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1.
A study of the changes in the ionic loads of NO, NH, SO and H+ in a boreal forest snowpack at Lake Laflamme, Québec was carried out using hydrological and chemical data from field lysimeters. The results showed that depletion of the N-containing species occurs periodically in the snowpack during meltwater discharge. Rain-on-snow events led to in-pack losses of NO and NH at a rate of 130 μeq m?2 day?1 and 101·3 μeq m?2day?1 respectively. On dry days, however, dry deposition and deposition of organic debris from the canopy resulted in increases of 183·3 μeq m?2day?1 for NO and 4·5 μeq m?2day?1 for NH in the pack. In contrast, SO42? showed continual in-pack increases due to deposition of 5·0 μeq m?2day?1 for wet days and 92·6 μeq m?2day?1 for dry days. The depletion of NO and NH is due to microbiological uptake of these nutrients during periods when the free water content of the pack is high. Controlled melts in a laboratory snowmelt simulator containing snow and organic matter from the forest canopy at Lake Laflamme showed losses of NO and NH similar to those observed in the field. As the microbiological uptake proceeds at a rate comparable to that of ionic load increases in the pack by dry deposition, models of the chemical dynamics of snowmelt should take the former into account in any system where organic content of the snowpack is appreciable.  相似文献   

2.
Errors in the kinematic wave and diffusion wave approximations for time-independent (or steady-state) cases of channel flow were derived for three types of boundary conditions: zero flow at the upstream end, and critical flow depth and zero depth gradient at the downstream end. The diffusion wave approximation was found to be in excellent agreement with the dynamic wave approximation, with errors in the range 1–2% for values of KF (? 7.5), where K is the kinematic wave number and F0 is the Froude number. Even for small values of KF (e.g. KF20 = 0.75), the errors were typically less than 15%. The accuracy of the diffusion wave approximation was greatly influenced by the downstream boundary condition. The error of the kinematic wave approximation was found to be less than 13% in the region 0.1 ? x ? 0.95 for KF = 7.5 and was greater than 30% for smaller values of KF (? 0.75). This error increased with strong downstream boundary control.  相似文献   

3.
The Krusné hory (Erzgebirge or Ore Mountains) has been heavily affected by high atmospheric pollutant deposition caused by fossil fuel combustion in an adjacent Tertiary coal basin. Long‐term routine sampling of bulk precipitation (1977–1996) and stream water (1977–1998) in a forested area on the south‐eastern slope of the mountains were used to evaluate trends and patterns in solute concentration and flux with respect to controlling processes. From 1977 to 1996, the annual volume‐weighted Ca2+ and SOconcentrations decreased in bulk precipitation. However, after 1989, when a pronounced and continuous decrease occurred in coal production, annual volume‐weighted concentrations decreased for most solutes, except H+. The concentration decreases were marked, with 1996 levels at or below 50% of those in 1989. The lack of a trend in H+ is attributed to similar decreases in both acid anions and neutralizing base cations. Stream water concentrations of most solutes, i.e. H+, Ca2+, Mg2+, SONOwere highest at the onset of sampling in 1977, decreased markedly from 1977 to 1983 and decreased more gradually from 1983 to 1998. The spruce forest die‐back and removal reduced dry deposition of these solutes by reducing the filtering action, which was provided by the forest canopy. A notable decrease in stream water Ca2+ concentrations occurred after 1995 and may be due to the depletion of Ca2+, which was provided by catchment liming in 1986, 1988 and 1989. Solute flux trends in bulk atmospheric deposition and stream water generally were not significant and the lack of trend is attributed to the large interannual variability in precipitation quantity and runoff, respectively. All solutes except Na+ varied seasonally. The average seasonal concentrations varied between the solutes, but for most solutes were highest in winter and spring and lowest in summer, correlating with the seasonal trend in runoff. For Ca2+, Mg2+ and SOthe concentration minimum occurs in September and the maximum occurs in February or March, correlating with the seasonal baseflow. These solutes are primarily controlled by the contribution of soil water and groundwater to stream flow. During snowmelt, the meltwater generally causes concentrations to decrease as soil water and groundwater are diluted. For NO3 , average minimum concentrations occur in August at the end of the growing season concurrent with the lowest stream flow, and the maximum occurs in February and March with high stream flow during snowmelt. Seasonal stream water NOconcentration variations are large compared with the long‐term decrease. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

4.
The uptake of phosphorus by Potamogeton pectinatus, P. lucens, Ranunculus fluitans, Elodea canadensis, Myriophyllum spicatum and Ceratophyllum demersum is investigated in batch tests at 0.02, 0.04, 0.4 and 4.0 mg/l PO in the medium for 4, 28 and 52 h. Uptake is strictly dependent on concentration, a saturation function being discernible already after 52 h. At rising concentration the mechanism of uptake is determined by a decreasing rate of incorporation. The rates of uptake are dependent also on the actual and maximum cell nutrient contents. Species with a low phosphorus content of <5 mg PO/g dry weight as Elodea canadensis, Potamogeton pectinatus and Myriophyllum spicatum show their maximum phosphorus incorporation at low substrate concentrations. At phosphorus contents >5 mg PO/g dry weight the phosphorus incorporation is increased only at substrate concentrations of 0.04… 0.4 mg/l PO.  相似文献   

5.
The knowledge of total inorganic carbon concentration (c) is important for characterizing natural waters. It is usually measured by the titration alkalinity (“m-value”) and pH which depend on temperature and ionic strength. This paper demonstrates that Ca (and Mg) can influence the calculation of from titration alkalinity, too. Errors result from neglecting this influence. In such cases the share of ion pair CaCO amounts to more than 50 % of . General relationships among the influencing factors are given by tables calculated with the help of a BASIC computer programme for calculation from titration alkalinity, pH and Ca concentration.  相似文献   

6.
Processes driving carbonate diagenesis in islands of the northern Bahamas are investigated using major ion, dissolved oxygen and dissolved organic carbon analyses of water samples from surface and ground waters, and measurements of soil gas P. Meteoric waters equilibrate with aragonite, but reactions are water controlled rather than mineral‐controlled and drive dissolution rather than concurrent precipitation of calcite. Surface runoff waters equilibrate with atmospheric P and rapidly recharge the vadose zone, limiting subaerial bedrock dissolution to only 6·6–15 mg l?1 Ca. P of soil gas measured in the summer wet season ((7·4 ± 3·7) × 10?3 atm) is elevated compared with that of the atmosphere, despite the thin skeletal organic nature of the soil and the discontinuous soil cover. Soil waters retained in surface pockets are equilibrated with respect to aragonite and have dissolved 51 ± 19 mg l?1 Ca. This is substantially less than the 93 ± 18 mg l?1 Ca in samples from pumping boreholes that sample meteoric waters from the freshwater lens. The high P of the freshwater lens ((16 ± 8·3) × 10?3 atm for pumping boreholes) suggests that significant additional CO2 may be derived by oxidation of soil‐ and surface‐derived organic carbon within the lens. The suboxic nature of the majority of the freshwater lens and the observed depletion in sulphate support this suggestion, and indicate that both aerobic and anaerobic oxidation may take place. Shallow lens samples from observation boreholes are calcite supersaturated and have a lower P than deeper lens waters, indicating that CO2 degasses from the water table, driving precipitation of calcite cements. We suggest that the geochemical evolution of waters in the vadose zone and upper part of the freshwater lens may be determined by the presence of a body of ground air with P controlled by production in the freshwater lens and soil and by degassing to the atmosphere. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

7.
It is shown that the new definition1 of strong motion local magnitude M leads to stable estimates of magnitudes for earthquakes in Yugoslavia, with epicentral distances R <100 km and for 2.5 < M < 6.5. Tables with magnitudes computed using this new procedure are presented for all earthquakes contributing to the strong motion accelerogram files in EQINFOS for Yugoslavia.2 The similarity of our findings with the analogous analyses for California suggests new possibilities for relative calibration between various local magnitude scales, which are used in southeastern Europe, and ML in California.  相似文献   

8.
One mechanism by which biochar application enhances soil nutrient availability is through direct nutrients release from biochar. However, factors controlling the release processes are poorly understood. In this study, the effects of pH, biochar to water ratio, temperature, ionic strength, and equilibration time on the release of PO, NO, NH, K+, Na+, Ca2+, and Mg2+ from biochar were evaluated in simulated experiments. The release of PO, K+, Ca2+, and Mg2+ was significantly affected by extraction pH, suggesting that their release from biochar was pH dependent or an H+‐consuming process. Correlation analysis indicated that PO and Ca2+, PO and Mg2+, and Ca2+ and Mg2+ were co‐solubilized with increasing soil acidity. To a lesser extent, the recovery of the nutrients was also affected by the ratio of biochar to water: more nutrients were soluble with more water supply. In contrast, the release of Na was not affected by pH while the concentration increased with decreasing biochar to water ratio. Meanwhile, other factors (temperature, ionic strength, and equilibration time) had less effect on nutrient release from biochar. Under the influence of pH, the patterns of NO and PO release from biochar were different: extractable NO concentration was not affected by the pH but more PO was released in strongly acidic conditions. Our data suggested that P was mainly retained in inorganic forms while N was in organic forms in biochar. We conclude that environmental factors have marked influences on nutrients release from biochar.  相似文献   

9.
Contamination of water due to bromate is a severe health hazard. The aim of the present study was to remove bromate from water using a crosslinked polystyrene based strongly basic anion exchange resin De‐Acidite FF‐IP. Batch experiments were performed to study the influence of various experimental parameters such as effect of pH, contact time, temperature, and effect of competing anions on bromate removal by De‐Acidite FF‐IP resin. At optimum parameters, the removal rate of bromate was very fast and 90% removal took place in 5 min and equilibrium was established within 10 min. The presence of competitive anions reduced the bromate adsorption in the order of Cl? > F? > CO > SO > NO > PO. The practical utility of this resin has been demonstrated by removing bromate in some of the commercial bottled water from Saudi Arabia. The level of bromate was determined using a very sensitive, precise and rapid method based on ultra‐performance liquid chromatography‐tendem mass spectrometry (UPLC‐MS/MS).  相似文献   

10.
The Manchester Ship Canal (MSC) has been the recipient of domestic and trade effluent since 1895, it continues to be grossly polluted. In 1985 the dock basins, now known as Salford Quays were isolated from the canal inorder to improve water quality and encourage redevelopment. Subsequent to isolation the dock basins received no effluent or drainage and Helixor pumps were installed to improve circulation, thereby preventing stratification and bottom water anoxia. Analysis of solid material, pore waters and phospholipid fatty acids (PLFA) in cores taken from Salford Quays and the MSC was carried out to assess changes in sediment characteristics that might affect water quality. Loss of carbon was apparent in the upper sediment of Salford Quays, as was a greater proportion of reducible Fe, Mn, Zn and Cd compared with the MSC. In Salford Quays a superficial peak in Fe and Zn concentration appeared to be attributable to migration of metals in the pore water and precipitation of Fe oxyhydroxide at the oxic sediment water interface. Despite these differences, NHSOconcentration pore water profiles were similar in both sediments if the MSC sediments were considered from a point below their top layers, which appeared to be composed of freshly deposited sewage. Bacterial biomass extrapolated from PLFA concentration also suggested that the upper sediment of the MSC was largely faecal. PLFA analyses to characterize changes in the microbial community, however, did not reveal any systematic changes. That this may have been because of an absence of vertical zonation was supported by pore water analyses. It was also apparent that the lack of systematic change might be due at least in part to an artefact of vestigial PLFA signatures, resulting from deposition and burial, and the need for finer vertical resolution in the sampling procedure. Despite incomplete and some contradictory findings it appears that although metal mobilization may result from the development of an oxic sediment water interface, the extremely high original organic content of the sediment ensures that even after 10 years it exerts a high oxygen demand. Consequently, sediment management is likely to be a long‐term commitment and as remediation proceeds the importance of continuity in management will increase. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

11.
A theoretical equation was developed to express the time variation of drainage density in a basin or geomorphic surface: Di(t, T) is the drainage density at time T on the i-th basin or geomorphic surface, which was formed at time t; β(τ) is a factor related to the erosional force causing the development of the rivers of the basin or surface at time τ; δi is the maximum drainage density; and Di is the initial drainage density on the i-th geomorphic surface or basin. The equation is based on the assumption that the drainage density increases with time until it reaches a specific upper limit δi(t)), the maximum drainage density, which is related to certain physical properties of the basin. The equations for various dated basins or geomorphic surfaces can be combined into one modified equation if the same relative erosional forces have acted on those basins or surfaces (β(t) = β(t) and if the basins or surfaces have the same physical properties δi(t) = δi(t), (Di = D0). The application of this equation to coastal terraces and glacial tills shows that the model is compatible with observed drainage densities on various dated basins or surfaces.  相似文献   

12.
The atmospheric chloride mass balance (CMB) method allows spatial evaluations of the average diffuse aquifer recharge by rainfall () in large and varied territories when long‐term steady conditions can be assumed. Often, the distributed average CMB variables necessary to calculate have to be estimated from the available variable‐length data series, which may be of suboptimal quality and spatial coverage. This paper explains the use of these data and the reliability of the results in continental Spain, chosen as a large and varied territory. The CMB variables have been regionalized by ordinary kriging at the same 4976 nodes of a 10 km × 10 km grid. Nodal values vary from 14 to 810 mm year–1, 90% ranging from 30 to 300 mm year–1. The recharge‐to‐precipitation ratios vary from 0.03 in low‐permeability formations and semiarid areas to 0.65 in some carbonate massifs. Integrated average results for the whole of continental Spain yield a potential aquifer recharge of 64 km3 year?1, the net recharge over permeable formations (40% of the territory) being 32 km3 year?1. Two main sources of uncertainty affecting (given by the coefficient of variation, CV), induced by the inherent natural variability of the variables (CVR) and from mapping (), have been segregated. The average CVR is 0.13 and could be improved with longer data series. The average is 0.07 and may be decreased with better data coverage. The estimates were compared with other regional and local recharge estimates, being 4% and 1% higher, respectively. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

13.
The present study deals with the application of the hierarchical cluster analysis and non‐parametric tests in order to interpret the Gdańsk Beltway impact range. The data set represents concentration values for major inorganic ions (Na+, NH, K+, Mg2+, Ca2+, F, Cl, NO, and SO) as well as electrolytic conductivity and pH measured in various water samples [precipitation, throughfall water, road runoff, and surface water (drainage ditches, surface water reservoirs, and spring water)] collected in the vicinity of the beltway. Several similarity groups were discovered both in the objects and in the variables modes according to the water sample. In the majority of cases clear anthropogenic (fertilizers usage and transport, road salting in winter) and semi‐natural (sea salt aerosols, erosion of construction materials) impacts were discovered. Spatial variation was discovered for road runoff samples and samples collected from surface water reservoirs and springs. Surprisingly no clear seasonal variability was discovered for precipitation chemistry, while some evidences for existing of summer and winter specific chemical profile was discovered for road runoff samples. In general, limited range of the Gdańsk Beltway impact was proven.  相似文献   

14.
Groundwater is a major source of water supply for domestic and irrigation uses in semiarid, remote but rapidly developing Kilasaifullah district part of Zhob River Basin, located at Pakistan–Afghanistan Border. Zhob River is among few major rivers of perennial nature in Balochistan, which flows from WSW to ENE and falls in Gomal River, a tributary of Indus River. Keeping in view the important geopolitical position and rapid development of the region, this study is primarily focused on groundwater chemistry for contamination sources as well as agriculture development. Water samples from open and tube wells are analyzed and calculated for electrical conductivity (EC), total dissolved solids (TDS), turbidity, pH, K+, Na+, Ca2+, Mg2+, HCO, Cl?, NO, SO, PO, sodium percent (Na%), sodium adsorption ratio (SAR), Kelly's index (KI), and heavy metals (Fe, Cu, Cr, Zn, Pb, and Mn). On the basis of the chemical constituents two zones within the study area are identified and possible causes of the contaminants are pointed out. Two recharge areas were responsible for the different chemical results in groundwater, e.g., zone A was recharged from NNW saline geological formations (Nisai, Khojak, Multana, Bostan formations, and Muslim Bagh ophiolites), which are concentrated with high sodium and chloride. On the other hand Zone B was sourced from SSW from carbonate rich rocks (Alozai, Loralai, Parh formations, and Muslim Bagh ophiolites). The groundwater is classified as C2–S1, C3–S1, C3–S2, C4–S2 on the basis of EC and SAR values which indicate that most of the water of both zones can be used for irrigation safely except the samples plotted in C3–S2 and C4–S2 categories which could be dangerous for soil and crops. Groundwater samples are plotted in good to permissible limits with some samples excellent to good and few samples belong to doubtful category based on sodium percent. Groundwater of zone A is unsuitable for irrigation use due to higher values of KI (more than one) but water of zone B are good for irrigation based on KI. In general, water of both zones is suitable for irrigation but care should be taken during the selection of crops which are sensitive to alkalinity or sodium hazards particularly in zone A.  相似文献   

15.
Major solute concentrations in overland flow water (OFW) were measured in an agricultural field of Brittany (western France). Two storm events were monitored in detail to examine the short time‐scale processes. During one year, samples were taken at different positions on the slope after each storm event to describe the spatial and seasonal variations of OFW chemistry. Although the total dissolved load in OFW is not much higher than in rain water, distinctive features are observed. K+, Ca2+, NH4 , Cl and SOare the major solutes. The main origin of the elements (sea salts, exchangeable soil complex or fertilizers) determined most of the variations observed. Spatial variations along the slope are mainly seen for exchangeable cations, while seasonal variations are predominant for sea salts. Rainfall intensity and suspended sediment load induce strong differences between the two storm events studied in detail. However, the within‐storm variations and the seasonal monitoring show that this relationship is complex. Within‐storm variations suggest that, in addition to desorption processes, mixing with pre‐event water may occur. The lack of a relationship between sediment load and dissolved load is attributed to the high rate of the exchange processes, which has been checked by a simple experiment in vitro. It is concluded that the conditions of the transit of water on the field (velocity, length, status of the surface, crusted or not) may well play a major role in the chemical changes between rain water and OFW. The results suggest that vegetated buffer strips designed to reduce the sediment load only, and not the amount of overland flow, will have little effect on the transfer of dissolved pollutants to the watercourses. Copyright © 1999 John Wiley & Sons, Ltd.  相似文献   

16.
Nutrient and Oxygen Balance of a Highly Polluted Treated Sewage Channel with Special Regard to the Submerged Macrophytes The changes of the concentrations of inorganic nitrogen compounds, orthophosphate, and oxygen were measured in the flowing wave along the flowing stretch of the Berlin treated sewage channel Wuhle monthly over a period of two years (1993/94) to estimate the nutrient and oxygen balances. This treated sewage channel is rich in nutrients and densely covered with submerged macrophytes. During the period of investigation in 1993 (1994), the effluent of the sewage treatment plant Falkenberg, which is lacking in adjustable nitrification and denitrification. contained in average 16.1 (12.7) mg/L of NH-N, 13.7 (9.4) mg/L of NO3?-N. 0.94 (0.69) mg/L of NO-N. and 0.36 (0.26) mg/L of PO-P. Due to the neglectable influence of other processes like nutrient uptake by submerged macrophytes and algae, desorption of ammonia or dilution, the changes of the concentrations of the inorganic nitrogen compounds are mainly influenced by nitrification and denitrification. The nitrification is mainly done by sessile nitrifiers in the treated sewage channel Wuhle. The nitrification rates. calculated from the decrease of the ammonium concentrations, were between 0.5 and 20 g/(m2d) related to the flowing stretch area. The ammonium concentrations decreased along the flowing stretch in average by 20 to 44%. The highest nitrification rates could be found at the stretches with a dense colonization with submerged macrophytes and a good oxygen supply due to low water depth and high flowing velocities. The denitrification rates, calculated from the decrease of the total of the concentrations of the inorganic nitrogen compounds, were between 0.5 and 23 g/(m2d) related to the flowing stretch area. The total loss of nitrogen due to denitrification was between 10 and 20% along the flowing stretch of the treated sewage channel Wuhle. This corresponds to a total amount of up to 530 kg nitrogen per day. The main part of the phosphorus occured as orthophosphate in concentrations between 0.04 and 0.87 mg/L of PO-P in the effluent of the treatment sewage plant Falkenberg. The orthophosphate concentration changed along the flowing stretch mostly in such a manner that it were at the same level at the end of the flowing stretch at the mouth into the river Spree. The self-purification capacity of the channel does not lead to a relevant reduction of the very high nutrient load under the present conditions. The rates of the photosynthetic production (P) and the community respiration (R) were calculated from the rates of the total changes of oxygen with regard to the physical aeration. The rates of the photosynthetic production were between 0 and 33 g/(m2d), the rates of the community respiration between 15 and 75 g/(m2d). Therewith, the Wuhle treatment sewage channel belongs to the very productive waters. A positive balance (P > R) could only be measured on two segments in May. The rates of oxygen production depend on the ratio width to depth of the water. It is possible that the positive influence of the submerged macrophytes on the oxygen balance also at higher biomasses than 250 g/m2 (as dry weight) predominates at the segments with a favourable ratio. The portion of the oxygen input through diffusion along the flowing stretch and at the weirs was 30%, respectively, that of the photosynthic production 40% in summer. The rates of community respiration decreased along the flowing stretch by 50 to 90%. The nitrification had the main portion of the oxygen depletion in the Wuhle treated sewage channel with 60…80%. Despite the high biomass, the respiration of the submerged macrophytes had only a small portion of the total oxygen depletion. Nevertheless, the submerged macrophytes contributed to the nearly total oxygen depletion at the most densely covered segment 2 at night. The decrease of the content of particular organic material and the ammonia concentrations at the effluent of the sewage treatment plant, a diminishing of the biomass of submerged macrophytes by shading, and the widening of a few flowing stretches are demanded for the improvement of the oxygen balance of the Wuhle treated sewage channel.  相似文献   

17.
Source apportionment of particulate matter <10 µm in diameter (PM10), having considerable impacts on human health and the environment, is of high priority in air quality management. The present study, therefore, aimed at identifying the potential sources of PM10 in an arid area of Ahvaz located in southwest of Iran. For this purpose, we collected 24‐h PM10 samples by a high volume air sampler. The samples were then analyzed for their elemental (Al, As, B, Ba, Be, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, Pb, Se, Si, Sn, Sr, Li, Ti, V, Zn, Mo, and Sb) and ionic (NH, Cl?, NO, and SO) components using inductively coupled plasma optical emission spectrometry and ion chromatography instruments, respectively. Eight factors were identified by positive matrix factorization: crustal dust (41.5%), road dust (5.5%), motor vehicles (11.5%), marine aerosol (8.0%), secondary aerosol (9.5%), metallurgical plants (6.0%), petrochemical industries and fossil fuel combustion (13.0%), and vegetative burning (5.0%). Result of this study suggested that the natural sources contribute most to PM10 particles in the area, followed closely by the anthropogenic sources.  相似文献   

18.
The water quality of an urban pond in the thickly populated area of Varanasi city (5 km apart) was studied and compared with a rural pond in the Banaras Hindu University campus for transparency, conductivity and nutrient richness (Cl?, SO, PO? P, NO? N, organic carbon, Ca2+, Mg2+, K+, Na+) at three depths (surface, 1.5 m, 3 m) at monthly intervals between February 1982 and February 1983. This was done to assess the effects of urban surroundings of a very ancient city sector on pond water quality in reference to that of a rural pond. The rural pond had a lush growth of 12 macrophytic species, whereas the urban one had only such a growth with many phytoplanktonic species. Transparency was maximum in the winter season and the rural pond water was more transparent, while the electrolytical conductance was maximum in the rainy season, being higher in the urban pond. Electrolytical conductivity was negatively correlated to transparency: urban: EC = 1081.612–6.575 T, r2 = 0.897, F1,11 = 96, P <0.005; rural: EC = 728.981–4.328 T, r2 = 0.892, F1,11 = 91, P <0.005. Chloride and sulphate concentrations were highest in summer months, but the former was much higher in the urban pond while the latter in the rural pond. NO3–N was highest in the rainy season in the rural pond and in early winter in the urban one and showed a definite trend with change in depth. PO4–P also varied with depth and time and it was higher in late summer and the early rainy season in the rural pond and in early winter in the urban pond. But both these nutrients were much higher in the urban pond. The maximum organic carbon concentration was found in the rainy season in the rural pond and in summer months in the urban pond. The variation of organic carbon with depth was distinct. Both summer and winter seasons showed almost similar values of calcium concentration in the rural pond, but in the urban pond it was maximum in summer. Organic carbon and calcium were higher in the urban pond. The magnesium concentration was highest in rainy months in both the ponds, but the periodicity of the minimum differed. The distribution of calcium with depth was not well defined. The highest concentration of potassium was found in the winter season in both the ponds. The sodium concentration in the rural pond was observed maximum in summer and minimum in the rainy season, but in the urban pond the trend was different. The variation of potassium and sodium with depth was not well defined. Magnesium and sodium were also higher in the urban pond but potassium was almost at the same concentration in both the ponds. The effect of urbanisation may be one of the factors which might be responsible to the shift of the species composition towards phytoplanktonic flora.  相似文献   

19.
The wet ammonia (NH3) desulfurization process can be retrofitted to remove nitric oxide (NO) and sulfur dioxide (SO2) simultaneously by adding soluble cobalt(II) salt into the aqueous ammonia solution. Activated carbon is used as a catalyst to regenerate hexaminecobalt(II), Co(NH3), so that NO removal efficiency can be maintained at a high level for a long time. In this study, the catalytic performance of pitch‐based spherical activated carbon (PBSAC) in the simultaneous removal of NO and SO2 with this wet ammonia scrubbing process has been studied systematically. Experiments have been performed in a batch stirred cell to test the catalytic characteristics of PBSAC in the catalytic reduction of hexaminecobalt(III), Co(NH3). The experimental results show that PBSAC is a much better catalyst in the catalytic reduction of Co(NH3) than palm shell activated carbon (PSAC). The Co(NH3) reduction reaction rate increases with PBSAC when the PBSAC dose is below 7.5 g/L. The Co(NH3) reduction rate increases with its initial concentration. Best Co(NH3) conversion is gained at a pH range of 2.0–6.0. A high temperature is favorable to such reaction. The intrinsic activation energy of 51.00 kJ/mol for the Co(NH3) reduction catalyzed by PBSAC has been obtained. The experiments manifest that the simultaneous elimination of NO and SO2 by the hexaminecobalt solution coupled with catalytic regeneration of hexaminecobalt(II) can maintain a NO removal efficiency of 90% for a long time.  相似文献   

20.
High‐resolution measurements of rainfall, water level, pH, conductivity, temperature and carbonate chemistry parameters of groundwater at two adjacent locations within the peak cluster karst of the Guilin Karst Experimental Site in Guangxi Province, China, were made with different types of multiparameter sonde. The data were stored using data loggers recording with 2 min or 15 min resolution. Waters from a large, perennial spring represent the exit for the aquifer's conduit flow, and a nearby well measures water in the conduit‐adjacent, fractured media. During flood pulses, the pH of the conduit flow water rises as the conductivity falls. In contrast, and at the same time, the pH of groundwater in the fractures drops, as conductivity rises. As Ca2+ and HCO3? were the dominant (>90%) ions, we developed linear relationships (both r2 > 0·91) between conductivity and those ions, respectively, and in turn calculated variations in the calcite saturation index (SIC) and CO2 partial pressure (P) of water during flood pulses. Results indicate that the P of fracture water during flood periods is higher than that at lower flows, and its SIC is lower. Simultaneously, P of conduit water during the flood period is lower than that at lower flows, and its SIC also is lower. From these results we conclude that at least two key processes are controlling hydrochemical variations during flood periods: (i) dilution by precipitation and (ii) water–rock–gas interactions. To explain hydrochemical variations in the fracture water, the water–rock–gas interactions may be more important. For example, during flood periods, soil gas with high CO2 concentrations dissolves in water and enters the fracture system, the water, which in turn has become more highly undersaturated, dissolves more limestone, and the conductivity increases. Dilution of rainfall is more important in controlling hydrochemical variations of conduit water, because rainfall with higher pH (in this area apparently owing to interaction with limestone dust in the lower atmosphere) and low conductivity travels through the conduit system rapidly. These results illustrate that to understand the hydrochemical variations in karst systems, considering only water–rock interactions is not sufficient, and the variable effects of CO2 on the system should be evaluated. Consideration of water–rock–gas interactions is thus a must in understanding variations in karst hydrochemistry. Copyright © 2004 John Wiley & Sons, Ltd.  相似文献   

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