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Abstract Coral calcification is essential to provide the structural foundation for coral reefs and is integral in supporting marine biodiversity reliant on reef ecosystems. The drivers for calcification in corals are undoubtedly highly complex and require several perspectives to identify vulnerabilities in the context of environmental change. Specifically, ocean acidification (OA) resulting from the rise of anthropogenic carbon dioxide (CO2) emissions poses a potential threat to the physiological mechanisms that drive calcification in corals. Therefore, this report goes beyond environmental seawater chemistry to examine the physiological mechanism of calcium ion homeostasis. Calcium's role in calcification physiology is well established, but how calcium homeostasis could shift under acidification has little been considered a significant driver in reduced calcification. Calcium is potentially the most actively transported substrate in coral calcification, though in high chemical abundance in seawater, corals are likely utilizing the most energy to concentrate calcium at the site of calcification. We argue for increased consideration of the calcium ion in the context of OA when identifying sensitivities. The concepts proposed here are justified through a combination of results from novel RAMAN spectroscopy and molecular work that provides insight into shifts in calcium homeostasis when exposed to acidification. We speculate that future work incorporating methodologies considering calcium dynamics in OA could benefit by narrowing in on what physiological mechanisms are potentially vulnerable. It is imperative that we identify what drives lower calcification in corals under OA to inform efficient directives in identifying species sensitivities to future climate change.
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Multiple carbonate system parameters independently govern shell formation in a marine mussel
Abstract Calcification is vital to marine organisms that produce calcium carbonate shells and skeletons. However, how calcification is impacted by ongoing environmental changes, including ocean acidification, remains incompletely understood due to complex relationships among the carbonate system variables hypothesized to drive calcification. Here, we experimentally decouple these drivers in an exploration of shell formation in adult marine mussels,Mytilus californianus. In contrast to models that focus on single parameters like calcium carbonate saturation state, our results implicate two independent factors, bicarbonate concentration and seawater pH, in governing calcification. While qualitatively similar to ideas embodied in the related substrate-inhibitor ratio (bicarbonate divided by hydrogen ion concentration), our data highlight that merging bicarbonate ion and hydrogen ion concentrations into a simple quotient obscures important features of calcification. Considering a dual-parameter framework improves mechanistic understanding of how calcifiers interact with complex and changing chemical conditions.
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- PAR ID:
- 10508571
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- Communications Earth & Environment
- Volume:
- 5
- Issue:
- 1
- ISSN:
- 2662-4435
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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