Seabird foraging behaviour indicates prey type
By K. Elliott, Kerry J. Woo, A. J. Gaston, S. Benvenuti, L. Dall'Antonia, G. Davoren. 2008
140 citations recorded by the source corpus.
Subfields: Ecology, Global and Planetary Change
View Paper: https://www.semanticscholar.org/paper/2a4005890e5c1679ddbe530cf60db2aaf39dcedd
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In Ecology
In Global and Planetary Change
Citations in the corpus
- Sexual segregation in a wide-ranging marine predator is a consequence of habitat selection (2015, background): “In particular, 342 when large aggregations of gannets form during feeding events, prey may descend to deeper 343 depths to escape predation forcing gannets to dive deeper as a result (Elliott et al. 2008, 344 Capuska et al. 2011).”
- Central-Place Foraging in an Arctic Seabird Provides Evidence for Storer-Ashmole's Halo (2009, methodology): “…TDRs) affect murre provisioning rates, trip duration, mass loss, dive depth, and time allocation during diving (Hamel et al. 2004; Paredes et al. 2004; Elliott et al. 2007, 2008a), our smaller, leg-mounted Lotek TDRs had no measurable effect on any of these parameters (Elliott et al. 2007, 2008d).”
- Prey preferences among the community of deep-diving odontocetes from the Bay of Biscay, Northeast Atlantic (2011, unknown): “As seabirds which exhibit different dive behaviors according to whether the prey was a fish, a squid or a crustacean (Elliott et al., 2008), these difference in prey types imply probably different diving strategies among these predators.”
- Confusion reigns? A review of marine megafauna interactions with tidal-stream environments (2015, background): “However, there are also distinct dietary variations at species-level, even within geographically similar areas, both between individuals (Elliott et al. 2008) and for the same individuals over time (Grémillet et al. 1998).”