Phylogenetic analyses of sexual selection and sexual size dimorphism in pinnipeds

Pinnipedia contains some of the most spectacular examples of sexual size dimorphism, examples that are therefore frequently used to illustrate the theory of sexual selection. This paper addresses the question of whether a significant relationship between sexual selection and size dimorphism exists in a comparative context. Thus, harem size and body size data gathered from the literature were analysed with independent contrasts analyses. These investigations showed that sexual size dimorphism is not a consequence of an allometric relationship between male and female size. Instead, there is a clear relationship between harem size and sexual size dimorphism. Further analyses also revealed a significant relationship between harem size and male size whereas no such relationship existed for females. These results support the hypothesis that sexual size dimorphism in pinnipeds is the product of an exclusively male response to sexual selection.     

Sex ratios,mating behavior and sexual size dimorphism of the northern water snake,Nerodia sipedon

Competition among males to mate is generally associated with male-biased size dimorphism. In this study we examine mating behavior in the northern water snake (Nerodia sipedon), a species in which males are much smaller than females despite substantial competition among males to mate. Competition among males was a consequence of a male-biased operational sex ratio due to slightly higher female mortality from a birth sex ratio of 1 : 1, and, in 1 year, more synchronous and longer mating activity by males. Approximately one-third of both males and females appeared not to mate in a given year. Larger males were generally more likely to attempt mating, but size did not explain the variance in the number of aggregations in which individual males participated. Within aggregations, males that were successful at achieving intromission were larger than unsuccessful males in 1 of 2 years. Variation in condition (mass relative to length) and relative tail length were not generally useful predictors of either mating effort or success in males. Because large size was often advantageous to males, sexual size dimorphism appeared not to be a consequence of sexual selection favoring smaller males. Because sexual dimorphism was evident at birth, and both males and females matured sexually at about 4 years, sexual dimorphism was not simply a consequence of one sex growing at the maximum rate for longer. Female fecundity increased with size, and sex differences in size-fecundity relations may underly the pattern of sexual size dimorphism. However, because multiple mating by females is common, sperm competition is likely to be important in determining male reproductive success. Therefore, allocation of energy to sperm rather than growth may also prove to be an important influence on male growth rates and sexual size dimorphism.     

Sex ratio, sexual dimorphism and mating structure in bethylid wasps

Sexual dimorphism has been linked to parasitoid mating structure by several authors. In turn mating structure has an important influence on predicted sex ratio optima. Here we test the relationship between sexual dimorphism and sex ratio using data from 19 species of bethylid wasps. Using phylogenetically based comparative methods we confirm the findings of a previous cross-species analysis that sex ratio (proportion of males) is strongly and negatively correlated with clutch size. Using cross-species comparisons we show an additional positive correlation of sex ratio and relative male size, as predicted. The relationship however is not significant when using phylogenetically based methods. The cross-species result is largely due to differences between two bethylid sub-families: the Epyrinae have relatively large males and relatively high sex ratios, whereas the Bethylinae have relatively small males and lower sex ratios. Our study illustrates the benefits and drawbacks of using cross-species versus phylogenetically based comparisons. Received: 13 May 1997 / Accepted after revision: 12 January 1998     

Parental care and sexual size dimorphism in wasps and bees

Sexual size dimorphism, in which one sex is larger than the other, occurs when body size has differential effects on the fitness of males and females. Mammals and birds usually have male-biased size dimorphism, probably because of strong sexual competition among males. Invertebrates usually have female-biased size dimorphism, perhaps because their inflexible exoskeletons limit ovary size, leading to a strong correlation between female body size and fecundity. In this paper, we test whether an additional factor, the type of parental care provided, affects the degree of sexual size dimorphism. Among wasps and bees, there is a contrast between provisioning taxa, in which females must gather and transport heavy loads of provisions to nests they have constructed, and non-provisioning taxa, in which females lay eggs but do not construct nests or transport provisions. Males have no role in parental care in either case. An analysis of British wasps and bees shows that provisioning taxa have significantly more female-biased size dimorphism than non-provisioning taxa. This is true for simple cross‑species comparisons and after controlling for phylogeny. Our data imply that the demands of carrying provision loads are at least part of the explanation for this pattern. Thus, sexual size dimorphism is greatest in pompilid wasps, which carry the heaviest prey items. Bees, which transport minute pollen grains, exhibit the least dimorphism. We also find that cavity‑nesting species, in which nest construction costs may be minimized, exhibit reduced dimorphism, but this was not significant after controlling for phylogeny.     

The genetic mating system of a sea spider with male-biased sexual size dimorphism: evidence for paternity skew despite random mating success

Male-biased size dimorphism is usually expected to evolve in taxa with intense male–male competition for mates, and it is hence associated with high variances in male mating success. Most species of pycnogonid sea spiders exhibit female-biased size dimorphism, and are notable among arthropods for having exclusive male parental care of embryos. Relatively little, however, is known about their natural history, breeding ecology, and mating systems. Here we first show that Ammothella biunguiculata, a small intertidal sea spider, exhibits male-biased size dimorphism. Moreover, we combine genetic parentage analysis with quantitative measures of sexual selection to show that male body size does not appear to be under directional selection. Simulations of random mating revealed that mate acquisition in this species is largely driven by chance factors, although actual paternity success is likely non-randomly distributed. Finally, the opportunity for sexual selection (I _s), an indirect metric for the potential strength of sexual selection, in A. biunguiculata males was less than half of that estimated in a sea spider with female-biased size dimorphism, suggesting the direction of size dimorphism may not be a reliable predictor of the intensity of sexual selection in this group. We highlight the suitability of pycnogonids as model systems for addressing questions relating parental investment and sexual selection, as well as the current lack of basic information on their natural history and breeding ecology.     

The length of growing season and adult sex ratio affect sexual size dimorphism in moose

While factors affecting body growth have been extensively studied, very little is known about the factors likely to affect the sexual size dimorphism (SSD) in polygynous mammals. Based on the carcass mass of 24420 male and female moose recorded in 14 Norwegian populations, we examine three hypotheses to explain geographical variation in SSD. First, SSD is expected to decrease when the relative density of animals (for a given habitat quality) increases, because resource limitation at high population densities is assumed to affect body growth of males more than females. Second, because males are selected to invest in growth more than females, environmental seasonality and related improvement of the forage quality during the short and intense growing season are expected to increase SSD. Third, by decreasing the proportion of adult males in the population, resulting in start of rutting earlier in life, hunting may decrease the SSD by increasing the reproductive cost of young males. We found that males grew faster and for a longer time of their life than did females and thus were heavier (-24%) when they reached adulthood. Sexual size dimorphism was independent of density but was higher in areas with short growing seasons. The low SSD in populations with largely adult female-biased sex ratios (males per female) shows that male body growth decreases with a decreasing proportion of adult males in the population. Our results indicate that geographical variation in moose SSD is influenced by divergent responses in the sexes to ecological factors affecting body growth.     

Changes in size and trends of North American sea duck populations associated with North Pacific oceanic regime shifts

Broad-scale multi-species declines in populations of North American sea ducks for unknown reasons is cause for management concern. Oceanic regime shifts have been associated with rapid changes in ecosystem structure of the North Pacific and Bering Sea. However, relatively little is known about potential effects of these changes in oceanic conditions on marine bird populations at broad scales. I examined changes in North American breeding populations of sea ducks from 1957 to 2011 in relation to potential oceanic regime shifts in the North Pacific in 1977, 1989, and 1998. There was strong support for population-level effects of regime shifts in 1977 and 1989, but little support for an effect of the 1998 shift. The continental-level effects of these regime shifts differed across species groups and time. Based on patterns of sea duck population dynamics associated with regime shifts, it is unclear if the mechanism of change relates to survival or reproduction. Results of this analysis support the hypothesis that population size and trends of North American sea ducks are strongly influenced by oceanic conditions. The perceived population declines appear to have halted >20 years ago, and populations have been relatively stable or increasing since that time. Given these results, we should reasonably expect dramatic changes in sea duck population status and trends with future oceanic regime shifts.     

Mating systems,parasites and plumage dimorphism in waterfowl

Summary Despite a tendency for males of polygynous bird species to show bright or elaborate plumage, comparative analyses have failed to show any consistent relationship between male brightness or plumage dimorphism and the form of breeding systems. Here we argue that this may be partly because the opportunity for sexual selection varies between species showing serial or seasonal monogamy and life-long monogamy. In waterfowl, both the brightness of male plumage and sexual dimorphism in colouration vary between these categories of monogamy. Other ecological factors related to male brightness or plumage dimorphism include male assistance in protecting young, latitude and an index of parasite sharing. The adaptive significance of these trends is discussed. Offprint requests to: D.K. Scott     

Intraspecific behaviors and major cheliped sexual dimorphism in three congeneric callianassid shrimp

Decapod callianassid shrimps are usually solitary occupants of their burrows. They are known to show distinct sexual dimorphism of the major cheliped, which is used as a weapon for intraspecific fighting. Three species of Nihonotrypaea occur in an estuary in southern Japan; they consist of two tidal flat species (N. harmandi; N. japonica) and one boulder beach species (N. petalura), with maximum population densities of 1,400, 340, and 12 m^–2, respectively. The major cheliped size and total length of shrimp were recorded from each population. The degrees of major cheliped sexual dimorphism were ordered as N. harmandi >N. japonica >N. petalura. In the laboratory, intra- and intersexual behaviors at forced encounters between two shrimps were recorded, for the former behavior throughout the year and the latter in the non-breeding season. At their intersected burrows, the shrimps either fought or retreated or filled the burrow crack. Males interacted aggressively with each other, with the intensity being N. petalura >N. harmandi N. japonica. Females of the tidal flat species were non-aggressive, while those of N. petalura were as aggressive with each other as were males. Intersexually, males of all species and females of N. petalura were much less aggressive than intrasexually. In N. petalura only, burrow-sharing behavior between sexes occasionally occurred. The interspecific difference in these behaviors is in parallel with the degree of major cheliped sexual dimorphism. Different intensities of intrasexual competition for mates could have been imposed by the different population densities of these species.Communicated by T. Ikeda, Hakodate     

Body size and sexual selection in the koala

Sexual selection is often characterized by polygynous breeding systems, size dimorphism, and skewed operational sex ratios. Koalas are sexually dimorphic in multiple domains, yet are absent from the literature on sexual selection and the structure of their mating system is unclear. We provide the first documentation of the strength of sexual selection in koalas by using microsatellite markers to identify sires. We combine the genetic data with morphological data in order to assess the role of body size in regulating reproductive output. During our 4-year study, 37% of males were identified as possible sires. Males were significantly larger than females, with sires heavier than non-sires. Male body mass correlated with annual reproductive output, with Crow’s Index of Opportunity for Selection revealing that variation in male reproductive success was threefold higher than that of females. Since it appears that male koalas rarely engage in physical confrontations over access to females, size dimorphism could be based upon non-agonistic competition and/or female mate choice. We propose that size dimorphism in koalas evolved as a consequence of endurance rivalry promoting vocal sexual advertisements that attract females. We suggest that female choice is a key mediator of male reproductive output.     

Sexual dimorphism and the mating ecology of polar bears (Ursus maritimus) at Svalbard

We assessed the role of size, mass, and age in mating and non-mating polar bears (Ursus maritimus) at Svalbard, Norway, during the spring breeding season. The ratio of male to female mass, in male-female pairs, ranged from 1.00 to 3.02 ([`(x)] = 1.99 overline x = 1.99 ) indicating that mating males were larger than mating females but with substantial variation. Paired males were older than unpaired males and male mass was related to age. However, males paired with females were not significantly different in body mass from those males caught alone. Wounds and scars resulting from fights between males began at about 6 years of age and peaked at about 17 and 20 years of age, respectively. The frequency of broken canines in males, presumably due to increased male-male conflicts, increased with age but showed little increase in females. The wide range of male size in male-female pairs and the age-related signs of injury suggest that male polar bears engage in both scramble competition and contest competition for access to breeding females. The mating system of polar bears is variable but is best described as female defense polygyny or serial monogamy.     

Male size,mating success,and mating strategy in the mosquitofish Gambusia affinis (Poeciliidae)

Summary In laboratory choice experiments, receptive female western mosquitofish Gambusia affinis affinis (deprived of contact with males 30 days) preferred the larger of two males. When two males differing in size were placed with a receptive female, the larger was generally able to monopolize access to her, but not when the female was not receptive. In other experiments, a single male was placed with a receptive or non-receptive female. These experiments showed size-correlated differences in male mating behavior. Smaller males were more likely to chase non-receptive females and attempt to inseminate them forcibly, while larger males continued to court females even if they were non-receptive. Even when the female was receptive, there was some evidence of size-correlated differences in levels of courtship and chasing.     

Mate choice,fecundity and sexual dimorphism in two pipefish species (Syngnathidae)

Summary In order to understand the causes of sexual dimorphism, mate choice and size-related fecundity were studied in two pipefish species, Syngnathus typhle and Nerophis ophidion. Sexual dimorphism is more pronounced in N. ophidion; females are larger, have sexual colourings, and are more active during courtship. In S. typhle the sexes are alike in all these respects. Males brood their offspring in both species. In N. ophidion fecundity was positively correlated with both body size and the amount of sexual colouring in females. In males no correlation between body size and fecundity, or between body size and embryo size existed. Predictably, in mate choice experiments with equal-sized females, males chose females with more extensive sexual colourings. We explain sexual dimorphism in this species as a consequence of both natural selection (fecundity increases with size in females but not in males) and sexual selection (males prefer larger females). We argue that sexual size dimorphism did not evolve by selection minimizing overlap in food niches between the sexes, because food production is high in the Zostera beds where the fishes live, and no size dimorphism was found in the sympatrically occurring S. typhle. Furthermore, in N. ophidion dimorphism is not greater in a particular mouth character than in overall body size. In S. typhle egg size and the average number of eggs transferred per spawning were positively correlated with female body size. Apparently more energy per offspring was provided by larger males than by smaller males, and larger males also carried more offspring. As predicted, large mates were preferred by both sexes in mate choice experiments. This is explicable in terms of both natural selection (fecundity increases with size in both sexes) and sexual selection (both sexes prefer large mates). As a consequence of selection acting in the same direction in both sexes, sexual dimorphism is absent in S. typhle.     

Aesthetascs in Lysmata spp. shrimp: sexual dimorphism and relationship with social environments

Aesthetascs are the olfactory receptor organs responsible for mate recognition in many decapod crustacean species. The number of aesthetascs varies greatly among species in different environments, but the functional significance of this variation is poorly understood. This study examined the relationship between social environment and the number of aesthetascs in six species of caridean shrimp in the genus Lysmata. Generally, the number of aesthetascs was greater in group-living species (L. boggessi and L. wurdemanni) than in low-density (L. ankeri and L. pederseni) and pair-living species (L. amboinensis and L. debelius). Aesthetascs are innervated by olfactory receptor neurons (ORNs). The total number of ORNs is related to the sensitivity of olfactory odor detection, and it was higher in group-living species than in pair-living species. Sexual dimorphism in the number of aesthetascs was present in L. boggessi, L. wurdemanni, and L. ankeri but not in L. pederseni and L. amboinensis.     

Evolution of variation in male secondary sexual characteristics

Summary The male pied flycatcher Ficedula hypoleuca exhibits sexual dimorphism in its plumage colour, varying from a female-like brown to jet black. The evoltution of this variation in male plumage colour can be explained by at least eight hypotheses viz., (I) neutral mutation; (II) individual recognition; (III) three forms of inter-sexual selection; (IIIa) mate selection for phenotypes, (IIIb) Fisherian selection, (IIIc) handicap selection; (IV) intrasexual selection; (V) delayed maturation; and (VI) female mimicry. The assumptions and predictions derived from all these hypotheses were tested by analysing the observed variation in male plumage colour in relation to age, body size, physical condition, survival rate, aggressivity in territorial defence, territorial quality, female choice of mate, sex ratio, and reproductive success. We found that: males became blacker with age; black males were larger than browner ones; however, browner males survived better between breeding seasons than did blacker ones; black males were more aggressive against black than brown intruders; blacker males occupied better territories; blacker males were paired earlier than browner males; and finally blacker males produced heavier offspring than did brown males. A reasonable conclusion from the results of these analyses is that four of the hypotheses considered, viz. mate selection for phenotypes (IIIa), Fisherian selection (IIIb), handicap selection (IIIc), and intra-sexual selection (IV) could not be rejected. We therefore suggest that the evolution of the observed variation in the secondary sexual characteristics of the male pied flycatcher can be explained by a combination of these hypotheses.     

Multiple mating affects offspring size in the opisthobranch Chelidonura sandrana

Offspring size can have pervasive effects throughout the life history stages of many marine invertebrates. Although maternal offspring investment is largely determined by the environmental conditions experienced by the mother, egg size might additionally vary in response to the number and quality of previous mating partners. Positive effects of mating multiply with several different males (polyandry) have been confirmed for a variety of species, whereas such investigations are lacking for marine invertebrates. Here we differentiated between the effects of ejaculate amount (repeatedly mated) and ejaculate diversity (polyandry) on maternal offspring investment in the simultaneously hermaphroditic sea slug Chelidonura sandrana. We found that focal “females” mated with four different “males” produced significantly larger egg capsules and larger veligers, while focal “females” mated four times with the same “male” suffered from reduced mid-term fecundity. We found no effect of veliger size on veliger survival. Our results show that female mating patterns are an important addition to understanding the variation in offspring size in internally fertilizing marine invertebrates.     

Foraging costs of a tail ornament: Experimental evidence from two populations of barn swallows Hirundo rustica with different degrees of sexual size dimorphism

Secondary sexual characters are assumed to be costly to produce or maintain. A test of this assumption was performed using the sexually exaggerated outermost tail feathers of male barn swallows Hirundo rustica, a trait currently subject of a directional female mate preference. A possible cost of sexual signalling in male barn swallows arises from increased flight cost during foraging in this aerially insectivorous species. A longer tail may impose a greater drag during flight and thereby affect foraging ability. This was tested by determining the relationship between experimentally modified male tail lengths and number and size of prey delivered to offspring in Spain, where sexual size dimorphism in tail length is small, compared to Denmark, where dimorphism is large. Food boluses contained significantly fewer small insects in Spain than in Denmark. Males with elongated tails captured more and smaller insects while males with shortened tails captured fewer and larger prey items at both sites. Males with naturally long tails were less affected by experimental treatment in terms of effects on the number and the size of prey delivered to their offspring, a finding consistent with a long tail being a condition-dependent viability indicator. The effect of a given degree of tail manipulation on prey size and number of prey per bolus was larger in Spain than in Denmark. These results demonstrate that (1) tail length in male barn swallows affects foraging, and (2) larger sexual size dimorphism occurs where the foraging cost of an increment in ornament size is smallest.Communicated by M. Zuk     

Sympatry and allopatry of song in North American tanagers

Summary The possibility that the hypotheses of character convergence and character displacement might explain interspecific variation in song features among North American tanagers is examined. Scarlet and summer tanagers (Piranga olivacea and P. rubra) are the most sympatric among the four species and have the largest differences in song characteristics. However, songs of scarlet tanagers do not differ significantly between sympatry and allopatry. Songs of summer tanagers more resemble those of scarlet tanagers in allopatry, but this geographical variation has been explained by variation in habitat characteristics. Both species countersing in sympatry, and react aggressively to each other's songs in sympatry as well as in allopatry, probably due to similarities in the song. The limited data from the narrow sympatric zone between western and hepatic tanagers (P. ludoviciana and P. flava) indicate that their songs differ to a great extent. Therefore, the results do not support the hypothesis of character convergence. Character displacement might explain partially interspecific differences in song features between scarlet and summer tanagers but cannot be tested further.     

The effect of mating on female sexual behavior of Teleogryllus commodus Walker

Summary Virgin Teleogryllus commodus females show rhythmic locomotor activity in light-dark (LD) and constant light (LL) conditions. A taped 3-h calling song stimulates them into further walking, and they lay few eggs. Successful mating suppresses or reduces circadian-controlled walking, but in LL-conditions the free-run still persists. Mated females no longer respond to the 3-h calling song. The number of eggs laid within 24–72 h after insemination increases, and the three effects of mating occur independently of one another. The possible physiological basis of these changes and their ecological and behavioral significance under field conditions are discussed.