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1.
An approach is presented to investigate the regional evolution of groundwater in the basin of the Amacuzac River in Central Mexico. The approach is based on groundwater flow cross-sectional modeling in combination with major ion chemistry and geochemical modeling, complemented with principal component and cluster analyses. The hydrogeologic units composing the basin, which combine aquifers and aquitards both in granular, fractured and karstic rocks, were represented in sections parallel to the regional groundwater flow. Steady-state cross-section numerical simulations aided in the conceptualization of the groundwater flow system through the basin and permitted estimation of bulk hydraulic conductivity values, recharge rates and residence times. Forty-five water locations (springs, groundwater wells and rivers) were sampled throughout the basin for chemical analysis of major ions. The modeled gravity-driven groundwater flow system satisfactorily reproduced field observations, whereas the main geochemical processes of groundwater in the basin are associated to the order and reactions in which the igneous and sedimentary rocks are encountered along the groundwater flow. Recharge water in the volcanic and volcano-sedimentary aquifers increases the concentration of HCO3 –, Mg2+ and Ca2+ from dissolution of plagioclase and olivine. Deeper groundwater flow encounters carbonate rocks, under closed CO2 conditions, and dissolves calcite and dolomite. When groundwater encounters gypsum lenses in the shallow Balsas Group or the deeper Huitzuco anhydrite, gypsum dissolution produces proportional increased concentration of Ca2+ and SO4 2–; two samples reflected the influence of hydrothermal fluids and probably halite dissolution. These geochemical trends are consistent with the principal component and cluster analyses.  相似文献   

2.
Major‐ and trace‐element chemistry (including rare‐earth elements), total‐rock Rb‐Sr and U‐Pb and zircon U‐Pb data are used in an attempt to distinguish between two essentially coeval, felsic volcanic suites: the predominantly submarine Woodlawn suite which is associated with massive Cu‐Pb‐Zn sulphide mineralization and the terrestrial Mt Painter suite, with minor vein‐type mineralization. The Woodlawn samples are the unmineralized equivalents of the volcanics in the immediate ore environment.

Alteration perturbs some of the major‐ and trace‐element chemistry, particularly Ca and alkalis, thereby precluding their usefulness. REE patterns exhibit a significant light to heavy rare‐earth enrichment with an average La/Yb of 12 in the Mt Painter volcanics compared with 5.6 in the Woodlawn volcanics. Both suites have a marked negative Eu anomaly, with that of the Woodlawn samples more pronounced (‐45.5) than in the Mt Painter volcanics (‐29.2). A hydrothermally‐altered sample from Woodlawn has apparently lost about 50% of its light rare‐earth elements.

Initial 87Sr/86Sr ratios at about 0.711 are the same for rocks from both suites and differences in initial lead‐isotopic ratios appear negligible.

Zircons from both suites are a mixture of clear euhedral crystals and rounded discrete crystals or rounded cores overgrown by clear zircon. The U‐Pb data substantiate the morphological features in that the zircon suites both contain older inherited Pb but the Mt Painter zircons contain a greater proportion.

Cs concentrations and Cs/Rb and Ti/Zr ratios can be used to distinguish between the Woodlawn suite and the Mt Painter suite.  相似文献   

3.
A base line study involving analysis of groundwater samples from the Jhansi district were carried out to determine the major and trace element chemistry and to assess the hydrogeochemical processes and water quality for domestic and irrigation uses. Study results show that groundwater is mildly acidic to alkaline in nature and HCO3 ?, Cl?, Ca2+, Na+ and Mg2+ are the major contributing ions for the dissolved loads. The data plotted on the Gibbs and Piper diagrams reveal that the groundwater chemistry is mainly controlled by rock weathering with secondary contribution from anthropogenic sources. In a majority of the groundwater samples, alkaline earth metals exceed alkalies and weak acid dominate over strong acids. Ca–Mg–HCO3 is the dominant hydrogeochemical facies in the majority of the groundwater samples. The computed saturation indices demonstrate that groundwater is oversaturated with respect to dolomite and calcite. Kaolinite is the possible mineral that is in equilibrium with the water, implying that the groundwater chemistry favors kaolinite formation. A comparison of groundwater quality parameters in relation to specified limits for drinking water shows that the concentrations of TDS, F?, NO3 ?, total hardness and Fe are exceeding the desirable limits in many water samples. Quality assessment for irrigation uses reveal that the groundwater is of good to suitable category. Higher salinity and residual sodium carbonate values at some sites restrict the suitability of groundwater and need an adequate drainage and water management plan for the area.  相似文献   

4.
This study applied a comprehensive quantitative approach including statistical, principal component and gray relation analyses to assess the groundwater chemistry based on monitored data from 840 samples collected from the lower reaches of Tarim River from 2000 to 2009. The main findings were: (1) there were six types of groundwater chemistry in the lower reaches of Tarim River where Cl·SO4–Na·Mg was the dominant type accounting for 73.57% in all samples. There were linear relationships among chemical parameters, where TDS had significant multiple correlations with Na+, K+, Mg2+, Ca2+ and Cl−, respectively. (2) Three principal components (PC1, PC2 and PC3) were extracted. They included comprehensive measurements for salinization, alkalinity and pH, respectively. Most parameters showed decreasing trends during the period of 2000–2009, as well as the scores on PC1, because the concentrations of various chemical substances were diluted due to the uplift of the groundwater table in the lower reaches and the implementation of the ecological water delivery project in 2000. (3) HCO3 − was the most sensitive chemical parameter affected by the groundwater table followed by TA, Mg2+, TH, SO42−, K+, TDS and TS. PC2 was the most sensitive principal component to the change of the groundwater table followed by PC1 and PC3.  相似文献   

5.
The reservoir temperature and conceptual model of the Pasinler geothermal area, which is one of the most important geothermal areas in Eastern Anatolia, are determined by considering its hydrogeochemical and isotope properties. The geothermal waters have a temperature of 51 °C in the geothermal wells and are of Na–Cl–HCO3 type. The isotope contents of geothermal waters indicate that they are of meteoric origin and that they recharge on higher elevations than cold waters. The geothermal waters are of immature water class and their reservoir temperatures are calculated as 122–155 °C, and their cold water mixture rate is calculated as 32%. According to the δ13CVPDB values, the carbon in the geothermal waters originated from the dissolved carbon in the groundwaters and mantle-based CO2 gases. According to the δ34SCDT values, the sources of sulfur in the geothermal waters are volcanic sulfur, oil and coal, and limestones. The sources of the major ions (Na+, Ca2+, Mg2+, Cl?, and HCO3 ?) in the geothermal waters are ion exchange and plagioclase and silicate weathering. It is determined that the volcanic rocks in the area have effects on the water chemistry and elements like Zn, Rb, Sr, and Ba originated from the rhyolite, rhyolitic tuff, and basalts. The rare earth element (REE) content of the geothermal waters is low, and according to the normalized REE diagrams, the light REE are getting depleted and heavy REE are getting enriched. The positive Eu and negative Ce anomalies of waters indicate oxygen-rich environments.  相似文献   

6.
Lake water, river water, and groundwater from the Lake Qinghai catchment in the northeastern Tibetan Plateau, China have been analyzed and the results demonstrate that the chemical components and 87Sr/86Sr ratios of the waters are strictly constrained by the age and rock types of the tributaries, especially for groundwater. Dissolved ions in the Lake Qinghai catchment are derived from carbonate weathering and part from silicate sources. The chemistry of Buha River water, the largest tributary within the catchment, underlain by the late Paleozoic marine limestone and sandstones, constrains carbonate-dominated compositions of the lake water, being buffered by the waters from the other tributaries and probably by groundwater. The variation of 87Sr/86Sr ratios with cation concentrations places constraint on the Sr-isotopic compositions of the main subcatchments surrounding Lake Qinghai. The relative significance of river-water sources from different tributaries (possibly groundwater as well) in controlling the Sr distribution in Lake Qinghai provides the potential to link the influence of hydrological processes to past biological and physical parameters in the lake. The potential role of groundwater input in the water budget and chemistry of the lake emphasizes the need to further understand hydrogeological processes within the Lake Qinghai system.  相似文献   

7.
A survey on quality of groundwater was carried out for assessing the geochemical characteristics and controlling factors of chemical composition of groundwater in a part of Guntur district, Andhra Pradesh, India, where the area is underlain by Peninsular Gneissic Complex. The results of the groundwater chemistry show a variation in pH, EC, TDS, Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, SO4 2?, NO3 ? and F?. The chemical composition of groundwater is mainly characterized by Na+?HCO3 ? facies. Hydrogeochemical type transits from Na+–Cl?–HCO3 ? to Na+–HCO3 ?–Cl? along the flow path. Graphical and binary diagrams, correlation coefficients and saturation indices clearly explain that the chemical composition of groundwater is mainly controlled by geogenic processes (rock weathering, mineral dissolution, ion exchange and evaporation) and anthropogenic sources (irrigation return flow, wastewater, agrochemicals and constructional activities). The principal component (PC) analysis transforms the chemical variables into four PCs, which account for 87% of the total variance of the groundwater chemistry. The PC I has high positive loadings of pH, HCO3 ?, NO3 ?, K+, Mg2+ and F?, attributing to mineral weathering and dissolution, and agrochemicals (nitrogen, phosphate and potash fertilizers). The PC II loadings are highly positive for Na+, TDS, Cl? and F?, representing the rock weathering, mineral dissolution, ion exchange, evaporation, irrigation return flow and phosphate fertilizers. The PC III shows high loading of Ca2+, which is caused by mineral weathering and dissolution, and constructional activities. The PC IV has high positive loading of Mg2+ and SO4 2?, measuring the mineral weathering and dissolution, and soil amendments. The spatial distribution of PC scores explains that the geogenic processes are the primary contributors and man-made activities are the secondary factors responsible for modifications of groundwater chemistry. Further, geochemical modeling of groundwater also clearly confirms the water–rock interactions with respect to the phases of calcite, dolomite, fluorite, halite, gypsum, K-feldspar, albite and CO2, which are the prime factors controlling the chemistry of groundwater, while the rate of reaction and intensity are influenced by climate and anthropogenic activities. The study helps as baseline information to assess the sources of factors controlling the chemical composition of groundwater and also in enhancing the groundwater quality management.  相似文献   

8.
Subduction related basalts display wide ranges in large ion lithophile element ratios (e.g., Rb/Ba and Rb/ Sr) which are unlikely to result from mixing, but suggest a role for small degree partial melting of a relatively Rb-poor mantle wedge source. However, these variations do not correlate with other trace element criteria, such as the depletions of high field strength elements (HFSE) and light rare earth elements (LREE) relative to the LILE, which characterise subduction related magmatism. Integration of radiogenic isotope and trace element data demonstrates that the elemental enrichment cannot be simply related to two component mixtures inferred from isotopic variations. Thus a minimum of three components is required to describe the geochemistry of subduction zone basalts. Two are subduction related: high Sr/Nd material is derived from the dehydration of subducted basaltic ocean crust, and a low Sr/Nd component is thought to be from subducted terrigenous sediment. The third component is in the mantle wedge, it is usually similar to the source of MORB, particularly in its isotopic composition. However, in some cases, notably continental areas, more enriched mantle wedge material with relatively high 87Sr/86Sr, low 143Nd/144Nd and elevated incompatible trace element contents may be involved Mixing of these three components is capable of producing both the entire range of Sr, Nd and Pb isotope signatures observed in destructive margin basalts, and their distinctive trace element compositions. The isotope differences between Atlantic and Pacific island arc basalts are attributed to the isotope compositions of sediments in the two oceans.  相似文献   

9.
Anders Lindh 《Lithos》1975,8(2):151-161
A population of 117 coexisting nonalkaline pyroxene pairs has been studied statistically to evaluate compositional and thermal effects on the element distribution. KDMgopx-cpx is influenced by the Fe/Mg-ratio, by the Ca content—especially of clinopyroxene—and by the content of tetrahedral Al. Fe and tetrahedral Al are found to be negatively correlated. A principal component analysis based on the variation of Si, AlIV, AlVI, Fe, Mg, Mn, Ca is performed. Dropping of highly correlated variables does not affect the result significantly. The first principal component reflects the major chemical variation in Fe and Mg. When using ferrous and ferric iron as separate entries of the analysis, either the second or the third component demonstrates a temperature dependence. It is, however, not possible to obtain pure temperature and chemical components due to the composition not being uncorrelated to temperature of formation. From these components a graph reflecting temperature of formation has been constructed.  相似文献   

10.
The River Ganges being the most sacred river and lifeline to millions of Indians in serving their water requirements is facing excessive threat of pollution. Under various river management and conservation strategies for its protection, the assessment of water quality of its main tributary Ramganga River is lacking. This study focuses on assessment of physicochemical and heavy metal pollution of the Ramganga River by application of multivariate statistical techniques. Sampling of Ramganga River at sixteen sampling sites was carried out in three seasons (summer, monsoon and winter) of 2014. The collected water samples were analyzed for physicochemical parameters and heavy metals. Results from cluster analysis (CA) of the data divided the whole stretch of the river into three clusters as elevation from 1304 to 259 m as less polluted, from 207 to 154 m as moderately polluted and from elevation 154 to 139 m as high-polluted stretches with anthropogenic as main sources of pollution in high-polluted stretch. Principal component analysis of the seasonal dataset resulted in three significant principal components (PC) in each season explaining 72–8% of total variance with strong loadings (>0.75) of PC1 on fluoride (F?), chloride (Cl?), sodium (Na+), calcium (Ca2+), magnesium (Mg2+), bicarbonate (HCO3 ?), total dissolved solids and electrical conductivity. Temporal variation by one-way ANOVA (Analysis of Variance) showed significant seasonal variation was in the pH, chemical oxygen demand, biochemical oxygen demand, turbidity, HCO3 ?, F?, Zn, cadmium (Cd) and Mn (p < 0.05). Turbidity showed approximately a twofold increase in monsoon season due to rainfall in the catchment area and subsequent flow of runoff into the river. Concentration of HCO3 ?, F? and pH also showed similar increase in monsoon. The concentration of Zn, Cd and Mn showed an increasing trend in summers compared to monsoon and winter season due to dilution effect in the monsoon season and its lasting effect in winters.  相似文献   

11.
This study investigated the effect of a pine/oak forest canopy on rainfall chemistry in the Qinling Mountains. The area is an important water source for China’s North-to-South Water Transfer Project. Rainfall and throughfall samples were collected at the Huoditang Natural Forest in 1999, 2004, and 2009. Analyses of the samples indicated that the forest canopy had several important effects on rainfall chemistry. Rainfall pH generally increased as water passed through the canopy. On average, the rainfall pH increased by 0.54 pH units. The canopy’s effect declined after deciduous trees lost their leaves late in the sampling season. Rainfall NO3 ? concentrations generally declined as water passed through the forest canopy, but PO4 3? concentrations generally increased. On average, rainfall NO3 ? concentration declined by 0.135 mg/L as it passed though the forest canopy and PO4 3? increased by 0.85 mg/L. The forest canopy had a mitigating effect on the base cation content of throughfall. Specifically, K+, Na+, Ca2+ and Mg2+ were leached from the canopy when the concentration of these cations in rainfall was low. In contrast, K+, Na+, Ca2+ and Mg2+ were absorbed by the canopy when the concentration of these cations in rainfall was high. The pH of rainfall, as well as its K+, Ca2+ and Mg+ concentration, influenced the effect of the forest canopy on the base cation content of throughfall. The concentration of Cd, Pb, and Zn in rainfall generally decreased as water passed through the forest canopy, but the concentration of Fe in rainfall generally increased. The Cd concentration decreased by an average of 3.938 μg/L, the Pb concentration decreased by an average of 8.457 μg/L, and the Zn concentration decreased by an average of 0.986 mg/L. The Fe concentration increased by an average of 0.009 mg/L. The canopy’s ability to absorb Cd declined after several rainfall events in which rainfall Cd concentrations were relatively high.  相似文献   

12.
Carbonate rocks and natural waters exhibit a wide range in the concentration and isotopic composition of strontium. This wide range and the quantifiable covariation of these parameters can provide diagnostic tools for understanding processes of fluid-rock interaction. Careful consideration of the uncertainties associated with trace element partitioning, sample heterogeneity and fluid-rock interaction mechanisms is required to advance the application of the trace element and isotope geochemistry of strontium to studies of diagenesis, goundwater evolution, ancient seawater chemistry and isotope stratigraphy. A principal uncertainty involved in the application of Sr concentration variations to carbonate systems is the large range of experimental and empirical results for trace element partitioning of Sr between mineral and solution. This variation may be a function of precipitation rate, mineral stoichiometry, crystal growth mechanism, fluid composition and temperature. Calcite and dolomite in ancient limestones commonly have significantly lower Sr concentrations (20–70 p.p.m.) than would be expected from published trace element distribution coefficient values and Sr/Ca ratios of most modern sedimentary pore waters. This discrepancy probably reflects the uncertainties associated with determining distribution coefficient values. As techniques improve for the analytical measurement and theoretical modelling of Sr concentration and isotopic variations, the petrological analysis of carbonate samples becomes increasingly important. The presence of even small percentages of non-carbonate phases with high Rb concentrations and high 87 Sr86 Sr values, such as clay minerals, can have significant effects on the measured 87 Sr/86 Sr values of carbonate rocks, due to the decay of 87Rb to 87 Sr. For example, a Permian marine limestone with 50 p.p.m. Sr and 1 p.p.m. Rb will have a present-day 87 Sr/86 Sr value that is >2 × 10?4 higher than its original value. This difference is an order of magnitude greater than the analytical uncertainty, and illustrates the importance of assessing the need for and accuracy of such corrections. A quantitative evaluation of the effects of water-rock interaction on Sr concentrations and isotope compositions in carbonates strengthens the application of these geochemical tracers. Geochemical modelling that combines the use of trace elements and isotopes can be used to distinguish between different mechanisms of water-rock interaction, including diffusive and advective transport of diagenetic constituents in meteoric pore fluids during the recrystallization of carbonate minerals. Quantitative modelling may also be used to construct diagnostic fluid-rock interaction trends that are independent of distribution coefficient values, and to distinguish between mixing of mineral end-members and fluid-rock interaction.  相似文献   

13.
The hydrochemistry of a perennial river has been investigated with multivariate cluster analysis (CA) and principal component analysis/factor analysis (PCA/FA). The aim was to investigate parameters responsible for spatial and temporal variations of river water quality. Water quality was monitored along the river basin at 20 different sites over a period of 1 year from July, 2008 to June, 2009. Multivariate statistics revealed that Ca2+, Mg2+, Na+, K+, HCO3 ?, Cl?, H4SiO4, SO4 2?, NO2 ?, and PO4 3? were influenced by seasonal and spatial variations and that water quality was in the first place determined more by natural weathering processes than by anthropogenic activities. We could prove by (a) Box and Whisker plot, (b) matrix scatter score mean plot, (c) ternary plot, and (d) Gibbs plot that the chemistry of river water is controlled by lithogenic weathering processes. The higher concentration of dissolved silica during summer and the pre-monsoon season is explained by natural and tropical climatic conditions of the environment.  相似文献   

14.
This paper focuses on the suitability of spring water for drinking and irrigation purposes in a part of eastern Himalaya, south Sikkim. There are many anthropogenic and geogenic factors contributing as a source of major cations and anions in the spring water. The spring water chemistry show a variation in EC, pH, TDS, Temperature, Na+, K+, Mg2+, Ca2+, Fe2+, Pb, Mn, Cu, HCO3-, Cl-, PO43-, NO3-, F- and SO42-. Mainly two types of water quality indexing has been used, one for suitability of spring water for drinking purposes and the other for irrigation purposes. For drinking purposes, Piper diagram used for determination of water type, water quality index (WQI) for quality monitoring and saturation index for mineral dissolution in water. % Na, RSC (Residual Sodium Carbon) and SAR (sodium absorption ratio) have been used for irrigation suitability. Piper diagram shows that CaHCO3 type of water was dominant in the study area. The WQI depicted excellent category and SAR, percent sodium and RSC (Residual Sodium Carbon) depict excellent, good and permissible category for irrigation purposes. Principle component analysis (PCA) was used to determine the major influencing factor responsible for the variability in the parameters analysed of spring water.  相似文献   

15.
To compare relative reaction rates of mineral dissolution in a mineralogically simple groundwater aquifer, we studied the controls on solute concentrations, Sr isotopes, and rare earth element and yttrium (REY) systematics in the Cape Cod aquifer. This aquifer comprises mostly carbonate-free Pleistocene sediments that are about 90% quartz with minor K-feldspar, plagioclase, glauconite, and Fe-oxides. Silica concentrations and pH in the groundwater increase systematically with increasing depth, while Sr isotopic ratios decrease. No clear relationship between 87Sr/86Sr and Sr concentration is observed. At all depths, the 87Sr/86Sr ratio of the groundwater is considerably lower than the Sr isotopic ratio of the bulk sediment or its K-feldspar component, but similar to that of a plagioclase-rich accessory separate obtained from the sediment. The Si-87Sr/86Sr-depth relationships are consistent with dissolution of accessory plagioclase. In addition, solutes such as Sr, Ca, and particularly K show concentration spikes superimposed on their respective general trends. The K-Sr-87Sr/86Sr systematics suggests that accessory glauconite is another major solute source to Cape Cod groundwater. Although the authigenic glauconite in the Cape Cod sediment is rich in Rb, it is low in in-grown radiogenic 87Sr because of its young Pleistocene age. The low 87Sr/86Sr ratios are consistent with equilibration of glauconite with seawater. The impact of glauconite is inferred to vary due to its variable abundance in the sediments. In the Cape Cod groundwater, the variation of REY concentrations with sampling depth resembles that of K and Rb, but differs from that of Ca and Sr. Shale-normalized REY patterns are light REY depleted, show negative Ce anomalies and super-chondritic Y/Ho ratios, but no Eu anomalies. REY input from feldspar, therefore, is insignificant compared to input from a K-Rb-bearing phase, inferred to be glauconite. These results emphasize that interpretation of groundwater chemistry, even in relatively simple aquifers, may be complicated by solute contributions from “exotic” accessory minerals such as glauconite. To detect such peculiarities, groundwater studies should combine the study of elemental concentration and isotopic composition of several solutes that show different geochemical behavior.  相似文献   

16.
Granitoid rocks of the compositionally zoned Late Cretaceous Toulumne Intrusive Suite in the central Sierra Nevada, California, have initial87Sr/86Sr values (Sri) and143Nd/144Nd values (Ndi) that vary from 0.7057 to 0.7067 and from 0.51239 to 0.51211 respectively. The observed variation of both Sri and Ndi and of chemical composition in rocks of the suite cannot be due to crystal fractionation of magma solely under closed system conditons. The largest variation in chemistry, Ndi, and Sri is present in the outer-most equigranular units of the Tuolumne Intrusive Suite. Sri varies positively with SiO2, Na2O, K2O, and Rb concentrations, and negatively with Ndi, Al2O3, Fe2O3, MgO, FeO, CaO, MnO, P2O5, TiO2, and Sr concentrations. This covariation of Sri, Ndi and chemistry can be modeled by a process of simple mixing of basaltic and granitic magmas having weight percent SiO2 of 48.0 and 73.3 respectively. Isotopic characteristic of the mafic magma are Sri=0.7047, Ndi=0.51269 and 18O=6.0, and of the felsic magma are Sri=0.7068, Ndi=0.51212 and 18O=8.9. The rocks sampled contain from 50 to 80% of the felsic component. An aplite in the outer equigranular unit of the Tuolumne Intrusive Suite apparently was derived by fractional crystallization of plagioclase and hornblende from magma with granudiorite composition that was a product of mixing of the magmas described above. Siliceous magmas derived from the lower crust, having a maximum of 15 percent mantle-derived mafic component, are represented by the inner prophyritic units of the Tuolumne Intrusive Suite.  相似文献   

17.
Many lunar highland rocks have been extensively metamorphosed during the late heavy bombardment of the Moon 3.9–4.0 AE ago. Rubidium and other, more volatile elements were preferentially mobilized during this event, which resulted in a considerable scatter of RbSr model ages. This scatter can be considerably reduced by estimating the original Rb content on the basis of Sm or other, less mobile, incompatible elements. The principal uncertainty on the corrected model ages of 4.25–4.45 AE comes from the original Sm/Rb ratio.Highland rocks enriched in incompatible elements in most cases are mixtures between KREEP-basalt and other highland rock types. After corrections for Rb mobilization 3.9–4.0 AE ago, slight isotopic differences among KREEP-enriched rocks from different landing sites becomes noticeable. These differences correspond to different meteoritic groups as defined by Morgan et al. (1974). Apparently there existed slightly different KREEP basalt reservoirs, with formation ages ranging from 4.25 to 4.45 AE. These reservoirs were partly exposed through impacts of basin-forming planetesimals 3.9–4.0 AE ago. The resulting impact melts were contaminated with meteoritic material from the bombarding planetesimals.The 4.63 ± 0.1 AE RbSr isochron of trace element poor highland rocks (Schonfeld, 1976) is determined by a K,Rb- and Ba-rich component, which formed earlier and independently of KREEP basalts.  相似文献   

18.
Numerous natural and anthropogenic processes in a watershed produce the geochemical composition of a river, which can be altered over time by snowmelt and rainfall events and by built infrastructure (i.e., dams and diversions). Trace element concentrations coupled with isotopic ratios offer valuable insights to disentangle the effects of these processes on water quality. In this study, we measured a suite of 40+ trace and major elements (including As, Cd, Ce, Cr, Cs, Fe, La, Li, Mo, Pb, Rb, Sb, Se, Sr, Ti, Tl, U, and Zn), Sr isotopes (87Sr/86Sr), and stable isotopes of H and O (δD and δ18O) to investigate natural and anthropogenic processes impacting the Provo River in northern Utah, USA. The river starts as a pristine mountain stream and passes through agricultural and urban areas, with two major reservoirs and several major diversions to and from the river. We sampled the entire 120 km length of the Provo River at 13 locations from the Uinta Mountains to Utah Valley, as well as two important tributaries, across the range of hydrologic conditions from low flow to snowmelt runoff during the 2013 water year. We also sampled the furthest downstream site in the Utah Valley urban area during a major flood event. Trace element concentrations indicate that a variety of factors potentially influence Provo River chemistry, including inputs from weathering of carbonate/siliciclastic rocks (Sr) and black shales (Se and U), geothermal groundwater (As, Cs, Li, and Rb), soil erosion during snowmelt runoff (Ce, Cr, Fe, La, Pb, and Ti), legacy mining operations (Mo, Sb, and Tl), and urban runoff (Cr, Pb, and Zn). Although specific elements overlap between different groups, the combination of different elements together with isotopic measurements and streamflow observations may act as diagnostic tools to identify sources. 87Sr/86Sr ratios indicate a strong influence of siliciclastic bedrock in the headwaters with values exceeding 0.714 and carbonate bedrock in the lower reaches of the river with values approaching 0.709. δD and δ18O changed little throughout the year in the Provo River, suggesting that the river is primarily fed by snowmelt during spring runoff and snowmelt-fed groundwater during baseflow. Based on nonmetric multidimensional scaling (NMS) water chemistry was unique across the upper, middle, and lower portions of the river, with high temporal variability above the first reservoir but minimal temporal variability below the reservoir. Thus, the results show that dams alter water chemistry by allowing for settling of particle-associated elements and also by homogenizing inflows throughout the year to minimize dilution during snowmelt runoff. Taken together, trace element concentrations and isotopic measurements can be used to evaluate the complex geochemical patterns of rivers and their variability in space and time. These measurements are critical for identifying natural and anthropogenic impacts on river systems.  相似文献   

19.
On a series of eight cruises conducted in the northern Gulf of Mexico, efforts were made to characterize temporal and spatial variability in parameters of the photosynthesis-irradiance saturation curve (P mas B , αB, Ik) and to relate the observed variations to environmental conditions. Experiments to examine the importance of diel variation in upper mixed layer populations were conducted in July–August 1990 and March 1991. During July–August 1990, P max B and Ik showed significant increases and αB decreased during the photoperiod in both river plume and shelf-slope populations. During March 1991, no consistent covariance of P-I parameters with local time was found, although highest values of αB in the river plume were observed in early morning. Seasonal variation in P max B and αB were correlated with temperature. Spatial variations of photosynthetic parameters in the upper mixed layer ranged from twofold to threefold within any given cruise. Variations of photosynthetic parameters in the upper mixed layer were related to principal components derived from environmental variables, including temperature, salinity, nutrients, mixed layer depth, attenuation coefficient, and daily photosynthetically available radiation (PAR). Greater than 70% of the variation in the environmental variables could be accounted for by two principal components; the majority of this variation was associated with the first principal component, which was generally strongly correlated with salinity, nutrients, mixed layer depth, and attenuation coefficient. Correlations of P max B , αB, and Ik with the first principal component were found to be significant in some cases, an indication that spatial variability in P-I parameters was related to river outflow. Variation of P-I parameters in relation to depth and PAR were evaluated by regressions with principal components derived from depth, temperature, and mean daily PAR. For most cruises, P max B and Ik were negatively correlated with the first principal component, which was strongly positively correlated with depth and negatively correlated with daily PAR. This was consistent with a decrease in both P max B and Ik with depth that could be related to decreasing daily PAR. Positive correlations of αB with the first principal component for two cruises, March 1991 and April 1992, indicated an increasing trend with depth. In conclusion, relationships between P-I parameters and environmental variables in the region of study were significant in some cases, but variation between cruises made it difficult to generalize. We attributed this variation to the physically dynamic characteristics of the region and the possible effects of variables that were not included in the analysis such as species composition. Our findings do support the view that a limited set of observations may be adequate to characterize P-I parameter distributions in a given region within a restricted period of time.  相似文献   

20.
Petrographic, trace element and isotopic evidence demonstrates that magma mixing preceded the eruption of the Garner Mountain andesite. The flow contains reversely zoned plagioclase phenocrysts and amphibole pseudomorphs composed of plagioclase, clinopyroxene, orthopyroxene and opaque oxides. Partially resorbed quartz grains are also present. In contrast to the isotopically uniform matrix, plagioclase phenocrysts have 87Sr/86Sr ratios that correlate negatively with matrix Sr and positively with matrix Rb abundances. These observations demonstrate increasing isotopic disequilibrium between the plagioclase and matrix in the more evolved varieties of the flow.Plagioclase phenocrysts and matrix are assumed to record fractionation-assimilation events in different parts of the magma chamber. Early formed plagioclase phenocrysts crystallized under AFC conditions close to the roof of the chamber and were subsequently entrained in a liquid mixture composed of evolved interstitial liquid held in the partly crystallized roof zone and newly injected parental magma.  相似文献   

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