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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/4000.rdf" xlink:actuate="onRequest">Mesoamerican Barrier Reef System coral buoyant weights for temperature experiments from Sapodilla Caye, Belize starting 2010 (OA - Ocean Acidification and Warming Impact on Calcification project)</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Ries, J. B. (2013) Mesoamerican Barrier Reef System coral buoyant weights for temperature experiments from Sapodilla Caye, Belize starting 2010 (OA - Ocean Acidification and Warming Impact on Calcification project). Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 22 July 2013) Version Date 2013-07-22 [if applicable, indicate subset used]. http://lod.bco-dmo.org/id/dataset/4000 [access date]</gco:CharacterString>
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        <gco:CharacterString>MBRS coral buoyant weights for temperature experiments Dataset Description: &amp;lt;p&amp;gt;MBRS coral buoyant weights for temperature experiments&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;In July 2011, eighteen colonies of the tropical coral &amp;lt;em&amp;gt;S. siderea&amp;lt;/em&amp;gt; were collected at 3 to 5 m depth on the Mesoamerican Barrier Reef System in southern Belize. Colonies were collected from nearshore, backreef, and forereef reef zones. &amp;lt;em&amp;gt;Siderastrea siderea&amp;lt;/em&amp;gt; corals were transported to the University of North Carolina at Chapel Hill and each coral colony was sectioned into 18 comparatively sized specimens (approximately 3 cm x 2 cm x 1 cm) using a rock saw and glued with cyanoacrylate on to plastic microscope slides.&amp;amp;nbsp; The corals were allowed to recover for approximately 30 days under laboratory conditions in two 500 L recirculating artificial seawater systems until the start of the 15-day acclimation period, in which the corals were incrementally exposed to the experimental treatment conditions.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
In the laboratory experiments, &amp;lt;em&amp;gt;Siderastrea siderea&amp;lt;/em&amp;gt; coral specimens from each of the 18 colonies were reared for 95 days (5 August − 8 November 2011) in each of twelve 38 L glass aquaria (18 specimens per tank; 216 specimens in total) filled with artificial seawater formulated at a salinity of 35 with &amp;lt;em&amp;gt;Instant Ocean Sea Salt&amp;lt;/em&amp;gt; and deionized water. Four pCO2 partial pressures [324, 477, 604, and 2553) ppm)], established by mixing pure CO2 with compressed air using &amp;lt;em&amp;gt;Aalborg&amp;lt;/em&amp;gt; mass flow controllers, were bubbled with microporous ceramic airstones into the triplicate glass aquaria (12 tanks total).&amp;amp;nbsp; Coral specimens from each of the 18 colonies were reared in each of the 12 replicate tanks.&amp;amp;nbsp; The pCO2 experiments were maintained at an average temperature of 28 ºC.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Experimental growth conditions for the seawater temperature experiment were similar to those for the CO2-induced ocean acidification experiment described above.&amp;amp;nbsp; &amp;lt;em&amp;gt;Siderastrea siderea&amp;lt;/em&amp;gt; coral specimens from each of the 18 colonies were reared for 95 days (5 August − 8 November 2011) in each of nine 38 L glass aquaria (18 specimens per tank; 162 specimens in total) filled with artificial seawater formulated at a salinity of 35 with &amp;lt;em&amp;gt;Instant Ocean Sea Salt&amp;lt;/em&amp;gt; and deionized water. Three experimental seawater temperatures [25, 28, and 32 ºC] were maintained in triplicate (9 tanks total) for this experiment. Coral specimens from each of the 18 colonies were reared in each of the 9 replicate tanks.&amp;amp;nbsp; Compressed air with an average pCO2 of 488 ppm was bubbled with microporous ceramic airstones into the triplicate glass aquaria.&amp;lt;br /&amp;gt;
&amp;lt;br /&amp;gt;
Coral calcification rates were estimated using a buoyant weight technique.&amp;amp;nbsp; &amp;lt;em&amp;gt;Siderastrea siderea&amp;lt;/em&amp;gt; specimens were weighed at the beginning of the experiment and a final measurement taken at approximately 95 days. Each coral specimen was suspended by aluminum wire at 10-cm depth from a &amp;lt;em&amp;gt;Cole-Parmer&amp;lt;/em&amp;gt; bottom-loading scale (precision ± 0.001; accuracy ± 0.002) in an aquarium filled with artificial seawater maintained at a temperature of 25 ºC and salinity of 33. A standardized plastic-coated zinc mass was intermittently weighed to ensure consistency of the buoyant weight method throughout the duration of the experiment.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/54819.rdf" xlink:title="OCE-1031995" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1031995 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1031995</gmx:Anchor>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/529179.rdf" xlink:title="OCE-1357665" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1357665 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1357665</gmx:Anchor>
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Anthropogenic elevation of atmospheric pCO2 is increasing the acidity of the oceans, thereby reducing the saturation state of seawater with respect to calcium carbonate (CaCO3). Of mounting concern is the potential impact of these changes on the ability of calcifying organisms to form their shells and skeletons. Recent studies, including pilot work conducted by investigator Ries and his colleagues on a suite of benthic marine calcifiers spanning broad taxonomic, mineralogical, and ecological ranges, have revealed that marine organisms exhibit a wide range of calcification responses to CO2-induced ocean acidification, including positive, negative, parabolic, threshold, and neutral responses. Marine calcifiers build their shells and skeletons from various forms (polymorphs) of CaCO3, most commonly aragonite, high-Mg calcite, and low-Mg calcite. These polymorphs differ greatly in their solubility in seawater and, therefore, in their potential response to CO2-induced ocean acidification. X-ray diffraction analysis of shells secreted by the organisms investigated in the pilot study reveals that the proportion of calcite (the less soluble form of CaCO3) to aragonite (the more soluble form) within their shells increases under elevated pCO2, while the Mg:Ca ratio of their calcite declines. These observations suggested that some marine calcifiers may partially adapt to a declining CaCO3 saturation state by accreting a greater proportion of the less-soluble form of CaCO3 (low-Mg calcite) at the expense of the more soluble forms (aragonite, high-Mg calcite). However, it is likely that such mineralogical and compositional changes in the shells and skeletons of marine organisms would alter their structural and biomechanical properties.&lt;/p&gt;
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&lt;p&gt;&lt;strong&gt;Note (02 Oct 2014):&lt;/strong&gt; Funding for this project has transferred from award OCE-1031995 to OCE-1357665, coincident with Principal Investigator's affiliation change from University of North Carolina at Chapel Hill to Northeastern University.&lt;/p&gt;</gco:CharacterString>
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&amp;lt;br /&amp;gt;
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&amp;lt;br /&amp;gt;
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&amp;lt;p&amp;gt;&amp;lt;strong&amp;gt;BCO-DMO Processing Notes&amp;lt;/strong&amp;gt;&amp;lt;br /&amp;gt;
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