Age, growth and mortality of the Mediterranean amberjack Seriola dumerili (Risso 1810) from the south-eastern Adriatic Sea

The age, growth and mortality of the Mediterranean amberjack Seriola dumerili (Risso 1810) were determined in 298 specimens collected in the south-eastern Adriatic Sea (Donji Molunat Bay) from 17 May to 26 June 1997. The total length ranged from 32.0 to 160.0 cm and weight from 0.5 to 46.5 kg. Ten age classes, ranging from 1° to 10° years were defined by scale readings. Mean total length and weight-at-age data were used to estimate the growth parameters of the von Bertalanffy equation: L _∞=174.6 cm, K =0.190, t ₀=–0.314; W _∞=79.01 kg, K =0.139 and t ₀=–0.746. The length–weight relationship was estimated at: W =0.000123 ×  L ^2.847. The overall sex ratio was 1 : 1.06 in favour of males. Total ( Z ) and natural ( M ) mortality were found to be 0.41 years⁻¹ and 0.30 years^–1, respectively. The exploitation ratio ( E =0.27) indicates that the fishing pressure on the Mediterranean amberjack was low in the investigated region.     

Differences in size and growth rates of male and female migrating Japanese eels in Pearl River, China

The Sr/Ca ratios in otoliths of silver Japanese eels Anguilla japonica , in Pearl River, China, indicated that both sexes did not stay in brackish water and grew in fresh water from the glass eel stage until spawning migration. This did not support the hypothesis that females tended to distribute upstream and males might be restricted to estuaries. The back-calculated total length of males at glass eel stage was not significantly different from that of females, indicating that the hypothesis that small glass eels became males and larger ones became females may not be true. The mean (±S.D.) age and total length of males at migration were 6·4±1·6 years and 48·3±4·5 cm, which were significantly smaller than for females, 8·3±1·6 years and 61·4±4·1 cm. The age of migration was related inversely to growth rate for both sexes. Growth parameters of the von Bertalanffy growth equation were K =0·21 cm year°1, L _∞=55·7 cm and t _o=-0·55 year for males and K =0·14 cm year⁻¹, L _∞=77·5 cm and t _o=-0·60 year for females. The difference in asymptotic length ( L _∞) between males and females may be because females postpone migration to achieve larger size for maximizing reproductive success.     

Growth rates of Lutjanidae (snappers) in tropical Australian waters

Growth rates of three commercial species of Lutjanidae were estimated from sections of vertebrae cross-checked with scales. The von Bertalanffy growth constants for Lutjanus malabaricus were K =0.168, L_∞ =70.7 cm standard length (S.L.). For Pristipomoides multidens these were K = 0.219, L _∞= 59.1cm, and for Pristipomoides typus K =0.254, L _∞= 51.5 cm. Length/weight was analysed in the form W= aL^b where W was fresh weight (g) and L = S.L. (cm). The constants were: L. malabaricus, a = 0.041, b = 2.842; P. multidens, a =0.032, b = 2.897; P. typus, a = 0.038, b = 2.822. The growth rates were considered low in comparison with demersal fish counterparts from temperate seas.     

Age and growth of Mediterranean albacore

Estimated ages of 1136 individual albacore Thunnus alalunga (57–92 cm L F) from the Aegean and Ionian Sea ranged from 1⁺ to 9 years. Males grew faster and reached a greater size and age than females. No significant differences were found in the mean lengths at estimated ages between the two sampling areas. The von Bertalanffy growth model was fitted to mean lengths of estimated ages of individual fish and estimated growth parameters for the combined sexes were: L _∞=94·7 cm, K =0·258, to=–1·354 years. Significant differences were found when the Mediterranean albacore growth parameters were compared with those determined for Atlantic Ocean albacore. It is not possible to determine if the differences in growth rates for the two populations are phenotypic or genotypic at the present time.     

Age, growth, sexual maturity and food composition of Sciaena umbra in the south-eastern Black Sea, Turkey

Studied were the age, growth, maturity and food composition of the brown meager, Sciaena umbra, caught off Trabzon, south-eastern Black Sea (Turkey) in 2002–2003. A total of 329 individuals was collected by spear fishing and hand nets. The thin sectioning method was used for aging the fish otoliths. Fitted von Bertalanffy growth parameters for all fish were: L _∞ = 51.14 (±1.19) cm, k  =   0.27 (±0.02) year⁻¹ and t ₀ = −0.93 (±0.07) year. This study revealed that S. umbra is a relatively slow-growing and long-lived species with a life span in excess of 18 years. Sexual maturity begins when they reach a length of about 15 cm. Lengths at which 50% of brown meagre become mature are 19.50 for males and about 22 cm for females. Spawning begins in June, when the temperature is approximately 18°C, and ends in August. Gut content analysis indicated that this species feeds mainly on crustaceans, then switches to fish as they grow. Sciaena umbra appears to be an apex predator in the upper littoral zone.     

Maturation, spawning and growth of rock soles off Kodiak Island in the Gulf of Alaska

Northern rock sole Lepidopsetta polyxystra females from the Kodiak Island area, Alaska, reached 50% maturity at 328 mm L _T and an average age of 7 years. In contrast, southern rock sole Lepidopsetta bilineata females reached 50% maturity at 347 mm L _T and an average age of 9 years. Spawning started in midwinter for northern rock sole and peaked during the spring, while spawning for southern rock sole occurred during the summer. The bottom depth for spawning northern rock sole ranged from 43 to 61 m and averaged 45 m; spawning depth for southern rock sole ranged from 35 to 120m and averaged 78m. Both species appeared to develop a single stock of oocytes and to ovulate them in a single spawning. Northern rock sole females grew faster overall ( K =0.24) than southern rock sole females ( K =0.12) but reached a smaller maximum length ( L _∞=430 mm) than southern rock sole ( L _∞=520mm). Males of both species grew more slowly than females after 5 years of age and reached a smaller maximum length.     

The biology of the bigeye grenadier at South Georgia

The biology of the bigeye grenadier Macrourus holotrachys caught as by‐catch in the Patagonian toothfish Dissostichus eleginoides longline fishery conducted around South Georgia was investigated to improve data available for fisheries management. Age estimates suggest that M. holotrachys is a moderately slow growing species ( K  = 0·10), reaching ages of >30 years and attaining total lengths ( L _T) >80 cm ( L _∞ = 33). The size at which 50% of females had started to mature ( L _int50) for M. holotrachys was 21 cm pre‐anal length ( L _PA) and occurred at c . 9 years old. Estimates of natural mortality and Pauly's growth performance index were found to be low ( M  = 0·09 and Φ = 2·82 respectively). Gonad maturity stage was described from macroscopic and histological investigation. Mature ovaries had oocytes at all developmental stages with between 22 and 55% likely to be spawned each year. Absolute fecundity ranged from 22 000 to 260 000 eggs and was positively correlated with both pre‐anal length and mass. A highly skewed sex ratio of 32 : 1, females : males, was found for specimens caught by longlines but not for a small sample of shallower trawl‐caught specimens. It is suggested that females are far more susceptible to longline capture than males. Macrourus holotrachys is a bentho‐pelagic predator and scavenger that feeds on a wide range of fishes and invertebrates. The fish are long lived, slow‐growing species typical of deep‐water grenadiers; fisheries management strategies should reflect their probable susceptibility to overfishing.     

Reproductive biology and growth of the goatfish, Parupeneus barberinus (Lacepede), in Aqaba, Jordan

Monthly changes in the gonadosomatic index indicate that the main spawning season of Parupeneus barberinus in Aqaba extends from May to August for females and from May to June for males. Males in the 4 years age-group (63–4%) and the 5 years age-group (65–1%) are predominant. The von Bertalanffy growth equation parameters calculated from mean total length data are: L_α= 32–8cm; K=0–225; (t_o=−0–73 for males and L_α= 32–7cm; K=0–206; t_o= −0.82 for females. The length-weight regression coefficients for males (2.85) and females (2.8) are not significantly different and they indicate a negative allometric growth. There is no significant change in condition factor with age.     

Reproduction in the dusky grouper from the southern Mediterranean

Demographic data and gonad histology confirmed that the dusky grouper Epinephelus marginatus is a protogynous hermaphrodite that follows a monandric pathway to sexual development. Females reached first sexual maturity at 36·7 cm L_s and estimated mean length at first maturity (L₅₀) was 43·8 cm L_s for females and 81·3 cm L_s for males. Adult sex ratios during the reproductive period were c. 3·5: 1 females to males. Females exhibited group-synchronous ovarian development and multiple ovulation occurred over the spawning period. Gonads were ripe from early May and spawning occurred from June until early September. The size of ripe testes (0·6% W )indicated strong oligospermy and suggested a mating system with no sperm competition. Sexual transition was protogynous involving regression of ovarian tissue and proliferation of testicular tissue in the gonads. Transitional individuals occurred from May through November and accounted for 9% of sampled adult population. Sex change occurred in fish 69–93 cm (L_s) long and the size distributions of males and females overlapped over 27% of the L_s range. Special zones were recognized as gathering areas for sexually mature dusky groupers during the reproductive period.     

Spatial and interannual patterns in growth of an exploited coral-reef fish

Patterns of growth in an exploited reef fish Lethrinus miniatus were examined over 5 years (1995–1999) at two spatial scales: (1) among regions of the Great Barrier Reef (GBR) separated by >100 km and (2) among reefs within each of these regions, separated by ≤10 km. Mean annual growth of L. miniatus varied significantly among years, but this variation was consistent among ages and regions, indicating that factors that influence temporal patterns in growth were not age-specific and operated at relatively large spatial scales. Significant variation in growth was also observed among some reefs within regions, although the greatest variation was among regions. The average maximum fork length ( ) and average maximum mass ( M _∞) varied significantly among regions, suggesting that productivity of L. miniatus is likely to vary among regions of the GBR. There was also significantly greater mass of fish for a given L _F in two regions, which magnified the regional differences in M _∞. The observed temporal and spatial variation in growth highlighted the importance of a multi-scale approach to population studies and assessment of fish stocks.     

Biology of the salema, Sarpa salpa (L. 1758) (Pisces, Sparidae) from the middle-eastern Adriatic

Salema Sarpa salpa (Linnaeus, 1758), were caught in the middle-eastern Adriatic Sea from August to November 2004. Length range of the samples was between 10.3 and 43.9 cm, with mean values of 25.5 cm in males, 32.6 cm in females, and 11.4 and 20.2cm in immature and hermaphrodite specimens, respectively. Sex ratio (males : females) was 3.1 : 1. Males were observed up to 37 cm length. Hermaphrodites showed lengths between 18 and 21 cm. The species was characterized by protandric hermaphroditism. Size at sexual maturity was 20.6 cm (2 years old) for males. Total length-total weight relationship for the entire population is described by the parameters a  = 0.00893, and b  = 3.1055. Otolith age readings showed that the population consisted of 15 age groups (1–15 years), including a very high proportion of individuals 1–7 years old. The von Bertalanffy growth parameters were L _∞ = 33.11cm, k  = 0.514, and t ₀ = −0.392 years for males and L _∞ = 40.85cm, k  = 0.179, and t ₀ = −2.606 years for females. Survival rate of females ( S  = 0.870) was much greater than for males ( S  = 0.769).     

Age, growth and reproduction of the barrelfish Hyperoglyphe perciformis (Mitchill) in the western North Atlantic

Otoliths ( n = 847) and gonads ( n = 817) were collected from barrelfish Hyperoglyphe perciformis that were captured by commercial fishermen in the waters off South Carolina and Georgia in 1995, 1997 and 2001–2006. Of the otoliths collected, 97% were aged successfully, and specimens sampled ranged from 5 to 85 years, with a median age of 12 years. The von Bertalanffy growth parameters yielded the equation: L_t = 857·8{1 − e^{−0·0985[ t −(−8·95)]}}, where L_t is fork length ( L _F) at time t . Through histological examination, 94% of the gonads assessed were assigned to a sex and reproductive class. Females spawned from September to May with a peak from November to January. Males spawned year round, but had a peak from September to April. The sex ratio (M:F) for this population was 1:1·34. The smallest mature female was 605 mm L _F and the youngest immature female was 697 mm L _F. Estimates of L _F and age at 50% maturity ( L ₅₀ and A ₅₀) for females were 660 mm L _F (95% CI = 633–667 mm L _F) and 6·08 years (95% CI = 3·50–7·27 years), respectively. The youngest mature male was 575 mm L _F and the oldest immature male was 762 mm L _F, and no estimates of L ₅₀ or A ₅₀ were made for males. It was determined that barrelfish exhibit the typical characteristics of long life span, slow growth and high age at maturity seen in other deepwater fishes, and that care should be taken to manage this species accordingly.     

Population variables and life-history characteristics of the alligator pipefish Syngnathoides biaculeatus, in Papua New Guinea

Population structure and life-history variables of the widely distributed alligator pipefish Syngnathoides biaculeatus were characterized in Bootless Bay, Papua New Guinea over the course of 11 months. There was little evidence of seasonality with four focal populations showing no significant change in abundance. Similarly, the sex ratio remained 1:1 for all but 1 month. Reproductive males carrying eggs (148–278 mm in total length, L _T) were found in all months. Brood size was significantly, positively related to male L _T for newly laid broods only. Maximum observed brood size was 351 and mean ± s . d . brood size was 238 ± 57 for newly laid broods. Juveniles and males showed no change in mean L _T over the year while slightly smaller females were captured in November 2006 and September 2007. Males were significantly longer than females so von Bertalanffy growth coefficients were estimated separately for each sex: males L _∞= 285 mm, K = 0·82 year⁻¹ and females L _∞= 261 mm, K = 1·10 year⁻¹. These estimates suggest that this species grows rapidly and has a short-life span. In the context of growing concern about overexploitation of syngnathids, a rapid growth rate combined with year round reproductive activity suggests that the tropical S. biaculeatus may be relatively resilient with regard to fishing pressure.     

Age and growth of eels Anguilla japonica in a Chinese river

Age and growth of Anguilla japonica sampled from the Qiulu River in southern China were studied. Mean body lengths and weights of the eels at each age were back-calculated from their otoliths. The growth parameters for the von Bertalanffy function gave L _∞= 98–2cm, K =0·07 and t ₀=− 1·94. Scales were observed to form firstly at the middle part of the lateral line, at a minimum body length of 160 mm and were inappropriate for ageing.     

Population biology and stock assessment of Pristipomoides filamentosus on the Mahe Plateau, Seychelles

The population of P. filamentosus around the periphery of the Mahe Plateau was studied using data derived from commercial handline fishing operations between November 1989 and December 1990. Sex ratio was close to one. Fork length was in the range 25.6–79.8 cm: at first sexual maturity, 36–38 cm for females and 40–42 cm for males. Spawning occurred from October to April peaking between February and April and in November.
The length ( f.l. , cm)–weight (kg) relationship was W =0.00005353 × f.l. ^2.7004. The von Bertalanffy growth parameters, estimated from length frequency data, were K =0.2875 and L _inf=81.7 cm. Mortality rates, estimated from length converted catch curve analysis, were Z =0.811, F =0.277 with M =0.534 derived from Pauly's empirical formula. Jones' length cohort analysis gave an estimate of F= 0.294 for the fully exploited part of the stock, and a density of 2.59 t km⁻² for the periphery of the plateau from 75 to 150 m depth. The Lesley constant catchability model, applied to the results of intensive fishing around isolated banks, derived a mean density estimate of 2.99t km⁻². The sustainable yield was estimated to be 233–268 tonnes per annum and the catch in 1990 was 200 tonnes.     

Age, growth and reproduction of the black scorpionfish, Scorpaena porcus (Pisces, Scorpaenidae), on the Black Sea coast of Turkey

Age, growth and reproduction of the black scorpionfish, Scorpaena porcus were studied in specimens from the coast of the Sinop Peninsula (Black Sea) between March 2002 and April 2003 in order to characterize these population parameters in comparison to specimens from populations of nearby regions. A total of 1086 specimens was captured by beam trawl at the depths between 0 and 30 m. The total number of females (510) was significantly higher than that of males (373). Total length of males and females ranged between 5.7 and 23.6 cm, and 4.9 and 31.7 cm, respectively. The length–weight relationship showed a positive allometric growth. Females grew faster and reached a larger size at age than males ( L _∞ = 111.9 cm, K  = 0.035 year⁻¹, φ' = 2.64 for females, and L _∞ = 74.6 cm, K  = 0.054 year⁻¹, φ' = 2.49 for males). The age range estimated was up to 8 years for females and 5 years for males. Reproduction likely occurs between June and September. Sex ratio varied greatly with season, perhaps indicating different seasonal migratory patterns in adults of different sex. An inverse correlation between gonadosomatic index (GSI) and hepatosomatic index (HSI) was evident during the reproduction seasons. The mean size at first sexual maturity was 17.5 cm TL for females, and 16.7 cm TL for males.     

Age determination and growth of turbot and brill in the Adriatic Sea: reversal of the seasonal pattern of otolith zone formation

The growth of two commercially important flatfish, turbot ( Psetta maxima ) (L.) and brill ( Scophthalmus rhombus ) (L.), was investigated in the Adriatic using whole otoliths (sagittae) and stained otolith sections. At variance with the pattern usually observed in temperate seas, the opaque zone was found to be laid down in autumn and winter, and the translucent zone in spring and summer. Growth rates differed according to sex, with the females attaining greater body lengths. The von Bertalanffy growth parameters were: L_∞=66.2 cm, K=0.31 years^–1, and t₀=–0.14 years for turbot males, L_∞=81.5 cm, K=0.21 years^–1, and t₀=–0.48 years for turbot females; L_∞=40.2 cm, K=0.49 years^–1, and t₀=–1.03 years for brill males; L_∞=50.1 cm, K=0.27 years^–1, and t₀=–1.75 years for brill females. Growth rates and maximum age recorded for turbot were comparable to those reported in the North Sea.     

Age, growth and mortality of picarel, Spicara smaris L. (Pisces: Centracanthidae), from the eastern Adriatic (Croatian coast)

Age, growth and mortality of picarel Spicara smaris L. collected in the eastern middle Adriatic during April and May in 1999 were studied. The total lengths of individuals ranged from 6.3 to 19.8 cm, and the weight from 2.2 to 78.3 g. The slopes ( b values) of the total length–weight regressions indicated negative allometric growth for females ( b =2.8± 0.03) and isometric growth for males ( b =3.08±0.04). The oldest female and male were 4 and 6 years, respectively. The von Bertalanffy growth parameters for the sexes combined were ( L _∞=22.76 cm, K =0.277, t ₀=−0.793). The overall sex ratio was 1 : 4.1 in favour of females. Individuals larger than 17.9 cm were all males.     

Growth and reproduction of the wedge clam (Donax trunculus) in the Sea of Marmara, Turkey

Reproduction, growth and mortality of the wedge clam Donax trunculus were studied in an unexploited population in the northern part of the Sea of Marmara. Age determination was based from counting shell increments by inspection of both the external ring structure and the internal structure on thin cross-sections of the shell. Maximum life span was observed as 6 years for the studied population, but 4 years (shell length 40–41 mm) were usually not exceeded. Maximum length was 44.8 mm. Growth parameters were estimated as L _∞   = 44.15 mm, k  =   0.62 year⁻¹, C  = 1 and WP = 0.83 from external ring structure, and L _∞   = 42.44 mm, k  =   0.75 year⁻¹, C  = 1 and WP = 0.79 from internal growth bands (thin section). Natural mortality ( M ) was estimated as 0.98 year⁻¹. Sex ratio was not significantly different from 1 : 1. The monthly maturation process was assessed macroscopically and from variation in the mean total ash-free dry weight per shell weight of adult individuals. Spawning occurred between April and July with a peak between May and June. The recruitment pattern was unimodal.     

Regional differences in length at sexual maturity for female blue whales based on recovered Soviet whaling data

New blue whale ovarian corpora data from illegal Soviet catches in the Southern Hemisphere and northern Indian Ocean were recovered from the original logbooks. Catches north of 52°S were assumed to be pygmy blue whales ( Balaenoptera musculus brevicauda , n = 1,272); those south of 56°S were assumed to be Antarctic (true) blue whales ( B. m. intermedia , n = 153). Three probable Antarctic blue whales north of 52°S were excluded. Lengths at which 50% and 95% of females become sexually mature ( L ₅₀ and L ₉₅) were estimated from a Bayesian logistic model. These estimates are more precise than previous Japanese estimates because Soviet catches below the legal minimum of 70 ft (21.3 m) were 32 times greater. For pygmy blue whales L ₅₀ was 19.2 m (95% interval 19.1–19.3 m) and L ₉₅ was 20.5 m (95% interval 20.4–20.7 m). Antarctic L ₅₀ (23.4 m, 95% interval 22.9–23.9 m) was much longer than L ₅₀ for pygmy blue whale regions (18.4–19.9 m). The median L ₅₀ for the northern Indian Ocean was 0.5–0.6 m shorter than for pygmy blue whales from other regions; although statistically significant, these small length differences provide little support for northern Indian Ocean blue whales being a separate subspecies, B. m. indica .