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1 Bureau of Mineral Resources, Division of Marine Geosciences and Petroleum Geology, PO Box 378, Canberra, ACT, Australia
2 CSIRO, Division of Water Resources, GPO Box 1666 Canberra, ACT Australia
3 Geological Research Division, Scripps Institution of Oceanography, La Jolla, California, 92093, USA
4 CSIRO, Division of Water Resources, Private Mail Bag #2, Glen Osmond, South Australia, 5064, Australia
5 CSIRO, Division of Fisheries, PO Box 120, Cleveland, Queensland, 4163, Australia
6 Department of Oceanography, Florida State University, Tallahassee, Florida, 32306, USA
7 CSIRO, Division of Soils, Private Bag #2, Glen Osmond, South Australia, 5064, Australia
During 1987, the Australian Bureau of Mineral Resources conducted a multidisciplinary investigation of the modern phosphorites on the continental margin of southeastern Australia between 28 and 32°S. The objectives of the work were to examine the processes controlling the cycling of organic carbon and bioactive elements, nitrogen, phosphorus, sulphur and iron in the sediments, and to investigate the roles which these processes played in the formation of the modern phosphorites. Bacterial productivities, sulphate-reduction rates, sedimentary oxygen and pore-water concentrations of nitrate, ammonia, phosphate, iron, sulphate and fluoride were measured at sea. The highest rates of microbial productivity were found in the surficial (0–20 mm) sediments of the modern phosphorite zone in 350–460 m water depth. These rates were about double those in shallower shelf (<300 m) sediments and 3–4 fold those rates in mid-slope (600–1000 m) sediments. Aerobic and anaerobic oxidation rates of organic matter, calculated from sediment oxygen profiles and sulphate-reduction rates were highest in the surface sediments in the modern phosphorite zone. The recycling of sedimentary iron, via reductive dissolution of iron oxyhydroxides and reprecipitation at the oxic/anoxic boundary results in a near-surface sedimentary trap for iron in the phosphorite zone sediments. Phosphate released from organic matter in the interfacial sediments, and fluoride from seawater, are scavenged by iron oxyhydroxides in the top few centimetres of sediment. Phosphorus, in this way, is decoupled from organic carbon in the near-surface sediments and linked to the redox cycling of iron. Phosphate and fluoride scavenged onto iron oxyhydroxides, and concentrated in the surficial sediments, are subsequently released to pore waters in the anoxic sediments when iron oxyhydroxides are buried and dissolve. The recycling process releases phosphate and fluoride for incorporation into apatite; fluoride is depleted from pore waters at depths <18 cm, phosphorite nodules form within anoxic sediments at depths <18 cm and continue to accumulate iron and phosphorus while resident in the mixed layer. Combinations of rapid sediment mixing rates, a slow sedimentation rate and a mixed layer to about 18 cm result in an average particle residence time in the phosphorite zone sediments which is about ten-fold that of the mid-slope sediments. Long residence times and rapid mixing promote the oxidation of organic carbon and release of phosphate, while the continuous recycling of iron and phosphate concentrates the phosphorus for apatite precipitation and accumulation into phosphorite nodules. Phosphorite nodules are not found in mid-slope sediments probably because of combinations of relatively rapid sedimentation rates, ineffective iron, phosphorus and fluoride recycling and trapping mechanisms, plus dilution and dissemination of any incipient apatite.
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