Bioenergetics of free-ranging juvenile scalloped hammerhead sharks (Sphyrna lewini) in Kāne'ohe Bay, Ō'ahu, HI
By Christopher G. Lowe. 2002
141 citations recorded by the source corpus.
View Paper: https://www.semanticscholar.org/paper/f9788c52580a2aa870dffebf1f3757680f22c59d
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- Emily L C Shepard
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- Y. Papastamatiou
- Jeremy J. Vaudo
- Christopher G. Lowe
- Y. Watanabe
Citations in the corpus
- Habitat use, growth rates and dispersal patterns of juvenile scalloped hammerhead sharks Sphyrna lewini in a nursery habitat (2006, background): “…without written consent of the publisher Mar Ecol Prog Ser 312: 211–221, 2006 ous studies have focused on (1) the physiology and behavior of S. lewini within the bay (Lowe 2001, 2002, Holland et al. 1993), (2) the population dynamics of the bay’s juvenile hammerhead population (Clarke 1971, Bush &…”
- Movement patterns of the round stingray Urobatis halleri(Cooper) near a thermal outfall (2006, background): “Juvenile scalloped hammerhead sharks and Hawaiian stingrays Dasyatis lata (Garman) in Kaneohe Bay both showed increased rates of movement during the summer when water temperatures were elevated (Lowe, 2002; Cartamil et al., 2003).”
- Nursery habitat use and foraging ecology of the brown stingray Dasyatis lata determined from stomach contents, bulk and amino acid stable isotopes (2011, unknown): “Future studies fo - cusing on the growth rates and energetics of brown stingrays would provide further insight into their role in ecosystem energy flow and their effect on prey populations (e.g. Lowe 2002).”
- Geographic and ontogenetic variation in the diet and daily ration of the bonnethead shark, Sphyrna tiburo, from the eastern Gulf of Mexico (2007, methodology): “Quantitative diet analysis, and its use in bioenergetic models, has become important to shark population and ecosystem modeling (See e.g., Kitchell et al. 2002; Lowe 2002; Schindler et al. 2002; Carlson 2007; Neer et al. 2007).”
- Diel movement patterns of the Hawaiian stingray, Dasyatis lata: implications for ecological interactions between sympatric elasmobranch species (2003, methodology): “lewini (Lowe 2002) were merged in ArcView to yield a combined activity space for all sharks.”
- Use of an acceleration data logger to measure diel activity patterns in captive whitetip reef sharks, Triaenodon obesus (2007, methodology): “…peduncle and a higher sampling rate may be required to detect more subtle changes in activity in constantly swimming species (Lowe et al. 1998; Lowe 2002), or to quantify specific behaviors that are difficult to observe directly in elasmobranchs (e.g. feeding, agonistic interactions,…”
- The slowest fish: Swim speed and tail-beat frequency of Greenland sharks (2012, background): “, 2007), or magnetic sensors (Lowe, 2002) attached to fish, (2) remote monitoring with echosounders (Handegard et al.”
- Making overall dynamic body acceleration work: on the theory of acceleration as a proxy for energy expenditure (2011, background): “Thus, quantification of energy expenditure is key to understanding issues such as life history (Hall, McConnell & Barker 2001), trophic flow (Lowe 2002), biogeography (McNab 2002) and behavioural strategies (Hinch & Rand 1998).”
- Communal or competitive? Stable isotope analysis provides evidence of resource partitioning within a communal shark nursery (2011, background): “Evidence of slow growth rates (Bush & Holland 2002, Lowe 2002, Duncan & Holland 2006) and high mortality rates of young sharks in nursery areas has been attributed in part to a lack of sufficient food resources (Manire & Gruber 1993, Duncan & Holland 2006).”