GEOCHEMISTRY OF GROUND WATERS FROM THE GREAT ARTESIAN BASIN, AUSTRALIA

被引:106
作者
HERCZEG, AL
TORGERSEN, T
CHIVAS, AR
HABERMEHL, MA
机构
[1] CSIRO,DIV WATER RESOURCES,GLEN OSMOND,SA 5064,AUSTRALIA
[2] UNIV CONNECTICUT,DEPT MARINE SCI,GROTON,CT 06340
[3] AUSTRALIAN NATL UNIV,RES SCH EARTH SCI,CANBERRA,ACT 2600,AUSTRALIA
[4] BUR MINERAL RESOURCES GEOL & GEOPHYS,DIV CONTINENTAL GEOL,CANBERRA,ACT 2601,AUSTRALIA
关键词
D O I
10.1016/0022-1694(91)90158-E
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Ground waters from the confined Lower Cretaceous-Jurassic aquifer of the Great Artesian Basin, Australia (GAB) are characterised by Na-HCO3 type waters throughout the eastern and central parts of the basin and Na-SO4-Cl type waters in the western part. Sodium and bicarbonate increase in concentration from the northeastern margins to the southwestern discharge areas along the regional groundwater flowlines. A mass-balance and equilibrium model for major dissolved species and stable carbon isotopes of dissolved inorganic carbon show that the chemical trends observed are caused by mass transfer reactions involving cation exchange of Na for Ca-Mg, carbonate dissolution and reactions between Na and kaolinite to form Na-smectite. The stable carbon isotopic composition of dissolved inorganic carbon (DIC) increases from values of about -15 parts per thousand near the basin margins to -6 parts per thousand in the interior of the basin. An inverse relationship exists between delta-C-13 and DIC indicating addition of enriched carbon as the ground waters move basinwards. A C-12-C-13 mass balance indicates that the trend toward heavier delta-C-13 values in the interior of the basin results from bacterial reduction of carbon dioxide to produce methane rather than dissolution of, and equilibration with, carbonate minerals. The GAB aquifer system is apparently open to CO2 which is the product of in situ anaerobic fermentation producing CO2 enriched in C-13. The chemical evolution of the major dissolved species and carbon isotope distribution in the eastern and central parts of the GAB can then be envisaged as an initial pCO2 up to several orders of magnitude above atmospheric level is acquired within the recharge area by plant respiration and oxidation of organic matter in the soil zone. Initially, silicate and carbonate minerals may dissolve, at least in some parts of the basin, resulting in increased alkalinity, higher Ca and Mg concentrations, and a delta-C-13 concentration of the DIC of around -12 parts per thousand. Processes such as cation exchange of Na for Ca and Mg in addition to the removal of some Na by 'reverse weathering' which produces a Na smectite dominate in the interior of the GAB. The chemistry of ground waters derived from the western recharge areas is controlled by evaporite dissolution as indicated by very high Cl/Br ratios.
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页码:225 / 245
页数:21
相关论文
共 22 条
[1]  
Airey P., 1979, ISOTOPE HYDROLOGY, V1, P205
[2]   THE OCCURRENCE AND ORIGIN OF METHANE IN SOME GROUNDWATER-FLOW SYSTEMS [J].
BARKER, JF ;
FRITZ, P .
CANADIAN JOURNAL OF EARTH SCIENCES, 1981, 18 (12) :1802-1816
[3]   CL-36 DATING OF VERY OLD GROUNDWATER .1. THE GREAT ARTESIAN BASIN, AUSTRALIA [J].
BENTLEY, HW ;
PHILLIPS, FM ;
DAVIS, SN ;
HABERMEHL, MA ;
AIREY, PL ;
CALF, GE ;
ELMORE, D ;
GOVE, HE ;
TORGERSEN, T .
WATER RESOURCES RESEARCH, 1986, 22 (13) :1991-2001
[4]   SALINITY OF ATMOSPHERIC PRECIPITATION IN THE MURRAY-DARLING DRAINAGE DIVISION, AUSTRALIA [J].
BLACKBURN, G ;
MCLEOD, S .
AUSTRALIAN JOURNAL OF SOIL RESEARCH, 1983, 21 (04) :411-434
[5]  
BLAKE R, 1989, WATER ROCK INTERACTI, P83
[6]  
CALF GE, 1984, ISOTOPE HYDROLOGY 19, P397
[7]  
CHAPELLE FH, 1988, GEOLOGY, V16, P117, DOI 10.1130/0091-7613(1988)016<0117:BMATCC>2.3.CO
[8]  
2
[9]   CYCLIC WETTING AND DRYING OF SOIL ZONE AS AN INFLUENCE ON CHEMISTRY OF GROUND-WATER IN ARID TERRAINS [J].
DREVER, JI ;
SMITH, CL .
AMERICAN JOURNAL OF SCIENCE, 1978, 278 (10) :1448-1454
[10]   METHANE-PRODUCING BACTERIA - NATURAL FRACTIONATIONS OF STABLE CARBON ISOTOPES [J].
GAMES, LM ;
HAYES, JM ;
GUNSALUS, RP .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1978, 42 (08) :1295-1297