Dimethylsulfide and its precursors and derivatives constitute a major sulfate aerosol source. This dataset incorporates the potential for increased UV radiation effects due to stratospheric ozone depletion over spring and summer in Antarctica, using large-scale incubation systems and 13-14 day incubation periods. Surface seawater (200 micron filtered) from the Davis coastal embayment was incubated during four experiments over the 2002-03 Antarctic Summer. The data incorporates seawater measurements of DMS, DMSP and DMSO over a temporal progression during each incubation experiment. Six polyethylene tanks of varying PAR and UV irradiances were incubated. Water was collected stored and analysed by gas chromatography according to a specific sampling protocol, employed by all investigators associated with the project. The data are organised according to analysis day, with each days calibration data displayed at the top of each sheet. The sample code is followed by GC run number and then the raw count data from the GC. This is calculated to nanomoles DMS, DMSP or DMSO. Sample Codes: Codes for temporal data follow format X.XXXX 1st X gives experiment number, 1 to 4. 2nd X gives sampling day, 0, 0.5, 1, 2, 4, 7, 14 (will result in digit code for day no. less than 10 3rd X gives tank number relating to irradiance level(one to six) 4th and 5th X is replicate number, (01, 02, 03, DMS), (04, 05,06, DMSP total), (07, 08, 09, DMSP dissolved), (10, 11, 12, DMSO total). The fields in this dataset are: Sample Code Run Number from the GC Counts - GC generated raw data Log Counts - logarithmic conversion of the count data Log -c - logarithmic conversion minus the y-intercept determined by calibration of the GC. (log -c)/m - log -c divided by m, determined by calibration of the GC. ngS anti log - nanograms of Sulfur NaOH - NaOH adjustment ngS/L - adjustment per litre nM-DMSP/L - nanoMol's DMSP per litre nm-DMS/L - nanoMol's DMS per litre September 2013 Update: DMSO was analysed in these experiments according to an adaptation of the sodium borohydride (NaBH4) reduction method of Andreae (1980). The method has since been superseded and the data here probably displays inaccuracies as a result of the analytical method used. This DMSO data should be treated with caution.

Ozone depletion over Antarctica increases UVB irradiances reaching the Earth's surface in the region. Marine microbes, that support the Antarctic food web and play an integral part in carbon cycling, are damaged by UVB. This research determines Antarctic UV climate, biological responses to UV from the molecular to community level, and combines these elements to predict UV-induced changes in Antarctic marine microbiology. A season of field work was undertaken over November and December 1994 based from Davis Station with the intention of making field measurements of ultraviolet radiation in the fast ice environment, as well as some of the lakes in the Vestfold Hills. Instrumentation The instrument for the measurements was a Macam spectral radiometer, owned by Geography and Environmental Studies, University of Tasmania. Field personnel were Dr Kelvin Michael (IASOS) and Mr Michael Wall (Honours student, Geography and Environmental Studies, UTas). The radiometer was equipped with a 25-metre quartz light pipe, with a cosine sensor attachment at the end. To make a measurement of ultraviolet irradiance, the sensor would be oriented so that its sensing surface was horizontal, and it would collect light which was then transmitted along the light pipe to the radiometer - a suitcase-sized unit which ran on battery power in the field. The radiometer was encased in a wooden box lined with polystyrene foam to provide protection from the elements and heat insulation. The radiometer was controlled via a laptop PC and the data were stored on the hard disk of the PC. Measurements Measurements of the attenuation of ultraviolet and visible radiation as a function of wavelength in water were made at the ice edge and lake measurement sites. At the ice edge, the light pipe was spooled over a wheel and lowered to preset depths (typically 1,2,4,8,16 and 32 m below the water surface). On a lake, a 25-cm augur hole was drilled, and the light pipe was lowered by hand to various depths, the exact depths chosen depended on the depth of the lake. Where the lake ice conditions permitted, a frame was lowered through the hole and used to lever the light pipe against the underside of the ice and a measurement of the ultraviolet and visible transmission of the sea ice was collected. In all cases, measurements of the ultraviolet and visible surface irradiance were collected before and/or after the sub-surface measurements. When the sky conditions were sufficiently clear, the direct and diffuse components of the ultraviolet and visible irradiance values were estimated, via the use of a shading apparatus. This would ensure that the radiometer would measure the diffuse component of the radiation field, allowing the direct component to be estimated by subtraction of the diffuse from the global (unshaded) measurement. On some occasions, the upwelling irradiance from the snow or ice surface was also measured, providing information on the spectral albedo of the surface. At each measurement, spectral irradiance values were generally collected for two spectral ranges: UV-B (280 - 400 nm, in 1-nm steps) and visible (400 - 700 nm, in 5-nm steps). In some cases, the wavelength boundaries were different - eg 280 - 350 nm for the UV-B, or 550 - 680 nm in the visible (corresponding to channel 1 of the NOAA AVHRR sensor). The data were stored by the PC as raw data files. The names of these files are automatically defined from the time on the logging PC as 'hhmmss.dti'. Note that the PC was operating on Australian Eastern Summer Time, 4 hours ahead of DLT. These data files were later read into Excel spreadsheets for manipulation. See the linked report for further information. The measurements are all in units of watts per metre squared per nanometre (Wm^-2 nm_-1) The heading UV-B refers to the fact that the data are collected in the ultraviolet part of the spectrum (280 - 400 nm) The heading AVHRR refers to the fact that the data are collected in the visible part of the spectrum (400 - 700 nm) The fields in this dataset are: UV Radiation Wavelength Depth AVHRR

From the abstract of some of the papers: It has been suggested that increased springtime UVB radiation caused by stratospheric ozone depletion is likely to reduce primary production and induce changes in the species composition of Antarctic marine phytoplankton. Experiments conducted at Arthur Harbour in the Antarctic Peninsula revealed a reduction in primary productivity at both ambient and increased levels of UVB. Laboratory studies have shown that most species in culture are sensitive to high UVB levels, although the level at which either growth or photosynthesis is inhibited is variable. Stratospheric ozone depletion, with resultant increased springtime UVB irradiance, has been occurring with increasing severity since the late 1970's. Thus the phytoplankton community has already experienced about 20 years' exposure to increasing levels of UVB radiation. Here we present analyses of diatom assemblages from high-resolution stratigraphic sequences from anoxic basins in fjords of the Vestfold HIlls, Antarctica. We find that compositional changes in the diatom component of the phytoplankton community over the past 20 years cannot be distinguished from long-term natural variability, although there is some indication of a decline in the production of some sea-ice diatoms. We anticipate that our results are applicable to other Antarctic coastal regions, where thick ice cover and the timing of the phytoplankton bloom protect the phytoplankton from the effects of increased UVB radiation. Growth rate, survival, and stimulation of the production of UV-B (280 to 320 nm) absorbing compounds were investigated in cultures of five commonly occurring Antarctic marine diatoms exposed to a range of UV-B irradiances. Experimental UV-B exposures ranged from 20 to 650% of the measured peak surface irradiance at an Antarctic coastal site (0.533 J per square metre per second). The five diatom species (Nitzschia lecointei, Proboscia alata, P. inermis, Thalassiosira tumida and Stellarima microtrias) appear capable of surviving two to four times this irradiance. In contrast to Phaeocystis cf. pouchetti, another major component of the Antarctic phytoplankton, the concentrations of pigments with discrete UV absorption peaks in diatoms were low and did not change significantly under increasing UV-B irradiance. Absorbance of UV-B by cells from which pigments had been extracted commonly exceeded that of the pigments themselves. Most of this absorbance was due to oxidisable cell contents, with the frustule providing the remainder. Survival of diatoms did not correlate with absorption by either pigments, frustules or oxidisable cell contents, indicating that their survival under elevated UV-B irradiances results from processes other than screening mechanisms. Springtime UV-B levels have been increasing in Antarctic marine ecosystems since the 1970's. Effects on natural phytoplankton and sea-ice algal communities, however, remain unresolved. At the Marginal Ice Edge Zone, enhanced springtime UV-B levels coincide with a shallow, stratified water column and a major phytoplankton bloom. In these areas it is possible that phytoplankton growth and survival is adversely impacted by enhanced UV-B. In coastal areas, however, the sea ice, which attenuates most of the UV-B before it reaches the water column, remains until December/January, by which time UV-B levels have returned to long-term seasonal averages. Phytoplankton from these areas are unlikely to show long-term changes resulting from the hole in the ozone layer. Fjords of the Vestfold Hills, eastern Antarctica, have anoxic basins which contain high-resolution, unbioturbated sedimentary sequences. Diatom assemblages from these sequences reflect the diatom component of the phytoplankton and sea-ice algal assemblages at the time of deposition. Twenty-year records from these sequences show no consistent record of change in species composition, diversity or species richness. Six-hundred-year records from the same area also show changes in species abundance greater than those seen in the last 20 years. From these records it can be seen that recent changes in diatom abundances generally fall within the limits of natural variability and there is little evidence of recent changes that might be associated with UV-B-induced change.

Minicosm design: Three successive experiments to a maximum incubation of 14 days were performed from mid November to early January in the summer of 2002/03 in a temperature controlled shipping container housing six 500 L polythene tanks or minicosms. Domes of UV transmissive PMMA in the roof of the container directly above the minicosms allowed ambient sunlight to be reflected to the tanks through tubes of anodised aluminium. These tubes reflected greater than 96% of the incident radiation irrespective of wavelength. Light perturbation to each minicosm was achieved by screening materials that attenuated UV wavelengths. UV stabilised polycarbonate removed wavelengths shorter than 400 nm, transmitting only photosynthetically active radiation (PAR) and provided the control treatment (PAR). In minicosm 2, a mylar screen removed UVB wavelengths (280 - 320 nm), providing a treatment (UVA) with PAR and UVA. Minicosms 3, 4 and 5 (UVB1, 2 and 3 respectively) were screened by borosilicate glass of 9, 5, and 3 mm thickness, transmitting ambient light (including UVR) at the equivalent water depths (ED, k=0.4) of 7.15, 5.38 and 4.97 meters respectively. Minicosm 6 (UVB4) was screened with PMMA that transmitted ambient light at an ED of 4.43 m. Light measurements: Measurements of downwelling UV and PAR were obtained using biometer and Licor sensors mounted on the roof of the minicosm container. A Macam, double grating spectroradiometer measured the spectral irradiance on the roof of the container. This was then weighted with the erythemal action spectrum and correlated to that obtained by the UV biometer. The Macam was used to measure the spectral irradiance at the cross of the UV biometer. The spectral intensity of light wavelengths were measured laterally and vertically in the minicosm screened only by UV-transmissive PMMA irradiance. These measurements were used to model the light field within the minicosm. In all other light treatments the Macam measured the spectral irradiance immediately below the water surface and in the centre of the minicosm. The model was then used to predict the spectral distribution and intensity of other light treatments. These measurements were repeated at interval throughout the season to determine whether solar elevation influenced transmission of ambient downwelling irradiance to the minicosms. UV and PAR sensors fixed to the outside of the minicosm container, together with the modelled light climates within each minicosm beneath each light treatment, predicted the quantify the light to which each experimental treatment was exposed. This work was conducted as part of ASAC project 2210. The download file contains three excel spreadsheets, plus three accompanying word documents which provide detailed methods used in the collection of these data, plus more information about the experiments. The fields in this dataset are: Day Treatment UVA UVB PAR - photosynthetically active radiation

Minicosm design: Three successive experiments to a maximum incubation of 14 days were performed from mid November to early January in the summer of 2002/03 in a temperature controlled shipping container housing six 500 L polythene tanks or minicosms. Domes of UV transmissive PMMA in the roof of the container directly above the minicosms allowed ambient sunlight to be reflected to the tanks through tubes of anodised aluminium. These tubes reflected greater than 96% of the incident radiation irrespective of wavelength. Light perturbation to each minicosm was achieved by screening materials that attenuated UV wavelengths. UV stabilised polycarbonate removed wavelengths shorter than 400 nm, transmitting only photosynthetically active radiation (PAR) and provided the control treatment (PAR). In minicosm 2, a mylar screen removed UVB wavelengths (280 - 320 nm), providing a treatment (UVA) with PAR and UVA. Minicosms 3, 4 and 5 (UVB1, 2 and 3 respectively) were screened by borosilicate glass of 9, 5, and 3 mm thickness, transmitting ambient light (including UVR) at the equivalent water depths (ED, k=0.4) of 7.15, 5.38 and 4.97 meters respectively. Minicosm 6 (UVB4) was screened with PMMA that transmitted ambient light at an ED of 4.43 m. Light measurements: Measurements of downwelling UV and PAR were obtained using biometer and Licor sensors mounted on the roof of the minicosm container. A Macam, double grating spectroradiometer measured the spectral irradiance on the roof of the container. This was then weighted with the erythemal action spectrum and correlated to that obtained by the UV biometer. The Macam was used to measure the spectral irradiance at the cross of the UV biometer. The spectral intensity of light wavelengths were measured laterally and vertically in the minicosm screened only by UV-transmissive PMMA irradiance. These measurements were used to model the light field within the minicosm. In all other light treatments the Macam measured the spectral irradiance immediately below the water surface and in the centre of the minicosm. The model was then used to predict the spectral distribution and intensity of other light treatments. These measurements were repeated at interval throughout the season to determine whether solar elevation influenced transmission of ambient downwelling irradiance to the minicosms. UV and PAR sensors fixed to the outside of the minicosm container, together with the modelled light climates within each minicosm beneath each light treatment, predicted the quantify the light to which each experimental treatment was exposed. This work was conducted as part of ASAC project 2210. The download file contains three excel spreadsheets, plus three accompanying word documents which provide detailed methods used in the collection of these data, plus more information about the experiments. The fields in this dataset are: Day Treatment Carbon Hydrogen Nitrogen C:N ratio

This is a parent metadata record for work carried out as part of ASAC/AAS project 40. See the child metadata records for further information. More than 95% of the biomass in the Southern Ocean is microscopic - single celled plants, animals, bacteria and viruses. We are studying the factors that control their distribution and abundance - oceanographic and seasonal conditions, their physiology, and grazing - in order to model their vital roles as food for other organisms and their influence in moderating global climate change through absorption of CO2 and production of DMS. We are also addressing the changes expected in microbial communities through effects of climate change - global warming, sea ice retreat, ocean acidification and enhanced ultraviolet radiation. This project aims to determine the role of microorganisms in the Southern Ocean. The major objectives are to: * Identify and quantify key protistan components of the Southern Ocean ecosystem and study their autoecology. * Identify environmental and ecological processes that control abundance of key microbial components. * Determine interactions between key microbial components to quantify major pathways of carbon flow. * Determine the activity and viability of bacterioplankton and protists in the Southern Ocean. * Distinguish different microbial communities by identifying key taxa and associations so that processes such as primary production, respiration, grazing and particle flux can be readily parameterised in ecological models. * Determine the effect of elevated CO2 concentrations on microbial populations and processes. Taken from the 2008-2009 Progress Report: Progress against objectives: 1. Ongoing sampling from Astrolabe has continued, with 3 return voyages being sampled for phytoplankton species, chlorophyll a and other pigments, coccolithophorid counts and DNA profiles, in conjunction with measurements of CO2, ocean structure, fluorescence and ocean colour by CSIRO / CRC colleagues. 2. Three sets of minicosm experiments were conducted at Davis station with 7 staff spending 4.5 - 5.5 months on site. These experiments consistently found that acidification caused blooms of nanoplanktonic diatoms and increased bacterial activity, apparently by inhibition of microheterotroph grazers, at the expense of larger cells that are more readily ingested by grazers such as krill. We showed for the first time in Antarctic waters that pCO2 affects the structure and function Antarctic microbial communities in a way that may reduce food availability to large grazers. Over 100 cultures of "winners and losers" from such experiments were isolated and returned to Australia. These will form the basis for further physiological experiments including molecular assays. 3. Submission and acceptance of 8 papers from the BROKE-West cruise (5 as senior author). These showed the interactions between bottom-up (micronutient) top-down (grazing) control in structuring microbial populations in the marginal ice zone. Five biogeographic zones were identified on the basis of species composition, and the productivity was measured for each zone. Microzooplankton grazing experiments found that grazing within that microbial loop consumed a significant proportion of new productivity. In some areas later in the season, all productivity was consumed by microheterotrophs, rather than metazoans such as krill. A time sequence was identified for seeding and development of components of ice edge blooms, subsequent grazing and decline and a mechanism postulated for export of micronutrients (e.g. iron) by grazing and sedimentation that prevents subsequent development of surface water blooms and constrains populations to a deep chlorophyll maximum below the level of a nutricline. 4. Detailed analysis of greater than 30 strains of keystone species Emiliania huxleyi of two morphotypes in conjunction with Clara Hoppe (Masters student, Alfred Wegener Institute) and Suellen Cook (PhD student, University of Tasmania) showed consistent differences between strains in terms of pigmentation, responses to light and genetics. The two morphotypes appear to be adapted to different mixing regimes north and south of the Polar Front; the southern form may represent a new species. For a full list of references associated with this project, see the project link at the provided URL.

Increased ultraviolet radiation (UV-A and/or UV-B) may impact on the establishment and structure of a shallow water benthic invertebrate assemblages. A global experiment in more than 8 countries, using an identical methodology (transparent UV filters) will add significantly to our understanding of the impacts of anthropogenically induced global change on natural systems. To appraise the effects of increased UVR on shallow marine benthic assemblages, five experimental rafts were deployed in protected bays west of Shirley Island near Casey Station, Antarctica (66.16oS 110.30oE). Each raft consisted of eight experimental units, each of which contained a colonization panel (ceramic tile) positioned horizontally and submerged 4-6 cm underwater. Irradiation treatments were randomly assigned to each unit with the use of UV cut-off filters. The treatments were as follows: No UVR (transmits photosynthetically active radiation or PAR, 400-700nm), No UVB (transmits PAR + UVA, 320-700nm), Perspex (full spectrum, 280-700nm, procedural control), or No filter (full spectrum, treatment control). In addition there were three levels of consumer treatments: With consumption (container sides removed), without consumption (container sides perforated with 4 mm holes), and a control (3 sides perforated, 1 side removed). After seven weeks tiles were removed to the laboratory for examination. All tiles were dominated by diatoms and no sessile invertebrates were apparent. The first trial has been completed, but several other panels are still in place. A conference will be held in early 2002 between participating countries to discuss results and findings. The 2001\2002 summer season consisted of experimental designs divided up into three separate projects. The aims were all to provide a corrollary to the previous seasons data. Project 1 consisted of the extraction and redeployment of settlement depth arrays situated in Geoffrey's Bay and Hollin Island Channel. Due to prevailing weather conditions resulting in limited boating hours and diving program, only one array was retrieved. On inspection of the array it was decided to deploy further replicates to gain a better temporal understanding of the communities. Projects 2 and 3 consisted of a similar experimental design, however monitoring the shallower depths of settlement (depths of 1m and 2m below sea level) for a period of one month. Project 2 consisted of arrays with two depths and 2 panels per depth, triple replicated, under the icesheet in O'Brien Bay and Shirley Channel, with a substrate depth of 20m. Diatom samples are to be analyzed in Australia. Project 3 was of a similar design to project 2 though it was measuring recruitment in shallow open water. The two sites consisted of Noonan Cove and Geoffrey's Bay at substrate depths of 5m. These tiles are also to be analyzed on return to Australia. There were 5 rafts used in this study - they are listed as R1 to R5 there were two factors in the design -(i) predator access: Caged (C) Half caged (H) and Open (O) and ii) UV exposure: Perspex (P), Macrolon (M), No filter (N) and Film + perspex (F). A list of the diatoms found on the settlement panels is provided at the URL below. The fields in this dataset are: Species Sample