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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd
    Journal of fish biology 67 (2005), S. 0 
    ISSN: 1095-8649
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Age and growth rates of bull shark Carcharhinus leucas[n = 255; 555–2230 mm fork length (LF)] from the northern Gulf of Mexico were estimated from ring counts on vertebral sections collected from fishery-dependent and -independent surveys. Two growth models were fitted to observed data: the von Bertalanffy growth model (VBGM) with t0 as the third parameter and a modified version of the VBGM using a fixed size-at-birth intercept as the third parameter. To address the variability in size-at-birth, a Monte Carlo simulation was incorporated into the size-at-birth intercept. The sex-specific growth models were not significantly different, allowing a sexes combined model to be generated. The traditional VBGM predicted a theoretical maximum size (L∞) of 3007·1 mm LF, a growth coefficient (K) of 0·042 year−1 and a theoretical age at zero length (t0) of –6·844 years. The modified VBGM with a fixed size-at-birth intercept of 565 mm LF predicted an L∞ of 2289·2 mm LF and a K value of 0·089 year−1. When comparing model estimates to previously published information, the traditional VBGM predicted a significantly lower theoretical maximum size and a higher growth coefficient than those produced using data collected during the 1980s. Overall, results obtained using the VBGM with a fixed size-at-birth produced more biologically realistic parameters than that of the VBGM with t0. The Monte-Carlo simulation incorporating variability in size-at-birth produced similar results to the VBGM using a fixed size-at-birth. This study provides the first attempt to incorporate variability at size-at-birth and provide measurements of variability around the individual parameter estimates for an elasmobranch.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK; Malden, USA : Blackwell Science Ltd
    Journal of fish biology 64 (2004), S. 0 
    ISSN: 1095-8649
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: The reproductive biology of blacknose sharks Carcharhinus acronotus in the western North Atlantic Ocean was studied by examining specimens collected in the coastal waters of South Carolina. Males begin the maturation process between 875 and 910 mm fork length (LF), as indicated by the presence of functional claspers and siphon sacs. The presence of vitellogenic oocytes and developing oviducal glands and uteri indicated that females begin to mature at c. 870 mm LF. Length at which 50% of the population reached maturity was 896 and 964 mm LF, equivalent to 4·3 and 4·5 years, for males and females, respectively. Gonado-somatic indices suggested that spermatogenesis and vitellogenesis began after December. Mating took place during the end of May and the beginning of June. Fertilization occurred during late June and early July, suggesting that female blacknose sharks were capable of sperm storage. Based on the timing of fertilization and occurrence of females carrying near-term pups in late May and early June, the gestation period for blacknose sharks was c. 11 months. Female blacknose sharks reproduced biennially based on the absence of vitellogenic oocytes in near-term females and there being no indication of vitellogenesis in postpartum females. Male blacknose sharks were capable of reproducing annually as indicated by turgid genital ducts, which were observed in all mature males collected during late May and early June.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of fish biology 55 (1999), S. 0 
    ISSN: 1095-8649
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Routine oxygen consumption rates of bonnethead sharks, Sphyrna tiburo, increased from 141·3±29·7 mg O2 kg−1 h−1 during autumn to 218·6±64·2 mg O2 kg−1 h−1 during spring, and 329·7±38·3 mg O2 kg−1 h−1 during summer. The rate of routine oxygen consumption increased over the entire seasonal temperature range (20–30° C) at a Q10=2·34.
    Type of Medium: Electronic Resource
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