Females solicit sneakers to improve fertilization success in the bitterling fish (Rhodeus sericeus)

In most species there is greater variance in reproductive fitness among males than females. A consequence is the evolution of alternative male mating tactics, including sneaking behaviour whereby males attempt to mate with females courted by other males, which could undermine female choice. In bitterling (Rhodeus sericeus), fish that lay their eggs on the gills of living freshwater mussels, sneaking is common and successful. Here we show that female bitterling can significantly improve their fertility with an increase in the number of spawning partners. Females perform conspicuous behaviours associated with spawning more frequently close to sneakers, and spawn more eggs close to high-quality sneakers. This is the first time that females have been shown to engage in behaviour that increases the probability of sneaking, and raises the possibility of a sexual conflict over the number and source of ejaculates during spawning in this species.     

Synchronous female spawning and male mating behavior in a land-locked population of Japanese charr, Salvelinus leucomaenis japonicus

In resource-based promiscuous mating systems, synchronous spawning of females affects competition among males and variation in the reproductive success of males. We documented the mating behavior of Japanese charr (Salvelinus leucomaenis japonicus) through an annual breeding season to examine the relationship between female spawning synchrony and male mating behavior. Females spawned highly synchronously in the population studied, i.e., approximately half the spawning was finished within the first three days of the entire spawning season (11 days). The daily operational sex ratio (OSR) was nearly 1:1 through the spawning period. The number of males around a spawning female was very small (1.21+/-0.49 males per female) over the spawning ground and period, suggesting that a competitive male could effectively chase subordinate males away from a spawning female. A few males attempted to sneak near the oviposition site of females (16%; 9 of 57 breeding groups), while some males adopted sneaking tactics in the initial phase of females' spawning (24%). We did not observe any males to succeed in sneak fertilizations. We conclude that in this Japanese charr population, the synchronous spawning of females was related to the unbiased daily OSR, male aggregation around females, and consequently whether and how efficiently males engaged in sneak mating behavior.     

Is reduced female survival after mating a by-product of male-male competition in the dung fly <Emphasis Type="Italic">Sepsis cynipsea</Emphasis>?

Background  

In a number of species males damage females during copulation, but the reasons for this remain unclear. It may be that males are trying to manipulate female mating behaviour or their life histories. Alternatively, damage may be a side-effect of male-male competition. In the black scavenger or dung fly Sepsis cynipsea (Diptera: Sepsidae) mating reduces female survival, apparently because males wound females during copulation. However, this damage does not seem to relate to attempted manipulation of female reproduction by males. Here we tested the hypothesis that harming females during mating is an incidental by-product of characters favoured during pre-copulatory male-male competition. We assessed whether males and their sons vary genetically in their ability to obtain matings and harm females, and whether more successful males were also more damaging. We did this by ranking males' mating success in paired competitions across several females whose longevity under starvation was subsequently measured.     

Factors Affecting Mating Tactics in the Fiddler Crab, Uca vocans hesperiae

The mating strategies of male fiddler crabs are variable and highly flexible within species. In this study I examine three types of mating strategy used by individual male Uca vocans hesperaie. The most common strategy, termed a ‘standard gambit’, where males approached females at their burrow entrance and initiated courtship, accounted for 63% of mating attempts and 75% of successful matings. The rarest strategy (4% of mating attempts) was the ‘dig out’, where males attempted to mate with females whose burrows they had excavated. This strategy accounted for 19% of successful matings. ‘Herding’ behaviour which involved a male attempting to herd a female into a burrow and mate, contributed 33% of mating attempts but were generally unsuccessful, accounting for only 2.6% of successful matings. Males used more than one strategy during the study period. Smaller males used the standard gambit strategy more often than herding or dig outs while larger males used the herding strategy more often. There was no relationship between male size and mating success and males did not preferentially mate with females of a certain size. The predominant strategy adopted by males over the lunar cycle depended on female behaviour. Herding behaviour was induced by female wandering which escalated at full moon. Standard gambits were the commonest strategy adopted at and around new moon. The low success rate of male mating attempts (16%) indicates a reluctance by females to mate multiply. This may lead to conflict between the sexes because in fiddler crabs there is last male sperm precedence.     

Pre-oviposition Ejaculation in Externally Fertilizing Fish: How Sneaker Male Rose Bitterlings Contrive to Mate

Pre-oviposition ejaculation as a mating tactic of sneaker males in the rose bitterling, Rhodeus ocellatus, was studied under natural and artificial conditions. In a small pond in Yao city, Osaka, Japan, the operational sex ratio of males and females was found to be approximately 3.5:1 and the proportion of males to the mussels, which serve as spawning beds for the rose bitterling, was approximately 2:1. Competitively subordinate rose bitterling males which spawned into the mussels participated in mating by sneaking, because not all males could occupy territories around the mussels. The sneaker males often released sperm not only after but also before egg-laying (this ejaculation movement by the male before egg-laying is termed ‘pre-oviposition ejaculation’). In pair spawning with sneaker, the sneakers frequently performed pre-oviposition ejaculations, which territorial males never performed. In the field, pre-oviposition ejaculations by sneakers coincided with the leading of females by territorial males. Under artificial conditions, I demonstrated by using electrophoretic paternal analyses that the pre-oviposition ejaculations by the sneakers were more effective than the post-oviposition ejaculations by the territorial males. In addition, there were negative size-dependences in ejaculation achievement rate and fertilization success of the sneaker males.     

Female mating status affects male mating tactic expression in the wolf spider Rabidosa punctulata

Males and females have conflicting interests on the frequency and outcomes of mating interactions. Males maximize their fitness by mating with as many females as possible, whereas choosy females often reduce receptivity following copulation. Alternative male mating tactics can be adaptive in their expression to a variety of mating contexts, including interactions with a relatively unreceptive mated female. Male Rabidosa punctulata wolf spiders can adopt distinctive mating tactics when interacting with a female, a complex courtship display, and/or a more coercive direct mount tactic that often involves grappling with females for copulation. In this study, we set up female mating treatments with initial trials and then paired mated and unmated females with males to observe both female remating frequencies and the male mating tactics used during the interactions. Males adopted different mating tactics depending on the mating status of the female they were paired with. Males were more likely to adopt a direct mount tactic with already-mated females and courtship with unmated females. Already-mated females were considerably less receptive to males during experimental trials, although they did remate 34% of the time, the majority of which were with males using a direct mount tactic. Whereas males adjusting to these contextual cues were able to gain more copulations, the observation of multiple mating in female R. punctulata introduces the potential for sperm competition. We discuss this sexual conflict in terms of the fitness consequences of these mating outcomes for both males and females.     

Costs of Mate Guarding and Opportunistic Mating Among Wild Male Japanese Macaques

A trade-off relationship between mating and feeding effort is important when considering reproductive strategies of long-lived species. I compared the influence of male sexual activities, female mate-choice behaviors and the daily activity budget on male mating success among males in a group of wild Japanese macaques (Macaca fuscata yakui) on Yakushima Island. The 1st-ranking male, which had immigrated into the troop at this rank, more frequently approached peri-ovulatory females, spent more time grooming peri-ovulatory females and in mounting series and spent less time feeding than subordinate males did. The 1st-ranking male attained the highest mating success as a result of his high expenditure of time and energy in sexual behaviors directed toward peri-ovulatory females. Mating success of subordinate males did not relate to the amount of sexual effort, but instead to the frequency of female approaches, female rush toward males and the number of peri-ovulatory females within the group. The pattern of intermale competition shifted from nearly contest competition to scramble competition as the number of peri-ovulatory females in the group increased. Feeding time of subordinate males did not vary between the days when they copulated and the days when they did not. The findings demonstrate that mate guarding in the 1st-ranking male is a high-cost mating tactic, while opportunistic mating in subordinate males is a low-cost mating tactic. The differences in male mating tactics are probably related to male life history and to the formation of groups with a high socionomic sex ratio.     

Alternative mating tactics of arctic charr,Salvelinus alpinus,in Thingvallavatn,Iceland

Synopsis During the spawning season the operational sex ratio of the large benthivorous (LB) arctic charr morph in Thingvallavatn is skewed in favour of males which compete intensely on the spawning site. The skewness is caused by males staying longer on the spawning ground than females. LB males employ two mating tactics. Either they guard the female or they attempt sneak-matings with guarded females. The tactics seem to obey a pure conditional strategy where relative size is the important criterion. Generally, the larger males use the guarding tactic and the smaller the sneaking tactic. Assessment of size is a part of the strategy. Relative size influences male behaviour irrespective of which tactic they employ. Guarding is more successful when courting is considered, both with respect to relative frequency and duration of courting acts. Females are aggressive towards the sneakers especially when they are small. This could be interpreted as female choice in favour of large males, but also as a defence against egg predation. A small dwarflike benthivorous morph (SB) is found in the same area. It is mainly active during night and on rare occasions SB-males are seen sneaking into the nest of LB-females. In such cases they are attacked vigorously by both LB sexes.     

Condition-dependent reproductive tactics by large and small anadromous male sockeye salmon Oncorhynchus nerka

Reproductive tactics, aggression and courtship by large and small (jack) male sockeye salmon Oncorhynchus nerka with ripe females in temporary enclosures depended on the size and behaviour of the competitor, not the size of the focal male. When paired with other jacks or with large but less aggressive males, jacks fought for access to ripe females rather than sneaking, but used sneaking tactics when paired with large, aggressive males. Dominant males of both size groups courted actively and females spawned readily with all combinations of males.     

Copulation type affects parturition in the guppy

In some animals, females are often compelled to mate with less desirable males due to the males' alternative mating tactics. Male guppies, Poecilia reticulata, exhibit courtship displays and cooperatively copulate with females. However, they also exhibit sneaking behaviors and coercively copulate with females. To examine the consequences of these two mating patterns, we investigated the influence of copulation type, i.e., cooperative or coercive, on parturition and brood size of females. A single female was allowed to freely contact and copulate with a single male only once. Males that cooperatively copulated with females had larger orange spot areas (an important criterion of female mate choice) than males that copulated coercively. Most females that were coerced into copulation did not give birth to offspring within 100 days after mating. The probability of parturition was high when females copulated cooperatively, and when their mates exhibited frequent postcopulatory jerking behavior. However, the results suggest that copulation type did not affect brood size. Brood size was positively influenced by both female body size and male orange spot area. These results suggest that parturient success is low when females are coerced into mating by less desirable males, whereas brood size is independent of copulation type.     

Male Defense of the Breeding Cavity and Factors Affecting the Persistence of Breeding Pairs in the Stomatopod,Gonodactylus bredini (Manning) (Crustacea: Hoplocarida)

In Caribbean Panama, nonreproductive male and female stomatopods are solitary and defend their own coral-rubble cavities. When breeding pairs form, however, males assume all responsibility for cavity defense. To compare success in cavity defense and defensive tactics among paired and unpaired males, and to examine the tendency for paired stomatopods to exchange their present mates for larger (higher quality) individuals, we introduced same-sized and 15% larger male, and same-sized and 15% larger reproductive female intruders to paired and unpaired male residents in a balanced design. Paired males were more successful at cavity defense than unpaired males, evidently because paired males strike intruders more than unpaired males, and because intruders fight less intensely against paired males than against unpaired males. Paired males occasionally attempted extrapair copulations, but showed little tendency to abandon their mates in favor of larger females. Paired females, however, mated readily with intruder males that evicted resident males. Populationwide female breeding synchrony and prolonged female receptivity before oviposition reduce variance in male mating success and may force males to guard the breeding cavity to assure their paternity. Uncertainty about the reproductive condition of intruder females may prevent males from exchanging mates.     

Somatic and gametic resources in male rock shrimp, Rhynchocinetes typus: effect of mating potential and ontogenetic male stage

Investment in somatic and gametic resources may vary during the ontogeny of an organism. In the rock shrimp, Rhynchocinetes typus, males pass through several stages during ontogeny, and a dominance order reflects this developmental order (typus<intermedius<robustus). During mating in a competitive environment, subordinate males use a sneaking tactic characterized by rapid placement of many spermatophores, but dominant males transfer few spermatophores during matings. We therefore hypothesized that males in the different ontogenetic stages (1) invest differently in somatic and gametic growth and (2) differ in their ability to engage in multiple matings. The relative weight of the hepatopancreas (adjusted for total body weight), an organ related to somatic growth, was significantly lower in robustus males than in all other ontogenetic stages examined. The relative weight of the vas deferens (Vd), a measure of sperm reserves, was significantly higher in robustus males than in males in the other stages. In typus males that had mated once, the total weight of Vd was significantly lower than in unmated typus males, but no such difference was found in robustus males. All robustus males mated successfully with five females during 5 consecutive days, but many typus males failed to mate after the second or third day. Typus males that mated successfully with females placed significantly more spermatophores than did robustus males during the first mating but not in subsequent matings. The results suggest that robustus males, in contrast to typus males, can invest more in sperm production and due to their ability to defend a female, can use spermatic resources economically allowing them to mate with subsequent females. We conclude that, during ontogeny, R. typus males invest simultaneously in somatic and gametic growth in accordance with their mating behaviour and chance to mate. In this and other crustacean species, male resource investment during ontogeny thus may depend on their probabilities at different ontogenetic stages for obtaining mating opportunities. Copyright 2003 Published by Elsevier Ltd on behalf of The Association for the Study of Animal Behaviour.      

Multiple mating and its effect on the reproductive success of female Epiphyas postvittana (Lepidoptera: Tortricidae)

Abstract.

• 1 Multiple mating and its effect on reproductive performance of female Epiphyas postvittana (Walker) moths were studied under controlled conditions.
• 2 The age at which the moths mated for the first time ranged from the first to the tenth day after emergence, but 71% of first matings were during the first 3 days.
• 3 The majority (63%) of females had one or two spermatophores in the bursa copulatrix. Some (24%) were found with three to five spermatophores, whereas no successful mating occurred among 13% of individuals. The number of matings was partly dependent on the number of mates available to the female. Between the range of sex ratios of one male to one female and four males to one female maximal mating success occurred at the ratio of three males to one female.
• 4 Virgin females were capable of egg-laying, but mating stimulated and accelerated oviposition. Mated individuals laid twice as many eggs as unmated ones.
• 5 The level of copulatory activity did not influence the longevity of females irrespective of the number of males available to them.
• 6 Sex ratios with greater than one male to a female improved the reproductive success by marginally increasing fecundity and fertility.
• 7 It is concluded that multiple mating would enhance population growth, and is of particular benefit to populations with a preponderance of females, as is known to occur naturally in this species.

     

Alternative mate-finding tactics in a non-territorial damselfly (Odonata: Coenagrionidae)

Males of the non-territorial damselfly Enallagma hageni have two alternative tactics for finding mates: (1) they search the banks of the pond for unmated females (searching tactic), or (2) wait at oviposition sites for females that resurface prematurely from underwater oviposition (waiting tactic). Although the searching tactic yielded more fertilizations than the waiting tactic, for time invested, the waiting tactic became increasingly successful later in the reproductive season due to changes in female oviposition behaviour. The two tactics can be maintained in the population because males can mate by the waiting tactic during the afternoon when few females are available to searchers. Among males visiting the breeding site an equal number of times, males mating by a mixture of tactics were as successful as males mating only by the main tactic. Because marked males were found to use both tactics, these behaviours are interpreted as evidence of behavioural plasticity within individuals, representing one conditional evolutionary strategy.     

Courtship and copulation in Tarsius bancanus

The reproductive behavior of 6 paired, captive Bornean tarsiers was studied over an 8-month period. Seven copulations were observed. Females signalled males by visual displays and olfactory cues from vulval rubbing. Males signalled females with courtship calls heard before matings. After a courtship lasting from 1 to 2 h, copulation occurred with the male thrusting 61-190 times for 60-90 s, ending in ejaculation. The female regulated timing of mating by rejection or avoidance of the male. Multiple matings were not observed, and mating occurred once or twice a night during each night of estrus. This copulatory pattern of infrequent matings of short duration and active female solicitation and regulation of copulating timing suggests a harem or monogamous system.     

`Little Chipmunk' Syndrome? Male Body Size and Dominance in Captive Yellow‐Pine Chipmunks (Tamias amoenus)

In mammals, large males are often assumed to have higher mating success because they have greater success at contest competition. This relationship is often used to explain the prevalence of male-biased sexual size dimorphism in mammals. However, in many small vertebrates, large individuals are not always dominant. Using staged dyadic encounters, we examined the relationship between male body size and social dominance in captive male yellow-pine chipmunks ( Tamias amoenus ), a species with female-biased sexual size dimorphism. The yellow-pine chipmunk has a mating system in which males participate in mating chases and dominant males may have an advantage in acquiring matings with oestrous females. Captive male chipmunks were aggressive in only 28% of 144 paired encounters; however, several lines of evidence indicated that smaller chipmunks were dominant over large chipmunks: (1) small males were dominant in more dyads than large males; (2) within dyads, dominant males were smaller than subordinate males; and (3) small males performed more aggressive behaviour than large males. These results are not consistent with the prediction that large males are typically dominant. If large chipmunks are able to gain matings with females because of qualities other than dominance (such as the ability to successfully find and/or chase receptive females), then the costs of aggression to large chipmunks may outweigh any potential benefits. Small males, but not large males, may improve their mating success by being aggressive.     

A Potential Cost of Monandry in the Lekking Sandfly Lutzomyia Longipalpis

Multiple mating by females is a subject of considerable controversy. In some species, however, females appear to mate only once, and the potential costs and benefits of this behavior are equally intriguing. When male mating success is highly skewed, monandrous females potentially risk mating with a sperm depleted male. In lek-breeding species, a male may gain up to 80% of available matings, yet few studies have explored whether these highly successful males suffer sperm depletion. These points are investigated in a series of laboratory experiments on the lekking sandfly, Lutzomyia longipalpis. It is shown that females may actively reject males prior to and after genital contact and that mated females do not remate within a single egg-laying cycle regardless of the refractory period between the first and subsequent matings. Males mate multiply and suffer from the effects of sperm depletion after their fifth copulation. Despite this, they continue to court and copulate females with equal vigor and females do not appear to detect sperm-depleted males: they lay similar numbers of eggs irrespective of the number of females their mate has previously copulated with. The implications of a single mating for L. longipalpis females in natural and laboratory leks are discussed.     

Influence of Nutrition on Courtship and Mating in the Scorpionfly Panorpa cognata (Mecoptera, Insecta)

Scorpionflies have been used as model organisms for the study of alternative male mating tactics as well as sexual conflict and coercive mating. Here we describe the courtship and mating behaviour of the scorpionfly Panorpa cognata at different levels of nutrition. Alternative mating tactics in scorpionflies involve nuptial food gifts, and we expected an effect of nutrient availability and male individual condition on the relative frequency of these mating tactics. Subsequent to female attraction by means of male pheromonal emission (calling) and a conspicuous pairing prelude, the majority of matings were initiated by male secretion of one relatively large salivary mass on which females feed during copulation. Usually, males produced only a single salivary mass per mating, and the copulation was terminated after the female had consumed the salivary mass. Alternatively, in 40% of the copulations, males offered females a dead arthropod as nuptial gift. However, these matings were neither preceded by male calling nor by the pairing prelude. Copulations with no gifts were extremely rare, and forced copulations were absent. The manipulation of the clamp‐like notal organ used by male scorpionflies in coercive matings had no effect on the duration of copulation, suggesting that P. cognata males are not able to enforce longer matings. Copulations involving salivary mass gifts were significantly longer than copulations with prey provided as gifts. Although contrary to our expectations, nutrition had no effect on the relative frequency of the different male mating tactics, it had several effects on courtship and mating. First, well‐fed individuals copulated significantly more often, both with prey and salivary secretions, than individuals with limited nutrient resources available. This was true for both sexes, although the effect was stronger for males. Higher availability of nutrients decreased the time until male and female sexual maturity and increased male calling duration per day. Furthermore, high nutrient availability decreased the duration of the pairing prelude, and consequently pairs started copulating earlier at night in the high nutrient treatment.     

Age‐dependent male mating tactics in a spider mite—A life‐history perspective

Males often fight with rival males for access to females. However, some males display nonfighting tactics such as sneaking, satellite behavior, or female mimicking. When these mating tactics comprise a conditional strategy, they are often thought to be explained by resource holding potential (RHP), that is, nonfighting tactics are displayed by less competitive males who are more likely to lose a fight. The alternative mating tactics, however, can also be explained by life‐history theory, which predicts that young males avoid fighting, regardless of their RHP, if it pays off to wait for future reproduction. Here, we test whether the sneaking tactic displayed by young males of the two‐spotted spider mite can be explained by life‐history theory. We tested whether young sneaker males survive longer than young fighter males after a bout of mild or strong competition with old fighter males. We also investigated whether old males have a more protective outer skin—a possible proxy for RHP—by measuring cuticle hardness and elasticity using nanoindentation. We found that young sneaker males survived longer than young fighter males after mild male competition. This difference was not found after strong male competition, which suggests that induction of sneaking tactic is affected by male density. Hardness and elasticity of the skin did not vary with male age. Given that earlier work could also not detect morphometric differences between fighter and sneaker males, we conclude that there is no apparent increase in RHP with age in the mite and age‐dependent male mating tactics in the mite can be explained only by life‐history theory. Because it is likely that fighting incurs a survival cost, age‐dependent alternative mating tactics may be explained by life‐history theory in many species when reproduction of old males is a significant factor in fitness.     

Social grooming in assamese macaques (Macaca assamensis)

Reciprocity and social bonding hypotheses were evaluated as explanations for observed patterns of social grooming in assamese macaques (Macaca assamensis). In accordance with social bonding, females, as the long-term residents of this matrifocal group, groomed each other and juveniles more often than males groomed one another or juveniles. On the other hand, males groomed females more often and for longer durations than females groomed males and, whereas both males and females groomed juveniles more often than juveniles groomed them, juveniles groomed their elders for longer durations. Male grooming of females did not seem directly related to matings as males are single mount ejaculators and use coercive mating tactics. Male grooming of females could not be accounted for in terms of reciprocity; it was not a simple function of dominance. Although both sexes groomed subordinate females more than vice versa, males groomed dominant males more and females groomed subordinate males more than they received grooming from them. Grooming was concluded to function to establish and maintain affiliative social bonds rather than as a specific mechanism to obtain matings or any other specific reciprocation in terms of services or favors.