scholarly journals Habitat use, residency, and seasonal distribution of female leopard sharks Triakis semifasciata in Elkhorn Slough, California

2009 ◽  
Vol 380 ◽  
pp. 213-228 ◽  
Author(s):  
AB Carlisle ◽  
RM Starr
Keyword(s):  
Habitat Use ◽  
Seasonal Distribution ◽  
Elkhorn Slough ◽  
Triakis Semifasciata ◽  
Leopard Sharks

Reproduction, diet and habitat use of leopard sharks, Triakis semifasciata (Girard), in Humboldt Bay, California, USA

2005 ◽  
Vol 56 (8) ◽  
pp. 1089 ◽  
Author(s):  
David A. Ebert ◽  
Thomas B. Ebert
Keyword(s):  
Habitat Use ◽  
Sexual Segregation ◽  
Minor Importance ◽  
Nursery Ground ◽  
Relative Importance ◽  
Fish Eggs ◽  
Index Of Relative Importance ◽  
Diet Analyses ◽  
Triakis Semifasciata ◽  
Leopard Sharks

A total of 312 female leopard sharks (Triakis semifasciata) was sampled in Humboldt Bay, California, USA, an important nursery ground for this species, during the spring month of May from 1983 to 1984 and 1985. Sexual segregation is strong as only three males were observed in the study area. Females ranged in size from 120 to 154 cm total length, and all examined were determined to be mature. Overall, 130 out of 153 females examined in early May contained term embryos. The number of embryos per female ranged from 1 to 37 with larger females tending to possess more embryos. Of the 159 individuals examined in late May, no females were found carrying embryos and most were ovulating. Diet analyses revealed that, overall, fish eggs (Atherinopsis californiensis) at 48.0%, had the highest percentage Index of Relative Importance (%IRI), followed by the cancrid crabs, Cancer antennarius (29.8%) and C. magister (11.6%). All other prey were of relatively minor importance, cumulatively representing 10.6% of the overall diet. Adults shift their diet after parturition: early May sharks fed almost exclusively on fish eggs, while crabs were more important in those examined in late May.

Tissue-specific isotope trophic discrimination factors and turnover rates in a marine elasmobranch: empirical and modeling results

2012 ◽  
Vol 69 (3) ◽  
pp. 551-564 ◽  
Author(s):  
Luis Malpica-Cruz ◽  
Sharon Z. Herzka ◽  
Oscar Sosa-Nishizaki ◽  
Juan Pablo Lazo
Keyword(s):  
Natural Populations ◽  
Nitrogen Isotope ◽  
Cartilage Tissue ◽  
Turnover Rates ◽  
Isotopic Equilibrium ◽  
Isotope Turnover ◽  
Discrimination Factors ◽  
Triakis Semifasciata ◽  
Leopard Sharks ◽  
Trophic Discrimination

There are very few studies reporting isotopic trophic discrimination factors and turnover rates for marine elasmobranchs. A controlled laboratory experiment was conducted to estimate carbon and nitrogen isotope trophic discrimination factors and isotope turnover rates for blood, liver, muscle, cartilage tissue, and fin samples of neonate to young-of-the-year leopard sharks ( Triakis semifasciata ). Trophic discrimination factors varied (0.13‰–1.98‰ for δ13C and 1.08‰–1.76‰ for δ15N). Tissues reached or were close to isotopic equilibrium to the new diet after about a threefold biomass gain and 192 days. Liver and blood exhibited faster isotope turnover than muscle, cartilage tissue, and fin samples, and carbon isotopes turned over faster than those of nitrogen. Metabolic turnover contributed substantially to isotopic turnover, which differs from most reports for young marine teleosts. We modeled the relationship between muscle turnover rates and shark size by coupling laboratory results with growth rate estimates for natural populations. Model predictions for small, medium, and large wild leopard sharks indicate the time to isotopic equilibrium is from one to several years.

Demography of the central california population of the Leopard Shark (Triakis semifasciata)

1992 ◽  
Vol 43 (1) ◽  
pp. 183 ◽  
Author(s):  
GM Cailliet
Keyword(s):  
Population Growth ◽  
Reproductive Rate ◽  
Shark Species ◽  
Sandbar Shark ◽  
Lemon Shark ◽  
Carcharhinus Plumbeus ◽  
Net Reproductive Rate ◽  
Leopard Shark ◽  
Triakis Semifasciata ◽  
Leopard Sharks

Demographic analyses can be quite useful for effectively managing elasmobranch fisheries. However, they require valid estimates of age-specific mortality and natality rates, in addition to information on the distribution, abundance, habits and reproduction of the population, to produce reliable estimates of population growth. Because such detailed ecological information is usually unavailable, complete demographic analyses have been completed for only four shark species: the spiny dogfish, Squalus acanthias; the soupfin shark, Galeorhinus australis; the lemon shark, Negaprion brevirostris; and most recently the sandbar shark, Carcharhinus plumbeus. In California, reliable estimates of age, growth, mortality, age at maturity, and fecundity are available only for the leopard shark, Triakis semifasciata. A demographic analysis of this species yielded a net reproductive rate (Ro) of 4.467, a generation time (G) of 22.35 years, and an estimate of the instantaneous population growth coefficient (r) of 0.067. If the mean fishing pressure over 10 years (F= 0.084) is included in the survivorship function, Ro and r are reduced considerably, especially if leopard sharks first enter the fishery at early ages. A size limit of 120 cm TL (estimated age 13 years), especially for female sharks, is tentatively proposed for the leopard shark fishery.

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