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1.
To discriminate possible anthropogenic and lithogenic sources of Pb in Lower Silesia (SW Poland), the Pb isotope composition was investigated in a spectrum of rocks and anthropogenic materials as well as within 10 soil profiles. Silicate rocks in Lower Silesia have 206Pb/207Pb ratios that vary from 1.17 for serpentinites to 1.38 for gneisses, and this variability is reflected in the isotope composition of the mineral soil horizons. The Pb isotope composition of coals, ores and anthropogenic materials (slags and fly ashes) is rather uniform, with 206Pb/207Pb ratios ranging from 1.17 to 1.18. Similar ratios were observed in ore and coal samples from Upper Silesia. The O soil horizons also have uniform 206Pb/207Pb ratios of 1.17–1.18 and the heterogeneity of the 206Pb/207Pb ratios increases with depth in the soil profiles. Five soils, with varying Pb concentrations, analysed far from contamination centres, show consistent, approximately 2-fold enrichment in Pb concentration from the C to A horizons, which is consistent with natural re-distribution of Pb within the profiles. The increase in the Pb concentration is accompanied by a decrease in 206Pb/207Pb ratios, also attributed to natural Pb isotope fractionation. Four soil profiles from industrial areas show variable enrichments in Pb concentrations and these are attributed to anthropogenic input from air-borne pollutants or even slag particles at smelting sites. The implication is that a lithogenic Pb source can deviate from the basement rock composition, and detailed isotope characteristics of the geological background and natural enrichments in soils are often needed to determine the lithogenic/anthropogenic proportions of Pb in soils.  相似文献   

2.
Base metal–Ag mineralisation at Dikulushi and in other deposits on the Kundelungu Plateau (Democratic Republic of Congo) developed during two episodes. Subeconomic Cu–Pb–Zn–Fe polysulphide ores were generated during the Lufilian Orogeny (c. 520 Ma ago) in a set of E–W- and NE–SW-oriented faults. Their lead has a relatively unradiogenic and internally inhomogeneous isotopic composition (206Pb/204Pb = 18.07–18.49), most likely generated by mixing of Pb from isotopically heterogeneous clastic sources. These sulphides were remobilised and enriched after the Lufilian Orogeny, along reactivated and newly formed NE–SW-oriented faults into a chalcocite-dominated Cu–Ag mineralisation of high economic interest. The chalcocite samples contain only trace amounts of lead and show mostly radiogenic Pb isotope signatures that fall along a linear trend in the 207Pb/204Pb vs. 206Pb/204Pb diagram (206Pb/204Pb = 18.66–23.65; 207Pb/204Pb = 15.72–16.02). These anomalous characteristics reflect a two-stage evolution involving admixture of both radiogenic lead and uranium during a young fluid event possibly c. 100 Ma ago. The Pb isotope systematics of local host rocks to mineralisation also indicate some comparable young disturbance of their U–Th–Pb systems, related to the same event. They could have provided Pb with sufficiently radiogenic compositions that was added to less radiogenic Pb remobilised from precursor Cu–Pb–Zn–Fe polysulphides, whereas the U most likely originated from external sources. Local metal sources are also suggested by the 208Pb/204Pb–206Pb/204Pb systematics of combined ore and rock lead, which indicate a pronounced and diversified lithological control of the immediate host rocks on the chalcocite-dominated Cu–Ag ores. The Pb isotope systematics of polysulphide mineralisation on the Kundelungu Plateau clearly record a diachronous evolution.  相似文献   

3.
若尔盖高原牧场处于中国偏远洁净高海拔地区,大气沉降是污染物主要来源途径之一。由于季风的影响,污染源的辨析较为困难。本文通过多点大气气溶胶不同季节同时采样方式,利用热电离固体同位素质谱仪可有效校正质谱分析中同位素分馏效应的优点,对若尔盖地区土壤和大气气溶胶的铅同位素比值进行精确分析,并结合季风特征对该地区污染物的来源进行解析。结果表明:土壤的208Pb/204Pb比值变化范围为38.79059±0.00194~38.94461±0.00135,206Pb/207Pb为1.18551±0.00002~1.19362±0.00002;大气气溶胶的208Pb/204Pb比值变化范围为37.49571±0.00117~38.48980±0.00105,206Pb/207Pb为1.12894±0.00001~1.16734±0.00001。该地区土壤铅同位素的特征是放射成因铅高,来自于自身天然存在的岩石矿物,与大气污染关系不大;大气气溶胶的铅同位素组成与土壤差异较大,显示为多元混合模式,受到了天然物质和人类活动来源的混合影响,机动车尾气及来自北部(兰州)和西北部(青海、新疆、哈萨克斯坦、俄罗斯)的大气远程运移是若尔盖大气气溶胶及污染物质的主要来源。  相似文献   

4.
Lead isotope analyses of galena from five ore deposits and six prospects in the Aysén region of southern Chile are reported. Most of the deposits are either low sulfidation epithermal gold–silver veins or skarn and manto deposits; the majority are either suspected to be, or dated as, Late Jurassic to mid-Cretaceous. Galena lead isotope data for most of the deposits from southern Chile cluster near the “orogene” within a “plumbotectonic” model framework. Average values (206Pb/204Pb=18.53, 207Pb/204Pb=15.63, and 208Pb/204Pb=38.50) are near Jurassic to Cretaceous model ages on the “orogene” curve of Zartman and Doe (1981) and the second-stage curve of Stacey and Kramers (1975) on a 206Pb/204Pb versus 207Pb/204Pb plot. These model ages are compatible with absolute ages as currently known. The elongate trends in the general cluster indicate mainly an orogenic model fit, suggesting variable mixing of lead from different sources, mainly model upper crust and lesser model mantle and lower crust reservoirs. Galena lead associated with one deposit (El Faldeo) is relatively radiogenic, and lies near a Jurassic age on the “upper crustal” curve of Zartman and Doe (1981), which is compatible with the Ar/Ar age of the deposit. Galena lead isotope clusters define three main groups of deposits. These three groups appear to be related to three mineralizing events, dated by K–Ar and Ar/Ar, in the Late Jurassic (group 3), and in the Early and mid-Cretaceous (groups 1 and 2 respectively). Averages for group 1, the northern group including El Toqui and Katerfeld, are 206Pb/204Pb=18.51, 207Pb/204Pb=15.62, 208Pb/204Pb=38.48. Averages for group 2, the southern group with Fachinal and Mina Silva, are 206Pb/204Pb = 18.56, 207Pb/204Pb=15.63, 208Pb/204Pb=38.52. Averages for group 3, the southernmost group with the El Faldeo, Lago Chacabuco and Lago Cochrane prospects, are 206Pb/204Pb=18.83, 207Pb/204Pb=15.65, 208Pb/204Pb=38.63. The Cretaceous deposits (groups 1 and 2) contain orogene-type lead that becomes increasingly radiogenic southward. Lead from the Late Jurassic deposits (group 3) appears to reflect mixing of orogene lead with highly radiogenic lead. The observed linear array of lead in group 3 probably reflects mixing of orogene lead with highly radiogenic lead, which was likely extracted by selective leaching of mineralizing hydrothermal solutions from the metamorphic basement. Received: 10 July 1999 / Accepted: 15 July 2000  相似文献   

5.
Lead isotope ratios of galena from the carbonate-hosted massive sulphide deposits of Kabwe (Pb-Zn) and Tsumeb (Pb-Zn-Cu) in Zambia and Namibia, respectively, have been measured and found to be homogeneous and characteristic of upper crustal source rocks. Kabwe galena has average isotope ratios of 206/204Pb = 17.997 ± 0.007, 207/204Pb = 15.713 ± 0.010 and 208/204Pb = 38.410 ± 0.033. Tsumeb galena has slightly higher 206/204Pb (18.112 ± 0.035) and slightly lower 207/204Pb (15.674 ± 0.016) and 208/204Pb (38.276 ± 0.073) ratios than Kabwe galena. The isotopic differences are attributed to local differences in the age and composition of the respective source rocks for Kabwe and Tsumeb. The homogeneity of the ore lead in the two epigenetic deposits suggests lead sources of uniform isotopic composition or, alternatively, thorough mixing of lead derived from sources with relatively similar isotopic compositions. Both deposits have relatively high 238U/204Pb ratios of 10.31 and 10.09 for Kabwe and Tsumeb galenas, respectively. These isotope ratios are considered to be typical of the upper continental crust in the Damaran-Lufilian orogenic belt, as also indicated by basement rocks and Cu-Co sulphides in stratiform Katangan metasediments which have a mean μ-value of 10.25 ± 0.12 in the Copperbelt region of Zambia and the Democratic Republic of Congo (formerly Zaire). The 232Th/204Pb isotope ratios of 43.08 and 40.42 for Kabwe and Tsumeb suggest Th-enriched source regions with 232Th/235U (κ-values) of 4.18 and 4.01, respectively. Model isotopic ages determined for the Kabwe (680 Ma) and Tsumeb (530 Ma) deposits indicate that the timing of the mineralisation was probably related to phases of orogenic activity associated with the Pan-African Lufilian and Damaran orogenies, respectively. Galena from the carbonate-hosted Kipushi Cu-Pb-Zn massive sulphide deposit in the Congo also has homogeneous lead isotope ratios, but its isotopic composition is comparable to that of the average global lead evolution curve for conformable massive sulphide deposits. The μ (9.84) and κ (3.69) values indicate a significant mantle component, and the isotopic age of the Kipushi deposit (456 Ma) suggests that the emplacement of the mineralisation was related to a post-tectonic phase of igneous activity in the Lufilian belt. The isotope ratios (206/204Pb, 207/204Pb, 208/204Pb) of the three deposits are markedly different from the heterogeneous lead ratios of the Katangan Cu-Co stratiform mineralisation of the Copperbelt as well as those of the volcanogenic Nampundwe massive pyrite deposit in the Zambezi belt which typically define radiogenic linear trends on lead-lead plots. The host-rock dolomite of the Kabwe deposit also has homogeneous lead isotope ratios identical to the ore galena. This observation indicates contamination of the Kabwe Dolomite Formation with ore lead during mineralisation. Received: 8 September 1997 / Accepted: 21 August 1998  相似文献   

6.
A peat core from an ombrotrophic bog documents the isotopic evolution of atmospheric Pb in central Ontario since AD 1804 ± 53 (210Pb dating). Despite the introduction of unleaded gasoline in the mid-1970’s, the ratio 206Pb/207Pb in atmospheric deposition has not increased as expected, but rather continues to decline. In fact, snowpack sampling (2005 and 2009) and rainwater samples (2008) show that the isotopic composition of atmospheric Pb today is often far less radiogenic than the gasoline lead that had been used in Canada in the past. The peat, snow, and rainwater data presented here are consistent with the Pb isotope data for aerosols collected in Dorset in 1984 and 1986 which were traced by Sturges and Barrie (1989) to emissions from the Noranda smelter in northern Quèbec, Canada’s largest single source of atmospheric Pb. Understanding atmospheric Pb deposition in central Ontario, therefore, requires not only consideration of natural sources and past contributions from leaded gasoline, but also emissions from metal smelting and refining.Lead in the streams which enter Kawagama Lake today (206Pb/207Pb = 1.16 − 1.19) represents a mixture between the natural values (1.191 − 1.201 estimated using pre-industrial lake sediments) and the values found in the humus layer of the surrounding forest soils (206Pb/207Pb = 1.15 − 1.19). In the lake itself, however, Pb is much less radiogenic (206Pb/207Pb as low as 1.09) than in the streams, with the dissolved fraction less radiogenic than particulate material. The evolution of Pb isotope ratios within the watershed apparently reflects preferential removal by sedimentation of comparatively dense, radiogenic, terrestrial particles (derived from the mineral fraction of soils) from the humus particles with lower ratios of 206Pb/207Pb (because of atmospheric Pb contamination). Despite the contemporary enrichments of Pb in rain and snow, concentrations of dissolved Pb in the lake are extremely low (sometimes below 10 ng/l), with Pb concentrations and Pb/Sc ratios approaching “natural” values because of efficient binding to particles, and their subsequent removal in the watershed.  相似文献   

7.
Lead isotopic composition and uranium and lead concentrations have been determined for galena, sphalerite, pyrite and acetic acid soluble material from the McArthur area in order to test the hypothesis of a dual sulphur source suggested by the sulphur isotope data of Smith and Croxford (Sulphur isotope ratios in the McArthur lead-zinc-silver deposit, Nature Phys. Sci. 245, 10–12 (1973)). Galena, sphalerite and the acetic acid washes from the McArthur deposit have uniform isotopic ratios (206Pb/204Pb, 16.07–16.15; 207Pb/204Pb, 15.37–15.47; 208Pb/204Pb, 35.57–35.89) consistent with other conformable ore deposits, whereas the ratios for pyrite are variable and quite radiogenic (206Pb/204Pb, 16.24–16.49; 207Pb/204Pb, 15.42–15.58; 208Pb/204Pb, 35.82–36.98). Acid washes where dolomite is a major dissolved phase are also radiogenic. The lead in the pyrite appears to have been derived from at least two sources: the less radiogenic lead coming from an exhalative source as for galena and sphalerite and the more radiogenic lead probably being leached from the country rocks. It is proposed that analysis of pyrite for isotopic composition and concentration of lead could be used as an indicator for similar types of deposits in this area.  相似文献   

8.
Southern Ocean aerosols were collected at the Cape Grim Baseline Air Pollution Station from onshore air under baseline conditions between February 1999 and April 2000. Thermal ionization techniques (TIMS) and isotope dilution mass spectrometry (IDMS) were used to measure the isotopic composition and concentration of lead in the air giving concentrations as low as 0.6 ± 0.1 pg · m−3. Air collected under baseline conditions for 12 months (May 1999-April 2000) yielded an overall lead concentration of 11.0 ± 0.2 pg · m−3 and isotopic composition of 206Pb/207Pb = 1.154, 208Pb/207Pb = 2.387 and 206Pb/204Pb = 17.93. The range in isotopic ratios was consistent with the mixing of lead from major population centers in the Southern Hemisphere in the mid to high latitudes, except for the presence of highly radiogenic lead in some samples. Contributions from radiogenic lead of up to ∼0.8% were observed. Three periods with the highest percentage contribution of radiogenic lead (>0.5%) were investigated in more detail, and 4-d back-trajectories and radon concentrations were used to help identify the sources. The sources are probably associated with the mining and processing of uranium rich ores in southern Africa and possibly South Australia.  相似文献   

9.
The lead isotopic composition of galenas from low-temperature veins of the Catalonian Coastal Ranges (NE Spain) displays a small but distinct range of values: 18.318 ≤206Pb/204Pb ≤ 18.678; 15.678 ≤207Pb/204Pb ≤ 15.767 and 38.534 ≤ 208Pb/204Pb ≤ 39.189. The data define a linear trend in the 208Pb/204Pb versus 206Pb/204Pb diagram that can be interpreted in terms of mixing of lead from different reservoirs. The lead appears to be derived from a solution that preferentially leached granites of Late-Hercynian age. Sulphur isotopic compositions of the galenas range from −8.5 to + 7.3‰ but variations in a single deposit are small (1–2‰), pointing to different sources of sulphur. In a δ34S versus 206Pb/204Pb plot no clear correlation trends appear. Lead isotope data from deposits of similar characteristics situated within the Hercynian orogenic belt as the Linares-La Carolina district (S Spain) and the Inglesiente-Sulcis area (Sardinia) show slight differences indicating a source area of similar lead isotopic composition. In the CCR and Linares-La Carolina districts, the main source of lead is related to the Hercynian granites of each area, although small contributions from metasediments cannot be ruled out. The contribution of lead from metasedimentary rocks is particularly seen in the Sardinian (Hercynian vein-type) ores. Received: 8 August 1996 / Accepted: 5 December 1996  相似文献   

10.
We report the first precise U–Pb isotope data on cassiterite from the large Xianghualing tin-polymetallic deposit in the central Nanling district, South China. The results show that four separates from sample XF-51 have a relatively narrow range of 206Pb/238U apparent ages, varying from 152 to 157 Ma, and the three 206Pb/238U apparent ages yield a weighted average value of 156 ± 4 Ma (MSWD = 0.32). Separates from two other cassiterite samples do not have sufficient radiogenic Pb to generate a reliable 206Pb/238U age. Seven separates from the above three cassiterite samples define a well-constrained 238U–206Pb isochron corresponding to an age of 157 ± 6 Ma (MSWD = 34). A comparison of the U–Pb cassiterite ages with published Ar–Ar dates on muscovite from this deposit and K–Ar age data on biotite from the pluton genetically related to the tin mineralization in this area demonstrates that the U–Pb isotope system of cassiterite is a potential geochronometer. Combined with the Ar–Ar dates of muscovite from this deposit, we can constrain the absolute age of tin-polymetallic mineralization in Xianghualing at 154–157 Ma. The dates obtained in this study, consistent with the published geochronological results from other important deposits in this region, reveal that the large-scale tungsten–tin mineralization in the central Nanling region was predominantly emplaced during 150–161 Ma.  相似文献   

11.
Knowledge of the cause and source of Pb pollution is important to abate environmental Pb pollution by taking source-related actions. Lead isotope analysis is a potentially powerful tool to identify anthropogenic Pb and its sources in the environment. Spatial information on the variation of anthropogenic Pb content and anthropogenic Pb sources in rural topsoils is remarkably limited. This study presents results of a survey of approximately 350 topsoil samples from rural locations covering the entire Netherlands, for which the bulk geochemical and Pb isotope compositions were determined. The specific aim of this study is to determine the anthropogenic Pb sources in the topsoils from rural areas in The Netherlands. The spatial distribution of anthropogenic Pb in soils in The Netherlands will be explained in terms of land use and pollution sources.Nearly all studied topsoils display Pb contents that exceed the amount expected based on the soil lithology. The range in Pb isotope ratios of the additional Pb fraction in rural Dutch topsoils is established at 1.056–1.199, 2.336–2.486 and 0.452–0.490 for 206Pb/207Pb, 207Pb/208Pb and 206Pb/208Pb, respectively. Five land use types are distinguished (forest, open nature, moor, arable land and grassland) with distinct isotopic compositions for added Pb. Additional Pb in soils of natural areas (forest, open nature and moor) has on average lower 206Pb/207Pb, 208Pb/207Pb and 206Pb/208Pb ratios than the agricultural soils (arable land and grassland). Additional Pb in both natural area soils and agricultural soils is interpreted to be of anthropogenic origin: most likely a mixture of coal/galena, incinerator ashes and gasoline Pb. The dominant sources of additional Pb in the topsoil of open nature areas are most likely incinerator ash and gasoline Pb. In contrast, the on average higher 206Pb/207Pb, 208Pb/207Pb and 206Pb/208Pb ratios of additional Pb in agricultural soils are most likely caused by the presence of animal manure and N–P fertilizers.Several areas are observed with notably high additional Pb contents (26–211 mg/kg on an organic matter-free basis) in the topsoil. The largest area is the Randstad area, which has the highest population and traffic density, and hosts a considerable fraction of the Dutch chemical industry. Two other areas with high additional Pb contents in the topsoil are located near the Dutch borders and are most likely influenced by German and Belgian chemical industries. The topsoils in the coastal dunes and southern, central and northern forests are characterized by relatively low additional Pb contents (<10 mg/kg on an organic matter-free basis). The population, traffic and chemical industry density is low in these areas and no fertilizers are applied.  相似文献   

12.
Rare earth element (REE) distributions and Pb isotope compositions were explored in soils varying in age from ca. 0.4 to ?300 ka, developed on moraines in the Wind River Mountains, Wyoming. Soil extracts (0.6 M HCl) were used to examine the soil labile pool while the major element distribution in soil profiles was used to determine the extent of weathering at different soil depths. The results show that the chondrite-normalized REE patterns of the deepest bulk soil within each profile reflects the composition of the moraine till, except for the oldest soil. Up to ca. 12 ka, the soil extract fraction is enriched in light REE, indicating early release of light REE to the soil labile pool while that of the two oldest soils are relatively enriched in heavy REE. In the soil extracts the La/Sm ratio normalized to the deepest soil (LaD/SmD) decreases systematically with soil age. Similarly, the Eu-anomaly in the deepest soil from each profile (EuD/EuD*) decreases slightly with soil age in the three young soils; however, EuD/EuD* increases with soil age in the older soils. The systematic trends of these two ratios indicate the depletion of light REE in young soils and the enrichment of Eu and heavy REE in the older soils. Based on the Pb isotope ratios, the relative contribution of Pb to the soil labile pool via mineral weathering of U- or Th-rich phases was assessed for the different stages of weathering. The whole-soil profile 208Pb/204Pb ratio was found to decrease with soil age and with LaD/SmD, whereas it increased with the EuD/EuD* ratio. In each horizon, Pb isotope ratios (206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb) ratio generally decrease with soil age. In order to overcome possible effects from parent material heterogeneity, the amount of radiogenic Pb as compared to the whole-soil composition was calculated and this was found to decrease systematically with soil age.  相似文献   

13.
Three soil profiles taken from the Hartwood Research Station in Central Scotland have been analyzed using chemical digestion and extraction techniques to investigate the chemical association of heavy metals deposited from the atmosphere. Total digestion, EDTA extraction and the BCR (Bureau Communitaire de Reference) sequential extraction procedure were used. In addition, lead isotope ratios in the whole soils and in the fractions from the sequential extraction procedure were measured using thermal ionisation mass spectrometry. All the digestion and extraction procedures gave clear indication of enhanced concentrations of heavy metals in surface soils, in particular for lead and zinc. Whereas total digestion gave a good indication of the heavy metal status of the soils, the extraction procedures were necessary to provide information on chemical association of the metals with soil components, information needed to understand the soil processes involved in mobilization of metals. Lead isotope analysis of the whole soils revealed a consistent picture of lower 206Pb/207Pb ratios in surface soils (1.140-1.147) than in soils at 20-30 cm depth (1.182-1.190). The steady progression from the lower to higher ratios down the profile was clear indication that anthropogenic lead had penetrated to some degree into the deeper soils. The combination of sequential extraction and lead isotope analysis proved to be a powerful approach to studying this effect in more detail and showed that the fractions extractable from 20 to 30 cm soils contained lead with much lower 206Pb/207Pb ratios (1.174-1.178) than the residual fraction (1.196-1.200). As the extractable fractions contained ≥85% of the lead in the soil, a substantial portion of lead at 20-30 cm depth was of anthropogenic origin. The 206Pb/207Pb ratios of 1.174-1.178 found in the extractable fractions suggested that the mobile component of the anthropogenic lead was that deposited before the introduction of leaded petrol.  相似文献   

14.
Systematic variations in the Cd and Pb isotope ratios in polluted topsoils surrounding the Jinding Pb–Zn mine in China were measured so that the sources of the metals could be traced. The average δ114/110Cd value and 206Pb/207Pb isotope ratio in background soils from the region were +0.41‰ and 1.1902, respectively, whereas the contaminated soil samples had different values, with the δ114/110Cd values varying between −0.59‰ and +0.33‰ and the 206Pb/207Pb isotope ratios varying between 1.1764 and 1.1896. We also measured the Cd and Pb isotopic compositions in oxide ores, sulfide ores, and slags, and found that binary mixing between ores and background soils could explain almost all of the variations in the Cd and Pb isotope ratios in the contaminated soils. This suggests that Cd and Pb pollution in the soils was mainly caused by the deposition of dust emitted during anthropogenic activities (mining and refining). The Pb and Cd isotope ratios clearly showed that contamination in soils in the northeastern part of the area was caused by surface mines and zinc smelters and their slagheaps, while contamination in soils in the southwestern part of the area also came from tailing ponds and underground mines. The main area of soil polluted by dust from Pb–Zn mining processes roughly extended for up to 5 km from the mine itself.  相似文献   

15.
The island of Salina comprises one of the most distinct calc-alkaline series of the Aeolian arc (Italy), in which calc-alkaline, high-K calc-alkaline, shoshonitic and leucite-shoshonitic magma series are developed. Detailed petrological, geochemical and isotopic (Sr, Nd, Pb, O) data are reported for a stratigraphically well-established sequence of lavas and pyroclastic rocks from the Middle Pleistocene volcanic cycle (430–127 ka) of Salina, which is characterized by an early period of basaltic volcanism (Corvo; Capo; Rivi; Fossa delle Felci, group 1) and a sequence of basaltic andesites, and andesites and dacites in the final stages of activity (Fossa delle Felci, groups 2–8). Major and trace element compositional trends, rare earth element (REE) abundances and mineralogy reveal the importance of crystal fractionation of plagioclase + clinopyroxene + olivine/ orthopyroxene ± titanomagnetite ± amphibole ± apatite in generating the more evolved magma types from parental basaltic magmas, and plagioclase accumulation in producing the high Al2O3 contents of some of the more evolved basalts. Sr isotope ratios range from 0.70410 to 0.70463 throughout the suite and show a well-defined negative correlation with 143Nd/144Nd (0.51275–0.51279). Pb isotope compositions are distinctly radiogenic with relatively large variations in 206Pb/204Pb (19.30–19.66), fairly constant 207Pb/204Pb (15.68–15.76) and minor variations in 208Pb/204Pb ratios (39.15–39.51). Whole-rock δ18O values range from +6.4 to +8.5‰ and correlate positively with Sr isotope ratios. Overall, the isotopic variations are correlated with the degree of differentiation of the rocks, indicating that only small degrees of crustal assimilation are overprinting the dominant evolution by crystal–liquid fractionation (AFC-type processes). The radiogenic and oxygen isotope composition of the Salina basalts suggests derivation from primary magmas from a depleted mantle source contaminated by slab-derived fluids and subducted sediments with an isotopic signature of typical upper continental crust. These magmas then evolved further to andesitic and dacitic compositions through the prevailing process of low-pressure fractional crystallization in a shallow magma reservoir, accompanied by minor assimilation of crustal lithologies similar to those of the Calabrian lower crust. Received: 29 November 1999 / Accepted: 16 April 2000  相似文献   

16.
A collection of galena from the Nezhdaninsky gold deposit (62 samples), as well as galena from the Menkeche silver-base-metal deposit and the Sentyabr occurrence and K-feldspar from intrusive rocks of the Tyry-Dyby ore cluster have been studied using the high-precision (±0.02%) MC-ICP-MS method. Particular ore zones are characterized by relatively narrow variations of isotope ratios (no wider than σ6/4 = 0.26%). Vertical zoning of Pb isotopic composition is not detected. Variation in Pb isotope ratios mainly depends on the type of mineral assemblage. Galena of the gold-sulfide assemblage dominating at the Nezhdaninsky deposit is characterized by the following average isotope ratios: 206Pb/204Pb = 18.472, 207Pb/204Pb = 15.586, and 208Pb/204Pb = 38.605. Galena from the regenerated silver-base-metal assemblage is distinguished by less radiogenic lead isotope ratios: 18.420, 15.575, and 38.518, respectively. In lead from the Nezhdaninsky deposit, the component, whose source is identified as Permian host terrigenous rocks, is predominant. The data points of isotopic composition of lode lead make up a linear trend within the range of μ2 = 9.5-9.6. K-feldspar of granitic rocks has less radiogenic and widely varying lead isotopic composition compared to that of galena. The isotopic data on Pb and Sr constrain the contribution of Late Cretaceous granitic rocks as a source of gold mineralization at the Nezhdaninsky deposit. The matter from the Early Cretaceous fluid-generating magma chamber participated in the ore-forming system of the Nezhdaninsky deposit. The existence of such a chamber is confirmed by the occurrence of Early Cretaceous granitoid intrusions on the flanks of the Nezhdaninsky ore field. The greatest contribution of magmatic lead (～30%) is noted in galena from the silver-base-metal mineral assemblage. This component has isotopic marks characteristic of lower crustal lead: the elevated 208Pb/206Pb ratio relative to the mean crustal value and the lower 207Pb/204Pb ratio. Taken together, they determine a high Th/U ～ 4.0 in the source and μ2 = 9.37–9.50. This conclusion is consistent with the contemporary tectonic model describing evolution of the South Verkhoyansk sector of the Verkhoyansk Foldbelt and the Okhotsk Terrane.  相似文献   

17.
High-K mafic alkalic lavas (5.4 to 3.2 wt% K2O) from Deep Springs Valley, California define good correlations of increasing incompatible element (e.g., Sr, Zr, Ba, LREE) and compatible element contents (e.g., Ni, Cr) with increasing MgO. Strontium and Nd isotope compositions are also correlated with MgO; 87Sr/86Sr ratios decrease and ɛNd values increase with decreasing MgO. The Sr and Nd isotope compositions of these lavas are extreme compared to most other continental and oceanic rocks; 87Sr/86Sr ratios range from 0.7121 to 0.7105 and ɛNd values range from −16.9 to −15.4. Lead isotope ratios are relatively constant, 206Pb/204Pb ∼17.2, 207Pb/204Pb ∼15.5, and 208Pb/204Pb ∼38.6. Depleted mantle model ages calculated using Sr and Nd isotopes imply that the reservoir these lavas were derived from has been distinct from the depleted mantle reservoir since the early Proterozoic. The Sr-Nd-Pb isotope variations of the Deep Springs Valley lavas are unique because they do not plot along either the EM I or EM II arrays. For example, most basalts that have low ɛNd values and unradiogenic 206Pb/204Pb ratios have relatively low 87Sr/86Sr ratios (the EM I array), whereas basalts with low ɛNd values and high 87Sr/86Sr ratios have radiogenic 206Pb/204Pb ratios (the EM II array). High-K lavas from Deep Springs Valley have EM II-like Sr and Nd isotope compositions, but EM I-like Pb isotope compositions. A simple method for producing the range of isotopic and major- and trace-element variations in the Deep Springs Valley lavas is by two-component mixing between this unusual K-rich mantle source and a more typical depleted mantle basalt. We favor passage of MORB-like magmas that partially fused and were contaminated by potassic magmas derived from melting high-K mantle veins that were stored in the lithospheric mantle. The origin of the anomalously high 87Sr/86Sr and 208Pb/204Pb ratios and low ɛNd values and 206Pb/204Pb ratios requires addition of an old component with high Rb/Sr and Th/Pb ratios but low Sm/Nd and U/Pb ratios into the mantle source region from which these basalts were derived. This old component may be sediments that were introduced into the mantle, either during Proterozoic subduction, or by foundering of Proterozoic age crust into the mantle at some time prior to eruption of the lavas. Received: 28 February 1997 / Accepted: 9 July 1998  相似文献   

18.
Economic reform in China since 1978 has accelerated economic development nationwide hugely, but has also brought about some environmental pollution. In order to identify the primary Pb source to the atmosphere in the central Guizhou region, Pb isotopic ratios in the acid soluble fraction of sediment from Hongfeng Lake were investigated. Lead isotopes in the lake sediments record the history of regional atmospheric Pb pollution. Before the economic reform in 1978, the 208Pb/206Pb and 206Pb/207Pb ratios in the leachates of lake sediments were constant, with a range of 2.0060 to 2.0117 and of 1.2314 to 1.2355, respectively. In the early period of economic reform (1978 to 1988), with the rapid industrial growth in Guizhou province, the acid soluble Pb isotope ratios in the lake sediments changed sharply: the 208Pb/206Pb ratios increased from 2.0212 to about 2.05, while the 206Pb/207Pb ratios decreased from 1.2251 to 1.2060. Emissions from Pb-ore-related industries are suggested to be the major pollution source of Pb in this period. Due to output from a local power plant since 1988, the isotope ratios of the acid soluble Pb in sediments in 1990s are characterized by a little higher radiogenic Pb (208Pb/206Pb = 2.0340–2.0400; 206Pb/207Pb = 1.2122–1.2158) than for the 1980s.  相似文献   

19.
The Pb, Sr and Nd isotopic compositions of biomonitors (lichen, moss, bark) and soil litter from different regions in the Rhine valley, as well as of <0.45 μm particles separated out of ice of the Rhône and Oberaar glaciers and lichens from the Swiss Central Alps, have been determined in order to deduce the natural baseline of the atmospheric isotopic compositions of these regions, which are suggested to be close to the isotopic compositions of the corresponding basement rocks or soils at the same sites. 206Pb/207Pb and 87Sr/86Sr isotope ratios are positively correlated. Most polluted samples from traffic-rich urban environments have the least radiogenic Pb and Sr isotopic compositions with 206Pb/207Pb and 87Sr/86Sr ratios of 1.11 and 0.7094, respectively. These ratios are very different from those of the atmospheric baseline for the Vosges mountains and the Rhine valley (206Pb/207Pb: 1.158–1.167; 87Sr/86Sr: 0.719–0.725; εNd: −7.5 to −10.1). However, this study indicates that the baseline of the atmospheric natural Pb and Sr isotopic compositions is affected by anthropogenic (traffic, industrial and urban) emissions even in remote areas. Lichen samples from below the Rhône and Oberaar glaciers reflect the baseline composition close to the Grimsel pass in the Central Swiss Alps (87Sr/86Sr: 0.714 − 0.716; εNd: −3.6 to −8.1). The 143Nd/144Nd isotope ratios are highly variable (8ε units) and it is suggested that the variation of the 143Nd/144Nd is controlled by wet deposition and aerosols originating from the regional natural and industrial urban environments and from more distant regions like the Sahara in North Africa. The least anthropogenetically affected samples collected in remote areas have isotopic compositions closest to those of the corresponding granitoid basement rocks.  相似文献   

20.
This paper dealt with the Pb contents and Pb isotopic composition of the West Lake Longjing tea. The results showed that in the tea leaves, from young leaf →old leaf →tea limb, the Pb contents tend to increase gradu-ally from 1.63 →4.84 →6.07×10-6, wich revealed that the Pb was accumulated gradually in the tea. After cleaned, the Pb contents of tea leaves were significantly reduced. This indicated that the deposits on the surface of tea leaves made a great contributuion to Pb contents. The survey results for soils in the relevant tea gardens showed that soil from the Longjing tea garden has higher Pb contents, with an average level of 49.6×10-6, two times those of common soils (24×10-6) in China. Results of the systematic analysis for tea, tea garden soil and the samples with the relevant background of the Pb isotopic composition displayed that the Pb isotopic ratio of tea is 206Pb/207Pb=1.164±0.005 (2σ). The ratio of 206Pb/207Pb for the soil gradually decreased from residue phase, soil dilute acid extract phase, and then to urban topsoil, i.e., 1.175 →1.171 →1.170. The 208Pb/(206Pb+207Pb) ratios also show a similar variation trend. 206Pb/207Pb ratios in the samples with the relevant background were: vehicle exhaust, 1.124; coal-combustion, 1.156; atmosphere, 1.168; and water, 1.166. Comparative studies have shown that Pb pollution is popular in the environ-mental media (soil, atmosphere, water) in Hangzhou. With the aggravation of Pb pollution, the Pb isotopic composi-tion gradually changed from the natural background (soil residues) to the direction of automobile exhaust. This phe-nomenon could illustrate that the pollution source was the vehicle exhaust, while the coal-combustion contributed little to environmental pollution in Hangzhou. The Pb of the Longjing tea came mostly from soluble phase Pb in the polluted soil. Moreover, secondary pollution was caused by vehicle exhaust.  相似文献   

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