Food and feeding of Aurelia aurita in Tokyo Bay with an analysis of stomach contents and a measurement of digestion times

By Haruto Ishii, F. Tanaka. Hydrobiologia, 2001

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Citations in the corpus

Effects of low dissolved oxygen on planula settlement, polyp growth and asexual reproduction of Aurelia aurita (2008, background): “The scyphozoan jellyfish Aurelia aurita (L., 1758) is found in many coastal waters (e.g. Möller 1980), and is a dominant predator in Tokyo Bay (Ishii & Tanaka 2001).”
Predation on zooplankton by large jellyfish, Aurelia labiata, Cyanea capillata and Aequorea aequorea, in Prince William Sound, Alaska (2003, background): “…aequorea are similar to diets previously reported for A. aurita, C. capillata and A. victoria, respectively, which contained a variety of holo- and merozooplankton (Fancett 1988, Brewer 1989, Purcell 1989, Sullivan et al. 1994, Behrends & Schneider 1995, Graham & Kroutil 2001, Ishii & Tanaka 2001).”
Who is eating whom? Morphology and feeding type determine the size relation between planktonic predators and their ideal prey (2012, background): “…(1985), Brachionus plicatilis from Hansen & Hansen (1997), Aurelia aurita and Cyanea capillata from Martinussen & Båmstedt (1999), Stoecker et al. (1987), Ishii & Tanaka (2001), Olesen (1995), and Barz & Hirche (2005), and Doliolum denticulatum and Penilia avirostris from Katechakis et al. (2004).”
Clearance rates of jellyfish and their potential predation impact on zooplankton and fish larvae in a neritic ecosystem (Limfjorden, Denmark) (2005, methodology): “…temperature and digestion time in Aurelia aurita, values of digestion time reported in the literature were plotted against temperature (Matsakis & Conover 1991, Sullivan et al. 1994, Martinussen & Båmstedt 1999, 2001, Båmstedt & Martinussen 2000, Dawson & Martin 2001, Ishii & Tanaka 2001) (Fig.”
Pelagic coelenterates and eutrophication: a review (2001, unknown): “Aurelia aurita preferentially decreases the abundance of A. omorii rather than the smaller O. davisae in Tokyo Bay (Omori et al., 1995), although A. aurita can also utilize O. davisae (Ishii & Tanaka, 2001).”
Geographic variation and ecological adaptation in Aurelia (Scyphozoa, Semaeostomeae): some implications from molecular phylogenetics (2001, background): “Moreover, the benthic scyphistomae can reproduce asexually in more than half-a-dozen ways (Arai, 1997; Lucas, 2001; Watanabe & Ishii, 2001), allowing a population to persist and propagate even if environmental conditions do not foster sexual reproduction (via medusae) for one or more years.”
Extension of methods for jellyfish and ctenophore trophic ecology to large-scale research (2008, background): “Rapid digestion at warm temperatures may have been exacerbated by small prey sizes at those locations (Dawson & Martin, 2001; Ishii & Tanaka, 2001; Uye & Shimauchi, 2005; Lo & Chen, 2008).”
Population biomass, feeding, respiration and growth rates, and carbon budget of the scyphomedusa Aurelia aurita in the Inland Sea of Japan (2005, unknown): “Ishii and Tanaka (Ishii and Tanaka, 2001) employed the same method to estimate in situ feeding rates of A. aurita in Tokyo Bay, where small copepods such as O. davisae dominated.”