| scholarly article | Q13442814 |
| P50 | author | W. D. Hamilton | Q15451 |
| P2093 | author name string | M Zuk | |
| P433 | issue | 4570 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 384-7 | |
| P577 | publication date | 1982-10-22 | |
| P1433 | published in | Science | Q192864 |
| P1476 | title | Heritable true fitness and bright birds: a role for parasites? | |
| P478 | volume | 218 |
| Q51692424 | 'Good-genes' and 'compatible-genes' effects in an Alpine whitefish and the information content of breeding tubercles over the course of the spawning season. |
| Q36387701 | A PHYLOGENETIC PERSPECTIVE ON THE EVOLUTION OF SEXUAL DICHROMATISM IN TANAGERS (THRAUPIDAE): THE ROLE OF FEMALE VERSUS MALE PLUMAGE. |
| Q52227076 | A PRODUCT OF DISCRIMINATIVE LEARNING MAY LEAD TO FEMALE PREFERENCES FOR ELABORATE MALES. |
| Q30383363 | A Paradox of Genetic Variance in Epigamic Traits: Beyond "Good Genes" View of Sexual Selection |
| Q48802588 | A career of many colors |
| Q55969754 | A comparison of infestation patterns by Ixodes ticks in urban and rural populations of the Common Blackbird Turdus merula |
| Q51436032 | A conceptual framework for organismal biology: linking theories, models, and data. |
| Q26740112 | A conceptual review of mate choice: stochastic demography, within-sex phenotypic plasticity, and individual flexibility |
| Q55519955 | A dynamic threshold model for terminal investment. |
| Q52109031 | A female melanin ornament signals offspring fluctuating asymmetry in the barn owl. |
| Q33550584 | A female signal reflects MHC genotype in a social primate |
| Q47839969 | A field reciprocal transplant experiment reveals asymmetric costs of migration between lake and river ecotypes of three-spined sticklebacks (Gasterosteus aculeatus). |
| Q35978794 | A field test of female mate preference for male plumage coloration in eastern bluebirds |
| Q47918744 | A jack-of-all-trades and still a master of some: prevalence and host range in avian malaria and related blood parasites |
| Q52585986 | A mechanistic link between parasite resistance and expression of a sexually selected trait in a damselfly. |
| Q24673107 | A naked ape would have fewer parasites |
| Q44508225 | A restriction site to differentiate Plasmodium and Haemoproteus infections in birds: on the inefficiency of general primers for detection of mixed infections. |
| Q59068515 | A sexually selected character displacement in flycatchers reinforces premating isolation |
| Q51285408 | A structural colour ornament correlates positively with parasite load and body condition in an insular lizard species. |
| Q59178910 | A test of the effect of testosterone on a sexually selected carotenoid trait in a cardueline finch |
| Q35129061 | A tradeoff between immunocompetence and sexual ornamentation in domestic fowl |
| Q39538752 | A typological approach to testing the evolutionary functions of human female orgasm. |
| Q52225680 | ARE WARNING COLORS HANDICAPS? |
| Q60562639 | Abiotic and biotic predictors of macroecological patterns in bird and butterfly coloration |
| Q93009136 | Absence of reproduction-immunity trade-off in male Drosophila melanogaster evolving under differential sexual selection |
| Q107744609 | Acoustic signals in insects: A reproductive barrier and a taxonomic character |
| Q93604237 | Acquired resistance affects male sexual display and female choice in guppies |
| Q34341491 | Activity predicts male reproductive success in a polygynous lizard. |
| Q88641554 | Acute stress, steroid plasma levels, and innate immunity in Brazilian toads |
| Q53401882 | Adiposity signals predict vocal effort in Alston's singing mice. |
| Q51293152 | Adiposity, compared with masculinity, serves as a more valid cue to immunocompetence in human mate choice. |
| Q30450657 | Aesthetic evolution by mate choice: Darwin's really dangerous idea |
| Q30781807 | Afternoon shedding of a new species of Isospora (Apicomplexa) in the endangered Regent Honeyeater (Xanthomyza phrygia). |
| Q57020716 | Age and infection history are revealed by different ornaments in a warbler |
| Q42012182 | Age-dependent trade-offs between immunity and male, but not female, reproduction |
| Q38943534 | Age-dependent trajectories differ between within-pair and extra-pair paternity success. |
| Q52778084 | Age-related sex differences in body condition and telomere dynamics of red-sided garter snakes. |
| Q40114471 | Age-specific patterns of infection with haemosporidians and trypanosomes in a warbler: implications for sexual selection |
| Q64099970 | Air sac trematodes: as a newly identified cause of death in the common blackbird () |
| Q93604385 | Alternative hypotheses linking the immune system and mate choice for good genes |
| Q52676927 | Alternative measures of response to Pseudomonas aeruginosa infection in Drosophila melanogaster. |
| Q57922445 | An ecological role for assortative mating under infection? |
| Q70849889 | An evolutionary perspective on signaling in behavior and immunology |
| Q33277670 | An experimental test for indirect benefits in Drosophila melanogaster |
| Q59662730 | An exploration of the links between parasites, trophic ecology, morphology, and immunogenetics in the Lake Tanganyika cichlid radiation. |
| Q37639797 | An initial evaluation of the functions of human olfaction. |
| Q58422681 | An introduction to ecological immunology |
| Q52701253 | An unexpected advantage of whiteness in horses: the most horsefly-proof horse has a depolarizing white coat. |
| Q59827609 | Animal allure and health linked by plant pigments |
| Q56920386 | Annual changes in the winter song of bowhead whales (Balaena mysticetus) in Disko Bay, Western Greenland |
| Q89565590 | Antlers and parasites |
| Q64951931 | Are avian blood parasites pathogenic in the wild? A medication experiment in blue tits (Parus caeruleus). |
| Q46525906 | Are hotshots always hot? A longitudinal study of hormones, behavior, and reproductive success in male marine iguanas |
| Q44502078 | Are large wattles related to particular MHC genotypes in the male pheasant? |
| Q79968220 | Are secondary sex traits, parasites and immunity related to variation in primary sex traits in the Arctic charr? |
| Q33633321 | Are the immunocompetence and the presence of metazoan parasites in cyprinid fish affected by reproductive efforts of cyprinid fish? |
| Q43652283 | Arrested development of secondary sexual adornments in subordinate adult male mandrills (Mandrillus sphinx). |
| Q38138189 | Art and brain: the relationship of biology and evolution to art. |
| Q57775447 | Artificial selection for increased comb size and its effects on other sexual characters and viability in Gallus domesticus (the domestic chicken) |
| Q34675737 | Assessment of possible ecological risks and hazards of transgenic fish with implications for other sexually reproducing organisms |
| Q46916039 | Association between parasite load and orange, but not blue, male nuptial colouration in Etheostoma caeruleum |
| Q43707940 | Associations between innate immune function and ectoparasites in wild rodent hosts. |
| Q89566035 | Assortative pairing in Gammarus insensibilis (Amphipoda) infected by a trematode parasite |
| Q59071010 | Asymmetry in the evolution of female mating preferences |
| Q56213275 | Attractive Skin Coloration: Harnessing Sexual Selection to Improve Diet and Health |
| Q24522438 | Autumn tree colours as a handicap signal |
| Q46217717 | Avian blood parasites in an endangered columbid: Leucocytozoon marchouxi in the Mauritian Pink Pigeon Columba mayeri |
| Q46276436 | Avian haemosporidian detection across source materials: prevalence and genetic diversity |
| Q50260078 | Avian phenotypic traits related to feeding preferences in two Culex mosquitoes |
| Q57230308 | BLOOD PARASITES IN BRIGHT BIRDS: TESTING THE HAMILTON-ZUK HYPOTHESIS IN SUB-SAHARAN AFRICA WITH AN IMPROVED STATISTICAL METHOD |
| Q33950316 | Background considerations to facial aesthetics |
| Q59049197 | Bacteria mating preferences |
| Q56980509 | Balancing selection on MHC class I in wild brown troutSalmo trutta |
| Q77957015 | Bateman's principle and immunity |
| Q51467634 | Bateman's principle and immunity in a sex-role reversed pipefish. |
| Q82450944 | Beak condition and cage density determine abundance and spatial distribution of northern fowl mites, Ornithonyssus sylviarum, and chicken body lice, Menacanthus stramineus, on caged laying hens |
| Q27026735 | Behavioral Immunity in Insects |
| Q28260307 | Behavioral adaptations to pathogens and parasites: five strategies |
| Q41394631 | Behavioral correlates of extra-pair copulation in Indri indri. |
| Q48685358 | Behavioral genetic variation, adaptation and maladaptation: an evolutionary perspective. |
| Q35598482 | Behavioral reduction of infection risk. |
| Q33887395 | Behavioral, physiological and morphological correlates of parasite intensity in the wild Cururu toad (Rhinella icterica). |
| Q92228522 | Behavioural ecology and infectious disease: implications for conservation of biodiversity |
| Q38791378 | Behavioural, ecological, and evolutionary aspects of diversity in frog colour patterns |
| Q27329716 | Beyond species recognition: somatic state affects long-distance sex pheromone communication |
| Q57780013 | Bill colour pattern in Bewick’s swan: information on sex and body size displayed on face? |
| Q47992104 | Biogeographical patterns and co-occurrence of pathogenic infection across island populations of Berthelot's pipit (Anthus berthelotii). |
| Q29010693 | Birds of Paradise and Mating System Theory — Predictions and Observations |
| Q43256692 | Blood parasitaemia in a high latitude flexible breeder, the white-winged crossbill, Loxia leucoptera: contribution of seasonal relapse versus new inoculations |
| Q34462417 | Blood parasite infection differentially relates to carotenoid-based plumage and bill color in the American goldfinch |
| Q87590839 | Blood parasites and male fitness in the pied flycatcher |
| Q43596476 | Blood parasites in passerine birds from the Brazilian Atlantic Forest |
| Q56946283 | Blood parasites, leucocytes and plumage brightness in the Cirl Bunting, Emberiza cirlus |
| Q38874742 | Blood transcriptomes and de novo identification of candidate loci for mating success in lekking great snipe (Gallinago media). |
| Q40520577 | Body condition is negatively associated with infection with Syngamus trachea in the ring-necked pheasant (Phasianus colchicus). |
| Q101632966 | Body condition, sex and elevation in relation to mite parasitism in a high mountain gecko |
| Q28301642 | Body shape and women's attractiveness : The critical role of waist-to-hip ratio |
| Q28703607 | Bold colors in a cryptic lineage: do Eastern Indigo Snakes exhibit color dimorphism? |
| Q64060859 | Both candidate gene and neutral genetic diversity correlate with parasite resistance in female Mediterranean mouflon |
| Q61458332 | Bower quality, number of decorations and mating success of male satin bowerbirds (Ptilonorhynchus violaceus): an experimental analysis |
| Q81265070 | Brood parasitism by brown-headed cowbirds and the expression of sexual characters in their hosts |
| Q34309347 | By-product information can stabilize the reliability of communication |
| Q43039148 | COSTS AND BENEFITS OF MOSQUITO REFRACTORINESS TO MALARIA PARASITES: IMPLICATIONS FOR GENETIC VARIABILITY OF MOSQUITOES AND GENETIC CONTROL OF MALARIA. |
| Q54094190 | CROSS-RESISTANCE FOLLOWING ARTIFICIAL SELECTION FOR INCREASED DEFENSE AGAINST PARASITOIDS IN DROSOPHILA MELANOGASTER. |
| Q26748478 | Can Neglected Tropical Diseases Compromise Human Wellbeing in Sex-, Age-, and Trait-Specific Ways? |
| Q26747119 | Can environmental change affect host/parasite-mediated speciation? |
| Q28660999 | Can reduced predation offset negative effects of sea louse parasites on chum salmon? |
| Q34509308 | Can sexual selection theory inform genetic management of captive populations? A review |
| Q58937041 | Carotenoid content and reflectance of yellow and red nuptial plumages in widowbirds (Euplectes spp.) |
| Q46448441 | Carotenoid limitation and mate preference evolution: a test of the indicator hypothesis in guppies (Poecilia reticulata). |
| Q47411510 | Carotenoid metabolism strengthens the link between feather coloration and individual quality |
| Q56772841 | Carotenoid-based bill colour is an integrative signal of multiple parasite infection in blackbird |
| Q57921559 | Carotenoid-based colour expression is determined early in nestling life |
| Q53937062 | Carotenoid-based plumage coloration of male greenfinches reflects health and immunocompetence. |
| Q53879167 | Carotenoid-based plumage coloration predicts resistance to a novel parasite in the house finch. |
| Q50449310 | Carotenoid-based plumage colouration is associated with blood parasite richness and stress protein levels in blue tits (Cyanistes caeruleus). |
| Q59178902 | Carotenoid-based plumage colouration is predicted by age and parasites in the male European serin |
| Q80124412 | Carotenoid-dependent coloration of male American kestrels predicts ability to reduce parasitic infections |
| Q80478136 | Carotenoids, immune response and the expression of sexual ornaments in male greenfinches (Carduelis chloris) |
| Q46898679 | Cellular respiration: the nexus of stress, condition, and ornamentation |
| Q43188299 | Chemical composition of scent-gland secretions in an old world monkey (Mandrillus sphinx): influence of sex, male status, and individual identity |
| Q33532195 | Chewing lice (Phthiraptera) on manakins (Passeriformes: Pipridae) from Costa Rica, with description of a new species of the genus Tyranniphilopterus (Phthiraptera: Philopteridae). |
| Q57929325 | Childhood ecology influences salivary testosterone, pubertal age and stature of Bangladeshi UK migrant men |
| Q58992908 | Choosing parasite-free mates |
| Q46633247 | Choosy Wolves? Heterozygote Advantage But No Evidence of MHC-Based Disassortative Mating |
| Q35547625 | Chronic infection. Hidden costs of infection: chronic malaria accelerates telomere degradation and senescence in wild birds |
| Q33979851 | Cloacal bacterial diversity increases with multiple mates: evidence of sexual transmission in female common lizards |
| Q52592108 | Clonal variation and covariation in aphid resistance to parasitoids and a pathogen. |
| Q52048621 | Coevolution of costly mate choice and condition-dependent display of good genes. |
| Q28273046 | Coevolution of hosts and parasites |
| Q36238271 | Coevolution of parasite virulence and host mating strategies |
| Q42989391 | Coevolutionary interactions between host life histories and parasite life cycles |
| Q46281354 | Color Patterning in Hard Ticks (Acari: Ixodidae). |
| Q87342681 | Colorful displays signal male quality in a tropical anole lizard |
| Q54958066 | Colour for Behavioural Success. |
| Q28066919 | Coloured ornamental traits could be effective and non-invasive indicators of pollution exposure for wildlife |
| Q33291746 | Common HLA alleles associated with health, but not with facial attractiveness |
| Q34214276 | Comparative biology of aging in birds: an update |
| Q55100056 | Comparative study of semen traits and histomorphometric features of testes of broiler breeder males with different phenotypic traits. |
| Q52569857 | Complex Mhc-based mate choice in a wild passerine. |
| Q34142124 | Complex adaptive responses during antagonistic coevolution between Tribolium castaneum and its natural parasite Nosema whitei revealed by multiple fitness components |
| Q38335955 | Condition-dependence, pleiotropy and the handicap principle of sexual selection in melanin-based colouration |
| Q50690631 | Condition-dependent expression of red colour differs between stickleback species. |
| Q27330023 | Condition-dependent reproductive effort in frogs infected by a widespread pathogen |
| Q38952362 | Condition-dependent sex: who does it, when and why? |
| Q93605247 | Condition-dependent variation in the blue-ultraviolet coloration of a structurally based plumage ornament |
| Q57899043 | Conditional Handicaps in Exuberant Lizards: Bright Color in Aggressive Males Is Correlated with High Levels of Free Radicals |
| Q91706601 | Conspecific infection threat rapidly biases the social responses of female mice: Involvement of oxytocin |
| Q101402478 | Conspecifics of the Striped Lava Lizard are able to distinguish sex and male colour morphs in apparently homogeneous dull dorsal colouration |
| Q57515062 | Conspicuous sexual signals in a socially monogamous passerine: the case of neotropical Blue-black Grassquits |
| Q92134404 | Contrasting associations between breeding coloration and parasitism of male Arctic charr relate to parasite species and life cycle stage |
| Q51508365 | Contributions of natural and sexual selection to the evolution of premating reproductive isolation: a research agenda. |
| Q33910327 | Corticosterone: a costly mediator of signal honesty in sand lizards |
| Q35004460 | Costly infidelity: low lifetime fitness of extra-pair offspring in a passerine bird |
| Q35101094 | Costly parasite resistance: a genotype-dependent handicap in sand lizards? |
| Q34572750 | Costly resistance to parasitism: evidence from simultaneous quantitative trait loci mapping for resistance and fitness in Tribolium castaneum |
| Q92157015 | Costly signaling and the handicap principle in hunter-gatherer research: A critical review |
| Q52653580 | Costs of an induced immune response on sexual display and longevity in field crickets. |
| Q55485834 | Costs of injury for scent signalling in a strepsirrhine primate. |
| Q33900472 | Costs of reproduction in a long-lived female primate: injury risk and wound healing |
| Q34092376 | Costs of sexual traits: a mismatch between theoretical considerations and empirical evidence |
| Q30049339 | Courtship displays and coloration as indicators of safety rather than of male quality : the safety assurance hyposthesis |
| Q33861928 | Cultural sexual selection in monogamous human populations |
| Q50025159 | Cycle-specific female preferences for visual and non-visual cues in the horse (Equus caballus). |
| Q47232701 | Dance reveals symmetry especially in young men. |
| Q35559350 | Darwinian aesthetics: sexual selection and the biology of beauty. |
| Q24617156 | Darwinian medicine: applications of evolutionary biology for veterinarians |
| Q62564053 | Defences against brood parasites from a social immunity perspective |
| Q37905945 | Delayed plumage maturation and delayed reproductive investment in birds |
| Q40985387 | Demasculinization of male guppies increases resistance to a common and harmful ectoparasite |
| Q96230412 | Demographic and reproductive associations with nematode infection in a long-lived mammal |
| Q26315281 | Detection, prevalence, and transmission of avian hematozoa in waterfowl at the Arctic/sub-Arctic interface: co-infections, viral interactions, and sources of variation |
| Q52203564 | Developmental isolation and subsequent adult behavior of Drosophila paulistorum. II. prior experience. |
| Q48704929 | Developmental stress, condition, and birdsong: a case study in song sparrows |
| Q30477687 | Different Vocal Parameters Predict Perceptions of Dominance and Attractiveness |
| Q41330099 | Different ornaments signal male health and MHC variation in two populations of a warbler |
| Q73009723 | Differential effects of endoparasitism on the expression of carotenoid- and melanin-based ornamental coloration |
| Q55921325 | Differential parasitaemia in the tawny owl (Strix aluco): effects of colour morph and habitat |
| Q36016328 | Differential prevalence and diversity of haemosporidian parasites in two sympatric closely related non-migratory passerines |
| Q38883570 | Dim light at night interferes with the development of the short-day phenotype and impairs cell-mediated immunity in Siberian hamsters (Phodopus sungorus). |
| Q68347778 | Diploid models of the handicap principle |
| Q24807199 | Direct selection on male attractiveness and female preference fails to produce a response |
| Q26863545 | Disease avoidance as a functional basis for stigmatization |
| Q39240679 | Disease in the dark: molecular characterization of Polychromophilus murinus in temperate zone bats revealed a worldwide distribution of this malaria-like disease |
| Q57579412 | Distress calls reflect poxvirus infection in lesser short-toed lark Calandrella rufescens |
| Q35045231 | Distribution pattern of apicomplexan parasites (Sporozoa: Haemosporida) in Columba livia, Gmelin |
| Q101631391 | Diurnal colour change in a sexually dimorphic trait in the Andean lizard Anolis heterodermus (Squamata: Dactyloidae) |
| Q91155426 | Divergent color signals from homologous unfeathered ornaments in two congeneric grouse |
| Q36032747 | Diversifying Selection Between Pure-Breed and Free-Breeding Dogs Inferred from Genome-Wide SNP Analysis |
| Q64132938 | Do facial averageness and symmetry signal health? |
| Q50632099 | Do feather-degrading bacteria affect sexually selected plumage color? |
| Q90015623 | Do glucocorticoids or carotenoids mediate plumage coloration in parrots? An experiment in Platycercus elegans |
| Q36733532 | Do men's faces really signal heritable immunocompetence? |
| Q56935394 | Do parasites matter? Assessing the fitness consequences of haemogregarine infection in snakes |
| Q53960392 | Do pheromones reveal male immunocompetence? |
| Q51575946 | Does egg colouration reflect male condition in birds? |
| Q21562150 | Does masculinity matter? The contribution of masculine face shape to male attractiveness in humans |
| Q37105352 | Does multiple paternity influence offspring disease resistance? |
| Q48165381 | Does nonreproductive swarming adapt to pathogens? |
| Q34998250 | Does sexual selection explain human sex differences in aggression? |
| Q30393164 | Dominant male song performance reflects current immune state in a cooperatively breeding songbird. |
| Q51146560 | Dose-dependent effects of an immune challenge at both ultimate and proximate levels in Drosophila melanogaster. |
| Q80384847 | Dual functions of a melanin-based ornament in the common yellowthroat |
| Q33379426 | Dynamic feedback between phenotype and physiology in sexually selected traits |
| Q90142021 | Dynamic phenotypic correlates of social status and mating effort in male and female red junglefowl, Gallus gallus |
| Q39999881 | Dynamic selective environments and evolutionary traps in human-dominated landscapes |
| Q38288475 | Dynamics of Mhc evolution in birds and crocodilians: amplification of class II genes with degenerate primers |
| Q60503528 | Dynamics of an immune response in house sparrows Passer domesticus in relation to time of day, body condition and blood parasite infection |
| Q39362051 | EFFECT OF ECTOPARASITIC MITES ON SEXUAL SELECTION IN A SONORAN DESERT FRUIT FLY. |
| Q57915321 | Early Life-History Effects, Oxidative Stress, and the Evolution and Expression of Animal Signals |
| Q46845962 | Early life stress shapes female reproductive strategy through eggshell pigmentation in Japanese quail. |
| Q88884768 | Ecological and Evolutionary Consequences of Parasite Avoidance |
| Q37505445 | Ecological immunology of mosquito-malaria interactions: Of non-natural versus natural model systems and their inferences |
| Q34051578 | Economic game theory for mutualism and cooperation. |
| Q35540351 | Ectoparasites and fitness of female Columbian ground squirrels |
| Q87587620 | Ectoparasitism as a possible cost of social life: a comparative analysis using Australian passerines (Passeriformes) |
| Q59812738 | Effects of blood parasite infection and innate immune genetic diversity on mating patterns in a passerine bird breeding in contrasted habitats |
| Q51535391 | Effects of egg testosterone on female mate choice and male sexual behavior in the pheasant. |
| Q58376715 | Effects of heterozygosity and MHC diversity on patterns of extra-pair paternity in the socially monogamous scarlet rosefinch |
| Q57671693 | Effects of juvenile infection on adult immunity and secondary sexual characters in a wolf spider |
| Q37451850 | Effects of parasitism and morphology on squirrelpox virus seroprevalence in grey squirrels (Sciurus carolinensis). |
| Q51719525 | Effects of testosterone and corticosterone on immunocompetence in the zebra finch. |
| Q39617906 | Effects of the parasitic botfly Philornis carinatus on nestling house wrens, Troglodytes aedon, in Costa Rica |
| Q57920922 | Eggshell pigmentation in the blue tit: male quality matters |
| Q34131166 | Ejaculate economics: testing the effects of male sexual history on the trade-off between sperm and immune function in Australian crickets |
| Q37025431 | Embryonic development period and the prevalence of avian blood parasites |
| Q57898316 | Emerging infectious disease selects for darker plumage coloration in greenfinches |
| Q40569585 | Empirical evidence for key hosts in persistence of a tick-borne disease |
| Q39211181 | Endocrine-reproductive-immune interactions in female and male Galápagos marine iguanas |
| Q53811248 | Energetic cost of tail streamers in the barn swallow (Hirundo rustica). |
| Q51747367 | Energetic costs of parasitism in the Cape ground squirrel Xerus inauris. |
| Q39188945 | Enhanced male coloration after immune challenge increases reproductive potential |
| Q49146500 | Environmental tracking by females : Sexual lability |
| Q28261345 | Epidemiology and genetics in the coevolution of parasites and hosts |
| Q39027595 | Estimating heritable genetic contributions to innate immune and endocrine phenotypic correlations: A need to explore repeatability |
| Q37988614 | Estrogenic involvement in social learning, social recognition and pathogen avoidance |
| Q50120601 | Evidence for sexual selection on structural plumage coloration in female eastern bluebirds (Sialia sialis). |
| Q34277744 | Evidence for the 'good genes' model: association of MHC class II DRB alleles with ectoparasitism and reproductive state in the neotropical lesser bulldog bat, Noctilio albiventris |
| Q45215016 | Evidence that sensory traps can evolve into honest signals |
| Q39023932 | Evolution of Sex Differences in Trait- and Age-Specific Vulnerabilities |
| Q28755308 | Evolution of an avian pigmentation gene correlates with a measure of sexual selection |
| Q35816548 | Evolution of human mate choice |
| Q68660512 | Evolution of increased susceptibility to infectious diseases in age structured populations |
| Q56084289 | Evolution of sexual dichromatism: contribution of carotenoid- versus melanin-based coloration |
| Q59094005 | Evolution: Contentious issues in sexual selection |
| Q38967197 | Evolutionary associations between host traits and parasite load: insights from Lake Tanganyika cichlids |
| Q37899274 | Evolutionary causes and consequences of sequential polyandry in anuran amphibians. |
| Q39015328 | Evolutionary framework for identifying sex- and species-specific vulnerabilities in brain development and functions |
| Q46475458 | Evolutionary innovation and diversification of carotenoid-based pigmentation in finches |
| Q35721485 | Experimental constraints on mate preferences in Drosophila pseudoobscura decrease offspring viability and fitness of mated pairs |
| Q55434816 | Experimental evidence for paternal effects on offspring growth rate in Arctic charr (Salvelinus alpinus). |
| Q38567233 | Experimental evidence of genetic determinism in high susceptibility to intestinal pinworm infection in mice: a hybrid zone model |
| Q51712272 | Experimental evolution of parasite life-history traits in Strongyloides ratti (Nematoda). |
| Q37062608 | Experimental evolution reveals trade-offs between mating and immunity |
| Q40423055 | Experimental removal of the male parent negatively affects growth and immunocompetence in nestling great tits |
| Q47552698 | Experimental stress during molt suggests the evolution of condition-dependent and condition-independent ornaments in the king penguin |
| Q85028579 | Experimental test of a trade‐off between moult and immune response in house sparrows Passer domesticus |
| Q46879026 | Experimentally elevated levels of testosterone at independence reduce fitness in a territorial bird. |
| Q48490092 | Extending parasite-stress theory to variation in human mate preferences |
| Q50655752 | Extra-pair paternity in relation to male age in Bullock's orioles |
| Q60939215 | Facial Adiposity, Attractiveness, and Health: A Review |
| Q39904685 | Facial adiposity: a cue to health? |
| Q41287392 | Facial appearance reveals immunity in African men. |
| Q36159283 | Factors affecting male song evolution in Drosophila montana |
| Q46348622 | Family and population effects on disease resistance in a reptile. |
| Q43904621 | Fat stores in a migratory bird: a reservoir of carotenoid pigments for times of need? |
| Q55546277 | Female Japanese quail visually differentiate testosterone-dependent male attractiveness for mating preferences. |
| Q50983055 | Female Mice Avoid Male Odor from the Same Strain via the Vomeronasal System in an Estrogen-Dependent Manner. |
| Q60302802 | Female assortative mate choice functionally validates synthesized male odours of evolving stickleback river–lake ecotypes |
| Q54048206 | Female barn owls (Tyto alba) advertise good genes. |
| Q55627642 | Female blue tits adjust parental effort to manipulated male UV attractiveness. |
| Q57159508 | Female choice and annual reproductive success favour less-ornamented male house sparrows |
| Q51473204 | Female choice for male motor skills. |
| Q35762315 | Female choice reveals terminal investment in male mealworm beetles, Tenebrio molitor, after a repeated activation of the immune system |
| Q56287174 | Female choice selects for a viability-based male trait in pheasants |
| Q30050496 | Female choice selects for male sexual tail ornaments in the monogamous swallow |
| Q48648920 | Female choice via indicator traits easily evolves in the face of recombination and migration |
| Q51425431 | Female goats use courtship display as an honest indicator of male quality. |
| Q33456948 | Female host sex-biased parasitism with the rodent stomach nematode Mastophorus muris in wild bank voles (Myodes glareolus). |
| Q56940663 | Female lizards discriminate between potential reproductive partners using multiple male traits when territory cues are absent |
| Q92981039 | Female loggerhead sea turtles (Caretta caretta L.) rarely remate during nesting season |
| Q77333613 | Female mating strategy in an enclosed group of Japanese macaques |
| Q38063593 | Female ornaments revisited - are they correlated with offspring quality? |
| Q30443805 | Female partner preferences enhance offspring ability to survive an infection |
| Q59067825 | Female pied flycatchers choose territory quality and not male characteristics |
| Q37677508 | Female plumage colour influences seasonal oxidative damage and testosterone profiles in a songbird |
| Q37970472 | Female postmating immune responses, immune system evolution and immunogenic males |
| Q46443185 | Female soldier beetles display a flexible preference for selectively favored male phenotypes |
| Q44394983 | Female sticklebacks count alleles in a strategy of sexual selection explaining MHC polymorphism |
| Q56287978 | Female sticklebacks use male coloration in mate choice and hence avoid parasitized males |
| Q81281902 | Female throat ornamentation does not reflect cell-mediated immune response in bluethroats Luscinia s. svecica |
| Q51150499 | Females choose gentle, but not healthy or macho males in Campbell dwarf hamsters (Phodopus campbelli Thomas 1905). |
| Q48423249 | Fertility cycle patterns in motives for sexual behavior |
| Q38836772 | Field endocrinology of nonhuman primates: past, present, and future |
| Q93603545 | Fish pheromones and evolutionary enigmas: a reply to Smith |
| Q33354325 | Fitness consequences of female multiple mating: a direct test of indirect benefits |
| Q30483399 | Fluctuating asymmetry and preferences for sex-typical bodily characteristics |
| Q22252811 | Fluctuating asymmetry and sexual selection |
| Q91989492 | Flying into the future: avian haemosporidians and the advancement of understanding host-parasite systems |
| Q55564159 | Frequency-dependent incidence in models of sexually transmitted diseases: portrayal of pair-based transmission and effects of illness on contact behaviour. |
| Q57864478 | Gastrointestinal parasites of Asian elephants ( L. 1798) in south Wayanad forest division, Kerala, India |
| Q52576756 | Gender differences and individual variation in the immune system of the scorpionfly Panorpa vulgaris (Insecta: Mecoptera). |
| Q33915740 | Genetic compatibility, mate choice and patterns of parentage: invited review. |
| Q35939182 | Genetic conflict between sexual signalling and juvenile survival in the three-spined stickleback |
| Q48032979 | Genetic correlations and sex-specific adaptation in changing environments |
| Q24813939 | Genetic covariance between indices of body condition and immunocompetence in a passerine bird |
| Q34133342 | Genetic diversity and reproductive success in mandrills (Mandrillus sphinx) |
| Q34062170 | Genetic diversity in cytokines associated with immune variation and resistance to multiple pathogens in a natural rodent population |
| Q52661237 | Genetic linkage between a sexually selected trait and X chromosome meiotic drive. |
| Q35014050 | Genetic regulation of parasite infection: empirical evidence of the functional significance of an IL4 gene SNP on nematode infections in wild primates |
| Q42047831 | Genetic variability in the diapause response of the burnet moth Zygaena trifolii (Lepidoptera: Zygaenidae). |
| Q42055962 | Genetic variance of sexually selected traits in waxmoths: maintenance by genotype x environment interaction. |
| Q36571809 | Genetic variation affecting host-parasite interactions: different genes affect different aspects of sigma virus replication and transmission in Drosophila melanogaster |
| Q35741451 | Genetic variation in Drosophila melanogaster pathogen susceptibility |
| Q52646276 | Genetic variation in infestation with a directly transmitted ectoparasite. |
| Q60094100 | Genetics of long-spurred pheasants |
| Q36479169 | Genic capture and resolving the lek paradox. |
| Q35411661 | Genitalia-associated microbes in insects |
| Q57072628 | Genome Sequence of Peacock Reveals the Peculiar Case of a Glittering Bird |
| Q50440346 | Genome-wide association and genome partitioning reveal novel genomic regions underlying variation in gastrointestinal nematode burden in a wild bird |
| Q39323492 | Genomics of coloration in natural animal populations |
| Q54102453 | Good genes, oxidative stress and condition-dependent sexual signals. |
| Q21283973 | Good vs complementary genes for parasite resistance and the evolution of mate choice |
| Q93604922 | Good-genes effects in sexual selection |
| Q51368084 | Grasshopper calling songs convey information about condition and health of males. |
| Q87590028 | Gregariousness versus solitude: another look at parasite faunal richness in Canadian freshwater fishes |
| Q33459303 | HERITABILITIES OF DOMINANCE-RELATED TRAITS IN MALE BANK VOLES (CLETHRIONOMYS GLAREOLUS). |
| Q35015777 | Habitat, world geographic range, and embryonic development of hosts explain the prevalence of avian hematozoa at small spatial and phylogenetic scales |
| Q56946261 | Haematozoan Parasites and Migratory Behaviour in Waterfowl |
| Q41392816 | Haemoproteus infected birds have increased lifetime reproductive success |
| Q52287289 | Hamilton and Zuk meet heterozygosity? Song repertoire size indicates inbreeding and immunity in song sparrows (Melospiza melodia). |
| Q48545916 | Has the inbreeding load for a condition-dependent sexual signalling trait been purged in insular lizard populations? |
| Q45179407 | Helminth egg excretion with regard to age, gender and management practices on UK Thoroughbred studs |
| Q44743832 | Helminth parasites of the blue-footed booby on Isla Isabel, México |
| Q47918207 | Hematological responses to hematozoa in North American and neotropical songbirds |
| Q59088505 | Heritable variation in a plumage indicator of viability in male great tits Parus major |
| Q54085755 | Heritable variation in resistance to gastro-intestinal nematodes in an unmanaged mammal population. |
| Q51635991 | Heterozygosity-based assortative mating in blue tits (Cyanistes caeruleus): implications for the evolution of mate choice. |
| Q100503948 | High fidelity defines the temporal consistency of host-parasite interactions in a tropical coastal ecosystem |
| Q38648613 | Higher risk of gastrointestinal parasite infection at lower elevation suggests possible constraints in the distributional niche of Alpine marmots |
| Q51297235 | Highly polymorphic colour vision in a New World monkey with red facial skin, the bald uakari (Cacajao calvus). |
| Q42493689 | Histomorphological study of the preputial and clitoral glands in BALB/c mice with experimental Taenia crassiceps infections. |
| Q50463556 | Honest sexual signaling in turtles: experimental evidence of a trade-off between immune response and coloration in red-eared sliders Trachemys scripta elegans |
| Q60330312 | Honest sexual signalling mediated by parasite and testosterone effects on oxidative balance |
| Q57159544 | Hormonal basis of sexual dimorphism in birds: implications for new theories of sexual selection |
| Q34080545 | Hormones and mating system affect sex and species differences in immune function among vertebrates |
| Q36307092 | Host associations and turnover of haemosporidian parasites in manakins (Aves: Pipridae). |
| Q41735710 | Host behavior alters spiny lobster-viral disease dynamics: a simulation study |
| Q60537684 | Host specificity in avian blood parasites: a study of Plasmodium and Haemoproteus mitochondrial DNA amplified from birds |
| Q50504879 | Host-parasite coevolution induces selection for condition-dependent sex. |
| Q35956477 | Housing condition alters immunological and reproductive responses to day length in Siberian hamsters (Phodopus sungorus). |
| Q58200737 | How coccidian parasites affect health and appearance of greenfinches |
| Q46049083 | How do host sex and reproductive state affect host preference and feeding duration of ticks? |
| Q51198130 | How to get the most bang for your buck: the evolution and physiology of nutrition-dependent resource allocation strategies. |
| Q46932925 | Human body morphology, prevalence of nasopharyngeal potential bacterial pathogens, and immunocompetence handicap principal |
| Q39323546 | Human colour in mate choice and competition |
| Q58298944 | Human communication and contemporary evolutionary theory |
| Q47724610 | Human facial beauty : Averageness, symmetry, and parasite resistance. |
| Q73485266 | Human fertility variation, size-related obstetrical performance and the evolution of sexual stature dimorphism |
| Q79393502 | Human parental effort and environmental risk |
| Q51168775 | Humans as a model species for sexual selection research. |
| Q64102723 | Immune Defenses of a Beneficial Pest: The Mealworm Beetle, |
| Q51332203 | Immune activation decreases sperm viability in both sexes and influences female sperm storage. |
| Q43212663 | Immune activation suppresses plasma testosterone level: a meta-analysis. |
| Q51107249 | Immune challenges and visual signalling in tree frogs. |
| Q51698962 | Immune defense and reproductive pace of life in Peromyscus mice. |
| Q21090815 | Immune investment is explained by sexual selection and pace-of-life, but not longevity in parrots (Psittaciformes) |
| Q57064978 | Immune response costs are associated with changes in resource acquisition and not resource reallocation |
| Q34608905 | Immune responses of a native and an invasive bird to Buggy Creek Virus (Togaviridae: Alphavirus) and its arthropod vector, the swallow bug (Oeciacus vicarius). |
| Q53669815 | Immune system evolution among anthropoid primates: parasites, injuries and predators. |
| Q34044861 | Immune-mediated change in the expression of a sexual trait predicts offspring survival in the wild |
| Q93605842 | Immunocompetence of nestling great tits in relation to rearing environment and parentage |
| Q35954165 | Immunocompetence, ornamentation, and viability of male barn swallows (Hirundo rustica) |
| Q34310296 | Immunological sex differences in socially promiscuous African ground squirrels |
| Q48208913 | Impaired discrimination of and aversion to parasitized male odors by female oxytocin knockout mice. |
| Q41118085 | Imperfect past and present progressive: beak color reflects early-life and adult exposure to antigen |
| Q34573102 | Inadvertent social information and the avoidance of parasitized male mice: a role for oxytocin. |
| Q28257255 | Inbreeding affects sexual signalling in males but not females of Tenebrio molitor |
| Q79170352 | Inbreeding depresses immune response in song sparrows (Melospiza melodia): direct and inter–generational effects |
| Q37428662 | Individual Facial Coloration in Male Eulemur fulvus rufus: A Condition-dependent Ornament? |
| Q51703553 | Individual MHC class I and MHC class IIB diversities are associated with male and female reproductive traits in the three-spined stickleback. |
| Q51615504 | Individual quality: tautology or biological reality? |
| Q35292227 | Infection before pregnancy affects immunity and response to social challenge in the next generation |
| Q57230222 | Infection prevalence and absence of positive correlation between avian haemosporidian parasites, mass and body condition in the Cape Weaver Ploceus capensis |
| Q93034935 | Infestation of small seabirds by Ornithodoros maritimus ticks: Effects on chick body condition, reproduction and associated infectious agents |
| Q37220408 | Influence of HLA on human partnership and sexual satisfaction |
| Q33642423 | Influence of host reproductive state on Sphaerothecum destruens prevalence and infection level |
| Q51664595 | Influence of major histocompatibility complex genotype on mating success in a free-ranging reptile population. |
| Q46556907 | Influence of temporal variation and host condition on helminth abundance in the lizard Tropidurus hispidus from north-eastern Brazil |
| Q104207851 | Insect Immunity: An Evolutionary Ecology Perspective |
| Q33789115 | Insularity effects on bird immune parameters: A comparison between island and mainland populations in West Africa |
| Q73179386 | Integrating different levels of analysis in the study of mate choice and mating systems in vertebrates |
| Q57159470 | Interspecific variation in plumage colour among birds: species recognition or light environment? |
| Q43148286 | Introduction. Ecological immunology |
| Q28603606 | Invaded Invaders: Infection of Invasive Brown Treesnakes on Guam by an Exotic Larval Cestode with a Life Cycle Comprised of Non-Native Hosts |
| Q56945937 | Is bill colouration in wild male Blackbirds (Turdus merula) related to biochemistry parameters and parasitism? |
| Q56078415 | Is cod lekking or a promiscuous group spawner? |
| Q98946745 | Is it best on the nest? Effects of avian life-history on haemosporidian parasitism |
| Q35080113 | Is sexual ornamentation an honest signal of male quality in the Chinese grouse (Tetrastes sewerzowi)? |
| Q92141440 | It's Not about Him: Mismeasuring 'Good Genes' in Sexual Selection |
| Q52657195 | Juvenile immune system activation induces a costly upregulation of adult immunity in field crickets Gryllus campestris. |
| Q28250761 | Koinophilia groups sexual creatures into species, promotes stasis, and stabilizes social behaviour |
| Q37413521 | Lab and field experiments: are they the same animal? |
| Q56020649 | Lekking in the black grouse— a test of male viability |
| Q54284258 | Leucocytozoon toddiin British sparrowhawksAccipiter nisus: observations on the dynamics of infection |
| Q58298808 | Life History Theory and Evolutionary Psychology |
| Q40328438 | Life-history strategy determines constraints on immune function |
| Q35696836 | Liking the good guys: amplifying local adaptation via the evolution of condition-dependent mate choice. |
| Q31094222 | Linkage between mitochondrial cytochrome b lineages and morphospecies of two avian malaria parasites, with a description of Plasmodium (Novyella) ashfordi sp. nov. |
| Q45039726 | Linkage between nuclear and mitochondrial DNA sequences in avian malaria parasites: multiple cases of cryptic speciation? |
| Q57134787 | Links between blood parasites, blood chemistry, and the survival of nestling American crows |
| Q83497798 | Litter quality and inflammatory response are dependent on mating strategy in a reptile |
| Q57127503 | Long-term epidemiology, effect on body condition and interspecific interactions of concomitant infection by nasopharyngeal bot fly larvae (Cephenemyia auribarbis and Pharyngomyia picta, Oestridae) in a population of Iberian red deer (Cervus elaphus h |
| Q35701655 | Long-term maternal effect on offspring immune response in song sparrows Melospiza melodia |
| Q51580125 | Low prevalence of Haemoproteus infections in Chiffchaffs. |
| Q33294709 | MHC adaptive divergence between closely related and sympatric African cichlids |
| Q35614762 | MHC class II-assortative mate choice in European badgers (Meles meles). |
| Q48046565 | MHC diversity and mate choice in the magellanic penguin, Spheniscus magellanicus |
| Q51339398 | MHC genotype predicts mate choice in the ring-necked pheasant Phasianus colchicus. |
| Q43968586 | MHC variation is related to a sexually selected ornament, survival, and parasite resistance in common yellowthroats |
| Q40863893 | MHC, parasites and antler development in red deer: no support for the Hamilton & Zuk hypothesis. |
| Q34261452 | Macroevolutionary Immunology: A Role for Immunity in the Diversification of Animal life |
| Q34784229 | Maintaining microendemic primate species along an environmental gradient - parasites as drivers for species differentiation |
| Q36943825 | Maintenance of genetic variation in sexual ornaments: a review of the mechanisms |
| Q51171426 | Major histocompatibility complex and mate choice in the polygynous primate: the Sichuan snub-nosed monkey (Rhinopithecus roxellana). |
| Q47833900 | Malaria and risk of predation: a comparative study of birds |
| Q41176943 | Malarial parasites of lizards: diversity and ecology |
| Q47989501 | Malarial parasitism and male competition for mates in the western fence lizard, Sceloporus occidentalis |
| Q57064568 | Male Aggression and Mating Opportunity in a Poeciliid Fish |
| Q44691517 | Male attractiveness, fertility and susceptibility to oxidative stress are influenced by inbreeding in Drosophila simulans. |
| Q54043924 | Male calling song provides a reliable signal of immune function in a cricket. |
| Q56287170 | Male characteristics, viability and harem size in the pheasant, Phasianus colchicus |
| Q38906602 | Male eastern bluebirds trade future ornamentation for current reproductive investment |
| Q21284106 | Male mate choice scales female ornament allometry in a cichlid fish |
| Q59024994 | Male morph predicts investment in larval immune function in the dung beetle, Onthophagus taurus |
| Q35604775 | Male ornament size as a reliable cue to enhanced offspring viability in the barn swallow |
| Q58393363 | Male quality, dominance rank, and mating success in free-ranging rhesus macaques |
| Q42609177 | Male reproductive strategy and the importance of maternal status in the Antarctic fur seal Arctocephalus gazella |
| Q21131910 | Males of a strongly polygynous species consume more poisonous food than females |
| Q58307106 | Manipulation of parasite load induces significant changes in the structural-based throat color of male iberian green lizards |
| Q21124201 | Markedly Elevated Antibody Responses in Wild versus Captive Spotted Hyenas Show that Environmental and Ecological Factors Are Important Modulators of Immunity |
| Q37645481 | Mate choice for major histocompatibility complex complementarity in a strictly monogamous bird, the grey partridge (Perdix perdix) |
| Q35038215 | Mate choice in modern societies : Testing evolutionary hypotheses with behavioral data |
| Q35132242 | Mate preference of female blue tits varies with experimental photoperiod |
| Q51542191 | Maternal investment of female mallards is influenced by male carotenoid-based coloration |
| Q37153065 | Maternal transfer of antibodies in vertebrates: trans-generational effects on offspring immunity |
| Q52459403 | Mating ability in laboratory-adapted and field-derived Drosophila melanogaster: the stress of domestication. |
| Q46324175 | Mechanisms and consequences of diversity-generating immune strategies. |
| Q28072124 | Meeting the Vitamin A Requirement: The Efficacy and Importance of β-Carotene in Animal Species |
| Q52572231 | Meiotic drive and evolution of female choice. |
| Q77071250 | Melatonin, immunity and cost of reproductive state in male European starlings |
| Q46475643 | Meta-analysis suggests choosy females get sexy sons more than "good genes". |
| Q33778300 | Microbes and masculinity: Does exposure to pathogenic cues alter women's preferences for male facial masculinity and beardedness? |
| Q40748047 | Mite choice generates sex- and size-biased infection in Drosophila hydei |
| Q91791504 | Mite load predicts the quality of sexual color and locomotor performance in a sexually dichromatic lizard |
| Q38907926 | Mitochondrial function, ornamentation, and immunocompetence |
| Q28084988 | Mitonuclear Ecology |
| Q57897386 | Modeling the impact of selective harvesting on red deer antlers |
| Q37657401 | Molecular biology and parasites |
| Q48086651 | Molecular characterization of three Mhc class II B haplotypes in the ring-necked pheasant |
| Q58779000 | Molecular survey of coccidian infections of the side-blotched lizard Uta stansburiana on San Benito Oeste Island, Mexico |
| Q50901164 | Monogamy versus Consensual Non-Monogamy: Alternative Approaches to Pursuing a Strategically Pluralistic Mating Strategy. |
| Q55439062 | Mothers produce less aggressive sons with altered immunity when there is a threat of disease during pregnancy. |
| Q46903754 | Multi-mode fluctuating selection in host-parasite coevolution |
| Q58307116 | Multiple color patches and parasites in Sceloporus occidentalis: differential relationships by sex and infection |
| Q101564277 | Mutual mate choice and its benefits for both sexes |
| Q50481022 | Negative correlation between nuptial throat colour and blood parasite load in male European green lizards supports the Hamilton-Zuk hypothesis. |
| Q35960944 | Negative relationships between cellular immune response, Mhc class II heterozygosity and secondary sexual trait in the montane water vole |
| Q34117911 | Neighbours' breeding success and the sex ratio of their offspring affect the mate preferences of female zebra finches |
| Q36645470 | Nematode parasites reduce carotenoid-based signalling in male red grouse |
| Q34080537 | Nest desertion is not predicted by cuckoldry in the Eurasian penduline tit. |
| Q36666005 | Nestling immune response to phytohaemagglutinin is not heritable in collared flycatchers |
| Q37191058 | Neural computations with mammalian infochemicals |
| Q46631199 | Neural network for female mate preference, trained by a genetic algorithm. |
| Q37482475 | Neuroendocrinology of social information processing in rats and mice. |
| Q46276519 | New Host Records for Haemoproteus Spp. (Apicomplexa: Haemosporidiasina) in Passeriformes from North-West of Iran |
| Q50859294 | New perspectives on mate choice and the MHC. |
| Q46015266 | New(t)s and views from hybridizing MHC genes: introgression rather than trans-species polymorphism may shape allelic repertoires. |
| Q57566228 | Next steps for understanding the selective relevance of female-female competition |
| Q41464656 | No evidence for MHC class I-based disassortative mating in a wild population of great tits. |
| Q57136434 | No evidence for MHC-based mate choice in wild giant pandas |
| Q55033958 | No evidence for the immunocompetence handicap hypothesis in male humans. |
| Q46314002 | No mutual mate choice for quality in zebra finches: Time to question a widely held assumption |
| Q38651275 | No speed dating please! Patterns of social preference in male and female house mice |
| Q50997320 | Non-random fertilization in mice correlates with the MHC and something else. |
| Q51295499 | Nongenetic inheritance and the evolution of costly female preference. |
| Q51902584 | Odour signals major histocompatibility complex genotype in an Old World monkey. |
| Q41987924 | Oil pollution increases plasma antioxidants but reduces coloration in a seabird |
| Q85632905 | Olfactory sexual inhibition and the westermarck effect |
| Q51998411 | Olfactory-mediated parasite recognition and avoidance: linking genes to behavior. |
| Q54695040 | On partitioning the opportunity for sexual selection |
| Q53857244 | On sex differences in optimal immunity. |
| Q30486901 | On sexual dimorphism in immune function |
| Q55456912 | On the function of female ornaments: male bluethroats prefer colourful females. |
| Q57893524 | On the measurement and classification of colour in studies of animal colour patterns |
| Q58575238 | Opposed elevational variation in prevalence and intensity of endoparasites and their vectors in a lizard |
| Q50675287 | Ornamental comb colour predicts T-cell-mediated immunity in male red grouse Lagopus lagopus scoticus. |
| Q58601397 | Overcoming mechanical adversity in extreme hindleg weapons |
| Q45419859 | Oxidative damage and plasma antioxidant capacity in relation to body size, age, male sexual traits and female reproductive performance in the collared flycatcher (Ficedula albicollis). |
| Q37273846 | Oxidative stress in ecology and evolution: lessons from avian studies. |
| Q36392657 | PARASITE LOAD, BODY SIZE, AND AGE OF WILD-CAUGHT MALE FIELD CRICKETS (ORTHOPTERA: GRYLLIDAE): EFFECTS ON SEXUAL SELECTION. |
| Q53914005 | PARASITE-MEDIATED SELECTION AGAINST INBRED SOAY SHEEP IN A FREE-LIVING ISLAND POPULATON. |
| Q42040772 | PCR diagnostics underestimate the prevalence of avian malaria (Plasmodium relictum) in experimentally-infected passerines |
| Q36388580 | PHYLOGENETIC ANALYSIS OF THE EVOLUTION OF ALTERNATIVE SOCIAL BEHAVIOR IN THE MANAKINS (AVES: PIPRIDAE). |
| Q56228483 | POLYGYNY IN GREAT REED WARBLERS: A LONG-TERM STUDY OF FACTORS CONTRIBUTING TO MALE FITNESS |
| Q51430838 | Pairing success and sperm reserve of male Gammarus pulex infected by Cyathocephalus truncatus (Cestoda: Spathebothriidea). |
| Q35992018 | Parallel and nonparallel behavioural evolution in response to parasitism and predation in Trinidadian guppies |
| Q58419496 | Parasite avoidance behaviours in aquatic environments |
| Q35552754 | Parasite diversity declines with host evolutionary distinctiveness: a global analysis of carnivores |
| Q36363912 | Parasite escape through trophic specialization in a species flock |
| Q36801164 | Parasite infection and host group size: a meta-analytical review |
| Q40850310 | Parasite infection negatively affects PHA-triggered inflammation in the subterranean rodent Ctenomys talarum |
| Q53651057 | Parasite infection, host resistance and mate choice: battle of the genders in a simultaneous hermaphrodite. |
| Q34227686 | Parasite manipulation of the proximate mechanisms that mediate social behavior in vertebrates |
| Q43784600 | Parasite mediated mortality and host immune response explain age-related differences in blood parasitism in birds |
| Q35326498 | Parasite prevalence corresponds to host life history in a diverse assemblage of afrotropical birds and haemosporidian parasites |
| Q52642167 | Parasite removal and its impact on litter size and body condition in Columbian ground squirrels (Spermophilus columbianus). |
| Q56881305 | Parasite species richness in carnivores: effects of host body mass, latitude, geographical range and population density |
| Q50220904 | Parasite transmission among relatives halts Red Queen dynamics |
| Q47169169 | Parasite-associated mortality in a long-lived mammal: Variation with host age, sex, and reproduction |
| Q36083386 | Parasite-mediated heterozygote advantage in an outbred songbird population |
| Q47229805 | Parasite-stress promotes in-group assortative sociality: the cases of strong family ties and heightened religiosity |
| Q52038220 | Parasites affect song complexity and neural development in a songbird. |
| Q46313725 | Parasites and Host Performance: Incorporating Infection into Our Understanding of Animal Movement |
| Q42052087 | Parasites and altruism: converging roads |
| Q33783906 | Parasites and behavior: an ethopharmacological analysis and biomedical implications |
| Q34076797 | Parasites and behaviour: an ethopharmacological perspective |
| Q51034186 | Parasites and carotenoid-based signal intensity: how general should the relationship be? |
| Q60319888 | Parasites and health affect multiple sexual signals in male common wall lizards, Podarcis muralis |
| Q44510947 | Parasites and sexual selection |
| Q59046910 | Parasites and sexual selection |
| Q47989519 | Parasites and showy males: malarial infection and color variation in fence lizards |
| Q56228247 | Parasites and the blackcap's tail: implications for the evolution of feather ornaments |
| Q34255781 | Parasites, desiderata lists and the paradox of the organism |
| Q37433200 | Parasites--the new frontier: celebrating Darwin 200. |
| Q50473394 | Parasitic castration promotes coevolutionary cycling but also imposes a cost on sex. |
| Q51580850 | Parasitic infection and oxidative status are associated and vary with breeding activity in the Seychelles warbler. |
| Q35116016 | Parasitism and the expression of sexual dimorphism |
| Q79240008 | Parasitism and the platyhelminthes |
| Q52573283 | Parasitism of Sympetrum dragonflies by Arrenurus planus mites: maintenance of resistance particular to one species. |
| Q33316846 | Parasitism, life history traits and immune defence in cyprinid fish from Central Europe. |
| Q74822490 | Parasitized female mice display reduced aversive responses to the odours of infected males |
| Q47147523 | Parental investment matters for maternal and offspring immune defense in the mouthbrooding cichlid Astatotilapia burtoni |
| Q35769305 | Parting ways: parasite release in nature leads to sex-specific evolution of defence. |
| Q87585741 | Paternal effects on offspring traits in Scaphiopus couchi (Anura: Pelobatidae) |
| Q24791565 | Patterns in abundance and diversity of faecally dispersed parasites of tiger in Tadoba National Park, central India |
| Q43527436 | Patterns in avian malaria at founder and source populations of an endemic New Zealand passerine |
| Q38793923 | Patterns of MHC-dependent mate selection in humans and nonhuman primates: a meta-analysis. |
| Q37519626 | Perfect genetic correlation between number of offspring and grandoffspring in an industrialized human population. |
| Q34733255 | Phagocytosis by invertebrate hemocytes: causes of individual variation in Panorpa vulgaris scorpionflies |
| Q56287168 | Pheasant sexual ornaments reflect nutritional conditions during early growth |
| Q55966924 | Phenotypic plasticity and the handicap principle |
| Q35091150 | Pheromone evolution and sexual behavior in Drosophila are shaped by male sensory exploitation of other males. |
| Q39831783 | Phylogenetic Targeting of Research Effort in Evolutionary Biology |
| Q30054085 | Phylogeny of Laniarius: Molecular data reveal L. liberatus synonymous with L. erlangeri and “plumage coloration” as unreliable morphological characters for defining species and species groups |
| Q30396992 | Physiological Costs of Repetitive Courtship Displays in Cockroaches Handicap Locomotor Performance |
| Q46104484 | Physiological Trade-Offs in Lizards: Costs for Individuals and Populations |
| Q37911987 | Physiological and behavioural interactions between parasites and invertebrate hosts |
| Q40591672 | Physiological bases for parasite-induced alterations of host behaviour |
| Q59329176 | Physiological condition of nestling great tits in response to experimental reduction in nest micro- and macro-parasites |
| Q27012651 | Physiological control of elaborate male courtship: female choice for neuromuscular systems |
| Q85784628 | Physiological costs enforce the honesty of lek display in the black grouse (Tetrao tetrix) |
| Q33421734 | Physiological stress mediates the honesty of social signals. |
| Q50478262 | Pigment-based skin colour in the blue-footed booby: an honest signal of current condition used by females to adjust reproductive investment. |
| Q57898409 | Plasma carotenoid levels in passerines are related to infection by (some) parasites |
| Q38961360 | Plasmodium prevalence across avian host species is positively associated with exposure to mosquito vectors |
| Q31138827 | Plasticity of fertilization rates under varying temperature in the broadcast spawning mussel, Mytilus galloprovincialis |
| Q56689069 | Plumage coloration is a sexually selected indicator of male quality |
| Q57515057 | Plumage coloration, body condition and immunological status in Yellow-billed Cardinals (Paroaria capitata) |
| Q57899077 | Population Social Structure Facilitates Indirect Fitness Benefits from Extra-Pair Mating |
| Q82689977 | Population genetics: XYZW as nature's language of love? |
| Q35680576 | Population-Specific Covariation between Immune Function and Color of Nesting Male Threespine Stickleback |
| Q47196227 | Positive genetic correlation between parasite resistance and body size in a free-living ungulate population |
| Q57699050 | Postcopulatory cost of immune system activation in Poecilia reticulata |
| Q58557835 | Potential genetic benefits of mate selection in whitefish |
| Q37623136 | Predictors of facial attractiveness and health in humans. |
| Q33398043 | Preferences across the menstrual cycle for masculinity and symmetry in photographs of male faces and bodies |
| Q60319957 | Prevalence and intensity of blood and intestinal parasites in a field population of a Mediterranean lizard, Lacerta lepida |
| Q46531931 | Prevalence and intensity of haemogregarine blood parasites and their mite vectors in the common wall lizard, Podarcis muralis |
| Q45059480 | Prevalence and intensity of haemogregarinid blood parasites in a population of the Iberian rock lizard, Lacerta monticola |
| Q51770420 | Prevalence and intensity of intestinal helminths found in free-ranging golden lion tamarins (Leontopithecus rosalia, Primates, Callitrichidae) from Brazilian Atlantic forest. |
| Q53888782 | Prevalence of blood parasites in European passeriform birds. |
| Q61050616 | Primate sexual swellings as coevolved signal systems |
| Q28749670 | Promiscuity and the rate of molecular evolution at primate immunity genes |
| Q30473112 | Protozoan parasite Toxoplasma gondii manipulates mate choice in rats by enhancing attractiveness of males |
| Q28607963 | Proximate causes of the red face of the bald uakari monkey (Cacajao calvus) |
| Q52661255 | Pterin pigments amplify iridescent ultraviolet signal in males of the orange sulphur butterfly, Colias eurytheme. |
| Q40191575 | Puumala hantavirus infection alters the odour attractiveness of its reservoir host |
| Q84580234 | Quantitative genetic architecture of parasite-induced cataract in rainbow trout, Oncorhynchus mykiss |
| Q33786725 | RNAi screen of DAF-16/FOXO target genes in C. elegans links pathogenesis and dauer formation |
| Q33352821 | Rapid and adaptive evolution of MHC genes under parasite selection in experimental vertebrate populations |
| Q55136771 | Reactive oxygen species as universal constraints in life-history evolution. |
| Q59088164 | Reassessment of comparative evidence for Hamilton and Zuk theory on the evolution of secondary sexual characters |
| Q56608232 | Receiver psychology and the evolution of animal signals |
| Q51288907 | Reciprocal relationships between behaviour and parasites suggest that negative feedback may drive flexibility in male reproductive behaviour. |
| Q55132681 | Relatedness, body size and paternity in the alpine newt, Triturus alpestris. |
| Q58790836 | Reproduction and immunity trade-offs constrain mating signals and nuptial gift size in a bushcricket |
| Q64074493 | Reproductive Strategy Inferred from Major Histocompatibility Complex-Based Inter-Individual, Sperm-Egg, and Mother-Fetus Recognitions in Giant Pandas () |
| Q61766488 | Reproductive and aggressive behavior in male broiler breeders with varying fertility levels |
| Q37243346 | Reproductive decisions under ecological constraints: it's about time |
| Q38863553 | Reproductive investment is connected to innate immunity in a long-lived animal |
| Q30376158 | Robust calling performance in frogs infected by a deadly fungal pathogen. |
| Q38753032 | SEXUAL DICHROMATISM IN BIRDS: IMPORTANCE OF NEST PREDATION AND NEST LOCATION FOR FEMALES VERSUS MALES. |
| Q46272803 | SEXUAL SELECTION AND MALE CHARACTERISTICS IN THE BLUEHEAD WRASSE, THALASSOMA BIFASCIATUM: MATING SITE ACQUISITION, MATING SITE DEFENSE, AND FEMALE CHOICE. |
| Q46509607 | SEXUAL SELECTION IN THE MONOGAMOUS BARN SWALLOW (HIRUNDO RUSTICA). I. DETERMINANTS OF TAIL ORNAMENT SIZE. |
| Q47241402 | SEXUAL SELECTION ON BODY SIZE, TERRITORY AND PLUMAGE VARIABLES IN A POPULATION OF DARWIN'S FINCHES. |
| Q36388379 | SEXUAL SELECTION THROUGH FEMALE CHOICE IN LAWES' PAROTIA, A LEK-MATING BIRD OF PARADISE. |
| Q52202018 | SEXUAL SELECTION, VIABILITY SELECTION, AND DEVELOPMENTAL STABILITY IN THE DOMESTIC FLY MUSCA DOMESTICA. |
| Q39018422 | Scarification in Sub-Saharan Africa: Social Skin, Remedy and Medical Import |
| Q63437956 | Scent-marking by male mammals: Cheat-proof signals to competitors and mates |
| Q38493390 | Seasonal and age-related changes in blood parasite prevalence in Dark-eyed Juncos (Junco hyemalis, Aves, Passeriformes). |
| Q93604603 | Seasonal changes in the relationship between ornamentation and immune response in red jungle fowl |
| Q36885729 | Seasonal changes in vertebrate immune activity: mediation by physiological trade-offs |
| Q93605593 | Secondary sex traits, parasites, immunity and ejaculate quality in the Arctic charr |
| Q51760183 | Secondary sexual ornamentation and non-additive genetic benefits of female mate choice. |
| Q28705023 | Selection and phylogenetics of salmonid MHC class I: wild brown trout (Salmo trutta) differ from a non-native introduced strain |
| Q45834790 | Selection at the MHC class IIB locus across guppy (Poecilia reticulata) populations. |
| Q52642155 | Selection for parasitoid resistance alters mating success in Drosophila. |
| Q38608385 | Selection on an extreme weapon in the frog legged leaf beetle (Sagra femorata). |
| Q50955980 | Senescence in immune priming and attractiveness in a beetle. |
| Q36838253 | Sensory genes and mate choice: evidence that duplications, mutations, and adaptive evolution alter variation in mating cue genes and their receptors |
| Q51750287 | Serial monogamy and sex ratio bias in Nazca boobies. |
| Q33840643 | Serial monogamy as polygyny or polyandry? : marriage in the tanzanian pimbwe |
| Q55983641 | Sex Role Reversal in Pipefish |
| Q39036728 | Sex differences in immune responses: Hormonal effects, antagonistic selection, and evolutionary consequences. |
| Q55894177 | Sex differences in the anatomical locations of human body scarification and tattooing as a function of pathogen prevalence |
| Q47276687 | Sex differences in the brain: Implications for behavioral and biomedical research. |
| Q34176454 | Sex is not a solution for reproduction: the libertine bubble theory |
| Q58573124 | Sex roles and sexual selection: lessons from a dynamic model system |
| Q93605171 | Sex, death, and genetic variation: natural and sexual selection on cricket song |
| Q34128406 | Sex, war, and disease: the role of parasite infection on weapon development and mating success in a horned beetle (Gnatocerus cornutus) |
| Q90373699 | Sex-dependent changes in the louse abundance of red-footed falcons (Falco vespertinus) |
| Q35870095 | Sex-specific consequences of an induced immune response on reproduction in a moth |
| Q79738415 | Sex-specific effects of carotenoid intake on the immunological response to allografts in guppies (Poecilia reticulata) |
| Q52649430 | Sex-specific response of a mosquito to parasites and crowding. |
| Q34708415 | Sex: differences in mutation, recombination, selection, gene flow, and genetic drift |
| Q89792795 | Sexual Dimorphisms in Innate Immunity and Responses to Infection in Drosophila melanogaster |
| Q58557670 | Sexual Selection and Life-History Decisions: Implications for Supportive Breeding and the Management of Captive Populations |
| Q38710756 | Sexual Selection and the differences between the sexes in Mandrills (Mandrillus sphinx). |
| Q51550129 | Sexual dichromatism in frogs: natural selection, sexual selection and unexpected diversity. |
| Q28749591 | Sexual dimorphism in primate aerobic capacity: a phylogenetic test |
| Q35202498 | Sexual ornamentation reflects antibacterial activity of ejaculates in mallards |
| Q61050726 | Sexual selection and exaggerated sexual swellings of female primates |
| Q34981456 | Sexual selection and human life history. |
| Q52686085 | Sexual selection and immune function in Drosophila melanogaster. |
| Q22162496 | Sexual selection and mate choice |
| Q86699347 | Sexual selection and physical attractiveness : Implications for mating dynamics |
| Q36660289 | Sexual selection and the evolution of evolvability. |
| Q33311622 | Sexual selection and the evolution of obligatory sex |
| Q55691063 | Sexual selection and the evolutionary dynamics of the major histocompatibility complex. |
| Q28511125 | Sexual selection by female immunity against paternal antigens can fix loss of function alleles |
| Q51372207 | Sexual selection explains more functional variation in the mammalian major histocompatibility complex than parasitism. |
| Q56287171 | Sexual selection in the ring-necked pheasant: a review |
| Q91784230 | Sexual selection reveals a cost of pathogen resistance undetected in life-history assays |
| Q56227340 | Sexual selection, Handicaps and true fintess |
| Q92650940 | Sexual selection, environmental robustness, and evolutionary demography of maladapted populations: A test using experimental evolution in seed beetles |
| Q24799773 | Sexual selection, germline mutation rate and sperm competition |
| Q34308599 | Sexual selection, honest advertisement and the handicap principle: reviewing the evidence |
| Q35021820 | Sexual selection: an evolutionary force in plants? |
| Q54296140 | Sexual showiness and parasite load: correlations without parasite coevolutionary cycles. |
| Q33694332 | Sexual signals reflect telomere dynamics in a wild bird. |
| Q51183604 | Sexually dichromatic coloration reflects size and immunocompetence in female Spanish terrapins, Mauremys leprosa. |
| Q36921071 | Sexually selected traits: a fundamental framework for studies on behavioral epigenetics |
| Q47434895 | Sexually transmitted disease and the evolution of mating systems |
| Q41077172 | Sexually transmitted diseases in animals: ecological and evolutionary implications |
| Q56432232 | Sexually transmitted diseases in polygynous mating systems: prevalence and impact on reproductive success |
| Q51024405 | Sexually transmitted infection and the evolution of serial monogamy. |
| Q36622129 | Sexually transmitted infections in polygamous mating systems |
| Q30437872 | Sexy faces in a male paper wasp |
| Q102053944 | Shifts in the developmental rate of spadefoot toad larvae cause decreased complexity of post-metamorphic pigmentation patterns |
| Q34261676 | Short-term enrichment makes male rats more attractive, more defensive and alters hypothalamic neurons |
| Q51789498 | Signal content of red facial coloration in female mandrills (Mandrillus sphinx). |
| Q35862595 | Size Dependent Male Reproductive Tactic in the Two-Spotted Goby (Gobiusculus flavescens). |
| Q50318468 | Smelling fit: scent marking exposes parasitic infection status in the banded mongoose. |
| Q56688097 | Soay Sheep |
| Q47662531 | Social Cognition and the Neurobiology of Rodent Mate Choice |
| Q51304425 | Social and extra-pair mating in relation to major histocompatibility complex variation in common yellowthroats. |
| Q46111338 | Social behaviour and gut microbiota in red-bellied lemurs (Eulemur rubriventer): In search of the role of immunity in the evolution of sociality |
| Q47374457 | Social behaviour and susceptibility to infection in house mice (Mus musculus): effects of group size, aggressive behaviour and status-related hormonal responses prior to infection on resistance to Babesia microti |
| Q70516375 | Social behaviour, stress and susceptibility to infection in house mice (Mus musculus): effects of duration of grouping and aggressive behaviour prior to infection on susceptibility to Babesia microti |
| Q36477835 | Social pairing of Seychelles warblers under reduced constraints: MHC, neutral heterozygosity, and age. |
| Q54950146 | Social status and parasitism in male and female vertebrates: a meta-analysis. |
| Q38419690 | Social status, immune response and parasitism in males: a meta-analysis |
| Q42587444 | Sociality and health: impacts of sociality on disease susceptibility and transmission in animal and human societies |
| Q35750585 | Sociality, exotic ectoparasites, and fitness in the plural breeding rodent Octodon degus. |
| Q37940904 | Sociality, pathogen avoidance, and the neuropeptides oxytocin and arginine vasopressin. |
| Q73902744 | Some thoughts on William D. Hamilton (1936-2000) |
| Q46328954 | Song complexity, song rate, and variation in the adrenocortical stress response in song sparrows (Melospiza melodia). |
| Q55393480 | Song predicts immunocompetence in male European starlings (Sturnus vulgaris). |
| Q28595824 | Song sparrows Melospiza melodia have a home-field advantage in defending against sympatric malarial parasites |
| Q55514954 | Spatiotemporal and gender‐specific parasitism in two species of gobiid fish. |
| Q26749152 | Speciation by Symbiosis: the Microbiome and Behavior |
| Q42655976 | Species-specific evolution of class I MHC genes in iguanas (order: Squamata; subfamily: Iguaninae). |
| Q58554287 | Specific MHC class I supertype associated with parasite infection and color morph in a wild lizard population |
| Q64235439 | Specificity of the female's local cellular immune response in genital plug producing scorpion species |
| Q46253768 | Stabilising selection on immune response in male black grouse Lyrurus tetrix. |
| Q107744263 | Stable and variable parameters in courtship songs of grasshoppers of the subfamily Gomphocerinae (Orthoptera, Acrididae) |
| Q33234649 | Steroid hormone related male biased parasitism in chamois, Rupicapra rupicapra rupicapra |
| Q91921027 | Stress hypothesis overload: 131 hypotheses exploring the role of stress in tradeoffs, transitions, and health |
| Q42945304 | Stress, social behaviour, and secondary sexual traits in a male primate |
| Q47946844 | Strong but flexible: How fundamental social motives support but sometimes also thwart favorable attractiveness biases |
| Q30382290 | Structural (UV) and carotenoid-based plumage coloration - signals for parental investment? |
| Q84203659 | Structural coloration signals condition, parental investment, and circulating hormone levels in Eastern bluebirds (Sialia sialis) |
| Q56211908 | Structural plumage colour and parasites in satin bowerbirds Ptilonorhynchus violaceus: implications for sexual selection |
| Q58307151 | Structural- and carotenoid-based throat colour patches in males of Lacerta schreiberi reflect different parasitic diseases |
| Q58512557 | Superciliums in white-eared hummingbirds as badges of status signaling dominance |
| Q34674184 | Superinfection drives virulence evolution in experimental populations of bacteria and plasmids. |
| Q57264684 | Survival costs and reproductive benefits of floral display in a sexually dimorphic dioecious shrub, Leucadendron xanthoconus |
| Q51715649 | Susceptibility to infection by a haemogregarine parasite and the impact of infection in the Australian sleepy lizard Tiliqua rugosa. |
| Q34608927 | Symbiont survival and host-symbiont disequilibria under differential vertical transmission |
| Q21144567 | Symmetry is related to sexual dimorphism in faces: data across culture and species |
| Q33618887 | Sympatric and allopatric divergence of MHC genes in threespine stickleback |
| Q52690788 | Systematic temporal changes in host susceptibility to infection: demographic mechanisms. |
| Q38753532 | THE EVOLUTION OF PLUMAGE BRIGHTNESS IN BIRDS IS RELATED TO EXTRAPAIR PATERNITY. |
| Q39415647 | THE SENSORY BASIS OF SEXUAL SELECTION FOR COMPLEX CALLS IN THE TÚNGARA FROG, PHYSALAEMUS PUSTULOSUS (SEXUAL SELECTION FOR SENSORY EXPLOITATION). |
| Q37734844 | Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates |
| Q56621829 | Temporal change in mite abundance and its effect on barn swallow reproduction and sexual selection |
| Q90264541 | Temporally consistent species differences in parasite infection but no evidence for rapid parasite-mediated speciation in Lake Victoria cichlid fish |
| Q35837635 | Testing Local Adaptation in a Natural Great Tit-Malaria System: An Experimental Approach |
| Q36137397 | Testing for links between face color and age, dominance status, parity, weight, and intestinal nematode infection in a sample of female Japanese macaques. |
| Q46886975 | Testing the Hamilton-Zuk hypothesis: past, present, and future |
| Q79653909 | Testosterone and oxidative stress: the oxidation handicap hypothesis |
| Q53402936 | Testosterone increases perceived dominance but not attractiveness in human males. |
| Q50713811 | Testosterone levels and gular pouch coloration in courting magnificent frigatebird (Fregata magnificens): variation with age-class, visited status and blood parasite infection. |
| Q73895740 | Testosterone treatment is immunosuppressive in superb fairy-wrens, yet free-living males with high testosterone are more immunocompetent |
| Q56454734 | The Body and Face of Woman |
| Q58486962 | The Effect of Hemosporidian Infections on White-Crowned Sparrow Singing Behavior |
| Q41676929 | The Hamilton-Zuk theory and initial test: an examination of some parasitological criticisms |
| Q56385849 | The Mating System of Foragers in the Standard Cross-Cultural Sample |
| Q40834648 | The Red Queen lives: Epistasis between linked resistance loci |
| Q92736405 | The Reproductive Microbiome: An Emerging Driver of Sexual Selection, Sexual Conflict, Mating Systems, and Reproductive Isolation |
| Q58703864 | The Role of Parasitism in Adaptive Radiations—When Might Parasites Promote and When Might They Constrain Ecological Speciation? |
| Q51710907 | The attractiveness fragment--AFLP analysis of local adaptation and sexual selection in a caeliferan grasshopper, Chorthippus biguttulus. |
| Q51733563 | The capture of heritable variation for genetic quality through social competition. |
| Q56213272 | The carotenoid beta-carotene enhances facial color, attractiveness and perceived health, but not actual health, in humans |
| Q54129115 | The coevolution of host resistance and parasitoid virulence. |
| Q24678266 | The coevolution theory of autumn colours |
| Q39994527 | The color genes of speciation in plants |
| Q37714363 | The contagion indicator hypothesis for parasite-mediated sexual selection |
| Q51703390 | The correlation between immunocompetence and an ornament trait changes over lifetime in Panorpa vulgaris scorpionflies. |
| Q68542722 | The costs of choice in sexual selection |
| Q34418961 | The costs of dominance: testosterone, cortisol and intestinal parasites in wild male chimpanzees |
| Q34565879 | The design and function of birds' nests |
| Q46901135 | The effect of a nematode parasite on feeding and dung-burying behavior of an ecosystem engineer |
| Q44532268 | The effect of an acute phase response on tissue carotenoid levels of growing chickens (Gallus gallus domesticus). |
| Q56156977 | The effect of dietary carotenoid access on sexual dichromatism and plumage pigment composition in the American goldfinch |
| Q45330666 | The effect of exogenous testosterone on ectoparasite loads in free-ranging western fence lizards |
| Q35178448 | The effect of parasites on sex differences in selection. |
| Q37286562 | The effect of rearing environment on blue structural coloration of eastern bluebirds (Sialia sialis) |
| Q21146602 | The effects of mite parasitism on the reproduction and survival of the Taiwan field mice (Apodemus semotus) |
| Q40072666 | The effects of sex hormones on immune function: a meta-analysis |
| Q92963856 | The efficacy of good genes sexual selection under environmental change |
| Q51640740 | The energetic basis of acoustic communication. |
| Q61458481 | The energetic cost of display in male sage grouse |
| Q28765066 | The evolution of avian parental care |
| Q47769631 | The evolution of magnanimity : When is it better to give than to receive? |
| Q24669654 | The evolution of mate choice and mating biases |
| Q68510672 | The evolution of mate choice in a fluctuating environment |
| Q56020653 | The evolution of mating preferences and the paradox of the lek |
| Q77827999 | The evolution of risky behaviour in the presence of a sexually transmitted disease |
| Q54943534 | The evolution of song repertoires and immune defence in birds. |
| Q33632793 | The evolution of trophic transmission |
| Q59620290 | The evolutionary psychology of extrapair sex: The role of fluctuating asymmetry |
| Q57253292 | The frontal shield of the moorhen: sex differences and relationship with body condition |
| Q37786600 | The hidden benefits of sex: Evidence for MHC‐associated mate choice in primate societies |
| Q46864326 | The history of ecoimmunology and its integration with disease ecology |
| Q24682803 | The hypothesis of reproductive compensation and its assumptions about mate preferences and offspring viability |
| Q73490855 | The immunocompetence handicap hypothesis: testing the genetic predictions |
| Q87590843 | The impact of tick load on the fitness of their lizard hosts |
| Q73048899 | The influence of intensity of infection by a trematode parasite on the reproductive biology of Gammarus insensibilis (Amphipoda) |
| Q51306071 | The influence of male age and simulated pathogenic infection on producing a dishonest sexual signal. |
| Q39216455 | The influence of parasites on the retention of long-term partnerships in the Australian sleepy lizard, Tiliqua rugosa. |
| Q35211306 | The interplay between gonadal steroids and immune defence in affecting a carotenoid-dependent trait |
| Q48376259 | The looks matter; aggression escalation from changes on phenotypic appearance in the domestic fowl |
| Q51214130 | The mitonuclear compatibility hypothesis of sexual selection. |
| Q33302213 | The odor of origin: kinship and geographical distance are reflected in the marking pheromone of male beewolves (Philanthus triangulum F., Hymenoptera, Crabronidae) |
| Q48457597 | The parasite-stress theory may be a general theory of culture and sociality |
| Q52001065 | The parasitic mite Varroa destructor affects non-associative learning in honey bee foragers, Apis mellifera L. |
| Q33291117 | The population dynamical implications of male-biased parasitism in different mating systems |
| Q40805431 | The proximate and the ultimate: past, present, and future |
| Q37655915 | The relationship between health and mating success in humans. |
| Q36793187 | The role of chemical communication in mate choice. |
| Q52641515 | The role of juvenile hormone in immune function and pheromone production trade-offs: a test of the immunocompetence handicap principle. |
| Q58610852 | The role of parasitism in the energy management of a free-ranging bird |
| Q57566216 | The role of pigment based plumage traits in resolving conflicts |
| Q46422028 | The role of sexual and natural selection in shaping patterns of sexual dichromatism in the largest family of songbirds (Aves: Thraupidae). |
| Q88984845 | The role of social cognition in parasite and pathogen avoidance |
| Q47968003 | The sensitivity of microscopy and PCR-based detection methods affecting estimates of prevalence of blood parasites in birds. |
| Q34248127 | The sexual cascade and the rise of pre-ejaculatory (Darwinian) sexual selection, sex roles, and sexual conflict |
| Q22065942 | The sexual selection continuum |
| Q28081583 | The sociality-health-fitness nexus: synthesis, conclusions and future directions |
| Q35995071 | The strength of indirect selection on female mating preferences |
| Q51595109 | The validity of composite photographs for assessing masculinity preferences. |
| Q57454142 | The value of a smile: Game theory with a human face |
| Q30470575 | Towards an integrative model of sociality in caviomorph rodents |
| Q50547104 | Toxoplasma gondii infection enhances testicular steroidogenesis in rats. |
| Q35685823 | Toxoplasma gondii: sexual transmission in mice |
| Q55632095 | Trade-offs between sexual advertisement and immune function in the pied flycatcher (Ficedula hypoleuca). |
| Q42627268 | Trans-species polymorphism, HLA-disease associations and the evolution of the MHC. |
| Q51111119 | Transgenerational interactions involving parental age and immune status affect female reproductive success in Drosophila melanogaster. |
| Q36939294 | Two sexes, one genome: the evolutionary dynamics of intralocus sexual conflict |
| Q36550747 | Ultraviolet plumage colors predict mate preferences in starlings. |
| Q51145912 | Understanding immune function as a pace of life trait requires environmental context. |
| Q62085684 | Understanding parasite strategies |
| Q34202099 | Unraveling the enigma: the role of melatonin in seasonal processes in birds |
| Q57898911 | Urban Impacts on Oxidative Balance and Animal Signals |
| Q28607669 | Urinary neopterin, a non-invasive marker of mammalian cellular immune activation, is highly stable under field conditions |
| Q95322164 | Using a multistate occupancy approach to determine molecular diagnostic accuracy and factors affecting avian haemosporidian infections |
| Q28255812 | Using theories of sexual selection and sexual conflict to improve our understanding of plant ecology and evolution |
| Q37625443 | Validation of a Method for the Assessment of Urinary Neopterin Levels to Monitor Health Status in Non-human-primate Species |
| Q58998283 | Validity of sexual selection in birds |
| Q56837912 | Variation in haematozoan parasitism at local and landscape levels in the red-billed quelea Quelea quelea |
| Q51197964 | Variation in immune defence as a question of evolutionary ecology. |
| Q101632922 | Variation in male ornaments in two lizard populations with contrasting parasite loads |
| Q50582145 | Variation in sex pheromone emission does not reflect immunocompetence but affects attractiveness of male burying beetles-a combination of laboratory and field experiments. |
| Q51733729 | Variation in the peacock's train shows a genetic component. |
| Q92923390 | Veiled preferences and cryptic female choice could underlie the origin of novel sexual traits |
| Q51528201 | Vertical transmission of feather lice between adult blackbirds Turdus merula and their nestlings: a lousy perspective. |
| Q59064395 | Viability costs of male tail ornaments in a swallow |
| Q37986597 | Virulence of lizard malaria: the evolutionary ecology of an ancient parasite-host association |
| Q59282854 | Visual Attention to Plain and Ornamented Human Bodies: An Eye-Tracking Study |
| Q36939220 | Water temperature, not fish morph, determines parasite infections of sympatric Icelandic threespine sticklebacks (Gasterosteus aculeatus). |
| Q36123454 | Weak link between dispersal and parasite community differentiation or immunogenetic divergence in two sympatric cichlid fishes |
| Q38070902 | What do we really know about the signalling role of plumage colour in blue tits? A case study of impediments to progress in evolutionary biology |
| Q38769915 | What maintains signal honesty in animal colour displays used in mate choice? |
| Q53785199 | When can host shifts produce congruent host and parasite phylogenies? A simulation approach. |
| Q36238474 | When sex makes you sick |
| Q51700588 | Who is in control of the stickleback immune system: interactions between Schistocephalus solidus and its specific vertebrate host. |
| Q45986504 | Why do gentlemen prefer blondes? |
| Q57069754 | Widespread loss of sexually selected traits: how the peacock lost its spots |
| Q55251629 | Within- and between-population variation for resistance of Daphnia magna to the bacterial endoparasite Pasteuria ramosa. |
| Q46377401 | Worldwide patterns of bird colouration on islands |
| Q95830063 | You're Just My Type: Mate Choice and Behavioral Types |
| Q99617275 | Young but not defenceless: antifungal activity during embryonic development of a social insect |
| Q35972494 | α2u-globulins mediate manipulation of host attractiveness in Toxoplasma gondii-Rattus novergicus association. |
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