Ocean acidification refugia of the Florida Reef Tract.

Ocean acidification (OA) is expected to reduce the calcification rates of marine organisms, yet we have little understanding of how OA will manifest within dynamic, real-world systems. Natural CO(2), alkalinity, and salinity gradients can significantly alter local carbonate chemistry, and thereby cr...

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Published in:PLoS ONE
Main Authors: Derek P Manzello, Ian C Enochs, Nelson Melo, Dwight K Gledhill, Elizabeth M Johns
Format: Article in Journal/Newspaper
Language:English
Published: Public Library of Science (PLoS) 2012
Subjects:
R
Q
Online Access:https://doi.org/10.1371/journal.pone.0041715
https://doaj.org/article/0e4e5cff601d41988c8152afe6fefbc7
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spelling ftdoajarticles:oai:doaj.org/article:0e4e5cff601d41988c8152afe6fefbc7 2023-05-15T17:50:44+02:00 Ocean acidification refugia of the Florida Reef Tract. Derek P Manzello Ian C Enochs Nelson Melo Dwight K Gledhill Elizabeth M Johns 2012-01-01T00:00:00Z https://doi.org/10.1371/journal.pone.0041715 https://doaj.org/article/0e4e5cff601d41988c8152afe6fefbc7 EN eng Public Library of Science (PLoS) http://europepmc.org/articles/PMC3407208?pdf=render https://doaj.org/toc/1932-6203 1932-6203 doi:10.1371/journal.pone.0041715 https://doaj.org/article/0e4e5cff601d41988c8152afe6fefbc7 PLoS ONE, Vol 7, Iss 7, p e41715 (2012) Medicine R Science Q article 2012 ftdoajarticles https://doi.org/10.1371/journal.pone.0041715 2022-12-31T01:43:05Z Ocean acidification (OA) is expected to reduce the calcification rates of marine organisms, yet we have little understanding of how OA will manifest within dynamic, real-world systems. Natural CO(2), alkalinity, and salinity gradients can significantly alter local carbonate chemistry, and thereby create a range of susceptibility for different ecosystems to OA. As such, there is a need to characterize this natural variability of seawater carbonate chemistry, especially within coastal ecosystems. Since 2009, carbonate chemistry data have been collected on the Florida Reef Tract (FRT). During periods of heightened productivity, there is a net uptake of total CO(2) (TCO(2)) which increases aragonite saturation state (Ω(arag)) values on inshore patch reefs of the upper FRT. These waters can exhibit greater Ω(arag) than what has been modeled for the tropical surface ocean during preindustrial times, with mean (± std. error) Ω(arag)-values in spring = 4.69 (±0.101). Conversely, Ω(arag)-values on offshore reefs generally represent oceanic carbonate chemistries consistent with present day tropical surface ocean conditions. This gradient is opposite from what has been reported for other reef environments. We hypothesize this pattern is caused by the photosynthetic uptake of TCO(2) mainly by seagrasses and, to a lesser extent, macroalgae in the inshore waters of the FRT. These inshore reef habitats are therefore potential acidification refugia that are defined not only in a spatial sense, but also in time; coinciding with seasonal productivity dynamics. Coral reefs located within or immediately downstream of seagrass beds may find refuge from OA. Article in Journal/Newspaper Ocean acidification Directory of Open Access Journals: DOAJ Articles PLoS ONE 7 7 e41715
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Derek P Manzello
Ian C Enochs
Nelson Melo
Dwight K Gledhill
Elizabeth M Johns
Ocean acidification refugia of the Florida Reef Tract.
topic_facet Medicine
R
Science
Q
description Ocean acidification (OA) is expected to reduce the calcification rates of marine organisms, yet we have little understanding of how OA will manifest within dynamic, real-world systems. Natural CO(2), alkalinity, and salinity gradients can significantly alter local carbonate chemistry, and thereby create a range of susceptibility for different ecosystems to OA. As such, there is a need to characterize this natural variability of seawater carbonate chemistry, especially within coastal ecosystems. Since 2009, carbonate chemistry data have been collected on the Florida Reef Tract (FRT). During periods of heightened productivity, there is a net uptake of total CO(2) (TCO(2)) which increases aragonite saturation state (Ω(arag)) values on inshore patch reefs of the upper FRT. These waters can exhibit greater Ω(arag) than what has been modeled for the tropical surface ocean during preindustrial times, with mean (± std. error) Ω(arag)-values in spring = 4.69 (±0.101). Conversely, Ω(arag)-values on offshore reefs generally represent oceanic carbonate chemistries consistent with present day tropical surface ocean conditions. This gradient is opposite from what has been reported for other reef environments. We hypothesize this pattern is caused by the photosynthetic uptake of TCO(2) mainly by seagrasses and, to a lesser extent, macroalgae in the inshore waters of the FRT. These inshore reef habitats are therefore potential acidification refugia that are defined not only in a spatial sense, but also in time; coinciding with seasonal productivity dynamics. Coral reefs located within or immediately downstream of seagrass beds may find refuge from OA.
format Article in Journal/Newspaper
author Derek P Manzello
Ian C Enochs
Nelson Melo
Dwight K Gledhill
Elizabeth M Johns
author_facet Derek P Manzello
Ian C Enochs
Nelson Melo
Dwight K Gledhill
Elizabeth M Johns
author_sort Derek P Manzello
title Ocean acidification refugia of the Florida Reef Tract.
title_short Ocean acidification refugia of the Florida Reef Tract.
title_full Ocean acidification refugia of the Florida Reef Tract.
title_fullStr Ocean acidification refugia of the Florida Reef Tract.
title_full_unstemmed Ocean acidification refugia of the Florida Reef Tract.
title_sort ocean acidification refugia of the florida reef tract.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doi.org/10.1371/journal.pone.0041715
https://doaj.org/article/0e4e5cff601d41988c8152afe6fefbc7
genre Ocean acidification
genre_facet Ocean acidification
op_source PLoS ONE, Vol 7, Iss 7, p e41715 (2012)
op_relation http://europepmc.org/articles/PMC3407208?pdf=render
https://doaj.org/toc/1932-6203
1932-6203
doi:10.1371/journal.pone.0041715
https://doaj.org/article/0e4e5cff601d41988c8152afe6fefbc7
op_doi https://doi.org/10.1371/journal.pone.0041715
container_title PLoS ONE
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