A 12-month program was developed and implemented in order to obtain baseline information on water quality (salinity, water temperature, dissolved oxygen, turbidity, pH, dissolved nutrients, silica), ecological condition as shown by Chlorophyll a, benthic macroinvertebrates, pathogens, and habitat extent determined from habitat mapping. Five key estuaries and coastal waters were assessed in the Southern NRM Region of Tasmania. The data represented by this record was collected in North West Bay.

The spatial extent of C. rodgersii "barrens" was estimated by surveying rocky reef habitat with a towed underwater video system. Sampling took place at 13 regions along the east coast of Tasmania, each comprising 3 subsites, this dataset refers to the Four-mile Creek region, and its 3 subsites: Falmouth, Ironhouse Point and Saltwater Inlet.

Data were collected from 28 artificial reefs varying in size and supporting different densities of transplanted kelp (Ecklonia radiata). We used rope fibre habitats (RFHs) attached to the benthos of the reefs and destructive sampling of understory algae to collect data on epifaunal invertebrates that naturally colonised the reefs (e.g. secondary productivity, species richness, Shannon diversity). The goal of the research was to understand how kelp structure influences the biodiversity and secondary productivity of epifauna.

Phytoplankton was counted and identified from five sites over the 5-year period. Annual cycles in abundance are available (as cells mL-1), along with detailed species identification. Cell measurements and approximate geometric shape were also recorded for the calculation of biovolume (μL cell-1). Diatoms and dinoflagellates dominated the samples in terms of biomass, however, small cells were also very abundant throughout each year. The data are restricted to an integrated sample from the top 12 m of the water column. Fluorescence profiles elsewhere in this dataset can provide an indication of phytoplankton presence lower in the water column.

Belt transect surveys (50m) were used to monitor the benthic community structure through time at experimental (lobster additions/ research reserve sites or abalone diver urchin culls) and control sites in eastern Tasmania. Measures of percentage cover of key algal guilds, percentage of reef grazed by sea urchins, number of sea urchins (Centrostephanus rodgersii, Heliocidaris erythrogramma), Abalone (Haliotis Rubra), Rock lobsters (Jasus edwardsii) and type of substratum were recorded.

The spatial extent of C. rodgersii "barrens" was estimated by surveying rocky reef habitat with a towed underwater video system. Sampling took place at 13 regions along the east coast of Tasmania, each comprising 3 subsites, this dataset refers to the South Bruny Island region, and its 3 subsites: Mangana Bluff, Bay of Islands and Cape Conella.

Data is PCR amplification results of southern rock lobster (Jasus edwardsii) faecal material tested for sea urchin DNA (using unique primers for Centrostephanus rodgersii and Heliocidaris erythrogramma) in an attempt to determine in situ rates of consumption of sea urchins by lobsters. An efficient and non-lethal method was used to source and screen lobster faecal samples for the presence of DNA from ecologically important sea urchins. Lobster faecal samples were collected from trap caught specimens sourced in winter & summer seasons over 2 years (2009-2011) within two no-take research reserves; declared specifically for the purpose of rebuilding large predatory-capable lobsters to assess the potential for predator-driven remediation of kelp beds on rocky reefs extensively overgrazed by sea urchins (North Eastern Tasmania) and reefs showing initial signs of overgrazing (South Eastern Tasmania). Data for molecular assays showed high variability in the proportion of lobsters testing positive to sea urchins, with significant variability detected across different years and seasons but this was found to vary depending on different lobster size-classes. Sea urchin DNA was also amplifiable from sediments and urchin faeces collected from the reef surface where urchins occurred in high abundance. Furthermore, positive sea urchin DNA assays were obtainable from lobster faeces after lobsteres were fed sediment and urchin faecal material. Rates of predation obtained with genetics tests can also be compared to independent rates of urchin losses given known lobster abundances within research reserves (and at control sites). Data of changes in urchin abundances and lobster abundances are therefore also lodged as part of this record.

The spatial extent of C. rodgersii "barrens" was estimated by surveying rocky reef habitat with a towed underwater video system. Sampling took place at 13 regions along the east coast of Tasmania, each comprising 3 subsites, this dataset refers to the Fortescue Bay region, and its 3 subsites: Lanterns, Munroe Bight and Thumbs.

The spatial extent of C. rodgersii "barrens" was estimated by surveying rocky reef habitat with a towed underwater video system. Sampling took place at 13 regions along the east coast of Tasmania, each comprising 3 subsites, this dataset refers to the St Helens region, and its 3 subsites: Binalong Bay, St Helens Island and St Helens Point

The spatial extent of C. rodgersii "barrens" was estimated by surveying rocky reef habitat with a towed underwater video system. Sampling took place at 13 regions along the east coast of Tasmania, each comprising 3 subsites, this dataset refers to the Nubeena region, and its 3 subsites: Cape Raoul, Salters Point and Wedge.