Responses of territorial and floater male Red‐winged Blackbirds to models of receptive females

Red‐winged Blackbirds (RWBL; Agelaius phoeniceus) have a polygynous mating system and, because territorial males commonly have harems of two to five females, some second‐year (SY) and after‐second‐year (ASY) males do not establish nesting territories, but become floaters. Previous studies have revealed high rates of extra‐pair copulations in this species and that sexually mature male floaters and territory owners do not differ in size, testosterone levels, or reproductive capability, suggesting that floaters may occasionally gain paternity. During May and June 2008, we observed the behavioral responses of floater males to taxidermic mounts (models) of female RWBL placed in a precopulatory position. Floaters intruded into territories during 46% of model presentations, with 20% of intrusions by ASY floaters and 80% by SY floaters. During intrusions, ASY floaters attempted to copulate with models 93% of the time compared to 80% for SY floaters. Copulations were successful during 30% of attempts by ASY males and 25% of attempts by SY floaters. The frequency of intrusions by ASY and SY floaters, attempted copulations by SY floaters, and successful copulations by ASY floaters increased as territorial males spent more time off their territories. Responses of floater males toward models in our study suggest that floater male RWBL attempt to exploit available breeding opportunities. The lack of evidence for extrapair young (EPY) fathered by floater male RWBL in previous studies, combined with our results indicating that the presence of territorial males limits floater intrusions, copulation attempts, and successful copulations, suggests that the reproductive success of floater males is limited in part by the aggressive behavior of territorial males.     

黄山短尾猴交配叫声及其影响因素

哺乳动物在交配过程中经常会发出独特且有节奏的交配叫声(Copulation call),这通常被认为是雌雄双方交配策略的一种体现.交配叫声的发生及其影响因素在不同物种间差异较大,对其深入研究有助于比较和揭示不同动物交配策略的差异及其适应性功能.为了阐明交配叫声的生物学和社会学因素,我们在安徽黄山记录了野生黄山短尾猴(M...     

Courtship Disruptions and Male Mating Strategies: Examples from Female-Defense Mating Systems

Males frequently interrupt the copulation attempts of other males, and these courtship disruptions may limit the extent to which a few males are able to monopolize mating access to females. Males actively defend sexually receptive females in many species in which females form dense aggregations during the breeding season. Across and within such species there is considerable variation in the mating tactics adopted by males, with males in some cases defending groups of females and in other cases sequentially consorting with individual females. Colonial blackbirds have been central to studying this mating system, and we develop a conceptual model for how courtship disruption may account for variation in male mating tactics in this group. Our model assumes that the frequency of disruptions increases with greater colony size. As a consequence, successful copulations are less likely to occur at large colonies than at small colonies, and males are expected to switch from defending multiple females at the colony to consorting individual females away from it. Results from two species of blackbird support the basic assumptions of this model. In one species, the Montezuma oropendola, disruptions occur rarely and males defend groups of females, whereas in the other species, the yellow-rumped cacique, disruptions are frequent and males defend single females. Moreover, consistent with a key prediction, within each species, males associated with small colonies remain at the colony and defend groups of females, whereas males spend little time defending groups of females at large colonies and rarely attempt copulations there. This model has the potential to explain variation in male mating strategies and female monopolization for other taxa in which females form breeding aggregations.     

Female mate preferences and subsequent resistance to copulation in the mallard

In the majority of socially monogamous bird species, femalessolicit or accept copulations from males other than their partner.Females may gain direct benefits from extrapair males, suchas greater access to resources, or indirect genetic benefitsthat will influence the future success of their offspring. However,one group of birds appears to be the exception to this generalrule; in the wildfowl (Anseriformes), all extrapair copulationsappear to be resisted by females. It has been suggested thatresistance behavior may be a strategy to allow females a greaterchoice of mates, either at the precopulatory level (to promotechoice of copulation partner) and/or the postcopulatory level(to promote multiple mating to increase their choice of sperm).This paper examines the function of female resistance behaviorin one of the dabbling ducks, the mallard (Anas platyrhynchos).Observations on a marked population of wild mallard and experimentswith captive birds found that although females showed a strongpreference for particular males that are the first to molt intotheir breeding plumage, male attractiveness did not influencefemale responses to pair or extrapair copulation attempts. Femaleresistance decreased the likelihood that copulation attemptswould end in successful insemination. The findings did not supportthe hypothesis that females resist copulations to promote femalechoice and the reasons why waterfowl may benefit from avoidingall extrapair copulations are discussed.     

Field bioassays show heterospecific mating preference asymmetry between hybridizing North American Papilio butterfly species (Lepidoptera: Papilionidae)

Few studies of interspecific mating preferences of naturally hybridizing species have been done in the field. Yet this is the only way potentially critical habitat-specific factors can be included in mating behavior evaluations. We conducted mate selection (male preference) studies using tethered pairs of heterospecific, size-matched virgin yellow females of Papilio glaucus and P. canadensis with free-flying male P. glaucus populations in south-central Florida, and with free-flying male P. canadensis populations in northern Michigan. Florida males clearly preferred the conspecific P. glaucus females of the pairs, as indicated by the touches/attempted matings and by the actual copulations observed. In 1997, 66.7% of the total attempts (n=168) and 94.2% of all copulations (n=69) were with the conspecific. In 1998 the same pattern of conspecific male preference was observed, with 67.3% of the touches/attempts (n=49) and 100% of the copulations (n=30) being with the P. glaucus females. In contrast, the natural populations of P. canadensis males did not show the expected conspecific preference. In fact, with wild P. canadensis males in 1997 a very strong preference was observed for the heterospecific P. glaucus females of the pairs, accounting for 75.8% of all touches/attempted matings (n=483) and 81.7% of all copulations (n=476). The strong asymmetry in interspecific mating preferences among these hybridizing Papilio species may reflect an ancestral trait in P. glaucus females that elicits strong preference in P. canadensis males, due perhaps to previously possessed male sensory bias or "good genes" indicators in the females. However, reinforcement of reproductive isolation in or near the hybrid zone of species overlap (sympatry) cannot be ruled out. Electronic Publication     

Post-copulatory Mounting Behavior of the West Indian Sweetpotato Weevil, Euscepes postfasciatus (Fairmaire) (Coleoptera: Curculionidae)

Post‐copulatory associations between males and females have been found in a variety of insects and are often described as mate guarding. Males of the West Indian sweetpotato weevil Euscepes postfasciatus (Fairmaire) mount the female's back after copulation. Two hypotheses have been advanced to explain this behavior: mate guarding to prevent future copulations by rivals (hypothesis 1), and mate guarding to gain additional copulations (hypothesis 2). We conducted three experiments to test predictions from these hypotheses. Our results disproved hypothesis 1 because the duration of the post‐copulatory association was very brief in comparison with the length of the refractory phase all females showed after copulation. When we prevented females from resisting copulations during the post‐copulatory mounted phase males copulated again, while under normal conditions, a second copulation was never observed. This result may indicate the presence of a sexual conflict over mating. However, we propose an alternative interpretation of the result, namely that after mating, males test whether the copulation has successfully reduced female receptivity by attempting to remate. If females resist the mating, males leave.     

Strategic male mating effort and cryptic male choice in a scorpionfly

In animal species with high male mating effort, males often find themselves in a dilemma: by increasing their mating effort, the gain from each copulation increases but simultaneously reduces available resources and, thus, the opportunity for future copulations. Therefore, we expect males to spend less reproductive resources on matings that provide low reproductive potential, thereby saving resources for future copulations, possibly with high-quality females, a sort of cryptic male choice. However, the strength of the trade-off between investment in a current mating and resources available for future matings must not be the same for all males. Males with relatively high mating costs should allocate their limited resources more cautiously than males with more plentiful resources. Here, we examine this prediction in the scorpionfly Panorpa cognata. Prior to copulation, males produce a large salivary mass on which females feed during copulation. We show that the production of larger salivary masses leads to longer copulations. Moreover, the size of the salivary gland and salivary mass increases with increasing male condition. However, males in poor condition make a relatively higher mating investment than males in good condition. We therefore expect male condition to influence cryptic male choice. In accordance with our hypothesis, only males in poor condition choose cryptically, producing larger salivary masses in copulations with females of high fecundity.     

Sexual harassment in live-bearing fishes (Poeciliidae): comparing courting and noncourting species

Sexual harassment by males has been reported from several live-bearingfishes (Poeciliidae) and has been shown to inflict costs onfemales. For example, poeciliid females have reduced feedingopportunities when accompanied by a male because females dedicateattention to avoiding male copulation attempts. Poeciliid speciesdiffer considerably in male mating behavior, such as the presenceor absence of courtship. Courting males display in front ofthe females, but males attempting to sneak-copulate approachfemales from behind, that is, in the blind portion of theirvisual field, and force copulations, which can be viewed asa male persistence trait. We predicted that poeciliid femalesneed to be more vigilant in the presence of noncourting males,and costs of harassment by noncourting males might be stronger.In a comparative approach we examined the costs of male sexualharassment for females as reduced feeding time in 9 speciesof live-bearing fishes, including courting (Poecilia latipinna,Poecilia reticulata, Xiphophorus cortezi, Xiphophorus variatus)and noncourting species (Poecilia mexicana [surface- and cave-dwellingform], Poecilia orri, Gambusia affinis, Gambusia geiseri, Heterandriaformosa). In all species examined except for the cave form ofP. mexicana, focal females spent significantly less time feedingin the presence of a male than when together with another female.The time females spent feeding was found to significantly declinewith increasing male mating activity (sum of all sexual behaviors),but there was no support for the idea that females would spendmore time feeding in the presence of courting males comparedwith noncourting ones.     

Why Do Female Birds Reject Copulations from their Mates?

Female birds frequently reject copulations from their mates, suggesting a conflict between the sexes. This study analyses behavioural data of socially monogamous razorbills, Alca torda, to examine whether females rejected their mates because of conflicts over fertilization or the pair bond. Among pairs, females rejected 9–70 % of their mates’ copulation attempts and prevented their mates from completing 42–100 % of successful copulations. Copulations terminated by females were half the duration of those terminated by males, and females terminated fewer first copulations than subsequent ones on the same day. These findings indicate that females were motivated to copulate less frequently and for shorter durations than their mates. The sperm competition hypothesis predicts that females reject their mates to increase the probability of being fertilized by extra-pair males. This hypothesis was not supported because females rejected extra-pair males similarly to their mates. The female-mate-guarding hypothesis predicts that females guard their pair bond by copulating frequently with their mates, thereby depriving the males of time and energy to copulate with and form bonds with other females. This prediction was consistent with a significant negative correlation between the percentage of copulation attempts that females accepted from their mates, and the number of extra-pair copulations that their mates attempted. However, this correlation was not caused by a trade-off of males copulating with their mates instead of attempting extra-pair copulation because males attempted most extra-pair copulations on days when their mates were absent. A new hypothesis is proposed, namely, that females reject their mates to test the male's commitment to provide essential parental contributions after egg-laying. The ‘testing-of-the-bond’ hypothesis is consistent with the findings but requires testing.     

Female resistance and male force: context and patterns of copulation in the New Zealand stitchbird Notiomystis cincta

The New Zealand stitchbird or hihi Notiomystis cincta is unique in that it has two distinct mating positions, in addition to the male standing on the female's back, as is seen in all other birds, it also copulates face‐to‐face. In this study, 43 male stitchbirds first attracted a female to their territory and supplemented their within‐pair matings by intruding into other territories and attempting forced copulations – often resulting in high levels of female harassment. I recorded the temporal variation of both attempted and successful copulations relative to the female's fertile period in order to understand the function of copulation variation in this species. Each of 105 observed copulations were classified according to whether they were: (1) within‐pair or extra‐pair, (2) forced or unforced, and (3) face‐to‐face or standing. Two copulation categories ‘within‐pair unforced standing’ (50%) and ‘extra‐pair forced face‐to‐face’ (27%) accounted for the majority of all observed copulations, and this supported the previous categorisation of face‐to‐face copulation being forced by extra‐pair males in this species. However, in 10% of copulations the female conceded to copulate with an extra‐pair male in a standing position while displaying only subtle signs of resistance, thus, female stitchbirds may show convenience polyandry when the costs of resistance are high. The peak in copulation frequency centred on two days prior to the laying of the first egg and occurred within a period of six days before and seven days after the first egg was laid. Unsuccessful extra‐pair forced copulation attempts closely followed the distribution of all copulations. Male age and morphometrics did not predict whether a female would resist or accept extra‐pair copulation attempts, and female resistance did not appear to depend on male quality. Despite the current trend focussing on female fitness benefits associated with EPCs, it appears that male stitchbirds gain EPCs through forced copulation and females gain no apparent benefit.     

Soay rams target reproductive activity towards promiscuous females' optimal insemination period

Female promiscuity is thought to have resulted in the evolution of male behaviours that confer advantages in the sperm competition that ensues. In mammalian species, males can gain a post-copulatory advantage in this sperm 'raffle' by inseminating females at the optimal time relative to ovulation, leading to the prediction that males should preferentially associate and copulate with females at these times. To the best of our knowledge, we provide the first high-resolution test of this prediction using feral Soay sheep, which have a mating system characterized by male competition for access to highly promiscuous females. We find that competitive males time their mate guarding (and hence copulations) to occur close to the optimal insemination period (OIP), when females are also increasingly likely to 'cooperate' with copulation attempts. Subordinate males practice an alternative mating tactic, where they break the integrity of the consort pair and force copulations on females. The timing of these forced copulations is also targeted towards the OIP. We thus provide quantitative evidence that female promiscuity has resulted in the evolution of reproductive strategies in which males 'load' the sperm raffle by targeting their mating activity towards female OIPs, when the probability of sperm-competition success is at its greatest.     

Rotifers from Andhra Pradesh,India — III., family Lecanidae including two new species

Seventeen species of rotifers of the family Lecanidae, including two new species: Lecane donnerianus sp.nov. and L. bidentata sp.nov., have been described.     

Male mating strategies and reproductive constraints in a group of wild tufted capuchin monkeys (Cebus apella nigritus)

Tufted capuchin monkeys (Cebus apella) provide an extreme example of active female sexual solicitation of males. In spite of being targeted by females for sex, males may delay copulation for hours or days. Data were collected on the sexual interactions in one wild capuchin group at the Estação Biológica de Caratinga in Brazil from September 1996 to August 1997. All successful conceptions during this year occurred in the dry season, yet sexual behavior was observed during 9 months of the year. This study tested whether male sexual response to female proceptivity was seasonally‐mediated. Male consortship participation, solicitation of females, latency to copulation, and copulation frequency were compared between fertile and nonconceptive females. Seasonal patterns in copulation interference, mating style, and alternative mating strategies were also examined. Thirty‐two copulations were observed. The alpha male was solicited for significantly more consortship days per female, but his mating success, in terms of copulation frequency, did not differ from that of two other adult males in the group. In the dry season, when the females were fertile, the males showed increased contest competition for mates, a higher frequency of alternative mating strategies against copulation interference, and increased monitoring of the females' condition. However, contrary to expectations, the alpha male's latency to copulation was significantly longer in the fertile season than in the nonconceptive months, and no males were observed to mate more than one time per day, even at the conceptive peak. Male mating strategies were affected by both season and rank, and there was evidence for reproductive constraints on males throughout the year. Limited male ejaculatory capacity and male choice in the timing of copulations within female proceptive phases may both be important factors in driving the sexual dynamics of this species. Am. J. Primatol. 67:313–328, 2005. © 2005 Wiley‐Liss, Inc.     

Ultrasonic courtship songs of male Asian corn borer moths assist copulation attempts by making the females motionless

Males of the Asian corn borer moth Ostrinia furnacalis (Guenée) produce an ultrasonic courtship song of extremely low‐intensity during copulation attempts. The song has been shown to significantly increase the mating success of the male; however, the mode of action of the sound in courtship remains to be resolved. Behavioural experiments using pairs with deafened females or muted males show that, without the aid of the sound, 63% of males eventually succeed in mating after several copulation attempts, whereas the remainder (37%) make repeated attempts in vain until interrupted by the escape of the female. Because few (2%) males fail to copulate when females hear the courtship song, it is evident that the song has an effect on females, promoting the success of copulation attempts. In support of this view, males produce louder songs if the first copulation attempt fails, suggesting that the males increase their sound levels to achieve successful copulation. It is suggested that the ultrasonic songs of the male render the females motionless, which is the same response as that to ultrasonic bat calls. Because even slight movements by the female can interfere with the attempt of the male to copulate, it is likely that, by making her motionless, the success rate of a single copulation attempt is increased greatly.     

Sex‐specific repeatabilities and effects of relatedness and mating status on copulation duration in an acridid grasshopper

In species with direct sperm transfer, copulation duration is a crucial trait that may affect male and female reproductive success and that may vary with the quality of the mating partner. Furthermore, traits such as copulation duration represent the outcome of behavioral interactions between the sexes, for which it is important—but often difficult—to determine which sex is in phenotypic control. Using a double‐mating protocol, we compared copulation durations between (1) virgin and nonvirgin and (2) sibling and nonsibling mating pairs in rufous grasshoppers Gomphocerippus rufus. Nonvirgin copulations took on average approximately 30% longer than virgin copulations, whereas relatedness of mating partners was not a significant predictor of copulation duration. Longer nonvirgin copulations may represent a male adaptation to sperm competition if longer copulations allow more sperm to be transferred or function as postinsemination mate guarding. The absence of differences between pairs with different degrees of relatedness suggests no precopulatory or preinsemination inbreeding avoidance mechanism has evolved in this species, perhaps because there is no inbreeding depression in this species, or because inbreeding avoidance occurs after copulation. Controlling for the effects of male and female mating status (virgin vs. nonvirgin) and relatedness (sibling vs. nonsibling), we found significant repeatabilities (R) in copulation duration for males (R = 0.33; 95% CI: 0.09–0.55) but not for females (R = 0.09; 95% CI: 0.00–0.30). Thus, copulation durations of males more strongly represent a nontransient trait expressed in a consistent manner with different mating partners, suggesting that some aspect of the male phenotype may determine copulation duration in this species. However, overlapping confidence intervals for our sex‐specific repeatability estimates indicate that higher sampling effort is required for conclusive evidence.     

Male age and sexual experience affect male mating behavior in the hawthorn spider mite,Amphitetranychus viennensis

As is reported, in species with first-male sperm precedence, male age and previous sexual experience play crucial roles in male mating behavior. In the hawthorn spider mite, Amphitetranychus viennensis Zacher, previous studies showed that only females that copulated for the first time could achieve fertilization. Based on this, the effects of male age and mating history on male mate choice and male mate competition were investigated. It was confirmed that males could distinguish virgins from fertilized females but they were unable to discriminate between virgins and unfertilized females. Interestingly, the copulation duration of males mated with fertilized females was much shorter than that of males mated with virgins or unfertilized females. Additionally, for male mating choice, males of all ages and more experienced males preferred 5-day-old virgin females, whereas only less experienced males preferred 1-day-old virgin females. In male-male competition, 3-day-old males were more competitive and obtained more copulations compared with others. Copula duration was closely related to male age. Though no significant differences were observed in mating competition between virgin and mated males, copula duration of males in first copulation was the longest and gradually shortened in subsequent copulations. In all, this investigation demonstrated that male age and sexual experience affected male mate choice and male-male competition, leading to further insight into the influences of male age and sexual experience on the reproductive fitness of both sexes.

     

Mating behavior and contact pheromones of Batocera horsfieldi (Hope) (Coleoptera: Cerambycidae)

The mating behavior of Batocera horsfieldi (Hope) was observed in the laboratory. The results showed that copulation of this longhorned beetle consisted of three phases: (i) encountering and pair‐bonding; (ii) mating attempt and ejaculation; and (iii) post‐copulatory guarding. Frozen females, with cuticular hydrocarbons stripped by hexane extraction, showed no attraction for males. Reapplying the solvent extract of frozen females to both washed dead males and females caused mating attempts by males, confirming that cuticular hydrocarbons (contact sex pheromones) played an important role in recognition of females by male B. horsfieldi.