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1.
Diffusion of four rare-earth elements and gallium has been measured in yttrium aluminum garnet (YAG). Sources of diffusant were mixtures of alumina and rare-earth element oxides for REE diffusion, and mixtures of gallium and yttrium oxides for Ga diffusion. Diffusion profiles were measured with Rutherford backscattering spectrometry (RBS). For the rare-earth elements investigated, the following Arrhenius relations were obtained: DLa=6.87×10–1 exp (–582±21 kJ mol–1 /RT) m2s–1 DNd=1.63×10–1 exp (–567±15 kJ mol–1 /RT) m2s–1 DDy=2.70×100 exp (–603±35 kJ mol–1 /RT) m2s–1 DYb=1.50×10–2 exp (–540±26 kJ mol–1 /RT) m2s–1 Diffusion rates for the rare earths are quite similar, in contrast with trends noted for zircon. It is likely that these differences are a consequence of the relative ionic radii of the REE and the cations for which they substitute in the mineral lattice. For gallium, the following Arrhenius relation was determined: DGa=9.96×10–6 exp (–404±19 kJ mol–1 /RT) m2s–1 Gallium diffuses faster than the REE in YAG and has a smaller activation energy for diffusion. These data mirror relative trends in diffusion rates for YIG, in which trivalent cations occupying tetrahedral and octahedral sites (i.e., Al, Ga, Fe) diffuse faster than trivalent cations occupying dodecahedral sites (i.e., Y and the REE), and suggest that the rate-limiting process in the diffusion-controlled regime of solid-state creep of YAG is the diffusion of yttrium. Received: 10 November 1997 / Revised; accepted: 13 March 1998  相似文献   

2.
The main goal of this investigation is estimating volume of volatile emission, atmospheric and climatic impact of the Kurile Lake caldera-forming eruption, one of the Earth’s largest Holocene explosive eruptions. The volatile content of magma before the eruption was estimated by comparing H2O, S, Cl and F contents in natural quenched glassy melt inclusions trapped by plagioclase phenocrysts. The volatile content of igneous rocks after eruption was estimated by comparing concentrations of degassed matrix glasses. As a result of KO-eruption not more than (3.7–4.2) × 1012 kg of water, (4.3–4.9) × 1010 kg of chlorine, (8.6–9.8) × 109 kg of fluorine and (2.6–2.9) × 1010 kg of sulphur were injected into the atmosphere. This eruption had to produce an important climatic impact.  相似文献   

3.
A large pool of nitrogen in the sediment pore fluid of a eutrophic lake in Iowa, USA, was mapped in this study. Previously, the lake had supported fishing and boating, but today it no longer supports its designated uses as a recreational water body. In the top 5 cm of the lake bottom, the pore water nitrogen ranges between 3.1 and 1,250 μg/cm3 of sediments, with an average of 160.3 μg/cm3. Vertically, nitrate concentrations were measured as 153 μg/cm3 at 0–10 cm, 162 μg/cm3 at 10–20 cm, and 32 μg/cm3 at 20–30 cm. Nitrate mass distribution was quantified as 3.67 × 103 kg (65%) in the bottom sediments, 172 kg (3%) in suspended particulates, and 1.83 × 103 kg (32%) in the dissolved phase. Soil runoff nutrients arrive at the lake from the heavily fertilized lands in the watershed. Upon sedimentation, a large mass of nitrogen desorbs from mineral particles to the relatively immobile pore fluid. Under favorable conditions, this nitrogen diffuses back into the water column, thereby dramatically limiting the lake’s capability to process incoming nutrients from farmlands. Consequently, a condition of oxygen deficiency disrupts the post-season biological activities in the lake.  相似文献   

4.
The technique of competitive ligand-exchange/anodic stripping voltammetry (CLE-SV) was used to investigate effects of pH and Ca concentration on cadmium complexation by fulvic acid (FA), as well as Cd speciation in two different freshwaters, a hardwater Lake Greifen and a softwater River Wyre. Binding of Cd to Suwannee river FA (10 mg/l) was determined at different pH (7–8.5) and in the presence of various concentration of Ca2+ (0–2 mmol/l). The results from one-ligand discrete models were compared to simulations by the WHAM VI model. In Lake Greifen, the determined dissolved [Cd2+] ranged from 10−13 to 10−12 mol/l, and the conditional stability constant with natural ligands was log K CdL about 9.5–10.5 (pH 8.6–8.8) with ligand concentrations of 1.2–7.8 × 10−6 mol/g C. In the softwater River Wyre, dissolved [Cd2+] ranged from 4 × 10−12 to 1 × 10−11 mol/l, and the ligands were weaker (log K CdL 8.9–9.8, pH 8.0) with lower ligand concentrations (0.9–2.3 × 10−6 mol/g C). The titration curves of FA samples were close to the simulated curves by the WHAM VI model at pH 8.0–8.5, but deviated more from the model at lower pH, indicating that the results determined with CLE-SV for Cd-FA complexation are relevant to the data base in the model. Calculation of the Ca competition for Cd binding by FA showed a competition effect of similar strength as the measured one, but indicated a systematic difference between measured and modeled data at pH 7.5. Using the WHAM model for comparison with FA, the complexation of Cd by the River Wyre ligands was close to that of FA, whereas stronger complexation was observed in the Lake Greifen water. These differences may originate from different ligand composition in the lake and the river.  相似文献   

5.
 Shallow, anaerobic groundwater near a former manufactured-gas plant (MGP) in Charleston, South Carolina, USA, contains mono- and polycyclic aromatic hydrocarbons (MAHs and PAHs, respectively). Between 1994 and 1997, a combination of field, laboratory, and numerical-flow and transport-model investigations were made to assess natural attenuation processes affecting MAH and PAH distributions. This assessment included determination of adsorption coefficients (K ad ) and first-order biodegradation rate constants (K bio ) using aquifer material from the MGP site and adjacent properties. Naphthalene adsorption (K ad =1.35×10–7 m3/mg) to aquifer sediments was higher than toluene adsorption (K ad =9.34×10–10 m3/mg), suggesting preferential toluene transport relative to naphthalene. However, toluene and benzene distributions measured in January 1994 were smaller than the naphthalene distribution. This scenario can be explained, in part, by the differences between biodegradation rates of the compounds. Aerobic first-order rate constants of 14C-toluene, 14C-benzene, and 14C-naphthalene degradation were similar (–0.84, –0.03, and 0.88 day–1, respectively), but anaerobic rate constants were higher for toluene and benzene (–0.002 and –0.00014 day–1, respectively) than for naphthalene (–0.000046 day–1). Both areal and cross-sectional numerical simulations were used to test the hypothesis suggested by these rate differences that MAH compounds will be contained relative to PAHs. Predictive simulations indicated that the distributions of toluene and benzene reach steady-state conditions before groundwater flow lines discharge to an adjacent surface-water body, but do discharge low concentrations of naphthalene. Numerical predictions were "audited" by measuring concentrations of naphthalene, toluene, and benzene at the site in early 1997. Measured naphthalene and toluene concentrations were substantially reduced and the areal extent of contamination smaller than was both observed in January 1994 and predicted for 1997. Measured 1997 benzene concentrations and distribution were shown to be relatively unchanged from those measured in 1994, and similar to predictions for 1997. Received: 26 June 1997 · Accepted: 25 August 1997  相似文献   

6.
Using powder X-ray diffraction of heated solids to pressures reaching 68 GPa, the pressure-volume-temperature (PVT) data on corundum Al2O3 and ɛ-Fe were determined with the following results: *Corundum,*Iron, *Al2O3*ɛ-Fe Isothermal bulk*258 (2)*164 (3)  modulus K'300, 1 (GPa) Pressure derivative K300, 1*4.88 (4)*5.36 (16) Temperature derivative*–0.020 (2)*–0.043 (3)  (∂K T,1 /∂T) P (GPa/K) Molar volume V300,1*25.59 (2)*6.76 (2)  (cm3/mol) Isobaric thermal expansion at 1 atm (0.101 MPa) is given by (K–1): α T =2.6 (2) 10–5+1.81 (9) 10–9 T–0.67 (6)/T 2 for corundum, and α T =5.7 (4) 10–5+4.2 (4) 10–9 T–0.17 (7)/T 2 for iron ɛ-Fe. Received: 1 March 1997 / Revised, accepted: 21 August 1997  相似文献   

7.
A review of published and newly measured densities for 40 hydrous silicate glasses indicates that the room-temperature partial molar volume of water is 12.0 ± 0.5 cm3/mol. This value holds for simple or mineral compositions as well as for complex natural glasses, from rhyolite to tephrite compositions, prepared up to 10–20 kbar pressures and containing up to 7 wt% H2O. This volume does not vary either with the molar volume of the water-free silicate phase, with its degree of polymerization or with water speciation. Over a wide range of compositions, this constant value implies that the volume change for the reaction between hydroxyl ions and molecular water is zero and that, at least in glasses, speciation does not depend on pressure. Consistent with data from Ochs and Lange (1997, 1999), systematics in volume expansion for SiO2–M2O systems (M=H, Li, Na, K) suggests that the partial molar thermal expansion coefficient of H2O is about 4 × 10−5 K−1 in silicate glasses. Received: 30 June 1999 / Accepted: 5 November 1999  相似文献   

8.
We investigated seasonal variability in organic carbon (OC) budgets using a physical-biological model for the Mississippi River turbidity plume. Plume volume was calculated from mixed layer depth and area in each of four salinity subregions based on an extensive set of cruise data and satellite-derived suspended sediment distributions. These physical measurements were coupled with an existing food web model to determine seasonally dependent budgets for labile (reactive on time scales of days to weeks) OC in each salinity subregion. Autochthonous gross primary production (GPP) equaled 1.3×1012 g C yr−1 and dominated labile OC inputs (88% of the budget) because riverine OC was assumed mostly refractory (nonreactive). For perspective, riverine OC inputs amounted to 3.9×1012 g C yr−1, such that physical inputs were 3 times greater than biological inputs to the plume. Annually, microbial respiration (R) accounted for 65% of labile OC losses and net metabolism (GPP—R) for the entire plume was, autotrophic, equaling 5.1×1011 g C yr−1. Smaller losses of labile OC occurred via sedimentation (20%), advection (10%), and export to higher trophic levels (5%). In our present model, annual losses of labile OC are 10% higher than inputs, indicating future improvements are required. Application of our model to estimate air-sea carbon dioxide (CO2) fluxes indicated the plume was a net sink of 2.0×109 mol CO2 yr−1, of which 90% of the total drawdown was from biotic factors. In all seasons, low salinity waters were a source of CO2 (pCO2=560–890 μatm), and intermediate to high salinity waters were a sink of CO2 (pCO2=200–370 μatm). Our model was also used to calculate O2 demand for the development, of regional hypoxia, and our spring and early summer budgets indicated that sedimentation of autochthonous OC from the immediate plume contributed 23% of the O2 demand necessary for establishment of hypoxia in the region.  相似文献   

9.
Sulfate transport in a Coastal Plain confining unit, New Jersey, USA   总被引：1，自引：0，他引：1  
 A transient 1-D, two-pathway non-equilibrium deterministic advective dispersion model was used to examine the distribution of chloride (43–100 mg/L) and sulfate (57–894 mg/L) concentrations in the 35-m-thick section of the Lower confining unit, Atlantic Coastal Plain, New Jersey, USA. The model was used to constrain hypotheses about how pore-water chemistry changed over time. Explanations of the solute concentrations were explored by inverse and direct methods given a few known constraints, including concentrations of pore-water constituents from 12 core samples, reported simulated flow rates, and estimated hydrogeologic properties. The hypothesis that is best supported by the model results is that the distribution of chloride and sulfate concentrations in the confining unit reflect the history of the aquifer system since it was filled with seawater at the last eustatic high, about 84×103yr BP. The model simulates fresh-water flushing of the seawater-permeated silts at a steady upward pore-water flow velocity of 8.8×10–6 m/d, with a dispersion coefficient of 9.2×10–7 m2/d, a dimensionless partition expression for chloride, βCl=0.981, and a dimensionless exchange coefficient, ωCl=0.31×10–2. Sulfate concentrations were simulated over the flow path using flow and dispersion values calculated for chloride transport plus a retardation term. Parameters for sulfate transport include retardation coefficient=4.51, βSO4=0.994, and ωSO4=0.31×10–2. Sensitivity analysis indicates that the model is most sensitive to flow velocity, and that fresh-water flushing of the confining unit is best simulated by having seawater concentration levels at the inflow boundary of the confining unit exponentially decrease with a concentration half-life rate of 825 yr. Received, January 1997 / Revised, April 1998, October 1998, January 1999 / Accepted, January 1999  相似文献   

10.
Thermal behavior of two new exhalation copper-bearing minerals, bradaczekite and urusovite, from the Great Tolbachik Fissure Eruption (1975–1976, Kamchatka Peninsula, Russia) has been studied by X-ray thermal analysis within the range 20–700°C in air. The following major values of the thermal expansion tensor have been calculated for urusovite: α11 = 10, α22 = αb = 7, α33 = 4, αV = 21 × 10−6°C−1, μ = c∧α33 = 49° and bradaczekite: α11aver = 23, α22 = 8, α33aver = 6 × 10−6°C−1, μ(c∧α33) = 73°. The sharp anisotropy of thermal deformations of these minerals, absences of phase transitions, and stability of the minerals in the selected temperature range corresponding to conditions of their formation and alteration during the posteruption period of the volcanic activity are established.  相似文献   

11.
We investigated the electrical conductivity of amphibole-bearing rocks under the conditions of the middle to lower crust. Alternating current measurements were performed in the frequency range of 10–106 Hz in a cubic-anvil high-pressure apparatus at 0.5–1.0 GPa and 373–873 K. The electrical conductivity of these rocks is weakly temperature dependent below ~800 K with modest anisotropy and relatively low conductivity (~5 × 10−3 S/m at ~750 K with the activation enthalpy of 64–67 kJ/mol). However, the electrical conductivity starts to increase with temperature more rapidly above ~800 K (activation enthalpy of 320–380 kJ/mol). The infrared spectroscopy observations indicate that dehydration occurs in this high temperature regime. The observed high activation enthalpy and the reproducibility suggest that the enhanced conductivity is not due to the direct effect caused by the generation of conductive fluids. Dehydration of amphibole is associated with the oxidation of iron (from ferrous to ferric), and we suggest that the increased conductivity associated with dehydration is caused by oxidation. This effect may explain high electrical conductivity observed in some regions of the continental crust.  相似文献   

12.
The accepted standard state entropy of titanite (sphene) has been questioned in several recent studies, which suggested a revision from the literature value 129.3 ± 0.8 J/mol K to values in the range of 110–120 J/mol K. The heat capacity of titanite was therefore re-measured with a PPMS in the range 5 to 300 K and the standard entropy of titanite was calculated as 127.2 ± 0.2 J/mol K, much closer to the original data than the suggested revisions. Volume parameters for a modified Murgnahan equation of state: V P,T  = V 298° × [1 + a°(T − 298) − 20a°(T − 298)] × [1 – 4P/(K 298 × (1 – 1.5 × 10−4 [T − 298]) + 4P)]1/4 were fit to recent unit cell determinations at elevated pressures and temperatures, yielding the constants V 298° = 5.568 J/bar, a° = 3.1 × 10−5 K−1, and K = 1,100 kbar. The standard Gibbs free energy of formation of titanite, −2456.2 kJ/mol (∆H°f = −2598.4 kJ/mol) was calculated from the new entropy and volume data combined with data from experimental reversals on the reaction, titanite + kyanite = anorthite + rutile. This value is 4–11 kJ/mol less negative than that obtained from experimental determinations of the enthalpy of formation, and it is slightly more negative than values given in internally consistent databases. The displacement of most calculated phase equilibria involving titanite is not large except for reactions with small ∆S. Re-calculated baric estimates for several metamorphic suites yield pressure differences on the order of 2 kbar in eclogites and 10 kbar for ultra-high pressure titanite-bearing assemblages.  相似文献   

13.
The rare-earth element （REE） concentrations of representative granite samples from the southeast of the Obudu Plateau, Nigeria, were analyzed with an attempt to determine the signatures of their source, evolutionary history and tectonic setting. Results indicated that the granites have high absolute REE concentrations （190×10^-6-1191×10^-6; av.=549×10^-6） with the chondrite-normalized REE patterns characterized by steep negative slopes and prominent to slight or no negative Eu anomalies. All the samples are also characterized by high and variable concentrations of the LREE （151×10^-6-1169×10^-6; av.= 466×10^-6）, while the HREE show low abundance （4×10^-6-107×10^-6; av.=28×10^-6）. These are consistent with the variable levels of REE fractionation, and differentiation of the granites. This is further supported by the range of REE contents, the chondrite-normalized patterns and the ratios of LaN/YbN （2.30-343.37）, CeN/YbN （5.94-716.87）, LaN/SmN （3.14-11.68） and TbN/YbN （0.58-1.65）. The general parallelism of the REE patterns, suggest that all the granites were comagmatic in origin, while the high Eu/Eu＊ ratios （0.085-2.807; av.=0.9398） indicate high fo2 at the source. Similarly, irregular variations in LaN/YbN, CeN/YbN and Eu/Eu＊ ratios and REE abundances among the samples suggest behaviors that are related to mantle and crustal sources.  相似文献   

14.
The Liuyuan area,which is located on the southern margin of the Beishan orogenic belt,develops abundant Early Paleozic granitoids.SHRIMP zircon U-Pb dating yielded a weighted mean 206Pb/238U age of 421±8 Ma for the Liuyuan granodiorite(Zhao Zehui et al.,2007),implying its Late Silurian intrusion.Geochemical compositions showed that the Liuyuan granodiorite is characterized by high SiO2(65.01%-67.31%),A12O3(17.17%-18.05%) and Na2O(Na2O/K2O=1.67-1.87) but low Mg# contents calculated as 100×Mg2+/(Mg2++∑Fe2+) from 28.77 to 31.15,as well as being enriched in Sr(472×10-6-517×10-6) but depleted in Yb(1.2×10-6-1.42×10-6) and Y(12.8×10-6-14×10-6).The REEs are characterized by right-inclined patterns with LREE enrichment,HREE depletion and slightly negative Eu anomalies(Eu/Eu*=0.91-0.97).Major and trace elements indicate that the granodiorite is an adakite.The Nb/Ta values of the granodiorite vary from 10.80 to 18.01 and Nb/U from 6.32 to 10.09,both lying between the values of the crust and the mantle.The rock has low εNd(t) values(-2.5--0.8) and high ISr(0.706321-0.706495).Geochemical and Sr-Nd isotopic compositions indicate that the Liuyuan granodiorite is possibly derived from partial melting of thickening lower crust,related to mantle underplating.The Yb-Ta and Y+Nb-Rb discriminant diagrams imply the Liuyuan granodiorite intruded in a local extensional tectonic setting during late collision.Combined with previous studies on geochronology,geochemistry and tectonic setting of granitoids,we interprete that the constraint of this adakite in the Liuyuan area indicates that the tectonic setting may have transformed from collision to extension during the Early Devonian.  相似文献   

15.
The extent of authigenic alteration of biogenic and reactive silica in Pearl River estuarine sediments has been estimated using wet-chemical digestion methods. Results show relatively constant distributions of biogenic and reactive Si horizontally and vertically. Based on three core measurements, the biogenic and total reactive Si average 77.91 and 264.77 μmol Si g−1, respectively. Their extents of authigenic alteration are correspondingly estimated as ~55.6 and ~70.6%. The average biogenic Si accumulation rate is calculated as 1.91 × 109 mol Si year−1, which translates into storage of ~7.15% of the annual riverine dissolved silica input. By contrast, the total reactive Si accumulation rate is as high as 6.49 × 109 mol Si year−1, improving annual riverine silicic acid storage to ~24.19%. Detailed investigation is required for a good understanding of early diagenetic process of biogenic and reactive silica in this subtropical area.  相似文献   

16.
Analysis of 3-m sediment cores revealed that profiles of carbon (C), sulfur (S), and iron (Fe) varied with relative distance from marine and terrestrial sediment sources in Tomales Bay California. Despite relatively high sedimentation rates throughout the bay (historically 3–30 mm yr−1), sulfate reduction of deposited organic matter led to free-sulfide accumulation in sediments only at the location farthest from terrestrial runoff, the source of reactive iron. Acid-volatile sulfide concentrations in all sediments (<10 μmol g−1) were low relative to concentrations of chromiumreducible sulfide (up to 400 μmol g−1 farthest from the reactive iron source). A calculated index of iron availability, used to describe sediment resistance to build-up of free sulfide, was lowest at this location. Recent, upward shifts in reactive Fe concentration and in the relative contribution of terrestrial orgnic carbon (measured as a shift in δ13C of bulk sediment organic matter) in all cores indicated that erosion and transport of sediments from the watershed surrounding Tomales Bay increased after European settlement in the 1850s.  相似文献   

17.
A 52-yr record of dissolved oxygen in Chesapeake Bay (1950–2001) and a record of nitrate (NO3 −) loading by the Susquehanna River spanning a longer period (1903, 1945–2001) were assembled to describe the long-term pattern of hypoxia and anoxia in Chesapeake Bay and its relationship to NO3 − loading. The effect of freshwater inflow on NO3 − loading and hypoxia was also examined to characterize its effect at internannual and longer time scales. Year to year variability in river flow accounted for some of the observed changes in hypoxic volume, but the long-term increase was not due to increased river flow. From 1950–2001, the volume of hypoxic water in mid summer increased substantially and at an accelerating rate. Predicted anoxic volume (DO<0.2 mg I−1) at average river flow increased from zero in 1950 to 3.6×109 m3 in 2001. Severe hypoxia (DO<1.0 mg I−1) increased from 1.6×109 to 6.5×109 m3 over the same period, while mild hypoxia (DO<2.0 mg I−1) increased from 3.4×109 to 9.2×109 m3. NO3 − concentrations in the Susquehanna River at Harrisburg, Pennsylvania, increased up to 3-fold from 1945 to a 1989 maximum and declined through 2001. On a decadal average basis, the superposition of changes in river flow on the long-term increase in NO3 − resulted in a 2-fold increase in NO3 − loading from the Susquehanna River during the 1960s to 1970s. Decadal average loads were subsequently stable through the 1990s. Hypoxia was positively correlated with NO3 − loading, but more extensive hypoxia was observed in recent years than would be expected from the observed relationship. The results suggested that the Bay may have become more susceptible to NO3 − loading. To eliminate or greatly reduce anoxia will require reducing average annual total nitrogen loading to the Maryland mainstem Bay to 50×106 kg yr−1, a reduction of 40% from recent levels.  相似文献   

18.
In this study rates of oxygen, ammonium (NH4 +), nitrate (NO3 −), nitrite (NO2 −), and nitrous oxide (N2O) fluxes, nitrogen (N) fixation, nitrification, and denitrification were compared between two intertidal sites for which there is an abundant global literature, muddy and sandy sediments, and two sites representing the rocky intertidal zone where biogeochemical processes have scarcely been investigated. In almost all sites oxygen production rates greatly exceeded oxygen consumption rates. During daylight, NH4 + and NO3 − uptake rates together with ammonification could supply the different N requirements of the primary producer communities at all four sites; N assimilation by benthic or epilithic primary producers was the major process of dissolved inorganic nitrogen (DIN) removal; N fixation, nitrification, and denitrification were minor processes in the overall light DIN cycle. At night, distinct DIN cycling processes took place in the four environments, denitrification rates ranged from 9 ± 2 to 360 ± 30 μmol N2 m−2 h−1, accounting for 10–48% of the water column NO3 − uptake; nitrification rates varied from 0 to 1712 ± 666 μmol NH4 + m−2 h−1. A conceptual model of N cycle dynamics showed major differences between intertidal sediment and rocky sites in terms of the mean rates of DIN net fluxes and the processes involved, with rocky biofilm showing generally higher fluxes. Of particular significance, the intertidal rocky biofilms released 10 times the amount of N2O produced in intertidal sediments (up to 17 ± 6 μmol N2O m−2 h−1), representing the highest N2O release rates ever recorded for marine systems. The biogeochemical contributions of intertidal rocky substrata to estuarine and coastal processes warrant future detailed investigation.  相似文献   

19.
The crystal structure of orthorhombic (Pbnm) ScAlO3 perovskite has been refined to 5 GPa using single-crystal X-ray diffraction. The compression of the structure if anisotropic with β a =1.39(3)×10−3 GPa−1, β b =1.14(3)×10−3 GPa−1 and β c =1.84(3)×10−3 GPa−1. The isothermal bulk modulus of ScAlO3, K T , determined from fitting a Birch-Murnaghan equation of state (K ′ T =4) to the volume compression data is 218(1) GPa. The interoctahedral angles to not vary significantly with pressure, and the compression of the structure is entirely attributable to compression of the AlO6 octahedra. The compressibilities of the constituent AlO6 and ScO12 are well matched: βAl−O=1.6×10−3 GPa−1 and βSc−O=1.5×10−3 GPa−1. Therefore the distortion of the structure shows no significant change with increasing pressure. Received: 18 August 1997 / Revised, accepted: 11 November 1997  相似文献   

20.
The study was designed to establish the distributions of trace metals, dissolved organic carbon, and inorganic nutrients as well as to assess the extent of anthropogenic inputs into the Narmada and Tapti rivers. Water and sediment qualities are variable in the rivers, and there are major pollution problems at certain locations, mainly associated with urban and industrial centers. The metal concentrations of samples of the aquatic compartments investigated were close to the maximum permissible concentration for the survival of aquatic life, except for higher values of Cu (5–763 μg l−1), Pb (24–376 μg l−1), Zn (24–730 μg l−1), and Cr (70–740 μg l−1) and for drinking water except for elevated concentrations of metals such as Pb, Fe (850–2,060 μg l−1), Cr, and Ni (20–120 μg l−1). In general, the concentrations of trace metals in the rivers vary down stream which may affect the “health” of the aquatic ecosystem and may also affect the health of the rural community that depends on the untreated river water directly for domestic use. The assessment of EF, I geo, and PLI in the sediments reveals overall moderate pollution in the river basins.  相似文献   

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