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1.
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   

2.
The Upper Cretaceous Torul pluton, located in the Eastern Pontides, is of sub-alkaline affinity and displays features typical of volcanic arc granitoids. It is a composite pluton consisting of granodiorite, biotite hornblende monzogranite, quartz monzodiorite, quartz monzonite and hornblende biotite monzogranite. The oldest syenogranite (77.9 ± 0.3 Ma) and the youngest quartz diorite form small stocks within the pluton. Samples from the granodiorites, biotite hornblende monzogranites, quartz monzodiorites, quartz monzonites and hornblende biotite monzogranites have SiO2 between 57 and 68 wt% and display high-K calc-alkaline, metaluminous to peraluminous characteristics. Chondrite-normalized REE patterns are fractionated (Lacn/Lucn = 6.0?14.2) with pronounced negative Eu anomalies (Eu/Eu* = 0.59–0.84). Initial ?Nd(i) values vary between ?3.1 and ?4.1, initial 87Sr/86Sr values between 0.7058 and 0.7072, and δ18O values between +4.4 and +7.3‰. The quartz diorites are characterized by relatively high Mg-number of 36–38, low contents of Na2O (2.3–2.5 wt%) and SiO2 (52–55 wt%) and medium-K calc-alkaline, metaluminous composition. Chondrite-normalized REE patterns are relatively flat [(La/Yb)cn =  2.8–3.3; (Tb/Yb)cn =  1.2] and show small negative Eu anomalies (Eu/Eu* = 0.74–0.76). Compared to the other rock types, radiogenic isotope signatures of the quartz diorites show higher 87Sr/86Sr (0.7075–0.7079) and lower ?Nd(i) (–4.5 to –5.3). The syenogranites have high SiO2 (70–74 wt%) and display high-K calc-alkaline, peraluminous characteristics. Their REE patterns are characterized by higher Lacn/Lucn (12.9) and Eu/Eu* (0.76–0.77) values compared to the quartz diorites. Isotopic signatures of these rocks [?Nd(i) =  ?4.0 to ?3.3; 87Sr/86Sr(i) =  0.7034?0.7060; δ18 O =  + 4.9 to + 8.2] are largely similar to the other rock types but differ from that of the quartz diorites. Fractionation of plagioclase, hornblende, pyroxene and Fe–Ti oxides played an important role in the evolution of Torul granitoids. The crystallization temperatures of the melts ranged from 800 to 900°C as determined from zircon and apatite saturation thermometry. All these characteristics, combined with low K2O/Na2O, low Al2O3/(FeOT + MgO + TiO2), and low (Na2O + K2O)/(FeOT + MgO + TiO2) ratios suggest an origin through dehydration melting of mafic lower crustal source rocks.  相似文献   

3.
Groundwater of an aquifer located in the vicinity of a large coal washery near Zarand City, Iran consists of two hydrochemically differing facies, which have been informally designated as groundwater (A) and groundwater (B). Groundwater (A) is native, brackish in composition and is characterized by Na+ > Mg2+ > Ca2+ > K+ and SO4 2? > HCO3 ? > Cl? > NO3 ?. Spearman’s rank correlation coefficient matrices, factor analysis data, and values of chloro-alkaline indices, C ratio and Na+/Cl? molar ratio indicate that in the groundwater (A), the ionic load of Ca2+, Mg2+, Na+, K+, SO4 2? and HCO3 ? is derived essentially from weathering of both carbonates and aluminosilicates and direct cation and reverse cation–anion exchange reactions. Groundwater (B) is the polluted variant of the groundwater (A), brackish to saline in composition, and unlike the groundwater (A), consists of HCO3 ? as the dominant anion. In comparison with the groundwater (A), the groundwater (B) contains higher concentrations of all ions, and its average ionic load (av. = 59.74 me/L) is 1.43 times higher than that of the groundwater (A) (av. = 41.54 me/L). Additional concentrations of Ca2+, Mg2+, K+, SO4 2?, Cl? and HCO3 ? in the groundwater (B) are provided mainly by downward infiltrating water from the coal washery tailings pond and reverse cation–anion exchange reaction between tailings pond water and exchanger of the aquifer matrix during non-conservative mixing process of groundwater (A) and tailings pond water. Certain additional concentrations of Na+, K+ and NO3 ? in the groundwater (B) are provided by other anthropogenic sources. Quality wise, both groundwaters are marginally suitable for cultivation of salt-tolerant crops only.  相似文献   

4.
Carbonate, largely in the form of dolomite, is found throughout the host rocks and ores of the Nchanga mine of the Zambian Copperbelt. Dolomite samples from the hanging wall of the mineralization show low concentrations of rare-earth elements (REE) and roof-shaped, upward convex, shale-normalized REE patterns, with positive Eu*SN anomalies (1.54 and 1.39) and marginally negative Ce anomalies (Ce*SN 0.98,0.93). In contrast, dolomite samples associated with copper and cobalt mineralization show a significant rotation of the REE profile, with HREE enrichment, and La/LuSN ratios <1 (0.06–0.42). These samples also tend to show variable but predominantly negative Eu*SN and positive cerium anomalies and an upwardly concave MREE distribution (Gd-Er). Malachite samples from the Lower Orebody show roof-tile-normalized REE patterns with negative europium anomalies (Eu*SN 0.65–0.80) and negative cerium anomalies (Ce*SN 0.86–0.9). The carbonate 87Sr/86Sr signature correlates with the associated REE values. The uppermost dolomite samples show Neoproterozoic seawater-like 87Sr/86Sr ratios ranging from 0.7111 to 0.7116, whereas carbonate from Cu–Co mineralized samples show relatively low concentrations of strontium and more radiogenic 87Sr/86Sr, ranging between 0.7136–0.7469. The malachite samples show low concentrations of strontium, but give a highly radiogenic 87Sr/86Sr of 0.7735, the most radiogenic 87Sr/86Sr ratio. These new data suggest that the origin and timing of carbonate precipitation at Nchanga is reflected in the REE and Sr isotope chemistry. The upper dolomite samples show a modified, but essentially seawater-like signature, whereas the rotation of the REE profile, the MREE enrichment, the development of a negative Eu*SN anomaly and more radiogenic 87Sr/86Sr suggests the dolomite in the Cu–Co mineralized samples precipitated from basinal brines which had undergone significant fluid–rock interaction. Petrographic, REE, and 87Sr/86Sr data for malachite are consistent with the original sulfide Lower Orebody being subject to a later oxidizing event.  相似文献   

5.
《Applied Geochemistry》2000,15(6):695-723
Ground and surface waters collected from two undisturbed Zn–Pb massive sulphide deposits (the Halfmile Lake and Restigouche deposits) and active mines in the Bathurst Mining Camp (BMC), NB, Canada were analysed for the rare earth elements (REE). REE contents are highly variable in waters of the BMC, with higher contents typical of waters with higher Fe and lower pH. There are significant differences between ground- and surface waters and between groundwaters from different deposits. The REE contents of surface waters are broadly similar within and between deposit areas, although there are spatial variations reflecting differences in pH and redox conditions. Surface waters are characterised by strong negative Ce anomalies ([Ce/Ce*]NASC as low as 0.08), produced by oxidation of Ce3+ to Ce4+ and preferential removal of Ce4+ from solution upon leaving the shallow groundwater environment. Groundwaters and seeps typically lack significant Ce anomalies reflecting generally more reducing conditions in the subsurface environment and indicating that Ce oxidation is a rapid process in the surface waters. Deeper groundwaters at the Halfmile Lake deposit are characterised by REE patterns that are similar to the host lithologies, whereas most groundwaters at the Restigouche deposit have LREE-depleted patterns compared to NASC. Halfmile Lake deposit groundwaters have generally lower pH values, whereas Restigouche deposit groundwaters show greater heavy REE-complexation by carbonate ions. Shallow waters at the Halfmile Lake and Stratmat Main Zone deposits have unusual patterns which reflect either the adsorption of light REE onto colloids and fracture-zone minerals and/or precipitation of REE–phosphate minerals. Middle REE-enrichment is typical for ground- and surface waters and is highest for neutral pH waters. The labile portion of stream sediments are generally more middle REE-enriched than total sediment and surface waters indicating that the REE are removed from solution by adsorption to Fe- and Mn-oxyhydroxides in the order middle REE≥light REE>heavy REE.  相似文献   

6.
Hydrogeochemical investigation of groundwater has been carried out in the coastal aquifers of southern Tamil Nadu, India. Seventy-nine dug well samples were collected and analyzed for various physicochemical parameters. The result of the geochemical analysis indicates the groundwater in the study area is slightly alkaline with moderate saline water. The cation and anion concentrations confirm most of the groundwater samples belong to the order of Na+ > Mg2+ > Ca2+ > K+ and Cl? > SO4 2? > HCO3 ?. Thereby three major hydrochemical facies (Ca–Cl, mixed Ca–Mg–Cl and Na–Cl) were identified. Based on the US Salinity diagram, majority of the samples fall under medium to very high salinity with low to high sodium hazard. The cross plot of Ca2+ + Mg2+ versus chloride shows 61 % of the samples fall under saline water category. Higher EC, TDS and Cl concentrations were observed from Tiruchendur to Koodankulam coastal zone. It indicates that these regions are significantly affected by saltwater contamination due to seawater intrusion, saltpan deposits, and beach placer mining activities.  相似文献   

7.
Atmospheric dust is one of the important indicators of urban air quality. In this study, atmospheric dust and topsoil samples were collected monthly from four sites in Beijing and surrounding areas, and analyzed for rare earth elements (REEs). Total REE concentrations (∑REE) in the dusts ranged from 43.10 to 164.43 mg kg?1; concentrations in Beijing and Miyun were higher than those in Zhangbei and Fengning. Most of sampling sites showed the same seasonal depletion in dust ∑REE concentrations in summer, probably caused by the “dilution effect” of added organic matter in summertime samples. Most of the dusts have consistent Ce-anomaly (Ce/Ce*) values (0.91–1.00) and Eu anomaly (Eu/Eu*) values (0.93–1.36); some dusts show slight positive Eu anomalies. The REE patterns of both the dusts and topsoils (normalized to post-Archean shales from Australia, PASS) show different signatures at different sites, whereas the temporal patterns are consistent at each site. These results suggest that local topsoils are likely to be the main provenance of the dusts in the study area.  相似文献   

8.
Groundwater survey has been carried out in the area of Gummanampadu sub-basin located in Guntur District, Andhra Pradesh, India for assessing the factors that are responsible for changing of groundwater chemistry and consequent deterioration of groundwater quality, where the groundwater is a prime source for drinking and irrigation due to non-availability of surface water in time. The area is underlain by the Archaean Gneissic Complex, over which the Proterozoic Cumbhum rocks occur. The results of the plotting of Ca2+ + Mg2+ versus HCO3 ? + CO3 2?, Ca2+ + Mg2+ versus total cations, Na+ + K+ versus total cations, Cl? + SO4 2? versus Na+ + K+, Na+ versus Cl?, Na+ versus HCO3 ? + CO3 2?, Na+ versus Ca2+ and Na+: Cl? versus EC indicate that the rock–water interaction under alkaline condition is the main mechanism in activating mineral dissociation and dissolution, causing the release of Ca2+, Mg2+, Na+, K+, HCO3 ?, CO3 2?, SO4 2? and F? ions into the groundwater. The ionic relations also suggest that the higher concentrations of Na+ and Cl? ions are the results of ion exchange and evaporation. The influences of anthropogenic sources are the other cause for increasing of Mg2+, Na+, Cl?, SO4 2? and NO3 ? ions. Further, the excess alkaline condition in water accelerates more effective dissolution of F?-bearing minerals. Moreover, the chemical data plotted in the Piper’s, Gibbs’s and Langelier–Ludwig’s diagrams, computed for the chloro-alkaline and saturation indices, and analyzed in the principal component analysis, support the above hypothesis. The groundwater quality is, thus, characterized by Na+ > Ca2+ > Mg2+ > K+: HCO3 ? + CO3 2? > Cl? > SO4 2? > NO3 ? > F? facies. On the other hand, majority of groundwater samples are not suitable for drinking with reference to the concentrations of TDS, TH, Mg2+ and F?, while those are not good for irrigation with respect to USSL’s and Wilcox’s diagrams, residual sodium carbonate, and magnesium hazard, but they are safe for irrigation with respect to permeability index. Thus, the study recommends suitable management measures to improve health conditions as well as to increase agricultural output.  相似文献   

9.
Twenty groundwater samples were collected from Enugu metropolis over two seasonal periods in order to characterize the groundwater and to determine its quality for domestic and irrigation purposes. The results show that groundwater of the area is strongly acidic to slightly alkaline in nature and varied from “soft water” to “moderately hard” water type. The major ionic trend is in the order Cl? > Na+ > HCO3 ? > K+ > Mg2+ > Ca2+ > SO4 2?and Mg2+ > Cl? > Na+ > K+ > Ca2+ > HCO 3 ?  > SO4 2? in abundance for dry and rainy seasons, respectively. The results also reveal that there is an increase in trend of the ionic concentrations during the dry season, which arises from weathering of the host rocks and anthropogenic activities. Two hydrochemical facies were identified, namely, Na+ –K+ –Cl? –SO4 2?and Ca2+ –Mg2+ –Cl? –SO4 2? , with Na+ –K+ –Cl? –SO4 2? as the dominant facies for the two seasons. Groundwater quality ranges from “very poor water” to “good water” and “water unsuitable for drinking purposes” to “good water” for the dry season and rainy season investigations, respectively. The groundwater is suitable for irrigation purposes for the two seasons.  相似文献   

10.
Triassic granodiorites in South China (SC) provide an opportunity to examine crust–mantle interactions that may have been caused by a mantle plume. Here we present a combined study of chronological, geochemical, and Sr–Nd–Hf isotopic compositions for Dashenshan granodiorites. These are high-K, calc-alkaline, I-type granodiorites that yield a U–Pb zircon age of 211 ± 3 Ma. They are metaluminous to weakly peraluminous (A/CNK < 1.1), with 3.04–3.89 wt.% Na2O and 3.24–3.86 wt.% K2O, and Na2O/K2O ratio ranging from 0.79 to 1.11. These granodiorites contain 67.7–72.6 wt.% SiO2 but show moderate Mg# values (44.2–57.8) and variable contents of Ni (3.6–29.9 ppm) and Cr (7.6–53.5 ppm). They exhibit light rare earth element (REE) enrichment and flat, heavy REE patterns with negative Eu anomalies (Eu/Eu* = 0.52–0.87). They also display strongly negative Ba, Sr, Nb, Ta, P, and Ti anomalies and positive Rb, Th, K, and Pb anomalies. Dashenshan granodiorites have high whole-rock initial 87Sr/86Sr ratios (0.7121–0.7172), negative εNd (t) values (–8.8 to –6.8), and negative zircon εHf (t) values (–6.6 to –3.3). These results suggest that the Dashenshan granodiorites were generated by a mixing between crustal melt and mantle-derived magma in an extensional setting. We conclude that generation of the Dashenshan pluton may reflect an interaction between a mantle plume and the overlying SC crust.  相似文献   

11.
A large variety of barites collected from marine and continental environments was analyzed by neutron activation for the rare-earth elements (REE) La, Ce, Sm, Eu and Dy. Relative to chondrites, all barites show a decrease of the lighter REE from La toward Eu. The abundance and distribution of rare earths in barites show a distinction of barite types. Deep-sea barites have large REE concentrations as do other authigenic deep-sea minerals and display the chondrite normalized Eu minimum, but not the negative Ce anomaly, of sea water. Other barites, mostly on land, some hydrothermal, and others of shallow marine origin, display lower total Ree concentrations. Chondrite normalized positive Eu anomalies are displayed by those varieties of reducing sedimentary and metamorphic origin.Distribution of REE in barite can be attributed both to crystallographic constraints of substitution, and to solution complexing of REE in the precipitating medium. Plots of rare earth partitioning versus effective ion size suggest that the decreasing enrichment toward Eu for all barite types is caused by crystallographic constraints due to contraction of the substituting REE ion sizes relative to the size of the host Ba ion. Solution effects on REE substitution in barite can be evaluated by writing solid solution distribution equations based on mass action of REE and Ba sulfates and the lanthanide (Ln) solution species Ln (CO3)?54), LnSO+4, LnCl+2 and LnF+2. Under normal sea water conditions, solution complexing plays a minor role. However, increased alkalinities of reducing sediments and increased brine chlorinities could cause significant complexing and deplete REE heavier than Eu. Besides Dy in barites, this could be true for aqueous precipitation of REE in general.  相似文献   

12.
The assessment of hydrogeochemical processes that govern the water quality of inland freshwater aquifers in coastal environment, especially in Indian sub-continent, is occasionally attempted. To bridge the gap, a detail hydrochemical evaluation of groundwater occurring in coastal alluvium is attempted. Single set of high-density water sampling is done from a limited area to gain an in-depth knowledge of the processes that govern the water chemistry of the sandy aquifers. The water is of weak alkaline nature and less mineralized, EC being < 1,000 μS/cm in many samples. Major ion composition indicates that water is contaminated with excess concentration of nitrates. Ionic abundance is in the order of Cl? > Na+  > Ca2+ > HCO3 ? > SO4 2? > Mg2+  > NO3 ?. Na+ and Cl? are almost in similar proportions implying the influence of coastal climate on water quality. The water shows modest variation in their ionic assemblage among different sample points as evident from Schoeller scheme. Groundwater can be classified into three distinct facies viz. Cl?–Ca2+–Mg2+, Na+–Cl? and Ca2+–Mg2+–HCO3 ? types. The ionic assemblages, their indices, ratios and cross-plots substantiate that multiple processes were involved in the evolution of the water chemistry. Among them, silicate weathering, halite dissolution, ion exchange and base exchange played prominent role in the ion enrichment of groundwater. The aquatic chemistry is further influenced and modified by marine environment, evapotranspiration and anthropogenic inputs which is authenticated by good correlation (r 2 = 1) among the Na+–Cl?, EC–Mg2+, Na+ and Cl?. Gibbs plots established that evaporation is more responsible for contribution of minerals to the groundwater than aquifer material. Nitrate contamination can be attributed for poor sewerage disposal mechanism which is aggravated by fertilizer inputs, irrigation practices and agriculture activity. A contrasting correlation (r 2 ≥90 to <0.40) among select pairs of ions reassures dissimilar source of those ions, involvement of multiple processes and limited interaction of formation water with aquifer material.  相似文献   

13.
Low to medium grade crystalline rocks locally known as Bomdila Group extensively covers the Lesser Himalayan region in Western Arunachal Himalaya. This Group consists dominantly of mylonitic gneisses of granitic composition of Palaeoproterozoic age, named as Bomdila mylonitic gneiss (BMG) and a small body of hornblende bearing granite of Mesoproterozoic age known as Salari granite (SG). The BMG is affinity to peraluminous (A/CNK > 1.1) with high content of SiO2, K2O/Na2O ratio, normative corundum, high ratio of FeOt/MgO in biotite (3.21–5.11) that shows characteristics of S-type granite whereas SG has granodiorite composition with high Na2O, low K2O, presence of hornblende, normative diopside, low A/CNK ratio (<1.1) and low FeOt/MgO ratio in biotite (1.58–1.60) indicates metaluminous I-type granite affinity. The SG has more fractionated nature of REE [(Ce/Yb)N = 9.06–18.53] and minor negative Eu anomalies [EuN/Eu* = 0.69–0.94] as compared to BMG which has less fractionation of REE [(Ce/Yb)N = 5.95–9.16] and strong negative Eu anomalies [EuN/Eu* = 0.37–0.43]. Geochemical and petrological studies suggest that the SG and BMG are not genetically related; SG appears to have derived from igneous source whereas the BMG have been derived from sedimentary source, however these granitoids might have produced during the same thermal event.  相似文献   

14.
We conducted geochemical and isotopic studies on the Oligocene–Miocene Niyasar plutonic suite in the central Urumieh–Dokhtar magmatic belt, in order better to understand the magma sources and tectonic implications. The Niyasar plutonic suite comprises early Eocene microdiorite, early Oligocene dioritic sills, and middle Miocene tonalite + quartzdiorite and minor diorite assemblages. All samples show a medium-K calc-alkaline, metaluminous affinity and have similar geochemical features, including strong enrichment of large-ion lithophile elements (LILEs, e.g. Rb, Ba, Sr), enrichment of light rare earth elements (LREEs), and depletion in high field strength elements (HFSEs, e.g. Nb, Ta, Ti, P). The chondrite-normalized rare earth element (REE) patterns of microdiorite and dioritic sills are slightly fractionated [(La/Yb)n = 1.1–4] and display weak Eu anomalies (Eu/Eu* = 0.72–1.1). Isotopic data for these mafic mantle-derived rocks display ISr = 0.70604–0.70813, ?Nd (microdiorite: 50 Ma and dioritic sills: 35 Ma, respectively) = +1.6 and ?0.4, TDM = 1.3 Ga, and lead isotopic ratios are (206Pb/204Pb) = 18.62–18.57, (207Pb/204Pb) = 15.61–15.66, and (208Pb/204Pb) = 38.65–38.69. The middle Miocene granitoids (18 Ma) are also characterized by relatively high REE and minor Eu anomalies (Eu/Eu* = 0.77–0.98) and have uniform initial 87Sr/86Sr (0.7065–0.7082), a range of initial Nd isotopic ratios [?Nd(T)] varying from ?2.3 to ?3.7, and Pb isotopic composition (206Pb/204Pb) = 18.67–18.94, (207Pb/204Pb) = 15.63–15.71, and (208Pb/204Pb) = 38.73–39.01. Geochemical and isotopic evidence for these Eocene–Ologocene mafic rocks suggests that the magmas originated from lithospheric mantle with a large involvement of EMII component during subduction of the Neotethyan ocean slab beneath the Central Iranian plate, and were significantly affected by crustal contamination. Geochemical and isotopic data of the middle Miocene granitoids rule out a purely crustal-derived magma genesis, and suggest a mixed mantle–crustal [MASH (melting, assimilation, storage, and homogenization)] origin in a post-collision extensional setting. Sr–Nd isotope modelling shows that the generation of these magmas involved ～60% to 70% of a lower crustal-derived melt and ～30% to 40% of subcontinental lithospheric mantle. All Niyasar plutons exhibit transitional geochemical features, indicating that involvement of an EMII component in the subcontinental mantle and also continental crust beneath the Urumieh–Dokhtar magmatic belt increased from early Eocene to middle Miocene time.  相似文献   

15.
Shallow groundwater and hot springs were collected from northeastern Guangdong Province, Southeast China, to determine the concentrations and fractionation patterns of rare-earth elements(REE). The results show that the La, Ce and Nd of REEs are abundant in groundwater and rock samples, and the ∑REE contents in groundwater and rock samples range from 126.5 to 2875.3 ng/L, and 79.44 to 385.85 mg/L, respectively. The shallow groundwater has slightly HREE-enriched PAAS-normalized patterns. However, the granitic rocks PAAS-normalized patterns, with remarkable negative Eu anomalies, are different from that of shallow groundwater. The enrichment of HREE is considered to be controlled by REE complexation and readsorption for most groundwater has Ce and Eu positive anomalies. The Ce and Eu anomalies in groundwater are controlled by redox conditions. Moreover, the Fe-contain sediments dissolution and/or the reduction of Fe oxyhydroxides are another factor contributing to Ce anomalies. The Eu anomalies in groundwater are controlled by the preferential mobilization of Eu2+ during water-rock interaction compared to Eu3+.  相似文献   

16.
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17.
We have collected ∼500 stream waters and associated bed-load sediments over an ∼400 km2 region of Eastern Canada and analyzed these samples for Fe, Mn, and the rare earth elements (REE + Y). In addition to analyzing the stream sediments by total digestion (multi-acid dissolution with metaborate fusion), we also leached the sediments with 0.25 M hydroxylamine hydrochloride (in 0.05 M HCl), to determine the REE + Y associated with amorphous Fe- and Mn-oxyhydroxide phases. We are thus able to partition the REE into “dissolved” (<0.45 μm), labile (hydroxylamine) and detrital sediment fractions to investigate REE fractionation, and in particular, with respect to the development of Ce and Eu anomalies in oxygenated surface environments. Surface waters are typically LREE depleted ([La/Sm]NASC ranges from 0.16 to 5.84, average = 0.604, n = 410; where the REE are normalized to the North America Shale Composite), have strongly negative Ce anomalies ([Ce/Ce∗]NASC ranges from 0.02 to 1.25, average = 0.277, n = 354), and commonly have positive Eu anomalies ([Eu/Eu∗]NASC ranges from 0.295 to 1.77, average = 0.764, n = 84). In contrast, the total sediment have flatter REE + Y patterns relative to NASC ([La/Sm]NASC ranges from 0.352 to 1.12, average = 0.778, n = 451) and are slightly middle REE enriched ([Gd/Yb]NASC ranges from 0.55 to 3.75, average = 1.42). Most total sediments have negative Ce and Eu anomalies ([Ce/Ce∗]NASC ranges from 0.097 to 2.12, average = 0.799 and [Eu/Eu∗]NASC ranges from 0.39 to 1.43, average = 0.802). The partial extraction sediments are commonly less LREE depleted than the total sediments ([La/Sm]NASC ranges from 0.24 to 3.31, average = 0.901, n = 4537), more MREE enriched ([Gd/Yb]NASC ranges from 0.765 to 6.28, average = 1.97) and Ce and Eu anomalies (negative and positive) are more pronounced.The partial extraction recovered, on average ∼20% of the Fe in the total sediment, ∼80% of the Mn, and 21-29% of the REEs (Ce = 19% and Y = 32%). Comparison between REEs in water, partial extraction and total sediment analyses indicates that REEs + Y in the stream sediments have two primary sources, the host lithologies (i.e., mechanical dispersion) and hydromorphically transported (the labile fraction). Furthermore, Eu appears to be more mobile than the other REE, whereas Ce is preferentially removed from solution and accumulates in the stream sediments in a less labile form than the other REEs + Y. Despite poor statistical correlations between the REEs + Y and Mn in either the total sediment or partial extractions, based on apparent distribution coefficients and the pH of the stream waters, we suggest that either sediment organic matter and/or possibly δ-MnO2/FeOOH are likely the predominant sinks for Ce, and to a lesser extent the other REE, in the stream sediments.  相似文献   

18.
The rare earth element (REE) contents of sixteen surficial calcareous sediments from the southwestern Carlsberg Ridge, Indian Ocean, have been determined. The total REE vary from 35 ppm to 126 ppm and are inversely related to the calcium carbonate content. REEs show a strong positive correlation with Al + Fe + K + Mg + Na (r 2= 0.98) and Mn + Fe + Cu + Ni (r 2= 0.86) suggesting that the REE is associated with a combined phase of clays (mainly illite) and Mn-Fe oxyhydroxides. The aeolian input into these sediments is suggested from the weak positive Eu/Eu* anomaly. Shale-normalized (NASC) pattern along with La(n)/Yb(n) ratio suggest enrichment of heavy REE (HREE) relative to the light REE (LREE) with a negative Ce/Ce* anomaly implying retention of a bottom water REE pattern. An erratum to this article is available at .  相似文献   

19.
Deepawali is one of the main festivals for Hindu religion which falls in the period October–November every year with great fireworks display. In this study, we investigated the levels of water soluble ions and heavy metals—during the fireworks festival in Rajnandgaon, Central India. The chemical compositions and noise level distributions are reported from the sampling site. First time during Deepawali, air quality was studied in this area, The Aerosol samples of PM10 (particle aerodynamic diameter <10 μm) are collected in October 24–28, 2011. Aims of the present studies are (1) To describe the particulate concentrations and associated chemical species during Deepawali festival, (2) To recognize the noise level in Deepawali festival. For study, the samples were collected in glass fiber filter paper and analyzed for the major water soluble ions F?, Cl?, NO3 ?, SO4 2?, Na2+, NH4 +, K+, Ca2+, and Mg2+ employing ion chromatograph. Concentration of heavy metals was analyzed by ICP-MS and was observed to occur in order Fe > Zn > Pb > Ni > Cr > Cd. The result revels that all concentration are above the permissible limit fixed by CPCB, USPEA, and WHO standard. It is concluded that the burning of fireworks during Deepawali festival was the main source of heavy metals and ion.  相似文献   

20.
In order to constrain the timing and petrogenesis of both the hosting rocks and the inner mafic microgranular enclaves (MMEs) of the Liangnong pluton, SE China, we have performed a series of bulk-rock geochemistry, zircon U–Pb, and Hf isotopic analysis, respectively. Zircon laser ablation–inductively coupled plasma–mass spectrometry U–Pb isotopic analysis yielded ages of 106.3 ± 1.1 Ma for the granodiorite and 103.9 ± 1.6 to 105 ± 1.8 Ma for monzogranite phases within the hosting pluton, as well as an age of 104.7 ± 0.8 Ma for the associated MMEs. The host rocks are metaluminous, have A/CNK values of 0.91–1.09, contain relatively high concentrations of SiO2 and K2O, are enriched in Rb, Th, Ba, Zr, and Hf, are depleted of Sr, P, Ti, Nd, and Ta, contain high concentrations of the rare earth elements (REE) and the light REE, and have moderately negative Eu anomalies (Eu*/Eu = 0.6–0.8). In comparison, the MMEs contain high concentrations of Al2O3, FeO, MgO, and TiO2, are relatively enriched in Ba, U, and Sr, and are depleted in Th, Nd, and Zr. They have lower total REE concentrations and higher Eu*/Eu values than the hosting granites. The zircons within the hosting granites have Hf crustal model ages (TDMC) that show a peak at 1.29–1.85 Ga. Zircons within the MMEs have different εHf(t) values (–3.7 to +4.9) than the zircons within the hosting granites (–10.8 to –1.9). The results indicate that the MMEs and the hosting granites crystallized from magmas with different sources, thereby showing that the Early Cretaceous magmatism in the coastal areas of SE China was generated by the widespread injection of mantle-derived magmas caused by rollback of the subducting palaeo-Pacific Plate.  相似文献   

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