scholarly article | Q13442814 |
P50 | author | Janne S. Kotiaho | Q51724060 |
Jacek Radwan | Q51815017 | ||
Thomas Tregenza | Q56435262 | ||
Joseph L. Tomkins | Q60658929 | ||
P2860 | cites work | MULTIFACTORIAL GENETICSUNDERSTANDING QUANTITATIVE GENETIC VARIATION | Q22121996 |
Condition-dependent signalling of genetic variation in stalk-eyed flies | Q28141741 | ||
Mate selection—A selection for a handicap | Q28214988 | ||
Heritable true fitness and bright birds: a role for parasites? | Q28278977 | ||
Sexual selection and the maintenance of sexual reproduction | Q33950344 | ||
Negative genetic correlation for adult fitness between sexes reveals ontogenetic conflict in Drosophila | Q34097980 | ||
Toward a realistic model of mutations affecting fitness | Q34191607 | ||
Sexual selection, honest advertisement and the handicap principle: reviewing the evidence | Q34308599 | ||
When does conservation genetics matter? | Q34459256 | ||
Experimental tests of the adaptive significance of sexual recombination | Q34609885 | ||
The strength of indirect selection on female mating preferences | Q35995071 | ||
Evolutionary quantitative genetics: how little do we know? | Q38763387 | ||
Quantitative genetics and fitness: lessons from Drosophila | Q41480365 | ||
Sexual selection fails to promote adaptation to a new environment | Q46336847 | ||
Deleterious mutations and genetic variation for flower size in Mimulus guttatus | Q47207345 | ||
Coevolution of costly mate choice and condition-dependent display of good genes. | Q52048621 | ||
How should we explain variation in the genetic variance of traits? | Q52237139 | ||
Genotype-environment interactions and the estimation of the genomic mutation rate in Drosophila melanogaster. | Q52540947 | ||
Male courtship song frequency as an indicator of male genetic quality in an insect species, Drosophila montana. | Q52563183 | ||
Inbreeding and outbreeding depression in male courtship song characters in Drosophila montana. | Q52578155 | ||
Evolution of ejaculates: patterns of phenotypic and genotypic variation and condition dependence in sperm competition traits. | Q52599531 | ||
The chemical composition of the spermatophore in some species of phaneropterid bushcrickets (Orthoptera: Tettigonioidea). | Q52607489 | ||
The effect of past condition on a multicomponent sexual signal. | Q52610900 | ||
Nonlinear and correlational sexual selection on 'honest' female ornamentation. | Q52640981 | ||
THE EVOLUTION OF COSTLY MATE PREFERENCES II. THE "HANDICAP" PRINCIPLE. | Q53246092 | ||
MUTATION, SELECTION, AND THE MAINTENANCE OF LIFE-HISTORY VARIATION IN A NATURAL POPULATION. | Q54162641 | ||
Inbreeding depression and genetic load of sexually selected traits: how the guppy lost its spots | Q54432829 | ||
Evolution of genetic variation for condition-dependent traits in stalk-eyed flies. | Q55173159 | ||
The Lek Paradox and the Capture of Genetic Variance by Condition Dependent Traits | Q55895821 | ||
A Resolution of the Lek Paradox | Q55895824 | ||
Colour bands, dominance, and body mass regulation in male zebra finches (Taeniopygia guttata) | Q56060505 | ||
Female choice selects for extreme tail length in a widowbird | Q56836087 | ||
Daytime calibration of magnetic orientation in a migratory bird requires a view of skylight polarization | Q56873939 | ||
On the misuse of residuals in ecology: testing regression residuals vs. the analysis of covariance | Q57062417 | ||
The Evolution of Mate Preferences for Multiple Sexual Ornaments | Q57065605 | ||
Natural selection on the genetical component of variance in body condition in a wild bird population | Q57237107 | ||
Towards a resolution of the lek paradox | Q57266153 | ||
Estimating Fitness: Comparison of Body Condition Indices Revisited | Q57266155 | ||
Differential allocation: tests, mechanisms and implications | Q57614441 | ||
What is genetic quality? | Q57669767 | ||
Perspective: Spontaneous Deleterious Mutation | Q57933462 | ||
Genetic Covariance of Fitness Correlates: What Genetic Correlations are Made of and Why it Matters | Q57933534 | ||
Sexual selection and the maintenance of sex | Q59086453 | ||
What does sexual trait FA tell us about stress? | Q73549769 | ||
An experimental method for evaluating the contribution of deleterious mutations to quantitative trait variation | Q78058680 | ||
Effectiveness of sexual selection in preventing fitness deterioration in bulb mite populations under relaxed natural selection | Q79733597 | ||
Do sexual ornaments demonstrate heightened condition-dependent expression as predicted by the handicap hypothesis? | Q80343313 | ||
Alternative hypotheses linking the immune system and mate choice for good genes | Q93604385 | ||
Good-genes effects in sexual selection | Q93604922 | ||
Fluctuating asymmetry of sexual and nonsexual traits in stalk-eyed flies: a poor indicator of developmental stress and genetic quality | Q104206900 | ||
P433 | issue | 6 | |
P1104 | number of pages | 6 | |
P304 | page(s) | 323-328 | |
P577 | publication date | 2004-06-01 | |
P1433 | published in | Trends in Ecology & Evolution | Q15265725 |
P1476 | title | Genic capture and resolving the lek paradox | |
P478 | volume | 19 |
Q48047671 | A mechanism of extreme growth and reliable signaling in sexually selected ornaments and weapons. |
Q51154393 | A multivariate analysis of genetic variation in the advertisement call of the gray treefrog, Hyla versicolor. |
Q52623101 | A performance-based cost to honest signalling in male green anole lizards (Anolis carolinensis). |
Q24685527 | A potential resolution to the lek paradox through indirect genetic effects |
Q36702186 | A tale of two matrices: multivariate approaches in evolutionary biology. |
Q30451077 | Adaptive plasticity in wild field cricket's acoustic signaling |
Q52705140 | Additive genetic breeding values correlate with the load of partially deleterious mutations. |
Q57266119 | Age-related decrease in male reproductive success and song quality in Drosophila montana |
Q38755559 | An epigenetic resolution of the lek paradox |
Q51686461 | An introduction to genetic quality in the context of sexual selection. |
Q48125650 | Assortative mating by fitness and sexually antagonistic genetic variation |
Q46452880 | Autism as the Low-Fitness Extreme of a Parentally Selected Fitness Indicator |
Q38874742 | Blood transcriptomes and de novo identification of candidate loci for mating success in lekking great snipe (Gallinago media). |
Q35754662 | Body Condition Indices Predict Reproductive Success but Not Survival in a Sedentary, Tropical Bird |
Q28540629 | Body morphology, energy stores, and muscle enzyme activity explain cricket acoustic mate attraction signaling variation |
Q33747893 | Breeding experience and the heritability of female mate choice in collared flycatchers |
Q59175517 | COMPARISON OF MATING OF TEN EUMENINAE WASP SPECIES WITH A BRIEF REVIEW OF SEXUAL SELECTION THEORIES: A FRAMEWORK FOR FUTURE RESEARCH |
Q30456118 | Calling, courtship, and condition in the fall field cricket, Gryllus pennsylvanicus |
Q28257122 | Cheating can stabilize cooperation in mutualisms |
Q50937757 | Choosing mates: good genes versus genes that are a good fit. |
Q39579420 | Comparing evolvabilities: common errors surrounding the calculation and use of coefficients of additive genetic variation |
Q28602968 | Comparing pre- and post-copulatory mate competition using social network analysis in wild crickets |
Q35849759 | Complex sperm evolution |
Q51104996 | Condition dependence and the maintenance of genetic variance in a sexually dimorphic black scavenger fly. |
Q36539247 | Condition dependence of male and female reproductive success: insights from a simultaneous hermaphrodite. |
Q36288063 | Condition-dependence and sexual ornamentation: Effects of immune challenges on a highly sexually dimorphic grasshopper |
Q51692417 | Condition-dependence, genotype-by-environment interactions and the lek paradox. |
Q37058735 | Condition-dependent expression of pre- and postcopulatory sexual traits in guppies |
Q36058415 | Condition-dependent trade-offs between sexual traits, body condition and immunity: the effect of novel habitats |
Q51600935 | Condition-dependent traits as signals of the functionality of vital cellular processes. |
Q57899043 | Conditional Handicaps in Exuberant Lizards: Bright Color in Aggressive Males Is Correlated with High Levels of Free Radicals |
Q45096263 | Correlational selection does not explain the evolution of a behavioural syndrome. |
Q29027832 | Crickets detect the genetic similarity of mating partners via cuticular hydrocarbons |
Q36268064 | DNA repair pathway choice is influenced by the health of Drosophila melanogaster |
Q55462006 | Defining individual quality over lifetimes and selective contexts |
Q51842459 | Developmental instability as phenodeviance in a secondary sexual trait increases sharply with thermal stress. |
Q51372943 | Differential effects of genetic vs. environmental quality in Drosophila melanogaster suggest multiple forms of condition dependence. |
Q36709164 | Differential sperm expenditure reveals a possible role for post-copulatory sexual selection in a lekking moth |
Q52701256 | Dispersal and ejaculatory strategies associated with exaggeration of weapon in an armed beetle. |
Q36572068 | Dissecting the complex genetic basis of mate choice |
Q38078466 | Do male secondary sexual characters signal ejaculate quality? A meta-analysis |
Q39108953 | Do males pay for sex? Sex-specific selection coefficients suggest not. |
Q60054902 | Do slower movers have lower reproductive success and higher mutation load? |
Q58044030 | Does Breeding Ornamentation Signal Genetic Quality in Arctic charr, Salvelinus alpinus? |
Q33632955 | Does segregating variation in sexual or microhabitat preferences lead to non-random mating within a population of Drosophila melanogaster? |
Q33328494 | Does sex trade with violence among genotypes in Drosophila melanogaster? |
Q90142021 | Dynamic phenotypic correlates of social status and mating effort in male and female red junglefowl, Gallus gallus |
Q33837363 | Ecology, sexual selection and speciation |
Q37743826 | Effect of diet on the structure of animal personality |
Q58376715 | Effects of heterozygosity and MHC diversity on patterns of extra-pair paternity in the socially monogamous scarlet rosefinch |
Q51347702 | Environment-dependent selection on mate choice in a natural population of birds. |
Q34691103 | Evaluating indices of body condition in two cricket species |
Q51711887 | Evolution of frequency-dependent mate choice: keeping up with fashion trends. |
Q54960079 | Evolutionary divergence in competitive mating success through female mating bias for good genes. |
Q36069032 | Evolutionary optimum for male sexual traits characterized using the multivariate Robertson-Price Identity |
Q90591699 | Experimental evidence for effects of sexual selection on condition-dependent mutation rates |
Q48013796 | Experimental evidence for sexual selection against inbred males |
Q33924574 | Experimental mutation-accumulation on the X chromosome of Drosophila melanogaster reveals stronger selection on males than females |
Q36159283 | Factors affecting male song evolution in Drosophila montana |
Q51767429 | Female fur seals show active choice for males that are heterozygous and unrelated. |
Q51291983 | Female preference for male courtship effort can drive the evolution of male mate choice. |
Q30863621 | Females prefer the scent of outbred males: good-genes-as-heterozygosity? |
Q46480654 | From beavis to beak color: a simulation study to examine how much qtl mapping can reveal about the genetic architecture of quantitative traits |
Q26824819 | Gene duplication, tissue-specific gene expression and sexual conflict in stalk-eyed flies (Diopsidae) |
Q35939182 | Genetic conflict between sexual signalling and juvenile survival in the three-spined stickleback |
Q42014676 | Genetic variation in a female genital trait evolved by sexual coevolution |
Q39323492 | Genomics of coloration in natural animal populations |
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 |
Q58461272 | Genotype-by-Environment Interactions and Reliable Signaling of Male Quality in Bank Voles |
Q57915313 | Genotype-by-Environment Interactions when the Social Environment Contains Genes |
Q51295489 | Genotype-by-environment interactions for cuticular hydrocarbon expression in Drosophila simulans. |
Q46752243 | Genotype-by-environment interactions underlie the expression of pre- and post-copulatory sexually selected traits in guppies |
Q51595054 | Genotype × environment interaction is weaker in genitalia than in mating signals and body traits in Enchenopa treehoppers (Hemiptera: Membracidae). |
Q51538054 | Genotype‐by‐environment interactions for female preference |
Q21135572 | Good genes and sexual selection in dung beetles (Onthophagus taurus): genetic variance in egg-to-adult and adult viability |
Q29305745 | Good genes sexual selection in nature |
Q57432884 | Gustatory adaptation affects sexual maturation in male German cockroaches,Blattella germanica |
Q48545916 | Has the inbreeding load for a condition-dependent sexual signalling trait been purged in insular lizard populations? |
Q46960700 | Heterozygosity and orange coloration are associated in the guppy (Poecilia reticulata). |
Q22122485 | High-quality male field crickets invest heavily in sexual display but die young |
Q51458673 | Immature performance linked with exaggeration of a sexually selected trait in an armed beetle. |
Q51615477 | Inbreeding and courtship calling in the cricket Teleogryllus commodus. |
Q35265248 | Inbreeding reveals stronger net selection on Drosophila melanogaster males: implications for mutation load and the fitness of sexual females |
Q47290493 | Increase in song frequency decreases spermatophore size: correlative evidence of a macroevolutionary trade-off in katydids (Orthoptera: Tettigoniidae). |
Q42028437 | Indirect genetic effects and the lek paradox: inter-genotypic competition may strengthen genotype x environment interactions and conserve genetic variance. |
Q51771281 | Influence of developmental environment on male- and female-mediated sperm precedence in Drosophila melanogaster. |
Q44581073 | Inter- and intrasexual genetic correlations of exaggerated traits and locomotor activity |
Q30497825 | Intrasexual competition facilitates the evolution of alternative mating strategies in a colour polymorphic fish. |
Q47375093 | Is bigger better? Male body size affects wing-borne courtship signals and mating success in the olive fruit fly, Bactrocera oleae (Diptera: Tephritidae). |
Q90273091 | Juvenile diet quality and intensity of sexual conflict in the mite Sancassania berlesei |
Q47730564 | Life history trade-offs at a single locus maintain sexually selected genetic variation |
Q57133292 | Lineages evolved under stronger sexual selection show superior ability to invade conspecific competitor populations |
Q57920868 | Longevity, calling effort, and metabolic rate in two populations of cricket |
Q57432057 | Macronutrient balance mediates the growth of sexually selected weapons but not genitalia in male broad-horned beetles |
Q36943825 | Maintenance of genetic variation in sexual ornaments: a review of the mechanisms |
Q50146939 | Male choice generates stabilizing sexual selection on a female fecundity correlate |
Q51596558 | Male cockroaches prefer a high carbohydrate diet that makes them more attractive to females: implications for the study of condition dependence. |
Q35080249 | Male courtship behavior and weapon trait as indicators of indirect benefit in the bean bug, Riptortus pedestris |
Q51707635 | Male courtship song and female preference variation between phylogeographically distinct populations of Drosophila montana. |
Q33304589 | Male dominance linked to size and age, but not to 'good genes' in brown trout (Salmo trutta) |
Q50890097 | Male-female genotype interactions maintain variation in traits important for sexual interactions and reproductive isolation. |
Q33305233 | Mate choice for genetic quality when environments vary: suggestions for empirical progress. |
Q57266130 | Mate choice for indirect genetic benefits: scrutiny of the current paradigm |
Q51672618 | Mate choice for nonadditive genetic benefits and the maintenance of genetic diversity in song sparrows. |
Q51703871 | Maternal inheritance, epigenetics and the evolution of polyandry. |
Q50999035 | Mating behavior as an indicator of quality of Drosophila subobscura males? |
Q52703669 | Mating tactics determine patterns of condition dependence in a dimorphic horned beetle. |
Q104282980 | Melanin-based ornament darkness positively correlates with across-season nutritional condition |
Q46475643 | Meta-analysis suggests choosy females get sexy sons more than "good genes". |
Q64056163 | Molecular evidence supports a genic capture resolution of the lek paradox |
Q27332178 | Natural allelic variations of xenobiotic-metabolizing enzymes affect sexual dimorphism in Oryzias latipes |
Q57266138 | Negatively condition dependent predation cost of a positively condition dependent sexual signalling |
Q38068803 | New perspectives on the evolution of exaggerated traits |
Q43967555 | No evidence for condition-dependent expression of male genitalia in the dung beetle Onthophagus taurus. |
Q51631569 | Nutritional correlates and mate acquisition role of multiple sexual traits in male collared flycatchers. |
Q89607459 | Nutritional geometry of paternal effects on embryo mortality |
Q51519381 | On the evolution of heightened condition dependence of male sexual displays. |
Q26827418 | Oxidative stress and condition-dependent sexual signals: more than just seeing red |
Q47865213 | Partitioning of resources: the evolutionary genetics of sexual conflict over resource acquisition and allocation |
Q37481026 | Pattern of inbreeding depression, condition dependence, and additive genetic variance in Trinidadian guppy ejaculate traits |
Q90579214 | Phenological mismatch drives selection on elevation, but not on slope, of breeding time plasticity in a wild songbird |
Q30469661 | Phenotypic covariance structure and its divergence for acoustic mate attraction signals among four cricket species |
Q52053715 | Phenotypic plasticity in the developmental integration of morphological trade-offs and secondary sexual trait compensation. |
Q85784628 | Physiological costs enforce the honesty of lek display in the black grouse (Tetrao tetrix) |
Q48470373 | Plastic flies: the regulation and evolution of trait variability in Drosophila. |
Q44747131 | Predicting Life-History Trade-Offs with Whole-Organism Performance |
Q44130339 | Rapid adaptation to a novel host in a seed beetle (Callosobruchus maculatus): the role of sexual selection. |
Q34762348 | Reaction norm variants for male calling song in populations of Achroia grisella (Lepidoptera: Pyralidae): toward a resolution of the lek paradox. |
Q52744414 | Reduced genetic variance among high fitness individuals: inferring stabilizing selection on male sexual displays in Drosophila serrata. |
Q50320085 | Reinforcement as an initiator of population divergence and speciation |
Q64990908 | Relative costs and benefits of alternative reproductive phenotypes at different temperatures - genotype-by-environment interactions in a sexually selected trait. |
Q34290976 | Relative effectiveness of mating success and sperm competition at eliminating deleterious mutations in Drosophila melanogaster |
Q51760183 | Secondary sexual ornamentation and non-additive genetic benefits of female mate choice. |
Q89664847 | Selection for Male Weapons Boosts Female Fecundity, Eliminating Sexual Conflict in the Bulb Mite |
Q52765246 | Selective harvest focused on sexual signal traits can lead to extinction under directional environmental change. |
Q51630172 | Separate and combined effects of nutrition during juvenile and sexual development on female life-history trajectories: the thrifty phenotype in a cockroach. |
Q52659278 | Sex, mutation and fitness: asymmetric costs and routes to recovery through compensatory evolution. |
Q34700185 | Sex-specific effect of juvenile diet on adult disease resistance in a field cricket. |
Q51317464 | Sex-specific genotype-by-environment interactions for cuticular hydrocarbon expression in decorated crickets, Gryllodes sigillatus: implications for the evolution of signal reliability. |
Q39282789 | Sex-specific selection under environmental stress in seed beetles |
Q57915057 | Sexual Selection and Life History Allocation |
Q55469367 | Sexual Selection on Leks: A Fruit Fly Primer. |
Q49075064 | Sexual Selection: The Weevils of Inbreeding |
Q36870658 | Sexual selection and conflict in the bulb mite, Rhizoglyphus robini (Astigmata: Acaridae). |
Q35701436 | Sexual selection and its effect on the fixation of an asexual clone |
Q22162496 | Sexual selection and mate choice |
Q36660289 | Sexual selection and the evolution of evolvability. |
Q51172405 | Sexual selection can remove an experimentally induced mutation load. |
Q43532949 | Sexual selection in the cricket Gryllus bimaculatus: no good genes? |
Q47193661 | Sexual selection on male body size, genital length and heterozygosity: Consistency across habitats and social settings. |
Q47693642 | Sexual selection on spontaneous mutations strengthens the between-sex genetic correlation for fitness. |
Q40928256 | Sexual selection protects against extinction |
Q91784230 | Sexual selection reveals a cost of pathogen resistance undetected in life-history assays |
Q92650940 | Sexual selection, environmental robustness, and evolutionary demography of maladapted populations: A test using experimental evolution in seed beetles |
Q52656227 | Sexual selection, genetic architecture, and the condition dependence of body shape in the sexually dimorphic fly Prochyliza xanthostoma (Piophilidae). |
Q92982836 | Sexual selection, phenotypic plasticity and female reproductive output |
Q30415861 | Sexual traits are sensitive to genetic stress and predict extinction risk in the stalk-eyed fly, Diasemopsis meigenii |
Q38769907 | Signal function drives phenotypic and genetic diversity: the effects of signalling individual identity, quality or behavioural strategy |
Q51987637 | Sounds different: inbreeding depression in sexually selected traits in the cricket Teleogryllus commodus. |
Q39909037 | Strong sexual selection in males against a mutation load that reduces offspring production in seed beetles |
Q33730557 | Superoxide dismutase deficiency impairs olfactory sexual signaling and alters bioenergetic function in mice. |
Q51695533 | Swingin' in the rain: condition dependence and sexual selection in a capricious world. |
Q39516985 | Telomere length and dynamics predict mortality in a wild longitudinal study |
Q46800732 | Territory defense as a condition-dependent component of male reproductive success in Drosophila serrata |
Q51733563 | The capture of heritable variation for genetic quality through social competition. |
Q47906072 | The complex interplay between macronutrient intake, cuticular hydrocarbon expression and mating success in male decorated crickets |
Q44563035 | The condition dependency of fitness in males and females: the fitness consequences of juvenile diet assessed in environments differing in key adult resources |
Q48372694 | The deleterious effects of high inbreeding on male Drosophila melanogaster attractiveness are observed under competitive but not under non-competitive conditions |
Q52579692 | The effect of sexual selection on adaptation and extinction under increasing temperatures. |
Q92963856 | The efficacy of good genes sexual selection under environmental change |
Q37926222 | The evolution and significance of male mate choice |
Q47598352 | The evolution of costly mate choice against segregation distorters. |
Q28235787 | The genetic basis of traits regulating sperm competition and polyandry: can selection favour the evolution of good- and sexy-sperm? |
Q30396395 | The incredible shrinking dewlap: signal size, skin elasticity, and mechanical design in the green anole lizard (Anolis carolinensis). |
Q30465478 | The juvenile social environment introduces variation in the choice and expression of sexually selected traits. |
Q47849965 | The lek mating system of the worm pipefish (Nerophis lumbriciformis): a molecular maternity analysis and test of the phenotype-linked fertility hypothesis |
Q51395738 | The nutritionally responsive transcriptome of the polyphenic beetle Onthophagus taurus and the importance of sexual dimorphism and body region. |
Q46390903 | The origins of extraversion: joint effects of facultative calibration and genetic polymorphism |
Q36793187 | The role of chemical communication in mate choice. |
Q21563530 | The sexually antagonistic genes of Drosophila melanogaster |
Q57266134 | The stability of genetic variance?covariance matrix in the presence of selection |
Q30389513 | The static allometry of sexual and non-sexual traits in vervet monkeys |
Q47262025 | The tale of the shrinking weapon: seasonal changes in nutrition affect weapon size and sexual dimorphism, but not contemporary evolution. |
Q36576404 | The transcriptomic basis of tissue- and nutrition-dependent sexual dimorphism in the beetle Onthophagus taurus |
Q34537790 | Timing of arrival from spring migration is associated with flight performance in the migratory barn swallow |
Q52722102 | Trade-off between warning signal efficacy and mating success in the wood tiger moth. |
Q50981570 | Transcriptome-wide effects of sexual selection on the fate of new mutations. |
Q55894384 | Understanding Heritability: What it is and What it is Not |
Q51542356 | Variation in acoustic signalling traits exhibits footprints of sexual selection |
Q36725682 | Variation in body condition indices of crimson finches by sex, breeding stage, age, time of day, and year |
Q51733729 | Variation in the peacock's train shows a genetic component. |
Q38952345 | What can we infer about the origin of sex in early eukaryotes? |
Q57669767 | What is genetic quality? |
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