Alteration of abyssal peridotites is a major sink in the W geochemical cycle

Author(s):  
Ramon Reifenröther ◽  
Carsten Münker ◽  
Holger Paulick ◽  
Birgit Scheibner
Keyword(s):  
1986 ◽  
Vol 286 (5) ◽  
pp. 361-389 ◽  
Author(s):  
J. F. Kasting ◽  
S. M. Richardson ◽  
J. B. Pollack ◽  
O. B. Toon

2016 ◽  
Vol 8 (1) ◽  
pp. 11-28 ◽  
Author(s):  
. Najamuddin ◽  
Tri Prartono ◽  
Harpasis s. Sanusi ◽  
I Wayan Nurjaya

ABSTRACTDissolved and particulate heavy metals play a role in geochemical cycle as an agent in adsorption-desorption, deposition-resuspension, and dispersion mechanisms of heavy metals in water environment. The objectives of this research were to determine the distribution and behaviour of dissolved and particulate heavy metals Pb and Zn in different seasons (west and east seasons) at Jeneberang Estuary of Makassar. Concentrations of Pb and Zn were analysed using Atomic Adsorption Spectrophotometry based on APHA, AWWA, WEF (2005). The concentration of dissolved Pb in the riverine, estuarine, and marine waters were in the range (average) of <0.002 mg/L (below detectable limit), 0.013-0.144 mg/L (0.047 mg/L), 0.016-0.198 mg/L (0.079 mg/L); and the concen-tration of dissolved Zn were in the range (average) of <0.002 mg/L (below detectable limit), <0.002-0.014 mg/L (0.005 mg/L), <0.002-0.083 mg/L (0.017 mg/L). Meanwhile, the concentration of parti-culate Pb were in the range (average) of 1.807-2.569 mg kg-1 (2.215 mg kg-1), 0.521-1.272 mg kg-1 (0.911 mg kg-1), 0.465-2.182 mg kg-1 (1.033 mg kg-1), and the concentration of particulate Zn were in the range (average) of 19.151-90.942 mg kg-1 (51.710 mg kg-1), 16.999-63.059 mg kg-1 (31.694 mg   kg-1), 19.439-80.283 mg kg-1 (45.554 mg kg-1) in the riverine, estuarine and marine waters, respecti-vely. Behaviour of dissolved heavy metals Pb and Zn showed that the concentrations tended to increase (desorption) along the gradient of high salinity as a  result of the higher heavy metals input from coastal region than that riverine regimes.Keywords: distribution, behaviour, dissolved, particulate, heavy metal, Jeneberang Estuary


2020 ◽  
Vol 117 (18) ◽  
pp. 9747-9754 ◽  
Author(s):  
Carole Nisr ◽  
Huawei Chen ◽  
Kurt Leinenweber ◽  
Andrew Chizmeshya ◽  
Vitali B. Prakapenka ◽  
...  

Sub-Neptunes are common among the discovered exoplanets. However, lack of knowledge on the state of matter in H2O-rich setting at high pressures and temperatures (P−T) places important limitations on our understanding of this planet type. We have conducted experiments for reactions between SiO2 and H2O as archetypal materials for rock and ice, respectively, at high P−T. We found anomalously expanded volumes of dense silica (up to 4%) recovered from hydrothermal synthesis above ∼24 GPa where the CaCl2-type (Ct) structure appears at lower pressures than in the anhydrous system. Infrared spectroscopy identified strong OH modes from the dense silica samples. Both previous experiments and our density functional theory calculations support up to 0.48 hydrogen atoms per formula unit of (Si1−xH4x)O2 (x=0.12). At pressures above 60 GPa, H2O further changes the structural behavior of silica, stabilizing a niccolite-type structure, which is unquenchable. From unit-cell volume and phase equilibrium considerations, we infer that the niccolite-type phase may contain H with an amount at least comparable with or higher than that of the Ct phase. Our results suggest that the phases containing both hydrogen and lithophile elements could be the dominant materials in the interiors of water-rich planets. Even for fully layered cases, the large mutual solubility could make the boundary between rock and ice layers fuzzy. Therefore, the physical properties of the new phases that we report here would be important for understanding dynamics, geochemical cycle, and dynamo generation in water-rich planets.


1980 ◽  
Vol 28 (2) ◽  
pp. 199 ◽  
Author(s):  
PM Attiwill

Uptake of phosphorus, potassium, magnesium, and calcium by mature Eucalyptus obliqua forest was measured over a period of 22 years. during which the forest reached maximum net annual primary production. The concentration of phosphorus in components of the trees was less than that recorded for other tree species, while the concentrations of the other nutrients in E. obliqua were similar to those in other trees. Since the biomass of E. obliqua is typical of temperate evergreen forests, the total mass of phosphorus in the stand is less than that found in other forests. Gross annual demand of the stand over the 22-year period 1955-1977 decreased in the order calcium > potassium > magnesium > phosphorus. The gross annual demand for phosphorus is 0.298 g m-2 year-1 of which 46% is supplied by biochemical cycling and 36% is supplied by biogeochemical cycling. Since the geochemical input of phosphorus is insignificant, the remaining 18%, or 0.054 g m-2 year-1, must be supplied from soil reserves. At the other extreme, gross annual demand for calcium is 3.37 g m-2 year-1 of which 82% is supplied by biogeochemical cycling and only 2% by biochemical cycling. Since the balance of the geochemical cycle of calcium supplies 0.11 g m-2 year-1 to the forest, the remaining 0.44 g m-2 year-1 is supplied from soil reserves. Annual demand for all nutrients increased slightly as the forest aged, but the proportion of this demand supplied by both biochemical cycling and biogeochemical cycling also increased. The annual supply of nutrients to the stand from available sources in the soil therefore decreased with increasing age. A major contribution to biochemical cycling is shown to result from heartwood formation; the sapwood-heartwood transition accounts for 31% of the total biochemical cycle of phosphorus. Comparison with other forests suggests that the eucalypt is no more efficient at keeping phosphorus within the stand than are other genera. The low concentrations of phosphorus in the eucalypt stand therefore suggest a low absolute requirement for phosphorus.


2017 ◽  
Vol 114 (52) ◽  
pp. E11092-E11100 ◽  
Author(s):  
William H. Schlesinger ◽  
Emily M. Klein ◽  
Avner Vengosh

Synthesizing published data, we provide a quantitative summary of the global biogeochemical cycle of vanadium (V), including both human-derived and natural fluxes. Through mining of V ores (130 × 109 g V/y) and extraction and combustion of fossil fuels (600 × 109 g V/y), humans are the predominant force in the geochemical cycle of V at Earth’s surface. Human emissions of V to the atmosphere are now likely to exceed background emissions by as much as a factor of 1.7, and, presumably, we have altered the deposition of V from the atmosphere by a similar amount. Excessive V in air and water has potential, but poorly documented, consequences for human health. Much of the atmospheric flux probably derives from emissions from the combustion of fossil fuels, but the magnitude of this flux depends on the type of fuel, with relatively low emissions from coal and higher contributions from heavy crude oils, tar sands bitumen, and petroleum coke. Increasing interest in petroleum derived from unconventional deposits is likely to lead to greater emissions of V to the atmosphere in the near future. Our analysis further suggests that the flux of V in rivers has been incremented by about 15% from human activities. Overall, the budget of dissolved V in the oceans is remarkably well balanced—with about 40 × 109 g V/y to 50 × 109 g V/y inputs and outputs, and a mean residence time for dissolved V in seawater of about 130,000 y with respect to inputs from rivers.


Icarus ◽  
1967 ◽  
Vol 6 (1-3) ◽  
pp. 100-107
Author(s):  
Yasuo Shimazu

1985 ◽  
Vol 22 (12) ◽  
pp. 1890-1892 ◽  
Author(s):  
R. W. Macqueen

The following seven papers were presented on May 16, 1984, at the Geological Association of Canada and Mineralogical Association of Canada joint annual meeting. The special session, organized by R. W. Macqueen and J. A. Coope, contained 10 papers and was sponsored by the Mineral Deposits Division of the Geological Association of Canada.Our objective in organizing the special session was to examine organically based processes and relationships that may be of major importance to the origin of ore deposits. As noted by Fyfe (1984), the concept of the geochemical cycle focuses attention on pathways of chemical elements and isotopes of the Earth's system during geologic history. It is clear from the chemistry of carbon-rich materials that a wide range of elements is concentrated directly or indirectly by biological processes operating as part of the geochemical cycle. Two of the papers of the special session examine some of these concentration processes, although definitive links to actual ore deposits cannot be made yet. Beveridge and Fyfe document the remarkable ability of the anionic cell walls of certain bacteria to concentrate metals and to provide sites for nucleation and growth of minerals. In a related paper, Mann and Fyfe show that several species of simple freshwater green algae readily concentrate large amounts of uranium under both experimental and natural conditions (Elliot Lake and Thames River, Ontario).Two papers deal with aspects of sulphate reduction. Birnbaum and Wireman describe controlled experiments that suggest that sulphate-reducing bacteria may be involved in the selective replacement of sulphate-evaporite minerals by silica and in the precipitation of silica in association with sulphide mineral phases in banded iron formations. Their work focuses directly on the effect that bacterial sulphate reduction has on silica solubility. Trudinger et al. examine the question of mechanisms of sulphate reduction at temperatures less than 200 °C and the bearing this has on origin of sulphide for low-temperature sulphide ore deposits. Although there is empirical evidence favouring abiological sulphate reduction at temperatures in the vicinity of 100 °C, Trudinger et al. have not been able to demonstrate abiological reduction of sulphate under controlled laboratory conditions and at temperatures under about 200 °C. Perhaps catalysts, as yet undiscovered, are involved in this process in nature.Impressive progress has been made in understanding the diagenetic evolution of organic matter in response to heat and pressure in geological environments: excellent reviews are found in Barnes et al. (1984) and Bustin et al. (1985). Simoneit's paper examines and reviews the genesis of petroleum in a most unusual setting, that of the active ocean ridge spreading centre of Guaymas Basin, Gulf of California. There, in the vicinity of black smokers and associated metallic sulphide deposits, petroleum originates instantaneously geologically as a result of hydrothermal activity. The question of genetic involvement of organic matter in the origin of the metallic sulphides (e.g., reduction of sulphate to H2S) cannot be answered yet for this setting with the available data.The final two special session papers included here are concerned with organic matter associated with mineralization in Canadian Shield Precambrian settings. Willingham et al. demonstrate that Elliot Lake – Blind River Early Proterozoic uranium deposits with minor amounts of associated gold also contain kerogen-like organic matter. Some of this organic matter has anomalously rich amounts of gold and uranium and appears to have originated as mats of cyanobacteria, possibly with the ability to concentrate these metals. For a number of settings in the Archean-aged Abitibi greenstone belt of Ontario and Quebec, Springer demonstrates that carbon, at least partly of organic origin, is closely associated with some gold deposits. Her interpretation is that carbon activated by shear-zone-associated hydrothermal fluids has provided sites for fixing some of the gold.Three of the papers given at the special session are not included here. H. T. Shacklette reviewed metal uptake by young conifer trees, demonstrating that nursery-grown seedlings of several species readily concentrated a variety of metals, including lead, zinc, tin, and gold, over a 7 year period. This work is of interest to those involved in geochemical prospecting and is now published elsewhere (King et al. 1984). R. W. Macqueen presented quantitative data on the genesis of sulphide by abiological bitumen–sulphate reactions at the Pine Point lead–zinc property, Northwest Territories, Canada (Macqueen and Powell 1983; Powell and Macqueen 1984). Although Trudinger et al. have not been able to demonstrate abiological reduction of sulphate at temperatures approximating those of Pine Point [Formula: see text], the data presented by Macqueen (Powell and Macqueen 1984) are consistent with the amounts, alteration, and composition of bitumens at Pine Point, as well as with the presence of native sulphur and the sulphur isotope compositions of the various Pine Point sulphur species. This work is continuing, and a more extensive account is in preparation. J. R. Watterson examined relationships between freezing climates and the local chemical behaviour of gold in the weathering cycle, concluding that ice-induced accumulation of organic acids, bacteria, and other organic matter at mineral surfaces may increase rates of chemical attack, leading to dissolution of normally insoluble metals such as gold (Watterson 1986).Interest in organic aspects of the geochemical cycle, including ore deposition, is growing dramatically (e.g., Fyfe 1984). Although the following papers address a limited range of topics within the field, they do indicate some of the diversity and variety of active processes and associations between metallic elements and organic components. Perhaps, in the not too distant future, we will be able to identify or even discover whole classes of ore deposits that owe their origin directly to organic influences operating within the geochemical cycle.


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