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1.
Alaknanda and Bhagirathi (AB) river basins in the Himalayan region in India expose lithologies comprising mainly of granites, low–high-grade metamorphics, shales and carbonates which, in conjunction with the monsoon rains and glacial melt, control water chemistry and dissolved elemental flux rates. In the present study, we monitored two locations: (a) Srinagar on the Alaknanda river and (b) Maneri on the Bhagirathi river for daily variations in total suspended sediments, major ions and dissolved silica over one complete year (July 2004–June 2005). Based on long-term discharge data, discharge-weighted composition and dissolved elemental flux rates (with respect to Ca, Mg, HCO3, Si) of the river were estimated. The information thus obtained has substantially added up to the existing chemical data of these rivers and has refined the flux rates. Our high-frequency samples provide informations such as (a) water chemical compositions that show a large temporal and spatial variation and (b) carbonate lithology that controls water chemistry predominantly. The dissolution kinetics of various lithologies namely leucogranite, gneiss, quartzite, phyllite and shale of the AB river basins were studied through batch experiments at controlled temperature (25 and 5°C) and pH (8.4) condition. In laboratory, these lithologies undergo slow rates of dissolution (10−13 to 10−15 mol/m2 s), while field weathering rates based on dissolved elemental flux rates in the AB rivers are much higher (10−8 to 10−9 mol/m2 s). Extremely high physical weathering rates in AB rivers, which enhance chemical weathering significantly, mainly attribute this wide discrepancy in laboratory-derived rates of representative basin rocks and dissolved elemental fluxes in the field. However, laboratory-simulated experiments facilitate to quantify elemental release rates, understand the kinetics of the dissolution reactions, and compare their roles at individual level.  相似文献   

2.
The influx of Sr responsible for increase in marine Sr has been attributed to rise of Himalaya and weathering of the Himalayan rocks. The rivers draining Himalaya to the ocean by the northern part of the Indian sub-continent comprising the Ganga Alluvial Plain (GAP) along with Central parts of the Himalaya and the northern part of the Indian Craton are held responsible for the transformation of Sr isotopic signature. The GAP is basically formed by the Himalayan-derived sediments and serves as transient zone between the source (Himalaya) and the sink (Bay of Bengal). The Gomati River, an important alluvial tributary of the Ganga River, draining nearly 30,500 km2 area of GAP is the only river which is originating from the GAP. The river recycles the Himalayan-derived sediments and transport its weathering products into the Ganga River and finally to Bay of Bengal. 11 water samples were collected from the Gomati River and its intrabasinal lakes for measurement of Sr isotopic composition. Sr concentration of Gomati River water is about 335 μg/l, which is about five times higher than the world’s average of river water (70 μg/l) and nearly three times higher than the Ganga River water in the Himalaya (130 μg/l) The Sr isotopic ratios reported are also higher than global average runoff (0.7119) and to modern seawater (0.7092) values. Strong geochemical sediment–water interaction appearing on surface is responsible for the dissolved Sr isotopic ratios in the River water. Higher Sr isotopic rations found during post-monsoon than in pre-monsoon season indicate the importance of fluxes due to monsoonal erosion of the GAP into the Gomati River. Monsoon precipitation and its interaction with alluvium appear to be major vehicle for the addition of dissolved Sr load into the alluvial plain rivers. This study establishes that elevated 87Sr/86Sr ratios of the Gomati River are due to input of chemical weathering of alluvial material present in the Ganga Alluvial Plain.  相似文献   

3.
 The Bengal basin, Bangladesh, represents one of the most densely populated recent floodplains of the world. The sediment flux through the basin is one of the highest on a global scale. A significant portion of this sediment load find its sink in the basin itself because of its lower elevation and frequent flooding. The textural, mineralogical and chemical nature of the sediments thus have an important bearing on the environmental quality of the basin as well as for the Bay of Bengal. The sediment load of the Ganges-Brahmaputra-Meghna (GBM) river system consists exclusively of fine sand, silt and clay at their lower reaches within the Bengal basin, Bangladesh, and is deposited under uniformly fluctuating, unidirectional energy conditions. The sediments have a close simitarity in grain size with the sediments of the surrounding floodplain. The mineral assemblage is dominated by quartz and feldspars. Illite and kaolinite are the major clay minerals, and occur in almost equal proportion in bed sediments. The heavy mineral assemblage is dominated by unstable minerals which are mostly derived from high-rank metamorphic rocks. The characteristic smaller grain-size, i.e. having large surface-to-mass ratios, and the mineralogy of sediments suggests that they are susceptible to large chemical adsorptive reactions and thus could serve as a potential trap for contaminants. However, the sediments of the GBM river system in the Bengal basin, Bangladesh, shows lower concentration of Pb, Hg and As, and a marginally higher value for Cd as compared to that of standard shale. Considering population density and extensive agricultural practice in the basin, the sediments can in the long run become contaminated. Received: 9 November 1994 · Accepted: 18 June 1996  相似文献   

4.
Sixty-eight groundwater samples from the Ganges-Brahmaputra floodplain in the Bengal Basin were analyzed to assess the groundwater geochemistry, the subsurface hydrology, the buffering effects of sediments on trace metal concentrations and their isotopic compositions, and the magnitude of the subsurface trace element flux to the Bay of Bengal and to the global ocean. Samples obtained from depths of 10 to 350 m were measured for major and trace elements, dissolved gas, and tritium. On the basis of the 3He/3H ages, the groundwater at depth (30-150 m) appears to be continually replenished, indicating that this recharge of groundwater to depth must ultimately be balanced by a significant quantity of submarine discharge into the Bay of Bengal. Using the 3He/3H groundwater age-depth relationship to calculate a recharge rate of 60 ± 20 cm/yr, we estimate a subsurface discharge into the Bay of Bengal of 1.5 ± 0.5 × 1011 m3/yr, or 15% of the surface Ganges-Brahmaputra river (GBR) flux. Several trace elements, especially Sr and Ba, display elevated concentrations averaging 7 to 9 times the surface GBR water values. The submarine groundwater fluxes of Sr and Ba to the oceans are 8.2 ± 2 × 108 and 1.5 ± 0.3 × 108 mol/yr, or 3.3 and 1.2%, respectively, of the world total, or equal to the surface GBR Sr and Ba estimated fluxes. Our groundwater flux for Ba agrees with the estimate of Moore (1997) (3 × 108-3 × 109 mol/yr), on the basis of measured Ba and Ra excesses in the Bay of Bengal. Other trace metals, such as U and Mo, are at low but measurable levels and are not major contributors to the global flux in this river system. A comparison of the Sr and Ba concentrations, plus 87Sr/86Sr ratios in groundwater to the oxalate extractable fractions of a coastal sediment core, suggests that weathering of carbonates and minor silicates, coupled with cation exchange plus adsorption and desorption reactions, controls the trace element concentrations and 87Sr/86Sr isotopic compositions in both the groundwater and river water. Our data also imply that other coastal floodplains (e.g., the Mekong and the Irrawaddy rivers) that have high precipitation rates and rapid accumulation of immature sediments are likely to make significant contributions to the global oceanic trace metal budgets and have an impact on the Sr isotopic evolution in seawater.  相似文献   

5.
We report osmium concentrations and isotopic compositions of 40 groundwater samples from the Bengal plain. Groundwaters have Os concentrations (16.9-191.5 pg/kg), about 5-10 times higher than those published for most rivers or seawater. 187Os/188Os varies widely (from 0.96 to 2.79) and is related to the isotopic signatures of the sediments constituting local aquifers. Os contents are correlated with those of soluble elements such as Sr, Mg, and Ca, suggesting that differing extents of solid-solution interaction explain most of the variation in measured Os concentrations. The covariation between Os and Sr allows us to estimate the mean Os content of Bengal groundwater (∼70 pg/kg). This concentration is too low to allow Bengal groundwater to significantly influence the marine Os isotopic composition, if likely fresh groundwater discharge rates to the Bay of Bengal are assumed. However, if Bengal groundwater Os concentrations are typical, the global Os groundwater flux would be expected to be around 180 kg/year, making it the second largest input of Os to the ocean after the river flux. Including this flux in the current Os marine budget, and assuming that this and other fluxes have remained constant with time, would decrease the calculated residence time of Os in the ocean by about 30%.  相似文献   

6.
Water samples were collected from different formations of Gadilam river basin and analyzed to assess the major ion chemistry and suitability of water for domestic and drinking purposes. Chemical parameters of groundwater such as pH, electrical conductivity (EC), total dissolved solids (TDS), Sodium (Na + ), Potassium (K + ), Calcium (Ca + ), Magnesium (Mg + ), Bicarbonate (HCO3  -_{3}^{\ \,-}), Sulphate (SO4  -_{4}^{\ \,-}), Phosphate (PO4  -_{4}^{\ \,-}) and Silica (H4SiO4) were determined. The geochemical study of the aquatic systems of the Gadilam river basin show that the groundwater is near-acidic to alkaline and mostly oxidizing in nature. Higher concentration of Sodium and Chloride indicates leaching of secondary salts and anthropogenic impact by industry and salt water intrusion. Spatial distribution of EC indicates anthropogenic impact in the downstream side of the basin. The concentration levels of trace metals such as Iron (Fe), Lead (Pb), Nickel (Ni), Bromide (Br), Iodide (I) and Aluminium (Al) have been compared with the world standard. Interpretation of data shows that some trace metals such as Al, Ni and Pb exceed the acceptable limit of world standard. Geophysical study was carried out to identify the weathered zone in the hard rock and contaminated zone by anthropogenic impact in the downstream of river Gadilam. A few of the groundwater samples in the study area were found to be unsuitable for domestic and drinking purposes.  相似文献   

7.
The changes in the water chemistry of rivers can reflect influence of anthropogenic activities on the water environment to some extent. To understand the relationship between the spatial distribution of the eco-environment of the watershed and the characteristics of water chemistry and geochemistry of rivers, firstly, the digital Wujiang watershed was built, and then the sub-watersheds were delineated, taking the sample points as sub-watershed outlets based on GIS. Secondly, using the function of spatial analyst of GIS, the statistical features of eco-environment (such as lithology and land use/cover) of each sub-watershed were calculated according to their respective classification. Finally, the correlation between the spatial distribution of lithology of the sub-watersheds and their corresponding 87Sr/86Sr ratio of river water, the correlation between NO3 −/HCO3 −, Cl−/HCO3 −, SO4 2−/HCO3 − and anthropogenic activities, respectively, and the correlation between the fraction of green vegetation of the sub-watershed and their corresponding flux of TDS (total dissolved solids) were analyzed quantitatively. The results justify that the 87Sr/86Sr ratio of river water is highly dependent on the lithologic feature of the watershed and indicate that anthropogenic activities are one of the main sources of NO3 − and SO4 2− of river waters. The output of TDS is highly dependent on the percentage of vegetation cover of the watershed.  相似文献   

8.
 The lower Ganges-Brahmaputra-Meghna (G-B-M) drainage basin occupies the total Bengal Basin, which is one of the unique basins of the world because of its location and size, density of population, and catastrophic deposition of sediments. The increased heavy metal concentration in the 63 m fraction of surface sediments shows similarity among major segments of the G-B-M system in the basin, which reflects the homogenization of lithologic and chemical diversity of the greater denudation regime by the river processes. The differences in heavy metal concentation in the lower G-B-M system with that of its upper and middle counterpart is mainly related to the contrast between Himalayan rivers and the other major South Asian rivers, and may be due to the geological differences of their denudation regime. Heavy metals in the Lower G-B-M system have an affinity towards the clay fraction of the sediments. The correlation matix of heavy metals in the lower Brahmaputra and Meghna suggests the importance of Fe-Mn oxyhydroxides in their accumulations. Iron, Ti and Mn are higher in the Meghna main channel, Zn is higher in the Meghna tributaries, and Cr is higher in both the Brahmaputra and Meghna compared to the value for standard shale. The enrichment factor is ≤1 for most of the metals except Mn which is relatively higher in the Meghna and lower Ganges main channels. The geoaccumulation index (Igeo) for most of the heavy metals lies below grade zero, suggesting unpolluted sediment quality. The lower Ganges system shows relatively higher concentration in the nondetrital fraction of heavy metals, probably due to the presence of petroleum refinery, industrial and mining effluents, and agricultural runoff in the drainage basin. The relative uniformity in concentration of heavy metals in vertical profiles may be due to the uniformity in sediment grain size and catastrophic deposition of sediments, where the time period represented by the vertical sediment column is not enough to reflect the cultural accumulation of heavy metals. The Bengal basin thus represents a relatively unperturbed alluvial basin with regards to heavy metal pollution. Received: 21 July 1997 · Accepted: 13 October 1997  相似文献   

9.
Systematic hydrogeochemical survey has been carried out for understanding the sources of dissolved ions in the groundwaters of the area occupied by Sarada river basin, Visakhapatnam district, Andhra Pradesh, India. Khondalites, charnockites and granite gneisses and calc-granulites of Precambrians and alluvial deposits of Quaternaries underlie the study area. Groundwaters are both fresh and brackish; the latter waters being a dominant. Most groundwaters are characterized by Na+:HCO3− facies due to chemical weathering of the rocks. Enrichment of Na+, K+, Cl−, SO42−, NO3− and F− in some groundwater samples is caused by seawater intrusion, locally accompanied by ion-exchange, and anthropogenic activities, resulting in an increase of brackish in the groundwaters. Based on the results of this hydrogeochemical study, suitable management measures are recommended to solve the water quality problems.  相似文献   

10.
The study was designed to establish the distributions of trace metals, dissolved organic carbon, and inorganic nutrients as well as to assess the extent of anthropogenic inputs into the Narmada and Tapti rivers. Water and sediment qualities are variable in the rivers, and there are major pollution problems at certain locations, mainly associated with urban and industrial centers. The metal concentrations of samples of the aquatic compartments investigated were close to the maximum permissible concentration for the survival of aquatic life, except for higher values of Cu (5–763 μg l−1), Pb (24–376 μg l−1), Zn (24–730 μg l−1), and Cr (70–740 μg l−1) and for drinking water except for elevated concentrations of metals such as Pb, Fe (850–2,060 μg l−1), Cr, and Ni (20–120 μg l−1). In general, the concentrations of trace metals in the rivers vary down stream which may affect the “health” of the aquatic ecosystem and may also affect the health of the rural community that depends on the untreated river water directly for domestic use. The assessment of EF, I geo, and PLI in the sediments reveals overall moderate pollution in the river basins.  相似文献   

11.
This study examined freshwater discharge of dissolved organic matter (DOM) to the shallow Lavaca–Matagorda (LM) Bay estuarine system along the central Texas coast and investigated whether chromophoric DOM (CDOM) photochemical reactions have the potential to stimulate microbial activity within LM estuarine waters. Dissolved organic carbon (DOC) concentrations ranged from 3 to 10 mg C l−1 and CDOM levels (reported as a 305) ranged from 8 to 77 m−1 during April and July, 2007, when the LM system was experiencing very high freshwater inputs. DOC and CDOM levels were well-correlated with salinities > 3, but exhibited considerable variability at salinities < 3. CDOM photobleaching rates (i.e., decrease in a 305 resulting from exposure to solar radiation) for estuarine samples ranged from 0.014 to 0.021 h−1, corresponding to photobleaching half-lives of 33–50 h. Our data indicate when Matagorda Bay waters photobleach; dissolved organic carbon utilization is enhanced perhaps due to enhanced microbial respiration of biologically labile photoproducts (BLPs). Net ecosystem metabolism calculations indicate that most of the LM system was net heterotrophic during our study. We estimate that BLP formation could support up to 20% of the daily microbial respiratory C demand in LM surface waters and combined with direct photochemical oxygen consumption could have an important influence on O2 cycles in the LM system.  相似文献   

12.
In order to investigate how monsoons influence biogeochemical fluxes in the ocean, twelve time-series sediment traps were deployed at six locations in the northern Indian Ocean. In this paper we present particle flux data collected during May 1986 to November 1991 and November 1987 to November 1992 in the Arabian Sea and Bay of Bengal respectively. Particle fluxes were high during both the SW and NE monsoons in the Arabian Sea as well as in the Bay of Bengal. The mechanisms of particle production and transport, however, differ in both the regions. In the Arabian Sea, average annual fluxes are over 50gm-2y-1 in the western Arabian Sea and less than 27gm-2 y-1 in the central part. Biogenic matter is dominant at sites located near upwelling centers, and is less degraded during peak flux periods. High particle fluxes in the offshore areas of the Arabian Sea are caused by injection of nutrients into the euphotic zone due to wind-induced mixed layer deepening. In the Bay of Bengal, average annual fluxes are highest in the central Bay of Bengal (over 50gm-2y-1) and are least in the southern part of the Bay (37gm-2y-1). Particle flux patterns coincide with freshwater discharge patterns of the Ganges-Brahmaputra river system. Opal/carbonate and organic carbon/carbonate carbon ratios increase during the SW monsoon due to variations in salinity and productivity patterns in the surface waters as a result of increased freshwater and nutrient input from rivers. Comparison of S years data show that fluxes of biogenic and lithogenic particulate matter are higher in the Bay of Bengal even though the Arabian Sea is considered to be more productive. Our results indicate that in the northern Indian Ocean interannual variability in organic carbon flux is directly related to the strength and intensity of the SW monsoon while its transfer from the upper layers to the deep sea is partly controlled by input of lithogenic matter from adjacent continents.  相似文献   

13.
Among several salt lakes in the Thar Desert of western India, the Sambhar is the largest lake producing about 2 × 105 tons of salt (NaCl) annually. The “lake system” (lake waters, inflowing river waters, and sub-surface brines) provides a unique setting to study the geo-chemical behavior of uranium isotopes (238U, 234U) in conjunction with the evolution of brines over the annual wetting and evaporation cycles. The concentration of 238U and the total dissolved solids (TDS) in lake water increase from ~8 μg L−1 and ~8 g L−1 in monsoon to ~1,400 μg L−1 and 370 g L−1, respectively, during summer time. The U/TDS ratio (~1 μg g−1 salt) and the 234U/238U activity ratio (1.65 ± 0.05), however, remain almost unchanged throughout the year, except when U/TDS ratio approaches to 3.8 at/or beyond halite crystallization. These observations suggest that uranium behaves conservatively in the lake waters during the annual cycle of evaporation. Also, uranium and salt content (TDS) are intimately coupled, which has been used to infer the origin and source of salt in the lake basin. Furthermore, near uniform ratios in evaporating lake waters, when compared to the ratio in seawater (~0.1 μg g−1 salt and 1.14 ± 0.02, respectively), imply that aeolian transport of marine salts is unlikely to be significant source of salt to the lake in the present-day hydrologic conditions. This inference is further consistent with the chemical composition of wet-precipitation occurring in and around the Sambhar lake. The seasonal streams feeding the lake and groundwaters (within the lake’s periphery) have distinctly different ratios of U/TDS (2–69 μg g−1 salt) and 234U/238U (1.15–2.26) compared to those in the lake. The average U/TDS ratio of ~1 μg g−1 salt in lake waters and ~19 μg g−1 salt in river waters suggest dilution of the uranium content by the recycled salt and/or removal processes presently operating in the lake during the extraction of salt for commercial use. Based on mass-balance calculations, a conservative estimate of "uranium sink" (in the form of bittern crust) accounts for ~5 tons year−1 from the lake basin, an estimate similar to its input flux from rivers, i.e., 4.4 tons year−1.  相似文献   

14.
Respiration and calcification rates of the Pacific oyster Crassostrea gigas were measured in a laboratory experiment in the air and underwater, accounting for seasonal variations and individual size, to estimate the effects of this exotic species on annual carbon budgets in the Bay of Brest, France. Respiration and calcification rates changed significantly with season and size. Mean underwater respiration rates, deducted from changes in dissolved inorganic carbon (DIC), were 11.4 μmol DIC g−1 ash-free dry weight (AFDW) h−1 (standard deviation (SD), 4.6) and 32.3 μmol DIC g−1 AFDW h−1 (SD 4.1) for adults (80–110 mm shell length) and juveniles (30–60 mm), respectively. The mean daily contribution of C. gigas underwater respiration (with 14 h per day of immersion on average) to DIC averaged over the Bay of Brest population was 7.0 mmol DIC m−2 day−1 (SD 8.1). Mean aerial CO2 respiration rate, estimated using an infrared gas analyzer, was 0.7 μmol CO2 g−1 AFDW h−1 (SD 0.1) for adults and 1.1 μmol CO2 g−1 AFDW h−1 (SD 0.2) for juveniles, corresponding to a mean daily contribution of 0.4 mmol CO2 m−2 day−1 (SD 0.50) averaged over the Bay of Brest population (with 10 h per day of emersion on average). Mean CaCO3 uptake rates for adults and juveniles were 4.5 μmol CaCO3 g−1 AFDW h−1 (SD 1.7) and 46.9 μmol CaCO3 g−1 AFDW h−1 (SD 29.2), respectively. The mean daily contribution of net calcification in the Bay of Brest C. gigas population to CO2 fluxes during immersion was estimated to be 2.5 mmol CO2 m−2 day−1 (SD 2.9). Total carbon release by this C. gigas population was 39 g C m−2 year−1 and reached 334 g C m−2 year−1 for densely colonized areas with relative contributions by underwater respiration, net calcification, and aerial respiration of 71%, 25%, and 4%, respectively. These observations emphasize the substantial influence of this invasive species on the carbon cycle, including biogenic carbonate production, in coastal ecosystems.  相似文献   

15.
Four surveys of the adjacent Cocheco, Bellamy, and Oyster estuaries reveal spatial heterogeneity with respect both to river-born carbon dioxide (CO2) fluxes and CO2 exchange with the atmosphere (−17 to 51 mmol m−2 day−1), a finding partially explained by CO2 inputs from contributing watersheds. Nonuniform nutrient and organic carbon loading from upstream rivers and within the estuaries is considered as a mechanism resulting in the variability between estuaries. Conditions during the surveys included spring river runoff and phytoplankton blooms, drought with baseline river flow, and a historic flood which led to a large CO2 release to the atmosphere. This study highlights the variability of CO2 transport and release found between proximate estuaries over a wide range of flow conditions.  相似文献   

16.
The Hanjiang River, the largest tributaries of the Changjiang (Yangtze) River, is the water source area of the Middle Route of China’s South-to-North Water Transfer Project. The chemical and strontium isotopic compositions of the river waters are determined with the main purpose of understanding the contribution of chemical weathering processes and anthropogenic inputs on river solutes, as well as the associated CO2 consumption in the carbonate-dominated basin. The major ion compositions of the Hanjiang River waters are characterized by the dominance of Ca2+ and HCO3 −, followed by Mg2+ and SO4 2−. The increase in TDS and major anions (Cl−, NO3 −, and SO4 2−) concentrations from upstream to downstream is ascribed to both extensive influences from agriculture and domestic activities over the Hanjiang basin. The chemical and Sr isotopic analyses indicate that three major weathering sources (dolomite, limestone, and silicates) contribute to the total dissolved loads. The contributions of the different end-members to the dissolved load are calculated with the mass balance approach. The calculated results show that the dissolved load is dominated by carbonates weathering, the contribution of which accounts for about 79.4% for the Hanjiang River. The silicate weathering and anthropogenic contributions are approximately 12.3 and 6.87%, respectively. The total TDS fluxes from chemical weathering calculated for the water source area (the upper Hanjiang basin) and the whole Hanjiang basin are approximately 3.8 × 106 and 6.1 × 106 ton/year, respectively. The total chemical weathering (carbonate and silicate) rate for the Hanjiang basin is approximately 38.5 ton/km2/year or 18.6 mm/k year, which is higher than global mean values. The fluxes of CO2 consumption by carbonate and silicate weathering are estimated to be 56.4 × 109 and 12.9 × 109 mol/year, respectively.  相似文献   

17.
The concentrations of water and carbon dissolved in an icelandite glass quenched from 1400 °C and 10 kbar were measured using Fourier transform infra-red spectroscopy and elemental analyses of carbon and hydrogen. Only carbon dioxide and water were observed in the fluid phase as analysed after quenching with a qudrupole mass analyser. The mole fraction of carbon dioxide in the fluid phase ranged from 0.36 to 0.95. Carbon is dissolved as carbonate except at the highest CO2 fluid fugacity, where a small amount of molecular CO2 is observed. Dissolved carbon in the glasses, calculated as CO2, remained constant at approximately 1 wt %, in spite of the different CO2 fluid fugacities. Water was dissolved as molecular water and as hydroxyl groups, the hydroxyl concentration in the quenched glasses remaining almost constant over the whole interval, whereas the molecular water dissolves in accordance with Henry's law. Molecular water peaks at 5200␣cm−1 and 1630 cm−1, the hydroxyl peak at 4500␣cm−1, and the carbonate peaks at 1400 cm−1–1550 cm−1 have been calibrated using elemental analyses of C and H in the quenched glasses. As molecular water decreases in the melt the higher wavenumber carbonate peak is observed to move towards the molecular water peak at 1630 cm−1 causing a split of the carbonate peaks, ranging from 45 cm−1 to 100 cm−1. Received: 15 November 1995 / Accepted: 21 September 1996  相似文献   

18.
A sulfur hexafluoride (SF6) tracer release experiment was conducted in the Stockton Deep Water Ship Channel (DWSC) to quantify mixing and transport rates. SF6 was injected in the San Joaquin River upstream of the DWSC and mapped for 8 days. From the temporal change in SF6 distributions, the longitudinal dispersion coefficient (K x ) was determined to be 32.7 ± 3.6 m2 s−1 and the net velocity was 1.75 ± 0.03 km day−1. Based on the decrease in SF6 inventory during the experiment, the pulsed residence time for waters in the DWSC was estimated at ∼17 days. Within the DWSC from Stockton downstream to Turner Cut, dissolved oxygen concentrations maintained a steady state value of 4 mg l−1. These values are below water quality objectives for the time of year. The low flow rates observed in the DWSC and the inability of oxygen-rich waters from downstream to mix into the DWSC upstream of Turner Cut contribute to the low dissolved oxygen concentration.  相似文献   

19.
The lithium concentration of the dissolved load from the Lena River, together with major element chemistry and GIS-based area and runoff data demonstrate the importance of evaporites in controlling dissolved Li in river waters. Eighty-four percent of the Li in the dissolved load of upper Lena tributaries comes from evaporites in these drainage basins. Altogether, at least ~20% of the total Li flux of the Lena River originates from this source. This finding has important implications for using lithium as a proxy for silicate weathering. The Li flux and the 87Sr/86Sr ratio are compared in order to address a difference between the two silicate weathering rate proxies. The proposed controls on the dissolved δ7Li values in rivers (kinetic vs. equilibrium isotopic fractionation; Rayleigh-type preferential extraction of the heavy isotope) (Huh et al., Earth Planet Sci Lett 194:189–199, 2001) are evaluated using data from both the Siberian rivers and the Orinoco River. Neither of the proposed mechanisms satisfactorily explains the comprehensive data set. Instead, a ‘mineralogy-specific view’ that emphasizes the difference in the secondary mineralogy (i.e., fractionation factor) is presented as a potential rationalization in the form of the refined Rayleigh-type extraction.  相似文献   

20.
A 52-yr record of dissolved oxygen in Chesapeake Bay (1950–2001) and a record of nitrate (NO3 −) loading by the Susquehanna River spanning a longer period (1903, 1945–2001) were assembled to describe the long-term pattern of hypoxia and anoxia in Chesapeake Bay and its relationship to NO3 − loading. The effect of freshwater inflow on NO3 − loading and hypoxia was also examined to characterize its effect at internannual and longer time scales. Year to year variability in river flow accounted for some of the observed changes in hypoxic volume, but the long-term increase was not due to increased river flow. From 1950–2001, the volume of hypoxic water in mid summer increased substantially and at an accelerating rate. Predicted anoxic volume (DO<0.2 mg I−1) at average river flow increased from zero in 1950 to 3.6×109 m3 in 2001. Severe hypoxia (DO<1.0 mg I−1) increased from 1.6×109 to 6.5×109 m3 over the same period, while mild hypoxia (DO<2.0 mg I−1) increased from 3.4×109 to 9.2×109 m3. NO3 − concentrations in the Susquehanna River at Harrisburg, Pennsylvania, increased up to 3-fold from 1945 to a 1989 maximum and declined through 2001. On a decadal average basis, the superposition of changes in river flow on the long-term increase in NO3 − resulted in a 2-fold increase in NO3 − loading from the Susquehanna River during the 1960s to 1970s. Decadal average loads were subsequently stable through the 1990s. Hypoxia was positively correlated with NO3 − loading, but more extensive hypoxia was observed in recent years than would be expected from the observed relationship. The results suggested that the Bay may have become more susceptible to NO3 − loading. To eliminate or greatly reduce anoxia will require reducing average annual total nitrogen loading to the Maryland mainstem Bay to 50×106 kg yr−1, a reduction of 40% from recent levels.  相似文献   

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