The effect of distribution of iron-oxyhydroxide grain coatings on the transport of bacterial cells in porous media

 Among the demonstrated processes influencing the transport of bacteria through aquifers, the deposition of cells on mineral surfaces is one of the most important. For example, understanding the transport of introduced bacteria through aquifers is essential to designing some in situ bioremediation schemes. The impact of the presence and distribution of Fe(III)-oxyhydroxide-coated sand grains on bacterial transport through porous media was evaluated in column experiments in which bacteria (short rods; 1.2 μm length) were eluted through columns of quartz sand (0.5–0.6 mm in diameter) for several conditions of chemical heterogeneity of mineral substrate. Fe(III)-oxyhydroxide-coated sand was present as 10% of the mass, and it was arranged in three treatments: (1) homogeneously distributed, and present as a discrete layer (2) at the top and (3) at the bottom of 14-cm-long sand columns. A pulse input of 10⁸ cells ml^–1 was introduced in an artificial groundwater solution flowing at 14 cm h^–1 through the column, and eluted cells were counted. Peak breakthrough occurred at 1.0 pore volume. A large proportion of cells were retained; 14.7–15.8% of the cells were recovered after three pore volumes of solution had eluted through clean quartz sand, and only 2.1–4.0% were recovered from the Fe(III)-oxyhydroxide-coated sand mixtures. The three physical arrangements of the chemical heterogeneity resulted in essentially the same breakthrough of cells, indicating that the spatial distribution of iron coating does not affect the transport of bacteria. The results of the column transport experiments, which mimic hydrogeological conditions encountered in field problems, are consistent with our mechanistic understanding of bacterial sorption. Received: 10 April 1996 · Accepted: 17 February 1997     

Identification of non-indigenous phytoplankton species dominated bloom off Goa using inverted microscopy and pigment (HPLC) analysis

An unusual phytoplankton bloom dominated by unidentified green coloured spherical algal cells (∼5μm diameter) and dinoflagellates (Heterocapsa, Scripsiella and Gymnodinium) was encountered along the coast of Goa, India during 27 and 29 January, 2005. Pigment analysis was carried out using both fluorometric and HPLC methods. Seawater samples collected from various depths within the intense bloom area showed high concentrations of Chl a (up to 106 mg m^− 3) associated with low bacterial production (0.31 to 0.52 mg C m^− 3 h^− 1) and mesozooplankton biomass (0.03 ml m^− 3). Pigment analyses of the seawater samples were done using HPLC detected marker pigments corresponding to prasinophytes, dinoflagellates and diatoms. Chlorophyll b (36–56%) followed by peridinin (15–30%), prasinoxanthin (11–17%) and fucoxanthin (7–15%) were the major diagnostic pigments while pigments of cryptophytes and cyanobacteria including alloxanthin and zeaxanthin formed <10%. Although microscopic analysis indicated a decline in the bloom, pheaophytin concentrations in the water column measured by both techniques were very low, presumably due to fast recycling and/or settling rate. The unique composition of the bloom and its probable causes are discussed in this paper.     

The impact of paleo-channel on groundwater contamination,Andhra Pradesh,India

 Nakka vagu, a tributary of the River Manjira in the Medak district of Andhra Pradesh, has a catchment area of ∼500 km². Patancheru is an industrial development area (IDA) near the vagu. There are about 350 industries of varied nature (pulp, plastic, bulk drugs, pharmaceuticals, paints and steel rolling mills) that are engaged in the manufacture/processing of their respective products and that use water extensively. The hydrogeological setup has a bearing on the widespread contamination in the area because of discharge of industrial effluents into open land and streams. Several dug wells and boreholes situated in the study area have been monitored for water level fluctuations and quality variations. Pumping tests have been conducted to evaluate aquifer parameters. The geology, drainage, chemistry and other related anthropogenic factors play a major role in the spread of pollution in the area. Hence, it is very important to determine the degree of vulnerability to pollution based on hydrogeological factors. Amidst the granite terrain, the Nakka vagu has been identified as a paleo-channel (composed of clay–silt–sand facies); its presence in the area has immensely increased the spread of groundwater contamination. The transmissivity of the alluvial aquifer varies from 750 to 1315 m²/day. The adjoining granite has a transmissivity that varies from 30–430 m²/day. The thickness of the valley fill in the discharge region is about 10–12 m, with a lateral spread of 500–700 m, east of Nakka vagu. Received: 17 November 1999 · Accepted: 14 March 2000     

Seepage measurements from Long Lake,Indiana Dunes National Lakeshore

 Long Lake, located near Lake Michigan within the dune-complexes of Indiana Dunes National Lakeshore, USA, was formed some time during the Pleistocene and Holocene epochs. A surficial aquifer underlies Long Lake, which is either a source or sink for the later. The hydrologic processes in the lakeshore and surrounding environs have been significantly altered during the agricultural, municipal, and industrial development of the region. Limited data suggest that the organisms of Long Lake have elevated levels of several contaminants. This study attempts to quantify seepage within the lake to assess the potential threat to groundwater quality. Seepage measurements and minipiezometric tests were used to determine seepage within the lake. Seepage measurements and minipiezometric tests suggest that water seeps out of Long Lake, thus recharging the groundwater that flows southwest away from the lake. There is a great deal of variability in the seepage rate, with a mean of 11.5×10^–4±11.2×10^–4 m d^–1. The mean seepage rate of 0.3 m yr^–1 for Long Lake is greater than the 0.2 m yr^–1 recharge rate estimated for the drainage basin area. The Long Lake recharge volume of 2.5×10⁵ m³ yr^–1 is approximately 22% of the volume of the lake and is significant when compared to the total surface recharge volume of 4.8×10⁵ m³ yr^–1 to the upper aquifer of the drainage area. There is a potential for contamination of the groundwater system through seepage from the lake from contaminants derived from aerial depositions. Received: 16 August 1995 · Accepted: 18 September 1995     

Comparison of soil erosion and deposition rates using radiocesium, RUSLE, and buried soils in dolines in East Tennessee

 Three dolines (sinkholes), each representing different land uses (crop, grass, and forest) in a karst area in East Tennesse, were selected to determine soil erosional and depositional rates. Three methods were used to estimate the rates: fallout radiocesium (¹³⁷Cs) redistribution, buried surface soil horizons (Ab horizon), and the revised universal soil loss equation (RUSLE). When ¹³⁷Cs redistribution was examined, the average soil erosion rates were calculated to be 27 t ha^–1 yr^–1 at the cropland, 3 t ha^–1 yr^–1 at the grassland, and 2 t ha^–1 yr^–1 at the forest. By comparison, cropland erosion rate of 2.6 t ha^–1 yr^–1, a grassland rate of 0.6 t ha^–1 yr^–1, and a forest rate of 0.2 t ha^–1 yr^–1 were estimated by RUSLE. The ¹³⁷Cs method expressed higher rates than RUSLE because RUSLE tends to overestimate low erosion rates and does not account for deposition. The buried surface horizons method resulted in deposition rates that were 8 t ha^–1 yr^–1 (during 480 yr) at the cropland, 12 t ha^–1 yr^–1 (during 980 yr) at the grassland, and 4 t ha^–1 yr^–1 (during 101 yr) at the forest site. By examining ¹³⁷Cs redistribution, soil deposition rates were found to be 23 t ha^–1 yr^–1 at the cropland, 20 t ha^–1 yr^–1 at the grassland, and 16 t ha^–1 yr^–1 at the forest site. The variability in deposition rates was accounted for by temporal differences;¹³⁷Cs expressed deposition during the last 38 yr, whereas Ab horizons represented deposition during hundreds of years. In most cases, land use affected both erosion and deposition rates – the highest rates of soil redistribution usually representing the cropland and the lowest, the forest. When this was not true, differences in the rates were attributed to differences in the size, shape, and closure of the dolines. Received: 10 October 1995 · Accepted: 13 October 1995     

The influence of marine inflows on the chemical composition of groundwater in small islands: the example of the Cyclades (Greece)

 Marine contamination of groundwater may be caused by seawater intrusion and by salt spray. The role of both processes was studied in the Cyclades archipelago on four small islands (45–195 km²) whose aquifers consist essentially of fractured, weathered metamorphic rocks. Annual rainfall ranges from 400 to 650 mm and precipitation has high total dissolved solids contents of 45–223 mg l^–1. The chemical characteristics of the groundwater, whose salinity is from 0.4 to 22 g l^–1, are strongly influenced by seawater intrusion. However, the effect of atmospheric input is shown in certain water sampling locations on high ground elevation where the dissolved chloride contents may attain 200 mg l^–1. Received: 14 November 1995 · Accepted: 9 September 1996     

Suspended particulate matter and dynamics of the Mfolozi estuary,Kwazulu-Natal: Implications for environmental management

 The Mfolozi Estuary on the KwaZulu-Natal coast of South Africa is the most turbid estuary in Natal due to poor catchment management, leading to large quantities of suspended particulate matter (SPM) entering the estuary from the Mfolozi River. This paper quantities some of the solute and sediment dynamics in the Mfolozi Estuary where the main documented environmental concern is the periodic input of SPM from the Mfolozi Estuary to the St. Lucia system, causing reduction of light penetration and endangering biological productivity in this important nature reserve. Synoptic water level results have allowed reach mean bed shear stresses and velocities to be calculated for an observed neap tidal cycle. Results indicate that ebb velocities dominate the sediment transport processes in the estuary when fluvial input in the Mfolozi River is of the order of 15–20 m³ s^–1. Observed and predicted flood tide velocities are too low (<0.35 m s^–1) to suspend and transport significant amounts of SPM. Observed results indicate that although the SPM load entering the estuary is dominantly from the Mfolozi River, the Msunduzi River flow plays a major role in the composition of the estuary's salinity and velocity fields. It is calculated that the Mfolozi Estuary would fill with sediment in 1.3 years if it was cut off from the sea. The major fluvial flood events help maintain the estuary by periodically pushing sediment seawards (spit progrades seawards 5 m yr^–1) and scouring and maintaining the main flow channel in the estuary. During low fluvial flow conditions, tidal flow velocities will become the dominant control on sediment transport in the estuary. Interchange of SPM between the St. Lucia and Mfolozi estuaries under present conditions is complicated by the strong transverse velocity shear between the two systems at their combined mouth. This is creating a salinity-maintained axial convergence front that suppresses mixing of solutes and SPM between the systems for up to 10 h of the tidal cycle during observed conditions. Received: 22 May 1995 · Accepted: 31 July 1995     

Source of pollution as a factor controlling distribution of heavy metals in bottom sediments of Chechło River (south Poland)

 The influence of sources of effluents on pollution of bottom sediments of the small Chechło River (23 km long, mean discharge 1.5 m³ s^–1) in southern Poland was examined through analysis of heavy metals distribution in transverse and longitudinal cross sections. Underground waters from a Pb–Zn mine cause very high concentrations of Zn, Cd, and Pb in both fractions investigated (<1 mm and <0.063 mm) of sediments in the active channel zone, whereas sedimentation of huge amounts of suspended matter discharged from oil refinery cause concentrations of heavy metals in fine fractions rather uniform in cross sections. In the lowest reach, with relatively reduced contamination, the highest concentration both in fine and coarse fractions occurs close to the river banks and in the deepest points of the channel. The lowest concentrations have been found at the points of strongest reworking and accumulation of sandy material in the riverbed. Received: 25 April 1995 · Accepted: 11 September 1995     

Surface analysis of particles in mine tailings by time-of-flight laser-ionization mass spectrometry (TOF-LIMS)

  Time-of-flight laser-ionization mass spectrometry was applied to study the chemical composition of mineral particle surfaces in a sulphide-rich mine-tailings impoundment. This surface-sensitive technique provides chemical information from surfaces of irregularly shaped mineral particles (both conductive and insulators) less than 100 μm in diameter, which are considered to be representative of particle surface coatings in the tailings pile (after drying). In addition, depth profiles in the mineral particles were obtained. The combination of speed of analysis (1 min), small beam-diameter (2–4 μm), surface sensitivity (2–10 nm), trace-element sensitivity, and capability to analyze rough surfaces makes this method useful as a complement to studies of pore-water geochemistry and tailings mineralogy. As an example, the behavior of Pb and As in the Kidd Creek tailings dam near Timmins, Ontario, Canada, was studied, using a combination of surface analyses, and pore-water geochemical data. Received: 22 February 1995 / Accepted: 6 January 1996     

Hydrogeologic and hydrochemical framework of the shallow groundwater system in the southern Voltaian Sedimentary Basin, Ghana

 The southern Voltaian Sedimentary Basin underlies an area of about 5000 km² in east-central Ghana. Groundwater in the basin occurs in fractures in highly consolidated siliciclastic aquifers overlain by a thin unsaturated zone. Aquifer parameters were evaluated from available aquifer-test data on 28 shallow wells in the basin. Hydraulic-conductivity values range from 0.04–3.6 m/d and are about two orders of magnitude greater than the hydraulic conductivity calculated using Darcy's Law and the average groundwater velocity estimated from carbon-14 dating. Linear-regression analysis of the transmissivity and specific-capacity data allowed the establishment of an empirical relationship between log transmissivity and log specific capacity for the underlying aquifers. Groundwater chemistry in the basin is controlled by the weathering of albitic plagioclase feldspar. The weathering rates of various minerals were estimated using ¹⁴C-derived average velocity in the basin. The weathering rate of albite was calculated to be 2.16 μmol L^–1 yr^–1 with the resulting formation of 3.3 μmol L^–1 yr^–1 of kaolinite and 0.047 μmol L^–1 yr^–1 of calcite. The low porosity and permeability of the aquifers in the basin are attributed to the precipitation of secondary minerals on fracture surfaces and interlayer pore spaces. Received, September 1997 Revised, July 1998, August 1998 Accepted, August 1998     

Composition and processes of the mantle lithosphere in northeastern Brazil and Fernando de Noronha: evidence from mantle xenoliths

Spinel–peridotite facies mantle xenoliths in Cenozoic alkali basalts of the Pico Cabuji volcano (Rio Grande do Norte State, Northeast Brazil) and the adjacent South Atlantic oceanic island of Fernando de Noronha are studied for: (1) the information they provide on the composition of the lithospheric component in the erupted basalt geochemistry, and (2) to check the effects of the Fernando de Noronha plume track on the mantle lithosphere. Xenoliths from Pico Cabuji are protogranular lherzolites and porphyroclastic harzburgites recording average equilibrium temperatures of 825 ± 116 and 1248 ± 19 °C, respectively. Pressure in the porphyroclastic xenoliths ranges from 1.9 to 2.7 GPa (Ca-in-olivine geobarometer). Both groups show major element chemical variation trends in whole-rock and Ti and HREE (Er, Yb) variations in clinopyroxene consistent with fractional melting and basalt extraction. REE (rare earth element) profiles of clinopyroxenes vary from LREE (La, Ce) enriched (spoon shaped) to LREE depleted in the protogranular group, whereas they are slightly convex upward in most porphyroclastic clinopyroxenes. HFSE (Ti and Zr) negative anomalies are in general modest in the clinopyroxenes of both groups. Xenoliths from Fernando de Noronha have textural variations similar to those of Pico Cabuji. Protogranular and porphyroclastic samples have similar temperature (1035 ± 80 °C) and the pressure is 1–1.9 and 2.3 GPa, respectively. Whole-rock chemical variation trends overlap and extend further than those of Pico Cabuji. The trace element profiles of the clinopyroxenes of the porphyroclastic xenoliths are enriched in La up to 30 × PM and are smoothly fractionated from LREE to HREE, with deep, negative, Zr and Ti anomalies. The geochemical heterogeneities of the xenoliths from both localities are interpreted in terms of reactive porous percolation. The porphyroclastic xenoliths from Pico Cabuji represent the lower part of a mantle column (the head of a mantle diapir, at the transition conductive–adiabatic mantle), where OIB infiltration triggers melting, and the protogranular xenoliths the top of the mantle column, chromatographically enriched by percolation at a low melt/rock ratio. This interpretation may also apply for Fernando de Noronha, but the different geochemical signature recorded by the clinopyroxenes requires a different composition of the infiltrated melt. Nd and Sr isotopes of the Pico Cabuji porphyroclastic clinopyroxenes (¹⁴³Nd/¹⁴⁴Nd= 0.51339–0.51255, ⁸⁷Sr/⁸⁶Sr=0.70275–0.70319) and of Fernando de Noronha (¹⁴³Nd/¹⁴⁴Nd=0.51323–0.51285, ⁸⁷Sr/⁸⁶Sr=0.70323–0.70465) plot on distinct arrays originating from a similar, isotopically depleted composition and trending to low Nd–low Sr (EMI) and low Nd–high Sr (EMII), respectively. Correlation of the isotope variation with geochemical parameters indicates that the isotopic variation was induced by the metasomatic component, of EMI type at Pico Cabuji and of EMII type at Fernando de Noronha. These different components enriched a lithosphere isotopically similar to DMM (depleted MORB mantle) at both localities. At Fernando de Noronha, the isotopic signature of the metasomatic component is similar to that of the ∼ 8 Ma old lavas of the Remedios Formation, suggesting that this is the age of metasomatism. At Pico Cabuji, the mantle xenoliths do not record the high ⁸⁷Sr/⁸⁶Sr component present in the basalts. We speculate that the EMII component derives from a lithospheric reservoir, which was not thermally affected during mantle metasomatism at Pico Cabuji, but was mobilized by the hotspot thermal influence at Fernando de Noronha. This interpretation provides a plausible explanation for the presence of distinct metasomatic components at the two localities, which would be difficult to reconcile with their genetic relationship with the same plume. Received: 12 June 1999 / Accepted: 13 December 1999     

Contrasting P-T conditions recorded in ultramafic high-pressure rocks from the Variscan Schwarzwald (F.R.G.)

 This paper presents mineralogical and textural data as well as thermobarometric calculations on ultramafic high-pressure rocks from the Variscan basement of the Schwarzwald (F.R.G.). The rocks form small isolated bodies within low-pressure / high-temperature gneisses and migmatites. The results of this study constrain contrasting P-T evolutions for four garnet-bearing ultramafic high-pressure rocks. Two magnesian garnet-spinal peridotites sampled near the southern margin of the Central Schwarzwald Gneiss Complex (CSGC) were equilibrated at 670–740^° C and 1.4–1.8 GPa. These P-T conditions are similar to those recorded by eclogites intercalated in the same basement unit. Two garnet websterites sampled from the northern part of the CSGC have comparatively low Mg/(Mg+Fe) and low Cr and Ni abundances and are interpreted as former cumulates. These rocks most probably experienced an initial high-temperature stage within the spinel peridotite stability field, followed by re-equilibration at 740–850^° C / 3.2–4.3 GPa and subsequent recrystallization at lower pressures. Further petrologic studies have to reveal whether ultramafic high-pressure rocks of the Schwarzwald can generally be assigned to these two groups which are mainly defined by contrasting peak pressures. Received: 22 August 1994 / Accepted: 19 January 1995     

Syngenetic inclusions in diamond from the Birim field (Ghana) – a deep peridotitic profile with a history of depletion and re-enrichment

Diamonds and their syngenetic mineral inclusions from placer deposits (Akwatia mine) along the Birim River, Ghana were studied, thus providing the first detailed data collection for the West African Craton. Inclusion contents indicate an almost exclusively peridotitic diamond suite, with the vast majority being part of the harzburgitic paragenesis. Chemically the Akwatian diamond inclusions differ from those in our 1100 sample world-wide data base mainly by shifts towards lower Mg/Fe ratios for harzburgitic olivines and orthopyroxenes, extremely high Ni contents in both harzburgitic and lherzolitic olivines, and a higher mean Cr content in chromites. The inconsistency between the low Mg/Fe ratios and the highly refractory compatible trace element signature seems best to be explained by re-fertilisation of a previously depleted source, similar to the metasomatic re-enrichment of deformed, Fe-Ti-rich and hot peridotites discussed by Harte (1983). Geothermometry shows Akwatian inclusions to be 140–190 °C hotter than the peridotitic average (1050 °C) given by Harris (1992). Since garnet-opx equilibria (1100 °C/50 kbar to 1370 °C/67 kbar) indicate a typical shield geotherm (40–42 mW/m²), these elevated temperatures imply an origin of the Akwatian diamonds unusually deep for a peridotitic suite. This is consistent with the presence of extraordinary amounts of silicate spinel component in chromite inclusions, indicative of crystallisation under higher pressures than recorded for most peridotitic suites. In addition, one garnet showed the highest knorringite component (66.4 mol%) so far observed in an inclusion in diamond. The same garnet also contained a minor enstatite solid-solution component, which indicates crystallisation at pressures just below 80 kbar. Akwatian diamond inclusions, therefore, represent the most complete cross-section through peridotitic subcontinental lithospheric upper mantle so far observed, down to a maximum depth between 200–240 km. Received: 1 November 1995 / Accepted 5 January 1997     

Cation ordering of orthopyroxenes from the Skaergaard Intrusion: implications for the subsolidus cooling rates and permeabilities

 We have determined the quenched cation ordering states of five orthopyroxene crystals collected from the marginal border group and the lower zone a and b of the Skaergaard intrusion, and modeled these data to retrieve their closure temperatures (T _c) of Fe–Mg ordering and cooling rates. According to existing thermal models for the Skaergaard pluton, conductive cooling dominated the high and low temperature regimes, which were separated by an intermediate temperature regime in which the cooling was controlled primarily by convective fluid circulation. The cooling rates retrieved from the quenched cation ordering states of the orthopyroxene crystals strictly apply to temperatures around the closure temperatures of the ordering states, ∼340–400^° C, which fall at the transition from convective to the lower temperature conductive cooling. The cooling rates obtained from the cation ordering states of orthopyroxene vary from ∼1 to 270 K/ka. These results agree well with a thermal model calculated using an assumed average permeability of 10^-12 cm² for the pluton, but not completely with a model calculated on the basis of an average permeability of 10^-13 cm², although both values produced shifts of δ¹⁸O that are comparable to those observed in the pluton. Received: 27 February 1995/Accepted: 20 July 1995     

Geochemistry and petrogenesis of sodic and potassic mafic alkaline rocks in the Deccan Volcanic Province, Mumbai Area (India)

Summary Major element, trace element, Sr- and Nd-isotopes and mineral chemical data are reported for alkaline rocks (lamprophyres, tephrites, melanephelinites, nephelinites and nepheline syenites) cross-cutting the Deccan Trap lava flows south (Murud-Janjira area) and north of Mumbai (Bassein). These rocks range from sodic to potassic and have a large span in MgO (12–2 wt%). The lamprophyres have high content of incompatible elements (e.g., TiO₂ > 3.8 wt%, Nb > 130 ppm, Zr > 380 ppm, Ba > 1200 ppm), and relatively high initial (at 65 Ma) ¹⁴³Nd/¹⁴⁴Nd (0.5128) and low ⁸⁷Sr/⁸⁶Sr (0.7038–0.7042). They are likely to be small-degree melts (2–3%) of volatile- and incompatible element-enriched mantle sources, similar to other alkaline rocks in the northern Deccan, though slightly more potassium-rich. The nepheline-rich rocks have highly porphyritic textures (up to 57% phenocrysts of diopside ± olivine), and anomalously low contents of incompatible elements (e.g., TiO₂ < 1.3 wt%, Nb < 24 ppm, Zr < 100 ppm) indicating that they could not represent liquid compositions. Moreover, their very low initial ¹⁴³Nd/¹⁴⁴Nd ratios (0.5116–0.5120), at ⁸⁷Sr/⁸⁶Sr = 0.7045–0.7049, are unusual in the rocks related to the Deccan Traps and identify a new end-member in this province, that could be identified as “Lewisian-type” lower crust and/or enriched mantle. The melting episode that generated these alkaline rocks likely occurred close to the base of the ca. 100 km-thick Indian lithosphere, very shortly after the main eruption of the Deccan tholeiites. Received January 14, 2000; revised version accepted September 28, 2001     

Supercooled diopside melt: confirmation of temperature-dependent expansivity using container-based dilatometry

The expansivity of supercooled diopside liquid has been determined using techniques of container-based dilatometry. Two thermal strategies have been employed, one in which the sample is brought to volumetric equilibrium by long-duration dwells at low temperatures (817 °C) and one in which scanning dilatometry of the sample has been performed at somewhat higher temperatures (890–913 °C). The results of both experiments yield a supercooled liquid expansivity for diopside liquid in the temperature range of 817–913 °C of 84.4 ± 2.8 × 10⁻⁴ cm³/mol K. The expansivity is 65% higher than that obtained for diopside melt obtained at superliquidus temperatures using the double bob Archimedean method. Combined fitting of the new low temperature, volume–temperature data from the present study and the superliquidus data from the literature has been performed. The combined fit yields the following equations for the volume–temperature relationship of diopside liquid (T=temperature in °C):

Groundwater problems resulting from CO2 pollution and overexploitation in Alto Guadalentín aquifer (Murcia,Spain)

 The Alto Guadalentín detrital aquifer is both overexploited and polluted. Water conductivity ranges between 1200 and 4900 μS cm^–1, HCO₃ ^– between 1000 and 1990 mg l^–1, and PCO₂ between 0.041 and 1.497 bars. The temperature and chemical composition of the water show a positive thermal anomaly directly attributable to the neotectonic activity in the area. The high CO₂ content has caused the abandonment of numerous wells due to water corrosiveness which attacks pumping equipment. Received: 10 October 1995 · Accepted: 14 November 1995     

Effects of quarry mining and of other environmental impacts in the mountainous Chicam-Toctina drainage basin (Córdoba, Argentina)

 The environmental conditions prevailing in the Chicam-Toctina drainage system (approx. 138 km² in Córdoba, Argentina) are considered representative of a number of catchments in Argentina's Sierras Pampeanas Range. Two groups of ions reflect the sources of dissolved species in the catchment: a) a group (Cl^–, SO^2– ₄, and Na⁺) which recognizes natural and anthropogenic sources, and which exhibits significant correlations with N^– ₃ and NO^– ₂, and b) another group of components (Ca²⁺, Mg²⁺, and HCO^– ₃) which is clearly controlled by carbonate rocks and their waste rock products. In the headwaters, stockpiled marble quarry mining wastes provide a more open system to CO₂ gaseous exchange than the outcropping rocks, thus promoting the increase of carbonate dissolution (up to 4.88 g km^–2 s^–1 during the rainy season). This specific yield was 20% higher than the amount estimated for an area with fewer extended mining activities. The dissolved load delivered by the upper reaches is subjected in the lower drainage area to various processes, mainly controlled by the presence of the city of Alta Gracia (approx. 40,000 inhabitants). In the dry season, due to nutrient inputs supplied by the city, photosynthetic activity plays a major role controlling stream pH. Hence, the high values of calcite saturation indexes and the increase of CaCO₃ concentration in bed sediments can be explained by calcite precipitation. Such a process could be accompanied by the coprecipitation on calcium carbonate of low solubility heavy metal carbonates. Received : 17 January 1997 · Accepted : 31 March 1997     

Agronomic impact of tephra fallout from the 1995 and 1996 Ruapehu Volcano eruptions, New Zealand

 Eruptions from Ruapehu Volcano on 11 and 14 October 1995 and 17 June 1996 distributed at least 36×10⁶ m³ of sulphur(S)-rich tephra over the central and eastern North Island of New Zealand. The tephras added between 30–1500 kg ha^–1 S to at least 25 000 km² of land in primary production. Smaller but beneficial amounts of selenium (Se) and in some areas potassium and magnesium were also supplied. Addition of S to the soils in the form of sulphate and elemental S resulted in a drop in soil pH and an increase in pasture S contents within seven weeks of the eruptions. The soils affected by the tephra are naturally low in S and Se, but following the eruptions S was not required in fertilizer applications in many areas. The strongest and longest lasting effects of S and Se deposition were in high anion-retention soils particularly Hapludands (moist, moderately weathered soils, derived from volcanic ash). Soluble fluorine concentrations within the tephras were low compared to historic Icelandic and Chilean examples. However, pastoral livestock deaths were apparently caused by fluorosis in addition to starvation when tephra covered feed. The Ruapehu tephra contained very low concentrations of other soluble toxic elements. Received: 17 January 1997 · Accepted: 31 March 1997     

Hydroxyl defects in garnets from mantle xenoliths in kimberlites of the Siberian platform

A suite of more than 200 garnet single crystals, extracted from 150 xenoliths, covering the whole range of types of garnet parageneses in mantle xenoliths so far known from kimberlites of the Siberian platform and collected from nearly all the kimberlite pipes known in that tectonic unit, as well as some garnets found as inclusions in diamonds and olivine megacrysts from such kimberlites, were studied by means of electron microprobe analysis and single-crystal IR absorption spectroscopy in the v _OH vibrational range in search of the occurrence, energy and intensity of the v _OH bands of hydroxyl defects in such garnets and its potential use in an elucidation of the nature of the fluid phase in the mantle beneath the Siberian platform. The v _OH single-crystal spectra show either one or a combination of two or more of the following major v _OH bands, I 3645–3662 cm⁻¹, II 3561–3583 cm⁻¹, III 3515–3527 cm⁻¹, and minor bands, Ia 3623–3631 cm⁻¹, IIa 3593–3607 cm⁻¹. The type of combination of such bands in the spectrum of a specific garnet depends on the type of the rock series of the host xenolith, Mg, Mg-Ca, Ca, Mg-Fe, or alkremite, on the xenolith type as well as on the chemical composition of the respective garnet. Nearly all garnets contain band systems I and II. Band system III occurs in Ti-rich garnets, with wt% TiO₂ > ca. 0.4, from xenoliths of the Mg-Ca and Mg-Fe series, only. The v _OH spectra do not correspond to those of OH⁻ defects in synthetic pyropes or natural ultra-high pressure garnets from diamondiferous metamorphics. There were no indications of v _OH from inclusions of other minerals within the selected 60 × 60 μm measuring areas in the garnets. The v _OH spectra of pyrope-knorringite- and pyrope-knorringite-uvarovite-rich garnets included in diamonds do not show band systems I to III. Instead, they exhibit one weak, broad band (Δv _OH 200–460 cm⁻¹) near 3570 cm⁻¹, a result that was also obtained on pyrope-knorringite-rich garnets extracted from two olivine megacrysts. The quantitative evaluation, on the basis of relevant existing calibrational data (Bell et al. 1995), of the sum of integral intensities of all v _OH bonds of the garnets studied yielded a wide range of “water” concentrations within the set of the different garnets, between values below the detection limit of our single-crystal IR method, near 2 × 10⁻⁴ wt%, up to 163 × 10⁻⁴ wt%. The “water” contents vary in a complex manner in garnets from different xenolith types, obviously depending on a large number of constraints, inherent in the crystal chemistry as well as the formation conditions of the garnets during the crystallization of their mantle host rocks. Secondary alteration effects during uplift of the kimberlite, play, if any, only a minor role. Despite the very complex pattern of the “water” contents of the garnets, preventing an evaluation of a straightforward correlation between “water” contents of the garnets and the composition of the mantle's fluid phase during garnet formation, at least two general conclusions could be drawn: (1) the wide variation of “water” contents in garnets is not indicative of regional or local differences in the composition of the mantle's fluid phase; (2) garnets formed in the high-pressure/high-temperature diamond-pyrope facies invariably contain significantly lower amounts of “water” than garnets formed under the conditions of the graphite-pyrope facies. This latter result (2) may point to significantly lower f _H2O and f _O2 in the former as compared to the latter facies. Received: 25 November 1997 / Accepted: 9 March 1998