ライフサイエンスコーパス: mate choice

1 often driven by social constraints on female mate choice.

2 contrasts with previous observations of male mate choice.

3 nces across a diverse set of case studies of mate choice.

4 aits may be more important in intra-specific mate choice.

5 avoided by active kin discrimination during mate choice.

6 tion about the signaler's quality, and allow mate choice.

7 nstruct and decorate bowers that function in mate choice.

8 quality of the offspring owing to nonrandom mate choice.

9 orrelation, same sex competition, and mutual mate choice.

10 conflict can restore the genetic benefits of mate choice.

11 enotypic traits and functional components of mate choice.

12 ex factors contributing to romantic love and mate choice.

13 are thought to use these different traits in mate choice.

14 own to be important for mate recognition and mate choice.

15 ossibly reflecting diverse tactics in female mate choice.

16 that cycle variability may facilitate female mate choice.

17 lfactory system is required for heterosexual mate choice.

18 complex interactions such as cooperation or mate choice.

19 s that pregnancy block is a manifestation of mate choice.

20 supporting the role of vocal consistency in mate choice.

21 iscrimination against first-order kin during mate choice.

22 as an honest signal of individual quality in mate choice.

23 ridization), but this did not lead to social mate choice.

24 in general, and specifically the potency of mate choice.

25 d moths, both males and females may exercise mate choice.

26 ng on the fitness advantages accrued through mate choice.

27 d, suggesting that local adaptation affected mate choice.

28 or genetic quality of competing mates during mate choice.

29 e, host plant preference, sex pheromones and mate choice.

30 en by either male-male competition or female mate choice.

31 be a widespread but unappreciated benefit of mate choice.

32 ness-determining in resource competition and mate choice.

33 and assortative mating apply to BT-dependent mate choice.

34 be associated with lizard territoriality and mate choice.

35 ral compatibility between partners with free mate choice.

36 feeding niches [5] also predicted F2 female mate choice.

37 have in such a way as to facilitate adaptive mate choice.

38 local adaptation, dominance, epistasis, and mate choice.

39 n Drosophila simulans and D. sechellia: male mate choice.

40 ffspring communication, kin recognition, and mate choice.

41 ue to sexual selection for ornamentation and mate choice.

42 a reduced reliance on pre-copulatory female mate choice.

43 lects the costs and benefits associated with mate choice.

44 ssociated with reduced pre-copulatory female mate choice.

45 volved differences in the expression of male mate choice.

46 dentified factors likely to influence female mate choices.

47 vide unparalleled insight into the chooser's mate choices.

48 Preliminary tests indicate slope-specific mate choices.

49 plays pivotal roles in social signaling and mate choice [2, 3].

50 , thereby conserving energy and facilitating mate choice-a primary aspect of reproduction.

51 Female mate choice acts as an important evolutionary force, yet

52 is similarly due to mate choice, or whether mate choice affects only part of the facial shape differ

53 rkable ability mediates sexual signaling and mate choice, although other potential functions of circu

54 versity and serves as an important signal in mate choice and aggressive interactions.

55 erred MHC genotypes, external traits used in mate choice and contributions to reproductive outputs.

56 pecific variants are potentially involved in mate choice and early speciation.

57 Here we report on mate choice and hybrid viability experiments in a pair o

58 Sexual selection, including mate choice and intrasexual competition, is responsible

59 raits-those traits traditionally ascribed to mate choice and male fighting.(6)(,)(7) A crucial predic

60 his topic has focused on the consequences of mate choice and mate change on annual reproductive succe

61 cisely establish which genes are involved in mate choice and mating activity--behaviors that are surp

62 and chemosensory genes that are involved in mate choice and mating behavior.

63 umenting the current fitness consequences of mate choice and mating patterns provides insight into th

64 re crucial for both intra- and interspecific mate choice and mating success.

65 Animals often use sex pheromones for mate choice and reproduction.

66 fferent contexts and features prominently in mate choice and reproduction.

67 yle, and ovary is critical to the process of mate choice and reproductive isolation.

68 lications for understanding the evolution of mate choice and sexual conflict in mammals, as well as t

69 number of independent traits contributing to mate choice and sexual isolation.

70 raction between males and females leading to mate choice and successful reproduction.

71 procity underlie conflicts over who controls mate choice and the origins of cross-cousin marriage pre

72 any opportunity for competition for mates or mate choice and thereby aligning the evolutionary intere

73 ful in sexual selection, both through female mate choice and through aggressive interactions.

74 This economic principle also applies to mate choice and, perhaps surprisingly, pregnancy.

75 This study demonstrates that mate choice and/or male-male competition are correlated

76 evolutionary processes of sexual selection (mate choice) and natural selection (predation), and prop

77 l roles of premating sexual selection (e.g., mate choice) and natural selection have received little

78 h members derive the benefits of protection, mate choice, and centralized information, balanced by th

79 on may be important in the evolution of sex, mate choice, and diploid life-cycles, and in the extinct

80 to variation in plumage, social behavior and mate choice, and is maintained in the population by nega

81 ighlight the importance of variation in male mate choice, and of identifying mechanisms in order to u

82 rtant implications for conventional views of mate choice, and offers inspiration for the design of mi

83 they relate to signal-receiver coevolution, mate choice, and reproductive isolation.

84 focused on natural behaviors like foraging, mate choice, and social interactions.

85 MHC) has implications for adaptive immunity, mate choice, and social signalling, how diversity at the

86 and birds express mate preferences and make mate choices, and data suggest that this "attraction sys

87 ent aggression and copulation, exhibits male mate-choice, and employs multiple mating tactics.

88 quality cues play an important role in human mate-choice, and height and waist interact to signal hea

89 how the evolution of self and interspecific mate choice are linked.

90 on and the adaptive logic (if any) of female mate choice are subjects of lively debate.

91 This evolution occurs if the benefits of mate choice are sufficiently large relative to the cost

92 mation and influence social interactions and mate choices as contributing factors to perceived beauty

93 This pattern was confirmed in mate-choice assays in cages.

94 Initially, female mate choice attracted the interest of behavioral ecologi

95 however, also be direct precopulatory female mate choice based on male genital traits.

96 Like mate-choice based on tenure, choice based on dispersal s

97 thought to overwhelm the genetic benefits of mate choice because preferred males incur a cost through

98 hysiology to investigate the architecture of mate choice behavior in Heliconius cydno butterflies, a

99 eflectance and polarization-dependent female mate choice behavior with no polarization-dependent cour

100 lts suggest that the genetic architecture of mate choice behavior, in this case, is more complex than

101 Mate choice behaviors are among the most important repro

102 This pattern of results is consistent with mate choice being mediated by a general preference for l

103 data robustly discriminate patterns of male mate choice between humans and chimpanzees.

104 se of the variation in costs and benefits of mate choice both between females and within individual f

105 sexual selection not only depends on initial mate choice but also mate switching.

106 s affected by survival of individuals and by mate choice, but how sexual selection affects adaptation

107 ion, competition between (usually) males and mate choice by (usually) females create important intras

108 influenced the perceptual processes used in mate choice by female tungara frogs.

109 hifts are probably because of flexibility in mate choice by individual females and that they parallel

110 tional post-mating (that is, cryptic) female mate choice can also occur in species with external fert

111 Our results show that mate choice can play an important role in improving repr

112 that behavioural traits such as shoaling and mate choice can promote population mixing if individuals

113 e, we propose a new model that explains this mate choice complexity with one general hypothesized mec

114 Polarization cues in mate choice contexts may provide aquatic vertebrates wit

115 ate choice, particularly shown by studies on mate choice copying.

116 n selecting mates, challenging the view that mate-choice copying should not occur in species with bip

117 r results support the hypothesis that female mate choice could have driven the evolution of larger pe

118 , species recovery should benefit if natural mate choice could improve reproductive output (i.e. pair

119 hlight a new potential route by which female mate choice could influence social evolution.

120 of the matings was varied so cryptic female mate choice could operate either in concert or antagonis

121 tween condition-dependent and disassortative mate choice criteria suggest a mechanism by which female

122 cent finding that female Drosophila copy the mate-choice criteria of other females introduces a mains

123 les mate only once in their lifetime, making mate choice critically important for reproductive succes

124 transmission, and receipt of crucial sensory mate-choice cues that affect fitness.

125 es affect the fitness consequences of female mate choice decisions and we determine how the magnitude

126 ng series of studies on mice have shown that mate choice decisions can be made on the basis of indivi

127 ong series of studies on mice has shown that mate choice decisions can be made on the basis of indivi

128 The uncertainty of mate choice decisions induced by unobserved male attribu

129 spective mates determines the uncertainty of mate choice decisions-the reliability of an observed mal

130 ency can make behavior an adaptive trait for mate choice decisions.

131 em's processing of social signals related to mate choice decisions.

132 d with the to-be-realized fitness benefit of mate choice decisions.

133 Queens of social insects make all mate-choice decisions on a single day, except in honeybe

134 se-induced errors in evolutionarily critical mate-choice decisions.

135 Transitivity in mate choice demonstrates that the quality of potential m

136 speciation is possible even when fitness and mate choice depend on different quantitative traits, so

137 mitted traits that influence the fitness and mate choice determined by another focal cultural trait.

138 In their investigation into whether female mate-choice drives male dispersal, Honer et al. argue th

139 First, why does mate choice evolve at all?

140 In mate choice experiments, matings between the two species

141 By using a combination of genetic mapping, mate-choice experiments, field observations, and populat

142 However, by using mate-choice experiments, we reveal disassortative mate p

143 our-pattern analysis, landscape genetics and mate-choice experiments, we show that a mimetic shift in

144 By using mate-choice experiments, we show that female brown anole

145 These results indicate that by exercising mate choice female Utetheisa receive both direct phenoty

146 Our results highlight the apparent strong mate choice for close kin in parent pairs of surviving o

147 We found that previously demonstrated male mate choice for conspecific over heterospecific females

148 characteristics and body morphology mediate mate choice for underlying genetic MHC variation.

149 any tasks that affect their fitness, such as mate-choice, foraging, and predator avoidance.

150 Male mate choice has been reported in the fruit fly, Drosophi

151 Moreover, environmentally dependent mate choice has evolved only in populations and species

152 s widely appreciated but diversity in female mate choice has received little attention.

153 ase in the number of variable loci affecting mate choice has the opposite effect.

154 If resource use and mate choice have a common genetic basis through pleiotro

155 Whereas many studies on mate choice have measured the relative attractiveness of

156 The perceptual mechanisms underlying female mate choice have not been identified, complicating effor

157 otheses, including a modified version of the mate choice hypothesis, are discussed.

158 by mapping both divergent traits and female mate choice in a classic model of ecological speciation:

159 multiple sensory modalities, are involved in mate choice in a wide range of animal taxa.

160 l importance of learning and memory on adult mate choice in an arthropod.

161 only drift in small populations and bias in mate choice in an invasive context may explain our resul

162 ing in a direct experimental test for mutual mate choice in captive populations of Zebra finches (r =

163 ed contrasting patterns of variation in male mate choice in D. melanogaster.

164 f social learning and cultural conformity in mate choice in Drosophila might allow for the investigat

165 that affects both desiccation resistance and mate choice in Drosophila serrata.

166 By measuring mate choice in F2 hybrid females, we allowed for recombi

167 stic/developmental processes associated with mate choice in flowering plants is sparse.

168 eveal costly traits that govern evolution of mate choice in humans and the importance of trade-offs a

169 new insight into the mechanisms that govern mate choice in humans and warrant the search for the gen

170 been believed to be a critical component of mate choice in humans.

171 date to examine the fitness benefits of free mate choice in humans.

172 strong evidence for inbreeding avoidance via mate choice in kin classes with relatedness >=0.25.

173 accumulating evidence of condition-dependent mate choice in many species, that is, individual prefere

174 ls the potential advantages of idiosyncratic mate choice in monogamous animal species.

175 in their study and so could be irrelevant to mate choice in nature.

176 ncompatibilities may affect the evolution of mate choice in plants.

177 t also reveals phenotypic plasticity in male mate choice in response to cues encountered in each choi

178 e for a primary role of both male and female mate choice in sexual selection.

179 , there exists only scant evidence of female mate choice in species mating on arenas, so-called leks.

180 Here we demonstrate that mate choice in the fruit fly Drosophila melanogaster res

181 al (imitative) factors in determining female mate choice in the guppy, Poecilia reticulata.

182 ing the cognitive processes underlying human mate choice in Western society: (i) mate preference is c

183 esponse to sexual signals or the strength of mate choice) in more than one environment, and used a ph

184 However, human mate choice, in many cultures, is heavily controlled by

185 in how effectively they avoid inbreeding via mate choice-in turn, demanding detailed demographic and

186 Many key issues regarding patterns of mate choice, including sensory biases, context dependenc

187 effects, determine how sexual selection and mate choice influence broader-scale processes like repro

188 Female mate choice influences the maintenance of genetic variat

189 These experiments assessing the role of mate-choice information on the brain using a paradigm of

190 involves strong selection within species on mate choice interactions.

191 tion occurs inside or close to an adult, (2) mate choice involves long-distance signals, (3) adults o

192 The evolution of mate choice is a function of the heritability of prefere

193 owerbirds (Ptilonorhynchus violaceus) female mate choice is a multistage process, where females of di

194 Sexual selection by mate choice is a powerful force that can lead to evoluti

195 those in which females engage in polyandry, mate choice is a sequential process in which a female mu

196 Mate choice is an evolutionarily critical decision that

197 The evolution of mate choice is believed to be important in speciation.

198 e morphological traits are highly heritable, mate choice is expressed as a positive correlation betwe

199 ng have led animal biologists to assume that mate choice is generally biased against relatives.

200 onsistent with the conclusion that Hutterite mate choice is influenced by HLA haplotypes, with an avo

201 t this cross-culturally universal pattern of mate choice is most consistent with a Euclidean model of

202 , including humans, indicates that MHC-based mate choice is not restricted to the genus Mus.

203 gs demonstrate that a conclusion of adaptive mate choice is not yet justified.

204 gregations and the extent of male and female mate choice is poorly understood.

205 To understand the evolution of male mate choice it is important to understand variation in m

206 n mate detection and assessment, as rational mate choice largely persists when visual or chemical sen

207 ow gradual divergence in a trait involved in mate choice leads to the formation of new species.

208 ans and other species that benefit from free mate choice led us to hypothesize that it also confers r

209 of assortative mating arises primarily from mate choice ("like attracts like"), which can be constra

210 les experimentally evolved in the absence of mate choice lost this preference for symmetry, suggestin

211 initially suggested that differences in male mate choice may be due to a couple loci with large effec

212 gametophyte (sperm) competition and maternal mate choice may have been key features of the earliest a

213 ts that odor-based mechanisms of MHC-related mate choice may occur in birds.

214 derstanding the relationship between BTs and mate choice may offer insights into patterns of variatio

215 s involved in both ecological divergence and mate choice may produce reproductive isolation and speci

216 lysis of the "taste"; an increasing focus on mate choice mechanisms before, during, and after mating

217 Focusing on mate-choice mechanisms may clarify longstanding evolutio

218 same species can illuminate trade-offs among mate-choice mechanisms.

219 Mate choice models derive from traditional microeconomic

220 eeding pairs to that expected under multiple mate-choice models, finding that pair relatedness is con

221 eromone components that play a major role in mate choice, namely the (Z)-9-tetradecenol and hexadecan

222 ge color, an "observer" female will copy the mate choice of another ("model") female.

223 lection will be low as more females copy the mate choice of other copiers without assessment.

224 ppies will, however, also copy (imitate) the mate choice of other females in that when two males are

225 d the less colorful male and thus copied the mate choice of others, despite a strong heritable prefer

226 the more colorful male and did not copy the mate choice of the other female.

227 lations could be exploited to manipulate the mate choice of transgenic release stocks are discussed.

228 play a major role in sexual selection, with mate choice often depending on conspicuous coloration an

229 ions have examined the effects of sequential mate choice on the operation of sexual selection, how fe

230 The effect of free mate choice on the relative magnitude of fitness benefit

231 both animal perception and the influences of mate choice on the tempo and mode of evolution.

232 icate that socializing animals and providing mate choice opportunities increase breeding success of r

233 not distinguish between phenotypes in either mate choice or cannibalism frequency.

234 re is overestimated and may not be driven by mate choice or mating competition for preferred mates.

235 are insufficient to explain the evolution of mate choice or of sexual ornamentation.

236 ggests that these differences are related to mate choice or species isolation.

237 cond, what factors determine the strength of mate choice (or intensity of sexual selection) in each s

238 cesses like those associated with viability, mate choice, or local adaptation, and "speciation genes"

239 s not clear whether this is similarly due to mate choice, or whether mate choice affects only part of

240 viors, including mate and food localization, mate choice, oviposition site selection, kin recognition

241 s across vertebrate taxa, focusing on female mate choice, pair-bonding, and aggressive behavior.

242 e for symmetric males in Drosophila, using a mate-choice paradigm where males with environmentally or

243 in long-range attraction and in close-range mate choice; parapheromones may be very useful in pest m

244 uably the most important sense, underpinning mate choice, parental care, territoriality and even dise

245 ion obtained from conspecifics can influence mate choice, particularly shown by studies on mate choic

246 ex (MHC or H-2) have been shown to influence mate choice, pregnancy block, and maternal behavior in m

247 Much of the evolutionary literature on mate choice presumes that individual mate preferences fu

248 ds of information in different stages of the mate choice process, or function as redundant signals to

249 ce for male cognition at three stages of the mating choice process: social pairing, extra-pair mating

250 During mate choice, receivers often assess the magnitude (durat

251 The mechanisms controlling mate choice remain poorly understood.

252 , and decision-making logics that facilitate mate choice, rival deterrence, and monogamy, gating spre

253 effect can comprise a substantial portion of mate choice's overall effect as a postzygotic barrier to

254 ulti-pronged study, combining the effects of mate choice, shoaling behaviour and genetics.

255 ts that affect ecological performance and/or mate choice show remarkably localized genomic differenti

256 spersal status itself is important in female mate-choice, such that females prefer immigrants over na

257 Both habitat slope selection and mate choices suggest ongoing incipient sympatric speciat

258 ive trait loci (QTLs) associated with female mate choice that also predicted female morphology along

259 s of sexual selection, in addition to female mate choice, that drive the origin and maintenance of sp

260 be used as visual cues during intraspecific mate choice, the strong resemblance of the iridescent si

261 Predominant mate choice theories assume preferences are determined s

262 llowing hypotheses from optimal foraging and mate choice theories: (a) raiding decisions are time con

263 ction and reconciles inconsistencies between mate choice theory and observed behavior.

264 ntroduced to sociality and promiscuity (free mate choice), they adapted within two generations.

265 erception and affect diverse behaviors, from mate choice to foraging decisions.(1-3) Although recepto

266 so considerable potential for cryptic female mate choice to operate on the basis of sperm karyotype.

267 ift from a reliance on pre-copulatory female mate choice to polyandry in conjunction with post-zygoti

268 een close relatives, ranging from pre-mating mate choice to post-mating gamete selection, have evolve

269 We conducted mate choice trials in an experimental tank that illumina

270 ideopolarimetry and polarization-manipulated mate choice trials, we found sexually dimorphic polarize

271 liar or unfamiliar manipulated phenotype for mate-choice trials.

272 isms in order to understand the evolution of mate choice under varying ecological conditions.

273 Thus, when the benefits of mate choice vary, females may radically alter their mate

274 Heritable BTs can enable informed mate choice via indirect benefits.

275 ods used in one study in which variable male mate choice was found, using the stock population from t

276 Across 222 studies, the strength of mate choice was significantly context-dependent, and mos

277 evidence that each parameter plays a role in mate choice, we have little understanding of the relativ

278 However, the fitness consequences of mate choice were dependent on environmental conditions e

279 variants most strongly associated with male mate choice were tightly linked to the gene controlling

280 us represent a proximate mechanism of female mate choice when ejaculates from multiple males overlap

281 ory as adaptations to mating competition and mate choice, whereas no unifying theory explains traits

282 n of gender characteristics is an outcome of mate choice, which has been assumed to be genetically me

283 pulated to test its role in eliciting female mate choice, which may be driving a speciation event, by

284 on in species recognition and may also guide mate choice within a species.

285 When LMSP and cryptic female mate choice work in concert a high level of LMSP was fou

286 strongly support the hypothesis that female mate choice yields genetic benefits for offspring.