Length-based growth,maturity and natural mortality of the cockfish <Emphasis Type="Italic">Callorhinchus callorhynchus</Emphasis> (Linnaeus, 1758) off Coquimbo,Chile

The growth rate, reproductive aspects, and natural mortality of chimaeras and ratfish are poorly known. In this study, life-history parameters for cockfish Callorhinchus callorhynchus (Holocephali—Callorhinchidae) are estimated, which is an important fish resource exploited in Chile. Specimens were sampled from the artisanal fishery captures, from November 2006 to November 2007. The standard length (SL) of males fluctuated between 20 and 62 cm, and between 21 and 70 cm for females. Von Bertalanffy growth parameters were estimated through length-frequency data analysis using MULTIFAN. The length-weight relationship and von Bertalanffy growth parameters were significantly different for males and females, as well as the length at 50% maturity. For males a model with 5 age-classes was the best, with asymptotic length L _∞ = 52 cm SL, growth coefficient K = 0.473 yr⁻¹, and age at length zero t ₀ = −0.690 yrs. For females the best model was represented by 10 age-classes (L _∞ = 70.3 cm SL, K = 0.193 yr⁻¹, t ₀ = −1.158 yrs) in the length-frequency data sets. Length at 50% maturity of males was estimated in 43.7 cm SL, and in 50.2 cm SL for females. The natural mortality rate fluctuated between 0.42 and 0.82 yr⁻¹ for males and between 0.12 and 0.37 yr⁻¹ for females, depending upon the method used. It is concluded that C. callorhynchus is a species with life-history parameters significantly different between males and females, and such differences should be taken into account in future population dynamics analysis.     

Age and growth of Schizopygopsis younghusbandi younghusbandi in the Yarlung Zangbo River in Tibet, China

Schizopygopsis younghusbandi younghusbandi is an endemic species whose distribution is restricted to the middle reaches of the Yarlung Zangbo River, being one of the most important commercial fishes in this area. Age and growth of 606 specimens captured between October 2002 and April 2005 were studied. The range in standard length (L) was 65.7–387.3 mm and total weight (W) was 3.3–772.0 g. The relationship between L and W was W = 0.000909L^2.2493 for males and W = 0.000259L^2.4781 for females. Age, determined from anal scales and lapillus otoliths, ranged from 3 to 18 years. The parameters of von Bertalanffy growth functions, estimated by back-calculated length, were L_￥ = 442.7mm  LL_\infty = 442.7mm\;L, k = 0.0738 year⁻¹ and t ₀  = −1.4 year for males, and L_￥ = 471.4mm  LL_\infty = 471.4mm\;L, k = 0.0789 year⁻¹ and t ₀ = 0.2 year for females. Males and females exhibited statistically significant differences in growth. χ ²-test indicated that von Bertalanffy growth functions could well describe the growth of S. y. younghusbandi. The longevities were 39.2 and 38.2 years for males and females, respectively. Growth inflexion points were 10.2 and 12.0 years for males and females, respectively, but 84.8% of the captures were at the smaller ages. So conservation and management schemes for this population should be considered urgently. In addition, we found that populations from the upstream of the Lhasa River, the downstream of the Lhasa River and the middle reaches of the Yarlung Zangbo River showed statistically significant differences in growth patterns.     

Life history characteristics of the protogynous parrotfish Calotomus japonicus from northwest Kyushu, Japan

In this study, we examined the life history characteristics of the parrotfish Calotomus japonicus, using individuals collected between May 2003 and May 2008 off the Nagasaki Peninsula in northwest Kyushu, Japan. Age determinations were performed using scales. Marginal increment analysis revealed that growth rings were formed annually around July. Growth in both sexes was fitted to the von Bertalanffy growth function (L _∞ = 513, k = 0.28, t ₀ = 0.03, where L _∞ is the theoretical asymptotic total length in mm, k is the growth rate coefficient and t ₀ is the theoretical time at zero length). Observed maximum age for both sexes was 8 years. We also characterized the reproductive biology of this species based on a gonadosomatic index and histological examinations of the gonads. The spawning season extends from July to October, with peak spawning activity occurring during July and August. Fish reach sexual maturity by the second year of life. Females are assumed to be multiple spawners, since we observed specimens with postovulatory follicles in ovaries containing either yolk globule oocytes or migratory nucleus oocytes. All males had secondary testes, which were characterized by the presence of an ovarian lumen structure and sperm sinuses in the gonadal wall. This indicates that all males, irrespective of whether they were initial or terminal phase males, had undergone a sexual transition. Sex change appears to occur during the spawning season, and thereafter sex-changed males are able to fertilize female eggs throughout the remainder of the current spawning season.     

Age and growth of the blackchin guitarfish Glaucostegus cemiculus (Geoffroy Saint-Hilaire, 1817) from Iskenderun Bay (Northeastern Mediterranean)

Between September 2010 and June 2012, a total 291 (166 females and 125 males) blackchin guitarfish Glaucostegus cemiculus were captured by a commercial bottom trawler (F/V Coşkun Reis) in Iskenderun Bay, Turkey (northeastern Mediterranean Sea). The total length (L) and total weight (W) of the female and male guitarfish ranged between 32.0–165.0 cm and 88 g–16.68 kg, and 34.3–128.3 cm and 112 g–6.00 kg, respectively. Vertebral age estimates ranged from 0 to 8 years for females and 0 to 5 years for males. The growth models of von Bertanlanffy and Gompertz were fitted to the length at age data using the nonlinear regression method. Model selection was based on the values of the residual standard error and the Akaike's information criterion corrected for small sample size (AIC_C) associated with each fit. The von Bertalanffy growth model provided the best fitting growth curves for each sex with parameters reaching L_∞ = 187.17 cm, K = 0.195 year^-1, t₀ = −1.38 year for females, and L_∞ = 144.85 cm, K = 0.321 year^-1, t₀ = −1.13 year^-1 for males. The W–L relationship parameters did not differ significantly between sexes, the estimated values of a and b were 0.0018 and 3.11, respectively. By using these values of a and b, and also respective estimates of L_∞, the values of W_∞ were obtained as 20.53 kg for females and 9.25 kg for males. The overall percentage ratios of females and males in the samples were 57% and 43% respectively.     

A re-examination of the age and growth of sand tiger sharks, Carcharias taurus, in the western North Atlantic: the importance of ageing protocols and use of multiple back-calculation techniques

Age and growth estimates for sand tiger sharks, Carcharias taurus, in the western North Atlantic were derived from 96 vertebral centra collected from sharks ranging from 94 to 277 cm total length (TL), and compared to previously published age and growth data. The oldest female and male sand tiger sharks aged in this study were 17 and 15 years of age, respectively. von Bertalanffy growth parameters derived from vertebral length-at-age data are L _∞ = 295.8 cm TL, k = 0.11 year⁻¹, and t ₀ = −4.2 years for females, and L _∞ = 249.5 cm TL, k = 0.16 year⁻¹, and t ₀ = −3.4 years for males. Sexual maturity is estimated to be 9–10 years for females and 6–7 years for males. Weight-to-length relationships determined for female and male sand tiger sharks in the western North Atlantic are; W = 1.3 × 10⁻⁴ × L ^2.4 (r ² = 0.84, n = 55) and W = 9.0 × 10⁻⁵ × L ^2.5 (r ² = 0.84, n = 47), respectively, and 7.9 × 10⁻⁵ × L ^2.5 (r ² = 0.84) for the sexes combined. Our results show sand tigers possess a slower rate of growth than previously thought. This information is crucial for accurately assessing this population’s ability to recover, and further justifies the need for this species to be fully protected.     

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.     

Age and growth of the nototheniid fishTrematomus bernacchii Boulenger from Terra Nova Bay,Antarctica

Age and growth of the nototheniid fishTrematomus bernacchii Boulenger 1902 were estimated by reading the sagittal otoliths of 457 adult specimens caught off Terra Nova Bay (Ross Sea) in the austral summer 1990–1991. Annuli in ground and polished otoliths were examined using a dissecting microscope under reflected light. The Von Bertalanffy growth equation was L_t=273.5 [1 − e^{−0.109(t+2.10)}] for males (n=122) and L_t=422.2 [1 − e^{−0.055(t+1.92)}] for females (n=211) where L is total length in millimetres. Maximum estimated age was 21 years for females and 16 years for males. This is in agreement with the hypothesis that considers slow growth and old age as a typical feature of Antarctic fishes.     

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).     

Age and Growth of the Whiskery Shark, Furgaleus macki, from Southwestern Australia

Age and growth of the whiskery shark, Furgaleus macki, from southwestern Australia were examined using vertebral ageing and tag-recapture data. The readability of bands on the vertebral centra varied markedly between individuals. Four readers were used to make band counts, with the most experienced reader having the lowest index of average percent error and the highest level of agreement with final counts. Marginal increment analysis indicated that opaque bands form in January. With parturition occurring from August to October, size data suggests that the first band is probably formed 15–17 months after birth. The age at maturity was estimated to be 4.5 years for males, and 6.5 years for females. The oldest male was 10.5 years, and oldest female was 11.5 years. Von Bertalanffy growth parameters for males were L =121.5cm fork length, K=0.423 year^–1, t ₀=–0.472 years, were L =120.7cm fork length, K=0.369 year^–1, t ₀=–0.544 years for females, and were L =118.1cm fork length, K=0.420 year^–1, t ₀=–0.491 years for combined sexes. Data from a tag recapture study were analysed using a maximum likelihood method to verify the estimates of growth parameters from vertebral ageing. Von Bertalanffy growth parameters from the tag recapture study were L =128.2cm fork length, K=0.288 year^–1, t ₀=–0.654 years. The two methods of estimating growth parameters produced similar results, with rapid growth until approximately 5 years of age, after which there was little increase in length.     

Age and growth of the sandbar shark, Carcharhinus plumbeus, in Hawaiian waters through vertebral analysis

Age and growth estimates were determined for the sandbar shark, Carcharhinus plumbeus, from Oahu, Hawaii in the central Pacific Ocean. Age estimates were obtained through vertebral centra analysis of 187 sharks. We verified our age estimates through marginal increment analysis of centra and oxytetracycline marking methods of at liberty sandbar sharks. Sizes of sampled sharks ranged from 46 to 147 cm pre-caudal length. Four growth models were fitted to length-at-age data; two forms of the von Bertalanffy growth model, the Gompertz growth model, and a logistic growth model. Males and females exhibited statistically significant differences in growth, indicating that females grow slower and attain larger sizes than males. Growth parameter estimates revealed slower growth rates than previously estimated (based on captive specimens) for Hawaiian sandbar sharks. The von Bertalanffy growth model using empirical length-at-birth provided the best biological and statistical fit to the data. This model gave parameter estimates of L _∞ = 138.5 cm PCL and k = 0.12 year⁻¹ for males and L _∞ = 152.8 cm PCL, k = 0.10 year⁻¹ for females. Male and female sandbar sharks mature at approximately 8 and 10 years of age, respectively.     

Life history of the nonnative convict cichlid <Emphasis Type="Italic">Amatitlania nigrofasciata</Emphasis> in the Haebaru Reservoir on Okinawa-jima Island,Japan

Life history parameters associated with reproductive biology, age, and growth of the convict cichlid (also known as the zebra cichlid) Amatitlania nigrofasciata, which was introduced into the Haebaru Reservoir on Okinawa-jima Island, were estimated using 437 specimens that ranged from 13.7 to 82.9 mm standard length (SL). Lengths of females at first maturity (SL) and 50% maturity (L ₅₀) were estimated to be 32.2 and 37.3 mm SL, respectively. The spawning period continued throughout the year, with a peak spawning cycle from March to May 2006–2007. Observations of postovulatory follicles and tertiary yolk stage oocytes indicate that convict cichlids spawn multiple times within a year. Female cichlids that hatched during the peak spawning seasons matured after October of the same year. Batch fecundity of females (32.2–61.2 mm SL) ranged from 65 to 345 (mean ± SD = 155 ± 63). Opaque zones along the outer margins of otoliths formed annually. The maximum age of male and female cichlids was 3 years. The von Bertalanffy growth formulae (VBGF) were expressed as L_t = 57.4( 1 - e ^{- 0.78( t + 0.91 )} ) {{\hbox{L}}_{\rm{t}}}{ = 57}{.4}\left( {1 - {e^{ - 0.78\left( {t + 0.91} \right)}}} \right) for females and L_t = 69.5( 1 - e ^{- 1.07( t + 0.24 )} ) {{\hbox{L}}_{\rm{t}}}{ = 69}{.5}\left( {1 - {e^{ - 1.07\left( {t + 0.24} \right)}}} \right) for males. Males grew larger than females beginning from the first year. Certain life history characteristics, such as year-round spawning and early maturation, probably contributed to the successful establishment of the convict cichlid, and this species in particular is thought to adapt and become established quickly upon introduction to freshwater systems on Okinawa-jima Island.     

Age,growth and reproduction of the white seabream Diplodus sargus sargus (Linneaus, 1758) off the eastern coast of Algeria

The objective of this study was to determine the basic population‐specific parameters necessary for fish stock assessment in the area and to compare these with data from other Mediterranean regions. White seabream Diplodus sargus sargus (n = 449) were caught along the Algerian coast between December 2005 and December 2006. Total length ranged from 12.2 to 34.6 cm, representing age classes between 0 and 10 years. Validity of the otolith readings for estimating age and growth was supported using the back‐calculation method. The von Bertalanffy growth parameters for all fish were calculated as: TL = 36.3 cm, k = 0.154 year⁻¹, t₀ = −0.488 year. The growth performance index (φ) showed a relatively slow growth of the local population. The length‐weight relationship showed an isometric growth (b = 2.98; r = 0.98). Subspecies Diplodus sargus sargus was characterized as being a proterandric hermaphrodite. Overall ratio of males to females was 1 : 1.4, with males predominant in the smaller size intervals and females in the larger ones. The reproductive season extended from January to May, with a March–April peak in spawning activity. Fifty per cent maturity of the tested cohort was reached at a total length of 20.2 cm for males and 20.0 cm for females.     

Using cross-dating techniques to validate ages of aurora rockfish (<Emphasis Type="Italic">Sebastes aurora</Emphasis>): estimates of age,growth and female maturity

Since fishery management regulations have shifted much of the groundfish trawl effort in the northeastern Pacific from the continental shelf to the slope, fishery impacts on unassessed demersal slope rockfish species like the aurora rockfish (Sebastes aurora) may have increased. Understanding the life history of these species is a critical first step in developing management strategies to protect them from overharvest. In this study we employ cross-dating methods to validate the annual periodicity of growth increments and investigate the age, growth and maturity of aurora rockfish, a species for which life history information is quite limited. Specimens were collected on an opportunistic basis from Oregon commercial landings and from research cruises, over the years 2003–2006. Age was estimated for 438 individuals using otoliths processed via the break-and-burn method. The maximum estimated age was 118 years for females (n = 324) and 81 years for males (n = 114). The von Bertalanffy growth function showed that males grow faster and reach a smaller maximum size than females (males: L _inf = 34, K = 0.09, t ₀ = −1.9; females: L _inf = 37, K = 0.06, t ₀ = −5.5), though both sexes demonstrate relatively slow growth. Visual assessment of ovaries showed that the aurora rockfish is a synchronous spawner with parturition occurring in May and June off Oregon. Female age and length at 50% maturity were calculated at 12.6 years and 26 cm, respectively (n = 307). Maturity and age data provided evidence for a protracted adolescence in this species.     

Length‐weight relationships,condition factor,gonadosomatic index‐based size at first sexual maturity,spawning season and fecundity of Aspidoparia morar (Cyprinidae) in the Jamuna River (Brahmaputra River distributary), northern Bangladesh

The present study describes the length‐weight relationships (LWRs), length‐length relationships (LLRs), Fulton's condition factor (K_F), size at first sexual maturity, spawning season, sex ratio and fecundity of the Morari Aspidoparia morar (Hamilton, 1822) (Cyprinidae). Sampling was done using traditional fishing gear jhaki jal (cast net) from July 2010 to June 2011. Total length (TL), fork length (FL) and standard length (SL) were measured with digital slide calipers. Individual body weight (BW) and gonad weight (GW) were determined to an accuracy of 0.01 g for all specimens. The gonadosomatic index (GSI) was calculated and size at first maturity for males and females estimated using GSI and TL as indicators. Female ≥ size at first maturity was used to determine fecundity. A total of 1200 specimens (males = 552, females = 648) ranging from 4.06–12.84 cm TL and 0.53–16.75 g BW were analyzed. The overall coefficient b for the LWR indicated positive allometric growth (>3.00) in males and isometric growth in females (~ 3.00). ancova (analysis of covariance) revealed significant differences between males and females (P < 0.001). All LLRs were highly correlated (r² > 0.973, P < 0.001). Sizes at first sexual maturity for males and females were 6.0 and 7.0 cm TL, respectively. K_F changed little throughout the year and GSI peaked in November to April, indicating the spawning season (GSImax = 15.0 in females, 2.0 in males). Mature females were dominant during the entire spawning season except in April. Mean total fecundity was 6700 ± 3500, ranging from 1860 to 19680. In addition, relative fecundity ranged from 190 to 1200 (mean 560 ± 235) in the Jamuna River. To ensure sustainable management of this species, the protection of mature individuals during the peak spawning season is highly recommended.     

Growth and mortality of bigeye tuna <Emphasis Type="Italic">Thunnus obesus</Emphasis> (Scombridae) in the eastern and central tropical Pacific Ocean

Biological parameters such as age, growth and age (or size) at maturity are vital for stock assessment and management. Aging is essential in yielding such information. However, limited aging studies have been conducted for large tropical pelagic species in the eastern and central tropical Pacific Ocean. The objective of this study is to conduct a length frequency analysis for estimating growth and mortality of bigeye tuna in the eastern and central tropical Pacific Ocean using samples from the Chinese longline fishery during February to November 2006. The von Bertalanffy growth parameters of asymptotic fork length L _∞ and growth coefficient k were estimated at L _∞ = 207.4 cm fork length, k = 0.23 year^-1, and theoretical age at zero length t ₀ = −0.40 year. The total mortality rate (Z) was estimated to be 0.60; the fishing mortality rate (F) and the natural mortality rate (M) were 0.25 year^-1 and 0.35 year^-1, respectively. The exploitation rate (E) was 0.16. This study provides the estimates of growth and mortality rate for bigeye tuna in the eastern and central tropical Pacific Ocean, which can be used as biological input parameters in further stock evaluations in this region. However, age analysis, further validation of the age composition and stock structure are needed for future studies.     

Age,growth and sexual development of solenette,Buglossidium luteum (Risso, 1810), in the central Aegean Sea

Age, growth, spawning period and maturity of the solenette (Buglossidium luteum Risso, 1810) were studied in the central Aegean Sea to provide fisheries managers with essential data for science‐based management. A total of 1220 samples were collected by trawl hauls from July 2004 to June 2007 in ?zmir Bay (Turkey). Sample sizes ranging from 5.3 to 11.6 cm total length were composed of 46% females, 32% males and 22% immature individuals, with a female to male ratio of 1 : 0.7. Age composition stages of the females were from I to IV, and males between I and III. The length–weight relationship was calculated as W = 0.0101L^3.008 for all samples. Estimated von Bertalanffy growth parameters were L = 13.30 cm, t_o = ?0.440 year and k = 0.481 year^?1, with a growth performance index of 1.93 (?’). The spawning period began in April and continued until July. Lengths at first maturity of females and males were 8.1 and 7.9 cm total length, respectively. Both sexes matured at the age of 2 years.     

Preliminary observations on the life history of the white-streaked grouper, <Emphasis Type="Italic">Epinephelus ongus</Emphasis>, from Okinawa,Japan

A preliminary analysis of 175 specimens of the white-streaked grouper, Epinephelus ongus (Serranidae), was undertaken to determine life history characteristics of the species. Sagittal otoliths, stomachs, and a subsample of gonads were removed to determine age at length, diet, and reproductive strategy. The von Bertalanffy growth equation was used to describe growth in this species and yielded the growth parameters L^∞ = 438.3, K = 0.04334, and t₀ = −8.752. Fish ranged in age from 1 to 20 years. Diet was consistent with other serranid species and included crabs, shrimps, octopi, and fishes. Based on a very limited number of specimens (n = 12), the larger size and older age of males compared to females suggests that E. ongus may be a protogynous hermaphrodite.     

Biology of the bottom-dwelling shrimp Nauticaris marionis Bate, 1888 at the sub-Antarctic Prince Edward Islands

Sub-Antarctic bottom-dwelling caridean shrimps Nauticaris marionis were collected in April/May between 1984 and 1997 over the shelf region of the Prince Edward Islands (37 °50′E, 46 °45′S). N. marionis is a partially protandric hermaphrodite. Hatching probably occurs just before April each year, but may persist until May. During the 1st year N. marionis seem to survive in undetected localities, moult into juveniles, and then settle amongst the benthos from the plankton beginning probably after November. Diel vertical migration then occurs up to an unknown larger size. The vast majority of juveniles develop into males, most of which transmutate into females by April/May of their 3rd year. Reproduction can occur before all male secondary characteristics have been lost. A minority of individuals develop directly into females without passing through a male phase. Individuals older than 5 years are undetectable using samples of the sizes analysed, but they may well persist in the population. The von Bertalanffy growth parameters for N. marionis are tentatively identified as k=0.2353/year, L _∞=12.6 mm, t ₀=−0.2828 years and WW _∞=2.03 g. Sex-reversal in N. marionis at Marion Island may be affected by the changing environment as sexual differentiation is probably determined during the planktonic stage. Accepted: 3 January 2000     

Age,growth, and population structure of the smooth clam <Emphasis Type="Italic">Callista chione</Emphasis> in the eastern Adriatic Sea

The age, growth, and population structure of the smooth clam Callista chione were determined from samples collected by hydraulic dredge and SCUBA at four locations in the eastern Adriatic during 2007 and 2008. The age of 436 clam shells was determined from internal growth lines present in shell sections, and the timing of growth line formation was ascertained from monthly collections of clams to occur between August and September when sea water temperatures were maximal. In addition, age of 30 older individuals was verified with acetate peels of polished and etched shell sections. Differences were apparent in the age structure and growth rates of clams collected from the four locations studied. Von Bertalanffy growth (VBG) curves obtained for clams from these locations were L _t  = 72.4 (1−e^{−0.25(t − 2.68)}) (Rab Island), L _t  = 74.5 (1−e^{−0.15(t + 0.57)}) (Pag Bay), L _t  = 79.3 (1−e^{−0.34(t − 0.97)}) (Cetina estuary), and L _t  = 82.5 (1−e^{−0.11(t + 2.88)}) (Kaštela Bay). The age of the clams ranged between 3 and 44 years; median clam ages were similar at three of the four locations (14, 12, and 12 years, respectively), but was significantly lower in the Cetina estuary (4 years). The VBG growth constants recorded from clams were within the range of values obtained for this species by previous authors. The observed local differences in population structure indicate different levels of exploitation and illustrate the need to establish long-term strategies for a sustainable exploitation of smooth clams in the Croatian Adriatic.     

Length‐weight relationship and reproductive parameters of Botia dario (Hamilton, 1822) in Assam,India

The length‐weight relationships, spawning season, sex ratio, size at first maturity and fecundity of Botia dario (Hamilton, 1822), also known as the Bengal loach, were analyzed based on 556 specimens collected from the wetlands of Majuli Island, Assam between June 2012 and May 2013. The sex ratio (M : F) was 1 : 0.68, differing significantly (P < 0.05) from a 1 : 1 ratio. Size at first maturity (L_m50) was estimated as 6.8 cm for males and 7.4 cm for females. Analysis of monthly variations in the gonado‐somatic index (GSI), the monthly proportions of macroscopic gonadal maturity, and the ova diameter suggest a prolonged spawning season of B. dario from May to August, with a peak in July for both males and females (GSI = 15.0 in females; 7.0 in males). Absolute fecundity varied from 2523 to 51 377, with a mean of 18 367 ± 1254 oocytes per ovary. A positive correlation was recorded between total fecundity and body weight (r² = 0.678).