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            <gco:CharacterString>Cite this dataset as: Glass, B., Brown, K., Speer, K., Barott, K., Schmitt, A. (2024) Larval respiration performance of Nematostella vectensis following parental exposure to ocean acidification during lab experiments conducted in spring 2022. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2024-03-24 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.920260.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>OA experiment: Nematostella larval respiration Dataset Description: &amp;lt;p&amp;gt;Data generated as part of a Nematostella ocean acidfication experiment published in Glass et al., 2023. (see Related Publications). Related Zenodo datasets provides further analysis and plotting of the BCO-DMO dataset here. (see Related Dataset).&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;&amp;lt;em&amp;gt;Nematostella vectensis&amp;lt;/em&amp;gt;&amp;amp;nbsp;(Stephenson, 1935) anemones were collected from a salt marsh in Brigantine, New Jersey in the fall of 2020. Females were identified by inducing spawning, and 14 individuals that released eggs were chosen as the genotype pool for this experiment. Each female was then horizontally bisected through the body column using a razor blade, resulting in two genotypically identical individuals that were divided between the two experimental groups (ambient and acidic).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;A clonal male population, also originating from the United States Atlantic coast, was obtained from the laboratory of Dr. Katerina Ragkousi (Amherst College) in the spring of 2021. The male population size was increased via bisection, resulting in a total of 20 genetically identical males for the experiment (N=10 per treatment).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;All anemones were kept in 12 parts per thousand (ppt) artificial seawater (ASW; Instant Ocean Reef Crystals&amp;lt;sup&amp;gt;Ⓡ&amp;lt;/sup&amp;gt;&amp;amp;nbsp;reef salt, Spectrum Brands, Blacksburg, VA, USA) at pH 7.7–8.1 and 18°C. The animals were maintained in a dark incubator (Boekel Scientific, Feasterville-Trevose, PA, USA) and fed approximately every other day with Artemia nauplii. The experiment was performed approximately 1–1.5 years after animal collection.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/843346.rdf" xlink:title="OCE-1923743" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-1923743 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=1923743</gmx:Anchor>
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Coral reefs are incredibly diverse ecosystems that provide food, tourism revenue, and shoreline protection for coastal communities. The ability of coral reefs to continue providing these services to society is currently threatened by climate change, which has led to increasing ocean temperatures and acidity that can lead to the death of corals, the animals that build the reef framework upon which so many species depend. This project examines how temperature and acidification stress work together to influence the future health and survival of corals. The scientists are carrying out the project in Hawaii where they have found individual corals with different sensitivities to temperature stress that are living on reefs with different environmental pH conditions. This project improves understanding of how an individual coral's history influences its response to multiple stressors and helps identify the conditions that are most likely to support resilient coral communities. The project will generate extensive biological and physicochemical data that will be made freely available. Furthermore, this project supports the education and training of undergraduate and high school students and one postdoctoral researcher in marine science and coral reef ecology. Hands-on activities for high school students are being developed into a free online educational resource.&lt;/p&gt;
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                <gco:CharacterString>&amp;lt;p&amp;gt;To quantify larval respiration rates, sperm and eggs were first combined by treatment in glass finger bowls in weeks 11 and 13. At 3 DPF, swimming larvae from each parental treatment were pipetted in three groups of ten (week 11) or nine groups of 15 (week 13) into wells of a 24-well plate equipped with oxygen sensor spots (Loligo Systems, Viborg, Denmark).&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Wells containing larvae as well as larvae-free wells containing water from the fertilization bowl as a bacterial control (‘blanks’;&amp;amp;nbsp;&amp;lt;em&amp;gt;N&amp;lt;/em&amp;gt;=3 in week 11;&amp;amp;nbsp;&amp;lt;em&amp;gt;N&amp;lt;/em&amp;gt;=6 in week 13) were filled to capacity (80 μL) with 12 ppt ASW and sealed with an adhesive plate cover before being placed on a PreSens SensorDish&amp;lt;sup&amp;gt;Ⓡ&amp;lt;/sup&amp;gt;&amp;amp;nbsp;Reader (Precision Sensing, Regensburg, Germany), which was previously calibrated according to the manufacturer's instructions.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Dissolved oxygen concentrations in each well were read every 15 s for at least 1 h, during which no wells experienced near or total oxygen depletion. The rate of oxygen consumption over time was determined from the slopes of linear regressions of oxygen levels multiplied by the volume of the wells. The average oxygen consumption rate for the blank wells was subtracted from the larval rates, which were then converted to nmol O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;amp;nbsp;minute&amp;lt;sup&amp;gt;−1&amp;lt;/sup&amp;gt;&amp;amp;nbsp;larva&amp;lt;sup&amp;gt;−1&amp;lt;/sup&amp;gt;.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;For respiration data, the average oxygen consumption rate for the blank wells was subtracted from the larval rates, which were then converted to nmol O&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;amp;nbsp;minute&amp;lt;sup&amp;gt;−1&amp;lt;/sup&amp;gt;&amp;amp;nbsp;larva&amp;lt;sup&amp;gt;−1&amp;lt;/sup&amp;gt;&amp;lt;/p&amp;gt;</gco:CharacterString>
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