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            <gco:CharacterString>Cite this dataset as: Binder, B. (2017) Prochlorococcus in situ cell cycle phases fractions from RV Cape Hatteras cruises CH0409 and CH0510 in the Western Sargasso Sea in 2009 and 2010. Biological and Chemical Oceanography Data Management Office (BCO-DMO). (Version 1) Version Date 2017-10-12 [if applicable, indicate subset used]. doi:10.1575/1912/bco-dmo.716955.1 [access date]</gco:CharacterString>
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        <gco:CharacterString>Prochlorococcus in situ Cell Cycle Phases Fractions. Dataset Description: &amp;lt;p&amp;gt;Prochlorococcus in situ Cell Cycle Phases Fractions.&amp;lt;/p&amp;gt; Methods and Sampling: &amp;lt;p&amp;gt;Samples were taken using a rosette of Niskin bottles, fixed with freshly titrated paraformaldehyde (pH 7.4–8.1, 0.1% final concentration), held in the dark for 10 min, frozen in liquid nitrogen, and stored in a -80 deg C freezer (CH0409 samples) or in liquid nitrogen (CH0510 samples) until analysis. Preserved samples were analyzed by dual beam flow cytometry on a modified Coulter-EPICS 753 flow cytometer (Binder et al. 1996). Samples were chosen in random order, defrosted in a 30°C water bath (just long enough to melt, ~5 min), and stained with the DNA-specific stain Hoechst 33342 (0.5 ug mL-1 final concentration) (Invitrogen, Carlsbad, California) for a minimum of 20 min in the dark. Prior to analysis, polystyrene fluorescent beads (Flow Check® 1.0 um (YG) and 0.494 um (BB); Polysicences Inc., Washington, PA, USA), were added to each sample, and used to normalize cellular light scatter, red (chlorophyll-derived) fluorescence, and Hoechst fluorescence.&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;Samples were run at an infusion rate of 10 uL min-1 for 10 to 50 min, depending on cell abundance within the sample. A minimum of 10,000 Prochlorococcus cells were analyzed, except for samples in which low Prochlorococcus concentrations made this impractical.&amp;amp;nbsp;&amp;amp;nbsp;&amp;lt;/p&amp;gt;

&amp;lt;p&amp;gt;DNA frequency distributions for Prochlorococcus cells were obtained from Hoechst-derived blue fluorescence. These frequency distributions were deconvoluted into their component cell cycle stages (G1, S, G2) using Modfit software (Verity Software House, Topsham, ME, USA), and assuming a simple model comprised of two Gaussian populations (G1 and G2) and a broadened rectangle (S).&amp;amp;nbsp;&amp;lt;/p&amp;gt;</gco:CharacterString>
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