Hydrogeochemistry and groundwater quality in the coastal sandy clay aquifers of Alappuzha district, Kerala

Groundwater qualities of coastal aquifers in the Chennam-Pallippuram Panchayath of Alappuzha district, Kerala have been extensively monitored in summer from January to May, 2007 to assess its suitability in relation to domestic and agricultural uses. The water samples (n=36) were analyzed for various physico-chemical attributes like temperature, pH, electrical conductivity (EC), dissolved oxygen (DO), Na, K, Ca, Mg, alkalinity, hardness, silica, chloride, salinity, total dissolved solids (TDS) and sulphate (SO₄ ^2?). Values of most of these parameters fall within permissible limits. Major ionic relationships indicate that weathering reactions have insignificant role in the hydrochemical processes of the shallow groundwater system. Hydrogeochemical processes controlling the water chemistry are precipitation rather than rock-water interaction. Various determinants such as Sodium Absorption Ratio (SAR), Percent Sodium (Na %), Residual Sodium Carbonate (RSC), and Kelley’s Ratio revealed that most of the samples are suitable for irrigation.     

Identification of the influencing factors on groundwater drought and depletion in north-western Bangladesh

Groundwater drought is a specific type of hydrological drought that concerns groundwater bodies. It may have a significant adverse effect on the socio-economic, agricultural, and environmental conditions. Investigating the effect of different climatic and anthropogenic factors on groundwater drought provides essential information for sustainable planning and management of (ground) water resources. The aim of this study is to identify the influencing factors on groundwater drought in north-western Bangladesh, to understand the forcing mechanisms. A multi-step methodology is proposed to achieve this objective. The standardised precipitation index (SPI) and reconnaissance drought index (RDI) have been used to quantify the aggregated deficit between precipitation and the evaporative demand of the atmosphere, i.e. meteorological drought. The influence of land-cover patterns on the groundwater drought has been identified by calculating spatially distributed groundwater recharge as a function of land cover. Groundwater drought is defined by a threshold method. The results show that the evapotranspiration and rainfall deficits are determining meteorological drought, which shows a direct relation with groundwater recharge deficits. Land-cover change has a small effect on groundwater recharge but does not seem to be the main cause of groundwater-level decline (depletion) in the study area. The groundwater depth and groundwater-level deficit (drought) is continuously increasing with little correlation to meteorological drought or recharge anomalies. Overexploitation of groundwater for irrigation seems to be the main cause of groundwater-level decline in the study area. Efficient irrigation management is essential to reduce the growing pressure on groundwater resources and ensure sustainable water management.     

Effect of agricultural land use on the chemistry of groundwater from basaltic aquifers, Jeju Island, South Korea

Geochemical processes were identified as controlling factors of groundwater chemistry, including chemical weathering, salinization from seawater and dry sea-salt deposition, nitrate contamination, and rainfall recharge. These geochemical processes were identified using principal component analysis of major element chemistry of groundwater from basaltic aquifers in Jeju Island, South Korea, a volcanic island with intense agricultural activities. The contribution of the geochemical processes to groundwater chemistry was quantified by a simple mass-balance approach. The geochemical effects due to seawater were considered based on Cl contributions, whereas the effects due to natural chemical weathering were based on alkalinity. Nitrogenous fertilizers, and especially the associated nitrification processes, appear to significantly affect groundwater chemistry. A strong correlation was observed between Na, Mg, Ca, SO₄ and Cl, and nitrate concentrations in groundwater. Correspondingly, the total major cations, Cl, and SO₄ in groundwater were assessed to estimate relative effect of N-fertilizer use on groundwater chemistry. Cl originates more from nitrate sources than from seawater, whereas SO₄ originates mostly from rainwater. N-fertilizer use has shown the greatest effect on groundwater chemistry, particularly when nitrate concentrations exceed 6–7 mg/L NO₃–N. Nitrate contamination significantly affects groundwater quality and 18% of groundwater samples have contamination-dominated chemistry.     

The problem of sustainable groundwater management: the case of La Mancha aquifers, Spain

Gisser and Sánchez (Water Resour Res 16(4):638–642, 1980) compared two different strategies to manage aquifers: “free market” and policy regulation. They stated that the outcome of both is practically the same, and that policy regulation could not improve social welfare. This study challenges this argument by analyzing the management strategies in two large aquifers located in southern Spain, the Eastern La Mancha and the Western La Mancha aquifers. The appeal of this case stems from the fact that management of the Eastern La Mancha aquifer is almost sustainable. In stark contrast, its neighboring Western La Mancha aquifer is being grossly mismanaged. The results engage two major questions from previous groundwater literature. The first question is whether or not aquifer management requires policy intervention. The answer depends upon the consideration and magnitude of environmental damages in the model. The second question addresses the nature of groundwater policies. The contrast in management outcomes between the Western and the Eastern La Mancha aquifers is related to the different types of policy instruments implemented for each aquifer. The results of these policies underline the importance of nurturing the stakeholders’ collective action under the appropriate institutional setting.     

Precambrian fossils from the Hamersley range,Western Australia,and their use in stratigraphic correlation

The palaeontology, correlation and sedimentation of the Proterozoic sequence in the Hamersley Range, Western Australia, are discussed. Fossil calcareous algal growths, such as stromatolites and onkolites are described, as well as possible medusoid impressions. These indicate shallow water accumulation of the sediments and provide evidence of the extensive existence of plant and animal life in the Late Precambrian of Western Australia.

Distinctive stromatolites are shown to characterize various levels in the Proterozoic succession. A descending sequence of stromatolite assemblages is proposed denoted by:

• Collenia frequens—Conophyton cf. inclinatum

• Collenia australasica—C. undosa

• C. cf. kona—C. brockmani

• C. sp. aff. multiflabella.

Emphasis is placed on the possible significance of these calcareous algae for correlation and age subdivision of the Proterozoic of Western Australia and its relation to other Precambrian successions.     

Geological and geophysical exploration of the groundwater aquifers of As Suqah area, Makkah district, Western Arabian Shield, Saudi Arabia

As Suqah area is a NW–SE trending wadi present in the west central part of the Arabian Shield. It comprises Precambrian–Cambrian basement rocks, Cretaceous–Tertiary sedimentary succession, Tertiary–Quaternary basaltic lava flows, and Quaternary–Recent alluvial deposits. The magnetic anomalies indicated the presence of many recent local buried faults. These affected the distribution of the clastic sedimentary succession and seem to have controlled the deep groundwater aquifers. Groundwater movement is towards the west and northwest, following in general the surface drainage system. Hydraulic gradient varies greatly from one point to another depending on the pumping rates and cross-sectional area of the aquifer in addition to its transmissivity. The detailed results of the resistivity and seismic measurements were integrated with those obtained from test holes drilled in the study area. Groundwater occurs mainly in two water-bearing horizons, the alluvial deposits and within the clastic sedimentary rocks of Haddat Ash Sham and Ash Shumaysi formations. The shallow zone is characterized with a saturated thickness of 3–20 m and water is found under confined to semi-confined conditions. Water levels were encountered at depths varying from 3 to 16 m in the alluvial wadi deposits and from 18 to 62 m in the sedimentary succession. The combinations of vertical electrical sounding, horizontal electrical profiling, and drilling led to the identification of groundwater resources in the study area. Resistivity soundings clearly identified the nature of the lithological depth and proved useful at identifying water-bearing zones. Significantly, the majority of the groundwater was found within the deep confined aquifer gravelly sandstone, rather than in the shallow unconfined aquifer.     

Marymia: an Archean, amphibolite facies-hosted, orogenic lode-gold deposit overprinted by Palaeoproterozoic orogenesis and base metal mineralisation, Western Australia

The Marymia gold deposit, comprising two orebodies, Keillor 1 and Keillor 2, is at the northern end of the Plutonic Well greenstone belt in the Marymia Inlier, in the southern Capricorn Orogen, just north of the Yilgarn craton. The Marymia Inlier is a discrete fault-bounded Archean gneiss-granitoid-greenstone domain surrounded by sedimentary basins that were formed and variably metamorphosed and deformed during several Palaeoproterozoic orogenic cycles. The greenstone sequence at Marymia is stratigraphically and geochemically similar to greenstone sequences in the Yilgarn craton, but was subjected to further deformation and metamorphism in the Palaeoproterozoic. Late Archean deformation (D1-D2) was ductile to brittle-ductile in style, whereas Palaeoproterozoic deformation was predominantly brittle. Equilibrium mineral assemblages indicate that peak amphibolite-facies metamorphism (540-575 °C, <3 kb) was overprinted by greenschist-facies metamorphism (300-360 °C). Petrographic textures indicate that prograde metamorphism was coeval with D1-D2, with peak metamorphism early to syn D2. Gold mineralisation at Marymia is hosted in metamorphosed tholeiitic basalts and banded iron formation. On a gross scale, the distribution of gold is controlled by D2 folds and shear zones. Lithological contacts with strong rheological or chemical contrasts provide local controls. Gold-related alteration comprises subtle millimetre- to centimetre-wide zones of silicification with variable amounts of quartz, hornblende, biotite, K-feldspar, plagioclase, calcite/siderite, scheelite, titanite, epidote, sulfide and telluride minerals. Quartz veins are generally narrow and discontinuous with low total volume of quartz. Gold is sited in the wall rock, at vein salvedges or within stringers of wall rock within veins. There are two distinct opaque-mineral assemblages: pyrite-pyrrhotite-chalcopyrite-galena and hessite-petzite-altaite-Bi-telluride-galena. Ore samples are variably enriched in Ag, Te, Pb, W, Cu, S and Fe reflecting heterogeneity of the ore mineralogy. Structural timing and temperature of formation of alteration and ore minerals support deposition of gold during late peak amphibolite-facies metamorphism from neutral to alkaline (pH=5-6), moderately oxidising (log P_O2,-21-22) and CO₂-bearing (X_CO2 Ƹ.2) fluids. The total sulfur content of the fluid is estimated at 1mDS. Lead isotope compositions support derivation of lead from within the local greenstone sequence. Gold lodes were deformed by faults and shear zones in the Palaeoproterozoic, with only limited remobilisation. Subeconomic, carbonate vein- and breccia-hosted base metal mineralisation is locally hosted within Palaeoproterozoic fault zones, which clearly cut gold lodes. Base-metal-related alteration is characterised by intense carbonatisation, chloritisation, and albitisation of the mafic host rocks. Mineral assemblages are consistent with formation at greenschist facies conditions. Lead isotope compositions support crystallisation at ca. 1.7 Ga from lead that is similar in composition to earlier gold-related galena.     

Controls on the chemical composition of groundwater from alluvial aquifers in the Wanaka and Wakatipu basins, Central Otago, New Zealand

 Groundwater in alluvial aquifers of the Wakatipu and Wanaka basins, Central Otago, New Zealand, has a composition expressed in equivalent units of Ca²⁺≫Mg²⁺≅Na⁺>K⁺ for cations, and HCO₃ ^–≫SO₄ ^2->NO₃ ^–≅Cl^– for anions. Ca²⁺ and HCO₃ ^– occur on a 1 : 1 equivalent basis and account for >80% of the ions in solution. However, some groundwater has increased proportions of Na⁺ and SO₄ ^2-, reflecting a different source for this water. The rock material of the alluvial aquifers of both basins is derived from the erosion and weathering of metamorphic Otago Schist (grey and green schists). Calcite is an accessory mineral in both the grey and green schists at <5% of the rock. Geological mapping of both basins indicates that dissolution of calcite from the schist is the only likely mechanism for producing groundwater with such a constant composition dominated by Ca²⁺ and HCO₃ ^– on a 1 : 1 equivalent basis. Groundwater with higher proportions of Na⁺ and SO₄ ^2- occurs near areas where the schist crops out at the surface, and this groundwater represents deeper and possibly older water derived from basement fluids. Anomalously high K⁺ in the Wakatipu basin and high NO₃ ^– concentrations in the Wanaka basin cannot be accounted for by interaction with basement lithologies, and these concentrations probably represent the influence of anthropogenic sources on groundwater composition. Received, June 1996 Revised, March 1997, July 1997 Accepted, July 1997     

Suitability assessment of deep groundwater for drinking and irrigation use in the Djeffara aquifers (Northern Gabes,south-eastern Tunisia)

The multilayered Djeffara aquifer system, south-eastern Tunisia, has been intensively used as a primary source to meet the growing needs of the various sectors (drinking, agricultural and industrial purposes). The analysis of groundwater chemical characteristics provides much important information useful in water resources management. Detailed knowledge of the geochemical evolution of groundwater and assessing the water quality status for special use are the main objective of any water monitoring study. An attempt has been made for the first time in this region to characterize aquifer behavior and appreciate the quality and/or the suitability of groundwater for drinking and irrigation purposes. In order to attend this objective, a total of 54 groundwater samples were collected and analyzed during January 2008 for the major cations (sodium, calcium, magnesium and potassium), anions (chloride, sulfate, bicarbonate), trace elements (boron, strontium and fluoride), and physicochemical parameters (temperature, pH, total dissolved salts and electrical conductivity). The evolution of chemical composition of groundwater from recharge areas to discharge areas is characterized by increasing sodium, chloride and sulfate contents as a result of leaching of evaporite rock. In this study, three distinct chemical trends in groundwater were identified. The major reactions responsible for the chemical evolution of groundwater in the investigated area fall into three categories: (1) calcite precipitation, (2) gypsum and halite dissolution, and (3) ion exchange. Based on the physicochemical analyses, irrigation quality parameters such as sodium absorption ratio (SAR), percentage of sodium, residual sodium carbonate, residual sodium bicarbonate, and permeability index (PI) were calculated. In addition, groundwater quality maps were elabortaed using the geographic information system to delineate spatial variation in physico-chemical characteristics of the groundwater samples. The integration of various dataset indicates that the groundwater of the Djeffara aquifers of the northern Gabes is generally very hard, brackish and high to very high saline and alkaline in nature. The water suitability for drinking and irrigation purposes was evaluated by comparing the values of different water quality parameters with World Health Organization (WHO) guideline values for drinking water. Piper trilinear diagram was constructed to identify groundwater groups where the relative major anionic and cationic concentrations are expressed in percentage of the milliequivalent per liter (meq/l), and it was demonstrated that the majority of the samples belongs to SO₄–Cl–Ca–Na, Cl–SO₄–Na–Ca and Na–Cl hydrochemical facies. As a whole, all the analyzed waters from this groundwater have revealed that this water is unsuitable for drinking purposes when comparing to the drinking water standards. Salinity, high electric conductivity, sodium adsorption ratio and sodium percentages indicate that most of the groundwater samples are inappropriate for irrigation. The SAR vary from medium (S2) to very high (S4) sodicity. Therefore, the water of the Djeffara aquifers of the northern Gabes is dominantly of the C4–S2 class representing 61.23 % of the total wells followed by C4–S3 and C4–S4 classes at 27.27 and 11.5 % of the wells, respectively. Based on the US Salinity Classification, most of the groundwater is unsuitable for irrigation due to its high salt content, unless certain measures for salinity control are undertaken.     

Impacts of land use change and groundwater management on long-term nitrate-nitrogen and chloride trends in groundwater of Jeju Island,Korea

Impacts of land use changes and groundwater management actions on groundwater quality were evaluated at the island scale with spatiotemporal trends of NO₃-N and Cl concentrations in groundwater of Jeju Island, Korea. The temporal trends from 1993 to 2012 in the concentrations of NO₃-N and Cl from more than 3900 wells were estimated using the Mann–Kendall trend test and Sen’s slope analysis and compared with the land use change trend for the period 1995–2009. The results indicate that the upward trends in NO₃-N were associated with the expansion of agricultural lands, whereas Cl trends were considered to be affected by other factors in addition to the land use changes. In the mid-mountainous region, the deterioration in the groundwater quality by the both NO₃-N and Cl was expected due to the continuous expansion of agricultural lands. In the lowland area, the NO₃-N and Cl components showed different trends depending on the regions. In the eastern area, increasing trends in NO₃-N were observed due to the development of new agricultural areas, while the Cl concentration was observed to decrease as a result of the regulation on groundwater extraction to reduce seawater intrusion. Our study highlights that a comprehensive interpretation of trends in NO₃-N and Cl and land use changes for long-term periods can provide useful insights to prepare for suitable groundwater management plans in the whole island perspective.     

Salinity mapping of coastal groundwater aquifers using hydrogeochemical and geophysical methods: a case study from north Kelantan,Malaysia

Integrated hydrogeochemical and geophysical methods were used to study the salinity of groundwater aquifers along the coastal area of north Kelantan. For the hydrogeochemical investigation, analysis of major ion contents of the groundwater was conducted, and other chemical parameters such as pH and total dissolved solids were also determined. For the geophysical study, both geoelectrical resistivity soundings and reflection seismic surveys were conducted to determine the characteristics of the subsurface and groundwater contained within the aquifers. The pH values range from 6.2 to 6.8, indicating that the groundwater in the study area is slightly acidic. Low content of chloride suggests that the groundwater in the first aquifer is fresh, with an average concentration of about 15.8 mg/l and high geoelectrical resistivity (>45 ohm m). On the other hand, the groundwater in the second aquifer is brackish, with chloride concentration ranging from 500 mg/l to 3,600 mg/l and very low geoelectrical resistivity (<45 ohm m) as well as high concentration of total dissolved solids (>1,000 mg/l). The groundwater in the third aquifer is fresh, with chloride concentrations generally ranging from 2 mg/l to 210 mg/l and geoelectrical resistivity of greater than 45 ohm m. Fresh and saltwater interface in the first aquifer is generally located directly in the area of the coast, but, for the second aquifer, both hydrogeochemical and geoelectrical resistivity results indicate that the fresh water and saltwater interface is located as far as 6 km from the beach. The considerable chloride ion content initially suggests that the salinity of the groundwater in the second aquifer is probably caused by the intrusion of seawater. However, continuous monitoring of the chloride content of the second aquifer indicated no significant changes with time, from which it can be inferred that the salinity of the groundwater is not affected by seasonal seawater intrusion. Schoeller diagrams illustrate that sulphate concentrations of the groundwater of the second aquifer are relatively low compared to those of the recent seawater. Therefore, this result suggests that the brackish water in the second aquifer is probably from ancient seawater that was trapped within the sediments for a long period of time, rather than due to direct seawater intrusion.     

Effects of poor quality irrigation waters on the nutrient leaching and groundwater quality from sandy soil

Sodium (Na⁺) in poor quality irrigation water participate in ion-exchange processes results in the displacement of base cations into solution and a raised concentration in groundwater. Knowledge of the rate of decrease of nutrients from soils resulting from poor water quality application is essential for long-term planning of crop production while minimizing the impact on groundwater quality. In this study, we examined the effect of sodium adsorption ratio (SAR) of irrigation water on nutrients leaching and groundwater quality in columns of sandy soil. Three types of irrigation waters at three NaCl–CaCl₂ solutions with the following levels of SAR (5, 15, and 30) were synthesized in laboratory. With the application of solutions, exchange occurred between solution Na⁺ and exchangeable cations (Ca²⁺, Mg²⁺, and K⁺), resulting in the displacement of these cations and anions into solution. Increasing the level of SAR from 5 to 15 and 30 resulted in increase in the average exchangeable sodium percentage (ESP) of the soil from 10.4 to 20.3, and 32.5, respectively. Adverse effect of high Na⁺ concentration in the solutions on raising ESP was less pronounced in solution having low SAR. Leaching of Ca²⁺, Mg²⁺, K⁺, and P from soil with the application of solutions represents a significant loss of valuable nutrients. This sandy soil showed the high risk for nutrients transfer into groundwater in concentrations exceeding the groundwater quality standard. Irrigation with poor quality water, which is generally more sodic and saline than regional groundwater, increases the rate of sodification and salinization of shallow groundwater.     

Lead isotopes and ages of Galenas from the Pilbara region,Western Australia

One of six galena samples from the Pilbara of Western Australia, located in a ‘greenstone’ sequence, appears from its lead‐isotope ratios to be of great age. ‘Linear Model III’ ages of Cumming & Richards (1975) agree with available geological evidence for this, and for one other younger sample located in the Shaw Batholith. Two of the other samples, also from Archaean granitic host rock, appear to be significantly younger than the host; the other two, from within the Lower Proterozoic Fortescue Group, suggest that its age is not yet well known. Previously‐published age information has been adapted to the newly‐accepted values for the decay constants throughout this discussion.     

The distribution of saline groundwater and its relation to the hydraulic conditions of aquifers and aquitards: examples from Israel

The effect of separation by aquitard layers on the distribution of saline groundwater in coastal aquifers has been demonstrated in two Israeli coastal aquifers: the Mediterranean and the Dead Sea aquifers. There is vertical separation in the Dead Sea area, even where the clayey aquitard layers are <1?m thick, exhibited by large differences in hydraulic head (2?C5?m), salinity (TDS of 50?C340?g/L) and chemical composition (e.g. Na/Cl range 0.28?C0.55). Similar features are found in the Mediterranean coastal aquifer, where the separating aquitard layers are thicker (??5?C10?m). Here, the different subaquifers host fresh and saline groundwater of different ages (tritium and ¹⁴C ages range from tens to thousands of years), as well as different chemical compositions. This high resolution of results can be obtained only by drilling without fluids; otherwise, the spatial information may lead to incorrect representation of the studied aquifer. This is especially important in saline systems where only partial flushing occurs and, thus, large variations in salinity and chemical composition are expected. The main factors controlling the salinity of groundwater in subaquifers in coastal aquifers are their connection to the sea or saline lakes, existence of brines, salinization and flushing rates, and separation by aquitard layers.     

Strontium isotopic studies of alkalic rocks: Localities from Australia,Spain, and the Western United States

Initial Sr⁸⁷/Sr⁸⁶ ratios and rubidium and strontium contents have been measured in 83 specimens from 8 suites of alkalic and ultrabasic rocks. The range of initial Sr⁸⁷/Sr⁸⁶ ratio observed and the number of specimens (in parentheses) analysed for each suite are: West Kimberley, Australia (8), 0.7125–0.7215; Jumilla, Spain (6), 0.7136–0.7158; Bearpaw Mountains, Montana (9), 0.7062–0.7086; Highwood Mountains, Montana (10), 0.7072–0.7087; Hopi Buttes, Arizona (8), 0.7038–0.7094; Leucite Hills, Wyoming (17), 0.7055–0.7070; Montana diatremes (13), 0.7034–0.7073; Navajo Province, Arizona and New Mexico (12), 0.7052–0.7099.The initial Sr⁸⁷/Sr⁸⁶ ratios of the West Kimberley and Jumilla rocks are the highest yet found in strontium-rich basic rocks. Some of the individual specimens from West Kimberley have initial ratios as high as some estimates of the present Sr⁸⁷/Sr⁸⁶ ratio of average crustal material. This is interpreted to mean that the West Kimberley and Jumilla rocks contain substantial amounts of radiogenic strontium, and possibly other elements, from a crustal source.     

Mineralogy and geochemistry of atypical reduction spheroids from the Tumblagooda Sandstone,Western Australia

Reduction spheroids are small-scale, biogenic, redox-controlled, metal enrichments that occur within red beds globally. This study provides the first analysis of the compositionally unique reduction spheroids of the Tumblagooda Sandstone. The work aims to account for their composition and consequently improve existing models for reduction spheroids generally, which presently fail to account for the mineralogy of the Tumblagooda Sandstone reduction spheroids. Interstitial areas between detrital grains contained in the cores of these reduction spheroids are dominated by microplaty haematite, in addition to minor amounts of svanbergite, gorceixite, anatase, uraninite, monazite and illite. The haematite-rich composition, along with an absence of base metal phases and the vanadiferous mica roscoelite, makes these reduction spheroids notable in comparison to other global reduction spheroid occurrences. Analyses of illite crystallinity provide values for samples of the Tumblagooda Sandstone host rock corresponding to heating temperatures of ca 200°C. Consequently, while Tumblagooda Sandstone reduction spheroids formed via the typical metabolic processes of dissimilatory metal-reducing bacteria, the combination of a unique mineralogy and illite crystallinity analysis provides evidence of more complex late-stage heating and reoxidation. This has not previously been recognised in other reduction spheroids and therefore expands the existing model for reduction spheroid genesis by also considering the potential for late-stage alteration. As such, future reduction spheroid studies should consider the potential impact of post-formation modification, particularly where they are to be used as evidence of ancient microbial processes; such as in the search for early evidence of life in the geological record on Earth or other planets. Additionally, because of their potential for modification, reduction spheroids serve as a record of the redox history of red beds and their study could provide insights into the evolution of redox conditions within a given red bed during its diagenesis. Finally, this paper also provides insights into the relatively understudied diagenetic history of the Tumblagooda Sandstone; supplying the first reliable and narrow constraints on its thermal history. This has important implications for the thermal history of the Carnarvon Basin and its petroleum prospectivity more broadly.     

Origin of yellow sand from Tamala Limestone on the Swan Coastal Plain,Western Australia

There has been considerable debate concerning the origin of the Spearwood Dunes on the Swan Coastal Plain in Western Australia. In general, it is believed that the Spearwood Dunes are a complex of calcareous coastal dunes deposited during the Quaternary and now consist of an aeolianite core (the Tamala Limestone) plus tracts of surficial residual sand from dissolution thereof. However, in the mid‐seventies a counter view was presented suggesting that the sand was not residual but was transported by aeolian processes from inland sources. At 11 sites on the Swan Coastal Plain a combination of grainsize analysis and heavy‐mineral analysis was used to demonstrate that the sand of the Spearwood Dunes has evolved as a result of in situ weathering of the underlying Tamala Limestone. This supports previous work on the Swan Coastal Plain and other sandplains in Western Australia, suggesting that there has been very little long‐range aeolian transport of sands during the Late Pleistocene.     

Using soil and Quaternary geological information to assess the intrinsic groundwater vulnerability of shallow aquifers: an example from Lithuania

Lithuania, in the Baltic region of northern Europe, is heavily dependent on groundwater resources for its public water supply, with a large proportion, especially in rural areas, derived from shallow Quaternary aquifers. A national groundwater-vulnerability methodology, based upon the UK approach, has been developed on behalf of the Lithuanian Ministry of Environmental Protection as a possible basis for the future protection of shallow groundwater resources for the rural inhabitants. Some modifications to the UK methodology were required to enable archive data to be used. The four aquifer classes depicted on the final groundwater vulnerability map are based upon the assessed relative permeabilities of the uppermost Quaternary deposits. The derivation of the classification of soil-leaching potential required a reassessment of Soviet-based soil wetness and particle-size classes and a calculation of subsoil-saturated hydraulic conductivity. A preliminary validation of the final maps against available shallow groundwater samples suggests that the methodology satisfactorily predicts the intrinsic groundwater vulnerability. The final methodology, based upon its low-cost approach using archive data, is relevant to the current needs of Lithuania and can be applied in other regions of similar geology and climate. Electronic Publication     

Oxygen isotope fractionation and disequilibrium displayed by some granulite facies rocks from the Fraser Range,Western Australia

The granulites of the Fraser Range are assumed to have formed in a carbon-rich fluid, and are generally devoid of hornblende, and lack obvious hydrous retrograde features. In these granulites, pyroxene, garnet, plagioclase and quartz are the minerals most likely to retain the oxygen isotope ratios fixed at an early stage of initial granulite metamorphism. Temperature estimates using these minerals commonly suggest that oxygen isotopic exchange ceased in the range 600 to 680°C. The peak metamorphic temperature was probably ～ 850°C as based on the stability fields of the coexisting minerals and some cation temperatures from coexisting pyroxenes in these rocks. Ilmenite may be slightly out of isotopic equilibrium with the other minerals. Thus, grains of quartz, feldspar, pyroxene and ilmenite have suffered considerable oxygen isotopic exchange during the retrogressive phase of the metamorphism, in spite of the fact that very little water was present in these granulites. The observed deviation from the peak metamorphic temperatures can be explained by essentially closed system solid-state diffusion (on at least a scale of centimetres) during slow cooling of the rocks from ~850 to 650°C, followed by more rapid cooling down to ～ 300°C. Such an explanation is not at variance with the radiometric data available for rocks from the area, which suggest that the latter phase could have involved uplift rates of ?0.5 mm/yr for a period of about 40 Ma. Wholerock δ¹⁸O values on non-quartzose mafic granulites, about 7.2%., fall within the range of basalts affected by seafloor weathering.