutionary stasis and trends in first lower molar shape of extinct Italian populations of Terricola savii (Arvicolidae, Rodentia) by means of geometric morphometrics. |
Q52844269 | Testing for a genetic response to sexual selection in a wild Drosophila population. |
Q51184608 | Testing for evolutionary trade-offs in a phylogenetic context: ecological diversification and evolution of locomotor performance in emydid turtles. |
Q51617585 | Testing for mating isolation between ecotypes: laboratory experiments with lake, stream and hybrid stickleback. |
Q47412905 | Testing for microevolution in body size in three blue tit populations |
Q35789149 | Testing for parallel allochronic isolation in lake-stream stickleback. |
Q34080074 | Testing gradual and speciational models of evolution in extant taxa: the example of ratites. |
Q42021543 | Testing host-associated differentiation in a quasi-endophage and a parthenogen on native trees. |
Q33675367 | Testing hybridization hypotheses and evaluating the evolutionary potential of hybrids in mangrove plant species |
Q48340501 | Testing hypotheses for maternal effects in Daphnia magna. |
Q40012929 | Testing multiple hypotheses for the maintenance of male homosexual copulatory behaviour in flour beetles |
Q30884709 | Testing paleolimnological predictions with molecular data: the origins of Holarctic Eubosmina |
Q91839456 | Testing sensory drive speciation in cichlid fish: Linking light conditions to opsin expression, opsin genotype and female mate preference |
Q89348573 | Testing the Dutilleul syndrome: host use drives the convergent evolution of multiple traits in parasitic wasps |
Q113855142 | Testing the Red Queen Hypothesis |
Q46858819 | Testing the correlated response hypothesis for the evolution and maintenance of male mating preferences in Drosophila serrata. |
Q41081216 | Testing the cranial evolutionary allometric 'rule' in Galliformes |
Q45398526 | Testing the directionality of evolution: the case of chydorid crustaceans |
Q113855139 | Testing the generation time hypothesis using DNA/DNA hybridization between artiodactyls |
Q43034406 | Testing the interactive effects of testosterone and parasites on carotenoid-based ornamentation in a wild bird |
Q31028229 | Testing the link between the latitudinal gradient in species richness and rates of molecular evolution |
Q82525506 | Testing the molecular and evolutionary causes of a ‘leapfrog’ pattern of geographical variation in coloration |
Q48144140 | Testing the phenotype-linked fertility hypothesis in the presence and absence of inbreeding |
Q42612421 | Testing the phenotypic gambit: phenotypic, genetic and environmental correlations of colour |
Q80118023 | Testing the pluralist approach to sex: the influence of environment on synergistic interactions between mutation load and parasitism in Daphnia magna |
Q51583916 | Testing the role of phenotypic plasticity for local adaptation: growth and development in time-constrained Rana temporaria populations. |
Q80960948 | Testing the status-dependent ESS model: population variation in fighter expression in the mite Sancassania berlesei |
Q39232696 | Testosterone production ability predicts breeding success and tracks breeding stage in male finches. |
Q44585446 | Testosterone, growth and the evolution of sexual size dimorphism |
Q111375235 | Tests of sib diversification theories of outcrossing in Impatiens capensis: Effects of inbreeding and neighbour relatedness on production and infestation |
Q129669777 | The Clade Replacement Theory: a framework to study age-dependent extinction |
Q47929384 | The Drosophila simulans Y chromosome interacts with the autosomes to influence male fitness. |
Q104466214 | The Evolution of Age-specific Choosiness when Mating |
Q42662894 | The Isthmus of Panama: a major physical barrier to gene flow in a highly mobile pantropical seabird |
Q51835531 | The Price equation framework to study disease within-host evolution. |
Q50551668 | The Red Queen theory of recombination hotspots. |
Q51673562 | The accumulation of deleterious mutations within the frozen niche variation hypothesis. |
Q46617085 | The accumulation of reproductive isolation in early stages of divergence supports a role for sexual selection |
Q40197546 | The achaete-scute complex in Diptera: patterns of noncoding sequence evolution |
Q39661102 | The adaptive significance of mandibular symphyseal fusion in mammals |
Q90141898 | The adaptive value of epigenetic mutation: Limited in large but high in small peripheral populations |
Q51542391 | The adaptive value of gluttony: predators mediate the life history trade-offs of satiation threshold. |
Q47182748 | The allometric pattern of sexually size dimorphic feather ornaments and factors affecting allometry. |
Q34447328 | The anther smut disease on Gypsophila repens: a case of parasite sub-optimal performance following a recent host shift? |
Q116847819 | The association between personalities, alternative breeding strategies and reproductive success in dunnocks |
Q46664006 | The association between the emergence of cooperative breeding and clutch size |
Q40473689 | The association of feeding behaviour with the resistance and tolerance to parasites in recently diverged sticklebacks. |
Q29026847 | The basic body plan of arthropods: insights from evolutionary morphology and developmental biology |
Q48617591 | The benefits of interpopulation hybridization diminish with increasing divergence of small populations. |
Q51672621 | The benefits of male ejaculate sex peptide transfer in Drosophila melanogaster. |
Q81670541 | The benefits of polyandry in the free-spawning polychaete Galeolaria caespitosa |
Q36201724 | The biological limitations of transcriptomics in elucidating stress and stress responses |
Q51715485 | The biology of multivariate evolution. |
Q35682479 | The burgeoning field of statistical phylogeography |
Q47300704 | The causes and consequences of variation in offspring size: a case study using Daphnia |
Q80960894 | The close relationship between estimated divergent selection and observed differentiation supports the selective origin of a marine snail hybrid zone |
Q45384851 | The coevolution of long-term pair bonds and cooperation |
Q46475409 | The colour of paternity: extra-pair paternity in the wild Gouldian finch does not appear to be driven by genetic incompatibility between morphs |
Q90323197 | The combined effect of host and food availability on optimized parasitoid life-history traits based on a three-dimensional trade-off surface |
Q40429938 | The combined effects of pre- and post-copulatory processes are masking sexual conflict over mating rate in Gerris buenoi |
Q48172448 | The combined effects of temporal autocorrelation and the costs of plasticity on the evolution of plasticity. |
Q58890600 | The common cuckoo Cuculus canorus is not locally adapted to its reed warbler Acrocephalus scirpaceus host |
Q33668053 | The common patterns of nature. |
Q44630325 | The comparative biology of diving in two genera of European Dytiscidae (Coleoptera). |
Q101631257 | The comparative evolution of lizard claw and toe morphology and clinging performance |
Q47906072 | The complex interplay between macronutrient intake, cuticular hydrocarbon expression and mating success in male decorated crickets |
Q46472951 | The consequences of facultative sex in a prey adapting to predation |
Q34375366 | The consequences of lifetime and evolutionary exposure to toxic prey: changes in avoidance behaviour through ontogeny |
Q51583888 | The consequences of mating over a range of parental genetic similarity in a selfing allopolyploid plant species. |
Q33751650 | The consequences of phenotypic plasticity for ecological speciation. |
Q36536774 | The constant philopater hypothesis: a new life history invariant for dispersal evolution |
Q31105586 | The context dependence of assortative mating: a demonstration with conspecific salmonid populations |
Q112810465 | The continuity of microevolution and macroevolution |
Q42014940 | The contribution of a pollinating seed predator to selection on Silene latifolia females. |
Q51687279 | The contribution of parasitism to selection on floral traits in Heuchera grossulariifolia. |
Q50440744 | The contribution of structural-, psittacofulvin- and melanin-based colouration to sexual dichromatism in Australasian parrots |
Q110616045 | The contributions of programmed developmental change and phenotypic plasticity to within-individual variation in leaf traits in Dicerandra linearifolia |
Q46545196 | The copulatory plug delays ejaculation by rival males and affects sperm competition outcome in house mice |
Q47424941 | The correlation between coloration and exploration behaviour varies across hierarchical levels in a wild passerine bird. |
Q90694735 | The cost and benefit of quorum sensing-controlled bacteriocin production in Lactobacillus plantarum |
Q48247100 | The cost of conflict in aphid societies. |
Q39550085 | The cost of copy number in a selfish genetic element: the 2-μm plasmid of Saccharomyces cerevisiae. |
Q40529349 | The cost of immunity in the yellow fever mosquito, Aedes aegypti depends on immune activation |
Q45950194 | The cost of mating rises nonlinearly with copulation frequency in a laboratory population of Drosophila melanogaster. |
Q51760149 | The cost of multiple drug resistance in Pseudomonas aeruginosa. |
Q104466112 | The cost of travel: how dispersal ability limits local adaptation in host-parasite interactions |
Q60407053 | The costs and benefits in an unusual symbiosis: experimental evidence that bitterling fish (Rhodeus sericeus) are parasites of unionid mussels in Europe |
Q114621930 | The costs and benefits of larger brains in fishes |
Q58034964 | The costs and benefits of resource sharing: reciprocity requires resource heterogeneity |
Q44369624 | The costs of being dark: the genetic basis of melanism and its association with fitness-related traits in the sand cricket |
Q39580176 | The costs of parental care: a meta-analysis of the trade-off between parental effort and survival in birds |
Q51620497 | The danger of applying the breeder's equation in observational studies of natural populations. |
Q79515717 | The dangers of diagonalization |
Q48067596 | The decline in fitness with inbreeding: evidence for negative dominance-by-dominance epistasis in Drosophila melanogaster |
Q35137906 | The decoupling between genetic structure and metabolic phenotypes in Escherichia coli leads to continuous phenotypic diversity |
Q51706675 | The degree of adaptive phenotypic plasticity is correlated with the spatial environmental heterogeneity experienced by island populations of Rana temporaria. |
Q40279212 | The design of complex sexual traits in male barn swallows: associations between signal attributes |
Q47175247 | The determinants of queen size in a socially polymorphic ant. |
Q39190511 | The determinants of the molecular substitution process in turtles |
Q42021073 | The diapause decision as a cascade switch for adaptive developmental plasticity in body mass in a butterfly |
Q92530791 | The dicey dinner dilemma: Asymmetry in predator-prey risk-taking, a broadly applicable alternative to the life-dinner principle |
Q43766628 | The differential contributions of herkogamy and dichogamy as mechanisms of avoiding self-interference in four self-incompatible Epimedium species |
Q52758163 | The direct effects of male killer infection on fitness of ladybird hosts (Coleoptera: Coccinellidae). |
Q30558145 | The disparity of priapulid, archaeopriapulid and palaeoscolecid worms in the light of new data. |
Q29399389 | The dissimilar costs of love and war: age-specific mortality as a function of the operational sex ratio |
Q57671657 | The distribution of copia-type retrotransposons and the evolutionary history of tomato and related wild species |
Q47610001 | The divergence history of the perennial plant Linaria cavanillesii confirms a recent loss of self-incompatibility. |
Q35664966 | The diversification of Heliconius butterflies: what have we learned in 150 years? |
Q43870826 | The diversification of mate preferences by natural and sexual selection |
Q33665255 | The diversity and radiation of the largest monophyletic animal group on New Caledonia (Trichoptera: Ecnomidae: Agmina). |
Q51534979 | The dual function of barred plumage in birds: camouflage and communication. |
Q45885833 | The dynamics of sexual conflict over mating rate with endosymbiont infection that affects reproductive phenotypes |
Q50518477 | The ecological advantage of sexual reproduction in multicellular long-lived organisms. |
Q42687517 | The ecological benefits of larger colony size may promote polygyny in ants. |
Q40615384 | The ecological success of a social parasite increases with manipulation of collective host behaviour. |
Q33831372 | The ecology of sexual reproduction |
Q51935154 | The economics of altruism and cooperation in class-structured populations: what's in a cost? What's in a benefit? |
Q45883104 | The effect of Wolbachia on the lifetime reproductive success of its insect host in the field |
Q43887257 | The effect of a population bottleneck on the evolution of genetic variance/covariance structure |
Q56888629 | The effect of cheats on siderophore diversity in Pseudomonas aeruginosa |
Q51820794 | The effect of coil phenotypes and genotypes on the fecundity and viability of Partula suturalis and Lymnaea stagnalis: implications for the evolution of sinistral snails. |
Q51830630 | The effect of female polyandry and sperm precedence on the evolution of sexual difference in dispersal timing. |
Q40494766 | The effect of frequency-dependent selection on resistance and tolerance to herbivory. |
Q45803136 | The effect of habitat on modern shark diversification |
Q51356352 | The effect of historical legacy on adaptation: do closely related species respond to the environment in the same way? |
Q46833089 | The effect of hybrid transgression on environmental tolerance in experimental yeast crosses. |
Q48946652 | The effect of inbreeding on defence against multiple enemies in Datura stramonium. |
Q43483672 | The effect of inbreeding on natural selection in a seed-feeding beetle |
Q60307322 | The effect of life cycle stage and genotype on desiccation tolerance in the colonizing parthenogenetic cockroach Pycnoscelus surinamensis and its sexual ancestor P. indicus |
Q46903418 | The effect of maternal and paternal immune challenge on offspring immunity and reproduction in a cricket. |
Q51614198 | The effect of mating system on growth of Arabidopsis lyrata in response to inoculation with the biotrophic parasite Albugo candida |
Q45231971 | The effect of parity on morphological evolution among phrynosomatid lizards |
Q51652142 | The effect of pathogens on selection against deleterious mutations in Drosophila melanogaster. |
Q34557604 | The effect of phenotypic plasticity on evolution in multipeaked fitness landscapes |
Q33763823 | The effect of population bottlenecks on mutation rate evolution in asexual populations |
Q48108856 | The effect of selection history on extinction risk during severe environmental change. |
Q37822889 | The effect of sex on the mean and variance of fitness in facultatively sexual rotifers |
Q36671416 | The effect of size and sex ratio experiences on reproductive competition in Nicrophorus vespilloides burying beetles in the wild |
Q36542289 | The effect of spontaneous mutations on competitive ability |
Q52653094 | The effect of temperature and wing morphology on quantitative genetic variation in the cricket Gryllus firmus, with an appendix examining the statistical properties of the Jackknife-MANOVA method of matrix comparison. |
Q51549275 | The effects of competition on the strength and softness of selection. |
Q47424056 | The effects of familiarity and group size on mating preferences in the guppy, Poecilia reticulata. |
Q92513976 | The effects of heterospecific mating frequency on the strength of cryptic reproductive barriers |
Q92002445 | The effects of male social environment on sperm phenotype and genome integrity |
Q51370436 | The effects of migration and drift on local adaptation to a heterogeneous environment. |
Q52007554 | The effects of parasitism and inbreeding on the competitive ability in Daphnia magna: evidence for synergistic epistasis. |
Q40241703 | The effects of reproduction on courtship, fertility and longevity within and between alternative male mating tactics of the horned beetle, Onthophagus binodis |
Q46947029 | The effects of sexual selection on life-history traits: an experimental study on guppies. |
Q36356830 | The effects of stochastic and episodic movement of the optimum on the evolution of the G-matrix and the response of the trait mean to selection. |
Q38649465 | The effects of stress and sex on selection, genetic covariance, and the evolutionary response. |
Q52698678 | The efficiency of purifying selection in Mammals vs. Drosophila for metabolic genes. |
Q47367833 | The emergence of cetaceans: phylogenetic analysis of male social behaviour supports the Cetartiodactyla clade |
Q41045621 | The epidemiological feedbacks critical to the evolution of host immunity |
Q130127526 | The evolution and ecology of multiple antipredator defences |
Q37675071 | The evolution from females to hermaphrodites results in a sexual conflict over mating in androdioecious nematode worms and clam shrimp |
Q34087474 | The evolution of South American endemic canids: a history of rapid diversification and morphological parallelism. |
Q36366605 | The evolution of a complex trait: cuticular hydrocarbons in ants evolve independent from phylogenetic constraints. |
Q42013116 | The evolution of alternative developmental pathways: footprints of selection on life-history traits in a butterfly |
Q34500593 | The evolution of aquatic feeding in seals: insights from Enaliarctos (Carnivora: Pinnipedimorpha), the oldest known seal |
Q35902191 | The evolution of colour pattern complexity: selection for conspicuousness favours contrasting within-body colour combinations in lizards. |
Q88628151 | The evolution of colour polymorphism in British winter-active Lepidoptera in response to search image use by avian predators |
Q51755230 | The evolution of conspecific gamete precedence and its effect on reinforcement. |
Q123137063 | The evolution of conspicuousness in frogs: When to signal toxicity? |
Q36566579 | The evolution of cooperation and altruism--a general framework and a classification of models |
Q52671456 | The evolution of cooperation and altruism: the basic conditions are simple and well known. |
Q50107399 | The evolution of cooperation by negotiation in a noisy world. |
Q34082075 | The evolution of cranial form and function in theropod dinosaurs: insights from geometric morphometrics |
Q113855136 | The evolution of demographic tactics in lizards: a test of some hypotheses concerning life history evolution |
Q45886035 | The evolution of endosymbiont density in doubly infected host species |
Q51324055 | The evolution of experience-mediated plasticity in mate preferences. |
Q46698382 | The evolution of fecundity is associated with female body size but not female-biased sexual size dimorphism among frogs |
Q91569796 | The evolution of female genitalia |
Q40369506 | The evolution of fledging age in songbirds |
Q113270349 | The evolution of flower longevity in unpredictable pollination environments |
Q113036739 | The evolution of food-producing glands in eusocial bees (Apoidea, Hymenoptera)1 |
Q52655373 | The evolution of generalization? Parasitoid flies and the perils of inferring host range evolution from phylogenies. |
Q51645287 | The evolution of haplodiploidy by male-killing endosymbionts: importance of population structure and endosymbiont mutualisms. |
Q51902473 | The evolution of helping and harming on graphs: the return of the inclusive fitness effect. |
Q52667604 | The evolution of host preference in allopatric vs. parapatric populations of Timema cristinae walking-sticks. |
Q42040306 | The evolution of host use and unusual reproductive strategies in Achrysocharoides parasitoid wasps. |
Q84437869 | The evolution of host-specific variation in cuckoo eggshell strength |
Q123345879 | The evolution of infertility: does hatching rate in birds coevolve with female polyandry? |
Q46694677 | The evolution of inquilinism, host-plant use and mitochondrial substitution rates in Tamalia gall aphids |
Q39177117 | The evolution of intrinsic reproductive isolation in the genus Cakile (Brassicaceae). |
Q33861819 | The evolution of jumping performance in anurans: morphological correlates and ecological implications |
Q45844240 | The evolution of male genitalia: patterns of genetic variation and covariation in the genital sclerites of the dung beetle Onthophagus taurus |
Q30626626 | The evolution of mammal body sizes: responses to Cenozoic climate change in North American mammals. |
Q37799858 | The evolution of mutualism |
Q89839746 | The evolution of parasite host range in heterogeneous host populations |
Q51609156 | The evolution of parental care in stochastic environments. |
Q53851380 | The evolution of phenotypic plasticity in spatially structured environments: implications of intraspecific competition, plasticity costs and environmental characteristics. |
Q44803926 | The evolution of plumage polymorphism in birds of prey and owls: the apostatic selection hypothesis revisited |
Q113855134 | The evolution of polyandry: an examination of the genetic incompatibility and good-sperm hypotheses |
Q52659276 | The evolution of polyandry: intrinsic sire effects contribute to embryo viability. |
Q52641724 | The evolution of polyandry: patterns of genotypic variation in female mating frequency, male fertilization success and a test of the sexy-sperm hypothesis. |
Q37772564 | The evolution of polyembryony in parasitoid wasps. |
Q45851082 | The evolution of queen pheromones in the ant genus Lasius |
Q113105971 | The evolution of red blood cell shape in fishes |
Q40451409 | The evolution of repeated mating under sexual conflict. |
Q34459152 | The evolution of reproductive isolation in the Drosophila yakuba complex of species |
Q42249723 | The evolution of resistance against good and bad infections. |
Q38425024 | The evolution of respect for property |
Q44057266 | The evolution of self-fertilization and inbreeding depression under pollen discounting and pollen limitation |
Q38203949 | The evolution of selfing from outcrossing ancestors in Brassicaceae: what have we learned from variation at the S-locus? |
Q83775791 | The evolution of senescence through decelerating selection for system reliability |
Q40012922 | The evolution of sex-determining mechanisms: lessons from temperature-sensitive mutations in sex determination genes in Caenorhabditis elegans |
Q98157062 | The evolution of sexually dimorphic cuticular hydrocarbons in blowflies (Diptera: Calliphoridae) |
Q47297239 | The evolution of size of the uropygial gland: mutualistic feather mites and uropygial secretion reduce bacterial loads of eggshells and hatching failures of European birds. |
Q51755226 | The evolution of sperm morphometry in pheasants. |
Q38735320 | The evolution of strategic male mating effort in an information transfer framework. |
Q113791770 | The evolution of the additive variance of a trait under stabilizing selection after autopolyploidization |
Q46947200 | The evolution of the phenotypic covariance matrix: evidence for selection and drift in Melanoplus |
Q61603638 | The evolution of the reptilian hindfoot and the homology of the hooked fifth metatarsal |
Q45934304 | The evolution of trade-offs: geographic variation in call duration and flight ability in the sand cricket, Gryllus firmus. |
Q36738147 | The evolution of trade-offs: where are we? |
Q40253454 | The evolution of trans-generational altruism: kin selection meets niche construction |
Q56774623 | The evolution of unusual chromosomal systems in coccoids: extraordinary sex ratios revisited |
Q33514913 | The evolutionary consequence of the individualistic response to climate change |
Q56619215 | The evolutionary dynamics of evolvability in a gene network model |
Q39051776 | The evolutionary dynamics of timing of maternal immunity: evaluating the role of age-specific mortality. |
Q34623676 | The evolutionary ecology of individual phenotypic plasticity in wild populations |
Q79787813 | The evolutionary fate of recently duplicated retrogenes in mice |
Q57912706 | The evolutionary forces maintaining a wild polymorphism of Littorina saxatilis: model selection by computer simulations |
Q39488553 | The evolutionary genetics of egg size plasticity in a butterfly. |
Q57006783 | The evolutionary history of Drosophila buzzatii. XVI. Fitness component analysis in an original natural population from Argentina |
Q60576954 | The evolutionary history of Drosophila buzzatii. XX. Positive phenotypic covariance between field adult fitness components and body size |
Q57006762 | The evolutionary history of Drosophila buzzatti. XXVI. Macrogeographic patterns of inversion polymorphism in New World populations |
Q58387378 | The evolutionary history of colour polymorphism in Ischnura damselflies |
Q57317207 | The evolutionary history of the common chloroplast genome of Arabidopsis thaliana and A. suecica |
Q91699645 | The evolutionary response of mating system to heterosis |
Q87845555 | The evolutionary stability of attenuators that mask information about animals that social partners can exploit |
Q51552931 | The experimental evolution of herbicide resistance in Chlamydomonas reinhardtii results in a positive correlation between fitness in the presence and absence of herbicides. |
Q34163530 | The expression and impact of antifungal grooming in ants. |
Q34177316 | The expression of virulence during double infections by different parasites with conflicting host exploitation and transmission strategies |
Q52680781 | The extent of variation in male song, wing and genital characters among allopatric Drosophila montana populations. |
Q53056987 | The fate of balanced, phenotypic polymorphisms in fragmented metapopulations. |
Q51940367 | The fitness costs of developmental canalization and plasticity. |
Q35831322 | The fitness of drug-resistant malaria parasites in a rodent model: multiplicity of infection |
Q58299458 | The fitness of twin mothers: evidence from rural Gambia |
Q51354272 | The form of sexual selection arising from male-male competition depends on the presence of females in the social environment. |
Q36855872 | The formal Darwinism project: a mid-term report. |
Q35163117 | The founding of Mauritian endemic coffee trees by a synchronous long-distance dispersal event. |
Q47214742 | The frequency of multiple paternity predicts variation in testes size among island populations of house mice |
Q39544608 | The function and evolution of male and female genitalia in Phyllophaga Harris scarab beetles (Coleoptera: Scarabaeidae). |
Q46880219 | The function of multiple ejaculations in bitterling. |
Q40392576 | The future of a mutation-limited tool-box |
Q84258956 | The genetic and environmental basis of adaptive differences in shoaling behaviour among populations of Trinidadian guppies, Poecilia reticulata |
Q51709756 | The genetic architecture of a niche: variation and covariation in host use traits in the Colorado potato beetle. |
Q46728642 | The genetic architecture of male colour differences between a sympatric Lake Malawi cichlid species pair. |
Q51530193 | The genetic architecture of sexual conflict: male harm and female resistance in Callosobruchus maculatus. |
Q39901529 | The genetic basis of early-life morphological traits and their relation to alternative male reproductive tactics in Atlantic salmon |
Q47293455 | The genetic basis of intrinsic and extrinsic post-zygotic reproductive isolation jointly promoting speciation in the lake whitefish species complex (Coregonus clupeaformis). |
Q33410636 | The genetic consequences of fluctuating inbreeding depression and the evolution of plant selfing rates |
Q51174188 | The genetic structure of Borrelia afzelii varies with geographic but not ecological sampling scale. |
Q51145559 | The genetic variance but not the genetic co-variance of life history traits changes towards the north in a time-constrained insect. |
Q53435549 | The genetical theory of kin selection. |
Q35556980 | The genetical theory of multilevel selection. |
Q48140273 | The genetics of adaptation to discrete heterogeneous environments: frequent mutation or large-effect alleles can allow range expansion. |
Q110616033 | The genetics of phenotypic plasticity I. Heritability |
Q110616034 | The genetics of phenotypic plasticity I. Heritability |
Q110616036 | The genetics of phenotypic plasticity. II. Response to selection |
Q110616037 | The genetics of phenotypic plasticity. III. Genetic correlations and fluctuating asymmetries |
Q110616039 | The genetics of phenotypic plasticity. IV. Chromosomal localization |
Q59411548 | The genetics of phenotypic plasticity. V. Evolution of reaction norm shape |
Q110616042 | The genetics of phenotypic plasticity. VI. Theoretical predictions for directional selection |
Q110615417 | The genetics of phenotypic plasticity. VII. Evolution in a spatially-structured environment |
Q110616048 | The genetics of phenotypic plasticity. VII. Evolution in a spatially-structured environment |
Q44830578 | The genetics of primary and secondary sexual character trade-offs in a horned beetle. |
Q44999779 | The genetics of speciation: are complex incompatibilities easier to evolve? |
Q52716574 | The genetics of speciation: genes of small effect underlie sexual isolation in the Hawaiian cricket Laupala. |
Q56636796 | The genic view of the process of speciation |
Q46662790 | The genomic bases of morphological divergence and reproductive isolation driven by ecological speciation in Senecio (Asteraceae). |
Q97558710 | The genomic view of diversification |
Q51956113 | The geographic mosaic in predispersal interactions and selection on Helleborus foetidus (Ranunculaceae). |
Q50774589 | The geographic selection mosaic for squirrels, crossbills and Aleppo pine. |
Q45880958 | The global impact of Wolbachia on mitochondrial diversity and evolution. |
Q37650867 | The group selection controversy |
Q80404275 | The heritability of inducible defenses in tadpoles |
Q85480937 | The heritable basis and cost of colour plasticity in coastrange sculpins |
Q34191585 | The high-throughput yeast deletion fitness data and the theories of dominance |
Q45883095 | The impact of Wolbachia, male age and mating history on cytoplasmic incompatibility and sperm transfer in Drosophila simulans. |
Q46502319 | The impact of digging on craniodental morphology and integration. |
Q41012991 | The impact of high-order epistasis in the within-host fitness of a positive-sense plant RNA virus |
Q48275451 | The impact of high-throughput sequencing technology on speciation research: maintaining perspective |
Q51581740 | The impact of intraspecific variation in a fish predator on the evolution of phenotypic plasticity and investment in sex in Daphnia ambigua. |
Q58493827 | The impact of parasite dispersal on antagonistic host-parasite coevolution |
Q36139563 | The impact of rate heterogeneity on inference of phylogenetic models of trait evolution. |
Q51514997 | The impact of reproductive investment and early-life environmental conditions on senescence: support for the disposable soma hypothesis. |
Q52687718 | The impact of shared ancestral variation on hybrid male lethality--a 16 codon indel in the Drosophila simulans Lhr gene. |
Q43939397 | The impact of uniform and mixed species blood meals on the fitness of the mosquito vector Anopheles gambiae s.s: does a specialist pay for diversifying its host species diet? |
Q35835362 | The impacts of Wolbachia and the microbiome on mate choice in Drosophila melanogaster |
Q41208615 | The importance (or lack thereof) of niche divergence to the maintenance of a northern species complex: the case of the long-toed salamander (Ambystoma macrodactylum Baird). |
Q40279221 | The importance of growth and mortality costs in the evolution of the optimal life history |
Q39765039 | The importance of listening: juvenile allocation shifts in response to acoustic cues of the social environment. |
Q60557414 | The importance of phylogenetic scale in tests of Bergmann's and Rapoport's rules: lessons from a clade of South American lizards |
Q63379977 | The importance of social dimension and maturation stage for the probabilistic maturation reaction norm inPoecilia reticulata |
Q41362960 | The inbreeding strategy of a solitary primate, Microcebus murinus |
Q52586951 | The influence of developmental environment on courtship song in cactophilic Drosophila. |
Q46894747 | The influence of developmental environment on the evolution of olfactory foraging behaviour in procellariiform seabirds |
Q33449296 | The influence of environmental factors, the pollen : ovule ratio and seed bank persistence on molecular evolutionary rates in plants |
Q46814767 | The influence of feeding on the evolution of sensory signals: a comparative test of an evolutionary trade-off between masticatory and sensory functions of skulls in southern African horseshoe bats (Rhinolophidae). |
Q46394802 | The influence of geographic heterogeneity in predation pressure on sexual signal divergence in an Amazonian frog species complex |
Q38989162 | The influence of growth patterns on sexual size monomorphism in lemurs |
Q96163027 | The influence of immune activation on thermal tolerance along a latitudinal cline |
Q46650211 | The influence of landscape configuration and environment on population genetic structure in a sedentary passerine: insights from loci located in different genomic regions. |
Q40429196 | The influence of mating system on the intensity of parent-offspring conflict in primates |
Q46942339 | The influence of social structure on brood survival and development in a socially polymorphic ant: insights from a cross-fostering experiment |
Q40000176 | The influence of space and time on the evolution of altruistic defence: the case of ant slave rebellion. |
Q45729925 | The influence of territoriality and mating system on the evolution of male care: a phylogenetic study on fish |
Q112810468 | The influence of variation and of developmental constraints on the rate of multivariate phenotypic evolution |
Q50746746 | The interaction between reproductive lifespan and protandry in seasonal breeders. |
Q51647564 | The interaction of multiple environmental stressors affects adaptation to a novel habitat in the natterjack toad Bufo calamita. |
Q60394130 | The interplay between colonization history and gene flow in passively dispersing zooplankton: microsatellite analysis of rotifer resting egg banks |
Q60232176 | The invading parthenogenetic cockroach: a natural history comment on Parker and Niklasson's study |
Q34786010 | The joint effects of kin, multilevel selection and indirect genetic effects on response to genetic selection |
Q90179295 | The joint evolution of lifespan and self-fertilization |
Q45118908 | The joint evolution of mating system, floral traits and life history in Clarkia (Onagraceae): genetic constraints vs. independent evolution |
Q50789436 | The learning advantage: bird species that learn their song show a tighter adjustment of song to noisy environments than those that do not learn. |
Q47426408 | The life history legacy of evolutionary body size change in carnivores |
Q51543204 | The lifetime costs of increased male reproductive effort: courtship, copulation and the Coolidge effect. |
Q81145549 | The limitations of adaptive dynamics as a model of evolution |
Q38383902 | The locus of sexual selection: moving sexual selection studies into the post-genomics era. |
Q51564703 | The long and the short of sperm selection in vitro and in vivo: swim-up techniques select for the longer and faster swimming mammalian sperm. |
Q96585390 | The loss of self-incompatibility in a range expansion |
Q50598049 | The maintenance of sex: host-parasite coevolution with density-dependent virulence. |
Q46467018 | The masculinity paradox: facial masculinity and beardedness interact to determine women's ratings of men's facial attractiveness |
Q90354388 | The microevolutionary response to male-limited X-chromosome evolution in Drosophila melanogaster reflects macroevolutionary patterns |
Q37678587 | The mismeasurement of sexual selection |
Q39502522 | The mode of evolution of aggregation pheromones in Drosophila species. |
Q61662320 | The molecular basis of dominance relationships: the case of some recent adaptive genes |
Q34683982 | The molecular basis of white pericarps in African domesticated rice: novel mutations at the Rc gene |
Q56986178 | The need for archiving data in evolutionary biology |
Q44634950 | The normal distribution as appropriate model of developmental instability in Opuntia cacti flowers |
Q54352667 | The onion model, a simple neutral model for the evolution of diversity in bacterial biofilms. |
Q60728703 | The ontogenetic complexity of developmental constraints |
Q60490420 | The ontogeny of cross-sex genetic correlations: an analysis of patterns |
Q39205054 | The opportunity for sexual selection: not mismeasured, just misunderstood. |
Q47572103 | The opportunity to be misled in studies of sexual selection. |
Q80511439 | The origin and colonization history of the barley scald pathogen Rhynchosporium secalis |
Q33247048 | The origin and early radiation of the therapsid mammal-like reptiles: a palaeobiological hypothesis |
Q33199144 | The origin of a 'true' worker caste in termites: mapping the real world on the phylogenetic tree |
Q60232149 | The origin of a ‘true’ worker caste in termites: phylogenetic evidence is not decisive |
Q56506392 | The origin of interlocus sexual conflict: is sex-linkage important? |
Q52676930 | The origin of the Chorthippus parallelus hybrid zone: chromosomal evidence of multiple refugia for Iberian populations. |
Q51713120 | The origins of ecotypic variation of rainbow trout: a test of environmental vs. genetically based differences in morphology. |
Q83364546 | The outcome of sperm competition is affected by behavioural and anatomical reproductive traits in a simultaneously hermaphroditic land snail |
Q46422213 | The oxidation handicap hypothesis and the carotenoid allocation trade-off. |
Q39124333 | The oxidative costs of territory quality and offspring provisioning. |
Q92693044 | The paradox of obligate sex: The roles of sexual conflict and mate scarcity in transitions to facultative and obligate asexuality |
Q37060487 | The past and future influence of geographic information systems on hybrid zone, phylogeographic and speciation research |
Q51283380 | The pay-offs of maternal care increase as offspring develop, favouring extended provisioning in an egg-feeding frog. |
Q113791762 | The phenomenon of red and yellow autumn leaves: Hypotheses, agreements and disagreements |
Q34678637 | The plastic fly: the effect of sustained fluctuations in adult food supply on life-history traits. |
Q30401959 | The potential influence of morphology on the evolutionary divergence of an acoustic signal. |
Q46528972 | The precision of the hominid timescale estimated by relaxed clock methods |
Q34171784 | The primary feather lengths of early birds with respect to avian wing shape evolution |
Q39227439 | The probability of parallel genetic evolution from standing genetic variation |
Q52708101 | The purge of genetic load through restricted panmixia in a Drosophila experiment. |
Q51559934 | The quantitative genetic basis of adaptive divergence in the moor frog (Rana arvalis) and its implications for gene flow. |
Q34511426 | The quantitative genetic basis of sex ratio variation in Nasonia vitripennis: a QTL study |
Q30855674 | The quantitative genetics of sexually selected traits, preferred traits and preference: a review and analysis of the data |
Q40062779 | The rate of environmental change drives adaptation to an antibiotic sink |
Q34154985 | The red queen coupled with directional selection favours the evolution of sex. |
Q121660158 | The redlegged earth mite draft genome provides new insights into pesticide resistance evolution and demography in its invasive Australian range |
Q53847225 | The relationship between morphology, escape behaviour and microhabitat occupation in the lizard clade Liolaemus (Iguanidae: Tropidurinae: Liolaemini). |
Q44040402 | The relationship between multiple mating by queens, within-colony genetic variability and fitness in the ant Lasius niger |
Q33995045 | The relative contribution of band number to phylogenetic accuracy in AFLP data sets. |
Q44986078 | The relative contribution of drift and selection to transcriptional divergence among Babine Lake tributary populations of juvenile rainbow trout |
Q51545470 | The relative importance of genetic and nongenetic inheritance in relation to trait plasticity in Callosobruchus maculatus. |
Q50467813 | The relative role of male vs. female mate choice in maintaining assortative pairing among discrete colour morphs. |
Q36555274 | The repeatability of mating failure in a polyandrous bug |
Q51416626 | The robustness of the weak selection approximation for the evolution of altruism against strong selection. |
Q46419218 | The role of Bh4 in parallel evolution of hull colour in domesticated and weedy rice |
Q103008078 | The role of balancing selection in maintaining human RhD blood group polymorphism: A preregistered cross-sectional study |
Q91203808 | The role of common ancestry and gene flow in the evolution of human-directed play behaviour in dogs |
Q39703562 | The role of environment and core-margin effects on range-wide phenotypic variation in a montane grasshopper. |
Q51144922 | The role of epistatic interactions underpinning resistance to parasitic Varroa mites in haploid honeybee drones. |
Q30676347 | The role of founder effects on the evolution of reproductive isolation |
Q93095606 | The role of functional constraints in nonrandom mating patterns for a dance fly with female ornaments |
Q52739130 | The role of gene flow asymmetry along an environmental gradient in constraining local adaptation and range expansion. |
Q85331570 | The role of genetic structure in the adaptive divergence of populations experiencing saltwater intrusion due to relative sea-level rise |
Q37781099 | The role of genotype‐by‐environment interactions in sexual selection |
Q39372526 | The role of historical factors and natural selection in the evolution of breeding systems of Oxalis alpina in the Sonoran desert 'Sky Islands'. |
Q44495710 | The role of immigration and local adaptation on fine-scale genotypic and phenotypic population divergence in a less mobile passerine |
Q44543598 | The role of learning by a predator, Rivulus hartii, in the rare-morph survival advantage in guppies |
Q39421193 | The role of local ecology during hybridization at the initial stages of ecological speciation in a marine snail. |
Q50682179 | The role of marker traits in the assortative mating within red crossbills, Loxia curvirostra complex. |
Q34013272 | The role of mobility for the emergence of diversity in victim-exploiter systems. |
Q33531904 | The role of phenotypic plasticity in responses of hunted thinhorn sheep ram horn growth to changing climate conditions |
Q35065043 | The role of phylogeny and ecology in shaping morphology in 21 genera and 127 species of Australo-Papuan myobatrachid frogs |
Q50270642 | The role of physiology in the divergence of two incipient cichlid species. |
Q51583906 | The role of post-natal ontogeny in the evolution of phenotypic diversity in Podarcis lizards. |
Q38726566 | The role of recombination in evolutionary adaptation of Escherichia coli to a novel nutrient |
Q35896748 | The role of selection and historical factors in driving population differentiation along an elevational gradient in an island bird |
Q30841449 | The role of sex chromosomes in sexual dimorphism: discordance between molecular and phenotypic data |
Q42011959 | The roles of ecological fitting, phylogeny and physiological equivalence in understanding realized and fundamental host ranges in endoparasitoid wasps. |
Q34666366 | The roles of geography and founder effects in promoting host-associated differentiation in the generalist bogus yucca moth Prodoxus decipiens |
Q51425164 | The scent of senescence: sexual signalling and female preference in house mice. |
Q35155700 | The scope and strength of sex-specific selection in genome evolution. |
Q46931750 | The search for Pleiades in trait constellations: functional integration and phenotypic selection in the complex flowers of Morrenia brachystephana (Apocynaceae). |
Q30085659 | The seven deadly sins of comparative analysis |
Q89174323 | The sex chromosome system can influence the evolution of sex-biased dispersal |
Q33408310 | The shape of pterosaur evolution: evidence from the fossil record |
Q50577164 | The shape of things to come: linking developmental plasticity to post-metamorphic morphology in anurans. |
Q60060069 | The significance of wing pattern diversity in the Lycaenidae: mate discrimination by two recently diverged species |
Q90771183 | The skull evolution of oviraptorosaurian dinosaurs: the role of niche partitioning in diversification |
Q54775966 | The social evolution of dispersal with public goods cooperation. |
Q52660527 | The social parasite wasp Polistes atrimandibularis does not form host races. |
Q55872527 | The speciation revolution |
Q80831758 | The spread of apomixis and its effect on resident genetic variation |
Q57266134 | The stability of genetic variance?covariance matrix in the presence of selection |
Q34116848 | The standard of neutrality: still flapping in the breeze? |
Q51569974 | The stationary distribution of a continuously varying strategy in a class-structured population under mutation-selection-drift balance. |
Q44791192 | The stimulation of immune defence accelerates development in the red flour beetle (Tribolium castaneum). |
Q30847435 | The strength of assortative mating for flowering date and its basis in individual variation in flowering schedule |
Q47262025 | The tale of the shrinking weapon: seasonal changes in nutrition affect weapon size and sexual dimorphism, but not contemporary evolution. |
Q94540616 | The target of selection matters: An established resistance - development-time negative genetic trade-off is not found when selecting on development time |
Q85904828 | The targets of selection during reinforcement |
Q51662805 | The timing of food-deceptive flowers: a commentary on Internicola et al. (2008). |
Q51575063 | The timing of mating influences reproductive success in Drosophila melanogaster: implications for sexual conflict. |
Q38831723 | The total opportunity for sexual selection and the integration of pre- and post-mating episodes of sexual selection in a complex world. |
Q46817335 | The trade-off between rate and yield in the design of microbial metabolism |
Q55043254 | The universal ancestor and the ancestors of Archaea and Bacteria were anaerobes whereas the ancestor of the Eukarya domain was an aerobe. |
Q45081473 | The unpredictable impact of hybridization |
Q51617375 | The unstable dynamics of multiple alternative reproductive tactics. |
Q52675726 | The unusual inheritance pattern of the courtship songs in closely related grasshopper species of the Chorthippus albomarginatus-group (Orthoptera: Gomphocerinae). |
Q60490561 | The use of marker-based relationship information to estimate the heritability of body weight in a natural population: a cautionary tale |
Q52002136 | The utility of AFLPs for supporting mitochondrial DNA phylogeographical analyses in the Taiwanese bamboo viper, Trimeresurus stejnegeri. |
Q46893566 | The utility of cranial ontogeny for phylogenetic inference: a case study in crocodylians using geometric morphometrics |
Q45884220 | The value of an egg: resource reallocation in ladybirds (Coleoptera: Coccinellidae) infected with male-killing bacteria |
Q52857389 | The way the world might be. |
Q51722512 | Theoretical influence of female mating status and remating propensity on male sperm allocation patterns. |
Q46539677 | There is more than one way to skin a G matrix. |
Q51957803 | There is no heterotic effect upon developmental stability in the ventral side of the skull within the house mouse hybrid zone. |
Q39097078 | There is no such a thing as a free cigarette; lining nests with discarded butts brings short-term benefits, but causes toxic damage. |
Q48308902 | Thermal acclimation in Arabidopsis lyrata: genotypic costs and transcriptional changes. |
Q47317532 | Thermal evolution of pre-adult life history traits, geometric size and shape, and developmental stability in Drosophila subobscura. |
Q36108025 | Thermal plasticity in Drosophila melanogaster populations from eastern Australia: quantitative traits to transcripts |
Q33288436 | This is not déjà vu all over again: male guppy colour in a new experimental introduction |
Q47627170 | Though with constraints imposed by endosymbiosis, preferential attachment is still a plausible mechanism responsible for the evolution of the chloroplast metabolic network |
Q41884240 | Three epigenetic information channels and their different roles in evolution |
Q90124044 | Three-dimensional characterization of osteocyte volumes at multiple scales, and its relationship with bone biology and genome evolution in ray-finned fishes |
Q42025214 | Time-shifted reproductive behaviours among fall armyworm (Noctuidae: Spodoptera frugiperda) host strains: evidence for differing modes of inheritance |
Q46888795 | Timing and tempo of primate speciation |
Q52815160 | To be or not to be? Mating success and survival trade-offs when switching between alternative reproductive tactics. |
Q40297592 | To eject or to abandon? Life history traits of hosts and parasites interact to influence the fitness payoffs of alternative anti-parasite strategies |
Q51332740 | Tolerance to deer herbivory and resistance to insect herbivores in the common evening primrose (Oenothera biennis). |
Q46391241 | Toll-like receptor variation in the bottlenecked population of the Seychelles warbler: computer simulations see the 'ghost of selection past' and quantify the 'drift debt'. |
Q47182409 | Tooth and cranial disparity in the fossil relatives of Sphenodon (Rhynchocephalia) dispute the persistent 'living fossil' label. |
Q51873075 | Toward evolutionary graphs with two sexes: a kin selection analysis of a sex allocation problem. |
Q125299081 | Towards a global perspective for Salvia L.: Phylogeny, diversification and floral evolution |
Q51254036 | Towards robust evolutionary inference with integral projection models. |
Q47257046 | Toxic hydrogen sulphide and dark caves: pronounced male life-history divergence among locally adapted Poecilia mexicana (Poeciliidae). |
Q46104298 | Tracking changes in chromosomal arrangements and their genetic content during adaptation |
Q43419398 | Tracking the origin of an invasive species: Drosophila subobscura in Argentina. |
Q45955176 | Trade-off acquisition and allocation in Gryllus firmus: a test of the Y model |
Q48497839 | Trade-off between male and female allocation in the simultaneously hermaphroditic flatworm Macrostomum sp. |
Q33861811 | Trade-off between steady and unsteady swimming underlies predator-driven divergence in Gambusia affinis |
Q39116756 | Trade-off of ovarian lipids and total body lipids for fecundity and starvation resistance in tropical populations of Drosophila melanogaster |
Q57142100 | Trade-offs between sexual and clonal reproduction in an aquatic plant: experimental manipulations vs. phenotypic correlations |
Q46757148 | Trade-offs in female signal apparency to males offer alternative anti-harassment strategies for colour polymorphic females |
Q114080047 | Trade‐offs between weapons and testes do not manifest at high social densities |
Q47591507 | Traditional Amerindian cultivators combine directional and ideotypic selection for sustainable management of cassava genetic diversity. |
Q51148802 | Trait differentiation and adaptation of plants along elevation gradients. |
Q34120887 | Trait-dependent diversification and the impact of palaeontological data on evolutionary hypothesis testing in New World ratsnakes (tribe Lampropeltini). |
Q100516609 | Trait-specific trade-offs prevent niche expansion in two parasites |
Q57614336 | Trans-generational effects on ageing in a wild bird population |
Q39564811 | Transcontinental migratory connectivity predicts parasite prevalence in breeding populations of the European barn swallow |
Q41197151 | Transcriptional changes during Daphnia pulex development indicate that the maturation decision resembles a rate more than a threshold |
Q99206449 | Transcriptome-wide genotype-phenotype associations in Daphnia in a predator risk environment |
Q48437604 | Transcriptomic analysis of inbreeding depression in cold-sensitive Drosophila melanogaster shows upregulation of the immune response. |
Q113855141 | Transfer of a parasitic sex factor to the nuclear genome of the host: A hypothesis on the evolution of sex-determining mechanisms in the terrestrial Isopod Armadillidium vulgare Latr. |
Q46140401 | Transgenerational effects alter plant defence and resistance in nature |
Q50525232 | Transgenerational effects of nutrition are different for sons and daughters. |
Q39901523 | Transgenerational memory effect of ageing in Drosophila |
Q47751046 | Translocons on the inner and outer envelopes of chloroplasts share similar evolutionary origin in Arabidopsis thaliana |
Q57050581 | Transmission mode affects the population genetic structure of Daphnia parasites |
Q45881586 | Transmission modes and the evolution of feminizing symbionts. |
Q91604158 | Transmission, relatedness, and the evolution of cooperative symbionts |
Q51279367 | Transparency and reproducibility in evolutionary research. |
Q90902513 | Transparency improves concealment in cryptically coloured moths |
Q112796094 | Trees growing in Eastern North America experience higher autumn solar irradiation than their European relatives, but is nitrogen limitation another factor explaining anthocyanin‐red autumn leaves? |
Q112797841 | Trick or treat: the battle of the sexes |
Q34386457 | Turtle origins: insights from phylogenetic retrofitting and molecular scaffolds |
Q48339290 | Two different strategies of host manipulation allow parasites to persist in intermediate-definitive host systems. |
Q48655251 | Two reproductively isolated cytotypes and a swarm of highly inbred, disconnected populations: a glimpse into Salicornia's evolutionary history and challenging taxonomy |
Q52957194 | Two species of feminizing microsporidian parasite coexist in populations of Gammarus duebeni. |
Q50784098 | Two-module organization of the mandible in the yellow-necked mouse: a comparison between two different morphometric approaches. |
Q30558142 | Unconstrained evolution in short introns? - an analysis of genome-wide polymorphism and divergence data from Drosophila |
Q83331067 | Uncorrelated evolution between vocal and plumage coloration traits in the trogons: a comparative study |
Q33746797 | Uncoupling ecological innovation and speciation in sea snakes (Elapidae, Hydrophiinae, Hydrophiini) |
Q91366585 | Understanding policing as a mechanism of cheater control in cooperating bacteria |
Q61686307 | Unequal allelic frequencies at the self-incompatibility locus within local populations of Prunus avium L.: an effect of population structure? |
Q57760425 | Uneven segregation of sporophytic self-incompatibility alleles in Arabidopsis lyrata |
Q51186613 | Unicoloniality, recognition and genetic differentiation in a native Formica ant. |
Q51811591 | Unique genomic configuration revealed by microsatellite DNA in polyploid dogroses, Rosa sect. Caninae. |
Q53524442 | Unprecedented chromosomal diversity and behaviour modify linkage patterns and speciation potential: structural heterozygosity in an Australian spider. |
Q29013496 | Unravelling the effects of contemporary and historical range expansion on the distribution of genetic diversity in the damselfly Coenagrion scitulum |
Q84437864 | Up, up, and away: relative importance of horizontal and vertical escape from predators for survival and senescence |
Q51169247 | Use it or lose it: reproductive implications of ecological specialization in a haematophagous ectoparasite. |
Q81145520 | Useful ways of being wrong |
Q28242293 | Using creation science to demonstrate evolution 2: morphological continuity within Dinosauria |
Q34121573 | Using creation science to demonstrate evolution: application of a creationist method for visualizing gaps in the fossil record to a phylogenetic study of coelurosaurian dinosaurs |
Q34170585 | Using creation science to demonstrate evolution? Senter's strategy revisited |
Q114080048 | Using gradient Forest to predict climate response and adaptation in Cork oak |
Q34814734 | Using visual modelling to study the evolution of lizard coloration: sexual selection drives the evolution of sexual dichromatism in lacertids. |
Q83454800 | Variability and constraint in the mammalian vertebral column |
Q52659281 | Variable assortative mating in replicate mating trials using Drosophila melanogaster populations derived from contrasting opposing slopes of 'Evolution Canyon', Israel. |
Q51598468 | Variable discrimination and asymmetric preferences in laboratory tests of reproductive isolation between cichlid colour morphs. |
Q45378676 | Variable post-zygotic isolation in Drosophila melanogaster/D. simulans hybrids |
Q112582360 | Variable routes to genomic and host adaptation among coronaviruses |
Q39198525 | Variable selection in Platanthera bifolia (Orchidaceae): phenotypic selection differed between sex functions in a drought year |
Q51592212 | Variable selection patterns on the labellum shape of Geoblasta pennicillata, a sexually deceptive orchid. |
Q57955142 | Variable visual habitats may influence the spread of colourful plumage across an avian hybrid zone |
Q44361385 | Variance and variability, uncovering an underappreciated component of reproductive isolation |
Q50755406 | Variation among populations of Diodia teres (Rubiaceae) in environmental maternal effects. |
Q51162665 | Variation and evolution of sex ratios at the northern range limit of a sexually polymorphic plant. |
Q51330223 | Variation in adult sex ratio alters the association between courtship, mating frequency and paternity in the lek-forming fruitfly Ceratitis capitata. |
Q42244602 | Variation in costs of parasite resistance among natural host populations. |
Q92446090 | Variation in ecophysiological traits might contribute to ecogeographic isolation and divergence between parapatric ecotypes of Mimulus aurantiacus |
Q58042361 | Variation in female mate preference across a grasshopper hybrid zone |
Q46608088 | Variation in genetic architecture of olfactory behaviour among wild-derived populations of Drosophila melanogaster. |
Q36230122 | Variation in infectivity and aggressiveness in space and time in wild host-pathogen systems: causes and consequences |
Q118129988 | Variation in life history and genetic traits of Hawaiian mosquitofish populations |
Q46953682 | Variation in male effects on female fecundity in Drosophila melanogaster |
Q53890550 | Variation in natural selection for growth and phlorotannins in the brown alga Fucus vesiculosus. |
Q58274471 | Variation in pollen production and pollen viability in natural populations of gynodioecious Beta vulgaris ssp. maritima : evidence for a cost of restoration of male function? |
Q46626339 | Variation in scorpion metabolic rate and rate-temperature relationships: implications for the fundamental equation of the metabolic theory of ecology |
Q33345547 | Variation in sex ratio, morph-specific reproductive ecology and an experimental test of frequency-dependence in the gynodioecious Kallstroemia grandiflora (Zygophyllaceae). |
Q52664021 | Variation in synonymous codon use and DNA polymorphism within the Drosophila genome. |
Q57237076 | Variation in the degree and costs of adaptive phenotypic plasticity among Rana temporaria populations |
Q60575277 | Variation in the intensity of inbreeding depression among successive life-cycle stages and generations in gynodioecious Silene vulgaris (Caryophyllaceae) |
Q36341205 | Variation in the post-mating fitness landscape in fruit flies |
Q62767457 | Variation in the rate of convergent evolution: adaptation to a laboratory environment in Drosophila subobscura |
Q60481818 | Variation in thermal sensitivity of performance among colour morphs of a pygmy grasshopper |
Q42001045 | Variation in two phases of post-winter development of a butterfly |
Q112293580 | Variation of plastic responses to oxygen availability within the hybridogenetic Rana esculenta complex |
Q45904702 | Variation of telencephalon morphology of the threespine stickleback (Gasterosteus aculeatus) in relation to inferred ecology. |
Q80117964 | Various remarks on Lehmann and Keller's article |
Q47228888 | Ventilatory mechanics from maniraptoran theropods to extant birds. |
Q38901558 | Vertebrate host protective immunity drives genetic diversity and antigenic polymorphism in Schistosoma mansoni. |
Q33358348 | Vertically transmitted symbiont reduces host fitness along temperature gradient |
Q38645478 | Viability and expression of sexual ornaments in the barn swallow Hirundo rustica: a meta-analysis. |
Q80231862 | Viability effects and not meoitic drive cause dramatic departures from Mendelian inheritance for malic enzyme in hybrids of Tigriopus californicus populations |
Q83606695 | Viability selection on prey morphology by a generalist predator |
Q112578795 | Viral susceptibility across host species is largely independent of dietary protein to carbohydrate ratios |
Q58885289 | Virulence and age at reproduction: new insights into host-parasite coevolution |
Q40004898 | Virulence evolution and the trade-off hypothesis: history, current state of affairs and the future |
Q34160528 | Virulence evolution in response to anti-infection resistance: toxic food plants can select for virulent parasites of monarch butterflies |
Q45355044 | Virus adaptation to quantitative plant resistance: erosion or breakdown? |
Q57783873 | Viruses as indicators of contemporary host dispersal and phylogeography: an example of feline immunodeficiency virus (FIVP le ) in free-ranging African lion (Panthera leo ) |
Q101148579 | Visual and non-visual opsin genes of sharks and other non-osteichthyan vertebrates: genomic exploration of underwater photoreception |
Q50961581 | Visual modelling suggests a weak relationship between the evolution of ultraviolet vision and plumage coloration in birds. |
Q35642363 | Visual system evolution and the nature of the ancestral snake. |
Q48166898 | Visualizing unbiased and biased unweighted meta-analyses |
Q45729825 | Vitamins, stress and growth: the availability of antioxidants in early life influences the expression of cryptic genetic variation |
Q84822868 | WWDD? (What would Darwin do?) |
Q95337483 | Warmer temperatures enhance beneficial mutation effects |
Q39044948 | Water availability and population origin affect the expression of the tradeoff between reproduction and growth in Plantago coronopus |
Q57471491 | Weak and inconsistent associations between melanic darkness and fitness related traits in an insect |
Q57269579 | Weak evidence for anticipatory parental effects in plants and animals |
Q43732851 | Weak impact of fine-scale landscape heterogeneity on evolutionary potential in Arabidopsis lyrata. |
Q51195574 | Weak phylogenetic effects on ecological niches of Sylvia warblers. |
Q45969891 | Weak phylogenetic signal in physiological traits of methane-oxidizing bacteria. |
Q91366590 | Weak premating isolation between Clitarchus stick insect species despite divergent male and female genital morphology |
Q46297890 | Weakened purifying selection leads to elevated mutation load under environmental sex determination |
Q29037148 | Weapon allometry varies with latitude in the New Zealand giraffe weevil |
Q52586949 | Web building and silk properties functionally covary among species of wolf spider. |
Q58869831 | What controls haploid-diploid ratio in the red alga, Gracilaria verrucosa? |
Q58038145 | What determines dewlap diversity in Anolis lizards? An among-island comparison |
Q37361612 | What do human economies, large islands and forest fragments reveal about the factors limiting ecosystem evolution? |
Q51875932 | What drives variation in the corticosterone stress response between subspecies? A common garden experiment of swamp sparrows (Melospiza georgiana). |
Q57006748 | What factors shape rates of phenotypic evolution? A comparative study of cranial morphology of four mammalian clades |
Q88783292 | What happens to offspring when parents are inbred, old or had a poor start in life? Evidence for sex-specific parental effects |
Q45887088 | What maintains noncytoplasmic incompatibility inducing Wolbachia in their hosts: a case study from a natural Drosophila yakuba population. |
Q34839852 | What, if anything, is sympatric speciation? |
Q46926735 | When a clonal genome finds its way back to a sexual species: evidence from ongoing but rare introgression in the hybridogenetic water frog complex |
Q43979808 | When assumptions on visual system evolution matter: nestling colouration and parental visual performance in birds |
Q33268530 | When bigger is not better: selection against large size, high condition and fast growth in juvenile lemon sharks. |
Q53785199 | When can host shifts produce congruent host and parasite phylogenies? A simulation approach. |
Q46246145 | When do trade-offs occur? The roles of energy constraints and trait flexibility in a bushcricket. |
Q100729379 | When does parasitism maintain sex in the absence of Red Queen Dynamics? |
Q45923882 | When less means more: evolutionary and developmental hypotheses in rodent molars. |
Q52655368 | When morphometry meets genetics: inferring the phylogeography of Carabus solieri using Fourier analyses of pronotum and male genitalia. |
Q90249237 | When mother knows best: A population genetic model of transgenerational versus intragenerational plasticity |
Q52650404 | When mutualists are pathogens: an experimental study of the symbioses between Steinernema (entomopathogenic nematodes) and Xenorhabdus (bacteria). |
Q38864738 | When relative allocation depends on total resource acquisition: implication for the analysis of trade-offs. |
Q34332221 | When should we expect early bursts of trait evolution in comparative data? Predictions from an evolutionary food web model |
Q51248642 | When three traits make a line: evolution of phenotypic plasticity and genetic assimilation through linear reaction norms in stochastic environments. |
Q47366601 | When to be born? Prolonged pregnancy or incubation enhances locomotor performance in neonatal lizards (Scincidae). |
Q38435639 | Where have all the blue flowers gone: pollinator responses and selection on flower colour in New Zealand Wahlenbergia albomarginata. |
Q37860352 | Whither Pst? The approximation of Qst by Pst in evolutionary and conservation biology. |
Q57149317 | Why Are Red Flowers So Rare? Testing the Macroevolutionary Causes of Tippiness |
Q44684173 | Why acquiesce? Worker reproductive parasitism in the Eastern honeybee (Apis cerana). |
Q47809123 | Why are some species more commonly afflicted by arthritis than others? A comparative study of spondyloarthropathy in primates and carnivores |
Q50588619 | Why birds eat colourful grit: colour preferences revealed by the colour of gizzard stones. |
Q34714398 | Why care? Inferring the evolution of complex social behaviour |
Q39600675 | Why colour in subterranean vertebrates? Exploring the evolution of colour patterns in caecilian amphibians |
Q91824770 | Why cooperation is not running away |
Q45260919 | Why do Californian striders fly? |
Q39498532 | Why do stigmas move in a flexistylous plant? |
Q52664038 | Why does a grasshopper have fewer, larger offspring at its range limits? |
Q46056465 | Why get big in the cold? Size-fecundity relationships explain the temperature-size rule in a pulmonate snail (Physa). |
Q37081630 | Why h2 does not always equal V A/V P? |
Q47956429 | Why join a neighbour: fitness consequences of colony fusions in termites |
Q51596835 | Why migrate during the day: a comparative analysis of North American birds. |
Q57065596 | Why pollinators visit only a fraction of the open flowers on a plant: The plant's point of view |
Q128153879 | Why so many polyploids? Accounting for environmental stochasticity in unreduced gamete formation lowers the perceived barriers to polyploid establishment |
Q46620070 | Why wait? Three mechanisms selecting for environment-dependent developmental delays. |
Q26998671 | Widespread phenotypic and genetic divergence along altitudinal gradients in animals |
Q33326133 | Widespread unidirectional transfer of mitochondrial DNA: a case in western Palaearctic water frogs |
Q80960858 | Will two walk together, except they have agreed? Amos 3:3 |
Q51969721 | Wing morphology and fluctuating asymmetry depend on the host plant in cactophilic Drosophila. |
Q51710894 | Wing pointedness associated with migratory distance in common-garden and comparative studies of stonechats (Saxicola torquata). |
Q51338455 | Wing trait-inversion associations in Drosophila subobscura can be generalized within continents, but may change through time. |
Q28308022 | Wings or winds: inferring bat migration in a stepping-stone archipelago |
Q36667574 | Winter is coming: hibernation reverses the outcome of sperm competition in a fly |
Q47970519 | With a little help from my kin: barn swallow nestlings modulate solicitation of parental care according to nestmates' need |
Q90694788 | Withdrawn: Mating system drives the mate selection in aphidophagous ladybird, Menochilus sexmaculatus |
Q51701397 | Within and between generation phenotypic plasticity in trichome density of Mimulus guttatus. |
Q52976395 | Within clutch co-variation of egg mass and sex in the black-headed gull. |
Q60566643 | Within population genetic differentiation in traits affecting clonal growth: |
Q113181529 | Within population genetic differentiation in traits affecting clonal growth: Festuca rubra in a mountain grassland |
Q38929584 | Within-clutch variation in offspring sex determined by differences in sire body size: cryptic mate choice in the wild |
Q36669721 | Within-female plasticity in sex allocation is associated with a behavioural polyphenism in house wrens |
Q92240170 | Within-host interactions shape virulence-related traits of trematode genotypes |
Q51616719 | Within-host viral evolution in a heterogeneous environment: insights into the HIV co-receptor switch. |
Q46818807 | Within-plant variation in reproductive investment: consequences for selection on flowering time |
Q46692110 | Within-population Y-linked genetic variation for lifespan in Drosophila melanogaster |
Q46806019 | Within-population genetic effects of mtDNA on metabolic rate in Drosophila subobscura. |
Q44347251 | Within-population polymorphism of sex-determination systems in the common frog (Rana temporaria). |
Q98882787 | Within-population variation in female mating preference affects the opportunity for sexual selection and the evolution of male traits, but things are not as simple as expected |
Q39093369 | Within-season increase in parental investment in a long-lived bird species: investment shifts to maximize successful reproduction? |
Q35832963 | Within-species reproductive costs affect the asymmetry of satyrization in Drosophila |
Q46672817 | Within-species variation in long-term trajectories of growth, fecundity and mortality in the Collembola Folsomia candida. |
Q51749472 | Within/between population crosses reveal genetic basis for siring success in Silene latifolia (Caryophyllaceae). |
Q31062718 | Wolbachia affects oviposition and mating behaviour of its spider mite host |
Q44009229 | Wolbachia effects in natural populations of Chorthippus parallelus from the Pyrenean hybrid zone. |
Q59117971 | Wolbachia in leafcutter ants: a widespread symbiont that may induce male killing or incompatible matings |
Q60398279 | Wolbachia infection in crustaceans: novel hosts and potential routes for horizontal transmission |
Q45886030 | Wolbachia-induced unidirectional cytoplasmic incompatibility and the stability of infection polymorphism in parapatric host populations. |
Q47572468 | Women's attractiveness is linked to expected age at menopause. |
Q29027323 | Worker interests and male production in Polistes gallicus, a Mediterranean social wasp |
Q28277150 | Worker reproduction and policing in insect societies: an ESS analysis |
Q44603407 | Worker reproduction in the ant Formica fusca. |
Q61659106 | Wormy mice in a hybrid zone: A genetic control of susceptibility to parasite infection |
Q63980011 | Wrensch, D. L. and Ebbert, M. A. 1992. Evolution and diversity of sex ratio in insects and mites. Chapman and Hall. f45. ISBN: 0-412-02221-4 (pb) |
Q81145529 | Wright meets AD: not all landscapes are adaptive |
Q38840902 | X chromosome drive in a widespread Palearctic woodland fly, Drosophila testacea. |
Q34195662 | Year-round resource defence and the evolution of male and female song in suboscine birds: social armaments are mutual ornaments |
Q90656578 | Yes, correct context is indeed the key: An answer to Haave-Audet et al. 2019 |
Q51824589 | Yolk androgens in the barn swallow (Hirundo rustica): a test of some adaptive hypotheses. |
Q47262669 | You are where you live: parasitic nematode mitochondrial genome size is associated with the thermal environment generated by hosts |
Q101124013 | microRNA expression variation in a natural system as a potential molecular mechanism contributing to adaptation to hydrogen sulfide |
ISSN 1010-061X | wikimedia | |
bn | জার্নাল অব ইভোল্যুশনারী বায়োলজি | wikipedia |
Journal of Evolutionary Biology | wikipedia | |
Journal of Evolutionary Biology | wikipedia |
Search more.