Age,growth, mortality and sex ratio of the inshore population of the edible crab,Cancer pagurus (Linnaeus 1758) in South Wales (UK)

Age, growth, and mortality of the edible crab, Cancer pagurus, were determined for the native population in South Wales (UK). Sampling was carried out on a monthly basis between February 2001 and September 2002. Carapace width ranged between 10.4 and 163 mm. Based on the carapace width frequency distribution, the Swansea and Gower population was composed mainly of males belonging to the first and second age‐class (1 and 2), and of females belonging to the third and fourth age‐class (3 and 4). Sex ratio was 1.126 ± 0.27 in favour of males. Carapace width frequency distributions and weight‐at‐age data were used to estimate the von Bertalanffy growth equation parameters. For the population as a whole, these were: L∞ = 199 mm, W∞ = 1179.56 g, K = 0.24 year^?1, t₀ = ?0.1004 years. The overall carapace width–weight relationship was: W = 0.38(CW^2.69). Analysis of covariance indicated a significant difference in the carapace width–weight relationship between males and females in the study area. Total mortality Z and natural mortality M rates for combined sexes were 1.245 year^?1 and 0.567 year^?1, respectively. The exploitation ratio E was estimated to be 54.43%.     

Age,growth, reproduction and feeding of John Dory,Zeus faber (Pisces: Zeidae), in the Saros Bay (North Aegean Sea)

The age, growth, reproduction, sexual maturity and stomach content of John Dory (Zeus faber), caught in the Bay of Saros (North Aegean Sea) between September 2006 and September 2008, were investigated. The female‐male ratio was 1.6 : 1. The total length of females ranged from 13.8 cm to 52.8 cm, and of males from 12.2 cm to 42.9 cm. The length‐weight relationship was W = 0.0174*L^2.936. Age data derived from vertebral centra readings were used to estimate the growth parameters of the von Bertalanffy equation. Growth parameters for females were L_∞ = 58.50 cm K = 0.11 year^?1, t₀ = ?0.99 year and for males L_∞ = 45.01 cm, K = 0.13 year^?1, t₀ = ?1.17 year. Maximum age was 18 years for females and 17 years for males. Length at first maturity for both females and males was 25.4 cm. Monthly values of the gonadosomatic index indicated that spawning occurred mainly in two peaks: one between January and June, and the other from August to September. Stomach content analysis showed the most‐preferred prey to be Pisces (IRI% 97.3).     

Testing staining techniques to determine age and growth of Dasyatis pastinaca (Linnaeus, 1758) captured in Iskenderun Bay,northeastern Mediterranean

This study tested the suitability of several staining methods to determine the age of common stingray (Dasyatis pastinaca) from Iskenderun Bay, Turkey. A total of 384 specimens (16.6 cm–69.3 cm disc width) were obtained by trawling between September 2010 and December 2011. Sex ratio of the samples was 53% males and 47% females. Appropriate age determination was firstly demonstrated using Safranin‐O staining. Age readings were made by two independent readers and the index of average percent error (IAPE) determined as 6.3% for Safranin‐O, 6.8% for Crystal Violet, 7.9% for Alcian Blue, and 9.3% for Silver Nitrate. Safranin‐O and Crystal Violet staining methods provided the best results. Verification of temporal growth ring formation was by marginal increment analysis. Disc width–weight relationships were determined by W = 0.0272*DW^3.06 for females and W = 0.0247*DW^3.08 for males. Estimates of the von Bertalanffy growth parameters indicated a larger asymptotic disc width (DW_∞ = 127.06 cm) for females than for males (DW∞ = 114.54 cm); growth parameters were k = 0.058 year^?1, t_o = ?1.508 and k = 0.041 year^?1, t_o = ?3.632 for females and males, respectively.     

Reproductive strategy of the invasive sharpbelly,Hemiculter leucisculus (Basilewsky 1855), in Erhai Lake,China

This study describes the reproductive strategy of the sharpbelly Hemiculter leucisculus, an invasive and dominant species in Erhai Lake in China with the goal of understanding how reproductive strategy contributes to its environmental adaptability and invasive potential. Specimens (n = 3583) were collected monthly or bimonthly from July 2009 to June 2011 (min: 114‐Feb, max: 883‐Aug), using gill nets (inner/outer mesh = 30/110 mm, stretched mesh). Gonads were removed, weighed and preserved for further (histological) analyses. Oocyte size‐frequency distribution was continuous and had advanced vitellogenic oocytes with postovulatory follicles present in spawning females, both suggesting that sharpbelly is a multiple spawner with adhesive eggs. Spawning extended from April to September, with the peak period from May to August. Standard lengths (SL, cm) at minimal observed maturity/L₅₀/L_99.9 values were 4.6/5.6/10.5 for females and 5.1/5.5/7.5 cm for males, respectively. Females were over‐represented (P < 0.01) in SL‐classes over 9 cm and males completely absent from the 13 to 19 cm SL‐classes. Overall sex ratio was highly significantly (P < 0.01) biased towards females (♀ = 1518, ♂ = 685, ♀/♂  = 2.21), however this was reversed in the spawning stock (8.3–16 cm, ♀ = 58, ♂ = 142, ♂/♀  = 2.45, P < 0.01). Batch spawning, a long spawning period, high male investment in reproduction and adhesive eggs all represent local adaptations in reproductive strategy that, along with other environmental factors, contribute to the invasion success of sharpbelly in Erhai.     

Population biology of grey gurnard (Eutrigla gurnardus (L.); Triglidae) in the coastal waters of Northwest Wales

The grey gurnard Eutrigla gurnardus (L.) has been identified by ICES as a potential commercial species in the NE Atlantic with recommendations made to derive information on population biology for stock assessment purposes. However, data on the population biology of this species is limited. In this study, data on the age, growth and maturity of grey gurnard were collected by otter trawling in the coastal waters of northwest Wales and Eastern Anglesey. Total length (TL) of fish sampled ranged between 2.1–33.0 cm (male) and 1.9–36.9 cm (female) with the majority of female (70.8%) fish between 11 and 20 cm TL and male fish (70.5%) between 11 and 18 cm TL. The percentage of fish >20 cm TL was larger for females (30.4%) compared to males (17.6%). Total weight (TW) for female and male grey gurnard in the stratified subsample ranged from 1.9 to 499.9 g for females and 2.1–390.0 g for males, with the majority of female (66.3%) and male (76.1%) fish between 10 and 60 g. TL/TW relations for male and female fish and both sexes combined were: TW = 0.006TL^3.07, TW = 0.007TL^3.03 and TW = 0.007TL^3.05 respectively. Age structure (based on otolith reading) ranged between 0.5 and 7.5 years old for females and 0.5 to 5.5 years old for male with the majority of female (41.7%) and male (46.0%) fish aged as 1.5 years old. The age structure of female and male grey gurnards was significantly different with the majority of older fish (>2.5 years) being female. The von Bertalanffy growth functions were calculated as L_t = 32.4[1 ? e^{?0.24(t + 1.41)}] for males, L_t = 45.9[1 ? e^{?0.16(t + 1.37)}] for females and L_t = 44.0[1 ? e^{?0.18(t + 1.20)}] for both sexes combined. Instantaneous rates of total mortality were similar for males and females and the combined Z value 1.00 year^?1 with the natural mortality rate estimated as 0.33 year^?1. The size at 50% maturity (L₅₀) was estimated to be 25.3 cm TL for males, females and for both sexes combined. Age at 50% maturity (A₅₀) was 3.2 years for both males and females. The results of this study provide the first information on the population biology of E. gurnardus in the Irish Sea, the first detailed study in the NE Atlantic since 1985 and helps to address the data gap identified by ICES in knowledge of the population biology of this species.     

Population parameters of stargazer (Uranoscopus scaber Linnaeus, 1758) in the southeastern Black Sea region during the 2011–2012 fishing season

The population parameters of stargazer (Uranoscopus scaber Linnaeus, 1758) were studied regarding age composition, sex ratio, growth, survival and mortality rates, and the exploitation rate in the southeastern Black Sea near the coast of Turkey during the 2011–2012 fishing season. According to ageing analysis of the samples, age group 1 is the most abundant (47.76%), followed by age 2 (41.04%), age 3 (9.33%), age 0 (1.12%) and age 4 (0.75%). Mean totals as well as total lengths and weights for males and females were 14.5 ± 0.22 cm and 12.9 ± 0.19 g, 16.6 ± 0.24 cm and 62.1 ± 2.76 g, and 37.2 ± 1.92 cm and 87.1 ± 3.88 g, respectively. The mean condition factor was K = 0.0167, while the sex ratio was 53.98% female, 38.75% male and 7.27% immature. Length‐weight, age‐length and age‐weight equations were W = 0.014 × L^3.059, L_(t)=44.5*[1?e^{?0.148*(t +1.242)}] and W_(t)=1544.4*[1?e^{?0.148*(t + 1.242)}]^3.059, respectively. The computed survival rate (S), instantaneous total mortality rate (Z), annual mortality rate (A), natural mortality rate (M) and fishing mortality rate (F) were S = 28.94%, Z = 1.24 year^?1, A = 71.06%, M = 0.26 year^?1 and F = 0.98 year^?1, respectively. The exploitation rate was 0.79, which is above the optimum exploitation levels.     

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.     

A study on age and growth characteristics of spiny gurnard (Lepidotrigla dieuzeidei Blanc & Hureau, 1973), northeastern Mediterranean Sea

This study investigated the age and growth characteristics of spiny gurnard, Lepidotrigla dieuzeidei, from the northeastern Mediterranean. Samples were collected by commercial trawls during the 2012–2013 fishing seasons. A total 1,878 speciments ranged from 7.10 to 15.90 cm total length and 2.28–35.88 g in weight. Female/male ratio was 1.2/1. The total length–weight relationship was W = 0.002 TL^3.579 (r² = .909) for sexes combined, W = 0.0021 TL^3.551 (r² = .914) for males and W = 0.0019 TL^3.602 (r² = .904) for females. Age determination was conducted using the sagittal otoliths. Ages of examined individulas ranged from 3 to 11 years. Total length‐at‐age data were fitted using the von Bertalanffy growth model. Estimated growth functions were TL_t = 18.100 [1?e^{?0.14 (t + 0.63)}] for sexes combined, TL_t = 23.587 [1?e^{?0.08 (t + 1.56)}] for males and TL_t = 16.612 [1?e^{?0.19 (t + 0.15)}] for females.     

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.     

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.     

Reproductive biology of Chinese minnow Hemiculterella sauvagei Warpachowski, 1888 in the Chishui River,China

This study describes the reproductive biology of the Chinese minnow Hemiculterella sauvagei. The length‐weight relationship, sex ratio, spawning season, size at first maturity, and fecundity were analyzed based on 685 specimens collected from the Chishui River between July 2011 and July 2012. The relationship between standard length (SL) and body weight (BW) were estimated as BW = 2.14 × 10^?4 × SL^2.801 (R² = 0.839; N = 413; P < 0.05) for females and BW = 1.31 × 10^?4 × SL^3.001 (R² = 0.868; N = 272; P < 0.05) for males. The female to male sex ratio, 1.52 : 1, differed significantly from a 1 : 1 ratio. Females predominated in standard lengths >12 cm. Analyses of the monthly variation in the gonadosomatic index (GSI), the monthly proportions of macroscopic gonadal maturity, and the size distribution of oocytes consistently suggested a prolonged spawning season of H. sauvagei from March to August, with a peak from April to May. Logistic curves describing the relationship between proportion of maturity (P_r) at each length interval and standard length were estimated as P_r = 1/(1 + e^{26.867–0.306SL}) (R² = 0.999; N = 413; P < 0.05) for females and P_r = 1/(1 + e^{10.522–0.142SL}) (R² = 0.999; N = 272; P < 0.05) for males. Size at first maturity was estimated as 7.4 cm for males and 8.8 cm SL for females. Absolute fecundity varied from 563 to 5052, with a mean of 2413 ± 874 oocytes per ovary. The relative fecundity was estimated to be 41–299, with a mean of 171 ± 55 oocytes per ovary. The present study provides useful information for fishery management and resources conservation.     

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.     

Reproduction,growth and mortality of the exploited sillaginid,Sillago ciliata Cuvier, 1829

The goal of this study was to examine the age and size composition, growth, reproductive biology and mortality of Sillago ciliata Cuvier, 1829 in one of the largest estuarine commercial fisheries in south‐eastern Australia. The study also aimed to present a qualitative comparison of latitudinal variations in some of these characteristics along the eastern Australian coastline. The sampled population contained fish aged up to 10 years with a maximum size of 39.2 cm fork length (L_F), and was dominated by 1–5 year olds. Sexual divergence in both the age and size structure of the population was recorded. Female S. ciliata grew slightly faster and attained a greater maximum size (L_∞ = 33.79 cm L_F, k = 0.50 year^?1 and t₀ = ?0.57 years) than males (L_∞ = 29.73 cm L_F, k = 0.49 year^?1 and t₀ = ?0.67 years). Females also matured at a significantly larger size (19.13 cm) and older age (1.63 years) than males (size: 17.07 cm, age: 1.10 years). Reproductive activity was highest between September and March. There were no differences between males and females in terms of mortality rate; the estimated total population, natural and fishing mortality rates were Z = 0.64, M = 0.42 and F = 0.22, respectively. Although these mortality rates suggest that S. ciliata in the Clarence River are relatively resilient to current rates of exploitation, regular monitoring of their commercial and recreational catch as well as their population structure is recommended in order to maintain sustainable fisheries. Potential latitudinal shifts in the spawning period, age structure and growth of S. ciliata along eastern Australia were also revealed.     

Age and growth characteristics of Schizopygopsis younghusbandi Regan, 1905 in the Yarlung Tsangpo River in Tibet,China

To better understand the biology of Schizopygopsis younghusbandi Regan, 1905 and its relationship with management considerations, this study describes the relationships between otolith size and fish length and age, verifies annual periodicity of otolith annulus formation, and estimates the S. younghusbandi growth parameters. These age and growth characteristics were studied using 694 specimens collected from August 2008 to August 2009. Otoliths grew asymmetrically throughout the range of standard length (SL) studied, showing a clear pattern of alternating translucent and opaque bands. Marginal increment ration (MIR) analysis of specimens up to 6 years of age indicated that one opaque band and one translucent band were laid down each year. Maximum observed age was 17 years, corresponding to a female of 35.8 cm SL and 589.1 g body weight (BW). The SL‐BW relationship was described as BW = 1.122 × 10^?5 SL^3.030 for sexes combined. The von Bertalanffy growth function was used to model back‐calculated lengths as L_t = 338.4 (1?e^{?0.233 (t + 0.403)}) for males, and L_t = 433.9 (1?e^{?0.194 (t + 0.397)}) for females. Growth performance of S. younghusbandi was relatively higher than those of other Schizothoracinaes inhabiting the same river.     

Identifying growth parameters for two endemic species [Capoeta antalyensis (Battalgil, 1943) and Pseudophoxinus antalyae Bogutskaya, 1992] in Duden Creek,Antalya, Turkey

It is hypothesized that Capoeta antalyensis (Battalgil, 1943) and Pseudophoxinus antalyae (Bogutskaya, 1992) might display specific growth characteristics that differ from other species of their genus. Age and growth were described for species from Duden Creek (Antalya, Turkey) from February 2008 to January 2009. The length–weight relationship for all individuals were described by the parameters: a = 0.0143 and b = 2.946 for C. antalyensis and a = 0.0084 and b = 3.251 for P. antalyae. The von Bertalanffy growth parameters based on data from scales were L∞ = 35.78 cm, k = 0.251 year^?1 and t₀ = ?0.30 for C. antalyensis and L∞ = 22.59 cm, k = 0.232 year^?1 and t₀ = ?0.78 for P. antalyae. The growth characteristics for these two species are not much different from those of closely related species from the same genus.     

Evaluating bony structures for ageing and growth parameters of Capoeta banarescui inhabiting the lower Melet River (Ordu,Turkey)

The aim of this study was to investigate the reliability of bony structures for age determination. A total of 247 Capoeta banarescui individuals were analyzed. Fish were caught on the lower Melet River between July 2010 and October 2012. Sex ratio was 2.5 : 1. The specimens ranged from 8.1 to 21 cm in total length and 5.07 to 108.93 g in weight. Age determined from vertebrae, scales, asteriscus and lapillus otoliths were variable. The highest percent agreement (PA) (69.2%) and the lowest average percent error (APE) (4.24%) and coefficient of variation (CV) (8.71%) were obtained for vertebrae. Hence, it was determined that the vertebra is the most reliable ageing structure for C. banarescui in the lower Melet River. Females were age I–V years and males I–V years. The von Bertalanffy growth equation was established for females, males, and all individuals, respectively: L_t = 23.9 [1?e^{?0.22 (t+1.89)}], L_t = 21.8 [1?e^{?0.26 (t+1.58)}], L_t = 26.7 [1?e^{?0.17 (t+2.21)}].     

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 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.     

Age,growth, and age at sexual maturity of the commercially landed skate species,Dipturus chinensis (Basilewsky, 1855), in the northern East China Sea

Age, growth, and age at sexual maturity of the polkadot skate Dipturus chinensis, in the northern East China Sea were determined for a total of 614 specimens collected from April 2009 to December 2014. Vertebral centrum analysis was used to calculate the age of the skates. Annual band deposition was determined by marginal increment analysis. The von Bertalanffy growth model was fitted to the observed length‐at‐age data for each sex (males, L_∞ = 76.8, k = 0.109, t₀ = ?1.28; females, L_∞ = 83.1, k = 0.103, t₀ = ?1.20). Growth patterns of females and males were similar until the age of 6; thereafter, females grew larger than males. Maximum age recorded was 13 years for males and 15 years for females. Age at 50% sexual maturity was 8.22 years for males and 9.39 years for females. These results indicate that D. chinensis is slow growing, relatively long‐lived, and late maturing, and therefore vulnerable to exploitation.     

Population statistics of the migratory hilsa shad,Tenualosa ilisha,in Sindh,Pakistan

In order to estimate the population dynamics of the hilsa shad, Tenualosa ilisha, fishery in Sindh, the key population parameters of growth, mortalities, recruitment pattern, exploitation and maximum sustainable yield are discussed. Length frequency data were collected from April to October 2004 from the main commercial (hilsa) landings at Thatta, Sindh. Estimated parameters of the von Bertalanffy (Hum. Biol. 10, 181–213) growth model were L_∞ = 31.5 cm, K = 1.5 year^?1, t₀ = ?0.10 year as obtained by the electronic length frequency analysis (ELEFAN I). Estimated natural, fishing, and total mortalities were 2.21, 0.673, 2.89 year^?1, respectively. The relative biomass per recruit (B′/R) was 0.95 and yield per recruit (Y′/R) was 0.06 using the knife‐edge selection. The exploitation ratio at the maximum sustainable yield (MSY) was E_max = 1.0 year^?1, fishing mortality at MSY was F_max = 2.89 year^?1, average target F_opt = 0.5 year^?1 and F_limit = 1.47 year^?1. The catch and effort data from 1981 to 2004 (MFD, Karachi) were analyzed using the catch and effort data analysis (CEDA) computer programme. Estimated biological reference point of MSY for the Fox model was 891 tonnes (t), R² = 0.75; for the Schaefer and Pella‐Tomlinson models MSY = 744 t, R² = 0.49, the outputs of which appeared to be more conservative than the Fox model which indicated a better fit. The overall situation of hilsa fishery is in severe stress and appears vulnerable to overexploitation. On the basis of the present findings, serious attention is required to provide appropriate access of the fish to the Indus River during the spawning period as well as to impose a ban on fishing during upstream migration and on undersized catch to prevent this traditional fishery in this area.