Abstract: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 fema… Show more
“…In light of the experimental design, this difference is not entirely surprising. Although males had ad libitum access to food and water throughout the mating trials, most males chose to remain in close association with females rather than eating or drinking, presumably to engage in post‐copulatory mate guarding (Sakaluk 1991; Frankino & Sakaluk 1994; Bateman & MacFadyen 1999). Thus, males likely had fewer resources available with which to produce a second spermatophore.…”
Female decorated crickets, Gryllodes sigillatus, obtain genetic benefits by mating with different males and, when given a choice, prefer novel males over previous mates. It is unknown, however, whether males exhibit a similar preference for novel females. Although female crickets control copulation, there are at least two ways in which males can exercise choice: (1) the amount of courtship directed towards prospective mates and (2) the size of the spermatophore transferred to the female at mating. To determine whether males devote more courtship effort to novel females while controlling for female behavioral cues, male courtship effort toward two dead females, one, a previous mate and the other, a novel female, was measured. To determine whether males manufacture larger spermatophores when paired with novel females, males were mated to novel or previous mates, and the different components of the spermatophore weighed. Males did not spend more time courting dead novel females than previous mates. There was no difference in the latency to remating of males confined with novel females and those paired with previous mates, and there was no difference in the mass of spermatophores transferred to novel and familiar females. Contrary to previous studies in other taxa, this study suggests that male crickets do not prefer novel mates and thus, are not subject to the Coolidge effect. Although mating with novel females may be beneficial to males, selection on males to identify and discriminate against previous mates may be relaxed because of a strong female preference for novel males.
“…In light of the experimental design, this difference is not entirely surprising. Although males had ad libitum access to food and water throughout the mating trials, most males chose to remain in close association with females rather than eating or drinking, presumably to engage in post‐copulatory mate guarding (Sakaluk 1991; Frankino & Sakaluk 1994; Bateman & MacFadyen 1999). Thus, males likely had fewer resources available with which to produce a second spermatophore.…”
Female decorated crickets, Gryllodes sigillatus, obtain genetic benefits by mating with different males and, when given a choice, prefer novel males over previous mates. It is unknown, however, whether males exhibit a similar preference for novel females. Although female crickets control copulation, there are at least two ways in which males can exercise choice: (1) the amount of courtship directed towards prospective mates and (2) the size of the spermatophore transferred to the female at mating. To determine whether males devote more courtship effort to novel females while controlling for female behavioral cues, male courtship effort toward two dead females, one, a previous mate and the other, a novel female, was measured. To determine whether males manufacture larger spermatophores when paired with novel females, males were mated to novel or previous mates, and the different components of the spermatophore weighed. Males did not spend more time courting dead novel females than previous mates. There was no difference in the latency to remating of males confined with novel females and those paired with previous mates, and there was no difference in the mass of spermatophores transferred to novel and familiar females. Contrary to previous studies in other taxa, this study suggests that male crickets do not prefer novel mates and thus, are not subject to the Coolidge effect. Although mating with novel females may be beneficial to males, selection on males to identify and discriminate against previous mates may be relaxed because of a strong female preference for novel males.
“…Following spermatophore transfer, males in several field cricket species engage in post-copulatory mate guarding (Alcock 1994). The guarding male directs aggressive behavior towards intruding males to prevent the female from remating (Simmons 1986(Simmons , 1990Sakaluk 1991;Simmons 1991;Wynn and Vahed 2004) or to allow the guarding male to secure additional matings (Bateman and MacFadyen 1999). Aggression towards females has sometimes been interpreted as a by-product of this process (Simmons 1986).…”
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confidence: 99%
“…Alternatively, aggression could be selected for if it prolongs spermatophore attachment time (Loher and Rence 1978;Evans 1988;Hockham and Vahed 1997;Bateman and MacFadyen 1999;Bateman et al 2001). Several authors have proposed that male behavior during post-copulatory guarding might allow females to assess a male's health and vigor, such that vigilant or vigorous guards, being the most desirable mates, signal their genetic superiority by their ability to harass females (Thornhill and Alcock 1983;Simmons 1986Simmons , 1990Simmons , 1991Hockham and Vahed 1997).…”
“…Post-copulatory mate guarding intensity was found to be initially high following copulation, before declining and then increasing to be high just before the male re-entered courtship. We propose that this pattern may be explained by the interaction between two of the three hypotheses for the function of post-copulatory mate guarding in gryllid crickets: ejaculate protection and spermatophore renewal (Sakaluk 1991;Bateman and MacFadyen 1999). The relative importance of each of these strategies is likely to alter over the guarding period as the benefits of each strategy change in value.…”
Section: Discussionmentioning
confidence: 95%
“…Post-copulatory mate guarding has been well documented in gryllid crickets (Simmons 1990;Sakaluk 1991;Hockham and Vahed 1997;Bateman and Macfadyen 1999;Wynn and Vahed 2004;Bussiere et al 2006;Parker 2009). The occurrence of pre-copulatory mate guarding in gryllids, however, appears to have been largely overlooked.…”
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
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