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Microelectrode characterization of coral daytime interior pH and carbonate chemistry

delete2016-04-04
delete122
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OA
AI
W
Wei‐Jun Cai *
Y
Yuening Ma
B
Brian M. Hopkinson
A
Andréa G. Grottoli
M
Mark E. Warner
Q
Qian Ding
X
Xinping Hu
X
Xiangchen Yuan
V
Verena Schoepf
H
Hui Xu
C
Chenhua Han
T
Todd F. Melman
K
Kenneth D. Hoadley
D
D. Tye Pettay
Y
Yohei Matsui
J
Justin H. Baumann
S
Stephen Levas
Y
Ying Ye
Y
Yongchen Wang
DOI:10.1038/ncomms11144delete
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Abstract

Abstract

En 中文
Reliably predicting how coral calcification may respond to ocean acidification and warming depends on our understanding of coral calcification mechanisms. However, the concentration and speciation of dissolved inorganic carbon (DIC) inside corals remain unclear, as only pH has been measured while a necessary second parameter to constrain carbonate chemistry has been missing. Here we report the first carbonate ion concentration ([CO32-]) measurements together with pH inside corals during the light period. We observe sharp increases in [CO32-] and pH from the gastric cavity to the calcifying fluid, confirming the existence of a proton (H+) pumping mechanism. We also show that corals can achieve a high aragonite saturation state (Omega(arag)) in the calcifying fluid by elevating pH while at the same time keeping [DIC] low. Such a mechanism may require less H+-pumping and energy for upregulating pH compared with the high [DIC] scenario and thus may allow corals to be more resistant to climate change related stressors.
Keywords:
OCEAN ACIDIFICATION
INORGANIC CARBON
SEA-WATER
CALCIFICATION
REEF
TRANSPORT
CO2
BIOMINERALIZATION
PHOTOSYNTHESIS
RESPIRATION
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Journal

Nature Communications cover
Nature Communications
IF:
15.7
Papers:
9.2W
Citations:
91.2W

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U
University of Western Australia
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University System of Ohio
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university system of georgia
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University of Delaware
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University of Georgia
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