REE diffusion in calcite

Chemical diffusion of four rare-earth elements (La, Nd, Dy and Yb) has been measured in natural calcite under anhydrous conditions, using rare-earth carbonate powders as the source of diffusants. Experiments were run in sealed silica capsules along with finely ground calcite to ensure stability of the single-crystal samples during diffusion anneals. Rutherford backscattering spectroscopy (RBS) was used to measure diffusion profiles. The following Arrhenius relations were obtained over the temperature range 600–850°C: D_La =2.6×10⁻¹⁴ exp(−147±14 kJ mol⁻¹/RT) m² s⁻¹, D_Nd =2.4×10⁻¹⁴ exp(−150±13 kJ mol⁻¹/RT) m² s⁻¹, D_Dy =2.9×10⁻¹⁴ exp(−145±25 kJ mol⁻¹/RT) m² s⁻¹, D_Yb =3.9×10⁻¹² exp(−186±23 kJ mol⁻¹/RT) m² s⁻¹. In contrast to previous findings for refractory silicates (e.g. zircon), differences in transport rates among the REE are not pronounced over the range of temperature conditions investigated in this study. Diffusion of the REE is significantly slower than diffusion of the divalent cations Sr and Pb and slower than transport of Ca and C at temperatures above 650°C. Fine-scale zoning and isotopic and REE chemical signatures may be retained in calcites under many conditions if diffusion is the dominant process affecting alteration.     

Melting rates beneath Hawaii: Evidence from uranium series isotopes in recent lavas

²³⁸U, ²³²Th, ²³⁰Th and ²²⁶Ra abundances have been measured in six samples of recent Hawaiian basalt by high precision mass spectrometry, in an attempt to compare the melting process in plumes and at spreading ridges. The data reveal a very small range in (²³⁰Th/²³⁸U) activity ratio up to a maximum value of 1.02 ± 0.01, and (²²⁶Ra/²³⁰Th) activity ratios which lie between 1.10 ± 0.015 and 1.19 ± 0.02. UTh and RaTh abundances are linearly correlated demonstrating that the disequilibria predate crystallisation and differentiation. Using recently published estimates for the bulk partition coefficients of U and Th, the results are consistent with melting rates > 10⁻³ kg m⁻³ a⁻¹ at porosities < 10⁻³ for dynamic fractional melting in the garnet stability field.     

Desalinization of running waters: III. Changes in the structure of diatom assemblages caused by a decreasing salt load and changing ion spectra in the river Wipper (Thuringia, Germany)

Salt-loaded effluents were introduced into the river Wipper during the mining period for almost a century. Beginning with the year 1990, the waste water load was strongly reduced due to the termination of the potash industry. Prior to 1990, monthly means of the chloride concentrations at times exceeded 6,000 mg l⁻¹ in the strongly polluted sections. Maximum concentrations reached twice these values. Up to 1998, mean annual chloride concentrations decreased to values below 2,000 mg l⁻¹. This led to more balanced fluctuations in salinity which had been pronounced before, depending on discharge and short-term changes in production. Similarly, the physiologically adverse ion conditions improved due to decrasing potassium and increasing calcium proportions.

In 1963/64, 1986 and 1998, samples of epilithic, epiphytic and epipsammic diatoms were taken at locations of different salinities along the river and examined for the effects of the salinization on the structure of the diatom assemblages. These structures changed in dependence on salinity. Increasing salt concentrations coincided with decreasing oligohalophilic and increasing mesohalophilic and polyhalophilic species numbers. Above a chloride concentration of about 3,000 mg l⁻¹, the proportion of the latter exceed that of the former (halobion index > 50). Corresponding to different conditions of salinization along the river, characteristic diatom assemblages occur differring from each other and which are specific for the river section. Spring and autumn aspects of the diatom assemblages show also salt-dependent differences. The assemblages found in 1998 after decrease of salinization have changed markedly in comparison to those from 1963/64 and 1986. Halobiontic species predominating formerly occurred only occasionally or not at all. They were replaced by oligohalobic-indifferent forms.

An ecological assessment of the changes was performed based on the halobion index calculated from all the samples. For the strongly salinized section of the river Wipper, a shift from -mesohalobic/polyhalobic conditions in 1963/64 and 1986 to -oligohalobic/β-mesohalobic conditions in 1998 was found. However, constant -oligohalobic conditions are still not given. With regard to the transition from -oligohalobic (limnetic) to β-mesohalobic (brackish) conditions, a maximum chloride concentration of 600 mg l⁻¹ was found. To guarantee -oligohalobic conditions, a maximum chloride concentration of 400 mg l⁻¹ should not be exceeded.     

Impacts of domestic sewage effluent on phytoplankton from Bedford Basin, eastern Canada

The impact of domestic sewage effluent (SE) on the dynamics of phytoplankton assemblages from Bedford Basin was evaluated in the laboratory. Phytoplankton production and chlorophyll a increased proportionally with SE enrichment. Phytoplankton species composition also changed. The potentially harmful diatoms, Pseudonitzschia spp., present initially in small numbers (600 cells 1⁻¹) in Bedford Basin seawater, and became dominant (3–5×10⁶ cells 1⁻¹) when the seawater was enriched with 0.5–5% untreated SE. With higher proportions of SE, other harmful species such as Fragilaria spp. and Euglena spp. became dominant (7−15×10⁶ and 2.2×10⁴ cells 1⁻¹, respectively). Treatment of SE with UV light or activated charcoal seems to favour growth of benign species, such as Chaetoceros socialis, Skeletonema costatum and Thalassiosira spp., but not harmful species such as Pseudonitzschia spp. Further research on UV treatment of domestic sewage is recommended.     

U,U andTh in seawater

We have developed techniques to determine²³⁸U,²³⁴U and²³²Th concentrations in seawater by isotope dilution mass spectrometry. U measurements are made using a²³³U²³⁶U double spike to correct for instrumental fractionation. Measurements on uranium standards demonstrate that²³⁴U/²³⁸U ratios can be measured accurately and reproducibly.²³⁴U/²³⁸U can be measured routinely to ± 5‰ (2σ) for a sample of 5 × 10⁹ atoms of²³⁴U (3 × 10⁻⁸ g of total U, 10 ml of seawater). Data acquisition time is 1 hour. The small sample size, high precision and short data acquisition time are superior to-counting techniques.²³⁸U is measured to ± 2‰ (2σ) for a sample of 8 × 10¹² atoms of²³⁸U ( 3 × 10⁻⁹ g of U, 1 ml of seawater).²³²Th is measured to ± 20‰ with 3 × 10¹¹²³²Th atoms (10⁻¹⁰ g²³²Th, 1 1 of seawater). This small sample size will greatly facilitate investigation of the²³²Th concentration in the oceans. Using these techniques, we have measured²³⁸U,²³⁴U and²³²Th in vertical profiles of unfiltered, acidified seawater from the Atlantic and²³⁸U and²³⁴U in vertical profiles from the Pacific. Determinations of²³⁴U/²³⁸U at depths ranging from 0 to 4900 m in the Atlantic (7°44′N, 40°43′W) and the Pacific (14°41′N, 160°01′W) Oceans are the same within experimental error (± 5‰,2σ). The average of these²³⁴U/²³⁸U measurements is 144 ± 2‰ (2σ) higher than the equilibrium ratio of 5.472 × 10⁻⁵. U concentrations, normalized to 35‰ salinity, range from 3.162 to 3.281 ng/g, a range of 3.8%. The average concentration of the Pacific samples (31°4′N, 159°1′W) is 1% higher than that of the Atlantic (7°44′N, 40°43′W and 31°49′N, 64°6′W).²³²Th concentrations from an Atlantic profile range from 0.092 to 0.145 pg/g. The observed constancy of the²³⁴U/²³⁸U ratio is consistent with the predicted range of²³⁴U/²³⁸U using a simple two-☐ model and the residence time of deep water in the ocean determined from¹⁴C. The variation in salinity-normalized U concentrations suggests that U may be much more reactive in the marine environment than previously thought.     

Heat loss from the earth: A constraint on Archaean tectonics from the relation between geothermal gradients and the rate of plate production

The models suggested for the oceanic lithosphere which best predict oceanic heat flow and depth profiles are the constant thickness model and a model in which the lithosphere thickens away from the ridge with a heat source at its base. The latter is considered to be more physically realistic. Such a model, constrained by the observed oceanic heat flow and depth profiles and a temperature at the ridge crest of between 1100°C and 1300°C, requires a heat source at the base of the lithosphere of between 0.5 and 0.9 h.f.u., thermal conductivities for the mantle between 0.005 and 0.0095 cal cm⁻¹ °C⁻¹ s⁻¹ and a coefficient of thermal expansion at 840°C between 4.1 × 10⁻⁵ and 5.1 × 10⁻⁵ °C⁻¹. Plate creation and subduction are calculated to dissipate about 45% of the total earth heat loss for this model. The efficiency of this mechanism of heat loss is shown to be strongly dependent on the magnitude of the basal heat source. A relation is derived for total earth heat loss as a function of the rate of plate creation and the amount of heat transported to the base of plates. The estimated heat transport to the base of the oceanic lithosphere is similar to estimates of mantle heat flow into the base of the continental lithosphere. If this relation existed in the past and if metamorphic conditions in late Archaean high-grade terrains can be used to provide a maximum constraint on equilibrium Archaean continental thermal gradients, heat flow into the base of the lithosphere in the late Archaean must have been less than about 1.2–1.5 h.f.u. The relation between earth heat loss, the rate of plate creation and the rate of heat transport to the base of the lithosphere suggests that a significant proportion of the heat loss in the Archaean must have taken place by the processes of plate creation and subduction. The Archaean plate processes may have involved much more rapid production of plates only slightly thinner than at present.     

AMS analysis of I in Japanese soil samples collected from background areas far from nuclear facilities

Analytical procedures in the determination of iodine-129 (half-life: 1.6×10⁷ y) have been studied using accelerator mass spectrometry (AMS), with special references to the separation procedures of iodine from soil samples for the AMS measurement. Iodine was successfully volatilized from soil samples by pyrohydrolysis at 1000 °C and collected in a trap solution. Iodine was purified from the matrix by solvent extraction. Finally, it was precipitated as silver iodide to make a target for AMS. In order to obtain information on the ¹²⁹I/¹²⁷I ratio in a chemical blank (or iodine carrier), we have determined the ratios in several iodine reagents and found that the ratios fell in a narrow range around 1.7×10⁻¹³. The detection limit for soil sample (1 g material) by the present method was about 0.01 mBq/kg or 4×10⁻¹¹ as the ratio of stable iodine (¹²⁹I/¹²⁷I ratio), i.e. these values were much better than that by neutron activation analysis (NAA) used in our previous studies. We have applied this method in the analysis of soil samples collected from different places in Japan. We could successfully determine ¹²⁹I in soil samples with low ¹²⁹I concentrations, which could not be detected by NAA. Sample size necessary for the soil analysis by AMS was only about 0.5 g or less, whereas about 100 g of the sample were required for NAA [Muramatsu, Y., Ohmomo, Y., 1986. Iodine-129 and iodine-127 in environmental samples collected from Tokaimura/ Ibaraki, Japan. Sci. Total Environ. 48, 33-43]. Using this method, new data were obtained for the ¹²⁹I levels in 20 soil samples collected from background areas far from nuclear facilities, and the ranges were 1.4×10⁻⁵−4.5×10⁻³ Bq/kg as ¹²⁹I concentrations and 3.9×10⁻¹¹−2.2×10⁻⁸ as ¹²⁹I/¹²⁷I ratios. These values are useful in understanding the ¹²⁹I levels in Japanese environments. Higher ¹²⁹I concentrations were observed in forest soils than those in field and rice paddy soils should be related to the interception effect of atmospheric ¹²⁹I due to tree canopies. Relatively high ¹²⁹I/¹²⁷I ratios found in rice paddy soils could be explained by their low stable iodine concentrations which were caused by the desorption of stable iodine from the rice paddies during the cultivation.     

Implanted radiogenic and other noble gases in crustal diamonds from Northern Kazakhstan

Noble gases were extracted in steps from grain size fractions of microdiamonds ( < 100 μm) from the Kokchetav Massif, Northern Kazakhstan, by pyrolysis and combustion. The concentration of ⁴He in the diamonds proper (liberated by combustion) shows a 1/r dependence on grain size. For grain diameters > 15 μm the concentration also decreases with the combustion step. Both results are clear evidence that ⁴He has been implanted into the diamonds from -decaying elements in the surrounding matrix. The saturation concentration of ⁴He(5.6 × 10⁻⁴ cm³ STP/g) is among the very highest observed in any terrestrial diamonds. Fission xenon from the spontaneous fission of ²³⁸U accompanies the radiogenic ⁴He; the ¹³⁶Xe_f/⁴He ratio of (2.5 ± 0.3) × 10⁻⁹ agrees well with the production ratio of 2.3 × 10⁻⁹ expected in a reservoir where Th/U 3.3. Radiogenic ⁴⁰Ar is predominantly ( > 90%) set free upon combustion; it also resides in the diamonds and appears to have been incorporated into the diamonds upon their formation.

³He, on the other hand is mainly released during pyrolysis and hence is apparently carried by ‘contaminants’. The concentration in the diamonds proper is of the order of 4 × 10⁻¹² cm³ STP/g, with a ³He/⁴He ratio of 1 × 10⁻⁸. Excess ²¹Ne, similarly, appears to be present in contaminants as well as in diamonds proper. These two nuclides in the contaminants must have a nucleogenic origin, but it is difficult to explain their high concentrations.     

Pu, Cs and excess Pb in Russian Arctic sediments

The activity ratios of Pu and radiocesium isotopes have been used to delineate the major sources (such as global and close-in (debris) fallout, nuclear fuel reprocessing and fabrication plant effluents) in the environment. We have measured ²³⁸Pu, ^239,240Pu, ¹³⁷Cs, and excess ²¹⁰Pb concentrations in 107 surficial sediments as well as in 5 sediment cores collected in the summer months of 1993 and 1994 from the Ob and Yenisey Rivers (Russia) and the Kara sea. A comparison of the sediment core inventories of ^239,240Pu and ¹³⁷Cs, along with the ²³⁸Pu/^239,240Pu activity ratios, with those expected from global fallout allows us to estimate the relative amounts, if any, of reactor-derived ²³⁸Pu and ^239,240Pu from the dumped reactor sites in the study area.

In surficial sediment samples collected in 1993 and 1994, the ^239,240Pu concentrations varied between 4.2 and 856 mBq kg⁻¹, with a mean of 239 mBq kg⁻¹. In samples with a measurable ²³⁸Pu, the ²³⁸Pu/^239,240Pu activity ratios varied between 0.010 and 0.069, with an average value of 0.035 ± 0.014. This range can be compared to the average ²³⁸Pu/^239,240Pu activity ratio of 0.030 for the year 1993 from nuclear weapons testing and SNAP fallout obtained from soil studies, indicating very little (≤ 5%) additional sources of ²³⁸Pu to the sediments in the study area. The inventories of Pu in the 5 sediment cores from the study area varied between 2.67 ± 0.67 and 24.5 ± 2.2 Bq m⁻² with a mean value of 8.83 Bq m⁻². The ¹³⁷Cs concentrations in the upper 3 cm of the sediments varied between below detection limit to 71.4 Bq kg⁻¹, with a mean of 14.9 Bq kg⁻¹. The ¹³⁷Cs inventories in the 5 sediment cores varied between 156.7 ± 28.3 and 1600 ± 153.3 Bq m⁻², with a mean value of 583.3 Bq m⁻². The mean ratio of inventories of Pu to that of ¹³⁷Cs, 0.015, is comparable to the values in other places in the Arctic region. There is a significant correlation between total organic carbon and concentrations of ¹³⁷Cs, ^239,240Pu and ²¹⁰Pb, suggesting that organic matter-enriched fine particles are a likely carrier phase for these nuclides. The ratio of ¹³⁷Cs/^239,240Pu also suggests that most of these nuclides are derived from global fallout.     

Taxonomic composition and seasonality of diatoms in three Dinaric karstic lakes in Croatia

The composition and temporal distribution of planktonic diatoms were studied in three small shallow karstic lakes – Modro Oko, Desne, and Kuti – throughout the seasons in 1994, 1995, 1997, and 1998. Physico-chemical parameters did not differ among the three lakes, except for NO₃ concentrations. Altogether, 137 diatom taxa within 41 genera were found in all three lakes combined. The highest number of taxa belonged to the genera Surirella (13), Navicula (12), andCymbella (9). Most taxa were tychoplanktonic, with true panktonic taxa contributing only 14% of the total. Despite their physical-chemical similarity, the lakes showed differences in the structure and dynamics of their diatom communities. Blooms occurred at different times in each of the lakes, and community similarity (Jaccard index) among all three was low (17.6–29.1%). The highest mean values of surface diatom abundance in Modro Oko (2199 cells L⁻¹), Desne (7900 cells L⁻¹), and Kuti (20690 cells L⁻¹) were not significantly different. Margalef's species richness index did not differ either among the lakes or seasonally. Only five diatom taxa in quantitative samples, and 22 taxa in net-samples, were common to all lakes. The most frequent diatoms were Cyclotella striata (56–93%), Fragilaria ulna (50–67%), and Asterionella formosa (27–83%). The most abundant taxa in Modro Oko, Desne, and Kuti were, respectively, Cymbella sp. 1 (402 cells L⁻¹), Cyclotella striata (3000 cells L⁻¹) and Asterionella formosa (20690 cells L⁻¹). Eighteen taxa were recorded for the first time in Croatia: Amphora commutata, Caloneis amphisbaena var. subsalina, C. silicula var. peisonis, Campylodiscus echeneis, Coscinodiscus lacustris, Denticula elegans, Gyrosigma acuminatum var. lacustre, G. distortum var. parkeri, G. fasciola, Navicula menisculus var. menisculus, N. pusilla, N. helensis, Stauroneis parvula var. prominula, Staurosira construens f. subsalina, Stephanodiscus sp. 1, Surirella gracilis, S. ovalis, and S. striatula. The genus Stephanodiscus was recorded for the first time in Croatia.     

Natural remanent magnetization of carbonaceous chondrites

We have observed natural remanent magnetizations (NRM), ranging from 10⁻³ to 10⁻⁵ Gauss cm³/g, at least two orders of magnitude greater than 10⁻⁷, the noise level of our spinner magnetometer, in the carbonaceous chondrites, Orgueil, Cold Bokkeveld, Nogoya and Mighei. Preliminary alternating field demagnetization of two samples of Orgueil showed a moderate sized stable component of 10⁻⁴ Gauss cm³/g. Microscopic study reveals that a grey spinel oxide, Ni-Fe and an Fe sulphide are the principal opaque minerals in both Cold Bokkeveld and Orgueil; the oxide phase predominates in both, while the Ni-Fe is more visible in the former. Coercive force determinations in Orgueil and Cold Bokkeveld indicate single domain particles as the NRM carrier. These meteorites are suitable for the determination of the magnetic field intensity in the primary solar nebula.     

A soil-water flux sensor and its use for field studies of transfer processes in surface soil

A soil-water flux sensor was developed, which determines the flux value from the difference between downstream and upstream temperatures at some distances from an artificial heat source. It can detect flux values ranging from several mm hr.⁻¹ to as small as 0.01 mm hr.⁻¹. Design and calibration of the sensor are described.

The sensor was applied to the field studies of transfer processes in a surface soil, including rainwater infiltration, upward soil-water flow during evapotranspiration, and their effects on the water table level. Cl⁻ accumulation in the surface soil is discussed on the basis of upward water flux and Cl⁻ content observed.     

Sublethal effects of cupric ion activity on the grazing behaviour of three calanoid copepods

This research (1) characterized the effects of sublethal cupric ion activities on the grazing behavior of two estuarine copepods (Acartia tonsa, Acartia hudsonica) and one nearshore, neritic copepod (Temora longicornis) and (2) compared the sensitivity of short-term sublethal behavioral assays with that of longer-term acute toxicity tests. A nitrilotriacetate-trace-metal-ion buffer system at 27‰. S was used to quantify and control the free cupric ion activity. Acute toxicity tests were used to determine the mortality of A. tonsa and T. longicornis over 72 h within the approximate cupric ion activity range of 10⁻¹³ to 10^−9.5 M. 24 h survival was not affected within the approximate cupric ion activity range of 10⁻¹³ to 10^−9.7 M, the range used for subsequent grazing activity experiments after 24 h exposure to Cu. Grazing activity was significantly diminished at cupric ion activities of ≈ 10⁻¹⁰ M for A. tonsa and T. longicornis, and at ≈ 10⁻¹¹ M for A. hudsonica. A hormetic pattern of response in feeding activity was observed with A. tonsa and T. longicornis. Grazing activity was found to be a sensitive measure of sublethal Cu stress compared with the acute toxicity tests. Grazing activity was affected at environmentally relevant cupric ion activities.     

Water flow path interactions with soil hydraulic properties in till soil at Gårdsjön, Sweden

In 1989, in a hydrological research programme within a deacidification project in the Gårdsjön area in southwest Sweden, flow paths and residence times of soil water and groundwater in microcatchments were examined to support the interpretation of the hydrochemical changes. Saturated hydraulic conductivity and soil water retention were analysed on more than 100 cylinder samples. The catchments have shallow sandy-silty till soil with a mean depth in the main catchment of 43 cm. Porosity of the mineral soil in the main catchment was high and ranged from 38 to 85%. The samples from the B-horizon had generally higher porosity. Porosity and the content of organic matter were correlated. The soil water retention was relatively high at all tensions, likely owing to the high content of organic matter. Dissolved organic substances were most probably transported from the shallow soil on the steep sides of the catchment down to the valley where it precipitated. The high porosities could be a consequence of long-term weathering, provided that the organic substances present have increased the leaching of the weathering products. Measured values of saturated hydraulic conductivity were close to log-normally distributed with a mean for all samples of 3 × 10⁻⁵ m s⁻¹. There was a significant increase in conductivity toward the ground surface with the mean conductivity of the samples in the uppermost 10 cm of the mineral soil of 4 × 10⁻⁵ m s⁻¹, which was about 13 times higher than the conductivity of 3 × 10⁻⁶ m s⁻¹ at 1 m depth. From the relationship between runoff at the catchment outlet and groundwater levels, the conductivity was estimated to be 15–200 times higher in the upper soil layer than in the deeper ones. In one profile, 44–64% of the yearly lateral flow was estimated to occur above 30 cm depth. The conductivity was correlated with the content of drainable water, which indicated the importance of the largest pores for the saturated hydraulic conductivity.     

The toxicity of marine sediments in Victoria Harbour, Hong Kong

When the toxicity of marine sediment in Hong Kong was evaluated, it was found that the seven sediments collected within Victoria Harbour were severely contaminated with heavy metals, at concentrations many times higher than those in sediments collected from outside the harbour. The highest metal content was recorded in site VS14 (located near the airport runway and the industrialized area), with copper, zinc, lead and chromium values of 3789, 610, 138 and 601 mg kg⁻¹ dry wt, respectively. This site also had the greatest alkaline phosphatase activities (15 fluorescent intensity unit g⁻¹ wet wt), the largest number of total coliforms (910 CFU g⁻¹ wet wt) and sulphate-reducing bacteria (8.5 × 10⁴ cells g⁻¹ wet wt), implying that site VS14 was also contaminated with organic matter and nutrients. Sediment bioassays, Microtox and algal tests, demonstrated that sediment elutriates obtained from site VS14 were of greatest toxicity. The EC₁₀ value in Microtox tests was 17% elutriate, and the 96-h IC₅₀ values using Skeletonema costatum and Dunaliella tertiolecta were 40 and 79% elutriate, respectively. No toxic effects were found in sediment samples collected from the control site outside Victoria Harbour. Significant correlations were found between the results of the algal toxicity test (using S. costatum) and the coliform count and metal content of the sediments. The Microtox test was less sensitive than the algal bioassay, and no sediment elutriate, even from the site mostly contaminated by heavy metals, caused more than 50% inhibition of the light-emitting activity of the bacteria. In this study, S. costatum (the diatom) provided a more sensitive and reliable test species than D. tertiolecta (the flagellate) in differentiating the toxicity of marine sediments.     

Influence of artificial groundwater lakes on the abundance and activity of bacteria in adjacent subsurface systems

Bacterial abundances and activity, estimated by 4′,6-diamidino-2-phenylindole staining (DAPI) and the reduction of 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyl tetrazolium chloride (INT), were investigated in two oligotrophic artificial groundwater lakes and the surrounding aquifers. To evaluate the effect of lake water on groundwater downstream, samples were taken from wells at different distances from the lakes, and the total number of bacteria and the number of active bacteria in these samples were compared with samples collected upstream. In addition, sterilized sandy sediments were exposed in groundwater wells to measure the number and activity of bacteria attached to particles. At one of the study sites, where the lake sediments were disturbed by dredging, total bacterial abundance and the number of respiring bacteria in the groundwater aquifer was clearly influenced by the lake water. The average bacterial abundances decreased from 2.6 ± 1.9 × 10⁵ cells ml⁻¹ in the well closest to the lake (S2) to 2.9 ± 3.8 × 10⁴ cells ml⁻¹ in the most distant one (S4), which was equivalent to cell numbers in the upstream well. The number of respiring bacteria showed a similar tendency with 1.3 ± 2.7 × 10⁴ active cells ml⁻¹ in S2 and 1.9 ± 1.5 × 10³ active cells ml⁻¹ in S4. At the second study site, which was not influenced by dredging, bacteria in the downstream wells seemed not to be affected by the lake water. The number and activity of bacteria, which colonized exposed sediments, were not significantly different in the upstream and downstream wells, indicating a minor influence of lake water on this habitat. Our results suggest that gravel-pit lakes may influence the free living bacterial assemblages in nearshore groundwater systems, but do not visibly affect numbers and activity of bacteria attached to the surface of aquifer sediments.     

Noble gases in submarine pillow basalt glasses from the Lau Basin: Detection of a solar component in backarc basin basalts

Noble gas elemental and isotopic abundances have been analysed in eight samples of youthful basaltic glass dredged from three different locations within the Lau Backarc Basin: (1) the King's Triple Junction, (2) the Central Lau Spreading Centre at 18°S and (3) the Eastern Lau Spreading Centre at 19°S. Samples from the Lau central and eastern spreading centres have MORB-like helium isotopic ratios of approximately 1.2 × 10⁻⁵ (8.5 R/R_A). In contrast, the samples from the King's Triple Junction yield helium isotopic ratios averaging 9.4 (±0.8) × 10⁻⁶ (6.7 ± 0.6 R/R_A), systematically lower than the MORB-like value, which may be reflecting the addition of radiogenic ⁴He released from the descending slab. Neon isotopic ratios are enriched in ²⁰Ne and ²¹Ne with respect to atmospheric ratios by as much as 23% and 62% respectively. These observations further confirm that non-atmospheric neon is a common characteristic of samples derived from the mantle. The helium and neon isotopic signatures in the samples can be explained by mixing of a primordial solar component, radiogenic and nucleogenic components produced by radioactive processes inside the Earth, and an atmospheric component. This reconnaissance survey of noble gases in a backarc basin indicates that current volcanism is dominated by magmas from the mantle wedge, a source similar to that from which MORBs are derived. The heavier noble gases (argon, krypton and xenon), however, show more atmosphere-like compositions, either indicating strong interaction of the magmas with the atmosphere or the presence of a recycled component derived from the underlying subducting slab.     

Brine history indicated by argon, krypton, chlorine, bromine, and iodine analyses of fluid inclusions from the Mississippi Valley type lead-fluorite-barite deposits at Hansonburg, New Mexico

Argon, krypton, chlorine, bromine, and iodine were measured in a homogeneous population of high-salinity hydrothermal fluid inclusions from the Tertiary-age Mississippi Valley-type (MVT) lead-fluorite-barite deposits at Hansonburg, New Mexico to establish new types of evidence for the history of both the fluid and the major dissolved salts. Noble gases and halogens in fluid inclusions containing 10⁻¹⁰–10⁻⁹ L of brine (Cl= 3 molal) were analyzed by laser microprobe noble-gas mass spectrometry (lmngms) on neutron-irradiated samples.

The concentrations of³⁶Ar (4.7 × 10⁻⁸ molal) and⁸⁴Kr1.8 × 10⁻⁹ molal) in the fluid inclusions are equal to those of fresh surface waters in equilibrium with air at approximately20 ± 5°. The mole ratios ofBr/Cl (1.2 × 10⁻⁴) andI/Cl (1–2 × 10⁻⁶) are among the lowest measured in any natural waters, similar to those of modern brines formed by dissolution of Permian NaCl-bearing evaporites in southeast New Mexico.⁴⁰Ar/³⁶Ar ratios (600) are twice that of air, and indicate that the fluid inclusions had excess radiogenic⁴⁰Ar (1.4 × 10⁻⁵ molal) when trapped. The amount of excess⁴⁰Ar appears to be too large to have been acquired with Cl by congruent dissolution of halite-bearing evaporites, and possibly too small to have been acquired with Pb by congruent dissolution of granitic basement rocks with Proterozoic KAr ages.

From thelmngms data, combined with published Pb and S isotope data, we infer the following sequence of events in the history of the Hansonburg MVT hydrothermal brine: (1) the brine originated as relatively dilute meteoric water, and it did not gain or lose atmospheric Ar or Kr after recharge; (2) the originally dilute fluid acquired the bulk of its Cl and sulfate in the subsurface after recharge by dissolving halite-bearing Permian? marine evaporites; (3) the high salinity brine then acquired most of its Pb and excess radiogenic⁴⁰Ar from interactions with aquifer rocks other than evaporites, possibly clastic sedimentary rocks or basement rocks with Phanerozoic KAr “ages”; and (4) the brine deposited fluorite without having boiled or degassed.     

New evidence for age variation and scale effects of permeabilities of young oceanic crust from borehole thermal and pressure measurements

In 1996, long-term sealed-hole hydrological observatories with subseafloor temperature and pressure sensors were installed in four cased holes drilled by the Ocean Drilling Program into sedimented young oceanic crust east of the Juan de Fuca Ridge. Data recovered over a year later showed that all four holes displayed temperature profiles indicative of vertical fluid flow immediately prior to their being sealed. Warm water was being produced from basement in two cases, and cool ocean bottom water was being drawn into basement at the others. Linear flow rates of 60–200 m/h were estimated from the perturbation of the temperature profiles relative to undisturbed geothermal gradients at the sites. The pressure differentials driving the flow were also measured at the time of the observatory installations, allowing estimates of permeabilities of the upper crustal sections penetrated by the holes. Estimated permeabilities vary systematically with age, ranging from about 10⁻¹⁰ m² in the youngest site (0.9 Ma) to 10⁻¹² m² in the oldest site (3.6 Ma), confirming an apparent reduction of permeability with age determined with packer experiments at three of the same sites. Combined with other estimates of permeabilities in the same holes using methods with different scales of investigation, the new permeability estimates also provide evidence for a significant scale dependence of permeability in the upper oceanic crust.     

Ar/Ar geochronology of the West Greenland Tertiary volcanic province

Paleocene volcanic rocks in West Greenland and Baffin Island were among the first products of the Iceland mantle plume, forming part of a larger igneous province that is now submerged beneath the northern Labrador Sea. A ⁴⁰Ar/³⁹Ar dating study shows that volcanism commenced in West Greenland between 60.9 and 61.3 Ma and that 80% of the Paleocene lava pile was erupted in 1 million years or less (weighted mean age of 60.5±0.4 Ma). Minimum estimates of magma production rates (1.3×10⁻⁴ km³ year⁻¹ km⁻¹) are similar to the present Iceland rift, except for the uppermost part of the Paleocene volcanic succession where the rate decreases to <0.7×10⁻⁴ km³ year⁻¹ km⁻¹ (rift). The timing of onset of volcanism in West Greenland coincides with the opening of the northern Labrador Sea and is also strikingly similar to the age of the oldest Tertiary volcanic rocks from offshore SE Greenland and the British–Irish province. This is interpreted as manifesting the impact and rapid (>1 m/year) lateral spreading of the Iceland plume head at the base of the Greenland lithosphere at 62 Ma. We suggest that the arrival, or at least a major increase in the flux, of the Iceland mantle plume beneath Greenland was a contributing factor in the initiation of seafloor spreading in the northern Labrador Sea. Our study has also revealed a previously unrecognised Early Eocene volcanic episode in West Greenland. This magmatism may be related to movement on the transform Ungava Fault System which transferred drifting from the Labrador Sea to Baffin Bay. A regional change in plate kinematics at 55 Ma, associated with the opening of the North Atlantic, would have caused net extension along parts of this fault. This would have resulted in decompression and partial melting of the underlying asthenosphere. The source of the melts for the Eocene magmatism may have been remnants of still anomalously hot Iceland plume mantle which were left stranded beneath the West Greenland lithosphere in the Early Paleocene.