PREDATION STRUCTURES COMMUNITIES AT DEEP‐SEA HYDROTHERMAL VENTS

By Fiorenza Micheli, C. Peterson, L. Mullineaux, C. Fisher, S. Mills, G. Sancho, G. A. Johnson, H. Lenihan. 2002

167 citations recorded by the source corpus.

Subfields: Global and Planetary Change, Oceanography

View Paper: https://www.semanticscholar.org/paper/7316471faa25b8a221c9210458af72db9fd1d828

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In Global and Planetary Change

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2. S. Hourdez
3. Erik Cordes
4. J. Clements
5. P. Kelley
6. Joel W. Martin
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Citations in the corpus

• Using stable isotopes and quantitative community characteristics to determine a local hydrothermal vent food web (2007, background): “Vent production also can be transferred into the larger deep-sea food web via direct and indirect exploitation by benthic background fauna (Micheli et al. 2002) and exported in the vent plume (Burd & Thomson 1994, Mullineaux et al. 1995).”
• Are spatial variations in the diets of hydrothermal fauna linked to local environmental conditions (2009, background): “Nonendemic benthic background fauna take advantage of the enhanced productivity found near vents and contribute to the exportation of organic carbon in the surrounding deep-sea ecosystem (Micheli et al. 2002).”
• Predation in the marine fossil record: Studies, data, recognition, environmental factors, and behavior (2019, methodology): “…related to environmental energy also can affect the activities of predators, and environmental stress can reduce the abundance of predators (McClanahan, 1992); predator-prey interactions should be less important in structuring communities in physically stressful environments (Micheli et al., 2002).”
• Succession of hydrocarbon seep communities associated with the long-lived foundation species Lamellibrachia luymesi (2005, background): “…vents, community succession has been demonstrated on temporal scales of months to years (Shank et al. 1998) and is correlated to changes in chemistry, although biotic interactions have a significant influence on the progression of successional stages (Micheli et al. 2002, Mullineaux et al. 2003).”
• Decapod crustaceans from hydrothermal vents and cold seeps: a review through 2005 (2005, background): “Gorodezky & Childress, 1994); indeed, they are probably top predators at vent sites (see Jollivet, 1993; Voight, 2000; Micheli et al., 2002).”
• A comparison of statistical approaches to analyzing community convergence between natural and constructed oyster reefs (2006, methodology): “AlthoughMANOVA has been used extensively to analyze differences in community compositions (e.g., Menge et al., 1997; Hillebrand et al., 2000; Navarrete et al., 2000; Forbes and Chase, 2002; Micheli et al., 2002; Hoeinghaus et al., 2003; Allison, 2004), the approach is controversial (Legendre and And”
• Ecological role of large benthic decapods in marine ecosystems: a review (2012, background): “Predation generally plays a strong role in structuring marine benthic communities (Shurin et al. 2002), ranging from intertidal shores (e.g. Paine 1994) to the deep sea (e.g. Micheli et al. 2002), but few experimental studies have focused on large decapods.”