Impacts of ocean acidification on respiratory gas exchange and acid-base balance in a marine teleost, Opsanus beta.

Abstract

The oceanic carbonate system is changing rapidly due to rising atmospheric CO(2), with current levels expected to rise to between 750 and 1,000 μatm by 2100, and over 1,900 μatm by year 2300. The effects of elevated CO(2) on marine calcifying organisms have been extensively studied; however, effects of imminent CO(2) levels on teleost acid-base and respiratory physiology have yet to be examined. Examination of these physiological processes, using a paired experimental design, showed that 24 h exposure to 1,000 and 1,900 μatm CO(2) resulted in a characteristic compensated respiratory acidosis response in the gulf toadfish (Opsanus beta). Time course experiments showed the onset of acidosis occurred after 15 min of exposure to 1,900 and 1,000 μatm CO(2), with full compensation by 2 and 4 h, respectively. 1,900-μatm exposure also resulted in significantly increased intracellular white muscle pH after 24 h. No effect of 1,900 μatm was observed on branchial acid flux; however, exposure to hypercapnia and HCO(3)(-) free seawater compromised compensation. This suggests branchial HCO(3)(-) uptake rather than acid extrusion is part of the compensatory response to low-level hypercapnia. Exposure to 1,900 μatm resulted in downregulation in branchial carbonic anhydrase and slc4a2 expression, as well as decreased Na(+)/K(+) ATPase activity after 24 h of exposure. Infusion of bovine carbonic anhydrase had no effect on blood acid-base status during 1,900 μatm exposures, but eliminated the respiratory impacts of 1,000 μatm CO(2). The results of the current study clearly show that predicted near-future CO(2) levels impact respiratory gas transport and acid-base balance. While the full physiological impacts of increased blood HCO(3)(-) are not known, it seems likely that chronically elevated blood HCO(3)(-) levels could compromise several physiological systems and furthermore may explain recent reports of increased otolith growth during exposure to elevated CO(2).

• Authors: Andrew J Esbaugh, Rachael Heuer, Martin Grosell
• Journal: Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology (J Comp Physiol B) Vol. 182 Issue 7 Pg. 921-34 (Oct 2012) ISSN: 1432-136X [Electronic] Germany
• PMID: 22581071 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• Anion Transport Proteins
• Antiporters
• DNA Primers
• SLC4A Proteins
• Carbon Dioxide

Topics

• Acid-Base Equilibrium (drug effects, physiology)
• Acidosis (physiopathology, veterinary)
• Animals
• Anion Transport Proteins (metabolism)
• Antiporters (metabolism)
• Batrachoidiformes
• Carbon Dioxide (administration & dosage, metabolism, toxicity)
• Climate Change
• DNA Primers (genetics)
• Fish Diseases (physiopathology)
• Florida
• Hydrogen-Ion Concentration
• Hypercapnia (physiopathology, veterinary)
• Real-Time Polymerase Chain Reaction
• Respiratory Transport (drug effects, physiology)
• SLC4A Proteins
• Seawater (chemistry)