| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1558-5646.1998.TB05132.X |
| P8608 | Fatcat ID | release_5nglj3wrkzdwhhrywik72qiaqm |
| P698 | PubMed publication ID | 28568154 |
| P2093 | author name string | William R Rice | |
| Brett Holland | |||
| P2860 | cites work | Intra-sexual selection in Drosophila | Q22251111 |
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| Female Zebra Finches Choose Extra-Pair Copulations with Genetically Attractive Males | Q56268977 | ||
| Why have birds got multiple sexual ornaments? | Q56485630 | ||
| Female choice selects for extreme tail length in a widowbird | Q56836087 | ||
| The Processes of Evolution: Toward a Newer Synthesis | Q56961549 | ||
| A negative correlation between trait and mate preference inXiphophorus pygmaeus | Q57706864 | ||
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| Sexual activity reduces lifespan of male fruitflies | Q59092255 | ||
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| P433 | issue | 1 | |
| P921 | main subject | sexual selection | Q206913 |
| P1104 | number of pages | 7 | |
| P304 | page(s) | 1-7 | |
| P577 | publication date | 1998-02-01 | |
| P1433 | published in | Evolution | Q4038411 |
| P1476 | title | PERSPECTIVE: CHASE-AWAY SEXUAL SELECTION: ANTAGONISTIC SEDUCTION VERSUS RESISTANCE. | |
| P478 | volume | 52 |
| Q35058102 | A macroevolutionary perspective on multiple sexual traits in the phasianidae (galliformes) |
| Q89525285 | A pheromone antagonist liberates female sea lamprey from a sensory trap to enable reliable communication |
| Q59126126 | A sustained change in the supply of parental care causes adaptive evolution of offspring morphology |
| Q30475867 | Acoustic discrimination of sympatric morphs in Darwin's finches: a behavioural mechanism for assortative mating? |
| Q34109048 | Adaptations to sexual selection and sexual conflict: insights from experimental evolution and artificial selection. |
| Q36548802 | All males are not created equal: fertility differences depend on gamete recognition polymorphisms in sea urchins |
| Q33277670 | An experimental test for indirect benefits in Drosophila melanogaster |
| Q35038256 | Assessing sexual conflict in the Drosophila melanogaster laboratory model system |
| Q30482171 | Bending for love: losses and gains of sexual dimorphisms are strictly correlated with changes in the mounting position of sepsid flies (Sepsidae: Diptera) |
| Q35767771 | Biomechanical Diversity of Mating Structures among Harvestmen Species Is Consistent with a Spectrum of Precopulatory Strategies |
| Q33747893 | Breeding experience and the heritability of female mate choice in collared flycatchers |
| Q34509308 | Can sexual selection theory inform genetic management of captive populations? A review |
| Q38680488 | Coevolution of coloration and colour vision? |
| Q21090115 | Coevolution of male and female genital morphology in waterfowl |
| Q36646348 | Contrasting effects of intralocus sexual conflict on sexually antagonistic coevolution. |
| Q36412830 | Convergent and unidirectional evolution of extremely long aedeagi in the largest feather mite genus, Proctophyllodes (Acari: Proctophyllodidae): Evidence from comparative molecular and morphological phylogenetics |
| Q24678658 | Costly traumatic insemination and a female counter-adaptation in bed bugs |
| Q51164699 | Costs of deception and learned resistance in deceptive interactions. |
| Q51632834 | Courtship raises male fertilization success through post-mating sexual selection in a spider. |
| Q34445910 | Courtship song does not increase the rate of adaptation to a thermally stressful environment in a Drosophila melanogaster laboratory population |
| Q30524892 | Deceptive vibratory communication: pupae of a beetle exploit the freeze response of larvae to protect themselves |
| Q24670334 | Degree of male ornamentation affects female preference for conspecific versus heterospecific males |
| Q35038224 | Detecting sexual conflict and sexually antagonistic coevolution |
| Q37116085 | Detection of seminal fluid proteins in the bed bug, Cimex lectularius, using two-dimensional gel electrophoresis and mass spectrometry |
| Q30470673 | Determinants of natural mating success in the cannibalistic orb-web spider Argiope bruennichi |
| Q36830910 | Do female Nicrophorus vespilloides reduce direct costs by choosing males that mate less frequently? |
| Q37433034 | Does reproductive isolation evolve faster in larger populations via sexually antagonistic coevolution? |
| Q36338225 | Effect of male mating history and age on remating by female European corn borer |
| Q38954307 | Estimating mating rates in wild Drosophila melanogaster females by decay rates of male reproductive proteins in their reproductive tracts. |
| Q34285671 | Estimation of heritability, evolvability and genetic correlations of two pollen and pistil traits involved in a sexual conflict over timing of stigma receptivity in Collinsia heterophylla (Plantaginaceae). |
| Q45215016 | Evidence that sensory traps can evolve into honest signals |
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| Q29394949 | Evolution of genitalia: theories, evidence, and new directions |
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| Q36337430 | Experimental removal of sexual selection reverses intersexual antagonistic coevolution and removes a reproductive load |
| Q34166454 | Female burying beetles benefit from male desertion: sexual conflict and counter-adaptation over parental investment |
| Q42909623 | Female competition and aggression: interdisciplinary perspectives |
| Q64066944 | Female genitalia can evolve more rapidly and divergently than male genitalia |
| Q39435464 | Female mating preferences determine system-level evolution in a gene network model |
| Q60492107 | Female plasticity tends to reduce sexual conflict |
| Q92751328 | Female secondary sexual traits in spiders: Adaptive interpretations of the sternum projection in the pholcid Holocnemus pluchei |
| Q33288973 | Female sexual polymorphism and fecundity consequences of male mating harassment in the wild |
| Q51105359 | Female, but not male, nematodes evolve under experimental sexual coevolution. |
| Q81578179 | First copulation increases longevity and fecundity of Histiostoma feroniarum (Acari: Astigmata: Acaridida) females |
| Q51363435 | Foraging costs drive female resistance to a sensory trap. |
| Q47071690 | Genetic control and evolution of sexually dimorphic characters in Drosophila |
| Q42014676 | Genetic variation in a female genital trait evolved by sexual coevolution |
| Q35179070 | Genetic variation in the effect of monoamines on female mating receptivity and oviposition in the adzuki bean beetle, Callosobruchus chinensis (Coleoptera: Bruchidae). |
| Q50074879 | Genomic Signatures of Sexual Conflict |
| Q36243524 | Hidden female physiological resistance to male accessory gland substances in a simultaneous hermaphrodite |
| Q52877191 | How choosy should I be? The relative searching time predicts evolution of choosiness under direct sexual selection. |
| Q47282475 | Impact of male alternative reproductive tactics on female costs of sexual conflict under variation in operational sex ratio and population density |
| Q26810029 | Inbreeding and sex: canalization, plasticity and sexual selection |
| Q21562178 | Indiscriminate males: mating behaviour of a marine snail compromised by a sexual conflict? |
| Q52781545 | Inter-genomic sexual conflict drives antagonistic coevolution in harvester ants. |
| Q56656968 | Intersexual ontogenetic conflict |
| Q33302978 | Is reduced female survival after mating a by-product of male-male competition in the dung fly Sepsis cynipsea? |
| Q34931128 | Is sexual conflict an "engine of speciation"? |
| Q90273091 | Juvenile diet quality and intensity of sexual conflict in the mite Sancassania berlesei |
| Q55970638 | Layered sexual selection: a comparative analysis of sexual behaviour within an assemblage of piophilid flies |
| Q36943825 | Maintenance of genetic variation in sexual ornaments: a review of the mechanisms |
| Q60959704 | Making sense of intralocus and interlocus sexual conflict |
| Q34355309 | Male clasping ability, female polymorphism and sexual conflict: fine-scale elytral morphology as a sexually antagonistic adaptation in female diving beetles |
| Q36311545 | Male courtship behavior of the South American fruit fly, Anastrepha fraterculus, from an Argentinean laboratory strain |
| Q35112660 | Male dwarf chameleons assess risk of courting large, aggressive females |
| Q37243342 | Mate choice and sexual selection: what have we learned since Darwin? |
| Q46242656 | Mating system manipulation and the evolution of sex-biased gene expression in Drosophila |
| Q34361641 | Mating system variation drives rapid evolution of the female transcriptome in Drosophila pseudoobscura |
| Q51369617 | Mating with large males decreases the immune defence of females in Drosophila melanogaster. |
| Q60026571 | Miniscule differences between sex chromosomes in the giant genome of a salamander |
| Q35038234 | Natural variation in male-induced 'cost-of-mating' and allele-specific association with male reproductive genes in Drosophila melanogaster |
| Q34999399 | No evidence for reproductive isolation through sexual conflict in the bulb mite Rhizoglyphus robini |
| Q30542409 | No intra-locus sexual conflict over reproductive fitness or ageing in field crickets |
| Q34992051 | Offspring viability benefits but no apparent costs of mating with high quality males |
| Q35630745 | On the evolutionary origins of differences in sexual preferences |
| Q37458357 | On the function of cornuti, sclerotized structures of the endophallus of Lepidoptera |
| Q35092394 | Pathology from evolutionary conflict, with a theory of X chromosome versus autosome conflict over sexually antagonistic traits. |
| Q33834859 | Pervasive antagonistic interactions among hybrid incompatibility loci |
| Q33694363 | Phenotypic plasticity in female mate choice behavior is mediated by an interaction of direct and indirect genetic effects in Drosophila melanogaster. |
| Q50281371 | Phylogeny with introgression in Habronattus jumping spiders (Araneae: Salticidae). |
| Q24678576 | Post-copulatory sexual selection and female fitness in Scathophaga stercoraria |
| Q24656756 | Postcopulatory sexual selection: Darwin's omission and its consequences |
| Q36023988 | Postmating reproductive barriers contribute to the incipient sexual isolation of the United States and Caribbean Drosophila melanogaster |
| Q35038241 | Quantifying the gender load: can population crosses reveal interlocus sexual conflict? |
| Q52081332 | Rapid evolution of reproductive barriers driven by sexual conflict. |
| Q24678680 | Reducing a cost of traumatic insemination: female bedbugs evolve a unique organ |
| Q35134346 | Reduction of female copulatory damage by resilin represents evidence for tolerance in sexual conflict |
| Q35108841 | Remating and sperm competition in replicate populations of Drosophila melanogaster adapted to alternative environments |
| Q34095557 | Remating in Drosophila melanogaster: are indirect benefits condition dependent? |
| Q28651598 | Running with the Red Queen: the role of biotic conflicts in evolution |
| Q37384886 | Selection on an antagonistic behavioral trait can drive rapid genital coevolution in the burying beetle, Nicrophorus vespilloides |
| Q36622109 | Selection on female remating interval is influenced by male sperm competition strategies and ejaculate characteristics |
| Q34546411 | Seminal fluid-mediated fitness traits in Drosophila |
| Q35038270 | Sensory exploitation and sexual conflict |
| Q33583287 | Sequential male mate choice under sperm competition risk |
| Q39399230 | Sexual Conflict, Facultative Asexuality, and the True Paradox of Sex. |
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| Q33440628 | Sexual conflict and sexually antagonistic coevolution in an annual plant |
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| Q34931296 | Sexual conflict in hermaphrodites |
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| Q36779303 | Sexual conflict in plants |
| Q24676760 | Sexual conflict over mating and fertilization: an overview |
| Q51141404 | Sexual conflict over mating in Gnatocerus cornutus? Females prefer lovers not fighters. |
| Q34612852 | Sexual conflict over the maintenance of sex: effects of sexually antagonistic coevolution for reproductive isolation of parthenogenesis |
| Q33563242 | Sexual conflict predicts morphology and behavior in two species of penduline tits |
| Q24799265 | Sexual responsiveness is condition-dependent in female guppies, but preference functions are not |
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| Q30885755 | Shall we dance or shall we fight? Using DNA sequence data to untangle controversies surrounding sexual selection |
| Q33244107 | Slow fertilization of stickleback eggs: the result of sexual conflict? |
| Q51814971 | Strong association between a single gene and fertilization efficiency of males and fecundity of their mates in the bulb mite. |
| Q51825763 | Structure and function of the spermathecal complex in the phlebotomine sandfly Phlebotomus papatasi Scopoli (Diptera: Psychodidae): I. ultrastructure and histology. |
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| Q33927882 | The evolution of genomic imprinting: theories, predictions and empirical tests. |
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| Q36081207 | The evolution of optimal female mating rate changes the coevolutionary dynamics of female resistance and male persistence |
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| Q30105646 | When it pays to cheat: Examining how generalized food deception increases male and female fitness in a terrestrial orchid |
| Q52657193 | Why do multiple traits determine mating success? Differential use in female choice and male competition in a water boatman. |
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