Aggregations of the jellyfish Aurelia labiata:abundance, distribution, association with age-0 walleye pollock, and behaviors promoting aggregation in Prince William Sound, Alaska, USA

By Jennifer E. Purcell, E. Brown, Kevin D. E. Stokesbury, L. Haldorson, T. C. Shirley. 2000

95 citations recorded by the source corpus.

Subfields: Molecular Biology, Oceanography, Paleontology

View Paper: https://www.semanticscholar.org/paper/ac18bb45bd64e7ac33a1cba97d04dfe8b7b3520e

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

1. J. Davenport
2. Michael N. Dawson
3. Jennifer E. Purcell
4. M. Arai

In Oceanography

1. Jennifer E. Purcell
2. Wen-Tseng Lo
3. Michael N. Dawson
4. M. Arai
5. Hao Chang
6. Wenchen Liu
7. Tom Doyle
8. G. Hays

In Paleontology

1. Jennifer E. Purcell
2. M. Arai
3. G. Hays
4. Tom Doyle
5. Michael N. Dawson
6. Wen-Tseng Lo
7. Hao Chang
8. Wenchen Liu

Citations in the corpus

• The broad-scale distribution of five jellyfish species across a temperate coastal environment (2007, methodology): “Hence other methods for extensive surveys are required, with for example, acoustic methods being developed recently (Brierley et al., 2005) and aerial surveys for large jellyfish been used by Purcell et al. (2000) and Houghton et al. (2006).”
• Interactions of pelagic cnidarians and ctenophores with fish: a review (2001, background): “For example, ROV observations show up to five age-0 walleye pollock swimming among tentacles of Cyanea capillata and up to 30 with Chrysaora melanaster Brandt at depths of 30– 40 m during the day in Alaskan waters (Brodeur, 1998).”
• Growth-related advantages for survival to the point of replenishment in the coral reef fish Stegastes partitus (Pomacentridae) (2002, unknown): “Many of the predators of larval fishes display seasonal blooms or cycles in abundance (Purcell 1985, Purcell et al. 2000).”
• Predation on zooplankton by large jellyfish, Aurelia labiata, Cyanea capillata and Aequorea aequorea, in Prince William Sound, Alaska (2003, methodology): “Aerial surveys of PWS showed that in 1998, a larger number of aggregations (770) of A. labiata was observed (Brown et al. 1999) than previously reported for 1995, 1996 or 1997 (94, 493 or 28, respectively; Purcell et al. 2000).”
• Geographic variation and ecological adaptation in Aurelia (Scyphozoa, Semaeostomeae): some implications from molecular phylogenetics (2001, background): “1982; Martin, 1999), although aggregations of jellyfish typically have been related to behavioral (Hamner & Hauri, 1981; Larson, 1992; Hamner et al., 1994; Purcell et al., 2000) and hydrographic effects (Hamner & Schneider, 1986; Larson, 1992; Purcell et al.”
• Effects of temperature and light intensity on asexual reproduction of the scyphozoan, Aurelia aurita (L.) in Taiwan (2008, background): “The blooms may be related to the combinations of several factors (Purcell et al., 2000), including climate change, especially warming (Uye & Ueta, 2004; Purcell, 2005; Attrill et al.”
• Extension of methods for jellyfish and ctenophore trophic ecology to large-scale research (2008, background): “The numbers of Aurelia labiata Chamisso and Eysenhardt aggregations showed great inter-annual variation in Prince William Sound, Alaska, where between 28 and 770 occurred in 1995–1998 (Purcell et al., 2000).”
• Prey selection and dietary overlap among zooplanktivorous jellyfish and juvenile fishes in Prince William Sound, Alaska (2001, background): “Similarly, in July 1996, A. labiata and herring were more abundant and pollock less abundant than in 1999, and 20 to 25% of seine sets that targeted on fish schools also contained jellyfish (Purcell et al. 2000).”