The function of mate guarding in a field cricket (Orthoptera: Gryllidae;Teleogryllus natalensis otte and cade)

Three hypotheses relating to the function of postcopulatory mate guarding were tested for the cricketTeleogryllus natalensis. The hypothesis that guarding allows the male to remain with the female for repeated matings was rejected. This was because the mean intercopulatory interval for maleT. natalensis was found to be nearly twice as long as the mean duration of guarding. Nor do the results provide evidence to support the hypothesis that guarding functions to prevent copulation attempts by rival males (the rival exclusion hypothesis): the presence of a rival male was found to have no significant effect on the duration of spermatophore attachment for either guarded or unguarded females. The results do, however, support a third hypothesis, namely, that guarding functions to prevent the female from removing the spermatophore ampulla before complete sperm transfer. As predicted by this hypothesis, the presence of a guarding male was found to have a significant positive effect on the duration of spermatophore attachment. Further support for this hypothesis was provided by the fact that there was a significant positive correlation between the duration of mate guarding and the duration of spermatophore attachment.     

Strategic mate‐guarding behaviour in ladybirds

Mate‐guarding behaviour is regarded as a means of increasing paternity share by reducing sperm competition. It is known to be a plastic response which varies with operational sex ratios and competitor presence in the vicinity. In a recent study, prolonged mating duration in Menochilus sexmaculatus (Fabricius) (Coleoptera: Coccinellidae) has been found to incorporate mate‐guarding behaviour. The present investigation was conducted to assess its plasticity in the presence of competitors. The physical and chemical presence of competitors of both sexes at varying densities was provided to a pair of ladybirds, and their time to commence mating, latent period and mate‐guarding duration was observed. These were compared to a control treatment where other partners were absent. All treatments were conducted with sibling as well as non‐sibling competitors. It was our hypothesis that mate guarding would be increased in the presence of male competitors and would be reduced by female presence. The results revealed that while mate‐guarding duration was increased by the chemical presence of males it was decreased by their physical presence. The latter result was attributed to interference by other males who dislodge the mating male in order to access the female. Female chemical presence had no effect on mate guarding, while physical presence increased the duration of mate guarding. The reasons for the latter behaviour require further investigation. Responses were not significantly affected by the relationship between the focal pair and the competitor. The authenticity of the mate guarding in this ladybird is strongly affirmed by our results.     

Aggressiveness during monogamous pairing in the sleepy lizard, <Emphasis Type="Italic">Tiliqua rugosa</Emphasis>: a test of the mate guarding hypothesis

The Australian sleepy lizard, Tiliqua rugosa, maintains monogamous associations for an average of 6 weeks before mating each spring. One hypothesis to explain this prolonged partnership is that males are guarding their female partners from rival males. This hypothesis has three predictions, that males are more aggressive than females to conspecific males, that male aggression will increase as the time of mating gets closer, and that males will be more aggressive towards conspecific males when they are with their partner than when they are alone. We tested those predictions with indirect evidence of aggression, using counts of scale damage on randomly encountered lizards, and with direct observations of their responses to approaches by conspecific and heterospecific models. As predicted by the mate guarding hypothesis, males showed more evidence of aggression towards conspecifics than did females. However, in contrast to the hypothesis, males did not become more aggressive as the time of mating came closer, and males in pairs were less aggressive than males on their own. Mate guarding cannot be the only process that has led to the prolonged monogamous associations in this species. Parental care is also unknown in these lizards, and we suggest that monogamy may be maintained through some form of female coercion, allowing females to gain additional fitness from the enhanced vigilance that results from male proximity.     

Mate Guarding in the Cricket Gryllodes sigillatus: Influence of Multiple Potential Partners

There are several hypotheses as to the function of postcopulatory mate guarding. Control over the mate-guarding period by either sex could potentially influence relative reproductive success. Mate-guarding behaviour in Gryllodes sigillatus was studied under several conditions: 1. undisturbed pairs; 2. pairs with a single male intruder; 3. pairs exposed acoustically, visually and olfactorily to several other males; 4. pairs exposed freely to several other males; and 5. pairs exposed freely to several other females. The results provide support for the spermatophore retention and rival defence hypotheses. The efficacy of mate guarding was not compromised by the pair being in acoustic, visual and olfactory contact with several other males. Once pairs were exposed to free contact with several other males, the spermatophore retention time by the female declined significantly, indicating that the mate guarder's efficiency declines under competition from several rivals. In pairs exposed to contact with several females after mating, the mate-guarding period and spermatophore retention time declined as the mate guarder abandoned the mated female and pursued the other females. Termination of the effective mate-guarding period by either sex seems to be influenced by the number of other potential partners present.     

SEX‐SPECIFIC EVOLUTIONARY POTENTIAL OF PRE‐ AND POSTCOPULATORY REPRODUCTIVE INTERACTIONS IN THE FIELD CRICKET,TELEOGRYLLUS COMMODUS

Mate choice often depends on the properties of both sexes, such as the preference and responsiveness of the female and the sexual display traits of the male. Quantitative genetic studies, however, traditionally explore the outcome of an interaction between males and females based solely on the genotype of one sex, treating the other sex as a source of environmental variance. Here, we use a half‐sib breeding design in the field cricket, Teleogryllus commodus, to estimate the additive genetic contribution of both partners to three steps of the mate choice process: the time taken to mate; the duration of spermatophore attachment; and the intensity of mate guarding. Rather than each sex contributing equally to the interactions, we found that genetic variation for latency to mate and spermatophore attachment was sex‐specific, and in the case of mate‐guarding intensity, largely absent. For a given interaction, genetic variation in one sex also appears to be largely independent of the other, and is also uncorrelated with the other traits. We discuss how pre‐ and postcopulatory interactions have the potential to evolve as an interacting phenotype, but that any coevolution between these traits, due to sexual selection or sexual conflict, may be limited.     

The intensity of pre- and post-copulatory mate guarding in relation to spermatophore transfer in the cricket Gryllus bimaculatus

While post-copulatory mate guarding has been well documented in field crickets (Orthoptera: Gryllidae), the occurrence of pre-copulatory mate guarding in this family has been largely overlooked. We examined the relationship between the intensity of two components of mate guarding (body judders and antennal whips) and the time before and after copulation. We found that when male Gryllus bimaculatus encounter a female but do not have a spermatophore ready to transfer, they engage in pre-copulatory mate guarding that is very similar to post-copulatory mate guarding. The intensity of pre-copulatory mate guarding increased up to the point at which the male was ready to transfer his spermatophore. Following copulation, the intensity of mate guarding initially remained high before declining, after which it began to increase again just before the male resumed courtship stridulation. We interpret this pattern of post-copulatory mate guarding as being consistent with both the ejaculate-protection and spermatophore-renewal hypotheses for the function of mate guarding. We found no significant relationship between mate guarding intensity and male body mass.     

Competing for last place: Mating behaviour in a pill-box crab, Halicarcinus cookii (Brachyura: Hymenosomatidae)

The mating strategy of Halicarcinus cookii was investigated to ascertain how males maximised their fitness through mate choice. An intertidal population at Kaikoura, New Zealand, was dominated by mature crabs of both sexes in summer and by immature crabs in the colder months. More than 95% of mature females were ovigerous with early stage and late stage broods found in almost every month, indicating that egg production and larval release is continuous. The operational sex ratio was less than 1 male/female in summer, but often more than 1.0 in the colder months. The gonosomatic index increased along with brood development so that as soon as zoeae were released, the next clutch of eggs was ready to be fertilised. Males searched for receptive females and began pre-copulatory mate guarding without any courtship display. They mated preferentially with late stage or non-ovigerous females: copulation duration was longest for stage 5 females as was post-copulatory guarding (mean 18.3 h). Late stage females were up to 14% of the female population. Mate attraction seems to be the result of an ovarian signal rather than from the developing brood. Manipulation of the sex ratio had effects upon copulation duration and post-copulatory guarding: presence of a rival male increased duration of guarding. Females showed precocious mating in the penultimate instar and were able to lay fertilised eggs after their pubertal moult in the absence of males. H. cookii females have many mates, but males attempt to ensure paternity by preferentially pursuing mature females close to egg laying and by guarding these females after copulation. These behaviours are all elements of a competitive strategy to ensure that a male loses (not wins) the race to copulate because females have a ventral seminal receptacle, giving sperm precedence to the last male to mate. Male mating behaviour is a consequence and evolutionary response to female morphology.     

Chemosensory assessment of sperm competition levels and the evolution of internal spermatophore guarding

Males of many species adjust their reproductive behaviour according to the perceived risk of sperm competition. Although this phenomenon is widespread in insects and other animals, the mechanisms that allow mates to assess sperm competition levels remain largely unexplored. In this study, we analysed the mating behaviour of pairs of Tenebrio molitor beetles under three odour treatments representing increasing levels of sperm competition risk (SCR) and sperm competition intensity (SCI). Copula duration and male and female post-copulatory behaviour varied significantly with odour treatment. Both copula duration and post-copulatory associations (PCAs) increased significantly in odour treatments reflecting high male density. To our knowledge, this is the first study to report that insects may assess the actual density of potential competitors at the time of mating, a cue to SCR and SCI, on the basis of chemical cues. In T. molitor, males inhibit sperm release from the spermatophore of a rival male when remating takes place at short intervals. We show that, when sperm competition levels are high, PCAs increase female remating interval just above that necessary to prevent spermatophore inhibition by rival males. This finding strongly suggests that strategic male behaviour plays a 'spermatophore guarding' role in this species. Although common in insects with external spermatophore transfer, spermatophore guarding is not expected in species with rapid ejaculate transfer and internal spermatophore delivery. Our results reveal that spermatophore guarding may evolve, even under these circumstances, as an evolutionary response to short-term spermatophore inhibition or displacement mechanisms.     

Physiological Costs of Mate Guarding in the Japanese Beetle (Popillia japonica Newman)

Males of many insects directly defend their mates from rival males (i.e. mate guard) as a way to avoid sperm competition and thus increase their reproductive success. However, mate guarding may have associated costs for these males. We examined costs of mate guarding in Japanese beetles (Popillia japonica), a pest species which exhibits post‐copulatory mate guarding during which the guarding male cannot feed. In this species, food provides both energy and water for thermoregulation. Consequently, we focused on possible thermoregulatory and energetic costs of their mate guarding. In a field study, we found that guarding males had significantly higher thoracic temperatures than non‐guarding males, indicating a difference in their ability and/or need to thermoregulate. Paired males had significantly lower water levels than single males in the morning and evening, but not in the afternoon. In the laboratory, we found that mate‐guarding duration was significantly shorter at higher ambient temperature than at lower temperature, and males that had been starved guarded for less time than males that had not been starved. Our results suggest that because guarding males are unable to feed, they suffer energetic and thermoregulatory costs that appear to limit the amount of time that they can guard a female.     

Breeding in the crayfish, Austropotamobius pallipes: mating patterns, mate choice and intermale competition

1. The breeding behaviour of the white-clawed crayfish, Austropotamobius pallipes, which is in decline throughout Europe, was analysed. 2. Observations and experiments focused on: (i) several aspects of mating behaviour, showing the primary role of the female during courtship, the patterns of mature male receptivity and the possible existence of a mating stimulus produced by either a mating pair or a receptive female; (ii) the potential for mate choice either by males (males were not choosy, mating with the first receptive female they met) or by females (that rejected the smallest males and males with only one cheliped) and (iii) intermale fighting before copulation (larger males copulated more often, with the exception of some ’sneakers‘). 3. Sperm competition occurred when a new male was presented with a female after a previous male‘s spermatophore had been deposited; the new male cleaned the rival male‘s spermatophore by feeding on it before copulation. This behaviour has also been observed in some pseudoscorpions, millipedes and collembolans, but always in cases where the spermatophore is deposited on the substratum. Introduction     

同种雄性竞争对手的存在对星豹蛛雄蛛求偶和交配行为的影响

越来越多的研究发现,雄性产生精子(精液)也需付出代价。雄性除了依据配偶质量和竞争对手的竞争强度适应性调整生殖投入外,雄性在求偶和交配行为上也相应产生适应性反应,求偶和交配行为具有可塑性。目前雄性求偶和交配行为可塑性研究主要集中于雌性多次交配的类群中,在雌性单次交配的类群中研究甚少。以雌蛛一生只交配一次而雄蛛可多次交配的星豹蛛为研究对象,比较:(1)前一雄性拖丝上信息物质对后续雄蛛求偶和交配行为的影响,(2)雌雄不同性比对雄蛛求偶和交配行为的影响。研究结果表明,星豹蛛前一雄蛛拖丝上的信息物质对后续雄蛛求偶潜伏期、求偶持续时间和交配持续时间都没有显著影响,但前一雄蛛拖丝上的信息物质对后续雄蛛求偶强度有显著抑制作用。同时,性比对星豹蛛雄蛛求偶和交配行为都没有显著影响。可见,星豹蛛雄蛛对同种雄性拖丝上的化学信息可产生求偶行为的适应性调整,而对性比不产生适应性反应。     

Hang on or run? Copepod mating versus predation risk in contrasting environments

Mating durations of copepods were found to differ significantly between fishless high-altitude waters and lowland lakes containing fish. In lowland species the whole mating process was completed within a few minutes, but it averaged over an hour in high-altitude species. Alpine copepods showed a prolonged post-copulatory association between mates, during which the male clasped the female for an extended period after spermatophore transfer, while in lowland species males abandoned their partner immediately after copulation. Prolonged associations also occurred after transfer of spermatophores to heterospecific females with shorter conspecific mating duration, suggesting that male interests largely dictate the time spent in tandem. The differences observed may be adaptations to environments with different predation pressure, as pairs in tandem are more conspicuous and less reactive than single animals. We argue that differences in mating behavior and mating duration evolved under sexual versus natural selection, reflecting trade-offs between enhancement of fertilization success and reduction of vulnerability to visual predation. In fishless mountain lakes with high intrasexual competition, guarding males can reduce the risk of spermatophore displacement or the risk that the female will accept sperm from rival males without increased risk of being eaten, thereby maximizing paternity. Populations from fishless alpine lakes further differed from lowland species by exhibiting higher female/male size dimorphism and more intense pigmentation. While these traits vary between populations according to predation pressure, mating duration appears to be more species-specific.     

Rapid diversification of male genitalia and mating strategies in Ohomopterus ground beetles

We analysed evolutionary diversification and covariation in male genitalia and four mating traits related to sexual selection, i.e. testis size, spermatophore size, copulation duration and post-copulatory guarding duration, in Ohomopterus ground beetles using phylogenetically independent contrasts. Male genital size and mating duration have evolved more rapidly than body size and the other traits studied. Male genital size was negatively correlated with copulation duration, suggesting that elongated male genitalia may enable decreased time investment in a single copulation because it is more effective at facilitating spermatophore deposition. Male genital size was positively correlated with spermatophore size, suggesting coevolution between offensive and defensive male mating tactics because the elongated male genitalia may be advantageous in displacement of rivals' plug-like spermatophores, and decreased mating duration may intensify sperm competition. Thus, the remarkable diversity of male genitalia in Ohomopterus may have been facilitated by the interplay between inter- and intrasexual selection processes.     

Energetic costs of mate guarding behavior in male stream-dwelling isopods

In the stream-dwelling isopod Lirceus fontinalis, males and females engage in a precopulatory mate guarding phase prior to mating. We examined the energetic costs of mate guarding behavior in males by separately assaying glycogen and lipid content at different time increments following mating. We found that males that had recently mated possessed reduced glycogen reserves and that these reserves were fully replenished within 36 h. Conversely, we found that male lipid reserves were unaffected by time since mating. We concluded that precopulatory mate guarding behavior is energetically costly to males and that glycogen is the energy source utilized to pay that cost. We also examined whether food deprivation during the mate guarding phase affected male energy reserves (glycogen) at the end of that phase. We found that males that were held in the laboratory and starved during mate guarding possessed reduced glycogen at the termination of the phase when compared to fed males. This reduced quantity was equivalent to the glycogen reserves of recently mated males collected from the field. We propose that food deprivation during the mate guarding phase explains the reduction in glycogen reserves at the termination of that phase. We discuss these results with reference to patterns of refuge use behavior during the mate guarding phase.     

三突伊氏蛛雌蛛不同交配史对雄蛛交配行为的影响

近年来越来越多研究表明,雄性产生精子(精液)也需付出代价。在多次交配的动物中,雄性为获得最大生殖潜力,必须依据配偶的质量策略性地调整每次交配的生殖投入。雄性策略性的生殖投入主要体现在两个方面,一是精子竞争(sperm competition),二是柯立芝效应(Coolidge effect)。目前精子竞争研究主要集中于昆虫类群,而柯立芝效应研究集中于高等脊椎动物,同时验证结果也时常与假说不一致。以多次交配的三突伊氏蛛为材料,以雄蛛交配行为为指标,在蜘蛛类群中探讨和验证雄性精子竞争强度假说和柯立芝效应。设定3个交配组合:2只雄蛛依次与1只雌蛛各交配1次(A组)、2只雄蛛依次与2只雌蛛各交配1次(B组)和1只雄蛛与1只雌蛛交配2次(C组),分析比较3个交配组合的三突伊氏蛛第1次交配和第2次交配在交配潜伏期、交配持续时间和交配回合数方面的差异,比较三突伊氏蛛雌蛛不同交配史对雄蛛交配行为的影响,以此验证雄性精子竞争强度假说和柯立芝效应。研究结果表明A和B组的三突伊氏蛛第2次交配的交配潜伏期和交配持续时间显著长于第1次交配。同时,C组的三突伊氏蛛第1次交配的交配潜伏期和交配持续时间与第2次交配都没有显著差异。同时,A、B和C组的三突伊氏蛛第1次交配的交配回合数与第2次交配都没有显著差异。研究结果支持精子竞争强度假说,而不支持柯立芝效应。     

The Effects of Age and Previous Mating Experience on Pre- and Post-copulatory Mate Choice in Female House Crickets (<Emphasis Type="Italic">Acheta domesticus</Emphasis> L.)

Although females’ mating preferences are influenced by male characteristics, there are a number of factors intrinsic to females and unrelated to male phenotype that can modulate female choice. We assessed the effects of age and mating experience on mechanisms of pre- and post-copulatory mate choice in female house crickets, Acheta domesticus L., by randomly assigning males to females, but independently varying the age and number of previous matings of females at the time of experimental matings. Latency to mating, a measure of a female’s pre-copulatory preference, was influenced by female age at the time of mating, with older females mating sooner than younger females. The reduced selectivity of older females appears consistent with life-history theory, which predicts that the reproductive value of females should decline with age. The length of time that females retained the spermatophore after mating, a measure of a female’s post-copulatory mating preference, was not influenced by female age at the time of mating, the number of previous matings, or any interaction between the two main effects. Contrary to previous reports, male mass had no effect on either the latency to mating or female retention of the spermatophore in A. domesticus. We conclude that female age and mating experience can moderate female selectivity, but that their impact varies according to the mechanism by which females favor particular sires.     

Spermatophore and Sperm Allocation in Males of the Monandrous Butterfly Pararge aegeria: the Female’s Perspective

In insects, spermatophore production represents a non‐trivial cost to a male. Non‐virgin males have been shown to produce small spermatophores at subsequent matings. Particularly in monandrous species, it may be an issue to receive a sufficiently large spermatophore at the first and typically only mating. Females of the monandrous Speckled wood butterfly Pararge aegeria (L.) produce fewer offspring after mating with a non‐virgin male. After mating, females spend all their active time selecting oviposition sites and typically ignore other males. Here, we show that females did not discriminate between a virgin male and a recently mated male in our laboratory experiments. We demonstrate that the number of eupyrene sperm bundles relative to spermatophore mass differed with subsequent male matings. Males transferred a significantly smaller spermatophore after the first copulation, but the spermatophore mass did not decrease further with subsequent matings. However, the number of eupyrene sperm bundles decreased linearly. Therefore, there was proportionally more eupyrene sperm in the male’s second spermatophore compared with the first and the later spermatophores. Such a pattern has been shown in polyandrous species. Hence, it suggests that differences in sperm allocation strategy between polyandrous and monandrous butterflies may be quantitative rather than qualitative. There was also a tendency for females that had mated with a recently mated male to have higher propensity to remate than did females that had mated with a virgin male. We discuss the results relative to the mating system in P. aegeria, including female remating opportunities in the field and male mate‐locating behaviour.     

Body Size and Multiple Copulations in a Neotropical Grasshopper with an Extraordinary Mate-Guarding Duration

After copulation, male grasshoppers of Sphenarium purpurascens (Orthoptera: Pyrgomorphidae) remain in a postinsemination association with their mate. A male can spend as many as 17 days mounted on a female. Guarding duration is related to both male and female body size and the female's mating history. Longest guarding durations were recorded at the middle of the reproductive season, when the probability of encounter between the sexes (sex ratio and population density) was decreasing, at the beginning of the associated dry season. These guardings were associated with large individuals of both sexes and with females that had more previous partners. Moreover, a positive association was found among guarding duration, female and male body size and age, and number of copulations performed by the males. Maybe males invest time and sperm in females as a function of the probability of sperm competition. Nevertheless, guarding may provide benefits to both sexes. Males may reduce the possibility of sperm competition, and females may obtain nutritional benefit for themselves or their offspring as a result of multiple copulations. Changes in male investment in guarding duration and number of copulations may be the result of physiological constraints related to seminal and/or sperm production. Moreover, guarding duration could be constrained by ecological factors such as a reduction of food availability associated with the beginning of the dry season.     

Mating behavior and time budget of an androdioecious crustacean,Eulimnadia texana (Crustacea: Conchostraca)

The clam shrimp,Eulimnadia texana (Crustacea, Conchostraca), is found in freshwater ephemeral environments throughtout the United States. Individual clam shrimp of this species are either hermaphroditic or male, a relatively rare mating system for animals known as androdioecy. Comparison of sex ratios between four neighboring populations ofE. texana in Southern New Mexico showed wide variation in the ratio of males to hermaphrodites with males making up as much as 42% of some populations and not occurring at all within others. Since little is known about the behavior of this species, an ethogram and time budget were prepared based on observations of laboratory populations. Males attempt to clasp hermaphrodites prior to mating. Precopulatory mate guarding occurs in this species. Outcrossing generally occurs during mate guarding and after the hermaphrodite molts. Hermaphrodites, however, seem to control the mating process. Successful mating by males never occured if the hermaphrodite struggled with him; hermaphrodite will self in the presence of males.     

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.