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1.
During Li recovery from salar brines, Li concentration is typically increased to about 60,000 mg L?1 by evaporation. We investigated the concentration changes of Li, Na, K, Mg, Cl, SO4, and B during evaporation of both natural Uyuni and artificial Atacama brines. The Uyuni brine exhibited a maximum Li concentration of 6810 mg L?1 at 31 days of evaporation, at which point the majority of the Na and K in the brine was removed. The Li concentration decreased with further evaporation due to precipitation as Li2SO4, such that the level at the 56 day mark was approximately 4130 mg L?1. In contrast, the artificial Atacama brine showed no pronounced Li precipitation, even after 54 days, at which point the Li concentration was 21,800 mg L?1. The initial concentrations of Na and K in the Atacama brine were higher than those in the Uyuni brine, and the Atacama solution still retained K after 54 days of evaporation. The order of precipitation of cation species during the evaporation of both brines was: Na, followed by K, Mg, and Li. Thus, Li precipitation in the Atacama brine might be prevented due to the more favored precipitations of Na and K, such that significant Li removal did not occur in this brine.  相似文献   

2.
The present study examines the temporal variability of air–water CO2 fluxes (FCO2) and seawater carbonate chemistry in a Baja California coastal lagoon during an exceptionally warm anomaly that was developed in Northeast Pacific coasts during 2014. This oceanographic condition led to a summer-like season (weak upwelling condition) during the study period, which reached a maximum surface temperature anomaly of 2 °C in September 2014. San Quintín Bay acts as a source of CO2 to the atmosphere in 2014 (3.3 ± 4.8 mmol C m?2 day?1) with the higher positive fluxes mainly observed in summer months (9.0 ± 5.3 mmol C m?2 day?1). Net ecosystem production (NEP) switched seasonally between net heterotrophy and net autotrophy during the study period, with an annual average of 2.2 ± 7.1 mmol C m?2 day?1, which indicates that San Quintín Bay was a net autotrophic system during the atypical warm oceanographic condition in 2014. This pattern of seasonal variations in the carbon balance at San Quintín Bay appears to be linked to the life cycle of benthic communities, which play an important role in the whole-ecosystem metabolism. Under the limited input from external sources coupled with an increase in seawater temperatures, the recycled benthic carbon and nutrient fluxes play a major role to sustain water-column processes within the bay. Since the upwelling condition may influence the magnitude of the air–water CO2 fluxes, our results clearly indicated that San Quintín Bay is a net source of carbon to the atmosphere regardless of the adjacent oceanic conditions. Our study sheds light on the carbon dynamics and its metabolic implications in a shallow coastal ecosystem under a regional warm anomaly and contributes potentially relevant information in view of the likely future scenario of global climate change.  相似文献   

3.
Salt tolerance in eighteen advanced rice genotypes was studied under an artificially salinized (EC=8.5 dSm?1) soil conditions after 90 days of transplanting. The results showed that the yield per plant, chlorophyll concentrations, fertility percentage, and number of productive tillers, panicle length and number of primary braches per panicle of all the genotypes were reduced by salinity. However, genotypes viz. Jhona-349 x Basmati-370, NR-1, DM-59418, DM-63275, DM-64198 and DM-38-88 showed better salinity tolerance than others.  相似文献   

4.
Coherency stress and coherency strain energy generated by Na+?K+ ion exchange in alkali feldspars are calculated using an isotropic model, and deformation of single crystals of alkali feldspars exposed to molten alkali chlorides at \(P_{H_2 O} \) < 1 bar is described. Coherency stress in alkali feldspars can reach 10–20 kb. When it is large, partial relaxation by fracture and/or plastic deformation takes place under anhydrous conditions, but temporary build-up of stress is unavoidable even under hydrothermal conditions. Because of coherency strain energy, a thin layer of an end-member alkali feldspar produced by cation exchange on a grain of the other end-member alkali feldspar would be unstable with respect to dissolution. Therefore, under hydrothermal conditions one end-member alkali feldspar replaces the other by dissolution and precipitation. The mechanism of the reaction $$Na_x K_{1 - x} AlSi_3 O_{8_{(feld.)} } + yK^ + \rightleftharpoons Na_{x - y} K_{1 + y - x} AlSi_3 O_{8_{(feld.)} } + yNa^ + $$ is primarily controlled by \(P_{H_2 O} \) and by ΔK/(Na + K), the difference between the equilibrium value and the initial value of the atomic K/(Na + K) ratio of the feldspar. When ¦ΔK/(Na + K)¦ is small, the reaction proceeds by cation exchange. When ¦ΔK/(Na + K)¦ is large, cation exchange still occurs if \(P_{H_2 O} \) is very low, but under hydrothermal conditions replacement by dissolution and precipitation occurs.  相似文献   

5.
We studied organic matter cycling in two Gulf Coast tidal, nonsaline marsh sites where subsidence causes marine intrusion and rapid submergence, which mimics increased sea-level rise. The sites experienced equally rapid submergence but different degrees of marine intrusion. Vegetation was hummocked and much of the marsh lacked rooted vegetation. Aboveground standing crop and production, as measured by sequential harvesting, were low relative to other Gulf CoastSpartina patens marshes. Soil bulk density was lower than reported for healthyS. alterniflora growth but that may be unimportant at the current, moderate sulfate levels. Belowground production, as measured by sequential harvesting, was extremely fast within hummocks, but much of the marsh received little or no belowground inputs. Aboveground production was slower at the more saline site (681 g m?2 yr?1) than at the less saline site (1,252 g m?2 yr?1). Belowground production over the entire marsh surface averaged 1,401 g m?2 yr?1 at the less saline site and 585 g m?2 yr?1 at the more saline site. Respiration, as measured by CO2 emissions in the field and corrected for CH4 emissions, was slower at the less saline site (956 g m?2 yr?1) than at the more saline site (1,438 g m?2 yr?1), reflecting greater contributions byS. alterniflora at the more saline site which is known to decompose more rapidly thanS. patens. Burial of organic matter was faster at the less saline site (796 g m?2 yr?1) than at the more saline site (434 g m?2, yr?1), likely in response to faster production and slower decomposition at the less saline site. Thus vertical accretion was faster at the less saline site (1.3 cm yr?1) than at the more saline site (0.85 cm yr?1); slower vertical accretion increased flooding at the more saline site. More organic matter was available for export at the less saline site (1,377 g m?2 yr?1) than at the more saline site (98 g m?2 yr?1). These data indicated that organic matter production decreased and burial increased in response to greenhouse-like conditions brought on by subsidence. *** DIRECT SUPPORT *** A01BY069 00016  相似文献   

6.
The weathering rates and mechanisms of three types of glassy rocks were investigated experimentally at 25 °C, pH 1.0 to 6.2, and reaction times as much as to 3 months. Changes in major element chemistry were monitored concurrently as a function of time in the aqueous solution and within the near surface region of the glass. Leach profiles, obtained by a HF leaching technique, displayed near-surface zones depleted in major cations. These zones increased in depth with increasing time and decreasing pH of reactions. Release rates into the aqueous solution were parabolic for Na and K and linear for Si and Al. A coupled weathering model, involving surface dissolution with concurrent diffusion of Na, K, and Al, produced a mass balance between the aqueous and glass phases. Steady state conditions are reached at pH 1.0 after approximately 3 weeks of reaction. Steady-state is not reached even after 3 months at pH 6.2.An interdiffusion model describes observed changes in Na diffusion profiles for perlite at pH 1.0. The calculated Na self-diffusion coefficient of 5 × 10?19 cm2·s?1 at 25°C approximates coefficients extrapolated from previously reported high temperature data for obsidian. The self-diffusion coefficient for H3O+, 1.2 × 10?20 cm2·s?1, is similar to measured rates of water diffusion during hydration of obsidian to form perlite.  相似文献   

7.
Lake Qinghai in the Qinghai-Tibet plateau is the largest lake in China. This study firstly reported the geochemistry of Cd in the lake. Water samples were collected from Lake Qinghai (n = 69) and Buha River (n = 12), while sediment (n = 22) and topsoil (n = 45) samples were collected from the lake and around the lake area, respectively. In addition, pore water samples (n = 20) were separated from sediment samples. Water samples were analyzed for pH, K, Na, Ca, Mg, Cl, S, and Cd, while sediment and topsoil samples were analyzed for K, Na, Ca, Mg, Al, Fe, Mn, S, Sc, and Cd. The average concentration of Cd was 0.014 μg L?1 in the water of Lake Qinghai and 0.007 μg L?1 in the water of Buha River. However, the average concentration of Cd was 0.320 μg L?1 in the sediment pore water, much higher than that in the lake water and river water. Cadmium concentration in the lake water might be mainly controlled by salinity, while it in the pore water might be mainly controlled by carbonate minerals. Cadmium concentration in the river water might be controlled by alkalinity and pH. The average concentration of Cd in the sediment was 0.284 mg kg?1. The enrichment of Cd in the lake sediment was significantly higher than that in the topsoil around the lake. Anthropogenic atmospheric deposition of Cd did not led to the increase in dissolved Cd level in the lake water, but led to its enrichment in the lake sediment.  相似文献   

8.
Disposal of saline subsurface drainage waters from croplands into evaporation basins (or ponds) in the San Joaquin Valley of California causes excessive accumulation of salts and elevated concentrations of arsenic (As), a potentially high risk element with little information about its fate, in the agricultural evaporation ponds. We examined dissolved As concentration, speciation, and distribution in waters as well as As fractionation in sediments in the 10-cell South Evaporation Basin for better understanding of processes and conditions affecting As transformations and fate in a specific drainage disposal facility. The increase of total dissolved As concentrations were observed with higher Cl− and electric conductivity along flow path indicating that evaporation was an important factor regulating total dissolved As concentration. The increases of reduced As species such as arsenite [As(III)] and organic As (monomethylarsonic acid and dimethylarsinic acid) were found towards the terminal flow pathway. However, arsenate [As(V)], the oxidized species remained greater than 67% of total dissolved As in all cell waters. Sequential extractions of sediments indicated that reducing conditions may influence As behavior in sediments to be more soluble and exchangeable. Arsenic association with oxides was appreciable only under oxidizing condition. Carbonate minerals played an important role in immobilizing As into the sediments under alkaline condition and a broad range of redox conditions. However, these sink mechanisms did not significantly reduce As concentrations in the cell waters. The reducing condition facilitated by high concentration of organic matter might be a major factor for the increase in As mobility.  相似文献   

9.
San Quintin Bay, Mexico, is a hypersaline coastal lagoon where the main external forcing of physical and biogeochemical processes is oceanic. Non-conservative fluxes of inorganic N (ΔDIN) and P (ΔDIP), and aspects of net ecosystem metabolism were studied in this lagoon during August 1995, August 1996, and February 1996, by following the LOICZ budgetary modeling approach. The whole-system water exchange time during summer (≈13 d) was shorter than in winter (≈26 d) as northwesterly winds enhancing mixing with the ocean are more intense during the spring-summer upwelling season. Whole-bay ΔDIP values of +0.2 to +0.3 mmol m?2 d?1 in August, and <+0.01 mmol m?2 d?1 in February indicate that the system is a net source of dissolved inorganic phosphorus (DIP). DIP fluxes from the Bay to the ocean during August are probably balanced by a net import of particulate organic matter between 1,000–1,300 × 103 mol C d?1, equivalent to a net ecosystem production (NEP) between ?24 and ?31 mmol C m?2 d?1. ΔDIN showed opposite trends in August 1995 and August 1996, with a net import of 13×103 mol N d?1 and a net export of 30× 103 mol N d?1, respectively. However, N fixation minus denitrification (“apparent denitrification”) estimates of ≈?4 mmol N m?2 d?1 in both periods indicate that San Quintin Bay is a net sink of nitrogen. Results from a 3-box model indicate that during summer Box C, adjacent to the ocean, contributed 70–80% of the excess DIP produced in the whole-system. This observation and high apparent denitrification values of ≈?7 mmol N m?2 d?1 at the entrance of the Bay, suggest that the net heterotrophic condition of San Quintin Bay in summer is largely determined by imports of labile phytoplanktonic carbon generated in the adjacent ocean during upwelling.A net flux of organic carbon of 30×106 mol C yr?1 was estimated from Box C, adjacent to the ocean, to Box B, locally known as Bahia Falsa, which is the area designated for oyster aquaculture in the lagoon. It is estimated that this net organic carbon supply is almost equivalent to the annual oyster food demand; our estimate is that oyster aquaculture in San Quintin Bay accounts for the vast majority of the net heterotrophy of Bahia Falsa.  相似文献   

10.
Measurements of groundwater-dissolved inorganic nitrogen (nitrate?+?nitrite?+?ammonia) and phosphate concentrations were combined with recent, radium-based, submarine groundwater discharge (SGD) fluxes and prior estimates of SGD determined from Darcy’s Law, a hydrologic model, and total recharge to yield corresponding SGD nutrient fluxes to Ninigret, Point Judith, Quonochontaug, and Winnapaug ponds, located in southern Rhode Island. Results range from 80 to279 mmol N m?2 year?1 and 4 to 15 mmol P m?2 year?1 for Ninigret, 48 to 265 mmol N m?2 year?1 and 4 to 23 mmol P m?2 year?1 for Point Judith, 31 to 62 mmol N m?2 year?1 and 1 to 2 mmol P m?2 y?1 for Quonochontaug, and 668 to 1,586 mmol N m?2 year?1 and 29 to 70 mmol P m?2 year?1 for Winnapaug ponds, respectively. On a daily basis, the SGD supply of dissolved inorganic nitrogen and phosphorus is estimated to represent ～1–6 % of the total amount of these nutrients in surface waters of Ninigret, Point Judith, and Quonochontaug ponds and up to 84 and 17 % for Winnapaug, respectively, which may reflect a greater SGD nutrient supply to this pond because of the proximity of fertilized golf courses. With regard to the total external input of these essential nutrients, SGD represents 29–45 % of dissolved inorganic nitrogen input to Ninigret, Point Judith, and Quonochontaug ponds and as much as 93 % for Winnapaug pond. For phosphorus, the contribution from SGD represents 59–85 % of the total external input for Ninigret, Point Judith, and Quonochontaug ponds and essentially all of the phosphorus input to Winnapaug pond. Estimated rates of primary productivity potentially supported by the average supply of dissolved inorganic nitrogen from SGD range from 10 g C m?2 year?1 for Ninigret, 13 g C m?2 year?1 for Point Judith, 4 g C m?2 year?1 for Quonochontaug, and as high as 84 g C m?2 y?1 for Winnapaug pond. The imputed SGD-derived rates of primary productivity represent 4–9 % of water column primary production for Ninigret, Point Judith, and Quonochontaug ponds, and 74 % for Winnapaug pond, a result that is reasonably comparable to several other coastal environments where estimates of SGD nutrient supply have been reported. The implication is that SGD represents an ecologically significant source of dissolved nutrients to the coastal salt ponds of southern Rhode Island and, by inference, other coastal systems.  相似文献   

11.
Wheat being a glycophyte crop, responds differently to saline-sodic soil environmental conditions. The application of calcium is multidimensional with respect to sodium ion and plant part response. This study was conducted to record the response of shoot and root to sodium and calcium interaction under saline environment. Wheat seed of variety Punjab 85 were raised in quartz sand. Later on the seedlings were transplanted to pots containing Hoagland’s nutrient solution along with NaCl at 0 mM. and 50 mM. Calcium was applied as CaSO2 2H2O at 3 mM. and 6 mM. Under saline conditions shoot showed positive response to sodium ion in the presence of higher calcium. Relative water contents were higher in the root system at 6 mM of CaSO4. 2H2O under saline condition. Growth responses to potassium and Magnesium in the presence of sodium induced salinity with calcium ion interaction remained variable.  相似文献   

12.
Benthic fluxes of soluble reactive phosphorus (SRP) and dissolved inorganic carbon (DIC) were measured in situ using autonomous landers in the Gulf of Finland in the Baltic Sea, on four expeditions between 2002 and 2005. These measurements together with model estimates of bottom water oxygen conditions were used to compute the magnitude of the yearly integrated benthic SRP flux (also called internal phosphorus load). The yearly integrated benthic SRP flux was found to be almost 10 times larger than the external (river and land sources) phosphorus load. The average SRP flux was 1.25?±?0.56?mmol?m?2?d?1 on anoxic bottoms, and ?0.01?±?0.08?mmol?m?2?d?1 on oxic bottoms. The bottom water oxygen conditions determined whether the SRP flux was in a high or low regime, and degradation of organic matter (as estimated from benthic DIC fluxes) correlated positively with SRP fluxes on anoxic bottoms. From this correlation, we estimated a potential increase in phosphorus flux of 0.69?±?0.26?mmol?m?2?d?1 from presently oxic bottoms, if they would turn anoxic. An almost full annual data set of in situ bottom water oxygen measurements showed high variability of oxygen concentration. Because of this, an estimate of the time which the sediments were exposed to oxygenated overlying bottom water was computed using a coupled thermohydrodynamic ocean?Csea and ecosystem model. Total phosphorus burial rates were calculated from vertical profiles of total phosphorus in sediment and sediment accumulation rates. Recycling and burial efficiencies for phosphorus of 97 and 3%, respectively, were estimated for anoxic accumulation bottoms from a benthic mass balance, which was based on the measured effluxes and burial rates.  相似文献   

13.
Long-term intake of high-fluoride groundwater causes endemic fluorosis. This study, for the first time, discovered that the salt lake water intrusion into neighboring shallow aquifers might result in elevation of fluoride content of the groundwater. Two cross-sections along the groundwater flow paths were selected to study the geochemical processes controlling fluoride concentration in Yuncheng basin, northern China. There are two major reasons for the observed elevation of fluoride content: one is the direct contribution of the saline water; the other is the undersaturation of the groundwater with respect to fluorite due to salt water intrusion, which appears to be more important reason. The processes of the fluorine activity reduction and the change of Na/Ca ratio in groundwater induced by the intrusion of saline water favor further dissolution of fluorine-bearing mineral, and it was modeled using PHREEQC. With the increase in Na concentration (by adding NaCl or Na2SO4 as Na source, calcium content kept invariable), the increase of NaF concentration was rapid at first and then became slower; and the concentrations of HF, HF2−, CaF+, and MgF+ were continuously decreasing. The geochemical conditions in the study area are advantageous to the complexation of F− with Na+ and the decline of saturation index of CaF2, regardless of the water type (Cl–Na or SO4–Na type water).  相似文献   

14.
Si, Al, Ca, Mg, Fe, Na, K, CO 3 ?2 , F, etc. are detected from the fluid inclusion leachates. Among these constituents, Si, Na, and CO 3 ?2 are predominant, amounting to more than 80 percent. This indicates that the ore-forming solution must be alkaline with Si, Na, and CO 3 ?2 as its dominant components. Homogenization temperatures for the solution range from 80 to 360°C. Although rock quartz can crystallize at the above temperature interval, perfect crystals of economic importance are largely formed below 260°C. The temperature of formation increases toward the granite intrusives at a rate of about one degree per meter. It is estimated from the lithostatic load that the salinity of rock quartz is 17–23 (NaCl wt%), while that of vein quartz is relatively high as compared with the former. There is a tendency for the salinity of the ore-forming solution to increase with depth.  相似文献   

15.
Seasonal responses in estuarine metabolism (primary production, respiration, and net metabolism) were examined using two complementary approaches. Total ecosystem metabolism rates were calculated from dissolved oxygen time series using Odum’s open water method. Water column rates were calculated from oxygen-based bottle experiments. The study was conducted over a spring-summer season in the Pensacola Bay estuary at a shallow seagrass-dominated site and a deeper bare-bottomed site. Water column integrated gross production rates more than doubled (58.7 to 130.9 mmol O2 m?2 day?1) from spring to summer, coinciding with a sharp increase in water column chlorophyll-a, and a decrease in surface salinity. As expected, ecosystem gross production rates were consistently higher than water column rates but showed a different spring-summer pattern, decreasing at the shoal site from 197 to 168 mmol O2 m?2 day?1 and sharply increasing at the channel site from 93.4 to 197.4 mmol O2 m?2 day?1. The consistency among approaches was evaluated by calculating residual metabolism rates (ecosystem ? water column). At the shoal site, residual gross production rates decreased from spring to summer from 176.8 to 99.1 mmol O2 m?2 day?1 but were generally consistent with expectations for seagrass environments, indicating that the open water method captured both water column and benthic processes. However, at the channel site, where benthic production was strongly light-limited, residual gross production varied from 15.7 mmol O2 m?2 day?1 in spring to 86.7 mmol O2 m?2 day?1 in summer. The summer rates were much higher than could be realistically attributed to benthic processes and likely reflected a violation of the open water method due to water column stratification. While the use of sensors for estimating complex ecosystem processes holds promise for coastal monitoring programs, careful attention to the sampling design, and to the underlying assumptions of the methods, is critical for correctly interpreting the results. This study demonstrated how using a combination of approaches yielded a fuller understanding of the ecosystem response to hydrologic and seasonal variability.  相似文献   

16.
In this study, analysis of hydrogeological conditions, as well as hydrochemistry and isotopic tools were used to get an insight into the processes controlling mineralization, recharge conditions, and flow pattern of groundwater in a typical arid alluvial-lacustrine plain in Qaidam Basin, northwest China. Analysis of the dissolved constituents reveals that groundwater evolves from fresh water (TDS =300–1000 mg/l) to saline water (TDS ≥5000 mg/l) along the flow paths, with the water type transiting from HCO 3?Cl–Na ?Mg to HCO 3?Cl–Na, and eventually to Cl–Na. Groundwater chemical evolution is mainly controlled by water–rock interaction and the evaporation–crystallization process. Deuterium and oxygen-18 isotopes in groundwater samples indicate that the recharge of groundwater is happened by meteoric water and glacier melt-water in the Kunlun Mountains, and in three different recharge conditions. Groundwater ages, estimated by the radiogenic (3H and 14C) isotope data, range from present to Holocene (～28 ka). Based on groundwater residence time, hydrogeochemical characteristics, field investigation, and geological structure distribution, a conceptual groundwater flow pattern affected by uplift structure is proposed, indicating that shallow phreatic water is blocked by the uplift structure and the flow direction is turned to the northwest, while high pressure artesian water is formed in the confined aquifers at the axis of the uplift structure.  相似文献   

17.
Hypoxia is emerging as a major threat to marine coastal biota. Predicting its occurrence and elucidating the driving factors are essential to set successful management targets to avoid its occurrence. This study aims to elucidate the effects of warming on the likelihood of hypoxia. High-frequency dissolved oxygen measurements have been used to estimate gross primary production (GPP), net ecosystem production (NEP) and community respiration (CR) in a shallow macroalgae (Caulerpa prolifera) ecosystem in a highly human-influenced closed Mediterranean bay. Daily averaged GPP and CR ranged from 0 to 1,240.9 and 51.4 to 1,297.3?mmol?O2?m?2?day?1, respectively. The higher GPP and CR were calculated for the same day, when daily averaged water temperature was 28.3?°C, and resulted in a negative NEP of ?56.4?mmol?O2?m?2?day?1. The ecosystem was net heterotrophic during the studied period, probably subsidized by allochthonous organic inputs from ground waters and from the surrounding town and boating activity. Oxygen dynamics and metabolic rates strongly depend on water temperature, with lower oxygen content at higher temperatures. The probability of hypoxic conditions increased at a rate of 0.39?% °C?1 (±0.14?% °C?1). Global warming will increase the likelihood of hypoxia in the bay studied, as well as in other semi-enclosed bays.  相似文献   

18.
Experiments on the partitioning of Cu between different granitic silicate melts and the respective coexisting aqueous fluids have been performed under conditions of 850 °C, 100 MPa and oxygen fugacity（f O2） buffered at approaching Ni–Ni O（NNO）. Partition coefficients of Cu（DCu= cfluid/cmelt） were varied with different alumina/alkali mole ratios [Al2O3/（Na2O·K2O）, abbreviated as Al/Alk], Na/K mole ratios, and Si O2 mole contents. The DCu increased from 1.28 ± 0.01 to 22.18 ± 0.22 with the increase of Al/Alk mole ratios（ranging from 0.64 to 1.20）and Na/K mole ratios（ranging from 0.58 to 2.56）. The experimental results also showed that DCuwas positively correlated with the HCl concentration of the starting fluid.The DCuwas independent of the Si O2 mole content in the range of Si O2 content considered. No DCuvalue was less than 1 in our experiments at 850 °C and 100 MPa, indicating that Cu preferred to enter the fluid phase rather than the coexisting melt phase under most conditions in the melt-fluid system, and thus a significant amount of Cu could be transported in the fluid phase in the magmatichydrothermal environment. The results indicated that Cu favored partitioning into the aqueous fluid rather than themelt phase if there was a high Na/K ratio, Na-rich, peraluminous granitic melt coexisting with the high Cl-fluid.  相似文献   

19.
Insufficient knowledge of the hydrogeochemistry of aquifers in the Central Region of Ghana has necessitated a preliminary water quality assessment in some parts of the region. Major and minor ions, and trace metal compositions of groundwater have been studied with the aim of evaluating hydrogeochemical processes that are likely to impair the quality of water in the study area. The results show that groundwater in the area is weakly acidic with mean acidity being 5.83 pH units. The dominant cation in the area is Na, followed by K, Ca, and Mg, and the dominant anion is Cl?, followed by HCO3 ? and SO4 2?. Two major hydrochemical facies have been identified as Na–Cl and Na–HCO3, water types. Multivariate statistical techniques such as cluster analysis (CA) and factor analysis/principal component analysis (PCA), in R mode, were employed to examine the chemical compositions of groundwater and to identify factors that influenced each. Q-mode CA analysis resulted in two distinct water types as established by the hydrochemical facies. Cluster 1 waters contain predominantly Na–Cl. Cluster 2 waters contain Na–HCO3 and Na–Cl. Cluster 2 waters are fresher and of good quality than cluster 1. Factor analysis yielded five significant factors, explaining 86.56% of the total variance. PC1 explains 41.95% of the variance and is contributed by temperature, electrical conductivity, TDS, turbidity, SO4 2?, Cl?, Na, K, Ca, Mg, and Mn and influenced by geochemical processes such as weathering, mineral dissolution, cation exchange, and oxidation–reduction reactions. PC2 explains 16.43% of the total variance and is characterized by high positive loadings of pH and HCO3 ?. This results from biogenic activities taking place to generate gaseous carbon dioxide that reacts with infiltrating water to generate HCO3 ?, which intend affect the pH. PC3 explains 11.17% of the total variance and is negatively loaded on PO4 3? and NO3 ? indicating anthropogenic influence. The R-mode PCA, supported by R-mode CA, have revealed hydrogeochemical processes as the major sources of ions in the groundwater. Factor score plot revealed a possible flow direction from the northern sections of the study area, marked by higher topography, to the south. Compositional relations confirmed the predominant geochemical process responsible for the various ions in the groundwater as mineral dissolution and thus agree with the multivariate analysis.  相似文献   

20.
The detailed hydro-chemical study of meltwater draining from Khangri glacier Arunachal Pradesh has been carried out to evaluate the major ion chemistry and weathering processes in the drainage basin. The investigative results shows that the meltwater is almost neutral to slightly acidic in nature with Mg–HCO3-dominated hydro-chemical facies. In glacial meltwater, Ca+?2 is the most dominated cation followed by Mg+2, Na+, and K+, while HCO3? is the most dominant anion followed by SO42?, NO3?, and Cl?. The dominant cations such as Ca+2 and Mg+2 show a good relation with the minerals abundance of the rocks. Calcite (CaCO3) and biotite [K(Mg,Fe)3AlSi3O10(F,OH)2] are the most abundant minerals in the deformed carbonate-rich metasedimentary rocks near to the snout with some K feldspar (KAlSi3O8) and quartz (SiO2). This suggests Ca+2 have definitely entered into the water due to the dissolution of calcite and Ca feldspar (CaAl2Si2O8), while one of the source of Mg+2 is biotite. Na feldspar (NaAlSi3O8) has contributed towards the availability of sodium ion, while potassium ion is derived from the chemical weathering of K feldspar and biotite. The chemical weathering is the foremost mechanism controlling the hydro-chemistry of the Khangri glacier because of the least anthropogenic interferences. The mineralogy of surrounding rocks is studied to understand better, the rock–water interaction processes, and their contribution towards ionic concentration of meltwater. The meltwater discharge and individual ion flux of the catchment area have also been calculated, to determine the ionic denudation rate for the ablation season. The high elemental ratio of (Ca?+?Mg)/(Na?+?K) (7.91?±?0.39 mg/l) and low elemental ratio of (Na?+?K)/total cations (0.11?±?0.004) indicate that the chemical composition of meltwater is mainly controlled by carbonate weathering and moderately by silicate weathering. The scatter plot result between (Ca?+?Mg) and total cations confirms that carbonate weathering is a major source of dissolved ions in Khangri glacier meltwater. In addition, the statistical analysis was also used to determine the correlation between physical parameters of glacier meltwater which controlled the solute dynamics.  相似文献   

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