Growth and body weight of European hares in southern Sweden

Body weight and growth of European hares Lepus europaeus Pallas in relation to environmental conditions, population density, age, sex, and reproduction were studied in three populations in southern Sweden on the basis of hares shot during October-December. There were no significant differences in mean body weight of juveniles in the three areas. Differences in juvenile growth, as indicated by the correlation between eye lens weight (age indicator) and body weight, between areas and years were related to variations in nutrient conditions, in an island population it was probably also related to population density. Adult body weights did not differ between two mainland areas despite differences in food supply and population density, whereas island adult hares were, on average, significantly lighter than mainland hares. Also this difference was ascribed to nutrient conditions and/or population density. There were no significant differences in body weight between adult hares of different age classes. But reproductive females showed a significant positive correlation between number of litters produced annually and body weight. This relation indicates that reproduction is favoured by large body size and body weight, which also might explain the average higher mean body weight in females than in males. Juvenile hares showed no clear tendency in sex dimorphism of body weight.     

人工饲养条件下东方田鼠指名亚种繁殖特性及其幼仔的生长发育

在实验室饲养条件下, 对东方田鼠指名亚种繁殖特性和幼仔生长发育进行了初步观察。该鼠全年均可繁殖, 平均每胎产仔3.8 ±1.5 只, 妊娠期20～21 d , 繁殖间隔期39.3 ±26.4 d , 雌雄比为1.48。幼鼠3 日龄耳壳完全直立, 4 日龄开始长下门齿, 5 日龄长上门齿, 7～8 日龄睁眼, 20 日龄可断奶, 55 日龄左右性成熟。3 种生长模型(Logistic 方程、Gompertz 方程和Von Bertalanffy 方程) 对体重、体长、尾和后足的生长过程的拟合优度均很高,择优选用Von Bertalanffy 方程对体重、体长和尾长进行描述, 选用Logistic 方程对后足长的生长过程进行描述。将该鼠的生长发育过程划分为4 个阶段, 乳鼠阶段: 初生至10 日龄; 幼鼠阶段: 11 日龄至20 日龄; 亚成年阶段: 21至55 日龄; 成年阶段: 56 日龄以后。对指名亚种和长江亚种生长、繁殖特性异同亦作了初步分析。     

Flying distance of frass kicked by the grasshopper Atractomorpha lata and factors affecting the flying distance

Adults of the grasshopper Atractomorpha lata use a hind leg kick to project their frass a considerable distance from themselves. To clarify the defecation behavior quantitatively and collect basic information that aids in clarification of the adaptive significance of this behavior, we measured the flying distance of kicked frass and examined the factors affecting the flying distance in adult A. lata. Males and females kicked their frass an average of 252 and 487 mm away, respectively. This represented more than ten times the body length or 100 times the length of the frass pellet for either sex. Only sex affected the flying distance of frass. There were sexual differences in hind‐femur length (females longer than males), volume of frass pellet (females larger than males) and ratio of diameter to length of frass pellet (RFP; larger in males than in females). The flying distance appears to be affected by the femur length, volume of frass pellet and RFP when data of both males and females were combined for analysis. However, none of these effects were observed when testing the effects within each sex. These results suggest that the sex difference in the flying distance does not result from the sex difference in femur length, volume of frass pellet or RFP. Because A. lata kicked their frass far away in both sexes, the frass‐kicking behavior might give benefit common to both males and females.     

Reproductive constraints,not environmental conditions,shape the ontogeny of sex‐specific mass–size allometry in roe deer

In polygynous mammals, sex‐specific patterns of body growth are linked to divergent selection pressures on male and female body size, resulting in sexual dimorphism (SD). For males, reproductive success is generally linked to body size, hence, males should prioritise early growth. For females, reproductive success is linked to resource availability, so they may adopt a more conservative growth tactic. Using longitudinal monitoring of known‐age animals in two contrasting populations and an allometric approach to disentangle the relative contribution of structural size and physiological condition to SD, we addressed these issues in the weakly polygynous roe deer. Despite very different environmental conditions, we found remarkably similar patterns in the two populations in the mass–size allometric relationship at each life history stage, suggesting that relative allocation to structural size and physiological condition is highly constrained. SD in structural size (indexed by hind foot length) involved sex‐specific growth trajectories governed by a single mass–size allometric relationship during the juvenile stage, such that males were both bigger and heavier than females. In contrast, SD in physiological condition (indexed by the allometric relationship between body mass and hind foot length, expressed as body mass for a given body size) developed markedly during the sub‐adult stage in relation to sex differences in the timing of first reproduction. Among adults, males were heavier for a given size than females, suggesting that, relative to females, males express a capital breeder tactic, accumulating fat reserves to offset reproductive costs. By the senescent stage, SD in physiological condition had disappeared, with both sexes governed by a single allometric relationship, suggesting more rapid senescence in males than females. Individuals born into poor cohorts were generally lighter for a given size, indicating growth priority for skeletal size over physiological condition in both sexes. However, sex differences in cohort effects among sub‐adults resulted in lower size‐specific SD in poor cohorts, indicating that body condition of sub‐adult females is buffered against environmental harshness. We conclude that sex‐differences in reproductive tactics impose constraints on the ontogeny of SD in roe deer, leading to sex‐specific trajectories in structural size and physiological condition.     

Demographics of the European hare (Lepus europaeus) in the Mediterranean climate zone of Australia

Demographic parameters of the European hare (Lepus europaeus) in southern Australia were investigated by dissecting hares shot by hunters during each month of the year. Gender, body weight, age, sucking, lactation, weight of the abdominal alimentary canal, weight of the left peri-renal fat body, pregnancy status, presence and counts of placental scars, litter size, and stage of gestation were recorded. From those data, growth rates, age at weaning, age and weight at puberty, date of conception, projected birth date, recruitment, survivorship, and the relationships between lactation and fat stores and alimentary capacity were determined.Fecundity of the southern Australian hares followed the seasonal pattern reported for northern hemisphere populations. However, output was lower per female and particularly per older female. Females began breeding at an earlier age such that recruitment into the southern Australian population was more dependent on females in their first year of life than on older females. Growth rates were comparable with European rates. Although high chill factors were apparently associated with higher leveret mortality, there was paradoxically higher overall mortality during the spring-early summer period of higher plant growth than in the late summer–winter period of lower plant growth and more extreme weather conditions. Fat was accumulated during pregnancy and would act as a buffer against the possibility of inadequate food availability during lactation, but hares increased the capacity of the alimentary canal during lactation and presumably with it their ability to assimilate energy to meet the demands of lactation.     

Somatic characteristics and reproduction of common vole, <Emphasis Type="Italic">Microtus arvalis</Emphasis> (Microtus arvalis

Reproduction potential and biometry of somatic characteristics of the common vole Microtus arvalis were evaluated and discussed. The results were processed on the basis of an extensive material (2,171 individuals) from the whole territory of Slovakia (315 sites situated at altitudes from 100 to 1500 m above sea level). Among the somatic characteristics studied, the highest variability was found in body length and the smallest in hind foot length. Highly significant differences were also found between the foot length of adult males and females. Populations of M. arvalis at low altitudes were less numerous than at higher altitudes. Altitudinal differences in average embryo numbers in female uteri as well as differences in follicle length in males during the reproductive season were also observed.     

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.     

Age and growth of Far Eastern staghorn sculpin <Emphasis Type="Italic">Ggymnocanthus herzensteini</Emphasis> (Cottidae) in peter the Great Bay (the Sea of Japan)

In a sample of Far Eastern staghorn sculpin Gymnocanthus herzensteini with a length up to 40 cm, age and growth were assessed from the results of analysis of thin longitudinal sections of otolith (sagitta). Males attained to an age not less than 13 years and females attained to an age not less than 17 years. Maximum length of males is much smaller than that of females. The absolute gains of females are greater than those of males; however, there are no considerable differences in the specific rate of growth. The most intensive growth is observed in the first two to three years of life. During sexual maturation, its rate decreases. The next noticeable decrease in the rate of growth occurs in fish of elder age groups. In catches of Far Eastern staghorn sculpin in Peter the Great Bay, females dominate; however, in groups of small and medium-sized individuals, the proportion of males increases, which is related to their smaller, as compared to females, absolute gains. The subsequent decrease in the proportion of large-sized males is determined by their greater natural mortality, as compared to similar-sized females.     

Somatometrical features of Japanese monkeys in the Koshima islet: In viewpoint of somatometry,growth, and sexual maturation

The Japanese monkeys inhabiting Koshima islet were investigated morphologically, and compared with those living in other areas of Japan. The morphological features of the Koshima monkeys are thought to reflect many interrelated factors. Their body size is the smallest inMacaca fuscata fuscata. The lower latitude and the warmer winter of the islet represent the major factors in this small body size. Another physical characteristic is their longer limbs, which may be related to the same environmental factors. The adult males of the Koshima troop show the widest variation, while the variation in the adult females is the narrowest, among the troops ofMacaca fuscata examined. This may be explained either by sexually differentiated growth, that is, males continue to grow considerably after 8 years of age, whereas females do not; or by isolation, that is, males sometimes immigrate into or emigrate from the islet, whereas almost of all the females remain there. It was found that the influence of food limitations on body weight depends on sex and age; babies and juveniles, and adult males did not lose their body weight, but monkeys aged from 3 to 7 years and adult females had lost much weight compared to those of the same ages and sexes measured in 1963 (feeding was not limited). This fact may support the idea of “sex-age-class selection” proposed byMori (1979), but the weight loss pattern could be explained by changes of body composition with growth. The growth of the anterior trunk length, too, was restrained. Sexual maturation in males was delayed by at least one year.     

The effects of size, age and a cost of early breeding on reproduction in female mountain hares

Both age and size may influence female reproductive performance in mammals, and successful early reproduction may lead to reduced success at later attempts. The effects of age, size and early reproduction on distribution of reproductive effort throughout a single breeding season was examined in female mountains hares Lepus timidus L. Hind foot length was used as an index of body size, because, unlike body weight, it did not fluctuate with reproductive status. Fifty-six female carcasses were collected from March to October 1984, and their litters were assigned to one of three chronologically equal'litter periods'(1–3) of equal length. Whereas number of ova shed was always independent of age, large females shed more ova than did smaller females in litter periods 1 and 2. Prenatal mortality of ova and embryos was highest during litter period 1, when it was independent of age and size. Although prenatal mortality remained high in first year females in litter period 2, there was an overall decline through to the final litter period when it was negligible. Total number of young produced through the season increased with skeletal size in old females (age > 1), but not significantly in first year females. It is concluded that large size, rather than age, favours early reproduction in mountain hares. Every additional offspring produced in litter periods 1 and 2 reduced that female's production in period 3. After correcting for this cost of early reproduction the number of young produced in the final litter period also increased with maternal size.     

How does environmental variation influence body mass,body size,and body condition? Roe deer as a case study

We tested the influence of population density and of drought intensity (measured as the Gaussen Index in spring and summer of the year of birth) on winter body mass, hind foot length, and body condition of roe deer fawns. Body mass decreased with increasing density and increased with increasing Gaussen Index in summer, in a similar way for both males and females. Hind foot length of males showed the same response. On the other hand, hind foot length of females decreased with increasing density only after dry summers, hence when environmental conditions were very harsh. Body condition was affected neither by density nor by drought intensity. Our results indicate that body mass and size are much better indicators of phenotypic quality than body condition in roe deer. The sex-specific responses of body size to environmental conditions could correspond to a differential allocation in favour of daughters by heavier than average roe deer mothers.     

Implications of individual growth status on the future sex of the European eel

Sex-related differences in growth status was demonstrated in eels Anguilla anguilla reared indoors at 17, 20 or 26° C, from the elver stage. Growth status was defined as length increase, weight increase and length–weight relationship. Eels attaining at least 10 g body weight (180–220 mm body length) were tagged with Passive Integrated Transponders (PIT). Length and weight were measured at 6-week intervals, until individuals stopped growing or had attained 150 g weight (380–450 mm). Sex-specific data from potentially undifferentiated eels were provided by retrospective classification of sex. Comparisions between sexes were made within groups graded by length or weight data from the beginning of each 6-week period. There was no consistent difference in absolute length increase between small males and females, but below 40–60 g initial body weight, males displayed on average a higher weight increase than females. Males also had lower length at weight than females, even in the smallest weight groups. Early growth status may influence the future sex of undifferentiated eels, but other approaches are needed for distinction between cause and effect.     

Growth and reproductive biology of the foxfish Bodianus frenchii,a very long‐lived and monandric protogynous hermaphroditic labrid

Samples of the foxfish Bodianus frenchii, collected over reefs on the lower west and south coasts of Western Australia, contained individuals ranging up to 78 years old. Although B. frenchii is far smaller than many other species within the Labridae, its maximum age is the greatest yet recorded for this highly speciose family and, together with Achoerodus gouldii, provides an example of a temperate hypsigenyine with exceptional longevity. Length and age compositions of females and males and the histological characteristics of gonads of a wide length range of individuals demonstrated that B. frenchii is a protogynous hermaphrodite. Furthermore, as, on both coasts, the length of the smallest male was greater than that at which all females had become mature, B. frenchii is a monandric protogynous hermaphrodite, i.e. all of its males are derived from functional females. Attainment of maturity by females is related more to length than age, whereas the reverse is true for sex change. On the basis of Schnute growth equations and length‐to‐body mass regression equations, the predicted length at age and body mass at length of fish on the south coast were greater than those on the west coast throughout life. Although B. frenchii spawns daily during the main spawning season, which extends from October to February on both coasts, its fecundity at any given length is substantially greater on the south than on the west coast. The more rapid growth of juveniles and earlier attainment of maturity by B. frenchii on the south coast than on the warmer west coast, together with maturation at a similar size on both coasts, run counter to the trends observed in many species and certain ecological theories regarding the relationships between life‐cycle traits and latitude and temperature. The attainment by B. frenchii of a larger body length at age, of greater body mass at length and of greater fecundity at both length and body mass in fish on the south than on the west coast strongly suggests that conditions on the former, cooler coast are more favourable for this labrid, which belongs to a sub‐genus whose other species typically live in cool, deep, temperate waters.     

Body size and craniometry of the herb field mouse from Lithuania in the context of species range

We present morphometric and craniometric measurements of the herb field mouse (Apodemus uralensis) from Lithuania and analyze variation of body and skull size across species range. We suppose species is characterized by high size variability, not following Bergmann’s or Murphy’s rules. Preliminary, distinct size differences have been registered in the eastern and southern edges of the distribution range, with these populations having largest individuals according to average body and skull size. In terms of tail length and condylobasal length of the skull, Lithuanian mice on the north-western edge of the species range are among the largest, but in terms of body weight, body length, zygomatic skull width and the length of maxillary toothrow, adult A. uralensis from Lithuania are small and correspond to those from populations on the western edge of the range. The relative skull width (ratio of zygomatic skull width to condylobasal length) of Lithuanian A. uralensis is the smallest across the entire range. In A. uralensis from Lithuania, sex dimorphism is weakly expressed, with hind foot length and postorbital constriction larger in adult males, while the height of the mandibula and length of the mandibular diastema is larger in adult females. Juvenile and subadult A. uralensis from Lithuania differ in body weight, but not in size.     

Reproduction, development and growth of Akodon lindberghi (Hershkovitz, 1990) (Rodentia, Muridae, Sigmodontinae) raised in captivity

The reproduction, development and growth of Akodon lindberghi were studied in captivity. The colony was derived from animals captured in Sim?o Pereira, Minas Gerais state, which represents a new area of geographical distribution known for this species. Twelve males and twelve females were crossed, producing 144 young in 53 litters. Post-partum oestrus was observed and gestation length was estimated in 23 days. Litter size ranged from 1 to 4 with a mean of 2.72 (SD = 0.97, n = 53) and modal size of 3. Sexual dimorphism was neither present in body mass at birth nor at weaning. There was a significant negative correlation between litter size and mass at birth or weaning. Permanent emergence of adult external appearance occurred at 15 days. Puberty for males and females was 43 and 42 days, respectively, and the first fecundation event for two females was recorded at 47 and 54 days of age. The weight growth was described by fitting a Gompertz model. No significant difference was found in any parameter of growth curves for males and females. Measurements (head-body, tail, hind foot and internal and external ear lengths) obtained for adult individuals also did not reveal the presence of sexual dimorphism.     

Fluctuating asymmetry,body size and sexual selection in the dung fly Sepsis cynipsea — testing the good genes assumptions and predictions

In the dung fly Sepsis cynipsea large and more symmetric males have been shown to enjoy a mating advantage, but we still do not know which mechanism of sexual selection is responsible. Here we test several assumptions and predictions relating to the hypothesis that either trait is indicative of ‘good genes’. We tested for good genes by regressing fitness in good and bad environments (no and high larval competition, respectively) on the family mean for size or asymmetry as expressed in the good environment, separately for both sexes. Body size (hind tibia length or head width) was positively correlated with female fecundity, growth rate of both sexes and larval survivorship for males, but only in the good environment. The corresponding evidence for asymmetry is more equivocal. Mean standardised asymmetry was weakly associated with lower survivorship in the good environment, while growth rates and female fecundity were not. As predicted by sexual selection theory, fore tibia length showed greater asymmetry than other, presumably not sexually selected traits, and asymmetry in fore tibia length was greater for males than females. However, a negative correlation between trait size and asymmetry was only evident for male seta length but not for fore tibia length, fore femur length, or any composite measure of asymmetry. Most crucially, asymmetry was heritable for some female morphological traits (hind tibia length: h² = 0.15; fore femur length: h² = 0.16; mean of all measured traits: h² = 0.27), but not for any male trait. Also, asymmetry of the various traits measured was not correlated within males and only weakly so within females. The crucial assumption that asymmetry of sexually selected traits reflects overall, heritable developmental stability of an individual is thus only partly substantiated by our data. In contrast, large body size is heritable, associated with high fitness and consequently could be indicative of good genes. Fore leg asymmetry may influence male mating success by simply mechanically constraining his ability to hold on to the female.     

Size and scaling of sexually-selected traits in the lizard, Uta palmeri

Differences between the sexes in overall body size and in the size of other morphological traits, relative to overall body size, are common in many animals. In this study, patterns of growth and scaling of sexually dimorphic tratis are assessedin a lilzard and then used to sugest general developmental mechanisms responsible for sexual size dimorphism (SSD). Adult make Uta palmeri lizards are larger than adult females inoverall body size (snout-vent length, SVL), body mass, jaw length head width, and head depth. Two general growth processes produce this adult SSD. First, juvenile males have greater annual SVL growth rates than do juvenile females, contributing to adult SSD because males will be larger than females in any trait positively correlated with SVL. Secondly, males and females differ in age-related changes in growth of the three head size traits, relative to growth in SVL. Comparing slopes from reduced major axis regressions of each trait on SVL reveals that the sexes do not differ in the scaling of these traits as juveniles, but as adults males have greater slopes than adult females, indicating ontogenetic differences in scaling of these traits in males. Two other topics in SSD are addressed with these data. First, comparing these data on scaling to those of an earlier analysis that used ordinary least squares regression reveals that conclusions about underlying mechanisms in an analysis of scaling can be altered by the choice of a regression model. Secondly, these data indicate that postmaturational differences in scaling contribute to adult sexual size differences, contrary to an earlier study. Shine (1990) found that for many ectotherms, which continue to grow after sexual maturation, post-maturational events contribute little to sexual differences in overall body size. Results for U. palmeri suggest that these findings may only hold for measures of overall body size (e.g. SVL) and may not generalize to traits that exhibit sex difference in scaling.     

Protandry, sexual selection and climate change

Protandry refers to the earlier appearance of males before females at sites of reproduction. Sexual selection has been hypothesized to give rise to sex differences in benefits and costs of early arrival, thereby selecting for earlier appearance by the sex subject to more intense sexual selection. If sexual selection is more intense, there is a greater premium on early arrival among individuals of the chosen sex because of direct selection for earlier arrival. This hypothesis leads to the prediction that changes in the costs and benefits of early arrival related to changes in environmental conditions should particularly affect the sex that arrives first and hence the degree of protandry. I tested this hypothesis using the Barn Swallow Hirundo rustica. During 1971–2003, the degree of protandry increased significantly in a Danish population because males advanced arrival date while females did not. This earlier arrival by males compared with females was correlated with a significant increase by over 1.2 standard deviations in the length of the outermost tail feathers of males, a secondary sexual character, suggesting direct selection on both protandry and the secondary sexual character. Environmental conditions during spring migration in Northern Africa, as reflected by the normalized difference vegetation index, have deteriorated since 1984, resulting in increased mortality among males during spring migration, but not among females, and this deterioration of climatic conditions was positively correlated with an increasing degree of protandry. Likewise, an increase in April temperatures at the breeding grounds during recent decades is positively correlated with increased protandry, apparently because males can arrive earlier without increasing the fitness cost of early arrival. Local population size did not predict changes in arrival date. These findings suggest that rapid changes in climate can cause a change in degree of protandry and secondary sexual characters.     

Sexual Selection of Zorion guttigerum Westwood (Coleoptera: Cerambycidae: Cerambycinae) in Relation to Body Size and Color

Zorion guttigerum is a flower-visiting longhorned beetle endemic to New Zealand. Sexual selection of this species in relation to the body size and color form of different sexes was investigated in the field. The population sex ratio, based on censuses of feeding and mating sites (flowers), is male-biased. Females are significantly larger than males. Both sexes have antennae of similar length but the antennal length relative to the elytral length is greater in males than in females, and the antennal length of males increases more with an increase in body size than that of females. Both sexes have dark blue (DB) and yellowish-brown (YB) individuals. Both pair-bonded and solitary males are similar in elytral and antennal length. In pair-bonded males, DB individuals are significantly more numerous than YB ones, but in solitary males, the number of both color forms is similar. Males tend to have territory protection behavior, fighting with and chasing away rival males from feeding and mating sites. Larger males usually win the fight but the size-dependent fighting advantage does not translate into mating success. Male color plays an important role in mating success, with DB males having a significantly better chance to mate than YB males. Furthermore, male body size and color also have interactions in mating success: males of DB color morph obtain a greater mating advantage according to body size. Pair-bonded females are significantly larger and have longer antennae than solitary females, suggesting that males prefer larger females for mating. In addition, females of DB color morph with longer antennae are also preferred by males for mating. The significance of these findings is discussed.     

Female‐biased dimorphism in size and age at maturity is reduced at higher latitudes in lake whitefish Coregonus clupeaformis

Female‐biased sexual dimorphism in size at maturity is a common pattern observed in freshwater fishes with indeterminate growth, yet can vary in magnitude among populations for reasons that are not well understood. According to sex‐specific optimization models, female‐biased sexual size dimorphism can evolve due to sexual selection favouring earlier maturation by males, even when sexes are otherwise similar in their growth and mortality regimes. The magnitude of sexual size dimorphism is expected to depend on mortality rate. When mortality rates are low, both males and females are expected to mature at older ages and larger sizes, with size determined by the von Bertalanffy growth equation. The difference between size at maturity in males and females becomes reduced when maturing at older ages, closer to asymptotic size. This phenomenon is called von Bertalanffy buffering. The predicted relationship between the magnitude of female‐biased sexual dimorphism in age and size at maturity and mortality rate was tested in a comparative analysis of lake whitefish Coregonus clupeaformis from 26 populations across a broad latitudinal range in North America. Most C. clupeaformis populations displayed female‐biased sexual dimorphism in size and age at 50% maturity. As predicted, female‐biased sexual size dimorphism was less extreme among lower mortality, high‐latitude populations.