Age and growth estimates of the bull shark,Carcharhinus leucas,from the northern Gulf of Mexico

Synopsis Length at age and growth rates for 59 bull sharks, Carcharhinus leucas, collected from the northern Gulf of Mexico were estimated from the band patterns formed seasonally in the vertebral centra. The combined age at length data for both sexes were applied to a von Bertalanffy growth model producing parameter estimates of L = 285 cm TL, K = .076, t₀ = –3.0 yr. Lengths at age for males and females were similar except that males did not attain as great a length as females. Growth was apparently slow and varied among individuals, but in general, was estimated to be 15–20 cm yr^–1 for the first five years, 10 cm yr^–1 for years 6–10, 5–7 cm yr^–1 for years 11–16, and less than 4–5 cm yr^–1 thereafter. Males mature at 210–220 cm TL or 14–15 yr of age; females mature at>225 cm TL or 18+ yr of age. The largest male (245 cm TL) was 21.3 yr old; the largest female (268 cm TL) was 24.2 yr old.     

Age and growth of the bonnethead shark, Sphyrna tiburo, from northwest Florida, with comments on clinal variation

Age and growth rates of the bonnethead shark, Sphyrna tiburo, from northwest Florida were estimated from vertebrae collected between October 1992 and October 1995. The von Bertalanffy growth equation was fit to male and female vertebral age data. Initial growth was rapid (≈ 200 mm TL) for both sexes from age 0–1. At age 2 growth slowed for males but continued for females. Similar to many species of sharks, females grew slower than males (K = 0.28 and K = 0.69, respectively) but attained a larger maximum size (L_∞=1226 and L_∞=897). Maximum age was estimated in males and females to be 8+ and 12+ years, respectively. Growth of young-of-year sharks was 21 to 30 mm TL per month determined by three different methods. A comparison of age and growth estimates from populations at more southerly latitudes suggest that clinal variation in total length may be evident among bonnethead sharks in the Gulf of Mexico with females reaching larger sizes in northern areas as compared to south Florida. This revised version was published online in July 2006 with corrections to the Cover Date.     

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.     

Age and growth of the blacknose shark, <Emphasis Type="Italic">Carcharhinus acronotus</Emphasis>, in the western North Atlantic Ocean with comments on regional variation in growth rates

We examined the age and growth of the blacknose shark, Carcharhinus acronotus, in the western North Atlantic Ocean by obtaining direct age estimates using vertebral centra. We verified annual deposition of growth increments with marginal increment analysis and validated it by analyzing vertebrae marked with oxytetracycline from a female blacknose shark held in captivity. Von Bertalanffy growth parameters indicated that female blacknose sharks have a lower growth constant (k), a larger theortical maximum size (L), and are longer lived than males. We compared these growth parameters for blacknose sharks in the western North Atlantic Ocean to growth parameters for blacknose sharks collected in the eastern Gulf of Mexico to test for differences between regions. Females in the western North Atlantic Ocean have a significantly lower L, lower k, and a higher theoretical longevity than females in the Gulf of Mexico. Males in the western North Atlantic Ocean have a higher L<>, lower k, and higher theoretical longevity than males in the Gulf of Mexico. The significant differences between these life history parameters for blacknose sharks suggest that, when possible, future management initiatives concerning blacknose sharks should consider managing the populations in the western North Atlantic and the Gulf of Mexico as separate stocks.     

Age, Growth Rates, Sex Change and Feeding Habits of Notothenioid Fish Eleginops Maclovinus from the Central-southern Chilean Coast

The róbalo, Eleginops maclovinus, a protandrous hermaphrodite species, is an important component of the ichthyofauna in the coastal areas and estuaries of southern Chile. However, there are many aspects about its life history that are unknown. Three hundred and eighty-three specimens of E. maclovinus (19–79 cm total length, TL) were collected between November 2002 and December 2003 from central-southern Chile. Marginal increment analysis from sagittal otoliths showed a single annual minimum in March, demonstrating that a single growth ring is formed each year. The growth of E. maclovinus was described by the von Bertalanffy growth model by following parameters: L _∞ = 105.4 cm TL, K = 0.08 per year, and t ₀ = −1.03 years. E. maclovinus can live for 10 years. The length and age at which the 50% of the males in the population transformed into females was estimated at ~36 cm TL and ~5-years old. A total of 27 prey items were identified. The most important prey items were the crustaceans Hemigrapsus crenulatus and Emerita analoga associated with estuarial and marine habitats respectively. Ontogenetic changes in the diet were related to the spatial distributional pattern of males (1–4 years old, in the estuary) and females (5–8 years old, in the sea). Also, diet changes are associated with the type of available prey in each habitat occupied, indicating a generalized opportunist strategy.     

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.     

Morphometric relationships for some species of elasmobranch from tropical eastern Pacific

This study proposes length relationship equations to determine total length of four species of sharks (Carcharhinus falciformis, Mustelus lunulatus, Sphyrna lewini and Carcharhinus limbatus) based on trunk lengths (TrL) and interdorsal lengths (IL) caught in Colombia and Central America Pacific Ocean. In Central American Pacific, data were recorded for C. falciformis, C. limbatus and S. lewini between 2006 and 2012. In the Colombian Pacific, data was recorded in 1994–1995 and from 2006 to 2012 for C. falciformis, S. lewini and M. lunulatus. In the Central American Pacific the IL – TL relationship was acceptable for C. falciformis (r² = .69) and C. limbatus which presented a good relationship (r² = .81) where most specimens were juveniles; the same trend was found for S. lewini (r² = .96). The TL‐TrL relationship estimated for species caught in the Colombian Pacific was significant for C. falciformis (r² = .98) and for M. lunulatus (r² = .84); however, for S. lewini this relationship was low (r² = .55). Results indicate this is a useful tool for fishery statistics and fishery management for elasmobranch species of the Eastern Tropical Pacific.     

Validated age and growth of the leopard shark,Triakis semifasciata,with comments on reproduction

Synopsis The age, growth, and sexual maturation of the leopard shark, Triakis semifasciata, from central California were studied. Growth band counts in vertebral centra of 162 leopard sharks produced von Bertalanffy growth curves with L, K. and t_o parameters of 1536 mm. 0.082, and -2.31, respectively, for both sexes combined. The L₈ value for females (1602 mm TL) was slightly but insignificantly higher than for males (1499 mm TL), but the K and t_o values were almost identical. Seasonal changes in size modes of young-of-the-year leopard sharks, centrum edge characteristics, and growth and tetracycline mark-recapture from the field were used to validate annual deposition of vertebral centrum band pairs. Sexual maturity was evaluated by the gonads and presence of sperm and eggs; males mature at 7 yr and at about 63% of asymptotic length, and females mature at 10 yr, and at about 72% of asymptotic length. This slow growth, late maturity, and relatively low fecundity may increase their susceptibility to over-exploitation.     

Age and growth of ocellated icefish, Chionodraco rastrospinosus DeWitt and Hureau, 1979, from the South Shetland Islands

Age and growth of ocellated icefish, Chionodraco rastrospinosus, were investigated using counts of annual growth increments from sagittal otoliths. Samples were collected during research surveys by benthic trawl carried out around Elephant and South Shetland Islands in January–February 2002 and December 2006–January 2007. A total of 290 specimens were selected for the study, consisting of 120 females and 170 males. The age of fish was estimated by counting annuli on transverse sections obtained by grinding and polishing whole otoliths embedded in epoxy resin. The precision-of-age estimates within and between readers were tested applying both the average percent error (APE) and the coefficient of variation (CV). The estimated age-range was 1–12 for both sexes of C. rastrospinosus. Applying the von Bertalanffy growth function to the age–length data, a growth curve was obtained for each sex. The estimated values of VB growth parameters L _∞ and k were, respectively, 47.9 cm and 0.28 for females and 42.9 cm and 0.36 for males. Compared to other congeneric species, the growth performance of C. rastrospinosus was relatively high, being 2.82 and 2.81 in males and females, respectively. Age at sexual maturity was estimated to be about 4 years in both sexes. C. rastrospinosus captured in the studied area consisted mainly of adult specimens between 3 and 8 years, with few older fish.