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Collections of 23 macroinvertebrate taxa associated with Durvillaea antarctica holdfasts and 58 invertebrate taxa associated with artificial substrata collectors are described from shallow-water and intertidal habitats at Heard Island. The fauna sampled possessed strong biogeographic affinities with the Kerguelen Island fauna and, to a slightly lesser extent, the fauna recorded at Macquarie Island. The fauna possessed negligible affinity with the Antarctic. Experiments involving the offshore tethering of Durvillaea antarctica holdfasts indicated epifaunal invertebrates rapidly abandoned detached holdfasts, but that the few species surviving after one day can probably survive long periods adrift. The fields in this dataset are: Taxon (species) Distribution Locality Date Control
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Abstract from ANARE Research Notes 72 The Antarctic fur seal Arctocephalus gazella has increased in numbers at Heard Island since the Australian National Antarctic Research Expeditions (ANARE) station was established in 1947. Increases have also been recorded at other breeding sites in the South Atlantic and South Indian Oceans this century, particularly at South Georgia. In the 1987-88 summer, fur seals at Heard Island were counted in several age and sex categories. The aims of the project were to determine the location of pupping sites, the extent of the pupping season and the size of the population, and to record the changes in numbers of animals ashore during the summer. Maps of the colonies and main haul-out areas, together with descriptions of census areas and tabulations of counts, provide a basis for future comparison. This dataset contains the results from surveys of Antarctic Fur Seals (Arctocephalus gazella) on Heard Island during the summer of 1987-1988. As well as habitat descriptions, age, sex, count of adults and pups were determined. The three major aims of the study include: to determine accurately the location of pupping sites; to determine the extent of the pupping season, the median date of birth and the number of pups born; and to census fur seals on as much of the island as possible in order to determine the number of animals ashore and to document changes in numbers during the summer. The results are listed in the document, which includes detailed tabulations of counts made at colonies and major haul-out sites on Macquarie Island during summer 1987-88, and descriptions and maps of these locations. Tagging, mainly of pups, was also undertaken, and a total of 234 pups, 8 under-yearlings, 9 yearlings, 2 juveniles and 1 sub-adult male were tagged. Counts at 3-day intervals (pups) were made between 25 November and 19 December 1987, and major censuses were made between 19 December 1987 and 25 February 1988. The fields in this dataset are: Locality Age Class Date Colony Bulls Cows Pups
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Introduction: During the seasons of 1954-1956 samples of liver and blood were collected from animals at Heard Island and Antarctica by members of the Australian Antarctic Expeditions. These samples were obtained primarily for determination of copper levels (see reference). Iron determinations were made concurrently by Beck and histological examinations were made on some of the liver samples by the late Dr H.W. Bennetts, at that time the Veterniary Pathologist of the Department of Agriculture. The data were not extensive enough for publication, but they are presented here for the information of other workers. Experimental: Blood was collected as it flowed from the bullet-hole after shooting. Samples were collected in bottles containing purified potassium oxalate and were subsequently preserved with purified thymol. Liver samples for analyses were preserved in a purified ethanol-formalin mixture. Those for histological studies were stored in buffered formal-saline. No special precautions were taken to remove all blood from the liver samples. Iron was estimated by the thioglycollic acid method of Mayer and Bradshaw (Analyst, 1951, 76, 715) after oxidation of organic matter with nitric, sulphuric and perchloric acids. Blood iron results are expressed as micrograms Fe per ml. If seal and penguin haemoglobin is similar to that of terrestrial species, 680 micrograms Fe per ml will equal about 20g haemoglobin per 100 ml blood. Liver results are expressed as parts per million Fe on dry matter. No correction was made for fat content as all samples (except for one leopard seal) were low in fat. The sample from the leopard seal contained 28% fat and the iron content has been calculated to a fat free basis. As it was possible that the high levels of iron are related to the diving habits of the seals, iron determinations were also made on livers from whales taken along the Australian coast. Some blood and liver iron levels for terrestrial species and for the Australian salmon are included for comparison. Results and Discussion: Detailed results for the seals and penguins and other animals are available at the url below. The levels of iron in the seal blood samples are extremely high and similar observations have been made by numerous other workers. The levels in Weddell seals Nos. 18 and 20 contain the equivalent of 30-35g haemoglobin per 100 ml blood. This level may be compared with 10-15g per 100 ml of terrestrial species. The levels of iron in the livers of the Weddell seals and in the penguins is generally higher than the corresponding values in terrestrial species. The values for elephant seals are however consistently higher than all other species. Several possible reasons can be advanced for the high iron content of the livers from elephant seals. 1) Contamination by blood is undoubtedly a factor. This is born out by the histological report of congestion of the sinusoids. Dr Budd, in a personal letter on April 17 1955, comments on the rather extraordinary slowness with which blood drains from seal liver. The fact that the very high liver iron levels are associated with heavy haemosiderin deposits indicates that blood contamination is only part of the reason for the high iron levels. 2) A small amount of contamination by black sand occurred in some of the Heard Island livers. We obtained a sample of this black sand but it contained only 3.3% soluble Fe. If there were 1% sand in the samples it would only increase the liver Fe by 330 ppm. As the sand contamination was far less than 1% I do not consider that it has contributed significantly to the liver iron values. 3) The haemosiderin may possibly be due to some virus or organism which caused blood breakdown. However, there was no comment of any sign of disease by those who collected the samples. Dr L.G.C.E. Pugh (Nature, Jan 10th 1959, 183, 74) comments on the ease of hydrolysis of Weddell seal blood and considers that the cell fragility may contribute to the high rate of destruction of red cells. If a very high destruction rate occurs in the blood of elephant seals this could account for the liver haemosiderin. 4) The high liver haemosiderin may merely be a normal iron reserve for what must be a very high iron requirement for blood production in this species. On the other hand the Weddell seals have just as high haemoglobin levels and yet the iron levels in the liver are much lower. The fields in this dataset are: antarctic blood duck fowl haemoglobin iron liver penguins petrels rabbit seals sheep skuas subantarctic whales animal No. common name scientific name taxon id locality date details blood Fe (ug/ml) liver Fe (p.p.m. on dry liver) Haemo-siderin in liver comments specials No. of samples iron content blood (micro grams per ml) iron content liver (ppm on dry matter)