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1.
Scorpionflies have been used as model organisms for the study of alternative male mating tactics as well as sexual conflict and coercive mating. Here we describe the courtship and mating behaviour of the scorpionfly Panorpa cognata at different levels of nutrition. Alternative mating tactics in scorpionflies involve nuptial food gifts, and we expected an effect of nutrient availability and male individual condition on the relative frequency of these mating tactics. Subsequent to female attraction by means of male pheromonal emission (calling) and a conspicuous pairing prelude, the majority of matings were initiated by male secretion of one relatively large salivary mass on which females feed during copulation. Usually, males produced only a single salivary mass per mating, and the copulation was terminated after the female had consumed the salivary mass. Alternatively, in 40% of the copulations, males offered females a dead arthropod as nuptial gift. However, these matings were neither preceded by male calling nor by the pairing prelude. Copulations with no gifts were extremely rare, and forced copulations were absent. The manipulation of the clamp‐like notal organ used by male scorpionflies in coercive matings had no effect on the duration of copulation, suggesting that P. cognata males are not able to enforce longer matings. Copulations involving salivary mass gifts were significantly longer than copulations with prey provided as gifts. Although contrary to our expectations, nutrition had no effect on the relative frequency of the different male mating tactics, it had several effects on courtship and mating. First, well‐fed individuals copulated significantly more often, both with prey and salivary secretions, than individuals with limited nutrient resources available. This was true for both sexes, although the effect was stronger for males. Higher availability of nutrients decreased the time until male and female sexual maturity and increased male calling duration per day. Furthermore, high nutrient availability decreased the duration of the pairing prelude, and consequently pairs started copulating earlier at night in the high nutrient treatment.  相似文献   

2.
Persistent mating attempts by males (sexual harassment) are frequently observed among animals. For females, resisting persistent males can be costly because vigorous resistance increases both energy expenditure and the possibility of injury. Although one tactic for coping with male harassment is to cease resistance and mate with the persistent partner, the females of several species are able to prevent the fertilization of their egg(s) despite copulation. In this study, we used three different sex ratios to investigate whether a male’s mating persistence affects his mating success in the West Indian sweet potato weevil Euscepes postfasciatus, in which males mount females both before and after copulation. Consistent with our predictions, we found that female weevils resist and manipulate sperm transfer either before or during copulation according to their preferences. Female weevils were able to reject the sperm of persistent males despite having copulated with them. However, neither copulation and/or post-copulatory mounting affected insemination success. We speculate that the intensive resistance shown by females before copulation may induce mechanical sterility in E. postfasciatus.  相似文献   

3.
The nuptial prey gift in the spider Pisaura mirabilis has been suggested to function as a male protection against sexual cannibalismduring courtship and mating. This hypothesis together withtwo alternatives—male mating effort and paternal investment hypotheses—were tested in a laboratory experiment withsexually inexperienced males and females. One group of malesoffered no gift to the female while three groups of males offeredsmall, medium, or large sized gifts, respectively. No malewas cannibalized among 82 trials. Aggression was observed onlyin encounters where a gift was presented. Males without a gift courted females, and 40% of these males managed to copulate,compared to 90% of males offering a gift. The copulation durationwas positively correlated with gift size. In general, the femaleterminated the copulation and ran away with the gift. The proportionof eggs fertilized increased with copulation time. Presenceor size of the nuptial gift did not affect female fecundityor spiderling size significantly. The results refute the hypothesesof sexual cannibalism and paternal investment. The nuptialgift represents a male mating effort; it entices the femaleto copulate, facilitates coupling during copulation, and byprolonging copulation it may increase the amount of sperm transferred.I conclude that the nuptial prey gift in Pisaura mirabilisis maintained by sexual selection.  相似文献   

4.
Darwin first identified female choice and male—male competitionas forms of sexual selection resulting in the evolution of conspicuoussexual dimorphism, but it has proven challenging to separatetheir effects. Their effects on sexual selection become evenmore complicated when sperm competition occurs because spermprecedence may be either a form of cryptic female choice ora form of male—male competition. We examined the effectsof tail height on male—male competition and female choiceusing the sexually dimorphic red-spotted newt (Notophthalmusviridescens viridescens). Experiment 1 examined whether maletail height influenced male mating success. Males with deeptails were more successful at mating with females than thosewith shallow tails. Successful, deep-tailed males also were bigger(snout-vent length; SVL) than unsuccessful, shallow-tailed males,but they did not vary in tail length or body condition. Of these,only tail height and tail length are sexually dimorphic traits.Experiment 2 tested the hypothesis that the differential successof males with deeper tails was due to female choice by examiningboth simultaneous female preference for association and sequentialfemale choice. We found no evidence of female choice. When maleswere not competing to mate with females, tail height did notinfluence male mating success. Successful males did not havedifferent SVL and tail lengths than unsuccessful males. Thus,tail height in male red-spotted newts appears to be an intrasexuallyselected secondary sexual characteristic. Experiment 3 usedpaternity exclusion analyses based on molecular genetic markersto examine the effect of sperm precedence on sperm competitionin doubly-mated females. Sperm precedence likely does not havea pervasive and consistent effect on fertilization success becausewe found evidence of first, last, and mixed sperm usage.  相似文献   

5.
Male’s copulation investment, including spermatophore and sperm investment were very high in the Chinese bushcricket Gampsocleis gratiosa. The effects of mating status of both males and females on male’s copulation investment were examined in this study. The fresh weight of spermatophylax increased positively with the weight of males’ body. This indicated that the nutritional investment during copulation depended on male’s quality. Spermatophore investment showed insignificant differences in every copulation protocols. This finding supported the paternal investment hypothesis, that is, males contributed to their offspring with little attention to their partners. Sperm releasing per ejaculation varied significantly among the trials. Males decreased 54.19% sperm in second mating than in its first mating, demonsrated that males regarded the first mating highly, and were more prudent in subsequent mating. These males’ strategies may contribute to the viability of the offspring.  相似文献   

6.
Male’s copulation investment, including spermatophore and sperm investment were very high in the Chinese bushcricket Gampsocleis gratiosa. The effects of mating status of both males and females on male’s copulation investment were examined in this study. The fresh weight of sper-matophylax increased positively with the weight of males’ body. This indicated that the nutritional in-vestment during copulation depended on male’s quality. Spermatophore investment showed insig-nificant differences in every copula...~  相似文献   

7.
Although mate preferences are most commonly examined in females, they are often found in both sexes. In the parasitoid wasp Urolepis rufipes, both female and male mating status affected certain aspects of sexual interactions. Female mating status mattered only in the later stages of mating. Males did not discriminate between virgin and mated females in terms of which they contacted or mounted first. However, once mounted, most virgin females were receptive to copulation, whereas very few mated females were. Whether a male’s mating status affected his own sexual response depended on the female’s ability to respond and the stage of mating. Examining male behavior toward dead females allowed elimination of the role of female behavior in how males responded. Virgin and mated males are both attracted to dead females as evidenced by their fanning their wings at such females. However, mated males were quicker than virgin males to contact and to mount in an experiment with dead females, whereas there was no such differential response in an experiment with live females. This difference is consistent with greater female sexual responsiveness to virgin males. Male mating status also affected female receptivity to copulate. Once mounted, live virgin females were less likely to become receptive to copulation by mated males than to virgin males, but only in a choice experiment, not in a no-choice experiment.  相似文献   

8.
Individual condition is expected to be an important determinantof many behaviors, including mating dynamics and habitat choice.In this study we experimentally investigated the linkages betweenindividual condition, habitat use, and mating dynamics in thewild. We manipulated recent feeding history of the water strider,Aquarius remigis, and then quantified the habitat use and matingactivity of males and females. Females could choose from threehabitats (refuge, near shore, and open). On the water surface(open and near-shore habitats), in contrast to refuge, femalescan forage, but they are exposed to predation and sexual harassmentby males. We tested three main hypotheses. First, we predictedthat single females that were fed, relative to those that werenot, would reduce their exposure to predators and male harassmentby increasing their use of refuge. Similarly, we predicted thatfed females that were mating would spend more time in refugethan those that were not fed. Our results support these twopredictions. Fed single and mating females significantly increasedtheir use of refuge. Third, we predicted that mating activity(proportion of time spent mating) of fed females would be reducedrelative to starved females, because of reduced exposure tomales while in refuge, and perhaps because of decreased receptivityto male mating attempts while on the water surface. Mating activityof fed females was about one third that of starved females.The decrease in mating activity could not be accounted for byany change in female receptivity, but could be accounted forby change in habitat use. The decrease in mating activity mayhave resulted from decreases in both mating frequency and matingduration. Our estimates of minimum mating frequency indicatea large and significant decrease, but we were unable to assessmating duration. We found no significant effect of our manipulationon habitat use or mating activity of males.[Behav Ecol 7: 474–479(1996)]  相似文献   

9.
The set of mating behaviours expressed by an individual may depend upon the state of that individual and local environmental conditions. Understanding how these factors affect mating behaviours may elucidate how a mating system operates, and its consequences for the form and strength of sexual selection. We conducted two experiments on the water striderGerris buenoi to (1) determine the effect of hunger on the mating behaviour of both sexes and (2) examine female choice for large males. In our first experiment, we manipulated hunger (20 h starvation) in both sexes and recorded mating, male harassment, copulation duration and guarding duration. We predicted that hunger would increase female reluctance to mate because mating conflicts with foraging. Female hunger (20 h starvation) decreased mating rate by two-thirds but had no significant effect on male mating behaviour. In a second experiment, we examined the effect of female hunger, and resulting reluctance, on sexual selection for large male size. Hungry females (5 h starvation) were placed with two fed males (one large, one small) and we recorded male premating and mating behaviours. We observed significant large-male mating advantage when females were hungry, but not when satiated. Mating efforts (harassment, premating struggles) were similar for both male phenotypes in both female hunger treatments, suggesting that the mating advantage of large males resulted from increased reluctance of hungry females to mate. Neither male body size nor female hunger explained a significant amount of variation in copulation duration or guarding duration. We discuss our results in light of two competing hypotheses for female choice (active and passive) on male body size and suggest that passive choice for large males acts in this system. Copyright 2002 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour  相似文献   

10.
Sexual coercion in the form of forced copulation has been used as a typical example to illustrate the conflict of interests between females and males. Among arthropods, forced copulation has been reported for some groups of insects and crustaceans, but not for arachnids. In the present work, we analyse and describe the behavioral patterns of mating behavior of the climbing camel-spider, Oltacola chacoensis, relating it to relevant morphological features, In this species, the male forcefully clasps the female’s genital region with his chelicerae and locks her fourth pair of legs with his pedipalps. In some cases, the cuticle of the female’s abdomen was damaged by this cheliceral clasping. In contrast to other camel-spiders, the female O. chacoensis never remained motionless during mating, but continuously shook her body, opening her chelicerae notably towards the male. Despite this coercive context, males performed copulatory courtship (tapping with pedipalps) and females showed an apparent cooperative behavior (they remained still during a short period of the sperm transfer phase). These results strengthen the idea that sexual coercion (in the form of forced copulation) and luring behavior (in the form of copulatory courtship) are not two mutually-exclusive male’s strategies during a single copulation.  相似文献   

11.
Males of Panorpa vulgaris Imhoff and Labram, 1836 (Insecta: Mecoptera) can apply three alternative mating tactics to gain access to female mating partners: (1) without nuptial feeding, (2) providing females with a dead arthropod or (3) producing salivary masses. Providing females with salivary masses during copulation leads to the highest reproductive success, as it results in longer mating durations relative to the other tactics. While the number of sperm transferred correlates with the duration of copulation, the sperm of different males are used according to the fair raffle model. Therefore, salivary mass production is an important fitness determining factor for males. In order to provide females with salivary masses, males must first produce and store saliva secretion inside their salivary glands. The present study was concerned with the development of male salivary glands (= production of saliva) in the course of time after adult emergence. We can show that saliva production did not start before adult emergence, that the state of development of salivary glands was affected by larval nutrition as well as by adult nutrition and, moreover, by age. Older individuals had developed glands of greater mass than had younger animals. After receiving a one‐time feeding immediately after eclosion salivary gland mass increased, while body mass decreased with age. Therefore, male P. vulgaris were able to enlarge the amount of their mating resources (= saliva) independently from external nutritional supply (after the initial feeding) and at the expense of losing weight. Possible reasons and functional explanations are discussed.  相似文献   

12.
Sexual selection is thought to have driven the diversificationof courtship behavior and associated ornamentation between geographicallyisolated populations of the jumping spider Habronattus pugillisGriswold. In an attempt to understand the pathways of sexualselection during this diversification, we conducted reciprocalmating trials between two populations of H. pugillis (SantaRita [SR] and Atascosa [AT]) that differ in both male courtshipdisplay and secondary sexual ornamentation. Observations ofmating frequencies show a xenophilic mating preference in whichSR females have a stronger response to AT males than to SR males,while AT females show no difference in mating frequency. Theseresults are not consistent with a coevolutionary process inwhich male traits and female preferences evolve in concert,positively reinforcing each other. We discuss alternative pathwaysof sexual selection that may have acted in this system, includingthe possibility that female preferences and male traits haveevolved antagonistically. In addition, we found that SR femalesspent a higher proportion of time prior to copulation visuallyattentive to AT males versus SR males. This difference in visualattention prior to copulation was not seen in AT females andmay provide insights into our observations of xenophilic matingpreference.  相似文献   

13.
We examined the relationships between male body and horn sizes and mating duration in the Japanese horned beetle, Allomyrina dichotoma. Smaller males possessing shorter horns spent more time for copulation with a female and mounting the female without copulation. The results of multiple regression analyses indicate that the horn length is a determining factor for the time spent by the males during mating. A previous study has documented that the horn length of male A. dichotoma primarily determined the outcomes of aggressive male–male interactions; hence, predicts access to females. Therefore, instead of fighting for females, males possessing short horns may maximize their fertilization success by mating longer with the few females they have access to.  相似文献   

14.
1. One explanation of the evolution of sexual cannibalism, the female’s consumption of a male during or following courtship or copulation, is that this behaviour increases the female’s fitness. This study tests the assumption that a single meal increases female reproductive output significantly in the sexually cannibalistic praying mantid Iris oratoria L. 2. In 38 mating trials, seven of the females cannibalised the males. In order to augment the number of females that fed, an additional nine females were each fed one cricket nymph at the end of the mating trial. 3. Three measures of female reproductive output – the occurrence of oviposition, the mass of the first ootheca, and the number of eggs in the first ootheca – increased significantly with female feeding condition, which was a reflection of food consumed before the mating trial. Females that copulated later in the season tended to lay lighter oothecae. 4. The females’ consumption of a meal during the mating trial, either a conspecific male or a cricket, did not influence any measure of reproductive output significantly, although possible effects upon subsequent oothecae cannot be ruled out. 5. If, as the present study suggests, a single meal provides a negligible or delayed benefit to female reproductive output, the evolution of sexual cannibalism might lie in alternative explanations, which include possible fitness benefits to cannibalistic females in the nymphal stage or possible paternity benefits to the cannibalised males.  相似文献   

15.
Recent studies have indicated that mating success of large malesmay improve under increasing levels of mating competition. Thisoutcome is explained 1) if male mating competition is overridingfemale preferences for male traits that are unrelated to, ornegatively correlated with, male size and dominance and, inso doing, dictates the distribution of matings or 2) if femalesalter their preferences with respect to large males when male–malecompetition is intense. Under both hypotheses, one could expectlarge, dominant males to be more successful under intense competitionthan under weak competition. However, only the first explanationpredicts that male mating success under intense competitionshould be determined by dominance; traits that are unrelatedto male dominance should be uncorrelated to mating success.In contrast, if females change their preferences (explanation2), males with traits beneficial to females independent of thecompetitive environment can maintain a high mating success underall levels of male–male competition. We tested these alternativesusing a small marine fish, the sand goby, Pomatoschistus minutus.The mating success of large males increased under conditionsallowing intense male competition, whereas females showed apreference for good nest building independent of the level ofcompetition. These findings suggest that females are in controlof their choice by altering their preference for male size inresponse to the intensity of male–male competition ratherthan female preference being overshadowed by male dominance.This plasticity of preferences implies that the strength ofsexual selection is not constant at the population level.  相似文献   

16.
Where males can increase their mating success by harassing femalesuntil they accept copulation, harassing tactics can be expectedto evolve to a point where they have costs to the longevityof both sexes. By experimentally manipulating the sex ratioin captive groups of tsetse flies Glossina morsitans morsitans,we demonstrated that the longevity of females declines wheresex ratios are biased toward males, while the longevity of malesdeclines where the sex ratio is biased toward females. Neitherirradiation of males nor prevention of copulation by blockingor damaging the external male genitalia increased the longevityof females caged with them, suggesting that female longevitywas reduced by the physical aspects of male harassment ratherthan by components of the ejaculate  相似文献   

17.
Cryptic female choice in crickets occurs through the prematureremoval of a male's spermatophore after copulation, which terminatessperm transfer. Although it is known that this behavior candirectly influence the paternity of offspring, its effects onfemale fitness have not been directly assessed. We tested thehypothesis that spermatophore removal by female house crickets(Acheta domesticus) confers fitness benefits on females, byrandomly assigning mates to females but permitting some femalesto freely remove spermatophores after mating (cryptic-choicetreatment) while forcing others to accept complete ejaculates(no-choice treatment). Although there was about a two-fold differencein the volume of ejaculate received by females of the two treatments,there were no significant differences in female longevity, reproductiveoutput, or offspring quality, as measured by offspring massand developmental time. Although differential spermatophoreremoval by females imposes strong sexual selection on males,the absence of a clear treatment effect suggests that femalesobtain no direct or indirect genetic benefits through theirpostcopulatory mating preferences.  相似文献   

18.
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.  相似文献   

19.
Conflict between the sexes over mating decision may result in antagonistic coevolution in structures that increase control over copulation. In Aquarius paludum both females and males have long abdominal spines. We tested the hypothesis that abdominal spines increase female ability to resist male mating attempts and reduce the costs of mating in A. paludum. We manipulated female spine length and observed female mating and egg-production rate in two different studies. We found that females with intact spines succeeded to reject male mating attempt more often than females with removed spines. Intact females also mated less often than females with removed or shortened spines. Male presence and mating rate increased female egg number. Our results thus support the hypothesis that abdominal spines help female to reject male mating attempts but contrary to predictions, we found that A. paludum females somehow benefit from multiple matings in spite of the sexual conflict.  相似文献   

20.
Male sagebrush crickets (Cyphoderris strepitans) permit femalesto engage in an unusual form of sexual cannibalism during copulation:females feed on males' fleshy hind wings and ingest hemolymphoozing from the wounds they inflict. These wounds are not fatal,and normally only a portion of the hind wings are eaten at anyone mating, so that mated males are not precluded from matingagain. As a result, nonvirgin males have fewer material resources tooffer females than do virgin males, such that females shouldbe selected to preferentially mate with high-investment virginmales. We tested the hypothesis that female mating preferencesfavor males capable of supplying females with the highest materialinvestment. Our results indicate that both female diet and opportunitiesfor sexual cannibalism influence female mating behavior. Femalesmaintained on a low-nutrient diet mounted males significantlysooner than females maintained on a high-nutrient diet, indicatingthat a female's overall nutrient intake may determine her propensityto mate. In addition, females were significantly more reluctantto mount and mate with males whose hind wings had been surgicallyremoved and thus were incapable of providing females with awing meal. Finally, females initially mated to dewinged malesremated with winged males significantly sooner than femalesallowed to feed freely during their initial mating, resultingin cryptic female choice of investing males.  相似文献   

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