COMPARATIVE DIVING PATTERNS OF PINNIPEDS AND SEABIRDS
By J. F. Schreer, Kit M. Kovacs, R. Hines. 2001
185 citations recorded by the source corpus.
Subfields: Ecology, Global and Planetary Change, Nature and Landscape Conservation
View Paper: https://www.semanticscholar.org/paper/81bc89b3d7a01c8e544b4f8411b0d59fb0b6fac5
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In Ecology
- C. Guinet
- K. Elliott
- A. J. Gaston
- Mark A. Hindell
- L. Dall'Antonia
- S. Benvenuti
- Kerry J. Woo
- G. Davoren
In Global and Planetary Change
- K. Elliott
- A. J. Gaston
- G. Davoren
- L. Dall'Antonia
- S. Benvenuti
- Kerry J. Woo
- C. Guinet
- T. Doniol‐Valcroze
In Nature and Landscape Conservation
Citations in the corpus
- Satellite telemetry of marine megavertebrates: the coming of age of an experimental science (2009, methodology): “Thus, we refer the readers to other recent reviews of bio-logging and marine wildlife tracking (Schreer et al. 2001, RopertCoudert & Wilson 2005, Wilson & McMahon 2006, Hooker et al. 2007).”
- In-depth studies of Magellanic penguin (Spheniscus magellanicus) foraging: can we estimate prey consumption by perturbations in the dive profile? (2003, background): “…over time is now commonly recorded by devices deployed on marine endotherms and used to classify dive types (usually V, U and W types) and, through these types, derive the proportion of searching and foraging dives (e.g. Wilson and Wilson 1990; LunaJorquera and Culik 1999; Schreer et al. 2001).”
- Fine-scale three-dimensional spatial use by diving, lactating female Weddell seals Leptonychotes weddellii (2002, background): “The variables were chosen to discriminate between directional (as opposed to ‘looping’) dives, benthic and mid-water dives, sit-and-wait and continuous search dives and dives with many changes in direction (Simpkins et al. 2001).”
- Seabird foraging behaviour indicates prey type (2008, methodology): “…avoidance (Schreer et al. 2001), travel in pinnipeds (Schreer et al. 2001) and penguins (Chappell et al. 1993, Wilson et al. 1996, Kirkwood & Robertson 1998), or exploration in pinnipeds (Schreer et al. 2001) and penguins (Kirkwood & Robertson 1998, RopertCoudert et al. 2002, Lescroël & Bost 2005).”
- Mesoscale eddies as foraging area of a deep-diving predator, the southern elephant seal (2010, background): “On any dive, a seal was assumed to be at the bottom of the dive whenever depth exceeded 80% of the maximum depth (Lesage et al. 1999, Schreer et al. 2001).”
- Southern elephant seals from Kerguelen Islands confronted by Antarctic Sea ice. Changes in movements and in diving behaviour (2007, methodology): “A dive’s bottom phase defined as the time spent at depths greater than or equal to 80% of the maximum depth was used to complete the analysis (Lesage et al., 1999; Schreer et al., 2001).”
- Optimal foraging theory predicts diving and feeding strategies of the largest marine predator (2011, background): “Previous studies of rorquals and other pelagic feeders have reliedmostly on visual examination of time-depth profiles for the detection of feeding events, usually identified by the occurrence of vertical excursions greater than an arbitrary threshold, called ‘‘wiggles’’ (Croll et al. 2001; Schreer e”
- Identifying foraging events in deep diving southern elephant seals, Mirounga leonina, using acceleration data loggers (2013, background): “In most species of pinnipeds and diving seabirds, dives with long bottom durations are thought to be associated with feeding (Schreer et al., 2001).”