4.7 Article

Membrane lipid sensitivity to ocean warming and acidification poses a severe threat to Arctic pteropods

Journal

FRONTIERS IN MARINE SCIENCE
Volume 9, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmars.2022.920163

Keywords

ocean warming; ocean acidification; arctic; pteropods; lipids

Funding

  1. German Federal Ministry of Education and Research (BMBF)
  2. [FKZ 03F06550]

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Ocean warming and acidification pose a severe threat to pteropods in the Arctic by reducing their survival and causing the dissolution of their shells. Lipids, especially phospholipids, play a crucial role in the early-stage pteropods. Our experimental study shows that elevated temperatures and high CO2 concentrations lead to a significant decrease in total lipids, mainly due to the reduction of phospholipids. This reduction may compromise cell differentiation and energy balance in the early-stage larvae. The negative effects of warming on lipid metabolism may be a more immediate threat to pteropods than shell dissolution effects caused by acidification.
Ocean warming and acidification will be most pronounced in the Arctic. Both phenomena severely threaten thecosome pteropods (holoplanktonic marine gastropods) by reducing their survival (warming) and causing the dissolution of their aragonitic shell (acidification). Lipids, particularly phospholipids, play a major role in veligers and juveniles of the polar thecosome pteropod Limacina helicina comprising more than two-thirds of their total lipids. Membrane lipids (phospholipids) are important for the temperature acclimation of ectotherms. Hence, we experimentally investigated ocean warming and acidification effects on total lipids, lipid classes, and fatty acids of Arctic early-stage L. helicina. The temperature and pCO(2) treatments chosen resembled Representative Concentration Pathway model scenarios for this century. We found a massive decrease in total lipids at elevated temperatures and at the highest CO2 concentration (1,100 mu atm) of the in situ temperature. Clearly, temperature was the overriding factor. Total lipids were reduced by 47%-70%, mainly caused by a reduction of phospholipids by up to 60%. Further, based on pH(T) development in the incubation water of pteropods during the experiment, some evidence exists for metabolic downregulation in pteropods at high factor levels of temperature and pCO(2). Consequently, the cell differentiation and energy balance of early-stage larvae were probably severely compromised. Comparison of our experimental with 'wild' organisms suggests phospholipid reduction to values clearly outside natural variability. Based on the well-known significance of phospholipids for membranogenesis, early development, and reproduction, negative warming effects on such a basal metabolic function may be a much more immediate threat for pteropods than so far anticipated shell dissolution effects due to acidification.

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