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1.
Three large-scale experimental waste rock piles (test piles) were constructed and instrumented at the Diavik Diamond Mine in the Northwest Territories, Canada, as part of an integrated field and laboratory study to measure and compare physical and geochemical characteristics of experimental, low sulfide waste rock piles at various scales. This paper describes the geochemical response during the first season from a test pile containing 0.053 wt.% S. Bulk drainage chemistry was measured at two sampling points for pH, Eh, alkalinity, dissolved cations and anions, and nutrients. The geochemical equilibrium model MINTEQA2 was used to interpret potential mineral solubility controls on water chemistry. The geochemical response characterizes the initial flushing response of blasting residues and oxidation products derived from sulfides in waste rock exposed to the atmosphere for less than 1 year. Sulfate concentrations reached 2000 mg L−1 when ambient temperatures were >10 °C, and decreased as ambient temperatures declined to <0 °C. The pH decreased to <5, concomitant with an alkalinity minimum of <1 mg L−1 (as total CaCO3), suggesting all available alkalinity is consumed by acid-neutralizing reactions. Concentrations of Al and Fe were <0.36 and <0.11 mg L−1, respectively. Trends of pH and alkalinity and the calculated saturation indices for Al and Fe (oxy)hydroxides suggest that dissolution of Al and Fe (oxy)hydroxide phases buffers the pH. The effluent water showed increased concentrations of dissolved Mn (<13 mg L−1), Ni (<7.0 mg L−1), Co (<1.5 mg L−1), Zn (<0.5 mg L−1), Cd (<0.008 mg L−1) and Cu (<0.05 mg L−1) as ambient temperatures increased. Manganese is released by aluminosilicate weathering, Ni and Co by pyrrhotite [Fe1−xS] oxidation, Zn and Cd by sphalerite oxidation, and Cu by chalcopyrite [CuFeS2] oxidation. No dissolved metals appear to have discrete secondary mineral controls. Changes in SO4, pH and metal concentrations indicate sulfide oxidation is occurring and effluent concentrations are influenced by ambient temperatures and, possibly, increasing flow path lengths that transport reaction products from previously unflushed waste rock. 相似文献
2.
Three large-scale instrumented waste rock piles were constructed at the Diavik Diamond Mine in the Northwest Territories, Canada. These experimental waste rock piles (test piles) are 15 m high and are part of an integrated field and laboratory research program to characterize and compare low-sulfide waste rock and drainage at various scales. During test pile construction, samples of the <50 mm fraction of waste rock were collected from two types of waste rock that are segregated during mining operations based on S content. The samples were analyzed for S content and particle size distribution. One test pile contained waste rock with an average of 0.035 wt.% S in the <50 mm fraction, within the operational S target of <0.04 wt.% S for the lower S waste rock type. The second test pile contained waste rock with an average of 0.053 wt.% S in the <50 mm fraction, lower than the operational S target of >0.08 wt.% S for the higher S waste rock type. The third test pile has a low permeability till layer and a low sulfide waste rock thermal layer covering a core of waste rock with average 0.082 wt.% S in the <50 mm fraction, which is within the operational S target of >0.08 wt.% S for the higher S waste rock. Particle size distributions for the lower and higher S waste rock are similar, but the higher S waste rock has a higher proportion of fine-grained particles. Sulfur determinations for discrete particle sizes of the <50 mm fraction illustrate higher S concentrations in smaller particles for both the lower S waste rock and the higher S waste rock. Similarly, S concentrations calculated for the >10 m scale, from composite blast hole cuttings, are lower than those calculated for the <50 mm scale. Acid–base accounting using standard methods and site-specific mineralogical information was used to calculate the ratio of neutralization potential to acid generating potential. A comparison of calculation approaches to pH and alkalinity data from humidity cell and test pile effluent suggest that ratios are very sensitive to the calculation method. The preferred calculation method was selected by comparing calculation results to pH and alkalinity data from humidity cell effluent collected over 95 weeks and test pile effluent collected over five field seasons. The preferred acid–base accounting values were obtained by calculating the average neutralization potential divided by the average acid potential of a sample set. This approach indicates that waste rock with >0.05 wt.% S is of uncertain acid-generating potential and effluent data indicate this waste rock generates acidic effluent; whereas lower S waste rock does not produce acidic effluent, consistent with the acid–base accounting predictions. 相似文献
3.
The physicochemical processes that affect acid mine drainage (AMD) in unsaturated waste rock piles and the capabilities of small-scale laboratory experiments to predict AMD from waste rock are not well understood. An integrated laboratory and field study to measure and compare low sulfide waste rock and drainage characteristics at various scales has been initiated. This paper describes the design, construction and instrumentation of three field-scale experimental waste rock piles (test piles), and six active zone lysimeters at the Diavik diamond mine in the Northwest Territories, Canada. The test piles are comprised of granitic and sulfide-bearing metasedimentary waste rock excavated during open pit mining operations. One test pile contains waste rock with a target S content of <0.04 wt.% S; the second test pile contains waste rock with a target S content of >0.08 wt.% S; and the third test pile contains the higher sulfide waste rock (>0.08 wt.% S) and was re-sloped and capped with a low permeability till layer and a low sulfide waste rock cover. The first two test piles are approximately 15 m high with bases of 50 m by 60 m, and the re-sloped test pile has a larger base of 80 m by 125 m. Instrumentation was selected to measure matrix flow, geochemistry of pore water and drainage, gas-phase O2 concentration, temperature evolution, microbiological populations, waste rock permeability to air, and thermal conductivity, as well as to resolve mass and flow balances. Instrument locations were selected to characterize coupled physicochemical processes at multiple scales and the evolution of those processes over time. Instruments were installed at a density such that the number of instruments that survived construction (40% to >80% by instrument type) was sufficient to allow adequate characterization of the physicochemical processes occurring at various scales in the test piles. 相似文献
4.
Philip Deline 《Quaternary Science Reviews》2009,28(11-12):1070-1083
Rock avalanches are common in the Mont Blanc massif, which is bordered by valleys with large resident and tourist populations and important highways. This paper combines historical data with detailed geomorphological mapping, stratigraphic observation, and absolute and relative dating, to interpret several deposits resulting from rock avalanching onto glaciers.Nineteen rock falls and rock avalanches are described, ranging in volume from 10,000 m3 to 10 × 106 m3. They occurred between 2500 BP and AD 2007 at six sites. The events at three sites (Miage and Drus Glaciers, and Tour des Grandes Jorasses) are characterised by short travel distances; those at Brenva, Triolet, and Frébouge Glaciers exhibit excessive travel distances.Interactions between rock avalanches and glaciers are of four types: (i) rock-avalanche triggering, where glacial and paraglacial controls include debuttressing of rockwalls due to glacier thinning and retreat, oversteepening of rock slopes by glacial erosion, and effects of glaciers on permafrost; (ii) rock-avalanche mobility, in which mobility and travel distance are modified by channelling of rock-avalanche debris by moraines and valleys, incorporation of ice and snow (often >50% for large events), and irregularities on the glacier surface; (iii) deposit sedimentology, where melting of incorporated ice transforms the final deposit by reducing its thickness typically to <5 m, and debris of variable thicknesses is juxtaposed in a hummocky deposit with chaotic piles of angular rock debris; and (iv) glacier dynamics where insulating debris deposited upon a glacier produces a debris-covered glacier of different dynamics, and high elevated scars can favour the formation of small glaciers. 相似文献
5.
We evaluated the concentration, size and distribution, and temporal variation of insoluble dust micro-particles in the snow, rainfall and water taken from the areas surrounding the Mt. Yulong to define the characteristics of modern atmospheric dust deposition and the contributions of different dust sources. The mean mass concentration (4511 μg kg−1) of micro-particles with 0.57 < d < 26 μm, and the diameter (11.5 μm) of dust contained in the water bodies of the Mt. Yulong are roughly similar to those observed in other sites, implying that dust is primarily supplied through short-range transport from proximal source regions (several or hundreds of km distances). The mean mass concentrations of micro-particles with 0.57 < d < 26 μm is lower in the rainfall than in the snow and the river water, suggesting the rain water is an ideal source/carrier for detecting the characteristics of modern atmospheric micro-particles. Volume size distributions of micro-particles in the snow and water showed single modal structures having volume median diameters from 3 to 26 μm. Number concentrations of micro-particles in the snow were higher than that in the rainfall, the river water contains the least amount of micro-particles. Vertical profiles of the snowpits show that there is a strong lateral correlation among the dust peaks, indicating a regional uniformity of dust deposition and suitability of snow analysis for dust deposition. In addition, the bare rock of snow-free terrain in the Mt. Yulong region and the mineral particles from local rock weathering are also important sources for the dust deposition. 相似文献
6.
Boom Clay is studied as a potential host formation for the disposal of high-and intermediate level long-lived radioactive waste in Belgium. In such a geological repository, generation of gases (mainly H2 from anaerobic corrosion) will be unavoidable. In order to make a good evaluation of the balance between gas generation vs. gas dissipation for a particular waste form and/or disposal concept, good estimates for gas diffusion coefficients of dissolved gases are essential. In order to obtain an accurate diffusion coefficient for dissolved hydrogen in saturated Boom Clay, diffusion experiments were performed with a recently developed through-diffusion set-up for dissolved gases. Due to microbial activity in the test set-up, conversion of hydrogen into methane was observed within several experiments. A complex sterilisation procedure was therefore developed in order to eliminate microbiological disturbances. Only by a combination of heat sterilisation, gamma irradiation and the use of a microbial inhibitor, reliable, reproducible and accurate H2(g) diffusion coefficients (measured at 21 °C) for samples oriented parallel (Deff = 7.25 × 10−10 m2/s and Deff = 5.51 × 10−10 m2/s) and perpendicular (Deff = 2.64 × 10−10 m2/s) to the bedding plane were obtained. 相似文献
7.
Phosphorite from the Meade Peak Phosphatic Shale member of the Permian Phosphoria Formation has been mined in southeastern Idaho since 1906. Dumps of waste rock from mining operations contain high concentrations of Se which readily leach into nearby streams and wetlands. While the most common mineralogical residence of Se in the phosphatic shale is elemental Se, Se(0), Se is also an integral component of sulfide phases (pyrite, sphalerite and vaesite–pyritess) in the waste rock. It may also be present as adsorbed selenate and/or selenite, and FeSe2 and organo-selenides.Se release from the waste rock has been observed in field and laboratory experiments. Release rates calculated from waste rock dump and column leachate solutions describe the net, overall Se release from all of the possible sources of Se listed above. In field studies, Se concentration in seepage water (pH 7.4–7.8) from the Wooley Valley Unit 4 dump ranges from 3600 µg/L in May to 10 µg/L by Sept. Surface water flow, Q, from the seep also declines over the summer, from 2 L/s in May to 0.03 L/s in Sept. Se flux ([Se] ? Q) reaches a steady-state of < 150 mg/day in 1–4 months, depending upon the volume of Q. Se release (mg/L) follows a first order reaction with a rate constant, k, = 1.35 – 6.35e?3 h? 1 (11.8–55.6 yr? 1).Laboratory experiments were performed with the waste shale in packed bed reactors; residence time varied from 0.09 to 400 h and outlet pH ～ 7.5. Here, Se concentration increased with increasing residence time and release was modeled with a first order reaction with k = 2.19e?3 h? 1 (19.2 yr? 1).Rate constants reported here fall within an order of magnitude of reported rate constants for oxidation of Se(0) formed by bacterial precipitation. This similarity among rate constants from both field and laboratory studies combined with the direct observation of Se(0) in waste shales of the Phosphoria Formation suggests that oxidation of Se(0) may control steady-state Se concentration in water draining the Wooley Valley waste dump. 相似文献
8.
Streams and rivers are major exporters of C and other dissolved materials from watersheds to coastal waters. In streams and rivers, substantial amounts of terrigenous organic C is metabolized and degassed as CO2 to the atmosphere. A long-term evaluation of CO2 dynamics in streams is essential for understanding factors controlling CO2 dynamics in streams in response to changes in climate and land-use. Long-term changes in the partial pressure of CO2 (pCO2) were computed in the Anacostia River and the lower Potomac River in the Chesapeake Bay watershed. Long-term estimates were made using routine monitoring data of pH, total alkalinity, and dissolved nutrients from 1985 to 2006 at 14 stations. Longitudinal variability in pCO2 dynamics was also investigated along these rivers downstream of the urban Washington D.C. metropolitan area. Both rivers were supersaturated with CO2 with respect to atmospheric CO2 levels (392 μatm) and the highly urbanized Anacostia waters (202–9694 μatm) were more supersaturated than the Potomac waters (557–3800 μatm). Long-term variability in pCO2 values may be due to changes in river metabolism and organic matter and nutrient loadings. Both rivers exchange significant amounts of CO2 with the atmosphere (i.e., Anacostia at 0.2–72 mmol m−2 d−1 and Potomac at 0.12–24 mmol m−2 d−1), implying that waterways receiving organic matter and nutrient subsidies from urbanized landscapes have the potential to increase river metabolism and atmospheric CO2 fluxes along the freshwater–estuarine continuum. 相似文献
9.
The interaction of groundwater with cement in a geological disposal facility (GDF) for intermediate level radioactive waste will produce a high pH leachate plume. Such a plume may alter the physical and chemical properties of the GDF host rock. However, the geochemical and mineralogical processes which may occur in such systems over timescales relevant for geological disposal remain unclear. This study has extended the timescale for laboratory experiments and shown that, after 15 years two distinct phases of reaction may occur during alteration of a dolomite-rich rock at high pH. In these experiments the dissolution of primary silicate minerals and the formation of secondary calcium silicate hydrate (C–S–H) phases containing varying amounts of aluminium and potassium (C–(A)–(K)–S–H) during the early stages of reaction (up to 15 months) have been superseded as the systems have evolved. After 15 years significant dedolomitisation (MgCa(CO3)2 + 2OH− → Mg(OH)2 + CaCO3 + CO32−(aq)) has led to the formation of magnesium silicates, such as saponite and talc, containing variable amounts of aluminium and potassium (Mg–(Al)–(K)–silicates), and calcite at the expense of the early-formed C–(A)–(K)–S–H phases. This occured in high pH solutions representative of two different periods of cement leachate evolution with little difference in the alteration processes in either a KOH and NaOH or a Ca(OH)2 dominated solution but a greater extent of alteration in the higher pH KOH/NaOH leachate. The high pH alteration of the rock over 15 years also increased the rock’s sorption capacity for U(VI). The results of this study provide a detailed insight into the longer term reactions occurring during the interaction of cement leachate and dolomite-rich rock in the geosphere. These processes have the potential to impact on radionuclide transport from a geodisposal facility and are therefore important in underpinning any safety case for geological disposal. 相似文献
10.
Continuous monitoring of a 15 m high heavily instrumented experimental waste rock pile (0.053 wt.% S) since 2006 at the Diavik diamond mine in northern Canada provided a unique opportunity to study the evolution of fresh run-of-mine waste rock as it evolved over annual freeze–thaw cycles. Samples were collected from soil water solution samplers to measure pore water properties, from twelve 4 to 16 m2 basal collection lysimeters to measure basal leachate properties in the region underlying the crest of the pile (the core), and from basal drains to measure aggregate total pile leachate properties. By 2012, monitoring of pore water geochemistry within the core structure of the test pile revealed an apparent steady state with respect to weathering geochemistry, represented by (i) a flush of pre-existing blasting residuals and applied tracers, (ii) declining pH, (iii) a stepwise progression and subsequent equilibrium with acid-neutralizing phases (depletion of available carbonates; equilibrium with respect to aluminum hydroxide phases and subsequent iron (III) hydroxide phases), and (iv) concordant release of SO4, major cations (Ca, Mg, K, Na, Si), and trace metals (Al, Fe, Ni, Co, Cu, Zn). Distinct, high concentration ‘spring flushes’, characteristic of drainage in northern environments and primarily explained by a combination of fluid residence time and the build-up of oxidation products over the winter, were released from core drainage each season. Following the initial flush, the concentration of all dissolved constituents steadily declined, with distinct minimums prior to freeze-up. The opposite trend was observed in the cumulative pile drainage, in which early season leachate dominated by snowmelt and batter flow had low concentrations and late season leachate dominated by contributions from the core of the pile (indicated by season end merging of core and cumulative drainage geochemistry) had higher concentrations. Northern waste rock pile drainage geochemistry is strongly influenced by freeze–thaw cycling and varying core and batter subsystem contributions to total drainage. A comprehensive understanding of thermal cycling in waste rock piles is an important component of temporal predictions of drainage water composition based on up-scaling or reactive transport modeling. 相似文献
11.
《Applied Geochemistry》2005,20(5):961-972
The temperature dependence of the self-diffusion of HTO, 22Na+ and 36Cl− in Opalinus Clay (OPA) was studied using a through-diffusion technique, in which the temperature was gradually increased in the steady state phase of the diffusion. The measurements were done on samples from two different geological locations. The dependence of the effective diffusion coefficient on temperature was found to be of an Arrhenius type in the temperature range between 0 and 70 °C. A slight difference between the two locations could be observed. The average value of the activation energy of the self-diffusion of HTO in OPA was 21.1 ± 1.6 kJ mol−1, and 21.0 ± 3.5 and 19.4 ± 1.5 kJ mol−1 for 22Na+ and 36Cl−, respectively. The measured values for HTO are slightly higher than the values found for the bulk liquid water (HTO: 18.8 ± 0.4 kJ mol−1). This indicates that the structure of the confined water in OPA might be slightly different from that of bulk liquid water. Also for Na+ and Cl−, slightly higher values than in bulk liquid water (Na+: 18.4 kJ mol−1; Cl−: 17.4 kJ mol−1) were observed.The Stokes–Einstein relationship, based on the temperature dependency of the viscosity of bulk water, could not be used to describe the temperature dependence of the diffusion of HTO in OPA. This additionally indicates the slightly different structure of the pore water in OPA. 相似文献
12.
Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) are persistent organic pollutants (POPs) that are formed and released unintentionally from anthropogenic sources. The high persistence of PCDD/Fs results in the concentrations of these contaminants in environment decreasing only very slowly. Two transport pathways, air and water, carry PCDD/Fs into all regions of the world. Recently, more frequent extreme weather events, such as storms and floods, have been projected to occur as a result of global warming. Extreme weather events have a documented impact on the remobilization and subsequent bioavailability of POPs. In this study, three specific episodes, namely winter monsoon, southeast biomass burning and tropical cyclone (typhoon) events, which influence the environmental fate and transport of PCDD/Fs in Taiwan, were evaluated based on a climate change scenario. During the winter (northeast) monsoon period, the temperature and relative humidity observed in northern Taiwan decreases sharply. During this time, the quantity of PCDD/Fs adsorbed onto suspended particles, as observed at background sites, was found to increase from 300 ± 127 to 630 ± 115 pg I-TEQ g-TSP−1, which is even higher than that measured in Taipei City (438 ± 80 pg I-TEQ g-TSP−1). Hence, the winter monsoon not only brings cold air but also transports air pollutants and dust over long distances from mainland China to Taiwan. During the 2010 Southeast Asia biomass burning events (2010/3/22–3/28), the level of atmospheric PCDD/Fs were measured in central Taiwan (Mt. Lulin) and in the source region of northern Thailand (Chiang Mai); this revealed that the variations in atmospheric PCDD/F concentrations at these two sites followed a similar pattern. On 25 March 2010, the atmospheric PCDD/F concentration increased dramatically from 1.43 to 6.09 fg I-TEQ m−3 at Mt. Lulin and from 7.64 to 12.1 fg I-TEQ m−3 in northern Thailand. However, the atmospheric PCDD/F concentration decreased dramatically 1 day after the biomass burning event. Based on the measurements from a dated sediment core collected at a reservoir in northern Taiwan, the sharp increases in input fluxes of PCDD/Fs and mineral-derived elements levels in 1990 (20 ng I-TEQ m−2 year−1), 2001 (17 ng I-TEQ m−2 year−1), 2004 (16 ng I-TEQ m−2 year−1) and 2005 (15 ng I-TEQ m−2 year−1) seem to be a result of a deep turbid layer formed upstream due to landslides and/or mud flows during the typhoon season. This finding demonstrates the effect of typhoon events on the long-term remobilization of PCDD/Fs as well as supporting the hypothesis that such events would have the potential to remobilize pollutants that have been deposited previously. 相似文献
13.
《Applied Geochemistry》2006,21(11):1955-1968
Elemental Hg–Au amalgamation mining practices are used widely in many developing countries resulting in significant Hg contamination of surrounding ecosystems. The authors examined for the first time Hg contamination in air, water, sediment, soil and crops in the Tongguan Au mining area, China, where elemental Hg has been used to extract Au for many years. Total gaseous Hg (TGM) concentrations in ambient air in the Tongguan area were significantly elevated compared to regional background concentrations. The average TGM concentrations in ambient air in a Au mill reached 18,000 ng m−3, which exceeds the maximum allowable occupational standard for TGM of 10,000 ng m−3 in China. Both total and methyl-Hg concentrations in stream water, stream sediment, and soil samples collected in the Tongguan area were elevated compared to methyl-Hg reported in artisanal Au mining areas in Suriname and the Amazon River basin. Total Hg concentrations in vegetable and wheat samples ranged from 42 to 640 μg kg−1, all of which significantly exceed the Chinese guidance limit for vegetables (10 μg kg−1) and foodstuffs other than fish (20 μg kg−1). Fortunately, methyl-Hg was not significantly accumulated in the crops sampled in this study, where concentrations varied from 0.2 to 7.7 μg kg−1. 相似文献
14.
The radioactive isotope 36Cl, with a half-life of 301 ka, is a valuable chronometer for estimation of groundwater residence time up to 2 millions of years. Aerial thermonuclear fission bomb tests, performed during the late 1950s, injected a massive amount of this isotope into the atmosphere, which exceeded the natural fallout signal. Since this bomb pulse, atmospheric 36Cl deposition tends to return to natural fallout rate. The monitoring of this attenuation can provide a good opportunity to extend the use of this chronometer to shorter time spans. Venice’s lagoon alimentation zone shows groundwaters with residence times distributed over last fifty years. This permits the estimation of a continuous 36Cl deposition curve, free from latitudinal and seasonal variations of the signal. Three old groundwater samples, with residence times comprised in the range −900 to −8000 BP, allow the estimation of a mean natural deposition of 49 at m−2 s−1 and are in good agreement with 36Cl fallout observed for the last 40,000 years by (Plummer et al., 1997). For the bomb pulse period, a fallout of 5300 at m−2 s−1 was calculated. This was followed by a strong attenuation period, taking place until the 1980s, during which the fallout reached values ranging between 167 and 354 at m−2 s−1. The attenuation reached then a plateau: it experienced a slower lowering until the actual deposition, with fallout values calculated between 124 and 252 at m−2 s−1. This persistence of high deposition rate was classically attributed to biological and atmospherical recycling processes or underestimation of the natural atmospheric production of the 36Cl. Additional source of 36Cl production has been envisaged through the activation of chlorine radicals from stratospherical CFCs, leading to a 36Cl production rate comparable with that of Ar spallation from the first approximation. Lastly, the latitudinal factor of the attenuation of the fallout rate is discussed and the impact of the jet streams is proposed as an explanation for the discrepancies in the attenuation rate. 相似文献
15.
《Journal of Structural Geology》2001,23(2-3):343-353
Field measurements were made of 1717 mineral-filled veins in the damage zone of an active dextral strike-slip fault zone in Iceland. Most veins are composed of quartz, chalcedony and zeolites, strike roughly parallel or perpendicular to the fault zone, and are members of dense palaeo-fluid transporting networks. A common vein frequency in these networks is 10 veins per metre. Cross-cutting relationships indicate that 79% of the veins are extension (mode I) cracks and 21% are shear cracks. The apertures of most veins, measured as mineral-fill thicknesses, are from 0.1 to 85 mm, and the aperture frequency distribution is a power law. The outcrop trace lengths of 384 veins (of the 1717) could be measured accurately. These 384 veins are mostly small and range in length from 2.5 to 400 cm, in aperture from 0.01 to 0.9 cm, and have an average length/aperture ratio of about 400. Simple analytical models are derived and used to make rough estimates of the volumetric flow rates in hydrofractures of dimensions equal to those of typical veins. The results indicate that volumetric flow rates for a horizontal fracture and a vertical fracture in a rigid (non-deforming) host rock would be around 1.5×10−4 and 8.9×10−4 m3s−1, respectively. The volumetric flow rate in a vertical fracture of equal size but in a deforming host rock, with buoyancy added to the pressure gradient, is around 1.3×10−3 m3s−1. Thus, vertical fluid transport is favoured under these conditions. 相似文献
16.
《Applied Geochemistry》1998,13(5):651-671
Highly saline fluids were encountered during the German Continental Deep Drilling Project (KTB) from depths ranging between 2 and 3 km to about 9 km. The most reliable data were obtained from samples extracted during a long-term pumping test in the 4000-m deep KTB pilot hole. Some 460 m3 Ca–Na–Cl brines with about 68 g l−1 total dissolved solids (TDS) and some 270 m3 associated gases, mainly N2 and CH4 were pumped to the surface from the main fracture system situated near the bottom of the pilot hole. Geochemical and isotopic data support the hydraulic tests which suggest the presence of an open and large fluid reservoir at depth. The pumped fluids from this main fracture system were released from a deep reservoir situated at more than 5500 m depth which is hydraulically connected with the 9101 m deep KTB main hole, drilled some 250 m to the northeast of the pilot hole.While Ca and Sr contents of the extracted brines may be the result of water–rock interaction, Cl is most likely of external origin. The Cl is hypothesized to derive from geotectonic processes rather than to descending infiltration of paleo-seawater (evaporitic brines). The sampled fluids have probably migrated from a deeper reservoir to their present position since the Cretaceous–Tertiary period due to tectonic activity. However, several isotopic studies have identified an admixture of descending paleowaters down to more than 4000 m depth. The high 36Cl/Cl ratio of the fluids sampled during the long-term pumping test point to a host rock highly enriched in U–Th, unlike the sampled KTB country rocks. The fluid reservoir is believed to be in contact with the Falkenberg granite massif situated about 2 km to the E of the KTB holes, capable of supplying sufficient neutron flux for considerable subsurface production of 36Cl. The Na–Cl–(K-, SO4) precursor fluids of the Ca–Na–Cl brines were produced in the course of extensive tectonic processes since the Late Caledonian within the Bohemian Massif. 相似文献
17.
River water infiltration into an unconfined porous aquifer (∼73% gravels, ∼12% sands, ∼15% silts and clays) in the Petrignano d’Assisi plain, central Italy, was traced combining isotopic techniques (222Rn) with hydrochemical and hydrogeologic techniques in order to characterize the system under study. The 222Rn gave information about the river water residence times within the aquifer and hydrochemical data, in a two-component mixing model, which allowed estimating the extent of mixing between surface waters and groundwater in wells at increasing distances from the river. The mixing measured in the well closer to the riverbank indicated a higher contribution of river water (up to 99%) during the groundwater recession phase and a moderate contribution (up to 64%) during the recharge phase. A model describing 222Rn concentrations in groundwater as the result of both parent/daughter nuclide equilibrium and mixing process (222Rn mixing/saturation model) was used to describe observed Rn concentrations and mixing index trends with the aim of evaluating water mean infiltration velocities along the transect. The stream bank infiltration velocities obtained by the model ranged from 1 m day−1 during groundwater recharge periods, when river water infiltration is lower, to 39 m day−1 during recession phases, when river water infiltration is larger. 相似文献
18.
《Russian Geology and Geophysics》2014,55(9):1103-1112
The state of Azad Kashmir is rich in three types of rocks, namely, sedimentary, metamorphic, and igneous rocks. These rocks contain extensive deposits of graphite, marble, limestone, quartzite, granite, dolerite, and sandstone, which are widely used for the construction of dwellings in Azad Kashmir and Pakistan. Therefore, knowledge about the presence of natural radioactivity in these materials is desirable to assess the radiological hazards associated with it. In this context, 30 rock samples were collected from different geologic formations of the Muzaffarabad Division, Azad Kashmir. After processing the samples, the specific activities of 226Ra, 232Th, and 40 K in them were measured using a P-type coaxial high-purity germanium detector. The observed highest dose rate values for sedimentary, metamorphic, and igneous rocks have been found to be 83.16 ± 1.08, 135.87 ± 1.18, and 115.98 ± 1 nGy ⋅ h–1, respectively. The radium equivalent activity (Raeq) varied from 23.76 ± 1.15 for dolerite sample (igneous rock) to 293.69 ± 2.60 Bq ⋅ kg–1 for marble (metamorphic rock). The Raeq values of all rock samples are lower than the limit mentioned in the Organization for Economic Cooperation and Development (OECD, 1979) report (370 Bq ⋅ kg–1, equivalent to γ-dose of 1.5 mSv ⋅ y–1). The values of external (Hex) and internal hazard indices (Hin) are less than unity. The mean outdoor and indoor annual effective dose equivalents are 0.073 mSv ⋅ y–1 and 0.29 mSv ⋅ y–1, respectively. The mean (over all types of rock samples) annual effective dose equivalent is reported as 0.36 mSv ⋅ y–1. 相似文献
19.
Assessing soil erosion and control factors by radiometric technique in the source region of the Yellow River,Tibetan Plateau 总被引：1，自引：0，他引：1
《Quaternary Research》2014,81(3):538-544
Measurements of 137Cs concentration in soils were made in a representative catchment to quantify erosion rates and identify the main factors involved in the erosion in the source region of the Yellow River in the Tibetan Plateau. In order to estimate erosion rates in terms of the main factors affecting soil loss, samples were collected taking into account the slope and vegetation cover along six selected transects within the Dari County catchment. The reference inventory for the area was established at a stable, well-preserved, site of small thickness (value of 2324 Bq·m− 2). All the sampling sites had been eroded and 137Cs inventories varied widely in the topsoil (14.87–25.56 Bq·kg− 1). The effective soil loss values were also highly variable (11.03–28.35 t·km− 1·yr− 1) in line with the vegetation cover change. The radiometric approach was useful in quantifying soil erosion rates and examining patterns of soil movement. 相似文献
20.
The interior thermal regime of a field-scale experimental waste rock pile in the Northwest Territories, Canada, was studied. Test pile construction was completed in the summer 2006, and temperature data was collected continuously since that time to February 2009. The temperature data indicates the test pile cooled over the study period, with an average heat energy release of −2.5 × 104 and −2.6 × 104 MJ in 2007 and 2008, respectively. The mean annual air temperature (MAAT) at the site was −8.9 °C during the period between 2006 and 2009, with a permafrost table at a depth of 4 m in bedrock away from the pile. Because of this cold environment, the upward movement rate of the 0 °C isotherm into the test pile at its base was approximately 1.5 m a−1 during 2007 and 2008. Thermistor strings installed immediately below the base of the test pile showed the test-pile basal temperatures remained near and below 0 °C during the study period. Furthermore, due to low rates of sulfide mineral oxidation, elevated temperatures in the interior of the test pile were not observed. The average air velocity in the pore space in July 2007 and 2008 was about one third of that during January of each year based on temperature distributions. Therefore, due to higher air velocity during the winter, it is expected that heat transfer is greater during winter. 相似文献