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1.
Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) are persistent organic pollutants (POPs) that are formed and released unintentionally from anthropogenic sources. The high persistence of PCDD/Fs results in the concentrations of these contaminants in environment decreasing only very slowly. Two transport pathways, air and water, carry PCDD/Fs into all regions of the world. Recently, more frequent extreme weather events, such as storms and floods, have been projected to occur as a result of global warming. Extreme weather events have a documented impact on the remobilization and subsequent bioavailability of POPs. In this study, three specific episodes, namely winter monsoon, southeast biomass burning and tropical cyclone (typhoon) events, which influence the environmental fate and transport of PCDD/Fs in Taiwan, were evaluated based on a climate change scenario. During the winter (northeast) monsoon period, the temperature and relative humidity observed in northern Taiwan decreases sharply. During this time, the quantity of PCDD/Fs adsorbed onto suspended particles, as observed at background sites, was found to increase from 300 ± 127 to 630 ± 115 pg I-TEQ g-TSP−1, which is even higher than that measured in Taipei City (438 ± 80 pg I-TEQ g-TSP−1). Hence, the winter monsoon not only brings cold air but also transports air pollutants and dust over long distances from mainland China to Taiwan. During the 2010 Southeast Asia biomass burning events (2010/3/22–3/28), the level of atmospheric PCDD/Fs were measured in central Taiwan (Mt. Lulin) and in the source region of northern Thailand (Chiang Mai); this revealed that the variations in atmospheric PCDD/F concentrations at these two sites followed a similar pattern. On 25 March 2010, the atmospheric PCDD/F concentration increased dramatically from 1.43 to 6.09 fg I-TEQ m−3 at Mt. Lulin and from 7.64 to 12.1 fg I-TEQ m−3 in northern Thailand. However, the atmospheric PCDD/F concentration decreased dramatically 1 day after the biomass burning event. Based on the measurements from a dated sediment core collected at a reservoir in northern Taiwan, the sharp increases in input fluxes of PCDD/Fs and mineral-derived elements levels in 1990 (20 ng I-TEQ m−2 year−1), 2001 (17 ng I-TEQ m−2 year−1), 2004 (16 ng I-TEQ m−2 year−1) and 2005 (15 ng I-TEQ m−2 year−1) seem to be a result of a deep turbid layer formed upstream due to landslides and/or mud flows during the typhoon season. This finding demonstrates the effect of typhoon events on the long-term remobilization of PCDD/Fs as well as supporting the hypothesis that such events would have the potential to remobilize pollutants that have been deposited previously.  相似文献   

2.
Rapid weathering and erosion rates in mountainous tropical watersheds lead to highly variable soil and saprolite thicknesses which in turn impact nutrient fluxes and biological populations. In the Luquillo Mountains of Puerto Rico, a 5-m thick saprolite contains high microorganism densities at the surface and at depth overlying bedrock. We test the hypotheses that the organisms at depth are limited by the availability of two nutrients, P and Fe. Many tropical soils are P-limited, rather than N-limited, and dissolution of apatite is the dominant source of P. We document patterns of apatite weathering and of bioavailable Fe derived from the weathering of primary minerals hornblende and biotite in cores augered to 7.5 m on a ridgetop as compared to spheroidally weathering bedrock sampled in a nearby roadcut.Iron isotopic compositions of 0.5 N HCl extracts of soil and saprolite range from about δ56Fe = 0 to ? 0.1‰ throughout the saprolite except at the surface and at 5 m depth where δ56Fe = ? 0.26 to ? 0.64‰. The enrichment of light isotopes in HCl-extractable Fe in the soil and at the saprolite–bedrock interface is consistent with active Fe cycling and consistent with the locations of high cell densities and Fe(II)-oxidizing bacteria, identified previously. To evaluate the potential P-limitation of Fe-cycling bacteria in the profile, solid-state concentrations of P were measured as a function of depth in the soil, saprolite, and weathering bedrock. Weathering apatite crystals were examined in thin sections and an apatite dissolution rate of 6.8 × 10? 14 mol m? 2 s? 1 was calculated. While surface communities depend on recycled nutrients and atmospheric inputs, deep communities survive primarily on nutrients released by the weathering bedrock and thus are tightly coupled to processes related to saprolite formation including mineral weathering. While low available P may limit microbial activity within the middle saprolite, fluxes of P from apatite weathering should be sufficient to support robust growth of microorganisms in the deep saprolite.  相似文献   

3.
《Applied Geochemistry》2006,21(11):1955-1968
Elemental Hg–Au amalgamation mining practices are used widely in many developing countries resulting in significant Hg contamination of surrounding ecosystems. The authors examined for the first time Hg contamination in air, water, sediment, soil and crops in the Tongguan Au mining area, China, where elemental Hg has been used to extract Au for many years. Total gaseous Hg (TGM) concentrations in ambient air in the Tongguan area were significantly elevated compared to regional background concentrations. The average TGM concentrations in ambient air in a Au mill reached 18,000 ng m−3, which exceeds the maximum allowable occupational standard for TGM of 10,000 ng m−3 in China. Both total and methyl-Hg concentrations in stream water, stream sediment, and soil samples collected in the Tongguan area were elevated compared to methyl-Hg reported in artisanal Au mining areas in Suriname and the Amazon River basin. Total Hg concentrations in vegetable and wheat samples ranged from 42 to 640 μg kg−1, all of which significantly exceed the Chinese guidance limit for vegetables (10 μg kg−1) and foodstuffs other than fish (20 μg kg−1). Fortunately, methyl-Hg was not significantly accumulated in the crops sampled in this study, where concentrations varied from 0.2 to 7.7 μg kg−1.  相似文献   

4.
The cirques of Snowdonia, North Wales were last occupied by glacier ice during the Younger Dryas Chronozone (YDC), c. 12.9–11.7 ka. New mapping presented here indicates 38 small YDC cirque glaciers formed in Snowdonia, covering a total area of 20.74 km2. Equilibrium line altitudes (ELAs) for these glaciers, calculated using an area–altitude balance ratio (AABR) approach, ranged from 380 to 837 m asl. A northeastwards rise in YDC ELAs across Snowdonia is consistent with southwesterly snow-bearing winds. Regional palaeoclimate reconstructions indicate that the YDC in North Wales was colder and drier than at present. Palaeotemperature and annual temperature range estimates, derived from published palaeoecological datasets, were used to reconstruct values of annual accumulation and ‘winter balance plus summer precipitation’ using a degree-day model (DDM) and non-linear regression function, respectively. The DDM acted as the best-estimate for stadial precipitation and yielded values between 2073 and 2687 mm a?1 (lapse rate: 0.006 °C m?1) and 1782–2470 mm a?1 (lapse rate: 0.007 °C m?1). Accounting for the potential input of windblown and avalanched snow onto former glacier surfaces, accumulation values dropped to between 1791 and 2616 mm a?1 (lapse rate: 0.006 °C m?1) and 1473–2390 mm a?1 (lapse rate: 0.007 °C m?1). The spatial pattern of stadial accumulation suggests a steep precipitation gradient and provides verification of the northeastwards rise in ELAs. Glaciers nearer the coast of North Wales were most responsive to fluctuations in climate during the YDC, responding to sea-ice enforced continentality during the coldest phases of the stadial and to abrupt warming at the end of the stadial.  相似文献   

5.
《Applied Geochemistry》2006,21(11):1855-1867
Methylmercury (MeHg) and total Hg (THg) concentrations in soil profiles were monitored in the Thur River basin (Alsace, France), where a chlor-alkali plant has been located in the city of Vieux-Thann since the 1930s. Three soil types were studied according to their characteristics and location in the catchment: industrial soil, grassland soil and alluvial soil. Contamination of MeHg and THg in soil was important in the vicinity of the plant, especially in industrial and alluvial soil. Concentrations of MeHg reached 27 ng g−1 and 29,000 ng g−1 for THg, exceeding the predictable no effect concentration. Significant ecotoxicological risk exists in this area and remedial actions on several soil types are suggested. In each type of soil, MeHg concentrations were highest in topsoil, which decreased with depth. Concentrations of MeHg were negatively correlated with soil organic matter and total S, particularly when MeHg concentrations exceeded 8 ng g−1. Under these conditions, MeHg concentrations in soil seemed to be influenced by THg, soil organic matter and total S concentrations. It was found that high MeHg/THg ratios (near 2%) in soil were mainly related to the combined soil environmental conditions such as low THg concentrations, low organic C/N ratios (<11) and relatively low pH (5–5.5). Nevertheless, even when the MeHg/THg ratio was low (∼0.04%), MeHg and THg concentrations were elevated, up to 13 ng g−1 and to 29,000 ng g−1, respectively. Thus, both THg and MeHg concentrations should be taken into account to assess potential environmental risks of Hg.  相似文献   

6.
Mercury concentrations were determined in stream sediments from the Camaquã River Basin, located in the shield region of the state of Rio Grande do Sul, southern Brazil. The resulting geochemical data show that overbank floodplain deposits exhibit higher concentrations than sediments collected from the active channel bed. In addition, higher Hg concentrations were measured in the fine(<63 μm) sediment fraction of the samples. Total Hg concentrations in the fine fraction of active stream sediments from Lavras do Sul County, which have been influenced by past gold mining activities, have decreased during the last five years to values ≤142 ng g−1. However, in a settling pond containing abandoned mine wastes, the Hg concentration of a bulk sample remained exceptionally high (5220 ng g−1). Preliminary speciation results show that Hg0 is the predominant species in most of the samples. This was the form of Hg released by the gold amalgamation activities in the area, and appears to be relatively stable under the existing Eh and pH conditions.  相似文献   

7.
《Applied Geochemistry》2005,20(3):627-638
Concentrations of total Hg and methylmercury (MMHg) in riparian soil, mine-waste calcine, sediment, and moss samples collected from abandoned Hg mines in Wanshan district, Guizhou province, China, were measured to show regional dispersion of Hg-contamination. High total Hg and MMHg concentrations obtained in riparian soils from mined areas, ranged from 5.1 to 790 mg kg−1 and 0.13 to 15 ng g−1, respectively. However, total Hg and MMHg concentrations in the soils collected from control sites were significantly lower varying from 0.1 to 1.2 mg kg−1 and 0.10 to 1.6 ng g−1, respectively. Total Hg and MMHg concentrations in sediments varied from 90 to 930 mg kg−1 and 3.0 to 20 ng g−1, respectively. Total Hg concentrations in mine-waste calcines were highly elevated ranging from 5.7 to 4400 mg kg−1, but MMHg concentrations were generally low ranging from 0.17 to 1.1 ng g−1. Similar to the high Hg concentrations in soil and sediments, moss samples collected from rocks ranged from 1.0 to 95 mg kg−1 in total Hg and from 0.21 to 20 ng g−1 in MMHg. Elevated Hg concentrations in mosses suggest that atmospheric deposition might be an important pathway of Hg to the local terrestrial system. Moreover, the spatial distribution patterns of Hg contamination in the local environment suggest derivation from historic Hg mining sites in the Wanshan area.  相似文献   

8.
Empirically derived algorithms are suggested by means of which it is possible to evaluate relations between physical properties in silty salt marsh clay. A relation between loss on ignition, sand content and bulk dry density in the topmost 5 cm was found to explain 84% of the variation of the latter. The bulk dry density in the topmost ≈ 0.5 m was found to vary as a logarithmic function of depth below the surface controlled by two constants directly dependent on the bulk dry density in the topmost 5 cm. Integration of this function illustrates that mass depth (MSDz) down core can be directly related to the bulk dry density of the surface layer. For sediments with a surface bulk dry density between 400 kg m? 3 and 800 kg m? 3 the porosity was found to vary (+/?10%) with MSDz as another logarithmic function. The results allow for an evaluation of the use of marker horizons in the topmost layers. Right after such a layer has been spread on the surface, sedimentation measured in length per time (accretion), will be significantly larger than for subsequent periods. Using marker horizons, it is therefore not trivial to know the level of the marker, as deeper located markers will indicate successively smaller accretion rates with the same sediment input.  相似文献   

9.
Increased seismicity and occurrences of hot springs having surface temperature of 36–58 °C are observed in the central part of India (74–81° E, 20–25° N), where the NE trending Middle Proterozoic Aravalli Mobile Belt meets the ENE trending Satpura Mobile Belt. Earlier Deep Seismic Sounding (DSS) studies along Thuadara-Sendhwa-Sindad profile in the area has showed Mesozoic Sediments up to around 4 km depth covered by Deccan Trap and the Moho depth with a boundary velocity (Pn) of 8.2 km/s. In the present study, surface heat flow of 48 ± 4 mW m?2 has been estimated based on Pn velocity, which agrees with the value of heat flow of 52 ± 4 mW m?2 based on Curie point isotherms estimates. The calculated temperature-depth profile shows temperature of 80–120 °C at the basement, which is equivalent to oil window temperature in Mesozoic sediments and around 570–635 °C at Moho depth of 38–43 km and the thermal lithosphere is about 110 km thick, which is comparatively higher than those of adjoining regions. The present study reveals the brittle–ductile transition zone at 14–41 km depth (temperature around 250–600 °C) where earthquake nucleation takes place.  相似文献   

10.
Phosphorite from the Meade Peak Phosphatic Shale member of the Permian Phosphoria Formation has been mined in southeastern Idaho since 1906. Dumps of waste rock from mining operations contain high concentrations of Se which readily leach into nearby streams and wetlands. While the most common mineralogical residence of Se in the phosphatic shale is elemental Se, Se(0), Se is also an integral component of sulfide phases (pyrite, sphalerite and vaesite–pyritess) in the waste rock. It may also be present as adsorbed selenate and/or selenite, and FeSe2 and organo-selenides.Se release from the waste rock has been observed in field and laboratory experiments. Release rates calculated from waste rock dump and column leachate solutions describe the net, overall Se release from all of the possible sources of Se listed above. In field studies, Se concentration in seepage water (pH 7.4–7.8) from the Wooley Valley Unit 4 dump ranges from 3600 µg/L in May to 10 µg/L by Sept. Surface water flow, Q, from the seep also declines over the summer, from 2 L/s in May to 0.03 L/s in Sept. Se flux ([Se] ? Q) reaches a steady-state of < 150 mg/day in 1–4 months, depending upon the volume of Q. Se release (mg/L) follows a first order reaction with a rate constant, k, = 1.35 – 6.35e?3 h? 1 (11.8–55.6 yr? 1).Laboratory experiments were performed with the waste shale in packed bed reactors; residence time varied from 0.09 to 400 h and outlet pH ～ 7.5. Here, Se concentration increased with increasing residence time and release was modeled with a first order reaction with k = 2.19e?3 h? 1 (19.2 yr? 1).Rate constants reported here fall within an order of magnitude of reported rate constants for oxidation of Se(0) formed by bacterial precipitation. This similarity among rate constants from both field and laboratory studies combined with the direct observation of Se(0) in waste shales of the Phosphoria Formation suggests that oxidation of Se(0) may control steady-state Se concentration in water draining the Wooley Valley waste dump.  相似文献   

11.
The solubility of synthetic ZnS(cr) was measured at 25–250 °C and P = 150 bars as a function of pH in aqueous sulfide solutions (~ 0.015–0.15 m of total reduced sulfur). The solubility determinations were performed using a Ti flow-through hydrothermal reactor. The solubility of ZnS(cr) was found to increase slowly with temperature over the whole pH range from 2 to ~ 10. The values of the Zn–S–HS complex stability constant, β, were determined for Zn(HS)20(aq), Zn(HS)3?, Zn(HS)42?, and ZnS(HS)?. Based on the experimental values the Ryzhenko–Bryzgalin electrostatic model parameters for these stability constants were calculated, and the ZnS(cr) solubility and the speciation of Zn in sulfide-containing hydrothermal solutions were evaluated. The most pronounced solubility increase, about 3 log units at m(Stotal) = 0.1 for the temperatures from 25 to 250 °C, was found in acidic solutions (pH ~ 3 to 4) in the Zn(HS)20(aq) predominance field. In weakly alkaline solutions, where Zn(HS)3? and Zn(HS)42? are the dominant Zn–S–HS complexes, the ZnS(cr) solubility increases by 1 log unit at the same conditions. It was found that ZnS(HS)? and especially Zn(HS)42? become less important in high temperature solutions. At 25 °C and m(Stotal) = 0.1, these species dominate Zn speciation at pH > 7. At 100 °C and m(Stotal) = 0.1, the maximum fraction of Zn(HS)42? is only 20% of the total Zn concentration (i.e. at pHt ~ 7.5), whereas at 350 °C and 3 <pHt <10, the fraction of Zn(HS)42? and ZnS(HS)? is less than 0.05% and 2.5% respectively, of the total Zn concentration and Zn(HS)20 and Zn(HS)3? predominate. The measured equilibrium formation constants were combined with the literature data on the stability of Zn–Cl complexes in order to evaluate the concentration and speciation of Zn in chloride solutions. It was found that at acidic pH, and in more saline fluids having total chloride > 0.05 m, Zn–Cl complexes are responsible for hydrothermal Zn transport with no significant contribution of Zn–S–HS complexes. The hydrosulfide/sulfide complexes will play a more important role in lower salinity (< 0.05 m chloride) hydrothermal solutions which are characteristic of many epithermal ore depositing environments. The value of ΔfG° (β-ZnS(cr)) = ? 198.6 ± 0.2 kJ/mol at 25 °C was determined via solubility measurements of natural low-iron Santander (Spain) sphalerite.  相似文献   

12.
Tidal marshes act as a buffer system for nutrients in the pore water and play important roles in controlling the budget of nutrients and pollutants that reach the sea. Spatial and seasonal dynamics of pore water nutrients were surveyed in three tidal marshes (Chongming Island, Hengsha Island, and Fengxian tidal flat) near the Yangtze Estuary and Hangzhou Bay from August 2007 to May 2008. Nutrient variations in pore water closely followed seawater quality in the estuaries, while the average concentration of NH4 +–N, the main form of inorganic nitrogen in pore water, was over two orders of magnitude higher than that in seawater which was dominated by nitrate. NH4 +–N export (13.81 μmol m?2 h?1) was lower than the import of (NO3 ?+NO2 ?)–N (?24.17 μmol m?2 h?1) into sediment over the 1-year period, hence reducing N-eutrophication in coastal waters. The export of SiO3 2?–Si and PO4 3?–P from tidal marshes regulated nutrient level and composition and lifted the ratio beyond potentidal element limitation in the coastal system. Moreover, macrophyte plants (Spartina alterniflora and Phragmites australis) played significant roles in controlling nutrient concentration in pore water and its exchange between marshes and estuaries. Fengxian marsh was characterized by higher nutrient concentrations and fluxes than other marshes in response to the more serious eutrophication in Hangzhou Bay than in the Yangtze Estuary.  相似文献   

13.
Dissolved and particulate Zn and Ni concentrations were determined at 76 locations along the Yangtze River basin from the headwaters to the estuary during flood and dry seasons. Spatial and temporal variations of Zn and Ni were investigated and six major source zones were identified. The Three Gorges Dam (TGD) blocked most of the suspended loads and extremely low concentration of Zn and Ni were observed downstream of the dam. Dissolved (ranging from 0.062 to 8.0 μg L−1) and particulate (ranging from 12 to 110 mg kg−1) Ni showed similar levels of concentrations during flood and dry seasons, whereas dissolved (ranging from 0.43 to 49 μg L−1) and particulate (ranging from 54 to 1100 mg kg−1) Zn were slightly and much lower in the flood season than dry season, respectively. This was attributed to the increased water discharge during the flood season causing a dilution effect and sediment resuspension. In the flood season, average concentrations of Zn and Ni were higher in the main channel than in tributaries, due to soil erosion and mining activities providing the dominant inputs. The situation was opposite in the dry season, attributed to the contribution of municipal sewage, industrial activities, and waste disposal. During the flood season, dissolved Zn and Ni concentrations were negatively correlated with pH. Water and suspended particulate matter (SPM) from the upper reaches, middle reaches, and lower reaches of the Yangtze River were characterized by their Zn and Ni concentrations. The Panzhihua, Nanling and Tongling mining areas were considered as the most important source zones of particulate Zn and Ni. The Chongqing region, Wuhan region and the Yangtze River Delta provided most of the dissolved Zn and Ni inputs into the river. Annual net flux of Zn (10–72 × 105 kg a−1) and Ni (5.0–19 × 105 kg a−1) in each source zone were estimated according to their respective influent and effluent fluxes. Contributions of the source zones to Zn and Ni transport decreased from the upper reaches to the lower reaches.  相似文献   

14.
Soils act as sources and sinks for greenhouse gases (GHG) such as carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O). Since both storage and emission capacities may be large, precise quantifications are needed to obtain reliable global budgets that are necessary for land-use management (agriculture, forestry), global change and for climate research. This paper discusses exclusively the soil emission-related processes and their influencing parameters. It reviews soil emission studies involving the most important land-cover types and climate zones and introduces important measuring systems for soil emissions. It addresses current shortcomings and the obvious bias towards northern hemispheric data.When using a conservative average of 300 mg CO2e m−2 h−1 (based on our literature review), this leads to global annual net soil emissions of ≥350 Pg CO2e (CO2e = CO2 equivalents = total effect of all GHG normalized to CO2). This corresponds to roughly 21% of the global soil C and N pools. For comparison, 33.4 Pg CO2 are being emitted annually by fossil fuel combustion and the cement industry.  相似文献   

15.
146Sm–142Nd and 147Sm–143Nd systematics were investigated in garnet inclusions in diamonds from Finsch (S. Africa) and Hadean zircons from Jack Hills (W. Australia) to assess the potential of these systems as recorders of early Earth evolution. The study of Finsch inclusions was conducted on a composite sample of 50 peridotitic pyropes with a Nd model age of 3.3 Ga. Analysis of the Jack Hills zircons was performed on 790 grains with ion microprobe 207Pb/206Pb spot ages from 3.95 to 4.19 Ga. Finsch pyropes yield 100 × ?142Nd = ? 6 ± 12 ppm, ?143Nd = ? 32.5, and 147Sm/144Nd = 0.1150. These results do not confirm previous claims for a 30 ppm 142Nd excess in South African cratonic mantle. The lack of a 142Nd anomaly in these inclusions suggests that isotopic heterogeneities created by early mantle differentiation were remixed at a very fine scale prior to isolation of the South African lithosphere. Alternatively, this result may indicate that only a fraction of the mantle experienced depletion during the first 400 Myr of its history. Analysis of the Jack Hills zircon composite yielded 100 × ?142Nd = 8 ± 10 ppm, ?143Nd = 45 ± 1, and 147Sm/144Nd = 0.5891. Back-calculation of this present-day ?143Nd yields an unrealistic estimate for the initial ?143Nd of ? 160 ?-units, clearly indicating post-crystallization disturbance of the 147Sm–143Nd system. Examination of 146,147Sm–142,143Nd data reveals that the Nd budget of the Jack Hills sample is dominated by non-radiogenic Nd, possibly contained in recrystallized zircon rims or secondary subsurface minerals. This secondary material is characterized by highly discordant U–Pb ages. Although the mass fraction of altered zircon is unlikely to exceed 5–10% of total sample, its high LREE content precludes a reliable evaluation of 146Sm–142Nd systematics in Jack Hills zircons.  相似文献   

16.
Uranium(VI) sorption onto kaolinite was investigated as a function of pH (3–12), sorbate/sorbent ratio (1 × 10?6–1 × 10?4 M U(VI) with 2 g/L kaolinite), ionic strength (0.001–0.1 M NaNO3), and pCO2 (0–5%) in the presence or absence of 1 × 10?2–1 × 10?4 M citric acid, 1 × 10?2–1 × 10?4 M EDTA, and 10 or 20 mg/L fulvic acid. Control experiments without-solids, containing 1 × 10?6–1 × 10?4 M U(VI) in 0.01 M NaNO3 were used to evaluate sorption to the container wall and precipitation of U phases as a function of pH. Control experiments demonstrate significant loss (up to 100%) of U from solution. Although some loss, particularly in 1 × 10?5 and 1 × 10?4 M U experiments, is expected due to precipitation of schoepite, adsorption on the container walls is significant, particularly in 1 × 10?6 M U experiments. In the absence of ligands, U(VI) sorption on kaolinite increases from pH ～3 to 7 and decreases from pH ～7.5 to 12. Increasing ionic strength from 0.001 to 0.1 M produces only a slight decrease in U(VI) sorption at pH < 7, whereas 10% pCO2 greatly diminishes U(VI) sorption between pH ～5.5 and 11. Addition of fulvic acid produces a small increase in U(VI) sorption at pH < 5; in contrast, between pH 5 and 10 fulvic acid, citric acid, and EDTA all decrease U(VI) sorption. This suggests that fulvic acid enhances U(VI) sorption slightly via formation of ternary ligand bridges at low pH, whereas EDTA and citric acid do not form ternary surface complexes with the U(VI), and that all three ligands, as well as carbonate, form aqueous uranyl complexes that keep U(VI) in solution at higher pH.  相似文献   

17.
Isotopic characteristics of river sediments on the Tibetan Plateau   总被引：1，自引：0，他引：1  
We systematically collected 40 modern clastic sediment samples from rivers in different tectonic units of the Tibetan Plateau and measured their Sr–Nd isotopic compositions. The isotopic characteristics provide insight into the controversial paleo-tectonic affinity of terranes of the Tibetan Plateau and the provenance of Songpan–Ganzi flysch complex. The Qilian Terrane and Himalaya Terrane have more negative εNd(0) values (from ? 14.3 to ? 11.8 and from ? 20.64 to ? 13.26, respectively) and high 87Sr/86Sr values (from 0.719674 to 0.738818 and from 0.721020 to 0.824959, respectively), reflecting old and mature continental crust origin of these two terranes. The southern Lhasa Terrane is more radiogenic in εNd(0) values (from ? 8.82 to ? 3.8) and low in 87Sr/86Sr values (from 0.711504 to 0.719489), implying the combined impact of the Neo-Tethys mantle and Himalaya old continental crust. Sr–Nd isotopic compositions of the Qilian Terrane are similar to those in the Yangtze Craton, indicating that the Qilian Terrane was probably separated from the Yangtze Craton. Sr–Nd isotopic characteristics of the Songpan–Ganzi Terrane are similar to the Yangtze Craton and are remarkably different to those in the North China Craton, eastern Kunlun–Qaidam and the central Qiangtang metamorphic belt, implying that the widely distributed flysch complex of the Songpan–Ganzi Terrane was sourced from the Yangtze Craton.  相似文献   

18.
LA–ICP–MS zircon U–Pb ages, geochemical and Sr–Nd–Pb isotope data are presented for mafic–ultramafic complexes from the southern Liaoning–southern Jilin area with the aim of determining the nature of the Mesozoic lithospheric mantle and to further constrain the spatial extent of destruction of the North China Craton (NCC). The complexes consist of olivine-websterite, gabbro, dolerite, and gabbro-diorite. Zircons from the complexes show typical zoning absorption, are euhedral–subhedral in shape, and yield high Th/U ratios (1.23–2.87), indicating a magmatic origin. Zircon U–Pb age data indicate that they formed in the Early Cretaceous (129–137 Ma). Geochemically, they have SiO2 = 44.3–49.8%, MgO = 6.8–26.5%, Cr = 102–3578 ppm, and Ni = 31–1308 ppm, and are characterized by enrichment in large ion lithophile elements (LILEs) and light rare earth elements (LREEs), and depletion in high field strength elements (HFSEs) and heavy rare earth elements (HREEs), as well as a wide range of Sr–Nd–Pb isotopic compositions [(87Sr/86Sr)i = 0.70557–0.71119; εNd (t) = ?5.4 to ?20.1; (206Pb/204Pb)i = 15.13–17.85; Δ7/4 = ?11.49 to 16.00; Δ8/4 = 102.64–203.48]. Compared with the southern Liaoning mafic–ultramafic rocks, the southern Jilin mafic–ultramafic rocks have high TiO2 and Al2O3 contents, high εNd (t) values, low (La/Yb)N values, low initial 87Sr/86Sr ratios, and low radiogenic Pb isotopic compositions. These findings indicate that the primary magmas of the southern Jilin complexes were derived from lithospheric mantle that was previously metasomatized by a melt derived from the delaminated ancient lower crust, whereas the primary magmas of the southern Liaoning complexes originated from partial melting of a lithospheric mantle source that was previously modified by melt derived from the broken-off Yangtze slab. Therefore, the lateral extent of the NCC destruction should include the southern Liaoning–southern Jilin area.  相似文献   

19.
A Human Health Risk Assessment (HHRA) was required for a closed landfill located in Cerdanyola del Vallès (Barcelona, Spain). The HHRA had two objectives, to evaluate the present risk of the identified receptors in the area and to safely develop the future urban planning of the area, therefore 3 scenarios for the current situation and 4 for the future situation were developed.After reviewing the existing data and exploring the needs of information, the assessment in this study was focused on the measurement of volatile organic compounds (VOCs) fluxes from the subsoil (emission from the landfill at 5 points), concentrations of VOCs in the air (immission in 4 urban sites) and concentration of VOCs in soil–gas (measurements at 5 m below ground surface outside the landfill at 8 sites). Around 70 VOCs were analyzed by using multi-sorbent tubes and Thermal Desorption Gas Chromatography (TD–GC–MS). The VOCs that were detected and quantified include alkanes, aromatic hydrocarbons, alcohols, ketones, halocarbons, aldehydes, esters, terpenoids, ethers and some nitrogenated and sulfur compounds, furans and carboxylic acids. Specific mercury flux measurements were performed in a hot spot by using carulite tubes, that were also analyzed by using Thermal Decomposition, Amalgamation, and Atomic Absorption Spectrophotometry.Results showed average values of volatile emission fluxes ranging from non-detected to 331 μg m−2 day−1 (dichlorodifluoromethane). In the case of immission, the concentration of VOCs measured in the air of populated area surrounding the landfill ranged values from non-detected to 42.0 μg m−3 (acetic acid). The soil–gas measurements in piezometers around the landfill showed individual VOC values with a maximum 830 μg m−3 for dichlorodifluoromethane.With the obtained fluxes and concentrations in air and soil–gas, USEPA methodology and modeling was used to evaluate equivalent concentration in the scenarios considered. Toxicity values from IRIS database were used to finally obtain chemical risk indicators. Admissible risk indicators were obtained in all scenarios. The VOCs that contributed more to risk indexes in RH2 were trichloroethylene, trimethylbenzene, chloroform, 1,2-dichloroethane and carbon tetrachloride. The carcinogenic risk in RH7 was linked to the presence of benzene and chloroform. The comparison of the measurements of the present work with other landfills evidence that HHRA in ambient air would be needed in order to perform a correct landfill management.  相似文献   

20.
Trace element contents and distributions in authigenic quartz cement in deeply buried (2500–4000 m) Haushi Group sandstones from wells in Oman have been investigated in order to determine the factors that control trace element uptake during precipitation.Scanning electron microscope-cathodoluminescence images show well developed growth zones within the quartz cement, which correlate with chemical zonations observed in electron microprobe Al distribution maps. The most abundant trace elements are Al (50–3000 μg g?1), Li (1–100 μg g?1), Na (1–40 μg g?1), and Ge (0.3–5 μg g?1) with a strong linear correlation between Li and Al and a weaker one between Ge and Al. The molar concentration of Li (+ Na) accounts only for ~ 15% of the charge compensation for Al3+ substitution of Si4+. Though H was not measured in this study, these data indicate a major role of H in charge balancing Al3+. The samples belong to the same stratigraphic unit and have similar petrography, but show considerable variability in absolute trace element concentrations between different wells. This variability does not correlate with either sample depth or temperature and shows no regional pattern, but seems to reflect petrophysical and tectonic differences within the sedimentary basin.Petrographic observations of the cogenetic mineral assemblages and hydrochemical modelling indicate that a change from the equilibrium assemblage quartz–kaolinite (–dolomite) to quartz–illite (–dolomite) reflects a decrease in the CO2 concentration and concurrent variations of the Al concentration. It is concluded that changes in the CO2 concentrations are responsible for fluctuations in fluid Al concentrations and thus likely also in the investigated quartz cements.  相似文献   

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