Mate choice by males of the hermit crab Pagurus filholi: Do males assess ripeness and/or fecundity of females?

Males of the hermit crab, Pagurusfilholi, often grasp the edges of shells occupied by females and drag them during the mating season. This behavior was experimentally confirmed to be a precopulatory guarding behavior displayed by males for ripe females, and males were found to recognize females which were within about 5 days of spawning. Most theoretical models for mating preference assume the choosing sex (the male in the present case) has complete reproductive information about potential mates, and predict that males will preferably choose more fecund females and/or females that will require less guarding time (i.e. that will spawn sooner) as partners. Several male-choice experiments between two ripe females, both previously guarded by other males, were carried out to examine the above predictions. Males did not prefer females of larger size, higher fecundity or with less time remaining until spawning. These results suggest that males may not have complete information about potential partners, rather that male hermit crabs may adopt a mating strategy of pairing with the first ripe female they encounter. Even with such incomplete mate assessment, males may enhance their reproductive success by recognizing ripe females that will spawn within a given time (about 5 days in the present case).     

Indirect female choice mediated by sex pheromones in the hermit crab Pagurus filholi

Males of the hermit crab Pagurus filholi perform precopulatory guarding behavior, and solitary males often show aggressive behavior to take away guarded females. Males behave coercively while guarding females, so direct mate choice by females seems difficult in such a situation. By performing several experiments we examined possible indirect female choice of hermit crab. Males were attached to a shell by their left cheliped to look like guarding pairs (fake guarding pairs). The shells were filled with cotton containing either seawater or pheromone water. The fake guarding pair with only seawater caused male–male combat in 60% of trials whereas with pheromone water combats occurred in 88% of trials. Mean duration of male–male combat was significantly longer in trials with drops of seawater containing pheromones than in those without pheromones. These results suggest guarding pairs themselves cause male–male combat by visual stimulation, that female sex pheromones have further significant function in the recognition of guarding pairs and intensification of male–male combat, and that females release sex pheromones while they are guarded. As a result of the combat, the larger male ended up guarding a female. This strongly suggests that females choose males indirectly by exploiting male–male competition induced by sex pheromones under male coercive behavior.     

Behavioral Interaction Between Males of Cephalonomia tarsalis (Ashmead) (Hymenoptera: Bethylidae) Competing for Females

Male Cephalonomia tarsalis (Ashmead) compete with one another for mates. The behavioral interactions between males for mates occur both on and off females. Males winning the first copulation do not exhibit apparent postcopulatory mate-guarding behaviors, and females accept subsequent copulations with losing males soon after separation. The duration of copulation when a second male is present is shorter than when only one male is present. However, females receive sufficient sperm for their life-time female progeny production in copulations disrupted artificially at 10 s (1/5 of the regular copulation duration) under normal noncompetition situations. This suggests that shorter copulations because of male–male competition could still result in adequate sperm transfer. Larger males were not more successful in competition than small males, but male competitive ability decreased with age.     

Sexual selection in hermit crabs: a review and outlines of future research

The information currently available on sexual selection in hermit crabs is reviewed to identify the role of males and females before, during and after mating. According to this information, possible mechanisms of male–male competition, female choice and/or sexual conflict are suggested. Important male components that may affect mating success include dragging the female shell, rotations of the female's shell and male cheliped palpations, and male size and/or shell characteristics (species and size). Possible female determinants of male mating/fertilization success include size (as an indicator of egg production capacity), signalling of sexual receptivity to males, delay from mate guarding to copulation and mating duration. Avenues for deeper exploration in males include the role of the number and morphometry of male sexual tubes during sperm transfer, and whether ejaculate size and sperm number can be adjusted with variable situations of sperm competition intensity and risk. In females it would be interesting to investigate the chemical and behavioural mechanisms affecting spermatophore breakage for sperm release and the variable duration from sperm transfer to spawning. Given these possibilities, and that sperm is externally deposited on the female's body but inside her shell (except for those species that do not use shells, e.g. Birgus , or species where shells are rather small and do not cover the body totally, e.g. Parapagurus ), we conclude that hermit crabs are unique subjects for separating male and female effects, particularly with respect to the applicability of current ideas in sexual selection such as female choice and sexual conflict. Some practical ideas are provided to disentangle both hypotheses using these animals.     

Eye and clasper damage influence male mating tactics in the horseshoe crab, Limulus polyphemus

In the horseshoe crab mating system, mated pairs are frequently accompanied by unattached satellite males as they spawn on intertidal beaches. Previous studies have shown that males locate females visually using their lateral (compound) eyes, and that attached (mated) males generally have less heavily worn or damaged carapaces than unattached males. The purpose of this study was to investigate the influences of lateral eye condition and clasper abnormalities on male mating tactics. Sexually mature males had two kinds of eye damage: deterioration caused by disease, and overgrowth by sessile invertebrates, such as bryozoans, mussels, and tube-building polychaetes. The lateral eyes of attached males had significantly less decay than unattached males. On the other hand, coverage of the lateral eyes by encrusting invertebrates was more extensive among attached than unattached males. Although overgrowth did not appear to impair a males ability to pair with a female as severely as eye decay, it is conceivable that amplexus may have occurred before epibiont coverage was sufficient to obscure vision. Male crabs that were experimentally blindfolded by painting their lateral eyes with black nail polish were less likely to reattach to a female than controls. Appendage injuries were more frequent among unattached males than among attached males; in particular, 6.4% of unattached males but 0.0% of attached males had damaged claspers (the modified first legs required for amplexus). Unattached males in the population were older, as judged by the degree of carapace wear, than attached males. Severe visual impairment and/or clasper damage may explain the reduced pairing success of older male horseshoe crabs, and underlie their choice of the alternative satellite male mating tactics.     

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.     

Costs and benefits for water strider (Aquarius paludum) females of carrying guarding, reproductive males

We describe the mating system of Aquarius paludum insularis based on field observations and test hypotheses about the effects of body size, hunger level and post-copulatory guarding on reproductive performance. The mating sequence of this species was typical for temperate water striders, except that most oviposition was carried out by tandem pairs, most of which were submerged. Mate guarding continued until the end of oviposition, lasting up to 18.2h, which was much longer than that recorded for other species of water striders. Pair partners changed after oviposition. Extended contact guarding reduced female mobility. In the case of females that carried long-winged males, there was a significant reduction in speed and stride between tandem as opposed to single females. However, when short-winged males were carried, there was not a significant difference. Short-term foraging efficiency did not differ significantly between tandem and single females, and thus did not reflect the difference in mobility. Hunger level did not significantly affect female mating receptivity. Although the number of harassment bouts by unpaired males did not differ between single and tandem females, single females suffered significantly more harassment. Females were able to lay fertilized eggs for about 15 days after a single copulation, but they accepted long guarding and multiple mating during this period as well. The cost of resisting male mating attempts appears to be greater than the cost of carrying males.     

Multiple Copulations and Post-Copulatory Guarding in a Free-Living Population of Sika Deer (Cervus nippon)

Multiple copulations by females and post‐copulatory guarding by males, were studied in a free‐living sika deer population, on Nozaki, an island of the Goto Group, off the coast of Kyushu, Japan. In 1990, 1991, and 1993, observations were carried out mainly on open grassland in the central section of the island. It was found, that 10 of 22 females in estrus copulated more than once and five of them copulated with several males (multi‐male copulations), while the remainder copulated with a single male (repeated copulation). Almost all copulations were followed by guarding behavior. Dominant males (DMs) guarded significantly longer and more effectively than subordinate males (SMs). Guarding was interrupted in four of the SMs, when the guarding male was forcibly driven away from a female by higher ranked males (‘take‐over’) and in three cases when the female left the guarding male spontaneously (‘escape’). The only interruption of guarding of a DM was caused when a lower ranked male sneaked towards the guarded female and mated with her briefly (sneak). Interruptions of guarding initiated by females (escapes) occurred more when they were guarded by SMs than by DMs. Our results suggest that female sika deer indulge in multiple copulations to seek better genetic quality, rather than insuring fertility, enhancing genetic diversity, or avoiding harassment. The post‐copulatory guarding by DMs appears to be more effective in the prevention of additional copulations by females with other males than guarding by SMs. Moreover, SMs decrease the duration of the pre‐copulatory phase to achieve copulation before having to give way to DMs.     

Last-Male Sperm Priority and the Mating System of the Haplogyne Spider Tetragnatha extensa (Araneae: Tetragnathidae)

Austad (1984) proposed a relation between female spermathecal anatomy and sperm priority, such that in a haplogyne spider with cul-de-sac spermathecae a last-male sperm priority was expected. A laboratory experiment using both normal and irradiated males (sterile-male technique) confirmed this prediction; last males fertilized ca. 70% of eggs in the first egg sac of double-mated females. Mating series with up to four males indicate an antichronological order of male success. Thus, when females laid multiple egg sacs, earlier males fertilized an increasing proportion of eggs in successive sacs. In nature this effect may be counteracted by the fact that females remate between sacs. These statistical patterns emerged in spite of considerable randomness in paternity order. Field observations showed that males survived as long as females (constant sex ratio throughout the breeding season), an unusual feature for a spider population. Mating frequency could not be determined in the field, but laboratory trials indicated that encounters between the sexes usually resulted in immediate copulation. No guarding of females or serious fights between males were observed. Males were observed to steal prey from females and to prey on subadult females. High feeding rates and lack of aggressiveness in males are tactics that secure survival into the egg-laying period. However males also mated frequently early in the maturity season; this is seen as a tactic to maximize the total amount of sperm surviving to the time of fertilization. Thus, survival and multiple matings are the key factors for male success.     

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.     

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.     

Spawning behavior of Arctic charr (Salvelinus alpinus): Spawning synchrony,vibrational communication,and mate guarding

A mismatch in synchrony between male and female gamete release in external fertilizers can result in reduced or failed fertilization, sperm competition, and reduced paternity. In Arctic charr (Salvelinus alpinus), males can adopt either a guard or sneak tactic resulting in both pre‐ and postcopulatory competition between males with alternative reproduction tactics. Here, spawning behavior of free‐living Arctic charr was video‐recorded, and their reproductive behavior was analyzed. From evaluating 157 spawning events, we observed that females mainly spawned with a guarding male and that the female and the guarding male synchronized timing of gamete release under sperm competition. Although sneakers spawned with higher synchrony than the guarding male in single‐male spawning events, the average sneaker released his milt less synchronized with the female than the guarding male under sperm competition. Approximately 50% of the recorded spawning events occurred under sperm competition, where each event included an average of 2.7 males. Additionally, sneakers were more exposed to sperm competition than guarding males. An influx of males, in close proximity to the female, occurred during the behavioral sequences leading up to egg release, but this influx seemed not dependent on egg release, suggesting that something else than gonadal product attracts sneaker males to the spawning female. Just before and during the actual release of gametes, the spawning couple vibrates their bodies in close contact and it seems likely that this vibrational communication between the spawning couple, which results in a larger amplitude sound wave than seen under regular courting, reveals time of gamete release to sneaker males. Thus, vibrational communication may enable synchrony between the guarding male and the female, and this might be traded against the cost of higher detectability from surrounding sneaker males, eavesdropping in close proximity.     

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.     

Flyingfish Spawning (Parexocoetus brachypterus) in the Northeastern Gulf of Mexico

A spawning aggregation of Parexocoetus brachypterus was observed in the northeastern Gulf of Mexico over the outer continental shelf, 100km south of Mobile, Alabama. The event was considered to be a spawning aggregation given the remarkably high abundance of flyingfish observed, together with unusually vigorous flying, jumping, and swimming activity near the surface, and observations of both males and females exuding ripe sex products when landed. The spawn occurred during May 2001 just after moonrise 2 days post full moon. More than 1000000 flyingfish were estimated to have participated in the spawn. Male flyingfish were three times more abundant than females, consistent with observations of 3–4 flyingfish grouped together before and after the spawning aggregation, if several males were simultaneously pursuing a single female. Although egg attachment to flotsam is the only reproductive mode previously described for flyingfishes with demersal eggs, the P. brachypterus spawn occurred in the absence of flotsam. Other possible egg development modes include egg suspension upon current, mid-water suspension above pycnocline or upon topographically induced turbulence, or benthic.     

Male sperm expenditure under sperm competition risk and intensity in quacking frogs

In the frog Crinia georgiana, reproductive behavior comprisesa "guarding tactic," in which males defend spawn sites and attractfemales by calling, and a "sneak tactic," in which males joinspawning pairs. The aims of the present study were to (1) relateejaculate expenditure by "guarding" and "sneak" males to theirprobability of mating with other males present (sperm-competitionrisk), and (2) determine if males adjust their ejaculate expenditureaccording to the number of males involved in a spawning (sperm-competitionintensity). Theory predicts that because sneak males alwaysmate with other males present, they will experience a highersperm-competition risk and should release larger ejaculatesrelative to that of guarding males. However, as the proportionof sneaks in a population increases so does the risk of spermcompetition to guarders, so expenditure by each tactic shouldmove toward equality. Given that the incidence of sneak behavioris high in C. georgiana, guarders and sneaks were expected toexperience similar risks of sperm competition and show similarinvestment in spermatogenesis. Comparison of testes size andejaculate size showed no difference between tactics. Modelsof sperm-competition intensity predict that males should increasetheir ejaculate size when spawning in the presence of one othermale but decrease their ejaculate size when spawning in thepresence of multiple males. Here, males maintained a constantsperm number irrespective of whether a mating involved one,two, or three males. This result suggests that male C. georgianado not facultatively adjust ejaculate investment in responseto fluctuating intensities of sperm competition.     

Costs of intersexual conflict in the isopod Idotea baltica

In sexual reproduction one sex can increase its reproductive success at the cost of the other, a situation known as intersexual conflict. In the marine isopod Idotea baltica, males guard females before copulation. The guarding phase is preceded by struggles as females resist males’ attempts to initiate guarding. We determined whether the struggle and/or mate‐guarding result in fitness costs in the form of decreasing fecundity and lower levels of the energy storage compounds, glycogen and lipids. Females that underwent the period of struggles with males had decreased glycogen levels compared with females maintained alone. No such cost was found for males. Females guarded by a male also had smaller eggs than females that were not guarded. Thus the intersexual conflict, imposed by the fitness maximization strategy of the males, gave rise to both a fecundity cost and an energetic cost for females. The fecundity cost confirms the existence of intersexual conflict in I. baltica. This cost is shared by males, suggesting that the intersexual conflict restrains the reproductive output of both sexes.     

Mate guarding and male mate choice in the chameleon grasshopper <Emphasis Type="Italic">Kosciuscola tristis</Emphasis> (Orthoptera: Acrididae)

In the wild, male chameleon grasshoppers (Kosciuscola tristis) are frequently observed mounted on the back of females even when not in copula, and will fight off other usurping males. If this behaviour is mate guarding and reflects investment in male mate choice, then we expect males to preferably guard females based on reliable cues of quality. Cues for female quality likely include female size and egg development that together may indicate fecundity. We investigated male mate choice in the field expressed as mate-guarding preference, by comparing size and egg development in guarded and unguarded females. We found no difference between guarded and unguarded females in measures of fecundity or body size. The majority of females sampled did not contain any viable eggs. This finding suggests that male K. tristis indiscriminately guard females in a scramble mating system.     

Sex-specific spawning behavior and its consequences in an external fertilizer

Identifying the target of sexual selection in externally fertilizing taxa has been problematic because species in these taxa often lack sexual dimorphism. However, these species often show sex differences in spawning behavior; males spawn before females. I investigated the consequences of spawning order and time intervals between male and female spawning in two field experiments. The first involved releasing one female sea urchin's eggs and one or two males' sperm in discrete puffs from syringes; the second involved inducing males to spawn at different intervals in situ within a population of spawning females. In both, fertilization success was measured as the fraction of eggs fertilized and the paternity share of each male. The results indicate that spawning after females imposes a cost on males but only during sperm competition. Further, the optimal interval between the initiations of male and female spawning depends on degree of sperm competition, distance between males and females, and water velocity. The results show that sex differences in spawning timing of marine invertebrates can be explained on the basis of the differential costs and benefits of spawning out of synchrony with the other sex and that the result of sexual selection on external fertilizers may be behavioral rather than morphological differentiation of the sexes.     

Nest use by territorial males in a shell-brooding cichlid: the effect of reproductive parasitism

Male Telmatochromis vittatus, a substrate-brooding Tanganyikan cichlid, exhibit two parasitic reproductive tactics: takeover of spawning by larger males (pirates) and sneaking by smaller males (sneakers). Medium-sized males are territorial and pair-spawn within nests of clumped shells that harbor several resident females that are potential mates of the territory owner. To study nest use by territorial males, we analyzed the relationship between the body size of territorial males and nest quality, the number of females per nest, the distance between nests, and the frequency and intensity of reproductive parasitism. The size of males was not correlated with nest quality, the number of females, or the number of sneakers, but was negatively correlated with the frequency of intrusion by pirates and was positively correlated with the distance between nests. Territorial males effectively defended nests against sneakers but failed to defend against pirates. These results suggest that larger territorial males selected nests that have a lower risk of usurpation of spawning. We hypothesize that the risk of intrusion by pirate males affects the selection of nests by territorial males in this species.