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1.
The hydrochemistry of naled and upwelling water sampled from the forefields of Finsterwalderbreen, Svalbard, during spring are used for the first time to infer the hydrology of overwinter meltwaters at a polythermal‐based glacier. Hydrochemical variations in naled are explained in terms of different water sources and their chemical alteration during freezing. Two water sources to naled are identified: surficially routed snowmelt and subglacial water. Naled that results from the freezing of the former is enriched in atmospherically derived ions such as Na+ and Cl−, and is believed to be formed during winter warm periods. Naled of subglacial origin contains relatively high proportions of crustally derived solute. It reflects the freezing of subglacial meltwaters that continue to issue from a subterranean upwellling during winter. An increasing dominance of SO2−4 Mg2+, Na+ and Cl− in subglacial naled with increasing distance from the upwelling reflects the progressive freezing of this water body and the associated removal of Ca2+ and HCO by calcite precipitation. These spatial trends are accentuated by the leaching of soluble ions from the naled close to its source by subsequent upwelling waters. The chemistry of spring upwelling waters, also of subglacial origin, strongly reflects this process. Meltwater produced by geothermal heating of glacier basal ice is believed to be the principal source of water to the subglacial drainage system during winter. Solute acquisition by this meltwater is limited by a scarcity of proton suppliers. Evolution of this dilute meltwater carries an imprint of ion exchange processes. Some stored subglacial water from the end of the previous ablation season may supplement the basal meltwater component in early winter. Copyright © 2000 John Wiley & Sons, Ltd. 相似文献
2.
Solute and runoff time-series at Finsterwalderbreen, Svalbard, provide evidence for considerable basal routing of water and the existence of at least two contrasting subglacial chemical weathering environments. The hydrochemistry of a subglacial upwelling provides evidence for a snowmelt-fed subglacial reservoir that dominates bulk runoff during recession flow. High concentrations of Cl− and crustal ions, high pCO2 and ratios of [*SO2−4/(*SO2−4+HCO−3)] close to 0·5 indicate the passage of snowmelt through a subglacial weathering environment characterized by high rock:water ratios, prolonged residence times and restricted access to the atmosphere. At higher discharges, bulk runoff becomes dominated by icemelt from the lower part of the glacier that is conveyed through a chemical weathering environment characterized by low rock:water ratios, short residence times and free contact with atmospheric gases. These observations suggest that icemelt is routed via a hydrological system composed of basal/ice-marginal, englacial and supraglacial components and is directed to the glacier margins by the ice surface slope. Upwelling water flows relatively independently of icemelt to the terminus via a subglacial drainage system, possibly constituting flow through a sediment layer. Cold basal ice at the terminus forces it to take a subterranean routing in its latter stages. The existence of spatially discrete flow paths conveying icemelt and subglacial snowmelt to the terminus may be the norm for polythermal-based glaciers on Svalbard. Proglacial mixing of these components to form the bulk meltwaters gives rise to hydrochemical trends that resemble those of warm-based glaciers. These hydrochemical characteristics of bulk runoff have not been documented on any other glacier on Svalbard to date and have significance for understanding interactions between thermal regime and glacier hydrology. © 1998 John Wiley & Sons, Ltd. 相似文献
3.
Waters were sampled from 17 boreholes at Haut Glacier d'Arolla during the 1993 and 1994 ablation seasons. Three types of concentrated subglacial water were identified, based on the relative proportions of Ca2+, HCO3? and SO42? to Si. Type A waters are the most solute rich and have the lowest relative proportion of Si. They are believed to form in hydrologically inefficient areas of a distributed drainage system. Most solute is obtained from coupled sulphide oxidation and carbonate dissolution (SO–CD). It is possible that there is a subglacial source of O2, perhaps from gas bubbles released during regelation, because the high SO42? levels found (up to 1200 µeq/L) are greater than could be achieved if sulphides are oxidized by oxygen in saturated water at 0 °C (c.414 µeq/L). A more likely alternative is that sulphide is oxidized by Fe3+ in anoxic environments. If this is the case, exchange reactions involving FeIII and FeII from silicates are possible. These have the potential to generate relatively high concentrations of HCO3? with respect to SO42?. Formation of secondary weathering products, such as clays, may explain the low Si concentrations of Type A waters. Type B waters were the most frequently sampled subglacial water. They are believed to be representative of waters flowing in more efficient parts of a distributed drainage system. Residence time and reaction kinetics help determine the solute composition of these waters. The initial water–rock reactions are carbonate and silicate hydrolysis, and there is exchange of divalent cations from solution for monovalent cations held on surface exchange sites. Hydrolysis is followed by SO–CD. The SO42? concentrations usually are <414 µeq/L, although some range up to 580 µeq/L, which suggests that elements of the distributed drainage system may become anoxic. Type C waters were the most dilute, yet they were very turbid. Their chemical composition is characterized by low SO42? : HCO3? ratios and high pH. Type C waters were usually artefacts of the borehole chemical weathering environment. True Type C waters are believed to flow through sulphide‐poor basal debris, particularly in the channel marginal zone. The composition of bulk runoff was most similar to diluted Type B waters at high discharge, and was similar to a mixture of Type B and C waters at lower discharge. These observations suggest that some supraglacial meltwaters input to the bed are stored temporarily in the channel marginal zone during rising discharge and are released during declining flow. Little of the subglacial chemical weathering we infer is associated with the sequestration of atmospheric CO2. The progression of reactions is from carbonate and silicate hydrolysis, through sulphide oxidation by first oxygen and then FeIII, which drives further carbonate and silicate weathering. A crude estimate of the ratio of carbonate to silicate weathering following hydrolysis is 4 : 1. We speculate that microbial oxidation of organic carbon also may occur. Both sulphide oxidation and microbial oxidation of organic carbon are likely to drive the bed towards suboxic conditions. Hence, we believe that subglacial chemical weathering does not sequester significant quantities of atmospheric CO2 and that one of the key controls on the rate and magnitude of solute acquisition is microbial activity, which catalyses the reduction of FeIII and the oxidation of FeS2. Copyright © 2002 John Wiley & Sons, Ltd. 相似文献
4.
There are still relatively few hydrochemical studies of glacial runoff and meltwater routing from the high latitudes, where non-temperate glacier ice is frequently encountered. Representative samples of glacier meltwater were obtained from Scott Turnerbreen, a ‘cold-based’ glacier at 78° N in the Norwegian high Arctic archipelago of Svalbard, during the 1993 melt season and analysed for major ion chemistry. Laboratory dissolution experiments were also conducted, using suspended sediment from the runoff. Significant concentrations of crustal weathering derived SO2−4 are present in the runoff, which is characterized by high ratios of SO2−4: (SO2−4+HCO−3) and high p(CO2). Meltwater is not routed subglacially, but flows to the glacier terminus through subaerial, ice marginal channels, and partly flows through a proglacial icing, containing highly concentrated interstitial waters, immediately afront the terminus. The hydrochemistry of the runoff is controlled by: (1) seasonal variations in the input of solutes from snow- and icemelt; (2) proglacial solute acquisition from the icing; and (3) subaerial chemical weathering within saturated, ice-cored lateral moraine adjoining drainage channels at the glacier margins, sediment and concentrated pore water from which is entrained by flowing meltwater. Diurnal variations in solute concentration arise from the net effects of variable sediment pore water entrainment and dilution in the ice marginal streams. Explanation of the hydrochemistry of Scott Turnerbreen requires only one major subaerial flow path, the ice marginal channel system, in which seasonally varying inputs of concentrated snowmelt and dilute icemelt are modified by seepage or entrainment of concentrated pore waters from sediment in lateral moraine, and by concentrated interstitial waters from the proglacial icing, supplied by leaching, slow drainage at grain intersections or simple melting of the icing itself. The ice marginal channels are analogous neither to dilute supra/englacial nor to concentrated subglacial flow components. © 1998 John Wiley & Sons, Ltd. 相似文献
5.
Bulk runoff and meteorological data suggest the occurrence of two meltwater outburst events at Finsterwalderbreen, Svalbard, during the 1995 and 1999 melt seasons. Increased bulk meltwater concentrations of Cl? during the outbursts indicate the release of snowmelt from storage. Bulk meltwater hydrochemical data and suspended sediment concentrations suggest that this snowmelt accessed a chemical weathering environment characterized by high rock:water ratios and long rock–water contact times. This is consistent with a subglacial origin. The trigger for both the 1995 and 1999 outbursts is believed to be high rates of surface meltwater production and the oversupply of meltwater to areas of the glacier bed that were at the pressure melting point, but which were unconnected to the main subglacial drainage network. An increase in subglacial water pressure to above the overburden pressure lead to the forcing of a hydrological connection between the expanding subglacial reservoir and the ice‐marginal channelized system. The purging of ice blocks from the glacier during the outbursts may indicate the breach of an ice dam during connection. Although subglacial meltwater issued continually from the glacier terminus via a subglacial upwelling during both melt seasons, field observations showed outburst meltwaters were released solely via an ice‐marginal channel. It is possible that outburst events are a seasonal phenomenon at this glacier and reflect the periodic drainage of meltwaters from the same subglacial reservoir from year to year. However, the location of this reservoir is uncertain. A 100 m high bedrock ridge traverses the glacier 6·5 km from its terminus. The overdeepened area up‐glacier from this is the most probable site for subglacial meltwater accumulation. Copyright © 2001 John Wiley & Sons, Ltd. 相似文献
6.
The significance of the baseflow component of glacier river discharge in summer varies with geographical location, altitude, glacier geometry and glacier size. Baseflow is maintained by meltwater generated above the transient equilibrium line and by water released from temporary storage on, in or beneath the glacier. At the Norwegian glacier Austre Okstindbreen, where precipitation is generally high throughout the year and the summers are cool and wet, observations in three successive, but contrasting, years have shown that Na+ ion concentrations in the glacier river water are influenced strongly by the amount of snowmelt. This itself depends on the preceding winter conditions, which determine the amount of accumulation, and on the current summer's weather. The efficiency of the glacier's drainage systems depends on the general progress of summer ablation. The speed with which the systems develop influences ion provision from subglacial sources. Ca2+ ion concentrations are largely determined by subglacial conditions. Oxygen isotope variations in glacier river water reflect the relative contributions made to total discharge by snow meltwater and other sources; the composition of the snow cover, which is a function of winter temperatures, has a strong influence. Ice meltwater has low isotopic variability, but the isotopic composition of rainfall varies markedly. A simple model of mixing of englacial and subglacial waters, each of a constant composition, cannot be applied to a high-latitude glacier of the size and altitudinal range of Austre Okstindbreen. 相似文献
7.
The anion compositions (SO24, HCO−3 and Cl−) of runoff from the Haut Glacier d'Arolla, Switzerland and Austre Brøggerbreen, Svalbard are compared to assess whether or not variations in water chemistry with discharge are consistent with current understanding of the subglacial drainage structure of warm- and polythermal-based glaciers. These glacial catchments have very different bedrocks and the subglacial drainage structures are also believed to be different, yet the range of anion concentrations show considerable overlap for SO2−4 and HCO−3. Concentrations of Cl− are higher at Austre Brøggerbreen because of the maritime location of the glacier. Correcting SO2−4 for the snowpack component reveals that the variation in non-snowpack SO2−4 with discharge and with HCO−3 is similar to that observed at the Haut Glacier d'Arolla. Hence, if we assume that the provenance of the non-snowpack SO2−4 is the same in both glacial drainage systems, a distributed drainage system also contributes to runoff at Austre Brøggerbreen. We have no independent means of testing the assumption at present. The lower concentrations of non-snowpack SO2−4 at Austre Brøggerbreen may suggest that a smaller proportion of runoff originates from a distributed drainage system than at the Haut Glacier d'Arolla. 相似文献
8.
The Agua Negra drainage system (30 12′S, 69 50′ W), in the Argentine Andes holds several ice‐ and rock‐glaciers, which are distributed from 4200 up to 6300 m a.s.l. The geochemical study of meltwaters reveals that ice‐glaciers deliver a HCO3?? Ca2+ solution and rock‐glaciers a SO42?? HCO3?? Ca2+ solution. The site is presumably strongly influenced by sublimation and dry deposition. The main processes supplying solutes to meltwater are sulphide oxidation (i.e. abundant hydrothermal manifestations), and hydrolysis and dissolution of carbonates and silicates. Marine aerosols are the main source of NaCl. The fine‐grained products of glacial comminution play a significant role in the control of dissolved minor and trace elements: transition metals (e.g. Mn, Zr, Cu, and Co) appear to be selectively removed from solution, whereas some LIL (large ion lithophile) elements, such as Sr, Cs, and major cations, are more concentrated in the lowermost reach. Daily concentration variation of dissolved rare earth elements (REE) tends to increase with discharge. Through PHREEQC inverse modelling, it is shown that gypsum dissolution (i.e. sulphide oxidation) is the most important geochemical mechanism delivering solutes to the Agua Negra drainage system, particularly in rock‐glaciers. At the lowermost reach, the chemical signature appears to change depending on the relative significance of different meltwater sources: silicate weathering seems to be more important when meltwater has a longer residence time, and calcite and gypsum dissolution is more conspicuous in recently melted waters. A comparison with a non‐glacierized semiarid drainage of comparable size shows that the glacierized basin has a higher specific denudation, but it is mostly accounted for by relatively soluble phases (i.e. gypsum and calcite). Meltwater chemistry in glacierized arid areas appears strongly influenced by sublimation/evaporation, in contrast with its humid counterparts. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
9.
&#x;ukasz Stachnik Jacob C. Yde Adam Nawrot &#x;ukasz Uzarowicz Elbieta &#x;epkowska Katarzyna Kozak 《水文研究》2019,33(12):1638-1657
The aluminium (Al) cycle in glacierised basins has not received a great deal of attention in studies of biogeochemical cycles. As Al may be toxic for biota, it is important to investigate the processes leading to its release into the environment. It has not yet been ascertained whether filterable Al (passing through a pore size of 0.45 μm) is incorporated into biogeochemical cycles in glacierised basins. Our study aims to determine the relationship between the processes bringing filterable Al and glacier‐derived filterable nutrients (particularly Fe and Si) into glacierised basins. We investigated the Werenskiöldbreen basin (44.1 km2, 60% glacierised) situated in SW Spitsbergen, Svalbard. In 2011, we collected meltwater from a subglacial portal at the glacier front and at a downstream hydrometric station throughout the ablation season. The Al concentration, unchanged between the subglacial system and proglacial zone, reveals that aluminosilicate weathering is a dominant source of filterable Al under subglacial conditions. By examining the Al:Fe ratio compared with pH and the sulphate mass fraction index, we found that the proton source for subglacial aluminosilicate weathering is mainly associated with sulphide oxidation and, to a lesser degree, with hydrolysis and carbonation. In subglacial outflows and in the glacial river, Al and Fe are primarily in the forms of Al(OH)4‐ and Fe(OH)3. The annual filterable Al yield (2.7 mmol m‐2) was of a magnitude similar to that of nutrients such as filterable Fe (3.0 mmol m‐2) and lower than that of dissolved Si (18.5 mmol m‐2). Our results show that filterable Al concentrations in meltwater are significantly correlated to filterable and dissolved glacier‐derived nutrients (Fe and Si, respectively) concentrations in glaciers worldwide. We conclude that a potential bioavailable Al pool derived from glacierised basins may be incorporated in biogeochemical cycles, as it is strongly related to the concentrations and yields of glacier‐derived nutrients. 相似文献
10.
Recent models of chemical weathering in alpine glacial meltwaters suggest that sulphide oxidation is a major source of solute in the distributed component of the subglacial hydrological system. This reaction requires O2, and may lower dissolved oxygen levels to below saturation with respect to the atmosphere. This should result in an inverse association between SO72- and dissolved oxygen saturation. However, measurements of O2 saturation in bulk meltwaters draining the Haut Glacier d'Arolla, Switzerland, show that there is a positive association between SO42- and O2 saturation. The O2 content of glacial meltwaters depends on the initial content of snow and icemelt, which may be controlled by the rate of melting, and the kinetic balance between O2 losses (e.g. sulphide oxidation, microbial respiration) and gains (e.g. diffusion of O2 into solution). 相似文献
11.
12.
Results from hydrometric and isotopic investigations of unsaturated flow during snowmelt are presented for a hillslope underlain by well-sorted sands. Passage of melt and rainwater through the vadose zone was detected from temporal changes in soil water 2H concentrations obtained from sequential soil cores. Bypassing flow was indicated during the initial snowmelt phase, but was confined to the near-surface zone. Recharge below this zone was via translatory flow, as meltwater inputs displaced premelt soil water. Estimates of premelt water fluxes indicate that up to 19 per cent of the premelt soil water may have been immobile. Average water particle velocities during snowmelt ranged from 6.2 × 10?7 to 1.1 × 10?6 ms?1, suggesting that direct groundwater recharge by meltwater during snowmelt was confined to areas where the premelt water table was within 1 m of the ground surface. Soil water 2H signatures showed a rapid response to isotopically-heavy rain-on-snow inputs late in the melt. In addition, spatial variations in soil moisture content at a given depth induced a pronounced lateral component to the predominantly vertical transport of water. Both factors may complicate isotopic profiles in the vadose zone, and should be considered when employing environmental isotopes to infer recharge processes during snowmelt. 相似文献
13.
Pathways and fate of road deicing salt (NaCl) applied during the 1994–1995 winter were studied for a 14-km section of a major highway that crosses the Oak Ridges Moraine in southern Ontario. Total salt applications over the winter ranged from 29 to 74 kg m−1 of highway, and NaCl concentrations in snow banks adjacent to the roadway reached 9400 mg l−1 during the later stages of snow cover development. This salt was released to the ground surface during snowmelt. Sodium chloride (NaCl) loadings to soil from snow cover during the final melt phase were relatively uniform along the study section (3–5 kg NaCl m−1 of highway). However, the snowpack at all transects retained <50% of applied NaCl, and this shortfall probably reflected direct runoff and infiltration of saline meltwater from the road surface into the adjacent shoulder and right-of-way. Cation exchange with Ca2+ in near-surface soils most likely resulted in preferential retention of Na+ relative to Cl−, although total storage of NaCl in upper soil horizons by winter's end was <15% of deicing salt applications. An environmental tracer (18O) was used to trace movement of saline meltwater through the unsaturated zone underlying the highway. Average meltwater particle velocities at a site underlain by loam soils were 0.02 m d−1, and ca. 280 mm of water was displaced below a depth of 1.86 m over a 78-day period in the spring and summer of 1995. Sodium ion and chloride ion concentrations in water sampled in late summer 1995 at depths >2 m exceeded 500 mg l−1 and 1000 mg l−1, respectively. Approximately 75% of the net flux of NaCl below the upper soil was retained in the 0–2.8 m depth interval at this site, and results from more permeable soils traversed by the highway indicate an even greater penetration of the annual NaCl application into the unsaturated zone along the moraine. This saline water likely recharges groundwater in this portion of the Oak Ridges Moraine. 相似文献
14.
Marty D. Frisbee Fred M. Phillips Andrew R. Campbell Jan M. H. Hendrickx Emily M. Engle 《水文研究》2010,24(7):834-849
Twelve modified passive capillary samplers (M‐PCAPS) were installed in remote locations within a large, alpine watershed located in the southern Rocky Mountains of Colorado to collect samples of infiltration during the snowmelt and summer rainfall seasons. These samples were collected in order to provide better constraints on the isotopic composition of soil‐water endmembers in the watershed. The seasonally integrated stable isotope composition (δ18O and δ2H) of soil‐meltwater collected with M‐PCAPS installed at shallow soil depths < 10 cm was similar to the seasonally integrated isotopic composition of bulk snow taken at the soil surface. However, meltwater which infiltrated to depths > 20 cm evolved along an isotopic enrichment line similar to the trendline described by the evolution of fresh snow to surface runoff from snowmelt in the watershed. Coincident changes in geochemistry were also observed at depth suggesting that the isotopic and geochemical composition of deep infiltration may be very different from that obtained by surface and/or shallow‐subsurface measurements. The M‐PCAPS design was also used to estimate downward fluxes of meltwater during the snowmelt season. Shallow and deep infiltration averaged 8·4 and 4·7 cm of event water or 54 and 33% of the measured snow water equivalent (SWE), respectively. Finally, dominant shallow‐subsurface runoff processes occurring during snowmelt could be identified using geochemical data obtained with the M‐PCAPS design. One soil regime was dominated by a combination of slow matrix flow in the shallow soil profile and fast preferential flow at depth through a layer of platy, volcanic rocks. The other soil regime lacked the rock layer and was dominated by slow matrix flow. Based on these results, the M‐PCAPS design appears to be a useful, robust methodology to quantify soil‐water fluxes during the snowmelt season and to sample the stable isotopic and geochemical composition of soil‐meltwater endmembers in remote watersheds. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
15.
Yan Guo Herong Gui Jiuchuan Wei Zhi Zhang Mancong Hu Pei Fang Guangping Li Chuan Gao Xin Wang 《Ground water》2021,59(2):256-265
Permian coal measure sandstone fissure water (referred to as “coal measure water,” that is, water in coal measures) is one of the important water sources for industrial and agricultural activities in mining areas. However, the regional high-pressure grouting, one of the most widely used floor control methods, may affect the coal measure water which is connected with limestone aquifer. This study used Taoyuan mine, a typical coal mine in Huaibei coalfield, as the research area to study the influencing mechanism of a grouting treatment on the hydrogeochemical evolution of coal measure water. The hydrogeochemical characteristics and water-rock interaction mechanism of the coal measure water before and during the treatment were evaluated using a Piper trigram, ion combination ratio, and hydrogen-oxygen stable isotope. The anions and cations in the coal measure water before and during the treatment had the same trends at SO42− > HCO3− > Cl− and Na+ > Ca2+ > Mg2+, respectively. Hydrochemical types of coal measure water before treatment were mainly SO4·Cl-Ca·Mg, SO4·Cl-Na, and HCO3-Na, and during treatment they were mainly SO4·Cl-Na and HCO3-Na. The formation of chemical components of coal measure water before treatment was mainly caused by carbonate dissolution, sulfate dissolution, and pyrite oxidation. During the treatment, sulfate dissolution and pyrite oxidation were the main geochemical processes, and ion exchange was enhanced. Atmospheric precipitation was the source of all water samples, and all showed an obvious 18O drift. 相似文献
16.
C. H. TAYLOR Methodological issues associated with isotopic hydrograph separations (IHSs) in built-up environments are explored using results from the 1990 spring melt in a suburban basin in Peterborough, Ontario, Canada. The hetrogeneous nature of suburban environments complicates the selection of appropriate isotopic signatures for event and pre-event waters. Near-stream groundwater δ18O sampled from wells was poorly mixed, such that the pre-event water signature was best characterized by δ18O in pre-melt baseflow or discharge from a headwater spring. The event water signature during snowmelt can be characterized using δ18O in the pre-melt snowpack, surface runoff samples or meltwater from lysimeters. However, the use of snowpack δ18O may be inappropriate in suburban basins where meltwater from thin snowcover may exhibit pronounced responses to δ18O in rainfall contributions. Intensive sampling of the spatial variability of runoff or meltwater δ18O may be required to characterize the average event water signature adequately. Rainfall δ18O provided an appropriate event water signal during a large rain on snow event, and differences between this IHS and one generated using an event water signature that included meltwater contributions from snow-covered surfaces were within the uncertainty attributable to the analytical error in δ18O values. Event water supplied 55-63% of the peak discharge and 48-58% of total runoff from the basin during the melt, which is consistent with the fraction of the basin that has been developed. These results contrast with IHSs conducted in forested basins that suggest that stormflow is dominated by pre-event water contributions. 相似文献
17.
A. Zuber S. Witczak K. Ra&#x;ski I.
liwka M. Opoka P. Mochalski T. Kuc J. Karlikowska J. Kania M. Jackowicz‐Korczy&#x;ski M. Duli&#x;ski 《水文研究》2005,19(11):2247-2275
A comprehensive study of a sandy aquifer of deltaic origin in southern Poland included water chemistry, isotopes, dissolved trace gases and transport modelling. Tritium, sulphur hexafluoride (SF6) and freons (F‐11, F‐12 and F‐113) showed the presence of modern waters in the recharge areas and shallow confined parts of the aquifer. The presence of older Holocene waters farther from the recharge areas was indicated by lack of 3H, SF6 contents ≤0·02 fmol l−1 and relatively low 14C values. The discharge from the system is by upward seepage in the valley of a major river. Pre‐Holocene waters of a cooler climate, identified on the basis of δ18O, δ2H, 14C, Ne and Ar data, were found in some distant wells. Concentrations of N2, Ne and Ar determined by gas chromatography were used for calculating the noble gas temperatures, air excess needed for correction of SF6, and nitrogen content released by denitrification process. The time series of 3H content available for some wells supplied quantitative information on age distributions and the total mean ages of flow through the unsaturated and saturated zones. The derived 3H age distributions turned out to be very wide, with mean values in the range of about 30 to 160 years. For each well with determined 3H age, the SF6 data showed either a lower age range or the possibility of a lower age as expected due to shorter travel times of SF6 through the unsaturated zone, which most probably also resulted in different types of age distributions of these tracers. Freons appeared to be of little use for individual age determinations. A quantitative estimation of two‐component mixing from SF6 3H relations is not possible unless the travel time of 3H through the unsaturated zone is comparable to that of SF6. The ratio of integrals of the response function over the age range with tracer and the whole response function yields the ratio of water with tracer to total flow of water. That ratio is a tracer‐dependent function of time. Transport modelling of SF6 tracer done with MT3D code yielded initially large discrepancies between calculated and measured tracer concentrations. Some discrepancies remained even after calibration of the transport model with SF6. Simulation of tritium contents with a calibrated transport model yielded reasonable agreement with measured contents in some wells and indicated a need for further investigations, particularly in the eastern part of the aquifer. The existence of distinct hydrochemical zones is consistent with the tracer data; young waters with measurable 3H and SF6 contents are aerobic and of HCO3 Ca or HCO3 SO4 Ca types. Slightly elevated Na and Cl contents, as well as the highest concentrations of SO4 and NO3 within this zone are due to anthropogenic influences. Anaerobic conditions prevail in the far field, under the confining cover, where pre‐bomb era Holocene waters dominate. In that zone, dissolved oxygen, NO3 and U contents are reduced, and Fe, Mn and NH4 contents increase. In the third zone, early Holocene and glacial waters occur. They are of HCO3 Ca Na or HCO3 Na types, with TDS values higher than 1 g l−1 and Na content higher than 200 mg l−1, due to either small admixtures of ascending or diffusing older water or freshening of marine sediments, a process that is probably occurring till the present time. Copyright © 2005 John Wiley & Sons, Ltd. 相似文献
18.
Recent understanding of chemical weathering in glacierized catchments has been focused on mid-latitude, Alpine catchments; comparable studies from the high latitudes are currently lacking. This paper attempts to address this deficiency by examining solute provenance, transport and denudation in a glacierized catchment at 78°N in the Svalbard High Arctic archipelago. Representative samples of snow, glacier ice, winter proglacial icing and glacier meltwater were obtained from the catchment during spring and summer 1993 and analysed for major ion chemistry. Seasonal variations in the composition of glacier meltwater occur and are influenced by proglacial solute acquisition from the icing at the very start of the melt season, and subsequently by a period of discharge of concentrated snowmelt caused by snowpack elution; weathering within the ice-marginal channels that drain the glacier, particularly carbonation reactions, continues to furnish solute to meltwater when suspended sediment concentrations increase later in the melt season. Partitioning the solute flux into its various components (sea-salt, crustal, aerosol and atmospheric sources) shows that c. 25% of the total flux is sea salt derived, consistent with the maritime location of the glacier, and c. 71% is crustally derived. Estimated chemical denudation, 160 meq m−2 a−1 sea salt-corrected cation equivalent weathering rate, is somewhat low compared with other studied glacierized catchments (estimates in the range 450–1000 meq m−2 a−1), which is probably attributable to the relatively short melt season and low specific runoff in the High Arctic. A positive relationship was identified between discharge and CO2 drawdown owing to carbonation reactions in turbid meltwater. © 1997 John Wiley & Sons, Ltd. 相似文献
19.
Water sources and flow paths contributing to stream chemistry were evaluated in four Japanese forested watersheds with steep topography (slopes ≥30°). Stream chemistry during periods without rainfall and during events with less than 100 mm of precipitation was similar to seepage water chemistry, but markedly different from that of soil water which had higher concentrations of NO−3 and Ca2+ and lower concentrations of Na+ and HCO−3. Also, stream Cl− concentrations in a Cl−‐treated watershed did not increase either during events with less than 100 mm of total rainfall or at baseflow conditions, even three years after the Cl− treatment. These results suggest that groundwater within bedrock fissures of Paleozoic strata had a long residence time and was a major contributor to steam water under baseflow conditions and even during small precipitation events (≤100 mm). In contrast, for large precipitation events (≥100 mm), stream chemistry became more similar to soil water chemistry, especially within the steepest watershed. Also, for large precipitation events, stream Cl− concentrations in the Cl−‐treated watershed increased markedly. These results suggest that soil water was a major contributor to stream waters only during these large events. Copyright © 1999 John Wiley & Sons, Ltd. 相似文献
20.
The molecular characteristics of dissolved organic matter (DOM) reflect both its source material and its biogeochemical history. In glacial systems, DOM characteristics might be expected to change over the course of a melt season as changes in the glacier drainage system cause the mobilization of DOM from different OM pools. To test this hypothesis we used Principal Components Analysis (PCA) of synchronous fluorescence spectra to detect and describe changes in the DOM in meltwater from a glacier system in the Coast Mountains of northern British Columbia, Canada. For most of the melt season, the dominant component of subglacially routed meltwater DOM is characterized by a tyrosine‐like fluorophore. This DOM component is most likely derived from supraglacial snowmelt. During periods of high discharge, a second component of DOM is present which is humic in character and similar to DOM sampled from a nearby non‐glacial stream. This DOM component is inferred to be derived from a moss‐covered soil environment that has been glacially overrun. It is probably entrained into glacial melt waters when the supraglacial meltwater flux exceeds the capacity of the principal subglacial drainage channels and water floods areas of the glacier bed that are normally isolated from the subglacial drainage system. Another source of DOM also appears to be mobilized during periods of high air temperatures. It is characterized by both humic and proteinaceous fluorophores and may be derived from the drainage of supraglacial cryoconite holes. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献