Tropospheric,stratospheric and mesospheric ozone observed using the Umkehr method

Ozone vertical profiles have been obtained above the “Observatoire de Haute-Provence” from 9 to 19 June 1981, with both conventional and short Umkehr methods: the mesospheric and stratospheric ozone variability has been found to be very small while the ozone variability was large in the troposphere and maximum at the tropopause level.     

Organic matter diagenesis in the anoxic sediments of saanich inlet,British Columbia,Canada: a case for highly evolved community interactions

Cytochrome c and ferricyanide reducing activities are measured in a Desulfovibrio desulfuricans (strain ATCC No. 17990) that indicate that the APS reductase activity is constitutive. This enzymatic activity is also measured in a Saanich Inlet isolate identified as Desulfovibrio salexigens (Saanich). Successful measurement of the Cytochrome c reducing activity was also made in the sediment extracts from Saanich Inlet, and this activity was found to be present in sediments as deep as 50 cm. Bacterial biomass distributions were estimated using measurements of ATP in the Saanich Inlet sediments. ETS activity measurements correlated well with the in situ [³⁵S]-SO₄^2? reduction rate measurements; both of the methods showing a subsurface maximum in activity at a depth of about 10 cm. However, some differences between the results obtained from these two procedures were also found, e.g., the in situ [³⁵S]-SO₄^2? reduction activity approximated zero values at or near 25 cm depth, while 5–10% of the surface ETS activity was present at a depth of as much as 50 cm. The hypothesis presented is that the subsurface maximum may be due to the anaerobic oxidation of methane by [³⁵S]-SO₄^2? ions as mediated by the sulfate-reducing bacteria. A discussion of the strong interactive relationships between a variety of organisms in an ecosystems context, so necessary in bringing about organic matter diagenesis in anoxic marine environments, is also presented.     

An estimate of the duct life time from low latitude ground observations of whistlers at Varanasi

The observed periodicity in the whistler occurrence rate recorded at our low latitude ground station at Varanasi (geomagnetic latitude, 14°55'N) is interpreted in terms of duct life time at lowL values. Power spectrum analysis of the whistler data yields a period of about 50 min for the growth and decay of ducts. Further dispersion analysis of the whistlers has qualitatively confirmed the existence of separate ducts during the period of observations.     

Benzene contamination at a metal plating facility

A metal plating facility in central Kentucky was required to complete a RCRA Facility Investigation to address a number of Solid Waste Management Units at the site. Twenty monitoring wells were installed at the facility. Ground water from the wells was sampled for total and dissolved metals, polychlorinated biphenyls, acid extractable compounds, base neutral compounds, and volatile organic compounds. Unexpectedly, relatively large concentrations of benzene, up to 120 μg/l, were detected in samples from some of the wells, including wells that should have been hydraulically upgradient from the facility. As a result of the detection of benzene, the facility completed an investigation to identify the source. A nearby facility had completed a gasoline underground storage tank (UST) closure at about the time of the installation of the 20 wells. Reportedly the UST had small holes when removed. Three potential pathways of migration (a ditch, sanitary sewer, and a sink hole) from the nearby facility to the metal-plating facility and residual soils with very large concentrations of benzene, toluene, ethylbenzene, and xylenes have been identified.     

Relationship of environmental geochemistry to soil degradation in Helwan catchment, Egypt

Environmental geochemistry plays an important role in understanding the distribution of major cations (Ca²⁺, Mg²⁺, Na⁺, K⁺) in Helwan catchment, south Cairo, Egypt. Evaluation of soil mechanical erosion rate, depletion rate, exchangeable rates of base cations and sodium adsorption ratios are essential for understanding soil degradation problems in the representative Helwan catchment. Soil erosion is a natural process. It often becomes a problem when human activity causes it to occur much faster than under natural conditions. The results of the mechanical erosion rate of soil and the exchangeable rates of base cations are 1845 and 80.3 kg ha⁻¹ yr⁻¹, respectively. The high intensity of the mechanical erosion rate is probably attributed to the high specific surface area of the studied type of Vertisol, intensive application of fertilizer and industrial activities. Mechanical erosion of soil, exchangeable rate of base cations and the depletion rate of base cations are almost inexhaustible sources of sodium, and all these increase the problem of sodic soils and may affect plant productivity in Helwan catchment.     

L'upwelling de la côte atlantique du Maroc entre 1994 et 1998

The pelagic ecosystem of the Moroccan Atlantic coast is influenced by the spatiotemporal variability of upwelling. The changes in the physicochemical and biological parameters as well as their interrelationship and regrouping by the principal components analysis allowed us to subdivide the Atlantic coast in four active areas: two areas located at the north of Cape Juby (28°N), characterised by a summery activity and two areas located at the south, active permanently, with a variable intensity. To cite this article: A. Makaoui et al., C. R. Geoscience 337 (2005).     

Fluid inclusions in chromite from a pyroxenite dike of the Pindos ophiolite complex

Chromitite occurrences in the Pindos ophiolite complex are located in elongated dunite bodies hosted in harzburgite of the mantle sequence, and show a compositional variation from high-Al to high-Cr type. Although the majority of the chromite ores is characterized by paucity in fluid inclusions, abundant fluid inclusions were found in chromite hosted by a coarse-grained pyroxenite dike at the Spanos Valley, Pindos complex. Chromite occurs in highly variable proportion in an orthopyroxene matrix or as inclusions in orthopyroxenes. Its composition is homogeneous and has an average Cr/(Cr+Al) ratio 0.73.The investigation of chromitites revealed the presence of primary and secondary fluid inclusions. The primary inclusions are of following types: Three-phase solid-liquid-gas, three-phase liquid-liquid-gas, two-phase liquid-gas and one-phase octahedron crystal-shaped. The secondary fluid inclusions are two-phase liquid-gas and mono-phase fluid inclusions.The presence of fluid inclusions in chromite aggregates hosted in orthopyroxenite dikes, in combination with the trace element contents in chromite concentrates and the mineralogical composition of the dikes may indicate that an aqueous phase separated from the magma.     

A menagerie of graphite morphologies in the Acapulco meteorite with diverse carbon and nitrogen isotopic signatures: Implications for the evolution history of acapulcoite meteorites

Morphologies, petrographic settings and carbon and nitrogen isotopic compositions of graphites in the Acapulco meteorite, the latter determined by secondary ionization mass spectrometry, are reported. Seven different graphite morphologies were recognized, the majority of which occur enclosed exclusively in kamacite. Individual graphite grains also rarely occur in the silicate matrix. Kamacite rims surrounding taenite cores of metal grains are separated from the Ni-rich metal cores by graphite veneers. These graphite veneers impeded or prevented Ni-Fe interdiffusion during cooling. In addition, matrix FeNi metal contains considerable amounts of phosphorous (≈ 700 ppm) and silicon (≈ 300 ppm) (Pack et al., 2005 in preparation) thus indicating that results of laboratory cooling experiments in the Fe-Ni binary system are inapplicable to Acapulco metals. Graphites of different morphologies display a range of carbon and nitrogen isotopic compositions, indicating a diversity of source regions before accretion in the Acapulco parent body. The isotopic compositions point to at least three isotopic reservoirs from which the graphites originated: (1) A reservoir with heavy carbon, represented by graphite in silicates (δ¹³C = 14.3 ± 2.4 ‰ and δ¹⁵N = −103.4 ± 10.9 ‰), (2) A reservoir with isotopically light carbon and nitrogen, characteristic for the metals. Its C- and N-isotopic compositions are probably preserved in the graphite exsolutions that are isotopically light in carbon and lightest in nitrogen (δ¹³C = −17 to −23 ‰ δ¹⁵N = −141 to −159 ‰). (3) A reservoir with an assumed isotopic composition (δ¹³C ∼ −5 ‰; δ¹⁵N ∼ −50 ‰). A detailed three-dimensional tomography in reflected light microscopy of the decorations of metal-troilite spherules in the cores of orthopyroxenes and olivines and metal-troilite veins was conducted to clarify their origin. Metal and troilite veins are present only near the fusion crust. Hence, these veins are not pristine to Acapulco parent body but resulted during passage of Acapulco in Earth’s atmosphere. A thorough search for symplectite-type silicate-troilite liquid quench textures was conducted to determine the extent of closed-system partial silicate melting in Acapulco.Metal-troilite spherules in orthopyroxenes and olivines are not randomly distributed but decorate ferromagnesian silicate restite cores, indicating that the metal-spherule decoration around restite silicates took place in a silicate partial melt. Graphite inclusions in these spherules have C- and N- isotopic compositions (δ¹³C = −2.9 ± 2.5 ‰ and δ¹⁵N = −101.2 ± 32 ‰) close to the average values of graphite in metals and in the silicate matrix, thus strongly suggesting that they originated from a mixture of graphite inclusions in metals and silicate matrix graphite during a closed system crystallization process subsequent to silicate-metal-sulfide partial melting. Troilite-orthopyroxene quench symplectite textures in orthopyroxene rims are clear evidence that silicate-sulfide partial melting took place in Acapulco. Due to petrographic heterogeneity on a centimeter scale, bulk REE abundances of individual samples or of individual minerals provide only limited information and the REE abundances alone are not entirely adequate to unravel the formational processes that prevailed in the acapulcoite-lodranite parent body. The present investigations demonstrate the complexity of the evolutionary stages of acapulcoites from accretion to parent body processes.     

Two-dimensional modeling of contaminant transport in porous media in the presence of colloids

It has long been known that colloids can facilitate the transport of contaminants in groundwater systems by reducing the effective retardation factor. A significant effort has been devoted to study colloid-facilitated contaminant transport during the past decade. Many of the previous studies were restricted to one-dimensional analyses and comparisons with finite-column experiments. In this work, a two-dimensional numerical model is developed and used to study the different interactions between colloids, contaminants, and porous media under homogeneous conditions. The numerical formulation of the model is based on discretizing mass balance equations and reaction equations using finite differences having a third-order, total variance-diminishing scheme for the advection terms. This scheme significantly reduces numerical dispersion and leads to greater accuracy compared to the standard central-differencing scheme. The model is tested against analytical solutions under simplified conditions as well as against experimental data, and the results are favorable. The model is used to investigate the impact of the various reaction rates and parameter values on the movement of contaminant plumes in two dimensions. The model is also used to investigate the hypothesis that colloids may increase the effective retardation factor of contaminant plumes. The analysis shows that assuming kinetic mass exchange between contaminant and colloids with constant reaction rate coefficients that are not related to the concentrations may lead to inaccurate results. These inaccurate results are exemplified in the finding that under the kinetic assumption the ratio of the initial concentration of colloids to the initial concentration of contaminant does not affect the amount of facilitation or retardation that occurs in the system. It is also found that colloids can increase the effective retardation factor for the contaminant under certain combinations of reaction rates and distribution coefficients. A quantitative empirical expression to identify whether colloids retard or facilitate the contaminant movement is presented.