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1.
Effects of short‐term (1 h exposure) and long‐term (7 d exposure) aluminium stress on photosynthesis and reproductive capacity have been studied in Euglena gracilis strain Z. Following concentrations of Altot (added as AlCl3) were tested: 0.5 mg L‐1, 1.0 mg L‐1, 1.5 mg L‐1, 2.5 mg L‐1, 5.0 mg L‐1, 7.5 mg L‐1, 10.0 mg L‐1, and 15.0 mg L‐1 Al, respectively. Growth rates at different aluminium concentrations did not show significant differences, except at 15.0 mg L‐1Al. Initial respiration was higher in long‐term than in the short‐term experiments. It is supposed that an energy‐dependent mechanism of excretion of aluminium ions has been active in the stressed cells. Consequently, the cells of E. gracilis after long‐term exposure to aluminium are believed to be more acclimatised to the aluminium stress. Photosynthetic efficiency (PE) has been negatively affected by aluminium in all experiments performed. Differences between control algae and those treated with aluminium were significant in all cases. PE in long‐term experiments was in general significantly higher at all concentrations of aluminium studied, compared to the short‐term experiments. The aluminium concentrations tested led only to a general decrease in PE while the level of decrease was not especially concentration‐dependent. In general, aluminium tolerance of E. gracilis can be estimated as low, especially by short‐term exposure. However, good acclimatisation capacity of this green flagellate to aluminium doses by long‐term exposure can be supposed.  相似文献   

2.
The aluminium (Al) cycle in glacierised basins has not received a great deal of attention in studies of biogeochemical cycles. As Al may be toxic for biota, it is important to investigate the processes leading to its release into the environment. It has not yet been ascertained whether filterable Al (passing through a pore size of 0.45 μm) is incorporated into biogeochemical cycles in glacierised basins. Our study aims to determine the relationship between the processes bringing filterable Al and glacier‐derived filterable nutrients (particularly Fe and Si) into glacierised basins. We investigated the Werenskiöldbreen basin (44.1 km2, 60% glacierised) situated in SW Spitsbergen, Svalbard. In 2011, we collected meltwater from a subglacial portal at the glacier front and at a downstream hydrometric station throughout the ablation season. The Al concentration, unchanged between the subglacial system and proglacial zone, reveals that aluminosilicate weathering is a dominant source of filterable Al under subglacial conditions. By examining the Al:Fe ratio compared with pH and the sulphate mass fraction index, we found that the proton source for subglacial aluminosilicate weathering is mainly associated with sulphide oxidation and, to a lesser degree, with hydrolysis and carbonation. In subglacial outflows and in the glacial river, Al and Fe are primarily in the forms of Al(OH)4‐ and Fe(OH)3. The annual filterable Al yield (2.7 mmol m‐2) was of a magnitude similar to that of nutrients such as filterable Fe (3.0 mmol m‐2) and lower than that of dissolved Si (18.5 mmol m‐2). Our results show that filterable Al concentrations in meltwater are significantly correlated to filterable and dissolved glacier‐derived nutrients (Fe and Si, respectively) concentrations in glaciers worldwide. We conclude that a potential bioavailable Al pool derived from glacierised basins may be incorporated in biogeochemical cycles, as it is strongly related to the concentrations and yields of glacier‐derived nutrients.  相似文献   

3.
Attenuation of Heavy Metals and Sulfate by Aluminium Precipitates in Acid Mine Drainage During the mixing of acid mine waters with nearly neutral tributaries, often precipitates are formed which are high in iron or aluminium. These precipitates cover the river bed for many kilometres. Near the town of Lehesten (Thuringian slate mining area), leachates of slate quarries and waste rock dumps contain high amounts of aluminium, sulfate, copper, nickel, zinc, manganese, and H+ ions as a result of the oxidation of incorporated pyrite. These leachates enter the brooks Loquitz, Kleine Sormitz, and Rehbach leading to the phenomenon named above. The contribution of the forming aluminium‐rich precipitates on the attenuation of sulfate and heavy metals by sorption or coprecipitation was studied by analysing the composition of water and sediment samples as well as samples of suspended matter. Sulfate is often considered as conservative tracer in acid mine drainage. However, sulfate does not behave conservatively in this system what might be explained by the adsorption of sulfate to the aluminium precipitates. Instead, conservative behaviour was found for calcium, potassium, chloride, zinc, manganese, and nickel. A formation of jurbanite can be excluded because of the low sulfate contents. The sulfate content of the sediment depends on the pH. At low pH values (4.8) the S/Al ratio corresponds to the theoretical ratio in basaluminite and decreases with rising pH. Sulfate is weakly bound to the solid phase and can easily be replaced by OH– ions. A formation of basaluminite is possible at low pH values with a fluent transition to aluminium hydroxide. Therefore the precipitates are assumed to consist predominantly of aluminium hydroxide with sulfate being adsorbed to the surface.  相似文献   

4.
Little is known about the spatial and temporal variability of the stable isotopic composition of precipitation in the North Atlantic and its relationship to the North Atlantic Oscillation (NAO) and anthropogenic climate change. The islands of the Azores archipelago are uniquely positioned in the middle of the North Atlantic Ocean to address this knowledge gap. A survey of spatial and temporal variability of the stable isotope composition of precipitation in Azores is discussed using newly presented analyses along with Global Network of Isotopes in Precipitation data. The collected precipitation samples yield a new local meteoric water line (δ2H = 7.1 * δ18O + 8.46) for the Azores region and the North Atlantic Ocean. The annual isotopic mean of precipitation shows a small range for the unweighted and precipitation mass‐weighted δ18O‐H2O values. Results show an inverse relation between the monthly δ18O‐H2O and the amount of precipitation, which increases in elevation and into the interior of the island. Higher amounts of precipitation (from convective storm systems) do not correspond to the most depleted values of stable isotopes in precipitation. Precipitation shows an orographic effect with depleted δ18O‐H2O values related to the Rayleigh effect. Monthly δ18O‐H2O values for individual precipitation sampling stations show little relationship to air temperature. Results show a local source of moisture during the summer with the characteristics of the first vapour condensate. The stable isotope composition of precipitation is strongly correlated to the NAO index, and δ18O‐H2O values show a statistically significantly trend towards enrichment since 1962 coincident with the increased air temperature and relative humidity due to climate change. Results are in line with observations of increasing sea surface temperature and relative humidity.  相似文献   

5.
Immediately before the extinction of the end‐Guadalupian (Middle Permian; ca 260 Ma), a significant change to the global carbon cycle occurred in the superocean Panthalassa, as indicated by a prominent positive δ13C excursion called the Kamura event. However, the causes of this event and its connection to the major extinction of marine invertebrates remain unclear. To understand the mutual relationships between these changes, we analyzed the sulfur isotope ratio of the carbonate‐associated sulfate (CAS) and HCl‐insoluble residue, as well as the carbon isotope ratio of bulk organic matter, for the Middle‐Upper Permian carbonates of an accreted mid‐oceanic paleo‐atoll complex from Japan, where the Kamura event was first documented. We detected the following unique aspects of the stable carbon and sulfur isotope records. First, the extremely high δ13C values of carbonate (δ13Ccarb) over +5 ‰ during the Capitanian (late Guadalupian) were associated with large isotopic differences between carbonate and organic matter (Δ13C = δ13Ccarb ? δ13Corg). We infer that the Capitanian Kamura event reflected an unusually large amount of dissolved organic matter in the expanded oxygen minimum zone at mid‐depth. Second, the δ34S values of CAS (δ34SCAS) were inversely correlated with the δ13Ccarb values during the Capitanian to early Wuchiapingian (early Late Permian) interval. The Capitanian trend may have appeared under increased oceanic sulfate conditions, which were accelerated by intense volcanic outgassing. Bacterial sulfate reduction with increased sulfate concentrations in seawater may have stimulated the production of pyrite that may have incorporated iron in pre‐existing iron hydroxide/oxide. This stimulated phosphorus release, which enhanced organic matter production and resulted in high δ13Ccarb. Low δ34SCAS values under high sulfate concentrations were maintained and the continuous supply of sulfate cannot by explained only by the volcanic eruption of the Emeishan Trap, which has been proposed as a cause of the extinction. The Wuchiapingian δ34SCAS–δ13Ccarb correlation, likely related to low sulfate concentration, may have been caused by the removal of oceanic sulfate through the massive evaporite deposition.  相似文献   

6.
Solid‐contacted Potentiometric Electrodes for Measurements of Sulfate Ions in Aqueous Solutions A solid‐contact electrode for potentiometric measurement of sulfate ions in aqueous solutions was developed and examined. The electrode is based on a PVC membrane which contains the ionophore 3‐decyl‐1,5,8‐triazacyclodecan‐2,4‐dione (DTADD). Instead of the usual inner fluid junction, a polypyrrole layer applied on the inner side of the PVC membrane was employed as inner solid contact. The performance of this electrode was compared to solid‐state sulfate‐selective electrodes with the ionophore α,α′‐bis(N′‐phenylthioureylene)‐m‐xylene (BTH) and to electrodes in the coated‐wire configuration. For the parameters sensitivity, selectivity, and long‐term stability, electrodes with the DTADD ionophore show improved properties. In the sulfate concentration range of 5·10–5...10–2 mol L–1 the slope of the response is –(26.8 ± 0.5) mV/decade. The new solid contact sulfate electrodes showed a very low drift of the electrode potential within a period of 150 days when the electrode was stored in 10–2 M Na2SO4. In Na2SO4 solutions of the pH range of 4...9 the electrode potentials were constant. The 95% response time was about 10 s when the sulfate concentration was changed from 10–4 mol L–1 to 10–3 mol L–1. The selectivity with DTADD ionophore relating to the nitrate ions is higher than the selectivity with BTH. Improvements are also made in comparison with sulfate‐selective electrodes described in the literature which contain other ionophores with fluid inner reference electrolytes.  相似文献   

7.
A bloom of Chlamydomonas botryopara was observed in an extremely acid coal mining pond (pH 2.5) with high concentrations of iron and aluminium (1160...3760 mg L–1 Fe, 133...387 mg L–1 Al). Cell density of algae was counted as 6.45 · 106 mL–1 corresponding to 700 mg L–1 fresh weight and 2660 μg L–1 chlorophyll‐a. The nutrient concentrations were 3.5 mg L–1 soluble reactive phosphorus and 0.15 mg L–1 dissolved inorganic nitrogen. This observation supports the hypothesis that a low nutrient availability rather than extreme conditions (e.g. high acidity and low pH) limit the development of phytoplankton in many acidified lakes.  相似文献   

8.
Dissolved organic carbon (DOC) originating in peatlands can be mineralized to carbon dioxide (CO2) and methane (CH4), two potent greenhouse gases. Knowledge of the dynamics of DOC export via run‐off is needed for a more robust quantification of C cycling in peatland ecosystems, a prerequisite for realistic predictions of future climate change. We studied dispersion pathways of DOC in a mountain‐top peat bog in the Czech Republic (Central Europe), using a dual isotope approach. Although δ13CDOC values made it possible to link exported DOC with its within‐bog source, δ18OH2O values of precipitation and run‐off helped to understand run‐off generation. Our 2‐year DOC–H2O isotope monitoring was complemented by a laboratory peat incubation study generating an experimental time series of δ13CDOC values. DOC concentrations in run‐off during high‐flow periods were 20–30 mg L?1. The top 2 cm of the peat profile, composed of decaying green moss, contained isotopically lighter C than deeper peat, and this isotopically light C was present in run‐off in high‐flow periods. In contrast, baseflow contained only 2–10 mg DOC L?1, and its more variable C isotope composition intermittently fingerprinted deeper peat. DOC in run‐off occasionally contained isotopically extremely light C whose source in solid peat substrate was not identified. Pre‐event water made up on average 60% of the water run‐off flux, whereas direct precipitation contributed 40%. Run‐off response to precipitation was relatively fast. A highly leached horizon was identified in shallow catotelm. This peat layer was likely affected by a lateral influx of precipitation. Within 36 days of laboratory incubation, isotopically heavy DOC that had been initially released from the peat was replaced by isotopically lighter DOC, whose δ13C values converged to the solid substrate and natural run‐off. We suggest that δ13C systematics can be useful in identification of vertically stratified within‐bog DOC sources for peatland run‐off.  相似文献   

9.
Delivery of sulfate to petroleum hydrocarbons (PHCs) source zones and groundwater plumes is desirable to enhance biodegradation rates when treatment has become limited due to depletion of sulfate. Sulfate land application involves spreading sulfate salts on ground surface and allowing their dissolution and infiltration of sulfate into subsurface. The objectives of this pilot-scale investigation were to capture the vertical transport of sulfate beneath an application area, confirm that sulfate reduction was occurring, and explore how the added sulfate affected biodegradation of benzene and toluene. Approximately 4000 kg of gypsum was spread over a 30 m × 30 m study area above a smear zone located approximately 2 m below-ground surface. Precipitation was augmented by two irrigation events. Groundwater samples, collected over 1058 days from multilevel wells and a conventional long-screened monitoring well, were analyzed for benzene, toluene, ethylbenzene, and xylenes (BTEX), sulfate, bromide, dissolved inorganic carbon (DIC) and methane. Compound-specific isotope analyses (CSIA) for benzene and toluene, and isotope analyses of 13C-DIC and 34S-SO42− were performed. Following application, an increase in sulfate concentration was noted in the smear zone. 34S-SO42− enrichment and 13C-DIC depletion indicated that sulfate reduction and mineralization of PHCs were enhanced. CSIA results provided unequivocal evidence of anaerobic biodegradation of benzene and toluene. After 1058 days when sulfate was depleted, methane concentrations were about three times greater than baseline conditions suggesting syntrophic benefit of the delivered sulfate. Observations from this investigation support the viability of sulfate land application to enhance biodegradation rates in shallow PHC smear zones.  相似文献   

10.
To improve quantitative understanding of mixed‐land‐use impacts on nutrient yields, a nested‐scale experimental watershed study design (n = 5) was applied in a 303(d), clean water act impaired urbanizing watershed of the lower Missouri River Basin, USA. From 2010 to 2013, water samples (n = 858 sample days per site) were analysed for total inorganic nitrogen (TIN‐N), nitrite (NO2–N) nitrate (NO3–N), ammonia (NH3–N), and total phosphorus (TP‐P). Annual, seasonal, and monthly flow‐weighted concentrations (FWCs) and nutrient yields were estimated. Mean nutrient concentrations were highest where agricultural land use comprised 58% of the drainage area (NH3 = 0.111 mg/l; NO2 = 0.045 mg/l; NO3 = 0.684 mg/l, TIN = 0.840 mg/l; TP = 0.127 mg/l). Average TP‐P increased by 15% with 20% increased urban land use area. Highly variable annual precipitation was observed during the study with highest nutrient yields during 2010 (record setting wet year) and lowest nutrient yields during 2012 (extreme drought year). Annual TIN‐N and TP‐P yields exceeded 10.3 and 2.04 kg ha?1 yr?1 from the agricultural dominated headwaters. Mean annual NH3–N, NO2–N, NO3–N, TIN‐N, and TP‐P yields were 0.742, 0.400, 4.24, 5.38, and 0.979 kg ha?1 yr?1, respectively near the watershed outlet. Precipitation accounted for the majority of the explained variance in nutrient yields (R2 values from 0.68 to 0.85). Nutrient yields were also dependent on annual precipitation of the preceding year (R2 values from 0.87 to 0.91) thus enforcing the great complexity of variable mixed‐land‐use mediated source‐sink nutrient yield relationships. Study results better inform land managers and best management practices designed to mitigate nutrient pollution issues in mixed‐land‐use freshwater ecosystems. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

11.
This study analysed the importance of precipitation events from May 2003 to April 2004 on surface water chemistry and solute export from a 696 ha glaciated forested watershed in western New York State, USA. The specific objectives of the study were to determine: (a) the temporal patterns of solutes within individual storm events; (b) the impact of precipitation events on seasonal and annual export budgets; and (c) how solute concentrations and loads varied for precipitation events among seasons as functions of storm intensity and antecedent moisture conditions. Analysis of solute trajectories showed that NH4+, total Al and dissolved organic nitrogen (DON) peaked on the hydrograph rising limb, whereas dissolved organic carbon (DOC) concentrations peaked following the discharge peak. Sulphate and base‐cations displayed a dilution pattern with a minimum around peak discharge. End‐member mixing analysis showed that throughfall contributions were highest on the rising limb, whereas valley‐bottom riparian waters peaked following the discharge peak. The trajectories of NO3? concentrations varied with season, indicating the influence of biotic processes on the generation, and hence flux, of this solute. Storm events had the greatest impact on the annual budgets for NH4+, K+, total dissolved Al, DON and DOC. Storm events during summer had the greatest impact on seasonal solute budgets. Summer events had the highest hourly discharges and high concentrations of solutes. However, NO3? and DOC exports during a spring snowmelt event were considerably more than those observed for large events during other periods of the year. Comparisons among storms showed that season, precipitation amount, and antecedent moisture conditions affected solute concentrations and loads. Concentrations of solutes were elevated for storms that occurred after dry antecedent conditions. Seven of the largest storms accounted for only 15% of the annual discharge, but were responsible for 34%, 19%, 64%, 13%, 39% and 24% of the annual exports of NH4+, K+, Al, NO3?, DON and DOC respectively. These results suggest that the intense and infrequent storms predicted for future climate‐change scenarios will likely increase the exports of solutes like DOC, DON, NH4+, Al and K+ from watersheds. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

12.
The present report describes the set-up and first operation results of a novel carousel magnetic separator. This carousel magnetic separator is suitable for continuous separation of magnetized particles from water. Continuous operation is achieved by a segmented rotating separation matrix. This matrix also allows the use of low-cost permanent magnets, by means of which magnetic fields of up to 0.5 T can be generated without energy consumption. The suitability of a first prototype of this carousel magnetic separator was tested for elimination of magnetite-containing iron phosphate and iron hydroxide flocs. These flocs result from conventional precipitation/flocculation of municipal sewage with FeCl3 and the addition of magnetite particles generated by wet-chemical processes. First results demonstrate that the carousel magnetic separator can reduce phosphate concentrations of up to 14 mg/L PO43–-P in the inlet to below 1 mg/L PO43–-P in the outlet at filtration rates of about 40 m/h. Magnetite dosage in the range of 50 mg/L affects phosphate precipitation positively via a slight reduction of the precipitant volume. However, the total amount of chemicals required for phosphate elimination is increased by the substances needed for magnetite production. Therefore, a further reduction of magnetite dosage must be achieved.  相似文献   

13.
Exchange of groundwater and lake water with typically quite different chemical composition is an important driver for biogeochemical processes at the groundwater‐lake interface, which can affect the water quality of lakes. This is of particular relevance in mine lakes where anoxic and slightly acidic groundwater mixes with oxic and acidic lake water (pH < 3). To identify links between groundwater‐lake exchange rates and acid neutralization processes in the sediments, exchange rates were quantified and related to pore‐water pH, sulfate and iron concentrations as well as sulfate reduction rates within the sediment. Seepage rates measured with seepage meters (?2.5 to 5.8 L m‐2 d‐1) were in reasonable agreement with rates inverted from modeled chloride profiles (?1.8 to 8.1 L m‐2 d‐1). Large‐scale exchange patterns were defined by the (hydro)geologic setting but superimposed by smaller scale variations caused by variability in sediment texture. Sites characterized by groundwater upwelling (flow into the lake) and sites where flow alternated between upwelling and downwelling were identified. Observed chloride profiles at the alternating sites reflected the transient flow regime. Seepage direction, as well as seepage rate, were found to influence pH, sulfate and iron profiles and the associated sulfate reduction rates. Under alternating conditions proton‐consuming processes, for example, sulfate reduction, were slowed. In the uppermost layer of the sediment (max. 5 cm), sulfate reduction rates were significantly higher at upwelling (>330 nmol g‐1 d‐1) compared to alternating sites (<220 nmol g‐1 d‐1). Although differences in sulfate reduction rates could not be explained solely by different flux rates, they were clearly related to the prevailing groundwater‐lake exchange patterns and the associated pH conditions. Our findings strongly suggest that groundwater‐lake exchange has significant effects on the biogeochemical processes that are coupled to sulfate reduction such as acidity retention and precipitation of iron sulfides. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

14.
The sorption of Co(II) from aqueous solutions on granulated titanium dioxide was investigated in dependence on pH-value (pH = 6 … 10) and solution concentration (cL = 10?7 … 10?2 mol/kg) at 83 °C. The precipitation in the solution occurred at high pH-values and solution concentrations was determined by control experiments without the adsorber. The adsorption isotherms are S-shaped. This can be interpreted as transition from chemisorption at the basic material to surface precipitation.  相似文献   

15.
Iron-rich spherules (> 90% Fe2O3 from electron microprobe analyses) ∼10-100 μm in diameter are found within sulfate-rich rocks formed by aqueous, acid-sulfate alteration of basaltic tephra on Mauna Kea volcano, Hawaii. Although some spherules are nearly pure Fe, most have two concentric compositional zones, with the core having a higher Fe / Al ratio than the rim. Oxide totals less than 100% (93-99%) suggest structural H2O and/or OH− 1. The transmission Mössbauer spectrum of a spherule-rich separate is dominated by a hematite (α-Fe2O3) sextet whose peaks are skewed toward zero velocity. Skewing is consistent with Al3+ for Fe3+ substitution and structural H2O and/or OH− 1. The grey color of the spherules implies specular hematite. Whole-rock powder X-ray diffraction spectra are dominated by peaks from smectite and the hydroxy sulfate mineral natroalunite as alteration products and plagioclase feldspar that was present in the precursor basaltic tephra. Whether spherule formation proceeded directly from basaltic material in one event (dissolution of basaltic material and precipitation of hematite spherules) or whether spherule formation required more than one event (formation of Fe-bearing sulfate rock and subsequent hydrolysis to hematite) is not currently constrained. By analogy, a formation pathway for the hematite spherules in sulfate-rich outcrops at Meridiani Planum on Mars (the Burns formation) is aqueous alteration of basaltic precursor material under acid-sulfate conditions. Although hydrothermal conditions are present on Mauna Kea, such conditions may not be required for spherule formation on Mars if the time interval for hydrolysis at lower temperatures is sufficiently long.  相似文献   

16.
Spatial and temporal variations of the isotopic composition of precipitation were investigated to better understand their controlling factors. Precipitation was collected from six locations in Hokkaido, Japan, and event‐based analyses were conducted for a period from March 2010 to February 2013. Relatively low δ values and a high d‐excess for annual averages were observed at three sites located along the Japan Sea compared to the three sites at Pacific Ocean side. Lower δ values in spring and fall and higher d‐excess in winter were observed for the region along the Japan Sea. In total, 264 precipitation events were identified. Precipitation originated predominantly from low‐pressure system (LPS) events, which were classified as northwest (LPS‐NW) and southeast (LPS‐SE) events according to the routes of the low‐pressure center, that passed northwest and southeast of Hokkaido, respectively. LPS‐SE events showed lower δ18O than LPS‐NW events, which is attributable to the lower δ18O of water vapor resulting from heavy rainfalls in the upstream region of the LPS air mass trajectories over the Pacific Ocean. This phenomenon observed in Hokkaido can be found in other midlatitude coastal regions and applied for hydrological, atmospheric, and paleoclimate studies. A characteristic spatial pattern was found in LPS‐NW events, in which lower δ18O was observed on the Japan Sea side than on the Pacific Ocean side in each season. This is likely due to the location of the sampling sites and their distance from the LPS: Precipitation with lower δ18O in the region along the Japan Sea occurs in a well‐developed cloud system near the low‐pressure center in cold and warm sectors of LPS, whereas precipitation with higher δ18O on the Pacific side mainly occurs in a warm sector away from the low‐pressure center. Air mass from the north does not always cause low δ in precipitation, and the precipitation process in the upstream region is another important factor controlling the isotopic composition of precipitation, other than the local temperature and precipitation amount.  相似文献   

17.
Temporal variation of runoff chemistry and its seasonal controls relating to chemical weathering processes and drainage system evolution were examined at Urumqi Glacier No.1 in Xinjiang, China, over a full melt season. The dominant ions in meltwater runoff are HCO3?, Ca2+, and SO42?; and Fe, Sr, and Al are dominant elements. Concentrations of major ions and some elements show periodic variations with seasons and negatively correlate with discharge, whereas other elements (e.g., Al, Ni, Cu, Zn, Cd, and Pb) show a random change, providing insights into the hydrological and physicochemical controls. HCO3? and Ca2+ are primarily derived from calcite, SO42? and Fe mainly come from pyrite, and Sr and Al principally originate from silicate. Hydrochemical fluxes of solutes exhibit strong seasonality but are positively related to discharge, suggesting an increasing release of solutes during higher flow conditions. Solute yields, cation denudation rate, and chemical weathering intensity observed at Urumqi Glacier No.1 are higher than those at most basins worldwide. This suggests that chemical weathering in central Asia may be stronger than at other glacial basins with similar specific discharge. Concentrations of some elements (e.g., Fe, Al, As, Pb, and Zn) are close to or exceed the guidelines for drinking water standards in meltwater‐fed rivers. These rivers may face future challenges of water quality degradation, and relationships between changing flow and water quality conditions should be established soon, given that development of channelized flow is expected to be earlier over a melt season in a warming climate.  相似文献   

18.
In the present research, laundry wastewater treatment is studied using the electrocoagulation/electroflotation process. For the optimization of treatment conditions such as electrode type (Al–Al, Al–Fe, Fe–Fe, and Fe–Al), initial pH (5–9), current (0.54–2.16 A), and application time (15–60 min), response surface methodology is used. Removal efficiencies of chemical oxygen demand (COD), color, anionic surfactant, microplastic, and phosphate are studied. It is determined that the most effective removal is obtained with 2.16 A current, pH 9, and 60 min reaction time using Fe–Al electrode. Here, 91%, 94%, 100%, and 98% removal efficiencies are achieved for COD, surfactant, color, and microplastic, respectively. The operating cost of the combined process is calculated as $1.32 m?3 for the optimum removal parameters. The adsorption kinetics study shows that the removal follows second‐order kinetics. The laboratory‐scale test results indicate that the electrocoagulation/electroflotation process is feasible for the treatment of laundry wastewater.  相似文献   

19.
Inclusions of ferropericlase and former (Mg,Fe)(Si,Al)O3 perovskite in diamonds from Kankan, Guinea believed to originate in the lower mantle were studied using Mössbauer spectroscopy to determine Fe3+/ΣFe. Fe3+ concentration in the (Mg,Fe)(Si,Al)O3 inclusion is consistent with empirical relations relating Fe3+/ΣFe to Al concentration, supporting the inference that it crystallised in the perovskite structure at lower mantle conditions. In ferropericlase there is a nearly linear variation of trivalent cation abundance with monovalent cation abundance, suggesting a substitution of the form Na0.5M0.53+O (M=Fe3+, Cr3+, Al3+). Excess positive charge is likely balanced by cation vacancies, where their abundance is observed to increase with increasing iron concentration, consistent with high-pressure experiments. The abundance of cation vacancies is related to oxygen fugacity, where ferropericlase inclusions from Kankan and São Luiz (Brazil) are inferred to have formed at conditions more oxidising than Fe-(Mg,Fe)O equilibrium, but more reducing than Re-ReO2 equilibrium. Fe2+/Mg partition coefficients between (Mg,Fe)(Si,Al)O3 and ferropericlase were calculated for inclusions co-existing in the same diamond using Mössbauer data and empirical relations based on high-pressure experimental work. Most values are consistent with high-pressure experiments, suggesting that these inclusions equilibrated at lower mantle conditions. The measured ferropericlase Fe3+ concentrations are consistent with diamond formation in a region of redox gradients, possibly arising from the subduction of oxidised material into reduced lower mantle. Reduction of carbonate to form ferropericlase and diamond is consistent with a slight shift of Kankan δ13C values to isotopically heavy compositions compared to the worldwide dataset, and could supply the oxygen necessary to satisfy the high Fe3+ concentration in (Mg,Fe)(Si,Al)O3 perovskite, as well as account for the high proportion of ferropericlase in the lower mantle paragenesis. The heterogeneity of lower mantle diamond sources indicates that the composition of lower mantle diamonds do not necessarily reflect those of the bulk mantle.  相似文献   

20.
According to the precipitation and δ18O data obtained during the GEWEX Asian Monsoon Experiment–Tibet Intensive Observation Period, based on the knowledge that δ18O is lower in precipitation formed from ocean air mass vapour than that from local evaporation vapour, the water vapour sources can be identified from the δ18O values in precipitation. We attempt to give the identification criterion of δ18O values in precipitation. The threshold values chosen to distinguish between ocean and local sources are δ18O < ?20‰ and δ18O > ?13‰ respectively. According to this criterion, the proportion of local evaporation‐formed precipitation and ocean air‐mass‐formed precipitation in total precipitation was estimated. The average value of precipitation at three sites (NODA, Amdo and AQB) is 249·76 mm. Among this, precipitation formed directly by the ocean air mass vapour is 80·08 mm at most. Precipitation formed by water vapour evaporated from local places is 117·05 mm at least. That is to say that precipitation formed directly by the ocean air mass vapour accounts for 32·06% of the total precipitation at most. Precipitation formed by water vapour evaporated from local places accounts for 46·86% of the total precipitation at least. At least 21·8% of the total precipitation came from water vapour that was evaporated on the way and transported by the monsoon circulation. Copyright © 2005 John Wiley & Sons, Ltd.  相似文献   

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