Morphometric variation in the Hooded seal (Cystophora cristata)

Intra- and intersexual variation in 16 skull dimensions and total body length of 233 aged Hooded seals caught in the north-west Atlantic were investigated. Absolute growth was described by asymptotic growth curves applied to single dimensions, as well as to scores on the first principal component of logarithmically transformed cranial data, which are believed to reflect the multivariate nature of growth. All dimensions were found to be fully developed later in males than in females. The growth of the male skulls was found to continue for more than 20 years, while the females approach final size about–7 years earlier than males, according to the scores on the first principal component. Female seals were found to reach 86 % of final total body length at the time of maturation, which is a generalized pinniped pattern. In both sexes, a yearling skull was characterized by a large brain-case, which decreased relatively with growth. The male skulls were further characterized by an increase in zygomatic width and orbital width in relation to basal length, a pattern which was not found in females.
All the asymptotic values were significantly larger in males than in females. The dimorphism develops mainly as a result of prolonged growth of males after the attainment of sexual maturity.     

Roentgen cephalometric studies on skull development in rats. II. Normal and hypophysectomized males; sex differences

Growth of the skull in normal male rats of the Long-Evans strain has been studied by serial roentgen cephalometry (under anesthesia) from 27 to 280 days of age, and has been compared with the retardation following hypophysectomy and with growth data obtained on females in an earlier similar study. The dimensions measured represented major skull regions and segments, and in some instances allowed calculation of indices (e.g., neurocranial width/length ratio) which would show changing proportions. In general, the skull showed the more rapid and prolonged growth characteristic of male rats' skeletal development when compared with that of females. Viscerocranial (“facial”) length and width were notable in this respect. On the other hand, growth in neurocranial width and height ceased at a time and size much like that in females. Examination of the possibility that the adult female skull might correspond closely to that of an immature male disclosed that though this might be true for the neurocranium, facial dimensions showed distinctive sex differences. After hypophysectomy at 27 days of age males (as also females) showed marked reduction of growth but not complete cessation. Dimensional increases were between one-fifth and one-fourth of the normal gains. The ratios computed showed that the proportions of infancy were retained after early hypophysectomy.     

The evolution of sexual size dimorphism in the house finch. IV. Population divergence in ontogeny

Differences among taxa in sexual size dimorphism of adults can be produced by changes in distinct developmental processes and thus may reflect different evolutionary histories. Here we examine whether divergence in sexual dimorphism of adults between recently established Montana and Alabama populations of the house finch (Carpodacus mexicanus) can be attributed to population differences in growth of males and females. In both populations, males and females were similar at hatching, but as a result of sex-specific growth attained sexual size dimorphism by the time of independence. Timing and extent of growth varied between the sexes: Females maintained maximum rates of growth for a longer time than males, whereas males had higher initial growth rates and achieved maximum growth earlier and at smaller sizes than females. Ontogeny of sexual dimorphism differed between populations, but in each population, sexual dimorphism in growth parameters and sexual dimorphism at the time of nest leaving were similar to sexual dimorphism of adults. Variation in growth of females contributed more to population divergence than did growth of males. In each population, we found close correspondence between patterns of sexual dimorphism in growth and population divergence in morphology of adults: Traits that were the most sexually dimorphic in growth in each population contributed the most to population divergence in both sexes. We suggest that sex-specific expression of phenotypic and genetic variation throughout the ontogeny of house finches can result in different responses to selection between males and females of the same age, and thus produce fast population divergence in the sexual size dimorphism.     

The growth and maturation of the "tarantula", Avicularia avicularia L.

The growth of the theraphosid spider, Avicularia avicularia L. was studied principally by taking measurements of the fang length of exuviae and dead specimens. The relatic ships between fang length and increment at ecdysis and fang length and instar duration were investigated and used to construct a projected growth curve for the species. This suggests that males reach sexual maturity in approximately 13 instars and at a minimum age of about two and a half years. In males the adult instar is terminal and rarely lasts more than three months. Reproductive maturity in females is probably not reached earlier than the XIVth instar or three years from birth. The females continue to moult annually after maturity and have a longevity in excess of seven years. The pattern of colouration shows characteristic changes in early immature life and develops a slight sexual dimorphism in adults. Type II urticating hairs are present throughout life and occur in light and dark forms in the IInd instar. The mean length of the urticating hairs increases during the life cycle and a sexual dimorphism develops in the XIIth or XIIth instar. In adult males the urticating hairs are uniformly barbed whereas in the adult females the barbs are restricted to the proximal end.     

Sex differences in body size and body condition in breeding Temminck’s Stints Calidris temminckii

There have been very few reports of body size measurements of live Temminck’s Stints, but earlier studies have shown sex differences in body mass and tarsus length. Here we use molecular techniques to determine the sex of Temminck’s Stints from a Norwegian breeding population. In total, we report measurements of body weight, wing length, tarsus length, bill length, skull length and keel length from 17 males and 30 females. We found significant sex differences in all of these variables, with the exception of tarsus length. The differences in skull length disappeared after the bill lengths had been subtracted from the measurements. A discriminant function analysis based on wing length and bill length correctly classified 86% of the cases (12/16 males, 25/27 females). Female Temminck’s Stints are known to regularly lay more than one clutch of eggs per season and could therefore be expected to be physiologically deprived of bodily energy stores. Nevertheless, we found females to be in better body condition than males.     

Protein content in urine of male and female water vole (Arvicola amphibius) at the period of spring growth and sexual maturation

The study was carried out on the water voles Arvicola amphibius reared in vivarium. For the first decade of January, March, and June, the body length, the anogenital distance, and the body mass were measured, and urine was collected for determination of its protein content. The obtained results have shown that the protein content depends on the animal gender and is connected with the reproductive status of males and their size-weight characteristics. The urinary protein excretion level in females remained stable at different months, whereas in males its sharp rise was noted at the period of spring growth and sexual maturation. The significant sexual differences were established in March and enhanced in June. In March the urine protein content in males was noted to correlate positively with the body mass and length and with the anogenital distance. The males reached sexual maturity at the earlier calendar terms than the females did; in sexually mature males the urine protein content was significantly higher than in the sexually immature ones.     

Growth and mortality in mountain hares: the effect of sex and date of birth

Summary Current theory suggests that high juvenile growth effort, may result in higher mortality. This prediction is tested in mountain hares (Lepus timidus), by examination of post-weaning growth and mortality of males and females. Dates of birth were estimated from weight at first capture and growth in body weight and hind foot length was described by the logistic growth equation. Although adult female hares are on average larger than males, this results from a longer period of growth and not from a faster growth rate. There was no clear sex bias in mortality, a slight but not significantly greater proportion of males suffered mortality during the growth period. Predictions as to sex difference in mortality should specify which aspects of growth (rate or duration) are the agents of mortality, since the two parameters are not necessarily positively associated. Overall asymptotic body size decreased and rate of growth increased from early through to late-born young. Rate of growth in hind foot length was greater in late-born males but not in late-born females as compared with those born earlier. It is hypothesized that late-born males are more tightly constrained to complete growth and subsequent sexual maturation earlier than late-born females.     

Growth differences and dimorphic expression of growth hormone (GH) in female and male Cynoglossus semilaevis after male sexual maturation

Half-smooth tongue sole, Cynoglossus semilaevis, is an ideal model to investigate the regulatory mechanisms of sexual growth dimorphism in fish species. The aim of the study was to investigate the effect of differential age of sexual maturity for females and males on growth and GH mRNA expression in C. semilaevis. The body weight differences between the sexes were not significant in C. semilaevis at age 5 months when females and males were all immature. Significant differences in body weight between the sexes were found after early sexual maturation of males at the age of 9 months. The body weight of 21-month-old females (621.4 ± 86.4g), still not immature, was even 3.28 times higher than that of the males (189.7 ± 14.4g). The cDNAs encoding GH in C. semilaevis was cloned. The GH gene is 2924bp long and consists of six exons and five introns. The results of qRT-PCR showed that GH mRNA levels of the immature females were not significantly different from that of immature males at age 5 months. However, GH mRNA levels of the immature females were significantly higher compared with those of the mature males at age 9 months (P<0.05). At age 11 months, GH mRNA levels of females were even 6.4-fold higher than that of males. In conclusion, for the first time we show that early sexual maturity of males is the main cause of sexual growth dimorphism in C. semilaevis and exert significant effect on GH mRNA expression.     

Morphometric variation of the skull during postnatal development in the Lowland European bisonBison bonasus bonasus

We studied the variation of linear measurements and skull capacity in Lowland European bisonBison bonasus bonasus (Linnaeus, 1758) during postnatal development, and the dependencies of the parameters in relation to sex, age, and body mass of the animals. Material consisted of 599 bison skulls (310 males and 289 females), within the age range of 1 month to 21 years (males) and to 27 years (females). In the group of calves to 1 year old, no sex connected differences in skull measurements were observed, whereas the skull capacity in older calves was significantly larger (0.01>p>0.001) in males than in females. From the third year of life, most skull measurements display characteristics of sexual dimorphism. Skull development in both sexes is most intensive during the first three years of life, and slows from the age of 5. In older individuals of both sexes (≥ 6 years), orbital breadth continues growing and, in females, breadth of splanchnocranium continues increasing. Growth in a bison’s skull capacity is most intensive up to the third year of life and slows from the age of 5. During postnatal development, a bison skull grows proportionally except the neurocranium, which grows slightly slower in comparison with basal length and its development finishes earlier than that of splanchnocranium. In ontogenesis, a bison skull grows much slower compared to body mass. In relation to body mass, skull capacity and the height of neurocranium grow most slowly while orbital breadth grows most intensively. The results obtained were compared with data on skull sizes of bison born in 1930–1950 and bred in captivity and with skulls of the American bisonBison bison. Inbreeding is probably responsible for some types of phenotypic abnormalities in the skull which appear in modern European bison.     

Correlation of kidney weight and volume and selected skeletal parameters to sex in the adult rhesus monkey (Macaca mulatta)

This report outlines a comparison of renal weight and volume and selected skeletal parameters to sex in 22 adult male and 156 adult female rhesus macaques. Means and standard deviations for kidney weight and volume, body weight, and radiographic measurements for both males and females are reported. Ninety-five percent confidence intervals and P-values for the mean differences between the sexes for these parameters were also compiled. Male monkeys were larger, but had kidneys of similar size to those of the females. Joint distributions of the radiographic measurements of the first lumbar vertebra and the skull showed that males were larger in both measurements. The distributions of these parameters were clearly separate in males and females, while joint distributions of kidney weight and volume for males and females overlapped almost completely. We found that, regardless of age, sex, weight, or skeletal size, all normal adult rhesus monkeys generally have similar-sized kidneys.     

Reproductive migrations of the sex role reversed pipefish Nerophis lumbriciformis(Pisces; Syngnathidae)

Using an individual identification technique, a population of worm pipefish Nerophis lumbriciformis was followed during 19 months, in order to determine the exact use of the intertidal and, considering the specific movement patterns of males and females, the mating system exhibited by this population. Field observations showed that the number of adults increased during the breeding season, with males arriving 1 month earlier than females. Furthermore, males and females presented distinct permanence periods, showing that the intertidal is used as a mating arena. It was also observed that both male and female worm pipefish mated repeatedly over the span of a reproductive season, but females exhibited shorter remating intervals. Also, females stayed for longer periods on the mating grounds, the intertidal zone, whereas males typically left for the subtidal after mating, usually returning within 2 months. These inter‐sexual differences in the occupation of the intertidal suggest that females breed with different males but also that males accept eggs from various females since, on their return, a new group of mating partners was now available. Thus, N. lumbriciformis might be considered polygynandric. It is a clearly dimorphic species in spite of the observed polygynandry, suggesting that differences in remating intervals may be influential in determining the strength of sexual selection along with what may be expected from the polygynandrous mating system alone.     

Ontogeny of sexual size dimorphism in monitor lizards: males grow for a longer period, but not at a faster rate

Monitor lizards belong to the largest and the most sexually dimorphic lizards in terms of size, making this group an ideal model for studies analyzing ontogenetic causes of sexual dimorphism. Understanding of these ontogenetic factors is essential to the current discussion concerning patterns of sexual dimorphism in animals. We examined the ontogenetic trajectories of body weight and snout-vent length to analyze the emergence of sexual size dimorphism. Experimental animals were 22 males and 13 females of mangrove-dwelling monitors (Varanus indicus) hatched at the Prague Zoo. They were regularly weighed and measured up to the age of 33-40 months, and subsequently sexed by ultrasonographic imaging. The logistic growth equation was used to describe and analyze the observed growth patterns. Our results confirm considerable sexual size dimorphism in the mangrove monitor. The mean asymptotic body weight of males was nearly three times higher than that of females. As the body size of male and female hatchlings is almost equal, and the growth rate parameter (K) of the logistic growth equation as well as the absolute growth rate up to the age of 12 months do not differ between the sexes, size differences between fully grown males and females should be attributed to timing of the postnatal growth. Males continue to grow several months after they reach the age when the growth of females is already reduced. Therefore, the sexual size dimorphism emerges and sharply increases at this period.     

The ontogeny of cranial sexual dimorphism in two old world monkeys:Macaca fascicularis (Cercopithecinae) andNasalis larvatus (Colobinae)

Allometric and heterochronic approaches to sexual dimorphism have contributed much to our understanding of the evolutionary morphology of the primate skull and dentition. To date, however, extensive studies of sexual dimorphism have been carried out only on the great apes and a few cercopithecine monkeys. To fill this gap, representative dimensions of the skull were collected among ontogenetic series of two dimorphic Old World monkeys:Macaca fascicularis (Cercopithecinae) andNasalis larvatus (Colobinae). The ontogeny of cranial sexual dimorphism was evaluated with least-squares bivariate regression, analysis of covariance (ANCOVA), and analysis of variance (ANOVA). Results indicate that within each species the sexes typically exhibit nonsignificant differences in ANCOVAs of ontogenetic trajectories, except for bivariate comparisons with bicanine breadth. AmongMacaca fascicularis, ANOVAs between males and females of common dental ages show that adult, and frequently subadult, males are significantly larger than females, i.e., sexual dimorphism develops via time and rate hypermorphosis (males primarily grow for a longer time period as well as faster). AmongNasalis larvatus, however, comparisons between males and females of common dental ages indicate that only adult males are significantly larger than females, i.e., sexual dimorphism develops primarily via time hypermorphosis (males grow for a longer time period). Within both species, females appear to exhibit an early growth spurt at dental age 2; that is, many cranial measures for females tend to be larger than those for males. Measures of the circumorbital region (e.g., browridge height), body weight, and bicanine breadth exhibit typically the highest sexual dimorphism ratios. The fact that postcanine toothrow length and neurocranial volume (less so inNasalis) demonstrate very low dimorphism ratios generally supports assertions that postnatal systemic growth (and associated selective pressures thereon) exerts a greater influence on facial, but not neural, dental, or orbital, development (Cochard, 1985, 1987; Shea, 1985a,b, 1986; Shea and Gomez, 1988; Sheaet al., 1990). Additional consideration of ontogenetic differences between species generally supports previous functional interpretations of subfamilial differences in cranial form related to agonistic displays in cercopithecine monkeys (Ravosa, 1990).     

Sex-specific impact of prenatal stress on growth and reproductive parameters of guinea pigs

Body condition and reproductive maturation are parameters of reproductive success that are influenced by sexual hormones rising in the circulation during the time of puberty. Various endocrine systems can be programmed by conditions experienced during early life. Stress for instance is supposed to be capable of influencing fetal development, leading to adjustments of offspring??s later physiology. We examined whether prenatal stress (induced by exposure to strobe light) during early- to mid-gestation was capable of affecting later reproductive parameters in guinea pigs (Cavia aperea f. porcellus). Therefore, we measured the levels of testosterone and progesterone from the age of day 12?C124 in prenatally stressed (PS, n?=?20) and unaffected control animals (n?=?24). Furthermore, we determined the timing of puberty and growth. Body weight development revealed significantly faster growth in PS females compared to control animals. The onset of first estrus was slightly earlier in PS females, however not significantly so. Cycle lengths and levels of progesterone differed between groups over the course of time with higher progesterone levels and more constant cycles among PS females compared to control females who displayed marked differences between first and subsequent cycles. Levels of testosterone did not differ between groups. We conclude that prenatal stress accelerates growth and maturity in females, but not in males.     

SEXUAL DIMORPHISM IN BOTTLENOSE DOLPHINS FROM THE EAST COAST OF FLORIDA

Skulls of 69 bottlenose dolphins (genus Tursiops ) from the Indian/Banana River on the east coast of Florida were examined for evidence of sexual dimorphism. The only sexual dimorphism shown by t -tests on 28 morphological and four meristic skull characters was that males have, on average, more teeth than females in all four arcades. Results of covariance analysis, employed to account for variation in size, indicate minor dimorphism in parietal width of the skull. Twenty body measurements of 29 Tursiops originating in the same area were also analysed for differences between males and females. Statistical results indicate the possibility of sexual dimorphism in the length from the snout to the umbilicus and in flipper width. No evidence was found for differences in overall skull or body length between the sexes.     

Variation in the growth of the preweaning Syrian hamster (Cricetus auratus)

An assessment of the growth rate spectrum based on a longitudinal weight study of golden hamsters was undertaken over the preweaning period. The period covered 23 days with data probes at 24-hourly intervals and encompassed 16 litters providing a birth number of 120 young and a weaning survival number of 82. Subsequent analysis directed initially at the pooled or averaged data showed sex differences with males gaining weight faster than females. Further analysis showed the total period to have three definitive break-points and therefore four phases of growth activity. The segmented linear regression line calculations showed that the phasic duration of males in the second and third phases were two days later than the females. Following data-analysis adjustments and taken into account aberrations of the sample, final indications pointed to the preweaning hamster growth spectrum as quadrophasic, exhibiting a stable first phase, a second and third phase terminating earlier in females and a final weaning weight being heavier in males. The growth curves demonstrated a 'U' shaped outline and formed an integral part of hamster preweaning precocity.     

Allometry of the postnatal cranial ontogeny and sexual dimorphism in Otaria byronia (Otariidae)

We studied the cranial postnatal ontogeny of Otaria byronia in order to detect sexual dimorphism in allometric terms, analyzing the rate of growth of functional variables linked to specific capacities as bite and head movements. We used 20 linear measurements to estimate allometric growth applying bivariate and multivariate analyses in females and males separately. Males were also analyzed in two partitioned subsets considering non-adult and adult stages, when the dimorphism is accentuated in order to reach optimal performance for intra-sexual competition. In the comparison of the employed techniques, we detected an empirical relationship between our multivariate results and the ordinary least square bivariate analysis. The quantitative analyses revealed different ontogenetic trajectories between non-adult and adult males in most variables, suggesting that the adult skull is not a scaled version of subadult skull. For instance, variables related with longitudinal dimensions decreased their allometric coefficients when the adult stage was reached, whereas those related with breadth or vertical dimensions increased their values. In adult males this could indicate that skull breadth and height are more important than longitudinal growth, relative to overall skull size. Conversely, inter-sexual comparisons showed that females and non-adult males shared similar ontogenetic growth trends, including more allometric trends than did males along their own ontogenetic trajectory. In general, adult males exhibited higher allometric coefficients than non-adult males in variables associated with bite and sexual behavior, whereas in comparison to females the latter showed higher coefficients values in these variables. Such patterns indicate a complex mode of growth in males beyond the growth extension, and are in partial agreement with changes previously reported for this and other species in the family Otariidae.     

Temporal changes in the reproductive population structures and males’ secondary sexual character of the hermit crab <Emphasis Type="Italic">Diogenes nitidimanus</Emphasis>

We investigated the reproductive ecology of D. nitidimanus in the Waka-River estuary with special reference to temporal change in the relative size of chelae length for males, i.e., secondary sexual character. Ovigerous females were observed from April to October, peaking in June–July with over 90% of females being ovigerous. Adult female carapace size ranged from 3.5 to 8.5 mm, but with the majority of females falling between 5–6 mm. Male carapace length was more evenly distributed between 3.5 and 10 mm. Juvenile settlement occurred mostly in July, during which time the frequency of both large females (over 6.5 mm in carapace length) and large males (over 8.5 mm in carapace length) clearly decreased. The carapace length of precopulatory-guarded females varied from 4.8 to 8.0 mm, while guarding males were almost over 7 mm and always larger than their paired females. The relative growth of the major chelae differed significantly between small and large males during the early months of the year, including the reproductive peak months (April–June). During these early months, large males had relatively larger chelae for their body size than did small crabs. This difference, however, was not evident later in the year (July–September). Large males may grow their chelae relatively long in the early months in order to take advantage of the mating opportunities during April–June. This is the first report in animals, to our knowledge, that relative size of the secondary sexual character for males temporarily change during a single reproductive season.     

Growth and reproduction in the Icelandic common seal (Phoca vitulina L., 1758)

Length, weight and maturity were studied in relation to age in the common seal (Phoca vitulina vitulina L., 1758), collected during the periods 1979-1983 and 1990-2000 in Icelandic waters. The maximum age of common seal observed was 36 years for females and 30 years for males. For common seal females and males, asymptotic length and weight were 161 cm and 93 kg and 174 cm and 97 kg, respectively, showing slight sexual dimorphism in size. The condition of adult females, measured as fat thickness at the lower end of the sternum, was lower in the period 1979-1983 than in 1990-2000 during June-September, the breeding and mating time of the Icelandic common seal. Males reached sexual maturity between 5 and 7 years, whereas 50% of females did so at age 4 years. Including the length and age interaction term in the logistic regression model for the maturity of females significantly improved it. Thus, body size matters in the onset of maturity. The mean birthing date for the Icelandic common seal was found to be in early June. A comparison of animals collected in the two periods 1979-1983 and 1990-2000 did not show significant differences in growth and the average age of sexual maturity for either males or females. The observed decline of the Icelandic common seal population is most probably caused by increased mortality, due to exploitation and accidental by-catch in gill-nets, rather than a decrease in fecundity.     

Growth in the myopathic Syrian hamster (Cricetus auratus)

The objective was to assess the effect of the hereditary myopathic disease (muscular dystrophy) on 4 growth parameters: body-weight, head-body length, skull weight and cranial length in the Syrian hamster over a 4-13 month period. A control colony of 34 males and 32 females was compared to a muscular dystrophy colony consisting of 37 males and 27 females. The monthly means of the 4 growth parameters were computed and full data were used for computations of analysis of variance with regression of each group, sex and growth parameter. Intersex and intergroup comparisons of the same parameters were made using analysis of covariance. In the controls, the male bodies were heavier and longer than the female bodies; males grew over the total period. In dystrophic hamsters, males were heavier than females, but females were longer. In both control and dystrophic hamsters, female skulls were longer and heavier. In all parameters the means of the control colony were greater than those of the dystrophic colony relative to age. The disease factor in the muscular dystrophy colony adversely influenced all 4 growth parameters.