Cape Darnley Early-Autumn Phytoplankton Bloom, March 2012

Progress Code: completed Statement: We were only able to obtain samples through the uncontaminated seawater line, with the intake positioned at 4.8 m below the ship. However, we think the majority of the bloom was at the surface associated with ice. Our data therefore likely under-represents the tru...

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Bibliographic Details
Format: Dataset
Language:unknown
Published: Australian Ocean Data Network
Subjects:
AMD
Online Access:https://researchdata.edu.au/cape-darnley-early-march-2012/2816271
Description
Summary:Progress Code: completed Statement: We were only able to obtain samples through the uncontaminated seawater line, with the intake positioned at 4.8 m below the ship. However, we think the majority of the bloom was at the surface associated with ice. Our data therefore likely under-represents the true surface phenomenon. 2018-10-10 The original files was reformatted to fit OBIS/GBFI/IPT Biodiversity.AQ tracking standards, and a new datasheet "CapeDarnelyBloom_2012.csv" was created. The new dataset contains datasetID, occurrenceID, recordNumber, verbatimLatitude, verbatimLongitude, decimalLatitude, decimalLongitude, locationID, locality, eventRemark, eventDate, year, month, basisOfRecord, occurrenceStatus, organismQuantity, organismQuantityType, preparations, institutionCode, continent. The lowest taxonomical rank of the species identified that could be determined is provided, after matched in WoRMS (World Register of Marine Species). These data relate to a large-scale early-autumn phytoplankton bloom that occurred off Cape Darnley, East Antarctica, in March 2012. The bloom was detected by Dr Jan Lieser (Antarctic Climate and Ecosystems Cooperative Research Centre, ACE-CRC) through MODIS satellite and was opportunistically sampled from RSV Aurora Australis using the uncontaminated seawater line. Samples were analysed for protist species and abundances using light and scanning electron microscopy, and pigment analyses were conducted using high performance liquid chromatography. Additional water samples were taken for dissolved nutrient analyses. Specific details of the files are: Cape Darnley Protist Counts Samples were preserved with 1 % vol:vol Lugols iodine and stored in glass bottles in the dark at 4 degrees C. Protists were identified and counted using phase and Nomarski interference optics using Olympus IX71 and IX81 inverted microscopes at 400X to 640X magnification. Bright field optics were also used to discriminate taxa that contained chloroplasts. Protistan taxa were counted in 20 randomly chosen ...