Microsoft Access database containing a compilation of CTD data collected in the Southern Ocean from Australian Antarctic Division (AAD), Antarctic Climate and Ecosystems Co-operative Research Centre (ACE CRC) and Hydrographic Atlas of the Southern Ocean (SOA) data sources. This SOA data contains discrete CTD (Conductivity, Temperature and Depth) station data along with a 1 x 1 degree gridded CTD data set interpolated in space and time. Parameters include pressure, temperature, salinity, dissolved oxygen, nutrients (phosphate, nitrate+nitrite, and silicate). Ocean Tools software developed by AAD is available in conjunction with this database to manipulate, extract and visualise data (including station map, transect selection, xy plots, vertical cross sections, geostrophic velocity/transport calculations). The download file contains an access database of the compiled CTD data, a word document containing further information about the structure of the database and the data (AAD CTD Data.doc), and a folder of the original source data, including readmes providing reference details, and specific information.

From 1991 to 2000 14 voyages have been completed in the Southern Ocean. Measurements of DMS (Dimethylsulfide) and DMSP (Dimethylsulfoniopropionate) have been carried out on surface and subsurface waters together with physical and biological measurements, with a view to understanding the main processes that affect DMS in the Southern Ocean. The first flux measurements have been carried out for DMS (see Curran and Jones 2000) in the last 3 years a concerted study has been carried out in the seasonal ice zone this study aims to identify the major phytoplankton assemblages responsible for DMS and DMSP production in the sea ice zone. It is thought that the sea ice zone also contributes to DMS in the atmosphere. This is being quantified. The fields in this dataset are: Site Date Time (local) Latitude Longitude Snow Cover (metres) Core Length (metres) DMSPt (nano Mols) Chlorophyl a (micrograms per litre) Sea Ice depth (metres) Pigments Fucoxanthin (micrograms per litre) Peridinin (micrograms per litre) 19' hexanoyloxyfucoxanthin (micrograms per litre) Salinity (ppt) Nitrate (micro Mols) Nitrite (micro Mols) Silicate (micro Mols) Phosphate (micro Mols)

Preliminary Metadata record for data expected from ASAC Project 1343 See the link below for public details on this project. Comparative study of the processes controlling carbon export in Southern Ocean environments characterised by a different hydrodynamical and ecological functioning. Work on this project was carried out on Voyage 3 of the Aurora Australis (CLIVAR) of the 2001 and 2002 season. Work at sea target sampling sites were the 8 'particle stations' along the CLIVAR SR3 repeat transect: the SAZ at 47 degrees and 49 degrees S; the SAF at 51 degrees S; the PFZ at 54 degrees S; the IPFZ at 57 degrees S; the SPZ at 59 degrees and 61 degrees S; the SACCF at 63 degrees S and the SSIZ at 64 degrees S. Some of these (64 degrees, 61 degrees and 51 degrees S) were sampled again on the way back to assess temporal evolution. All proxy studies (new production; Ba; delta30Si; 234Th-deficit) were done at each particle station but not necessarily on the same CTD casts. New production assessment Surface water (at 5, 25, 50 and 70m) was sampled with the CTD rosette at all particle stations. Different aliquots of 1L seawater were spiked with 15N-nitrate, 15N-ammonium or 15N-urea. All samples were spiked with 13C-bicarbonate; the latter in order to assess net primary production rates. Incubations (12 H) were done in a thermo stated algal cabinet, using appropriate neutral density screens for samples from depths below 5m. The samples were submitted to a constant light flux of 0.7x10power16 quanta/cm2/sec. Furthermore, samples from 5m depth were amended with increasing doses of ammonium (+0.1 micro M; +0.25 micro M; +0.5 micro M and +1 micro M) having natural 15N/14N abundance to assess susceptibility of N-uptake (ammonium, nitrate, urea) to ammonium. Similar experiments were run for three iron amended and control cultures in collaboration with Pete Sedwick, Dave Hutchins and Phil Boyd. Analysis of ammonium related to the incubation work was done on board by colorimetry. As a side product we obtained ammonium profiles at all particle stations and also six shallow CTD's in the southern part of the transect (greater than 61 degrees S). Suspended particle sampling for trace element analysis and isotopic composition of Si For biogenic-Ba was also carried out. Typically 14 depths were sampled between the surface and 1000m. On board filtration was performed on Nuclepore membranes. These were dried (60 degrees C) and stored for analysis in the shore-based lab. Occasionally, we also sampled large particles - size fractions (greater than 70 micro m and 20 less than 70 micro m) - from the upper 150m for Ba, using the bow pump system of Tom Trull. Ba and Sr incubations on large settling particles sampled with the Snatcher were also performed at 5 particle stations. For delta30Si, all 24 depths of the deep CTD casts at the particle stations 1 to 8 were sampled. Filtered seawater and suspended matter filtered on Nuclepore membranes (dried at 60 degrees C) were saved for later analysis in the home based laboratory. 234Th work - we refer to the report by Ken Buesseler for the major part of this work. In addition we performed some work using the 'Snatcher' Large Volume sampler and sedimentation column. Total 234Th deficit and 234Th activity on particles and solution was assessed at T0 and T4 H after return of the sampling device on board, in an attempt to construct the 234Th mass balance and eventually get at the settling speed (and flux) of 234Th carrying particles. These analyses went together with flow cytometry analyses (collaboration with Clive Crossley) to check for sedimentation by (fluorescent) particles and also with POC and biogenic silica in order to determine the elemental ratios of suspended and sinking particles. Flow cytometer results did not indicate there was significant sedimentation of life cells going on at this time of the year. Dissolved Ba Seawater samples were taken at all depths sampled by deep CTD's during the southward transect. Samples were acidified and kept for later analysis of dissolved barium by isotope dilution ICP-MS. Comparison of the dissolved Ba distribution along the transect with the one reconstructed through a multiple end-member mixing model will help understanding of the relative contribution of in-situ processes (uptake, dissolution) versus conservative mixing, thus improving our understanding of the oceanic Ba biogeochemistry. Analysis New production. Isotope ratio analysis of the 15N and 13C spiked natural plankton samples will be conducted in the home lab., using emission spectrometry and mass spectrometry. Mass balance calculations will allow assessing relative importance of new production as well as the fraction of new production that is in the particulate form and represents the potential for export. Ba and trace elements. Suspended matter samples will be acid digested (HNO3, HCl, HF) and analysed per ICP-MS and ICP-AES for contents of Ba, Ca, Sr, Al, Fe, Mn, Th, U, REE, Ti. The vertical concentration profiles will inform on the latitudinal and temporal variability of the biogeochemical control processes between SAZ, PFZ, ACC and SSIZ subsystems. For the sites with sediment trap deployments, particulate trace element distributions in the water column will be compared with trace element composition of fast settling particles intercepted by the traps. Ba-uptake / barite formation. Isotope ratio analysis (135Ba/138Ba; 86Sr/87Sr) of suspended matter incubated after spiking with 135Ba and 86Sr will be analysed by ICP-MS to investigate on the barite formation process. Abundance and type of barite crystals will be studied by SEM-EMP (mapping + photographs). delta30Si, In the home based lab. particle samples will be extracted using base (NaOH). Silicates in filtered seawater will be precipitated and analysed using a multi collector ICP-sectorial Mass Spectrometer (MC-ICP-MS) once this new method is set up. 234Th. Total, particulate and dissolved 234Th measurements were performed on board using low beta counters. Background (after 6 months decay) and chemical yields will be measured at Ken Buesseler's lab (WHOI, USA), using beta counters and ICP-MS respectively. The worksheets contained in the excel spreadsheet are: Phyo biomass New production and cell counts Particulate barium Dissolved barium d29Si isotope signature of dissolved silicic acid The fields in this dataset are: Carbon Seawater CLIVAR temperature pressure salinity depth barium latitude longitude oxygen silicate phophate nitrate flagellates diatoms picoplankton plankton urea ammonia coccolithophores

This dataset contains CTD (conductivity, temperature, depth) and nutrient (nitrate, nitrite (insignificant concentrations), phosphate, silicate) data obtained from the Second International BIOMASS Experiment (SIBEX II) cruise of the Nella Dan, during January 1985. This cruise is the fourth in a series of six cruises, conducting a long term field survey on krill and other zooplankton. 64 CTD casts were taken in the Prydz Bay region, and nutrient data were collected at 44 of the stations. Casts were made to 1000 m or to near bottom if shallower. Oceanographic and nutrient sampling was done a supplement to the krill research program, and therefore was not always ideal for oceanographic purposes. The fields in this dataset are: cruise name station number date start time ship name station position cast depth sea bottom depth Depth Nitrate Nitrite Phosphate Silicate Manganese (Mn) Pressure Temperature Salinity Sigma-T Specific Volume Anomaly Geopotential Anomaly Number of samples Temperature Deviation Conductivity Deviation This dataset was updated by Angela McGaffin to include a summary excel file. This download file also contains the original datasets.

1.The lakes and ponds in the Larsemann Hills and Bolingen Islands (East-Antarctica) are characterised by cyanobacteria-dominated, benthic microbial mat communities. A 56-lake dataset representing the limnological diversity among the more than 150 lakes and ponds in the region was developed to identify the nature and quantify the effects of the abiotic conditions structuring the cyanobacterial and diatom communities. 2.Limnological diversity in the lakes of the Larsemann Hills and Bolingen Islands is primarily determined by salinity and salinity related variables (concentrations of major ions, conductivity and alkalinity), and variation in lake morphometry (depth, catchment and lake area). Low pigment, phosphate and nitrogen concentrations, and DOC and TOC levels in the water column of most lakes underscore the ecological success of benthic microbial mats in this region. 3.Benthic communities consisted of prostrate, sometimes finely laminated mats, flake mats, epilithic and interstitial microbial mats. Mat physiognomy and chlorophyll/carotenoid ratios were strongly related to lake depth, but not to salinity. 4.Morphological-taxonomic analyses revealed the presence of 27 diatom morphospecies and 34 cyanobacterial morphotypes. Mats of shallow lakes (interstitial and flake mats) and those of deeper lakes (prostrate mats) were characterized by different dominant cyanobacterial morphotypes. No relationship was found between the distribution of these morphotypes and salinity. In contrast, variation in diatom species composition was strongly related to both lake depth and salinity. Shallow ponds are mainly characterised by aerial diatoms (e.g. Diadesmis cf. perpusilla and Hantzschia spp.). In deep lakes, communities are dominated by Psammothidium abundans and Stauroforma inermis. Lakes with conductivities higher than 1.5 mS/cm become susceptible to freezing out of salts and hence pronounced salinity fluctuations. In these lakes Psammothidium abundans and Stauroforma inermis are replaced by Amphora veneta. Stomatocysts were only important in shallow freshwater lakes. 5.Ice cover influences microbial mat structure and composition both directly by physical disturbance in shallow lakes and by influencing light availability in deeper lakes, as well as indirectly by generating salinity increases and promoting the development of seasonal anoxia. 6.The relationship between diatom species composition and salinity and depth is statistically significant. Transfer functions based on these data can therefore be used in paleolimnological reconstruction to infer changes in the precipitation-evaporation balance in continental Antarctic lakes. These data were also collected under the auspices of the Micromat Project, Biodiversity of Microbial mats in Antarctica (see the URL below). The fields in this dataset are: Lake Lake number Location Latitude Longitude Altitude (m) Area (ha) Catchment (ha) Depth (m) Distance from Plateau Distance from Sea Geology Substrate Presence Absence pH Alkalinity Nitrate Nitrite Ammonium Silicate Phosphate Oxygen Salinity Turbidity Conductivity Sodium Potassium Calcium Magnesium Chlorine Sulphur Bicarbonate Hydrocarbonate Total Organic Carbon Dissolved Organic Carbon