Does constrained oviposition influence offspring sex ratio in the solitary parasitoid wasp Venturia canescens?

Abstract.  1. In haplodiploid organisms, virgin or sperm-depleted females can reproduce but are constrained to produce only male progeny. According to Godfray's constrained model, when p , the proportion of females constrained to produce only male progeny, is not null in a panmictic population, unconstrained females should bias their sex allocation towards females to compensate for the excess of males. These unconstrained females should be able to adjust the sex ratio in response to local variation of p .
2. In this paper an experimental approach is used to test the hypotheses of this model in the solitary endoparasitoid Venturia canescens under both field and laboratory conditions. Specifically, it is tested whether unconstrained females use their encounters with conspecifics (either male or female) to estimate p and then adjust their sex ratio accordingly.
3. As assumed by Godfray's model, constrained females actively search for host patches in the field and under laboratory conditions produce the same number of offspring during their lifetime as unconstrained females. As predicted by the model, unconstrained females produce a sex ratio biased towards females both in the laboratory and in the field.
4. The results show that this bias is not a response to encounters with conspecifics previous to oviposition. The hypothesis that the bias is due to differential mortality between sexes during ontogeny is also rejected. The proportions of constrained ovipositions estimated in two natural populations explain only a small fraction of the sex ratio bias observed in V. canescens.     

Environmentally induced changes in carotenoid-based coloration of female lizards: a comment on Vercken et al

Colouration may either reflect a discrete polymorphism potentially related to life-history strategies, a continuous signal related to individual quality or a combination of both. Recently, Vercken et al. [J. Evol. Biol. (2007) 221] proposed three discrete ventral colour morphs in female common lizards, Lacerta vivipara, and suggested that they reflect alternative reproductive strategies. Here, we provide a quantitative assessment of the phenotypic distribution and determinants of the proposed colour polymorphism. Based on reflectance spectra, we found no evidence for three distinct visual colour classes, but observed continuous variation in colour from pale yellow to orange. Based on a 2-year experiment, we also provide evidence for reversible colour plasticity in response to a manipulation of the adult population sex ratio; yet, a significant portion of the colour variation was invariant throughout an adult female's life. Our results are thus in agreement with continuous colour variation in adults determined by environmental factors and potentially also by genetic factors.     

Sex differences in mortality of Japanese macaques: Twenty-one years of data from the Arashiyama West population

Theorists argue that mortality in male mammals should be higher than that of females, and many studies of primates followed across the life course have found this to be the case. This study examines mortality patterns in the rapidly expanding Arashiyama West (Texas) population of Japanese macaques (Macaca fuscata) and finds that males have a significantly lower median survival age (12.2 years) in comparison to females (20.5 years). Males and females are born in equal proportions, but by adulthood there are 2–5 females to every male. Males are at higher risk of falling victim to infectious diseases and human-related causes of death, and they are more likely to “disappear” from the population, which is inferred to result largely from emigration. There are no significant sex differences in the risks of dying from predation, non-infectious illnesses, neonatal defect, or social stress. Males become more susceptible to mortality than females once they reach sexual maturity, and they remain at greater risk than females until their old age. There is no evidence that one sex or the other is at greater risk of dying as infants, or as juveniles. Comparing males of different age classes, adolescent and adult males are more likely to die and to disappear than are juvenile males. These findings support the “high-risk, high-gain” hypothesis that males are mainly lost to the population because of their risk-taking behaviors after sexual maturity, rather than the “fragile male” hypothesis that males are more vulnerable to mortality during the period of growth and development. Am J Phys Anthropol 102:161–175, 1997 © 1997 Wiley-Liss, Inc.     

All-female broods and mimetic polymorphism in Acraea encedon (L.) (Lepidoptera: Acraeidae) in Tanzania

In some populations of the African butterfly, Acraea encedon, there are two kinds of females, one producing offspring in a normal 1:1 sex ratio, the other producing females only; in other populations the sex ratio is apparently normal. All-female broods had hitherto been mainly associated with populations in which field sampling revealed an excess of females. The all-female brood trait is described from a population at Dar es Salaam which field sampling suggested was normal, and this indicates that the trait may be much more widespread and common than had previously been supposed. This discovery also extends the known distribution of the trait across Africa from Sierra Leone to eastern Tanzania. The butterfly is also a polymorphic Müllerian mimic of Danaus chrysippus, which is a highly unusual phenomenon as Müllerian mimicry is almost invariably monomorphic. The relative frequencies of two corresponding colour forms of the two species of butterflies at Dar es Salaam adds support to the hypothesis that they are indeed Mullerian mimics. The results of breeding experiments suggest that the polymorphic forms in Acraea encedon are allelic with dominance.     

The year cycle of Eudiaptomus vulgaris (Schmeil, 1896) (Copepoda,Calanoida) in a small,acid water body during 1973. Development in the natural habitat and relationships between temperature and duration of development stages

The development of a population of Eudiaptomus vulgaris (Schmeil, 1896) in the Meeuwenven, a shallow acid guanotrofic moorland pool, has been described during one year. The population hibernates as copepodite 5 stages, adults and, to a small extent as naupliar stages N1, N2 and N3 (which could not develop further at low temperatures in autumn). In spring the population development starts at temperatures above 10°C and shows 3 or 4 pulses a year. An attempt has been made to explain seasonal changes in the size of adult males and females and in the sex ratio.In order to establish the duration of the various development stages, the animals have been cultured at different temperatures under illumination with 2000 Lux at a daylength of 14 hours. An adequate quantity of food from the natural habitat was available.Total egg development and total naupliar and copepodite development have been compared with the results of other workers, especially with those from Eckstein (1964), who studied Eudiaptomus vulgaris in the deep Schluchsee. The duration curves do not differ markedly with those of Eckstein and are strongly temperature dependent.The relation between the development times of the various stages with temperature can be generally expressed as parabolic regressions of the type D = a + b₁T + b₂T², the C₅ and adult stages being the only exception at higher temperatures. Comparison of the relative duration of the stages at different temperatures did show that younger stages can take a larger share of the total development time at lower temperatures, stage N6 being the most temperature-sensitive.     

Sex-chromosome differentiation and ‘sex races’ in the common frog (Rana temporaria)

Sex-chromosome differentiation was recently shown to vary among common frog populations in Fennoscandia, suggesting a trend of increased differentiation with latitude. By rearing families from two contrasted populations (respectively, from northern and southern Sweden), we show this disparity to stem from differences in sex-determination mechanisms rather than in XY-recombination patterns. Offspring from the northern population display equal sex ratios at metamorphosis, with phenotypic sexes that correlate strongly with paternal LG₂ haplotypes (the sex chromosome); accordingly, Y haplotypes are markedly differentiated, with male-specific alleles and depressed diversity testifying to their smaller effective population size. In the southern population, by contrast, a majority of juveniles present ovaries at metamorphosis; only later in development do sex ratios return to equilibrium. Even at these later stages, phenotypic sexes correlate only mildly with paternal LG₂ haplotypes; accordingly, there are no recognizable Y haplotypes. These distinct patterns of gonadal development fit the concept of ‘sex races’ proposed in the 1930s, with our two populations assigned to the ‘differentiated’ and ‘semi-differentiated’ races, respectively. Our results support the suggestion that ‘sex races’ differ in the genetic versus epigenetic components of sex determination. Analysing populations from the ‘undifferentiated race’ with high-density genetic maps should help to further test this hypothesis.     

Genetic conflict and changes in heterogametic mechanisms of sex determination

The consequences of cytoplasmic sex‐ratio distortion and host repression for the evolution of host sex‐determining mechanisms are examined. Analytical models and simulations are developed to investigate whether the interplay between sex‐ratio distorters and host masculinizers or resistance genes can cause heterogamety switching (changes between male and female heterogamety). Switches from female heterogamety to a system analogous to male heterogamety can occur when selection favours the spread of autosomal masculinizers. However, the evolutionary outcome depends on the type of repressor and costs associated with repression, and also on aspects of population structure. Under most conditions, systems evolved to a polymorphic sex‐determining state although many systems were characterized by numerical dominance of male heterogamety.     

Do males have a better chance of mating when the number of estrous females is equal to or greater than the males' ordinal rank? Testing the hypothesis in Japanese macaques

This study was designed to test the hypothesis that male primates in multi-male/multi-female social groups with a clear male dominance hierarchy have a better chance of mating when the number of estrous females is equal to or greater than, as opposed to less than, the males' ordinal rank. I studied a Japanese macaque (Macaca fuscata fuscata) troop during mating seasons from 1992 to 1995. The mean daily operational sex ratio (OSR; the number of estrous females per troop male), which was calculated on observation days, was 0.21, 1.9, 0.48, and 3.1 in 1992-1995, respectively. Overall, focal animal sampling of males yielded 118 male-day records. The male-day records for each male were divided into the two estrous female number conditions: 1) the male-day records when the number of estrous females was equal to or greater than the male's ordinal rank, and 2) the male-day records when the number of estrous females was less than the male's ordinal rank. In the 1993 and 1995 mating seasons, when the number of estrous females was equal to or greater than the ordinal rank of each male, all of the males were observed mating. Conversely, when the number of estrous females was less than the ordinal rank of some male, they were not observed mating in the 1992 and 1994 mating seasons. The percentage for each male across each male's total mating opportunity was <20% when the number of estrous females was less than the male's ordinal rank. By contrast, the percentage for each male across each male's total mating opportunity exceeded 45% when the number of estrous females was equal to or greater than the male's ordinal rank, except for one male. Of all the male-day records for males observed mating with ejaculation, 41 were obtained when the number of estrous females was equal to or greater than the male's rank; conversely, only three records were obtained when the number of estrous females was less than the male's ordinal rank. Therefore, it appears that males have a better chance of mating when the number of estrous females is equal to or greater than the males' ordinal rank, as opposed to when the number is less than their ordinal rank.     

Temperature-induced changes in spider mite fitness: offsetting effects of development time, fecundity, and sex ratio

Temperature affects many life history parameters in poikilotherms. Temperature clearly affects development time and fecundity, which affect the intrinsic rate of increase. In haplodiploid mites, ambient temperature may also affect offspring sex ratio which, in turn, affects intrinsic rate of increase. The combined effect of all these processes determines the fitness of individual females. However, sex ratio also affects mating structure and, potentially, rate of local adaption. We investigated the direct effect of temperature variation on sex ratio, development time, and fecundity in the twospotted spider mite (Tetyranychus urticae), and calculated the effect of their interaction on mite intrinsic rate of increase. We conducted experiments at 2 temperatures and designed the experiment to separate pre-adult and adult sensitivity to temperature variation. Mites were reared from eggs to adult ecdysis at either 22°C or 32°C. Upon emergence as adults, these 2 groups were each split between 22°C and 32°C and allowed to oviposit. Not surprisingly, development from egg to adult was accelerated when mites were exposed to the higher temperature during offspring development, regardless of the temperature experienced by the mother during her development. Fecundity and the proportion of female offspring were affected by temperature only when mothers were exposed during both development and oviposition. About 12 offspring were gained and female bias was increased by 26% when the mother's development occurred at 22°C, whereas oviposition at 22°C added only 6 more offspring and increased female bias by only 7%. There was no correlation between sex ratio and fecundity; both were related to temperature but not to each other. Furthermore, development time, not fecundity or sex ratio, appeared to the main factor affecting the intrinsic rate of increase. Our results support other evidence that sex ratio varies independently of development time and fecundity.     

Influence of fluctuation in the operational sex ratio to mating of troop and non-troop male Japanese macaques for four years on Kinkazan Island, Japan

Taking advantage of a marked yearly fluctuation in the number of estrous females, I studied the differences in mating success between troop males and non-troop males in an unprovisioned group of Japanese macaques. Fluctuation in the defendability of estrous females by troop males, as predicted by the operational sex ratio (the number of estrous females per troop male), strongly affected the mating with ejaculation (successful mating) per observation day of both troop and non-troop males. When operational sex ratio was low, troop males monopolized successful mating inside the troop. No successful mating of non-troop males was observed inside the troop. In contrast, both troop and non-troop males were able to mate often inside the troop when operational sex ratio was high. These findings suggest that troop males obtained the benefit of secured successful mating in the troop because troop males could mate successfully even in mating seasons with a low operational sex ratio, and the chance of successful mating for non-troop males will increase as the ability of troop males to monopolize estrous females decreases.     

Fitness effects of X chromosome drive in the stalk-eyed fly, Cyrtodiopsis dalmanni

Sex-ratio (SR) males produce predominantly female progeny because most Y chromosome sperm are rendered nonfunctional. The resulting transmission advantage of XSR chromosomes should eventually cause population extinction unless segregation distortion is masked by suppressors or balanced by selection. By screening male stalk-eyed flies, Cyrtodiopsis dalmanni, for brood sex ratio we found unique SR alleles at three X-linked microsatellite loci and used them to determine if SR persists as a balanced polymorphism. We found that XSR/XST females produced more offspring than other genotypes and that SR males had lower sperm precedence and exhibited lower fertility when mating eight females in 24 h. Adult survival was independent of SR genotype but positively correlated with eye span. We infer that the SR polymorphism is likely maintained by a combination of weak overdominance for female fecundity and frequency dependent selection acting on male fertility. Our discovery of two SR haplotypes in the same population in a 10-year period further suggests that this SR polymorphism may be evolving rapidly.     

Reproductive cycle of the winged pearl oyster,Pteria penguin (Röding 1793) (Pteriidae) in north-eastern Australia

The spawning cycle of the winged pearl oyster, Pteria penguin, was studied at Orpheus Island, north-eastern Queensland to observe seasonal changes in gonad development, mean oocyte diameter and sex ratio over time. A total of 201 oysters were collected over 10 sampling periods, approximately every 5–6 weeks (mean?=?20 oysters/sample). Histological analysis of gonads showed that spawning activity occurred mainly through the austral mid-spring to late summer (November to March), when mean monthly water temperature ranged between 27.5°C and 29.4°C. There was a primary spawning peak at the beginning of the spawning season in December, followed by a secondary peak in March. Mean oocyte diameter (µm) was highest during the warmer months, ranging from 31.2?±?2.4 in November to 36.2?±?3.2 in March, and sex ratio analysis showed the percentage of females in the population also peaked between 30% and 50% during this period.