ライフサイエンスコーパス: mate choice

1 ex factors contributing to romantic love and mate choice.

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

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

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

5 ossibly reflecting diverse tactics in female mate choice.

6 that cycle variability may facilitate female mate choice.

7 lfactory system is required for heterosexual mate choice.

8 complex interactions such as cooperation or mate choice.

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

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

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

12 ffspring communication, kin recognition, and mate choice.

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

14 lects the costs and benefits associated with mate choice.

15 ssociated with reduced pre-copulatory female mate choice.

16 ral compatibility between partners with free mate choice.

17 volved differences in the expression of male mate choice.

18 contrasts with previous observations of male mate choice.

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

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

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

22 nstruct and decorate bowers that function in mate choice.

23 quality of the offspring owing to nonrandom mate choice.

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

25 conflict can restore the genetic benefits of mate choice.

26 enotypic traits and functional components of mate choice.

27 Preliminary tests indicate slope-specific mate choices.

28 dentified factors likely to influence female mate choices.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

94 First, why does mate choice evolve at all?

95 In mate choice experiments, matings between the two species

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

129 Female mate choice influences the maintenance of genetic variat

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

131 involves strong selection within species on mate choice interactions.

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

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

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

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

136 Mate choice is an evolutionarily critical decision that

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

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

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

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

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

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

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

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

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

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

147 Focusing on mate-choice mechanisms may clarify longstanding evolutio

148 Mate choice models derive from traditional microeconomic

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

167 The mechanisms controlling mate choice remain poorly understood.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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