Growth Studies and Ageing Methods for Adult Triturus vulgaris L. and T. cristatus Laurenti (Urodela, Salamandridae)

Growth of adult newts in southwestern Sweden has been studied from 1969 to 1972 in two ways: (1) The age of alcohol-preserved specimens has been determined by counting dark zones, which are thought to indicate hibernations, on transverse sections of bones (femur or humerus); and average body length and head width of the different age classes have been recorded and compared; (2) Free-living individuals have been identified by their ventral pattern, and body length and head width in different years have been recorded for each specimen. There was generally a small annual increase in body length and in head width, although the individual variation was large because some do not grow at all. Differences in growth were found between years, between populations and between sexes. It is concluded from these results that size should not be used for estimating the age of adult newts.     

Sex differences in age structure, growth rate and body size of common frogs Rana temporaria in the subarctic

The thermal environment and length of the activity season are important factors in shaping life-history trait variation in ectotherms. Many ectothermic vertebrates living at high latitudes or altitudes tend to be larger and older than their conspecifics living at lower latitudes or altitudes. However, detailed data on age, body size and growth variation—and how they may differ between males and females—are still scarce, especially from extreme high-latitude environments. We studied growth (body length increment), age and size structure of common frogs (Rana temporaria) in subarctic Finland (69°04′N) by applying skeletochronological methods to individually marked adults (n?=?169) captured and recaptured between 1999 and 2003. We found that breeding males were on average younger (mean?=?8.5?years) than females (11.9?years) and that males started reproducing earlier (≥3–4?years of age) than females (>4–5?years). The oldest encountered individual was an 18-year-old female, which to our knowledge is the oldest wild common frog ever reported. Females were on average larger (mean body length?=?76.6?mm) than males (70.7?mm), and this appeared to be mainly due to their older age as compared to males. While body length increased and growth rate decreased with age in both sexes, growth rate declined significantly faster with age in males than in females. The latter finding provides a proximate explanation for the observation that even after accounting for age differences among sexes (females?>?males), females were longer than males.     

Dynamics of telomere length in captive Siamese cobra (Naja kaouthia) related to age and sex

Telomeres comprise tandem repeated DNA sequences that protect the ends of chromosomes from deterioration or fusion with neighboring chromosomes, and their lengths might vary with sex and age. Here, age‐ and sex‐related telomere lengths in male and female captive Siamese cobras (Naja kaouthia) were investigated using quantitative real‐time polymerase chain reaction based on cross‐sectional data. A negative correlation was shown between telomere length and body size in males but not in females. Age‐related sex differences were also recorded. Juvenile female snakes have shorter telomeres relative to males at up to 5 years of age, while body size also rapidly increases during this period. This suggests that an accelerated increase in telomere length of female cobra results from sex hormone stimulation to telomerase activity, reflecting sexually dimorphic phenotypic traits. This might also result from amplification of telomeric repeats on sex chromosomes. By contrast, female Siamese cobras older than 5 years had longer telomeres than males. Diverse sex hormone levels and oxidative stress parameters between sexes may affect telomere length.     

Growth and development of the European ferret (Mustela putorius)

Body weight, body length, and other developmental parameters were studied in the European ferret, Mustela putorius, from birth to 26 weeks of age. Males and females did not differ in weight until the seventh week of live, and they did not differ in length until the ninth week of life, when the males began to grow faster. Adult males (1400--1500 g) were heavier than adult females (800--900 g), but females reached adult size faster than males.     

Ontogeny and sexual dimorphism in a captive population of juvenile striped skunks <Emphasis Type="Italic">Mephitis mephitis</Emphasis>

Three main hypotheses can explain the origin of the sexual size dimorphism: (1) the birth-size hypothesis, which states that birth size of males is larger than that of females; (2) the growth-rate hypothesis, which states that males grow faster than females; (3) the growth-length hypothesis, which states that males grow for a longer period of time than females. We examined the factors that may contribute to sexual size dimorphism with growth data of striped skunks Mephitis mephitis Schreber, 1776 held in captivity in Manitoba (Canada), from 7 to 72 days of age. At seven days of age, the mass of male skunks (mean = 79.7 g ± 13.9 SE, n = 37) was significantly larger than that of females (mean = 71.2 g ± 15.0 SE, n = 35) but the head and body length was not statistically different between males (mean = 110.3 mm ± 8.0 SE, n = 37) and females (mean = 95.3 mm ± 7.4 SE, n = 35). There was no difference in growth rate for mass or for length between sexes. We were not able to test for a difference in growth length between sexes. Our results suggest that mass dimorphism occurs early in life.     

Body size, age and reproduction in the Smooth newt, Triturus vulgaris

Data on the relationships between individual body size, age and reproduction were obtained for a sample of Smooth newts collected from several sites in southern England. Age was determined by counting lines of arrested growth in histological sections of humerus. In males and females, body size increases with age, but only in the former sex is the correlation statistically significant. In both sexes, there is great inter-individual variability in body size within a year class. Measures of fecundity (testis size, ovary size, clutch size and oocyte size) are positively correlated with body size, but not age. The timing of first reproduction does not seem to depend on the attainment of a fixed body size; the earliest age at first reproduction is two or three years. Together with information obtained during previous studies, the data we present support the hypothesis that the Smooth newt may be an r -selected, colonizing species.     

Age, growth, reproduction and mortality of the striped seabream, Lithognathus mormyrus (Pisces, Sparidae), off the Canary Islands (Central-east Atlantic)

Striped seabream, Lithognathus mormyrus L. (n=731) caught off the Canary Islands from January 1999 to June 2000 were studied. Fish ranged in size from 113 to 372 mm total length, weighing from 21.1 to 748.2 g total weight. Weight increased allometrically with size (b=2.9071). Fish age was 0–10-years-old. Growth was relatively slow (k=0.88 years⁻¹), with females growing at a slightly faster rate than males. The species displayed protandric hermaphroditism. Male : female ratio was unbalanced in favour of males (1 : 0.85). Males predominated in smaller sizes, females in larger sizes, and intersexual individuals were in intermediate sizes. The reproductive season extended from June to December, with a peak in spawning activity in August–September. Males reached maturity at 207 mm (2 years) and females at 246 mm (3 years). The real value of instantaneous rate of natural mortality was between 0.30 and 0.45 years⁻¹.     

Life history of harbor porpoises (Phocoena phocoena) in Scottish (UK) waters

Life history parameters were determined for stranded and bycaught harbor porpoises (Phocoena phocoena) from Scottish (UK) waters (1992–2005). Fetal growth rate was 84.4 mm/mo and mean size at birth was 76.4 cm (range 65–88 cm). Males and females had a similar range of body lengths (65–170 cm and 66–173 cm, respectively), although asymptotic lengths were higher in females than males (approximately 158 cm and 147 cm, respectively). Nonpregnant females were significantly lighter, in relation to their length than males. Maximum estimated age was 20 yr for both sexes. Age at sexual maturity (ASM) was estimated as 4.35 yr in females and 5.00 yr in males. Conception occurred mainly in July and August although reproductively active males were recorded during April to July. Gestation lasted 10–11 mo, with calving mainly between May and July. Lactating females were recorded during June to November, while small calves with solid food in their stomachs were found mainly during February to May. Estimated pregnancy rate (0.34–0.40) is lower than recorded elsewhere, but is likely underestimated due to the prevalence of mature females of poor health status in the sample. Nevertheless, cetacean strandings can be an essential source of data on demographic parameters.     

Growth, size and age at maturity of the agile frog (Rana dalmatina) in an Iberian Peninsula population

The mean age of a population of agile frogs (Rana dalmatina) from the Iberian Peninsula was estimated using mark and recapture and skeletochronology. Life-history parameters, including growth rate, body length, age and size at maturity, sexual dimorphism and longevity, were studied. The regression between age and snout-vent length (SVL) was highly significant in both sexes. Males reached sexual maturity at two years of age, although sometimes they can reach it at only one year of age. The average SVL at maturity was 51.75 mm (standard error (SE) = 0.71; n = 45). Females reached sexual maturity at two years of age with an average SVL of 62.14 mm (SE = 2.20; n = 14). A subset of the female population reached sexual maturity at three years of age. Growth was rapid until sexual maturity was reached. There was an overlap of SVL between different age classes. Growth was continuous, fulfilling the conditions of Von Bertalanffy's model. The growth coefficient (K) was 0.840 in males and 0.625 in females. The maximum SVL was greater in females (73.00 mm) than in males (59.50 mm). Sexual dimorphism was significantly biased towards females in all age classes. The maximum longevity observed was 6 years in females and 8 years in males. Management strategies for agile frogs should take into account factors such as these life-history characteristics.     

水丰水库的池沼公鱼生物学

本文报道了1942年横断鸭绿江而成的水丰水库的池沼公鱼生物学,内容包括性状变异、年龄和生长、食性、繁殖、群体结构、群体消长变化及渔业利用。水丰水库的池沼公鱼一龄体长(到尾叉的体长,后同)74毫米,体重3克;二龄体长99毫米,体重6.5克。体长体重关系式:logW=2.5306logL-1.7590。主要以浮游动物为食,但不同栖息地点食物组成有明显差异。一龄即达性成熟;性比为1♀:1.24♂;个体繁殖力905—19051粒,平均4330粒;个体繁殖力Y(百粒鱼卵)与体长L(厘米)的相关方程式为Y=58.4860L-402.7606;群体增殖速度(Vp)等于1494;4至5月在水库岸边产卵,卵粘性,水温10—15℃,约经12天孵出仔鱼。群体由1—3龄3个龄组组成,1321尾标本的平均年龄为1.15;65.1—80毫米体长组的个体为主要渔获对象,占整个渔获的65.5%。池沼公鱼是目前水丰水库第一位的经济鱼类,1982年鱼产量120万斤,占总鱼产的57.8%。       

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.     

Ontogeny of sexual dimorphism in the Long-tailed Manakin Chiroxiphia linearis: long maturation of display trait morphology

Males of dimorphic species often show ornaments that are thought to have evolved through female choice or/and male–male competition. The sexual differentiation of similar morphologies occurs during ontogeny, resulting in differential sex and age-specific selection. The Long-tailed Manakin is a dimorphic species with a highly skewed mating system, the males of which delay plumage maturation over 3 to 4 years. We describe ontogenetic changes in feather morphology in this species through sexual maturity. Males showed a significant increase in length of the central rectrices with age, hence their degree of sexual dimorphism increased from zero in 1-year-old males to 189.5% in adults. In contrast, male tail length decreased with age. Wing length did not vary significantly with age, but females had relatively longer wings than males. Wing loading was greater in females and decreased with age in males. In adults, rectrix length was positively correlated with testis volume, supporting the hypothesis that secondary sexual characters can signal the condition of primary sexual characters. Rectrix length showed positive allometry with body size in males less than 4 years old, whereas older males showed negative allometry and females showed isometry. Wing area and wing loading shifted from negative to positive allometry in males of 2 to 3 years of age. Changes in male morphology during ontogeny in the Long-tailed Manakin appeared to be associated with their specific display behaviours. Age-related changes in allometric growth of rectrices in the Long-tailed Manakin suggested that young males invest disproportionately more in the length of this trait relative to their body size. This investment could act as a signal of competitive ability to move status position in their orderly queue.     

External morphology of the short-beaked common dolphin, Delphinus delphis: growth, allometric relationships and sexual dimorphism

Growth, allometric relationships and sexual dimorphism are described from measurements of 105 male, 149 female and 38 unsexed specimens of short‐beaked common dolphin, Delphinus delphis, stranded along the Irish coastline (53.8% of the sample) or by‐caught in fisheries (46.2% of the sample), from 1990 to 2003. For each dolphin, 24 external body length measurements were recorded. Ages were determined for 183 dolphins by analysis of growth layer groups in the dentine. Males ranged in total body length (TBL) from 105 to 231 cm and females from 93 to 230 cm, with a maximum age of 25 years obtained for both sexes. Using a single Gompertz growth curve, asymptotic values obtained for TBL were 211.6 cm and 197.4 cm for males and females, respectively. Asymptotic lengths were attained at 11 years in males and 9 years in females. The gestation period was estimated to last approximately 11.5 months. Sexual size dimorphism (SSD) was evident, with males being significantly larger than females for 20 of the characters measured, and an SSD ratio of 1.06 was obtained. Sexual shape dimorphism was lacking, except for the presence of prominent postanal humps in mature males.     

大凉螈繁殖生态

大凉螈是我国特有的珍稀有尾两栖动物,其种群数量目前呈现明显下降趋势,然而涉及该物种保护的繁殖生态学研究仍十分匮乏。通过融合围栏陷阱及标志重捕的样方调查法,对大凉螈石棉栗子坪种群繁殖个体和变态登陆幼体的迁徙、繁殖群体种群大小、繁殖场内雌雄有效性比变化等进行了研究。运用Jolly-Seber法估测了繁殖种群大小,运用单因素方差分析或Kruskal-Wallis秩和检验比较了不同时期进入繁殖场的雄性大凉螈头体长及体重,运用t检验或者Wilcoxon秩和检验比较了雌雄性间形态上的差异,运用t检验、t′检验或Wilcoxon秩和检验比较了野外抱对雄性与非抱对雄性间的体征差别,运用Pearson相关分析探讨了雌性产卵量与其身体形态的关系,同时观察了卵的孵化情况。研究结果表明:大凉螈的繁殖季为每年的4月下旬到7月下旬,幼体最早于8月上旬变态登陆。估测调查地繁殖场内雄性大凉螈繁殖种群大小约为391尾,雄螈较雌螈更早进入繁殖场且在场内停留时间更长,体重较轻的雄螈较晚迁入繁殖场。有效性比明显偏雄(雌/雄:0.03—0.10)。雌雄间具明显性二型性,雌性个体的头体长、体重及肥满度均大于雄性,而雄性的尾高和尾长占全长的比例则大于雌性。对比自然抱对雄性和非抱对雄性个体发现,抱对个体在头体长、体重和尾高等体征方面显著大于非抱对个体,暗示这些形态特征可能在雄性竞争配偶的过程中起到关键作用。雌螈在室内条件下平均产卵数为176枚,产卵历时2—4 d,产卵量与雌性肥满度正相关,卵的平均孵化期为15.7 d,孵出幼体平均全长为9.74 mm。     

Aspects of the biology of Pilot whales (Globicephala melaena) in recent mass strandings on the British coast

Five mass strandings of Pilot whales, involving from 23 to 40 animals, occurred on the British coast between 1982 and 1985. The sex ratio in all strandings was biased towards females (62% overall), but more than one mature male was present in each group. A multi-male, polygynous social system is suggested. Growth is rapid from a mean body length at birth of 1.78 m to about 3 m at 2–3 years. Thereafter, males grow faster than females and attain a greater body length by some 18–25%. Maximum body lengths in this study were of a 6.3 m male and a 5.5 m female. The greatest ages determined were of a 20-year-old male and a 25-year-old female, but there is a possibility that readable dentine is not deposited in the teeth of older animals and that some whales are thus of a greater age than can be detected. Females become sexually mature at about seven years of age and a body length of 3–4 m. Some reach sexual senility before death. Males mature at a greater age and at about 5 m in length. Annual calf production is about 11% and no seasonality in parturition could be detected. Pollutant levels are generally within the range of those published for odontocetes, but PCB levels are higher than any yet found in other Pilot whale populations. Evidence of squid was found in three digestive tracts. Blubber thickness increases with the size of the animal, reaching 35–65 mm in adults. The existence of an annual, rigid north-south migrational pattern is unlikely.     

The growth of charr, Salvelinus willughbii Günther, in Windermere

The growth of charr ( Salvelinus willughbii Günther ) caught in Windermere from 1941–1952 has been studied. Scales were used for determination of age and back-calculation of length for age. Autumn and spring spawners, males and females, and charr of normal and dwarf growth were treated separately. In fish of normal growth, the spring spawners were significantly smaller than the autumn spawners at ages 1 and 2 years, and significantly larger from age 4 years onwards. There was little difference in growth between males and females within the two spawning populations. Charr of lengths of less than 200 mm at age 4 years were considered to be dwarfs. Mean lengths at capture of male charr were: autumn spawners normal growth 272 mm, dwarf 218 mm; spring spawners normal growth 327 mm, dwarf 194 mm. The oldest recorded age was 8 years.     

东方蝾螈性二型性特征分析

以东方蝾螈大别山种群为实验材料,随机选取162只蝾螈(雄52只,雌110只),通过单变量、双变量、多变量分析的方法,进行11项体征的测量分析.结果表明,头体长是本研究的最适单变量,且头体长与腋胯距之间的相关性最高;PCl在雄性和雌性中均与头体长密切相关,且大多数体征与头体长进行比例分析均显示出异速生长关系,东方蝾螈性二型性普遍存在.本研究中11项体征呈现符合Renseh法则的雌性依赖性二型性演化特征,这种性二型性特征可能是一系列复杂的非对称性选择的结果.     

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 structure and body size of the Chuanxi Tree Frog Hyla annectans chuanxiensis from two different elevations in Sichuan (China)

Age, body size, and growth patterns in the subtropical anuran Hyla annectans chuanxiensis from high (Dengchigou Protection Station) and low (Lingguan Town) elevations in Baoxing County of Sichuan province (China) were described using skeletochronology. Females were significantly older than males at the low-elevation site, but there was no significant difference between the sexes at the high-elevation site. Age at sexual maturity of both males and females was 2 years at the high-elevation site, whereas males matured at 1 year and females at 2 years at the low-elevation site. Males and females from the low-elevation population reached a maximum age of 3 and 4 years, respectively, whereas males and females from the high-elevation population reached a maximum age of 4 and 5 years, respectively. At both sites, females were significantly larger than males. Females and males from the high-elevation population were larger than individuals from the low-elevation population. When the effect of age was controlled, the differences in body size of the two populations were significant only for females. Von Bertalanffy growth curves indicated that the growth rates in males was greater than in females in both populations. They also showed that the growth of both sexes slowed at an earlier age in the low-elevation population than in the high-elevation population. The findings suggest that age is a major factor underlying body size patterns for both sexes, but that the elevation of the locality affects the body size of females.