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  • These are phytoplankton pigment datasets collected on the BROKE voyage of the Aurora Australis during the 1995-1996 summer season. The readme file in the data download states: Data supplied by Dr Simon Wright. Details phytoplankton pigment data from BROKE. "BROKEPIGDBase.xls Contains 5 worksheets. 'Notes' repeats the information presented here. 'Key' describes the column headings, chemical names. 'Raw_Data' is the exact spreadsheet receieved from Dr Wright. 'Standard_sample_source' contains all the phyto-chemical data as taken from the CTD programme. 'Non_standard_sample_source' contains phyto-chemical data that seems to have been collected opportunistically, to test some assumptions. The details of the locations of the opportunistic samples are detailed in the column 'Sample_source'. Note- it is unsure whether the numbers in the CTD column describe the Station Number. This has to be verified. Converted into a MS Access database- 'BROKE_phytoplankton.mdb' by Natalie Kelly. This database contains 3 tables. One is a description of the column names, chemical etc. The other two contain both the Standard and Non-Standard Sample source phytochemical data. Natalie Kelly 19 November 2005"

  • The data reports the pigment concentrations and results of CHEMTAX analysis for 2 summer seasons in Antarctic. In 2008/09 three experiments in which 6 x 650 l minicosms (polythene tanks) were used to incubate natural microbial communities (less than 200 um diameter) at a range of CO2 concentrations while maintained at constant light, temperature and mixing. The communities were pumped from ice-free water ~60 m offshore on 30/12/08, 20/01/09 and 09/02/09. These experiments received no acclimation to CO2 treatment. A further experiment was performed in 2014/15 using water helicoptered from ~ 1 km offshore amongst decomposing fast ice on 19/11/14. This experiment included a 5 day period during which the community was exposed top low light and the CO2 was gradually raised to the target value for each tank, followed by a two day period when the light was raised to an irradiance that was saturating but not inhibitory for photosynthesis. A range of coincident measurements were performed to quantify the structure and function of the microbial community (see Davidson et al. 2016 Mar Ecol Prog Ser 552: 93–113, doi: 10.3354/meps11742 and Thomson et al 2016 Mar Ecol Prog Ser 554: 51–69, 2016, doi: 10.3354/meps11803). The data provides a matrix of samples against component pigment concentration and the output from CHEMTAX that best explained the phytoplankton composition of the community based on the ratios of the component pigments. For the 2008/09 experiments, samples were obtained every 2 days for 10, 12 and 10 days in experiments 1, 2 and 3 respectively. In 2014/15 samples were obtained from each incubation tank on days 1,3, 5, and 8 during th acclimation period and every 2 days until day 18 thereafter. For each sample a measured volume was filtered through 13 mm Whatman GF/F filters for 20 mins. Filters were folded in half, blotted dry, and immediately frozen in liquid nitrogen for analysis in Australia. Pigments were extracted, analysed by HPLC, and quantified following the methods of Wright et al. (2010). Pigments (including Chl a) were extracted from filters with 300 micro l dimethylformamide plus 50 micro l methanol, containing 140 ng apo-8'-carotenal (Fluka) internal standard, followed by bead beating and centrifugation to separate the extract from particulate matter. Extracts (125 micro l) were diluted to 80% with water and analysed on a Waters HPLC using a Waters Symmetry C8 column and a Waters 996 photodiode array detector. Pigments were identified by comparing retention times and spectra to a mixed standard sample from known cultures (Jeffrey and Wright, 1997), run daily before samples. Peak integrations were performed using Waters Empower software, checked manually for corrections, and quantified using the internal standard method (Mantoura and Repeta, 1997).

  • This dataset contains chlorophyll a data collected by the Aurora Australis on Voyage 6, 1997-1998 - the SAZ (Subantarctic Zone) cruise. Samples were collected in March of 1998. These data were collected as part of ASAC project 40 (The role of antarctic marine protists in trophodynamics and global change and the impact of UV-B on these organisms).

  • This dataset is derived from sediment trap records collected by Thomas Trull as part of the multidisciplinary SAZ Project initiated in 1997 by the Antarctic Cooperative Research Centre (ACE CRC) (Trull et al 2001b). The current submission provides data not included in Wilks et al. (submitted) 'Biogeochemical flux and phytoplankton assemblage variability: A unique year-long sediment trap record in the Australian Sector of the Subantarctic Zone.' This dataset contains three parts: Supplementary Table 1 describes sediment trap deployment information and current speed measured during deployment. Supplementary tables 2a and 2b are raw diatom counts of every species encountered at the site, at every sampling cup. Table 2a contains the 500 m trap depth record, while table 2b is for the 2000 m trap depth record. Supplementary table 3 contains environmental data (chlorophyll-a, photosynthetically active radiation, and sea surface temperature) for each cup record.

  • The ASPeCt - Bio dataset is a compilation of currently available sea ice chlorophyll a (chl-a) data from pack ice (i.e., excluding fast ice) cores collected during 32 cruises to the Southern Ocean sea ice zone from 1983 to 2008 (Table S1). Data come from peer-reviewed publications, cruise reports, data repositories and direct contributions by field-research teams. During all cruises the chl-a concentration (in micrograms per litre) was measured from melted ice core sections, using standard procedures, e.g., by melting the ice at less than 5 degrees C in the dark; filtering samples onto glassfibre filters; and fluorometric analysis according to standard protocols [Holm-Hansen et al., 1965; Evans et al., 1987]. Ice samples were melted either directly or in filtered sea water, which does not yield significant differences in chl-a concentration [Dieckmann et al., 1998]. The dataset consists of 1300 geo-referenced ice cores, consisting of 8247 individual ice core sections, and including 990 vertical profiles with a minimum of three sections. An updated dataset was provided in 2017-12-15, which included a compilation Net CDF file.

  • This dataset contains the chlorophyll a data from Voyage 6 (FISHOG) 1991-92 of the Aurora Australis. The observations were taken from the Heard Island area in January and February 1992. These data were collected as part of ASAC project 40 (The role of antarctic marine protists in trophodynamics and global change and the impact of UV-B on these organisms).

  • Chlorophyll a data collected on the AAMBER II cruise of the Aurora Australis from January to March of 1991. The voyage traveled to the Prydz Bay region, and data were collected en route and in the area.

  • This study employs data from two satellite-borne instruments namely, the Sea-Viewing Wide Field-of-view Sensor (SeaWiFS) and the Total Ozone Mapping Spectrometer (TOMS). This work was completed as part of an honours project under ASAC project 2210 (UV climate over the Southern Ocean south of Australia, and its biological impact). Further information about the project is available in the word document available for download (extract from the honours thesis). The fields in this dataset are: Region Year Day (Julian Day) Pixels (number of cloud free pixels from SeaWiFS sensor that were available for analysis) Mean Chlorophyll (milligrams per cubic metre) (derived from cloud free pixels) Standard Deviation Ozone (dobson units) from the TOMS sensor (average for whole region).

  • This dataset contains chlorophyll a data collected by the Aurora Australis on Voyage 7, 1992-1993 - the WOES (Wildlife Oceanography Ecosystem Survey) cruise. Samples were collected from March-May of 1993. These data were collected as part of ASAC project 40 (The role of antarctic marine protists in trophodynamics and global change and the impact of UV-B on these organisms).

  • This dataset contains chlorophyll a data collected by the Aurora Australis on Voyage 7 1992-93, taken in the Prydz Bay region between January and February 1993. These data were collected as part of ASAC project 40 (The role of antarctic marine protists in trophodynamics and global change and the impact of UV-B on these organisms).