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            <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/dataset/959925.rdf" xlink:actuate="onRequest">Nutrient data for mesocosm incubation experiment simulating a phytoplankton bloom in Chesapeake Bay August 2021</gmx:Anchor>
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            <gco:CharacterString>Cite this dataset as: Ward, B. B., Lee, J. (2025) Nutrient data for mesocosm incubation experiment simulating a phytoplankton bloom in Chesapeake Bay August 2021. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2025-04-28 [if applicable, indicate subset used]. doi:10.26008/1912/bco-dmo.959925.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Mesocosm CB 2021 Nutrients Dataset Description:  Methods and Sampling: &amp;lt;p&amp;gt;The mesocosm experiment was performed in August 2021 on the R/V Hugh Sharp, cruise HRS2110, at a station near the mouth of Chesapeake Bay.&amp;amp;nbsp;Surface water (2–5 m) was collected from the study site (37.27&amp;lt;sup&amp;gt;o&amp;lt;/sup&amp;gt;&amp;amp;nbsp;N, 76.09&amp;lt;sup&amp;gt;o&amp;lt;/sup&amp;gt;&amp;amp;nbsp;W), located near the mouth of the bay. Incubation medium was prepared by pumping surface water (~5 m) directly from the sample site through a series of nylon mesh and glass fiber filters, ending with a 0.3&amp;amp;nbsp;&amp;lt;em&amp;gt;μ&amp;lt;/em&amp;gt;m filter, using a double diaphragm pump into three 24-L translucent polycarbonate (PC) carboys. Surface water inoculum was collected using a rosette system with 12–L Niskin bottles and a CTD profiler from 2–4 m depth and pre–filtered through 210&amp;amp;nbsp;&amp;lt;em&amp;gt;μ&amp;lt;/em&amp;gt;m nylon mesh before being added to the mesocosms to produce a 10 % inoculation.&amp;amp;nbsp;Carboys were incubated for eight days in an on–deck water bath, using a seawater flow–through system drawn from surface water and a plastic screen shade covering to keep incubation temperature and light similar to in situ conditions.&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples for nutrient concentrations were collected from each carboy three times per day, at approximately 06:00, 12:00, and 18:00 local time. Samples were filtered through a 0.22 &amp;lt;em&amp;gt;μ&amp;lt;/em&amp;gt;m syringe filter into 50–mL plastic conical tubes and stored at –20&amp;lt;sup&amp;gt;o &amp;lt;/sup&amp;gt;C until analysis. Reactive nitrite (NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt;) and silicate (silicic acid, H&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;SiO&amp;lt;sub&amp;gt;4&amp;lt;/sub&amp;gt;) concentrations were measured on a ThermoScience Genesys150 UV–Vis spectrophotometer using colorimetric methods (sulfanilamide + &amp;lt;em&amp;gt;N&amp;lt;/em&amp;gt;–(1–naphthyl)–ethylenediamine and metol sulfite, respectively) modified from Strickland and Parsons (1972). NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; + NO&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; concentration was measured via chemiluminescent detection using a Teledyne NOx analyzer (NOxBox) according to Braman &amp;amp;amp; Hendrix (1989). NO&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;- &amp;lt;/sup&amp;gt;concentrations were calculated by subtracting the colorimetrically derived NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; concentrations from their paired NO&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; + NO&amp;lt;sub&amp;gt;3&amp;lt;/sub&amp;gt;&amp;lt;sup&amp;gt;-&amp;lt;/sup&amp;gt; NOxBox concentrations.&amp;lt;/p&amp;gt;</gco:CharacterString>
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        <gmx:Anchor xlink:href="http://lod.bco-dmo.org/id/award/869583.rdf" xlink:title="OCE-2149606" xlink:actuate="onRequest">Funding provided by NSF Division of Ocean Sciences (NSF OCE) Award Number: OCE-2149606 Award URL: https://www.nsf.gov/awardsearch/show-award?AWD_ID=2149606</gmx:Anchor>
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A recent global survey of surface ocean waters revealed that microbial parasites comprise half of the eukaryotic plankton diversity and suggested that biological interactions, including parasites, play an important role in the ecology of many types of microscopic algae, which are the base of the ocean food web, but not diatoms. Diatoms are among the most abundant microalgae, particularly in upwelling areas where nutrient-rich deep currents feed the ocean's surface and support the world's greatest fisheries. Yet this survey did not investigate high-productivity regions, leaving a significant knowledge gap. Diatoms may be successful in upwelling regions because they evade predators and parasites, but it seems more reasonable that they, like all other microalgae, also have biological enemies. In this study, the researchers use a large set of available samples from upwelling regions to investigate the effect of parasites on the proliferation of diatom communities and resulting primary production. The project supports a graduate student and provides hands-on research experiences for high school and undergraduate college students. The study data are also integrated into courses taught by the principal investigator.&lt;/p&gt;
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