TemperateReefBase Geonetwork Catalogue
CRUSTACEANS
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[This data has been superseded by a synthesised global dataset which includes additional ecological data contributed by non-RLS entities (National Reef Monitoring Network). Please visit the corresponding NRMN Collection (IMOS - National Reef Monitoring Network Sub-Facility - Global cryptobenthic fish abundance) for the most current version of this data. See "Downloads and Links" section below.] Reef Life Survey is designed to develop and resource a network of skilled recreational divers for rapid and cost-effective assessment of the state of the inshore marine environment at the global scale. The project uses standardised underwater visual census methods employed by trained SCUBA divers to survey fish and invertebrate species and to record habitat type using photo quadrats - this dataset refers to the cryptic fish and invertebrate survey component only.
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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.
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[This data has been superseded by a synthesised global dataset which includes additional ecological data contributed by non-RLS entities (National Reef Monitoring Network). Please visit the corresponding NRMN Collection (IMOS - National Reef Monitoring Network Sub-Facility - Global mobile macroinvertebrate abundance) for the most current version of this data. See "Downloads and Links" section below.] Reef Life Survey is designed to develop and resource a network of skilled recreational divers for rapid and cost-effective assessment of the state of the inshore marine environment at the global scale. The project uses standardised underwater visual census methods employed by trained SCUBA divers to survey fish and invertebrate species and to record habitat type using photo quadrats - this dataset refers to the cryptic fish and invertebrate survey component only.
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Instantaneous growth rates (IGR) of Antarctic krill kept under experimental conditions were measured. The measured appendages included the uropods, telson (both standard length measurements with the IGR technique) and the pleopod endopodite and pleopod exopodite were investigated as an alternate length measurement. IGR measurements were recorded on 90 experimental animals. The total carbon content of 45 krill of various size ranges (collected directly from the field) was determined. The relationship between the change in length in carbon as a function of growth was investigated. The parameters measured were total length, mean uropod length, telson length, wet weight, dry weight and total carbon content. This dataset was collected as part of ASAC project 141. See metadata record ASAC_141 - Collection of live Antarctic krill 'Euphausia superba'. The fields in this dataset are: Krill Total length (mm) Telson length (mm) Mean uropod length (mm) Wet weight (g) Dry weight (g) Dry Weight (mg) Carbon content as a % of dry weight Total carbon content (g) Moult Sex
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Crustaceans are an important component of the Antarctic marine ecosystem. Large numbers live in or close to the sea-ice cover, using it as a refuge from predation and a source of food. However, the impact of these animals on algae that grows in the sea ice is unknown. This study is examining the diets and grazing rates of crustaceans in the Antarctic sea-ice ecosystem. These results will aid our understanding of the fate of algal production in sea-ice and will enable the construction of realistic carbon budgets for this ecosystem. This project was commenced in July 2002. A five-week voyage was undertaken on the RV Aurora Australis in October and November 2002, in the vicinity of the Mertz Glacier. Pack ice cores and sub-ice water samples were collected from 8 locations, with 3 to 5 samples of each type collected per site. The cores were sectioned in the field, melted and treated for further analysis. All samples were either preserved or frozen, depending on future requirements, and returned to Australia. Sea ice cores were processed for a range of analyses including microscopy, lipid class and fatty acid determination and stable isotope analysis. A physical description of the pack ice environment (ice type, ice thickness, snow cover, temperature profiles, salinity profiles) was also compiled. A second sampling of the pack ice occurred in Sept-Oct 2003. To date, the salinity and temperature profiles of the pack ice cores have been described and a database compiled of the physical description of the region. A large number of samples (10 sites; 5 ice/water/animal samples per site) was collected and analysis has begun of stable isotopic signatures, fatty acids, chlorophyll a and species identifications. Crustaceans have been sorted under the microscope and initial descriptions of gut contents begun. The third successful sampling trip was to the fast ice surrounding Davis Station during the 2003/04 summer. Two sites were sampled regularly, with a full suite of analyses undertaken. This will provide a temporal component to the project to complement the spatial approach used in the pack ice. Analysis of the fast ice samples is ongoing. Two more sampling trips were carried out during the 2004/05 season. The first in the pack ice offshore from Casey and the second in the fast ice at Casey. The same suite of analyses as listed above was carried out and analyses are ongoing. The download file contains five excel spreadsheets, as well as a word document which further explains data collection.
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The effect of barrens formed by the long spined sea urchin, Centrostephanus rodgersii, on the standing stocks of southern rock lobsters (Jasus edwardsii) and black lip abalone (Haliotis rubra) was estimated by divers using underwater visual census methods to compare lobster and abalone abundance in barrens with that in adjacent kelp habitat. Abalone (H. rubra) and rock-lobster (J. edwardsii) populations were compared on C. rodgersii barrens and in adjacent algal-dominated habitat at the same depth and on the same substratum type at three sites in eastern Tasmania (Elephant Rock:Binalong Bay, St Helens Is, and Mistaken Cape:Maria Island). At Elephant Rock and St Helens Island , the barrens are extensive and well established Type 1 barrens, while at Mistaken Cape the barrens in 8-14 m are incipient Type 4 barrens, comprising small barren patches in the algal bed (see FRDC report for classification of barren types). Note that while there are extensive barrens in deeper water (>18 m) at Mistaken Cape, at these depths working time is limited and it was difficult to locate intact macroalgal beds on equivalent substrata.