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    Parks Australia - Our Marine Parks Grants Round 2 Project: Nearshore marine habitat mapping of the Norfolk Marine Park (Grant Activity ID: 4-FIZ391E) The Norfolk Marine Park is the is the eastern-most Park in the Temperate East Network of Australian Marine Parks, located between the NSW coast and Norfolk Island. The Park encompasses 188,444 km² of ocean and ranges in depth from 0 m at the Norfolk Island high tide mark to more than 5,00 m off the edge of the Norfolk Ridge. The Park includes two key ecological features – the Norfolk Ridge, and the Tasman Front and associated eddy field – both of which are valued for their high productivity, aggregations of marine life, biodiversity, and endemism. Norfolk Marine Park supports a range of species, including those listed as threatened under the Environment Protection and Biodiversity Conservation (EPBC) Act (1999), and contains Biologically Important Areas for breeding, foraging, and migration of seabirds, marine turtles, and humpback whales. The objective of this project was to create the first marine habitat map for the nearshore shallow water surrounding Norfolk, Nepean, and Phillip Islands. This was conducted in collaboration with Norfolk residents to provide local knowledge input and to ground-truth the remotely-sensed habitat mapping. This high-level habitat map will be used for planning purposes, development applications, and EPBC Act referrals within the nearshore waters of the Norfolk Marine Park, where no specific zoning for recreational and commercial activities currently exists. The map provides a basis for any ongoing citizen-science-driven marine habitat impact and condition assessments, ecosystem monitoring, and to provide the Norfolk Island residents with ownership of any future zoning planning. The map can be further refined as more detailed information becomes available from subject matter experts in the future.

  • Data to accompany publication on wild diet of southern rock lobster on the east coast of Tasmania. In this study we collected 64 lobsters and analysed the diet of each individual using stomach contents, stable isotope analysis and DNA identification of prey species in faecal samples.

  • Southeastern Australia's marine waters are undergoing a trend of increased warming, surpassing the global average. This area has emerged as an alluring location for research on planktic microfossils, particularly dinoflagellate cysts, which are abundant in contemporary and Late Quaternary sediments. The composition of dinoflagellate cyst assemblages offers valuable information about the physical and biogeochemical properties of mid-latitude waters in this region. This study presents an analysis of cyst assemblages from marine sediment cores from waters inshore and offshore Maria Island, Tasmania, southeast Australia, up to 9 kyrs BP. The dominant cysts were Protoceratium reticulatum, Protoperidinium spp. (P. avellana, P. conicum, P.minutum, P. oblongum, P. subinerme, P. shanghaiense) and Spiniferites spp. (S. bulloideus, S. hyperacanthus, S. membranaceus, S. mirabilis, S. pachydermus, and S. ramosus). Inshore, Spiniferites spp. were more abundant (up to 61%), while P. reticulatum was dominant (up to 80%) at the offshore site. Impagidinium spp. and Nematosphaeropsis labyrinthus were exclusively detected offshore, with their increasing occurrence from 6 kyrs BP to present suggesting a transition from shallow coastal to stable deep-water habitat. Cysts of the Alexandrium tamarense complex were detected over the past 140 years and 9 kyrs BP at the inshore and offshore sites respectively, indicating an endemic long-term presence. Low abundances of Gymnodinium catenatum cysts were detected exclusively inshore from 50 years ago to present, suggesting recent bloom events. The limited southward penetration of the East Australian Current is indicated by the lack of warm-water cyst taxa such as Lingulodinium machaerophorum. Unlike coccolithophores, previously studied in the same sediment core, no discernible shift from cold to warm-water dinoflagellate cyst species was observed. The documentation of dinoflagellate cyst assemblages presented in this study will aid in predicting the effects of climate change, eutrophication, and introduction of novel species on local and broader community dynamics.

  • A compilation of existing literature on the characteristics of Southern Ocean diatom species.

  • This data record contains findings from bottom trawl dredging by the FV Southern Champion voyage SC26 (April to May 2003). The petrographic, geochemical and geochronological data provided here was organised by Prof. Pat Quilty and Dr. Trevor Falloon. Further research is underway to characterise dredged granites and gneisses as part of a PhD project facilitated by the Institute for Marine and Antarctic Studies (IMAS), University of Tasmania. The metadata record will be updated to reflect further publications related to this dataset.

  • These files contain the data recorded from a mesocosm experiment conducted in Bergen, Norway 2022 which assessed the effect of simualted mineral-based (silicate or calcium) ocean alkalinity enhancement (OAE) on diatom silicification. Ten mesocosms were used in total, divided into two groups either the silicate- or calcium based group and alkalinity was increased by either 0, 150, 300, 450 or 600 µmol L-1 above natrually occuring levels. The PDMPO-fluorescence (an appropriate proxy for silicification) of diatoms was recorded on eight seperate days during the experiment. Accompanying data includes measured; macronutrients (nitrate, nitrite, phophate, silicate), total alkalinity, biogenic silica in the water column and sediment trap.

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    At the inception of our project, no study had examined particle fluxes in the Subantarctic Zone (SAZ) of the Southern Ocean, despite the fact that the SAZ represents a large portion of the total area of the Southern Ocean, serve as a strong sink for atmospheric (~1G t C yr-1 [Metzl et al., 1999]), and is central to hypotheses linking particle fluxes and climate change [Francois et al., 1997; Kumar et al., 1995; Sigman et al., 1999]. The SAZ serves as an interface between the cold nutrient-rich waters to its south and the nutrient-depleted subtropical gyres to its north. SAZ upper layers are marked by a thick layer of relatively homogenous Subantarctic Mode Water (SAMW), which overlies Antarctic Intermediate Water (AAIW). Both water masses are subducted northward beneath the subtropical gyres. Thus particles leaving the surface in these regions contribute to carbon redistribution via both the fraction that reaches the deep sea by settling and the fraction that is remineralized within SAMW or AAIW and subsequently subducted. The SAZ exhibits surface water carbon dioxide partial pressures well below atmospheric equilibrium, but PFZ waters are closer to atmospheric equilibrium in this sector [Metal et al., 1999; Poppet al., 1999]. The relative physical and biological contributions to these carbon dioxide partial pressure variations are unclear, but it is important to determine them because physical and biological carbon dioxide transfers are expected to show different responses to climate change [ Matear et al., 1999; Sarmiento and LeQuere, 1996]. For these reasons we focused on the SAZ and, for comparative purposes, on the PFZ to its south. We measured particle fluxes using moored sinking particle traps at three sites in the SAZ, in the PFZ, and beneath the Subantarctic Front (SAF), which separates them. This record describes particle flux data collected between 2000 and 2001. The NetCDF data contains the following variables. Please note not all variables are supplied in all files, specifically there are not uncertainty estimates and no quality control flags for this data. -----DATA DICTIONARY----- Name, description, units, standard name TIME, time, YYYY-MM-DD, time of sample midpoint TIME_START, time sample open, YYYY-MM-DD, time sample open NOMINAL_DEPTH, depth, m, nominal depth LATITUDE, latitude, degrees_north, latitude of anchor LONGITUDE, longitude, degrees_east, longitude of anchor pressure_actual, actual, dbar, actual pressure sample, sample number, 1, sample number sample_quality_control, quality flag for sample number, unitless, quality flag for sample number mass_flux, <1mm, mg m-2 d-1, particulate total mass flux mass_flux_uncertainty, uncertainty for particulate total mass flux, mg m-2 d-1,), uncertainty for particulate total mass flux mass_flux_quality_control, quality flag for particulate total mass flux, unitless, quality flag for particulate total mass flux SAL_BRINE, supernatant, 1, sample supernatant practical salinity SAL_BRINE_uncertainty, uncertainty for sample supernatant practical salinity, 1, uncertainty for sample supernatant practical salinity SAL_BRINE_quality_control, quality flag for sample supernatant practical salinity, unitless, quality flag for sample supernatant practical salinity pH_BRINE, supernatant, 1, sample supernatant pH NBS scale pH_BRINE_uncertainty, uncertainty for sample supernatant pH NBS scale, 1, uncertainty for sample supernatant pH NBS scale pH_BRINE_quality_control, quality flag for sample supernatant pH NBS scale, unitless, quality flag for sample supernatant pH NBS scale PC_mass_flux, <1mm, mg m-2 d-1, particulate total carbon mass flux PC_mass_flux_uncertainty, uncertainty for particulate total carbon mass flux, mg m-2 d-1, uncertainty for particulate total carbon mass flux PC_mass_flux_quality_control, quality flag for particulate total carbon mass flux, unitless, quality flag for particulate total carbon mass flux PN_mass_flux, <1mm, mg m-2 d-1, particulate total nitrogen mass flux PN_mass_flux_uncertainty, uncertainty for particulate total nitrogen mass flux, mg m-2 d-1, uncertainty for particulate total nitrogen mass flux PN_mass_flux_quality_control, quality flag for particulate total nitrogen mass flux, unitless, quality flag for particulate total nitrogen mass flux POC_mass_flux, <1mm, mg m-2 d-1, particulate organic carbon mass flux POC_mass_flux_uncertainty, uncertainty for particulate organic carbon mass flux, mg m-2 d-1, uncertainty for particulate organic carbon mass flux POC_mass_flux_quality_control, quality flag for particulate organic carbon mass flux, unitless, quality flag for particulate organic carbon mass flux PIC_mass_flux, <1mm, mg m-2 d-1, particulate inorganic carbon mass flux PIC_mass_flux_uncertainty, uncertainty for particulate inorganic carbon mass flux, mg m-2 d-1, uncertainty for particulate inorganic carbon mass flux PIC_mass_flux_quality_control, quality flag for particulate inorganic carbon mass flux, unitless, quality flag for particulate inorganic carbon mass flux BSi_mass_flux, <1mm, mg m-2 d-1, particulate biogenic silicon mass flux BSi_mass_flux_uncertainty, uncertainty for particulate biogenic silicon mass flux, mg m-2 d-1, uncertainty for particulate biogenic silicon mass flux BSi_mass_flux_quality_control, quality flag for particulate biogenic silicon mass flux, unitless, quality flag for particulate biogenic silicon mass flux TIME_END, time sample closed, YYYY-MM-DD, time sample closed Reference, citable reference DOI, DOI

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    Parks Australia - Our Marine Parks Grants Round 3 Project: Satellite Mapping of Bathymetry and Habitats of Ashmore and Cartier Island Marine Parks This project aimed to map the satellite-derived bathymetry (SDB) and benthic habitats at 2m horizontal spatial resolution, for the shallow waters (~0-25 m) of the Ashmore Reef and Cartier Island Marine Parks. These critical geospatial data layers provide the essential environmental baseline information for the long-term monitoring and management of these Marine Parks. Mapping the shallow water zone is of importance both from an environmental and socioeconomic perspective. Having access to digital, georeferenced, high-resolution, satellite-derived maps of bathymetry and benthic habitats of shallow water areas, is of fundamental use in the areas of navigation, ecological research, environmental modelling, management and conservation, and monitoring the impacts from climate change.

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    At the inception of our project, no study had examined particle fluxes in the Subantarctic Zone (SAZ) of the Southern Ocean, despite the fact that the SAZ represents a large portion of the total area of the Southern Ocean, serve as a strong sink for atmospheric (~1G t C yr-1 [Metzl et al., 1999]), and is central to hypotheses linking particle fluxes and climate change [Francois et al., 1997; Kumar et al., 1995; Sigman et al., 1999]. The SAZ serves as an interface between the cold nutrient-rich waters to its south and the nutrient-depleted subtropical gyres to its north. SAZ upper layers are marked by a thick layer of relatively homogenous Subantarctic Mode Water (SAMW), which overlies Antarctic Intermediate Water (AAIW). Both water masses are subducted northward beneath the subtropical gyres. Thus particles leaving the surface in these regions contribute to carbon redistribution via both the fraction that reaches the deep sea by settling and the fraction that is remineralized within SAMW or AAIW and subsequently subducted. The SAZ exhibits surface water carbon dioxide partial pressures well below atmospheric equilibrium, but PFZ waters are closer to atmospheric equilibrium in this sector [Metal et al., 1999; Poppet al., 1999]. The relative physical and biological contributions to these carbon dioxide partial pressure variations are unclear, but it is important to determine them because physical and biological carbon dioxide transfers are expected to show different responses to climate change [ Matear et al., 1999; Sarmiento and LeQuere, 1996]. For these reasons we focused on the SAZ and, for comparative purposes, on the PFZ to its south. We measured particle fluxes using moored sinking particle traps at three sites in the SAZ, in the PFZ, and beneath the Subantarctic Front (SAF), which separates them. This record describes particle flux data collected between 2004 and 2005. The NetCDF data contains the following variables. Please note not all variables are supplied in all files, specifically there are not uncertainty estimates and no quality control flags for this data. -----DATA DICTIONARY----- Name, description, units, standard name TIME, time, YYYY-MM-DD, time of sample midpoint TIME_START, time sample open, YYYY-MM-DD, time sample open NOMINAL_DEPTH, depth, m, nominal depth LATITUDE, latitude, degrees_north, latitude of anchor LONGITUDE, longitude, degrees_east, longitude of anchor pressure_actual, actual, dbar, actual pressure sample, sample number, 1, sample number sample_quality_control, quality flag for sample number, unitless, quality flag for sample number mass_flux, <1mm, mg m-2 d-1, particulate total mass flux mass_flux_uncertainty, uncertainty for particulate total mass flux, mg m-2 d-1,), uncertainty for particulate total mass flux mass_flux_quality_control, quality flag for particulate total mass flux, unitless, quality flag for particulate total mass flux SAL_BRINE, supernatant, 1, sample supernatant practical salinity SAL_BRINE_uncertainty, uncertainty for sample supernatant practical salinity, 1, uncertainty for sample supernatant practical salinity SAL_BRINE_quality_control, quality flag for sample supernatant practical salinity, unitless, quality flag for sample supernatant practical salinity pH_BRINE, supernatant, 1, sample supernatant pH NBS scale pH_BRINE_uncertainty, uncertainty for sample supernatant pH NBS scale, 1, uncertainty for sample supernatant pH NBS scale pH_BRINE_quality_control, quality flag for sample supernatant pH NBS scale, unitless, quality flag for sample supernatant pH NBS scale PC_mass_flux, <1mm, mg m-2 d-1, particulate total carbon mass flux PC_mass_flux_uncertainty, uncertainty for particulate total carbon mass flux, mg m-2 d-1, uncertainty for particulate total carbon mass flux PC_mass_flux_quality_control, quality flag for particulate total carbon mass flux, unitless, quality flag for particulate total carbon mass flux PN_mass_flux, <1mm, mg m-2 d-1, particulate total nitrogen mass flux PN_mass_flux_uncertainty, uncertainty for particulate total nitrogen mass flux, mg m-2 d-1, uncertainty for particulate total nitrogen mass flux PN_mass_flux_quality_control, quality flag for particulate total nitrogen mass flux, unitless, quality flag for particulate total nitrogen mass flux POC_mass_flux, <1mm, mg m-2 d-1, particulate organic carbon mass flux POC_mass_flux_uncertainty, uncertainty for particulate organic carbon mass flux, mg m-2 d-1, uncertainty for particulate organic carbon mass flux POC_mass_flux_quality_control, quality flag for particulate organic carbon mass flux, unitless, quality flag for particulate organic carbon mass flux PIC_mass_flux, <1mm, mg m-2 d-1, particulate inorganic carbon mass flux PIC_mass_flux_uncertainty, uncertainty for particulate inorganic carbon mass flux, mg m-2 d-1, uncertainty for particulate inorganic carbon mass flux PIC_mass_flux_quality_control, quality flag for particulate inorganic carbon mass flux, unitless, quality flag for particulate inorganic carbon mass flux BSi_mass_flux, <1mm, mg m-2 d-1, particulate biogenic silicon mass flux BSi_mass_flux_uncertainty, uncertainty for particulate biogenic silicon mass flux, mg m-2 d-1, uncertainty for particulate biogenic silicon mass flux BSi_mass_flux_quality_control, quality flag for particulate biogenic silicon mass flux, unitless, quality flag for particulate biogenic silicon mass flux TIME_END, time sample closed, YYYY-MM-DD, time sample closed Reference, citable reference DOI, DOI

  • Diel partitioning of animals within ecological communities is widely acknowledged, yet rarely quantified. Investigation of most ecological patterns and processes involves convenient daylight sampling, with little consideration of the contributions of nocturnal taxa, particularly in marine environments. Here we assess diel partitioning of reef faunal assemblages at a continental scale utilizing paired day and night visual census across 54 shallow tropical and temperate reefs around Australia. Day/night differences were most pronounced in the tropics, with fishes and invertebrates displaying distinct and opposing diel occupancy on coral reefs. Tropical reefs in daytime were occupied primarily by fishes not observed at night (64% of all species sighted across day and night, and 71% of all individuals). By night, substantial emergence of invertebrates not otherwise detected during sunlit hours occurred (56% of all species, and 45% of individuals). Nocturnal emergence of tropical invertebrates corresponded with significant declines in the richness and biomass of predatory and herbivorous diurnal fishes. In contrast, relatively small diel changes in fishes active on temperate reefs corresponded to limited nocturnal emergence of temperate invertebrates. This reduced partitioning may, at least in part, be a result of strong top-down pressures from fishes on invertebrate communities, either by predation or competitive interference. For shallow reefs, the diel cycle triggers distinct emergence and retreat of faunal assemblages and associated trophic patterns and processes, which otherwise go unnoticed during hours of regular scientific monitoring. Improved understanding of reef ecology, and management of reef ecosystems, requires greater consideration of nocturnal interactions. Without explicit sampling of nocturnal patterns and processes, we may be missing up to half of the story when assessing ecological interactions.