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1.
Tracing groundwater flow and sources of organic carbon in sandstone aquifers using fluorescence properties of dissolved organic matter (DOM) 总被引：7，自引：0，他引：7
The fluorescence properties of groundwaters from sites in two UK aquifers, the Penrith Sandstone of Cumbria and the Sherwood Sandstone of South Yorkshire, were investigated using excitation–emission matrix (EEM) fluorescence spectroscopy. Both aquifers are regionally important sources of public supply water and are locally impacted by pollution. The Penrith Sandstone site is in a rural setting while the Sherwood Sandstone site is in suburban Doncaster. Fluorescence analysis of samples from discrete sample depths in the Penrith Sandstone shows decreasing fulvic-like intensities with depth and also shows a good correlation with CFC-12, an anthropogenic groundwater tracer. Tryptophan-like fluorescence centres in the depth profile may also provide evidence of rapid routing of relatively recent applications of organic slurry along fractures. Fluorescence analysis of groundwater sampled from multi-level piezometers installed within the Sherwood Sandstone aquifer also shows regions of tryptophan-like and relatively higher fulvic-like signatures. The fluorescence intensity profile in the piezometers shows tryptophan-like peaks at depths in excess of 50 m and mirrors the pattern exhibited by microbial species and CFCs highlighting the deep and rapid penetration of modern recharge due to rapid fracture flow. Fluorescence analysis has allowed the rapid assessment of different types and relative abundances of dissolved organic matter (DOM), and the fingerprinting of different sources of organic C within the groundwater system. The tryptophan:fulvic ratios found in the Penrith Sandstone were found to be between 0.5 and 3.0 and are characteristic of ratios from sheep waste sources. The Sherwood Sandstone has the lowest ratios (0.2–0.4) indicating a different source of DOM, most likely a mixture of terrestrial and microbial sources, although there is little evidence of pollution from leaking urban sewage systems. Results from these two studies suggest that intrinsic fluorescence may be used as a proxy for, or complementary tool to, other groundwater investigation methods in helping provide a conceptual model of groundwater flow and identifying different sources of DOM within the groundwater system. 相似文献
2.
The presence of methane (CH4) in groundwater is usually only noticed when it rises to high concentrations; to date rather little is known about its production or natural ‘baseline’ conditions. Evidence from a range of non-polluted groundwater environments in England, including water supply aquifers, aquicludes and thermal waters, reveals that CH4 is almost always detectable, even in aerobic conditions. Measurements of potable waters from Cretaceous, Jurassic and Triassic carbonate and sandstone aquifers reveal CH4 concentrations of up to 500 μg/l, but a mean value of < 10 μg/l. However, aquiclude and thermal waters from the Carboniferous and Triassic typically contain in excess of 1500 μg/l. Such high concentrations have so far only been found at redox (Eh) potentials below 0 mV, but in general CH4 concentration and Eh value are poorly correlated. This suggests a lack of thermodynamic equilibrium, which is confirmed by comparing pe values calculated from the redox couple C(4)/C(− 4) with those derived from Eh. Genesis of CH4 appears to occur on two timescales: a rapid if low rate of production from labile carbon in anaerobic microsites in the soil, and a much longer, millennium scale of production from more refractory carbon. Methane is rarely measured in groundwater; there is no single ionic determinand which acts universally as a proxy, but a combination of high HCO3 and low SO4 concentrations, or the reverse, is an indication that high amounts of CH4 may be present. 相似文献
3.
M.E. Stuart L. Maurice T.H.E. Heaton M. Sapiano M. Micallef Sultana D.C. Gooddy P.J. Chilton 《Applied Geochemistry》2010
The Maltese islands are composed of two limestone aquifers, the Upper and Lower Coralline Limestone separated by an aquitard, the ‘Blue Clay’. The Lower Coralline Limestone is overlain in part by the poorly permeable Globigerina Limestone. The upper perched aquifers are discontinuous and have very limited saturated thickness and a short water level response time to rainfall. Frequent detections of coliforms suggest a rapid route to groundwater. However, the unsaturated zone has a considerable thickness in places and the primary porosity of the Upper Coralline Limestone is high, so there is likely to be older recharge by slow matrix flow as well as rapid recharge from fractures. Measurement of SF6 from a pumping station in a deep part of one of the perched aquifers indicated a mean saturated zone age of about 15 a. The Main Sea Level aquifers (MSL) on both Malta and Gozo have a large unsaturated thickness as water levels are close to sea level. On Malta, parts of the aquifer are capped by the perched aquifers and more extensively by the Globigerina Limestone. The limited detection of coliform bacteria suggests only some rapid recharge from the surface via fractures or karst features. Transmissivity is low and 3H and CFC/SF6 data indicate that saturated zone travel times are in the range 15–40 a. On Gozo the aquifer is similar but is more-extensively capped by impermeable Blue Clay. CFC data show the saturated zone travel time is from 25 a to possibly more than 60 a. Groundwater age is clearly related to the extent of low-permeability cover. The δ13C signature of groundwater is related to the geochemical processes which occur along the flowpath and is consistent with residence time ages in the sequence; perched aquifers < Malta MSL < Gozo MSL. The 18O and 2H enriched isotopic signature of post 1983 desalinated water can be seen in more-modern groundwater, particularly the urbanized areas of the perched and Malta MSL aquifers. In all aquifers, movement of solutes from the surface travelling slowly through the matrix provide a long-term source of groundwater contaminants such as NO3. 相似文献
4.
The Swanscombe area of Kent, SE England represents a typical example of a heavily quarried Chalk area currently undergoing re-development. Because the Chalk is also an important aquifer, a good understanding of groundwater movement is required if environmental impacts are to be minimised and the water resource maximised. In particular, the nature of the relationship between the River Darent and groundwater in the Swanscombe Chalk Block requires better characterisation. Here, ‘environmental tracers’ in the form of ambient concentrations of stable isotopes, chlorofluorocarbons (CFCs), sulphur hexafluoride (SF6) and tritium (3H) are used to investigate this and other aspects of groundwater movement in the vicinity of the quarries. Stable isotopic contrasts indicate little evidence for widespread river infiltration to the regional Chalk aquifer, although stable isotope and 3H data suggest that 20–35% of the abstraction by river-valley public water supply boreholes may be derived from the river. The CFCs, while present at above-modern concentrations in almost all groundwaters, can be used as tracers, indicating basically S–N flowpaths in the area south of the quarries, though sub-karstic conduits associated with areas of Palaeogene cover add a level of uncertainty at the local scale. Simple piston flow residence times based on SF6 range from 1 to 17 a, but the data are probably better interpreted in terms of mixing between varying amounts of modern recharge derived from the south and deeper stored groundwater. The information gained from environmental tracers can therefore contribute to effective resource management. 相似文献
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6.
Knowledge of groundwater residence time is important in understanding key issues in the evolution of water quality, whether this occurs due to water–rock interaction or simply by mixing or contamination. The build-up in the atmosphere of the trace gases chlorofluorocarbons (CFCs) and sulphur hexafluoride (SF6) from the middle of the last century offers a convenient way of dating waters up to ∼60 a old. The gases are well-mixed in the atmosphere so their input functions are not area-specific as is the case with 3H. While any one of these trace gases can in principle provide a groundwater age, when two or more are measured on water samples the potential exists to distinguish between different modes of flow including piston flow, exponential flow and simple end-member mixing. As with all groundwater dating methods, caveats apply. Factors such as recharge temperature and elevation must be reasonably well-constrained. Primarily for SF6, the phenomenon of ‘excess air’ also requires consideration. Primarily for the CFCs, local sources of contamination need to be considered, as do redox conditions. For both SF6 and the CFCs, the nature and thickness of the unsaturated zone need to be factored into residence time calculations. However, as an inexpensive dating method, the trace gases can be applied to a wide range of groundwater problems where traditional age indicators might once have been used more sparingly. Examples include tracing flowlines, detecting small modern inputs in ‘old’ waters, and pollution risk assessment. In the future, with the main CFCs already declining in the atmosphere, new anthropogenic trace gases are likely to take their place. 相似文献
7.
Long‐term Holocene groundwater fluctuations in a chalk catchment: evidence from Rock‐Eval pyrolysis of riparian peats 
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下载免费PDF全文 Andrew J. Newell Christopher H. Vane James P.R. Sorensen Vicky Moss‐Hayes Daren C. Gooddy 《水文研究》2016,30(24):4556-4567
The depositional history of peat‐dominated wetlands can be used to understand palaeoclimate and palaeohydrology and also constrain the impacts of future climate change. However, in chalkland valleys, seasonal water table fluctuations and a high alkalinity have diminished key environment indicators such as pollen, and there is a need for alternative investigative techniques. The method of Rock‐Eval pyrolysis can track changes in organic matter source and degradation, potentially relating to historic changes in vegetation cover. This is the first Rock‐Eval on cores from a groundwater‐dependent riparian chalk valley wetland combined with radiocarbon dating. The dating showed that the cores represented approximately 4000 years of depositional history. Changes in hydrocarbon chemistry including normal alkane composition of the peat indicated shifts of around 500 to 1000 years between terrestrial and more aquatic species, relating to periods of climate wetness. These climatic shifts are broadly consistent with other evidence from ombrotrophic peatland and lacustrine sediments across northwest Europe. However, the connection between climate wetness and groundwater dependent chalkland wetlands is complicated by external anthropogenically driven factors relating to land use and vegetation cover changes in the catchment. Nonetheless, this study suggests that Rock‐Eval pyrolysis is a useful and cost‐effective tool that can provide evidence for long‐term Holocene groundwater fluctuations. Copyright © 2016 British Geological Survey. 相似文献
8.
The behavior of the herbicides isoproturon (IPU) and chlortoluron (CTU) in ground water and shallow unsaturated zone sediments were evaluated at a site situated on the Chalk in southern England. Concentrations of IPU in ground water samples varied from < 0.05 to 0.23 microgram/L over a five-year period of monitoring, and were found to correlate with application of the pesticide. Concentrations of pesticides in ground water samples collected during periods of rising water table were significantly higher than pumped samples and suggest that rapidly infiltrating recharge water contains higher herbicide concentrations than the native ground water. Significant variations in herbicide concentrations were observed over a three-month period in ground water samples collected by an automated system, with concentrations of IPU ranging from 0.1 to 0.5 microgram/L, and concentrations of a recent application of CTU ranging from 0.2 to 0.8 microgram/L. Different extraction methods were used to assess pore water concentrations of herbicides in the unsaturated zone, and samples were analyzed by standard HPLC analysis and immunoassay (ELISA) methods. These data indicated highly variable concentrations of herbicide ranging from 4 to 200 g/ha for HPLC and 0.01 to 0.04 g/ha for ELISA, but indicate a general pattern of decreasing concentrations with depth. The results of this study indicate that transport of IPU and CTU through the unsaturated zone to shallow ground water occurs and that this transport increases immediately following herbicide application. Measured concentrations of herbicides are generally lower than specified by the European Union Drinking Water Directive, but are observed to spike above this limit. These results imply that, while delivery of pesticides to ground water can occur as a result of normal agricultural practices, the impact on potable supplies is likely to be negligible due to the potential for degradation during the relatively long travel time through the unsaturated zone and high degree of dilution that occurs within the aquifer. As a result of the wide variation in concentrations detected by different techniques, it is suggested that for future site investigations more than one sampling strategy be employed to characterize the occurrence of pesticide residues and elucidate the transport mechanisms. 相似文献
9.
David J. Allen W. George Darling Daren C. Gooddy Daniel J. Lapworth Andrew J. Newell Ann T. Williams Debbie Allen Corinna Abesser 《Hydrogeology Journal》2010,18(5):1125-1141
Understanding the processes controlling groundwater/surface-water interaction is essential for effective resource management and for protecting sensitive ecosystems. Through intensive monitoring of Chalk groundwater, shallow gravel groundwater and surface water in the River Lambourn, UK, using a combination of hydrochemical and hydrophysical techniques, a complex pattern of interactions has been elucidated. The river is broadly in hydraulic contact with the streambed sediments and adjacent gravels and sands, but these deposits are mainly hydraulically separate from the underlying Chalk at the site. The hydraulic relationship between the river and underlying alluvium is variable, involving components of groundwater flow both parallel and transverse to the river and with both effluent and influent behaviour seen. While the gravel aquifer is significant in controlling groundwater/surface-water interaction, its importance as a route for flow down the catchment is likely to be modest compared with river discharge. The hydrological complexity revealed in a geological setting typical of lowland UK Chalk streams has implications both for investigation methods and for management such as in the setting of environmental objectives in the European Water Framework Directive. 相似文献
10.
Prediction of the arrival of peak nitrate concentrations at the water table at the regional scale in Great Britain 总被引：1，自引：0，他引：1
L. Wang M. E. Stuart J. P. Bloomfield A. S. Butcher D. C. Gooddy A. A. McKenzie M. A. Lewis A. T. Williams 《水文研究》2012,26(2):226-239
A simple process‐based approach to predict regional‐scale loading of nitrate at the water table was implemented in a GIS for Great Britain. This links a nitrate input function, unsaturated zone thickness, and lithologically dependent rate of nitrate unsaturated zone travel to estimate arrival time of nitrate at the water table. The nitrate input function is the loading at the base of the soil and has been validated using unsaturated zone porewater profiles. The unsaturated zone thickness uses groundwater levels based on regional‐scale observations infilled by interpolated river base levels. Estimates of the rate of unsaturated zone travel are attributed from regional‐scale hydrogeological mapping. The results indicate that peak nitrate loading may have already arrived at the water table for many aquifers, but that it has not where the unsaturated zone is relatively thick There are contrasting outcomes for the two main aquifers which have similar unsaturated zone velocities, the predominantly low relief Permo‐Triassic sandstones, and the Chalk, which forms significant topographic features. For about 60% of the Chalk, the peak input has not yet reached the water table and will continue to arrive over the next 60 years. The methodology is readily transferable and provides a robust method for estimating peak arrival time for any diffuse conservative pollutant where an input function can be defined at a regional scale and requires only depth to groundwater and a hydrogeological classification. The methodology is extendable in that if additional information is available this can easily be incorporated into the model scheme. British Geology Survey © NERC 2011. Hydrological Process © 2011 John Wiley & Sons, Ltd 相似文献