Why do female pied flycatchers mate with already mated males: deception or restricted mate sampling?

The polygyny threshold model suggests that females make an optimal choice between mated and unmated males. However; in birds in which males provide parental care, the fitness of secondary females is often lower than expected from this model. This has been explained by the deception hypothesis, which states that males hide their mating status and deceive females into polygyny. Yet there is no direct evidence that secondary females are unaware of male mating status when they settle. Alternatively, females settle with mated males as a result of mate competition and costs of searching. We used videofilming at nestboxes defended by males to study mate sampling of female pied flycatchers Ficedula hypoleuca. The females visited on average only 2.74 males (range 1–8, n = 43). Most (16 of 19) of the polygynous matings occurred because females had only visited mated males, or the unmated males visited became occupied by competitors during the sampling period. Among females that could choose between both mated and unmated males, the majority (13 of 16) settled with unmated males. These results lend little support to the deception hypothesis but are consistent with the view that females are able to detect male mating status but sometimes settle with mated males because of cost of searching. Prospecting females seemed willing and able to suffer the cost of fighting with aggressive primary females in the males' secondary territory if no alternative mating options were available. In addition to male mating status, females took male quality (plumage colour, age) into account in mate choice but the former appeared to be the more important. Correspondence to: T. Slagsvold     

Sex ratio,local mate competition and mating behaviour in the aphid Pemphigus spyrothecae

Summary The primary sex ratio and the selective factors associated with it were investigated in the aphid Pemphigus spyrothecae. The sexuparae gave birth to an average of 1.99 ± 0.01 (1–2) males and 5.06 ± 0.09 (2–6) females [± SE (range), n = 147]. The average weight of individual males was 16.2±0.86 (13–18) g (n = 5) and of females 40.7 ± 0.71 (38–46) g (n = 15). The overall investment ratio by the mother sexuparae was therefore 1:6.4, equivalent to a proportionate investment in sons of 0.135 (interquartiel range: 0.117–0.165). There was a highly significant correlation between the size of the sexupara and the number of her daughters: the number of sons was independent of sexupara size. Field observations and laboratory experiments showed that the sexuparae aggregate on poplar bark before giving birth to the sexuals: they appear to behave in such a way that there is always at least one other sexupara in the crevice with them. The average number of sexuparae forming a foundress group, within which offspring could potentially mate with each other, was 2.48±0.19 (1–9) (n = 80). The life-time activity patterns of the sexuals (which moult four times but do not feed) was described. Both sexes are active shortly after birth; they are then immobile for a long period but become very active again after emerging as adults (after about 42 h in males, 51 h in females). Each male can mate with up to 14 females. The females are receptive to a second male for only a relatively short period (ca. 15–20 min) after their first mating. There is considerable competition between males during mating (just as intense between clonal sibs as non-sibs) and evidence for post-copulatory mate-guarding by the males. There is no evidence that females prefer to mate with non-sibs rather than sibs. The observed sex ratios and the mating behaviour of the aphids are discussed in relation to models of local mate competition assuming variable female fecundity, as developed by Frank (1987a, b) and Yamaguchi (1985) (the constant male hypothesis) and by Stubblefield and Seger (1990).     

Measuring mate choice using correlation: the effect of female sampling behaviour

For intersexual selection to occur, it is necessary that females choose between males. It is now well appreciated that constraints exist, which preclude females sampling all the available males in a population. These constraints are likely to have caused the evolution of sampling rules (such as the “best-of-n” rule) by which females sample males. Here we investigate the impact of female subsampling of the male population, not on the evolution of sampling behaviour, but on the population-level correlation between a male trait and currencies such as reproductive success. This study is important as it illustrates when population-level correlations can be safely used to infer the presence and strength of sexual selection in the field. We find that the correlation between a male trait and a mate choice variable rises steeply as the number of males sampled by each female increases, flattening above seven to ten males sampled. This shape is found to be remarkably robust, and little affected by, for example, the mate choice variable used, by noise in assessment, by sampling behaviour depending on female quality, or by population size. The only variable found to have a large impact is male clumping according to their “quality”. If females are sampling about four males, the maximum correlation that can be found at the population level is in the range 0.4–0.6, perhaps as little as 0.1 if males are strongly clumped. A recent review of the literature suggests that four is the average number of males that females sample. Thus, the absence of a strong correlation cannot by itself be used to infer that sexual selection is weak, as it may be due to females sampling few males. Received: 18 May 1998 / Accepted after revision: 18 July 1998     

Does female aggression prevent polygyny? An experiment with pied flycatchers (Ficedula hypoleuca)

The female aggression hypothesis states that resident females may be able to prevent polygyny by behaving aggressively towards intruding females. A critical test of the hypothesis is to provide prospecting females with a choice between displaying mated males some of which have initial mates with artificially reduced levels of aggressiveness. Here we present a mate choice experiment on pied flycatchers Ficedula hypoleuca. The species is a cavity nester, and resident females were prevented from behaving aggressively by enclosing them within their own nestboxes: narrowing the entrance hole so that they could not escape but could still let their head out and have some contact with their mate. This treament had only a minor influence on male behaviour. We studied whether the experimental males were better able to attract a new female than a control group of mated males. Four predictions from the female aggression hypothesis were supported. (1) Mating success of control males was positively related to the distance between their primary and secondary territory. (2) For experimental males, mating success was unrelated to interterritorial distance. (3) Experimental males had higher mating success than control males when the interterritorial distance was short but (4) not when it was long. Experimental males had much lower mating success than unmated males, as would be expected if prospecting females are able to discover male mating status from cues other than visits by primary females to their mates' secondary nest sites. Received: 5 January 1998 / Accepted after revision: 30 December 1998     

Mate sampling behaviour of black grouse females (Tetrao tetrix)

We studied female mate sampling behaviour in lekking black grouse (Tetrao tetrix). Females mainly visited males occupying territories in the centre of the lek with relatively large territories. They were also more likely to visit males that had high attendance. The same factors were also correlated with male mating success. A multiple regression model including these factors explained more of the variance in female visits per male (53%) than in mating success (33%). The pattern of female sampling conformed with a pool comparison (best-of-n) tactic. Such a tactic is expected if the costs of sampling are low. Females of high body mass visited more males than lighter females, however, which indicates that females may vary in their search tactics and suggests that there may be search costs. The existence of costs is further suggested by the fact that if the mate from a previous year was still present, females always mated with the same male in the following year. Though search costs were not measured directly, our findings suggest that some costs are negligible (e.g. energetic exhaustion or predation) whereas others (timing of mating) may be more important.     

Mate sampling behaviour of female pied flycatchers: evidence for active mate choice

Summary This paper presents major new evidence for active mate choice of female pied flycatchers, Ficedula hypoleuca. Fifteen color-ringed females were released into a study area containing 23 unmated males defending one nestbox each. Through intensive surveillance, the behavior of the females was observed during 2 consecutive days. Twenty-two of the males received a total of 131 female visits. Six of the females settled in the study area, and their premating period lasted 1.3–2.5 days. The females were seen searching for mates for at least 6–32 h and were seen visiting at least 1–9 different males. Hence, some of the females rejected males before mating. Nevertheless, the females settled close to the site of release (range: 16–243 m), suggesting that they mated with one of the first males encountered. Females visited males most frequently in the morning, and the diurnal distribution of visits was significantly correlated with male song activity. Offprint requests to: S. Dale     

Behavioral strategies of American kestrels during mate replacement

Summary To determine the influence of mate replacement on the behavior and reproductive success of wild American kestrels (Falco sparverius) we removed 4 female and 16 male members of breeding pairs during incubation in 1983 and 1984. Eight males and 1 female were replaced within a mean time of 43 h. Widowed females that received a replacement spent less time hunting, but incubated and performed aerial displays more frequently than females that did not receive a replacement. After replacement, widowed females continued to incubate the original clutch, yet copulated and performed other courtship behaviors with the incoming male. Overlapping of normal temporally separate behavioral cues may be a female strategy to gain assistance from a replacement mate. However, none of the original clutches was successfully hatched. Of 8 pairs with replacement males, 2 pairs abandoned their territory, two remained on territory but did not renest, and 4 renested within a mean interval of 18 days. The lone female replacement and her mate copulated and performed nest inspections but then abandoned the territory. Incubation behavior was similar between replacement and control pairs; however, replacement males fed more invertebrate prey to nestling and made many more nest visits. All 3 replacement nests that hatched young failed within 8 days.     

Multiple mating in a lekking bird: why do peahens mate with more than one male and with the same male more than once?

Summary Approximately 50% of marked peahens (Pavo cristatus) mate more than once with lek males. Some females mate with more than one male, others copulate repeatedly with the same male. The frequency of courtship also shows marked variation. Some females repeatedly engage males in courtship interactions after they have succesfully copulated with them. The likelihood of mating with more than one male increases if a female first mates with a non-preferred (unsuccessful male). There is a non-significant tendency for females to copulate with a more successful male when remating. Peahens may mate with a non-preferred male first if they do not encounter a successful male during their initial period of choice, perhaps because the most successful male on a lek was courting another female and/or was defended by another female. There are more aggressive interactions between females in front of preferred males. Preferred males receive more repetitive courtship behaviour and repeated matings. Dominant females are more likely to engage in repetitive courtship and matings. The number of times a female initiates courtship on any one day increases with the number of other females actively courting males at a lek site on that day. We suggest that there is competition amongst females for access to preferred males and that dominant females try to monopolise these males by repeatedly engaging them in courtship interactions. We discuss the implications of these observations for the idea that female may gain directly from mate choice in a species where males contribute nothing but gametes to their offspring. Correspondence to: M. Petrie at the present address     

Male mate choice and male–male competition in the hermit crab Pagurus nigrofascia: importance of female quality

Male mate choice has recently been reported in some animals with male–male competition. In the laboratory, we examined whether males choose their mates based on female quality that was indicated by body size and/or days to prenuptial molt, and the effects of female quality on male–male competition in the hermit crab Pagurus nigrofascia. We collected samples from April to May 2009 at an intertidal shore in Hokkaido, Japan (41°N, 140°E). When a male simultaneously encountered two receptive females in the mate choice experiment, males chose females which require less time to molt. When a male guarding a female with less time to molt was challenged by an intruder, the guarding male defended the female for a longer period and was more likely to win the contest. These results indicate that male P. nigrofascia use time to molt to discriminate between females.     

Time constraints and multiple choice criteria in the sampling behaviour and mate choice of the fiddler crab,Uca annulipes

Active female sampling occurs in the fiddler crab Uca annulipes. Females sample the burrows of several males before remaining to mate in the burrow of the chosen partner. Females time larval release to coincide with the following nocturnal spring tide and must therefore leave sufficient time for embryonic development after mating. Here we show how this temporal constraint on search time affects female choosiness. We found that, at the start of the sampling period (when time constraints are minimal), females selectively sample the larger males in the population. Towards the end of the sampling period (when the temporal constraints increase the costs of sampling), females are less selective. Furthermore, we suggest that the number of males sampled (and other indices of ‘‘sampling effort’’) may not be reliable indicators of female choosiness and may not reflect the strength of female mating preferences under certain conditions. Burrow quality also emerged as an important criterion in final mate choice. Burrow structure potentially influences reproductive success, and mate acceptance based on burrow structure appears to involve a relatively invariant threshold criterion. Since there is no relationship between male size and burrow quality, females are using at least two independent criteria when choosing potential mates. We envisage mate choice as a two-stage process. First, females select which males to sample based on male size. They then decide whether or not to mate with a male based on burrow features. This sampling process explains how two unrelated variables can both predict male mating success. Received: 23 March 1995/Accepted after revision: 14 January 1996     

The effects of mating system on male mate choice in a coral reef fish

Summary We show how mate limitation appears to be critical in determining whether or not males exercise mate choice among available females. Thalassoma bifasciatum is a Caribbean reef fish with two distinct mating patterns: group-spawning and pair-spawning. In both mating systems, female fecundity is variable and size dependent, and female availability is high. However, sperm competition among group-spawning males apparently limits the number of effective matings in which a male may engage, whereas territorial pair-spawning males have little or no such limitation. Group-spawning males should be discriminating in their choice of mates and our data confirm this: there is strong evidence for assortative mating in group-spawns, with more large males joining in mating groups around large females. In contrast, pair-spawning males show no indication of mate preferences, and spawn with all females who arrive at their territories.     

Adaptive responses to local mate competition by the parasitoid,Telenomus remus

Summary The parasitic wasp, Telenomus remus, lays her eggs in diserete patches of moth eggs, where her offspring develop and mate before dispersal, satisfying conditions for local mate competition (LMC). In the presence of other ovipositing females, wasps lay a higher sex ratio (proportion males), as predicted by LMC theory, and achieve this by a combination of two mechanisms, (1) avoidance of superparasitism and a sequence of sex allocation initially biased towards males and (2) a direct increase in sex ratio in the presence of other wasps, sex ratio increases with the proportion of previously parasitized hosts, as predicted by LMC theory. In both cases, chemical traces left by foraging wasps are indicated as the stimuli causing wasps to increase the proportion of males allocated to hosts.     

Sperm competition risk affects male mate choice copying

Mate choice copying was mostly described as a strategy employed by females to assess the quality of potential mates, but also males can copy other males’ mate choice. An open question in this context is whether and how copying males evaluate sperm competition risk, as mating with a female that has already copulated with another male obviously sets the stage for intense sperm competition (i.e., in species with internal fertilization). Using the livebearing Atlantic molly (Poecilia mexicana) as a model, we asked (a) whether males of that species indeed copy other males’ choices, and if they do so, (b) whether copying males strategically adjust their behavior to sperm competition risk. We used an approach where focal males could first choose to associate with a large or a small stimulus female. Mate choice tests were then repeated after an “observation phase” during which either no model male was present (treatment 1, control) or the previously non-preferred female could be seen associating (treatment 2) or physically interacting (treatment 3) with a model male. We found that, after the observation phase, males spent considerably more time with the previously non-preferred female in treatment (2), i.e., they copied the model male’s choice. This effect was much weaker during treatment (3) where sexual interactions between the model male and the formerly non-preferred female were allowed. Males, therefore, seem to adjust their copying behavior strategically to the perceived risk of sperm competition.     

Female reactions to male absence after pairing in the pied flycatcher

Mating with an already mated pied flycatcher (Ficedula hypoleuca) male is costly for a female. Two hypotheses explain why some females still mate with already mated males. The deception hypothesis suggests that some females mate with already mated males since it is difficult to assess perfectly the mating status of a male with separate territories (polyterritoriality). The search cost hypothesis states that females are aware of male mating status but the costs of searching for an unmated male exceed costs associated with the status of secondary female. One potential cue that could disclose a male's mating status is the existence of brief visits to the primary territory by polyterritorial males. To mimic such visits I removed the male from the territory for 60 min soon after female settlement. Only few females abandoned their mates as a consequence of male removal even though they had available unmated males close by. This result is most consistent with the deception hypothesis. Females did not use occasional male absence as a cue to avoid presumably polyterritorial males and in this respect they were not perfect in assessing males.     

Do sex-changing male snails use mate choice to get a jump on their “size advantage”?

Individuals of species that change sex from male to female may gain a “size advantage” from that sex change; that is, as males become larger, they become female, thus increasing their fecundity with their size. However, males could also gain an early and different reproductive size advantage by choosing large females as mates. While male preference for large females has been observed in many dioecious species, we know little about male size preference in sex-changing species. In choice experiments, we examined whether males of two congeneric species of marine sex-changing snails, Crepidula fornicata and C. convexa, chose large females over small ones as partners. We also used choice tests to see whether males of C. fornicata, a species whose members form long-term, multi-animal stacks, would choose two females in a stack over a single female. Surprisingly, males of neither species showed a preference for large females, in spite of the documented fecundity advantage associated with large female-size. Males of C. fornicata chose slightly, but not significantly, more single females than stacks, suggesting that neither number nor size drives mate choice in these animals. Key factors that may influence this lack of size preference include long association time, the likelihood of sperm competition, and the cost of extended mate search; it may also be that sex-change itself, the very factor that creates female-biased sexual size dimorphism in these species, prevents size preference, as males may gain sufficient reproductive advantage from eventually becoming large females themselves to offset any benefit of choosing large females.     

Long-term mate and territory fidelity in neotropical buff-breasted wrens (Thryothorus leucotis)

Among sedentary species, mate and site fidelity may be imposed by year-round territoriality and high annual survivorship, both of which theoretically lead to few opportunities to move between mates and breeding territories. We examined mate and territory fidelity in sedentary neotropical buff-breasted wrens (Thryothorus leucotis) in relation to the opportunities to divorce (vacancies on neighbouring territories), breeding experience and site of origin (within vs outside local breeding population). Overall, buff-breasted wrens showed high rates of mate and territory fidelity between years, with individuals significantly more faithful to their territories than to their partners. Mate and territory fidelity was not forced upon buff-breasted wrens, as most individuals had opportunities to switch mates and territories. However, this was not uniform among all individuals. Individuals that had bred together displayed 100% mate and territory fidelity despite the fact that males and females in almost all experienced pairs had opportunities to switch mates and territories. Local recruits (philopatric offspring that acquired territories in the local breeding population) also displayed mate and territory fidelity, but fidelity occurred because recruits rarely had the opportunity to divorce prior to initiating their first breeding attempt. By contrast, almost half of all territorial individuals that originated outside the local breeding population (immigrants) had opportunity to divorce, with approximately two thirds of them switching mates and territories. Divorces occurred within the first 5 months of pairing, suggesting that immigrants may have sampled mates and territories before forming permanent partnerships.     

Interspecific interference competition and mate choice in the soldier beetle,Chauliognathus pennsylvanicus

Summary Interference competition directed at soldier beetles, Chauliognathus pennsylvanicus, by four aggressive wasp species changed the mate choice of females. In the absence of wasps, females mated more frequently with males of greater weight and greater antennal scape diameter. Only in the presence of wasps did females frequently mate when they did not contain mature ova. When wasps were abundant, the proportion of beetles mating was higher. Wasps reacted aggressively toward mating beetles less frequently than toward single beetles. Therefore, females may have fed more efficiently in the presence of wasps when coupled.     

Black Grouse leks on ice: Female mate sampling by incitation of male competition?

Male-male competition is assumed to limit female choice of mates, but it may also help females to choose the most vigorous males. We studied the mate sampling behaviour of female black grouse (Tetrao tetrix) at spatially unstable leks on ice-covered lakes. In the absence of territories and site-dependence in outcomes of fights, the male dominance hierarchy is very evident on ice. When being courted by dominant males, females frequently tried to approach other males. This was frequently prevented because (1) the courting male and the approached male were involved in physical fight, or (2) the dominant male followed the female and the approached male escaped and avoided contact with him. These behaviours express dominance relationships, and the female behaviour could be considered as incitive. Rank in dominance hierarchy was a significant predictor of male mating success. In this case competition between males and female choice worked in parallel favouring male traits correlated with dominance.     

Experimental manipulation of mate choice by male katydids: the effect of female encounter rate

Summary This study tests the general prediction that discrimination among potential mates increases with the availability of potential mates. Specifically, we conducted two experiments that examined mate choice by male zaprochiline katydids in relation to their prior encounter rate with females. The probability of mate acceptance or rejection was measured for males given either frequent or no contact with females in the laboratory (experiment 1) and males taken directly from natural areas of either high or low female abundance (experiment 2). In both experiments, males with low female encounter rates were more likely to mate than males with high female encounter rates. In both cases, the decreased mating probability of males in the high encounter treatment resulted from their tendency to reject lighter (and less fecund) females. Despite the presumed advantage to males of selecting heavier females, field data indicate that, unlike females, males do not aggregate in rich food patches. Possible explanations for this finding are discussed. Offprint requests to: T.E. Shelly at the present address     

Potential direct fitness consequences of ornament-based mate choice in a butterfly

Female mate choice has been shown to provide direct mating benefits in several animal groups. In butterflies, for which there are increasing reports of fine-scale color-based mate choice, the evolutionary benefits that accrue from such mating biases, if any, are largely unknown. We addressed this issue in the butterfly Colias eurytheme, a species in which females choose mates on the basis of iridescent ultraviolet (UV) wing ornamentation and in which males donate reproductively beneficial nuptial gifts. In the first experiment, we assessed the mass of gifts donated to 77 virgin females by males sampled directly from a field encounter site. Despite large variance in the male adult phenotype and ejaculate, no single aspect of dorsal wing coloration, including UV brightness, chroma, or hue, was related to ejaculate mass. There was, however, an interesting interaction between the effects of male body size and copula duration upon ejaculate mass, with size scaling positively with ejaculate mass among males involved in shorter copulations (those lasting <70 min) but negatively among males in longer copulations. In the second experiment, we assessed the lifetime fecundity, fertility, and longevity of 85 females mated under similar circumstances to free-flying wild males. Although several wing color parameters proved subtly informative in more sophisticated multivariable models, no model predicted more than about 20% of the variation in any single female fitness parameter. The duration of copulation, which ranged from 35 min to over 16 h and which carries putative costs for females, was, again, only very weakly predicted by male wing color parameters (i.e., R ² = 0.089). Given the overall minor predictive power of male wing coloration in general and of UV brightness in particular, our results do not strongly support the hypothesis that female C. eurytheme prefer bright UV males to obtain direct benefits or to minimize the costs associated with lengthy copulations.