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        <gco:CharacterString>Estimated frequency of lytic viral infection from the ETNP Dataset Description: &amp;lt;p&amp;gt;Estimated frequency of lytic viral infection from samples collected in the&amp;amp;nbsp;Eastern Tropical North Pacific oxygen minimum zone region (ETNP OMZ) on R/V New Horizon cruise NH1315 from 13-28 June 2013.&amp;amp;nbsp;Samples were deposited onto TEM grids, stained, and examined using a transmission electron microscope. Micrographs of cells were collected and characterized as infected or uninfected.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;Detailed protocols, including suggestions from the scientific community, are published on the lab website at &amp;lt;a href=&amp;quot;https://u.osu.edu/viruslab/protocols/&amp;quot; target=&amp;quot;_blank&amp;quot;&amp;gt;https://u.osu.edu/viruslab/protocols/&amp;lt;/a&amp;gt;&amp;amp;nbsp;and maintained on protocols.io at&amp;amp;nbsp;&amp;lt;a href=&amp;quot;https://www.protocols.io/workspaces/sullivan-lab&amp;quot; target=&amp;quot;_blank&amp;quot;&amp;gt;https://www.protocols.io/workspaces/sullivan-lab&amp;lt;/a&amp;gt;.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples were collected from the Eastern Tropical North Pacific oxygen minimum zone region (ETNP OMZ) during the OMZ Microbial Biogeochemistry Expedition cruise (R/V NewHorizon,13-28 June 2013). Seawater was collected from 16 depths spanning the mixed layer, oxycline, OMZ core, and below the OMZ. Collections were made using Niskin bottles on a rosette. Samples were preserved with EM-grade glutaraldehyde (2% final concentration), flash-frozen in liquid nitrogen and stored between -72 °C and -80 °C until analysis.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples were centrifuged for 1 h at 55 000 g using an ultracentrifuge (LM-80, Beckman, Brea, CA, USA) onto TEM grids (200 mesh copper grids with carbon- stabilized formvar support; Ted Pella, Redding, CA, USA). Grids were then stained with uranyl acetate and analyzed as previously described (Brum et al., 2005) to determine the frequency of visibly infected cells using a transmission electron microscope (CM12, Philips, Eindhoven, The Netherlands). The frequency of infected cells was then calculated from the frequency of visibly infected cells (Binder, 1999).&amp;lt;/p&amp;gt;</gco:CharacterString>
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