The CSIRO Global Atmospheric Sampling Laboratory (GASLAB) Flask Sampling Network archive for the carbon 13 isotope (C13) of atmospheric trace gas carbon dioxide (CO2) concentrations. GASLAB principally analyzes air samples that have been captured at eleven fixed geographic sites and one moving (aircraft over bass strait and Cape Grim), but also includes other sites at various locations globally on a less regular or as needed basis. The CO2C13 measurements are made by concentrating the CO2 from the air sample utilising a 3 step automated cryogenic trapping system connected to a dual inlet stable isotope ratio mass spectrometer (Finnigan MAT252) for analysis. The CO2 and N2O gas chromatography concentrations data for the sample are used for ion corrections on the stable isotope measurements. Alternatively the Cape Grim in situ air sample (cia) which has already had the trapping process applied to it on site, uses the data from the Cape Grim in situ CO2 analyser, with the N2O concentration determined by interpolation from the CSIRO global flask network data. There are 6 differant types of flask that are used to store and transport air samples from site and in the labratory:(i) glass 0.5 litre ("G050"), (ii) glass 5.0 litre ("G500"), (iii) glass 0.8 litre ("G080"), (iv) electropolished stainless steel 1.6 litre "Sirocans" ("S160"), (v) glass 2.0 litre, 1 stopcopck ("F", "FF", "FA", "FE", "EP", ALT"), (vi) glass 2.0 litre, 2 stopcocks(“M1”, “S”, “P2”, “TEMP”). Files containing a single species value for each sample are denoted by a filename of the form (XXX_XXXX_event.XXX), for the geographically fixed sites data is also provided in the form of monthly means (e.g. XXX_XXXX_mm.XXX) with all files being in ascii format.

The CSIRO Global Atmospheric Sampling Laboratory (GASLAB) Flask Sampling Network archive for the oxygen 18 isotope (O18) of atmospheric trace gas carbon dioxide (CO2) concentrations. GASLAB principally analyzes air samples that have been captured at eleven fixed geographic sites and one moving (aircraft over bass strait and Cape Grim), but also includes other sites at various locations globally on a less regular or as needed basis. The CO2O18 measurements are made by concentrating the CO2 from the air sample utilising a 3 step automated cryogenic trapping system connected to a dual inlet stable isotope ratio mass spectrometer (Finnigan MAT252) for analysis. The CO2 and N2O gas chromatography concentrations data for the sample are used for ion corrections on the stable isotope measurements. Alternatively the Cape Grim in situ air sample (cia) which has already had the trapping process applied to it on site, uses the data from the Cape Grim in situ CO2 analyser, with the N2O concentration determined by interpolation from the CSIRO global flask network data. There are 6 differant types of flask that are used to store and transport air samples from site and in the labratory:(i) glass 0.5 litre ("G050"), (ii) glass 5.0 litre ("G500"), (iii) glass 0.8 litre ("G080"), (iv) electropolished stainless steel 1.6 litre "Sirocans" ("S160"), (v) glass 2.0 litre, 1 stopcopck ("F", "FF", "FA", "FE", "EP", ALT"), (vi) glass 2.0 litre, 2 stopcocks(“M1”, “S”, “P2”, “TEMP”). Files containing a single species value for each sample are denoted by a filename of the form (XXX_XXXX_event.XXX), for the geographically fixed sites data is also provided in the form of monthly means (e.g. XXX_XXXX_mm.XXX) with all files being in ascii format.

This is a biological overview of data collected on Southern Surveyor voyage SS 09/2004. The voyage took place off the east coast of Queensland in September 2004. This dataset will be processed and archived within the CSIRO Marine and Atmospheric Research Data Centre in Hobart. Additional information regarding this dataset is contained in the cruise report for this voyage and/or the data processing report. For micronekton and zooplankton prey data contact Jock Young, acoustic biomass data was collected and stored by Rudy Kloser. The Phytoplankton biomass and speciation was processed by Lesley Clementson. The Stomach content data is in an ACCESS database, contact Jock Young. Mark Lewis has video from voyage and photographs of deck shots & equipment used during the voyage.

Process Study 2 was undertaken between 20-22 September 2005 in the Huon Estuary offshore from Hideaway Bay. During this Process Study, two sediment traps were deployed at each of two sites (near sites P3 and P4 from the spatial survey) on the bottom for 24 hours.Prior to the deployment of the traps surface sediment samples were collected with a benthic grab from each site. Each sediment trap consisted of three collection tubes, material from each tube was filtered on 47 mm GFF filters, with several filters required to filter all of the particualte matter from each tube. Combined filters from each of two tubes labeled A and B (typically 3 filters for each tube) were extracted for lipid analysis. Tube C was used either for isotopes or Fauna indent.

Process Study 3 was undertaken between 03-05 October 2006 in North West Bay. Sediment traps were deployed and sediment samples taken at five sites in NWB. The primary aim was to investigate the composition of material being deposited to the sediments from the water column at these times and to compare this organic matter with that found in the sediments at the same sites. Additionally, we wished to see whether any organic matter of obvious fish farm origin could be detected. One sediment trap was deployed at each North West Bay (NWB) site in water varying in depth from 10 m (site 9) to 20 m (site 2). The trap sites were numbered 2, 4, 5, 7, and 9. Traps were deployed at their respective sites and left for at least one hour before the caps were removed in order to eliminate sediment re-suspended during deployment from entering the traps. The traps were left in place for 48 hours and then retrieved, capped and returned to Hobart for recovery of the samples. Each trap had 3 tubes, each of these tubes was split into three. One litre was taken and filtered for lipids using pre-weighed 47 mm GFF filters, one litre for pigments and the rest was split in two and stored in 500ml bottles, one for zooplankton analysis and the other for microalgal samples. Several filters were required to filter the lipid sample depending on the amount of particles in the tube. Selected filters were then analysed for lipid biomarkers. Organic matter from selected filters was also analysed for stable isotope 13C and 15 N values and carbon content. The contents of one tube from each trap was inspected for identification of zooplankton remains and faecal pellets using light microscopy. Sediments were collected at each of the above trap sites using a Wilco box corer.

Process Study 1 was undertaken between 12-14 April 2005 in the Huon Estuary offshore from Hideaway Bay. During this Process Study, two sediment traps were deployed at each of two sites (near sites P3 and P4 from the spatial survey) on the bottom for 24 hours.Prior to the deployment of the traps surface sediment samples were collected with a benthic grab from each site. Each sediment trap consisted of three collection tubes, material from each tube was filtered on 47 mm GFF filters, with several filters required to filter all of the particualte matter from each tube. Combined filters from each of two tubes labeled A and B (typically 3 filters for each tube) were extracted for lipid analysis. Tube C was used either for isotopes or Fauna indent.

This dataset contains data from pollution monitoring in Jervis Bay, NSW. The data were obtained from various sites around Jervis Bay at different times between October 1988 and July 1991. Samples for trace metals from sediments were determined, together with grain size. Mercury in the tissues of Red morwong (Cheilodactylus fuscus), Oysters (Ostrea angasi), Mussels (Trichomya hirsuta) and heavy metals in the leaves of Posidonia australis and Zostera sp. were determined. Organochlorides and hydrocarbons from sediments, water column and biota were also determined. Tributyl tin experiments were conducted in tanks. The data are part of the Jervis Bay Marine Ecological Study. NB - As the database has been lost, the only data still available are those published in the JERVIS BAY BASELINE STUDIES Final Report.

The content and composition of the oil from nearly 200 species of Australian fish, shellfish and crustaceans were examined. The nutritional value of Australian species was determined with respect to oil composition, as was how oil content may differ with geographical region, taxonomic group and other factors. This knowledge has been transferred, in various formats, to the Fishing Industry, nutritionists and other consumer groups to better utilize the total catch, including waste products.