鹅喉羚的年龄鉴定

本文以鹅喉羚为材料,采用双重附贴磨片法及蚀刻法确定角磨片上显示的生长层与角鞘上凸“嵴”的关系,并以第一下门齿(I_1)作切片所显示的年轮线进行验证。证明其角鞘上的凸“嵴”数量多少并不表示年龄大小,在一龄内无凸“嵴”,二、三龄均包含有4—5个凸“嵴”,四龄后亦为2—3个凸“嵴”组成一龄,真正的年龄线是角表凸“嵴”之后有一粗糙微凹的环纹。实验结果可应用于野外生态学调查,用以判断种群年龄及结构。     

Age-related differences in social grooming among adult female Japanese monkeys ( Macaca fuscata)

The present study investigated the influence of dominance rank in combination with kinship on age-related differences in social grooming among adult females in a free-ranging group of Japanese monkeys (Macaca fuscata). Eighty-three adult females were divided into six sub-groups according to age-class (younger: 5–9 years old; middle: 10–14 years old; older: 15–22 years old) and dominance rank (high and low rank). The ratio of the number of unrelated females that each female groomed to the total number of available unrelated females and grooming bouts which she gave to unrelated females decreased with increasing age for both high- and low-ranking females, whereas age did not appear to affect corresponding values for related females. On the other hand, compared with low-ranking females, high-ranking females of all age-classes received grooming more often from a larger number of unrelated females. Moreover, older females of low rank received grooming less often from a smaller number of unrelated females than younger females of low rank. These results indicate that with increasing age females are more likely to concentrate on related females when they have grooming interactions with other females. This tendency seems to be more apparent for low-ranking females. Moreover, the present findings also indicate that older high-ranking females could maintain their social attractiveness as high as younger high-ranking females.     

Age and growth of the ajime-loach,niwaella delicata, in the yura river, kyoto, japan

The age of the Ajime-loach,Niwaella delicata (a species endemic to Japan), was determined from the number of concentric rings appearing on the cross-sectional surface of the erectile spine (peculiar to Cobitidae). The ages of loaches caught in the Yura River, Kyoto, were determined and growth rates for each sex estimated. It was found that size dimorphism in this species was due to different growth patterns between the sexes, 2.5 years old males being larger than females and usually sexually mature, unlike the latter. Females older than 3.5 years were sexually mature and larger than males of equivalent age.     

Growth of dark chub, Zacco temmincki (Cyprinidae), with a discussion of sexual size differences

I examined the annual and seasonal growth of dark chub, Zacco temmincki, in a Japanese river. Investigation of opercular rings showed that the fish reached a maximum age of 8 years. There was no significant sexual size difference at younger ages (3–5 years), but males were larger than females at older ages (6–7 years). Annual increments of length and weight for males that were recaptured were also larger than those for females. The fish spawn from June to August. Females grew for a short period from April to May, but males on average grew for a longer period from April to August. There was no sexual difference in growth rate except during the spawning period. Annual growth rate was negatively correlated with fish length in each sex. The sexual size differences at older ages of the fish might be due to the polygynous mating system in which most mature males could not obtain females and invested for somatic growth in the spawning period, and a short growing season that was overlapped considerably with the spawning period.     

Reproductive efficiency of captive Chinese- and Indian-origin rhesus macaque (Macaca mulatta) females

Reproductive and survival records (n=2,913) from 313 Chinese-origin and 365 Indian-derived rhesus macaques at the Tulane National Primate Research Center (TNPRC) spanning three generations were studied. Least-squares analysis of variance procedures were used to compare reproductive and infant survival traits while proportional hazards regression procedures were used to study female age at death, number of infants born per female, and time from last birth to death. Chinese females were older at first parturition than Indian females because they were older when placed with males, but the two subspecies had similar first postpartum birth interval (1st PPBI) and lifetime postpartum birth interval (LPPBI). Females that gave birth to stillborn infants had shorter first postpartum birth intervals (1st PPBI) than females giving birth to live infants. Postpartum birth intervals decreased in females from age 3 to 12 but then increased again with advancing age. Chinese infants had a greater survival rate than Indian infants at 30 days, 6 months, and 1 year of age. Five hundred and forty-three females (80.01%) had uncensored, or true records for age at death, number of infants born per female, and time from the birth until death whereas 135 females (19.91%) had censored records for these traits. Low- and high-uncensored observations for age at death were 3 and 26 years for Chinese, and 3 and 23 years for Indian females. Uncensored number of infants born per female ranged from 1 to 15 for Chinese females and 1 to 18 for Indian females. Each of these traits was significantly influenced by the origin×generation interaction in the proportional hazards regression analyses, indicating that probabilities associated with age at death, number of infants born per female, and time from last birth to death for Chinese and Indian females did not rank the same across generations.     

A statistical model for the prediction of the number of sapwood rings in Scots pine (Pinus sylvestris L.)

Dendrochronology is a well-established dating method for wooden objects, but due to surface processing of construction timber or natural degradation the dating of historical wood often relies on a prediction of the number of missing rings based on sapwood statistics. Since Scots pine (Pinus sylvestris L.) is one of the most common tree species in north-western Europe, the absence of reliable sapwood statistics and models for the prediction of missing sapwood rings for pine samples is remarkable. We have therefore produced sapwood statistics based on data from 776 pine trees with ages from 15 to 345 years. The material consists of both living trees and historical timber, with varying growth rates, geographic settings, and from different soil types. When the whole material is considered, the average age of the trees is 103 years, and the number of sapwood rings is 54 ± 15 (1 SD), but range from 18 to 129. Trees less than 100-years in age contained 46 ± 11 (1 SD) sapwood rings and had an average tree-ring width (TRW) of 1.76 mm. With increasing age, the average TRW decreased while the number of sapwood rings increased. The average TRW of 101–200-year-old trees is 0.99 mm while the samples contained 63 ± 12 (1 SD) sapwood rings. For trees older than 201 years, the average TRW is 0.64 mm while the number of sapwood rings increased to 85 ± 16 (1 SD). The two most important factors in determining the number of sapwood rings for a given tree when only heartwood statistics are available proved to be (i) the number of heartwood rings and (ii) the average TRW of the heartwood rings. For incomplete samples, we have therefore developed a statistical model based on the sample’s heartwood rings (number and average width) to compute a prediction interval for the total number of rings. The sapwood and heartwood statistics suggest a statistical model for the number of sapwood rings with mean that increase with the number of heartwood rings. Furthermore, the average number of sapwood rings decreases with the mean width of the heartwood rings. However, the predictive power of the mean width is limited when the number of heartwood rings has already been taken into account. Thus, we suggest making predictions for the number of sapwood rings using only the number of heartwood rings. Predictions of the number of sapwood rings based on the statistical model where convincing in the case of the three different datasets that were analysed. The certainty in these predictions was such that the width of the 80% and 95% prediction intervals ranged 28–34 and 45–52 sapwood rings, respectively. Additionally, we demonstrate how make predictions when there is information about the number of remaining sapwood rings in a given sample. To make the sapwood model available, we present a free online R package for fitting our models and an online software dashboard.     

Features of female reproductive senescence in tamarins (Saguinus spp.), a New World primate.

Cyclical changes in concentration of plasma progesterone, urinary oestrone-conjugates and urinary luteinizing hormone (LH) were compared in young and older cotton-top tamarins (Saguinus oedipus) and saddle-backed tamarins (S. fuscicollis). A group of six young adult tamarin females (4-5 years of age) was sampled over eight periods of 6-8 weeks and six older (14-20 years of age) females were sampled over thirteen periods. There was hormonal evidence of ovulation in all of the sampling periods for young females; in five of thirteen periods, older females displayed no evidence of ovulation. Of the six older females, two were anovulatory in one sampling period, while one female displayed no evidence of ovulation in any of three sampling periods. Generally, females over 17 years of age either did not ovulate or displayed abnormally long periods of moderate concentrations of progesterone and oestrone conjugates. Basal concentrations of LH differed in individuals, but were not always higher in older females. In contrast to patterns of reproductive senescence in other primates, older, anovulatory tamarins displayed moderate concentrations of urinary oestrone conjugates (5-50 micrograms/mg creatinine) and plasma progesterone (8-19 ng/ml), both of which are hormones of probable luteal origin in these species. This result suggests continued production of steroids by the luteal cells of the prominent interstitial gland in reproductively senescent tamarins. This suggestion was reinforced by histological examination of the ovaries of four older, anovulatory females; few primary follicles were found. Three females had no normal antral follicles, but all females had large luteal masses. The presence of functional luteal cells in the older ovaries, which do not experience regular follicular development, may distinguish ovarian ageing in New World primates from that of Old World primates.     

Age and growth of black seabream Acanthopagrus schlegelii (Sparidae) in Hong Kong and adjacent waters of the northern South China Sea

Age and growth of the black seabream Acanthopagrus schlegelii (family Sparidae) from the northern South China Sea (NSCS) were studied by reading growth rings in sectioned sagittal otoliths. Ring formation frequency was determined to be annual by using marginal increment analysis. The von Bertalanffy growth function parameters were estimated as: L_∞ = 43.7 cm L_S; K =0.22 year; t₀ = ?1.59 years. Functional males are significantly younger than functional females, with sexually transitional individuals between the modal ages of males and females supporting protandry in this species. Males become sexually mature within 1 year and 50% age at sex change is at 2 years. The maximum age recorded for both males and females sampled was 9 years which is lower than for conspecifics elsewhere and may reflect high fishing pressure in the study area when compared with conspecifics in other areas or could reflect latitudinal effects. Otolith mass was significantly and positively related to age, providing a cheap and quick alternative method for approximating age. Acanthopagrus schlegelii is a relatively fast‐growing and rapidly maturing species attaining a similar asymptotic length to conspecifics. A need for fishery management is indicated to protect both young juveniles and older adults, especially females, to increase reproductive output and safeguard fishery production.     

Age, growth and reproduction of the cyprinid Rutilus lemmingii (Steindachner, 1866) in the River Huebra, Central Spain

Age, growth and reproduction of the R. lemmingii population of the River Huebra, Duero basin are analysed. Females dominated older age classes and lived up to 6 years (5+) while males only reached 5 years (4+). The growing season extended from April to September; growth rates were similar for both sexes. 0+ fish condition increased during their first summer and spring. In older fish, condition cycle was related to gonad development and showed some differences between sexes. The number of females reaching maturity at age 1 + almost doubled that of males; females also matured at smaller size. Both fecundity and egg size increased with female length: mean egg counts varied between 974 for 1 + individuals and an estimated 10491 for 5+ fish. Eggs were produced as a single batch, but were released fractionally during April and May.     

Early age reproduction in female savanna elephants (Loxodonta africana) after severe poaching

A 10-year study revealed that after severe poaching (>93% killed) of elephants ( Loxodonta africana ) in Zambia's North Luangwa National Park (NLNP) during the 1970s and 1980s, the age of reproduction in females was greatly reduced. Fifty-eight per cent of births were delivered by females aged 8.5–14 years, an age at which elephants were reported to be sexually immature in nearby South Luangwa National Park (SLNP) before poaching. The mean age of females at first birth (AFB) (1993, 1994) was 11.3 years. Prior to poaching, the mean age AFB in SLNP was 16 years. The NLNP age structure and sex ratio were skewed, mean family unit size was reduced, and 37% of family units contained no females older than 15 years. Twenty-eight per cent of family units were comprised entirely of a single mother and her calf, and 8% of units consisted only of orphans who would have been considered sexually immature prior to poaching. Only 6% of survivors were older than 20 years, the age at which females in little-poached populations generally become most reproductively active. After a community-based conservation programme and the UN-CITES ban on the ivory trade were introduced, no elephants were recorded killed. In spite of a high reproductive rate, 6 years after poaching decreased, the density of the NLNP population had not increased, supporting predictions that the removal of older matriarchs from family units will have serious consequences on the recovery of this species.     

Relative allocation to horn and body growth in bighorn rams varies with resource availability

Males may allocate a greater proportion of metabolic resourcesto maintenance than to the development of secondary sexual characterswhen food is scarce, to avoid compromising their probabilityof survival. We assessed the effects of resource availabilityon body mass and horn growth of bighorn rams (Ovis canadensis)at Ram Mountain, Alberta, Canada over 30 years. The number ofadult ewes in the population tripled during our study, and theaverage mass of yearling females decreased by 13%. We used theaverage mass of yearling females as an index of resource availability.Yearling female mass was negatively correlated with the bodymass of rams of all ages, but it affected horn growth only duringthe first three years of life. Yearly horn growth was affectedby a complex interaction of age, body mass, and resource availability.Among rams aged 2–4 years, the heaviest individuals hadsimilar horn growth at high and at low resource availability,but as ram mass decreased, horn growth for a given body massbecame progressively smaller with decreasing resource availability.For rams aged 5–9 years, horn growth was weakly but positivelycorrelated with body mass, and rams grew slightly more hornfor a given body mass as resource availability decreased. Whenfood is limited, young rams may direct more resources to bodygrowth than to horn growth, possibly trading long-term reproductivesuccess for short-term survival. Although horn growth of olderrams appeared to be greater at low than at high resource availability,we found no correlation between early and late growth in hornlength for the same ram, suggesting that compensatory horn growthdoes not occur in our study population. Young rams with longerhorns were more likely to be shot by sport hunters than thosewith shorter horns. Trophy hunting could select against ramswith fast-growing horns.     

A skeletochronological analysis of a population of the Anatolia Newt,Neurergus strauchii (Steindachner, 1887) (Caudata: Salamandridae), in Eastern Anatolia,Turkey

This study presents data on age, growth and longevity of a population of Neurergus strauchii in Eastern Anatolia (Bingöl, Turkey) based on skeletochronological data. The phalangeal diaphyseal cross-sections of 54 individuals studied (12♂, 42♀) showed that females are on average older than males: the ages ranged from 6 to 14 years, with an average age of 8.8 years in males and 10.9 years in females. Sexual maturity is reached at an age of 4-5 years in both sexes. The slow growth and the longevity make the species vulnerable.     

Age-related changes in ovarian morphology of the South American tamarin Saguinus fuscicollis (Callitrichidae)

The aim of this histological study was to investigate the postnatal ontogeny of the ovaries in Saguinus fuscicollis to provide a detailed knowledge of the ovarian morphology for further endocrinological studies. Gonads from 43 animals between one day and 18 years of age were investigated. Based on the available material the ovarian development is characterized by seven distinct stages. 1. Neonatal stage : Folliculogenesis is still in progress. The ovarian medulla is filled with an intraovarian rete system, which forms open connections between the rete tubules and the cords containing oocytes. 2. Infantile stage : One month after birth the ovarian cortex is mainly composed of primordial follicles and a few primary follicles at the corticomedullary border, which are separated from each other by connective tissue. At two months, folliculogenesis is nearly completed. The first secondary follicles are present. 3. Juvenile stage : In six-month-old females weighing 184±9.5 g, folliculogenesis has reached the stage of secondary follicles with up to six layers of granulosa cells. In females of the same age weighing 251.5±37 g, antral follicles attain a maximum diameter of 925 μm m. 4. Pubertal stage : At the age of 8–10 months, corpora lutea accessoria (CLA) begin to form from atretic antral follicles. 5. Adult stage : The ovaries of all females older than 1.2 years are filled with large patches of interstitial gland tissue (IGT). In breeding females up to 58.4%of the antral follicles are intact. In non-breeding daughters living in the family group only 1.8%are intact, the rest are in various stages of atresia and form CLA. 6. Climacterial stage : With increasing age (8–13 years), the number of intact follicles decreases dramatically and IGT fills nearly the whole ovary. 7. Senile stage : In females older than 14 years, nearly all remaining follicles show signs of atresia.     

The growth of Tilapia mossambica Peters (Pisces: Cichlidae) in Lake Sibaya, South Africa

The scales of Tilapia mossambica Peters * from Lake Sibaya show clear rings formed by broken, widely-spaced circuli in the anterior field. In order to determine the rate and time of scale ring formation, the number of circuli in the marginal increment was determined. Five scales from the pectoral region of 2223 fishes caught at regular intervals over two years were examined. When plotted as histograms, the number of circuli in the marginal increment showed a sharp movement to the left in September–October and again in January, indicating that the rings were formed during these months in the majority of fish examined. Pre- and postbreeding feeding migrations, and increases in condition factor, were associated with scale ring formation. Otoliths and opercula were also examined for age determination. Annual length increments were calculated for 450 T. mossambica collected throughout the year, and growth curves plotted. T. mossambica from Sibaya reach maturity after one year at a standard length of about 8 cm in females, and after two years at 10 cm in males. The breeding population had a standard length mode of 11–12 cm in females and 17 cm in males. The maximum final size was about 24 cm.     

On the biology of the catfish Chrysichthys auratus (Geoffory) in the man-made Tiga Lake in Northern Nigeria

SUMMARY. (1) A study was made of the biology of Chrysichthys auratus , a bottom-feeding omnivore, in Tiga Lake, a man-made lake in Northern Nigeria.
(2) Ripe females were present from April to September, coinciding with the hot season and rise in water level. First spawning took place at age II in females. No ripe males were found, and this was attributed to their spatial separation. Absolute fecundity was related to length and ranged from 327 to 1466 in forty-six females.
(3) Hyaline rings on the centra of lumbar vertebrae were counted to age 235 fish. The first ring is laid down at the end of the second year, after which the rings were formed annually, probably during the breeding season. The fish live for up to 6 years. There is a good fit of the growth curve to the von Bertalanffy equation. Growth is slow and a smaller maximum size is attained than in rivers.     

骨龄学方法测定中国水蛇的年龄

取不同体长的中国水蛇（Ｅｎｈｙｄｒｉｓ ｃｈｉｎｅｎｓｉｓ）标本４４条（２９♀♀,１４♂♂,１胎蛇）,剥取心脏附近的椎骨５枚,按常规骨骼磨片方法磨制椎骨中部的横切片,于低倍光学显微镜下观察。可以看到,磨片上有清晰的生长层,年老的个体更典型。用椎骨半径对生长层厚度的回归方程和ｖｏｎ Ｂｅｒｔａｌａｎｆｆｙ的生长方程式估算在骨骼生长过程中被再吸收而消失了的生长层。结果,４４条标本的年龄范围是０～１１．     

Aggressive interventions and matrilineal dominance relations in semifree-ranging barbary macaques (Macaca sylvanus)

Female Barbary macaques (Macaca sylvanus) form matrilineal hierarchies, i.e. they come to rank below their mother in relation to non-kin females in the course of maturation. The stability of such hierarchies and the acquisition of the matrilineal rank are achieved through dyadic aggressions and third party interventions in conflicts. This study examines the dynamics of interventions in non-kin conflicts in a semifree-ranging group of 109 Barbary macaques at “La Montagne des Singes,” Kintzheim, France. Focal sampling on 13 females aged 3 and 4 years not yet dominant over all older females from lower ranking kin groups (lower born females) was carried out during 16 months in 1987 and 1988. Results on the direction of support in non-kin female conflicts (all samples pooled) show that interventions were generally provided on behalf of the female from the higher ranking kin group (higher born female). Rates of interventions (derived from focal samples) given and received were correlated with the hierarchy; higher born females received more support and intervened more often than lower born females. A subset of interventions (based on the age of the females involved) was analyzed according to the rank distance between the opponents and the type of support provided (spontaneous or solicited). On the basis of their representation, intermediate-ranking supporters (i.e. females ranking between the opponents) intervened more often than above-ranking supporters (i.e. females dominant to both opponents), and they intervened more often spontaneously than following a solicitation. The results on interventions are discussed in the perspective of benefits to supporters. Twenty-one instances of outranking of older females (matrilineal rank acquisition) were observed. By the end of the study, the number of older lower born females not yet outranked by the focal females was negatively correlated to the rank distance between the two sets of females. However no such correlation was found between these two groups when compared according to their age difference in years.     

Evaluation of the age of the red whelk Neptunea antiqua using statoliths, opercula and element ratios in the shell

Growth rings present in whole and sectioned statoliths were used to determine the age of red whelks Neptunea antiqua, from the North Sea. Validation of the periodicity of the rings was established in four whelks by comparing the number of statolith rings with the number of seasonal Mg:Ca ratio cycles present in shell calcium carbonate samples drilled sequentially from along the growth axis. There was exact correspondence between the number of growth rings and the number of element ratio cycles in two of the shells and a 1-year difference in the estimated age between the two methods in the other two shells, evidence which is strongly indicative of an annual periodicity of deposition to the statolith rings. The estimated age of the whelks using the statolith rings varied between 4 years (shell length 102 mm) and 17 years (shell length 148 mm). The age of the whelks ascertained from the statoliths was compared with age estimates from the number of adventitious layers in sectioned opercula. The number of adventitious layers in whelks from 51 to 148 mm shell length ranged between 1 and 12 years. No significant difference was observed between the number of strongly defined statolith rings and number of opercula adventitious layers.     

The use of sectioned otoliths to age barramundi (Lates calcarifer) (Bloch, 1790) [Centropomidae]

The relationship between the number of rings present in sagittal otoliths and the age of barramundi, Lates calcarifer (Bloch, 1790) [Centropomidae], was investigated by examining cross sectioned otoliths of 37 tagged fish of known age between 1 and 5 years from the Johnstone River, north Queensland. Concentric rings were clearly visible in all otolith sections and were validated as annual marks. The technique was then used to estimate the age and calculate von Bertalanffy growth parameters for 70 barramundi from the Fitzroy River, central Queensland. Growth appeared to be rapid but variable in the first year; the von Bertalanffy growth parameters for length versus age were L =690 mm, K=0.53, t ₀= 0.003 years. October 1 was designated as the birth date. Whole otolith length, width and thickness were also approximated well by the von Bertalanffy equation. We suggest that examination of otoliths is a useful technique for ageing barramundi but note that further validation of the ageing method is still needed for fish older than six years.     

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.