The assessment of female reproductive state during courtship and scramble competition in the fiddler crab, Uca paradussumieri

Male fiddler crabs, Uca paradussumieri, mate underground during a 4- to 7-day period each full and new moon. As soon as the tide recedes, males enter the burrows of females that will ovulate the following day ('pre-ovigerous' females). Males copulate with and guard these females until they ovulate. When interrupted by an intruding male, the first male to reach the female is usually able to defend her and successfully mate with her. In fiddler crabs, females mate multiply and there is last male sperm precedence. Before each semi-lunar mating period, male U. paradussumieri were more likely to court females with whom they would later mate than other nearby females with whom they did not mate. This suggests that males collect information on female reproductive state prior to the females becoming ovigerous. In this species, aggression was common between males that courted the same female. When previously courted females were approached by other males, the initial courter attempted to forcefully disrupt the courtship. This behavior may allow males the exclusive use of information on female reproductive condition. It also suggests a type of scramble competition between males over females. Furthermore, it indicates that males are able to locate receptive females prior to their becoming ovigerous. The shorter guarding period observed in this species, as compared with other fiddler crabs, is caused by females rejecting longer guarding periods. Male ability to assess female reproductive status may therefore be advantageous because it increases male mating success within a scramble type of competitive polygyny.     

Manipulating the perceived opportunity to cheat: an experimental test of the active roles of male and female zebra finches in mate guarding behavior

Birds are commonly sexually promiscuous, which can lead to conflict between the sexes and the evolution of paternity assurance strategies, such as mate guarding. Adaptive explanations for mate guarding have tended to focus on fitness consequences for males, but mate guarding and participation in being guarded is also likely adaptive for females in certain contexts. To better understand the adaptive explanations for mate guarding as well as the observed variation in paternity patterns, it is necessary to explore the relative costs and benefits of guarding (and being guarded) from both the male and female perspective. To investigate these costs and benefits, we conducted an experiment with the Australian zebra finch (Teniopygia guttata) in which we independently varied the perceived opportunity for each member of a captive breeding pair to engage in extra-pair copulation (EPC) solicitation behavior; as an individual’s EPC opportunity increased, the partner’s EPC opportunity remained constant. Our results indicate that, for males, mate guarding intensity increases when their female’s EPC opportunity increases but decreases when their own (i.e., male) EPC opportunity increases. We did not find evidence of flexible female guarding behavior, but we found that females do not evade their partners more as female EPC opportunity increases.     

Mate guarding in the swallowHirundo rustica

Summary The importance of mate guarding by males in the monogamous swallowHirundo rustica was studied by temporarily detaining the males. Mate guarding reduced the frequency of extra-pair copulations and of sexual chases involving female mates. Males participated in sexual chases more frequently if they had a non-fertile female. Neighbouring males of ‘widowed’ females increased their own mate guarding presumably in response to the experimentally increased rate of sexual chases. Neighbouring males with a fertile female increased their mate guarding more than did males with a non-fertile female. Addition of eggs to swallow nests in the post-fledging period of the first brood induced mate guarding by male nest owners. These males also copulated more frequently with their mates than did control males. Neighbouring male swallows responded to the increased mate guarding by showing sexual interest in the guarded females. removal of eggs from swallow nests during the laying period, leaving only one egg in the nest, resulted in reduced nest attendance by females. Male mates responded by increasing their mate guarding intensity as compared to controls, and neighbouring males showed an increased sexual interest in these females.     

Male reproductive tactics to increase paternity in the polygynandrous Columbian ground squirrel (<Emphasis Type="Italic">Urocitellus columbianus</Emphasis>)

In polyandrous and polygynandrous species where females mate with multiple partners, males are expected to maximize their fitness by exhibiting an array of reproductive behaviors to ensure fertilization success, such as competing for the best mating order within a mating sequence, optimizing their investment in copulation, and mate guarding. Though there is genetic evidence of a first-male precedence in siring success for many mammalian species, the causes of this effect are poorly understood. We studied influences on first-male precedence in Columbian ground squirrels (Urocitellus columbianus). We found that the time a male spent consorting and mate guarding declined with his mating order (both the highest for the first male to mate). Mate guarding by the first male significantly reduced, but did not exclude, the number of additional males a female accepted. Later mating males reduced the time spent consorting, suggesting a perceived decreased chance of fertilization success. Consortship and mate guarding durations were positively related to the male’s siring success and to each other, suggesting that males adjusted these behaviors strategically to increase their chances of fertilization success. Our results suggest that besides being the first male to consort, first-male sperm precedence is further enhanced through longer mating bouts and by suppressing the chances and/or efforts of later mating males.     

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     

Mate guarding and copulation behaviour in monogamous and polygynous blue tits: do males follow a best-of-a-bad-job strategy?

This study investigates the importance of mate guarding for males and females in the facultatively polygynous blue tit Parus caeruleus. We present observational data in combination with a paternity analysis using DNA fingerprinting to show that (1) male blue tits guard their mate, since they stay closer to their mate, initiate fewer flights and follow their mate more often during the female's presumed fertile period; (2) polygynous males do not suffer more from lost paternity despite lower mate guarding; (3) in monogamous pairs there is either no relation or a positive relation (depending upon the variable measured) between measures of mate guarding intensity and the proportion of extra-pair young in the nest; and (4) monogamous males that are more often followed by their fertile female suffered less from lost paternity. We conclude that, despite mate guarding, paternity seems to be largely under female control and unattractive males guarding their mate are making the best of a bad situation. Experimental evidence is provided showing that when males were temporarily removed from their territory, their mate suffered from increased harassment from neighbouring males that intruded in the territory and tried to copulate with the female. Almost all of these copulation attempts were unsuccessful because females refused to copulate. We conclude that mate guarding may be beneficial for females because harassment by neigbouring males is prevented.     

Mixed reproductive strategy and mate guarding in a semi-colonial passerine,the swallow Hirundo rustica

Summary Both male and female swallows Hirundo rustica have a mixed reproductive strategy (parental care for offspring and extra-pair couplations). Mate guarding protects females from male harassment and male swallows from being cuckolded. Females hide their fertile period by copulating successfully with their mates for an extended period during first clutches. Males guard in the pre-fertile period, when many unpaired males are present. Early breeding swallows guard more than late breeders since more sexual chases of females by non-mate males take place in the early period. Solitarily breeding females experience few chases by strange males; copulation frequency, length of copulation period and mate guarding is adjusted to a lower level than among colonial birds. Male guarding activity is more intense in the fertile than in the pre-fertile period. Guarding reduces success of extra-pair copulation attempts.Three female swallows each paired and copulated with a single male and later changed to a new male before starting to breed. Extra-pair copulations most often take place between neighbouring swallows in the fertile period of the female. Many old, early breeding males and many young, late breeding females participate in extra-pair couplations. Successful extra-pair copulations peak in the fertile period contrary to success of pair copulations which does not change during the copulation period.     

Discovery of postcopulatory mate guarding in Copepoda Harpacticoida (Crustacea)

Mating behaviour of four species of Tisbe (Tisbidae) and of Paramphiascella fulvofasciata (Diosaccidae) was filmed with a videocamera during 1992 and 1993 at the University of Oldenburg. This behaviour is complex and can be divided into different phases: grasping of the female; courtship; copula and postcopulatory mate guarding. During courtship both partners lie parallel in opposite directions with their ventral sides facing each other. The male strokes the abdomen of the female with his second to fourth peracopods. As a result the female becomes motionless. The copula is a quick process of only a few seconds during which spermatophore transfer takes place. When this has happened, males do not leave the females but become inactive and are carried around by them for varying lengths of time. This pattern and the fact that only adult partners are involved in these associations prove that this behaviour is very different from the precopulatory mate guarding presumed to be ubiquitous among Harpacticoida. Cases of postcopulatory mate guarding have never been explicitly demonstrated for Harpacticoida. The minimum duration of guarding was found to match the time necessary for spermatophore discharge. Guarding is, therefore, interpreted as a strategy to secure paternity. New definitions are given for courtship, copula and postcopulatory mate guarding in Harpacticoida to help avoiding misinterpretations of associations between adult partners. Such misinterpretations abound in the literature.     

Underwater oviposition in a damselfly (Odonata: Coenagrionidae) favors male vigilance,and multiple mating by females

Summary Female Enallagma hageni oviposit underwater where they are inaccessible to males. I demonstrate that males guard submerged females rather than perch sites, and are behaviorally distinct from lone males at the water. In contrast to lone males, which always attempt to copulate with females presented to them, guarding males exhibit a conditional latency to remating which corresponds closely to the time required by females to oviposit a complete clutch of eggs. By ovipositing underwater, females decrease the risk that their eggs become exposed. Risks associated with submerged oviposition favor both mate guarding, and multiple, within-clutch matings by females. Both guarding mates and lone males rescue females that float on the water surface as the result of improper resurfacing. Such behavior reduces the mortality risk to females from 0.06 to 0.02 per oviposition bout. By remating between bouts, females benefit from the additional vigilance of lone males, who rescue floating females 1.4 times as often as original mates. A second consequence of multiple mating is an increase in the selective advantage of vigilance by mates. Because receptive females become scarce by early afternoon, whereas male density remains high, a male has little (3%) chance of encountering a second receptive female that day. However, he incurs a 42% risk of losing fertilizations if he abandons a mate. For male E. hageni mate guarding functions in the context of both natural and sexual selection. It insures that a mate lives to lay a complete egg clutch in addition to protecting a male's sperm investment.     

Reproductive biology of a small isopod symbiont living on a large isopod host: from the maternal marsupium to the protective grip of guarding males

Mating systems of many symbiotic crustaceans are characterised by a high degree of mate guarding. A peculiar case of mate guarding has been reported for small symbiotic janirid isopods where males mate with immature females. Field samples of individual hosts and laboratory experiments were conducted to reveal the mating behaviour of the symbiont in a natural environment, that is, on their hosts. Along the coast of the Magellan Strait, Chile, the janirid isopod Iais pubescens was frequently found on the shore-living isopod Exosphaeroma gigas. Symbiont prevalence (percent hosts occupied) was high at eight of the nine sampling sites. Mean symbiont intensity was very low at one site (<<1 individual host^-1), intermediate at two sites (1-10 individuals host^-1) and high at the other sites (10-40 individuals host^-1). The mean sex ratio (males:females) was male biased at most sampling sites (n=7). Females of I. pubescens reached substantially larger sizes (1.5-3.0 mm body length, BL) than males (1.1-1.9 mm BL). The majority of males were carrying small juveniles (66.15%), and males with juveniles were significantly larger than males without juveniles - this suggests that males prefer virgin juveniles to adult females and that they compete for small juveniles. In laboratory observations, males were seen to manipulate the marsupium of adult females that were about to release small juveniles. Males obtained virgin juveniles in this manner. Juveniles were carried for ~7 days, and they moulted shortly before being fertilised and released by males. The high proportion of juveniles carried by males in the field (68.2%) supports previous observations that males initially are not able to distinguish male and female juveniles. It is suggested that the mating system of symbiotic janirid isopods with long-term sperm storage and continuous receptivity in females and male mating with virgin females has evolved in response to highly unpredictable encounter probabilities between the sexes. Mate guarding and manipulation of small virgin juveniles may be favoured on the highly mobile hosts of symbiotic janirid isopods. Furthermore, adult females may gain by leaving their emerging offspring in the protective grip of guarding males, thereby reinforcing the maintenance of this peculiar mating system.     

Mate preferences by male guppies (Poecilia reticulata) in relation to the risk of sperm competition

We investigated male mate preferences in relation to the perceived risk of sperm competition in the guppy (Poecilia reticulata), a freshwater fish with a promiscuous mating system. Our laboratory experiments revealed that male mate choice behaviour is not influenced by the presence of rival males that are merely in close proximity to a potential mate, as there was no significant difference in the amount of time that males spent with females that were recently either alone or in close proximity to four rival males. Male mate choice behaviour was, however, strongly influenced by the presence of rival males in a second experiment, where those rivals were permitted to copulate with one of the females. In that situation, males spent significantly more time with, and directed significantly more sigmoid courtship displays toward, females that they had recently seen alone compared to females they had seen receiving forced copulations from up to four rival males. Our results therefore indicate that male guppies are sensitive to the risk of sperm competition and alter their mate choice behaviour in an adaptive fashion.Communicated by K. Lindström     

Land or lover? Territorial defence and mutual mate guarding in the crimson-breasted shrike

Crimson-breasted shrikes produce duets which are used in interactions with neighbours and intruders. We examined two major hypotheses explaining duetting, the territorial defence and mate guarding hypotheses, using playback experiments. The responses of 12 pairs towards solo male, solo female and stereo duet playback were analysed using principal component analysis and ANOVA. The measures of response intensity revealed in most cases highly coordinated responses of the pair partners. Although these joint responses could suggest cooperative territorial defence or mutual mate defence, responses to the treatments differed between males and females in terms of three variables. Females increased their answer rates significantly in response to unpaired female intruders, compared to unpaired male intruders. During duet playback, females directed their responses equally at both intruding pair members. In contrast, males were equally responsive towards unpaired male intruders and intruding pairs, but in the latter case directed their responses at the male pair member. In the presence of unpaired female intruders, males increased their solo song rates, but in the presence of intruding pairs, they increased overlapping rates and duetted with their mates. These divergent responses suggest that females use duets for mate guarding against unpaired females, whereas males use solo songs for mate guarding and both solos and duets in territorial defence.     

Male mating history: effects on female sexual responsiveness and reproductive success in the parasitoid wasp Spalangia endius

Males frequently mate multiply, but are there negative fitness consequences for their later mates? Potential costs include less sperm and less nutrition. In most hymenopterans, daughters, but not sons, are produced sexually. This mean that effects of being a later mate on sperm received versus on nutrients received should be distinguishable. If later mates receive less sperm, it should manifest as a reduction in daughter production, whereas a reduction in nutrients should affect production of both sexes. Any cost to being a later mate may in turn select for polyandry or for female choice of virgin males. Males of the parasitoid wasp Spalangia endius were presented with up to five females in succession. Offspring production was compared among first, third, and fifth females; and it did not differ. However, about half of fifth females had begun producing only sons by their tenth day, whereas first and third females rarely had. Despite the reduction in daughter production, even fifth females rarely remated. However, females tended to mate with virgin males rather than mated males when given a choice. This tendency was dependent on male, not female, behavior, but should benefit the female nevertheless. Sex ratios in this species are one male for every one and a half to three females. Thus, the number of times that males could mate before daughter production was reduced coincided roughly with the mean number of times that males likely mate in this species. Nevertheless, some females are likely to experience the cost of being a fifth female because of skewed mating success among males.     

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.     

Tests of the mate-guarding hypothesis for social monogamy: does population density, sex ratio, or female synchrony affect behavior of male snapping shrimp (Alpheus angulatus)?

There are at least two mechanisms by which social monogamy in the absence of biparental care may evolve: as a form of territorial cooperation, in which one or both sexes benefits by sharing a territory with a partner, and as a form of extended mate guarding, in which males guard females through entire, and perhaps multiple, reproductive cycles. I examined the effects of population variables (density, sex ratio, female synchrony) on male pairing behavior in the snapping shrimp, Alpheus angulatus, to test the hypothesis that social monogamy in this genus has evolved as a result of selection on males for long-term mate guarding of females. There was no evidence that pairing behavior changes with differences in population density; in a natural population, there was a 1:1 relationship between the number in pairs and local population density. In a laboratory experiment, males altered their pairing behavior in response to manipulated differences in sex ratio. Males in female-biased sex ratios were significantly more likely to abandon recently mated females than males in equivalent sex ratios, though there was no significant difference in the duration of pairing or the number of times males switched females. Observations of shrimp maintained for an extended period in the laboratory revealed no evidence that females molt and become sexually receptive synchronously, which would reduce the likelihood that a searching male would encounter additional receptive females. These data suggest that sex ratio may have contributed to the evolution of social monogamy in snapping shrimp, but provide no evidence that population density or female synchronous receptivity have contributed to the evolution of social monogamy.     

Mate guarding behavior in clam shrimp: the influence of mating system on intersexual conflict

Mate guarding is a male strategy to gain access to receptive females but often results in antagonistic interactions between the sexes because of different costs/benefits of guarding. In addition to social, morphological, and physiological parameters, the type of mating system should also affect the strength of the conflict and thus the guarding duration. Specifically, when compared to females, self-compatible hermaphrodites might have reduced benefits of outcrossing. We investigated mate guarding in dioecious (co-presence of females and males) and androdioecious (co-presence of hermaphrodites and males) branchiopod crustaceans. Both sexes in androdioecious systems should shift their guarding times to lower values relative to dioecious systems because (1) androdioecious males are present in lower percentages than dioecious males and thus encounter rates with receptive mates are relatively greater for them; and (2) hermaphrodites should have low incentive to incur high costs of mate guarding, having the alternative of self-fertilization, and thus should be highly eager to resist. While females preferred short guarding times, when allowed to control the guarding duration (males tethered), dioecious males did not increase their guarding duration when females (treated with muscular relaxant) could not resist, in contrast to what has previously been found for androdioecious males. This indicates that hermaphrodites are more willing to resist mate guarding than females. The among-species comparisons supported our hypotheses: compromised guarding times were significantly lower in androdioecious than in dioecious species. The introduction of a parameter (mating system) not previously investigated in mate guarding models resulted in a powerful test of mate guarding theory, adding a valuable contribution to our understanding of intersexual conflict.     

Seasonal variation in the duetting behaviour of rufous-and-white wrens (<Emphasis Type="Italic">Thryothorus rufalbus</Emphasis>)

Seasonal variation in animal signalling behaviour has been well documented and has contributed much to our understanding of male signals. In contrast, we know little about seasonal variation in female signals or signals produced jointly by males and females, such as the vocal duets of birds. Here, we examine how singing behaviour changes in relation to time of year and breeding stage in rufous-and-white wrens (Thryothorus rufalbus), neotropical songbirds where both males and females sing and where breeding partners coordinate songs to produce vocal duets. We recorded a colour-marked population of birds over an extended time period encompassing multiple breeding stages. Across all time frames and breeding stages, males sang at higher rates than females and male solos were more common than duets or female solos. Males and females showed divergent seasonal patterns of singing. Females sang more often early in the year, during the pre-breeding season, and female song tapered off as the breeding season progressed. Duetting followed a parallel pattern, which resulted from females showing less duet responsiveness to their partner’s songs later in the year. Male independent song rate peaked at the onset of the rainy season – a time when females become fertile – and males showed the highest level of duet responsiveness during this period. Our results suggest that early in the year, duets appear to be cooperative displays, functioning in joint territory defence and/or the coordination of breeding activities. When females are fertile, however, increased duet responsiveness by males is consistent with mate or paternity guarding.     

Mechanisms of sexual fidelity in the monogamous California mouse,Peromyscus californicus

Summary Peromyscus californicus are exclusively monogamous in the wild. We examined in the laboratory whether established pairs of male and female P. californicus would remain faithful when given the opportunity to mate with an opposite sex stranger, either in the presence or absence of their partner. When the partner was present she or he was tethered and could not intervene. Females in postpartum estrus (day 0 postpartum) preferred to associate with their pairmate rather than the unfamiliar virgin male. Females also preferred to mate with their partner, but 15–20% of the females mated with the unfamiliar male both in the presence and absence of their partner. Paired males were tested with an unfamiliar, sexually inexperienced estrous female on days 4 and 8 postpartum with their partners either absent or present but not in postpartum estrus, and on day 0 in the absence of their partner. Males preferred to associate with their pairmate. Contrary to theoretical expectations, males did not copulate with the estrous female when given the opportunity regardless of whether their partner was present or not. Furthermore, few males (2/13) tested in the absence of their partner mated with a sexually experienced, postpartum estrous female. These results indicate that monogamy in P. californicus is maintained by a strong attraction and preference of pairmates for each other and by self-restraint from mating with others. Male mate guarding may further ensure female faithfulness. Males exhibit apparently more sexual fidelity than females.Correspondence to: D.J. Gubernick     

The influence of sexual selection and predation on the mating and postcopulatory guarding behavior of stone crabs (Xanthidae,Menippe)

Summary Postcopulatory mate guarding in crustaceans traditionally has been viewed as a behavioral mechanism that prevents predation on the soft post-molt female. This study tests the effects of sexual selection and predation on the postcopulatory guarding durations of male stone crabs, Menippe mercenaria, M. adina, and their hybrid. Male stone crabs were held with a pre-molt female, and either another adult male stone crab, an intermolt female, or a male blue crab, which corresponded to intermale competition, control, and predation treatments, respectively. The mating behavior of the heterosexual pair was recorded with a time lapse video system and the durations of copulation and postcopulatory guarding were measured. Males guarded longer in the intermale competition treatment than either the control or predation treatments. In the competition treatment, agonistic encounters occurred between the males at the den containing the female and several mate takeovers occurred. Females survived the predation treatment in trials in which the guarding durations were the longest, whereas females were eaten by the blue crab in trials with the shortest guarding durations. Sexual selection appears to be important in maintaining postcopulatory mate guarding in stone crabs.     

Re-copulation and post-copulatory mate guarding increase immediate female reproductive output in the dragonfly Nannophya pygmaea Rambur

After copulation, male Nannophya pygmaea dragonflies mate guard by hovering over ovipositing females and repelling conspecific males. Copulation is not always a prerequisite for oviposition in the females of this species because females can store the sperm received during previous visits/copulations. An oviposition episode consists of several bouts of oviposition separated by periods of perching. We conducted two types of male-removal experiments to examine the effects of mating and post-copulatory mate guarding on the oviposition behaviour of females. In the first experiment, we removed all males from the habitat to eliminate the effect of re-copulation, mate-guarding and harassment by males. In the second experiment, we removed males immediately after copulation to eliminate the effects of guarding and other post-copulatory male-female interactions. We compared these experimental data with data obtained under natural conditions. The dipping rate in an oviposition bout was not influenced by copulation or guarding. However, guarded females made more dips per episode than did solitary females. The proportion of time actually spent ovipositing (total bout duration/oviposition episode duration) of guarded females was higher than that of solitary females. Solitary females often oviposited in more than one territorial site, while guarded females usually oviposited within a single territorial site during an oviposition episode. Because males tend to hold territories at sites where egg survival is high, guarded females (and the male guardian) benefit from guarding in terms of egg hatchability. The possible benefits for solitary females are discussed.