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Individual juvenile copepods were isolated to prevent fertilization before the assay began. Developmental stage was monitored each day, and male\u2013female pairs were created within 3 days of individuals reaching maturity. During development and match making, copepods were fed ad libitum using the same mix of phytoplankton as the lab cultures. One day after pairing, adults were moved to petri dishes with fresh seawater and provided with 800 \u03bcg C\/L of food mix (split evenly based on carbon content between Tetraselmis and Thalasiossira). Females were given 3 days to produce eggs, after which mate pairs were removed. The produced eggs were then given an additional 3 days to hatch. After the hatching period, egg plates were preserved using non-acid Lugols solution. The number of eggs was then visually counted using a dissection microscope. Total egg production (recorded in the Total column) was calculated as the combined number of hatched and unhatched eggs. The number of eggs hatched is recorded in the Hatched column. Hatching success was calculated as the percentage of eggs that hatched (hatched\/total eggs produced), and is recorded in the Hatching_Success column. The number of eggs per day was calculated by dividing the total number of eggs produced by the duration of the assay (recorded in the Eggs_per_day column).\u00a0<\/p><\/div>","@type":"rdf:HTML"}],"http:\/\/ocean-data.org\/schema\/hasBriefDescription":[{"@value":"Individual egg production measurements from 10 copepod populations from 2017-07-15 to 2018-07-26 in coastal northwest Atlantic surface waters","@language":"en-US"}],"http:\/\/purl.org\/dc\/terms\/description":[{"@value":"
Detailed methods are presented in Sasaki & Dam 2019 (DOI: 10.1111\/gcb.14811). Copepods were collected from ten locations across the Northwest Atlantic (recorded in the Population column). Populations were maintained at the UConn Avery Point campus for three generations at 18oC, with a 12:12 light:dark cycle and a diet of Tetrasemis sp., Thalassiosira weissflogii, and Rhodomonas salina. F3 generation eggs were collected and split into two groups, which developed at either 18oC or 22oC. Egg production assays were performed at the temperature individuals developed at (recorded in the Temp column).\u00a0<\/p><\/div>","@type":"rdf:HTML"}],"http:\/\/www.w3.org\/2000\/01\/rdf-schema#label":[{"@value":"Acartia tonsa Egg Production","@type":"xsd:string"}],"http:\/\/ocean-data.org\/schema\/hasProcessingDescription":[{"@value":"
Data was not processed before analyses. All analyses were performed with the raw data in R version 3.0.\u00a0<\/p>\n
BCO-DMO Processing Notes:
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\n-\u00a0added Latitude, Longitude, and Collection_Date\u00a0columns<\/p>\n
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