Genes, copying, and female mate choice: shifting thresholds

Recent experimental work on guppies (Poecilia reticulata) hasexamined the strength of genetic and cultural (copying) factorsin determining female mate choice. Using females from a populationwith a heritable preference for the amount of orange body colorpossessed by males, prior work discovered that a threshold differencein orange color among males existed below which females wouldchoose a less orange male if they observed another female choosethat male, but above which they consistently preferred the moreorange of the males, regardless of whether they viewed anotherfemale prefer the less orange male. I tested whether this thresholdcan be shifted by increasing the amount of mate-copying informationavailable to a female. I demonstrate that when a female hasthe opportunity to see two different model females independentlyprefer the less orange of two males or a single female neara drab male for a longer period of time (twice as long as inprior work), the observer female prefers this drab male evenwhen males dramatically differ in orange coloration.     

Nonindependent mating in a coral reef damselfish: evidence of mate choice copying in the wild

Theoretical and experimental studies have shown that mate choicecopying is a viable mating strategy under certain conditions.Copying experiments in fish have been conducted primarily inthe laboratory, except for one study conducted in the fieldunder artificial conditions. We investigated whether in a wildpopulation of the coral reef whitebelly damselfish (Amblyglyphidodonleucogaster) females copy the choice of other females. Femalespreferentially spawn with males that have recently mated. Todetermine if the presence of new eggs in the nest was the reasonfemales chose mates or whether females were mate choice copying,we conducted egg-switching experiments. Eggs from males thatrecently mated were donated to males that had no eggs. If femalesare mate choice copying, then donor males with no eggs in thenest should continue to receive additional eggs. If femalesare using the presence of new eggs as the criterion for matechoice, then foster males with new eggs should receive additionaleggs. We found that donor males received new eggs significantlymore often than expected. More females mated with donor malesthan foster males. Furthermore, females preferentially choseto mate with males whom they had seen mating with another female.Females appear to remember the mate choice of other femalesand choose to mate with those same males even after 1 day. Theseresults suggest that females may be copying the mating decisionof other females rather than choosing males based on the presenceof new eggs in the nest.     

Male but not female pipefish copy mate choice

If mate choice is costly, an individual may reduce the costsof choice by observing and copying the mate choice of others.Although copying has received much attention during the past10 years, evidence of copying is not very strong, partly becauseof problems with distinguishing copying from other mechanismscreating similar mating patterns. I conducted an aquarium experimentusing the deep-snouted pipefish Syngnathus typhle, a specieswith reversed sex roles and mutual mate choice. I tested whethercopying occurred both during male and female mate choice. Theresults showed that males, but not females, displayed more towardan individual, which they perceived as popular among others,and this was interpreted as male mate choice copying. Whilebeing the first evidence of copying in a sex-role–reversedspecies, the sex difference in behavior mirrors the sex-rolepattern and begs the question whether we should predict copyingonly in females in other species with mutual choice but conventionalsex roles.     

Experimental tests of copying and mate choice in fallow deer (Dama dama)

In fallow deer (Dama dama), as well as in other lek-breedingungulates, receptive females arriving at leks commonly joinmales that are defending large harems. This tendency enhancesdifferences in harem size and mating success between males.It could occur because females independendy move to the samemales, because females are attracted to males with females,or because females are attracted to each other. Using controlledexperiments with estrous female fallow deer, we show that, althoughfemales are more attracted to males with harems than to thosewithout, they are as frequently attracted to groups of femaleswithout a male as to female groups with males. We conclude thatfemale fallow deer joining leks are attracted to each otherand copy each other's movements. As yet, there is no firm evidencein fallow deer or in other lek-breeding ungulates that femalescopy each other's choice of mating partners. Key words: Damadama, fallow deer, lek breeding, mate choice, copying behavior.[Behav Ecol 4: 191–193 (1993)]     

Designing mate choice experiments

The important role that mate choice plays in the lives of animals is matched by the large and active research field dedicated to studying it. Researchers work on a wide range of species and behaviours, and so the experimental approaches used to measure animal mate choice are highly variable. Importantly, these differences are often not purely cosmetic; they can strongly influence the measurement of choice, for example by varying the behaviour of animals during tests, the aspects of choice actually measured, and statistical power. Consideration of these effects are important when comparing results among studies using different types of test, or when using laboratory results to predict animal behaviour in natural populations. However, these effects have been underappreciated by the mate choice literature to date. I focus on five key experimental considerations that may influence choice: (i) should mating be allowed to occur, or should a proxy behavioural measure of preference be used instead? (ii) Should subjects be given a choice of options? (iii) Should each subject be tested more than once, either with the same or different stimuli? (iv) When given a choice, how many options should the subject choose between? (v) What form should the experimental stimuli take? I discuss the practical advantages and disadvantages of common experimental approaches, and how they may influence the measurement of mate choice in systematic ways. Different approaches often influence the ability of animals to perceive and compare stimuli presented during tests, or the perceived costs and benefits of being choosy. Given that variation in the design of mate choice experiments is likely unavoidable, I emphasise that there is no single ‘correct’ approach to measuring choice across species, although ecological relevance is crucial if the aim is to understand how choice acts in natural populations. I also highlight the need for quantitative estimates of the sizes of potentially important effects, without which we cannot make informed design decisions.     

A Comparative Bayes tactic for mate assessment and choice

Models of mate choice tactics have assumed that females randomlyencounter males when collecting information and the informationis perfect. Empirical observations of four bird species showthat females selectively visit males and repeat visits to malesbefore mating. This suggests that the assumptions of previousmodels have been too restrictive. An alternative model of informationgathering and mate choice, which relaxes the assumptions ofrandom encounters and perfect information, is presented. Inthis Comparative Bayes model, the decision of when and fromwhom to collect information is made using Bayesian estimatesof each male's quality. Predictions from the model are that:(1) the occurrence of mate assessment will increase as initialuncertainty about the quality of males increases, as the costof gathering information decreases, and as the signal perceivedby the female becomes a better representation of males' actualqualities; (2) the occurrence of repeat visits to males willbe highest when signals from males are of medium reliability;and (3) the decision of which male to assess will depend onthe estimated qualities of males, prior certainty about eachmale's quality, the reliability of each male's signal, and thecosts of assessment. Simulations compare the fitness outcomesof the Comparative Bayes tactic to other mate choice tactics.The fitness from the Comparative Bayes tactic is significantlyhigher than from the fixed threshold tactic and than from thebest-of-n tactic when the cost of assessment is low. [BehavEcol 7: 451–460 (1996)]     

Female mate choice in vervet monkeys (Cercopithecus aethiops sabaeus)

Female mate choice was examined in a captive group of vervet monkeys (Cercopithecus aethiops sabaeus). Male-female interactions were examined under both dyadic and group conditions to determine whether females mate with different males under the two conditions. Results showed that all females preferred to mate with the alpha male under both dyadic and group conditions. Alpha females, however, were more successful than subordinate females in rejecting the sexual solicitations of subordinate males. Thus female dominance status played an important role in determining the degree to which females exercised mate choice.     

Female within-nest spawning-site preference in a paternal brooding blenny and its effect on the female mate choice

Female spawning-site preference within a nest and its effect on the female mate choice in a paternal brooding blenny Rhabdoblennius ellipes , were examined in rocky intertidal pools using artificial nests. The number of eggs deposited at the nest entrance site was lower than the number deposited at the center and at deep sites. Moreover, the within-nest difference in the egg developmental stage indicated that eggs at the nest entrance site were deposited after those at the center and deep sites. These results indicated that females prefer to spawn eggs in the center and deep sites rather than at the entrance site. Owing to the higher egg mortality rate at the entrance site, females may avoid spawning at such sites. An analysis of the nests in the study area suggested that the within-nest site preference affects female mate choice that is females avoided nests where only the entrance site was available for spawning and instead spawned in nests where the center and deep sites were available.     

Indirect mate choice, direct mate choice and species recognition in a bower-building cichlid fish lek

Sexual selection arising through female mate choice typically favours males with larger, brighter and louder signals. A critical challenge in sexual selection research is to determine the degree to which this pattern results from direct mate choice, where females select individual males based on variation in signalling traits, or indirect mate choice, where male competition governs access to reproductively active females. We investigated female mate choice in a lekking Lake Malawi cichlid fish, Hemitilapia oxyrhynchus, in which males build and aggressively defend sand 'bowers'. Similar to previous studies, we found that male reproductive success was positively associated with bower height and centrality on the lek. However, this pattern resulted from males holding these territories encountering more females, and thus their greater success was due to indirect mate choice. Following initial male courtship, an increase in the relative mating success of some males was observed, but this relative increase was unrelated to bower size or position. Crucially, experimentally manipulating bowers to resemble those of a co-occurring species had no appreciable effect on direct choice by females or male spawning success. Together, these results suggest indirect mate choice is the dominant force determining male-mating success in this species, and that bowers are not signals used in direct mate choice by females. We propose that, in this species, bowers have a primary function in intraspecific male competition, with the most competitive males maintaining larger and more central bowers that are favoured by sexual selection due to higher female encounter rates.     

Parasites, male-male competition and female mate choice in the sand goby

Male sand goby Pomatoschistus minutus dominance in competition over nest sites was associated with higher body condition but not with the intensity of infection with any individual parasite of six different species, nor with an overall index combining relative levels of infection by all parasites. Body condition was not related to the intensity of infection with any individual parasite nor with the index of total relative parasite load. In trials in which females spawned, they showed a tendency to choose dominant over subordinate males as mates, but did not consistently choose less parasitized males. Variation in the relative size of the dorsal fins of males was detected, and this related to numbers of the ectoparasitic monogenean Gyrodactylus sp., suggesting that at least some infections have phenotypic effects that could allow females to detect and avoid the most heavily infected males.     

The evolution of male mate choice in insects: a synthesis of ideas and evidence

Mate choice by males has been recognized at least since Darwin's time, but its phylogenetic distribution and effect on the evolution of female phenotypes remain poorly known. Moreover, the relative importance of factors thought to underlie the evolution of male mate choice (especially parental investment and mate quality variance) is still unresolved. Here I synthesize the empirical evidence and theory pertaining to the evolution of male mate choice and sex role reversal in insects, and examine the potential for male mating preferences to generate sexual selection on female phenotypes. Although male mate choice has received relatively little empirical study, the available evidence suggests that it is widespread among insects (and other animals). In addition to 'precopulatory' male mate choice, some insects exhibit 'cryptic' male mate choice, varying the amount of resources allocated to mating on the basis of female mate quality. As predicted by theory, the most commonly observed male mating preferences are those that tend to maximize a male's expected fertilization success from each mating. Such preferences tend to favour female phenotypes associated with high fecundity or reduced sperm competition intensity. Among insect species there is wide variation in mechanisms used by males to assess female mate quality, some of which (e.g. probing, antennating or repeatedly mounting the female) may be difficult to distinguish from copulatory courtship. According to theory, selection for male choosiness is an increasing function of mate quality variance and those reproductive costs that reduce, with each mating, the number of subsequent matings that a male can perform ('mating investment') Conversely, choosiness is constrained by the costs of mate search and assessment, in combination with the accuracy of assessment of potential mates and of the distribution of mate qualities. Stronger selection for male choosiness may also be expected in systems where female fitness increases with each copulation than in systems where female fitness peaks at a small number of matings. This theoretical framework is consistent with most of the empirical evidence. Furthermore, a variety of observed male mating preferences have the potential to exert sexual selection on female phenotypes. However, because male insects typically choose females based on phenotypic indicators of fecundity such as body size, and these are usually amenable to direct visual or tactile assessment, male mate choice often tends to reinforce stronger vectors of fecundity or viability selection, and seldom results in the evolution of female display traits. Research on orthopterans has shown that complete sex role reversal (i.e. males choosy, females competitive) can occur when male parental investment limits female fecundity and reduces the potential rate of reproduction of males sufficiently to produce a female-biased operational sex ratio. By contrast, many systems exhibiting partial sex role reversal (i.e. males choosy and competitive) are not associated with elevated levels of male parental investment, reduced male reproductive rates, or reduced male bias in the operational sex ratio. Instead, large female mate quality variance resulting from factors such as strong last-male sperm precedence or large variance in female fecundity may select for both male choosiness and competitiveness in such systems. Thus, partial and complete sex role reversal do not merely represent different points along a continuum of increasing male parental investment, but may evolve via different evolutionary pathways.     

Female mate assessment and choice behavior affect the frequency of alternative male mating tactics

Explanations for the existence of alternative male mating tacticsfocus primarily on male–male competition. Mating systems,however, are composed of interactions both within and betweenthe sexes, and the role of female behavior in shaping male matingtactics should not be overlooked. By using a dynamic state variablegame model, I examine how female mate assessment and choicebehavior affect the frequency of alternative male mating tactics.When females can accurately assess the quality of males, onlymales with high quality are likely to be chosen as mates, andthus, lower-quality males gain little fitness from courtingfemales. This leads lower-quality males to switch to an alternativemating tactic that attempts to circumvent female mate choice.In contrast, if the abilities of females to accurately assessmales are constrained by assessment costs, imperfect information,or time constraints, or if the pool of available males is smaller,then lower-quality males are increasingly chosen as mates andthey less often use alternative mating tactics. Thus, femalebehavior shapes the frequency of alternative male mating tactics.A consequence of this game between the sexes is that male behavior(i.e., increased alternative mating tactics) decreases the benefitsfemales might otherwise gain from lower assessment costs, clearersignals of male quality, more time to choose a male, and moremales from which to choose a mate.     

The effect of male tenure and female mate choice on paternity in free-ranging Japanese macaques

In this study, the paternity of all the infants born in 2002 and 2003 in a free-ranging Japanese macaque (Macaca fuscata) group at Arashiyama in Kyoto, Japan, was analyzed in relation to males' age, dominance rank, and tenure and females' mate choice. The fathers of 20 out of 23 infants were determined by DNA analyses. Central adult (high-ranking) males sired two infants, whereas peripheral adult (low-ranking) males sired 14 infants. Young males sired only one infant. Among adult males, tenure was the most dominant factor that negatively affected male reproductive success. The mating behavior of females who gave birth was also analyzed. The number of male copulations in the peri-fertilization period was positively correlated with the number of infants that they sired. Females copulated with central males with a long tenure only when fertilization was unlikely or impossible. The females probably avoided insemination by males with a long tenure and selected males with a shorter tenure as their mating partners during the ovulation period.     

Bias in studies of heterozygosity and mate choice

A key question for molecular and behavioural ecologists who study mating systems is to understand why, in many species, females choose to mate with extra-pair males. Recently a possible explanation, 'genetic compatibility', has gained increasing empirical support (for a comprehensive review, see Kempenaers 2007 ). Genetic compatibility hypotheses assume that females seek extra-pair mates with alleles that complement their own. Typically, this will be achieved by mating with a male of a different genotype than her own, in order to maximise the heterozygosity of her offspring. Because numerous studies have indicated positive associations between heterozygosity and fitness (see Coltman & Slate 2003 ), it follows that mating with 'compatible' males will result in heterozygous, and therefore fit, offspring. Most empirical support for genetic compatibility has been obtained with microsatellite markers that have first been used to assess parentage and then to estimate relatedness and/or individual heterozygosity. A problem with this approach is a possible bias that favours the detection of extra-pair paternity when the extra-pair male has a genotype different from that of the female and her social mate. This in turn could lead to the erroneous conclusion that extra-pair males are less related to the female than within-pair males. In this issue of Molecular Ecology , Wetzel & Westneat 2009 (hereafter W&W), use simulation studies to assess the extent of this bias, using parameter estimates obtained from recent empirical data. They identify two forms of bias that may affect tests of the genetic compatibility hypothesis, and provide guidelines on how these biases may be avoided.