| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1111/J.1469-185X.1995.TB01439.X |
| P698 | PubMed publication ID | 7718697 |
| P2093 | author name string | Johnstone RA | |
| P2860 | cites work | Stimuli provided by Courtship of Male Drosophila melanogaster | Q59094862 |
| Precopulatory sexual interaction in an arctiid moth (Utetheisa ornatrix): Role of a pheromone derived from dietary alkaloids | Q58814172 | ||
| Mate choice increases a component of offspring fitness in fruit flies | Q59060312 | ||
| Viability costs of male tail ornaments in a swallow | Q59064395 | ||
| Heritable variation in a plumage indicator of viability in male great tits Parus major | Q59088505 | ||
| Courtship feeding increases female reproductive success in bushcrickets | Q59089940 | ||
| Pheromonal advertisement of a nuptial gift by a male moth (Utetheisa ornatrix) | Q24560399 | ||
| Models of speciation by sexual selection on polygenic traits | Q24634925 | ||
| Biparental defensive endowment of eggs with acquired plant alkaloid in the moth Utetheisa ornatrix | Q24651452 | ||
| Mate selection—A selection for a handicap | Q28214988 | ||
| Asymmetries in mating preferences between species: female swordtails prefer heterospecific males | Q28243136 | ||
| Heritable true fitness and bright birds: a role for parasites? | Q28278977 | ||
| Ecology, Sexual Selection, and the Evolution of Mating Systems | Q28294410 | ||
| Biological signals as handicaps | Q28298209 | ||
| The cost of honesty (further remarks on the handicap principle) | Q28304186 | ||
| Sexual selection when the female directly benefits | Q29030204 | ||
| Sensory exploitation and the evolution of male mating behaviour: a cladistic test using water mites (Acari: Parasitengona) | Q29031854 | ||
| Bower Destruction, Decoration Stealing and Female Choice in the Spotted Bowerbird Chlamydera maculata | Q29306012 | ||
| Patterns of Fluctuating Asymmetry in Avian Feather Ornaments: Implications for Models of Sexual Selection | Q29396601 | ||
| Female choice selects for male sexual tail ornaments in the monogamous swallow | Q30050496 | ||
| Sexual selection and the potential reproductive rates of males and females | Q34104846 | ||
| Sexually transmitted disease in birds: occurrence and evolutionary significance | Q34334963 | ||
| Parasites and Sexual Selection: A Macroevolutionary Perspective | Q36800945 | ||
| Sexual selection and the role of parasites | Q37827923 | ||
| Theories of sexual selection | Q37828230 | ||
| Sexual selection and communication in frogs | Q39415640 | ||
| Some general comments on the evolution and design of animal communication systems. | Q40711293 | ||
| Sexual selection for sensory exploitation in the frog Physalaemus pustulosus | Q41222695 | ||
| Paternal allocation of sequestered plant pyrrolizidine alkaloid to eggs in the danaine butterfly, Danaus gilippus | Q42073607 | ||
| Females' choice of "good genotypes" as mates is promoted by an insect mating system | Q42075168 | ||
| Evolution. A case of male opportunism | Q43454494 | ||
| Copying and sexual selection. | Q46145030 | ||
| Sexual competition among females: What causes courtship-role reversal? | Q46484745 | ||
| Reproductive strategies and disease susceptibility: an evolutionary viewpoint | Q46503176 | ||
| Recurrent origin of a sexually selected trait in Xiphophorus fishes inferred from a molecular phylogeny | Q47339201 | ||
| Sexual difference theory: mormon crickets show role reversal in mate choice | Q47890343 | ||
| Female swallow preference for symmetrical male sexual ornaments. | Q50543943 | ||
| Honesty, perception and population divergence in sexually selected traits. | Q52393181 | ||
| Selection of exaggerated male traits by female aesthetic senses. | Q52400961 | ||
| Sexual selection unhandicapped by the Fisher process. | Q52481005 | ||
| The evolution of aggression: can selection generate variability? | Q52560111 | ||
| MATE CHOICE IN HYLOBITTACUS APICALIS (INSECTA: MECOPTERA) AND ITS RELATION TO SOME MODELS OF FEMALE CHOICE. | Q52869696 | ||
| THE EVOLUTION OF COSTLY MATE PREFERENCES II. THE "HANDICAP" PRINCIPLE. | Q53246092 | ||
| SEXUAL SELECTION AND THE EVOLUTION OF FEMALE CHOICE. | Q54018405 | ||
| THE EFFECTS OF THE MATING SYSTEM ON PROGENY PERFORMANCE IN HYLA CRUCIFER (ANURA: HYLIDAE). | Q54038166 | ||
| Sexual Selection Through Female Choice in Lawes' Parotia, A Lek-Mating Bird of Paradise | Q54045120 | ||
| SEXUAL SELECTION IN A BRENTID WEEVIL. | Q54150375 | ||
| Mutual sexual selection in a monogamous seabird | Q54275342 | ||
| EFFECTS OF A HAEMATOPHAGOUS MITE ON THE BARN SWALLOW (HIRUNDO RUSTICA): A TEST OF THE HAMILTON AND ZUK HYPOTHESIS. | Q54319661 | ||
| Female preference predates the evolution of the sword in swordtail fish. | Q55044450 | ||
| Parasites, Bright Males, and the Immunocompetence Handicap | Q55871167 | ||
| Peahens prefer peacocks with elaborate trains | Q55881312 | ||
| Courtship in the water mite Neumania papillator: males capitalize on female adaptations for predation | Q55919112 | ||
| Phenotypic plasticity and the handicap principle | Q55966924 | ||
| Male Spawning-Partner Preference in an Arena-Breeding Teleost Cyprinodon macularius californiensis Girard (Atherinomorpha: Cyprinodontidae) | Q56020637 | ||
| Lekking in the black grouse— a test of male viability | Q56020649 | ||
| The evolution of mating preferences and the paradox of the lek | Q56020653 | ||
| Truth in Advertising: The Kinds of Traits Favored by Sexual Selection | Q56047500 | ||
| Mate Choice in Experimentally Parasitized Rock Doves: Lousy Males Lose | Q56093894 | ||
| Age-advertisement and the evolution of the peacock's train | Q56094892 | ||
| Peacocks with low mating success are more likely to suffer predation | Q56094893 | ||
| Species Recognition and Sexual Selection as a Unitary Problem in Animal Communication | Q56156966 | ||
| Female choice and the evolution of the conspicuous plumage coloration of monogamous male great tits | Q56210335 | ||
| Directional Patterns of Female Mate Choice and the Role of Sensory Biases | Q56212754 | ||
| Context and consequences of comb displays by male rock ptarmigan | Q56225923 | ||
| Sexual Selection: The Handicap Principle Does Work -- Sometimes | Q56227338 | ||
| Sexual response of female yellowhammers to differences in regional song dialects and repertoire sizes | Q56228008 | ||
| Mate sampling behaviour of female pied flycatchers: evidence for active mate choice | Q56235063 | ||
| Sexual selection and reproductive success in males of the bicolor damselfish, Eupomacentrus partitus (Pisces: Pomacentridae) | Q56268717 | ||
| Female Zebra Finches Choose Extra-Pair Copulations with Genetically Attractive Males | Q56268977 | ||
| Male characteristics, viability and harem size in the pheasant, Phasianus colchicus | Q56287170 | ||
| Female choice selects for a viability-based male trait in pheasants | Q56287174 | ||
| Female sticklebacks use male coloration in mate choice and hence avoid parasitized males | Q56287978 | ||
| Experimental investigations of the evolutionary significance of sexually dimorphic nuptial colouration in Gasterosteus aculeatus (L.): the relationship between male colour and female behaviour | Q56287979 | ||
| Costs and Benefits of Female Mate Choice: Is There a Lek Paradox? | Q56430257 | ||
| Sexual Selection and the Evolution of Song | Q56432237 | ||
| Why have birds got multiple sexual ornaments? | Q56485630 | ||
| Evolution of multiple sexual preferences by Fisher’s runaway process of sexual selection | Q56485633 | ||
| Genetic difference in female choice between two guppy populations | Q56518135 | ||
| The relationship between male ornamentation and swimming performance in the guppy, Poecilia reticulata | Q56518137 | ||
| Aerodynamics and the evolution of long tails in birds | Q56532220 | ||
| Epigamic selection by males as evidenced by courtship partner preferences in the checkered white butterfly (Pieris protodice) | Q56566665 | ||
| Exaptation—a Missing Term in the Science of Form | Q56611312 | ||
| Extra-pair paternity results from female preference for high-quality males in the blue tit | Q56637992 | ||
| The Red Queen Visits Sage Grouse Leks | Q56656958 | ||
| Plumage coloration is a sexually selected indicator of male quality | Q56689069 | ||
| Parasites and mate choice in red jungle fowl | Q56689072 | ||
| Male mate choice and female-female competition for mates in the pipefish Nerophis ophidion | Q56764233 | ||
| The Processes of Evolution: Toward a Newer Synthesis | Q56961549 | ||
| The Evolution of Costly Mate Preferences I. Fisher and Biased Mutation | Q57065637 | ||
| Female Strategy During Mate Choice: Threshold Assessment | Q57275182 | ||
| A mechanism for female choice of large males in the treefrog Hyla chrysoscelis | Q57706905 | ||
| Signals, Signal Conditions, and the Direction of Evolution | Q57893481 | ||
| Parasite load predicts mate choice in guppies | Q57893565 | ||
| The aerodynamic and mechanical effects of elongated tails in the scarlet-tufted malachite sunbird: measuring the cost of a handicap | Q57942463 | ||
| Mate assessment in a cockroach, Nauphoeta cinerea | Q57942469 | ||
| Female preferences, male social status, and sexual selection in Nauphoeta cinerea | Q57942476 | ||
| P433 | issue | 1 | |
| P921 | main subject | disability | Q12131 |
| sexual selection | Q206913 | ||
| P304 | page(s) | 1-65 | |
| P577 | publication date | 1995-02-01 | |
| P1433 | published in | Biological Reviews | Q2500948 |
| P1476 | title | Sexual selection, honest advertisement and the handicap principle: reviewing the evidence | |
| P478 | volume | 70 |
| Q46040687 | A cross-cultural study of noblesse oblige in economic decision-making |
| Q48047671 | A mechanism of extreme growth and reliable signaling in sexually selected ornaments and weapons. |
| Q51974966 | A primary role of developmental instability in sexual selection. |
| Q41621262 | Acoustic allometry revisited: morphological determinants of fundamental frequency in primate vocal production. |
| Q58243304 | Age estimation by skeletochronology and advertisement call variation in the black-spotted pond frog (Rana nigromaculata) |
| Q80441210 | Alternative phenotypes and sexual selection: can dichotomous handicaps honestly signal quality? |
| Q55040194 | Antlers honestly advertise sperm production and quality. |
| Q38529248 | Are aposematic signals honest? A review |
| Q30432741 | Barriers to gene exchange in hybridizing field crickets: the role of male courtship effort and cuticular hydrocarbons |
| Q27329716 | Beyond species recognition: somatic state affects long-distance sex pheromone communication |
| Q28727750 | Birds of a feather: Neanderthal exploitation of raptors and corvids |
| Q30503847 | Both male and female identity influence variation in male signalling effort. |
| Q55098780 | Bower decorations attract females but provoke other male spotted bowerbirds: bower owners resolve this trade-off. |
| Q26748478 | Can Neglected Tropical Diseases Compromise Human Wellbeing in Sex-, Age-, and Trait-Specific Ways? |
| Q59944115 | Chapter 6 Song and Female Mate Choice in Zebra Finches: A Review |
| Q30221197 | Ciliates learn to diagnose and correct classical error syndromes in mating strategies |
| Q31144288 | Climate change and micro-geographic variation in laying date |
| Q45954311 | Closed-loop bird–computer interactions: a new method to study the role of bird calls |
| Q38335955 | Condition-dependence, pleiotropy and the handicap principle of sexual selection in melanin-based colouration |
| Q51564881 | Condition-dependent expression of melanin-based coloration in the Eurasian kestrel. |
| Q26824275 | Condition-dependent ornaments, life histories, and the evolving architecture of resource-use |
| Q46983882 | Corticosterone regulates multiple colour traits in Lacerta [Zootoca] vivipara males |
| Q24555102 | Cost and conflict in animal signals and human language |
| Q51543213 | Costly signals in a field cricket can indicate high- or low-quality direct benefits depending upon the environment. |
| Q51671590 | Covariation between eumelanic pigmentation and body mass only under specific conditions. |
| Q64121200 | Crowd wisdom enhanced by costly signaling in a virtual rating system |
| Q51385841 | Darwinian balancing selection: predation counters sexual selection in a wild insect. |
| Q60502055 | Decreased sexual signalling reveals reduced viability in small populations of the drumming wolf spider Hygrolycosa rubrofasciata |
| Q50054404 | Diel Periodicity of 3-Methyl-2-Butenyl Butyrate Emissions by Bronze Bug Males Is Suppressed in the Presence of Females |
| Q36733532 | Do men's faces really signal heritable immunocompetence? |
| Q80343313 | Do sexual ornaments demonstrate heightened condition-dependent expression as predicted by the handicap hypothesis? |
| Q37631942 | Environmental change mediates mate choice for an extended phenotype, but not for mate quality |
| Q57063430 | Environmental factors affecting the balance of autotrophs versus heterotrophs in the microbial food web of temporary ponds |
| Q56993142 | Environmental heterogeneity generates opposite gene-by-environment interactions for two fitness-related traits within a population |
| Q51569841 | Eutrophication and predation risk interact to affect sexual trait expression and mating success. |
| Q39023932 | Evolution of Sex Differences in Trait- and Age-Specific Vulnerabilities |
| Q56985114 | Evolution of female choice under intralocus sexual conflict and genotype-by-environment interactions |
| Q39067500 | Evolution of risk-taking during conspicuous mating displays. |
| Q46041705 | Evolutionary ecology of endocrine-mediated life-history variation in the garter snake Thamnophis elegans |
| Q39015328 | Evolutionary framework for identifying sex- and species-specific vulnerabilities in brain development and functions |
| Q35095592 | Expression of multiple sexual signals by fathers and sons in the East-Mediterranean barn swallow: are advertising strategies heritable? |
| Q55653398 | Fear, food and sexual ornamentation: plasticity of colour development in Trinidadian guppies. |
| Q57159508 | Female choice and annual reproductive success favour less-ornamented male house sparrows |
| Q55413200 | Female choice in the sedge warbler Acrocephalus schoenobaenus: multiple cues from song and territory quality. |
| Q37333966 | Female mating preference for bold males in the guppy, Poecilia reticulata |
| Q51291983 | Female preference for male courtship effort can drive the evolution of male mate choice. |
| Q93604597 | Fisherian flies: benefits of female choice in a lekking sandfly |
| Q29011784 | Flat lizard female mimics use sexual deception in visual but not chemical signals |
| Q26824819 | Gene duplication, tissue-specific gene expression and sexual conflict in stalk-eyed flies (Diopsidae) |
| Q24813939 | Genetic covariance between indices of body condition and immunocompetence in a passerine bird |
| Q52848546 | Genetic variation but weak genetic covariation between pre- and post-copulatory episodes of sexual selection in Drosophila melanogaster. |
| Q36479169 | Genic capture and resolving the lek paradox. |
| Q39403208 | Geographical and seasonal variation in the intensity of sexual selection in the barn swallow Hirundo rustica: a meta-analysis |
| Q51090420 | Handicap principle implies emergence of dimorphic ornaments. |
| Q45329757 | Heightened condition-dependent growth of sexually selected weapons in the rhinoceros beetle, Trypoxylus dichotomus (Coleoptera: Scarabaeidae). |
| Q60074841 | Honesty in sexual selection |
| Q34407689 | Human preferences for sexually dimorphic faces may be evolutionarily novel |
| Q46206633 | INTRASEXUAL COMPETITION ALONE FAVORS A SEXUALLY DIMORPHIC ORNAMENT IN THE RUBYSPOT DAMSELFLY HETAERINA AMERICANA. |
| Q52142778 | Immunocompetence, developmental stability and wingspot size in the damselfly Calopteryx splendens L. |
| Q33952194 | Juvenile hormone regulates extreme mandible growth in male stag beetles |
| Q30463855 | Limited condition dependence of male acoustic signals in the grasshopper Chorthippus biguttulus |
| Q40376772 | Longevity cost of reproduction for males but no longevity cost of mating or courtship for females in the male-dimorphic dung beetle Onthophagus binodis. |
| Q46813496 | Male body size and condition affects sperm number and production rates in mosquitofish, Gambusia holbrooki |
| Q54043924 | Male calling song provides a reliable signal of immune function in a cricket. |
| 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 |
| Q47756527 | Male quality, signal reliability and female choice: assessing the expectations of inter-sexual selection |
| Q33361048 | Male sexual ornament size is positively associated with reproductive morphology and enhanced fertility in the stalk-eyed fly Teleopsis dalmanni |
| Q64898211 | Mate choice confers direct benefits to females of Anastrepha fraterculus (Diptera: Tephritidae). |
| Q50999035 | Mating behavior as an indicator of quality of Drosophila subobscura males? |
| Q28767958 | Mating system and brain size in bats |
| Q50283005 | No evidence for general condition-dependence of structural plumage colour in blue tits: an experiment. |
| Q51066669 | Noise affects the shape of female preference functions for acoustic signals. |
| Q33360836 | Non-cooperative game theory in biology and cooperative reasoning in humans |
| Q28749127 | Of Lion Manes and Human Beards: Some Unusual Effects of the Interaction between Aggression and Sociality |
| Q42480865 | On classical and quantum error-correction in ciliate mate selection |
| Q51519381 | On the evolution of heightened condition dependence of male sexual displays. |
| Q58601397 | Overcoming mechanical adversity in extreme hindleg weapons |
| Q55563945 | Pectoral fins and paternal quality in sticklebacks. |
| Q52607739 | Phenotypic plasticity of Rhyzopertha dominica pheromone signaling: the effects of different hosts and presence of conspecific females on male produced aggregation pheromone. |
| Q36797408 | Polyandrous females discriminate against previous mates |
| Q61050616 | Primate sexual swellings as coevolved signal systems |
| Q51685657 | Resource value and the context dependence of receiver behaviour. |
| Q30381446 | Rhythm Generation and Rhythm Perception in Insects: The Evolution of Synchronous Choruses. |
| Q38173259 | Role of sexual selection in speciation in Drosophila |
| Q47302177 | SIZE-DEPENDENT ASYMMETRY: FLUCTUATING ASYMMETRY VERSUS ANTISYMMETRY AND ITS RELEVANCE TO CONDITION-DEPENDENT SIGNALING. |
| Q38608385 | Selection on an extreme weapon in the frog legged leaf beetle (Sagra femorata). |
| Q55983641 | Sex Role Reversal in Pipefish |
| Q38710756 | Sexual Selection and the differences between the sexes in Mandrills (Mandrillus sphinx). |
| Q30415861 | Sexual traits are sensitive to genetic stress and predict extinction risk in the stalk-eyed fly, Diasemopsis meigenii |
| Q56485623 | Showing off, handicap signaling, and the evolution of men's work |
| Q35035095 | Signal design and courtship presentation coincide for highly biased delivery of an iridescent butterfly mating signal |
| Q30224667 | Social biases determine spatiotemporal sparseness of ciliate mating heuristics |
| Q96230617 | Social environment modulates investment in sex trait versus lifespan: red deer produce bigger antlers when facing more rivalry |
| Q46033557 | Socially selected ornaments and fitness: Signals of fighting ability in paper wasps are positively associated with survival, reproductive success, and rank. |
| Q35031818 | Spectacular phenomena and limits to rationality in genetic and cultural evolution |
| Q35165563 | Testosterone increases bioavailability of carotenoids: insights into the honesty of sexual signaling. |
| Q73895740 | Testosterone treatment is immunosuppressive in superb fairy-wrens, yet free-living males with high testosterone are more immunocompetent |
| Q58393373 | The High Price of Success: Costs of Mating Effort in Male Primates |
| Q97551039 | The Impact of Environmental Factors on the Efficacy of Chemical Communication in the Burying Beetle (Coleoptera: Silphidae) |
| Q48047445 | The Putative Son's Attractiveness Alters the Perceived Attractiveness of the Putative Father |
| Q55099890 | The cost of dishonesty. |
| Q28743205 | The dynamics of honesty: modelling the growth of costly, sexually-selected ornaments |
| Q53268775 | The evolution of index signals to avoid the cost of dishonesty. |
| Q55052679 | The health of a nation predicts their mate preferences: cross-cultural variation in women's preferences for masculinized male faces. |
| Q93079567 | The hidden cost of sexually selected traits: the metabolic expense of maintaining a sexually selected weapon |
| Q73490855 | The immunocompetence handicap hypothesis: testing the genetic predictions |
| Q51970203 | The psychology of social chess and the evolution of attribution mechanisms: explaining the fundamental attribution error. |
| Q37781099 | The role of genotype‐by‐environment interactions in sexual selection |
| Q56429897 | Theft of bower decorations among male Satin Bowerbirds (Ptilonorhynchus violaceus): why are some decorations more popular than others? |
| Q57266153 | Towards a resolution of the lek paradox |
| Q41619778 | Unpredictability of escape trajectory explains predator evasion ability and microhabitat preference of desert rodents. |
| Q51733729 | Variation in the peacock's train shows a genetic component. |
| Q38645478 | Viability and expression of sexual ornaments in the barn swallow Hirundo rustica: a meta-analysis. |
| Q28477941 | Vitamin E supplementation increases the attractiveness of males' scent for female European green lizards |
| Q38769915 | What maintains signal honesty in animal colour displays used in mate choice? |
| Q58831069 | What were “owls” doing in our ancestral photoperiodic environment? Chronobiological account for the evolutionary advantage of nocturnal lifestyle |
| Q52657193 | Why do multiple traits determine mating success? Differential use in female choice and male competition in a water boatman. |
| Q51496926 | Why not lie? Costs enforce honesty in an experimental signalling game. |
| Q58316036 | Women Express a Preference for Feminized Male Faces after Giving Birth |
| Q51816410 | Women use voice parameters to assess men's characteristics. |
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