Effects of the sex-linked dwarf gene (dw) on the expression of the muscular dystrophy gene (am) in chicken.

The sex-linked dwarf gene (dw) was introduced into companion muscular dystrophic (am) and nondystrophic (Am+) New Hampshire chicken lines to investigate influences of the dwarf gene on breast muscle weights, muscle fiber area, and the histological expression of muscular dystrophy. Dystrophic and nondystrophic chickens within dwarf or nondwarf genotypes were similar in body and carcass weights. Pectoralis and supracoracoideus muscle weights (as a percentage of adjusted carcass weight) were similar in nondystrophic dwarf and nondwarf males and females. In addition, pectoralis weight was similar in dystrophic dwarf males and dystrophic nondwarf males and females. However, pectoralis weight was significantly smaller in dystrophic dwarf females than in dystrophic nondwarf females, whereas supracoracoideus weight was significantly larger in dystrophic dwarf males than in dystrophic nondwarf males. Supracoracoideus weight was similar in dystrophic dwarf males and females and dystrophic nondwarf females. Pectoralis muscle fiber area was influenced by sex and by dwarf and dystrophy genotype. Muscle fiber area was larger in females than in males, smaller in dwarfs than in nondwarfs, and smaller in dystrophic than in nondystrophic muscles. Muscle fiber degeneration and adipose infiltration was more extensive in dystrophic than in nondystrophic females and males, and it was more advanced in dwarfs than in nondwarfs. Excessive acetylcholinesterase staining patterns were characteristic of dystrophic muscle in both dwarf and nondwarf genotypes. Nondystrophic and dystrophic dwarf male and female chickens are comparable substitutes for nondwarfs as biomedical models with respect to pectoralis histology, acetylcholinesterase staining pattern, and pectoralis muscle hypertrophy.     

Canine muscular dystrophy: confirmation of X-linked inheritance

The genetic basis of muscular dystrophy in golden retriever dogs was investigated by means of experimental matings and cytogenetic studies. An affected male golden retriever was mated to three normal females, producing an F1 generation of six males and 14 females, all of which were clinically normal. Of six F1 females retained for breeding, all were shown to be carriers of muscular dystrophy in outcrosses to unrelated normal male dogs or in backcrosses to the affected male golden retriever. In outcrosses of carrier females, three of seven male and none of nine female offspring were affected, as expected under the X-linked recessive hypothesis. Backcrosses of F1 females to their affected sire also yielded results that are consistent with this hypothesis: 15 of 32 males and 5 of 17 females had muscular dystrophy. Cytogenetic studies of a carrier female, an affected male offspring, and a normal male sibling revealed no detectable abnormalities of the X chromosome.     

Enhanced longevity in tau mutant Syrian hamsters,Mesocricetus auratus

The single-gene mutation tau in the Syrian hamster shortens the circadian period by about 20% in the homozygous mutant and simultaneously increases the mass-specific metabolic rate by about 20%. Both effects might be expected to lead to a change in longevity. To test such expectations, the life span of male and female hamsters from three genotypes (wild-type, heterozygous, and homozygous tau mutants, all derived from heterozygote crosses to randomize the genetic background) was recorded in constant darkness. Male hamsters lived significantly longer than females: the overall average life span was 96.9 weeks (SE = 2.5, n = 118) for males and 82.0 weeks (SE = 2.1, n = 99) for females. To our surprise, male and female homozygous mutant hamsters lived significantly longer rather than shorter compared to wild-types. For males, the difference between the two genotypes was on average 14%; for females, the difference was 16%. The mortality rate of wild-type males was significantly different from that of homozygous tau males but not different from that of heterozygotes. Overall, survival of wild-type females was statistically distinguishable from both heterozygous and homozygous mutant females. Male and female wild-type hamsters were heavier than homozygote mutants throughout the entire life span, and heterozygous mutants had intermediate weights. There was no correlation between body mass and life span, and the causes of the extended life span in tau mutant hamsters remain unresolved.     

Sexual selection is not the origin of long necks in giraffes

The evolutionary origin of the long neck of giraffes is enigmatic. One theory (the 'sexual selection' theory) is that their shape evolved because males use their necks and heads to achieve sexual dominance. Support for this theory would be that males invest more in neck and head growth than do females. We have investigated this hypothesis in 17 male and 21 female giraffes with body masses ranging from juvenile to mature animals, by measuring head mass, neck mass, neck and leg length and the neck length to leg length ratio. We found no significant differences in any of these dimensions between males and females of the same mass, although mature males, whose body mass is significantly (50%) greater than that of mature females, do have significantly heavier (but not longer) necks and heavier heads than mature females. We conclude that morphological differences between males and females are minimal, that differences that do exist can be accounted for by the larger final mass of males and that sexual selection is not the origin of a long neck in giraffes.     

Avian muscular dystrophy: Thyroidal influence on pectoralis muscle growth and glucose-6-phosphate dehydrogenase activity

The pectoralis muscles of dystrophic chickens (line 413) were hypertrophic on the basis of fresh weight and fat-free dry weight. They also had greater DNA content and greater glucose-6-phosphate dehydrogenase (G6PD) and 6-phosphogluconate dehydrogenase (6PGD) activities. Of the parameters measured, the largest differences between pectoralis muscles from dystrophic and normal (line 412) chickens were for DNA content and G6PD activity. These parameters were 4.3- and 6.7-fold, respectively, the values for control pectoralis at 5 wk of age. The average number of nuclei per unit length of isolated muscle fiber was also greater (approximately 3-fold) for the dystrophic pectoralis. Body weight and pectoralis fresh weight, fat-free dry weight, DNA content, G6PD activity and 6PGD activity were reduced significantly in propylthiouracil (PTU)-treated normal and dystrophic chickens. Moreover, the effects of PTU were more pronounced in the dystrophic strain. Thyroid deprivation significantly improved the righting ability of the dystrophic chickens, in addition to its influence on muscle hypertrophy and body growth. Thyroxine (T₄) replacement reversed the PTU effects in both strains. Of all the variables measured, total G6PD activity was the most affected by PTU treatment of dystrophic chickens and was only 16% of the control dystrophic value.In addition to the effects of thyroid deprivation on the expression of avian muscular dystrophy, we observed significant differences in thyroid-related variables in the two strains. The average thyroid weight at 4 wk and serum triiodothyronine level at 5 wk for dystrophic chickens were 65 and 76%, respectively, of the normal values. The results that we report here indicate that altered thyroid function affects the expression of avian muscular dystrophy.     

Canine X-linked muscular dystrophy in Japan (CXMDJ).

The purpose of this study was to develop a strain of canine X-linked muscular dystrophy (CXMD), a model of Duchenne muscular dystrophy, in Japan. A female beagle was artificially inseminated with frozen-thawed spermatozoa derived from an affected golden retriever. Subsequently, two carrier female dogs (G1 carriers) and four normal male littermates were produced. Thereafter, the two G1 carriers were mated with beagle sires. As a result, each bitch whelped three times, and out of 54 pups, 17 affected male descendants, and 11 carrier female descendants (G2 carriers) were detected. One G2 carrier was then mated with a beagle sire and 15 pups in two whelpings were produced, including five affected males and four carrier females (G3 carriers). A total of 10 female beagles were artificially inseminated to evaluate the fertility of the frozen-thawed spermatozoa from the two affected dogs. The whelping rates of the two affected dogs were 4/5 and the litter sizes were 5.0 +/- 1.41 and 6.0 +/- 0.82, respectively. These results indicate that a canine X-linked muscular dystrophy colony has been established in Japan. We called them CXMDJ.     

Polyphasic growth-weight response in the guinea pig

An assessment of the growth rate pattern based on longitudinal weight data of guinea pigs was conducted over the presumptive preweaning and early postweaning period. The study covered the minimum of 44 and maximum of 53 days with means calculated for 3-day intervals involving 13 litters and a total of 40 young. Initial analysis showed males heavier than females at birth and both sexes being inversely proportional to litter size at birth. At the end of the experimental period the males were still heavier than the females but their weight distribution peaked in litter of three while the females were heaviest in the largest litters of five and lightest in the litter of one. Phasic linear regression line analysis revealed 4 litters with a triphasic growth outline and 6 litters with quadrophasic growth outline. Final assessments indicate that the total period of 53 days manifests a quadrophasic growth outline while, in contrast, the period specifically involved with the process of lactation and weaning displays a definite diphasic growth spectrum and is comparable to the tri- or quadrophasic spectrum occurring in the albino rats, rice rats and hamsters.     

Growth and ontogeny of sexual size dimorphism in the mandrill (Mandrillus sphinx)

We present body mass (N = 419) and crown-rump length (CRL, N = 210) measurements from 38 male and 49 female mandrills born into a semifree-ranging colony in order to describe growth from birth to adulthood, and to investigate maternal influences upon growth. Adult male mandrills are 3.4 times the body mass, and 1.3 times the CRL, of adult females. Body mass dimorphism arises from a combination of sex differences in length of the growth period (females attain adult body mass at 7 years, males at 10 years) and growth rate. Both sexes undergo a subadult growth spurt in body mass, and this is much more dramatic in males (peak velocity 551 g/months +/- 89 SEM at 84-96 months). CRL dimorphism arises from bimaturism (females attain adult CRL at 6 years, males after 10 years), and neither sex shows a particular subadult growth spurt in CRL. Sexual size dimorphism thus represents important time and metabolic costs to males, who mature physically approximately 3-4 years after females. Considerable interindividual variation occurs in the size-for-age of both sexes, which is related to maternal variables. Older mothers have heavier offspring than do younger mothers, and higher-ranking mothers have heavier offspring than do lower ranking mothers. Mass advantages conferred upon offspring during lactation by older and higher-ranking mothers tend to persist postweaning in both sexes. Thus maternal factors affect reproductive success in both sexes, influencing the age at which offspring mature and begin their reproductive career.     

The individual counts: within sex differences in foraging strategies are as important as sex‐specific differences in masked boobies Sula dactylatra

Understanding how animals allocate their foraging time is a central question in behavioural ecology. Intrinsic factors, such as body mass and size differences between sexes or species, influence animals’ foraging behaviour, but studies investigating the effects of individual differences in body mass and size within the same sex are scarce. We investigated this in chick‐rearing masked boobies Sula dactylatra, a species with reversed sexual dimorphism, through the simultaneous deployment of GPS and depth‐acceleration loggers to obtain information on foraging movements and activity patterns. Heavier females performed shorter trips closer to the colony than lighter females. During these shorter trips, heavier females spent higher proportions of their flight time flapping and less time resting on the water than lighter females did during longer trips. In contrast, body mass did not affect trip duration of males, however heavier males spent less time flapping and more time resting on the water than lighter males. This may occur as a result of higher flight costs associated with body mass and allow conservation of energy during locomotion. Body size (i.e. wing length) had no effect on any of the foraging parameters. Dive depths and dive rates (dives h^?1) were not affected by body mass, but females dived significantly deeper than males, suggesting that other factors are important. Other studies demonstrated that females are the parent in charge of provisioning the chick, and maintain a flexible investment under regulation of their own body mass. Variation in trip length therefore seems to be triggered by body condition in females, but not in males. Consequently, shorter trips are presumably used to provision the chick, while longer trips are for self‐maintenance. Our findings underline the importance of accounting for the effects of body mass differences within the same sex, if sex‐specific foraging parameters in dimorphic species are being investigated.     

Compensatory adrenal growth in aldosterone-treated male and female hamsters

The aim of the study was to investigate the compensatory adrenal growth in aldosterone-treated male and female hamsters. Hemiadrenalectomised and sham-operated animals were treated for 5 days with a daily d-aldosterone dose of 25 micrograms/animal. In both male and female aldosterone-treated hamsters monoadrenalectomy did not change the relative adrenal weight if compared with sham-operated groups. The fasciculata zonae of monoadrenalectomised aldosterone-treated males was larger and contained more parenchymal cells than in appropriate control group. There was no difference in the volume of adrenocortical zones, average cell volume and in cell number between sham-operated and unilaterally adrenalectomised females. In vitro 3H-thymidine incorporation per adrenal was markedly higher in monoadrenalectomised than in sham-operated aldosterone-treated males while the opposite was true for female hamsters. Thus, the action of aldosterone on CAG in the hamster seems to depend on sex, with no effect in males and inhibitory action in females.     

SEX DIFFERENCES IN BODY SIZE AND BODY CONDITION OF CALIFORNIA SEA LION (ZALOPHUS CALIFORNIANUS) PUPS FROM THE GULF OF CALIFORNIA

The Gulf of California harbors about 15% of the total California sea lion ( Zalophus californianus californianus ) population. We studied pup morphometrics from eight Gulf of California rookeries during the 1996 and 1997 reproductive seasons to describe sex differences in body size and body condition indices. Newborn pup body size was not different from previous reports. Male pups were heavier and larger than female pups in terms of all linear dimensions. Morphometric relationships, however, showed that males were 3%-4% denser, and that after removing the effects of length, they were about 2% heavier than females. Sculp depth adjusted for length was 12% larger in female than in male pups. Our data provide further evidence that male otariid pups may allocate a larger fraction of milk energy to muscular and skeletal growth compared to female pups.     

SEXUAL DIMORPHISM IN MAMMALS

1. Life expectancy and mortality rates from diseases arising in various organs vary with sex because of differential exposure to external hazards and because of essential differences between males and females in aspects not directly connected with reproduction. This review attempts to collate data about the structural and functional dimorphism of mammals exclusive of the genital organs and psychological aspects. 2. The primary sex ratio is not certain and like the secondary and tertiary may vary with species. In many mammals more males are aborted and born than females. Later a higher mortality of males, due to sex-linked congenital diseases and greater exposure to external hazards, shifts the balance in favour of females at the time of sexual maturity. The average life span of females is longer than that of males, except in hamsters and in inbred strains of mice with a high incidence of mammary tumours. 3. Chromosomes as well as gonadal hormones are responsible for the development of male and female characteristics. The Y-chromosome initiates the differentiation of the testis, but gonadal hormones control the subsequent differentiation of the genital tract and other organs. In embryos the testicular secretion precedes that of the ovary. The Y-chromosome is devoid of, but the X-chromosome retains structural genes. The random heterochromatization of a paternal or a maternal X-chromosome in the somatic cells of female embryos equalizes the genetic information for both sexes and produces a mosaicism of female somatic cells except in the kangaroo where the paternal X-chromosome is selectively inactivated. Deficient genes on the X-chromosome become manifest in hemizygous males, in homozygous females and can be detected in heterozygous women in half of the somatic cell population in some conditions. 4. The testis grows faster than the ovary and starts to secrete earlier, but the maturation of female gonocytes precedes that of males. Spermatogenesis starts at puberty and is maintained throughout life, while multiplication of oogonia ceases in the perinatal period (except in lemurs), when the stage of the first meiotic division is reached. The stock of oocytes dwindles during life. 5. In many mammals the male grows faster than the female before and after birth, but is less mature. Puberty tends to start earlier in females and the associated growth spurt does not last as long as in males. Testosterone has a direct anabolic effect, promotes growth and delays differentiation. Oestrogens are considered katabolic, but promote growth indirectly by stimulating the production of growth hormone in the pituitary. Progesterone has an anabolic and slight androgenic effect. 6. A female pattern of differentiation of the hypothalamus, the pituitary and the pineal gland, manifested at puberty by cyclical activities of the reproductive organs requires the absence of androgens during a critical phase of ante- or perinatal development. Oestrogens given to males at that period produce effects similar to castration. Antiandrogens induce in males a cyclical pattern of function in the hypothalamus and the pituitary, enlargement of the breasts and formation of nipples in the rat and a female type of sexual behaviour. There is no complete sex reversal in mammals comparable to that of fish and amphibians. 7. With some exceptions (hamsters, rabbits, guinea-pigs) males are larger than females. Gender differences in weight of organs and in other parameters must be assessed as proportion to male or female weight, surface and activities. The relatively greater amount of fat in female and of connective tissue in male organs in relation to the active parenchyma complicate comparisons. 8. The head and shoulder region is proportionately larger in males and the pelvic region in females. Men and male mice have heavier bones, muscles, hearts, lungs, salivary glands, kidneys and gonads in proportion to body weight, while females have proportionately heavier brains, livers, spleens, adrenals, thymus, stomach and fat deposits. 9. The basal metabolic rate in women is lower than in males. A great variety of metabolic parameters, levels of enzyme activity, location of fat deposits, sensitivity to drugs is sexually dimorphic and responsive to the action of androgens, oestrogens and progestagens. 10. Males tend to have more red blood corpuscles, haemoglobin and erythropoietin per unit volume of blood than women, cows, mares, sows, bitches, female cats and hamsters, but there is no sex difference in this respect in rats, rabbits, goats or sheep. Females tend to have more granulocytes and a proportionately larger lymphomyeloid complex (bone marrow, spleen, thymus, lymph nodes and lymphoepithelial tissues) and greater immunological competence than males. The cortical epithelium of the thymus in mice and rats is sexually dimorphic, responsive to castration and treatment with sex hormones and varies with the oestrous cycle. 11. The kidney is proportionately larger in male mice, rats, cats and dogs, is reduced by castration and enlarged by treatment with testosterone. The kidneys of hamsters and guinea-pigs do not differ in size with sex, nor do they respond to castration or to androgens. The proportion of tubules to glomeruli is greater in the male than the female kidney. The tubular mass increases with androgenic medication, but not the juxtaglomerular apparatus. The parietal epithelium of Bowman's capsule, the histochemistry of the kidney and the composition of the urine vary with gender and respond to sex hormones according to species and strain. The bladder of male mice is proportionately larger than that of females. Some pheromones are present in the bladder urine of intact male mice and of spayed females given testosterone, but absent from that of castrated males. 12. Boars, male elephants, mastodons, horses, deer and monkeys have larger canines than the females. The submaxillary gland of male mice, rats and pigs is proportionately larger than in females, but smaller in hamsters. The proportion of mucous to serous acinar cells in female rodents is greater than in males; female hamsters produce more sialic acid. The secretory tubules of male rats and mice are larger than in females and produce a nerve- and an epidermal-growth factor. Apart from amylase the levels of enzyme activity vary with sex. The liver is sexually dimorphic as regards size, content and metabolism of glycogen, fat, vitamin A, levels of enzymatic activity, phagocytic activity and in its response to castration, sex hormones, to toxic agents, drugs and carcinogens. Sex hormones affect the production of insulin by the pancreas in vivo and in vitro. 13. The male larynx which enlarges and induces voice changes in many mammals at puberty or the onset of the breeding season, is affected by castration and by sex hormones. Male lungs are proportionately larger than female ones with a greater vital and maximal respiratory capacity. Breathing rate and manner varies with sex and is related to differences in the muscular development of the diaphragm. 14. The epidermis and dermis of males are thicker, but the subcutis thinner than in females. The skin is sexually dimorphic in respect of dermatoglyphics, the replacement of vellus by terminal hair and pigmentation of specific regions, the colour of the face and of the sexual skin in monkeys, the development of antlers and horns. The synchrony of the hair cycle and the growth wave of the hair coat in mice and rats depend on the sex of the animals. The X-chromosome mosaicism in the hair follicles of female mice accounts for the mosaicism in pigmentation. Apart from a genetic disorder, the sweat glands are not sexually dimorphic, but the apocrine, the sebaceous glands and their specialized forms are. The embryonic development of mammary glands depends on the absence of androgens and can be induced in male rats and guinea-pigs by antiandrogens. 15. An intact cerebral cortex is necessary for the performance of reproductive functions in male, but not in female rats, cats, rabbits and guinea-pigs. Removal of the olfactory bulb impairs reproduction in female, but not in male mice. Pinealectomy prevents the testicular atrophy of hamsters kept in the dark. The reproductive cycles in females are regulated by the hypothalamus through the control of the ratio of FSH to LH release in the pituitary. This in turn acts on the ovary and thus affects the activity of the thyroid, thymus and lung. In males FSH and LH act synergistically and their secretion is not controlled separately. Oestrogens are more effective than androgens in inhibiting pituitary functions. Sexual dimorphism in cytology, enzyme levels and oestrogen-binding is manifest in the preoptic area, the hypothalamus and the nucleus medialis amygdalae. The female brain is proportionately larger than the male with equal relative amounts of grey and white matter, but a bigger hypothalamic-pituitary-pineal complex. The pineal gland is more prone to tumour formation in boys than in girls and retains its cellularity longer in women than in men. Colour blindness is manifested less in heterozygous women than in hemizygous men. Mature women are more sensitive to the smell of synthetic musk than girls or men. Male rats and mice are more susceptible to audiogenic seizures than females. 16. The activity of the thyroid gland varies at different phases of the oestrous cycle in rats, mice and guinea-pigs. Female mice release more thyroid hormone into the blood than males or spayed animals. Oestrogens increase the level of thyroxin-binding protein. The concentration of TSH in the blood of mature women is double that of men and of menopausal women. The incidence of non-endemic thyroid disorders in women considerably exceeds that in men. 17. The adrenals of females are much larger than those of males except in hamsters. The gland of the female mouse contains more lipid than that of the male. The juxtamedullary X-zone of mice involutes at puberty in males and during the first pregnancy in females. Castration induces an X-zone in male mice, voles, hamsters and cats and an enlargement without stratification in rats. ACTH controls the secretion of glucocorticoids and since its formation is promoted by oestrogens and inhibited by androgens, sex hormones influence indirectly the size and activity of the adrenal cortex. Hepatic inactivation of glucocorticoids is 3 to 10 times greater in intact females than in males. 18. The implications of species variations in sexual dimorphism for the survival and the evolution of mammals are discussed.     

Individual differences in aggressiveness of female hamsters: response to intact and castrated males and to females

The aggressive behaviour of female hamsters was studied while they were housed in large enclosures with males and in brief tests with males or females. Some females are not aggressive with any male, whereas others are very aggressive toward all males in both testing conditions. Females that are not aggressive toward intact males may be very aggressive toward castrated males or females. When the animals are housed together for long periods of time, males dominate only if they are much heavier. Male dominance takes a relatively long time to establish and often there is an equivocal period characterized by reversals of dominance. Female dominance is rapidly established. Unless the male is much heavier, the female determines the presence or absence of agonistic behaviour.     

Statural growth in known-age African elephants (Loxodonta africana)

The shoulder heights of 224 females and 170 males, and hindfoot length of 236 female and 217 male known-age African elephants ( Loxodonta africana ) were measured, and growth curves constructed for each measure of size. A linear relationship between foot length and shoulder height was confirmed in simultaneous measures of 97 males and 110 females. Growth curves demonstrated the typical sexual dimorphism in both foot length and shoulder height, with males growing more rapidly than females from birth onwards. The size dimorphism in foot length and shoulder height becomes marked by the age of 10 years, with males on average being 60–70 cm taller than females at 65 years. This size dimorphism is produced through faster growth which continues for longer than does that of females. The variance in growth rates is slightly greater for females than for males. It is proposed that female growth after puberty is affected by a trade-off between growth and reproduction, while males who deviate markedly from typical patterns of growth may be subject either to mortality or energetic constraints limiting their potential variance.     

Effects of divergent selection for yolk testosterone content on growth characteristics of Japanese quail

Effects of yolk androgens on postnatal growth of offspring have been widely studied but their physiological role in the growth control is not fully understood due to an inconsistency in obtained results. We investigated androgen-mediated maternal effects on postnatal growth in relation to endocrine control mechanisms using two lines of Japanese quail divergently selected for high (HET) and low (LET) egg testosterone (T) content. Embryonic growth did not differ between the lines. During the growth period HET quail were heavier and displayed longer tarsi as compared with LET quail, with more pronounced line differences in males than females. HET males were heavier than LET males from the age of 2 weeks, reached the age of maximum growth rate earlier, and displayed higher asymptotic body weight than LET males. Accelerated growth in HET males was not accompanied by increased postembryonic plasma T concentrations. Plasma triiodothyronine levels did not differ between lines while plasma thyroxine levels were decreased in HET as compared with LET female chicks. Line differences in body weight disappeared in adult quail suggesting that yolk androgens, increased in a physiological way, resulted in stimulation of juvenile growth rate in precocial Japanese quail under stable social and environmental conditions.     

Can captivity lead to inter-species mating in two Mesocricetus hamster species?

In two closely related species, females generally prefer conspecific males over heterospecific males. We found that estrous (but not diestrous) female Syrian hamsters Mesocricetus auratus prefer the odors of conspecific males to odors of Turkish hamsters Mesocricetus brandti . However, female Syrian hamsters are not aggressive toward male Turkish hamsters and will readily mate with them. We hypothesize that many generations in captivity led to a reduction in females' ability to avoid inter-species mating, possibly related to the heightened sexual receptivity observed in Mesocricetus hamsters in captivity. To test this hypothesis, we replicated a study carried out with female Turkish hamsters soon after the current laboratory stock of this species was established. In that study, female Turkish hamsters showed lordosis toward male Syrian hamsters in only 20% of interactions and attacked heterospecific males in 80% of the pairings. Using animals descended from that original colony (after many generations in captivity and certain episodes of inbreeding), 100% of female Turkish hamsters mated with heterospecific males and none showed aggression toward heterospecific males. Thus female avoidance of inter-specific mating may be affected by captive rearing conditions.     

Sexual dimorphism and growth trade‐offs in Blue Tit Cyanistes caeruleus nestlings

The outcome of sibling competition for food is often determined by variation in body size within the brood and involves trade‐offs; traits that enhance competitive ability within the nest may be developed at the expense of traits that enable effective flight at fledging, or vice versa. We quantified growth of skeletal, body mass and feather traits in male and female Blue Tit Cyanistes caeruleus nestlings. Males were significantly heavier, had longer tarsi and tended to have greater head–bill lengths than females, whereas females were similar to males in wing flight feather growth. These differences in growth may result from sexual differences in selection of the traits. Females are likely to prioritize feather growth to facilitate synchronized fledging with the rest of the brood, and to enhance escape from predators. We suggest that males are heavier and develop longer tarsi because body size is an important determinant of male reproductive success.     

BODY SIZE DECLINES DESPITE POSITIVE DIRECTIONAL SELECTION ON HERITABLE SIZE TRAITS IN A BARNACLE GOOSE POPULATION

Analyses of more than 2000 marked barnacle geese (Branta leucopsis) in the largest Baltic colony, Sweden, showed that structurally large females generally produced larger clutches and larger eggs, hatched their broods earlier in the season, and produced more and heavier young than smaller females. In males, the corresponding relationships between reproductive parameters and structural body size were weaker or nonsignificant. Because structural body size traits have previously been found to be significantly heritable and positively genetically correlated, an increase in mean structural body size of individuals as a response to selection might have been expected. By contrast, we found that the mean adult head length and mean adult tarsus length decreased significantly in the largest colony by approximately 0.7 and 0.5 standard deviations, respectively, in both males and females during the 13-year study period. Environmental factors, such as the amount of rain in different years, were found to affect the availability of high-quality food for growing geese. As a consequence of this temporal variability in the availability of high-quality food, the mean adult structural body size of different cohorts differed by up to 1.3 standard deviations. Comparisons of mean body size of cohorts born in different colonies suggest that the most likely explanation for the body-size decline in the main study colony is that a density-dependent process, which mainly was in effect during the very early phase of colony growth, negatively affected juvenile growth and final size. We conclude that large environmental effects on growth and final structural body size easily can mask microevolutionary responses to selection. Analyses of environmental causes underlying temporal and spatial body size variation should always be considered in the reconstruction and prediction of evolutionary changes in natural populations.     

SEXUAL AND SEASONAL, VARIATION IN CONDITION AND SURVIVAL OF SWEDISH GOSHAWKS ACCIPITER GENTILIS

Winglength was the most powerful intersex discriminator, giving 99.5% separation by itself and 100% combined with bodyweight or keel length. Females but not males, had longer wings and were heavier as adults than as juveniles. Pectoral fat and muscle indices explained 81–91% of variation in total fat and 93–96% of variation in total lean dry weight for male and female hawks but bodyweight change explained only 56–60% of variation in the fat index compared with 75–76% for pectoral lean dry weight. The best size index, keel length, explained only 6.4% of bodyweight variation in males and 11.2% in females. Winglength was very weakly correlated with keel length. Taking size difference into account, females were heavier with higher wingloading than males but had relatively lighter flight muscles and therefore a lower power availability relative to their flight requirements than in males. On the other hand, females had greater maximum fat stores (17% of bodyweight) than males (14%) and could have survived longer than males without food. These differences would be adaptive for the different role of each sex during breeding. The weight of first capture of live-trapped adults and juveniles increased between September and December, possibly because moulting (in adults) or hunting inexperience (in juveniles) kept weights low in autumn but also perhaps because the benefit of having large reserves for surviving, relative to the cost of decreased agility in flight because of increased wingloading, was greatest in mid-winter. Shot hawks weighed more than the live-trapped birds but showed the same trends, as did retrapped individuals. Females but not males, tended to lose weight in January before a further increase in the spring. Records of hawks retaken more than two months after first capture showed that between October and January survival in females but not males, was enhanced by high bodyweight. Since female weights were also significantly lower in southern Sweden than in central and northern areas, it is suggested that changing agriculture or other factors in the south may have reduced prey for females more than for males.