AGE,GROWTH, AND REPRODUCTIVE PATTERNS OF DALL'S PORPOISE (PHOCOENOIDES DALLI) IN THE CENTRAL NORTH PACIFIC OCEAN

Life history parameters were estimated for Dall's porpoise, Phocoenoides dalli, from biological specimens collected in the western Aleutian Islands, during 1981–1987. Of 2,033 males and 3,566 females examined, reproductive data were available for 1,941 males and 1,906 females; ages were determined for 813 males and 1,297 females. Female sexual maturity was based on the presence of one or more corpus on either ovary; 845 were sexually immature and 1,061 were sexually mature. Two estimates of female average age at sexual maturity (ASM) were 3.8 and 4.4 yr; average length at sexual maturity (LSM) was 172 cm. Males were considered sexually mature when evidence of spermatogenesis was detected; 1,136 were sexually immature and 805 were sexually mature. Two estimates of male ASM were 4.5 and 5.0 yr; LSM was 179.7 cm. Physical maturity was assessed for 246 males and 446 females by examining the degree of fusion in thoracic vertebral epiphyses. For both sexes, the average age at physical maturity was 7.2 yr. Average length at physical maturity was 202.6 cm for males and 192.7 cm for females. Average lengths of physically mature males (x?= 198.1 cm, SE = 0.8566) and females (x?= 189.7 cm, SE = 0.4002) were significantly different(P < 0.0001). Early postnatal growth was rapid in both sexes. A secondary growth spurt in both mass and length was characteristic for both sexes; the increase in length preceded the mass increase by 1–2 yr. Average length at birth (LOB) was approximately 100 cm; birth mass averaged 11.3 kg (SE = 0.0772). By the time the umbilicus had healed (<2 mo), the average length and mass had increased to 114.1 cm and 23.8 kg, respectively. Gestation period based on projections using LOB was 12 mo, but this was considered an overestimate. Calving was modal, centered in early July; an annual reproductive interval was indicated. Among the sexually mature females, 120 were pregnant, 55 were pregnant and lactating, 321 were pregnant with colostrum, and 33 were “resting.” By 3 July (95% CI =x? 1 d), 50% of births had occurred, during each of the seven years sampled. The ovulation rate was estimated at 0.914 ovulations per average reproductive year. Enlarged follicles and recent ovulations were observed in postpartum females in late July.     

Reproduction and population growth in free-ranging mantled howling monkeys

Free-ranging mantled howling monkey (Alouatta palliata Gray) females experienced a regular estrus cycle averaging 16.3 days, demonstrated sexual skin changes, and participated in multiple matings before becoming pregnant. Gestation averaged 186 days. The average interval between births was 22.5 months. Sexual maturity occurred at approximately 36 and 42 months for females and males, respectively. Female age at first birth was about 3½ years. Births were scattered during some years and clustered during others. The age, rank, and parity of the females affected infant survival. More female than male infants survived to one year of age. Increased population size was the result of immigration rather than births.     

Social interactions among adult male langurs (Presbytis entellus) at Rajaji Wildlife Sanctuary

A population of langurs (Presbytis entellus)at the Rajaji Wildlife Sanctuary in northern India was investigated for 1820 hr throughout a 10-month period in 1978. Data were collected from four bisexual troops and the adult males that ranged outside of bisexual troops. Most (60%) of the observation hours occurred with a main study troop from which social and ecological data were collected. The langur population at Rajaji shows pronounced birth and mating seasons. The population density is high (ca. 80/km ²), with about 75% of the adult males living outside of bisexual troops, which typically are large and multimale. Males outside of bisexual troops occur in small all-male bands or as isolates. Relations between bisexual troops and all-male bands are characterized by relatively low levels of aggression, and members of all-male bands are able to associate with bisexual troops for prolonged periods during the mating season. As a result of these associations, nontroop males are about as successful as troop males in achieving reproductive access to troop females. These associations between bisexual troops and all-male bands occurred with a minimal amount of agonistic behavior and without mortality or injury to troop females or immatures.     

Birth dynamics in Hanuman langurs,Presbytis entellus of Jodhpur,India

Ten years data on birth peak, birth rate and interbiith interval inPresbytis entellus of Jodhpur have been presented. Although Hangman langur females breed round the year, there is some concentration of births during January–March while fewer births occur during October–December. It seems that provisioning and crop raiding together may provide better feeding opportunities to breed year round. However, it remains unclear whether environmental factors allow langur females to deliver more infants during January–March. During 1984–86 the birth rate was uniform for the whole population (0.63). While there was a variation within the troops from year to year, data suggest that resident male replacements do alter birth rate. It goes down when resident males are replaced frequently. The interbirth interval ranges between 7.0 and 76.5 months (average, 16.88 months;n = 112). Abortions and still-births reduced the interbirlh interval to 7.1 months (range 7.1-21.1; average, 11.4 months;n= 8) compared to the normal inlerbirth interval following infant survive its first 4.1 months of life (range 10.7-76.5 months; average, 17.28 months;n = 86). However, infant loss under the age of 4.1 months did not reduce the interbirth interval except in two cases (range 7.0-51.8 months; average, 17.27 months;n = 18). Maternal rejection or weaning begins at about 8 months of age and lasts until infants are 12 months old. In this population, the probability of twin births was worked out to be 0.79 per 100 births.     

Life history variables of wild troops of formosan macaques (Macaca cyclopis) in Kenting,Taiwan

A study on population dynamics of wild Formosan macaques (Macaca cyclopis) in Kenting, southern Taiwan, was conducted from March 1985 to August 1990. At first, only one monkey troop was studied. It fissioned in 1987 and both of the daughter troops have been observed since then. Total number of animals increased from 10 to 29 over the years, but the sizes of individual troops have never been more than 20. Seasonality in breeding has been detected: copulations were concentrated in the period from November to January and 75% of all the 28 births occurred between April and June. Time of birth by parous females without offspring from the preceding year was earlier than that of lactating females. Young females gave their first births at 4 or 5 years of age. Total birth rate over the study period was 0.8 infant per female per year. Hunting was the main cause of death while natural mortality rate was low for the animals. There was only one adult male in each troop for most of the time. Troop males in the two daughter troops have been replaced two or three times in the three years by some solitary males that moved around in the area. The reproductive parameters of Formosan macaques in Kenting were found to be more similar to that of rhesus monkeys than to Japanese macaques. And a case of higher reproductive success in a high-ranking matriline was reported.     

The growth and maturation of the "tarantula", Avicularia avicularia L.

The growth of the theraphosid spider, Avicularia avicularia L. was studied principally by taking measurements of the fang length of exuviae and dead specimens. The relatic ships between fang length and increment at ecdysis and fang length and instar duration were investigated and used to construct a projected growth curve for the species. This suggests that males reach sexual maturity in approximately 13 instars and at a minimum age of about two and a half years. In males the adult instar is terminal and rarely lasts more than three months. Reproductive maturity in females is probably not reached earlier than the XIVth instar or three years from birth. The females continue to moult annually after maturity and have a longevity in excess of seven years. The pattern of colouration shows characteristic changes in early immature life and develops a slight sexual dimorphism in adults. Type II urticating hairs are present throughout life and occur in light and dark forms in the IInd instar. The mean length of the urticating hairs increases during the life cycle and a sexual dimorphism develops in the XIIth or XIIth instar. In adult males the urticating hairs are uniformly barbed whereas in the adult females the barbs are restricted to the proximal end.     

Reproductive biology of brown trout, Salmo trutta macrostigma Dumeril 1858, in a tributary of the Ceyhan River which flows into the eastern Mediterranean Sea

The study describes some key elements of the reproductive biology, including spawning season, age at sexual maturity, fecundity and egg diameter of the native brown trout, Salmo trutta macrostigma, in a tributary of the Ceyhan River. A total of 197 brown trout (118 females and 79 males) were captured in 2000–2001 by electric fishing. In observations on monthly changes, the gonadosomatic index (GSI) and the monthly frequency distribution of egg diameter confirmed that spawning lasted from November to January. Some 27.7% of the females and 62.5% of the males attained sexual maturity in their second year. The smallest fork length (FL) of brown trout attaining sexual maturity was 17.4 cm for males and 17.8 cm for females. Mean fecundity in age groups II, III, IV and V were 360, 452, 693 and 1283 eggs per female, respectively. One 9‐year‐old female had a unique 3232 egg count. The mean fecundity of the sampled population was 554 eggs per fish, positively correlated with the FL (mm) (R = 0.8227 ) and body weight (R = 0.8130). The diameter of mature eggs in the spawning season ranged from 3.250 to 5.930 mm, with a 4.146 mm average. Mean egg diameter in age groups II, III, IV and V in the spawning season were 0.813, 3.799, 4.663 and 5.243 mm, respectively. Fecundity, egg weight and diameter were statistically different in all age groups.     

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.     

Reproductive cycle,sexual maturity and longevity of Odontophrynus americanus (Anura: Odontophrynidae) in South Brazil

Studies on the reproductive biology and age of amphibians provide primary information about the life history and population demographic parameters of species. Here, we describe the reproductive cycle, size–fecundity relationships, reproductive effort, sexual dimorphism and sexual maturity of Odontophrynus americanus, the flood frog, from South Brazil. A total of 96 individuals were analysed. The reproductive cycles of males and females were described through morphoanatomical analysis of testis and ovary. Age at onset of sexual maturity and estimated longevity were determined by skeletochronology. Individuals of O. americanus presented a potentially continuous reproductive cycle with a peak of reproductive activity in the warmer months. Females presented a higher reproductive investment than males. Sexual maturity was reached at around one year of age for both sexes while longevity differed between the sexes, with females living up to six years and males up to ten years. No evidence of sexual size dimorphism was found. This study is among the few that have assessed age at sexual maturity and longevity in a Neotropical anuran. Basic aspects of life history are of paramount importance because they allow comparisons and test of hypotheses to be made, which can help to build generalizations about the evolutionary meaning of ecological strategies.     

Reproductive biology of the swell shark Cephaloscyllium ventriosum (Carcharhiniformes: Scyliorhinidae)

The Cephaloscyllium ventriosum shark is present in the artisanal fisheries of elasmobranchs on the western coast of Baja California Sur, Mexico. The main characteristics of the sexual maturation of this species based on individuals captured from off north-west Mexico in 2013–2016 are described. The size at maturity of this species was determined for the first time (total length 82 cm for females and 76 cm for males). Most females had one egg case per one uterus, and two per one uterus was an isolated event of low incidence. From the histological analysis of females, it was possible to show sperm storage in the oviducal gland. Fully developed sperm in immature organisms were identified in the testes. The main indicator of the maturity stage of males and their mating activity is the clasper. The present study provides evidence for a reliable estimation of the sexual maturity of these organisms, demonstrating the need for the combination of macroscopic and microscopic methods.     

Temporal Variation in Japanese Macaque Bodily Mass

We investigated the bodily mass of infants and postpartum adult females longitudinally in provisioned free-ranging Japanese macaque (Macaca fuscata) troops of the Takasakiyama Natural Zoo, Oita, Japan. We investigated whether the rate of mass change in postpartum adult females and infants is more strongly associated with season (or calendar date) as opposed to the length of time since delivery/birth. Focal adult females' postpartum mass ranged between 7 and 10 kg for a year after delivery. For postpartum adult females, calender date (season) influenced the rate of mass change more than the length of time since delivery did. Rate of mass change in postpartum adult females was high in October (autumn) and April and May (spring) and low between December and February (winter). This may reflect seasonality in energy and protein intake from natural foods. Infant mass increased steadily from birth. Mass of infants varied between individuals, some infants reached 2 kg by about 240 days of age, and others by about 400 days of age. It was unclear, however, whether the rate of mass change in infants was influenced more by age or calendar date (season). Differences in trends between adult females and infants may reflect, to some degree, differences in sources of energy intake, i.e. solid foods for adult females and suckling and solid foods for infants.     

Abortions in free ranging Hanuman langurs (Presbytis entellus) — a male induced strategy?

During a 10-year long term study, 6 eye-witnessed and 1 pressumed cases of abortions occurred in 3 one-male bisexual troops of free ranging langurs (Presbytis entellus) near Jodhpur, Rajasthan, India. The age of the unborns varied from 35 to about 200 days. The subsequent birth interval ranged between 7.1–21.1 months. 2 miscarriages occurred during stable periods of residency of a single male. 5 cases occurred prior to or after infanticide in connection with male changes. In one case a female was attacked by the new male before she aborted. In one case a female presumably aborted after attacks on her semiweaned infant. Most of the reproductive losses hence seem to be related to psychical and physical stress exerted by new males on pregnant females. As part of their reproductive strategy, males reduce their waiting time to insemination in this way. Abortions may likewise represent an adaptive reproductive strategy of females, who prefer to abort instead of investing in a foetus which is likely to be killed after birth.     

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]。     

Social organization and space use in California voles: seasonal,sexual, and age-specific strategies

We intensively monitored space use and movement in Microtus californicus over a 2-year period that included 1 year of high density (maximum 618/ha) and one of low (minimum 5/ha); historically this population has exhibited cycles of 2 or 4 years. Adults of both sexes dispersed at the start of the breeding season, culminating in the establishment of intrasexually exclusive territories. In females, these territories persisted throughout life, except that many young females recruiting during the breeding season established contiguous, overlapping, or adjacent home ranges with their mothers. This female philopatry explains the conclusion of previous workers that females of this species are non-territorial. In the dry (non-breeding) season, females had smaller ranges that often overlapped and were clustered. Adult males moved breeding territories at a modal interval of 6 weeks; this is consistent with their avoidance of inbreeding with philopatric daughters. Ranges overlapped 1–4 adult females at any one time, and a cohort of 7 long-lived males overlapped an average of 16.4 females during their tenure on the grid. The period of maximum overlap with adult females varied among individual males, and did not correlate with the time of maximum body weight. Ranges of males in the dry season overlapped extensively, with persistent associations among some individuals. In the lowdensity year, ranges of some adults failed to overlap intersexually. Juvenile males dispersed gradually between 3 and 13 weeks of age (half before 9 weeks), with some leaving after reaching sexual maturity; a few remained philopatric. Of juvenile females, 47% remained philopatric with the rest disappearing before 9 weeks of age. New understanding of vole social behavior, dispersal, and space use is achieved by focusing on the seasonal dynamics of spatial relationships among individuals with respect to age, sex, and relatedness.     

The process of weaning in hanuman langursPresbytis entellus entellus

Twelve langur infants (seven males and five females) of three focal bisexual unimale troops of Hanuman langurs,Presbytis entellus entellus living near Kailana, Jodhpur, Rajasthan (India) were observed for their weaning behaviour. Weaning starts between 7.0 to 10.0 months of age, average 8.6 months. The process of weaning lasts between 3.2 to 5.6 months, average 4.2 months. A 13-month-old infant is fully weaned. Infants are independent at this age. Male infants are weaned earlier compared to females. Males react to their mothers' rejections more fearlessly and are more vocal compared to females. By and large, infants were found in stress during this period as their mothers are often very harsh, hostile, punitive, and indifferent to their infants. By severing ties with their infants, mothers serve dual purpose of allowing their infants to become independent and may be to become ready to bear offspring.     

Ecology and behavior ofPresbytis thomasi in Northern Sumatra

A field study of 23 bisexual troops, ranging in size from 3 to 21 members ( =8), and two all-male groups of the Thomas's leaf monkey (Presbytis thomasi) was conducted in North Sumatra from November 1981 to April 1984. Most troops (N=19 or 82.6%) contained only one adult male. Two troops and one group were most intensively studied. The home range was 12.3–15.7 ha for the two bisexual troops, and only 1.7 ha for the one, all-male, ten-member group. Fruits composed more than 50% of their diets. Vocalizations were classified into 13 types. Births occurred at any time of the year. Among three males of a bisexual troop, serious fights were observed: two males died of wounds and the former beta male became the new alpha male. After this social change, the home range area of this troop gradually shifted eastward. But, 3.5 months after the social change, a 9-month-old infant male stayed alone in the western part of its former range. Thereafter, he became a solitary male and sometimes went into the riverine area of the Bohorok river. The occurrence of male replacement suggests instability of multi-male organization in bisexual troops. Moreover, the different mortality rate between males and females and the unequal sex ratios forced by the formation of one-male troops, maintained high tension levels among males competing on females.     

A study of a black howling monkey (Alouatta caraya) population in northern Argentina

A population of Alouatta caraya in northern Argentina had an ecological density of 130 animals per km². Mean troop size varied from 7.2 to 8.9 individuals, and the ratio of adult males to adult females from 0.58 to 0.51. Infants comprised from 6% to 14% of the population, juveniles from 16% to 21%. These percentages probably vary seasonally in response to a birth peak at the beginning of the dry season. Males were age-graded in multi-male troops. Sexual dimorphism was extreme in this species. Males were all black and averaged 6.7 kg; females were yellow-brown and averaged 4.4 kg. Juvenile males retained the pelage color of the female until approximately 4.5 yr of age and 5 kg in weight. No genital mimicry or exaggeration occurred in this species. Vocalizations of A. caraya were similar to those of A. seniculus, both of which tend to be lower pitched than those of A. palliata.     

Reproduction of the lesser kudu (Tragelaphus imberbis) at Dvůr Králové Zoo

Reproductive data on captive lesser kudus (Tragelaphus imberis) were collected from 1972 to 1990. The estrous cycles of two females were 21 and 22 days. Mean gestation length of 18 pregnancies was 244 ± 5.5 days (range = 235–256 days), and 71.2% of interbirth intervals (n = 146) were from 248 to 365 days. Births occurred throughout the year, but 55% were from September to December. Females always gave birth to a single calf (n = 215), and the sex ratio did not differ from unity. Neonatal weights (1–3 days postpartum) of 32 males and 28 females surviving at least 30 days were 6.4 ± 0.8 kg and 5.8 ± 0.7 kg, respectively. Males and females reached sexual maturity at the ages of 16 and 19 months, respectively. The oldest male lived to slightly more than 14 years, 5 months, and the oldest female to more than 18 years, 11 months. Males were fertile until at least 14 years and females minimally to 14–18 years of age; however, the maximum age of successful lactation was 13–14 years. © 1992 Wiley-Liss, Inc.     

Intermale relations and troop male membership changes in langurs (Presbytis entellus) in Nepal

Data on intermale social relations and troop membership changes in one Nepalese high-altitude population of free-ranging langurs (Presbytis entellus)are reported here. Data were collected from six troops by three observers and cover 32 months of observations. The predominantly multi-male troops indicate an alternating pattern of exclusions and introductions with gradual adult male replacement. Takeovers and infant killing were not observed. Analysis of adult social behavior records show qualitative and quantitative differences in intrasexual relations, with primarily agonistic social contacts occurring between males. Agonistic encounters between females and between males differ in frequency of occurrence, types of be-haviors used, cause, and consistency in direction of threats between individuals. Individual adult male frequency of interaction with females and immatures varied significantly, with the majority of these interactions occurring between the dominant troop male and other troop members. Data indicate that intermale dominance is a major factor in determining male access to fertile females: This appears to be achieved by either directly excluding males from the troop or effectively “controlling” their inter-actions with troop females. Data from these studies are compared with data from other Presbytis entellusinvestigations. Review of these data suggests that intraspecific variability in intermale social dynamics and type of troop male membership change are correlated with the percentage of nontroop males. It is suggested that environmental pressures resulting in social crowding can be critical in determing the occurrence of takeovers in some populations of Presbytis entellus.     

Troop history,female reproductive strategies and timing of male change in Hanuman langurs,Presbytis entellus

Female reproductive data are presented from 9 years of longitudinal observations on two troops of Hanuman langurs (Presbytis entellus) living around Jodhpur, India. On the basis of 89 live births interbirth intervals were calculated to examine the effect of demographic factors on reproductive behaviour and troop composition. Sex of an infant seems to influence the length of intervals which are longer after the birth of female infants at an average of 1.7 months. It is suggested that this may be an outcome of differential maternal investment by allocating more time and energy towards female infants who run a higher mortality risk than male infants, at least up to an age of 27 months. Troopspecific interbirth intervals are influenced by social events. If the last infant is still alive when the next one is conceived, the intervals are significantly longer than after the premature loss of an infant (Bijolai troop: 15.6 vs. 12.1 months; Kailana-1 troop: 16.7 vs. 11.4 months). During undisturbed male tenureship intervals are shorter than after a male change (Bijolai troop: 14.3 vs. 16.0 months; Kailana-I troop: 15.6 vs. 17.5 months). Thus the frequency of male changes can influence the demography of a troop. Furthermore, the data suggest that take-overs are optimally timed by males. New males tend to take over a troop when most of the females are cycling.