The adaptive significance of temperature-dependent sex determination: experimental tests with a short-lived lizard

Abstract Why is the sex of many reptiles determined by the temperatures that these animals experience during embryogenesis, rather than by their genes? The Charnov‐Bull model suggests that temperature‐dependent sex determination (TSD) can enhance maternal fitness relative to genotypic sex determination (GSD) if offspring traits affect fitness differently for sons versus daughters and nest temperatures either determine or predict those offspring traits. Although potential pathways for such effects have attracted much speculation, empirical tests largely have been precluded by logistical constraints (i.e., long life spans and late maturation of most TSD reptiles). We experimentally tested four differential fitness models within the Charnov‐Bull framework, using a short‐lived, early‐maturing Australian lizard (Amphibolurus muricatus) with TSD. Eggs from wild‐caught females were incubated at a range of thermal regimes, and the resultant hatchlings raised in large outdoor enclosures. We applied an aromatase inhibitor to half the eggs to override thermal effects on sex determination, thus decoupling sex and incubation temperature. Based on relationships between incubation temperatures, hatching dates, morphology, growth, and survival of hatchlings in their first season, we were able to reject three of the four differential fitness models. First, matching offspring sex to egg size was not plausible because the relationship between egg (offspring) size and fitness was similar in the two sexes. Second, sex differences in optimal incubation temperatures were not evident, because (1) although incubation temperature influenced offspring phenotypes and growth, it did so in similar ways in sons versus daughters, and (2) the relationship between phenotypic traits and fitness was similar in the two sexes, at least during preadult life. We were unable to reject a fourth model, in which TSD enhances offspring fitness by generating seasonal shifts in offspring sex ratio: that is, TSD allows overproduction of daughters (the sex likely to benefit most from early hatching) early in the nesting season. In keeping with this model, hatching early in the season massively enhanced body size at the beginning of the first winter, albeit with a significant decline in probability of survival. Thus, the timing of hatching is likely to influence reproductive success in this short‐lived, early maturing species; and this effect may well differ between the sexes.     

孵化水热环境对渔异色蛇孵化卵和孵出幼体的影响

渔异色蛇卵孵化时能从环境中吸收水分导致质量增加,卵质量的增加与初始卵质量和孵化基质湿度有关。较大幅度的孵化基质湿度变化对孵化期、孵化成功率、胚胎动用孵内物质和能量、孵出幼体的性比、大小和质量无显著影响。孵化期随温度升高而缩短,并显示极强的窝间差异。温度对孵出幼体的性别无影响,但显著影响孵化成功率、胚胎对卵内物质和能量的动用、幼体的大小和质量、躯干和剩余卵黄的质量。孵出幼体总长的两性差异不显著,但雌体体长大于雄体而尾长小于雄体。３２℃不适于孵化渔异色蛇卵,该温度下孵出的幼体躯干发育不良,剩余孵黄较多,尾部均呈畸形,孵化过程中能量转化率较低。２４℃和２６℃中孵出的幼体躯干发育良好,孵化过程中能量转化率较高,各项被测定的幼体特征指标均极相似。     

Plasticity of brood patch development and its influence on incubation periods in the yellow-eyed penguin Megadyptes antipodes: an experimental approach

In many bird species, eggs laid late in the laying period hatch after a shorter incubation period than early-laid eggs. However, the mechanisms that explain these seasonal declines in incubation periods among clutches remain poorly understood. In this study we investigated the plasticity of brood patch development during incubation in yellow-eyed penguins Megadyptes antipodes and established whether differences exist in brood patch formation among early, mean and late-breeding penguins. We also examined whether brood patch development was influenced by sex and age of birds. We then placed an artificial egg in nests a few days prior to egg laying to investigate whether the presence of an egg influences brood patch development and whether an advanced brood patch development at the time of egg laying causes declines in incubation periods. Initial brood patch width on the day the first egg was laid was dependent on sex and age, while the development of brood patch width after first egg laying was slower in early-laying birds than in mean- and late-laying birds. Initial brood patch temperature as well as temperature throughout incubation was largely dependent upon sex, whereby males had higher brood patch surface temperatures than females. Placement of an artificial egg in nests stimulated successfully brood patch development in manipulated birds, so that by the time they laid their own first egg, their brood patches were wider and had higher temperatures than those of control birds. Moreover, incubation periods of first eggs from manipulated nests were significantly shorter (43.5 days) than were those from control nests (47.3 days). Thus, variation in brood patch development and related differences in incubation temperature during early incubation could contribute to seasonal declines in incubation periods.     

Patch leaving decision rules and the Marginal Value Theorem: an experimental analysis and a simulation model

The patch exploitation strategy of females of the insect parasitoid Trichogramma brassicae was studied on patches containing different proportions of hosts that were previously attacked by conspecificfemales. On average, T. brassicae females spent more time onpatches of higher quality, and all patches were reduced tothe same level of profitability before being left. This appearedto be in accordance to the optimal predictions of the CharnovMarginal Value Theorem. The proximate leaving mechanisms involvedwere analyzed by means of a Cox proportional hazards model.Each oviposition in a healthy host appeared to have an incremental influence on the patch residence time, whereas each rejectionof a healthy host or of a host that was previously attackedby the same female (i.e., self-superparasitism) had a decrementaleffect. These patch leaving mechanisms did not change accordingto the quality of the patch the females were exploiting. AMonte Carlo simulation was developed around the results of the Cox regression model. The results suggest that this set of patchleaving rules seems to provide the females with a sufficientway to reach the predictions of the Charnov model. Among thedifferent mechanisms involved, the incremental effect associatedwith each oviposition in a healthy host appeared to play the most important role. The relationship between the proximatemechanistic rules adopted by the females and the ultimate predictionof the Charnov model is discussed.     

High brood patch temperature of less colourful,less pheomelanic female Barn Swallows Hirundo rustica

In birds, even a minor difference in egg temperature (1–1.5 °C) has been shown to affect the fitness of offspring by changing hatching success, incubation period and nestling quality. Female, but not male, passerines develop brood patches. Thus if there are traits, such as plumage ornamentation, that indicate optimal egg temperature, males should pair with females that exhibit those traits. However, no study has yet investigated the relationship between female brood patch temperature, which would directly affect egg temperature, and female plumage ornamentation. In this study, we examined the surface temperature of female brood patches during nocturnal incubation and examined its relationship with female plumage ornaments in Asian Barn Swallows Hirundo rustica gutturalis. After controlling for ambient air temperature, brood patch temperature was negatively associated with colour saturation of the female throat patch. No other female ornaments, such as tail‐length, white tail spots or throat patch size, predicted brood patch temperature. When oral (mouth) temperature was statistically controlled, females with less colourful throats and longer tails showed higher brood patch temperature, indicating that these females had hotter brood patches in relation to the temperature of other body parts. Furthermore, we found a negative relationship between pheomelanin pigmentation and brood patch temperature after controlling for ambient air temperature or oral temperature. To our knowledge, this is the first study to show that female ornaments can predict the absolute/relative thermal investment in brood patches. This relationship, together with other aspects of female quality, may affect male mate preference and female ornamentation.     

SEX RATIOS AND CONDITIONS REQUIRED FOR ENVIRONMENTAL SEX DETERMINATION IN ANIMALS

Environmental sex determination (ESD) is a system of sexual determination that is influenced by a variable environment. Once sex is determined it is then fixed for life. The model of Charnov & Bull (1977) proposes that ESD is favoured by natural selection when an individual's fitness as a male or female is strongly influenced by environmental conditions and when the individual has little control over which environment it will experience. Adaptive sex ratio variation is considerably easier for organisms with ESD, and this feature is the ultimate cause for the evolution and maintenance of ESD. ESD is taxonomically widely expressed, and more cases are likely to be discovered. Both environmental and genotypic sex determination mechanisms are found in closely related species. Evidence of geographical variation in the degree and in the critical environmental values of ESD within the same species has also been discovered, e.g. in the fish Menidia menidia and in the crustacean Gammarus duebeni. The factors causing sex determination in invertebrates include temperature, daylength, nutrition, density, humidity, ionic composition of the environment, pH, carbon dioxide, UV light, metabolic products, parasites, exposure to the opposite sex of the same species, and in parasitoids also host size, age and type. In vertebrates temperature is the dominant factor causing sex determination, though in fish also pH, salinity, light, water quality and nutrition, and in turtles water potential of the substrate have some effect on the sex expression. Most of these factors influence growth through resource availability or developmental speed. In most cases of ESD in invertebrates and fish, the environmental factor has a gradual effect on the sex expression, in contrast to the typical steep threshold mode found in reptiles. These differences might be due to the fact that invertebrates exhibiting ESD are commonly parasitic or confined to aquatic environments, where less spatial microhabitat differentiation exists. Sex ratio data available from nature for animals with ESD are quite limited, except for reptiles. In the laboratory sex ratios can be varied more widely than what is observed in nature. There are a number of characteristic features some of which are found in each species exhibiting ESD: (1) Patchy environments, (2) variable sex ratios, (3) parthenogenesis in addition to bisexuality, (4) parasitism, (5) aquatic habitats, (6) sexual dimorphism, (7) females larger than males, and (8) local mate competition.     

Incubation temperatures, sex ratios and sex determination in a population of Nile crocodiles (Crocodylus niloticus)

A demographic study of the Nile crocodile Crocodylus niloticus at Lake Ngezi, Zimbabwe, revealed that females predominated in all size classes and among embryos. The sex of C. niloticus was shown to be determined by the temperature of egg incubation in constant temperature laboratory experiments. At 31 °C and below only females were produced. The threshold temperature for maleness was between 31 ° and 34 °C, but appeared to vary between clutches. The duration of the incubation period varied with temperature and was 110 days at 28 °C, falling to 85 days at 34 °C. Incubation temperature affected hatchling length, but not mass. Hatchlings from incubation at 34 °C were shorter on average than those from incubation at 28 °C and 31 °C, but by three months had outgrown them. There was no sex-related difference in length in a random sample of 200 two-year-old C. niloticus on a crocodile farm. Mean temperatures in wild nests were consistently lower than 31 °C and therefore the male threshold as determined in the laboratory. Embryonic development was slow and hatching success poor. The shallowest eggs in a nest had higher mean temperatures and more advanced embryos than the deepest eggs. They also experienced daily temperature fluctuations of up to 10 °C during which the maximum occasionally rose to 35 °C. Constant temperature incubation was not a good model of field conditions, but the correlation between nest temperatures and embryonic sex is consistent with temperature-dependent sex determination in the wild.     

The variance of incubation temperatures does not affect the phenotype of hatchlings in a colubrid snake, Xenochrophis piscator

It has been documented in some reptiles that fluctuating incubation temperatures influence hatchling traits differently than constant temperatures even when the means are the same between treatments; yet whether the observed effects result from the thermal variance, temperature extremes or both is largely unknown. We incubated eggs of the checkered keelback snake Xenochrophis piscator under one fluctuating (Ft) and three constant (24, 27 and 30 °C) temperatures to examine whether the variance of incubation temperatures plays an important role in influencing the phenotype of hatchlings. The thermal conditions under which eggs were incubated affected a number of hatchling traits (wet mass, SVL, tail length, carcass dry mass, fatbody dry mass and residual yolk dry mass) but not hatching success and the sex ratio of hatchlings. Body sizes were larger in hatchlings from incubation temperatures of 24 and 27 °C compared with the other two treatments. Hatchlings from the four treatments could be divided into two groups: one included hatchlings from the 24 and 27 °C treatments, and the other included hatchlings from the 30 °C and Ft treatments. In the Ft treatment, the thermal variance was not a significant predictor of all examined hatchling traits, and incubation length was not correlated with the thermal variance when holding the thermal mean constant. The results of this study show that the mean rather than the variance of incubation temperatures affects the phenotype of hatchlings.     

Phenotypic consequences of incubation temperature and feeding regimen in captive-bred tarantulas

Eighteen oothecae of the African selenocosmiine spider Pterinochilus murinus were incubated at 22.5, 27.0, or 31.5°C. Neonates were reared under high or low feeding regimens. Potential influences of incubation temperature on incubation period, secondary sex ratio, egg inviability, embryo mortality, and juvenile mass at eclosion were examined using chi-square analysis and analysis of covariance. Potential direct and interactive effects of the temperature of incubation and feeding regimen on juvenile mortality, mass at 35 weeks, and duration of immature/mature life span and body mass/size in males were tested using multivariate analysis of covariance. Secondary sex ratio did not depart from parity within any experimental treatment. The strikingly small mass of spiders reared under the low feeding regimen was unaffected by incubation temperature and was equivalent between the sexes. Under the high feeding regimen, females in the 22.5 and 31.5°C incubation treatments had surpassed the mass of their male counterparts by week 35, but male and female mass was equivalent at 27.0°C. The most massive high-fed females were produced from the 31.5°C incubation temperature, while high-fed males were largest from 27.0°C, which also produced mature males of the greatest mass and body size. Captive-management implications are discussed. Zoo Biol 17:405–414, 1998. © 1998 Wiley-Liss, Inc.     

Egg incubation temperature differently affects female and male hatching dynamics and larval fitness in a leafhopper

Temperature effects on ectotherms are widely studied particularly in insects. However, the life-history effects of temperature experienced during a window of embryonic development, that is egg stage, have rarely been considered. We simulated fluctuating temperatures and examined how this affects the operational sex ratio (OSR) of hatching as well as nymph and adult fitness in a leafhopper, Scaphoideus titanus. Specifically, after a warm or cold incubation we compared males and females hatching dynamics with their consequences on the sex ratio in the course of time, body size, weight, and developmental rate of the two populations, all reared on the same posthatching temperature. Males and females eggs respond differently, with females more sensitive to variation in incubation temperature. The different responses of both sexes have consequences on the sex ratio dynamic of hatchings with a weaker protandry after warm incubation. Temperatures experienced by eggs have more complex consequences on posthatching development. Later nymphal instars that hatched from eggs exposed to warm temperature were larger and bigger but developmental rate of the two populations was not affected. Our study demonstrates how incubation temperature could affect operational sex ratio and posthatching development in an insect and how this may be critical for population growth.     

Geographic variation in hatchling size in an oviparous skink: effects of maternal investment and incubation thermal environment

Geographic variation in offspring size can be viewed as an adaptive response to local environmental conditions, but the causes of such variation remain unclear. Here, we compared the size and composition of eggs laid by female Chinese skinks (Plestiodon chinensis) from six geographically distinct populations in southeastern China to evaluate geographic variation in hatchling size. We also incubated eggs from these six populations at three constant temperatures (24, 28 and 32 °C) to evaluate the combined effects of incubation temperature and population source on hatchling size. Egg mass and composition varied among populations, and interpopulation differences in yolk dry mass and energy content were still evident after accounting for egg mass. Population mean egg mass and thus hatchling mass were greater in the colder localities. Females from three northern populations increased offspring size by laying larger eggs relative to their own size. Females from an inland population in Rongjiang could increase offspring size by investing relatively more dry materials and thus more energy into individual eggs without enlarging the size of their eggs. The degree of embryonic development at oviposition was almost the same across the six populations, so was the rate of embryonic development and thus incubation length at any given temperature. Both incubation temperature and population source affected hatchling traits examined, but the relative importance of these two factors varied between traits. Our data show that in P. chinensis hatchling traits reflecting overall body size (body mass, snout‐vent length and tail length) are more profoundly affected by population source. © 2014 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 113 , 283–296.     

Offspring sex ratio skew in the sexually monomorphic house martin Delichon urbicum

Sex ratio at conception may be under selection pressure, given that male and female offspring differ in the cost of production or generate different fitness returns under specific conditions. We studied adjustments in the primary, secondary and tertiary sex ratio in house martin Delichon urbicum, which is a sexually monomorphic, socially monogamous, colonial bird. Males of this species engage in extra‐pair copulations with heavy males acquiring the highest fertilization success. We analyzed variation in the sex ratio in relation to clutch size and parental characteristics including body condition, wing length, as well as length and pigmentation of the white rump patch during three breeding seasons. The only variable which significantly explained the variation in the sex ratio was wing length of the social father and mother. The proportion of sons among offspring was positively correlated to wing length of the social father and negatively correlated to mother wing length. Social father wing length positively correlated with mean brood body mass at fledging, which may suggest that females that mated with long‐winged males produced sons, which acquired the highest total fertilization success. Consequently, our results indicate that house martin females may adaptively adjust offspring sex composition at egg laying in relation to the characteristics of their social mate.     

Fluctuations in incubation temperature affect incubation duration but not morphology,locomotion and growth of hatchlings in the sand lizard Lacerta agilis (Lacertidae)

Li, H., Zhou, Z.‐S., Ding, G.‐H. and Ji, X. 2011. Fluctuations in incubation temperature affect incubation duration but not morphology, locomotion and growth of hatchlings in the sand lizard Lacerta agilis (Lacertidae). —Acta Zoologica (Stockholm) 00 : 1–8. Studies looking for potential effects of temperature and temperature fluctuations on phenotypic traits of reptile hatchlings have shown species variation, but have not always allowed a distinction between effects of fluctuation per se and temperature extremes themselves. To examine whether incubation temperature fluctuation has a key role in influencing the phenotype of offspring, we incubated eggs of the sand lizard Lacerta agilis at one of the four temperature regimes (27, 27 ± 2, 27 ± 4 and 27 ± 6 °C). We found that: (1) hatchlings incubated under the four temperature regimes did not differ from each other in any of the morphological and physiological traits examined; (2) interactions that included temperature treatment did not affect any trait examined; (3) the mean incubation length was longer in the 27 ± 6 °C treatment than in the other three treatments; and (4) female hatchlings were shorter in head length and width but longer in snout‐vent length as well as abdomen length than males derived from the same‐sized egg. Our data show that both the type and the magnitude of temperature variation can affect incubation length. We found no evidence for phenotypic divergence in responses to temperature fluctuations during incubation and therefore suggest that temperature variation does not affect the phenotype of hatchlings in L. agilis.     

Microclimate of American crocodile nests in Banco Chinchorro biosphere reserve, Mexico: Effect on incubation length, embryos survival and hatchlings sex

Crocodilians have temperature-dependent sex determination (TSD) in which incubation temperature determines sex of embryo. Global warming is expected to alter hatchling sex ratio, leading to the extinction of small populations. Regional climate influence on crocodile nest microclimate and hatchlings' characteristics is poorly known. Here, microclimate in natural nests of American crocodile (Crocodylus acutus) and its relation with incubation length, hatchling sex and nesting success was studied in Banco Chinchorro Biosphere Reserve (Mexico) from 2007 to 2010. Temperature and relative humidity in different locations within and outside the nests were registered by data loggers. Incident solar radiation above nest was calculated from hemispheric photographs. Incubation length, proportion of hatchling reaching complete development and hatchling sex were determined at hatching. Nest temperatures exhibited a cyclic daily fluctuation due to solar radiation, which is the major heat source for nests. Clutch temperature was relatively stable and its daily amplitude was negatively correlated with clutch depth and size. Rainfall was the major source of clutch temperature decrease. Clutch and metabolic temperatures increased significantly during incubation. A small sample size failed to demonstrate a statistical relationship between length of incubation and mean clutch temperature. Proportion of embryos reaching complete development depended on maximum and minimum clutch temperature, maximum daily amplitude of clutch temperature and maximum decrease in clutch temperature on a period ≤4 day. Results confirmed a Female-Male-Female TSD pattern for C. acutus, with 31 and 32.5 °C as possible pivotal temperatures. Population and hatchling sex ratios were male-biased and fate of crocodiles of Banco Chinchorro could depend on the magnitude of temperature increase in the future.     

CULTURAL INHERITANCE AS A MECHANISM FOR POPULATION SEX-RATIO BIAS IN REPTILES

Abstract.— Although natural populations of most species exhibit a 1:1 sex ratio, biased sex ratios are known to be associated with non‐Mendelian inheritance, as in sex‐linked meiotic drive and cytoplasmic inheritance (Charnov 1982; Hurst 1993). We show how cultural inheritance, another type of non‐Mendelian inheritance, can favor skewed primary sex ratios and propose that it may explain the female‐biased sex ratios commonly observed in reptiles with environmental sex determination (ESD). Like cytoplasmic elements, cultural traits can be inherited through one sex. This, in turn, favors skewing the primary sex allocation in favor of the transmitting sex. Female nest‐site philopatry is a sex‐specific, culturally inherited trait in many reptiles with ESD and highly female‐biased sex ratios. We propose that the association of nest‐site selection with ESD facilitates the maternal manipulation of offspring sex ratios toward females.     

Influence of incubation temperature on hatching success,energy expenditure for embryonic development,and size and morphology of hatchlings in the oriental garden lizard,Calotes versicolor (Agamidae)

We incubated eggs of Calotes versicolor at four constant temperatures ranging from 24 degrees C to 33 degrees C to assess the effects of incubation temperature on hatching success, embryonic use of energy, and hatchling phenotypes that are likely to affect fitness. All viable eggs increased in mass throughout incubation due to absorption of water, and mass gain during incubation was dependent on initial egg mass and incubation temperature. The average duration of incubation at 24 degrees C, 27 degrees C, 30 degrees C, and 33 degrees C was 82.1 days, 60.5 days, 51.4 days, and 50.3 days, respectively. Incubation temperature affected hatching success, energy expenditure for embryonic development, and several hatchling traits examined, but it did not affect the sex ratio of hatchlings. Hatching success was lowest (3.4%) at 33 degrees C, but a higher incidence of deformed embryos was recorded from eggs incubated at this temperature compared to eggs incubated at lower temperatures. Most of the deformed embryos died at the last stage of incubation. Energy expenditure for embryonic development was, however, higher in eggs incubated at 33 degrees C than those similarly incubated at lower temperatures. A prolonged exposure of eggs of C. versicolor at 33 degrees C appears to have an adverse and presumably lethal effect on embryonic development. Hatching success at 24 degrees C was also low (43.3%), but hatchlings incubated at 24 degrees C did not differ in any of the examined traits from those incubated at two intermediate temperatures (27 degrees C and 30 degrees C). Hatchlings incubated at 33 degrees C were smaller (snout-vent length, SVL) than those incubated at lower incubation temperatures and had larger mass residuals (from the regression on SVL) as well as shorter head length, hindlimb length, tympanum diameter, and eye diameter relative to SVL. Hatchlings from 33 degrees C had significantly lower scores on the first axis of a principal component analysis representing mainly SVL-free head size (length and width) and fore- and hindlimb lengths, but they had significantly higher scores on the second axis mainly representing SVL-free wet body mass. Variation in the level of fluctuating asymmetry in eye diameter associated with incubation temperatures was quite high, and it was clearly consistent with the prediction that environmental stress associated with the highest incubation temperatures might produce the highest level of asymmetry. Newly emerged hatchlings exhibited sexual dimorphism in head width, with male hatchlings having larger head width than females.     

孵化温度对王锦蛇胚胎代谢和幼体适合度的影响

孵化温度所驱动的爬行动物的表型变异是生理生态学研究的热点。本研究以王锦蛇(Elaphe carinata)为实验动物,检验了24℃和28℃孵化温度对王锦蛇胚胎代谢速率、孵化过程中的卵重量、孵出幼体代谢和行为的影响。研究结果显示:卵重和胚胎的呼吸代谢均与孵化时间呈正相关;28℃下胚胎代谢速率大于24℃;幼蛇孵出15 d内体重随着生长时间的延长而减小,24℃孵出幼体的代谢速率大于28℃孵出幼体,两温度下孵出幼体的呼吸代谢速率和生长时间无显著关系;28℃孵出幼体的疾游速和吐信频次均大于24℃;两孵化温度孵出幼体的选择体温无显著差异,但在消耗完体内的剩余卵黄后28℃孵出幼体有60%的个体摄食,而24℃孵出幼体无摄食个体。总体而言,王锦蛇28℃孵出幼体适合度优于24℃孵出幼体。     

Sexual differentiation in the spiny softshell turtle (Apalone spinifera), a species with genetic sex determination

It is hypothesized on the basis of sex determination theory that species exhibiting genetic sex determination (GSD) may undergo sexual differentiation earlier in development than species with environmental sex determination (ESD). Most turtle species exhibit a form of ESD known as temperature-dependent sex determination (TSD), and in such species the chronology of sex differentiation is well studied. Apalone spinifera is a species of softshell turtle (Trionychidae) that exhibits GSD. We studied sexual differentiation in this species in order to facilitate comparison to TSD species. Eggs were incubated at two different temperatures and embryos were harvested at various stages of mid to late development. Gonad length was measured with image analysis software, then prepared histologically. Indifferent gonads have differentiated in stage 19 embryos. Histological details of gonadogenesis follow the same pattern as described for other reptiles. Regression of the male paramesonephric duct closely follows testicular differentiation. Gonad lengths are longer at the warmer incubation temperature, and ovaries are generally longer than testes at each stage and for each temperature. Although sexual differentiation takes place at about the same stage as in other turtles with TSD (18-20), in A. spinifera this differentiation is irreversible at this stage, while in some of the TSD species sex is reversible until about stage 22. This immutable, definitive sexual differentiation may support the hypothesis of an accelerated chronology of sex differentiation for this species. We also note that sexual dichromatism at hatching is known in this species and may provide additional evidence of early differentiation. J. Exp. Zool. 290:190-200, 2001.     

THE INCUBATION PATCH OF BIRDS

1. The incubation patch of birds forms in the areas of the ventrum devoid of contour feathers (apteria) by processes involving defeathering of down, dermal and subdermal hypervascularization, oedema, and hyperplasia of the epidermis and dermal connective tissue. Its formation facilitates the transfer of heat to the eggs and hatched young. 2. In general, the sex that incubates develops a patch; this may be the female, both sexes, or the male, and the species within any one order tend to exhibit a common pattern. In some orders (e.g. Pelecaniformes) no patch develops. 3. The incubation patch begins to form before egg laying in passerine birds and during egg laying in Galliformes. Most of the patch responses in passerines are completed earlier in the reproductive cycle (late egg laying to middle incubation) than in Galliformes (middle incubation to early brooding). 4. In the passerines studied, in which usually only the female develops a patch, oestrogen and prolactin synergize to cause patch development; oestrogen given alone is effective because it synergizes with endogenous prolactin in intact birds. The role of progesterone is unclear, but it seems to mimic the effects of prolactin and also plays a role in the increase in skin sensitivity characteristic of patch development in the canary. 5. In the one galliform studied (California quail), in which both sexes develop a patch, either oestrogen or androgen synergizes with prolactin; oestrogen alone is ineffective in non-breeding quail because of insufficient endogenous prolactin levels. Prolactin alone causes epidermal hyperplasia and vascularization, and progesterone seems mainly to be involved in defeathering. In the starling also both sexes develop a patch, but testosterone plus prolactin is not effective as it is in the quail. 6. In the phalaropes, birds in which only the male develops a patch, androgen and prolactin are the effective synergists in patch development. Thus, there is a correlation between the sex which develops a patch in the wild and the steroid (oestrogen or androgen) which synergizes with prolactin. 7. In the brown-headed cowbird, a parasitic species which neither develops a patch nor incubates, there are no responses to exogenous hormones. The absence of patch development in one sex or in both can be due either to an absence of appropriate hormone levels or to a lack of sensitivity of the skin to hormones. 8. More study is needed of the transfer of heat from the patch area to the eggs or young, including the relationships between patch structure, surface area, surface temperature, type of nest, and the number and size of eggs. 9. Patch formation is affected by and influences behaviour. 10. More research is needed in regard to (I) the natural development and endocrine control of the incubation patch in various orders of birds: (2) the effects of patch formation on behaviour, and vice versa; (3) the mode of action of the hormones in patch formation, that is, whether it is direct or indirect, e.g. through the release of another hormone; (4) the specificity of the ventral skin to hormone administration; (5) the effects of stimulation of the patch by eggs in the nest on prolactin and gonado-trophin secretion; (6) the possible role of other, as yet untested, hormones on patch development; (7) the levels of endogenous hormones in relation to natural patch formation; and (8) possible correlations between the structure of the patch, the chronology of its formation, the clutch size and the condition of the young when hatched in various species.     

Host size and sex allocation of parasitoids in a gall forming community

Summary The sex ratios of three Mesopolobus species were found to vary in different hosts in a gall-forming community in Berkshire. These relationships were consistent with Charnov's host size—sex ratio hypothesis (Charnov 1979). Due to the segregation of host species on different species of Quercus, it was possible to conduct a geographical variation experiment proposed by Charnov et al. (1981). The results of this experiment suggest that the parasitoids have a fixed rule of thumb and are not flexible in their sex allocation in response to changes in host size distribution. The data, therefore, do not support the prediction of Charnov's hypothesis. Problems associated with this kind of field experiment are discussed.