Stable lead isotopes reveal a natural source of high lead concentrations to gasoline-contaminated groundwater

Concentrations of total lead as high as 1,600 g/L were detected in gasoline-contaminated and uncontaminated groundwater at three gasoline-release sites in South Carolina. Total lead concentrations were highest in turbid groundwater samples from gasoline-contaminated and uncontaminated wells, whereas lower turbidity groundwater samples (collected using low-flow methods) had lower total lead concentrations. Dissolved lead concentrations in all wells sampled, however, were less than 15 g total lead/L, the current United States Environmental Protection Agency (US EPA) maximum contaminant level (MCL). Because many total lead concentrations exceeded the MCL, the source of lead to the groundwater system at two of the three sites was investigated using a stable lead isotope ratio approach. Plots of the stable isotope ratios of lead (Pb) in groundwater as ²⁰⁷Pb/²⁰⁶Pb versus ²⁰⁸Pb/²⁰⁶Pb, and ²⁰⁸Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb were similar to ratios characteristic of lead-based minerals in local rocks of the southeastern US, and were not similar to the stable lead isotopes ratios characteristic of distant lead ore deposits such as Broken Hill, Australia, used to produce tetraethyl lead in gasoline products prior to its phase-out and ban in the United States. Moreover, the isotopic composition of dissolved lead was equivalent to the isotopic composition of total lead in turbid samples collected from the same well, suggesting that the majority of the lead detected in the groundwater samples was associated with sediment particulates of indigenous aquifer material, rather than lead associated with spilled leaded gasoline. The results of this investigation indicate that (1) lead detected at some gasoline-release sites may be derived from the local aquifer material, rather than the gasoline release, and consequently may affect site-specific remediation goals; (2) non-low flow groundwater sampling methods, such as a disposable bailer, may result in turbid groundwater samples and high total lead concentrations, and; (3) stable lead isotopes can be used to clarify the source of lead detected above permissible levels in gasoline-contaminated groundwater systems.     

The removal kinetics of dissolved organic matter and the optical clarity of groundwater

Concentrations of dissolved organic matter (DOM) and ultraviolet/visible light absorbance decrease systematically as groundwater moves through the unsaturated zones overlying aquifers and along flowpaths within aquifers. These changes occur over distances of tens of meters (m) implying rapid removal kinetics of the chromophoric DOM that imparts color to groundwater. A one-compartment input-output model was used to derive a differential equation describing the removal of DOM from the dissolved phase due to the combined effects of biodegradation and sorption. The general solution to the equation was parameterized using a 2-year record of dissolved organic carbon (DOC) concentration changes in groundwater at a long-term observation well. Estimated rates of DOC loss were rapid and ranged from 0.093 to 0.21 micromoles per liter per day (μM d^?1), and rate constants for DOC removal ranged from 0.0021 to 0.011 per day (d^?1). Applying these removal rate constants to an advective-dispersion model illustrates substantial depletion of DOC over flow-path distances of 200 m or less and in timeframes of 2 years or less. These results explain the low to moderate DOC concentrations (20–75 μM; 0.26–1 mg L^?1) and ultraviolet absorption coefficient values (a ₂₅₄?<?5 m^?1) observed in groundwater produced from 59 wells tapping eight different aquifer systems of the United States. The nearly uniform optical clarity of groundwater, therefore, results from similarly rapid DOM-removal kinetics exhibited by geologically and hydrologically dissimilar aquifers.     

Detection of <Superscript>3</Superscript>H and <Superscript>85</Superscript>Kr in groundwater from arsenic-bearing crystalline bedrock of the Goose River basin,Maine

Presence of young groundwater (post-1950) in the Goose River basin is demonstrated with ³H and ⁸⁵Kr analyses. A total of 96 wells and four springs were sampled quarterly from 1999 to 2001 to determine the extent of any recent recharge and to what depth hydraulic continuity existed in the groundwatershed (33.3 km²). Recharge groundwater is less than 50 years in about 31% (³H) to 37% (⁸⁵Kr) of sampled wells and 75% of sampled springs. Young groundwater ages are recorded in wells up to 320 m in depth within fractured- and arsenic-bearing crystalline bedrock. Total arsenic 10 g L^–1 occurs significantly in drinking water with young groundwater flowing through the pumping well intervals. As_total occurs in 89% (⁸⁵Kr) to 93% (³H) of all wells with post-1950 groundwater ages. Young groundwater recharge and elevated geogenic arsenic were discovered only in the anatectic granitoids and migmatized country rock of the southwestern part of the Goose River basin.     

Arsenic Distribution Pattern in Different Sources of Drinking Water and their Geological Background in Guanzhong Basin,Shaanxi, China

To study arsenic(As) content and distribution patterns as well as the genesis of different kinds of water, especially the different sources of drinking water in Guanzhong Basin, Shaanxi province, China, 139 water samples were collected at 62 sampling points from wells of different depths, from hot springs, and rivers. The As content of these samples was measured by the intermittent flowhydride generation atomic fluorescence spectrometry method(HG-AFS). The As concentrations in the drinking water in Guanzhong Basin vary greatly(0.00–68.08 μg/L), and the As concentration of groundwater in southern Guanzhong Basin is different from that in the northern Guanzhong Basin. Even within the same location in southern Guanzhong Basin, the As concentrations at different depths vary greatly. As concentration of groundwater from the shallow wells(50 m deep, 0.56–3.87 μg/L) is much lower than from deep wells(110–360 m deep, 19.34–62.91 μg/L), whereas As concentration in water of any depth in northern Guanzhong Basin is 10 μg/L. Southern Guanzhong Basin is a newly discovered high-As groundwater area in China. The high-As groundwater is mainly distributed in areas between the Qinling Mountains and Weihe River; it has only been found at depths ranging from 110 to 360 m in confined aquifers, which store water in the Lishi and Wucheng Loess(Lower and Middle Pleistocene) in the southern Guanzhong Basin. As concentration of hot spring water is 6.47–11.94 μg/L; that of geothermal water between 1000 and 1500 m deep is 43.68–68.08 μg/L. The high-As well water at depths from 110 to 360 m in southern Guanzhong Basin has a very low fluorine(F) value, which is generally 0.10 mg/L. Otherwise, the hot springs of Lintong and Tangyu and the geothermal water in southern Guanzhong Basin have very high F values(8.07–14.96 mg/L). The results indicate that highAs groundwater in depths from 110 to 360 m is unlikely to have a direct relationship with the geothermal water in the same area. As concentration of all reservoirs and rivers(both contaminated and uncontaminated) in the Guanzhong Basin is 10 μg/L. This shows that pollution in the surface water is not the source of the high-As in the southern Guanzhong Basin. The partition boundaries of the high- and low-As groundwater area corresponds to the partition boundaries of the tectonic units in the Guanzhong Basin. This probably indicates that the high-As groundwater areas can be correlated to their geological underpinning and structural framework. In southern Guanzhong Basin, the main sources of drinking water for villages and small towns today are wells between 110–360 m deep. All of their As contents exceed the limit of the Chinese National Standard and the International Standard(10 μg/L) and so local residents should use other sources of clean water that are 50 m deep, instead of deep groundwater(110 to 360 m) for their drinking water supply.     

Surface and groundwater quality in the northeastern region of Buenos Aires Province, Argentina

This work studies the water quality of the Pergamino–Arrecifes River zone in the Rolling Pampa, northeast Buenos Aires Province, Argentina. Temperature, pH, specific conductivity, Na, K, Mg, Ca, , Cl⁻, , , Si, Ag, Al, As, B, Ba, Be, Br, Cd, Co, Cr, Cu, Fe, Hg, Li, Mn, Mo, Ni, P, Pb, Se, Tl, U, V, Zn, and the environmental stable δ¹⁸O and δ²H isotope ratios were determined in 18 sampling stations. Natural and anthropogenic features influence surface and groundwater quality. Point pollution sources (septic wells and other domestic and farming effluents) increase the nitrate concentration. The values of pH, , Al, As, B, Fe, and Mn exceed the respective Argentine reference thresholds in different sampling stations for human drinking water; B, Mo, U, and V for irrigation; and V and Zn for cattle consumption.     

Zur Röntgen-Fluoreszenz-Spektralanalyse von Rubidium,Strontium, Barium und Blei in Kaolinen und Tonen

An x-ray fluorescence spectrographic method is described for the determination of rubidium, strontium, barium and lead in kaolins and clays. The method is most usefull within a concentration range of 50–2000 p.p.m. Rb, Sr, Ba or Pb in the sample.Dried powder samples of kaolins resp. clays are compressed in a suitably shaped die and its x-ray radiations are compared with those of the same kaolins or clays to which small amounts of Rb, Sr, Ba or Pb had been added. A homogenous distribution of small amounts of these elements in kaolins and clays is obtained by precipitation of Pb, Ba and Sr as sulfate and Rb as Rb[B(C₅H₆)₄] in a concentrated clay resp. kaolin suspension. The prepared suspensions are filtered (by membran-filters) and dried before compressing and x-ray measuring.The instrumental conditions were: Siemens x-ray spectrograph Kristalloflex IV fitted with a lithium fluoride analysing crystall, molybdenum-target x-ray tube (type AG Mo 61), 50 kV 30 m.amp. for measuring of the Sr K-, Rb K-, Pb L/gB-lines and 60 kV 36 m.amp. for measuring of the Ba K-line.The standard deviations were: ± 3 p.p.m. Rb for samples containing 25– 150 p.p.m. of Rb ± 6 p.p.m. Sr for samples containing 200– 400 p.p.m. of Sr ± 60 p.p.m. Ba for samples containing 1000–2000 p.p.m. of Ba ± 9 p.p.m. Pb for samples containing 250– 800 p.p.m. of Pb

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Der Deutschen Forschungsgemeinschaft dankt der Verfasser für die gewährte Unterstützung zur Durchführung der vorgelegten Arbeit.     

Diagnosis of trace Pb in domestic wells,Upper Gloucester Catchment,Maine, USA

Dissolved Pb in 32 wells associated with corroding submersible pumps is examined within a rural water district after almost 20 years (1984–2002). Groundwater Pb ranged from 0.4–24.9 μg L⁻¹ after 24 h pump flushing. Preliminary geochemistry and representative borehole lithology examinations were extrapolated by Markov chain modeling. The first-order geostatistical realizations of glacial sediments coupled with the Monte Carlo Metropolis-Hasting method suggest that elevated trace Pb persists in sand and gravel units, and continues at least to 40 m depth in the catchment. The ²⁰⁷Pb/²⁰⁶Pb and ²⁰⁸Pb/²⁰⁶Pb isotope compositions of groundwater Pb were decisive in discriminating the importance of leached Pb from submersible pump materials among geogenic sources.     

Virus occurrence in private and public wells in a fractured dolostone aquifer in Canada

Groundwater samples from 22 wells completed in a regional fractured dolostone aquifer in the Guelph region of southern Ontario, Canada, were collected over an 8-month period and analyzed for viruses and Campylobacter jejuni. Only 8% of the 118 samples exhibited viruses at extremely low concentrations, but of the 22 wells sampled, 10 (45%) were positive for human enteric viruses (polyomavirus, adenovirus A, and GII norovirus) including 5 of the 8 public supply wells (62.5%) and 5 of the 11 private wells (45%). Each virus-positive well had only one virus occurrence with six sampling events during the 8-month sampling campaign and only one virus type was detected in each well. The probability of virus detection was positively associated with well open-interval length. Virus concentration (in the wells that were virus-positive) was negatively associated with well depth and open-interval length and positively associated with overburden thickness (i.e., the thickness of unconsolidated materials overlying bedrock facies) and the amount of precipitation 8–14 and 15–21 days prior to the sampling date. The ephemeral nature of the virus detections and the low detection rate on a per sample basis were consistent with previous studies. The percentage of virus-positive wells, however, was much higher than previous studies, but consistent with the fact that the hydrogeologic conditions of fractured bedrock aquifers create wide capture zones and short groundwater travel times to wells making them more vulnerable to contamination occurrence but at very low concentrations.     

Hydrogeochemical Processes in the Kafue River upstream from the Copperbelt Mining Area, Zambia

Frequent sampling during an annual cycle of dissolved(<0.45 m) and suspended (>0.45 m) elementshas been conducted in the Kafue River at Raglan'sFarm, upstream from the mining activities within theCopperbelt Province, Zambia. Additional sampling ofsediment and interstitial pore water was conductedduring low water discharge. The presence of carbonateswithin the drainage basin naturally gives rise to highelement concentrations in the dissolved phase(Ca = 626, Mg = 494, Na = 360 and K = 24 mmol l^-1).During the rainy season the relative composition ofthe dissolved elements indicated a wash out ofaccumulated weathering products and mineralisedorganic material from the unsaturated zone of the soilprofile. High concentrations of dissolved Al, Fe andMn were measured during high water discharge. At lowwater discharge the sediment was a major source of Fe,Mn and associated Co and Cu to the water column.Enhanced concentrations of dissolved and suspended S,Co and Cu during the rainy season indicated thatatmospheric deposited particles from the mining areawere washed out into the river. Autochthonousformation of particles rich in Si indicated diatomproduction during low water discharge.     

An enriched mantle source for potassic basanites: evidence from Karisimbi volcano,Virunga volcanic province,Rwanda

Lavas from Karisimbi, the largest volcano in the Virunga province in the Western Branch of the African rift on the Zaire-Rwandan border, constitute a suite of mafic potassic basanites and more evolved potassic derivatives. All of the lavas are potassic with K₂O/Na₂O1, and enriched in incompatible elements, with chondrite normalised (La/Yb)_n>18 and Nb/Zr>0.25. The ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios reflect these enriched compositions, varying from 0.7052 and 0.51258 respectively in the K-basanites to 0.7132 and 0.51226 in the most evolved K-trachyte, although at MgO abundances >4% there is no systematic variation of isotope ratios with fractionation. At >4% MgO, lava compositions were controlled by assimilation and fractional crystallization in a sub-volcanic magma chamber. Trace-element and isotope variations in the more mafic lavas appear to reflect mixing between a primitive K-basanite (PKB) magma and a Sr-rich end-member, similar to melilite nephelinites from the neighbouring volcano, Nyiragongo. Both endmembers are mantle-derived and isotopically distinct, with the PKB being characterised by ⁸⁷Sr/⁸⁶Sr up to 0.707 and ¹⁴³Nd/¹⁴⁴Nd as low as 0.51236. Alternatively, isotope variations may be the time-integrated response to trace-element fractionations in a variably enriched mantle source. The Pb isotope variations within Karisimbi are complex. In the more evolved lavas all three ratios increase coherently with fractionation, whereas in the mafic varieties ²⁰⁶Pb/²⁰⁴Pb remains roughly constant at 19.2 while ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb vary from 15.67 to 15.78 and 39.49 to 40.80 respectively, defining sub-vertical trends, consistent with PKB-nephelinite magma mixing. The Nd and Sr isotopes indicate trace-element fractionation in the PKB source at 1 Ga, similar to ages derived from the overlying crust and suggesting a lithospheric origin. Elevated ²⁰⁸Pb/²⁰⁴Pb and ²⁰⁸Pb^*/²⁰⁶Pb^* values of the PKB are also consistent with Th/U fractionation at a similar time. However, this 1Ga age contrasts with that derived from the elevated ²⁰⁷Pb/²⁰⁴Pb ratios which indicate U/Pb fractionation during the Archaean. Crustal contamination can be excluded as the major control of Pb isotope variation in the PKB because their high Ce/Pb ratios (27) are similar to those typical of oceanic basalts. Parent/daughter trace-element fractionation and the high Ti, Nb and Ta abundances of the PKB lavas are all consistent with enrichment of a lithospheric source region by small-degree silicate melts at 1Ga. Comparison between measured and time-integrated trace-element ratios suggests that the degree of melting associated with recent magmatism was 5%. These data show that significant Th/U and Rb/Sr fractionation can be produced by intra-mantle melting processes and that high ²⁰⁸Pb/²⁰⁴Pb and ²⁰⁸Pb^*/²⁰⁶Pb^* values can evolve within the upper mantle and do not necessarily require the recycling of crustal material. Comparable isotope features in continental flood basalts and DUPAL ocean island basalts may be explained in a similar way.     

Groundwater development in Lemoa, Guatemala

In the rural Guatemalan Central Highlands, drinking water wells are a rare commodity due to lack of data regarding depth and sustainability of groundwater. At a study well in Lemoa, aquifer sustainability and other characteristics were estimated using hydrograph data and Theiss recovery method for pumping tests. These tests showed that while specific capacity remained fairly constant, transmissivity increased, indicating development of the well subsequent to installation of the study well. The time domain electromagnetic (TDEM) method was evaluated at the site as a prospective groundwater prospecting technique. Characterization of subsurface conditions using TDEM is feasible with local subsurface data for correlation; however, it is limited to delineating low electrical resistive zones without geologic data for correlation. Data showed that groundwater produced from volcanic alluvium at approximately 79 m in depth is sustainable at the study area at current use rates.     

Measurements and interpretations of36Cl in groundwater,Milk River aquifer,Alberta, Canada

The³⁶Cl/Cl ratios of 12 groundwater samples from the Milk River aquifer were determined by accelerator mass spectrometry. Using known Cl concentrations,³⁶Cl concentrations were deduced. Approximately linear relations were observed between the logarithm of the³⁶Cl concentration, the Cl concentration, and the distance from the recharge area along two flow paths. The results are discussed in two approaches:

• (1)in an interpretation of the linear relation between logarithm of the³⁶Cl concentration and Cl concentration excluding and includingin situ production of³⁶Cl;
• (2)in a diffusion model. The increase of the Cl concentration with the distance from the recharge area is considered to be due to diffusion of Cl from the underlying confining Colorado shale to the aquifer.

Flow velocities ranging between 0.04 and 0.14 m/a, and ages of the groundwater between 0.6 and 2 Ma are obtained at a distance of 80 km from the recharge area.     

Nd,Sr, Pb,Ar, and 0 isotopic systematics of Sturgeon Lake kimberlite,Saskatchewan, Canada: constraints on emplacement age,alteration, and source composition

Rb-Sr isotopic dating of phlogopite megacryst samples separated from Sturgeon Lake kimberlite, Saskatchewan, yields a crystallization age of 98±1 Ma (2 , MSWD=1.2; ⁸⁷Sr/⁸⁶Sr(t)=0.7059). The ⁴⁰Ar/³⁹Ar analyses of a phlogopite megacryst sample indicate the presence of large amounts of excess ⁴⁰Ar and yield an excessively old age of 410 Ma. Assessment of the Ar data using isotope correlation plots indicates clustering of the data points about a mixing line between the radiogenic ⁴⁰Ar component at 98 Ma and a trapped component with uniform ³⁶Ar/⁴⁰Ar and Cl/⁴⁰Ar. Values of {ie212-1} as high as +20%. (VSMOW) for calcite from the groundmass and a whole-rock sample indicate pervasive lowtemperature alteration. The {ie212-2} of matrix carbonate is-11.3%. (PDB), slightly lighter than typical values from the literature. The {ie212-3} values of about +5%. (VSMOW) for brown phlogopite megacrysts may be primary, green phlogopites are interpreted to be an alteration product of the brown variety and are 2%. heavier. Initial Nd-Sr-Pb isotopic ratios for a whole-rock sample {ie212-4}; ⁸⁷Sr/⁸⁶Sr=0.7063, ²⁰⁶Pb/²⁰⁴Pb=18.67, ²⁰⁷Pb/²⁰⁴Pb=15.54, ²⁰⁸Pb/²⁰⁴Pb=38.97) suggest an affinity with group I kimberlites. Initial {ie212-5} values of +1.7 and +0.5 (⁸⁷Sr/ ⁸⁶Sr(t)=0.7053 and 0.7050) for eclogitic and lherzolitic garnet megacryst samples, and values of 0.0 for two phlogopite megacryst samples reflect an origin from an isotopically evolving melt due to assimilation of heterogeneous mantle. Lilac high-Cr lherzolitic garnet megacrysts give an unusually high {ie212-6} of +28.6 (⁸⁷Sr/⁸⁶Sr=0.7046) indicating a xenocrystic origin probably from the lithospheric mantle. The very radiogenic ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb ratios of the kimberlite are consistent with melting of EM II (enriched) mantle components.     

Unsupported radiogenic Pb in zircon: a cause of anomalously high Pb-Pb,U-Pb and Th-Pb ages

Ion microprobe U-Th-Pb isotopic analyses of zircons from a granodioritic orthogneiss from the Napier Complex, Mount Sones, Enderby Land, Antarctica, have identified an unambiguous example of unsupported radiogenic Pb in a 3,950 Ma-old crystal. At one 40 m spot on the crystal an unusually large heterogeneity in Pb content was found, the concentration of radiogenic Pb ranging from 5 to 50 percent higher than could have been generated in 3,950 Ma by radioactive decay of the co-existing U and Th. This relative excess of radiogenic Pb is attributed to Pb gain rather than to U and Th loss because first, the Pb content varied by more than the U or Th contents and secondly, changes in the Pb/U, Pb/Th and Pb isotopic composition correlated directly with changes in the Pb concentration. The individual ²⁰⁷Pb/²⁰⁶Pb apparent ages ranged from 4,000 Ma to 4,145 Ma, all greater than the inferred age of the crystal. A correlation between ²⁰⁷Pb/²⁰⁶Pb and Pb/U shows that the Pb excess has not resulted from recent Pb movement. The spot apparently gained radiogenic Pb about 2,500 Ma ago, at the same time as the majority of the other zircons in the rock suffered substantial Pb loss. The Pb movement occurred in response to a discrete geologic event. Reverse discordance is a phenomenon that must be considered when interpreting zircon U-Pb ages, especially ²⁰⁷Pb/²⁰⁶Pb ages of single crystals or portions of crystals. Decay constants. Ages in this paper are calculated using the decay constant convention recommended by the Subcommission on Geochronology (Steiger and Jaeger 1977).     

Evaluation of the thermal regime of the Valles Caldera,New Mexico,U.S.A., by downward continuation of temperature data

Downward continuation of temperature data from 73 wells extending to depths of 250 ft (76 m) provides constraints on the thermal regime of the Valles Caldera. Surface-temperature gradient data and bottom-hole temperatures were used as constraints in the downward continuation. Three factors were found to control the shallow thermal regime:

• 1.(1) heat associated with the main geothermal source;
• 2.(2) local topography; and
• 3.(3) west-southwest groundwater flow. Although the well density is relatively high, comparison with the topography shows that the wells are not randomly distributed and tend to be clustered in valleys. Many details in the thermal regime appear to be related to groundwater drainage in these valleys. Temperature gradients and temperatures generally increase in the same direction as the regional drainage of the caldera suggesting a long-wavelength, shallow component to this regional gradient trend. Inversion of gradient and temperature data show additional deep heat input in the west-southwest sector of the caldera which appears to be spatially associated to the youngest volcanism. A previously reported northeast displacement of the main heat source from the surface anomaly has not been confirmed.

     

Glacio-lacustrine stratigraphy,aquifer characterization and contaminant transport: a case study in South Lake Tahoe,California, USA

A hydrogeologic model that has been used by many researchers and consultants to describe an area of South Lake Tahoe, California, USA impacted by MTBE contamination describes a relatively homogeneous unconfined aquifer comprised of poorly sorted glacial outwash deposits, within which water-supply wells are able to exert significant alteration in natural groundwater flow. A re-examination of the area’s hydrogeology is presented, which supports a layered heterogeneous aquifer system constructed of alternating fine and coarser-grained glacio-lacustrine depositional units. This re-evaluation was accomplished through a review of lithologic logs across an area of approximately 1 km², combined with observations of significant hydraulic head differences and knowledge of the depositional environments controlled by Pleistocene Lake Tahoe high stands. Many of the fine-grained units observed at depths from 6 to 15 m, although relatively thin, are generally continuous and serve as significant barriers to groundwater flow. The vertical migration of contamination across these fine-grained units to deeper groundwaters was facilitated by cross-screened monitoring wells installed as part of site investigation activities. This conclusion highlights the importance of geologic characterization and proper monitoring well construction at contaminated site investigations.

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Pb and Nd isotope constraints on the origin of high Mg and tholeiitic amphibolites,Kolar Schist Belt,South India

The late Archean, north-south trending Kolar Schist Belt in south India, 4 km wide by 80 km long, is thought to be a suture between two gneiss terranes (Krogstad et al. 1989). Within this volcanics-dominated belt are recognized both tholeiitic and high Mg (komatiitic and picritic) amphibolites, which make up some 70% and 5% respectively of the exposed outcrops. A massive tholeiitic amphibolite separates the belt into western and eastern parts. A Pb-Pb whole-rock age of 2732±155 Ma on samples from a single outcrop of massive tholeiite is a minimum age for this rock. Samples of this rock have _Nd values at 2700 Ma that range between +3.8 and +6.8, ₁ (initial ²³⁸U/²⁰⁴Pb) of 7.5 and K ₁ (initial ²³²Th/²³⁸U) of about 4. Two different types of high-Mg amphibolites are recognized from the western part of the belt: a picritic or P-type, and a komatiitic or K-type. The P-type have highly variable Ce/Al ratios all greater than chondritic, Nd/Yb ratios greater than chondritic, _Nd at 2700 Ma of +1.5 to +8, and Pb isotope compositions variable in ²⁰⁷Pb/²⁰⁴Pb with ₁ of about 8.0 and k ₁ of about 4. The trace-element data suggest that the light-REE enrichment is a character of the mantle source and is not due to residual garnet. The K-type amphibolites have near chondritic Ce/Al and Nd/Yb ratios, _Nd at 2700 Ma of +1.5 to +8, and ₁ of about 8 and k ₁ of about 4. Although the P-type is light-REE enriched compared to the K-type, both types have similar Ce/Nd ratios as well as initial Pb and Nd isotopes. If the 2696±136 Ma age for the Sm-Nd isochron which includes both types of high-Mg amphibolite has any significance it dates the time of light-REE enrichment of the mantle source for the P-type komatiitic amphibolites. The high-Mg amphibolites in the eastern part of the belt are light-REE enriched, have Pb isotopic compositions that are variable in ²⁰⁷Pb/²⁰⁴Pb with a ₁ about 8.5 and _Nd at 2700 Ma of +1.8 to +4.5. Hydrothermal fluids associated with metamorphism and shearing prior to about 2400 Ma ago were responsible for the introduction of gold-quartz-carbonate veins into the Kolar Schist Belt. The Pb isotope composition of galena in these veins suggests that these fluids may have also introduced extraneous Pb from adjacent older granitoid gneisses into the amphibolites, which could be responsible for the variability in the ²⁰⁷Pb/²⁰⁴Pb ratios of the samples. This extraneous Pb probably is not responsible for the distinct Pb isotope character of each type of amphibolite.