A skeletochronological study of breeding females in a population of Japanese clouded salamanders (Hynobius nebulosus)

The age structure of breeding females of Hynobius nebulosus has not been studied sufficiently. We estimated the ages of 76 individuals from a population in Kyoto by using skeletochronology. The mean age and snout-vent length (SVL) of this population were 4.6 years and 55.7 mm, respectively. It was estimated that the youngest females breed two years post hatching at a mean SVL of 46.5 mm, but a larger number of individuals begins breeding at three years and a mean SVL of 52.2 mm. Because most males also start to breed at three years, there seems to be no gender difference in the timing of sexual maturation. The age of the oldest female was estimated to be 11.8 years. It is possible that the life history of H. nebulosus is characterized by early maturation and arrested growth, and short longevity.     

Annual survival rate and age structure of habu,Trimeresurus flavoviridis (Viperidae), on Minna island,Japan: Estimation from removal trapping

A population of a viperid snake,Trimeresurus flavoviridis, was studied over 10 years by removal trapping on a small subtropical island in Japan. The sex ratio of trapped individuals changed seasonally, but was not biased to either sex in the whole sample of 258 individuals. The age of each individual was estimated through the size structure and the age-size relationship. The minimum number of individuals at the beginning of the study was estimated through accumulating older individuals trapped in the subsequent years. By assuming an annual natural survival rate in the course of this accumulation, an age structure was simulated which led to calculate a resulted natural survival rate. The assumed rate of 0.62 fitted best to the resulted one. The annual trapped proportion estimated on the simulated absolute number of individuals was higher in older individuals than in younger ones with the overall mean of 16%.     

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.     

Demography of an island population of the lizard,Eumeces okadae,on Miyake-jima,Izu Islands

The demography of the lizard Eumeces okadae was studied for 4 years on Miyake-jima, in the Izu Islands, central Japan. Most males matured at 3 years of age with a mean snout-vent length of 77.5 mm. Females matured at 3–4 years with a mean SVL of 77.8 mm, and reproduced biennially thereafter. Growth continued after maturity with a decreasing rate. In females, annual growth was negligible in reproductive years, but resumed markedly in non-reproductive years. Clutch size increased with SVL and was used to construct a fecundity schedule. Population density (exclusive of hatchlings) was estimated to be ca. 4000 individuals/ha in August, an exceptionally high density for lizards. Before introduction of the weasel onto Miyake-jima, low predation pressure had allowed E. okadae to maintain a high population density. Estimated annual survival rates were 36% for hatchlings, 56% for yearlings, 80% for 2-year-olds, 63% for adult males and 76% for adult females. The cohort generation time (6.95 years) was so long that the E. okadae population can be characterized by a combination of low natality and slow turnover.     

A skeletochronological study of growth,longevity, and age at sexual maturity in a population of<Emphasis Type="Italic">Rana latastei</Emphasis> (Amphibia,Anura)

Longevity and age at sexual maturity in an Italian population ofRana latastei were studied by skeletochronology performed on the phalanges. Frogs collected in 1998 and 1999 by drift fences and pitfall traps were marked by toe-clipping. After marking, individuals were released and the cut phalanges were processed for skeletochronological analysis. The maximum age so far recorded was 3 years in males and 4 years in females. The smallest male and female that were sexually mature on the basis of histological analysis of the gonads were 36 and 35 mm snout vent length (SVL), respectively. In both sexes, most individuals were estimated to breed shortly after emergence from their first overwintering. Among the European Brown Frogs,Rana latastei appears to be one of the shortest-lived and one of the first to reach sexual maturity.     

Life history parameters and diet of Risso's dolphins,Grampus griseus,from southeastern South Africa

The life history of Risso's dolphins (Grampus griseus) remains poorly known and data from strandings can help provide important information. Data from 126 Risso's dolphins stranded or bycaught along the southeastern coastline of South Africa between 1958 and 2017 were analyzed in relation to their sex, age structure, and diet. Mean estimated length at birth was 146.9 cm, while maximum length was 325 cm for males and 313 cm for females; small sample sizes precluded detailed examination of sexual dimorphism. Age estimates for 33 individuals (14 males, 17 females, 2 unknown sex) indicated a maximum age of 13 years (males) and 17 years (females), respectively; the oldest animal was 19 years (unknown sex). Mean length and age at attainment of sexual maturity were estimated at 280 cm and 7.1 years in males and at 282 cm and 7.7 years in females. Stomach contents from 27 individuals showed that diets of immature and mature males and females overlapped and consisted predominantly of cephalopods. Reported strandings decreased between 2000 and 2017, possibly due to a lack of reporting associated with a ban on driving on beaches or related to the collapse of the local “chokka” squid (Loligo reynaudii) fishery in 2014–2015.     

Structure of the femora and autotomous (postpygal) caudal vertebrae in the three-toed skink Chalcides chalcides (Reptilia: Squamata: Scincidae) and its applicability for age and growth rate determination

The limbs of the three-toed skink Chalcides chalcides are reduced to such a degree that the three digits are too small for skeletochronology. This study, performed on animals collected near Isernia (central Italy), describes the structure of the caudal vertebrae, which are often naturally lost due to autotomy, in order to determine whether they can be used to obtain data on age and growth with skeletochronological techniques. The reliability of the autotomous caudal vertebrae for skeletochronology was verified by performing skeletochronological analyses also on femora. Although the identification of the lines of arrested growth (LAGs) was easier in femora than in autotomous caudal vertebrae, a high correspondence of the LAG count between the two bones was observed. Females were larger and lived longer than males (4 and 3 years, respectively). For both sexes, the snout vent length (SVL) was significantly correlated with age. For both sexes, sexual maturity was attained after two hibernations from birth, beginning at the 20th month of age. At first reproduction, males had an SVL of 91–106 mm and females one of 111–150 mm. Von Bertalanffy growth curves of age versus SVL showed that females had slower growth rates than males for attaining their asymptotic SVL (females: 197 mm; males: 143 mm). The results provide the first data on age and growth of C. chalcide, and show that autotomous caudal vertebrae are reliable alternatives for obtaining such data for limb-reduced reptiles, avoiding the need to sacrifice or disable animals, as occurs when long bones are used.     

Estimating preharvest density,adult sex ratio,and fecundity of white‐tailed deer using noninvasive sampling techniques

Adult sex ratio and fecundity (juveniles per female) are key population parameters in sustainable wildlife management, but inferring these requires abundance estimates of at least three age/sex classes of the population (male and female adults and juveniles). Prior to harvest, we used an array of 36 wildlife camera traps during 2 and 3 weeks in the early autumn of 2016 and 2017, respectively. We recorded white‐tailed deer adult males, adult females, and fawns from the pictures. Simultaneously, we collected fecal DNA (fDNA) from 92 20 m × 20 m plots placed in 23 clusters of four plots between the camera traps. We identified individuals from fDNA samples with microsatellite markers and estimated the total sex ratio and population density using spatial capture–recapture (SCR). The fDNA‐SCR analysis concluded equal sex ratio in the first year and female bias in the second year, and no difference in space use between sexes (fawns and adults combined). Camera information was analyzed in a spatial capture (SC) framework assuming an informative prior for animals’ space use, either (a) as estimated by fDNA‐SCR (same for all age/sex classes), (b) as assumed from the literature (space use of adult males larger than adult females and fawns), or (c) by inferring adult male space use from individually identified males from the camera pictures. These various SC approaches produced plausible inferences on fecundity, but also inferred total density to be lower than the estimate provided by fDNA‐SCR in one of the study years. SC approaches where adult male and female were allowed to differ in their space use suggested the population had a female‐biased adult sex ratio. In conclusion, SC approaches allowed estimating the preharvest population parameters of interest and provided conservative density estimates.     

High Proportion of Male Faeces in Jaguar Populations

Faeces provide relevant biological information which includes, with the application of genetic techniques, the sex and identity of individuals that defecated, thus providing potentially useful data on the behaviour and ecology of individuals, as well as the dynamics and structure of populations. This paper presents estimates of the sex ratio of different felid species (jaguar, Panthera onca; puma, Puma concolor; and ocelot/margay, Leopardus pardalis/Leopardus wiedi) as observed in field collected faeces, and proposes several hypotheses that could explain the strikingly high proportion of faeces from male jaguars. The proportion of male and female faeces was estimated using a non-invasive faecal sampling method in 14 study areas in Mexico and Brazil. Faecal samples were genetically analysed to identify the species, the sex and the individual (the latter only for samples identified as belonging to jaguars). Considering the three species, 72.6% of faeces (n = 493) were from males; however, there were significant differences among them, with the proportion from males being higher for jaguars than for pumas and ocelots/margays. A male-bias was consistently observed in all study areas for jaguar faeces, but not for the other species. For jaguars the trend was the same when considering the number of individuals identified (n = 68), with an average of 4.2±0.56 faeces per male and 2.0±0.36 per female. The observed faecal marking patterns might be related to the behaviour of female jaguars directed toward protecting litters from males, and in both male and female pumas, to prevent interspecific aggressions from male jaguars. The hypothesis that there are effectively more males than females in jaguar populations cannot be discarded, which could be due to the fact that females are territorial and males are not, or a tendency for males to disperse into suboptimal areas for the species.     

Different cost of reproduction for the males and females of the rare dioecious shrub Corema conradii (Empetraceae)

Males and females of dioecious plant species often differ in their reproductive investment. Such differences frequently result in differential demographic costs represented by lower growth, survival, and/or frequency of reproduction, and/or by more variable reproductive effort through time for females. We present the results of a study on Corema conradii, a rare dioecious shrub of the coastal dune heathlands of northeastern North America. We estimated the reproductive investment of both males and females, determined their age structure, and compared their spatial patterns in a population at ?les-de-la-Madeleine, Quebec. We also determined the sex ratio of the four populations known to occur on the islands. Males invested more in reproduction at flowering, but when fruit production was considered, female reproductive investment was higher in terms of biomass, Mg, and Ca, but not in terms of N, P, and K. The age frequency distribution of males and females did not differ significantly from one another. The population dispersion pattern was contagious, with patches of similar-age individuals. There was no spatial segregation between males and females, although the sex ratio varied somewhat spatially. Females did not start reproducing at a later age than males and did not appear to have a shorter longevity. However, the crown and radial growth rates of females were lower than those of males. When estimated by the crown intercept method, the sex ratio of all four populations was male biased. However, because males had a higher crown growth rate, genet sex ratio was in fact balanced. Higher investment in reproduction was associated with a lower growth rate, which represents a differential cost of reproduction according to sex in this species.     

Age,growth, and sex ratio among populations of least brook lamprey,Lampetra aepyptera,larvae: an argument for environmental sex determination

Synopsis Sex ratios of least brook lamprey,Lampetra aepyptera, larvae varied widely among 12 geographically-diverse streams of the eastern United States. The extremes were 29 and 71% male, and the proportion of males increased significantly with relative population density, which was estimated among the streams from the number of larvae collected per m2 of substrate. The skewed sex ratios were not likely due to differential mortality between the sexes or differential recruitment to the adult stock, since they were established at the time of gonadal differentiation (at ca. 2 years of age) and remained relatively constant over the subsequent 2–3 years of larval life. Furthermore, although females seemed to predominate in the oldest larval age class, thus appearing to metamorphose later than males, their numbers were small and were omitted from the overall sex ratio. Sex ratio did not vary significantly with water hardness, pH, annual thermal units, or latitude. The possible adaptive significance of density-dependent sex determination in lampreys, however, remains elusive. It has been proposed that growth-promoting conditions might yield female-biased sex ratios as a tactic for ensuring that relatively large individuals become females, thereby increasing their fecundity. As predicted, larval size at a given age was generally greater in low-density populations, but there was no relationship between sex ratio and larval size, and female larvae were not consistently larger than the males.     

Sex ratio, survival and territorial behaviour of polygynous Hen Harriers Circus c. cyaneus in Orkney

Polygyny is widespread among Orkney's Hen Harriers Circus cyaneus . From 1975–81, it was associated with a sex ratio estimated from resightings of colour-marked birds up to six years of age to be 29 females:ten males. The sex ratio of fledglings changed significantly from a greater proportion of females in the 1950s and early 1960s to a greater proportion of males subsequently. The mean estimated 'survival' rates (birds colour-marked in Orkney which were seen there in later years) of males and of females 0–2 years old were 14 and 29%. The mean estimated annual survival rates of males and females from 2–6 years old were 72 and 90%. It is suggested that the uneven sex ratio resulted in more frequent intra-sexual encounters and displays by females. The results of temporary removals of two females (immediately replaced) and of two males (not replaced) in spring indicates that there was a shortage of males in the population.     

Age ratio and survival of Common Rosefinch (<Emphasis Type="Italic">Carpodacus erythrinus</Emphasis>, Passeriformes,Fringillidae) in a local population based on ringing data

The ringing data on Common Rosefinch obtained during thirteen field seasons (2002–2014) at the National Park “Russky Sever” (Vologda region) are analyzed. Birds were trapped in two sites 59 km apart. The age of the birds (yearlings or first breeders and adults) was determined according to the plumage color in every male captured with mist nets. The apparent survival rate of adult individuals was determined using two methods: according to the ratio of males’ age and the CJS model (Lebreton et al., 1992; Bursky, 2011). A total of 713 captures of 657 individuals were analyzed. The ratios of ages in the males from the sites studied did not differ; yearlings amounted to 56% of all males. The rate of survival in the males based on the age ratios was estimated at 44 ± 2%. The apparent survival rate obtained using the CJS model was significantly higher (61 ± 6%). The survival rate of adult rosefinches in two sites did not differ and did not depend on sex. Literature materials on the age ratio and survival of rosefinches in local populations are analyzed. There is a suggestion that the mismatch of the survival rates obtained by two methods and the high proportion of yearling males in the banding captures can be explained by the fact that the majority of individuals of that age category did not participate in nesting.     

Age and growth of sailfish Istiophorus platypterus (Shaw in Shaw and Nodder, 1792) from Mazatlan, Sinaloa, Mexico

Age and growth of the sailfish Istiophorus platypterus were determined for the area off Mazatlan coast, Sinaloa, in the Gulf of California, between September 2002 and August 2003. The lower jaw-fork length and total weight of 572 specimens were measured, and the fourth dorsal spine was collected to determine age. The monthly variation of the sample size displayed a well-defined seasonal pattern, which peaked during the warm period (May?CNovember) and declined during the rest of the year (temperate period). Significant differences were detected in the size structure by sex during the temperate period, with females displaying larger sizes and greater abundance (Female:Male = 3.35:1). In the warm period the size structure was similar, with the sex ratio reaching F:M = 0.73:1. This suggests a different sex-related recruitment in the fishing zone, with males moving more actively than females. While female size remained relatively unchanged over the year, male size increased during the warm period. Age was estimated using the number of growth rings on the cross-sectioned fourth dorsal spine, after the number of absorbed growth rings in the vascularized zone had been estimated. Nine age groups were identified; group-5 was the most abundant, representing 31% of the catch. The trend of the monthly change in the percentage of opaque-edge spines and the average of the marginal increase rate indicated that the formation of growth rings displayed an annual pattern. The von Bertalanffy growth model was adequately fitted to age and back-calculated length data. Significant differences were detected when growth was compared between sexes; females grew faster than males.     

基于骨龄学方法鉴定吐鲁番沙虎的年龄

基于113个标本的吻肛长频次数据,初步划分吐鲁番沙虎(Teratoscincus roborowskii)的年龄组,各年龄组共选取54例个体,分别截取第2右前趾骨第3趾节,用常规石蜡切片法进行了骨龄学鉴定。同时,根据野外标记重捕方法获得个体的形态学生长指标来验证年龄组划分的合理性。结果表明,吐鲁番沙虎雌雄个体间吻肛长差异不显著,可以合并进行年龄鉴定;吐鲁番沙虎的吻肛长和骨龄间有显著的相关性;对于小于6龄的个体,骨龄学的方法适用于吐鲁番沙虎年龄的鉴定。     

Morphology,Reproduction and Diet in Australian and Papuan Death Adders (Acanthophis,Elapidae)

Death adders (genus Acanthophis) differ from most other elapid snakes, and resemble many viperid snakes, in their thickset morphology and ambush foraging mode. Although these snakes are widely distributed through Australia and Papua New Guinea, their basic biology remains poorly known. We report morphological and ecological data based upon dissection of >750 museum specimens drawn from most of the range of the genus. Female death adders grow larger than conspecific males, to about the same extent in all taxa (20% in mean adult snout-vent length,  =  SVL). Most museum specimens were adult rather than juvenile animals, and adult males outnumbered females in all taxa except A. pyrrhus. Females have shorter tails (relative to SVL) than males, and longer narrower heads (relative to head length) in some but not all species. The southern A. antarcticus is wider-bodied (relative to SVL) than the other Australian species. Fecundity of these viviparous snakes was similar among taxa (mean litter sizes 8 to 14). Death adders encompass a broad range of ecological attributes, taking a wide variety of vertebrate prey, mostly lizards (55%), frogs and mammals (each 21%; based on 217 records). Dietary composition differed among species (e.g. frogs were more common in tropical than temperate-zone species), and shifted with snake body size (endotherms were taken by larger snakes) and sex (male death adders took more lizards than did females). Overall, death adders take a broader array of prey types, including active fast-moving taxa such as endotherms and large diurnal skinks, than do most other Australian elapids of similar body sizes. Ambush foraging is the key to capturing such elusive prey.     

Structure of the femora and autotomous (postpygal) caudal vertebrae in the three-toed skink Chalcides chalcides (Reptilia: Squamata: Scincidae) and its applicability for age and growth rate determination

The limbs of the three-toed skink Chalcides chalcides are reduced to such a degree that the three digits are too small for skeletochronology. This study, performed on animals collected near Isernia (central Italy), describes the structure of the caudal vertebrae, which are often naturally lost due to autotomy, in order to determine whether they can be used to obtain data on age and growth with skeletochronological techniques. The reliability of the autotomous caudal vertebrae for skeletochronology was verified by performing skeletochronological analyses also on femora. Although the identification of the lines of arrested growth (LAGs) was easier in femora than in autotomous caudal vertebrae, a high correspondence of the LAG count between the two bones was observed. Females were larger and lived longer than males (4 and 3 years, respectively). For both sexes, the snout vent length (SVL) was significantly correlated with age. For both sexes, sexual maturity was attained after two hibernations from birth, beginning at the 20th month of age. At first reproduction, males had an SVL of 91–106 mm and females one of 111–150 mm. Von Bertalanffy growth curves of age versus SVL showed that females had slower growth rates than males for attaining their asymptotic SVL (females: 197 mm; males: 143 mm). The results provide the first data on age and growth of C. chalcide, and show that autotomous caudal vertebrae are reliable alternatives for obtaining such data for limb-reduced reptiles, avoiding the need to sacrifice or disable animals, as occurs when long bones are used.     

Gut microbiota are associated with sex and age of host: Evidence from semi‐provisioned rhesus macaques in southwest Guangxi,China

Host characteristics, such as sex and age, are closely associated with the structure and function of gut microbiota; however, less is known about the effects of age and sex on the gut microbiota of nonhuman primates, and therefore, our knowledge of interindividual variability in host gut microbiota is limited. In this study, 153 fecal samples from rhesus macaques (Macaca mulatta) were analyzed using high‐throughput 16S rRNA sequencing in order to explore associations between age and sex of the host and their gut microbiota. The results indicated that female macaques had higher alpha diversity and a more unique gut microbiota than did males. The proportion of Proteobacteria, Tenericutes, Cyanobacteria, unclassified bacteria, and Verrucomicrobia was higher in females than that in males. We also found that adults of both sexes had a higher alpha diversity, a higher proportion of norank Ruminococcaceae, Oscillospira, norank Lachnospiraceae, norank Clostridiales, and Succinivibrio, and a lower proportion of Enterococcus than immatures. Functional analyses revealed that the richness of metabolic pathways was higher in females than males and in adults compared with immatures. These results could be attributed to differences in the nutritional requirements and hormone levels of macaques of different sex and age classes. We conclude that variation in the gut microbiota of different sex and age classes of rhesus macaques may be linked to age‐ and sex‐specific differences in nutrient requirements and hormone levels. These results highlight the importance of host age and sex on the structure and function of the gut microbiota and the need to consider physiological traits when conducting studies on the gut microbiota.     

Association patterns and kinship in female reindeer (Rangifer tarandus) during rut

Non-random association of females has been reported in many social species, with kinship being the main mechanism in shaping these associations. Understanding the patterns of association during rut is particularly important in polygynous animals, as this may have implications for inbreeding vulnerability and genetic structuring of populations. However, these patterns are highly dynamic and may be influenced by the population sex ratio and male age structure. We examined females' association in reindeer (Rangifer tarandus), a highly polygynous ungulate, to determine whether genetically related females associate more often than non-kin during rut and whether this association was influenced by the aforementioned factors. During three rutting seasons the male age structure and the sex ratio of the herd was manipulated: two extremely female biased sex ratios, one with only adult males and one with only young males, whereas the third being closer to a more even sex ratio and male age structure. We found that genetic relatedness influenced female association in the mixed male age group, but not in the adult and young male age groups. Highly related females (relatedness ??0.5) associated more closely than unrelated females. Further, period of the rut as well as male age structure and sex ratio had a significant effect on female association. Our study suggests that the female reindeer association during rut is not only influenced by preference for kin but also by male?Cmale competition and male age as well.     

Growth and reproduction of the sea snake,Emydocephalus ijimae,in the central Ryukyus,Japan: a mark and recapture study

A mark and recapture study was carried out for three years on a population of the Ijima's sea snake, Emydocephalus ijimae, in the coastal shallow water of Zamamijima Island, central Ryukyus, Japan. The relatively high recapture (47% of 167 marked snakes) suggests that E. ijimae is a particularly philopatric, sedentary species among the sea snakes. The sex ratio (male: female), approximately 1.6:1, significantly skewed from 1:1. The growth rate in SVL declined with growth, with females thoroughly growing better than males. Males and females were estimated to begin reproductive activity in the second or third summer and the third spring after birth, respectively. Frequency of female reproduction is guessed to vary from annual to biennial, or even less frequent.