Data for flow cytometry, FlowCam, and microscopy comparison experiment

The minicosm experimental design measured the microbial community growth in six unreplicated fCO2 treatments. Therefore, sub-samples from each minicosm were within-treatment pseudoreplicates and thus, results of statistical analysis must be interpreted conservatively. This data set was collected fro...

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Bibliographic Details
Other Authors: AADC (originator), AU/AADC > Australian Antarctic Data Centre, Australia (resourceProvider)
Format: Dataset
Language:unknown
Published: Australian Ocean Data Network
Subjects:
biota
oceans
PLANKTON
EARTH SCIENCE
BIOSPHERE
AQUATIC ECOSYSTEMS
PHYTOPLANKTON
BIOLOGICAL CLASSIFICATION
PROTISTS
BACTERIA/ARCHAEA
FLAGELLATES
DINOFLAGELLATES
OCEAN ACIDIFICATION
FLOWCAM
FLOW CYTOMETRY
MICROSCOPES
FIELD INVESTIGATION
LABORATORY
AMD/AU
AMD
CEOS
GEOGRAPHIC REGION &gt
POLAR
OCEAN &gt
SOUTHERN OCEAN &gt
Prydz Bay
CONTINENT &gt
ANTARCTICA &gt
Davis Station
Southern Ocean
Davis-Station
Antarc*
Antarctica
Ocean acidification
Online Access:https://researchdata.edu.au/flow-cytometry-flowcam-comparison-experiment/1330632
https://data.aad.gov.au/metadata/records/AAS_4026_Variance_Experiment
https://data.aad.gov.au/aadc/metadata/citation.cfm?entry_id=AAS_4026_Variance_Experiment
https://data.aad.gov.au/eds/4809/download
https://secure3.aad.gov.au/proms/public/projects/report_project_public.cfm?project_no=AAS_4026
Description
Summary:The minicosm experimental design measured the microbial community growth in six unreplicated fCO2 treatments. Therefore, sub-samples from each minicosm were within-treatment pseudoreplicates and thus, results of statistical analysis must be interpreted conservatively. This data set was collected from two minicosm experiments conducted at Davis Station, Antarctica. 1. Variance experiment - 2013/14 summer season 2. Ocean acidification experiment - 2014/15 summer season It includes: - description of methods for all data collection and analyses. - environmental data logged throughout the experiment; nutrients, temperature, light climate. - flow cytometry counts; autotrophic cells, heterotrophic nanoflagellates, and prokaryotes. - FlowCam counts; individual phytoplankton species data. - microscopy counts; individual phytoplankton species data. The purpose of this data set is to compare the results of three commonly used techniques for microbial community composition and abundance counts.

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