Slow growth of the overexploited milk shark Rhizoprionodon acutus affects its sustainability in West Africa

Age and growth of Rhizoprionodon acutus were estimated from vertebrae age bands. From December 2009 to November 2010, 423 R. acutus between 37 and 112 cm total length (L_T) were sampled along the Senegalese coast. Marginal increment ratio was used to check annual band deposition. Three growth models were adjusted to the length at age and compared using Akaike's information criterion. The Gompertz growth model with estimated size at birth appeared to be the best and resulted in growth parameters of L_∞ = 139·55 (L_T) and K = 0·17 year^?1 for females and L_∞ = 126·52 (L_T) and K = 0·18 year^?1 for males. The largest female and male examined were 8 and 9 years old, but the majority was between 1 and 3 years old. Ages at maturity estimated were 5·8 and 4·8 years for females and males, respectively. These results suggest that R. acutus is a slow‐growing species, which render the species particularly vulnerable to heavy fishery exploitation. The growth parameters estimated in this study are crucial for stock assessments and for demographic analyses to evaluate the sustainability of commercial harvests.     

Age structure and multi-model growth estimation of longnose stingray Hypanus guttatus (Dasyatidae: Myliobatoidei) from north-east Brazil

We collected 729 Hypanus guttatus from the northern coast of the state of Rio Grande do Norte (RN), of which 196 were used to estimate age and growth. Ninety-five were male (12.7 to 57.0 cm disc width; W_D) and 101 were female (13.0 to 88.5 cm W_D); females were significantly larger than males. Cross sections of vertebrae showed band-pairs ranging from 0 to > 14 in females and from 0 to 9 in males. New-borns presented an opaque edge at birth in vertebrae without a birthmark. The average percentage of error (APE; %E) for the entire sample provided evidence that ages were repeatable. The mean monthly marginal increment (I_M) indicates annual band-pair formation from August to November. The annual cycle model for one band-pair deposition provided the best fit to data based on the AIC, with peaks between August and October, similar to that found in the I_M analysis, suggesting an annual formation pattern. A multi-model approach that included four models based on the observed mean W_D at age indicated a modified von Bertalanffy growth model as the best for describing the species growth: W₀ (W_D at birth) = 14.6 cm for both sexes; females W_∞ = 98.61 cm (95% CI = 87.34–114.61 cm); k = 0.112 year⁻¹ (CI = 0.086–0.148 year⁻¹); males W_∞ = 60.22 cm (CI = 55.66–65.35 cm); k = 0.219 year⁻¹ (CI = 0.185–0.276 year⁻¹). The age-at-maturity in males and females is 5 years and 7 years, respectively. The age composition shows that most (84%) specimens were aged 0 to 2 years. The information provided here is essential for analytical assessments of H. guttatus, which is subject to significant fishing pressure mainly on new-borns and juveniles.     

Basic characteristics of the population dynamic and state of exploitation of Moroccan white seabream Diplodus sargus cadenati (Sparidae) in the Canarian archipelago

Moroccan white seabream Diplodus sargus cadenati (n = 603) were caught off the Canary Islands from April 2000 to March 2001. Total length ranged from 46 to 404 mm. The subspecies was characterized as being dygynous with partial protandry. Overall ratio of males to females was 1 : 2.9. The reproductive season extended from December to May, with a peak in spawning activity in January–February. Fifty per cent maturity was reached at 201 mm total length in males and 216 mm in females. The length–weight relationship for all individuals was described by the following parameters: a = 0.000023, and b = 2.96, when length is given in millimeters and weight in grams. Fish of 0–12 years in age were found. The von Bertalanffy growth parameters for the entire population were: L_∞ = 467 mm, k = 0.143 year^?1 and t₀ = ?2.14 year. Growth parameters differed between males and females. For all fish, instantaneous rates of mortality were Z = 0.68 year^?1, M = 0.31 ± 0.6 year^?1 and F = 0.37 ± 0.6 year^?1; the exploitation ratio was E = 0.54 ± 0.9. Length at first capture for all individuals was 173 mm. The stock exploited above is an assumed optimum.     

Validated annual band‐pair periodicity and growth parameters of blue‐spotted maskray Neotrygon kuhlii from south‐east Queensland,Australia

Age and growth parameters were derived for blue‐spotted maskray Neotrygon kuhlii from Moreton Bay in subtropical eastern Australia. Maximum age estimates of 13 and 10 years were obtained from female (n = 76) and male (n = 44) N. kuhlii, respectively. Estimated ages at maturity for 50% of females and males were 6·32 and 3·95 years, respectively. A three‐parameter power function provided the best statistical fit to size at age data in both sexes, providing parameter estimates of y⁰ = 163·13, a = 58·52 and b = 0·58 for females and y⁰ = 165·13, a = 59·02 and b = 0·54 in males. The two‐parameter von Bertalanffy growth function was used to estimate biological parameters based on disc width (W_D) for both female (W_D∞ = 465·81 mm, K = 0·13 year^?1, b = 0·63) and male N. kuhlii (W_D∞ = 385·19 mm, K = 0·20 year^?1, b = 0·54). Annual band‐pair deposition was observed in three calcein‐injected N. kuhlii after periods of liberty ranging from 631 to 1081 days. Centrum edge analysis indicated that annual band‐pair formation was generally consistent within this population, with translucent bands formed over spring and summer and opaque bands formed in autumn and winter. Individual growth rates obtained from tagged specimens were similar to power function growth predictions. These results support previous characterizations of this common trawl by‐catch species as comparatively resilient to non‐targeted catches, although higher catch rates outside Australia infer a need for cautious management.     

Age,growth and maturity of the pelagic thresher Alopias pelagicus and the scalloped hammerhead Sphyrna lewini

Indonesia has the greatest reported chondrichthyan catches worldwide, with c.110,000 t caught annually. The pelagic thresher (Alopias pelagicus) and scalloped hammerhead (Sphryna lewini) together comprise about 25% of the total catches of sharks landed in Indonesia. Age and growth parameters were estimated for A. pelagicus and S. lewini from growth‐band counts of thin‐cut vertebral sections. Alopias pelagicus (n = 158) and S. lewini (n = 157) vertebrae were collected from three Indonesian fish markets over a 5 year period. A multi‐model analysis was used to estimate growth parameters for both species. The models of best fit for males and females for A. pelagicus was the three‐parameter logistic (L_∞ = 3169 mm L_T, k = 0·2) and the two‐parameter von Bertalanffy models (L_∞ = 3281 mm L_T, k = 0·12). Age at maturity was calculated to be 10·4 and 13·2 years for males and females, respectively, and these are the oldest estimated for this species. The samples of S. lewini were heavily biased towards females, and the model of best fit for males and females was the three‐parameter Gompertz (L_∞ = 2598 mm L_T, k = 0·15) and the two‐parameter Gompertz (L_∞ = 2896 mm L_T, k= 0·16). Age at maturity was calculated to be 8·9 and 13·2 years for males and females, respectively. Although numerous age and growth studies have previously been undertaken on S. lewini, few studies have been able to obtain adequate samples from all components of the population because adult females, adult males and juveniles often reside in different areas. For the first time, sex bias in this study was towards sexually mature females, which are commonly lacking in previous biological studies on S. lewini. Additionally, some of the oldest aged specimens and highest age at maturity for both species were observed in this study. Both species exhibit slow rates of growth and late age at maturity, highlighting the need for a re‐assessment of the relative resilience of these two globally threatened sharks at current high levels of fishing mortality throughout the eastern Indian Ocean.     

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,growth, reproduction and feed of longnosed skate,Dipturus oxyrinchus (Linnaeus, 1758) in Saros Bay,the north Aegean Sea

The age, growth, reproduction, and feeding of longnosed skate (Dipturus oxyrinchus) were studied using 179 specimens from the Saros Bay (North Aegean Sea) between March 2005 and December 2007. Composition was 49.7% females and 50.3% males. Total length of females ranged from 14.9 to 100 cm (disc width, 9.8–65 cm), and of males from 15.2 to 86.5 cm (disc width, 10–57.5 cm). Total length‐weight and disc width‐weight relationships are described by the equations W = 0.0008*TL^3.35 and W = 0.0043*DW^3.29, respectively. The age data, derived from vertebrae readings, were used to estimate the growth parameters of the von Bertalanffy equation: L_∞ = 256.46 cm, K = 0.04 year^?1, t₀ = ?1.17year. The maximum age was 9 years. Males matured at 64–65 cm (disc width, 43.5 cm) and females at 82–83 cm TL (disc width, 53 cm). The stomach contained mainly Parapenaus longirostris, IRI: 93.47%.     

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.     

Factors affecting estimates of size at age and growth in grey triggerfish Balistes capriscus from the northern Gulf of Mexico

Growth zones in dorsal spines of grey triggerfish Balistes capriscus from the northern Gulf of Mexico were utilized to estimate growth and examine factors that may affect estimates of size at age. Age was estimated from dorsal‐spine sections of 4687 individuals sampled from U.S. waters during 2003–2013, including both fishery‐independent (n = 1312) and fishery‐dependent (n = 3375) samples. Ninety‐six per cent (n = 4498) of these sections were deemed suitable for ageing; average per cent error between two independent readers was 10·8%. Fork length (L_F) ranged from 65 to 697 mm and age estimates from 0 to 14 years. Both sex and sample source (fishery‐independent v. recreational) significantly affected estimated size at age for 2–6 year‐old fish. Data were pooled between sources to fit sex‐specific von Bertalanffy growth functions. Results for the female model were L_∞ = 387 mm L_F, k = 0·52 year^?1 and t₀ = 0·01 year, while for males L_∞ = 405 mm L_F, k = 0·55 year^?1 and t₀ = 0·02 year. These results were significantly different between sexes and indicate clear sexual dimorphism. Thus, growth should be modelled separately by sex when examining population parameters or conducting stock assessment modelling. The positive bias in estimates of size at age computed for recreational v. fishery‐independent samples also has clear implications for stock assessment as growth functions computed with fishery‐dependent samples would tend to overestimate stock productivity.     

Life history of the red-banded seabream Pagrus auriga (Sparidae) from the coasts of the Canarian archipelago

Red‐banded seabream Pagrus auriga (N = 615) were caught off the Canary Islands from January 2003 to December 2004. Total length ranged from 120 to 780 mm. The species was characterized by protogynous hermaphroditism. The male :female ratio was in favour of females (1 : 8.2). The reproductive season extended from September to February, with a peak in spawning activity in October–November. Fifty percentage maturity was reached at 387 mm total length by females and 533 mm by males. The length–weight relationship for all individuals was described by the parameters: a = 0.0086 and b = 3.014, when length is given in mm and weight in grams. Otolith age readings indicated that the population consists of 19 age groups, including a very high proportion of individuals between 0 and 7 years old. Growth analysis reveals that the species is slow‐growing and relatively long lived (18 years). The von Bertalanffy growth parameters for the entire population were: L_∞ = 803 mm, k = 0.081 year⁻¹ and t₀ = −2.17 year. Growth differed between males and females. The instantaneous rate of natural mortality for all fish was: M = 0.164 year⁻¹.     

Validated age,growth and maturity of the bonnethead Sphyrna tiburo in the western North Atlantic Ocean

The age, growth and maturity of bonnetheads Sphyrna tiburo inhabiting the estuarine and coastal waters of the western North Atlantic Ocean (WNA) from Onslow Bay, North Carolina, south to West Palm Beach, Florida, were examined. Vertebrae were collected and aged from 329 females and 217 males ranging in size from 262 to 1043 mm and 245 to 825 mm fork length, L_F, respectively. Sex‐specific von Bertalanffy growth curves were fitted to length‐at‐age data. Female von Bertalanffy parameters were L_∞ = 1036 mm L_F, k = 0·18, t₀ = ?1·64 and L₀ = 272 mm L_F. Males reached a smaller theoretical asymptotic length and had a higher growth coefficient (L_∞ = 782 mm L_F, k = 0·29, t₀ = ?1·43 and L₀ = 266 mm L_F). Maximum observed age was 17·9 years for females and 16·0 years for males. Annual deposition of growth increments was verified by marginal increment analysis and validated for age classes 2·5+ to 10·5+ years through recapture of 13 oxytetracycline‐injected specimens at liberty in the wild for 1–4 years. Length (L_F50) and age (A₅₀) at 50% maturity were 819 mm and 6·7 years for females, and 618 mm and 3·9 years for males. Both female and male S. tiburo in the WNA had a significantly higher maximum observed age, L_F50, A₅₀ and L_∞, and a significantly lower k and estimated L₀ than evident in the Gulf of Mexico (GOM). These significant differences in life‐history parameters, as well as evidence from tagging and genetic studies, suggest that S. tiburo in the WNA and GOM should be considered separate stocks.     

Unravelling growth trajectories from complicated otoliths – the case of Brazilian codling Urophycis brasiliensis

Uncertainty regarding the age determination of the Brazilian codling Urophycis brasiliensis has hampered its stock assessment. Transverse sections of otoliths displayed up to seven (in males) and 12 (in females) alternate opaque and translucent bands that could not be conclusively validated as annuli, resulting in unrealistically high ages of first maturity (A₅₀) (A_50male = 4·5 years and A_50female = 6 years). Therefore, growth was described by the von Bertalanffy (VB) model using an alternative approach that combined microstructure data (daily growth increments) and a fixed asymptotic total length (L_∞). This approach was supported by applying it to two other co‐occurring species, the whitemouth croaker Micropogonias furnieri and the king weakfish Macrodon atricauda, for which daily and annual ring formation has previously been validated. The sensitivity to realistic errors associated with the choice of the L_∞ and the daily increment readings was shown to be low. The results show that U. brasiliensis has a fast growth rate (K_male = 1·19 year^?1, K_female = 0·71 year^?1) and early maturation (A_50male = 1·1–1·5 years, A_50female = 1·6–1·8 years); typical life‐history traits for a sub‐tropical coastal gadiform. This novel study offers an alternative approach for age and growth reconstruction for species with complex patterns of opaque and translucent bands provided that daily growth increments in the yearlings can be counted and L_∞ reliably estimated.     

Age and growth of the gulf toadfish Opsanus beta based on otolith increment analysis

In the present study, sagittal otoliths of confirmed male and female specimens of the gulf toadfish Opsanus beta that were collected monthly over the course of a year from Biscayne Bay, Florida, U.S.A. were analysed. The timing and frequency of O. beta spawning seasons are reported by examination of the gonado‐somatic index. The estimated ages of males and females ranged from < 1 year to 6 and 5 years, respectively. Strong sexual dimorphism in growth was apparent with von Bertalanffy parameter estimates for males of L_∞ = 393·8 mm, K = 0·30, t₀ = 0·36 and females of L_∞ = 201·1 mm, K = 0·79, t₀ = 0·47. Comparison with previously published growth trajectories of the more northerly distributed conspecific Opsanus tau showed that O. beta males had a higher growth rate. Female O. beta and O. tau growth trajectories appear similar, with an indication that the former becomes asymptotic at least a year before the latter. Results are discussed in the context of temperature regimes, reproductive energy allocation and waste urea excretion in the two species.     

Age and growth in pink cusk-eel (Genypterus blacodes) off the Chilean austral zone: evaluating differences between management fishing zones

The von Bertalanffy (vB) growth parameters for pink cusk‐eel (Genypterus blacodes) were estimated for the Chilean austral‐zone (41°28′–57°00′S) by gender and management fishing zones. A total of 47 026 samples were collected between March 1982 and May 2004, with total length ranging from 19 to 154 cm. Age determinations, based on the reading of saggital otoliths, were between 1 and 14 years in males and between 1 and 16 years in females. Statistical differences in growth were found between the sexes and management fishing zones. For the combined sexes the vB growth parameters for the northern‐austral zone (41°28′–47°00′S) were: l_∞=111.452 cm, k = 0.186 year⁻¹, t₀ = −0.912 year; and for the southern‐austral zone (47°00′–57°00′S): l_∞ = 123.447 cm, k = 0.147 year⁻¹, t₀ = −1.779 year.     

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.     

Reproductive biology of the guitarfish Rhinobatos percellens (Chondrichthyes,Rhinobatidae) from the São Paulo Coast,Brazil, western South Atlantic Ocean

The reproductive biology of the guitarfish Rhinobatos percellens was studied from 751 specimens caught by bottom pair trawlers off the coast of São Paulo, Brazil, between c. 24° 00′ S; 45° 15′ W and c. 25° 10′ S; 47° 52′ W, from September 2007 to August 2009. The total length (L_T) and total mass (M_T) relationship for males and females combined was M_T = 1·29E‐06 L_T^3·15 (r = 0·99, n = 751). The mean L_T of sexually mature specimens was 548 mm for males and 583 mm for females. Clasper growth was allometric and showed three distinct phases. Most claspers were calcified in specimens of c. 550 mm L_T. The mean diameter of the largest oocyte was 29·8 mm, the mean ovarian fecundity was seven oocytes and ovulation occurred between August and November. Uterine fecundity ranged from two to 13 embryos (mean of five embryos). Larger females had higher litter sizes and larger embryos; the size‐at‐birth was c. 200 mm L_T. The hepato‐somatic index oscillated seasonally for males and females; the gonado‐somatic index had little variation in males, but varied seasonally in females. The presence of many non‐pregnant adult females and of encapsulated eggs during two consecutive seasons suggests a resting period between gestations and the possibility of diapause.     

Life history of an unusual marine fish: survival, growth and movement patterns of Hippocampus guttulatus Cuvier 1829

The life history of the long‐snouted seahorse Hippocampus guttulatus was characterized using mark‐recapture data collected within a focal study site and catch data from 53 additional sites in the Ria Formosa coastal lagoon, southern Portugal. Population structure in benthic habitats was characterized by high local densities (0·3–1·5 m^?2), equal sex ratios and few juveniles <70 mm. Adult H. guttulatus maintained small (19·9 ± 12·4 m²), strongly overlapping home ranges during multiple reproductive seasons. Recruited (benthic) juveniles exhibited significantly lower site fidelity than adults. A Ford‐Walford plot of standard length (L_S) at time t against L_S measured during the previous year from tagged juveniles and adults led to estimates of the von Bertalanffy parameters K = 0·571 and L_∞ = 197·6 mm. The growth rate of planktonic juveniles (inferred from previous studies), was greater than predicted by the von Bertalanffy model, providing evidence of an ontogenetic shift in growth trajectory. The instantaneous rate of natural mortality, M, ranged from 1·13 to 1·22 year^?1(annual survival rate = 29·4–32·2%). Sexes did not differ in movement, growth or survival patterns. On average, H. guttulatus measured 12·2 ± 0·8 mm at birth. Planktonic juveniles recruited to vegetated habitat at 96·0 ± 8·0 mm (0·25 years), had mature brood pouches (males only) at 109·4 mm (0·49 years), began maintaining home ranges and reproducing at 125–129 mm (0·85–0·94 years), and lived for 4·3–5·5 years. Early age at maturity, rapid growth rates, and short generation times suggested that H. guttulatus may recover rapidly when direct (e.g. exploitation) and indirect (e.g. by‐catch and habitat damage) effects of disturbance cease, but may be vulnerable to extended periods of poor recruitment.     

Age and growth parameters of shark‐like batoids

Estimates of life‐history parameters were made for shark‐like batoids of conservation concern Rhynchobatus spp. (Rhynchobatus australiae, Rhynchobatus laevis and Rhynchobatus palpebratus) and Glaucostegus typus using vertebral ageing. The sigmoid growth functions, Gompertz and logistic, best described the growth of Rhynchobatus spp. and G. typus, providing the best statistical fit and most biologically appropriate parameters. The two‐parameter logistic was the preferred model for Rhynchobatus spp. with growth parameter estimates (both sexes combined) L_∞ = 2045 mm stretch total length, L_ST and k = 0·41 year^?1. The same model was also preferred for G. typus with growth parameter estimates (both sexes combined) L_∞ = 2770 mm L_ST and k = 0·30 year^?1. Annual growth‐band deposition could not be excluded in Rhynchobatus spp. using mark‐recaptured individuals. Although morphologically similar G. typus and Rhynchobatus spp. have differing life histories, with G. typus longer lived, slower growing and attaining a larger maximum size.     

Life histories of two deep‐water Australian endemic elasmobranchs: Argus skate Dipturus polyommata and eastern spotted gummy shark Mustelus walkeri

Two Australian endemic elasmobranchs, the Argus skate Dipturus polyommata and the eastern spotted gummy shark Mustelus walkeri, were collected from the by‐catch of a prawn Melicertus plebejus trawl fishery off Queensland. Age and growth parameters were estimated from growth band counts in vertebral sections of 220 D. polyommata and 44 M. walkeri. Dipturus polyommata males and females had an observed maximum age of 10 years and reached maximum sizes of 369 and 371 mm total length (L_T), respectively. Mustelus walkeri lived longer, with the oldest female aged 16 years and measuring 1050 mm stretched total length (L_ST), and oldest male aged 9 years and 805 mm L_ST. Dipturus polyommata grew relatively fast with a von Bertalanffy growth completion parameter of k = 0·208 year^?1 with males reaching maturity at 4·0 years (c. 278 mm L_T) and females at 5·1 years (c. 305 mm L_T). Mustelus walkeri grew more slowly with k = 0·033 year^?1 with males estimated to mature at 7–9 years (670–805 mm L_ST) and females at 10–14 years (833–1012 mm L_ST). Length at birth inferred from neonate D. polyommata was 89–111 mm L_T while for M. walkeri it was estimated to be 273 L_ST based on the value of L₀ from the von Bertalanffy growth model. Both species appeared to have continuous reproductive cycles and low fecundity with an average ovarian fecundity of eight follicles for D. polyommata and a litter size of five to seven pups for M. walkeri. Based on these life‐history traits, D. polyommata is more resilient to fishing pressure than M. walkeri.     

Age,growth and maturity for two highly targeted jack species: Caranx ignobilis and Caranx melampygus

This study provides growth rate, longevity and maturity estimates for the two important species of jack in Hawaiʻi: ulua aukea/giant trevally Caranx ignobilis and omilu/bluefin trevally Caranx melampygus. Maximum observed ages for C. ignobilis and C. melampygus were 31 years and 24 years, respectively. Combined sex von Bertalanffy growth parameter values for C. ignobilis and C. melampygus were as follows: L_∞ = 1064 mm and K = 0.18 year⁻¹; and L_∞ = 718 mm and K = 0.20 year⁻¹, respectively. Female size at maturity was significantly greater than males for both C. ignobilis and C. melampygus. Size and age at maturity for C. ignobilis was 594 mm and 4.4 years for females and 465 mm and 2.8 years for males. Size and age at maturity for C. melampygus was 372 mm and 4.1 years for females and 329 mm and 2.9 years for males. This study provides the first robust demographic data for both of these highly prized and ecologically important predatory species in Hawaiʻi, which can be used for future assessments or management.