Solute provenance,transport and denudation in a high arctic glacierized catchment

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.     

Influence of melt‐freeze‐cycles on the radionuclide transport in homogeneous laboratory snowpack

Radionuclides released to the environment and deposited with or onto snow can be stored over long time periods if ambient temperature stays low, particularly in glaciated areas or high alpine sites. The radionuclides will be accumulated in the snowpack during the winter unless meltwater runoff at the snow base occurs. They will be released to surface waters within short time during snowmelt in spring. In two experiments under controlled melting conditions of snow in the laboratory, radionuclide migration and runoff during melt‐freeze‐cycles were examined. The distribution of Cs‐134 and Sr‐85 tracers in homogeneous snow columns and their fractionation and potential preferential elution in the first meltwater portions were determined. Transport was associated with the percolation of meltwater at ambient temperatures above 0 °C after the snowpack became ripe. Mean migration velocities in the pack were examined for both nuclides to about 0.5 cm hr^?1 after one diurnal melt‐freeze‐cycle at ambient temperatures of ?2 to 4 °C. Meltwater fluxes were calculated with a median of 1.68 cm hr^?1. Highly contaminated portions of meltwater with concentration factors between 5 and 10 against initial bulk concentrations in the snowpack were released as ionic pulse with the first meltwater. Neither for caesium nor strontium preferential elution was observed. After recurrent simulated day‐night‐cycles (?2 to 4 °C), 80% of both radionuclides was released with the first 20% of snowmelt within 4 days. 50% of Cs‐134 and Sr‐85 were already set free after 24 hr. Snowmelt contained highest specific activities when the melt rate was lowest during the freeze‐cycles due to concentration processes in remaining liquids, enhanced by the melt‐freeze‐cycling. This implies for natural snowpack after significant radionuclide releases, that long‐time accumulation of radionuclides in the snow during frost periods, followed by an onset of steady meltwater runoff at low melt rates, will cause the most pronounced removal of the contaminants from the snow cover. This scenario represents the worst case of impact on water quality and radiation exposure in aquatic environments.     

Hydrological and hydrochemical response of a small canadian shield catchment to late winter rain-on-snow events

A study was undertaken during the winter of 1990–1991 in a small (3.7 ha) Canadian Shield catchment to examine the hydrological and hydrochemical response during rain-on-snow events. The results are presented of two large (37.9 and 34.6 mm) rain-on-snow events occurring in early and late March 1991. Peak and total runoff and the groundwater response from the two events are significantly different. Hydrological data indicate that these differences can be attributed to a combination of meteorological (temperature) and physical conditions (antecedent snowpack ripeness, soil moisture and groundwater levels). An immature snowpack (low temperature and density) combined with low antecedent soil moisture conditions significantly reduced the magnitude of the net hydrological input and runoff from the catchment during the early March event, whereas a more mature snowpack and high antecedent soil moisture conditions led to a large runoff event during late March. During both rain-on-snow events a significant portion of the pre-event snowpack chemical load was lost. Based on the maximum snowpack chemical load measured before the events, the two large rain-on-snow events and a brief mid-March warm period during which there were two much smaller rain-on-snow events removed 78% of the hydrogen ion and 63% of the sulphate and nitrate load from the snowpack, while only reducing snowpack water equivalence by 7%. A two-component (rain and snowmelt) isotopic (δ¹⁸O SMOW %₀) separation of snowmelt lysimeter water during the two events indicated that snowmelt was an important (50 and 65%, respectively) water source available for infiltration and runoff at the snow-soil interface. Considering the high hydrogen ion loadings to the catchment during these two events (3.3 and 3.0 mequiv.m^?2, respectively) streamflow pH was not significantly reduced due to an increase in the discharge of well-buffered groundwater. A two-component isotopic hydrograph separation of peak stream discharge during the 2–3 March event indicated that 75% of the total flow was groundwater. In mid-latitude acid-sensitive catchments, winter rain-on-snow events are an important hydrological occurrence due to their ability to elute much of the chemical load (H⁺, SO₄, NO₃) from the snowpack before the onset of spring melt when the maximum annual hydrological input typically occurs.     

Analysis of snowpack dynamics during the spring melt season for a sub‐alpine site using point measurements and numerical modeling

Snowpack dynamics through October 2014–June 2017 were described for a forested, sub‐alpine field site in southeastern Wyoming. Point measurements of wetness and density were combined with numerical modeling and continuous time series of snow depth, snow temperature, and snowpack outflow to identify 5 major classes of distinct snowpack conditions. Class (i) is characterized by no snowpack outflow and variable average snowpack temperature and density. Class (ii) is characterized by short durations of liquid water in the upper snowpack, snowpack outflow values of 0.0008–0.005 cm hr^?1, an increase in snowpack temperature, and average snow density between 0.25–0.35 g cm^?3. Class (iii) is characterized by a partially saturated wetness profile, snowpack outflow values of 0.005–0.25 cm hr^?1, snowpack temperature near 0 °C, and average snow density between 0.25–0.40 g cm^?3. Class (iv) is characterized by strong diurnal snowpack outflow pattern with values as high as 0.75 cm hr^?1, stable snowpack temperature near 0 °C, and stable average snow density between 0.35–0.45 g cm^?3. Class (v) occurs intermittently between Classes (ii)–(iv) and displays low snowpack outflow values between 0.0008–0.04 cm hr^?1, a slight decrease in temperature relative to the preceding class, and similar densities to the preceding class. Numerical modeling of snowpack properties with SNOWPACK using both the Storage Threshold scheme and Richards' equation was used to quantify the effect of snowpack capillarity on predictions of snowpack outflow and other snowpack properties. Results indicate that both simulations are able to predict snow depth, snow temperature, and snow density reasonably well with little difference between the 2 water transport schemes. Richards' equation more accurately simulates the timing of snowpack outflow over the Storage Threshold scheme, especially early in the melt season and at diurnal timescales.     

Hydrological characterization and connectivity of proglacial lakes to a stream,Adygine ice-debris complex,northern Tien Shan

ABSTRACT

In this study, we characterized the glacial meltwater flow through a proglacial area with a focus on proglacial lakes, their hydrological regime and their connection to the stream. The studied lakes – the Adygine ice-debris complex, northern Tien Shan – showed a distinct development throughout an ablation season: at Lake 2, the mean daily water-level fluctuation amplitude increased from 0.07 m to 0.18 m (June, August), then dropped to 0.07 m in September. Glacial meltwater flows through the lakes and further downstream through a rock glacier rather fast, moving at 0.085 m s^?1. However, based on the low dye recovery in the stream (0.03%), only a small portion of water was routed efficiently. The complexity of the site’s drainage system was supported by varying isotopic composition of water in the tarns situated on the rock glacier, with Tarn a (δ²H: –36.08‰; δ¹⁸O: –6.25‰) being the most enriched and Tarn c (δ²H: 78.68‰; δ¹⁸O: 11.9‰) the most depleted in heavy isotopes.     

The solute budget of a forest catchment and solute fluxes within a Pinus radiata and a secondary native forest site,southern Chile

Solute concentrations and fluxes in rainfall, throughfall and stemflow in two forest types, and stream flow in a 90 ha catchment in southern Chile (39°44′S, 73°10′W) were measured. Bulk precipitation pH was 6·1 and conductivity was low. Cation concentrations in rainfall were low (0·58 mg Ca²⁺ l^?1, 0·13 mg K⁺ l^?1, 0·11 mg Mg²⁺ l^?1 and <0·08 mg NH₄–N l^?1), except for sodium (1·10 mg l^?1). Unexpected high levels of nitrate deposition in rainfall (mean concentration 0·38 mg NO₃–N l^?1, total flux 6·3 kg NO₃–N ha^?1) were measured. Concentrations of soluble phosphorous in bulk precipitation and stream flow were below detection limits (<0·09 mg l^?1) for all events. Stream‐flow pH was 6·3 and conductivity was 28·3 μs. Stream‐water chemistry was also dominated by sodium (2·70 mg l^?1) followed by Ca, Mg and K (1·31, 0·70 and 0·36 mg l^?1). The solute budget indicated a net loss of 3·8 kg Na⁺ ha^?1 year^?1, 5·4 kg Mg²⁺ ha^?1 year^?1, 1·5 kg Ca²⁺ ha^?1 year^?1 and 0·9 kg K⁺ ha^?1 year^?1, while 4·9 kg NO₃–N ha^?1 year^?1 was retained by the ecosystem. Stream water is not suitable for domestic use owing to high manganese and, especially, iron concentrations. Throughfall and stemflow chemistry at a pine stand (Pinus radiata D. Don) and a native forest site (Siempreverde type), both located within the catchment, were compared. Nitrate fluxes within both forest sites were similar (1·3 kg NO₃–N ha^?1 year^?1 as throughfall). Cation fluxes in net rainfall (throughfall plus stemflow) at the pine stand generally were higher (34·8 kg Na⁺ ha^?1 year^?1, 21·5 kg K⁺ ha^?1 year^?1, 5·1 kg Mg²⁺ ha^?1 year^?1) compared with the secondary native forest site (24·7 kg Na⁺ ha^?1 year^?1, 18·9 kg K⁺ ha^?1 year^?1 and 4·4 kg Mg²⁺ ha^?1 year^?1). However, calcium deposition beneath the native forest stand was higher (15·9 kg Ca²⁺ ha^?1 year^?1) compared with the pine stand (12·6 kg Ca²⁺ ha^?1 year^?1). Copyright © 2002 John Wiley & Sons, Ltd.     

Wetland nitrogen dynamics in an Adirondack forested watershed

Wetlands often form the transition zone between upland soils and watershed streams, however, stream–wetland interactions and hydrobiogeochemical processes are poorly understood. We measured changes in stream nitrogen (N) through one riparian wetland and one beaver meadow in the Archer Creek watershed in the Adirondack Mountains of New York State, USA from 1 March to 31 July 1996. In the riparian wetland we also measured changes in groundwater N. Groundwater N changed significantly from tension lysimeters at the edge of the peatland to piezometer nests within the peatland. Mean N concentrations at the peatland perimeter were 1·5, 0·5 and 18·6 µmol L^?1 for NH₄⁺, NO₃^? and DON (dissolved organic nitrogen), respectively, whereas peatland groundwater N concentration was 56·9, 1·5 and 31·6 µmol L^?1 for NH₄⁺, NO₃^? and DON, respectively. The mean concentrations of stream water N species at the inlet to the wetlands were 1·5, 10·1 and 16·9 µmol L^?1 for NH₄⁺, NO₃^? and DON, respectively and 1·6, 28·1 and 8·4 µmol L^?1 at the wetland outlet. Although groundwater total dissolved N (TDN) concentrations changed more than stream water TDN through the wetlands, hydrological cross‐sections for the peatland showed that wetland groundwater contributed minimally to stream flow during the study period. Therefore, surface water N chemistry was affected more by in‐stream N transformations than by groundwater N transformations because the in‐stream changes, although small, affected a much greater volume of water. Stream water N input–output budgets indicated that the riparian peatland retained 0·16 mol N ha^?1 day^?1 of total dissolved N and the beaver meadow retained 0·26 mol N ha^?1 day^?1 during the study period. Nitrate dominated surface water TDN flux from the wetlands during the spring whereas DON dominated during the summer. This study demonstrates that although groundwater N changed significantly in the riparian peatland, those changes were not reflected in the stream. Consequently, although in‐stream changes of N concentrations were less marked than those in groundwater, they had a greater effect on stream water chemistry—because wetland groundwater contributed minimally to stream flow. Copyright © 2004 John Wiley & Sons, Ltd.     

The hydrochemistry of runoff from a ‘cold-based’ glacier in the High Arctic (Scott Turnerbreen,Svalbard)

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.     

Geochemical evidence for mixing of magmatic fluids with seawater,Nisyros hydrothermal system,Greece

The chemical and isotopic compositions (δD_H2O, δ¹⁸O_H2O, δ¹⁸O_CO2, δ¹³C_CO2, δ³⁴S, and He/N₂ and He/Ar ratios) of fumarolic gases from Nisyros, Greece, indicate that both arc-type magmatic water and local seawater feed the hydrothermal system. Isotopic composition of the deep fluid is estimated to be +4.9±0.5‰ for δ¹⁸O and ?11±5‰ for δD corresponding to a magmatic water fraction of 0.7. Interpretation of the stable water isotopes was based on liquid–vapor separation conditions obtained through gas geothermometry. The H₂–Ar, H₂–N₂, and H₂–H₂O geothermometers suggest reservoir temperatures of 345±15 °C, in agreement with temperatures measured in deep geothermal wells, whereas a vapor/liquid separation temperature of 260±30 °C is indicated by gas equilibria in the H₂O–H₂–CO₂–CO–CH₄ system. The largest magmatic inputs seem to occur below the Stephanos–Polybotes Micros crater, whereas the marginal fumarolic areas of Phlegeton–Polybotes Megalos craters receive a smaller contribution of magmatic gases.     

Transformations of runoff chemistry in the Arctic tundra,Northwest Territories,Canada

The transformation of snowmelt water chemical composition during melt, elution and runoff in an Arctic tundra basin is investigated. The chemistry of the water flowing along pathways from the surface of melting snow to the 95·5 ha basin outlet is related to relevant hydrological processes. In so doing, this paper offers physically based explanations for the transformation of major ion concentrations and loads of runoff water associated with snowmelt and rainfall along hydrological pathways to the stream outlet. Late‐lying snowdrifts were found to influence the ion chemistry in adjacent reaches of the stream channel greatly. As the initial pulse of ion‐rich melt water drained from the snowdrift and was conveyed through hillslope flowpaths, the concentrations of most ions increased, and the duration of the peak ionic pulse lengthened. Over the first 3 m of overland flow, the concentrations of all ions except for NO increased by one to two orders of magnitude, with the largest increase for K⁺, Ca²⁺ and Mg²⁺. This was roughly equivalent to the concentration increase that resulted from percolation of relatively dilute water through 0·25 m of unsaturated soil. The Na⁺ and Cl^? were the dominant ions in snowmelt water, whereas Ca²⁺ and Mg²⁺ dominated the hillslope runoff. On slopes below a large melting snowdrift, ion concentrations of melt water flowing in the saturated layer of the soil were very similar to the relatively dilute concentrations found in surface runoff. However, once the snowdrift ablated, ion concentrations of subsurface flow increased above parent melt‐water concentrations. Three seasonally characteristic hydrochemical regimes were identified in a stream reach adjacent to late‐lying snowdrifts. In the first two stages, the water chemistry in the stream channel strongly resembled the hillslope drainage water. In the third stage, in‐stream geochemical processes, including the weathering/ion exchange of Ca²⁺ and Mg²⁺, were the main control of streamwater chemistry. Copyright © 2006 John Wiley & Sons, Ltd.     

Trace element and major ion concentrations and dynamics in glacier snow and melt: Eliot Glacier,Oregon Cascades

We present concentrations of environmentally available (unfiltered acidified 2% v/v HNO₃) As, Cu, Cd, Pb, V, Sr, and major ions including Ca²⁺, Cl^?, and SO₄^2? in a July 2005 and a March 2006 shallow snow profile from the lower Eliot Glacier, Mount Hood, Oregon, and its proglacial stream, Eliot Creek. Low enrichment factors (EF) with respect to crustal averages suggests that in fresh March 2006 snow environmentally available elements are derived primarily from lithogenic sources. Soluble salts occurred in lower and less variable concentrations in July 2005 snow than March 2006. Conversely, environmentally available trace elements occurred in greater and more variable concentrations in July 2005 than March 2006 snow. Unlike major solutes, particulate‐associated trace elements are not readily eluted during the melt season. Additionally, elevated surface concentrations suggest that they are likely added throughout the year via dry deposition. In a 1‐h stream sampling, ratios of dissolved (<0·45 µm) V:Cl^?, Sr:Cl^?, and Cu:Cl^? are enriched in the Eliot Stream with respect to their environmentally available trace element to Cl^? ratios in Eliot Glacier snow, suggesting chemical weathering additions in the stream waters. Dissolved Pb:Cl^? is depleted in the Eliot Stream with respect to the ratio of environmentally available Pb to Cl^? in snow, corresponding to greater adsorption onto particles at greater pH values. Copyright © 2009 John Wiley & Sons, Ltd.     

The importance of oxygen isotope provenance in relation to solute content of bulk meltwaters at Imersuaq Glacier,West Greenland

Stable oxygen isotope analysis and measurement of several dissolved cations and anions of bulk meltwater samples have provided information about the hydrochemical environment of the glacial hydrological system at Imersuaq Glacier, an outlet tongue from the Greenland ice‐sheet, West Greenland. The samples were collected at frequent intervals during the period 20–28 July 2000 in a small (<20 L s^?1) englacial meltwater outlet at the glacier margin. The results document the following findings: (i) a marked diurnal variation of δ¹⁸O is related to the composition of oxygen isotope provenances, mainly near‐marginal local superimposed ice and basal up‐sheared ice further up‐glacier; (ii) a relationship is seen between all base cations (Na⁺, K⁺, Ca²⁺, Mg²⁺), SO₄^2? and δ¹⁸O, indicating that solute acquisition is provided by solid–solution contact with the up‐sheared ice—as the relationship with Cl^? is weak the influence of seasalt‐derived solutes is small in the area; (iii) when the melt rate is high, two diurnal maxima of δ¹⁸O values and solute concentrations are measured, and it is suggested that a snow meltwater component is responsible for the second maximum of δ¹⁸O—a short residence time leads to a delayed decrease in ion concentrations. Copyright © 2003 John Wiley & Sons, Ltd.     

Variation of hydrogeochemical characteristics of water in surface flows,shallow wells,and boreholes in the coastal city of Douala (Cameroon)

ABSTRACT

Groundwater is used by 3?million inhabitants in the coastal urban city of Douala, Cameroon, but comprehensive data are too sparse for it to be managed in a sustainable manner. Hence this study aimed to (1) assess the potability of the groundwater; (2) evaluate the spatial variation of groundwater composition; and (3) assess the interaction and recharge mechanisms of different water bodies. Hydrogeochemical tools and methods revealed the following results in the Wouri and Nkappa formations of the Douala basin, which is beneath Douala city: 30% of water samples from hand-dug wells in the shallow Pleistocene alluvium aquifer were saline and highly mineralized. However, water from boreholes in the deeper (49–92 m depth) Palaeocene aquifer was saline-free, less mineralized and potable. Water in the shallow aquifer (0.5–22 m depth) was of Na⁺-K⁺-Cl^?-NO₃^? type and not potable due to point source pollution, whereas Ca⁺-HCO₃^? unpolluted water dominates in the deeper aquifer. Water in the deep and shallow aquifers indicates the results of preferential flow pass and evaporative recharge, respectively. Possible hydrogeochemical processes include point source pollution, reverse ion exchange, remote recharge areas and mixing of waters with different chemical signatures.

EDITOR D. Koutsoyiannis ASSOCIATE EDITOR M.D. Fidelibus     

Seasonal controls of meltwater runoff chemistry and chemical weathering at Urumqi Glacier No.1 in central Asia

Temporal variation of runoff chemistry and its seasonal controls relating to chemical weathering processes and drainage system evolution were examined at Urumqi Glacier No.1 in Xinjiang, China, over a full melt season. The dominant ions in meltwater runoff are HCO₃^?, Ca²⁺, and SO₄^2?; and Fe, Sr, and Al are dominant elements. Concentrations of major ions and some elements show periodic variations with seasons and negatively correlate with discharge, whereas other elements (e.g., Al, Ni, Cu, Zn, Cd, and Pb) show a random change, providing insights into the hydrological and physicochemical controls. HCO₃^? and Ca²⁺ are primarily derived from calcite, SO₄^2? and Fe mainly come from pyrite, and Sr and Al principally originate from silicate. Hydrochemical fluxes of solutes exhibit strong seasonality but are positively related to discharge, suggesting an increasing release of solutes during higher flow conditions. Solute yields, cation denudation rate, and chemical weathering intensity observed at Urumqi Glacier No.1 are higher than those at most basins worldwide. This suggests that chemical weathering in central Asia may be stronger than at other glacial basins with similar specific discharge. Concentrations of some elements (e.g., Fe, Al, As, Pb, and Zn) are close to or exceed the guidelines for drinking water standards in meltwater‐fed rivers. These rivers may face future challenges of water quality degradation, and relationships between changing flow and water quality conditions should be established soon, given that development of channelized flow is expected to be earlier over a melt season in a warming climate.     

Etude de la phase gazeuse occluse dans les laves de «l’Ardoukôba», volcan éphémère d’une dorsale émergée (Afar)

Gases trapped in lavas of three main flows of the Ardoukôba eruption (8 to 15 November, 1978) have been analysed by mass spectrometry. These analyses concern both plagioclase phenocrysts and microcrystalline mesostasis. Fluids are released between 500°C and 1200°C, and consist of H₂O, CO₂, CO, N₂, SO₂, HCl, H₂, CH₄ with traces of hydrocarbons and H₂S. The total content is less than 0.3–0.4 wt. % of samples with about 0.1–0.15 wt % of H₂O. No significant variation among the three flows is observed. Plagioclase phenocrysts are less abundant in fluids than the mesostasis (～2/3). The gases trapped in these phenocrysts are richer in CO and organic compounds, whereas mesostasis contain more H₂O, CO₂ and SO₂. CO is likely produced by reduction of CO₂ and H₂O with carbon during either analyses or eruption itself, or is of primary origin. In the latter case, gas composition suggests an entrapment temperature of about 1200°C ± 75°C. Kinetic study of the water and carbon dioxide release allows to calculate the diffusion characteristics of these fluids. Water and carbon dioxide behave rather similarly. Plagioclase gives a single activation energy value (8 Kcal/mole), while mesostasis gives two values (8 Kcal/mole, 15 Kcal/mole). Diffusion coefficients at 20°C are estimated to fall in the range 10^?13 · 10^?12 cm² · sec^?1.     

Chemical dynamics of N-containing ionic species in a boreal forest snowcover during the spring melt period

A study of the changes in the ionic loads of NO, NH, SO and H⁺ in a boreal forest snowpack at Lake Laflamme, Québec was carried out using hydrological and chemical data from field lysimeters. The results showed that depletion of the N-containing species occurs periodically in the snowpack during meltwater discharge. Rain-on-snow events led to in-pack losses of NO and NH at a rate of 130 μeq m^?2 day^?1 and 101·3 μeq m^?2day^?1 respectively. On dry days, however, dry deposition and deposition of organic debris from the canopy resulted in increases of 183·3 μeq m^?2day^?1 for NO and 4·5 μeq m^?2day^?1 for NH in the pack. In contrast, SO₄^2? showed continual in-pack increases due to deposition of 5·0 μeq m^?2day^?1 for wet days and 92·6 μeq m^?2day^?1 for dry days. The depletion of NO and NH is due to microbiological uptake of these nutrients during periods when the free water content of the pack is high. Controlled melts in a laboratory snowmelt simulator containing snow and organic matter from the forest canopy at Lake Laflamme showed losses of NO and NH similar to those observed in the field. As the microbiological uptake proceeds at a rate comparable to that of ionic load increases in the pack by dry deposition, models of the chemical dynamics of snowmelt should take the former into account in any system where organic content of the snowpack is appreciable.     

Water quality and hydrogeochemical characteristics of the River Buyukmelen,Duzce, Turkey

The River Buyukmelen is located in the province of Duzce in northwest Turkey and its water basin is approximately 470 km². The Aksu, Kucukmelen and Ugursuyu streams flow into the River Buyukmelen. It flows into the Black Sea with an output of 44 m³ s⁻¹. The geological succession in the basin comprises limestone and dolomitic limestone of the Yılanlı formation, sandstone, clayey limestone and marls of the Akveren formation, clastics and volcano‐clastics of the Caycuma formation, and cover units comprised of river alluvium, lacutrine sediments and beach sands. The River Buyukmelen is expected to be a water source that can supply the drinking water needs of Istanbul until 2040; therefore, it is imperative that its water quality be preserved. The samples of rock, soil, stream water, suspended, bed and stream sediments and beach sand were collected from the Buyukmelen river basin. They were examined using mineralogical and geochemical methods. The chemical constituents most commonly found in the stream waters are Na⁺, Mg²⁺, SO²⁻₄, Cl⁻ and HCO₃⁻ in the Guz stream water, Ca²⁺ in the Abaza stream water, and K⁺ in the Kuplu stream water. The concentrations of Na⁺, K⁺, Ca²⁺, Mg²⁺, SO²⁻₄, HCO⁻₃, Cl⁻, As, Pb, Ni, Mn, Cr, Zn, Fe and U in the Kuplu and Guz stream waters were much higher than the world average values. The Dilaver, Gubi, Tepekoy, Maden, Celik and Abaza streams interact with sedimentary rocks, and the Kuplu and Guz streams interact with volcanic rocks. The amount of suspended sediment in the River Buyukmelen in December 2002 was 120 mg l⁻¹. The suspended and bed sediments in the muddy stream waters are formed of quartz, calcite, plagioclase, clay (kaolinite, illite and smectite), muscovite and amphibole minerals. As, Co, Cd, Cr, Pb, Ni, Zn and U have all accumulated in the Buyukmelen river‐bed sediments. The muddy feature of the waters is related to the petrographic features of the rocks in the basin and their mineralogical compositions, as most of the sandstones and volcanic rocks (basalt, tuffite and agglomerate) are decomposed to a clay‐rich composition at the surface. Thus, the suspended sediment in stream waters increases by physical weathering of the rocks and water–rock interaction. Owing to the growing population and industrialization, water demand is increasing. The plan is to bring water from the River Buyukmelen to Istanbul's drinking‐water reservoirs. According to the Water Pollution Regulations, the River Buyukmelen belongs to quality class 1 based on Hg, Cd, Pb, As, Cu, Cr, Zn, Mn, Se, Ba, Na⁺, Cl⁻, and SO²⁻₄; and to quality class 3 based on Fe concentration. The concentration of Fe in the River Buyukmelen exceeds the limit values permitted by the World Health Organization and the Turkish Standard. Because water from the River Buyukmelen will be used as drinking water, it will have an adverse effect on water quality and humans if not treated in advance. In addition, the inclusion of Mn and Zn in the Elmali drinking‐water reservoir of Istanbul and Fe in the River Buyukmelen water indicates natural inorganic contamination. Mn, Zn and Fe contents in the waters are related to geological origin. Moreover, the River Buyukmelen flow is very muddy in the rainy seasons and it is inevitable that this will pose problems during the purification process. Copyright © 2005 John Wiley & Sons, Ltd.     

Contribution of glacier meltwater to streamflow in the Wind River Range,Wyoming, inferred via a Bayesian mixing model applied to isotopic measurements

The Wind River Range (WRR) of Wyoming has the largest concentration of alpine glaciers in the American Rockies and contributes to several major river systems in the western United States. Declines in the areal extent and volume of these glaciers are well documented, and eventual loss of alpine glaciers will reduce the amount of water available for agricultural and domestic use. The contribution of glacial melt to streamflow remains largely unquantified in Wyoming. We used isotope measurements and Bayesian modeling to estimate the fractional contribution of glacier meltwater to Dinwoody Creek (DC) in the WRR on bi‐weekly and seasonal (spring, summer, and fall) time scales over 2 years. In 2007 and 2008, we made temporally intensive measurements of the stable isotope composition of water from the DC watershed. Samples of the primary sources of streamflow (snowmelt, glacier melt, rain, and baseflow) were collected during field campaigns, and automated collection of stream samples occurred over the melt season. Isotope data (D and ¹⁸O) were analyzed within a hierarchical Bayesian framework that incorporated temporal and spatial correlations. Glacial melt contributed a significant proportion (～53–59%) to streamflow in a low‐flow year (2007) or when streamflow was low during a high‐flow year (2008). In 2008, a large and persistent snowpack contributed significantly (～0·42–51%) to streamflow in mid‐summer. The large contribution of glacial melt to streamflow suggests that the loss of glaciers may impact riparian ecosystems and human water supplies in the late summer and in years with low snowpack. Copyright © 2011 John Wiley & Sons, Ltd.     

The influence of oxidation state on the electrical conductivity of olivine

The electrical conductivity of a single crystal of San Carlos olivine (Fo₉₂, 0.16 wt.% Fe₂O₃) has been measured as a function of temperature and oxygen fugacity (fO₂). After heating to 1338°C at fO₂ = 10^?12 atm., the conductivity at 950°C was 10^?5 (ohm-m)^?1, almost 3 orders of magnitude less than that measured in air. This decrease is due to the reduction of Fe³⁺ to Fe²⁺. Further heating to 1500°C at fO₂ = 10^?14 atm., decreased the electrical conductivity at 950°C to 10^?6 (ohm-m)^?1. When recovered at room temperature, the speciment had Fo₉₆ composition and contained small, opaque blebs distributed throughout the crystal. Derivations of temperature profiles for the earth's mantle from conductivity-depth models must take account of the important role played by iron oxidation state in the electrical conductivity of olivine.     

Applicability of isotopic hydrograph separation in a suburban basin during snowmelt

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.