Effects of the sea lice bath treatment pharmaceuticals hydrogen peroxide, azamethiphos and deltamethrin on egg-carrying shrimp (Pandalus borealis)

This study investigated effects of sea lice pharmaceuticals on egg-bearing deep-water shrimp (Pandalus borealis). Both mortality and sub-lethal effects (behavior, embryo development, and reproductive output) were studied for each of three pharmaceuticals alone and in different sequential combination...

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Bibliographic Details
Published in:Marine Environmental Research
Main Authors: Frantzen, Marianne, Bytingsvik, Jenny, Tassara, Luca, Reinardy, Helena C, Refseth, Gro Harlaug, Watts, Ellie J, Evenset, Anita
Format: Article in Journal/Newspaper
Language:English
Published: 2020
Subjects:
Online Access:https://pure.uhi.ac.uk/en/publications/b89d20ce-2b1f-4e61-933f-43fafa026b46
https://doi.org/10.1016/j.marenvres.2020.105007
https://pureadmin.uhi.ac.uk/ws/files/14429951/Frantzen_et_al_2020_preproof.pdf
https://www.sciencedirect.com/science/article/pii/S0141113619306543?via%3Dihub
Description
Summary:This study investigated effects of sea lice pharmaceuticals on egg-bearing deep-water shrimp (Pandalus borealis). Both mortality and sub-lethal effects (behavior, embryo development, and reproductive output) were studied for each of three pharmaceuticals alone and in different sequential combinations. The most severe effect was observed for deltamethrin where 2 h exposure to 330 times diluted treatment dose (alone and in sequential application with hydrogen peroxide and azamethiphos) induced almost 100% mortality within a few days after exposure. Similar effects were not observed for hydrogen peroxide or azamethiphos. However, sequential treatment of hydrogen peroxide and azamethiphos (2 h exposure to each pharmaceutical; 500 times dilution) resulted in >40% mortality during the first week following treatment. No sub-lethal effects or loss of eggs in female shrimp could be related to exposure to the bath treatments. Future studies should investigate potential sub-lethal effects at exposure concentrations close to the no-effect concentration.