Male Gryllus bimaculatus Guard Females to Delay Them from Mating with Rival Males and to Obtain Repeated Copulations

Three hypotheses for the function of postcopulatory mate guarding were tested in the field cricket Gryllus bimaculatus De Geer. The duration of spermatophore attachment was greater in the absence than in the presence of a guarding male. The ejaculate protection hypothesis was, therefore, rejected. The duration of mate guarding was found to be equal to the interval between copulations, supporting the spermatophore renewal hypothesis. In support of the rival exclusion hypothesis, the presence of a guarding male did increase the duration of spermatophore attachment when a rival male was also present. The presence of a guarding male also delayed the female from mating with the rival male. Female mating status had a significant effect on the duration of spermatophore attachment. Females mating for the first time retained the spermatophore for a significantly longer period of time than females that had mated previously.     

Vibratory signals enhance mate-guarding in a water strider (Hemiptera: Gerridae)

Mating males of the water strider Gerris remigisproduce vibratory signals when-single males grasp mating pairs. When played through live females with dead males on their backs, these signals repelled mating attempts by single males. A previous study showed that male mate-guarding enhances female foraging effectiveness in this species. Thus male mate-guarding signals also enhance female foraging effectiveness.     

Precopulatory mate guarding in Harpacticella inopinata Sars (Copepoda: Harpacticoida) from Lake Baikal

Precopulatory mate guarding is reported for the first time from a freshwater harpacticoid, Harpacticella inopinata. Adult males were observed grasping onto juvenile females from the third copepodid stage onwards, but most commonly with the fifth copepodid. This behaviour is interpreted as a plesiomorphic trait of the family Harpacticidae.     

Mating behavior of male deer ticksIxodes dammini (Acari: Ixodidae)

To analyze the sexual behavior of male black-legged deer ticks Ixodes dammini,we collected ticks infesting 202 white-tailed deer. On average, 17.7 males and 8.8 females infested each deer. Field-collected males copulated with a mean of 2.25 females, and virgin males mated with 2.4 females. On experimental hosts, males established sexual contact with feeding females and repelled other males, and about half remained paired after their mate detached. Engorged females continue to be receptive, and males mate more readily with them than with nonfed females. We conclude that male I. damminiare endowed with a repertoire of behaviors which favor an opportunistic mating before seeking a host and a preference for mating with feeding females on the host accompanied by tenacious mate guarding.     

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.     

Site-specific mate-finding strategies and oviposition behavior inCrocothemis erythraea (Brullé) (Odonata: Libellulidae)

Mate-finding strategies and adaptations in pre- and postcopulatory behaviors to avoid male disturbance were studied in Crocothemis erythraea at two different sites. At ponds without perch sites males patrolled with temporal partitioning of the limited oviposition sites and male-male disputes were rare. The arrival rate of females was high. At temporary marshes with dense emergent vegetation the oviposition sites were widely distributed. Males mainly perched and interacted with longer disputes. At both types of habitats with high male densities females showed a similar number of copulations per visit and oviposition durations. Postcopulatory behavior to avoid male disturbance and to decrease remating of the female differed in both sexes. At the ponds with patrolling males the probability of remating in guarded and unguarded ovipositions was similar and higher than at the marshes. At the marshes 78% of rematings occurred when the guarding male was still involved in disputes with the previously disturbing male. At the ponds females hovered before escaping successfully from approaching males and they changed to another oviposition site where they continued oviposition. Females at the marshes remated after surprise attacks by neighboring males.     

The adaptiveness of intense contact mate guarding by males of the emerald damselfly,Lestes sponsa (Odonata, Lestidae): The male’s perspective

We studied the mating system of the emerald damselflyLestes sponsa. All males showed intense contact mate guarding by holding the female in tendem during the entire oviposition period. Our findings support the predictions made by Alcock (1994) about the occurrence of intense mate guarding: (1) a high female receptivity after copulation, (2) a high male capacity to resist takeovers, (3) sperm precedence, (4) a high operational sex ratio, (5) a high male density, (6) high access by rivals to mated females, (7) low energy expenditure, (8) a low risk of guarding, and (9) a short interval between copula and oviposition. This indicates a positive cost-benefit balance for this behavior, at least in males. A comparison within the genusLestes suggests that the male-biased sex ratios and the ease with which mated females are detected have been strong selection pressures in the evolution of intense contact mate guarding.     

Delayed copulation as a means of female choice by the hermit crab Pagurus filholi

Male hermit crabs perform precopulatory mate-guarding behavior during their reproductive season. As females generally cannot reject guarding attempts by males, male guarding prevents females from inspecting and choosing other male mates. However, as guarding males are often replaced by other males through competition for females during the guarding phase, females may be able to select males by delaying their copulation. To examine the possibility of female choice by hermit crabs, we investigated whether female Pagurus filholi that were being guarded in the field were ready to copulate and spawn. We found that about 30% of females guarded in the field were ready to spawn, indicating that guarded females delayed copulation with their current male. Our results suggest that by delaying copulation females may exploit male–male competition to choose dominant males. However, delaying copulation reduced the spawning potential of females. Hence, there is a trade-off between waiting for the opportunity to mate with a dominant male and decreased spawning success if females exploit male–male competition.     

Male-biased sex ratios,female promiscuity,and copulatory mate guarding in an aggregating tropical bug,Dysdercus bimaculatus

The ecological and social bases of the mating system of the seed-feeding bug, Dysdercus bimaculatus(Hemiptera: Pyrrhocoridae), were studied in the lab and in aggregations at the host tree, Sterculia apetala(Malvales: Malvaceae), in Panama. On theoretical grounds, two factors are predicted to be of importance in determining the evolution of male mating tactics in Ms species: the operational sex ratio and the probability that undefended females will mate with other males, subjecting the gametes of deserters to sperm competition. Results of a study of a related species suggested that sperm displacement is probably substantial. Adult sex ratios at numerous sites were significantly male biased, and females whose mates were removed remated before oviposition (i. e., sperm utilization). These results predict that a mate defense tactic is likely to be superior to a nondefense tactic. The biological significance of the parameters is supported by observations that captive pairs often remained in copulafor several days, until just before oviposition. However, substantial variation in copulation duration was also observed, and possible causes of this variation are considered. Causes of male biased adult sex ratios were investigated by monitoring demographic changes within a single aggregation over 2 months. Both female juvenile and adult mortality rates were greater than male. In addition, dissections of reproductive adults showed that the flight muscles of females, but not males, had histolyzed, so that female reproduction is physiologically limited to a single site. Greater rates of immigration among both mature and young males suggests that an excess of males may also be found in the populations of bugs that subsequently colonize other host plants, so that female scarcity is typical of aggregations in all stages of development. The evolution of sex-limtied flight muscle histolysis may be explained by greater patchiness of females than males as mating resources, plus a lower energetic benefit/cost ratio of histolysis for males.     

The reproductive behavior of six species of Namib desert tenebrionid beetles (Coleoptera: Tenebrionidae)

The reproductive behavior of six species of tenebrionid beetles (Coleoptera: Tenebrionidae) was studied in the Namib Desert of southern Africa. In three species, males follow closely behind females (following behavior), while in the other three species, males mount females and remain clasped to them for extended periods (riding behavior). Following behavior occurs before and sometimes after copulation, while riding behavior occurs primarily after copulation. Males of all six species guard females from contesting males, although the effectiveness of guarding is greater in riding species. The evolution of the two male mating strategies does not appear to be related to operational sex ratio differences but, rather, to differential tendencies of females to remate. Variation in total pair duration within following and riding species may be attributed partly to species differences in operational sex ratio. However, pair durations are not affected by experimental manipulations of sex ratio in each species.     

Sex-specific chemical cues from immatures facilitate the evolution of mate guarding in Heliconius butterflies

Competition for mates has substantial effects on sensory systems and often leads to the evolution of extraordinary mating behaviours in nature. The ability of males to find sexually immature females and associate with them until mating is a remarkable example. Although several aspects of such pre-copulatory mate guarding have been investigated, little is known about the mechanisms used by males to locate immature females and assess their maturity. These are not only key components of the origin and maintenance of this mating strategy, but are also necessary for inferring the level to which females cooperate and thus the incidence of sexual conflict. We investigated the cues involved in recognition of immature females in Heliconius charithonia, a butterfly that exhibits mate guarding by perching on pupae. We found that males recognized female pupae using sex-specific volatile monoterpenes produced by them towards the end of pupal development. Considering the presumed biosynthetic pathways of such compounds and the reproductive biology of Heliconius, we propose that these monoterpenes are coevolved signals and not just sex-specific cues exploited by males. Their maintenance, despite lack of female mate choice, may be explained by variation in cost that females pay with this male behaviour under heterogeneous ecological conditions.