Fate of Point‐Source Pesticide Spill in Clayey Till after 15 Years

This study investigated the development of pesticide pollution two, three, and 17 years after spills of the herbicides dichlorprop, mecoprop (MCPP), MCPA, 2,4‐D (phenoxy acids), simazine, and terbutylazine (triazines) in a former orchard machinery service yard. The spills had occurred over several decades on a 23‐m thick, mainly anaerobic fractured clayey till aquitard. Angled monitoring wells were installed in the aquitard 3 years after the spills ceased in 1989. In 1993, monitoring revealed that high groundwater concentrations of dichlorprop (677 µg/L) and MCPP (139 µg/L) were accumulated as a zone of maximum pollution in anaerobic and largely immobile pore water at 5 to 6 m depth in the aquitard profile. In contrast, 2,4‐D was determined in only one water sample, and MCPA and simazine and terbutylazine were determined only in low concentrations (below10 µg/L), although these pesticides had been handled at the site in greater amounts than dichlorprop and MCPP according to detailed historic information obtained for the site. Repeated monitoring in the same wells after a further 14 years in 2007 revealed that no identifiable degradation of MCPP had occurred, while dichlorprop had degraded by 75% to 80% (estimated half‐life of approximately 5 years). Furthermore, degradation products related to the phenoxy acids had accumulated, especially 4‐CPP with a maximum concentration of 218 µg/L. In the same zone, MCPA and simazine had almost disappeared. As the pollution was mainly accumulated in largely immobile pore water of the aquitard clayey matrix, and the groundwater recharge was low (30 to 60 mm/year), only minor vertical displacement of the zone with maximum pollution zone had occurred during the 15 years of monitoring. However, concentrations of dichlorprop (0.01 to 0.02 µg/L), MCPP (0.1 to 0.2 µg/L), and 4‐CPP (0.6 to 0.7 µg/L) had spread along textural heterogeneities in the aquitard into the underlying sandy aquifer at 23‐m depth.     

Effects of ultrafiltration on salt migration and isotopic composition of pore water in groundwater depression area in Hengshui,NCP

Clay aquitards are semipermeable membranes that allow groundwater flow while retarding solute migration has been researched extensively but also subjected to much debate. At present, there is no evidence of whether the physical and chemical properties of clay soil and the isotopic composition of pore water affect the semipermeable membrane effect. In this study, we collected clay samples from drilling cores (30–90 m) in the Hengshui area located in the North China Plain (NCP), then extracted pore water using a high-pressure squeezing device. Vertical hydrochemical and isotopic profile variation trends for the pore water were revealed using hydrochemical (Cl⁻, Na⁺, Ca²⁺, K⁺, Mg²⁺, and SO₄²⁻) and stable isotopic measurements of H, O and Cl. The results showed that the hydrochemical clay interlayer pore water of the saline aquifer is Cl/SO₄-Na/Mg type and the average total dissolved solids (TDS) are 10.17 g/L. However, the hydrochemical clay aquitard pore water is of the Cl/SO₄-Na/Ca type with an average TDS of 1.90 g/L. The hydrochemical clay interlayer pore water of aquifer II is of Cl-Na/Ca type with an average TDS of 1.10 g/L. Our results showed that the water quality of the aquifer II is not affected by the upper part of the saline aquifer, thus the clay aquitard acts as a significant barrier to salt movement. A polarization layer concentrated in ions was formed between the upper part of the saline aquifer and the clay aquitard. The concentration polarization layer increases the salt-inhibition effect. H, O and Cl isotopic composition results showed significant fractionation. The pore water of aquifer II lacked heavy isotopes (²H, ¹⁸O, ³⁷Cl), but had significant heavy isotope enrichment in the concentrated polarized layer (the δ²H value was −76‰, the δ¹⁸O value was −8.4‰, and the δ³⁷Cl value was 1.59‰). Hyperfiltration thus played a significant role in isotope fractionation.     

The Apure River: geochemistry of major and selected trace elements in an Orinoco River tributary coming from the Andes,Venezuela

The analysis of physicochemical variables and selected dissolved elements was performed on the Apure River waters for 15 months. The variables pH, alkalinity, dissolved O₂, conductivity and Na, Ca, Mg and Cd concentrations showed maximum values during low water, whereas K, Si, Fe, Al, Mn, Zn, Cu, Cr and dissolved organic carbon (DOC) showed maximum concentrations during rising and high water. Five important factors were found to control the amount and temporal variability of the dissolved elements: lithology, hydrology, vegetation–floodplain processes, redox conditions and organic complexation. Weathering of silicates, carbonates and evaporites in the Andes provides most of the proportion of Na, Ca, Mg and HCO₃^? to waters. The temporal variability of these ions is controlled by a dilution process. Although Si can be taken up by the biomass, Si and K can be leached from the floodplain by weathering of clays. Microbial decay of the submerged plants in the floodplain during the inundation periods provides DOC and K to river waters and changes the redox conditions in water. The changing redox conditions control the solubility of Mn, Zn and Fe. Dissolved Mn is a function of pH‐dependent redox process, whereas Zn solubility is controlled by scavenging of Zn during the oxidation of Mn²⁺ to MnO₂. Positive relationships between Al, Fe, Cu, Cr and DOC suggest that these elements are complexed by organic colloids generated in the floodplain. Moreover, the binding capacity of Fe with DOC increases under reducing conditions. Although Cd seems to be provided by weathering in the Andes, several processes can affect the mobility of Cd during transport. Copyright © 2010 John Wiley & Sons, Ltd.     

Effect of water table drawdown on peatland dissolved organic carbon export and dynamics

Peatlands play an important role in the global carbon cycle, and loss of dissolved organic carbon (DOC) has been shown to be important for peatland carbon budgets. The objective of this study was to determine how net production and export of DOC from a northern peatland may be affected by disturbance such as drainage and climate change. The study was conducted at a poor fen containing several pool–ridge complexes: (1) control site–no water table manipulation; (2) experimental site–monitored for one season in a natural state and then subjected to a water table drawdown for 3 years; (3) drained site–subjected to a water table drawdown 9 years prior to monitoring. The DOC concentration was measured in pore water along a microtopographic gradient at each site (hummock, lawn and hollow), in standing water in pools, and in discharge from the experimental and drained sites. The initial water table drawdown released ～3 g of carbon per square metre in the form of DOC, providing a large pulse of DOC to downstream ecosystems. This value, however, represents only 1–9% of ecosystem respiration at this site. Seasonal losses of DOC following drainage were 8–11 g of carbon per square metre, representing ～17% of the total carbon exchange at the experimental study site. Immediately following water table drawdown, DOC concentrations were elevated in pore water and open water pools. In subsequent seasons, DOC concentration in the pool declined, but remained higher than the control site even 11 years after water‐table drawdown. This suggests continued elevated net DOC production under lower water table conditions likely related to an increase in vegetation biomass and larger water table fluctuations at the experimental and drained sites. However, the increase in concentration was limited to initially wet microforms (lawns and hollows) reflecting differences in vegetation community changes, water table and soil subsidence along the microtopographic gradient. Copyright © 2008 John Wiley & Sons, Ltd and Her Majesty the Queen in right of Canada.     

The estuarine chemistry and isotope systematics of U in the Amazon and Fly Rivers

Natural concentrations of ²³⁸U and δ²³⁴U values were determined in estuarine surface waters and pore waters of the Amazon and Fly (Papua New Guinea) Rivers to investigate U transport phenomena across river-dominated land–sea margins. Discharge from large, tropical rivers is a major source of dissolved and solid materials transported to the oceans, and are important in defining not only oceanic mass budgets, but also terrestrial weathering rates.On the Amazon shelf, salinity-property plots of dissolved organic carbon, pH and total suspended matter revealed two vastly contrasting water masses that were energetically mixed. In this mixing zone, the distribution of uranium was highly non-conservative and exhibited extensive removal from the water column. Uranium removal was most pronounced within a salinity range of 0–16.6, and likely the result of scavenging and flocculation reactions with inorganic (i.e., Fe/Mn oxides) and organic colloids/particles. Removal of uranium may also be closely coupled to exchange and resuspension processes at the sediment/water interface. An inner-shelf pore water profile indicated the following diagenetic processes: extensive (1 m) zones of Fe(III)—and, to a lesser degree, Mn(IV)—reduction in the absence of significant S(II) concentrations appeared to facilitate the formation of various authigenic minerals (e.g., siderite, rhodocrosite and uraninite). The pore water dissolved ²³⁸U profile co-varied closely with Mn(II). Isotopic variations as evidenced in δ²³⁴U pore waters values from this site revealed information on the origin and history of particulate uranium. Only after a depth of about 1 m did the δ²³⁴U value approach unity (secular equilibrium), denoting a residual lattice bound uranium complex that is likely an upper-drainage basin weathering product. This suggests that the enriched δ²³⁴U values represent a riverine surface complexation product that is actively involved in Mn–Fe diagenetic cycles and surface complexation reactions.In the Fly River estuary, ²³⁸U appears to exhibit a reasonably conservative distribution as a function of salinity. The absence of observed U removal does not necessarily imply non-reactivity, but instead may record an integration of concurrent U removal and release processes. There is not a linear correlation between δ²³⁴U vs. 1/²³⁸U that would imply simple two component mixing. It is likely that resuspension of bottom sediments, prolonged residence times in the lower reaches of the Fly River, and energetic particle–colloid interactions contribute to the observed estuarine U distribution. The supply of uranium discharged from humid, tropical river systems to the sea appears to be foremost influenced by particle/water interactions that are ultimately governed by the particular physiographic and hydrologic characteristics of an estuary.     

Quartz-Helium Method to Estimate Fluid Flow in Thick Aquitards,Gunnedah Basin,Australia

The hydraulic integrity of aquitards is generally assumed and relies on a few core-scale permeability measurements, drill-stem tests, or textbook values. This approach is because hydraulic data across the full aquitard thickness is generally lacking. Proper assessment of aquitard integrity should be studied at the formation (spanning its entire thickness at a single point) or regional (formation properties at multiple locations throughout the basin) scale. One formation-scale approach uses environmental tracers and advection-dispersion modeling to constrain fluid flow rates. This study demonstrates the use of helium concentrations in quartz as a method of constraining the rate of fluid flow in a 520-m thick aquitard in the Gunnedah Basin, NSW, Australia. Quartz was separated from existing core samples in the Watermark and Porcupine Formations at depths from 750 to 1200 m. The helium was released from these samples by heating and select samples were impregnated with helium to determine the rate of helium diffusion through the quartz. One-dimensional advection-dispersion modeling of the helium profile accounting for diffusive helium exchange between quartz and pore water revealed, that (1) vertical fluid velocity has been on the order of 0.02 mm/year or less for tens to thousands of years, (2) helium is in equilibrium between quartz and pore water, and (3) the helium profile is transient indicating that helium concentrations in the underlying Maules Creek Formation has varied over geological time. Further modeling identified aquitard conditions (thickness and temperature) for which equilibrium exists, a precondition for deriving formation-scale permeability.     

Dissolved Organic Carbon in Seepage Water – Production and Transformation during Soil Passage

Dissolved organic carbon (DOC) in seepage water can combine with organic pollutants, with Al and heavy metal ions and transport them through the soil profile with a potential to contaminate groundwater. We studied the production of DOC in aerobic decomposition experiments at 8 °C and moisture close to field capacity in soils from two sites with different microbial activities (spodic dystric Cambisols with moder (SLB) and mor‐moder (SLS) layers) using ¹³C‐depleted plants of differing decomposability (Epilobium angustifolium and Calamagrostis epigeios). Additionally, we investigated the DOC transformation during soil passage in decomposition experiments and in the field for the sites SLB and SLS. For SLS, decomposition of Epilobium resulted in a cumulative CO₂ production of 14% of the added C within 128 days. Priming effects were negligible. CO₂ production for the experiments using Calamagrostis was less with 11% for SLB and 10% for SLS. Cumulative DOC production was markedly high in the Epilobium decomposition experiment, being 25 g m^–2, out of which 11 g m^–2 were Epilobium‐derived (2% of the added C). For the Calamagrostis experiments, cumulative productions of DOC and Calamagrostis‐derived DOC (0.1% of the added C for SLS and SLB) were much less. During the soil passage, much of the DOC was removed by sorption or decomposition processes. Field studies at SLS and SLB using ¹³C natural abundance showed that ¹³C distribution of soil organic matter increased with depth, probably mainly due to a discrimination of C isotopes by decomposing microorganisms. DOC, however, showed a depletion of ¹³C from –28γ PDB to –29γ (SLB at 40 cm) or –28 to –30γ (SLS at 20 cm) with depth, owing to preferential decomposition of ¹³C‐enriched substances or preferential adsorption. This study indicates that DOC production is strongly affected by litter composition and that significant changes in DOC composition may occur during its passage through a soil depth of 40 cm.     

Three-Dimensional Numerical Investigation of Pore Water Pressure and Deformation of Pumped Aquifer Systems

Excessive groundwater withdrawal has caused severe land subsidence worldwide. The pore water pressure and the deformation of pumped hydrostratigraphic units are complex. A fully coupled three-dimensional numerical simulation was carried out for different pumping plans in this paper. When groundwater is pumped from a confined aquifer, the great compaction occurs in the pumped aquifer and its upper and lower adjacent aquitard units. Land subsidence is smaller and the area affected by land subsidence is greater when groundwater is pumped from the deeper confined aquifer. The pore water pressure in the pumped confined aquifer changes immediately with pumpage. In the adjacent aquitard units, however, the pore water pressure increases in the early pumping time and decreases in the early recharging time. The decrease in the pore water pressure vertically spreads from the interface between aquitard and pumped aquifer to the other surface of the aquitard. The pumped aquifer compacts and rebounds immediately with pumping and non-pumping or recharging actions, while the compaction and rebounding of the aquitard units clearly lag behind. The compaction of the adjacent aquitard unit first occurs near the interface between aquitard and pumped aquifer units, and the compaction zone spreads outward as the pumping goes on. The aquitards may expand vertically within some zones. Due to the inelastic deformation of soil skeleton, different pumping plans result in different land subsidence. For the same net pumpage, maximal land subsidence and horizontal displacement are the smallest for constant discharge and the greatest for recharge-discharge cycle.     

Organically Bound Nutrients in Dissolved Organic Matter Fractions in Seepage and Pore Water of Weakly Developed Forest Soils

Previous field and laboratory studies showed that organically bound nutrients can contribute largely to the export of N, P, and S from soil into aquatic systems. One possible determinant for the losses of dissolved organic nutrients leaving the soil environment could be their distribution between dissolved organic matter (DOM) fractions of different mobility in soil. To elucidate the potential influence of DOM fractions under varying flow conditions on the vertical translocation of organically bound nutrients, we determined the concentrations and fluxes of dissolved organic C (DOC) and nutrients (DON, DOP, DOS) in soil water under a Scots pine (Pinus sylvestris L.) and a European beech (Fagus sylvatica L.) forest. We sampled seepage water from the organic forest floor layer and the mineral subsoil using zero‐tension lysimeters and soil pore water using tension lysimeters and suction cups. DOM in soil water was fractionated into hydrophilic and hydrophobic compounds by XAD‐8 at pH 2. We found that the organic forest floor layers were large sources for DOC, DON, DOP, and DOS. The dissolved organic nutrients were mainly concentrated in the hydrophilic DOM fraction which proved to be more mobile in mineral soil pore water than the hydrophobic one. Consequently, the concentrations and fluxes of dissolved organic nutrients decreased less with depth than those of DOC. Concentrations as well as fluxes in subsoil pore water of DOC and dissolved organic nutrients in the studied weakly developed soils were high as compared with literature data on deeply developed forest soils. Under conditions of rapid water flow through the strongly structured mineral soil at the beech site, almost no retention of DOM took place and thus the influence of the distribution of organically bound nutrients between the DOM fractions on the export of DON, DOP, and DOS was negligible.     

长江中下游湖泊群落水平下沉水植物碳、氮、磷化学计量特征及其影响因素

以长江中下游14个湖泊沉水植物为研究对象,分析群落水平下沉水植物碳(C)、氮(N)、磷(P)的化学计量特征及其影响因素.结果显示,沉水植物群落C含量平均为386.93±25.80 mg/g,范围为315.98~441.97 mg/g,N和P含量的平均值分别为26.10±4.84和2.64±0.99 mg/g,范围分别为13.75~40.89和1.01~5.92 mg/g.与物种水平研究相比,群落水平下沉水植物C、N、P化学计量特征变异系数较小,内稳定性更强.群落C含量与P含量具有显著相关性,而与N含量不相关,这说明C元素与N和P之间的耦合关系并不一致;N∶P比与P含量之间具有极显著的负相关关系,但与N含量不相关,说明沉水植物群落P含量的变异对N∶P比起主导作用.冗余分析表明,环境因子解释了沉水植物群落化学计量特征总变异的30.2%,在P0.01水平下对沉水植物群落化学计量特征具有显著影响的环境因子为底泥总磷、底泥N∶P比、水深和消光系数.变差分解结果表明,底泥和上覆水分别独自解释了化学计量特征总变异的5.21%和10.19%,其交互作用解释了总变异的5.25%.通过该研究结果推测,在恢复湖泊水生植被的实践过程中,相对于底泥,对上覆水光照条件进行控制可能更加迫切.     

Lake metabolism scales with lake morphometry and catchment conditions

We used a comparative data set for 25 lakes in Denmark sampled during summer to explore the influence of lake morphometry, catchment conditions, light availability and nutrient input on lake metabolism. We found that (1) gross primary production (GPP) and community respiration (R) decline with lake area, water depth and drainage ratio, and increase with algal biomass (Chl), dissolved organic carbon (DOC) and total phosphorus (TP); (2) all lakes, especially small with less incident light, and forest lakes with high DOC, have negative net ecosystem production (NEP < 0); (3) daily variability of GPP decreases with lake area and water depth as a consequence of lower input of nutrients and organic matter per unit water volume; (4) the influence of benthic processes on free water metabolic measures declines with increasing lake size; and (5) with increasing lake size, lake metabolism decreases significantly per unit water volume, while depth integrated areal rates remain more constant due to a combination of increased light and nutrient limitation. Overall, these meta-parameters have as many significant but usually weaker relationships to whole-lake and benthic metabolism as have TP, Chl and DOC that are directly linked to photosynthesis and respiration. Combining water depth and Chl to predict GPP, and water depth and DOC to predict R, lead to stronger multiple regression models accounting for 57–63% of the variability of metabolism among the 25 lakes. It is therefore important to consider differences in lake morphometry and catchment conditions when comparing metabolic responses of lakes to human impacts.     

Fracture control of ground water flow and water chemistry in a rock aquitard

There are few studies on the hydrogeology of sedimentary rock aquitards although they are important controls in regional ground water flow systems. We formulate and test a three-dimensional (3D) conceptual model of ground water flow and hydrochemistry in a fractured sedimentary rock aquitard to show that flow dynamics within the aquitard are more complex than previously believed. Similar conceptual models, based on regional observations and recently emerging principles of mechanical stratigraphy in heterogeneous sedimentary rocks, have previously been applied only to aquifers, but we show that they are potentially applicable to aquitards. The major elements of this conceptual model, which is based on detailed information from two sites in the Maquoketa Formation in southeastern Wisconsin, include orders of magnitude contrast between hydraulic diffusivity (K/S(s)) of fractured zones and relatively intact aquitard rock matrix, laterally extensive bedding-plane fracture zones extending over distances of over 10 km, very low vertical hydraulic conductivity of thick shale-rich intervals of the aquitard, and a vertical hydraulic head profile controlled by a lateral boundary at the aquitard subcrop, where numerous surface water bodies dominate the shallow aquifer system. Results from a 3D numerical flow model based on this conceptual model are consistent with field observations, which did not fit the typical conceptual model of strictly vertical flow through an aquitard. The 3D flow through an aquitard has implications for predicting ground water flow and for planning and protecting water supplies.     

Inferring Heterogeneity in Aquitards Using High-Resolution δD and δ18O Profiles

Vertical depth profiles of pore water isotopes (δD and δ¹⁸O) in clay-rich aquitards have been used to show that solute transport is dominated by molecular diffusion, to define the timing of geologic events, and to estimate vertical hydraulic conductivity. The interpretation of the isotopic profiles in these studies was based on pore water samples collected from piezometers installed in nests (typically 4 to 15 piezometers) over depths of 10 to 80 m. Data from piezometer nests generally have poor vertical resolution (meters), raising questions about their capacity to reveal the impact of finer scale heterogeneities such as permeable sand bodies or fractured till zones on solute transport. Here, we used high-resolution (30-cm) depth profiles of δD and δ¹⁸O from two continuously cored boreholes in a till aquitard to provide new insights into the effects of sand bodies on solute transport. High-resolution core-derived profiles indicate that such heterogeneities can cause major deviations from one-dimensional diffusion profiles. Further, comparison of piezometer-measured values with best-fit diffusion trends shows subtle deviations, suggesting the presence of heterogeneities that should not be ignored. High-resolution profiles also more clearly defined the contact between the highly fractured oxidized zone and the underlying unoxidized zone than the piezometers.     

Hydrograph separation to improve understanding of Dissolved Organic Carbon Dynamics in Headwater catchments

Dissolved organic carbon (DOC) is a key component of the global carbon cycle, but, to date, large uncertainties still exist on its source and fate in first‐order streams. In a 23 ha rangeland and steep‐slope headwater of South Africa, our aim was to quantify the contribution of overland flow (OF), soil water (SW) and ground water (GW) to DOC fluxes (DOC_F), and to interpret the results in terms of DOC sources and fate. The average 2010–2011 DOC concentration (DOC_C) at the catchment outlet was 4.7 mg C l^?1 with a standard error of ±2.5 mg C l^?1, which was significantly lower than in SW (15.2 ± 1.6 mg C l^?1) and OF (11.9 ± 0.8 mg C l^?1), but higher than in GW (2.3 ± 0.6 mg C l^?1). Based on end‐member mixing using Si and Na concentration in the water compartments, the average SW contribution to DOC_F was 66.4%, followed by OF (30.0%) and GW (3.6%). The resulting estimated DOC_F at the catchment outlet was 8.05 g C m² y^?1. This was much higher than the observed value of 2.80 g C m² y^?1, meaning that 5.25 g C m² y^?1 or 65% of the DOC is lost during its downslope and/or downstream transport to the catchment outlet. Complementary investigations revealed that the DOC_C in SW dropped from 15.2 ± 1.6 to 2.6 ± 0.3 mg C l^?1 during its downslope transport to the river system, which corresponded to a net loss of 5.10 g C m² y^?1, or 97% of the catchment DOC losses. These results on DOC sources and potential fate in headwaters are expected to improve our understanding of the impact of hydrology on the global C‐cycle. Copyright © 2013 John Wiley & Sons, Ltd.     

Application of Ultrafiltration for Characterization of the DOC of Elbe River Water

An ultrafiltration methodology and the results of its application on Elbe river water are presented. Compared with other methods, Ultrafiltration allows fractionation of the molecular-weight fractions of DOC for higher volumes of solution in a shorter time. To characterize the molecular-weight fractions, the sum parameter DOC (β(DOC)) and the absorption coefficient at 254 nm a₂₅₄ were measured, together with determination of a₂₅₄/ β(DOC) for further characterization of the DOC fractions and to provide information about changes in parts of the UV-active substances of the total dissolved organic material. In the period May 1992 to November 1994, the DOC molecular-weight composition of 65 samples of Elbe river water were determined. At two sampling locations (Torgau-East and Meissen), the DOC content β(DOC) was approximately 6 mg/L. The high-molecular weight fraction (> 10000 g/mol) gave a mean of 13% of the total DOC content β₀(DOC). The measurements showed that the molecular composition of DOC in the Elbe does not greatly differ. There was also no clear seasonal influence on the molecular-weight composition of the DOC content. During the period of investigation, the percentage part of β(DOC) and a₂₅₄/β(DOC) of the high-molecular weight fraction of the total dissolved organic material increased, while the a₂₅₄/β(DOC) values of the middle molecular-weight fraction remained fairly constant. The dependence of β(DOC) on discharge of the Elbe river is low. Changes in molecularweight composition of DOC were only observed during the steepest increase in river discharge during a flood event, with another spectrum of substances responsible for the increase in β(DOC) when compared with the β(DOC) for low or middle water level.     

Dissolved Carbohydrate Concentration,Composition, and Bioavailability to Microbial Heterotrophs in Stream Water

Dissolved total carbohydrates (DTCH), dissolved free monosaccharides (DFMS), dissolved organic carbon (DOC), biodegradable DOC (BDOC), and humic substances (HS) were measured in White Clay Creek (WCC), a stream in southeastern Pennsylvania Piedmont, USA. Samples were collected over different seasons and under baseflow and stormflow conditions. DOC concentrations ranged from 1.0 to 12.8 mg/L C with the highest concentrations associated with stormflows. Carbohydrates ranged from 0.42 to 12.4 μM and accounted for 2.9 to 12.7% of the DOC. Humic substances represented the major DOC fraction, accounting for 55 to 72% of the DOC pool under all flow conditions. The humic fraction had a lower carbohydrate content (4.4%) than the non-humic fraction of DOC (7.2%). Stormflow DOC was enriched in carbohydrates relative to baseflow DOC, but the percentage of humic-C changed little. Carbohydrates were primarily present as dissolved polysaccharides (55%), but a significant fraction was bound to humic substances (40%), while a small proportion was present as monosaccharides (5%). The major monosaccharides in stream water, listed in order of decreasing concentration, included glucose, galactose, rhamnose, xylose, arabinose, mannose, and fucose. On average (30.6 ± 7.4)% (n = 44) of the stream water DOC was biodegradable, and carbohydrates accounted for 9.9 to 17.7% of the BDOC.     

Sorption behavior of U(VI), ~(234)U(VI) and ~(238)U(VI) onto fracture-filling clays in Beishan granite, Gansu: Application to selecting the site of high-level radwaste repository in China

Knowing the transport of uranium and radionu-clides through the environment is important for as-sessing the risk posed by long-term disposal of rad-waste. Granitic rocks have been selected as a host-rock type for the first high-level radwaste repository in China. According to the Chinese High-level Rad-waste Management Program, high-level radwaste (HLW) will be buried at 800―1000 m depth in a granitic pluton in Northwest China and, specifically, in the A granitic complex of Beishan area,…     

ANDRA underground research laboratory: interpretation of the mineralogical and geochemical data acquired in the Callovian–Oxfordian formation by investigative drilling

Under the ANDRA Meuse/Haute Marne underground research laboratory scientific programme, two boreholes (EST204 and EST205) were drilled to a depth of 510 m for the purposes of scientific characterisation. Twenty-nine core samples were taken in borehole EST205 every 3 m between 422 and 504 m depth. Physical property measurements (water content, porosity, density, specific surface), geochemical analyses (major and trace elements, cation exchange capacity [CEC] and surface cation occupancy, leaching anions, redox state, organic matter concentration), and a semi-quantitative mineralogical study were conducted on the samples.As the rocks are in a reduced state, the core samples were stored under nitrogen immediately after drilling. All the steps of the sampling and of the characterisation are done with a research of limitation of the oxidation to obtain representative samples of the in situ conditions.The top of the formation is more carbonate-rich, with interbedded clayey layers and carbonate rock. The formation is more homogeneous in its central section with a clay mineral concentration of 45–50%, which corresponds to a maximum of flooding within the area. In the upper part of this section, micas and mixed-layer illite/smectite R0 dominate, whereas in the lower part of the section we find an abrupt transition to mixed-layer illite/smectite R1 associated with kaolinite.A statistical analysis, including the data of major and trace elements with the semi-quantitative mineralogy, enabled the identification of some mineralogical traps for trace elements. The values of cation occupancy at the surface of the clay minerals provided a good image of the pore water chemistry; pore water is in equilibrium with the clay surfaces. Leaching experiments revealed the pore water salinity and provided profiles of Cl and Br concentrations. Cl/Br values in the centre of the formation are close to the present-day seawater ratio, which could indicate a seawater origin of the pore water. Some measurements of total reduced capacity, provide quantified results of the reduced state of the rock.Processing the data on water content, helium and petroleum pycnometry enabled calculation of total rock porosity and gave an uncertainty range for this value. Finally, the high BET(N₂) specific surfaces are consistent with the clayey nature of the rock.     

Maintenance of estuarine water quality by mangroves occurs during flood periods: A case study of a subtropical mangrove wetland

Seasonal changes in water quality were measured in samples taken at various distances from shallow water across mudflat to mangroves during flood period and from mangroves across mudflat to shallow water during ebb period in a subtropical mangrove estuary (Zhangjiang Estuary, Fujian, China). The TN (total dissolved nitrogen), TP (total dissolved phosphorus), COD (chemical oxygen demand), and DOC (dissolved organic carbon) contents during the flood period were significantly higher than those during the ebb period. In contrast, the opposite was true for the POC (particulate organic carbon) content and transparency. The mangroves at Zhangjiang Estuary may trap nutrients at rates of 90.5 g N/m²/yr, 2.2 g TP/m²/yr, and 13.7 g C/m²/yr in the form of DOC, and export POC at a rate of 81.8 g/m²/yr. Our results support the hypothesis that the maintenance of estuarine water quality by mangroves occurs during flood periods.