Sex ratio varies with egg investment in the red-necked phalarope (Phalaropus lobatus)

Fisher’s sex ratio theory predicts that on average parents should allocate resources equally to the production of males and females. However, when the cost/benefit ratio for producing males versus females differs, the theory predicts that parents may bias production, typically through underproduction of the sex with greater variation in fitness. We tested theoretical predictions in the red-necked phalarope, a polyandrous shorebird with sex-role reversal. Since females are larger and therefore potentially more expensive to produce and may have greater variation in reproductive success, we predicted from Fisher’s hypothesis a male bias in population embryonic sex ratio, and from sex allocation theory, female biases in the clutches of females allocating more resources to reproduction. We measured eggs and chicks and sexed 535 offspring from 163 clutches laid over 6 years at two sites in Alaska. The embryonic sex ratio of 51.1 M:48.9 F did not vary from parity. Clutch sex ratio (% male) was positively correlated with clutch mean egg size, opposite to our prediction. Within clutches, however, egg size did not differ by sex. Male phalarope fitness may be more variable than previously thought, and/or differential investment in eggs may affect the within-sex fitness of males more than females. Eggs producing males were less dense than those producing females, possibly indicating they contained more yolk relative to albumen. Albumen contributes to chick structural size, while yolk supports survivorship after hatch. Sex-specific chick growth strategies may affect egg size and allocation patterns by female phalaropes and other birds.     

Daring females,devoted males,and reversed sexual size dimorphism in the sand-dwelling spider <Emphasis Type="Italic">Allocosa brasiliensis</Emphasis> (Araneae,Lycosidae)

Sexual selection theory predicts that a higher investment in offspring will turn females into the selective sex, while males will compete for accessing and courting them. However, there are exceptions to the rule. When males present a high reproductive investment, sex roles can reverse from typical patterns, turning males into the choosy sex, while females locate males and initiate courtship. In many spiders, males are smaller than females, wandering in search of sedentary females and maximizing the number of copulations. In the present study, we present findings on the sand-dwelling wolf spider, Allocosa brasiliensis, evidencing a reversal in typical courtship roles reported for the first time in spiders. Males were bigger than females. Females located males and initiated courtship. Copulation always occurred in male burrows and took place mainly in long burrows. Males donated their burrows to the females after copulation, closing the entrance before leaving with female cooperation from inside. Males would provide females with a secure place for ovipositing, being exposed to predation and diminishing their future mating possibilities until constructing a new burrow. The cost of vacating the burrow and losing the refuge in an unpredictable habitat, such as sand dunes, would explain the courtship roles reversal in this spider species. Results turn A. brasiliensis as a promising model for discussing the determinants of sex roles and the pressures that drive their evolution and maintenance. Electronic supplementary material The online version of this article (doi: ) contains supplementary material, which is available to authorized users.     

Male backspace availability in the giant waterbug (Belostoma flumineum Say)

Summary Following bouts of courtship and copulation, female giant waterbugs (Belostoma flumineum Say) deposit eggs on the backs of their mates. Throughout a 6– to 12-day brooding period, males display several behaviors that are vital to egg-nymph survival. Consequently, females depend on male post-copulatory behaviors for successful reproduction and the possibility exists for male backspace availability to limit female reproduction in this species. I studied seasonal trends and factors that affect male backspace availability in populations of B. flumineum in east-central Illinois (USA). Early in the spring/summer, giant waterbug populations are relatively small and a large majority (188/205=91.7%) of the males are egg-laden; males experimentally added to the population during this period quickly became encumbered. In contrast, later in the summer after young-of-the-year emerge as adults, the waterbug population density increases dramatically and fewer (670/1274\2= 52.6%) of the males are encumbered (egg-laden). Of the males that are egg-laden both early and late in the season, significantly more are completely encumbered (i.e., 100% of the dorsum egg covered) early in the spring. The adult sex ratio is generally not biased and the number of eggs/pad that completely covers a male approximates a full ovarian complement. Therefore, these factors probably do not cause male backspace to become limited. The primary factor that appears to limit male backspace availability is the ability of females to synthesize a second partial clutch in a short time, often within 1 to 4 days. Females are capable of ovipositing partial clutches on 12 males within 30 days, whereas male brooding period is temperature dependent and ranges from 6 to 13 days. Newly emerged males are capable of breeding significantly sooner than can newly emerged females, thereby creating ample oviposition substrate for the females in the population after young-of-the-year adults appear. The evolution of sex-role reversal is not well understood; however it should not evolve in waterbugs unless male backspace limits female reproduction. Such a situation appears to exist in B. flumineum early in the season but not later in the summer.     

Histological investigation of the reproductive cycles of the limpets <Emphasis Type="Italic">Patella </Emphasis><Emphasis Type="Italic">vulgata</Emphasis> and <Emphasis Type="Italic">Patella ulyssiponensis</Emphasis>

This study devised a staging system for, and monitored, the gonad development of the limpet species Patella vulgata and Patella ulyssiponensis on the South West coast of Ireland using histological techniques. Maturation began in the males of both species in January and in the females it began in March. There was no statistical difference in gonad development between sexes and between species. Spawning in the male P. vulgata occurred from September to December 2003 and in September and October 2004. In female P. vulgata spawning occurred from October to December 2003, no spawning of females was observed in 2004. In male P. ulyssiponensis spawning occurred in November and December 2003 and from September 2004 to December 2004. Spawning was observed from November 2003 to January 2004 and in September 2004 in female P. ulyssiponensis. Sex ratios also varied between the species and between months sampled. Nevertheless more males were observed in both species.     

Zur sexuellen Differenzierung von Ophryotrocha puerilis (Polychaeta: Eunicidae)

Intact young males of Ophryotrocha puerilis Clap. Mecz. which are about to reach the female phase are capable of producing oocytes even under conditions of fasting. Intact isolated females may change sex under fasting conditions; their oocytes are not shed but resorbed. Decerebrated males which are about to reach the female phase at the moment of decerebration are unable to develop oocytes. Decerebrated females begin earlier with the production of spermatozoa than females under fasting conditions. The oocytes of decapitated females are either resorbed (young females with oocytes ranging in diameter up to 60 μm), or shed in egg masses capable of development after fertilization (older females with oocytes of 90 μm diameter or more). The effect of decerebration on females is compensated completely by implantation of isolated prostomia from female donors. Decerebrated males with implanted isolated prostomia from female donors immediately start oocyte production; these oocytes are not shed. In the majority of cases, decerebrated females change to the male phase after implantation of prostomia isolated from male donors. The mutual influence of a pair depends on direct contact of the partners. In isolated females, anterior fragments, consisting of prostomia and some segments, may induce change of sex and shedding of oocytes. On the other hand, intact females may induce sex reversal in anterior fragments. Even isolated prostomia from female donors may induce change of sex in intact females. A possible influence of intact females upon isolated prostomia was not found. Intact females and decerebrated females with implanted prostomia from female donors exhibit no mutual influence when placed together.     

Information content of female copulation calls in wild long-tailed macaques (<Emphasis Type="Italic">Macaca fascicularis</Emphasis>)

Primates are unusual in that many females display sexual signals, such as sex skin swellings/colorations and copulation calls, without any sex role reversal. The adaptive function of these signals remains largely unclear, although it has been suggested that they provide males with information on female reproductive status. For sex skin swellings, there is increasing evidence that they represent a graded signal indicating the probability of ovulation. Data on the functional significance of copulation calls are much scarcer. To clarify the information content of such calls, we recorded copulation calls in wild long-tailed macaques (Macaca fascicularis) and analysed the structure of these calls during the ovarian cycle. Specifically, we correlated selected call parameters with the female oestrogen to progestogen ratio (obtained from faecal samples), which are known to be elevated during the female's fertile phase. In addition, we ran a general linear mixed model for these call parameters, testing factors (cycle phase, occurrence/absence of ejaculation, male dominance status, occurrence/absence of mate guarding) which potentially influence female copulation calls in primates. Our results show that copulation calls of female long-tailed macaques signal mating outcome and rank of the mating partner, but not female reproductive status. They also show for the first time on primates that copulation calls can convey information on whether a female is mate guarded or not. We suspect that the function of these calls is manipulation of male mating and mate-guarding behaviour and that in this way the degree of sperm competition and ultimately male reproductive success is influenced.     

Male-male competition selects for delayed sex change in the protandrous shrimp<Emphasis Type="Italic"> Pandalus latirostris</Emphasis>

In most protandrous species, male size advantage is generally regarded as unimportant in determining the timing of protandrous sex change. In pandalid shrimp, the size/age of male sex change often fluctuates among years and populations, but the adaptive significance of late reversing males (LRMs) is not well understood. This study experimentally examined the adaptive significance of LRMs in the protandrous pandalid shrimp Pandalus latirostris Rathbun. Field and laboratory studies were carried out in August–September of 1998–2002 on P. latirostris in Notoro Lagoon, Japan (44°03′N; 144°10′E). Mature females that had molted (i.e. mate receptive) were tethered in the field and their mating behavior with wild males was observed. Copulations occurred with a single male at a time, although other males could sequentially mate with a tethered female. Because tethered females rejected male approaches, males had difficulty transferring their spermatophores. In the laboratory, males copulated with non-tethered, recently molted females for only 15 min after molting. Recently molted females are wary of potential predators, since their soft exoskeleton makes them particularly vulnerable. Fast access by males enhanced fertilization success in this shrimp. The effect of male size on mating success in the laboratory was examined. Both small and large males successfully inseminated females in the absence of competitors. In experiments where large, medium, and small males competed for a female, however, larger males guarded females longer than smaller males, until the female molted and became receptive. Moreover, large males were more successful at copulating once molting occurred. These results imply that male-male competition drives delayed sex change in some situations.     

Synchronized development of gonad and bioluminescent light organ in a highly sexually dimorphic leiognathid fish, Photoplagios rivulatus

In order to investigate the possible coupling between sexual maturation and the light organ system (LOS) development in leiognathid fish, we determined the seasonal changes in the gonad maturation and the light organ enlargement in Photoplagios rivulatus, one of the leiognathid species possessing highly sexually dimorphic LOS. The fish specimens collected from March 2001 to August 2002 were assessed for standard length (SL), body weight (BW), sex, gonad weight (GW) and the light organ weight (LW). Gonadosomatic index (GSI = 10²GW/BW) and percent weight of the light organ to body weight (PLW = 10² LW/BW) were used to demonstrate the extent of development of gonad and the LOS, respectively. Mean GSIs in both male and female increased in June through August. The mean PLW in males showed a similar trend to that of the GSI, while PLW in females showed no clear seasonal trends. A significant positive correlation was found between the GSI and the PLW in males but not in females. The onset of sexual maturity in males (55 mm SL) coincided with that of the light organ enlargement. These results strongly support the functional coupling between reproduction and bioluminescence in this species of leiognathid. From an evolutionary perspective, sexual dimorphism in the LOS is likely to have evolved through sexual selection for reproductive success in leiognathid fishes.     

Temporal shifts in the allocation of energy in the arrow squid,<Emphasis Type="Italic"> Nototodarus gouldi</Emphasis>: sex-specific responses

Squid typically display considerable intra-specific plasticity in size and age-at-maturity in response to ambient environmental conditions, yet little is known of the mechanisms driving these variations. We examined the intra-specific variability in Nototodarus gouldi reproductive traits to determine patterns of energy allocation between somatic and reproductive processes over short temporal scales. Females caught during the cool months of May and July were larger, had slower lifetime growth, lower gonad investment, and better somatic condition than females caught during the warmer months, suggesting a trade-off between gonad investment and somatic condition in females. On the other hand, males showed a tight coupling between somatic condition and gonad investment for most months, with increases in somatic and gonad tissue occurring concurrently. In male squid, an increase in lifetime growth rate was coupled with an increase in the relative weights of somatic and reproductive structures, whereas in females, percent increase in body weight per day was correlated only with gonad development. Patterns of repro-somatic investment in mature females had implications for spawning strategies, since female squid with higher levels of gonad investment apparently released batches of eggs together as a group, regardless of body size, whereas females with low gonad investment possibly spawned their eggs independently of one another. In terms of life-history theory, male squid were able to respond rapidly to environmental fluctuations without compromising either the gonad or the soma. However, although mature females did not appear to respond as quickly to ambient conditions, female squid possibly produced two different reproductive strategies, possibly to maximise offspring survival in either a stable or a variable environment. It seems from our study that monthly variations in ambient conditions may have large effects on life-history strategies.Communicated by M.S. Johnson, Crawley     

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.     

Male choice

Summary Male preference for large females as mates was demonstrated in the wood-boring weevil, Brentus anchorago (Coleoptera: Brentidae) by observation and by mate choice experiments in which the complicating factor of male rivalry was eliminated. Adult weight varied at least 23-fold in a large breeding aggregation in Panama. Drilling females guarded by males were larger than unguarded drilling females, and the number of males attending a drilling female increased with length of the female. Thus despite a sex ratio of about 1:1, males were unevenly distributed among the females. A male attending a female had on average about 1 rival male in his vicinity (Lloyd's Index of Mean Crowding). Male preference for large females in the absence of rival males was directly tested in choice arenas on the surface of the host tree. When a large and a small female were simultaneously presented, large and small males alike mated first with the large female. Male choice of large females is probably adaptive in Brentus anchorago because larger females lay larger eggs, which produce larger offspring in a competitive larval environment. Male choice in this species is associated with high male mating investment and time commitment per female, and not with high male parental investment.     

Body size preferences in the pot-bellied seahorse <Emphasis Type="Italic">Hippocampus abdominalis:</Emphasis> choosy males and indiscriminate females

Male seahorses (genus Hippocampus) provide all post-fertilization parental care, yet despite high levels of paternal investment, these species have long been thought to have conventional sex roles, with female mate choice and male–male competition. Recent studies of the pot-bellied seahorse (Hippocampus abdominalis) have shown that sex-role reversal occurs in high-density female-biased populations, indicating that male mating preferences may lead to sexual selection on females in this species. Egg size, egg number, and offspring size all correlate positively with female body size in Hippocampus, and by choosing large mating partners, male seahorses may increase their reproductive success. While male brood size is also positively correlated with body size, small H. abdominalis males can carry exceptionally large broods, suggesting that the fecundity benefits of female preference for large partners may be limited. We investigated the importance of body size in reproductive decisions of H. abdominalis, presenting focal individuals of both sexes with potential mating partners of different sizes. Mating preferences were quantified in terms of time spent courting each potential partner. Male seahorses were highly active throughout the mate-choice trials and showed a clear behavioral preference for large partners, while females showed significantly lower levels of activity and equivocal mating preferences. The strong male preferences for large females demonstrated here suggest that sexual selection may act strongly on female body size in wild populations of H. abdominalis, consistent with predictions on the importance of female body size for reproductive output in this species. An erratum to this article can be found at     

Effects of seasonality on the reproductive cycle of <Emphasis Type="Italic">Diadema</Emphasis> aff. <Emphasis Type="Italic">antillarum</Emphasis> in two contrasting habitats: implications for the establishment of a sea urchin fishery

Reproduction of Diadema aff. antillarum was examined between 2002 and 2005 at subtidal rocky bottoms around the Canary Islands. Two contrasting habitats (urchin barrens and grazing fronts) characterized by different levels of food availability were chosen, and factors thought to influence reproductive periodicity were monitored, including temperature, photoperiod, phytoplankton abundance and benthic food availability. Histological analyses showed that D. aff. antillarum had an annual reproductive cycle that was relatively synchronous across the studied sites and habitats. Photoperiod was the most significant factor that correlated with gonad periodicity; benthic food availability of 2 month lag was also correlated. However, some differences were detected between males and females in the timing of the onset of gametogenesis. Spawning was synchronized between both sexes from June to August. Results suggest that the optimum time of year to harvest urchin gonads would be between May and June when gonads were maximal in size but not full of gametes. This species may not provide optimal conditions for an industrial scale fishery, as sea urchins occurring in high density had small gonads and those producing larger volume or more marketable gonad tissue occurred in low densities where harvesting costs would exceed profit.     

Population structure and sex-change in the coral-inhabiting snailCoralliophila violacea at Hsiao-Liuchiu,Taiwan

Surveys of the coral-inhabiting snailCoralliophila violacea (Lamarck) (=C. neritoidea Kiener) were made on shallow fringing reefs (<8 m deep) around Hsiao-Liuchiu, Taiwan, between July and October 1990. The snails were aggregated into patches on the surface of massive poritid coral colonies. Coral colonies >40 cm in diameter were more likely to bear patches of snails than smaller colonies, and also to have more snails. The coralliophilids ranged from 5 to 30 mm in aperture length. The sex ratio of the population was biased toward males (539:279), with only a few small individuals of indistinguishable sex. Snails between 6 and 10 mm were all males, while most snails with aperture lengths 20 mm were females. Judging from the distinct size ranges of males and females within patches and from the observed degeneration of the penis, the snails may have changed sex from male to female with increasing size. Sex-change may occur across a wide size range (10 to 20 mm). The correlation of smallest female size and largest male size among patches indicates that snail size at sex-change is peculiar to each individual patch. Those females in patches with a single female (but many males) were significantly smaller than females in multiple-female patches. It is likely that in the absence of females males change sex at a smaller size, whereas in the presence of large females males delay sexchange until they have reached a larger size. The plasticity of size at sex-change may be adaptive and a result of natural selection at the individual level.     

Effect of female molt stage and sex ratio on courtship behavior of the blue crab Callinectes sapidus

In many species, males and females actively participate in courtship, and the outcome of pre-mating interactions influences the mating success of both sexes. Female blue crabs, Callinectes sapidus, mate soon after their final molt to maturity; thus female molt stage dictates the timing of mating. In a field experiment, we manipulated female molt stage and sex ratio to test their effects on the courtship behavior of both sexes, if female behavior influences the behavior and pairing success of males, and if male courtship influences male pairing-success. Early-molt-stage females avoided males during courtship, whereas late-molt-stage females sought out males. As a result, males had to pursue and capture early-molt-stage females whereas males displayed to late-molt-stage females and more easily physically controlled them. Males sometimes abandoned late-molt-stage females, but this occurred more often when females were abundant. The rate at which females avoided males was positively correlated with that of males abandoning females, and males that were unsuccessful at pairing met with higher rates of female resistance than successful males, suggesting that female behavior influences male pairing-success. Unlike unsuccessful males, successful males more often made the transition between display and maintaining physical control of the female. At high male sex ratios, males initiated courtship more readily; thus both sexual competition and female behavior influence male courtship in this species. Received: 7 July 1996 / Accepted: 10 January 1998     

Changes in gonadal development,androgenic gland cell structure,and hemolymph vitellogenin levels during male phase and sex change in laboratory-maintained protandric shrimp, <Emphasis Type="Italic">Pandalus hypsinotus</Emphasis> (Crustacea: Caridea: Pandalidae)

Most pandalid shrimps show protandric hermaphroditism, and male sexual differentiation is considered to be controlled by the androgenic gland. In the present study, we examined the histology of gonadal development during the male phase and sex change and the involvement of the androgenic gland in regulating male reproduction in laboratory-maintained Pandalus hypsinotus. Juvenile shrimps developed testicular tissues in the peripheral part of gonads during the age of 16–31 months and produced spermatozoa between 34 and 36 months. After reaching sexual maturity, male shrimps exhibited seasonal testicular development: active production of spermatozoa (February–May), disappearance of spermatozoa (spent, April–June), increase of spermatocytes (May–November), appearance of spermatids and spermatozoa in the gonads (November–February). The androgenic gland cells became larger and the rough endoplasmic reticulum in the cytoplasm developed at male sexual maturity. The cell structure shows that the androgenic gland hormone is a peptide. Furthermore, bilateral eyestalk ablation on immature male shrimps induced hypertrophy of the androgenic gland and acceleration of male sexual maturation. These results indicate the involvement of androgenic gland hormone and some eyestalk factor in regulating male sexual maturation. Over a 1-year laboratory-rearing period, some male shrimps (16.7%) changed sex. In transitional shrimps, testicular tissues in the gonads and androgenic glands degenerated; on the other hand, oocytes started yolk protein accumulation and hemolymph vitellogenin levels became high. These results suggest that androgenic gland degeneration is a trigger for sex change and that the vitellogenin level is a useful marker for sex change.     

No evidence of mate discrimination against males carrying a sex ratio distorter in <Emphasis Type="Italic">Drosophila pseudoobscura</Emphasis>

Selfish genetic elements (SGEs) that spread by manipulating spermatogenesis often have highly deleterious effects on males that carry them. Females that mate with male carriers of SGEs can also suffer significant costs: they receive fewer and poorer-quality sperm, their offspring will inherit the deleterious allele, and the sex ratio of their offspring will be biased towards the more common sex. To counter these costs, females are therefore expected to prefer to mate with males that do not carry sex ratio distorters or other deleterious selfish genetic elements. However, despite the potential costs, there are few examples of female choice against males carrying SGEs. We searched for evidence of a female preference in fruit fly Drosophila pseudoobscura against males carrying a costly meiotic driving X-chromosome Sex Ratio (SR). In a series of five non-competitive mate preference experiments, we find no evidence that females prefer to mate with non-SR males. Our use of five separate experiments, involving more than 800 females, makes it unlikely that this lack of a difference was due to low power or simple chance. We suggest that the lack of female choice against SGE-carrying males may be due to strong selection on SGEs to be indistinguishable from alternative alleles. Furthermore, polyandry, either in direct response to receiving an ejaculate from an SGE-carrying male or carried out indiscriminately when at risk of mating with carriers, may be an alternative response by females to limit the exposure of their offspring to SGEs.     

Independent effects of male and female density on sexual harassment, female fitness, and male competition for mates in the western mosquitofish Gambusia affinis

Operational sex ratio (the ratio of sexually active males to fertilizable females) has a major influence on male competition for mates and male–female interactions. The contributions of male and female density per se to mating system dynamics, however, are rarely examined, and the fitness consequences are often inferred rather than quantified. Male mosquitofish (Gambusia affinis) compete aggressively and frequently harass females for copulations, a behavior thought to reduce female fitness. Female fitness can also be reduced by increases in female density, which may affect food availability, cannibalism rates, and chemical interactions between females. I manipulated male and female densities of G. affinis to measure their effects on male–male aggression, male harassment toward females, and female fitness. I found that males chased rivals more often and attempted fewer copulations when female density decreased, but surprisingly male density had no significant effect on the frequency of these male behaviors. In contrast, males’ agonistic displays toward other males increased with male density, but display behavior was unaffected by female density. These results suggest that male and female density do not always contribute equally or at all to the patterns of behavior we observe. Female fitness declined as female density increased, the opposite pattern expected if male harassment is costly to females. This suggests that a strong, negative effect of female density overwhelmed any potential costs of male harassment. Sources of female density dependence and the consequences of changes in male and female density to patterns of male behavior are discussed.     

Male influence on sex allocation in the parasitoid wasp Nasonia vitripennis

Sex allocation is an important reproductive decision for parents. However, it is often assumed that females have substantial control over sex allocation decisions, and this is particularly true in haplodiploid insects, in which females apparently determine sex by deciding whether to fertilise an egg (and produce a diploid daughter) or not (and produce a haploid son). Mechanisms by which males may influence sex allocation are not so straightforward, and their potential influence on sex ratios has been somewhat neglected. Here, we test whether males influence offspring sex ratios in the parasitoid wasp Nasonia vitripennis. We show that some of the variation in observed sex ratios can be attributed to males when comparing the affect of male strain on sex ratio. We did not find among-male variation in sex ratio with a less powerful experiment using males from only one strain or an effect of male mating environment. Our data suggest that males can influence female sex ratios and contribute to the variation around the sex ratios optimal for females. However, the influence is not large, suggesting that females have more influence on sex allocation than do males. We conclude by considering whether male influences on sex ratio represent differences in male reproductive competence or deliberate attempts by males to increase their fitness by influencing daughter production.     

Female egg investment in relation to male sexual traits and the potential for transgenerational effects in sexual selection

Life-history theory predicts that individuals should increase their reproductive effort when the fitness return from reproduction is high. Females mated with high-quality males are therefore expected to have higher investment than females mated with low-quality males, which could bias estimates of paternal effects. Investigating the traits females use in their allocation decisions and the aspects of reproduction that are altered is essential for understanding how sexual selection is affected. We studied the potential for differential female allocation in a captive population of a precocial bird, the Chinese quail, Coturnix chinensis. Females paired with males with large sexual ornaments laid larger, but not more, eggs than females paired with males with small sexual ornaments. Furthermore, female egg mass was also significantly positively affected by male testis size, probably via some unknown effect of testis size on male phenotype. Testis size and ornament size were not correlated. Thus, both primary and secondary male sexual traits could be important components of female allocation decisions. Experimental manipulation of hormone levels during embryonic development showed that both male and female traits influencing female egg size were sensitive to early hormone exposure. Differences in prenatal hormone exposure as a result of maternal steroid allocation to eggs may explain some of the variation in reproductive success among individuals, with important implications for non-genetic transgenerational effects in sexual selection.Communicated by C. Brown