bzielins@mail.usf.edu<\/a>).<\/strong><\/p>\nAll the stations represent 2-3 true replicates, each replicate consisted of three separate readings. The reason not all of the stations had 3 replicates was because one day the machine malfunctioned and all the samples to be run that day needed to be discarded. The counts usually are very accurate and precise; however it seems that with these samples the precision was not as good as I would hope to see. This can be caused by two things. 1) small organics\/cell debris from the plume water could have been included in the viral counts, or 2) I have only briefly used these methods previously and these counts were taken along my learning curve.<\/p>\n
Related files and references:<\/strong>
\n1. Brussaard CPD (2004) Optimization of procedures for counting viruses by flow cytometry. Applied and Environmental Microbiology 70: 1506.<\/p><\/div>","@type":"rdf:HTML"}],"http:\/\/ocean-data.org\/schema\/hasBriefDescription":[{"@value":"Viral Counts","@language":"en-US"}],"http:\/\/purl.org\/dc\/terms\/description":[{"@value":"Viral counts determined by flow-cytometry<\/p><\/div>","@type":"rdf:HTML"}],"http:\/\/www.w3.org\/2000\/01\/rdf-schema#label":[{"@value":"Viral Counts - AN10","@type":"xsd:string"}],"http:\/\/ocean-data.org\/schema\/hasProcessingDescription":[{"@value":"
<\/p>\n
Related files and references:<\/strong>
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