Taking the metabolic pulse of the world’s coral reefs

Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety of anthropogenic perturbations including ocean warming and acidification, increased sedimentation, eutrophication, and overfishing, which could shift reefs to a condition of net calcium carbonate (CaCO3) dissolution...

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Published inPloS one Vol. 13; no. 1; p. e0190872
Main Authors Cyronak, Tyler, Andersson, Andreas J., Langdon, Chris, Albright, Rebecca, Bates, Nicholas R., Caldeira, Ken, Carlton, Renee, Corredor, Jorge E., Dunbar, Rob B., Enochs, Ian, Erez, Jonathan, Eyre, Bradley D., Gattuso, Jean-Pierre, Gledhill, Dwight, Kayanne, Hajime, Kline, David I., Koweek, David A., Lantz, Coulson, Lazar, Boaz, Manzello, Derek, McMahon, Ashly, Meléndez, Melissa, Page, Heather N., Santos, Isaac R., Schulz, Kai G., Shaw, Emily, Silverman, Jacob, Suzuki, Atsushi, Teneva, Lida, Watanabe, Atsushi, Yamamoto, Shoji
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 09.01.2018
Public Library of Science (PLoS)
Subjects
Online AccessGet full text
ISSN1932-6203
1932-6203
DOI10.1371/journal.pone.0190872

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Abstract Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety of anthropogenic perturbations including ocean warming and acidification, increased sedimentation, eutrophication, and overfishing, which could shift reefs to a condition of net calcium carbonate (CaCO3) dissolution and erosion. Herein, we determine the net calcification potential and the relative balance of net organic carbon metabolism (net community production; NCP) and net inorganic carbon metabolism (net community calcification; NCC) within 23 coral reef locations across the globe. In light of these results, we consider the suitability of using these two metrics developed from total alkalinity (TA) and dissolved inorganic carbon (DIC) measurements collected on different spatiotemporal scales to monitor coral reef biogeochemistry under anthropogenic change. All reefs in this study were net calcifying for the majority of observations as inferred from alkalinity depletion relative to offshore, although occasional observations of net dissolution occurred at most locations. However, reefs with lower net calcification potential (i.e., lower TA depletion) could shift towards net dissolution sooner than reefs with a higher potential. The percent influence of organic carbon fluxes on total changes in dissolved inorganic carbon (DIC) (i.e., NCP compared to the sum of NCP and NCC) ranged from 32% to 88% and reflected inherent biogeochemical differences between reefs. Reefs with the largest relative percentage of NCP experienced the largest variability in seawater pH for a given change in DIC, which is directly related to the reefs ability to elevate or suppress local pH relative to the open ocean. This work highlights the value of measuring coral reef carbonate chemistry when evaluating their susceptibility to ongoing global environmental change and offers a baseline from which to guide future conservation efforts aimed at preserving these valuable ecosystems.
AbstractList Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety of anthropogenic perturbations including ocean warming and acidification, increased sedimentation, eutrophication, and overfishing, which could shift reefs to a condition of net calcium carbonate (CaCO3) dissolution and erosion. Herein, we determine the net calcification potential and the relative balance of net organic carbon metabolism (net community production; NCP) and net inorganic carbon metabolism (net community calcification; NCC) within 23 coral reef locations across the globe. In light of these results, we consider the suitability of using these two metrics developed from total alkalinity (TA) and dissolved inorganic carbon (DIC) measurements collected on different spatiotemporal scales to monitor coral reef biogeochemistry under anthropogenic change. All reefs in this study were net calcifying for the majority of observations as inferred from alkalinity depletion relative to offshore, although occasional observations of net dissolution occurred at most locations. However, reefs with lower net calcification potential (i.e., lower TA depletion) could shift towards net dissolution sooner than reefs with a higher potential. The percent influence of organic carbon fluxes on total changes in dissolved inorganic carbon (DIC) (i.e., NCP compared to the sum of NCP and NCC) ranged from 32% to 88% and reflected inherent biogeochemical differences between reefs. Reefs with the largest relative percentage of NCP experienced the largest variability in seawater pH for a given change in DIC, which is directly related to the reefs ability to elevate or suppress local pH relative to the open ocean. This work highlights the value of measuring coral reef carbonate chemistry when evaluating their susceptibility to ongoing global environmental change and offers a baseline from which to guide future conservation efforts aimed at preserving these valuable ecosystems.
Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety of anthropogenic perturbations including ocean warming and acidification, increased sedimentation, eutrophication, and overfishing, which could shift reefs to a condition of net calcium carbonate (CaCO 3 ) dissolution and erosion. Herein, we determine the net calcification potential and the relative balance of net organic carbon metabolism (net community production; NCP) and net inorganic carbon metabolism (net community calcification; NCC) within 23 coral reef locations across the globe. In light of these results, we consider the suitability of using these two metrics developed from total alkalinity (TA) and dissolved inorganic carbon (DIC) measurements collected on different spatiotemporal scales to monitor coral reef biogeochemistry under anthropogenic change. All reefs in this study were net calcifying for the majority of observations as inferred from alkalinity depletion relative to offshore, although occasional observations of net dissolution occurred at most locations. However, reefs with lower net calcification potential (i.e., lower TA depletion) could shift towards net dissolution sooner than reefs with a higher potential. The percent influence of organic carbon fluxes on total changes in dissolved inorganic carbon (DIC) (i.e., NCP compared to the sum of NCP and NCC) ranged from 32% to 88% and reflected inherent biogeochemical differences between reefs. Reefs with the largest relative percentage of NCP experienced the largest variability in seawater pH for a given change in DIC, which is directly related to the reefs ability to elevate or suppress local pH relative to the open ocean. This work highlights the value of measuring coral reef carbonate chemistry when evaluating their susceptibility to ongoing global environmental change and offers a baseline from which to guide future conservation efforts aimed at preserving these valuable ecosystems.
Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety of anthropogenic perturbations including ocean warming and acidification, increased sedimentation, eutrophication, and overfishing, which could shift reefs to a condition of net calcium carbonate (CaCO3) dissolution and erosion. Herein, we determine the net calcification potential and the relative balance of net organic carbon metabolism (net community production; NCP) and net inorganic carbon metabolism (net community calcification; NCC) within 23 coral reef locations across the globe. In light of these results, we consider the suitability of using these two metrics developed from total alkalinity (TA) and dissolved inorganic carbon (DIC) measurements collected on different spatiotemporal scales to monitor coral reef biogeochemistry under anthropogenic change. All reefs in this study were net calcifying for the majority of observations as inferred from alkalinity depletion relative to offshore, although occasional observations of net dissolution occurred at most locations. However, reefs with lower net calcification potential (i.e., lower TA depletion) could shift towards net dissolution sooner than reefs with a higher potential. The percent influence of organic carbon fluxes on total changes in dissolved inorganic carbon (DIC) (i.e., NCP compared to the sum of NCP and NCC) ranged from 32% to 88% and reflected inherent biogeochemical differences between reefs. Reefs with the largest relative percentage of NCP experienced the largest variability in seawater pH for a given change in DIC, which is directly related to the reefs ability to elevate or suppress local pH relative to the open ocean. This work highlights the value of measuring coral reef carbonate chemistry when evaluating their susceptibility to ongoing global environmental change and offers a baseline from which to guide future conservation efforts aimed at preserving these valuable ecosystems.Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety of anthropogenic perturbations including ocean warming and acidification, increased sedimentation, eutrophication, and overfishing, which could shift reefs to a condition of net calcium carbonate (CaCO3) dissolution and erosion. Herein, we determine the net calcification potential and the relative balance of net organic carbon metabolism (net community production; NCP) and net inorganic carbon metabolism (net community calcification; NCC) within 23 coral reef locations across the globe. In light of these results, we consider the suitability of using these two metrics developed from total alkalinity (TA) and dissolved inorganic carbon (DIC) measurements collected on different spatiotemporal scales to monitor coral reef biogeochemistry under anthropogenic change. All reefs in this study were net calcifying for the majority of observations as inferred from alkalinity depletion relative to offshore, although occasional observations of net dissolution occurred at most locations. However, reefs with lower net calcification potential (i.e., lower TA depletion) could shift towards net dissolution sooner than reefs with a higher potential. The percent influence of organic carbon fluxes on total changes in dissolved inorganic carbon (DIC) (i.e., NCP compared to the sum of NCP and NCC) ranged from 32% to 88% and reflected inherent biogeochemical differences between reefs. Reefs with the largest relative percentage of NCP experienced the largest variability in seawater pH for a given change in DIC, which is directly related to the reefs ability to elevate or suppress local pH relative to the open ocean. This work highlights the value of measuring coral reef carbonate chemistry when evaluating their susceptibility to ongoing global environmental change and offers a baseline from which to guide future conservation efforts aimed at preserving these valuable ecosystems.
Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety ofanthropogenic perturbations including ocean warming and acidification, increased sedimentation,eutrophication, and overfishing, which could shift reefs to a condition of net calciumcarbonate (CaCO3) dissolution and erosion. Herein, we determine the net calcificationpotential and the relative balance of net organic carbon metabolism (net community production;NCP) and net inorganic carbon metabolism (net community calcification; NCC) within23 coral reef locations across the globe. In light of these results, we consider the suitabilityof using these two metrics developed from total alkalinity (TA) and dissolved inorganic carbon(DIC) measurements collected on different spatiotemporal scales to monitor coral reefbiogeochemistry under anthropogenic change. All reefs in this study were net calcifying forthe majority of observations as inferred from alkalinity depletion relative to offshore, although occasional observations of net dissolution occurred at most locations. However,reefs with lower net calcification potential (i.e., lower TA depletion) could shift towards netdissolution sooner than reefs with a higher potential. The percent influence of organic carbonfluxes on total changes in dissolved inorganic carbon (DIC) (i.e., NCP compared to thesum of NCP and NCC) ranged from 32% to 88% and reflected inherent biogeochemical differencesbetween reefs. Reefs with the largest relative percentage of NCP experienced thelargest variability in seawater pH for a given change in DIC, which is directly related to thereefs ability to elevate or suppress local pH relative to the open ocean. This work highlightsthe value of measuring coral reef carbonate chemistry when evaluating their susceptibility toongoing global environmental change and offers a baseline from which to guide future conservationefforts aimed at preserving these valuable ecosystems.
Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety of anthropogenic perturbations including ocean warming and acidification, increased sedimentation, eutrophication, and overfishing, which could shift reefs to a condition of net calcium carbonate (CaCO.sub.3) dissolution and erosion. Herein, we determine the net calcification potential and the relative balance of net organic carbon metabolism (net community production; NCP) and net inorganic carbon metabolism (net community calcification; NCC) within 23 coral reef locations across the globe. In light of these results, we consider the suitability of using these two metrics developed from total alkalinity (TA) and dissolved inorganic carbon (DIC) measurements collected on different spatiotemporal scales to monitor coral reef biogeochemistry under anthropogenic change. All reefs in this study were net calcifying for the majority of observations as inferred from alkalinity depletion relative to offshore, although occasional observations of net dissolution occurred at most locations. However, reefs with lower net calcification potential (i.e., lower TA depletion) could shift towards net dissolution sooner than reefs with a higher potential. The percent influence of organic carbon fluxes on total changes in dissolved inorganic carbon (DIC) (i.e., NCP compared to the sum of NCP and NCC) ranged from 32% to 88% and reflected inherent biogeochemical differences between reefs. Reefs with the largest relative percentage of NCP experienced the largest variability in seawater pH for a given change in DIC, which is directly related to the reefs ability to elevate or suppress local pH relative to the open ocean. This work highlights the value of measuring coral reef carbonate chemistry when evaluating their susceptibility to ongoing global environmental change and offers a baseline from which to guide future conservation efforts aimed at preserving these valuable ecosystems.
Audience Academic
Author McMahon, Ashly
Andersson, Andreas J.
Suzuki, Atsushi
Cyronak, Tyler
Corredor, Jorge E.
Kayanne, Hajime
Schulz, Kai G.
Watanabe, Atsushi
Silverman, Jacob
Lantz, Coulson
Teneva, Lida
Santos, Isaac R.
Yamamoto, Shoji
Erez, Jonathan
Koweek, David A.
Gattuso, Jean-Pierre
Manzello, Derek
Langdon, Chris
Shaw, Emily
Enochs, Ian
Eyre, Bradley D.
Carlton, Renee
Page, Heather N.
Kline, David I.
Lazar, Boaz
Albright, Rebecca
Meléndez, Melissa
Gledhill, Dwight
Dunbar, Rob B.
Bates, Nicholas R.
Caldeira, Ken
AuthorAffiliation 7 Cooperative Institute for Marine and Atmospheric Studies, Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, Florida, United States of America
16 Department of Earth and Planetary Science, The University of Tokyo, Tokyo, Japan
17 Smithsonian Tropical Research Institute, Balboa, Ancon, Republic of Panama
20 Department of Biology, California State University, Northridge, California, United States of America
19 School of Marine Science and Ocean Engineering, University of New Hampshire, Durham, New Hampshire
1 Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, United States of America
2 The Rosential School of Marine & Atmospheric Science, University of Miami, Miami, Florida, United States of America
5 University of Southampton, Southampton, United Kingdom
13 Sorbonne Universités, UPMC Univ Paris 06, Observatoire Océanologique, Villefranche-sur-mer, France
15 National Oceanic and Atmospheric Administration Ocean Acidificat
AuthorAffiliation_xml – name: 5 University of Southampton, Southampton, United Kingdom
– name: 19 School of Marine Science and Ocean Engineering, University of New Hampshire, Durham, New Hampshire
– name: 6 Atlantic Oceanographic and Meteorological Laboratory, NOAA, Miami, Florida, United States of America
– name: 21 National Institute of Oceanography, Haifa, Israel
– name: 4 Bermuda Institute of Ocean Sciences, St. George’s, Bermuda
– name: 13 Sorbonne Universités, UPMC Univ Paris 06, Observatoire Océanologique, Villefranche-sur-mer, France
– name: 22 Geological Survey of Japan, National Institute of Advanced Industrial Science and Technology, Tsukuba, Ibaraki, Japan
– name: 8 Department of Marine Sciences, University of Puerto Rico, Mayagüez, Puerto Rico
– name: 1 Scripps Institution of Oceanography, University of California San Diego, La Jolla, California, United States of America
– name: 24 Department of Mechanical and Environmental Informatics, Tokyo Institute of Technology, Meguro, Tokyo, Japan
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– name: 11 Centre for Coastal Biogeochemistry Research, Southern Cross University, Lismore, New South Wales, Australia
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– name: 17 Smithsonian Tropical Research Institute, Balboa, Ancon, Republic of Panama
– name: 14 Institute for Sustainable Development and International Relations, Sciences Po, Paris, France
– name: 20 Department of Biology, California State University, Northridge, California, United States of America
– name: 9 Department of Earth System Science, Stanford University, Stanford, California, United States of America
– name: 10 Institute of Earth Sciences, The Hebrew University, Jerusalem, Israel
– name: 15 National Oceanic and Atmospheric Administration Ocean Acidification Program, Silver Spring, Maryland, United States of America
– name: King Abdullah University of Science and Technology, SAUDI ARABIA
– name: 7 Cooperative Institute for Marine and Atmospheric Studies, Rosenstiel School of Marine and Atmospheric Science, University of Miami, Miami, Florida, United States of America
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/29315312$$D View this record in MEDLINE/PubMed
https://hal.science/hal-02345725$$DView record in HAL
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Snippet Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety of anthropogenic perturbations including ocean warming and acidification,...
Worldwide, coral reef ecosystems are experiencing increasing pressure from a variety ofanthropogenic perturbations including ocean warming and acidification,...
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StartPage e0190872
SubjectTerms Acidification
Alkalinity
Anthropogenic factors
Atmospheric sciences
Biogeochemistry
Biology and Life Sciences
Calcification
Calcification (Physiology)
Calcium
Calcium carbonate
Carbon
Carbon fixation
Conservation
Continental interfaces, environment
Coral reef ecosystems
Coral reefs
Depletion
Dissolution
Dissolved inorganic carbon
Earth science
Earth Sciences
Ecology and Environmental Sciences
Ecosystems
Environment and Society
Environmental aspects
Environmental changes
Environmental Sciences
Eutrophication
Fluxes
Global Changes
Human influences
Laboratories
Medicine and Health Sciences
Metabolism
Observations
Ocean temperature
Ocean warming
Ocean, Atmosphere
Oceanography
Oceans
Organic carbon
Overfishing
pH effects
Physical Sciences
Sciences of the Universe
Seawater
Seawater pH
Sedimentation
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Title Taking the metabolic pulse of the world’s coral reefs
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http://dx.doi.org/10.1371/journal.pone.0190872
Volume 13
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