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Bugula neritina<\/em> colonies were collected by hand off the sides of floating docks around Morehead City, NC (latitude: 34.7, longitude: -76.8). Larvae from individual colonies were collected and settled into 10 mL of filtered seawater with (treated) or without (control) 100 ug\/mL of gentamicin.\u00a0Larvae were allowed to settle overnight. The control and treated seawater was changed the next morning for the next 3 days. The plates were transported to Georgia Tech where they were placed in 2.5 gallon tanks with artificial seawater maintained in environmental chambers at 16 degrees C and 22 degrees C. They were fed ad libitum<\/em> an artificial diet of the phytoplankton Rhodomonas lens<\/em> for approximately one month.\u00a0After the 1-month period, the size of the colonies was measured by counting the number of bifurcations in each colony.\u00a0A Leica stereomicroscope was used while counting the number of colony bifurcations. Samples of larvae, juvenile, and the grown colonies were placed in RNAlater for symbiont quantification analysis by quantitative PCR (currently in progress).<\/p><\/div>","@type":"rdf:HTML"}],"http:\/\/ocean-data.org\/schema\/hasBriefDescription":[{"@value":"Size of Bugula neritina colonies with and without symbiont grown at different temperatures","@language":"en-US"}],"http:\/\/purl.org\/dc\/terms\/description":[{"@value":" Size of Bugula neritina<\/em> colonies with and without symbiont grown at different temperatures in laboratory mesocosms.<\/p><\/div>","@type":"rdf:HTML"}],"http:\/\/www.w3.org\/2000\/01\/rdf-schema#label":[{"@value":"Mesocosm Growth Data","@type":"xsd:string"}],"http:\/\/ocean-data.org\/schema\/hasProcessingDescription":[{"@value":" Data were\u00a0analyzed using IBM SPSS Statistics 24.<\/p>\n BCO-DMO Processing:
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