The role of ionotropic receptors in behavioural alterations at elevated CO2 in a cephalopod


SOCIETY FOR INTEGRATIVE AND COMPARATIVE BIOLOGY
2021 VIRTUAL ANNUAL MEETING (VAM)
January 3 – Febuary 28, 2021

Meeting Abstract


21-3  Sat Jan 2  The role of ionotropic receptors in behavioural alterations at elevated CO2 in a cephalopod Thomas, JT*; Spady, BL; Munday, PL; Watson, S-A; James Cook University, Townsville, Queensland, Australia; James Cook University, Townsville, Queensland, Australia; James Cook University, Townsville, Queensland, Australia; Museum of Tropical Queensland, Townsville, Australia jodi.thomas@my.jcu.edu.au https://www.coralcoe.org.au/person/jodi-thomas

Projected future CO2 levels in the ocean can alter the behaviour of marine animals. Disrupted functioning of the γ-aminobutyric acid type A (GABAA) receptor is suggested to underlie CO2-induced behavioural changes in fish, however, the mechanisms underlying behavioural changes of marine invertebrates at elevated CO2 levels are not well understood. We exposed two-toned pygmy squid Idiosepius pygmaeus to ambient (~450 µatm) or elevated (~1,000 µatm) CO2 levels for seven days. Squid were treated with sham, gabazine (GABAA receptor antagonist) or picrotoxin (chloride (Cl) channel blocker) immediately before measurement of conspecific-directed behaviours and activity levels upon mirror exposure. If disrupted function of GABAA-like and/or other Cl channel receptors underlies the behavioural changes, we predicted that gabazine and picrotoxin would attenuate the behavioural changes at elevated CO2. Elevated CO2 increased squid activity levels and altered some, but had no meaningful effect on other, conspecific-directed behaviours. Gabazine and picrotoxin attenuated some of the behavioural changes at elevated CO2, indicating altered GABAA-like and Cl channel receptor functioning may underlie these behavioural changes. However, gabazine and picrotoxin had the same effect at both CO2 levels on other behavioural traits, suggesting altered function of GABAA-like and Cl channel receptors was not responsible for other behavioural changes at elevated CO2. Our results suggest multiple mechanisms may be involved, which could explain variability in the effects of CO2 and drug treatment across behaviours.

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