Book reviews     

Yukio Fujinawa  A. V. Koloskov  Gerardo G. Tango  Lech Stefaníak  Douglas R. Schmitt  Kei Katsumata  Vernon F. Cormier  Wladislaw Lyatsky  Krzysztof Haman  P. Vincent  Konrad Bajer  Henryk Piwkowski 《Pure and Applied Geophysics》1991,136(2-3):343-367

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How to Determine the End of Active Remediation     

Evan K. Nyer  Douglas G. Mehan 《Ground Water Monitoring & Remediation》1991,11(3):89-91

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Heat flow in the Ozark Plateau, Arkansas and Missouri: relationship to groundwater flow     

Joseph G. Meert  Douglas L. Smith  Len Fishkin 《Journal of Volcanology and Geothermal Research》1991,47(3-4)

Heat flow values were calculated from direct measurements of temperature and thermal conductivity at thirteen sites in the Arkansas-Missouri Ozark Plateau region. These thirteen values are augmented by 101 estimates of heat flow, based on thermal conductivity measurements and temperature gradients extrapolated from bottom-hole temperatures. The regional heat flow profile ranges from 9 mW m⁻² to over 80 mW m⁻², but at least two distinct thermal regimes have been identified. Seven new heat flow determinations are combined with three previously published values for the St. Francois Mountains (SFM), a Precambrian exposure of granitic and rhyolitic basement rocks, average 47 mW m⁻². Radioactive heat production of 76 samples of the exposed rocks in the SFM averages 2.4 μW m⁻² and a typical continental basement contribution of 14 mW m⁻² is implied. Conversely, the sedimentary rock sequence of the plateau is characterized by an anomalously low heat flow, averaging approximately 27 mW m⁻². Groundwater transmissivity values that are based on data from 153 wells in deep regional aquifers demonstrate an inverse relationship to the observed heat flow patterns. The areas of high transmissivity that correspond to areas of low total heat flux suggest that the non-conservative vertical heat flow within the Ozark sedimentary sequence can be attributed to the effects of groundwater flow.  相似文献   

The Batu Hijau porphyry copper-gold deposit, Sumbawa Island, Indonesia   总被引：4，自引：0，他引：4  

Simon J. Meldrum  Romeo S. Aquino  Rene I. Gonzales  Robert J. Burke  Artha Suyadi  Bambang Irianto  Donald S. Clarke 《Journal of Geochemical Exploration》1994,50(1-3)

The Batu Hijau porphyry Cu---Au deposit lies in southwest Sumbawa Island, Indonesia. It is a world-class porphyry Cu deposit in an island are setting, and is typical of this deposit type in most features, including igneous association, morphology, hydrothermal alteration and mineralisation style.The region was not previously recognised as a porphyry Cu province; disseminated Cu sulphides were first recognised in float samples in southwest Sumbawa in 1987. Associated stream sediment sampling identified a broad area of anomalous Au and Cu in an area of greater than 5 km² around Batu Hijau, including 169 ppb Au in BLEG samples and 580 ppm Cu in stream silts 1 km from the deposit. Mineralisation in bedrock at surface contains > 0.1 wt % Cu and > 0.1 ppm Au over an area of 0.6 km × 1.2 km, including a zone 300 m × 900 m containing > 0.3 wt % Cu. Areas with elevated Mo (> 30 ppm) form a distinctive annulus around this Cu-rich zone.Batu Hijau mineralisation is hosted in a tonalite intrusive complex, and diorite and metavolcanic wallrocks. There are no post-mineralisation igneous intrusions or breccia pipes within the deposit. The main tonalite intrusion forms a stock in the centre of the deposit, where it generally displays intensely pervasive potassic (biotite with magnetite-quartz) alteration and hosts most of the higher grade mineralisation. Younger tonalite dykes intruding the centre of this stock are generally less altered and mineralised than the older tonalite.The core zone of potassic alteration grades outward into extensive propylitic alteration (chlorite-epidote), with both variably overprinted by widespread fracture controlled intermediate argillic alteration (sericite-chlorite), and minor phyllic (sericite-pyrite) and sodic (albite) alteration. Argillic (sericite-kaolinite) and advanced argillic (kaolinite-alunite-pyrophyllite) assemblages occur near surface.Copper and Au grades within the orebody show a positive correlation with quartz stockwork intensity, although disseminated Cu sulphides are also common. Chalcopyrite and bornite are the principle hypogenal minerals, with minor chalcocite. Oxidation extends to a depth of 5 m to 85 m below surface across the deposit, and is underlain by weak supergene mineralisation. Drill testing of the deposit down to 650 m below surface reveals a single cylindrical to conical orebody of 334 million tonnes grading 0.8 wt % Cu and 0.69 gm per tonne Au; the depth extent of mineralisation is unknown.  相似文献   

Mg²⁺ removal in the system Mg²⁺—amorphous SiO₂—H₂O by adsorption and Mg-hydroxysilicate precipitation     

Douglas B. Kent  Miriam Kastner 《Geochimica et cosmochimica acta》1985,49(5):1123-1136

Two chemical processes can remove Mg²⁺ from suspensions containing amorphous silica (am-SiO₂) at low temperatures: adsorption and precipitation of a Mg-hydroxysilicate resembling sepiolite. Mg²⁺ removal from am-SiO₂ suspensions was investigated, and the relative role of the two removal processes evaluated, as a function of: pH, ionic strength, Mg²⁺ concentration, and temperature.The extent of Mg²⁺ adsorption onto am-SiO₂ decreases with increasing NaCl concentration due to displacement of Mg²⁺ by Na⁺. At NaCl concentrations of 0.05 M and above, adsorption occurs only at pH values above 8.5, where rapid dissolution of am-SiO₂ gives rise to high concentrations of dissolved silica, resulting in supersaturation with respect to sepiolite. Removal of Mg²⁺, at concentrations of 40 to 650 μM, from am-SiO₂ suspensions in 0.70 M NaCl at 25 °C occurs at pH 9.0 and above. Experiments show that under these conditions adsorption and Mg-hydroxysilicate precipitation remove Mg²⁺ at similar rates. For 0.05 M Mg²⁺, at 0.70 M ionic strength and 25 °C, measurable Mg²⁺ removal occurs down to ca. pH 7.5 but is primarily due to Mg-hydroxysilicate precipitation. For the same solution conditions at 5°C, Mg²⁺ removal occurs above pH 8.0 and is primarily due to adsorption.Assuming that increasing pressure does not greatly enhance adsorption, Mg²⁺ adsorption onto am-SiO₂ is an insignificant process in sea water. The surface charge of pristine am-SiO₂ in sea water is primarily controlled by interactions with Na⁺. The principal reaction between Mg²⁺ and am-SiO₂ in marine sediments is sepiolite precipitation.The age distribution of sepiolite in siliceous pelagic sediments is influenced by temperatures of bottom waters and by geothermal gradients.  相似文献   

Erratum: T. Torgersen and W. B. Clarke (1985) Helium accumulation in groundwater,I: An evaluation of sources and the continental flux of crustal 4He in the Great Artesian Basin,Australia 49, 1211–1218     

T. Torgersen  W.B. Clarke 《Geochimica et cosmochimica acta》1985,49(11):2499

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The geography of tourism in France: definition,scope and themes   总被引：1，自引：0，他引：1  

Bernard Barbier  Douglas G. Pearce 《GeoJournal》1984,9(1):47-53

Conclusions The substantial body of literature produced in the last two decades bears witness to the marked development of the geography of tourism in France over this period. This research has been strongly influenced by traditional geographic thought and is notable for the logic which underlies it. At the same time much remains to be done, with various avenues for future research being suggested in this paper. French geographers might also look increasingly outwards and to the work of others. By considering new and different methodologies, theories and fields of interest, the conceptual base of the subject might be enlarged and a more systematic approach developed. This need is keenly felt and this opening up is starting to occur, particularly through the exchange of ideas with foreign geographers at meetings of the national or international (IGU) commissions on the geography of tourism.  相似文献   

The typing of Au and base-metal occurrences by plasma/mass spectrometry: initial results     

R.G. Smith  E.J. Brooker  D.J. Douglas  E.S.K. Quan  G. Rosenblatt 《Journal of Geochemical Exploration》1984,21(1-3)

This paper discusses the application of the newly developed ELAN 250 I.C.P./mass spectrometer to exploration geochemistry. This instrument combines an inductively coupled plasma with a quadrupole mass spectrometer. The combination of these two existing technologies makes it possible for the first time to perform stable-isotope and elemental analysis rapidly and concurrently.Particular attention is paid to the use of lead isotopes to type Au and base-metal occurrences. Data are presented on galena samples obtained from the Geological Survey of Canada and the Royal Ontario Museum. Consideration is also given to the potential usefulness of Pb isotopes and trace-element data to type mineral occurrences and to identify new ones.  相似文献   

Uranium geochemistry in groundwater from tertiary sediments     

Roy F. Spalding  A.Douglas Druliner  Lowell S. Whiteside  Arthur W. Struempler 《Geochimica et cosmochimica acta》1984,48(12):2679-2692

Dissolved U concentrations and activity ratios (ARs) of the U isotopes in the ²³⁸U decay series were measured in ground and surface waters as part of an investigation to delineate the water quality in a proposed uranium mining area of northwest Nebraska. In oxidizing groundwaters from 67 wells completed in the Tertiary sediments, increasing U concentrations in the direction of groundwater flow generally were associated with a maturation of the formation water as evidenced by evolutionary trends in major ion character. The increased U levels probably are associated with leaching as shown by the positive correlation between U concentrations and total dissolved solids (TDS) (r = +0.83). The inverse relationships between TDS and U ARs (r = ?0.73) and U levels and ARs (r = 0.72) indicate that the decay of excess U-234 is related to maturation of the formation water and to sediment leaching along the flowpath. The data are described by a model which incorporates etching, decay and recoil and suggests that aquifer residence time can be estimated from the TDS level.The levels of soluble U in a reducing uraniferous hydrogeologic unit near Crawford, Nebraska are affected by the proximity of the sample collection to ore. In groundwater samples having similar chemistries (Na-SO₄ + Cl type), similar Ehs, and collected from a close-knit pattern, U concentrations ranged from 0.01 to 2,037 μg l^?1 and ARs ranged from 0.75 to 12.6. This high variability in U levels and ARs is indicative of uranium ore in small areal studies where low ARs almost always are associated with high U concentrations.  相似文献   

Robust kriging—A proposal     

Douglas M. Hawkins  Noel Cressie 《Mathematical Geosciences》1984,16(1):3-18

Geological data frequently have a heavy-tailed normal-in-the-middle distribution, which gives rise to grade distributions that appear to be normal except for the occurrence of a few outliers. This same situation also applies to log-transformed data to which lognormal kriging is to be applied. For such data, linear kriging is nonrobust in that (1)kriged estimates tend to infinity as the outliers do, and (2)it is also not minimum mean squared error. The more general nonlinear method of disjunctive kriging is even more nonrobust, computationally more laborious, and in the end need not produce better practical answers. We propose a robust kriging method for such nearly normal data based on linear kriging of an editing of the data. It is little more laborious than conventional linear kriging and, used in conjunction with a robust estimator of the variogram, provides good protection against the effects of data outliers. The method is also applicable to time series analysis.  相似文献