Sexual size dimorphism,growth, and maturity of the fluvial eight-barbel loach in the Kako River,Japan

The maturation and growth pattern of the fluvial eight-barbel loach Lefua sp. (Japanese name: nagare-hotoke-dojo), an endangered species, was investigated using an individual identification-recapture method from 1995 to 1998 in an upper reach of a headwater tributary of the Kako River, Hyogo Prefecture, Japan. Based on observations of the gonads through the abdominal skin, the loach was estimated to breed mostly from May to July. All the males matured by age 1⁺, and all the females matured by age 2⁺. Gamete release in all individuals of both males and females was predicted from recaptured loaches during each breeding season. The standard length of mature females was significantly larger than that of males, showing sexual size dimorphism (SSD). The maximum sizes recorded were 75.4 mm SL for females and 61.2 mm SL for males. Both males and females of immature specimens grew mainly from May to November, including the breeding season, with no significant differences in growth rates between them. After sexual maturity, both males and females grew mainly from July to October (or November), after the breeding season, and the females exhibited higher growth rates than males. Therefore, SSD of the species seems to be attributable to the different growth rates after maturity. The longevity of the loach was estimated to exceed ten years based on individual growth patterns of various sizes during the survey period. It is likely that the loach has an iteroparous life history, breeding every year, and moderate growth rates after maturity.     

Reproduction and sexual dimorphism in the viviparous lizard Sceloporus palaciosi (Squamata: Phrynosomatidae) from the Trans‐Mexican Volcanic Belt,Mexico

In this study, sexual dimorphism, reproductive cycles, litter size and offspring size of a population of the little‐known species Sceloporus palaciosi in central Mexico were analysed. Significant male‐biased sexual size dimorphism was recorded in snout–vent length (SVL), head length, head width, forearm length and tibia length. Both sexes showed asynchronous reproductive cycles, and males reached sexual maturity at a smaller SVL (33 mm) than females (37 mm). Testes volumes were small from January to February, testicular recrudescence began from March to June, and decreased in July, but increased again in August and September, followed by a second decrease from October to December. In females, vitellogenesis began from May until ovulation in December. Embryonic development extended from November to March, and a small number of females carried embryos through July. Mean litter size was 4.0 and was positively correlated with female SVL. The length of the reproductive period in S. palaciosi recorded in this study is longer than that recorded for other populations in other parts of this species range. Further studies are needed to clarify reproductive cycles in the other isolated populations of S. palaciosi, and then extended to other species and chromosome races in the Sceloporus grammicus complex.     

Use of pleopod morphology to determine sexual dimorphism and maturity in hermit crabs: <Emphasis Type="Italic">Isocheles sawayai</Emphasis> as a model

In the Anomura, studies on growth patterns are infrequent, possibly because the heterogeneity of the group, especially in terms of morphology, makes it difficult to construct generalized growth models. Particularly hermit crabs are an interesting group to evaluate aspects of growth, because of their unique body. Isocheles sawayai, a hermit crab found only in the western Atlantic Ocean, poorly known with respect to its sexual dimorphism and maturity, was investigated here based on morphometry. Monthly collections (July 2001 through June 2003) were made from a shrimp fishing boat in the Caraguatatuba region on the northern coast of the state of São Paulo, Brazil. The specimens were measured and weighed, and had their sex checked. Throughout the sampling period, 374 specimens of I. sawayai were collected (11.23% nonovigerous females, 6.69% ovigerous females, 79.41% males and 2.67% intersexes). The size at which morphological sexual maturity was reached by both sexes ranged from 4.0 to 4.3 mm shield length, according to the relative growth and the size of the smallest ovigerous female. Sexual dimorphism was shown by males, which were significantly larger than females, and by differences in growth pattern between the sexes, especially for relationships that involved the pleopods, which is related to their different functions in males and females. The present study is one of the first to use pleopod morphometry to determine sexual maturity and dimorphism in hermit crabs, especially for species with intersexuality such as I. sawayai.     

Development of intraspecific size variation in black coucals,white-browed coucals and ruffs from hatching to fledging

Most studies on sexual size dimorphism address proximate and functional questions related to adults, but sexual size dimorphism usually develops during ontogeny and developmental trajectories of sexual size dimorphism are poorly understood. We studied three bird species with variation in adult sexual size dimorphism: black coucals (females 69% heavier than males), white-browed coucals (females 13% heavier than males) and ruffs (males 70% heavier than females). Using a flexible Bayesian generalized additive model framework (GAMM), we examined when and how sexual size dimorphism developed in body mass, tarsus length and bill length from hatching until fledging. In ruffs, we additionally examined the development of intrasexual size variation among three morphs (Independents, Satellites and Faeders), which creates another level of variation in adult size of males and females. We found that 27–100% of the adult inter- and intrasexual size variation developed until fledging although none of the species completed growth during the observational period. In general, the larger sex/morph grew more quickly and reached its maximal absolute growth rate later than the smaller sex/morph. However, when the daily increase in body mass was modelled as a proportion, growth patterns were synchronized between and within sexes. Growth broadly followed sigmoidal asymptotic models, however only with the flexible GAMM approach, residual distributions were homogeneous over the entire observation periods. These results provide a platform for future studies to relate variation in growth to selective pressures and proximate mechanisms in these three species, and they highlight the advantage of using a flexible model approach for examining growth variation during ontogeny.     

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.     

Diet and reproductive biology of the Starred Agama,Laudakia stellio (Linnaeus, 1758) (Squamata: Agamidae), in the northern Sinai,Egypt

We quantified sexual size dimorphism, diet and reproduction in the Starred Agama, Laudakia stellio, in northern Sinai. Males were larger than females in snout-vent length and head index. The species is a sit-and-wait predator and feeds on insects, mainly coleopterans. About 30% of stomachs included plant material. No difference between sexes existed in terms of prey size preference. The reproductive season is seen to be year round with no distinctive seasonality. The smallest sexually mature female measured 92 mm SVL, whereas the smallest sexually reproductive male was 89 mm SVL. Clutch size ranged from 6 to 18 eggs.     

Annual reproductive cycle and sexual dimorphism in the dragonet,repomucenus valenciennei, in tokyo bay, japan

The annual reproductive cycle of the dragonet,Repomucenus valenciennei, from Tokyo Bay, Japan, was studied by analysis of seasonal trends in gonadosomatic indices and histological observations of gonads. Sexual dimorphism in the growth of several body parts relative to standard length (SL) and changes in color pattern of the first dorsal fin with growth were also investigated. The spawning season lasted from spring (April [1991] or February [1992]) to autumn (October) with two spawning peaks, in spring and autumn. In spring, only one-year-old (age 1+) fish spawned, age 0+ females not spawning until autumn, at which time they had reached age 1+. Likewise, histological observations of males indicated that testes had reached full maturity by 80 mm SL (age 1+). The minimum mature size of females was estimated as 60 mm SL. In males 45–80 mm SL, the first spine of the first dorsal fin, last ray of the second dorsal fin, last ray of the anal fin, and caudal fin ray showed strongly positive allometry, indicating rapid growth of these structures relative to SL. Subsequently, their growth returned to an isometric pattern in males>80 mm SL. In females, on the other hand, the same body parts showed slightly positive allometry throughout their growth. The color pattern on the first dorsal fin also changed in males 45–80 mm SL.     

Variation in body size, sexual dimorphism and age-specific survival in stoats, Mustela erminea (Mammalia: Garnivora), with fluctuating food supplies

Most hypotheses attempting to explain the evolution of pronounced sexual dimorphism in body size in the three species of weasels (Mustela erminea, M. frenata, M. nivalis) assume that sexual dimorphism is a long-term adaptation, associated with the different reproductive strategies of the two sexes. We here examine an auxiliary hypothesis which predicts that the degree of sexual dimorphism may also vary over the short-term, because when food is temporarily abundant, sexual selection should favour a greater growth rate of males than of females. This hypothesis concerns a phenotypic response which could introduce temporarily increased variation into an existing genotypic trait. We document the present size and sexual dimorphism of stoats introduced last century to New Zealand from Britain in relation to between-year variation in food supply in a single habitat (forests of southern beech, Nothofagus sp.). Southern beech trees produce heavy crops of flowers and seed at 3–5 year intervals, which are associated with very variable supplies of important prey of stoats, including several species of seed-eating birds, litter-feeding insects, and feral house mice (Mus musculus). Alternative prey are scarce. Regressions of condylobasal length and head-body length on mouse population indices were significant in both sexes. Mean condylobasal length was larger in both male and female stoats born after a heavy seedfall compared with those born in non-seedfall years. However, the largest males born in years of heavy seedfall were removed by selective mortality before the age of 3 years, so the condylobasal lengths for old (≥ 3.0 yr) males converged on a common mean regardless of food supply in their birth year. Sexual dimorphism did not vary with food supplies (as reflected in seedfall records or mouse population indices) at any age. First-year survivorship, at least from the age of independence, was significantly negatively correlated with density of stoats in the summer of their birth year.     

Growth, mortality and reproduction of the blue tilapia Oreochromis aureus (Perciformes: Cichlidae) in the Aguamilpa Reservoir, Mexico

Tilapia production has increased in Aguamilpa Reservoir, in Nayarit, Mexico, in the last few years and represents a good economic activity for rural communities and the country. We determined growth parameters, mortality and reproductive aspects for 2413 specimens of blue tilapia Oreochromis aureus in this reservoir. Samples were taken monthly from July 2000 through June 2001, of which 1 371 were males and 1 042 were females. Standard length (SL) and total weight (TW) were measured in each organism. The SL/TW relationships through power models for sexes were determined. The growth parameters L infinity k, and t0 of the von Bertalanffy equation were estimated using frequency distribution of length through ELEFAN-I computer program. Finally the reproductive cycle and size of first maturity were established using morph chromatic maturity scale. The results suggested that the males and females had negative allometric growth (b < 3). Significant differences were found between SL/TW model for the sexes, suggesting separate models for males and females. Results indicate that there are no differences in growth rates between sexes; the proposed parameters were L infinity = 43.33 cm standard length, k = 0.36/year and t0 = -0.43 years. Natural and fishing mortality coefficients were 0.83/year and 1.10/year, respectively. The estimated exploitation rate (0.57/year) suggested that during the study period the fishery showed signs of overfishing. Blue tilapia reproduces year-round; the highest activity occurs from January through May and size of first maturity was 23 cm SL. We conclude that it is necessary to establish a minimum catch size in this reservoir based on the reproductive behavior of this species.     

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

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

Growth and survivorship as proximate causes of sexual size dimorphism in peninsula dragon lizards Ctenophorus fionni

Males and females differ in body size in many animals, but the direction and extent of this sexual size dimorphism (SSD) varies widely. Males are larger than females in most lizards of the iguanian clade, which includes dragon lizards (Agamidae). I tested whether the male larger pattern of SSD in the peninsula dragon lizard, Ctenophorus fionni, is a result of sexual selection for large male size or relatively higher mortality among females. Data on growth and survivorship were collected from wild lizards during 1991–1994. The likelihood of differential predation between males and females was assessed by exposing pairs of male and female lizards to a predator in captivity, and by comparing the frequency of tail damage in wild‐caught males and females. Male and female C. fionni grew at the same rate, but males grew for longer than females and reached a larger asymptotic size (87 mm vs. 78 mm). Large males were under‐represented in the population because they suffered higher mortality than females. Predation may account for some of this male‐biased mortality. The male‐biased SSD in C. fionni resulted from differences in growth pattern between the sexes. The male‐biased SSD was not the result of proximate factors reducing female body size. Indeed SSD in this species remained male‐biased despite high mortality among large males. SSD in C. fionni is consistent with the ultimate explanation of sexual selection for large body size in males.     

Sexual dimorphism in <Emphasis Type="Italic">Sebastes owstoni</Emphasis> (Scorpaenidae) from the Sea of Japan

Morphological and genetic differences between red and yellow morphotypes of Sebastes owstoni were investigated, utilizing 277 males [84.0–194.3 mm in standard length (SL)] and 542 females (92.3–251.5 mm SL) from the Sea of Japan. All males smaller than 120 mm SL were characterized by red body color. The frequency of specimens with yellow body color thereafter increased gradually with SL, all specimens larger than 170 mm SL being yellow. The specimens with yellow body color were observed throughout the year. All females smaller than 170 mm SL were characterized by red body color, the frequency of specimens with yellow body color tending to slightly increase with SL. However, most females had red body color, except for 16 specimens (177.7–241.5 mm SL) that were yellow, growth-related color change from red to yellow being uncommon. Morphological analysis of 49 males (107.6–193.3 mm SL) and 68 females (108.7–241.5 mm SL) showed the head length, orbit diameter, lower jaw length, and predorsal length to be relatively greater, but the distance between the pelvic and anal fins less, in males. A discriminant analysis using Mahalanobis distances resulted in 100% correct assignment of specimens to sex, regardless of SL and body color. In addition, no genetic differences were apparent between red and yellow individuals in mitochondrial DNA sequence analyses from the threonine tRNA to the first half of the control region (498 bp). Accordingly, the differences in body color, maximum size, and the five morphometric characters listed above were considered to represent sexual dimorphism. That evidenced by body color was considered to appear after that shown by morphometric characters, some exceptions in the former occurring in females. This is the first report of permanent sexual dimorphism in body color in Sebastes.     

Patterns of growth and sexual size dimorphism in two species of box turtles with environmental sex determination

An adaptive explanation for environmental sex determination is that it promotes sexual size dimorphism when larger size benefits one sex more than the other. That is, if growth rates are determined by environment during development, then it is beneficial to match developmental environment to the sex that benefits more from larger size. However, larger size may also be a consequence of larger size at hatching or growing for a longer time, i.e., delayed age at first reproduction. Therefore, the adaptive significance of sexual size dimorphism and environmental sex determination can only be interpreted within the context of both growth and maturation. In addition, in those animals that continue to grow after maturation, sexual size dimorphism at age of first reproduction could differ from sexual size dimorphism at later ages as growth competes for energy with reproduction and maintenance. I compared growth using annuli on carapace scales in two species of box turtles (Terrapene carolina and T. ornata) that have similar patterns of environmental sex determination but, reportedly, have different patterns of sexual size dimorphism. In the populations I studied, sexual size dimorphism was in the same direction in both species; adult females were, on average, larger than adult males. This was due in part to males maturing earlier and therefore at smaller sizes than females. In spite of similar patterns of environmental sex determination, patterns of growth differed between the species. In T. carolina, males grew faster than females as juveniles but females had the larger asymptotic size. In T. ornata, males and females grew at similar rates and had similar asymptotic sizes. Sexual size dimorphism was greatest at maturation because, although males matured younger and smaller, they grew more as adults. There was, therefore, no consistent pattern of faster growth for females that may be ascribed to developmental temperature. Received: 20 March 1996 / Accepted: 10 March 1998     

The evolution of sexual size dimorphism in the house finch. IV. Population divergence in ontogeny

Differences among taxa in sexual size dimorphism of adults can be produced by changes in distinct developmental processes and thus may reflect different evolutionary histories. Here we examine whether divergence in sexual dimorphism of adults between recently established Montana and Alabama populations of the house finch (Carpodacus mexicanus) can be attributed to population differences in growth of males and females. In both populations, males and females were similar at hatching, but as a result of sex-specific growth attained sexual size dimorphism by the time of independence. Timing and extent of growth varied between the sexes: Females maintained maximum rates of growth for a longer time than males, whereas males had higher initial growth rates and achieved maximum growth earlier and at smaller sizes than females. Ontogeny of sexual dimorphism differed between populations, but in each population, sexual dimorphism in growth parameters and sexual dimorphism at the time of nest leaving were similar to sexual dimorphism of adults. Variation in growth of females contributed more to population divergence than did growth of males. In each population, we found close correspondence between patterns of sexual dimorphism in growth and population divergence in morphology of adults: Traits that were the most sexually dimorphic in growth in each population contributed the most to population divergence in both sexes. We suggest that sex-specific expression of phenotypic and genetic variation throughout the ontogeny of house finches can result in different responses to selection between males and females of the same age, and thus produce fast population divergence in the sexual size dimorphism.     

蓝尾石龙子的头部两性异形和食性

通过测量头、体大小和胃检研究浙江泰顺产蓝尾石龙子 (Eumeceselegans)个体发育过程中两性异形和食性的变化。蓝尾石龙子成体个体大小和头部大小的两性差异显著 ,雄性大于雌性。不同发育阶段雌性头长与SVL的线性回归斜率无显著差异 ,头宽与SVL线性回归斜率的差异显著 ,成体和SVL <5 0mm幼体头宽随SVL的增长速率显著小于SVL为 5 0 - 6 9mm的幼体。雄性头部相对于SVL呈加速式异速生长。两性比较发现 :雌雄幼体头长和头宽随SVL的增长速率无显著差异 ,SVL <5 0mm幼体特定SVL的头长和头宽无显著的两性差异 ,但SVL为 5 0 - 6 9mm的雄性幼体头长和头宽大于SVL相同的雌性幼体 ;雄性成体头长和头宽随SVL的增长速率显著大于雌性。SVL <5 0mm的雌性幼体头部相对小于SVL为 5 0 - 6 9mm的同性幼体 ,性成熟雌体头部相对小于SVL为 5 0 - 6 9mm的同性幼体。雌性幼体、雄性幼体、雌性成体和雄性成体食物生态位宽度分别为 12 3、 12 5、 4 8和 14 4。雌雄幼体食物生态位重叠度最高 ,雌雄成体食物生态位重叠度次之 ,成体与幼体食物生态位重叠度较小。成体摄入食饵的大小 (用胃内完整食物长度的平均值表示 )和变化范围大于幼体。两性成、幼体摄入的食饵大小差异显著。两性个体摄入的食饵大小均与其SVL呈正相关 ,表明较大     

The reproductive biology, age and growth of the North American cyprinid, Notropis longirostris (Hay)

Notropis longirostris (Hay), the longnose shiner, in Catahoula Creek, Jourdan River drainage, Hancock County, Mississippi, was studied from May 1970 to May 1972. In 1971 reproduction occurred from late March into October, as indicated by gross examination of testes, breeding tubercles and breeding colour in males, and ovarian weights, measurements of ova, and gross examination of ovaries in females. Gross examination of ovaries in 1970 also indicated an extended reproductive season. Generally no significant differences from a 1 : 1 sex ratio or in the size of males and females in collections taken during the reproductive season were indicated. Males and females matured about the same size. Most females were sexually mature when 29–30 mm SL. The smallest female with mature ova was 28 mm; however, the majority of females did not have mature ova until 31–33 mm. The number of mature ova produced prior to spawning ranged from 15 to 129 for females 30.8–44 mm SL. There were significant differences in the number of mature ova with time, two peaks being indicated: the first in late March and April at the beginning of the reproductive period and the second in early July about the middle of the season. This conclusion is also supported by ovarian weight measurements and length frequency histograms. The mean diameters of mature ova ranged from 0.70–1.05 mm, averaging 0.90 mm, and were not significantly correlated with length. Most fish live about 1–1.5 years and do not live through two winters, indicating an annual turnover in the population. Maximum size was about 48 mm SL. Specific characteristics of the life history pattern of N. longirostris are discussed in relation to ecological conditions of the habitat.     

Extreme Sexual Brain Size Dimorphism in Sticklebacks: A Consequence of the Cognitive Challenges of Sex and Parenting?

Selection pressures that act differently on males and females produce numerous differences between the sexes in morphology and behaviour. However, apart from the controversial report that males have slightly heavier brains than females in humans, evidence for substantial sexual dimorphism in brain size is scarce. This apparent sexual uniformity is surprising given that sexually distinct selection pressures are ubiquitous and that brains are one of the most plastic vertebrate organs. Here we demonstrate the highest level of sexual brain size dimorphism ever reported in any vertebrate: male three-spined stickleback of two morphs in an Icelandic lake have 23% heavier brains than females. We suggest that this dramatic sexual size dimorphism is generated by the many cognitively demanding challenges that males are faced in this species, such as an elaborate courtship display, the construction of an ornate nest and a male-only parental care system. However, we consider also alternative explanations for smaller brains in females, such as life-history trade-offs. Our demonstration of unprecedented levels of sexual dimorphism in brain size in the three-spined stickleback implies that behavioural and life-history differences among the sexes can have strong effects also on neural development and proposes new fields of research for understanding brain evolution.     

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

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

Sexual size dimorphism and selection in the wild in the waterstrider Aquarius remigis: Body size,components of body size and male mating success

Sexual size dimorphism is assumed to be adaptive and is expected to evolve in response to a difference in the net selection pressures on the sexes. Although a demonstration of sexual selection is neither necessary nor sufficient to explain the evolution of sexual size dimorphism, sexual selection is generally assumed to be a major evolutionary force. If contemporary sexual selection is important in the evolution and maintenance of sexual size dimorphism then we expect to see concordance between patterns of sexual selection and patterns of sexual dimorphism. We examined sexual selection in the wild, acting on male body size, and components of body size, in the waterstrider Aquarius remigis, as part of a long term study examining net selection pressures on the two sexes in this species. Selection was estimated on both a daily and annual basis. Since our measure of fitness (mating success) was behavioral, we estimated reliabilities to determine if males perform consistently. Reliabilities were measured as ? statistics and range from fair to perfect agreement with substantial agreement overall. We found significant univariate sexual selection favoring larger total length in the first year of our study but not in the second. Multivariate analysis of components of body size revealed that sexual selection for larger males was not acting directly on total length but on genital length. Sexual selection for larger male body size was opposed by direct selection favoring smaller midfemoral lengths. While males of this species are smaller than females, they have longer genital segments and wider forefemora. Patterns of contemporary sexual selection and sexual size dimorphism agree only for genital length. For total length, and all other components of body size examined, contemporary sexual selection was either nonsignificant or opposed the pattern of size dimporhism. Thus, while the net pressures of contemporary selection for the species may still act to maintain sexual size dimorphism, sexual selection alone does not.     

Life-history strategies of Acrossocheilus fasciatus (Barbinae, Cyprinidae) in the Huishui Stream of the Qingyi watershed, China

Life-history traits of Acrossocheilus fasciatus were examined using 384 specimens collected monthly during May 2009 and April 2010 in the Huishui Stream of the Qingyi watershed, China. Using scales for age determination, female and male fish comprised five and four age groups, respectively. The monthly changes in marginal increment ratio suggested that annuli on scales were formed during March through May. Total lengths back-calculated significantly increased with age for both sexes and varied significantly between the two sexes at each age. The fact that females had larger body size and grew faster than males indicated the sexual size dimorphism for this species. Both sexes got their 50% maturity at age 3, when females and males were 105.3 and 112.1?mm total length, respectively. Based on the monthly changes in the gonado-somatic index and egg-development process, fish spawned from April through August. Absolute fecundity ranged from 295 to 3,573 eggs per fish and increased significantly with age. But relative fecundity, ranging from 11.77 to 69.96?eggs/g, was not significantly different among age groups. Compared with the life-history traits of an upstream population in the Puxi Stream (a headwater stream within this study watershed), the downstream population of A. fasciatus in the Huishui Stream (a 4th-order stream) exhibits larger body size, faster somatic growth, later sexual maturity, and lower reproductive investment. These variations in life-history strategies between the two populations could perhaps be explained by the spatial heterogeneity in habitat environment along the upstream–downstream gradient in this watershed.