Causes of a non-random pairing by size in the brine shrimp,Artemia salina: (Crustacea: Anostraca)

Summary Brine shrimp (Artemia salina) males and females entered precopula assortatively by size in the laboratory; large males also had a pairing advantage over smaller males. We investigated the causes of such nonrandom pairing to test hypotheses on size-assortative mating.We found precopulatory biases with respect to male size in the absence of direct competition among males (which produces pairing biases in other species). Large males encountered females significantly more often than did small males. Similarly, large females encountered males more often than did small females, but showed less willingness than small females to enter precopula when housed with small males. Consequently, large females took longer than small females to enter precopula with small males. Although large males entered precopula readily with small females, such size-mismatched pairs appeared short-lived.We conclude that non-random pairing by size in A. salina is determined by several factors including: encounter rates between males and females of different sizes, female behavior, and time following initial pair formation. Our results are likely applicable to other species and can help explain variation for selection on size or other traits.     

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.     

Strategic egg allocation in the zebra fish, Danio rerio

Females across a range of taxa have been shown to differentiallyallocate their reproductive resources according to the attractivenessof their mate. Previous studies demonstrated a female preferencefor larger males in the zebra fish but have so far failed touncover a size-mediated difference in male mating success, possiblydue to the effects of male–male competition. By controllingfor male–male competition in the present study, we showthat females strategically allocate their reproductive resources(i.e., eggs) toward larger males. When females were mated sequentiallywith a large and small male, they released a greater numberof eggs to the second male when he was large than when he wassmall. Furthermore, there was also a trend for females to releasea greater proportion of their eggs to the first male when hewas large. Across females, the total number of eggs laid byeach female increased with the average standard length of themale pair, whereas the number of eggs laid to the second malealso increased with his standard length. This study representsone of the first attempts at identifying differential allocationin a resource-free egg scatterer and suggests that female preferencesmay play a greater role in the reproductive success of malesin this species than previously envisaged.     

Male–male competition for large nests as a determinant of male mating success in a Japanese stream goby, Rhinogobius sp. DA

Males of the stream goby Rhinogobius sp. DA (dark type) court females in deep pools and care for the eggs under stones in shallow riffles. We studied male–male competition for access to females and nest sites to understand how male size influences the mating success of this species. In field observations, larger males won in fighting with other males. However, large males did not tend to monopolize courtship opportunities, and the frequency of successful courtships, after which males led the females to the nests, was not related to male body size. The fact that courted females always escaped from the fighting sites once males began fighting likely explains why male size was not positively related to courtship success. Large males occupied large nest stones, and the number of eggs received in the nest was correlated positively with nest size. In aquarium experiments with two tiles of different sizes provided as nesting materials, males always chose the larger nest and, when two males were introduced simultaneously, the larger one occupied the larger nest. These results suggested that male mating success of this goby is determined by male–male competition for large nests rather than for access to females. Received: June 9, 2000 / Revised: September 2, 2000 / Accepted: October 4, 2000     

Females decide whether size matters: plastic mate preferences tuned to the intensity of male-male competition

Recent studies have indicated that mating success of large malesmay improve under increasing levels of mating competition. Thisoutcome is explained 1) if male mating competition is overridingfemale preferences for male traits that are unrelated to, ornegatively correlated with, male size and dominance and, inso doing, dictates the distribution of matings or 2) if femalesalter their preferences with respect to large males when male–malecompetition is intense. Under both hypotheses, one could expectlarge, dominant males to be more successful under intense competitionthan under weak competition. However, only the first explanationpredicts that male mating success under intense competitionshould be determined by dominance; traits that are unrelatedto male dominance should be uncorrelated to mating success.In contrast, if females change their preferences (explanation2), males with traits beneficial to females independent of thecompetitive environment can maintain a high mating success underall levels of male–male competition. We tested these alternativesusing a small marine fish, the sand goby, Pomatoschistus minutus.The mating success of large males increased under conditionsallowing intense male competition, whereas females showed apreference for good nest building independent of the level ofcompetition. These findings suggest that females are in controlof their choice by altering their preference for male size inresponse to the intensity of male–male competition ratherthan female preference being overshadowed by male dominance.This plasticity of preferences implies that the strength ofsexual selection is not constant at the population level.     

Size-assortative pairing in Gammarus pulex (Crustacea: Amphipoda): a test of the timing hypothesis

We present the first empirical test of the timing hypothesis regarding the generation of size-assortative pairing in amphipods. The timing hypothesis proposes that, since large males are better able to afford the costs of mate guarding than small males, the former can take larger females into precopula earlier in the female moult cycle than is feasible for the latter. This leaves small males to form pairs with smaller females closer to moult, thus generating size assortment. We presented male Gammarus pulex, collected both in precopula and as singletons, with females that were (1) previously guarded and therefore near to copulatory moult and (2) previously unguarded and therefore far from copulatory moult. This comparison tested the prediction of the timing hypothesis, that size assortment should break down when the opportunity for time-based male decisions is removed, but that size assortment should occur where timing is not disrupted. Counter to the hypothesis, we found that size assortment did not break down upon removal of the time factor. Large males tended to initiate mate guarding earlier than small males in both female moult groups. However, only in the previously unguarded group did large males guard for longer than small males. This result suggests that, although size assortment occurred in all groups, the causative mechanisms that generated this pattern may differ between these groups. We therefore consider the possible importance of mechanisms such as aggression, simultaneous manipulation of females and female resistance in producing size assortment where males encounter numerous females that are close to moult. We also observed that prior recent guarding experience by males had no effect on latency to guard or size-assortative pairing. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.     

Social electric signals in freely moving dyads of <Emphasis Type="Italic">Brachyhypopomus pinnicaudatus</Emphasis>

Brachyhypopomus pinnicaudatus (pulse-type weakly electric fish) is a gregarious species that displays reproductive behavior and agonistic encounters between males only during the breeding season. During social interactions, in addition to its basal electric organ discharge (EOD), fish emit social electric signals (SESs) in the contexts of reproduction and intrasexual aggression. We reproduced natural behavior in laboratory settings: SESs recorded in the field are indistinguishable from those observed in our experimental setup. SESs are nocturnal, change seasonally and exhibit sexual dimorphism. This study provides an exhaustive characterization and classification of SESs produced by males and females during the breeding season. In male–female dyads, males produce accelerations and chirps while females interrupt their EODs. The same SESs are observed in male–male dyads. We present a novel, thorough classification of male chirps into four independent types (A, B, C, and M) based on their duration and internal structure. The type M chirp is only observed in male–male dyads. Chirps and interruptions, both in male–female and male–male dyads, are emitted in bouts, which are also grouped throughout the night. Our data suggest the existence of a sophisticated electric dialog during reproductive and aggressive interaction whose precise timing and behavioral significance are being investigated.     

Honesty of agonistic signalling and effects of size and motivation asymmetry in contests

Game theoretical models predict that the main function of fighting behaviour is to assess the relative fighting ability of opponents. The sequential assessment game has often been used to investigate contests, while honest signalling theory has received much less attention. With the wolf spider Hygrolycosa rubrofasciata we investigated whether male agonistic signalling can reveal honest information about fighting ability, and how size and motivation asymmetries affect male fighting behaviour. We also determined whether male–male competition affects the courtship behaviour of the males. We found that agonistic drumming activity is an honest indicator of male fighting ability, and that relative size asymmetry and motivation to fight both contribute to the fighting ability. We also found that male–male competition decreases the courtship drumming rate of subdominant males, suggesting that male–male competition limits the opportunities for female choice. We conclude that sequential assessment and honest signalling may both be used in settling contests, and that they may be used simultaneously. Received: 10 December 1998 / Received in revised form: 23 June 1999 / Accepted: 5 July 1999     

Intrasexual Competition and Mating Behavior in <Emphasis Type="Italic">Ptomascopus morio</Emphasis> (Coleoptera: Silphidae Nicrophorinae)

In nicrophorine beetles, genus Nicrophorus care their larva using small vertebrate carrion, whereas genus Ptomaucopusreproduce with small vertebrate carrion but show no parental care. Aggression and sexual behavior were examined in Ptomascopus morio and Nicrophorus quadripunctatus. Nicrophorus quadripunctatus had intense female–female as well as male–male contests. In Ptomascopus morio, by contrast, female–female aggression was rarely observed. Male–male aggression (pushing, biting, male–male mounting) in Ptomascopus morio was observed when a resource for breeding was present, whether or not a female was present. The lack of female–female aggression, and male–male aggression when resources but not females are present, suggest that the mating system of Ptomascopus morio is resource defense polygyny. Large males of Ptomascopus morio were also found to exhibit mate choice, preferring large females over small females.     

Sexual Size Dimorphism and Aggressive Interactions under Starvation Conditions in the Seed Bug <Emphasis Type="Italic">Togo hemipterus</Emphasis> (Heteroptera: Lygaeidae)

Males of the seed bug Togo hemipterus are larger in size and have considerably larger front legs compared to females. This size discrepancy is likely related to the fact that males fight for food using their enlarged forelegs. A “hungry” bug, i.e. one previously without food, is expected to behave in a certain way when food is present. Here, we demonstrate that aggressive “fighting and chasing” behavior was frequently observed only between males under starvation conditions and became especially severe when food was present. Togo hemipterus males may adopt a resource-defense mating system that is beneficial for males because females aggregate near food when it is scarce. This strategy strongly suggests that the aggressive behavior acts as male–male competition. In a second set of experiments, aggressive behavior occurred between two small males, two large males, or one large and one small male. Fighting ensued mainly when large males were involved, and larger males won fights. Consequently, the male-biased sexual size dimorphism in T. hemipterus appears to be partially attributable to sexual selection favoring larger males.     

The Role of Olfactory Cues in Short-Range Mate Finding by the Emerald Ash Borer, Agrilus planipennis Fairmaire (Coleoptera: Buprestidae)

We investigated the relative importance of olfaction versus vision in the mate-finding behavior of Agrilus planipennis. When coupled in male–female, male–male and female–female pairs, attempts to mate occurred only in the male–female pairs, suggesting that beetles can identify the opposite sex before attempting to mate. In a set of sensory deprivation experiments with male–female pairs, we evaluated whether males could find females when deprived of their sense of olfaction, vision or both. Males whose antennae were blocked with model paint took significantly longer to find females and spent less time in copula compared to untreated males. Males whose eyes were similarly blocked did not differ in their mate finding capacity compared to untreated males. In a third experiment that compared both olfaction and vision, olfactorily impaired beetles never mated whereas the mate finding potential of visually impaired beetles did not differ from that of untreated beetles. Our results indicate that males can identify females before coming into physical contact with them, and that at short range (≤5 cm), volatile cues detected by olfaction are involved in mate finding by A. planipennis.     

Reproductive ecology of a freshwater amphipod,Jesogammarus suwaensis Morino,inhabiting Lake Suwa in central Japan

The reproductive traits ofJesogammarus suwaensis Morino (1986) were estimated by field survey and rearing experiments. According to the relationship between clutch interval and water temperature, one clutch interval under 15°C corresponded to 212 degree days of the effective cumulative temperature. Thus a female could produce about three clutches during the reproductive period from November to early May in the field. Reproduction was somewhat inhibited at 20°C. The clutch size was positively correlated with female body length, and the regression coefficient was large (4.470 on log-transformed data). Oviposition was somewhat synchronized in the field, and the proportion of paired females increased as their reproductive development approached oviposition. The precopula duration was estimated to be 60–80% of the clutch interval in the field. Positive size-assortative mating was observed in precopula pairs and pairing males were usually larger than single ones.     

Mating Compatibility between Geographic Populations of the Seed Beetle <Emphasis Type="Italic">Callosobruchus maculatus</Emphasis>

Allopatric populations sometimes display reproductive barriers in incipient form, and may thus reveal potential mechanisms of speciation. We conducted mating trials to estimate the degree of precopulatory (behavioral) and postcopulatory (gametic) prezygotic isolation between African and Asian populations of the seed beetle Callosobruchus maculatus. The populations differ in several fitness-related traits, and have been associated with different legume hosts. In single-pair trials, the probability of copulation within 10 min was lower when Asian females were paired with African males than it was in the other three pairing combinations. This pairing also provided evidence for gametic isolation, as Asian females mated once to African males laid fewer eggs than did females in the other treatments. Variation in fecundity could not be explained by the duration of copulation, which did not differ among pairing combinations. There was also no effect of pairing combination on the number of copulation attempts, latency to copulation, or rate of egg hatch. When females were simultaneously presented a male from each population, Asian males obtained a disproportionate share of the matings, and were more likely to disturb a pair already in copulo. Surprisingly, male size did not influence the probability of copulation in the single-male trials, the outcome of male–male competition, or the fecundity of once-mated females. Although the African and Asian populations showed some evidence of mating incompatibility, the absence of symmetrical isolating factors suggests minimal barriers to gene flow.     

Comparison of colony foundation success between sexual pairs and female asexual units in the termite Reticulitermes speratus (Isoptera: Rhinotermitidae)

In termites, a male and a female usually found a colony cooperatively. However, pairing efficiency tends to be low in Reticulitermes speratus because of a limited mate-searching range, the female-biased sex ratio, and a relatively low calling ability. Females that fail to pair with males found colonies either in female–female pairs or even alone. In the laboratory, we examined colony foundation by single females (F), female–female pairs (FF), and normal male–female pairs (FM). The time until colony foundation (when termites began excavating wood baits) differed significantly among the unit types. Time until excavation was much longer for single females than for FF and FM units, which reflects the relative success of colony foundation. The survival rate of single females was also significantly lower than that of FF- and FM-unit females, although there was no difference between FF and FM units. This result demonstrates that cooperation, even female–female, promotes female survivorship. Nevertheless, the number of progeny per female was significantly lower in FF units than in FM units, possibly because females of FF units must share reproductive output. These results lead us to the conclusion that a normal monogamous pair is the best unit for colony foundation. Nevertheless, females alone can establish colonies by parthenogenesis, and even female–female cooperation promotes colony foundation success if pairing with males is not possible. Considering the functional decision for females in F and FF units of how much time to spend searching for a male mate, we believe that these facultative pathways of colony foundation by parthenogenesis have adaptive significance. Received: November 30, 2000 / Accepted: March 6, 2001     

Group unity of chimpanzees elucidated by comparison of sex differences in short-range interactions in Mahale Mountains National Park,Tanzania

Chimpanzees (Pan troglodytes) form multi-male and multi-female unit groups with fission–fusion grouping patterns. Short-range interaction (SRI) plays an important role in the unity of these groups and in maintaining social bonds among members. This study evaluated three models of chimpanzee social structure that differed according to the emphasis each placed on social bonds between the sexes, i.e., the male-only, the bisexual, and the male-bonded unit-group model. I investigated differences in SRI between the sexes among group members in well-habituated wild chimpanzees in Mahale Mountains National Park, Tanzania. I followed six focal adult males and six females, and quantified their respective SRI with other chimpanzees. Except between subordinate males and adult females, adults in general engaged in SRI with about 60–90% of the individuals with whom they made visual contact each day, whether in large or small parties. Although the number of social grooming (SGR) partners was limited, male–male SGR networks were wider than were either male–female or female–female SGR networks among adults. The number of contact-seeking behavior (CSB) partners was also limited, but dominant males had more CSB partners. Adult females mainly interacted by pant-grunt greeting (PGG) with adult males, but tended to do so mainly with the highest-ranking male(s) within visual contact. These results indicated that the social bonds among adult males were essential to group unity. Because of clear male dominance, adult females established peaceful coexistence with all group members despite less frequent SRI with subordinate males by maintaining affiliative social bonds with dominant males, thereby supporting the male-bonded unit-group model. Adult females had many female SRI partners, but these interactions did not involve performing conspicuous behaviors, suggesting that females maintain social bonds with other females in ways that differ from how such bonds are maintained with and between adult males.     

Assortative pairing and divergent evolution in Darwin’s Small Tree Finch, Camarhynchus parvulus

Size assortative mating has received increasing attention due to its potential to drive divergence and perhaps speciation. In this study, we examined assortative pairing at 17 nests of Darwin’s Small Tree Finches, Camarhynchus parvulus. We found positive assortative pairing for two traits: bill length and tarsus length, and these traits showed a significant positive correlation to each other. Assortative pairing could be driven by female choice for similar phenotypes because male–male competition has rarely been observed in the Small Tree Finch, nor have males been observed to reject potential mates. Given the high heritability of bill morphology in Darwin’s finches, it is possible that female preference for male bill length, a trait that is known to be important for foraging, will influence offspring bill size to maximise efficient exploitation of resources. The finding of size assortative pairing on the basis of tarsus length requires more research, but suggests different trait utilities for different foraging niches. Interestingly, the highland distribution of tarsus length across the population showed a unimodal distribution, but a bimodal distribution after pairing. While not significant, we found comparatively large differences across study plots in tarsus length, which suggests the possibility of phenotype–habitat matching at a small spatial scale in this species. Our findings are significant in the context of the adaptive radiation of Darwin’s finches as they are consistent with the allopatric model of speciation but also show potential for adaptive divergence in sympatry in Darwin’s tree finches.     

Host-size-dependent sex ratio in a parasitoid wasp

Charnov's host-size model explains parasitoid host-size-dependent sex ratio as an adaptive consequence when there is a differential effect of host size on the offspring fitness of parasitoid males versus females. This article tests the predictions and the assumptions of the host-size model. The parasitoid wasp Pimpla nipponica Uchida (Hymenoptera: Ichneumonidae) laid more female eggs in larger or fresher host pupae when choice among hosts of different sizes or ages was allowed. Then, whether an asymmetrical effect of host size and age on the fitness of females versus males existed in P. nipponica was examined. Larger or fresher host pupae yielded larger wasps. Larger females lived longer, whereas male size did not influence male longevity. Large males mated successfully with relatively large females but failed with small females, whereas small males could mate successfully either with small or with large females. Thus, small-male advantages were found, and this held true even under male–male competition. Ovariole and egg numbers at any one time did not differ among females of different sizes. Larger females attained higher oviposition success and spent less time and energy for oviposition in hosts. Larger females produced more eggs from a single host meal. Taken together, females gained more, and males lost more, by being large. Host size and age thus asymmetrically affected the fitness of offspring males versus females through the relationships between host size or hast age and wasp size, which means the basic assumption of the host-size model was satisfied. Therefore, sex ratio control by P. nipponica in response to host size and age is adaptive. Received: November 13, 1998 / Accepted: January 18, 1999     

Agonistic and courtship behaviour patterns in the skink Chalcides viridanus (Fam. Scincidae) from Tenerife

There have been relatively few attempts to quantitatively describe behaviours in scincid lizards. Chalcides viridanus is a small body-sized skink endemic of Tenerife (Canary Islands). We describe and quantify 18 behaviour patterns (both social and agonistic) of this species, some of which have not been described before for other scincids. Video recordings of male–male, female–female, and male–female interactions were made under laboratory conditions, with controlled light–dark cycle and temperature. We describe several agonistic and courtship behaviour patterns. Within the first context, we detected a new agonistic behaviour for a scincid, “Snout to body”, that appeared at the beginning of agonistic sequences; it consisted of each animal placing its snout in contact with the other individual’s lateral side of the body. The amplitude of head movement during “Head bobbing” was lower than that described for many other lizard species. Agonistic behaviours were shown in intrasexual staged encounters both within males and females. The comparison of behaviour patterns of both types of intrasexual encounters showed that females were more active, exhibiting significantly higher frequencies of behaviour than males. Specifically, females showed the “Snout to body” pattern more frequently than males. In male–female encounters we detected courtship and copulation patterns only in April, when males performed “Bites” and “Snout to body” directed at females.     

Is size assortative mating in Paracalliope fluviatilis (Crustacea: Amphipoda) explained by male–male competition or female choice?

Field and laboratory studies were used to assess: (1) whether size assortative mating occurred in the New Zealand amphipod Paracalliope fluviatilis and (2) hypotheses developed to explain size assortative mating. We found that assortative mating occurred and that larger females carried more eggs, suggesting they may be more valuable as mates. Laboratory experiments were then used to determine whether: (1) male size influenced the size of the female selected (mechanical constraints hypothesis); (2) male size influenced pairing success in the presence of competition (intrasexual selection hypothesis); (3) take‐overs of females occurred and whether large males were more successful (intrasexual selection hypothesis); (4) guard duration varied relative to male and female size (guard duration hypothesis); and (5) females had control over pairing success and guard duration (intersexual selection hypothesis). Although there was evidence to suggest the existence of intrasexual competition for mates (i.e. both small and large males preferred large females), there was no evidence of overt competition (i.e. takeovers of paired females). There was also no difference with respect to how long small and large males guarded females, but large females were guarded longer by both male size classes. Females handicapped by having their mobility reduced were guarded for the same duration as control females but males were more likely to pair with handicapped females, suggesting that they were easier to amplex. Given the lack of evidence for direct male–male competition or female choice, we suggest that assortative mating may be the result of: (1) indirect competition (e.g. in situ large males may be better able to access and amplex the largest females) or (2) female resistance to small males in combination with higher costs that small males may incur in securing large females. © 2007 The Linnean Society of London, Biological Journal of the Linnean Society, 2007, 92 , 173–181.     

Sexual conflict over mating in Gnatocerus cornutus? Females prefer lovers not fighters

Female mate choice and male–male competition are the typical mechanisms of sexual selection. However, these two mechanisms do not always favour the same males. Furthermore, it has recently become clear that female choice can sometimes benefit males that reduce female fitness. So whether male–male competition and female choice favour the same or different males, and whether or not females benefit from mate choice, remain open questions. In the horned beetle, Gnatocerus cornutus, males have enlarged mandibles used to fight rivals, and larger mandibles provide a mating advantage when there is direct male–male competition for mates. However, it is not clear whether females prefer these highly competitive males. Here, we show that female choice targets male courtship rather than mandible size, and these two characters are not phenotypically or genetically correlated. Mating with attractive, highly courting males provided indirect benefits to females but only via the heritability of male attractiveness. However, mating with attractive males avoids the indirect costs to daughters that are generated by mating with competitive males. Our results suggest that male–male competition may constrain female mate choice, possibly reducing female fitness and generating sexual conflict over mating.