The energetic cost of protogynous versus protandrous sex change in the bi-directional sex-changing fish Gobiodon histrio

To investigate the relative cost of protogynous versus protandrous sex change we induced sex change in each direction in Gobiodon histrio (Gobiidae) and then compared growth, body condition and biochemical condition between sex-changed and non-sex-changed fish in treatment and control groups. Sex change in each direction was induced by establishing pairs of adult males and pairs of adult females on isolated coral colonies. Heterosexual pairs were used as controls. For both males and females, growth and body condition did not vary between fish that changed sex and those that did not. The relatively low cost of sex change, compared to the likely costs of searching for a mate of the correct sex, appears to explain the evolution of bi-directional sex change in coral-dwelling gobies. Lipid concentrations in the liver of males and females that changed sex were reduced by similar amounts (34% and 41%, respectively) compared to male and female controls that did not change sex. Therefore, changes in biochemical condition were approximately equal for fish that sex change in each direction and cannot explain the unequal frequency of sex change in each direction in natural populations of G. histrio.     

Bi-directional sex change in a coral-dwelling goby

Bi-directional sex change has recently been reported among obligate coral-dwelling gobies of the genus Gobiodon. However, neither the functional role of this pattern of sex change nor the frequency of sex change in either direction in natural populations is known. We investigated the social structure and pattern of sex change of Gobiodon histrio at Lizard Island on the Great Barrier Reef. The social structure of G. histrio within coral colonies usually consisted of a single juvenile or a heterosexual adult pair. The size of adult social groups was not constrained by coral colony size. In contrast to expectations for pair-forming species, G.␣histrio was primarily a protogynous hermaphrodite. All immature G. histrio were females and sex change from female to male occurred readily when two mature females were placed in a coral colony. In addition, male G. histrio were able to change back to females when two mature males were placed in a coral. Sex change from female to male, however, occurred with over twice the frequency of sex change from male to female. Where two males were placed in a coral colony, heterosexual pairs were most frequently re-established by immigration of females from outside the treatment population. This pattern might be predicted if sex change from male to female is more expensive than sex change from female to male for G. histrio. Where sex change is expensive, movement may be favoured over sex change, particularly where coral densities are high and movement among corals incurs little mortality risk. Received: 10 November 1997 / Accepted after revision: 16 May 1998     

Gonad morphology, sexual development, and colony composition in the obligate coral-dwelling damselfish Dascyllus aruanus

Gonad morphology and colony composition support the existing supposition that the obligate coral-dwelling damselfish Dascyllus aruanus has a protogynous hermaphroditic sexual pattern. Adults had either an active ovary containing vitellogenic oocytes, an ovotestis, or a spermiated testis and were classified as adult female, hermaphrodite, or adult male, respectively. Among individuals having male function, the testis (or testis portion of the ovotestis) takes the form of an unrestricted spermatogonial lobular testis. Among hermaphrodites having an ovotestis, a small proportion of individuals had a gonad in which both the ovarian and testicular portions were inactive (inactive hermaphrodites), whereas the majority had a predominantly testicular ovotestis that contained spermatozoa (male-active hermaphrodites). The size range of individuals within gonadal classes indicates that all D. aruanus first develop an ovariform gonad. Some individuals then undergo ovarian maturation to become adult females while others develop testicular tissue to form an ovotestis and become male-active hermaphrodites. Subsequently, progressive loss of ovarian tissue results in the development of a secondary testis from an ovotestis with the retention of a residual, afunctional lumen among adult males. The wide size range of individuals having an ovotestis suggests that some hermaphrodites function as adult females before developing testicular tissue while other individuals do not pass through an adult female stage. If this is the case, D. aruanus exhibits a diandric protogynous hermaphroditic sexual pattern. The apparent prolonged retention of an ovotestis with both healthy oocytes and an ovarian-type lumen in a spermiated ovotestis, as well as a functional sex ratio of 1:1 for adult females:adult males plus male-active hermaphrodites also raises the possibility that D. aruanus may be capable of bidirectional sex change during the hermaphroditic stage. Such a capability would be highly adaptive for a species having limited mobility and unpredictable recruitment of new colony members resulting in unpredictable mating opportunities.     

Reproductive biology of a small isopod symbiont living on a large isopod host: from the maternal marsupium to the protective grip of guarding males

Mating systems of many symbiotic crustaceans are characterised by a high degree of mate guarding. A peculiar case of mate guarding has been reported for small symbiotic janirid isopods where males mate with immature females. Field samples of individual hosts and laboratory experiments were conducted to reveal the mating behaviour of the symbiont in a natural environment, that is, on their hosts. Along the coast of the Magellan Strait, Chile, the janirid isopod Iais pubescens was frequently found on the shore-living isopod Exosphaeroma gigas. Symbiont prevalence (percent hosts occupied) was high at eight of the nine sampling sites. Mean symbiont intensity was very low at one site (<<1 individual host^-1), intermediate at two sites (1-10 individuals host^-1) and high at the other sites (10-40 individuals host^-1). The mean sex ratio (males:females) was male biased at most sampling sites (n=7). Females of I. pubescens reached substantially larger sizes (1.5-3.0 mm body length, BL) than males (1.1-1.9 mm BL). The majority of males were carrying small juveniles (66.15%), and males with juveniles were significantly larger than males without juveniles - this suggests that males prefer virgin juveniles to adult females and that they compete for small juveniles. In laboratory observations, males were seen to manipulate the marsupium of adult females that were about to release small juveniles. Males obtained virgin juveniles in this manner. Juveniles were carried for ~7 days, and they moulted shortly before being fertilised and released by males. The high proportion of juveniles carried by males in the field (68.2%) supports previous observations that males initially are not able to distinguish male and female juveniles. It is suggested that the mating system of symbiotic janirid isopods with long-term sperm storage and continuous receptivity in females and male mating with virgin females has evolved in response to highly unpredictable encounter probabilities between the sexes. Mate guarding and manipulation of small virgin juveniles may be favoured on the highly mobile hosts of symbiotic janirid isopods. Furthermore, adult females may gain by leaving their emerging offspring in the protective grip of guarding males, thereby reinforcing the maintenance of this peculiar mating system.     

A histological study of reproduction in the serpulids<Emphasis Type="Italic"> Pomatoceros triqueter</Emphasis> and<Emphasis Type="Italic"> Pomatoceros lamarckii</Emphasis> (Annelida: Polychaeta)

The reproductive cycles of the serpulid polychaetes Pomatoceros lamarckii (Quatrefages, 1865, as Vermilia) and P. triqueter (Linnaeus, 1767, as Serpula triquetra) were studied by histological examination during 1999 and 2000 at Bantry Bay, south-west Ireland. Gametogenesis, sex ratios and hermaphroditism were also investigated. The male/female ratio in P. lamarckii was approximately equal, but in P. triqueter it deviated significantly in favour of females. There was no significant variation in the sex ratios throughout the year in either species. Results confirm that the species are protandric hermaphrodites. In P. lamarckii, but not in P. triqueter, sexual dimorphism was exhibited in body size, the females being larger than the males of the same species. In both species, the proportion of females increased with increasing body size. Simultaneous hermaphroditism was recorded in P. lamarckii, but not in P. triqueter. There was no clearly defined annual gametogenic cycle in either species. Both species appear to have an extended reproductive season, with numerous small-scale peaks in reproductive maturity that can vary annually. Spawning was broadly synchronous between sexes. Visual observation alone (i.e. without histology) was insufficient to accurately assess reproductive condition in individuals not in, or close to, a ripe state.     

Age,size, dominance and reproduction among male kudus: mating enhancement by attrition of rivals

Summary Size dimorphism with males larger than females has been related to the benefits for males of enhanced dominance and hence reproductive success. However, mating gains must outweigh the fitness costs of deferred reproduction and the mortality associated with further growth. The relationships between male age, size and reproduction were assessed for greater kudus (Tragelaphus strepsiceros) in the Kruger National Park in South Africa. Individually identifiable animals were monitored over 10 years, with detailed observations made during six breeding seasons. In the non-breeding season males formed loose all-male groups. Horn grappling and low intensity agonistic interactions fostered dominance rankings. Dominance was age-graded, until males reached full weight at 6 years of age. Males aged 6 and 7 years monopolized courtship and mating, but 5-year-old males secured about 10% of mating opportunities. Few males survived beyond 7 years. Male mortality rate rose steeply with age, so that the functional sex ratio of fertile females per mature male was about 14:1. During the breeding season many female groups remained unattended by a mature male. Reproductive sorting among males occurred largely through variation in survival to full size and maturity. Increased size enhances fighting success and hence dominance. Further growth ceases when the functional sex ratio exceeds the number of mating opportunities that males can effectively achieve during a breeding season. Predation amplifies the mortality cost of continued growth. In the absence of large predators, male-male interactions may be atypically exaggerated.     

Mouse lemurs in space and time: a test of the socioecological model

Socioecological theory predicts that the distribution of fertile females in space and time is the major determinant of male spacing behavior and mating strategies. Using a small nocturnal Malagasy primate, the gray mouse lemur (Microcebus murinus), we determined the spatiotemporal distribution of estrous females during the brief annual mating season to examine the predictive power of the socioecological model for male mating strategies. Mouse lemurs are particularly interesting in this respect because this polygynous species is characterized by seasonal reproduction, seasonally reversed sexual dimorphism, and relatively large testes. All resident animals in our 8-ha study area, a total of 30 adult males and 27 adult females, were individually marked and regularly recaptured to determine female reproductive status and to obtain home range data. We found that the mating season is limited to 4 weeks following female emergence from hibernation. Only 3-9 females could have synchronized estruses during a given week, indicating a moderately high male monopolization potential. However, receptive females were not spatially clumped and male ranges overlapped with those of many other rivals. Therefore, we suggest that individual powerful males may be unable to defend exclusive permanent access to receptive females because of prohibitive costs of range defense resulting from the strongly male-biased operational sex ratio and the corresponding intruder pressure. Our general conclusions are (1) that the socioecological model provides a useful heuristic framework for the study of mating systems, but that (2) it does not specify the degree of spatiotemporal clumping of receptive females at which male mating strategies switch among mate guarding, spatial exclusion of rivals, and roaming, and that (3) the operational sex ratio can have profound effects on male mating strategies as well.     

Selection for male choice based primarily on mate compatibility in the oldfield mouse, Peromyscus polionotus rhoadsi

Despite the consensus that mate choice acts as a mechanism for selection of secondary sexual traits, the evolutionary forces affecting mate preferences themselves remain controversial. In this study, we first demonstrated selection acting directly on the mate preferences of monogamous male oldfield mice, Peromyscus polionotus rhoadsi. One group of male oldfield mice were allowed to express a social preference between two potential mates, and were subsequently paired with either their preferred or rejected female. Among these pairs, those containing preferred females produced more offspring than did those containing rejected females. We next demonstrated that this fitness advantage depended primarily on compatibility between the members of a mated pair. A second group of male oldfield mice were not allowed the opportunity to express a social preference between potential mates. Rather, these males were paired with females that had been either preferred or rejected by males in the first group. Among these pairs, those containing preferred females did not produce more offspring than those containing rejected females. In other words, individual mate preferences had fitness consequences only for those males that expressed them, demonstrating that these preferences were based primarily on compatibility between mates.     

Reproduction in a simultaneous hermaphroditic shrimp, Lysmata wurdemanni: any two will do?

The caridean shrimp Lysmata wurdemanni (Gibbes) displays protandric simultaneous hermaphroditism with out-crossing, but not all males become simultaneous hermaphrodites (euhermaphrodites). In this laboratory study, we attempted to determine why some shrimp remain males. In our experiment, we grew L. wurdemanni from postlarvae to adults in several group sizes and observed their reproductive function. We found that all shrimp reared in isolation become euhermaphrodites. When cultured in a group, the proportion of shrimp remaining male decreased with increasing group size. Except for those that mated within a day, inter-molt euhermaphrodite-phase shrimp (with or without embryos) and inter-molt male-phase shrimp fertilized eggs successfully. On the other hand, euhermaphrodite shrimp can only mate as females and have their eggs fertilized during a narrow post-molt window (less than 12 h) in each molt cycle (10 days). The fertilization rate of male-euhermaphrodite pairs was similar to that of euhermaphrodite-euhermaphrodite pairs. There are at least two non-exclusive explanations for the persistence of male shrimp in a group. In certain group compositions, an individual may gain more reproductive fitness as a large male with multiple mating partners than as a small female with low clutch size. Alternatively, the presence of male-phase individuals, with variable molt-cycle duration (5-8 days), may be necessary to ensure mating. This study is the first direct experimental demonstration of social control of sex change in the decapod crustaceans.     

Reproduction in a simultaneous hermaphroditic shrimp, Lysmata wurdemanni: any two will do?

The caridean shrimp Lysmata wurdemanni (Gibbes) displays protandric simultaneous hermaphroditism with out-crossing, but not all males become simultaneous hermaphrodites (euhermaphrodites). In this laboratory study, we attempted to determine why some shrimp remain males. In our experiment, we grew L. wurdemanni from post-larvae to adults in several group sizes and observed their reproductive function. We found that all shrimp reared in isolation become euhermaphrodites. When cultured in a group, the proportion of shrimp remaining male decreased with increasing group size. Except for those that mated within a day, inter-molt euhermaphrodite-phase shrimp (with or without embryos) and inter-molt male-phase shrimp fertilized eggs successfully. On the other hand, euhermaphrodite shrimp can only mate as females and have their eggs fertilized during a narrow post-molt window (less than 12 h.) in each molt cycle (10 days). The fertilization rate of male-euhermaphrodite pairs was similar to that of euhermaphrodite-euhermaphrodite pairs. There are at least two non-exclusive explanations for the persistence of male shrimp in a group. In certain group compositions, an individual may gain more reproductive fitness as a large male with multiple mate partners than as a small female with low clutch size. Alternatively, the presence of male-phase individuals, with variable molt-cycle duration (5-8 days), may be necessary to ensure mating. This study is the first direct experimental demonstration of social control of sex change in the decapod crustaceans.     

Tests of the mate-guarding hypothesis for social monogamy: does population density, sex ratio, or female synchrony affect behavior of male snapping shrimp (Alpheus angulatus)?

There are at least two mechanisms by which social monogamy in the absence of biparental care may evolve: as a form of territorial cooperation, in which one or both sexes benefits by sharing a territory with a partner, and as a form of extended mate guarding, in which males guard females through entire, and perhaps multiple, reproductive cycles. I examined the effects of population variables (density, sex ratio, female synchrony) on male pairing behavior in the snapping shrimp, Alpheus angulatus, to test the hypothesis that social monogamy in this genus has evolved as a result of selection on males for long-term mate guarding of females. There was no evidence that pairing behavior changes with differences in population density; in a natural population, there was a 1:1 relationship between the number in pairs and local population density. In a laboratory experiment, males altered their pairing behavior in response to manipulated differences in sex ratio. Males in female-biased sex ratios were significantly more likely to abandon recently mated females than males in equivalent sex ratios, though there was no significant difference in the duration of pairing or the number of times males switched females. Observations of shrimp maintained for an extended period in the laboratory revealed no evidence that females molt and become sexually receptive synchronously, which would reduce the likelihood that a searching male would encounter additional receptive females. These data suggest that sex ratio may have contributed to the evolution of social monogamy in snapping shrimp, but provide no evidence that population density or female synchronous receptivity have contributed to the evolution of social monogamy.     

Swarming and mating behavior of a mayfly Baetis bicaudatus suggest stabilizing selection for male body size

Large size often confers a fitness advantage to female insects because fecundity increases with body size. However, the fitness benefits of large size for male insects are less clear. We investigated the mating behavior of the mayfly Baetis bicaudatus to determine whether the probability of male mating success increased with body size. Males formed mating aggregations (swarms) ranging from a few to hundreds of individuals, 1-4 m above the ground for about 1.5-2 h in the early morning. Females that flew near swarms were grabbed by males, pairs dropped to the vegetation where they mated and then flew off individually. Some marked males returned to swarms 1, 2 or 3 days after marking. Larger males swarmed near spruce trees at the edges of meadows, but the probability of copulating was not a function of male body size (no large male advantage). Furthermore, the potential fitness advantage of mating with larger, more fecund females was not greater for large males (no size-assortative mating). However, the sizes of copulating males were significantly less variable than those of non-mating males collected at random in swarms. Intermediate male size may be optimal during mating because of trade-offs between flight agility and longevity or competitive ability. Results of this study are consistent with the hypotheses that there is stabilizing selection on adult male body size during mating, and that male body size in this species may be influenced more by selection pressures acting on larvae than on adults.     

Trophic segregation between sexes in the Black Skimmer revealed through the analysis of stable isotopes

The degree of individual or gender variation when exploiting food resources is an important aspect in the study of foraging ecology within a population. Previous information on non-breeding skimmers obtained through conventional methodologies suggested sex-related differences in prey species. In this study, stable isotope techniques were used to investigate the intraspecific segregation in diet and foraging habits of the Black Skimmer (Rynchops niger intercedens) at Mar Chiquita Coastal Lagoon (37°40′S, 57°22′W), Argentina. These results were compared with contemporary data on the trophic composition obtained by conventional methodologies. Blood samples were taken from birds captured with mist-nets during their non-breeding season. The isotopic signatures of skimmers showed a diet mainly composed of marine prey with some degree of estuarine fish intake. When comparing diet between sexes, males showed enrichment in ¹⁵N compared to females, while no differences were observed in ¹³C. The use of mixing models revealed differences in the relative composition of prey in the diet of male and female skimmers. This study highlights stable isotope analysis as a valuable tool to test inter-individual differences and sexual segregation in trophic ecology of Black Skimmers as compared to conventional methodologies. The results show a trophic segregation in the Black Skimmer during the non-breeding season that can be explained by differences in prey species and larger prey sizes of male skimmers. Our findings have significant implications for conservation since any environmental change occurring at wintering areas might have profound effects on several avian life-history traits, and could be different for males and females due to trophic segregation.     

Seasonal variation in male-female competition,cooperation and selfish hoarding in a monogamous songbird

Both cooperation and conflict between the sexes are commonplace in monogamous mating systems. However, little is known about how cooperation and competition varies seasonally in monogamous species that maintain permanent territories. We presented territorial pairs of male and female New Zealand robins (Petroica australis) with a large supply of insect prey at monthly intervals for 2 years. Behavioural observations after food presentation were then made to quantify seasonal and sexual differences in aggressive interactions over prey, prey acquisition rates, mate provisioning, offspring provisioning, selfish food hoarding and cache retrieval. Data were used to evaluate sex-specific behavioural strategies of mediating competition for food. Results showed that males aggressively excluded females from experimental food sources year-round. Females only accessed food sources when males left them unattended. Consequently, females acquired fewer prey than males. After controlling for differences in prey acquisition, both sexes consumed similar amounts of prey in the non-breeding season. Even though males aggressively excluded females from accessing food sources directly, males fed large amounts of prey to females during the breeding season. Both sexes provisioned young at similar rates. Males cached less prey than females in the breeding season but more prey than females in the non-breeding season. Females showed similar caching intensities year-round. Although males tried to defend their hoards, females frequently retrieved male-made caches. Overall, results showed that although New Zealand robins cooperate to raise offspring during the breeding season, conflict between the sexes occurs year-round. Males and females display different behavioural strategies to gain access to experimental food sources, which appear to lessen male–female competition for food and evenly distribute food resources between the sexes.     

Influence of social factors on sex ratio at birth,maternal investment and young survival in a prosimian primate

Summary In order to determine whether social factors influence sex ratio at birth in lesser mouse lemurs, experiments were conducted during 5 successive breeding periods on 51 females. At the beginning of the breeding season, females were either isolated (I) or grouped (G) in heterosexual groups with an increasing number of females (2, 3 or 4). To ensure mating, I females were introduced in a group only during the oestrous period. After mating, both I and G females were isolated during pregnancy and lactation. Reproductive capacities of females in terms of oestrus occurrences (n = 324), impregnations (n–210), pregnancies (n = 136) or abortions (n = 38) or litter sizes (1–3 young) were affected neither by age and parity of females nor by group housing prior to conception. G females produced significantly more sons than daughters (67% males for 189 newborn) while females living alone except during the mating period demonstrated a significant inverse tendency (39.6% males for 96 newborn). Distribution of sexes in litters was statistically different from random and varied according to the shift of sex ratio at birth. In G females, the shift in the sex ratio towards males was consistent across the different groups, independent of the number of females living together, suggesting that the presence of only 1 female is sufficient to induce a bias in the sex ratio. No correlation was found between infant survival at weaning and age, parity or group housing of the mother. The maternal investment allocated to male or female newborn was similar provided the litter contained at least 1 male. In litters without males, growth and survival of female infants were significantly less. These results on sex ratio bias in captive female mouse lemurs agree with directions of bias predicted by the local resource competition model for facultative sex ratio adjustment (Clark 1978). Nevertheless, the pattern observed in mouse lemurs appears to be independent of the nutritional state of the female and of differential maternal investment.     

Territory defence in tropical birds: are females as aggressive as males?

Much of our knowledge concerning the functions of territorial behaviour and how territories are defended by individuals comes from research on birds. The vast majority of this work has focused on temperate zone breeding territoriality in which territories are defended most obviously by males. Our understanding of the female role in territory defence is limited because they are less conspicuous and much harder to observe. We studied sex roles in territory maintenance and defence in a duetting, resident neotropical passerine, the white-bellied antbird (Myrmeciza longipes). This species maintains territories and pair bonds year round and both sexes sing and actively participate in territory defence. We performed a series of playback experiments throughout the dry (non-breeding) and wet (breeding) seasons. We exposed territorial pairs to three types of stimuli including: (1) single sex, male only songs, (2) single sex, female only songs, and (3) both sex songs/duets. Contrary to findings for most other tropical species, individuals defended their territories with equal levels of aggression regardless of stimuli. Furthermore, sex roles were very different, with males responding more aggressively than females to all stimuli throughout both seasons. Both males and females consistently responded more aggressively to territorial intrusions during the dry season than during the wet season, likely because food abundance is low in the dry season and territory value is high. Our analysis of duetting behaviour suggests that duets do not serve a significant role in mate guarding, or territory defence.     

The cause of size-assortative mating in the leaf beetle Trirhabda canadensis (Coleoptera : Chrysomelidae)

Summary Examples of positive assortative mating by body size are abundant but its causes remain controversial. I show that size-assortative mating occurs in the chrysomelid beetle Trirhabda canadensis and I test a series of alternative hypotheses to explain how this mating pattern comes about. Results suggest that assortative mating in this beetle is due to the greater ease with which size-matched pairs can achieve intromission, and not due to size-biased skews in the availability of mates or mate choice favoring large individuals. There was no correlation between male and female elytron length (a measure of body size) at the initiation of courtship, but pairs assorted positively by size at the onset of intromission. Moreover, in the laboratory, there was a negative correlation between male and female size for pairs engaged in courtship that terminated without mating. Assortative mating was not associated with a large-male mating advantage and there was no evidence of female choice of large males. Nor was there unequivocal evidence for male choice of large females; although mating females were slightly larger and considerably heavier than solitary females, males did not differ in the frequency with which they rejected large and small females. Assortative mating in T. canadensis appeared to be caused by the lower ability of mismatched pairs to achieve intromission after an encounter, both when males were larger and when they were smaller than the female.     

Functional aspects of the pair bond in winter in Bewick's swans (Cygnus columbianus bewickii)

Summary The benefits to partners of monogamous pairs of maintaining continual spatial proximity in the non-breeding season were studied in Bewick's swans wintering in Norfolk, UK.When separated from their mates, females were less successful in aggressive encounters, were threatened more frequently and spent less time feeding than when close to them. Males also suffered reduced success in encounters and a higher frequency of threats by other flock members, though the effect was less pronounced than for females. This sex difference in effect of separation may be associated with the greater weight of males and the fact that success in encounters is related to weight.Partners appeared to assist each other by joining in aggressive encounters, as well as by inhibiting other birds from threatening their mates. However, the precise manner in which the female assisted the male is still obscure, since the highest intensity aggressive encounters — physical fights — involved only male partners. It is suggested that the male may fight harder in his mate's presence.Proximity of partners varied with situation and between different pairs. Partners maintained greater proximity in dense flocks than in dispersed flocks and showed a tendency to stay closer when feeding on winter wheat than on waste potatoes. Partners where the male was high-ranking spent more time together than those where the male was low-ranking.     

Dominance behaviour,body weight and fat variations,and partial migration in European blackbirds Turdus merula

Summary A partially migratory population of European blackbirds Turdus merula was studied in central Europe during the non-breeding season. Body weight and the amount of subcutaneous fat deposits showed seasonal variations typical for each age and sex category. Juveniles were fattest in autumn and spring and both juveniles and females lost fat and body weight in mid-winter. Adults and males reached their maximum body weight in mid-winter. These findings together with data from Schwabl (1983) suggest that juveniles and females constitute the main fraction of those birds migrating from the area in autumn. In winter mainly adults and males have access to food resources. These patterns may be regulated by dominance behaviour, since adults and males are usually dominant over juveniles and females throughout the non-breeding season. Subordinate birds that stay in the area probably suffer from a higher winter mortality but have the advantage of early breeding.     

Parental investment, adult sex ratios, and sexual selection in a socially monogamous seabird

Although most birds are monogamous, theory predicts that greater female parental investment and female-biased adult sex ratios will lower the polygyny threshold. This should result in polygynous mating, unless obligate biparental care or the spatial and temporal distribution of fertilizable females constrains a male’s ability to take advantage of a lowered polygyny threshold. Here we present data on the extent of male sexually dimorphic plumage, adult sex ratios and breeding season synchrony in three populations of a socially monogamous seabird, the brown booby Sula leucogaster. For one of these populations, San Pedro Mártir Island, we also present data on differences in male and female parental investment, mortality and probability of pairing. The extent of plumage dimorphism varied among populations. Sex ratios were female biased in all populations. On San Pedro Mártir Island, parental investment was female biased, females failed more often than males to find a mate, but there was no polygyny. We suggest that on San Pedro Mártir: (1) a period of obligate biparental care coupled with a relatively synchronous breeding season constrained the ability of males to take advantage of a high environmental polygamy potential and (2) the resulting socially monogamous mating system, in combination with the female-biased adult sex ratio, caused females to be limited by the availability of males despite their greater parental investment. Received: 18 November 1999 / Accepted: 24 January 2000