Impact of liquid waste disposal on potable groundwater resources near Perth,Western Australia

 Drilling of 15 boreholes at a disused liquid waste disposal site near Perth, Western Australia, has indicated that a contamination plume extends about 1000 m in a southerly direction from the site in the direction of groundwater flow. The plume is up to 600 m wide and 5–40 m thick. Chemical and microbiological analyses have indicated that contaminated groundwater contains high concentrations of ammonia, iron, and bacteria at levels that commonly exceed national drinking water guidelines. It is likely that a proposed water supply production well in the path of the contamination plume will have to be abandoned, and additional wells may have to be abandoned if the plume continues to extend in the direction of groundwater flow. There is currently insufficient information to indicate whether the plume is continuing to expand, but studies on similar plumes in the Perth metropolitan area have indicated that contaminated groundwater can move at rates up to 100 m yr^–1. Several other liquid waste disposal sites are now located in residential areas of Perth where wells are used for garden irrigation. Further work is required to ensure that there is no potential impact of groundwater contamination on public health in these areas. Received: 31 July 1995 · Accepted: 18 September 1995     

Case study: a 3D resistivity and induced polarization imaging from downstream a waste disposal site in Brazil

A contaminated site from a downstream municipal solid waste disposal site in Brazil was investigated by using a 3D resistivity and induced polarization (IP) imaging technique. This investigation purpose was to detect and delineate contamination plume produced by wastes. The area was selected based on previous geophysical investigations, and chemical analyses carried out in the site, indicating the presence of a contamination plume in the area. Resistivity model has successfully imaged waste presence (ρ < 20 Ωm), water table depth, and groundwater flow direction. A conductive anomaly (ρ < 20 Ωm) outside wastes placement was interpreted as a contamination plume. Chargeability model was also able to imaging waste presence (m > 31 mV/V), water table depth, and groundwater flow direction. A higher chargeability zone (m > 31 mV/V) outside wastes placement and following conductive anomaly was interpreted as a contamination plume. Normalized chargeability (MN = m/ρ) confirmed polarizable zone, which could be an effect of a salinity increase (contamination plume), and the clay presence in the environment.     

The effect of clay dehydration on land subsidence in the Yun-Lin coastal area, Taiwan

 The smectite dehydration theory developed by Ransom and Helgeson was applied for simulation of land subsidence in the Yun-Lin coastal area, Taiwan. The volumetric reduction of smectite clay at equilibrium state was computed by assuming that the dehydration of interlayer water in smectite clay can be described with a regular solid solution reaction. By using the in situ stratigraphic data collected from the subsidence monitoring wells in the simulated area, the amounts of land subsidence caused by smectite dehydration in three scenarios with pressure variation were calculated. The results indicate that significant amounts of land subsidence can be attributed to smectite dehydration. This finding reveals that smectite dehydration is of importance for assessment and prediction of land subsidence. Additionally, the results also indicate the overburden weight has a larger effect on clay dehydration than the effective stress change resulting from over-pumping, although both of them induce relatively minor variations on land subsidence. Received: 23 February 2000 · Accepted: 23 March 2000     

Detection of Hg pollution by stream sediment geochemistry in the Bisagno valley (Genoa, Italy)

 Systematic stream sediment investigation in a periurban area surrounding Genoa (Italy) revealed the existence of a significant mercury anomaly localized on the main (3rd rank) bed of the Bisagno river. Statistical multivariate analysis of elemental abundances points out the anthropic nature of this contamination. Because of the well-known bioaccumulation of Hg in contaminated media, attention must be focused on the risks associated with the discovered pollution. Received: 30 November 1999 · Accepted: 22 March 2000     

Geoenvironmental site investigation using different techniques in a municipal solid waste disposal site in Brazil

Different geoenvironmental site investigation techniques to assess contamination from a municipal solid waste disposal site in Brazil are presented here. Superficial geophysical investigation (geoelectrical survey), resistivity piezocone penetration tests (RCPTU), soil samples collected with direct-push samplers and water samples collected from monitoring wells were applied in this study. The application of the geoelectrical method was indispensable to identify the presence and flow direction of contamination plumes (leachate) as well as to indicate the most suitable locations for RCPTU tests and soil and water sampling. Chemical analyses of groundwater samples contributed to a better understanding of the flow of the contaminated plume. The piezocone presented some limitations for tropical soils, since the groundwater level is sometimes deeper than the layer which is impenetrable to the cone, and the soil genesis and unsaturated conditions affect soil behavior. The combined interpretation of geoelectrical measurements and soil and water samplings underpinned the interpretation of RCPTU tests. The interpretation of all the test results indicates that the contamination plume has already overreached the landfill’s west-northwest borders. Geoenvironmental laboratory test results suggest that contamination from the solid waste disposal site has been developing gradually, indicating the need for continuous monitoring of the groundwater.     

Oxygen isotope geochemistry of the Mesozoic anorogenic complexes of Damaraland,northwest Namibia: evidence for crustal contamination and its effect on silica saturation

 Fifty-six new oxygen isotope analyses of minerals separated from nine Mesozoic anorogenic complexes of Damaraland in northwest Namibia have been used to estimate the δ¹⁸O values of the original magmas (δ_magma). These complexes range in composition from nepheline syenite to alkaline and peraluminous granites, often with a variety of rock types present at a single centre. The silica-undersaturated rock types show a relatively small spread of values of δ_magma from 6.0 to 7.0‰ (mean 6.6‰), which is consistent with their derivation from the mantle with little or no subsequent crustal contamination. The silica-oversaturated rocks show a wide range of δ_magma values from 4.9 to 12.0‰, with a mean value of 8.3‰. The high values of δ_magma in the silica-oversaturated rocks can only be explained with considerable involvement of the continental crust in their petrogenesis, and those rocks with δ_magma>10‰ are interpreted as essentially crustal melts. It is generally accepted that the Damaraland complexes were generated as a result of rifting across the Tristan plume, with the plume providing both mantle-derived magma and with it the heat required for crustal melting. In addition to their mantle-like oxygen isotope ratios, the undersaturated rocks of the Damaraland complexes possess the trace element characteristics (e.g. low Zr/Nb ratios) of ocean island basalt, suggesting that their parental magmas were produced from the plume itself. In contrast, the oversaturated complexes generally have higher Zr/Nb ratios that are consistent with a larger crustal input. The highest values of δ_magma in the Damaraland complexes are found in granitic rocks that intrude the central zone of the Pan-African Damara Orogen where presumably there is a substantial component of sedimentary origin in the lower to middle crust. Received: 3 April 1995/Accepted: 24 July 1995     

Magma Genesis and Mantle Dynamics at the Harrat Ash Shamah Volcanic Field (Southern Syria)

A geochemical and petrological study of Miocene to recent alkalibasalts, basanites, hawaiites, mugearites, trachytes, and phonoliteserupted within the Harrat Ash Shamah volcanic field was performedto reconstruct the magmatic evolution of southern Syria. Themajor element composition of the investigated lavas is mainlycontrolled by fractional crystallization of olivine, clinopyroxene,± Fe–Ti oxides and ± apatite; feldspar fractionationis restricted to the most evolved lavas. Na₂O and SiO₂ variationswithin uncontaminated, primitive lavas as well as variably fractionatedheavy rare earth element ratios suggest a formation by variabledegrees of partial melting of different garnet peridotite sourcestriggered, probably, by changes in mantle temperature. The isotopicrange as well as the variable trace element enrichment observedin the lavas imply derivation from both a volatile- and incompatibleelement-enriched asthenosphere and from a plume component. Inaddition, some lavas have been affected by crustal contamination.This effect is most prominent in evolved lavas older than 3·5Ma, which assimilated 30–40% of crustal material. In general,the periodicity of volcanism in conjunction with temporal changesin lava composition and melting regime suggest that the Syrianvolcanism was triggered by a pulsing mantle plume located underneathnorthwestern Arabia. KEY WORDS: ⁴⁰Ar/³⁹Ar ages; intraplate volcanism; mantle plume; partial melting; Syria     

Longitudinal Petrochemical Variation in the Mackenzie Dyke Swarm, Northwestern Canadian Shield

Previous magnetic fabric studies of the giant, radiating, 1.27Ga Mackenzie dyke swarm concluded that flow patterns withinthe dykes support the concept of a mantle plume that is centredbeneath the swarm focus and supplies magma to overlying floodbasalts and developing radial dykes. To examine petrochemicalimplications of the model, compositional variation within thebasalt sequence is compared with that of the dykes along a ‘streamline’ of the swarm between 400 km (just beneath the lavas)and 2100 km from its focus and in a parallel segment farthereast. Evolution of tholeiitic magmas of the main sampled streamis recorded in the upward change of composition in the lavasequence from mg-numbers of 70 to 35. Underlying (feeder) dykeshave a comparable range, but outward along the swarm the rangeof compositions narrows progressively towards its more evolvedend, and at 2100 km, dyke compositions match those in upperlevels of the lava sequence. REE and other trace element abundancesshow a similar contraction in range, and a shift towards moreevolved compositions, both upward in the lava sequence and outwardalong the swarm. Apart from complications owing to crustal contamination,fundamental attributes of the magma (e.g. Zr/Y) change littlewith stratigraphic level or distance from the focus. The moreeasterly stream differs in its high proportion of alkalic compositions,suggesting the existence of distinctive subswarms. Normativemineral variation plots are consistent with fractionation inhigh- (main stream) to low-level (eastern stream) crustal magmachambers. Mackenzie magmatism is compatible with the plume model.Domal uplift related to plume activity initiated central grabencollapse and outward-extending radial fractures, thus providingaccess to plume-derived magmas and loci for magma chamber anddyke swarm development. Multiple magma chambers, forming aroundthe apex, each fed relatively independent subswarms of dykes.Uplift, accompanying fractionation, provided increasing magmatichead by which fractionating magmas could be dispatched to successivelygreater distances. This, and crystal settling in transport,accounts for the increasingly evolved nature of dykes with distancefrom the source. KEY WORDS: mantle plume; flood basalts; dyke swarm; petrochemistry; Precambrian ^*Corresponding author.     

Nd and Sr isotopic geochemistry of mafic layered intrusions in the eastern Baltic shield: implications for the evolution of Paleoproterozoic continental mafic magmas

 Nd and Sr isotopic data are presented for the 2449–2441 Ma Olanga and Burakovka layered mafic complexes in the eastern Baltic Shield. These complexes have similar tectonic position, but differ in two aspects: the age of the enclosing crust and the post-crystallization metamorphic history. The Sm–Nd isotopic results for the Kivakka and Lukkulaisvaara intrusions, Olanga Complex, are consistent with the model of closed-system crystallization of a single magma without significant wallrock assimilation. The Rb–Sr systems of minerals were disturbed by late Rb addition during 1.75–1.50 Ga metamorphism. The Nd and Sr isotopic systems in the Burakovka complex show no metamorphic disturbance and indicate mixing of at least four isotopically distinct components. Isotopic variations in the Burakovka Complex can be explained by a 4–20 per cent contamination of a primary komatiitic or picritic magma with a Mesoarchean crust, similar to that exposed in the region. A similar model, applied to the Olanga Complex using a Neoarchean crustal isotopic composition, cannot reproduce the observed isotopic signature. The nearly uniform initial ɛ_Nd values between −1 and −2.3, observed in the Kivakka and Lukkulaisvaara intrusions of the Olanga Complex, as well as in the other 2.50–2.44 Ga layered mafic intrusions throughout the eastern Baltic Shield, are better explained by a mantle plume model with small amounts of crustal contamination and minor involvement of asthenospheric material. This model is also consistent with the geological observations and the temporal distribution of the Paleoproterozoic mafic magmatism in the eastern Baltic Shield. As an alternative, the enriched isotopic characteristics may be explained by melting of a metasomatically modified lithospheric mantle source. Received: 4 August 1994/Accepted: 5 April 1996     

Petrogenesis of Tertiary Mafic Alkaline Magmas in the Hocheifel, Germany

Primitive nephelinites and basanites from the Tertiary Hocheifelarea of Germany (part of the Central European Volcanic Province;CEVP) have high Mg-number (>0·64), high Cr and Nicontents and strong light rare earth element enrichment butsystematic depletion in Rb, K and Ba relative to trace elementsof similar compatibility in anhydrous mantle. Alkali basaltsand more differentiated magmatic rocks have lower Mg-numberand lower abundances of Ni and Cr, and have undergone fractionationof mainly olivine, clinopyroxene, Fe–Ti oxide, amphiboleand plagioclase. Some nephelinites and basanites approach theSr–Nd–Pb isotope compositions inferred for the EAR(European Asthenospheric Reservoir) component. The Nd–Sr–Pbisotope composition of the differentiated rocks indicates thatassimilation of lower crustal material has modified the compositionof the primary mantle-derived magmas. Rare earth element meltingmodels can explain the petrogenesis of the most primitive maficmagmatic rocks in terms of mixing of melt fractions from anamphibole-bearing garnet peridotite source with melt fractionsfrom an amphibole-bearing spinel peridotite source, both sourcescontaining residual amphibole. It is inferred that amphibolewas precipitated in the asthenospheric mantle beneath the Hocheifel,close to the garnet peridotite–spinel peridotite boundary,by metasomatic fluids or melts from a rising mantle diapir orplume. Melt generation with amphibole present suggests relativelylow mantle potential temperatures (<1200°C); thus themantle plume is not thermally anomalous. A comparison of recentlypublished Ar/Ar ages for Hocheifel basanites with the geochemicaland isotopic composition of samples from this study collectedat the same sample sites indicates that eruption of earlierlavas with an EM signature was followed by the eruption of laterlavas derived from a source with EAR or HIMU characteristics,suggesting a contribution from the advancing plume. Thus, theHocheifel area represents an analogue for magmatism during continentalrift initiation, during which interaction of a mantle plumewith the overlying lithosphere may have led to the generationof partial melts from both the lower lithosphere and the asthenosphere. KEY WORDS: alkali basalts; continental volcanism; crustal contamination; partial melting; Eifel, Germany     

Heavy metal distribution and environmental status of Doon Valley soils, Outer Himalaya, India

 Doon Valley is surrounded by two major river systems (Ganga and Yamuna) on either side, with a water divide passing nearly across the centre of the valley, and is sandwiched between two mountain ranges in the fragile ecological systems of the Himalayan foothills. In total 398 soil samples were collected from the valley in a grid pattern (∼1 sample per 2 km²) and investigated for their heavy metal (Cr, Cu, Ni, Pb and Zn) abundances that are environmentally sensitive. Comparison of the heavy metal abundances with the contamination threshold values (CTV) revealed that most of these elemental abundances in Doon Valley soils fall well within the range of the uncontaminated to slightly contaminated category. In the case of Cr and Ni, a sizeable number of samples exceeded the CTV (250 and 100 mg kg^–1 respectively) with an overall background value of 109 and 52 mg kg^–1 respectively. Sites of high Cr and Ni mostly occur in the Ganga Catchment (GC) sector that includes even relatively undisturbed forestland. The source of this contamination is attributed to geological factors which indicate contribution from the mafic volcanics of the Lesser Himalaya. This is also consistent with the distribution pattern of Mn and Fe, though their abundance levels are not alarming. The background concentration of Pb is low (22 mg kg^–1) in Doon Valley soils; however, signs of gradual Pb contamination are palpable in and around the centre of the Dehra Dun city and along the highways. Aluminium normalized heavy metal ratios were found to exhibit narrow variability in the case of Cu, Ni and Cr and had good correlation with Al, indicating their affinity and association with the clay minerals. On the other hand, Pb and Zn seem to be associated with non-silicate sources. Received: 7 January 2000 · Accepted: 30 July 2000     

Limitations in the use of compound-specific stable isotope analysis to understand the behaviour of a complex BTEX groundwater contamination near Brussels (Belgium)

The application of compound-specific stable isotope analysis (CSIA) was evaluated to characterise a complex groundwater contamination. For this purpose, δ¹³C and δ²H analysis of benzenes and alkylated derivatives were used to interpret both the impact of different sources on a contaminant plume and the presence of degradation processes. The different contaminant sources could be distinguished based on their combined δ¹³C–δ²H signature of the benzene, toluene, ethylbenzene and xylenes (BTEX) dissolved in the groundwater. Despite this source differentiation, plume characterisation was not possible due to the complex mixing of the respective contaminant plumes. Furthermore, the original isotope signatures of the sources were not preserved across these plumes. To estimate the level of in situ biodegradation independently from concentration data, the Rayleigh equation was used. Although current literature identifies the application of CSIA as very promising in the frame of characterising organic groundwater pollution, this study has indicated that this approach can be limited with respect to successfully distinguish the different plumes and their relation to the known source zones.     

Kankan diamonds (Guinea) II: lower mantle inclusion parageneses

Frequent inclusions of ferropericlase, some coexisting with phases of MgSiO₃, CaSiO₃ and SiO₂ composition, suggest that a large proportion of diamonds from Guinea are derived from the lower mantle. Low aluminium contents in MgSiO₃ inclusions indicate derivation from the uppermost lower mantle, where Al solubility in perovskite is low. Trace element analyses (SIMS) of CaSiO₃ inclusions reveal extreme degrees of LREE (200–2000 times chondritic) and Sr enrichment (70–1000 times chondritic) together with negative and positive Eu anomalies. This implies a highly enriched lower mantle source, possibly a product of a subducted oceanic slab. A number of phases that are only stable in the upper mantle are found to coexist with lower mantle phases and thereby indicate retrograde equilibration during slow exhumation within a rising plume or convection cell. In one case, however, an inclusion paragenesis of ferropericlase and olivine can be shown to have formed within the upper mantle, indicating that the occurrence of ferropericlase inclusions alone is an unreliable indicator of lower mantle origin. Received: 26 January 2000 / Accepted: 18 May 2000     

The origin of salinity and sulphate contamination of groundwater in the Colima State, Mexico, constrained by stable isotopes

Chemical compositions and stable isotope ratios of water and sulphate were used to characterise sources and processes responsible for elevated concentrations of sulphate and other constituents in groundwater from aquifers at Colima State along Mexico’s Pacific Coast. The δ¹⁸O and δ²H values of the groundwater were similar to those of precipitation indicating a meteoric origin, and recharge processes are relatively uniform in large parts of the study area with only slight local evaporation effects. δ³⁴S_sulphate and δ¹⁸O_sulphate analyses indicated that high sulphate concentrations of up to 1,480 mg/l are mainly due to dissolution of evaporites and volcanic exhalations. Chloride is largely related to sources other than seawater. The Marabasco sub basin is affected by anthropogenic contamination through manganese and iron ore mining activities. The obtained knowledge regarding sources and areas of contamination will be essential for the development and design of a water quality monitoring program in the study area.     

Post-injection spreading and trapping of CO2 in saline aquifers: impact of the plume shape at the end of injection

We use an analytical model for the post-injection spreading of a plume of CO₂ in a saline aquifer under the action of buoyancy and capillary trapping to show that the spreading behavior is at all times strongly influenced by the shape of the plume at the end of the injection period. We solve the spreading equation numerically and confirm that, at late times, the volume of mobile CO₂ is given by existing asymptotic analytical solutions. The key parameters governing plume spreading are the mobility ratio, M, and the capillary trapping number, Γ—the former sets the shape of the plume at the end of the injection period, and the latter sets the amount of trapping. As a quantitative measure of the dependence of the spreading behavior on the initial shape, we use a volume ratio. That is, we evolve the plume from a true end-of-injection initial shape and also from an idealized “step” initial shape, and we take the ratio of these mobile plume volumes in the asymptotic regime. We find that this volume ratio is a power-law in M, where the exponent is governed exclusively by Γ. For conditions that are representative of geologic CO₂ sequestration, the ratio of mobile volumes between “true” and “step” initial plume shapes can be 50% or higher.     

The Mesozoic to Early Cenozoic Magmatism of the Benue Trough (Nigeria); Geochemical Evidence for the Involvement of the St Helena Plume

The Benue Trough is a continental rift related to the openingof the equatorial domain of the South Atlantic which was initiatedin Late Jurassic-Early Cretaceous times. Highly diversifiedand volumetrically restricted Mesozoic to Cenozoic magmaticproducts are scattered throughout the rift. Three periods ofmagmatic activity have been recognized on the basis of ⁴⁰ Ar-³⁹Ar ages: 147–106 Ma, 97–81 Ma and 68–49 Ma.Trace element and Sr, Nd and Pb isotope determinations, performedon selected basaltic samples, allow two groups of basaltic rocksto be identified: (1) a group with a tholeiitic affinity, withZr/Nb=7–11.1; La/Nb = 0.77–1; ⁸⁷Sr/⁸⁶Sr; =0.7042–0.7065¹⁴³Nd/¹⁴⁴Nd;_i = 0.5125–0.5127; ²⁰⁶Pb/²⁰⁴Pb_i = 17.59–18.48;(2) a group with an alkaline affinity, with Zr/Nb = 3.6–6.8;La/Nb=0.53–0.66; ⁸⁷Sr/⁸⁶ Sr_i=0.7029–0.7037; ¹⁴³Nd/¹⁴⁴Nd_i=0.5126–0.5129;²⁰⁶Pb/²⁰⁴Pb_i = 18.54–20.42. The geochemical data leadto the conclusion that three types of mantle sources were involvedin the genesis of the Mesozoic to Cenozoic basaltic rocks ofthe Benue, without significant crustal contamination: (1) anenriched subcontinental lithospheric mantle from which the tholeiiticbasalts were derived; (2) a HIMU-type (plume) component fromwhich the alkaline basalticrocks originated; (3) a depletedasthenospheric mantle (N-MORB-type source), which was involvedin the genesis of the alkaline basaltic magmas. According to(1) the postulated location of the St Helena hot spot in theEquatorial Atlantic at about 130 Ma and (2) the isotopic compositionof the alkaline basaltic rocks of the Benue Trough and theirgeochemical similarity with the basalts of St Helena, we concludethat the St Helena plume was involved in the genesis of thealkaline magmatism of the Benue at the time of opening of theEquatorial Atlantic. Moreover, the geochemical similarity betweenthe alkaline magmatism of the Benue Trough and that of the CameroonLine suggests that both magmatic provinces were related to theSt Helena plume. Finally, the temporal change of the mantlesources observed in the Benue Trough can be accounted for bythe recent models of plume dynamics, in the general frameworkof opening of the Equatorial Atlantic. KEY WORDS: Benue Trough; Mesozoic to Cenozoic magmatism; Equatorial Atlantic; mantle sources; St Helena plume ^*;Corresponding author.     

Distribution and environmental impact of coal-mining wastes in Upper Silesia, Poland

 About 50 million tonnes/year of waste rock from coal-mining is generated in the limited area of the thickly populated Upper Silesian Coal Basin (USCB) in Poland. There are 380 coal-mining waste dumps, including 76 active dump sites covering over 2,000 ha. About 15-16 million tonnes/year of waste rock is being reused for civil engineering purposes in the same area. This brings about a problem of ground water deterioration by constituents leached from waste rock exposed to atmospheric conditions. The major factors determining the ground water contamination potential from waste rock are chloride salinity, sulfur content and acid generation potential. The concept behind the presented studies was to provide data for correct evaluation and prediction of contaminant release from the waste rock, based on the characterization of coal-mining waste properties, as well as on long-term laboratory, lysimetric and field studies. The results show that coal-mining waste dumps can be a long-term source of ground water contamination, lasting for decades and increasing with time. Ground water down-gradient from the disused 15–30-years-old part of the studied dump displays high and increasing acidification, high TDS, SO₄, and the highest, still increasing concentrations of Mn, Fe and Zn. Cost-effective and efficient pollution control measures, similar to the presented design and construction elements of the dump site, can mitigate the negative environmental impacts. Received: 3 July 1997 · Accepted: 9 September 1998     

Spatial distribution of nitrate and related factors in the High Plains Aquifer,Texas

Utilizing geographic information systems (GIS) and statistics, objectives of this study were to evaluate: (a) the spatial distribution of nitrate concentrations in groundwater, and (b) associations between nitrate concentrations and: proximity to playa lakes, hydraulic conductivity of soil, well depth, and land use in the High Plains Aquifer, Texas. Data were compiled from wells sampled during 2000–2008. Nitrate concentrations in approximately 9% of wells exceeded the maximum contaminant level for drinking water. Concentrations were generally higher beneath urban and agricultural land, under permeable soil, and in shallow wells (especially in the southern part of the study area). However, concentrations were lower near playa lakes. While playas focus recharge to groundwater, denitrification in reducing environments lower nitrate concentrations beneath them. This study identifies areas vulnerable to nitrate contamination that warrant continued monitoring and mitigation efforts.     

Geochemical and hydrologic controls on the mobilization of arsenic derived from herbicide application

The fate and transport of As was examined at an industrial site where soil- and groundwater contamination are derived from the application of As₂O₃ as a herbicide. Application of arsenical herbicides was discontinued in the 1970s and soils in the source area were partially excavated in 2003. Arsenic contamination (up to 280 mg/kg) remains in the source area soils and a plume of As-contaminated groundwater persists in the surficial aquifer downgradient of the source area with maximum observed As concentrations of 1200 μg/L near the source area. The spatial extent of As contamination as defined by the 10 μg/L contour appears to have remained relatively stable over the period 1996–2006; the boundary of the 1000 μg/L contour has retreated over the same time period indicating a decrease in total As mass in the surficial groundwater.In column experiments conducted with source area soil, the As concentrations in the column effluent were comparable to those observed in groundwater near the source area. A substantial fraction of the As could be leached from the source area soil with ammonium sulfate and ammonium phosphate. Exhaustive extraction with background groundwater removed most of the total As. These results indicate that As in the source area soils is geochemically labile. Source area soils are low in extractable Fe, Mn and Al, and characterization by X-ray absorption spectroscopy and electron microscopy indicated that As is present primarily as arsenate sorbed to (alumino)silicate minerals. Batch sorption experiments showed much less sorption on surficial aquifer sediments than on sediments from the Jackson Bluff Formation (JBF), a presumed confining layer. This limited capacity of the surficial aquifer sediments for As sorption is consistent with the similar As contents observed for these sediments within and upgradient of the As plume. The apparent stability of the As plume cannot be explained by sequestration of As within the surficial aquifer. Sorption to JBF sediments may contribute to As sequestration, but As enrichment in JBF sediments within the plume (i.e., as compared with JBF sediments upgradient) was not observed. These results indicate that neither the persistence of As in the source area soils or the apparent stability of the plume of As-contaminated groundwater at this site can be explained by geochemical controls on As mobility. The absence of demonstrable geochemical bases for such observations suggests that possible hydrologic controls should be further investigated at this site.     

Delineation of a landfill leachate plume and flow channels in coastal sands near Christchurch, New Zealand, using a shallow electromagnetic survey method

The Burwood landfill, which serves the city of Christchurch, New Zealand, is situated on coastal sands underlain by a sequence of aquifers and aquitards. Groundwater flow is toward the coast, located approximately 700 m from the landfill boundary. Shortly after completion of the first phase of the landfill, an array of wells was installed to detect any contaminant from the landfill. Leachate was detected in the wells closest to the landfill. A shallow electromagnetic (EM31) survey was carried out between the landfill and the coast, in order to delineate any leachate plume that may be present. On the basis of the geophysical results, a contaminant plume and buried channels connected to the coast were identified. Leachate flow initially occurs in what is probably a channel or pair of channels. Downgradient, the plume spreads out to the north and south as it moves eastward toward the coast. Using the geophysical results as a guide, a new set of wells was installed to confirm the presence of high leachate concentrations. Pore-water sampling confirms the presence of a leachate plume. Received, June 1998 /Revised, March 1999, January 2000/Accepted, January 2000