Intraspecific variation in movement patterns: modeling individual behaviour in a large marine predator

By Deborah Austin, W. Bowen, J. McMillan. 2004

310 citations recorded by the source corpus.

Subfields: Ecology, Ecology, Evolution, Behavior and Systematics, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/98c169ae23c7c9b2d3eae5e2e67c18b3f99e15e7

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In Ecology

In Ecology, Evolution, Behavior and Systematics

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Citations in the corpus

Males in the shade: habitat use and sexual segregation in the Galápagos sea lion (Zalophus californianus wollebaeki) (2005, background): “Sexual segregation has been reported for both the marine (Stewart 1997; Thompson et al. 1998; Le Boeuf et al. 2000; Austin et al. 2004) and the terrestrial habitat (Bartholomew 1970; Kovacs et al. 1990).”
Should we consider individual behavior differences in applied wildlife conservation studies (2017, background): “…in movement pattern and capacity contributes to variability in conspecific and heterospecific interactions, resource use, and competition (Austin et al., 2004; Spiegel et al., 2015) and can influence gene flow, population dynamics, and the distribution and colonization potential of…”
State-space models of individual animal movement. (2008, methodology): “Such analyses have been used to identify modes of behaviour [27‐30], to support hypotheses about search behaviour [31‐33], or to classify individuals into subgroups based on their movements [34, 35 ].”
Corridors for Conservation: Integrating Pattern and Process (2006, background): “Even if real organisms usually violate some of the assumptions of general movement models (Bergman et al. 2000), CRWs can be useful null models for distinguishing different movement types (Austin et al. 2004) and identify opportunities for corridors.”
Behavioural drivers of the ecological roles and importance of marine mammals (2015, background): “…3 main movement types, differentiated by variation in home range size, travel speed and move length, have been observed in adult grey seals Halichoerus grypus (Austin et al. 2004) that would result in individual variation in the spatiotemporal pattern of their potential impacts to ecosystems.”
L\'evy walks (2014, background): “…al., 2014; Hays et al., 2006), dolphins (Bailey and Thompson, 2006), mussels (de Jager et al., 2011), cuttlefish, octopus, various rays, sole and anglerfish (Wearmouth et al., 2014), jelly fish (Hays et al., 2012), grey seals (Austin et al., 2004), and, finally, fishermen (Bertrand et al., 2007).”
A comparison of indirect measures of feeding behaviour based on ARGOS tracking data (2007, methodology): “FPT and fractal D methods also can be used to identify the location of ARS behaviour along a ARTICLE IN PRESS P.W. Robinson et al. / Deep-Sea Research II 54 (2007) 356–368366 track (Fauchald and Tveraa, 2003; Austin et al., 2004).”
Patch density determines movement patterns and foraging efficiency of large herbivores (2007, background): “This is mostly done within the realm of microorganisms, insects, birds, and small mammals (e.g., Kareiva and Shigesada 1983; Turchin 1991; Crist et al. 1992; Cole 1995; Viswanathan et al. 1996, 1999; Levandowsky et al. 1997; Atkinson et al. 2002; Bartumeus et al. 2003; Austin et al. 2004; Ramos-Fern”
Lévy trajectories of Peruvian purse-seiners as an indicator of the spatial distribution of anchovy ( Engraulis ringens ) (2005, background): “The Lévy flight type of spatial behaviour has been documented for a variety of foraging natural predators: Drosophila (Cole, 1995), albatross (Viswanathan et al., 1996), reindeer (Mårell et al., 2002), jackal (Atkinson et al., 2002), and seals (Austin et al., 2004).”
Turn designation, sampling rate and the misidentification of power laws in movement path data using maximum likelihood estimates (2011, methodology): “of the hypothesis (Atkinson et al. 2002 ;M arell et al.2002; Bartumeus et al. 2003; Austin et al. 2004; Boyer et al. 2004, 2006; Ramos-Fernandex et al. 2004 ;R eynolds et al. 2007 ;S ims et al.2008), and others criticising some of the methods employed in these (Sims et al. 2007; Edwards et al. 200”
Home range size of adult Indo-Pacific bottlenose dolphins (Tursiops aduncus) in a coastal and estuarine system is habitat and sex-specific (2016, background): “Home range size can be sex-specific for both marine (e.g., spottail shark, Carcharhinus sorrah, Knip et al. 2012; gray seal, Halichoerus grypus, Austin et al. 2004) and terrestrial species (e.g., chimpanzee, Pan troglodytes, Chapman and Wrangham 1993; grizzly bear, Ursus arctos horribilis, Mace and…”