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.     

Avoidance of egg parasitism through submerged oviposition by tandem pairs in the water strider, Aquarius paludum insularis (Heteroptera: Gerridae)

Abstract.  1. Females of the water strider Aquarius paludum insularis (Motschulsky) (Heteroptera: Gerridae) carry males on their backs and oviposit under water after copulation. This study focuses on the benefit  A. paludum insularis receives by ovipositing in tandem.
2. Males guarded females in tandem through to the end of oviposition in 85% of copulations. Females in tandem dived deeper than single females, and the density of A. paludum insularis eggs increased with water depth. The proportion of eggs parasitized by a scelionid wasp, Tiphodytes gerriphagus Marchal (Hymenoptera: Scelionidae) decreased with increasing water depth.
3. These results suggest that during oviposition guarding by males is beneficial for females, because it enables pairs to dive and lay eggs deeper and in oviposition sites where the risk of egg parasitism is lower.     

Mate disruption in the water strider Aquaris remigis Say, 1832 (Hemiptera: Gerridae)

This report describes the behaviour of a previously uncharacterised mating tactic amongst male water striders (Aquarius remigis Say, 1832), involving the physical break up of existing mating pairs. Using data from four separate laboratory observations on the water strider mating system, we show that this behaviour represents roughly 12.6% of all mating attempts by males. Furthermore, we demonstrate that males are successful in breaking up the existing mating pair in 15.6% of the cases, resulting in secure matings with the disrupted female 6.2% of time. We suspect that mate disruption may serve as an alternative means for acquiring mates by males with low mating success using conventional behaviours. Further research should be performed to determine the prevalence of this behaviour in various natural populations and the specific contexts in which this behaviour occurs.     

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.     

Cost of oviposition site selection in a water strider Aquarius paludum insularis: Egg mortality increases with oviposition depth

Females generally avoid selecting sites for oviposition which have a high predation risk to increase offspring survival. Previous studies have focused on costs to ovipositing females. However, although offspring may also incur costs by being oviposited at low predation risk sites, no studies have focused on costs to offspring. Such costs to offspring were examined by using Aquarius paludum insularis, females of which avoid eggs parasitism by ovipositing at deep sites. Deep sites are safe from egg parasitism but may be unsuitable for hatching due to environmental factors. We examined the costs to offspring at deep sites by comparing the hatching rate, the duration to hatching and the proportion of drowned larvae between eggs that were set at three levels of water depth (0 cm, 25 cm and 50 cm depth). While the hatching rate at 50 cm was lower than that at 0 cm, the rate at 25 cm did not differ from that at 0 cm. Duration to hatching and the proportion of drowned larvae did not differ between the three depths. It is suggested that the declining survival rate of A. paludum eggs was due to increased water pressure at greater depth. Such a cost may exist in other species and such an observation may aid in understanding oviposition site selection.     

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.     

The adaptive significance of mate guarding in the soapberry bug,Jadera Haematoloma (Hemiptera: Rhopalidae)

Male soapberry bugs (Jadera haematoloma)face severe mating competition at the northern edge of their range due to male-biased adult sex ratios. Copulations lasting up to 11 days may serve a mate guarding function (encompassing four or more ovipositions), but copulation duration is highly variable, with some pairings lasting as little as 10 min. Data were gathered to describe factors that influence the reproductive costs and benefits of prolonged copulation. Estimated copulation durations (mean ± SD) were 20 ± 23 h in the lab and 50 ± 8 h in the field and were only weakly affected by sex ratio. Females mated for 5 min produced as many fertile eggs as those mated for 600 min laid; they became depleted of fertile sperm after about 25 days. In twicemated females, the first male's paternity was reduced by about 60%, and all females (N = 13) whose mates were removed experimentally mated again within an average of 6 min. The outcome of sperm competition on a perclutch basis was not highly predictable. The possibility of increased sperm displacement in longer copulations was not tested. Males often guarded females during oviposition and successfully defended them from intruding single males by recopulating. Such intrusions occurred in the majority of oviposition attempts observed in nature. Even though most females mated promiscuously, in a focal aggregation with a mean sex ratio of 2.2 ± 0.4 males/female, the interval between matings by males was commonly several days. Males appeared to respond facultatively to several aspects of the distribution and availability of females. The intensities of mating competition and sperm competition indicate that monogamous mate guarding should be favored over nonguarding in nature. Unpredicted brief. pairings may result from assessment by males of female reproductive value or of their own physical condition, or from female resistance.     

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.     

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.     

Comparing salinity tolerance in embryonic and larval development of two species of water strider,Aquarius paludum and Gerris latiabdominis (Hemiptera: Gerridae)

Water strider Aquarius paludum (Fabricius) is a cosmopolitan species colonizes mainly freshwater but occasionally brackish habitats throughout the Palearctic and Oriental regions. Water strider Gerris latiabdominis (Miyamoto) is a common species in Japan lives in temporary habitats as freshwater paddy fields. These two species often occur syntopically. We investigated differences in the developmental response to brackish water during embryonic and larval stages between the two species. Eggs were exposed to 0–1.8% NaCl solutions within 24 h of oviposition. Larvae of G. latiabdominis were exposed to salinities of 0, 0.5%, and 0.9% from the first instar until adult emergence. Limits of NaCl concentration for hatching were 1.3% and 1.0% for A. paludum and G. latiabdominis, respectively. The hatching rate of G. latiabdominis was lower than that of A. paludum at salinities ≥0.9%. The period of embryonic development of G. latiabdominis was more prolonged than that of A. paludum at a given salinity. Although the salinity tolerance of G. latiabdominis was lower than that of A. paludum, our results suggest G. latiabdominis has the physiological capacity to expand into brackish waters. High and low salinity tolerances of A. paludum and G. latiabdominis, respectively, reflect the relatively wide range of habitat salinities utilized by A. paludum and the relatively restricted habitats preferred by G. latiabdominis. The high salinity tolerance of A. paludum could be an important factor contributing to their cosmopolitan distribution because high tolerance to salinity means the possibility of them to be dispersed via ocean or sea to other continents and islands.