The determinants of sexual segregation in the scalloped hammerhead shark,Sphyrna lewini
By A. P. Klimley. Environmental Biology of Fishes, 2004
297 citations recorded by the source corpus.
Subfields: Global and Planetary Change, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/06bc92fdf98656ccbfebca7675856b162618dfed
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In Global and Planetary Change
- Darren P. Croft
- D. Jacoby
- Barbara V. Hight
- D. W. Sims
- A. Marshall
- C. Dudgeon
- H. L. Pratt
- Christopher G. Lowe
In Nature and Landscape Conservation
Citations in the corpus
- Social behaviour in sharks and rays: analysis, patterns and implications for conservation (2012, background): “Therefore, it is perhaps unsurprising that sexual segregation is relatively common among elasmobranchs (Ford 1921; Klimley 1987; Sims et al. 2001; Litvinov 2006; Mucientes et al. 2009).”
- Size and structure of a photographically identified population of manta rays Manta alfredi in southern Mozambique (2011, background): “Sexual biases occur at the population level in many species of elasmobranches in space and time (Springer 1967; Klimley 1987; Anderson and Pyle 2003).”
- Environmental variables affecting the sexual segregation of great white sharks Carcharodon carcharias at the Neptune Islands South Australia (2007, background): “Available at http://www.marine.csiro.au/;lband/web_point/ # 2007 The Author Journal compilation # 2007 The Fisheries Society of the British Isles, Journal of Fish Biology 2007, 70, 1350–1364”
- Inter-island movements of scalloped hammerhead sharks (Sphyrna lewini) and seasonal connectivity in a marine protected area of the eastern tropical Pacific (2014, background): “…near Wolf, Darwin, and roca redonda, most likely offshore, considering that the most important prey items of hammerheads are oceanic cephalopods in ecuadorian Mar Biol 1 3 waters (Castañeda-Suárez and Sandoval-londoño 2007) and mesopelagic cephalopods in the gulf of California (Klimley 1987).”
- Advances in the Study of Feeding Behaviors, Mechanisms, and Mechanics of Sharks (2001, background): “Females therefore grow to reproductive size more rapidly than males (reviewed by Klimley 1987).”
- Analysis of whale shark Rhincondon typus aggregations near South Ari Atoll, Maldives Archipelago (2010, background): “Age or sexual segregation has been reported in basking sharks Cetorhinus maximus, another large planktivorous shark, and is widespread in Selachimorphs (e.g. Klimley 1987, Bres 1993, Robbins 2007).”
- Behavioural response of sicklefin lemon sharks Negaprion acutidens to underwater feeding for ecotourism purposes (2010, unknown): “This spatial and temporal sexual segregation is commonly encountered in carcharhinids (Klimley 1987, Economakis & Lobel 1998) and other shark families (Bansemer & Bennett 2008, Mucientes et al. 2009).”
- Abundance and demography of a seasonal aggregation of zebra sharks Stegostoma fasciatum (2008, background): “Furthermore, sex and size segregation in aggregations are common, and have been found to be correlated with reproductive strategy (Klimley 1987, Economakis & Lobel 1998, Sims et al. 2001, Hight & Lowe 2007).”
- A Review of Elasmobranch Reproductive Behavior with a Case Study on the Nurse Shark, Ginglymostoma Cirratum (2001, background): “The discovery of large groupings of scalloped hammerheads, Sphyrna lewini(Klimley 1987), dominance hierarchies in sand tigers, Carcharias taurus (Gordon 1993) and bonnetheads, S.”
- Assessing the size, growth rate and structure of a seasonal population of whale sharks (Rhincodon typus Smith 1828) using conventional tagging and photo identification (2007, unknown): “Itispossiblethatfemales feed on more pelagic prey, to grow faster and reach a larger size at maturity, similar to scalloped hammerheads near the El Bajo Espiritu Santo seamount in Baja California (Klimley, 1987).”
- Reproduction, abundance and feeding habits of the broadnose sevengill shark Notorynchus cepedianus in north Patagonia, Argentina (2005, background): “Also, the highly female-biased sex ratio of juveniles suggests that juvenile females might use Anegada Bay as a rich foraging area allowing them to increase their growth rate, and then acquire a larger size at maturity (Klimley 1987).”
- Elevated body temperatures of adult female leopard sharks, Triakis semifasciata, while aggregating in shallow nearshore embayments: Evidence for behavioral thermoregulation? (2007, background): “Sexual segregation is common in elasmobranchs, in which females are typically found at shallower depths than males (Klimely 1987; Wetherbee et al., 1997).”