<Superscript>238</Superscript>U and <Superscript>235</Superscript>U isotope fractionation upon oxidation of uranium-bearing rocks by fracture waters

The variations in ²³⁸U/²³⁵U values accompanying mobilization of U by fracture waters from uranium-bearing rocks, in which U occurs as a fine impregnation of oxides and silicates, were studied by the high-precision (±0.07‰) MC–ICP–MS method. Transition of U into the aqueous phase in the oxidized state U(VI) is accompanied by its isotope fractionation with enrichment of dissolved U(VI) in the heavy isotope ²³⁸U up to 0.32‰ in relation to the composition of the solid phases. According to the sign, this effect is consistent with the tendency of the behavior of ²³⁸U and ²³⁵U upon interaction of river waters with rocks of the catchment areas [11] and with the effect observed during oxidation of uraninite by the oxygen-bearing NaHCO₃ solution [12].     

Hydrochemical and isotopic characterisation of groundwaters to define aquifer type and connectivity in a subtropical coastal setting,Fraser Coast,Queensland

Physico-chemical parameters, major ion chemistry and isotope composition of surface and groundwaters were determined in forested coastal catchments and adjacent coastal plains. Results showed obvious characterisation related to physical and hydrological setting, and highly variable spatial differences reflecting the complexities of these areas. All these coastal waters are dominated by Na–Cl and fall on a common dilution line; hydrochemical grouping is largely due to anionic differences (Cl, SO₄ and HCO₃), although Na and Mg ratios also vary. Six major hydrochemical facies were determined. For groundwaters, compositional differences are largely related to aquifer material and level of confinement; for coastal groundwaters important are tidal effects and proximity to the shoreline. Differentiation for surface waters is mainly by drainage morphology, flow regime plus proximity to the coast. Connectivity between water bodies is reflected by minor base flow to catchment streams, including with flood plain wetlands, but mostly occurs in low-lying zones where there is mixing of fresh and saline water within surface water and subterranean estuaries, or by seawater intrusion enhanced by overuse. Oxygen and hydrogen isotopic data for confined and semi-confined groundwaters along the coast indicates local recharge; fresh surface waters in the elevated catchments are shown to be sourced further inland plus have experienced evaporation.     

Hydrochemical evolution and water quality along the groundwater flow path in the Sandıklı plain, Afyon, Turkey

 An unconfined aquifer system suggests an open system in the study area. Hydrochemical evolution is related to the flow path of groundwater. The groundwaters are divided into two hydrochemical facies in the study area, 1) Ca–Mg–HCO₃ and 2) Ca–Mg–SO₄HCO₃. Facies 1 has shallow (young) waters which dominate in recharge areas during rapid flow conditions, whereas facies 2 may show shallow and mixed waters which dominate intermediate or discharge areas during low flow conditions. Ionic concentrations, TDS, EC and water quality are related to groundwater residence time and groundwater types. The groundwaters in the plain are chemically potable and suitable for both domestic and agricultural purposes. Received: 20 May 1996 · Accepted: 30 July 1996     

Correlation of δ<Superscript>18</Superscript>O and initial<Superscript>87</Superscript>Sr/<Superscript>86</Superscript>Sr ratios in Kirkpatrick basalt on Mt. Falla,transantarctic mountains

Theδ¹⁸O (SMOW) values of the Kirkpatrick Basalt (Jurassic) on Mt. Falla, Queen Alexandra Range, vary between +6.3‰ and +8.6‰ The apparent enrichment of these rocks in¹⁸O excludes the possibility that they were altered by interaction with aqueous solutions of meteoric origin. Theδ¹⁸O values of the flows correlate significantly with the initial⁸⁷Sr/⁸⁶Sr ratios and all major elements. These correlations confirm the hypothesis that the basalt magma was contaminated by rocks of the continental crust through which it was extruded. Estimates of the chemical composition of the basalt magma and the contaminant, based on extrapolations of the new oxygen data, generally confirm earlier estimates based on extrapolations of initial⁸⁷Sr/⁸⁶Sr ratios. The⁸⁷Sr/⁸⁶Sr ratio of the uncontaminated basalt was 0.7093 which indicates that magma may have originated by melting either in old Rb-enriched lithospheric mantle under Antarctica or in the overlying crust, or both.     

Relationship between electrical conductivity, <Superscript>18</Superscript>O of water and NO<Subscript>3</Subscript> content in different streamflow stages

The Ballenera Creek has 160 km² being a small catchment in the Pampa Plain in Argentina. This area has been deeply modified by human action through agricultural activities. From 2013 to 2017, electrical conductivity, stable isotopes of water and nitrate concentration monitoring program were conducted. The sampling included weekly and bimonthly samples in two sites along the stream, several groundwater wells and monthly precipitation. Chemical and isotopic tracers are used to discriminate the streamflow components and to evaluate their incidence in the nitrate concentration. The easiest conceptual model for gaining streams contemplates two main elements: direct runoff and groundwater (baseflow and pre-event water). The direct runoff has the lowest electrical conductivity and ¹⁸O_w variable content. The baseflow component is characterized by the highest electrical conductivity and isotope composition quite constant. Finally, pre-event water has an intermediate electrical conductivity and isotopic content close to the rainfall-weighted average composition. The nitrate concentration obtained was in general related to the different stream stages and was a useful indicator to evaluate the fertilization in agricultural zones.     

Compositional controls on <Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar ages of zoned mica from a rare-element pegmatite

A high spatial resolution Ar–Ar dating study of compositionally zoned micas using UV laser extraction has been used to investigate the effect of composition and compositional boundaries upon argon diffusion in mica. The crystals are characterised by muscovite cores and Li–F–Rb–Cs-rich lepidolite rims produced by the interaction of a residual melt-vapour phase with the original muscovite during the late stages of pegmatite crystallisation. Single crystals exhibit dramatic intra-grain age variations, with a maximum range of 2,880–2,117 Ma. Backscattered electron images combined with UV-laser analyses reveal that apparent ages younger than 2,600 Ma are directly associated with the compositionally distinct rims, suggesting that Ar diffusion was faster in the lepidolite than in muscovite. Although it is not possible to be fully quantitative using the present data, it seems that argon diffusion rates in lepidolite are similar to those in biotite. Major rearrangements of the crystal structure needed to accommodate high concentrations of lithium, fluorine and large interlayer cations (Rb⁺, Cs⁺) in muscovite account for lower argon retentivity of the crystal rims. In most cases the age profiles show no disturbance at the compositional boundary, despite the transition from a di-octahedral to tri-octahedral mica, indicating that in general the boundaries do not act as fast diffusion pathways. However, in some cases there is a clear drop in ages at the compositional boundary, which acts as an effective sub-grain boundary. The difference between the two types may be related to the internal structure of the compositional boundaries or their degree of contact with the grain boundary network of the rock.     

Extreme <Superscript>15</Superscript>N Depletion in Seagrasses

Seagrass beds form an important part of the coastal ecosystem in many parts of the world but are very sensitive to anthropogenic nutrient increases. In the last decades, stable isotopes have been used as tracers of anthropogenic nutrient sources and to distinguish these impacts from natural environmental change, as well as in the identification of food sources in isotopic food web reconstruction. Thus, it is important to establish the extent of natural variations on the stable isotope composition of seagrass, validating their ability to act as both tracers of nutrients and food sources. Around the world, depending on the seagrass species and ecosystem, values of seagrass N normally vary from 0 to 8?‰ δ¹⁵N. In this study, highly unusual seagrass N isotope values were observed on the east coast of Qatar, with significant spatial variation over a scale of a few metres, and with δ¹⁵N values ranging from +2.95 to ?12.39?‰ within a single bay during March 2012. This pattern of variation was consistent over a period of a year although there was a seasonal effect on the seagrass δ¹⁵N values. Seagrass, water column and sediment nutrient profiles were not correlated with seagrass δ¹⁵N values and neither were longer-term indicators of nutrient limitation such as seagrass biomass and height. Sediment δ¹⁵N values were correlated with Halodule uninervis δ¹⁵N values and this, together with the small spatial scale of variation, suggest that localised sediment processes may be responsible for the extreme isotopic values. Consistent differences in sediment to plant ¹⁵N discrimination between seagrass species also suggest that species-specific nutrient uptake mechanisms contribute to the observed δ¹⁵N values. This study reports some of the most extreme, negative δ¹⁵N values ever noted for seagrass (as low as ?12.4?‰) and some of the most highly spatially variable (values varied over 15.4?‰ in a relatively small area of only 655 ha). These results are widely relevant, as they demonstrate the need for adequate spatial and temporal sampling when working with N stable isotopes to identify food sources in food web studies or as tracers of anthropogenic nutrients.     

Hydrochemical characteristics of Lastochka Spa (Primorye, Far East of Russia)

This study presents new data on major, trace and REE element concentration of groundwaters in Lastochka spa located in the northern part of Primorye, Far East of Russia. The studied area is characterized by two types of groundwaters issued from a spring and wells: fresh waters with low mineralization (Total Dissolved Solids is up to 400 mg/l) and high pCO₂ waters with high mineralization (TDS is up to 4700 mg/l). New data and previous δ¹³C_(TIC), oxygen (δ¹⁸O) and hydrogen (δ²H) isotope data indicate that these waters result from meteoric water infiltration in the Sikhote–Alin mountain, circulating at shallow depths in sedimentary rocks. CO₂ in groundwater is of mantle origin.     

The barents sea magmatic province: Geological-geophysical evidence and new <Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar dates

Resulting from study of the geological structure of the Franz Josef Land and Svalbard archipelagoes, this work presents new 17 ⁴⁰Ar/³⁹Ar age datings for basalts taken during coastal expeditions in 2006–2010. Radiological age determination for intrusive units (sills) located in the western part of Nordensciold Land (Spitzbergen Island) has been made for the first time. In relation to use of the interpretation results of marine geological-geophysical data, the distribution peculiarities and time ranges for Jurassic-Cretaceous basic magmatism within the studied regions of the Barents Sea continental margin and within the Arctic as a whole are discussed.     

Br/Cl ratios and O, H, C, and B isotopic constraints on the origin of saline waters from eastern Canada

Saline groundwaters were recovered from undisturbed (Restigouche deposit) and active (Brunswick #12 mine) Zn-Pb volcanogenic massive sulfide deposits in the Bathurst Mining Camp (BMC), northern New Brunswick, Canada. These groundwaters, along with fresh to brackish meteoric ground and surface waters from the BMC, have been analyzed to determine their major, trace element and stable isotopic (O, H, C, and B) compositions. Saline groundwaters (total dissolved solids = 22-45 g/L) are characterized by relatively high Na/Ca ratios compared to brines from the Canadian Shield and low Na/Cl_molar and δ¹¹B isotopic compositions (−2.5‰ to 11.1‰) compared to seawater. Although saline waters from the Canadian Shield commonly have oxygen and hydrogen isotopic compositions that plot to the left of the global meteoric water line, those from the BMC fall close to the water line. Fracture and vein carbonate minerals at the Restigouche deposit have restricted carbon isotopic compositions of around −5‰ to −6‰. The carbon isotopic compositions of the saline waters at the Restigouche deposit (+12‰ δ¹³C_DIC) are the result of fractionation of dissolved inorganic carbon by methanogenesis. We suggest that, unlike previous models for shield brines, the composition of saline waters in the BMC is best explained by prolonged water-rock reaction, with no requirement of precursor seawater. We suggest that elevated Br/Cl ratios of saline waters compared to seawater may be explained by differential uptake of Br and Cl during groundwater evolution through water-rock reaction.     

Detecting inter-aquifer leakage in areas with limited data using hydraulics and multiple environmental tracers,including <Superscript>4</Superscript>He, <Superscript>36</Superscript>Cl/Cl, <Superscript>14</Superscript>C and <Superscript>87</Superscript>Sr/<Superscript>86</Superscript>Sr

The investigation of regionally extensive groundwater systems in remote areas is hindered by a shortage of data due to a sparse observation network, which limits our understanding of the hydrogeological processes in arid regions. The study used a multidisciplinary approach to determine hydraulic connectivity between the Great Artesian Basin (GAB) and the underlying Arckaringa Basin in the desert region of Central Australia. In order to manage the impacts of groundwater abstraction from the Arckaringa Basin, it is vital to understand its connectivity with the GAB (upper aquifer), as the latter supports local pastoral stations and groundwater-dependent springs with unique endemic flora and fauna. The study is based on the collation of available geological information, a detailed analysis of hydraulic data, and data on environmental tracers. Enhanced inter-aquifer leakage in the centre of the study area was identified, as well as recharge to the GAB from ephemeral rivers and waterholes. Throughout the rest of the study area, inter-aquifer leakage is likely controlled by diffuse inter-aquifer leakage, but the coarse spatial resolution means that the presence of additional enhanced inter-aquifer leakage sites cannot be excluded. This study makes the case that a multi-tracer approach along with groundwater hydraulics and geology provides a tool-set to investigate enhanced inter-aquifer leakage even in a groundwater basin with a paucity of data. A particular problem encountered in this study was the ambiguous interpretation of different age tracers, which is attributed to diffusive transport across flow paths caused by low recharge rates.     

Atacamite formation by deep saline waters in copper deposits from the Atacama Desert,Chile: evidence from fluid inclusions,groundwater geochemistry,TEM, and <Superscript>36</Superscript>Cl data

The presence of large amounts of atacamite in oxide zones from ore deposits in the Atacama Desert of northern Chile requires saline solutions for its formation and hyperarid climate conditions for its preservation. We investigated the nature and origin of atacamite-forming solutions by means of coupling groundwater geochemical analyses with fluid inclusion data, high-resolution mineralogical observations, and chlorine-36 (³⁶Cl) data in atacamite from the Mantos Blancos and Spence Cu deposits. In both deposits, the salinities of fluid inclusions in atacamite are comparable to those measured in saline groundwaters sampled from drill holes. The average salinity of fluid inclusions in atacamite for the Mantos Blancos and Spence deposits (~7–9 and 2–3 wt.% NaCl_eq, respectively) are strongly correlated to the salinities at which gypsum supersaturates from groundwaters in both deposits (total dissolved solids ~5–9 and 1–3 wt.% NaCl_eq, respectively). This correlation is confirmed by transmission electron microscopy observations of atacamite-bearing samples, revealing an intimate association between atacamite and gypsum that can be traced down to the nanometer scale. ³⁶Cl data in atacamite provide new lines of evidence concerning the origin and age of the saline waters that formed atacamite in various stratabound and porphyry Cu deposits from the Atacama Desert. All atacamite samples show very low ³⁶Cl-to-Cl ratios (11 × 10⁻¹⁵ to 28 × 10⁻¹⁵ at at⁻¹), comparable to previously reported ³⁶Cl-to-Cl ratios of deep formation waters and old groundwaters. In addition, ³⁶Cl-to-Cl ratios in atacamite correlate with U and Th concentration in the host rocks but are independent from distance to the ocean. This trend supports an interpretation of the low ³⁶Cl-to-Cl ratios in atacamite as representing subsurface production of fissiogenic ³⁶Cl in secular equilibrium with the solutions involved in atacamite formation. Therefore, ³⁶Cl in atacamite strongly suggest that the chlorine in saline waters related to atacamite formation is old (>1.5 Ma) but that atacamite formation occurred more recently (<1.5 Ma) than suggested in previous interpretations. Our data provide new constraints on the origin of atacamite in Cu deposits from the Atacama Desert and support the recent notion that the formation of atacamite in hyperarid climates such as the Atacama Desert is an ongoing process that has occurred intermittently since the onset of hyperaridity.     

The distribution and hydrogeological controls of fluoride in the groundwater of central Ethiopian rift and adjacent highlands

Occurrence of fluoride (F) in groundwater has drawn worldwide attention, since it has considerable impact on human health. In Ethiopia high concentrations of F in groundwaters used for community water supply have resulted in extensive dental and skeletal fluorosis. As a part of a broader study, the distribution of F in groundwater has been investigated, and compared with bedrock geology and pertinent hydrochemical variables. The result indicates extreme spatial variations. High F concentration is often associated with active and sub-active regional thermal fields and acidic volcanics within high temperature rift floor. Variations in F can also be related to changes in calcium concentration resulting from dissolution of calcium minerals and mixing with waters of different chemical composition originated from variable hydrogeological environment across the rift valley. The concentration of F dramatically declines from the rift towards the highlands with the exception of scattered points associated with thermal springs confined in local volcanic centers. There are also interactions of F-rich alkaline lakes and the surrounding groundwater. Meteoric waters recharging volcanic aquifers become enriched with respect to F along the groundwater flow path from highland recharge areas to rift discharge areas. Locally wells drilled along large rift faults acting as conduits of fresh highland waters show relatively lower F. These areas are likely to be possible sources of better quality waters within the rift. The result of this study has important implications on site selection for water well drilling.     

Interpreting high-pressure phengite <Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar laserprobe ages: an example from Saih Hatat,NE Oman

New single grain fusion and core-rim ⁴⁰Ar/³⁹Ar laserprobe phengite data from the Saih Hatat high-pressure terrane in NE Oman show that individual samples yield a range of apparent ages which is similar to that previously reported from across the entire terrane. The majority of the determined ages are older than the previously reported U-Pb zircon peak metamorphic age. Core to rim age variations within individual grains range from no discernible difference across the grain to grains with older cores, or, rarely, older rims; some samples manifest all three patterns. Numerical diffusion modelling shows that due to the peak temperature of ca. 550°C, the measured apparent ages cannot be explained by simple cooling or by partial retention of crystallisation or detrital ages in an open system. The age variability is better explained by spatially and temporally variable open or closed system behaviour at the mm-cm scale coupled with pervasive and heterogeneously distributed excess argon. Anomalously old eclogite phengite ⁴⁰Ar/³⁹Ar ages are due either to internally derived ⁴⁰Ar inherited from a K-bearing precursor, or externally derived ⁴⁰Ar distributed by grain boundary fluids. Mica-rich schists within the eclogite boudins yield younger phengite ages, suggesting excess argon was absent or diluted. Pelites hosting the eclogite appear to have been affected by later fluid ingress during deformation and greenschist-facies overprint and yield very variable ages commonly with apparently older rims on younger cores. The grain- and sample-scale age variations measured in Saih Hatat indicate that the grain boundary network in eclogite pods was not an efficient transfer pathway for argon transport, whereas the grain boundary network in the surrounding pelites acted as a more efficient pathway on the timescale of the metamorphic cycle.     

Polyphosphates as a source of enhanced P fluxes in marine sediments overlain by anoxic waters: Evidence from <Superscript>31</Superscript>P NMR

Sedimentary phosphorus (P) composition was investigated in Effingham Inlet, a fjord located on the west coast of Vancouver Island in Barkley Sound. Solid-state ³¹P nuclear magnetic resonance (NMR) spectroscopy was applied to demineralized sediment samples from sites overlain by oxic and anoxic bottom waters. The two sites were similar in terms of key diagenetic parameters, including the mass accumulation rate, integrated sulfate reduction rate, and bulk sediment organic carbon content. In contrast, P benthic fluxes were much higher at the anoxic site. ³¹P NMR results show that P esters and phosphonates are the major organic P species present at the surface and at depth in sediments at both sites. Polyphosphates were only found in the surface sediment of the site overlain by oxic waters. The varying stability of polyphosphates in microorganisms under different redox conditions may, in part, explain their distribution as well as differences in P flux between the two sites.     

Comparison of the behaviour of rare earth elements in surface waters,overburden groundwaters and bedrock groundwaters in two granitoidic settings,Eastern Sweden

This work, which was done within the Swedish nuclear waste management program, was carried out in order to increase the understanding of the mobility and fate of rare earth elements (REEs) in natural boreal waters in granitoidic terrain. Two areas were studied, Forsmark and Simpevarp, one of which will be selected as a site for spent nuclear fuel. The highest REE concentrations were found in the overburden groundwaters, in Simpevarp in particular (median ∑REE 52 μg/L), but also in Forsmark (median ∑REE 6.7 μg/L). The fractionation patterns in these waters were characterised by light REE (LREE) enrichment and negative Ce and Eu anomalies. In contrast, the surface waters had relatively low REE concentrations. They were characterised either by an increase in relative concentrations throughout the lanthanide series (Forsmark which has a carbonate-rich till) or flat patterns (Simpevarp with carbonate-poor till), and had negative Ce and Eu anomalies. In the bedrock groundwaters, the concentrations and fractionation patterns of REEs were entirely different from those in the overburden groundwaters. The median La concentrations were low (just above 0.1 μg/L in both areas), only in a few samples were the concentrations of several REEs (and in a couple of rare cases all REEs) above the detection limit, and there was an increase in the relative concentrations throughout the lanthanide series. In contrast to these large spatial variations, the temporal trends were characterised by small (or non existent) variations in REE-fractionation patterns but rather large variations in concentrations. The Visual MINTEQ speciation calculations predicted that all REEs in all waters were closely associated with dissolved organic matter, and not with carbonate. In the hydrochemical data for the overburden groundwater in particular, there was however a strong indication of association with inorganic colloids, which were not included in the speciation model. Overall the results showed that within a typical boreal granitoidic setting, overburden groundwaters are enriched in REEs, organic complexes are much more important than carbonate complexes, there is little evidence of significant mixing of REEs between different water types (surface, overburden, bedrock) and spatial variations are more extensive than temporal ones.     

Cosmogenic radionuclide <Superscript>7</Superscript>Be concentration in seven species of lichens and its correlation with <Superscript>40</Superscript>K, <Superscript>137</Superscript>Cs and <Superscript>226</Superscript>Ra

In this work, accumulation of cosmogenic radionuclide ⁷Be in seven species of lichens was determined using HPGe detectors in autumn season. Ramsar city which is located in the north of Iran as one of the high-level natural radiation areas in the world was considered. Lichen species represented good potential in accumulation of ⁷Be radionuclide. The foliose species of Xanthoria parietina with the highest activity concentration value of 112.8 ± 1.8 Bq kg^?1 was introduced as bioindicator for accumulation of ⁷Be radionuclide. Cladonia rangiformis species has got minimum concentration of 64.5 ± 0.8 Bq kg^?1. Also from thallus morphology viewpoint, results showed that ⁷Be accumulation in foliose species is higher than in fruticose and crustose lichens species. Also there was relatively large positive correlation between ⁷Be and ²²⁶Ra activity concentrations in lichens species.     

Factors of <Superscript>18</Superscript>O/<Superscript>16</Superscript>O fractionation in corundum estimated from the calculation of isotopic shifts on vibration frequencies

The β-factors of corundum were estimated on the basis of DFT calculations of vibrational frequency changes due to ¹⁶O–¹⁸O isotope substitution in a harmonic approximation using an all-electron Gaussian-type basis set and the B3LYP hybrid functional (the CRYSTAL program). Calculations were performed accounting for eight phonon wave vectors within the first Brillouin zone. The results are approximated by the relation 1000ln β _crn = 9.19874x–0.12326x ² + 0.00213x ³ (x = 10⁶/T(K)², 400 < T(K) < 1300), which can be used in isotope geochemical studies in combination with the known temperature effects on the β-factors of other phases.     

Oxygen isotope and deuterium indication of the origin and <Superscript>14</Superscript>C age of the massive ice,Bovanenkovo, Central Yamal peninsula

The conditions and forming time of massive ice were specified (Bovanenkovo gas condensate field, Central Yamal). Here, massive ice lies as stratums, laccoliths, stocks, and lenses. Three thousand boreholes 10–100 m in depth were analyzed. In 260 of them massive ice was broached. The ice foot is situated from 1 to 57 m deep. The maximal thickness of ice broached with boreholes came to 28.5 m; on average, it was about 8 m. The extension of massive ice is sometimes more than 2000 m, and its area is quite often more than 10 km². According to the radiocarbon method, loams of the third terrace, containing and overlapping ice deposits, were formed from 25 000 to 20 000 years ago or somewhat later. These strongly peat loams containing massive ice formed either in shallow sea conditions or during periodical draining conditions of beaches or low laida, where organic matter appeared due to erosion and deposition and accumulated during draining and overgrowing of drains. In more inclement conditions than at present, loam deposits were frozen immediately, forming massive ice, which occupied the barely water-saturated layers. The oxygen isotope composition (δ18O) of massive ice samples varied from −12.49‰ (here and further, relative to SMOW) to −22.95‰. The deuterium concentration (δD) varied from −91.7 to −177.1‰. Deuterium kurtosis (d _exc) varied from 3.4 to 10.6‰. In one seam outcrop, the content of stable isotopes varied significantly. Here, at a depth of 0.2–0.8 m, the δ¹⁸O content varied by more than 10‰ (from −12.49 to −22.75), and the δD content, from −91.7 to −171.9‰. Such variations testify about ice extraction upon freezing of water-saturated grounds in a closed system. According to palynological analysis of ice stratums, numerous remains of unicellular green algae and diatoms were revealed. It is possible that this is evidence of the existence of a fresh well, which was a source of water, feeding the layer. Most probably these were near-bottom silt waters of a large lake or desalted bay, which were frozen syngenetically. This accentuates the new type of massive ice, syncriogenic segregative ice, which probably formed 25 000–20 000 yr BP.     

Probing the relationship between surface waters and aquifers by <Superscript>18</Superscript>O measurements on the top of the Araripe Plateau/NE Brazil

The Araripe Plateau in northeastern Brazil has an area of about 8,000 km², confined by 39°05E and 40°55E, and 7°10S and 7°50S. Due to high permeability of soils, a surface drainage system is practically inexistent. Water is stored in excavations with clayey soil, the barreiros. Monthly samples were taken for ¹⁸O measurements, from September 1999 to August 2000, from four barreiros, three dug wells and five drilled wells. Results show that (1) groundwaters in the eastern part of the plateau are derived from present-day rainfall (¹⁸O–3.2), whereas groundwaters in the western portion are isotopically different (¹⁸O–5.0); (2) barreiros are strongly marked seasonally by elevated ¹⁸O during the dry period due to elevated evaporation; (3) a dug well at a distance of 30 m from a barreiro exhibits ¹⁸O similar to that of the reservoir, indicating a strong interaction between groundwater and surface water; and (4) a tubular well of 242-m depth, located in a fault, exhibits strong seasonal changes in ¹⁸O and electrical conductivity, revealing downward leakage between aquifers.