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Methodology:\u00a0
\nDuplicate cultures of Synechococcus WH8102 (axenic), Synechococcus WH7805 (xenic) and Prochlorococcus marinus MED4 (xenic and axenic) were sampled every other day for 17-19 days for the quantification of single cells, suspended aggregates (aggregates ca. 5-60 \u03bcm), and TEP. Single cell abundance was determined using epifluorescence microscopy.
\n\u00a0
Growth rates of xenic and axenic marine Prochlorococcus and Synechococcus cultures from laboratory experiments conducted in 2016 and 2017.
\nThese data were published in\u00a0Cruz and Neuer, 2019.
\nRelated datasets from the same laboratory experiments:
\nPicocyanobacteria TEP: Cell Abundance https://www.bco-dmo.org/dataset/774628
\nPicocyanobacteria TEP: Suspended Aggregates https://www.bco-dmo.org/dataset/774639
\nPicocyanobacteria TEP: TEP Concentration https://www.bco-dmo.org/dataset/774646
BCO-DMO Data Manager Processing Notes: Growth Rates
\n\u200b* Excel sheet extracted to a csv file
\n* added a conventional header with dataset name, PI name, version date
\n* modified parameter names to conform with BCO-DMO naming conventions
\n* blank values in this dataset are displayed as \"nd\" for \"no data.\"\u00a0 nd is the default missing data identifier in the BCO-DMO system.