Hydrocarbon-based indicators for characterizing potential sources of coal-derived pollution in the vicinity of the Ostrava City     

Eva Geršlova  Jan Schwarzbauer 《Environmental Earth Sciences》2014,71(7):3211-3222

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Brick kiln exhaust as a source of polycyclic aromatic hydrocarbons (PAHs) in the surrounding soil and plants: a case study from the city of Peshawar, Pakistan     

F. Akbar Jan  Sabir Khan  M. Ishaq  M. Naeem  I. Ahmad  Sajjad Hussain 《Arabian Journal of Geosciences》2014,7(1):13-19

The purpose of the present study was to investigate the effects of brick kiln exhaust on the quantity of polycyclic aromatic hydrocarbons in surrounding soils and plants. In Pakistan, a big problem is the rapid conglomeration of the brick kilns in out skirt of nearly all urban centers to cope with the rapid construction work in big cities. A huge amount of low-grade coal, rubber, tires is used in non-scientific manner. The study was conducted in the City of Peshawar the capital of Kyber Pakhtunkhwa where many brick kilns are located in the periurban areas. Soil and medicinal plants samples were collected from different locations around the bricks kiln and were analyzed for selected polycyclic aromatic hydrocarbons (PAHs), i.e., benzo(a)pyrene, anthracene, chrysene, flourene, flouranthene, phenanthrene, naphthalene, and acenapthylene. Quantitative and qualitative analysis was carried out by UV spectrophotometer and high-performance liquid chromatography. Benzo[a]pyren and Chrysene were found to be the most abundant compounds. The total load of PAHs in the central location was found to be 0.4014 mg/kg. General trend of PAHs distribution was such that the concentration of individual PAHs was found to increase with depth clearly indicating their absorption in the soil. PAHs concentration increased with the distance up to 300 m and then gradual decreased which showed their movement with the water and air. The PAHs load was found high in the leaves as compared to stem and roots. This high load in the aerial parts indicated their excretion route as well as air deposition.  相似文献   

Fluid-assisted retrogression of garnet and P–T history of metapelites from HP/UHP metamorphic terrane (Pohorje Mountains, Eastern Alps)     

Vratislav Hurai  Marian Janák  Rainer Thomas 《Contributions to Mineralogy and Petrology》2010,160(2):203-218

Fluid inclusions in garnet combined with element X-ray mapping, phase equilibrium modelling and conventional thermobarometry have been used to constrain the metamorphic evolution of metapelitic gneiss from the HP/UHP metamorphic terrane of Pohorje Mountains in the Eastern Alps, Slovenia. Retrograde P–T trajectory from ~2.75 GPa and 780°C is constrained by the composition of matrix phengite (6.66 apfu Si) coexisting with garnet cores, kyanite and quartz. The intersection of the X _Prp = 0.25 isopleth for the garnet with the upper stability boundary for K-feldspar in the matrix indicates near-isothermal decompression to ~0.9 GPa at 720°C. Temperatures over 650°C during this stage are corroborated by the high degree of ordering of graphite inclusions associated with Zn, Mg-rich staurolite and phlogopite in the Mg-rich (X _Prp = 0.22–0.25) garnet cores. Majority of garnet porphyroblasts are depleted in Mg (down to X _Prp = 0.09) and enriched in Mn (up to X _Sps = 0.12) along cracks and at their margins. The associated retrograde mineral assemblage comprises Zn, Mg-poor staurolite, muscovite, biotite–siderophyllite, sillimanite and quartz. The onset of the retrogression and the compositional modification of the garnet porphyroblasts were accompanied by the addition of fluid-deposited graphite around older graphite inclusions, probably due to removal of water from a graphite-buffered COH fluid by dissolution in partial silicic melt. Instantaneous expulsion of water near the melt solidus (640°C, max. 0.45 GPa) caused dissolution of the graphite at redox conditions corresponding to 0.25–1.25 logfO₂ units below the QFM buffer, giving rise to a H₂O–CO₂–CH₄ fluid trapped in primary inclusions in Mn-rich, Mg-poor, almandine garnet that reprecipitated within the retrogressed domains. The absence of re-equilibration textures and consistent densities of the fluid inclusions reflect a near-isochoric cooling postdating the near-isothermal decompression. Bulk water content in the metapelite attained 2 wt% during this stage. The low-degree partial melting and extensive hydration due to the release of the internally derived, low-pressure aqueous fluids led to the reset of peak-pressure mineral assemblage.  相似文献   

Quantifying inorganic sources of geochemical energy in hydrothermal ecosystems, Yellowstone National Park, USA     

Everett L. Shock  Melanie Holland  D’Arcy Meyer-Dombard  Jan P. Amend  Tobias P. Fischer 《Geochimica et cosmochimica acta》2010,74(14):4005-4845

Combining analytical data from hot spring samples with thermodynamic calculations permits a quantitative assessment of the availability and ranking of various potential sources of inorganic chemical energy that may support microbial life in hydrothermal ecosystems. Yellowstone hot springs of diverse geochemical composition, ranging in pH from <2 to >9 were chosen for this study, and dozens of samples were collected during three field seasons. Field measurements of dissolved oxygen, nitrate, nitrite, total ammonia, total sulfide, alkalinity, and ferrous iron were combined with laboratory analyses of sulfate and other major ions from water samples, and carbon dioxide, hydrogen, methane, and carbon monoxide in gas samples to evaluate activity products for ∼300 coupled oxidation-reduction reactions. Comparison of activity products and independently calculated equilibrium constants leads to values of the chemical affinity for each of the reactions, which quantifies how far each reaction is from equilibrium. Affinities, in turn, show systematic behavior that is independent of temperature but can be correlated with pH of the hot springs as a proxy for the full spectrum of geochemical variability. Many affinities are slightly to somewhat dependent on pH, while others are dramatically influenced by changes in chemical composition. All reactions involving dissolved oxygen as the electron acceptor are potential energy sources in all hot spring samples collected, but the ranking of dominant electron donors changes from ferrous iron, and sulfur at high pH to carbon monoxide, hydrogen, and magnetite as pH decreases. There is a general trend of decreasing energy yields depending on electron acceptors that follows the sequence: O₂(aq) > NO₃⁻ ≈ NO₂⁻ ≈ S > pyrite ≈ SO₄⁻² ≈ CO(g) ≈ CO₂(g) at high pH, and O₂(aq) ≈ magnetite > hematite ≈ goethite > NO₃⁻ ≈ NO₂⁻ ≈ S ≈ pyrite ≈ SO₄⁻² at low pH. Many reactions that are favorable sources of chemical energy at one set of geochemical conditions fail to provide energy at other conditions, and vice versa. This results in energy profiles supplied by geochemical processes that provide fundamentally different foundations for chemotrophic microbial communities as composition changes.  相似文献   

Iron isotope fractionation during proton- and ligand-promoted dissolution of primary phyllosilicates     

Mirjam Kiczka  Jan G. Wiederhold  Jakob Frommer  Bernard Bourdon 《Geochimica et cosmochimica acta》2010,74(11):3112-6415

We studied stable iron isotope fractionation during dissolution of a biotite and chlorite enriched mineral fraction from granite by HCl and 5 mM oxalic acid in a pH range of 4-5.9. Batch experiments covered a time period from 2 h to 100 days and were performed at initial potassium concentrations of 0, 0.5, and 5 mM to induce different levels of biotite exfoliation. All experiments were kept anoxic to investigate solely the dissolution step without the influence of oxidation and precipitation of secondary Fe oxyhydroxides. Oxalic acid increased the release of Fe by a factor of ∼15 compared with the HCl experiments. Addition of 0.5 mM K to initial solutions in proton-promoted dissolution decreased the release of Fe by 30-65% depending on the dissolution stage. In ligand-controlled dissolution, K reduced the Fe release only to a minor extent. All solutions of the early dissolution stages were enriched in light Fe isotopes by up to −1.4‰ in δ⁵⁶Fe compared with the isotopic composition of biotite and chlorite mineral separates, which we explained by a kinetic isotope effect. In proton-promoted dissolution, early released fractions of K-enriched experiments were significantly lighter (−0.7‰ to −0.9‰) than in the initially K-free experiments. The evolution of Fe isotope ratios in solution was modeled by a linear combination of kinetic isotope effects during two independent dissolution processes attacking different crystallographic sites. In ligand-controlled dissolution, K did not influence the kinetic isotope effect and the Fe isotope composition in solution in the late dissolution stages remained slightly lighter than the bulk composition of the biotite/chlorite enriched mineral fraction. This study demonstrates that the initial Fe weathering flux should be enriched in light Fe isotopes and that Fe isotope data in combination with dissolution kinetics and stoichiometry provide new insights into dissolution mechanisms.  相似文献   

Energetics of potential heterotrophic metabolisms in the marine hydrothermal system of Vulcano Island, Italy     

Karyn L. Rogers  Jan P. Amend   《Geochimica et cosmochimica acta》2006,70(24):6180-6200

Values of overall Gibbs free energy of 144 organic oxidation (respiration) and disproportionation (fermentation) reactions are calculated at the temperatures and chemical compositions that exist in nine submarine vents, sediment seeps and geothermal wells in the hydrothermal system of Vulcano Island, Italy. The organic compounds considered here include four carboxylic acids (formic, acetic, propanoic and lactic), two C₅ aldoses (arabinose and xylose), three C₆ aldoses (galactose, glucose and mannose), and 15 protein-forming amino acids (Ala, Arg, Asp, Glu, Gly, His, Ile, Leu, Lys, Met, Phe, Ser, Thr, Tyr, and Val). Oxidation of these compounds is coupled to five redox pairs: O₂/H₂O, , S⁰/H₂S, and Fe₃O₄/Fe²⁺. Energy yields from potential respiration reactions range from 6 to 118 kJ/mol of electrons transferred and show systematic behavior with respect to the terminal electron acceptor. Overall, respiration with O₂ yields the most energy (98–118 kJ/mol e⁻), followed by reactions with (53– 86 kJ/mol e⁻), magnetite (29–91 kJ/mol e⁻), S⁰ (11–33 kJ/mol e⁻) and (6–34 kJ/mol e⁻). Energy yields show little correlation with organic compound family, but are correlated with fluid pH. Variability in energy yields across the nine sites is greatest for Fe(III) reduction and is primarily influenced by pH and the activity of Fe²⁺. In addition to the potential respiration reactions, the energetics of 24 potential fermentation reactions are also calculated. As expected, fermentation reactions generally yield much less energy than respiration. Normalized to the number of moles of carbon transferred, fermentation yields−8 to 71 kJ/mol C, compared with 16 to 531 kJ/mol C for respiration reactions. All respiration and fermentation reactions, except for methionine (Met) fermentation, are exergonic under the in situ hydrothermal conditions and represent a plethora of potential metabolisms for Vulcano’s diverse thermophilic heterotrophs.  相似文献   

Comparing the activity of aluminum in two B horizons developed from volcanic ash deposits in Japan, dominated by short-range ordered aluminosilicates and crystalline clay minerals, respectively     

Yasumi Yagasaki  Jan Mulder 《Geochimica et cosmochimica acta》2006,70(1):147-163

Mechanisms controlling the activity of free aluminum (Al) in Bw1 horizons of soils developed from volcanic ash deposits in Japan were investigated by means of acid-base titrations and kinetic studies. In a Bw1 horizon, with a high content of acid-oxalate extractable Al, soil solution reached equilibrium with short-range ordered aluminosilicates in the order of days. Relatively fast kinetics of the release and precipitation of Al and Si indicate a high reactivity of short-range ordered aluminosilicates in the soil. In the Bw1 horizon of an adjacent soil, with a high content of crystalline clay minerals like halloysite and interlayered vermiculite, solution remained well undersaturated with respect to short-range ordered aluminosilicates and aluminum hydroxide. Apparent equilibrium with respect to halloysite occurred after more than 30 days. This halloysite ( (25 °C)) has a solubility that is less than that reported in the literature ( (25°C)). Our findings suggest that different reactive aluminosilicates may control the activity of free Al in sub-surface horizons of volcanic ash soils with different mineralogy.  相似文献   

Determination of first-order degradation rate constants from monitoring networks   总被引：1，自引：0，他引：1  

Beyer C  Chen C  Gronewold J  Kolditz O  Bauer S 《Ground water》2007,45(6):774-785

In this article, different strategies for estimating first-order degradation rate constants from measured field data are compared by application to multiple, synthetic, contaminant plumes. The plumes were generated by numerical simulation of contaminant transport and degradation in virtual heterogeneous aquifers. These sites were then individually and independently investigated on the computer by installation of extensive networks of observation wells. From the data measured at the wells, that is, contaminant concentrations, hydraulic conductivities, and heads, first-order degradation rates were estimated by three 1D centerline methods, which use only measurements located on the plume axis, and a two-dimensional method, which uses all concentration measurements available downgradient from the contaminant source. Results for both strategies show that the true rate constant used for the numerical simulation of the plumes in general tends to be overestimated. Overestimation is stronger for narrow plumes from small source zones, with an average overestimation factor of about 5 and single values ranging from 0.5 to 20, decreasing for wider plumes, with an average overestimation factor of about 2 and similar spread. Reasons for this overestimation are identified in the velocity calculation, the dispersivity parameterization, and off-centerline measurements. For narrow plumes, the one- and the two-dimensional strategies show approximately the same amount of overestimation. For wider plumes, however, incorporation of all measurements in the two-dimensional approach reduces the estimation error. No significant relation between the number of observation wells in the monitoring network and the quality of the estimated rate constant is found for the two-dimensional approach.  相似文献   

Changes in nematode communities at the long-term sand extraction site of the Kwintebank (southern bight of the north sea)     

Vanaverbeke J  Deprez T  Vincx M 《Marine pollution bulletin》2007,54(9):1351-1360

We investigated the long-term effects of sand extraction activities on the nematode communities from the Kwintebank. Although changes in nematode community composition cannot be completely uncoupled from natural processes, we suggest that the morphological changes in the sandbank and physical disturbance associated with the dredging activities indeed affected nematode community composition. Nematode diversity did not change since the start of the extraction activities but nematode community composition changed significantly. The SIMPER routine identified predatory nematodes to be important for the within group similarity at the start of the exploitation, while similarity in 1997 and 2001 was determined by the contribution of deposit feeding nematodes. In addition, long nematodes, vulnerable to physical disturbance became less important. These changes are attributed to long term changes in sediment characteristics in combination with additional short-term disturbances by the creation and filling of dredge furrows which are related to the extraction activities.  相似文献   

Compound response of marine and terrestrial ecosystems to varying climate: pre-anthropogenic perspective from bivalve shell growth increments and tree-rings     

Helama S  Schöne BR  Kirchhefer AJ  Nielsen JK  Rodland DL  Janssen R 《Marine environmental research》2007,63(3):185-199

Annual growth increments were examined from shells of the ocean quahog (Arctica islandica L.) from northwest Norway and from tree-ring samples of the Scots pine (Pinus sylvestris L.) from nearby coastal areas. The reconstructed annual growth increments were used to compare growth variability in marine and terrestrial ecosystems. Spatiotemporal comparison of the growth records showed statistically significant correlation during the 19th century A.D., indicative of ecosystem-independent response to pre-anthropogenic climate variations. Geographical correlation between marine and terrestrial records was only observed at the local scale. Years with particularly low winter or high summer North Atlantic Oscillation (NAO) indices showed the best synchronization of marine and terrestrial growth. Despite strong correlation during historical time, our palaeoecological evidence suggests that marine and terrestrial ecosystems may show dissimilar growth reaction to recently observed positive winter-NAO phases.  相似文献