Age,growth and mortality of invasive sharpbelly,Hemiculter leucisculus (Basilewski, 1855) in Erhai Lake,China

The sharpbelly Hemiculter leucisculus, an invasive species, has expanded its range throughout much of Asia and into the Middle East. However, little is known of its adaptive changes regarding life history traits such as age, growth and mortality that could possibly explain its success as an invasive species. A detailed study of the invasive sharpbelly was conducted based on 4539 samples collected from July 2009 to June 2011 in Erhai Lake, China. Standard length ranged from 4.3–19.1 cm for females and 4.6–12.3 cm for males. Length–weight relationships for females and males were significantly different and described as W = 0.0076SL^3.2608 and W = 0.0084SL^3.1901, respectively. Otoliths are ideal for age determination because of the single annulus formed each year. Based on marginal increment analysis, the total mean CV for age estimate between two readings was 3.55%. The von Bertalanffy growth curves computed by observed length‐at‐age data were expressed as L_t = 25.6 (1 ? e^{?0.176 (t + 1.347)}) for females and L_t = 16.4 (1 ? e^{?0.354 (t + 0.819)}) for males. According to the age, growth and mortality data, there are three possible reasons for H. leucisculus attaining such dominance within a short time in Erhai Lake. First, because of the simple age structure of this species: 97.58% of males were 1–2 years old with a maximum age of only 3 years; 93.14% of females were 1–3 years old, with a maximum age of 6 years. Second, females grew larger than males at any age. Third, instantaneous mortality rates were much higher for males (4.22 year^?1) than for females (1.17 year^?1).     

Growth and life history traits of Aegean chub,Squalius fellowesii (Günther, 1868) in streams in Muğla Province,Aegean coast,Turkey

To aid in species' conservation, the aim of this study was to provide initial findings on age, growth and reproduction of an endemic species, Aegean chub Squalius fellowesii (Günther, 1868) populations from streams in the Aegean region of Mu?la Province, Turkey. The species is relatively short‐lived (maximum 6 years), attaining a size of about 200 mm total length with a rapid growth to first maturity (≈60 mm TL), and relatively little growth thereafter. The male:female ratio was 1.0 : 0.6, males significantly outnumbering females in the majority of the streams. General condition values of individual fish varied between 2.9 and 3.4. Sexual maturity was usually achieved later and at larger sizes in females than in males. Sexual maturation in most populations was at the age of 2 years in females and 1 year in males. The species spawns between early April and late May. Mean absolute and relative fecundity were about 4440 eggs and 57 eggs·g^?1, respectively. Mean egg diameter was 1.00 ± 0.03 mm, ranging from 0.70 to 1.20 mm. Suggestions for the conservation of Aegean chub are discussed.     

Life history traits of Aphanius ginaonis Holly, 1929 (Cyprinodontidae) and potential risks of extinction in the Geno hot spring (Iran) population

This study presents some traits of the Aphanius ginaonis life history in the Geno hot spring and explains the potential risks of its extinction. Sampling was from March 2009 to February 2010. A total of 61 males and 71 females were measured (total length) and weighed, with data on reproductive biometry also taken. Growth parameters were determined in addition to weight–length relationships: W (t) = 0.012TL^3.42, R² = 0.96 for females and W (t) = 0.0101TL^3.38, R² = 0.94 for males. A. ginaonis females showed an asymptotic total length (TL_∞) of 53.03 mm; the growth coefficient, K (year^?1) 0.15, t₀ (year) 1.01; and natural mortality coefficient M (year^?1) 0.62. In males the value for TL_∞ was 48.83 mm; for K (year^?1) 0.2, t₀ (year) 0.44; and M (year^?1) 0.49. The relationship between absolute fecundity and fish size (total length, body weight or age) showed a strong correlation to body weight. The A. ginaonis population is threatened with extinction – and a co‐management in cooperation with the local population for strong protection measures is urgently needed.     

Life‐history traits of Aphanius danfordii (Boulenger, 1890) (Pisces: Cyprinodontidae), endemic to Kızılırmak Basin (Turkey)

The life‐history traits of Aphanius danfordii in Hirfanl? Reservoir were studied on the basis of 2252 specimens caught between April 2008 and April 2009. Maximum age was determined as five years for both sexes. The overall sex ratio of males to females was 1 : 1.21; however, this ratio varied by age and season. Mean total length at age data derived from scale readings were used to estimate growth. The von Bertalanffy growth parameters were: L_∞ = 126.63 mm, K = ?0.09, t₀ = 2.35 for females; and L_∞ = 61.2 mm, K = ?0.19, t₀ = 2.76 for males. The gonadosomatic index (GSI) values indicated spawning to be from May to September. Absolute fecundity varied from a minimum of 143 eggs for age one to a maximum of 698 eggs for age five. Relationships between fecundity–length and fecundity–weight were described by the equations: F = 0.0002 TL^3.3222 and F = 36.032 W^1.0053, respectively. The equation of the relation between absolute fecundity and age was F = 25.372 t^1.2343.     

Age,growth and reproduction of the sand smelt Atherina boyeri Risso, 1810 in Mellah Lagoon (Eastern Algeria)

This aim of this paper was the study of the reproductive biology and growth of the sand smelt, Atherina boyeri, in Mellah Lagoon (Algeria). These data are important for the sustainable exploitation of the stocks of this species. Examined was a total of 1402 Atherina boyeri specimens captured monthly from March 2010 to March 2011, in a population with a 3‐year life cycle. Length–weight relationship was estimated as W = 0.0047 L^3.077 (r² = 0.935) for males and W = 0.0047 L^3.176 (r² = 0.935) for females. Using scales, the von Bertalanffy growth function fitted to back‐calculated size‐at‐age data was Lt = 9.49 [1 ? e^{?0.316 (t + 0.928)}] for males, and Lt = 11.67 [1 ? e^{?0.179 (t + 1.514)}] for females; using otoliths this was Lt = 9.68 [1 ? e^{?0.3 (t + 1.02)}] for males, and Lt = 11.93 [1 ? e^{?0.171 (t + 1.55)}] for females. The growth performance index (Φ) indicated that males (Φ_scales = 3.34, Φ_otoliths = 3.33) grew at the same rate as females (Φ_scales = 3.19, Φ_otoliths = 3.24), with a sex ratio of 1 : 1.6 in favor of females. The reproductive season extended from February to June. Individual length at first sexual maturity was 4.20 cm for 1‐year‐old males and 4.35 cm for 1‐year‐old females.     

Life history characteristics and age validation of southern kingfish (Menticirrhus americanus (Linnaeus, 1758)) in the middle South Atlantic Bight

The purpose of this study was to determine critical components of the life history including otolith age validation, growth estimation, and reproductive characteristics for southern kingfish Menticirrhus americanus. A total of 2233 southern kingfish were collected from March 2009 to December 2010. Ages were estimated and validated using thin‐sectioned otoliths. Marginal increment analysis showed a single annulus was deposited once a year between April and May. Growth was significantly different (P < 0.0001) between sexes L_inf = 418.97 ± 16.58 mm, k = 0.29 ± 0.03, t₀ = ?1.30 ± 0.10 for females and L_inf = 290.74 ± 6.93 mm, k = 0.52 ± 0.05, t₀ = ?1.08 ± 0.11 for males. Southern kingfish spawn from March to August with a peak spawn in April. Based on evidence of multiple oocyte maturation stages and post‐ovulatory follicles (POFs) southern kingfish are multiple spawners exhibiting indeterminate fecundity. Spawning frequency for females ranging from 222 to 351 mm TL (age 1–5) was estimated as one spawning event every 2.0–4.2 days with up to 6 million total ova produced per spawning season per female.     

Life‐history traits of gaur Bos gaurus: a first analysis

In this first detailed analysis of gaur Bos gaurus life‐history traits, data were collected from a 20‐month field study in South India and from captive gaur populations. Mean age of females at first parturition was 3 years; females remained fertile beyond the age of 15 years. Adult females were three times more abundant than adult males in the wild; survival of females was greater than males beyond three years of age. Life span of both sexes has not exceeded 24 years in captivity. Gaur life‐history traits are similar to those of other similar‐sized Bovini species.     

Reproductive biology,growth, and age composition of non‐native Indian glassy fish Parambassis ranga (Hamilton, 1822) in Haebaru Reservoir,Okinawa‐jima Island,southern Japan

Age composition, growth, and reproductive biology of the non‐native Indian glassy fish Parambassis ranga (Hamilton, 1822) were surveyed in the Haebaru Reservoir on Okinawa‐jima Island, southern Japan. Standard lengths (SLs) of males and females ranged from 19.7 to 44.0 mm and from 19.2 to 52.4 mm, respectively. The overall sex ratio was significantly female‐biased, with the monthly percentage of females ranging from 71.4 to 100.0. Marginal growth analysis of sectioned otoliths revealed opaque zones formed annually from November to May. Observed age ranged from 0 to 3 years for both sexes, although the 1‐year age class comprised the majority of the sampled population. Von Bertalanffy growth parameters were L_∞ = 48.8 mm (SL), K = 0.43 year^?1, and t₀ = ?1.47 years for males, and L_∞ = 43.7 mm, K =0.72 year^?1, and t₀ = ?1.29 years for females. Length at 50% maturity was estimated to be 25.8 mm SL, and maturation was within 1 year after hatching. The main spawning season of P. ranga was estimated to occur from February to October, peaking in April.     

Reproductive biology of Metaschistura cristata in northeastern Iran

The study purpose was to investigate the reproductive biology, growth and length‐weight of the Turkmenian crested loach, Metaschistura cristata, in the Radkan River of northeastern Iran. Age and growth are described for 1029 specimens from January 2009 to December 2010. The sex ratio was 1:1. Maximum age, based on opercula readings, was 6⁺ years for both sexes. Specimens ranged in size from 24 to 98 mm total length and weighed from 0.08 to 7.32 g. The length‐weight relationships were described as W = 0.005166 TL^3.225 (R² = 0.97) for males and W = 0.006192 TL^3.125 (R² = 0.97) for females. Growth was expressed in length and the von Bertalanffy growth parameters were estimated as L_∞ = 354.9 mm, k = 0.0038, t₀ = ?26.82 for males and L_∞ = 339.0 mm, k = 0.0043, t₀ = ?24.88 for females. Growth performance indexes were also estimated as Φ′ = 6.17 for males and Φ′ = 6.20 for females. The gonadosomatic index showed that peak reproduction occurred during April and June, with highest average values of 2.1% for males and 25.3% for females in May. Oocyte diameter ranged from 0.09 to 1.58 mm, with a mean value of 0.54 ± 0.42 mm.     

Age,growth and maturity of tub gurnard (Chelidonichthys lucerna Linnaeus 1758; Triglidae) in the inshore coastal waters of Northwest Wales,UK

The tub gurnard Chelidonichthys lucerna has been identified by ICES as a potential commercial species in the northeast Atlantic with recommendations made to monitor landings and discards and to derive information on population biology for stock assessment purposes, however, data are lacking for the species in the northeast Atlantic. Therefore, aims of this study were to provide data on the size/age‐structure and patterns of growth, maturity and mortality of C. lucerna in Northwest Wales, UK, and in doing so to provide data on the biological characteristics of the most northerly population studied to date for comparison with the existing data for southerly Mediterranean populations. Data on the age, growth and maturity of C. lucerna were collected by otter trawling (73 mm cod‐end stretched mesh size) in the coastal waters of Northwest Wales, UK in October (2000–2011, excluding 2006). Total length (TL) of fish sampled ranged between 10.5–41.0 cm (males) and 10.4–57.5 cm (females). The majority of the female fish were between 20–30 cm TL (60.2%) and the majority of the male fish between 20–30 cm TL (58.3%) respectively. TL/weight (W) relations for male and female fish were similar and the combined data was described by W = 0.0067 TL^3.10. Age of fish ranged between 1–7 years old for female fish and 1–5 years old for male fish respectively with the majority of female fish 3 years old (40%) and the majority of male fish 3 years old (37%). The age structures of female and male tub gurnards were not significantly different with the older age classes consisting predominantly of female fish. Both males and females exhibited similar asymptotic growth patterns and the combined von Bertalanffy growth function was TL_t = 51.6 (1 ? e ^{[?0.25(t + 0.41)]}). Instantaneous rates of total mortality were calculated as 1.04 year^?1 for males and 1.11 year^?1 for females. The size (L₅₀) and age at first maturity (A₅₀) were estimated to be 29.1 cm TL and 2.8 years for males, 27.7 cm TL and 2.7 years for females and 28.0 cm TL and 2.8 years for both sexes combined. The results of this study provide the first information on the biology and population dynamics of C. lucerna in the Irish Sea, the first data collected in the northeast Atlantic since 1985 and the most northerly population studied to date.     

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.     

Age at mating and male quality influence female patterns of reproductive investment and survival

The trade‐off between the allocation of resources toward somatic maintenance or reproduction is one of the fundamentals of life history theory and predicts that females invest in offspring at the expense of their longevity or vice versa. Mate quality may also affect life history trade‐offs through mechanisms of sexual conflict; however, few studies have examined the interaction between mate quality and age at first mating in reproductive decisions. Using house crickets (Acheta domesticus), this study examines how survival and reproductive trade‐offs change based on females’ age at first reproduction and exposure to males of varying size. Females were exposed to either a large (presumably high‐quality) or small male at an early (young), middle (intermediate), or advanced (old) age, and longevity and reproductive investment were subsequently tracked. Females mated at a young age had the largest number of eggs but the shortest total lifespans while females mated at older ages produced fewer eggs but had longer total lifespans. The trade‐off between age at first mating and eggs laid appears to be mediated through higher egg‐laying rates and shorter postmating lifespans in females mated later in life. Exposure to small males resulted in shorter lifespans and higher egg‐laying rates for all females indicating that male manipulation of females, presumably through spermatophore contents, varies with male size in this species. Together, these data strongly support a trade‐off between age at first reproduction and lifespan and support the role of sexual conflict in shaping patterns of reproduction.     

Growth and longevity of the protogynous parrotfish,Hipposcarus harid,Scarus ferrugineus and Chlorurus sordidus (Teleostei,Scaridae), off the eastern coast of the Red Sea

Growth and longevity were studied for three species of the family scaridae, the longnose parrotfish (Hipposcarus harid), rusty parrotfish (Scarus ferrugineus) and bullethead parrotfish (Chlorurus sordidus), sampled at the eastern coast of the Red Sea, off Saudi Arabia. The three species are protogynous hermaphrodites presenting two distinct phases whereby the initial phase includes females and primary males, and the terminal phase is exclusively secondary males transformed from females. Annual marks in the ctenoid scales from the three species were used to develop size‐at‐age plots. Linear relationships were found between the scale radius and standard length for the three species, and the relationships between body weight (w) and standard length (L) were estimated. Scales of these species increased in size consistently throughout life, even though the somatic growth rate decreased with age. Sex‐specific growth effects in the three species were demonstrated. Growth of initial phase females was the lowest, followed by the initial phase males and terminal phase males, the latter showing the fastest growth rates. Thus, transition to the terminal male identity was associated with enhanced growth, resulting in larger terminal males than females of equivalent size. The von Bertalanffy growth formula (VBGF) was estimated for H. harid, S. ferrugineus and C. sordidus (L_∞ = 43.92, 27.4 and 23.3; K = 0.067, 0.27 and 0.56; t₀ = ?6.92, ?4.98 and ?4.6, respectively). The relationship between growth and reproduction of these species is also discussed.     

Age and growth of damselfish Chromis notata (Temminck & Schlegel, 1843), Jeju Island,Korea

This study investigated the age and growth of damselfish, Chromis notate, from Jeju Island in Korea. Samples were collected monthly by lift net from September 2013 to August 2014. Total lengths of the damselfish ranged from 6.4 to 15.3 cm. The relationship between total length and wet weight was WW = 0.0125TL^3.1631 for females, and WW = 0.0091TL^3.2769 for males. The slopes in the relationship between length and weight were not significantly different between sexes, but were significantly different in the intercepts. There were more female than male specimens (1.3:1). Age determination was conducted using the otoliths. Marginal increment (MI) declined in summer and winter, which suggests that two rings are formed each year. Ages of sampled individuals ranged from 1 to 5 years. Length‐at‐age data were fitted using the von Bertalanffy growth model. The estimated growth functions were L_t = 19.93 [1 ? exp^{?0.21 (t + 0.811)}] total length and wet weight was females, and L_t = 16.47 [1 ? exp^{?0.32 (t + 0.499)}] for males.     

Sexuality, sex change and maturation patterns in the yellowfin seabream, Acanthopagrus latus (Teleostei: Sparidae) (Houttuyn, 1782)

Macroscopic and histological studies were carried out to describe the reproductive styles and sex reversal and to follow gonadal changes in captive yellowfin seabream during the second year of life. Four reproductive styles are found in Acanthopagrus latus (Houttuyn, 1782): (i) males and females (gonochorism), (ii) functional males, (iii) transitionals and (iv) functional females. The species is a protandric hermaphrodite and begins life as a functional male with testicular zone undergoing active spermatogenesis, while the ovarian zone is arrested at the primary growth (perinucleolar) phase. Males and females were encountered in virtually all size‐classes. Functional males outnumbered the functional females in all size‐classes in which they were encountered. Sex reversal begins in the transitionals from July to August, after spawning in the functional males, at 14.9–20.2 cm standard length (SL) and, by November, maturation of the ovarian tissue begins. A. latus in cages in Kuwait waters spawns from January to April with a peak in February for males, and a peak in March for females and transitionals. Spawning begins in the 18.3–20.2 cm size‐range fish, peaking in the 20.3–22.2 cm size‐range in both males and females and also in the transitionals, although a few of the latter spawn from 14.9 cm SL. In relation to age, spawning begins at 20 months in males and peaks at 21 months. Females begin to spawn at 21 months with a peak at 22 months, while transitionals generally begin to spawn at 20 months, although a few 14–15‐month‐old sex‐changing individuals were encountered. Temperature, either alone or in combination with other unknown factors, triggers spawning in A. latus.     

Comparative morphology of dark-eyed juncos Junco hyemalis breeding at two elevations: a common aviary experiment

Morphologies of bird species often vary along elevation gradients, yet causes of the variation have not been examined experimentally. We investigated variation in morphological traits of the dark‐eyed junco Junco hyemalis, breeding at 1,000 m a.s.l. (low‐elevation; i.e. low) and 2,000 m asl (high‐elevation; i.e. high) in the Rocky Mountains, Canada. Eight morphological traits were measured in free‐living birds. We found two consistent differences in populations between elevations: at high‐elevation sites, females had longer wings and males had longer tails than birds from low‐ elevation sites. Other age‐ and gender‐ specific results were observed in free‐living birds between elevations: tarsi were shorter in high‐elevation second year (SY) females and after second year (ASY) males, beak lengths were slightly longer in low‐elevation SY females, and high‐elevation ASY females tended to have lower fat than low‐elevation ASY females. Morphological differences may result from genetic differences between elevations, or phenotypic flexibility resulting from exposure to the different environmental conditions. To identify which mechanism caused the difference in morphometrics, hand‐reared birds from low‐ and high‐elevation habitats were raised in identical conditions with unlimited access to high quality food until they had replaced all feathers. The traits measured in the lab (wing and rectrix length, weight and fat score) tended to increase in magnitude compared to field values. Juncos from high‐ and low‐elevations had similar responses to the aviary environment, with one exception: males from high‐elevation sites had greater weight gain relative to free‐living juncos than males from low‐elevation sites. Thus, morphological traits in dark‐eyed juncos were phenotypically flexible, capable of growing larger in the laboratory environment. However, there were also persistent genetic or perinatal/maternal differences underlying population responses that prevented traits from converging under aviary conditions. As a result, trait size differences between high‐ and low‐elevation populations were maintained or exacerbated in the common aviary environment.     

Sex‐specific telomere length and dynamics in relation to age and reproductive success in Cory’s shearwaters

Individuals in free‐living animal populations generally differ substantially in reproductive success, lifespan and other fitness‐related traits, but the molecular mechanisms underlying this variation are poorly understood. Telomere length and dynamics are candidate traits explaining this variation, as long telomeres predict a higher survival probability and telomere loss has been shown to reflect experienced “life stress.” However, telomere dynamics among very long‐lived species are unresolved. Additionally, it is generally not well understood how telomeres relate to reproductive success or sex. We measured telomere length and dynamics in erythrocytes to assess their relationship to age, sex and reproduction in Cory's shearwaters (Calonectris borealis), a long‐lived seabird, in the context of a long‐term study. Adult males had on average 231 bp longer telomeres than females, independent of age. In females, telomere length changed relatively little with age, whereas male telomere length declined significantly. Telomere shortening within males from one year to the next was three times higher than the interannual shortening rate based on cross‐sectional data of males. Past long‐term reproductive success was sex‐specifically reflected in age‐corrected telomere length: males with on average high fledgling production were characterized by shorter telomeres, whereas successful females had longer telomeres, and we discuss hypotheses that may explain this contrast. In conclusion, telomere length and dynamics in relation to age and reproduction are sex‐dependent in Cory's shearwaters and these findings contribute to our understanding of what characterises individual variation in fitness.     

Age and growth of Boops boops (Linnaeus, 1758) in Izmir Bay,Aegean Sea,Turkey

The present study was conducted to determine the age relationships in lengths and weights of Boops boops (Linneaus, 1756) in Izmir Bay, central Aegean Sea. A total of 932 specimens (503 females and 429 males) were caught by gillnet, trammel net and a combination thereof on a monthly sampling basis from November 2008 through October 2009. Total length and weight of sampled fish ranged from 11.3 to 27.9 cm and from 12.2 to 261.7 g, with a mean of 19.6 cm and 82.7 g, respectively. Length‐weight relationships for all individuals were described by the parameters a = 0.0050, b = 3.237 and r² = 0.956. The von Bertalanffy growth curve fitted to the lengths‐at‐age provided parameters of L_∞ = 29.87 cm k = 0.243 and t_o = ?0.98 for males and L_∞ = 30.79 cm, k = 0.239 and t_o = ?0.90 for females. Based on otolith readings, age determinations varied from 1 to 5 years. Maximum age was 5 years in age group 2, with 29.84 and 37.97% for males and females, respectively. The overall 1 : 1.17 sex ratio of males to females was significantly biased toward females (P < 0.05). There was no statistical difference in the mean condition factor (P > 0.05), with a value of 1.028 for the entire population. The growth performance index (Φ^’) was 2.33 and 2.36 for males and females, respectively. Results were similar to other geographical areas, which suggests that a common fisheries management might be possible.     

The relationship between otolith size and estimated age of tigertooth croaker (Otolithes ruber Bloch and Schneider, 1801) in Oman Sea,Iran

The relationships between somatic growth and otolith dimensions, otolith size to estimated age and growth parameters of the tigertooth croaker (Otolithes ruber) were investigated in 100 specimens (size range: 19.1–52.0 cm, total length) from the Oman Sea area, September 2014. All 100 otoliths were sectioned and determined by age. The oldest specimen was a 4.5‐year‐old female with a total length of 40.6 cm; the youngest specimen was also a female estimated at 1 year of age with a total length of 19.1 cm. The von Bertalanffy growth equation was estimated as L_t = 54.70 (1 ? exp (?0.37 (t + 0.21))). Concluded was that there is a significant relationship between body size, otolith dimensions and estimated age of Otolithes ruber.     

On the biological characteristics of Capoeta fusca Nikolskii, 1897 in eastern Iran

It is hypothesized that Capoeta fusca might display specific life‐history traits that differ from other species of this genus. To test this hypothesis a total of 354 specimens of C. fusca (listed by ICUN in the category DD = data deficient) were caught in the Qanat of Shadmehr (a well‐known active man‐made water well system in eastern Iran) on a monthly basis to cover fully the reproductive season from April to October 2007. Based on opercula readings the maximum ages of the population were 5+ years for both sexes. Sizes ranged from 57 to 190 mm total length (weight 2.14–84.76 g). Length‐weight relationship implied that the growth was negatively allometric for males and isometric for females. The von Bertalanffy growth model was estimated as L_t=18.74(1‐e^{?0.33(t+0.473)}) and L_t=22.35(1‐e^{?0.32(t+0.333)}) for males and females, respectively. Sex ratio was 1 : 2.42 in favour of females. The GSI indicated that reproduction of the fish in the qanat system occurred between May and August, with the highest average value of 6.12 for males in June and 9.55 for females in July. Oocyte diameters ranged from 0.30 to 2.05 mm, with a mean value of 0.92 mm. Absolute fecundity ranged between 506 and 22 800 eggs, with a mean of 4961 eggs. Fecundity relative to total weight fluctuated from 34 to 583, with a mean value of 133 eggs per g. Absolute fecundity and oocyte diameter to fish size (length and weight) were significantly correlated.