Early growth in male and female fallow deer fawns

In this paper we present data from a long-term study on earlygrowth and related variables in fallow deer fawns living inlarge enclosures. Pre-winter body mass was constantly higherand more strongly correlated to subadult body mass in malesthan in females. To find out the mechanism for this higher pre-wintermass in males, we analyzed the variation in pre-winter massin relation to sex, year, mother's body mass, age and parityof mother, birth date, birth mass, growth rate, suckling behavior,and other behaviors. Birth mass was higher for male fawns, andgestation length, birth date, and weaning date did not differbetween the sexes. Consequently, both pre- and postnatal growthwere faster in males than in females. No behavioral differenceswere found between the sexes that could explain the differencein postnatal growth. Pre-winter mass was positively relatedto mother's body mass. Heavy mothers gave birth earlier andto larger offspring who grew at a higher rate, independent ofoffspring sex. However, male fawns born to primiparous mothershad relatively lower growth than male fawns born to multiparousmothers. This was not the case for female fawns. Suckling timeafter the first 2 weeks was positively related to mother's bodymass and growth of offspring. However, no measurements of sucklingbehavior differed between male and female fawns. Our results,except for the effect of parity on male and female growth, indicatethat selection has not acted on mothers to promote faster earlygrowth in males.     

Effects of cohort,sex, and birth date on body development of roe deer (Capreolus capreolus) fawns

We investigated the effects of the year of birth (cohort effect), sex and birth date on the variations observed in birth weight and postnatal growth rate in 209 newborn fawns marked during eight consecutive fawning seasons from a highly productive roe deer population under good nutritional conditions. Roe deer exhibited a fast body development with a birth weight of 1628 g and a postnatal growth rate of 139 g/day constant over the first 20 days of their life. As previously reported for dimorphic and polygynous ungulates, there was a marked cohort effect on the rate of body development. This variability was partly explained by climatic conditions during late gestation. When fewer than 5 days with rainfall over 5 mm occurred in April, fawns were heavier. High temperatures during April and during the winter could also be involved in fast body development of roe deer fawns. Sex of fawn did not affect roe deer growth pattern. This was expected on the basis of low sexual dimorphism in size and low polygyny level characteristic of roe deer. Lastly, the date of birth did not affect the body development of roe deer fawns. High constancy of mean birth dates and high synchrony of births observed in this population could account for this result.     

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.     

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.     

Body size, age and paternity in common brushtail possums (Trichosurus vulpecula)

Sexual selection should produce sexual size dimorphism in species where larger members of one sex obtain disproportionately more matings. Recent theory suggests that the degree of sexual size dimorphism depends on physical and temporal constraints involving the operational sex ratio, the potential reproductive rate and the trade-off between current reproductive effort and residual reproductive value. As part of a large-scale experiment on dispersal, we investigated the mating system of common brushtail possums inhabiting old-growth Eucalyptus forest in Australia. Paternity was assigned to 20 of 28 pouch-young (maternity known) genotyped at six microsatellite loci. Male mating success was strongly related to body size and age; male body weight and age being highly correlated. Despite disproportionate mating success favouring larger males, sexual size dimorphism was only apparent among older animals. Trapping and telemetry indicated that the operational sex ratio was effectively 1 : 1 and the potential reproductive rate of males was at most four times that of females. Being larger appeared to entail significant survival costs because males 'died-off' at the age at which sexual size dimorphism became apparent (8-9 years). Male and female home ranges were the same size and males appeared to be as sedentary as females. Moreover, longevity appears to be only slightly less important to male reproductive success than it is to females. It is suggested that a sedentary lifestyle and longevity are the key elements constraining selection for greater sexual size dimorphism in this 'model' medium-sized Australian marsupial herbivore.     

Reproductive strategies and the influence of date of birth on growth and sexual development of an aseasonally-breeding ungulate: Reeves' muntjac (Muntiacus reevesi)

Unlike most species of deer, Reeves' muntjac does not have a seasonal reproductive cycle. Births are equally distributed throughout the year and, irrespective of season of birth, females start breeding when they have reached a minimum body weight of about 10 kg. A significantly smaller proportion of females is born in the autumn/winter than the spring/summer, but there is no effect of maternal age or condition on foetal sex ratios for first or subsequent pregnancies. Whilst aseasonal breeding increases female productivity, males are only able to hold territories encompassing the ranges of a number of does for a relatively short period of time. It is argued that for muntjac there is much less inter-sexual variation in lifetime reproductive success than for seasonally-breeding polygynous cervids. Hence, although muntjac are sexually dimorphic and polygynous, females do not invest preferentially in male offspring.
Young males can be fertile from 36 weeks of age, when their first antlers are still in velvet. Whilst season of birth has no effect on the rate of sexual development in females, it does for males, with autumn-born male fawns attaining sexual maturity earliest. This accelerated development occurs in the period following independence from the mother, and there is no evidence of a maternal cost in producing male fawns. Since the canine tusks are the main weapons for intra-sexual conflict, there could be clear gains in terms of reproductive success for males that attain sexual maturity, adult weight and adult tusk size quickly, even though their first antlers are much smaller than those of older bucks. The hypothesis is presented that, for muntjac, the majority of a male's lifetime reproductive success is achieved relatively early in life when the canine tusks are in pristine condition, and that bucks lose their territories, and associated access to oestrous does, once the canines are broken.     

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 Role of Sex-specific Plasticity in Shaping Sexual Dimorphism in a Long-lived Vertebrate,the Snapping Turtle <Emphasis Type="Italic">Chelydra serpentina</Emphasis>

Sex-specific plasticity, the differential response that the genome of males and females may have to different environments, is a mechanism that can affect the degree of sexual dimorphism. Two adaptive hypotheses have been proposed to explain how sex-specific plasticity affects the evolution of sexual size dimorphism. The adaptive canalization hypothesis states that the larger sex exhibits lesser plasticity compared to the smaller sex due to strong directional selection for a large body size, which penalizes individuals attaining sub-optimal body sizes. The condition-dependence hypothesis states that the larger sex exhibits greater plasticity than the smaller sex due to strong directional selection for a large body size favoring a greater sensitivity as an opportunistic mechanism for growth enhancement under favorable conditions. While the relationship between sex-specific plasticity and sexual dimorphism has been studied mainly in invertebrates, its role in long-lived vertebrates has received little attention. In this study we tested the predictions derived from these two hypotheses by comparing the plastic responses of body size and shape of males and females of the snapping turtle (Chelydra serpentina) raised under common garden conditions. Body size was plastic, sexually dimorphic, and the plasticity was also sex-specific, with males exhibiting greater body size plasticity relative to females. Because snapping turtle males are larger than females, sexual size dimorphism in this species appears to be driven by an increased plasticity of the larger sex over the smaller sex as predicted by the condition-dependent hypothesis. However, male body size was enhanced under relatively limited resources, in contrast to expectations from this model. Body shape was also plastic and sexually dimorphic, however no sex by environment interaction was found in this case. Instead, plasticity of sexual shape dimorphism seems to evolve in parallel for males and females as both sexes responded similarly to different environments.     

Ontogenetic scaling of the human nose in a longitudinal sample: Implications for genus Homo facial evolution

Researchers have hypothesized that nasal morphology, both in archaic Homo and in recent humans, is influenced by body mass and associated oxygen consumption demands required for tissue maintenance. Similarly, recent studies of the adult human nasal region have documented key differences in nasal form between males and females that are potentially linked to sexual dimorphism in body size, composition, and energetics. To better understand this potential developmental and functional dynamic, we first assessed sexual dimorphism in the nasal cavity in recent humans to determine when during ontogeny male‐female differences in nasal cavity size appear. Next, we assessed whether there are significant differences in nasal/body size scaling relationships in males and females during ontogeny. Using a mixed longitudinal sample we collected cephalometric and anthropometric measurements from n = 20 males and n = 18 females from 3.0 to 20.0+ years of age totaling n = 290 observations. We found that males and females exhibit similar nasal size values early in ontogeny and that sexual dimorphism in nasal size appears during adolescence. Moreover, when scaled to body size, males exhibit greater positive allometry in nasal size compared to females. This differs from patterns of sexual dimorphism in overall facial size, which are already present in our earliest age groups. Sexually dimorphic differences in nasal development and scaling mirror patterns of ontogenetic variation in variables associated with oxygen consumption and tissue maintenance. This underscores the importance of considering broader systemic factors in craniofacial development and may have important implications for the study of patters craniofacial evolution in the genus Homo. Am J Phys Anthropol 153:52–60, 2014. © 2013 Wiley Periodicals, Inc.     

Variation in maternal investment in a small cervid; the effects of cohort,sex, litter size and time of birth in roe deer (Capreolus capreolus) fawns

 We investigated the effects of cohort, sex, litter size and time of birth on birth weights and postnatal growth rates of roe deer fawns in a highly reproductive Norwegian population. By repeatedly recapturing radio-collared individuals, a total of 950 weights were obtained from 231 fawns of known age. In accordance with earlier studies, there was a period of linear growth during the first month following birth. Mean postnatal growth rates of 155 g/day are the highest yet recorded for roe deer; however, the mean birth weights of fawns were lower than those reported from populations in continental Europe. During the period of linear growth, we found no sex differences. However, growth rates were affected both by time of birth and litter size; fawns born early had lower growth rates than fawns born during or after the peak calving period, and fawns in triplet – groups had lower growth rates than either fawns in twin – groups or single fawns. Despite a fourfold increase in population density during the study, this factor was not able to explain variation in postnatal growth rates, although cohort effects on birth weight were evident. Received: 13 May 1996 / Accepted: 26 June 1996     

云南星云湖长臀云南鳅两性异形及其生境适应性

云南鳅属鱼类是云贵高原及邻近区域特有鱼类,其独特两性异形现象可能是对喀斯特高原特定生境的一种重要适应。本文对云南星云湖特有鱼类长臀云南鳅两性异形、个体繁殖力及与之关联的雌雄摄食分化问题进行了研究,以揭示其两性异形特征并探讨其与生境的关系。结果表明: 长臀云南鳅两性异形指数为0.23,表明它是偏向于雌性体型较大的两性异形类型。同时,雌雄外部形态存在明显的色斑差异,雌鱼体侧密布横向色斑,而雄鱼体侧则有一明显的纵向条纹,横向色斑稀少或缺乏。单因素方差分析、主成分分析、判别分析及单因素相似性分析(ANOSIM)等进一步证实长臀云南鳅雌雄形态性状明显分离,全长、叉长、体长、头宽/头长、腹鳍起点-胸鳍起点(JK)/体长等对两性形态差异起主导作用。雌鱼繁殖力为(1364.5±489.3)粒,变化幅度为470~2430粒,其繁殖力随体长的增长而增大。食物分析显示,长臀云南鳅以摇蚊幼虫、蜉蝣稚虫为主要食物,食性较为狭窄。雌雄长臀云南鳅食物组成较为相似,但两者具有统计学意义上的显著差异。繁殖力选择压力、食物分化等可能对星云湖长臀云南鳅两性异形的形成起重要驱动作用,而两性异形的出现是长臀云南鳅对喀斯特贫营养龙潭生境的一种重要适应。     

Sexual dimorphism and ontogenetic allometry of soft tissues in Rattus norvegicus.

Most studies of sexual dimorphism in mammals focus on overall body size. However, relatively little is known about the differences in growth trajectories that produce dimorphism in organ and muscle size. We weighed six organs and four muscles in Rattus norvegicus to determine what heterochronic and allometric scaling differences exist between the sexes. This cross-sectional growth study included 113 males and 109 females with ages ranging from birth to 200 days of age. All muscle and organ weights were ultimately greater in males than in females, because males grew for a longer period of time, had a greater maximum rate of growth, and spent more time near the maximum rate. No ontogenetic scaling differences existed between the sexes in organ weight except for lungs and gonads. During growth, organ weights were negatively allometric to body weight. No scaling differences relative to body weight existed between the sexes for muscles; however, there was variation in the allometric relations among muscles relative to body weight. Sexual dimorphism in muscles and organs appears to be a size difference resulting from differences in the duration and rates of growth.     

Relations among measures of body composition, age, and sex in the common marmoset monkey (Callithrix jacchus)

Few studies of body composition have been done in New World primates. In the study reported here, four methods of assessing body composition (body weight, anthropometry, labeled-water dilution, and total body electroconductivity) were compared in 20 marmosets, aged 0.96 to 7.97 years. Males and females did not differ in any measure (P > 0.05). Body weight ranged from 272 to 466 g, and body fat estimates varied from 1.6 to 19.5%. Strong positive correlations were observed between total body water and total body electroconductivity (R2 = 0.77), body weight and fat-free mass (males R2 = 0.95; females R2 = 0.91), and body weight and fat mass (males R2 = 0.86; females R2 = 0.85; P < 0.01). Male and female slopes were equivalent (P > 0.05) for the regressions of fat and fat-free mass against body weight. Positive correlations also were observed between girth measures and fat-free mass (R2 = 0.48 to 0.78) and fat mass (R2 = 0.60 to 0.74; P < 0.01). A good second- order polynomial relationship was observed between age and fat-free mass for the combined sample (R2 = 0.64). Results indicated that: subjects were lean; there was no sexual dimorphism relative to measures; body weight provided a reliable estimate of fat and fat-free mass; and within-subject body weight changes reflected a similar relationship between body weight and fat-free mass as did that across subjects.     

Sexual dimorphism and species differences in the neurophysiology and morphology of the acoustic communication system of two neotropical hylids

We examined auditory tuning and the morphology of the anatomical structures underlying acoustic communication in female Hyla microcephala and H. ebraccata and compared our findings to data from a previous study (Wilczynski et al. 1993) in which we showed species differences in the traits that in males relate to differences in the species-typical calls. Female species differences in the best excitatory frequency (BEF) of the basilar papilla (BP) were similar to the differences seen in males, and females had a significantly lower BEF in H. ebraccata, but not H. microcephala. In both species, females had lower BP thresholds. Snout-vent length, head width, and tympanic membrane diameters were sexually dimorphic in both species and larger in females, whereas laryngeal components were sexually dimorphic and larger in males. Middle and inner ear volumes were not sexually dimorphic. Despite the significant species differences in laryngeal morphology seen in males, female larynges are not significantly different. Furthermore, the interaction of species and sex differences resulted in significantly different degrees of sex dimorphism in the species, particularly for the larynx, which is more sexually dimorphic in H. microcephala, and measures of body size, which are more dimorphic in H. ebraccata. Accepted: 6 December 1996     

Patterns of growth in wild bottlenose dolphins, Tursiops truncatus

The growth of bottlenose dolphins is described from observations made during a capture release programme that has operated in coastal waters of the eastern Gulf of Mexico from 1970 to the present. Measurements of standard length, girth and body mass were recorded from 47 female and 49 male dolphins, some captured as many as nine times. Ages were known from approximate birth dates or estimated from counts of dentinal growth layers. In all three measurements. females grew at a faster initial rate than males, but reached asymptotic size at an earlier age. This extended period of growth in males resulted in significant sexual dimorphism in length, girth and mass at physical maturity. The growth of both sexes was well described by three-parameter Gompertz models using either cross-sectional data or a mixture of longitudinal and cross-sectional data. There was considerable variation in size-at-age for both sexes in all year classes. Residuals of size measurements were used to derive measures of relative size for individual dolphins; most dolphins demonstrated little ontogenetic change in relative size. Body mass was adequately predicted by multiple regression equations that incorporated both length and girth as independent variables.     

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.     

ORIGINAL ARTICLE: Leptin associations with age,weight, and sex among chimpanzees (Pan troglodytes)

Background Leptin is a hormone secreted primarily by adipocytes, a lipostatic signal to the hypothalamus, and is often correlated with adiposity. Associations between leptin, age, and development are unknown in human’s closest evolutionary relative, the common chimpanzee (Pan troglodytes). Methods Serum leptin was assessed cross sectionally in association with age, weight, and sex in healthy captive chimpanzee males (n = 47) and females (n = 49) to test hypotheses related to predicted differences in leptin levels with body mass, development, and sexual dimorphism. Results Leptin increased with age and weight among females, but not in males. Leptin was overall higher in females compared to males. Conclusions Sex differences in leptin were most evident during adolescence and adulthood, despite similar increases in weight in both sexes indicating that sexual maturation is a key divergence point for differential somatic investment in adiposity and leptin levels between male and female chimpanzees.     

圈养条件下仔狍的生长与发育

2003 年4 月至2004 年10 月对12 只狍东北亚种雌性生产的16 只仔狍进行了生长发育观察。记录仔狍出生日期,观察生长过程的毛色变化,定期检查牙齿生长状况,测定体尺和体重,所得数据采用SPSS13. 0 软件处理,绘制生长曲线并建立体长与体重的拟合曲线方程。结果表明,圈养条件下仔狍出生主要集中在5 月中旬至6
月中旬,出生时毛色呈暗棕黄色,身体两侧分布不规则的白斑,翌年换毛后白斑消失;出生仔狍的齿式为(0 03 0 /4 0 3 0)×2 = 20,成年狍的齿式为(0 1 3 3/4 0 3 3)×2 = 34,乳齿6 ～7 月龄开始脱换,8 ～9 月龄完成,脱换的顺序为中央切齿→两侧切齿→隅齿;(上、下颌)后臼齿的第一后臼齿2 月龄萌发、3 ～ 4 月龄生长完成,第
二后臼齿6 ～ 7 月龄萌发,8 ～9 月龄生长完成,第三后臼齿12 ～ 13 月龄萌发,14 ～ 15 月龄生长完成;乳齿的前臼齿从12 月龄开始脱换,14 月龄完成,脱换的顺序是上颌第一前臼齿和下颌第三前臼齿→上、下颌第二前臼齿→上颌第三前臼齿和下颌第一前臼齿;仔狍体尺增长率顺序为体长> 臀高> 肩高> 胸围> 腰围。仔狍体长与体重的拟合曲线方程是Y = 63.1084 - 0.0070x + 1.1e ^{- 6} x² - 3e^{- 11} x³ ,生长发育过程可分为生长快速期、生长缓慢期和雌雄狍生长差异期3 个阶段。     

Patterns of sexual dimorphism from birth to senescence

Sexual dimorphism is expressed as median of the female values in percent of the median of the male values, of 4 length measurements, 3 circumferences, and 5 measurements of corpulence respectively fat. Data were obtained from a cross-sectional sample of more than 41.000 German subjects, aged from birth to age 62. The pattern of sexual dimorphism is similar in the length measurements. Girls are shorter at birth, but they increase in length at higher rates than boys and even temporarily overgrow the boys up to age 12. Thereafter, males show an obvious growth advantage leading to some 6 to 9% more length in adult males. In contrast, female circumferences are always smaller, from birth to senescence. Though, the differences between the sexes are low in circumferences, up to age 13, sexual dimorphism increases to 17% in the thoracic circumference at adulthood. Sexual dimorphism in weight and BMI is comparably with that in length measurements while subcutaneous fat and total body fat content are always higher in females. The results highlight that sexual dimorphism develops at different pace in the various components of the body and that it associates with a sex specific growth tempo.     

Costs of parturition and rearing in female sika deer (Cervus nippon)

The costs of parturition and lactation of female sika deer on Kinkazan Island (9.6 km(2) in size), northern Japan, which live at a high density (about 50 deer/km(2)), were evaluated by comparison of body weights of 481 females measured during a 15 year study (1993-2008). Weight data were chosen from only females that did not give birth in the preceding year. The mean body weight of females that did not give birth ("yelds") was significantly lower (P < 0.001) than that of females who gave birth ("milks"); yelds' body weight was 93.1% and 83.5% that of milks in the preceding and parturition years, respectively. The yelds increased in body weight by the following March by 8.2% (P < 0.001), whereas milks did not. Among the milks, those whose fawns survived until the following May ("rearing milks") lost body weight by 14.9% (P < 0.001). Milks who lost fawns within a week after birth ("early fawn-less milks") did not lose body weight (P = 0.583), while those whose fawns died after the first autumn but died before May ("late fawn-less milks") lost body weight by 19.9% (P < 0.001). These results indicate that sika deer females do not enter estrus unless they are heavy enough, and that both parturition and rearing are costly for sika deer mothers living in high-density conditions.