Abstract

Anti-parasitic drugs used in the aquaculture industry are discharged to the sea after treatment of salmon. In this study, the effects of azamethiphos (AZA) in the Salmosan® formulation and deltamethrin (DEL) in the Alpha Max® formulation, have been assessed in Northern shrimp larvae (Pandalus borealis) when administered both separately and in combination. The exposure concentrations were 100 ng/L for AZA and 2 ng/L for DEL, each representing a 1000-fold dilution of the prescribed concentrations for salmon. These two chemicals were combined at these concentrations to give a third treatment (AZA + DEL). When larvae were exposed for two hours on the first, second and third days post hatch (dph), significantly increased mortality and reduced swimming activity were observed for larvae from the DEL and combined AZA + DEL treatments 4 dph, though not in larvae from the AZA treatment. A single pulse exposure, delivered on the first day post hatch, caused similar effects on mortality and swimming activity 4 dph as the three-pulse exposure. Mortality was driven by the presence of DEL in both experiments, with no amplification or reduction of effects observed when DEL and AZA were combined. Larvae were observed for 13 days following the single pulse exposure, with food limitation introduced as an additional stressor on day 4. In the DEL and AZA + DEL treatments mortality continued to increase regardless of food level, with no larvae completing development to stage II. The overriding toxicity of DEL masked any potential effects the reduced food ration may have exerted. Swimming activity was lower for AZA treated larvae than Control larvae 13 dph, when both groups were fed daily, though no other significant changes to mortality, development to stage II, feeding rate or gene expression were observed. Food limited Control and AZA larvae had lower swimming activity and feeding rate than daily fed Control larvae, with expression of pyruvate kinase and myosin genes also downregulated. However, there was no negative effect on survival or successful development to stage II in these treatments. In addition, mesencephalic astrocyte-derived neurotropic factor was downregulated in food limited Control larvae when compared with the daily fed Controls.Results from this study together with reported estimates of dispersion plume concentrations of discharged pesticides indicate that toxic concentrations of deltamethrin could reach shrimp larvae several kilometers from a treated salmon farm.

Highlights

  • Chemicals are used to treat farmed salmon against the crustacean ectoparasitic salmon louse (Lepeophtheirus salmonis)

  • Four replicate aquaria were used in the Control, AZA, DEL and AZA + DEL treatment

  • Six replicate aquaria were used in the Control, AZA, DEL and AZA + DEL treatment

Read more

Summary

Introduction

Chemicals are used to treat farmed salmon against the crustacean ectoparasitic salmon louse (Lepeophtheirus salmonis). Data are available regarding the toxicity of AZA and DEL to non-target species when exposed to a single compound (Burridge et al, 2014; Burridge and Van Geest, 2014; Urbina et al, 2019) These studies provide estimates of lethal thresholds and show, not surprisingly, that exposures of short duration require higher concentrations of the chemicals to produce the same level of toxicity. Burridge et al (2014) showed that the American lobster was more sensitive to DEL than the shrimp species tested by Brokke (2015), but all three species were far less sensitive to AZA than to DEL under the same exposure scenario These studies show that there are interspecies differences in sensitivity, and it is important to study other relevant non-target crustaceans, and life-stages, to determine their sensitivity to AZA and DEL separately and in combination. Northern shrimp is a keystone species in the marine ecosystem and an important commercial crustacean species (Bergström, 2000), with high sensitivity to anti-parasitic chemicals used in salmon farms (Bechmann et al, 2017, 2018, 2019)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call