池塘中斑索蟾的种群结构、个体生长与存活率

在澳大利亚新南威尔士南部沿海,作者搜集了一个池塘繁殖的斑索蟾(Crinia signifera)的种群统计资料。通过捕捉进出池塘的1 612只个体,获得种群大小、结构、生长率、性成熟时的大小和年龄、死亡率及寿命资料。迁移高峰从6月持续到11月,蛙的最高、最低遇见数量分别出现在春季和秋季。但第2年,该池塘蛙的数量明显减少,可能是由于补充到种群中的幼体数量很少的缘故。6个月后个体的重捕率很低;但距第一次捕获18个月以后,仍有个别个体再次被捕获。性成熟时,雌性比雄性的身体大一些。生长曲线显示,雌性比雄性的生长更快,所以更早地达到性成熟。研究种群的数量、结构和死亡率趋势等与已知的其它Crinia signifera种群基本一致。但研究种群迁移活动的高峰出现较晚,并且夏季的活动水平明显很高。这种长的活动时间可能会导致存活率的下降,同时有利于选择迅速性成熟的雌性[动物学报51 (3) : 393 -400 , 2005]。     

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.     

Determination of growth and maturation in the common frog, Rana temporaria, by skeletochronology

Growth and maturation in a Swiss population of Rana temporaria were studied in 1983 and 1984 by means of skeletochronology. Resting line (growth ring) diameters were used to back-calculate individual body sizes in previous years; these permitted establishment of an average growth curve and determination of individual ages and sizes at first reproduction. Growth was rapid up to maturation, but continued thereafter at a decreased rate. Males were larger than females at age two but females grew faster thereafter, causing sexual dimorphism in adult body sizes. Body size distributions for both years and for frogs recaptured and first captured in 1984 were established. Growth in immatures was positively, but in adults negatively correlated with body size, with considerable variation at all sizes. Individual adult sizes were positively correlated with body sizes at the end of the first year. Average individual age at first reproduction was 2.8 years in males and 3.1 years in females (range in both sexes two to four years). There is no evidence for a two-year-cycle of reproduction.     

The effects of density,rainfall and environmental temperature on body condition and fecundity in the common toad,Bufo bufo

The body length and body weight of all adult common toads (Bufo bufo) breeding at a pond in south Dorset were measured between 1983 and 1993. Each toad was placed into one of four categories depending on its sex and whether it was either a first time breeder or an animal that had previously bred. The body condition of each male and female toad for each year was compared with the average body condition of all the male and female toads captured over the 11 years of the study so that between-year differences in condition could be detected. Changes in body condition were compared with changes in body condition were compared with changes in toad density, rainfall and climatic temperature during the previous summer (March–September), during hibernation (October–February) and during the month preceding the start of spawning. During the study there was a decline in the body condition of all toad categories and these changes were significantly correlated with changes in toad density and climatic temperature. Toads were also more likely to enter hibernation in poor condition following a hot dry summer than after either cool wet or hot wet summers. Body condition explained 41% of the size-specific variation in fecundity.     

Body size, age and reproduction in the leopard toad, Bufo pardalis

Data on the relationships between body size and age were obtained for a sample of leopard toads Bufo pardalis from a breeding population of this species from the Cape Peninsula, South Africa. Age was determined by counting the number of lines of arrested growth in histological sections of a digit clipped from each individual. In males there was a positive, but weak, correlation (explaining only 18% of the variance) between body size and age, and in females no correlation at all existed between these two variables. Males which were successful in obtaining matings were not older than unsuccessful males. Age of males at the breeding site ranged from one to three years, whereas females ranged from two to six years old. This represents both the earliest age of reproduction, as well as the greatest difference in longevity between the sexes, documented for an anuran species.     

Growth patterns,and age and size at maturity in femaleCottus hangiongensis,with special reference to their life-history variation

Growth patterns of the 1982 year-class, individual growth patterns, age and size at sexual maturity and longevity in females of the river-sculpin,Cottus hangiongensis (Cottidae), were examined along the course of the Daitobetsu River of southern Hokkaido, Japan. Growth of females slightly varied both along the river course and among individual fishes: slow growth occurs in females from the lower reaches, while more rapid growth occurs in females from upstream areas. Body size and age at the first sexual maturity of females slightly increased towards the upstream, from 52 mm SL and 2 years in the most downstream area to 72 mm SL and 2–3 years in the uppermost site. Longevity was estimated to be 7 years in the downstream areas and 8–9 years in the upstream sites. These results suggest that female life history varies along the course of the river and thus allow us to consider the following alternative reproductive tactics: when females stay in the lower reaches, they attain sexual maturity at a smaller body size and younger age, and have a small clutch size, but when females migrate into the upper reaches, their maturity is delayed until they reach a larger body size and older age, and have a greater clutch size.     

Estimation of age structure by skeletochronology of a population of Hynobius nebulosus in a breeding season (Amphibia,Urodela)

Using skeletochronology, we determined the age structure of adult Hynobius nebulosus from Kyoto in the breeding season of 1998. From previously marked individuals, the lines of arrested growth proved to be formed once per year, indicating the number of winters each salamander experienced. The age at first reproduction was estimated to be 2.8-2.9 yrs of age in males and 3.8-3.9 yrs in females. The oldest males and females were 9.8-9.9 and 5.8-5.9 yrs of age, respectively, and, therefore the longevity in this species was estimated to be more than 9 yrs for males and 5 yrs for females. The growth curve of male's body size estimated indicated that the growth rate much decreases after males attained sexual maturity. Because body sizes of adults greatly vary even within an age class, it is dangerous to estimate individual age from the size frequency data at least in adults. We discussed age properties in Hynobius by comparing lentic and lotic breeders.     

Body mass, age and sexual maturity in short-beaked echidnas, Tachyglossus aculeatus

During the course of this 12 year field study body masses of 11 hatchling echidnas (Tachyglossus aculeatus multiaculeatus) and 25 pouch young between the ages of 5 and 60 days were recorded. Body mass increased from 0.3 to approximately 50 g in the first half of pouch life. It then quadrupled before young were placed in a burrow at 45 to 55 days of age. There was a positive correlation between the body mass of the female and that of her young at weaning. From 33 subadult echidnas located, tagged and radio tracked during this study, body masses of 10 were monitored to sexual maturity, i.e. when first encountered in a courtship train. Minimum age of sexual maturity ranged between 5 and 12 years. As subadults, there was no difference between mean body masses of males and females. At sexual maturity, mean body mass of females was significantly higher. No correlation was found between age at sexual maturity and body mass nor was there a significant difference in age of males and females at sexual maturity.     

Non-random mating by size in American toads, Bufo americanus

Male American toads, Bufo americanus, captured in amplexus at least once during the season were significantly longer than males captured only singly in the same breeding population in all three cases studied. Absence of any correlation between the body lengths of the members of amplexing pairs argues against selection for optimal relative size. Males successful at breeding were those that (1) were larger, (2) were at the pond more nights, and (3) spent more time calling than unsuccessful males. Residency, per se, did not enhance breeding success, however, as on any given day successful males were equally likely to come from recaptured males previously present at the pond and unmarked males presumed new to the pond. Amount of movement about the pond did not vary with breeding success; all males tended to remain in one area on any given night and to change areas between nights. A very low displacement rate (about 7%) of males in amplexus argues against primacy of this form of male-male competition in producing differential mating by size. Rather it appears that some combination of other forms of intrasexual competition and female choice caused the mating pattern seen.     

Predation by grass snakes (Natrix natrix) at a site in southern England

The prey and feeding frequency in free-living grass snakes was studied during 1993 and 1994 at a site in southern England. Individual snakes and common toads were recognized using PIT tags and a small number of adult snakes were radio-tracked over long periods to determine predation rates.
Grass snakes fed, almost exclusively, on common toads (adult, juvenile, and tadpoles). A positive correlation was found between prey size and snake size. Large snakes did not appear to prey upon small toads, although clearly capable of doing so.
Male and female snakes ate large meals (toads) approximately every 20 days between May and September, with females fasting for a period of about 45 days during gestation and egg-laying. After allowing for differences in the number and size of toads predated by male and female snakes, the mean amount of food consumed per day was estimated to be 2.3% and 1.6% of body weight.     

Size and age at sexual maturity of female bluefin tuna (Thunnus thynnus L. 1758) from the Mediterranean Sea

The ovaries of 501 female eastern Atlantic bluefin tuna (Thunnus thynnus Linnaeus, 1758) captured in the Mediterranean Sea from May to September between 1998 and 2004 were analysed histologically. Body size at median sexual maturity (L₅₀) was 103.6 cm fork length (FL), while 100% maturity was reached above 135 cm FL. The age analysis, based on the count of the translucent zones of the first spiniform ray of the first dorsal fin, showed that most of the specimens with FL = L₅₀ were 3 years old while 100% maturity was reached between 4 to 5 years. The reported evidence indicates that for the eastern Atlantic bluefin tuna stock, the size and age of first sexual maturity of females was lower than in the western Atlantic stock.     

Sexual size dimorphism in a landlocked Pacific salmon in relation to breeding habitat features

Many animal species exhibit size dimorphism between sexes. Sexual selection, whereby male–male competition favors larger body sizes, has been considered a likely cause of sexual size dimorphism. Habitat features in breeding areas could affect the outcome of male–male competition, yet few attempts have been made to relate breeding habitat features with interpopulation variation in sexual size dimorphism. In this study, we examined interpopulation variation in sexual size dimorphism by studying the landlocked amago salmon (Oncorhynchus masou ishikawae) at a microgeographic scale. We found that female body size was independent of stream size but that male body size decreased with smaller stream sizes. A likely explanation is that the relationship between reproductive success and the size of males is influenced by the availability of refuges that are only available to small-bodied males. Sexual differences in body size increased with decreasing stream sizes, supporting the hypothesis that the reproductive success of larger males is reduced in smaller streams. In contrast, the maturation-length threshold increased with stream size for both sexes. The stream-size-based interpopulation variation in sexual size dimorphism and size at maturity in landlocked amago salmon may therefore have arisen through a combination of sexual and natural selection.     

Mixed-stock aging analysis reveals variable sea turtle maturity rates in a recovering population

Quantifying demographic parameters and variable vital rates, such as somatic growth rates, time to maturity, and reproductive longevity, is important for effective management of threatened and endangered populations such as sea turtles (Cheloniidae). To address these knowledge gaps, we applied skeletochronology to analyze and compare somatic growth rates and variation in life-history traits such as age and size at sexual maturity for 65 green turtles (Chelonia mydas) in the eastern Pacific Ocean (EP), along the west coast of the United States; turtles belonged to ≥2 nesting subpopulations that differed in body size (mean nesting size). Green turtles in the EP spend approximately 5 years in the oceanic stage before recruiting to nearshore habitats, males may be smaller and younger than females at maturation (x̅ = 17.7 ± 5.5 yr vs. 28.0 ± 8.2 yr), and younger age at sexual maturity was associated with smaller size at sexual maturity, suggesting that mean nesting body size may be reflective of maturation timing for subpopulations. Smaller body sizes for females nesting at Michoacán, Mexico (continental) rookeries, yielded a younger predicted age at sexual maturity (x̅ = ~17 yr) compared to females from Revillagigedo Islands, Mexico rookeries, which displayed larger body sizes and older age at sexual maturity (x̅ = ~30 yr). We consider possible mechanisms driving the observed divergence in life-history traits, including the possibility that earlier maturation (reduced generation length) for turtles in the Michoacán nesting subpopulation may be a response to intense harvesting in the past 50 years, and consideration of such anthropogenic impacts is warranted by population managers. Finally, our results indicate green turtles moved into nearshore neritic habitats at a young age (4–6 yr), emphasize the importance of protecting neritic habitats along the southwestern United States and northwestern Mexican coasts, and encourage the incorporation of variable maturation time in population recovery assessments.     

Determinate growth in a paternal mouthbrooding fish whose reproductive success is limited by buccal capacity

The life history of the paternal mouthbrooding cardinal fish Apogon doederleini was investigated in the temperate waters of Japan, with particular reference to its growth and reproductive rate. Both males and females almost ceased to grow at age 3 years, although living to 7 years of age. Their growth pattern, represented by the relative size at sexual maturity to the asymptotic size and the von Bertalanffy growth coefficient, was among the most determinate in ectothermic vertebrates. Brood size just before hatching increased in proportion to the second power of the body size of the brooding male, and correlated more positively with the male's than the female's body size, suggesting that it was limited by the male's buccal capacity. The estimated total number of broods hatched in a breeding season showed a weak or no correlation with the body size or age in either sex. Using life-history parameters based on data of A. doederleini, a simulation model of energy allocation without considering sexual interaction revealed that the optimal growth pattern shows an indeterminate growth that differs greatly from the actual growth pattern of A. doederleini. This suggests that there are some brooding constraints to size-advantage of reproductive success in this species. The possible mechanism of such reproductive constraint is discussed.     

Sexual maturity and shape development in cranial appendages of extant ruminants

Morphological disparity arises through changes in the ontogeny of structures; however, a major challenge of studying the effect of development on shape is the difficulty of collecting time series of data for large numbers of taxa. A proxy for developmental series proposed here is the age at sexual maturity, a developmental milestone potentially tied to the development of structures with documented use in intrasexual competition, such as cranial appendages in Artiodactyla. This study tested the hypothesis that ruminant cranial appendage shape and size correlate with onset of sexual maturity, predicting that late sexual maturity would correlate with larger, more complicated cranial appendages. Published data for cranial appendage shape and size in extant taxa were tested for correlations with sexual maturity using linear mixed‐effect models and phylogenetic generalized least‐squares analyses. Ancestral state reconstructions were used to assess correlated variables for developmental shifts indicative of heterochrony. These tests showed that phylogeny and body mass were the most common predictors of cranial appendage shape and sexual maturity was only significant as an interaction with body mass. Nevertheless, using developmental milestones as proxies for ontogeny may still be valuable in targeting future research to better understand the role of development in the evolution of disparate morphology when correlations exist between the milestone and shape.     

Population fluctuations, reproduction and survival in the Striped fieldmouse Rhabdomys pumilio on the Cape Flats, South Africa

A wild population of Striped fieldmice was studied for a continuous period of five years in an area of alien Acacio bush about 24 km from Cape Town, South Africa. Mice were live-trapped, marked by toe-clipping and released on a 60-station grid, and also kill-trapped in a separate area. Marked annual fluctuations in the population size were correlated with a 6–8 month summer breeding season. There were also marked inter-annual differences in peak population size. The age of sexual maturity of females was determined from the first pregnancy which occurred at 6–7 weeks old; and of males from the presence of visible spermatozoa in the vas deferens which occurred at about 11 weeks old. Litter size was affected by both the age and the body mass of the female. It appeared that mean survival from birth was only approximately 1.5 months and that survival from first capture was about 1.9–2.5 months. This high mortality appeared to be the major reason for the sharp seasonal fluctuations in population size and may also have been responsible for the interannual differences since marked changes in survival were recorded between some years.     

Differences in life-history traits in two clonal strains of the self-fertilizing fish, <Emphasis Type="BoldItalic">Rivulus marmoratus</Emphasis>

Synopsis We compared life-history traits such as fecundity, sex ratio, reproductive cycle, age at sexual maturity, embryonic period, egg size, early growth and morphology in two clonal strains (PAN-RS and DAN) of the mangrove killifish, Rivulus marmoratus, under constant rearing conditions. We found a positive relationship between growth and reproductive effort. Fecundity was significantly higher in the PAN-RS strain than in the DAN strain. The sex ratio was significantly different, with DAN producing more primary males than PAN-RS. Spawning and ovulation cycle did not clearly differ between the strains. PAN-RS showed a significantly higher growth rate than DAN from 0 to 100 days after hatching, however, age at sexual maturity, embryonic period, egg size, and morphometric and meristic characteristics (vertebral and fin-ray counts) did not differ between the two strains. The high fecundity of PAN-RS may provide an increased chance of offspring survival, while the attainment of sexual maturity at a smaller size in DAN may allow them to invest earlier in reproduction to increase breeding success. Variations in the life-history traits of PAN-RS and DAN may be adaptive strategies for life in their natural habitat, which consists of mangrove estuaries with a highly variable environment.     

Relationships of reproductive traits and body size with attainment of sexual maturity and age in Blanding's turtles (Emydoidea blandingi)

To place associations among body size, age at maturity, age, and reproductive traits of a long-lived organism in the context of current life history models based on the concept of norms of reaction, we examined data from a mark-recapture study of Blanding's turtles (Emydoidea blandingi) in southeastern Michigan during 24 of the years between 1953 and 1988. Females matured between 14 and 20 years of age. Both the smallest and largest adult females in the population were reproducing for the first time in their lives. This result suggests that a combination of differences in juvenile growth rates and ages at maturity, and not indeterminate growth, are the primary cause of variation in body size among adults. Body size variation among individuals was not related to age at sexual maturity. Females that had slower growth rates as juveniles matured later at similar mean body size compared to those with more rapid growth that matured at an earlier age. As a result, a linear model of age at sexual maturity with growth rates of primiparous females between hatching and maturity was significant and negative (R² = 0.76). Frequency of reproduction of the largest and smallest females was not significantly different. Clutch size did not vary significantly with age among either primiparous or multiparous females. Clutch sizes of primiparous females and multiparous females were not significantly different. However, older females (>55 years minimum age) reproduced more frequently than did younger females (minimum age <36 y).     

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.