Age and growth of albacore Thunnus alalunga in the North Pacific Ocean

The age and growth of North Pacific albacore Thunnus alalunga were investigated using obliquely sectioned sagittal otoliths from samples of 126 females and 148 males. Otolith edge analysis indicated that the identified annulus in a sagittal otolith is primarily formed during the period from September to February. The assessments of the fish age at first annulus formation indicated that the first annulus represents an age of <1 year. This study presents an age estimate (0·75 years) for the formation of the first annulus. The oldest fish ages observed in this study were 10 years for females and 14 years for males. The von Bertalanffy growth parameters of females estimated were L(∞) = 103·5 cm in fork length (L(F) ), K = 0·340 year(-1) and t(0) = -0·53 years, and the parameters of males were L(∞) = 114·0 cm, K = 0·253 year(-1) and t(0) = -1·01 years. Sexual size dimorphism between males and females seemed to occur after reaching sexual maturity. The coefficients of the power function for expressing the L(F) -mass relationship obtained from sex-pooled data were a = 2·964 × 10(-5) and b = 2·928.     

The life histories of endangered hammerhead sharks (Carcharhiniformes, Sphyrnidae) from the east coast of Australia

The life histories of two globally endangered hammerhead sharks, Sphyrna lewini and Sphyrna mokarran, were examined using samples collected from a range of commercial fisheries operating along the east coast of Australia. The catch of S. lewini was heavily biased towards males, and there were significant differences in von Bertalanffy growth parameters (L(∞) and k) and maturity [stretched total length (L(ST)) and age (A) at which 50% are mature, L(ST50) and A(50)] between those caught in the tropics (L(∞) = 2119 mm, k = 0·163, L(ST50) = 1471 mm, A(50) = 5·7 years) and those caught in temperate waters (L(∞) = 3199 mm, k = 0·093, L(ST50) = 2043 mm, A(50) = 8·9 years). The best-fit estimates for a three-parameter von Bertalanffy growth curve fit to both sexes were L(∞) = 3312 mm, L(0) = 584 mm and k = 0·076. Males attained a maximum age of 21 years and grew to at least 2898 mm L(ST). The longevity, maximum length and maturity of females could not be estimated as mature animals could not be sourced from any fishery. Length at birth inferred from neonates with open umbilical scars was 465-563 mm L(ST). There was no significant difference in length and age at maturity of male and female S. mokarran, which reached 50% maturity at 2279 mm L(ST) and 8·3 years. Sphyrna mokarran grew at a similar rate to S. lewini and the best-fit estimates for a two-parameter von Bertalanffy equation fit to length-at-age data for sexes combined with an assumed mean length-at-birth of 700 mm were L(∞) = 4027 mm and k = 0·079. Females attained a maximum age of 39·1 years and grew to at least 4391 mm L(ST). The oldest male S. mokarran was 31·7 years old and 3691 mm L(ST). Validation of annual growth-band deposition in S. mokarran was achieved through a mark, tag and recapture study.     

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.     

Population dynamics and life history of a geographically restricted seahorse, Hippocampus whitei

The aim of this study was to collect data on population dynamics and life history for White's seahorse Hippocampus whitei, a geographically restricted species that is listed as data deficient under the IUCN Red List. Data from H. whitei populations were collected from two regions, Port Stephens (north) and Sydney Harbour (south) in New South Wales, Australia, covering most of the known range of H. whitei, from 2005 to 2010. Over 1000 individuals were tagged using fluorescent elastomer and on subsequent recaptures were re-measured for growth data that were used in a forced Gulland-Holt plot to develop growth parameters for use in a specialized von Bertalanffy growth-function model. Growth parameters for Port Stephens were: females L(∞) = 149·2 mm and K = 2·034 per year and males L(∞) = 147·9 mm and K = 2·520 per year compared with estimates from Sydney Harbour: females L(∞) = 139·8 mm and K = 1·285 per year and males L(∞) = 141·6 mm and K = 1·223 per year. Whilst there was no significant difference in growth between sexes for each region, H. whitei in Port Stephens grew significantly quicker and larger and matured and reproduced at a younger age than those from Sydney Harbour. The life span of H. whitei is at least 5 years in the wild with six individuals recorded reaching this age. Data collected on breeding pairs found that H. whitei displays life-long monogamy with three pairs observed remaining pair bonded over three consecutive breeding years. Baseline population densities were derived for two Port Stephens' sites (0·035 and 0·110 m(-2) ) and for Manly in Sydney Harbour (1·050 m(-2) ). Even though the life-history parameters of H. whitei suggest it may be reasonably resilient, precaution should be taken in its future management as a result of its limited geographical distribution and increasing pressures from anthropogenic sources on its habitats.     

Growth differences between naturally recruited and stocked European eel Anguilla anguilla from different habitats in Lithuania

European eels Anguilla anguilla from freshwater lakes in Lithuania had slower growth rates and lower backcalculated total lengths ( L _T) than those from lagoons and coastal waters, but no significant differences were found among fish with different migratory histories or between naturally recruited and stocked fish except a higher L _T at age of stocked European eels at ages 5 to 8 years. The asymptotic L _T did not differ among habitats or migratory histories, but the stocked eels in the lakes had smaller K (coefficient from the von Bertalanffy growth function) than did the both naturally recruited and stocked eels in the lagoon and coastal waters. The growth rate of European eels in Lithuania might be influenced mainly by different habitats rather than different migratory histories and stocking. The lower L _T at age of naturally recruited fish at ages 5–8 years compared to stocked fish might result from the extra energy costs entailed in migration from the Atlantic and across the Baltic Sea.     

Influence of oceanic factors on Anguilla anguilla (L.) over the twentieth century in coastal habitats of the Skagerrak,southern Norway

The European eel (Anguilla anguilla L.) is distributed in coastal and inland habitats all over Europe, but spawns in the Sargasso Sea and is thus affected by both continental and oceanic factors. Since the 1980s a steady decline has been observed in the recruitment of glass eels to freshwater and in total eel landings. The eel is considered as critically endangered on the International Union for the Conservation of Nature and Natural Resources Red List of species. The Skagerrak beach seine survey from Norway constitutes the longest fishery-independent dataset on yellow/silver eels (starting in 1904). The Skagerrak coastal region receives larvae born in the Sargasso Sea spawning areas that have followed the Gulf Stream/North Atlantic Drift before they penetrate far into the North Sea. The Skagerrak coastal time series is therefore particularly valuable for exploring the impacts of oceanic factors on fluctuations in eel recruitment abundance. Analyses showed that Sargasso Sea surface temperature was negatively correlated with eel abundance, with a lag of 12 years revealing a cyclic and detrimental effect of high temperatures on the newly hatched larvae. The North Atlantic Oscillation index and inflow of North Atlantic water into the North Sea were negatively correlated with eel abundance, with a lag of 11 years. Increased currents towards the North Atlantic during high North Atlantic Oscillation years may send larvae into the subpolar gyre before they are ready to metamorphose and settle, resulting in low recruitment in the northern part of the distribution area for these years. The Skagerrak time series was compared with glass eel recruitment to freshwater in the Netherlands (Den Oever glass eel time series), and similar patterns were found revealing a cycle linked to changes in oceanic factors affecting glass eel recruitment. The recent decline of eels in the Skagerrak also coincided with previously documented shifts in environmental conditions of the North Sea ecosystem.     

Diet and feeding niches of juvenile Gadus morhua, Melanogrammus aeglefinus and Merlangius merlangus during the settlement transition in the northern North Sea

A study on the feeding ecology of juvenile cod Gadus morhua, haddock Melanogrammus aeglefinus and whiting Merlangius merlangus during the pelagic to demersal transition was carried out on fishes sampled throughout their settlement season at a local nursery ground in the north-western North Sea, off the Scottish east coast. A comprehensive quantitative taxonomic analysis of the diets, as described in the paper, showed the emergence of distinctive feeding niches, minimizing the potential for competition between species and size categories. The diet of the juveniles changed with fish size, water depth, time of year and distance offshore. Small G. morhua were present in the study area earlier in the season, settled further inshore and ate a higher proportion of pelagic prey (copepods) and as size increased they moved into deeper waters and targeted larger, more benthic prey. As M. aeglefinus grew larger and moved into deeper waters, a diet of largely copepods, amphipods, pelagic Ammodytes spp., cyprids and pelagic gastropods evolved to one dominated predominantly by fishes and benthic invertebrates. In the case of M. merlangus, widespread ages and sizes throughout the sampling season, a consequence of their more protracted spawning season, resulted in dietary changes which were more likely to be influenced by seasonal changes in the prey field, in addition to developmental (size) changes, than the diets of the other two species.     

Modelling the growth of Japanese eel Anguilla japonica in the lower reach of the Kao-Ping River, southern Taiwan: an information theory approach

Information theory was applied to select the best model fitting total length ( L _T)-at-age data and calculate the averaged model for Japanese eel Anguilla japonica compiled from published literature and the differences in growth between sexes were examined. Five candidate growth models were the von Bertalanffy, generalized von Bertalanffy, Gompertz, logistic and power models. The von Bertalanffy growth model with sex-specific coefficients was best supported by the data and nearly overlapped the averaged growth model based on Akaike weights, indicating a similar fit to the data. The Gompertz, generalized von Bertalanffy and power growth models were also substantially supported by the data. The L _T at age of A. japonica were larger in females than in males according to the averaged growth mode, suggesting a sexual dimorphism in growth. Model inferences based on information theory, which deal with uncertainty in model selection and robust parameter estimates, are recommended for modelling the growth of A. japonica .     

Effect of spatial differences in growth on distribution of seasonally co‐occurring herring Clupea harengus stocks

The mechanisms most likely to determine the distribution of the two major herring Clupea harengus stocks in their common early summer feeding ground in the eastern North Sea, Skagerrak and Kattegat were investigated through analysis of acoustic survey data from six consecutive years. No change was detected in biomass of North Sea autumn spawning C. harengus (NSAS) over time, whereas the biomass of western Baltic spring spawning C. harengus (WBSS) declined severely. Analyses of centre of abundance by stock showed no change in NSAS distribution, whereas the WBSS changed to a more western distribution over time. Contrary to previous perception of the juvenile migration, NSAS were found to leave the study area at the age between 1 and 2 years and WBSS 1 year olds were encountered in the Skagerrak. The estimated parameters of von Bertalanffy growth equations showed marked differences between areas with fish in the eastern part of the area having the lowest size at age at all ages. Further, their growth conditions appeared to deteriorate progressively over the period studied. Both NSAS and WBSS showed the highest condition in the North Sea and Skagerrak while condition was substantially lower in age Kattegat. The westward movement of spring spawners over time suggests that growth rate and possibly density of conspecifics influence the migration pattern and distribution of C. harengus in the area. In contrast, there was no evidence to suggest that distribution was constant over time within stocks or that distribution reflected size‐dependent limitations on migration distance.     

Age and growth of longnose trevally (Carangoides chrysophrys) in the Arabian Sea

The ages and growth of longnose trevally (Carangoides chrysophrys), caught in the northwest Arabian Sea between April 2005 and September 2006, were investigated. Age and growth of 336 fish specimens were determined using sectioned sagittae otoliths. Annual opaque growth rings were formed between December and March, with the majority being laid down in February and March, coinciding with the spawning period and high water temperatures. Marginal zone or edge analysis was used to validate the annual deposition of the opaque zone in the otoliths. This species showed large variations in length‐at‐age, suggesting large growth variations among individuals of the same cohort. The estimated von Bertalanffy growth model differed significantly between the sexes, with males having larger mean lengths at age and reaching a larger asymptotic size. The von Bertalanffy growth models were TL (cm) = 73.34[1‐exp (?0.25 (t + 1.21))] and TL(cm) = 73.26[1‐exp (?0.24 (t + 1.20))] for males and females, respectively.     

Decadal variability in growth of the Caribbean spiny lobster Panulirus argus (Decapoda: Paniluridae) in Cuban waters

Annual von Bertalanffy growth parameters of the Caribbean spiny lobster (Panulirus argus) in Cuban waters were estimated from a long term study (40 years) by length-based methods ELEFAN and the new version of SLCA. Data of around 800 000 lobsters (with carapace length ranging 14 to 199mm) were randomly sampled in artificial shelters (a non selective fishing gear very common in the lobster fishery), through the field monitory program established for this species since 1963 in 14 localities of southwestern Cuban shelf. The software ELEFAN showed problems to converge in an optimal combination of the instantaneous growth coefficient (K) and the asymptotic length (Linfinity) of the von Bertalanffy equation, whereas the new SLCA software produced value estimates of K between 0.20 and 0.27 year(-1) and values of Linfinity between 177 and 190 mm carapace length, all within the range reported in the literature. The standardized anomalies of both parameters showed the presence of cycles along the analyzed time series. Decadal variability in growth parameters was revealed through the spectral analysis indicating cycles of 16 and 20 years for K and of 16 years for Linfinity. The incidence of some factors such as biomass and temperature that modulate growth in this crustacean was explored, using a nonlinear multiple regression model. These combined factors explained 33% and 69% of the variability of K and Linfinity respectively. The growth coefficient appeared to be maximum with annual mean sea surface temperature of 28. 1 degrees C and the largest Linfinity is reached at a annual men biomass level of 23,000 t. These results should be the basis to understand the Cuban lobster population dynamics.     

The food of five gadoid species during the pelagic O-group phase in the northern North Sea

The diets of five gadoid species in the northern North Sea are described: the cod, Gadus morhua (L.); haddock, Melanogrammus aeglefinus (L.); whiting, Merlangius merlangus (L.); saithe, Pollachius virens (L.); and the Norway pout, Trisopterus esmarkii (L.). The diet of each species was shown to be a gradual progression to different prey species as the predators increased in length. There were differences in the food taken by each species with respect to numbers, species and size. These differences in diet suggest that the degree of competition between pelagic O-group gadoids is not great.     

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.     

Female‐biased dimorphism in size and age at maturity is reduced at higher latitudes in lake whitefish Coregonus clupeaformis

Female‐biased sexual dimorphism in size at maturity is a common pattern observed in freshwater fishes with indeterminate growth, yet can vary in magnitude among populations for reasons that are not well understood. According to sex‐specific optimization models, female‐biased sexual size dimorphism can evolve due to sexual selection favouring earlier maturation by males, even when sexes are otherwise similar in their growth and mortality regimes. The magnitude of sexual size dimorphism is expected to depend on mortality rate. When mortality rates are low, both males and females are expected to mature at older ages and larger sizes, with size determined by the von Bertalanffy growth equation. The difference between size at maturity in males and females becomes reduced when maturing at older ages, closer to asymptotic size. This phenomenon is called von Bertalanffy buffering. The predicted relationship between the magnitude of female‐biased sexual dimorphism in age and size at maturity and mortality rate was tested in a comparative analysis of lake whitefish Coregonus clupeaformis from 26 populations across a broad latitudinal range in North America. Most C. clupeaformis populations displayed female‐biased sexual dimorphism in size and age at 50% maturity. As predicted, female‐biased sexual size dimorphism was less extreme among lower mortality, high‐latitude populations.     

Long‐term patterns in growth of Oneida Lake walleye: a multivariate and stage‐explicit approach for applying the von Bertalanffy growth function

Total length ( L _T) and its inter annual variation of walleye Sander vitreus from Oneida Lake, New York, based on 51 years (1950–2000) of data for ages 1 to 7 years were analysed. Growth increased over time at young ages, did not change at intermediate ages and decreased at old ages. Total length at age increased over time to age 4 or 5 years, but was stable at older ages. Principle component analysis was used to study the pattern of variations in annual L _T increments among years. More than 92 and 91% of inter annual variability in growth was described by the first three principal components for males and females, respectively. The first principal component was a general indicator of annual growth at all ages, but was dominated by annual growth at intermediate ages. The second and third principal components represented contrasts among yearling L _T, yearling growth and growth at older ages. Therefore, changes in the three stage‐specific parameters, yearling L _T, yearling growth and asymptotic L _T, explained most of the variance in observed growth. Using these three stage‐specific parameters for the von Bertalanffy growth function facilitated interpretations of growth comparisons.     

Evidence of sustained populations of a small reef fish on artificial structures. Does depth affect production on artificial reefs?

The length frequencies and age structures of resident Pseudanthias rubrizonatus (n = 407), a small protogynous serranid, were measured at four isolated artificial structures on the continental shelf of north-western Australia between June and August 2008, to determine whether these structures supported full (complete size and age-structured) populations of this species. The artificial structures were located in depths between 82 and 135 m, and growth rates of juveniles and adults, and body condition of adults, were compared among structures to determine the effect of depth on potential production. All life-history stages, including recently settled juveniles, females and terminal males, of P. rubrizonatus were caught, ranging in standard length (L(s)) from 16·9 to 96·5 mm. Presumed ages estimated from whole and sectioned otoliths ranged between 22 days and 5 years, and parameter ±s.e. estimates of the von Bertalanffy growth model were L(∞) = 152 ± 34 mm, k = 0·15(±0·05) and t(0) = -1·15(±0·15). Estimated annual growth rates were similar between shallow and deep artificial structures; however, otolith lengths and recent growth of juveniles differed among individual structures, irrespective of depth. The artificial structures therefore sustained full populations of P. rubrizonatus, from recently settled juveniles through to adults; however, confirmation of the maximum age attainable for the species is required from natural populations. Depth placement of artificial reefs may not affect the production of fish species with naturally wide depth ranges.     

Temperature,salinity tolerance,and buoyancy during early development and starvation of Clyde and North Sea herring,cod, and flounder larvae

Tolerance limits, at which 50% of larvae could survive high temperature and low salinity for 24 h, were determined for the yolk-sac larvae of Clyde and North Sea herring (Clupea harengus L.), cod (Gadus morhua L.) and flounder (Platichthys flesus L.) during early development and starvation. Clyde and North Sea herring, cod and flounder from hatching to the end of the yolk-sac stage, could withstand 21–23.5 °C, 20.5–23 °C, 15.5–18 °C and 21.5–24°C, respectively. The temperature tolerance was reduced by about 3.5–4 °C for Clyde herring and cod, 4–4.5 °C for North Sea herring and 8–8.5 °C for flounder when the larvae reached the point-of-no-return (PNR, when 50% of larvae, although still alive, are no longer strong enough to feed). The lowest salinity tolerance between hatching and the end of yolk-sac stage was 1–1.5‰ for Clyde and North Sea herring, 2–3‰ for cod and 0–1‰ for flounder. In no instance was there a loss of tolerance to low salinity during starvation. In fact, tolerance improved somewhat until the larvae became moribund. At hatching Clyde and North Sea herring larvae were negatively buoyant with a sinking rate of 0.35–0.4cm · s⁻¹ which steadily decreased until the larvae became moribund. Cod and flounder larvae, however, were positively buoyant at hatching but became progressively less buoyant and, by the end of the yolk-sac stage they were negatively buoyant with a sinking rate of 0.06–0.07 cm · s⁻¹. This sinking rate then decreased slightly until the PNR stage. The low salinity tolerance of all three species varied in a similar fashion to buoyancy.     

Immature digeneans from the alimentary tract of larval and juvenile pelagic stages of haddock, Melanogrammus aeglefinus (L.)

Immature specimens of Opechona sp. are described from the stomach, pyloric caeca and intestine of larval and O-group haddock, Melanogrammus aeglefinus (L.), taken in the northern North Sea and to the west of Scotland. This appears to be a new host record and possible sources of infection are discussed, together with the occurrence of this normally intestinal parasite in the stomach. It is suggested that these infections may be worth taking into account when considering possible factors contributing to mortalities of haddock and other teleost larvae.     

尖头塘鳢(Eleotris oxycephala Temmiuck et Schlegel)的年龄、生长和生活史类型的研究

本文采用胸鳍第二支鳍骨为研究东江尖头塘鳢的年龄鉴定材料。胸鳍第二支鳍骨(远侧部)长的骨(R)与体长(L)的关系L=10.6565 54.3848R。用von Bertalanffy生长方程可表达体长、体重与年龄的关系:L=298.6(1-e~(-0.2313(t 0.3028))];W_t=577.4(1-e~(-0.2313(t 0.3028))]~3。根据r-选择和K-选择的典型特征以及渐近体长(L_∞)、渐近体重(W_∞)、生长系数(K)、瞬时自然死亡率(M)、初次生殖年龄(T_m)、最大年龄(T_(max))和性腺指数(GI)等7个生态学参数值,可以判断尖头塘鳢偏向r-选择。应用平衡产量模式计算改变瞬时捕捞死亡率(F)和渔业补充年龄(t_c)时的产量变化,同样证实尖头塘鳢生活史偏向r-选择。作为渔业管理对策,尖头塘鳢的捕捞年龄可定为2—3龄,以2龄为主,这样既能保护资源,又能获得较好的经济效益。     

Growth, mortality, parasitism, and potential yields of two Priacanthus species in the South China Sea

In the northern part of the South China Sea the 'big-eye', Priacanthus tayenus , spawned once a year in June, had von Bertalanffy growth parameters of k = 0.8 and L ∞= 30 cm, and a mean total annual instantaneous mortality of Z = 2.0, calculated from adjusted catch curves and a mean length equation. The natural mortality rate M = 1.4, fishing mortality rate F = 0.6, and the exploitation rate (E) was 0.27. The maximum potential yield, calculated using Marten's method, was 0.06 kg/recruit when F = 5.4. The fish were heavily parasitised by the protozoan Pleistophora priacanthicola .
A second big-eye, P. macracanthus , spawned twice a year in May-June and September, had growth parameters of κ= 0.7 and L∞= 32, and population parameters of Z = 2.0, . F = 0.7, and E = 0.34. The maximum potential yield was 0.13 kg/recruit when F = 5.8.
A marked reduction in fishing mortality occurred for both species between 1965 and 1966, coinciding with the onset of the Chinese Cultural Revolution. Our estimates of maximum potential yield correspond to fishing mortalities eight times estimated levels, though such heavy exploitation could risk recruitment failure.