Effects of hypoxia on an estuarine predator-prey interaction : foraging behavior and mutual interference in the blue crab Callinectes sapidus and the infaunal clam prey Mya arenaria
By David L. Taylor, D. Eggleston. 2000
128 citations recorded by the source corpus.
Subfields: Ecology, Global and Planetary Change, Oceanography
View Paper: https://www.semanticscholar.org/paper/3329f7a9abd406b261261c98374806cf1ee8d6a0
How researchers see this paper
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In Ecology
In Global and Planetary Change
- J. Craig
- Jennifer E. Purcell
- Rochelle D. Seitz
- G. Bell
- A. Hines
- D. Eggleston
- W. Christopher Long
- M. B. Decker
In Oceanography
- J. Craig
- Jennifer E. Purcell
- Rochelle D. Seitz
- M. B. Decker
- G. Bell
- A. Hines
- D. Eggleston
- W. Christopher Long
Citations in the corpus
- Behavioral effects of low dissolved oxygen on the bivalve Macoma balthica (2008, background): “In laboratory experiments, hypoxia changed the predator-prey relationship, likely due to a change in both predator and prey behavior (Breitburg et al., 1994; Breitburg et al., 1997; Taylor and Eggleston, 2000; Sagasti et al., 2001; Seitz et al., 2003).”
- Broad-scale effects of hypoxia on benthic community structure in Chesapeake Bay, USA (2009, background): “Sessile organisms may stretch bodies or body extensions (e.g., bivalve siphons) into the water column in an attempt to reach higher oxygen levels farther up in the water column (Jørgensen, 1980; Taylor and Eggleston, 2000; Seitz et al., 2003).”
- Effects of hypoxia on predator-prey dynamics of the blue crab Callinectes sapidus and the Baltic clam Macoma balthica in Chesapeake Bay (2003, background): “Similar to the reduction in blue crab predation upon Macoma balthica under hypoxia in our experiment, Taylor & Eggleston (2000) reported lower consumption by blue crabs of M. arenaria despite the clams’ migration toward the sediment surface under hypoxia.”
- Effects of low dissolved oxygen on zooplankton predation by the ctenophore Mnemiopsis leidyi (2004, background): “…rates can be affected by hypoxia due to decreased foraging activity of predators (Bejda et al. 1987, Breitburg et al. 1994, Petersen & Pihl 1995, Taylor & Eggleston 2000) and changes in the behaviors of prey that make them more susceptible to predation (Poulin et al. 1987, Rahel & Kolar 1990,…”
- Species-specific avoidance responses by blue crabs and fish to chronic and episodic hypoxia (2005, background): “Clam and polychaete prey migrate vertically to the sediment surface during exposure to hypoxia (Diaz and Rosenberg 1995; Taylor and Eggleston 2000; Tallqvist 2001).”
- DENSITY‐DEPENDENT PREDATION, HABITAT VARIATION, AND THE PERSISTENCE OF MARINE BIVALVE PREY (2001, background): “Experimentally, if the ‘‘low density’’ range for a particular prey species is known, then the difference between a type II and type III FR can be determined from as few as two data points within that range (Taylor and Eggleston 2000).”
- Hypoxia-induced growth rate reduction in two juvenile estuary-dependent fishes (2004, background): “Most marine hypoxia investigations concentrate on infauna and benthic macrofauna (Dauer, et al., 1992; Pihl, et al., 1992; Rosenberg, et al., 1992; Pihl, 1994; Diaz and Rosenberg, 1995; Nestlerode and Diaz, 1998; Taylor and Eggleston, 2000).”
- Hypoxia-induced habitat shifts and energetic consequences in Atlantic croaker and brown shrimp on the Gulf of Mexico shelf (2005, background): “Indirect effects of hypoxia on trophic interactions can be positive or negative depending on trophic level and speciesspecific details of foraging and predation processes (e.g. Breitburg et al. 1999, Taylor & Eggleston 2000, Seitz et al. 2003).”