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    Neil your Flaffing...your research is wanting to say the least...just another for you to chew on..

    Tracas and Modelling in Hydrogeology (Proceedings of the TraM '2000 Conference
    held at Liège, Belgium, May 2000). IAHS Publ. no. 262, 2000. 347
    Measurements and models of solute behaviour in
    the dual-porosity Chalk aquifer of the UK: the
    applicability of tracer tests
    SALLY WATSON, WILLIAM BURGESS, JOHN BARKER
    Groundwater Tracing Unit, Hydrogeology' Group, Department of Geological Sciences,
    University College London, Gower Street, London WC1E 6BT, UK
    e-mail: sally.watson@ucl.ac.uk
    JULIO CARNEIRO
    Universidade de Evora, Dep. Geociências, Col. Luis Verney, Apartado 94,
    7002-554 Evora Codex, Portugal
    SARA HAZELL
    Dames & Moore, Wimbledon, London SW19 4DR, UK
    Abstract Tracer tests provide direct observations of solute transport in
    groundwater, but how relevant are small-scale tests to the prediction of longterm
    behaviour of contaminants in a dual-porosity aquifer? To address this
    question for the Chalk aquifer of the UK, a catchment at Tilmanstone
    (southeast England) is being investigated; disposal of coalfield brine directly
    to the Chalk aquifer took place over many decades and a large plume of
    contamination has developed. Transport properties of the Chalk are being
    established across a range of space and time scales. Results of laboratory-scale
    diffusion experiments, single-borehole dilution tests, and borehole-to-borehole
    tracer tests in the Chalk are reviewed in the context of observations of chloride
    flux through the Eastry valley at Tilmanstone over several decades. Modelling
    of groundwater flow and chloride transport, using a dual-porosity framework,
    provides both the context and the criteria for judging the applicability of the
    field-scale tracer tests.
    INTRODUCTION
    Groundwater-mediated solute transport in fractured porous media is dominated by advection
    in fractures and diffusive exchange between fracture water and the matrix pore water (e.g.
    Barker, 1993), their relative significance depending on the scale and duration of transport.
    Limited knowledge of the complexity of aquifer properties and flow geometry severely
    restricts our ability to predict solute migration at the field scale. Tracer tests have the
    advantage of revealing aquifer transport characteristics directly, but there is a discrepancy
    between the scales and durations of practicable tracer tests and of contaminant plumes.
    To address this issue, we present observations at various scales of solute transport
    in the Chalk aquifer, the epitome of the dual-porosity aquifer. We concentrate on the
    Tilmanstone catchment in Kent, southeast England, where disposal of coalfield brine
    in open lagoons over many decades has resulted in a large plume of contamination of
    over 25 km2 in area (Fig. 1). Results of historical reviews and field investigations in
    the 1970s (Ffeadworth et al, 1980) and predictions of an early model (Bibby, 1981),
    form the basis for our current research.
    348 Sally Watson et al.
    ^ D i s c h a r g e lagoon ©Town o 4km
    y- Stream
    "150 Chloride concentration mg/l (1994)
    Fig. 1 Site location , indicating the extent of the saline plume.
    The Tilmanstone catchment
    A number of deep coalmines were active in southeast Kent from the early 1900s until
    final closure in 1986. The Tilmanstone mine is situated at the head of a valley in the
    Upper Chalk, which dips to the northeast and drains to springs in the northeast (Fig. 1).
    The hydraulic gradient along the valley is approximately 0.008.
    Brine pumped from the deep coalfield was discharged to unlined lagoons on the
    Chalk surface at the head of the valley between 1906 and 1974. Flow rates and
    chloride concentration increased from 1.4 Ml day"1 and 45 mg l"1 in 1906 to
    11.8 Ml day"1 and over 2000 mg l"1 in 1958; thereafter the flow remained approximately
    steady as the concentration increased further to 5200 mg l"1. About 190 Mm3
    of brine, close to 320 x 106 kg of chloride, entered the Chalk aquifer over a 68 year
    period. The resultant contaminant plume provides an opportunity to test the value of
    tracer tests at different scales in predicting the long term plume development.
    OBSERVATIONS OF CHLORIDE MOVEMENT IN THE CHALK
    Catchment-scale chloride transport
    The background chloride content of the Chalk aquifer is low: 30-40 mg l"1. By 1929,
    chloride had reached 200 mgl"1 immediately to the north of the mine. By 1949 the
    maximum chloride concentration in the aquifer was 900 mg l"1. By 1977, groundwater
    chloride concentration had increased to 5000 mg l"1 within 1000 m of the lagoons, and
    1000 mg l"1 at Eastry (Fig. 2). The aquifer was considered polluted over an area of
    27 Ion", the plume being 8 km long in the direction of the valley and 2 to 5 km wide.
    Headworth et al. (1980) estimated that 98 x 106 kg of chloride (30% of the total load),
    had been discharged at the springs by the early 1970s. A fairly steady concentration of
    slightly above 200 mg l"1 corresponds to an annual flux of 2-3 x 106 kg of chloride to
    the streams since then. Since 1977 the centre of the plume has moved 2 km down the
    Measurements and models of solute behaviour in the dual-porosity Chalk aquifer of the UK 349
    SW NE
    Tilmanstone
    settling lagoons
    Lower Venson ^
    Farm E a s t rV
    \1000 f..._2I>be „_,.____, ^
    ~ I 1 ™ / ; ; / -»
    d o o '• I / :
    - - i ~ f- Y
    » - —JQQ. -
    V * - : —
    Key
    Lined borehole
    Unlined borehole
    Borehole ID numbers
    Porewater chloride (mg/l)
    Fissure water chloride (mg/l)
    \ 5 0 0
    ••-,200
    Scale
    1
    500
    20
    - 10
    - 0 S
    •150
    metres
    0 250 _
    metres
    Fig. 2 Extent of contamination (1974) with pore water and fissure water profiling (after
    H e a d w o r d s a/., 1980).
    valley and the maximum chloride content (in pumped groundwater) has declined to
    1500 mgl"1 , yet the total extent of pollution, as defined by the 150 mg F1 contour
    (Fig. 1), has expanded, (Peedell, 1994; Ffazell, 1998).
    A chloride pore water profile determined in 1999 (Fig. 3) suggests that the active
    fractures are quite closely spaced, since the profile is locally smooth. The low
    CI concentration mg/l
    0 500 1000 1500

    1

    1 *
    * t

    Fig. 3 Chloride pore water profile 1999. Data collected as part of EU FRACFLOW
    project (www.fracflow.dk) by British Geological Survey.
    350 Sally Watson et al.
    concentrations between 45 and 58 m b.g.l. and below 80 m b.g.l, at which depths bulk
    permeability is low (Fig. 4), indicate that less chloride was transported into these zones.
    Permeability variation with elevation EastryBHA
    Permeability m/d
    0 20 40 60 80 100 120
    E
    TO
    Q
    -20
    S -30
    <
    E
    i X
    MX.
    f•• • i
    x A A
    A à •- *
    • 1
    A
    A K A
    A X
    •f
    °n
    ®BH3
    • BH4
    ABH5
    *BHA
    ABH8
    OBH7
    I
    Ct-Cb/Co-Cb
    0 1
    -50
    / .7
    / ,•;
    - i - . . . -'-.\
    " - \ - n.
    \\ vw
    / 4
    \ tj
    \ v
    Minutes since start
    • 45
    -165
    915
    Fig. 4 Single borehole dilution test results.
    Borehole-to-borehole tracer tests
    Natural-gradient borehole-to-borehole tracer tests are currently underway at the site.
    Such tests provide information most effectively at the intermediate scale (Ward et al.,
    1998), where the significance of diffusion depends on the distances between the
    boreholes and the characteristics of the rock. For tracer residence times of a few
    minutes, diffusion is negligible. The tracer test reveals the kinematic porosity of the
    fractures but nothing about the matrix. For tracer residence times of a few hours, there
    will be time for diffusion of a few millimetres into the matrix, which is significant in
    comparison to the fracture apertures. The test will reveal behaviour characterized by
    the fracture porosity and the area for diffusive exchange which is only significant
    during early plume development. Where channelling is important the effective
    apertures may be of the order of 1 cm and diffusion will have less effect. It is unlikely
    that borehole-to-borehole tracer tests will provide suitable information to assess
    pollutant transport over distances of kilometres and time scales of years or decades.
    Single-borehole dilution tests
    Interval dilution tracer tests can yield vertical profiles of the Darcy velocity of
    groundwater flow (e.g. Hazell, 1998). With knowledge of the local groundwater head
    Measurements and models of solute behaviour in the dual-porosity Chalk aquifer of the UK 351
    gradient these can be interpreted as profiles of hydraulic conductivity which are more
    appropriate for solute transport modelling than values from pumping tests, as they
    involve smaller volumes of aquifer. Dilution tests at six boreholes at Tilmanstone
    (Fig. 4) show that the Chalk becomes more permeable down-valley, and a marked
    reduction in hydraulic conductivity is evident at a depth of 40 m. Our results show
    considerably more detail than previous pumping tests and are consistent with
    geophysical logs, which confirm a greater degree of fracturing in the upper 40 m.
    Laboratory scale diffusion experiments
    Diffusive exchange occurs between matrix pore water and mobile groundwater in
    fractures and fissures at the sub-metre scale: the kinematic porosity, fracture and
    matrix porosities, and the diffusion coefficient of the saturated matrix are the key
    parameters (Barker et al, 2000; Fretwell et al, 2000). Diffusion coefficients for
    chloride in the Chalk of southern England, summarized in Fretwell (1999), range from
    5.2 x 10"11 to 1.3 x 10 - 9mV, but none relate specifically to Tilmanstone. Tests are
    being conducted on recently acquired core material.
    MODELLING CHLORIDE FLUX IN THE TILMANSTONE VALLEY
    A finite-element dual-porosity model, calibrated against the field observations up to
    and including the surveys of the 1970s, was developed by Bibby (1981). Transport was
    described according to a parallel plate representation, and diffusion within the matrix
    water was described by Fick's second law. The model was two-dimensional, it ignored
    density effects, and transmissivity and storativity were independent of saturated
    thickness. It was probably the first catchment-scale dual-porosity model applied to a
    groundwater contamination incident.
    The Bibby model predicted the future development of the plume, the chloride
    concentration at the Eastry borehole (Fig. 5) and of the springs, and the flux of chloride
    from the springs up to the year 2008. However, the parameters of the calibrated
    transport model were far from realistic (Carneiro, 1996), and the aquifer is
    rehabilitating at a rate considerably slower than the model predicted. The effects of the
    seasonal desaturation of fractures (Fretwell et al, 2000), accentuated by droughts, and
    1600
    1930 1940 1950 1960 1970 1980 1990 2000 2010 2020 2030 2040 2050 2060
    Year;
    [ Model prediction •» Field data |
    Fig. 5 Comparison of 1970s numerical model predictions and recent field data.
    352 Sally Watson et al.
    the three-dimensionality of the plume due to density effects, aquifer heterogeneity and
    vertical hydraulic gradients, are considered the most likely causes of discrepancy.
    A new model of chloride transport in the Eastry valley is being developed that will
    incorporate these features, and include recent pore water chloride profiles and tracer
    test results in its calibration and validation. The model will be used to assess the value
    both of the tracer tests and of the various observations of plume development, in
    making predictions.
    We anticipate a particular challenge will be to make predictions on time scales
    which are intermediate between those of tracer tests (weeks) and plume development
    (decades).
    Acknowledgements A Research grant from the Natural Environment Research
    Council (no. GST/2/1811) under the DAEC/Envirorrmental Diagnostics Programme is
    gratefully acknowledged. The matrix chloride profile illustrated in Fig. 3 resulted from
    collaboration with the British Geological Survey, working on the EU FRACFLOW
    project (www.ffacflow.dk), which is also gratefully acknowledged.

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