E
E. J. Baxter
Researcher at University College Cork
Publications - 14
Citations - 477
E. J. Baxter is an academic researcher from University College Cork. The author has contributed to research in topics: Jellyfish & Aurelia aurita. The author has an hindex of 11, co-authored 14 publications receiving 397 citations. Previous affiliations of E. J. Baxter include Wildlife Trusts.
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Journal ArticleDOI
Gill disorders in marine-farmed salmon: investigating the role of hydrozoan jellyfish
TL;DR: A significant positive correlation between daily fish mortality and the abundance of these jellyfish but not with any other factors is revealed, which raises concerns for the expected growth of the industry, especially as jellyfish populations are predicted to increase in some areas.
Book ChapterDOI
Jellyfish as products and problems of aquaculture
TL;DR: This chapter begins by reviewing the fisheries and culture of jellyfish for human food, multi-million-dollar industries with markets currently centered in Asia, and presents guidelines for culture conditions and tank construction for display or study of 27 jellyfish species.
Journal ArticleDOI
Gill damage to Atlantic salmon (Salmo salar) caused by the common jellyfish (Aurelia aurita) under experimental challenge
E. J. Baxter,Michael M. Sturt,Neil M. Ruane,Thomas K. Doyle,Rob McAllen,Luke Harman,Hamish D. Rodger +6 more
TL;DR: The findings clearly demonstrate that A. aurita can cause severe gill problems in marine-farmed fish.
Journal ArticleDOI
Development of a novel histopathological gill scoring protocol for assessment of gill health during a longitudinal study in marine-farmed Atlantic salmon (Salmo salar)
TL;DR: Throughout the longitudinal study, the scoring system provided an accurate and effective means of assessing gill health, demonstrating the ability of this practical tool to be used in future studies of gills health and disease.
Journal ArticleDOI
Development of a quantitative real-time PCR for the detection of Tenacibaculum maritimum and its application to field samples.
TL;DR: The development and the application of a quantitative real-time PCR for the detection of Tenacibaculum maritimum DNA was described and was shown to be very sensitive, able to detect as little as 4.8 DNA copies number μL(-1) .