The isotope hydrology of the Muskoka River Watershed,Ontario, Canada

Stable isotope tracers of δ¹⁸O and δ²H are increasingly being applied in the study of water cycling in regional-scale watersheds in which human activities, like river regulation, are important influences. In 2015, δ¹⁸O and δ²H were integrated into a water quality survey in the Muskoka River Watershed with the aim to provide new regional-scale characterization of isotope hydrology in the 5,100-km² watershed located on the Canadian Shield in central Ontario, Canada. The forest dominated region includes ~78,000 ha of lakes, 42 water control structures, and 11 generating stations, categorized as “run of river.” Within the watershed, stable isotope tracers have long been integrated into hydrologic process studies of both headwater catchments and lakes. Here, monthly surveys of δ¹⁸O and δ²H in river flow were conducted in the watershed between April 2015 and November 2016 (173 surface water samples from 10 river stations). Temporal patterns of stable isotopes in river water reflect seasonal influences of snowmelt and summer-time evaporative fractionation. Spatial patterns, including differences observed during extreme flood levels experienced in the spring of 2016, reflect variation in source contributions to river flow (e.g., snowmelt or groundwater versus evaporatively enriched lake storage), suggesting more local influences (e.g., glacial outwash deposits). Evidence of combined influences of source mixing and evaporative fractionation could, in future, support application of tracer-enabled hydrological modelling, estimation of mean transit times and, as such, contribute to studies of water quality and water resources in the region.     

Assessment of annual high‐water events for the Mackenzie River basin,Canada

River ice break‐up is known to have important morphological, ecological and socio‐economic effects on cold‐regions river environments. One of the most persistent effects of the spring break‐up period is the occurrence of high‐water events. A return‐period assessment of maximum annual nominal water depths occurring during the spring break‐up and open‐water season at 28 Water Survey of Canada hydrometric sites over the 1913–2002 time period in the Mackenzie River basin is presented. For the return periods assessed, 13 (14) stations are dominated by peak events occurring during the spring break‐up (open‐water) season. One location is determined to have a mixed signal. A regime classification is proposed to separate ice‐ and open‐water dominated systems. As part of the regime classification procedure, specific characteristics of return‐period patterns including alignment, and difference between the 2 and 10‐year events are used to identify regime types. A dimensionless stage‐discharge plot allows for a contrast of the relative magnitudes of flows required to generate maximum nominal water‐depth events in the different regimes. At sites where discharge during the spring break‐up is approximately one‐quarter or greater than the magnitude of the peak annual discharge, nominal water depths can be expected to exceed those occurring during the peak annual discharge event. Several physical factors (location, basin area, stream order, gradient, river orientation, and climate) are considered to explain the differing regimes and discussed relative to the major sub‐regions of the MRB. Copyright © 2008 John Wiley & Sons, Ltd and Her Majesty the Queen in right of Canada.     

Element geochemistry of weathering profile of dolomitite and its implications for the average chemical composition of the upper-continental crust

Geochemical behavior of chemical elements is studied in a dolomitite weathering profile in upland of karst terrain in northern Guizhou. Two stages can be recognized during the process ofin situ weathering of dolomitite: the stage of sedentary accumulation of leaching residue of dolomitite and the stage of chemical weathering evolution of sedentary soil. Ni, Cr, Mo, W and Ti are the least mobile elements with reference to Al. The geochemical behavior of REE is similar to that observed in weathering of other types of rocks. Fractionation of REE is noticed during weathering, and the two layers of REE enrichments are thought to result from downward movement of the weathering front in response to changes in the environment. It is considered that the chemistry of the upper part of the profile, which was more intensively weathered, is representative of the mobile components of the upper curst at the time the dolomitite was formed, while the less weathered lower profile is chemically representative of the immobile constitution. Like glacial till and loess, the “insoluble” materials in carbonate rocks originating from chemical sedimentation may also provide valuable information about the average chemical composition of the upper continental crust.     

Effects of shield brine on the safe disposal of waste in deep geologic environments

The salinity of groundwater increases with depth in the Canadian Shield (up to 1.3 kg/L of density). The existence of brine can be critically important for the safe geologic disposal of radioactive wastes, as dense brine can significantly retard the upward migration of radionuclides released from repositories. Static and flushing conditions of the deep brine are analyzed using a U-tube analogy model. Velocity reduction due to the presence of dense brine is derived under flushing conditions. A set of illustrative numerical simulations in a two-dimensional cross section is presented to demonstrate that dense brine can significantly influence regional groundwater flow patterns in a shield environment. It is implied from the results that (1) the existence of Shield brine can be an indicator of a hydrogeologically stable environment, (2) activities near ground surface may not perturb the stable groundwater environment in the deep brine region, and thus, (3) the deep brine region can be considered as a candidate geologic site for the safe disposal of waste. In addition to brine, other issues associated with long-term waste disposal, such as geological, glacial and seismic events, may need to be considered for the safe storage of spent nuclear fuel in a shield environment.     

Comparing various approaches for assessing groundwater recharge at a regional scale in the Canadian Shield

ABSTRACT

Estimating groundwater recharge is crucial to ensuring the proper management of aquifers. In this study, net regional recharge and spatial potential recharge are estimated at four watersheds within the Charlevoix–Haute-Côte-Nord (CHCN) regions, Quebec Province, Canada. Four methods are applied based on available data. The first two approaches are regional water budget methods. These two methods differ in their estimation of vertical inflow (VI), which is estimated from two hydrological models: GR4J and HYDROTEL. The third method estimates potential recharge spatially over the study area. Finally, the streamflow data are analysed using the Eckhardt baseflow separation method to obtain an estimation of recharge, assuming that discharge is equal to recharge. According to the results of all investigated methods, the mean annual recharge for the CHCN region is approximately 183 mm, which is 18% of the total annual precipitation (P). The discussion section highlights uncertainties due to the assumptions of each method and the reliability of the data.     

Element geochemistry of weathering profile of dolomitite and its implications for the average chemical composition of the upper-continental crust--Case studies from the Xinpu profile,northern Guizhou Province,China

Geochemical behavior of chemical elements is studied in a dolomitite weathering profile in upland of karst terrain in northern Guizhou.Two stages can be recognized during the process of in situ weathering of dolomitite:the stage of sedentary accumulation of leaching residue of dolomitite and the stage of chemical weathering evolution of sedentary soil.Ni,Cr,Mo,W and Ti are the least mobile elements with reference to Al.The geochemical behavior of REE is similar to that observed in weathering of other types of rocks.Fractionation of REE is noticed during weathering,and the two layers of REE enrichments are thought to result from downward movement of the weathering front in response to changes in the environment.It is considered that the chemistry of the upper part of the profile,which was more intensively weathered,is representative of the mobile components of the upper curst at the time the dolomitite was formed,while the less weathered lower profile is chemically representative of the immobile constitution.Like glacial till and loess,the "insoluble" materials in carbonate rocks originating from chemical sedimentation may also provide valuable information about the average chemical composition of the upper continental crust.     

粤东五华河流域的化学风化与CO2吸收

基于对粤东五华河干流和支流水体的物理、化学组成测试数据,应用质量平衡法和相关分析法探讨湿热山地丘陵地区岩石化学风化过程对大气CO₂的吸收.结果表明:五华河水体的总溶解性固体含量(77.11 mg/L)接近于世界河流的平均值(65 mg/L);离子组成以Ca²⁺、Na⁺和HCO₃^-为主,可溶性Si次之.五华河流域化学径流组成主要源自硅酸盐矿物化学风化过程的贡献,碳酸盐矿物的贡献较少;大气和土壤CO₂是流域内岩石化学风化的主要侵蚀介质.与同一气候带其他河流相比较,五华河流域岩石化学风化过程对大气CO₂的吸收通量(2.14×105mol/(km²·a))较低,这主要是由于流域内缺乏碳酸盐岩所导致.     

Assessment of the WATCLASS hydrological model result of the Mackenzie River basin using the GRACE satellite total water storage measurement

Earlier efforts have been geared towards modelling the hydrological water balance of the Mackenzie River basin and its sub‐basins using a coupled land surface–hydrological model for the Canadian cold region known as WATCLASS. The goal of this current study is to effectively inter‐compare the resulting total water storage anomalies estimated from the gravity recovery and climate experiment (GRACE) satellite analysis with those estimated from the atmospheric‐based water balance approach as well as the model output from WATCLASS over the 1 · 8 × 10⁶ km² Mackenzie River basin in Canada. Since the success of the parameter estimation stage of the coupled land surface–hydrological model, WATCLASS over this large catchment, was entirely based on a goodness of fit between the simulated and observed flows, it is often desirable to assess the reliability of the generated state variables prior to concluding on the overall efficiency of this model in reproducing the relevant hydrological processes over this region. A major challenge here lies in finding suitable dataset with which this comparison can be made to further assess the ability of the model in accurately reproducing other mass fluxes. The outcome of this inter‐comparison reveals the potential application of the GRACE‐based approach as a veritable tool required for the closure of the hydrological water balance of the Mackenzie River basin as well as serving as a dependable source of data for the calibration of traditional hydrological models. Copyright © 2009 John Wiley & Sons, Ltd.     

Early Paleozoic whole-rock Ce anomalies and secular eustatic changes in the Upper Yangtze region

The 65 whole-rock REE samples studied come from the classic sections of Early Cambrian to Early Silurian in the Yichang area, Hubei Province. REE concentrations tested on ICP-AES are normalized to the North American Shale Composite (NASC), and Ce anomaly values are calculated based on log[ 3Cen/(2Lan+Ndn)] . With the whole-rock Ce anomaly used as a quantitative index of sea-level changes, 5 prominent eustatic circles are recognized, and a good corresponding relationship is observed between the black shale episodes and the transgressive events. On account of the global distributions of coeval black shales and the specified paleogeographic background of South China, a genetic hypothesis based on the model of O2-minimum zone expansion is suggested for the Early Paleozoic multi-episode black shales in South China.     

腾格里沙漠盐湖氯同位素地球化学特征

δ~(37)Cl值可以用来指示盐湖演化过程中卤水的蒸发浓缩程度、可能的补给来源和控制因素,本文对腾格里沙漠地区12个代表性盐湖卤水样品开展了氯同位素组成研究.结果表明,研究区内沙漠盐湖卤水的δ~(37)Cl值变化范围为-0.10‰~1.36‰,平均值为0.55‰;其中,硫酸钠亚型卤水的δ~(37)Cl值范围为-0.10‰~1.36‰(平均值为0.56‰),硫酸镁亚型卤水的δ~(37)Cl值范围为0.14‰~0.82‰(平均值为0.48‰).对比柴达木盆地现代盐湖分析数据,发现区内沙漠盐湖的δ~(37)Cl平均值明显大于柴达木盆地盐湖的δ~(37)Cl平均值,并且,硫酸钠亚型卤水δ~(37)Cl最高,硫酸镁亚型卤水次之,氯化物型卤水最小.基于不同盐湖地下水咸化程度以及盐湖卤水中δ~(37)Cl值与Br/Cl系数关系的研究,揭示了研究区东部和东北部盐湖可能受到第三系地层咸水的补给,而其他盐湖主要受蒸发浓缩作用影响.δ~(37)Cl值分布特征则显示,腾格里沙漠地区部分盐湖在形成过程中可能受到区域构造活动诱发的第三系深部水补给及水-岩作用等多重因素的影响.     

A study of interaction between surface water and groundwater using environmental isotope in Huaisha River basin

The surface water and groundwater are important components of water cycle, and the interaction between surface water and groundwater is the important part in water cycle research. As the effective tracers in water cycle research, environmental isotope and hydrochemistry can reveal the interrelationships between surface water and groundwater effectively. The study area is the Huaisha River basin, which is located in Huairou district, Beijing. The field surveying and sampling for spring, river and well water were finished in 2002 and 2003. The hydrogen and oxygen isotopes and water quality were measured at the laboratory. The spatial characteristics in isotope and evolution of water quality along river lines at the different area were analyzed. The altitude effect of oxygen isotope in springs was revealed, and then using this equation, theory foundation for deducing recharge source of spring was estimated. By applying the mass balance method, the annual mean groundwater recharge rate at the catchment was estimated. Based on the groundwater recharge analysis, combining the hydrogeological condition analysis, and comparing the rainfall-runoff coefficients from the 1960s to 1990s in the Huaisha River basin and those in the Chaobai River basin, part of the runoff in the Huaisha River basin is recharged outside of this basin, in other words, this basin is an un-enclosed basin. On the basis of synthetically analyses, combining the compositions of hydrogen and oxygen isotopes and hydrochemistry, geomorphology, geology, and watershed systems characteristics, the relative contributions between surface water and groundwater flow at the different areas at the catchments were evaluated, and the interaction between surface water and groundwater was re- vealed lastly.     

Major- and trace-element systematics and isotope geochemistry of Cenozoic mafic volcanic rocks from the Vogelsberg (central Germany): Constraints on the origin of continental alkaline and tholeiitic basalts and their mantle sources

The Cenozoic basaltic province of the Vogelsberg area (central Germany) is mainly composed of intercalated olivine to quartz tholeiites and near-primary nephelinites to basanites. The inferred mantle source for the alkaline and tholeiitic rocks is asthenospheric metasomatized garnet peridotite containing some amphibole as the main hydrous phase. Trace element modelling indicates 2 to 3% partial melting for the alkaline rocks and 5 to 7% partial melting for the olivine tholeiites. Incompatible trace element abundances and ratios as well as Nd and Sr radiogenic isotope compositions lie between plume compositions and enriched mantle compositions and are similar to those measured in Ocean Island Basalts (OIB) and the Central European Volcanic Province elsewhere. The mafic olivine tholeiites have similar Ba/Nb, Ba/La and Nd–Sr isotope ratios to the alkaline rocks indicating derivation of both magma types from chemically comparable mantle sources. However, Zr/Nb ratios are slightly higher in olivine tholeiites than in basanites reflecting some fractionation of Zr relative to Nb during partial melting. Quartz tholeiites have higher Ba/Nb, Zr/Nb, La/Nb, but lower Ce/Pb ratios and lower Nd isotope compositions than the alkaline rocks which can be explained by interaction of the basaltic melt with lower (granulite facies) crustal material or partial melts thereof during stagnation within the lower crust. It appears most likely that upwelling of hot, asthenospheric material results in the generation of primitive alkaline rocks at the base of the lithosphere at depths of 75–90 km. Lithospheric extension together with minor plume activity and probably lower lithosphere erosion induced melting of shallower heterogenous upper mantle generating a spectrum of olivine tholeiitic melts. These olivine tholeiitic rocks evolved via crystal fractionation and probably limited contamination to quartz tholeiites.     

The role of wetland coverage within the near‐stream zone in predicting of seasonal stream export chemistry from forested headwater catchments

Stream chemistry is often used to infer catchment‐scale biogeochemical processes. However, biogeochemical cycling in the near‐stream zone or hydrologically connected areas may exert a stronger influence on stream chemistry compared with cycling processes occurring in more distal parts of the catchment, particularly in dry seasons and in dry years. In this study, we tested the hypotheses that near‐stream wetland proportion is a better predictor of seasonal (winter, spring, summer, and fall) stream chemistry compared with whole‐catchment averages and that these relationships are stronger in dryer periods with lower hydrologic connectivity. We evaluated relationships between catchment wetland proportion and 16‐year average seasonal flow‐weighted concentrations of both biogeochemically active nutrients, dissolved organic carbon (DOC), nitrate (NO₃‐N), total phosphorus (TP), as well as weathering products, calcium (Ca), magnesium (Mg), at ten headwater (<200 ha) forested catchments in south‐central Ontario, Canada. Wetland proportion across the entire catchment was the best predictor of DOC and TP in all seasons and years, whereas predictions of NO₃‐N concentrations improved when only the proportion of wetland within the near‐stream zone was considered. This was particularly the case during dry years and dry seasons such as summer. In contrast, Ca and Mg showed no relationship with catchment wetland proportion at any scale or in any season. In forested headwater catchments, variable hydrologic connectivity of source areas to streams alters the role of the near‐stream zone environment, particularly during dry periods. The results also suggest that extent of riparian zone control may vary under changing patterns of hydrological connectivity. Predictions of biogeochemically active nutrients, particularly NO₃‐N, can be improved by including near‐stream zone catchment morphology in landscape models.     

Variations in chemical compositions of the eolian dust in Chinese Loess Plateau over the past 2.5 Ma and chemical weathering in the Asian inland

Major and trace elements as well as strontium isotopic composition have been analyzed on the acid-insoluble (AI) phase of the loess-paleosol sequence from Luochuan, Shaanxi Province, China. Results show that the chemical composition of AI phase of loess and paleosols is distinctive to the average composition of upper continental crust (UCC), characterized by depletion of mobile elements Na, Ca and Sr. The distribution pattern of elements in AI phase reveals that initial dust, derived from a vast area of Asian inland, has suffered from Na- and Ca-removed chemical weathering compared to UCC. Some geochemical parameters (such as CIA values, Na/K, Rb/Sr and⁸⁷Sr/⁸⁶Sr ratios) display a regular variation and evolution, reflecting that the chemical weathering in the source region of loess deposits has decreased gradually since 2.5 Ma with the general increase of global ice volume. This coincidence reflects that the aridity of Asian inland since the Quaternary is a possible regional response to the global climate change.     

Space weathering processes on airless bodies: Fe isotope fractionation in the lunar regolith

Nanophase Fe metal grains (np-Fe°) are a product of space weathering, formed by processes related to meteorite impacts, and solar-wind sputtering on airless planetary bodies, such as the Moon. Iron isotopes of lunar soils are fractionated during these processes, and the np-Fe° in the finest (<10 μm), mature, size fractions of the soil become enriched in heavier isotopes by ∼0.3‰ in ⁵⁶Fe/⁵⁴Fe in comparison to the bulk rocks (0.03±0.05‰), from which the soil was formed. A positive correlation of δ⁵⁶Fe values with the soil maturity index, I_S/FeO, suggests that the high δ⁵⁶Fe values reflect production of nanophase Fe metal that is produced by space weathering that occurs on airless planetary bodies. Furthermore, the enrichment of δ⁵⁶Fe in the smallest size fraction of lunar soils supports a model for creation of np-Fe° through vapor deposition induced by micrometeorites, as well as that by solar-wind sputtering.     

Strontium isotope identification of water mixing and recharge sources in a river system (Oder River,central Europe): A quantitative approach

This study uses Sr isotope composition (⁸⁷Sr/⁸⁶Sr) and Sr content of waters of the Oder, one of the largest rivers in central Europe, to fingerprint natural and anthropogenic contributions to its Sr budget and to evaluate water mixing processes in its hydrological system. It also demonstrates a simple method of quantifying natural and anthropogenic Sr inputs in the watershed. The method has potential for environmental and archaeological research because past Sr geochemistry of river water can easily be reconstructed. For the first time, a catchment‐scale impact of anthropogenic sources on the Sr budget of a middle‐size river is shown in a quantitative way. The water of the Oder is characterized by a relatively uniform Sr isotope composition, from 0.7100 to 0.7108, contrasting with strong variations in Sr concentration, from 0.25 to 1.27 mg/L. There is a general seasonal trend in variability, with waters becoming more radiogenic and dilute with respect to the Sr in the spring time. This Sr systematics differs significantly from the Sr budgets of the majority of the Oder tributaries that exhibit more radiogenic composition and systematically lower Sr concentrations. A mixing scenario in the Oder involves Sr contribution from four principal water sources: (a) shallow ground waters with Sr derived from near‐surface weathering of silicates, (b) moderately radiogenic mine waters from the Upper Silesian Coal Basin, (c) unradiogenic mine waters from the Permian sequence of the copper district, and (d) unradiogenic ground waters from shallow‐seated Palaeogene, Neogene, and Mesozoic aquifers. The Sr budget of the Oder is primarily controlled by inputs of dissolved Sr from anthropogenic sources, which overprint the natural background, controlled by geology. Thus, about 47.5% of Sr originates from agriculture, industrial, and municipal additions, 31.5% from mine water inputs, and only 21% from natural sources, that is, rock weathering and atmospheric precipitation. Reconstruction of the past Sr chemistry of the Oder reveals that its present‐day Sr isotope composition is temporary and significantly different from that of the preindustrial times.     

Ionic and stable isotope chemistry as indicators of water sources to the Upper Mendoza River basin,Central Andes of Argentina

The Mendoza River is mainly dependent on the melting of snow and ice in the Upper Andes. Since predicted changes in climate would modify snow accumulation and glacial melting, it is important to understand the relative contributions of various water sources to river discharge. The two main mountain ranges in the basin, Cordillera Principal and Cordillera Frontal, present differences in geology and receive differing proportions of precipitation from Atlantic and Pacific moisture sources. We propose that differences in the origin of precipitation, geology and sediment contact times across the basin generate ionic and stable isotopic signatures in the water, allowing the differentiation of water sources. Waters from the Cordillera Principal had higher salinity and were more isotopically depleted than those from the Cordillera Frontal. Stable isotope composition and salinity differed among different water sources. The chemical temporal evolution of rivers and streams indicated changes in the relative contributions of different sources, pointing to the importance of glacier melting and groundwater in the river discharge.     

Hydrocarbon accumulation in network and its application in the continental rift basin

The concept of hydrocarbon accumulation in network was presented on basis of the overall analysis of the formation and evolution characteristics of the continental faulted basin and of the systemic re-search on the major controlling factors on the hydrocarbon accumulation. The hydrocarbon accumu-lation in network can be defined as hydrocarbon accumulation in a three-dimensional network system which is constituted by the hydrocarbon migration passages under multiple dynamics,following the hydrocarbon generation from source rocks. The research shows that the hydrocarbon accumulation in network is composed of four elements,i.e.,hydrocarbon source (source rock kitchen),hydrocarbon accumulation terminal (trap),network pathway connecting source and terminal (transporting system),and network potential driving hydrocarbon migration in the network pathway (migration dynamics). Compared with other networks,hydrocarbon accumulation in network has three basic characteristics: the irreversible geological process of material and information flow in the network; the loss of material and information in the flow process in the network; the multiple dynamics in the flow process. Interac-tion of all the elements in the geological process can be called hydrocarbon accumulation in network. There are three basic models for hydrocarbon accumulation in network,that is,hydrocarbon accumu-lation in the network source area,hydrocarbon accumulation in the network pathway,and hydrocarbon accumulation in the network terminal. The key in the application of the hydrocarbon accumulation models in network in practice is to confirm the major accumulation stage and the function range of the four elements controlling the hydrocarbon firstly,to predict the profitable accumulation region by su-perposition of the favorable areas confirmed by four elements consequently,and to evaluate the oil-bearing property of the trap as well as confirm drilling targets. This paper takes the Dongying De-pression in the Bohai Bay Basin as an application example.     

Chemocline instability and isotope variations of the Ediacaran Doushantuo basin in South China

Stable isotope analyses in sections across a shelf to basinal transect of the Ediacaran Doushantuo basin show substantial isotope variabilities. In Songlin section where sediments were deposited in an intrashelf basin, δ 13C values are persistently negative (_3‰ to _5‰, VPDB) through the entire Doushantuo Formation, similar to those obtained from the slope section in Wuhe (_5‰ to _10‰, VPDB). Shallow water sections in Weng'an and Duoding show two broad δ 13C anomalies overprinted with significant meter-scale variations, but none of the curves has similar absolute δ 13C values compared to the Yangtze Gorges areas in South China and other sections globally. Such isotope variations, if partially recording ancient seawater signature, imply spatial and temporal chemocline instability in the Doushantuo basin. In combination with available δ 13C records from other Ediacaran successions globally, the data from the Doushantuo basin are consistent, in first order, with the existence and oxidation of a large dissolved organic carbon (DOC) reservoir in Ediacaran oceans, but imply local environmental controls on Neoproterozoic isotope values and call attentions for using δ 13C anomalies as time lines in stratigraphic correlation.