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HYDC03  12/5/05  5:37 PM  Page 104






                 104    Chapter Three


                 c   = c    − c                     eq. 3.24  c   = f  · c    + (1 − f  )c      eq. 3.25
                 i,react  i,sample  i,mix                     Na,mix  saline  Na,saline  saline Na,fresh
                                                                                          −
                 As an example calculation, the data shown in   Now, using the mixed and saline Cl concentration
                 Table 3.8 are for samples 0, 14 and 19 of Fig. 3.19   values (samples 14 and 19) to indicate the fraction of
                 representing fresh, mixed and saline groundwaters  the saline water ( f  = 114/1100), and assuming a
                                                                            saline
                                                                                 −
                 present in the Lincolnshire Limestone aquifer. To cal-  freshwater end-member Cl concentration value equal
                                 +
                 culate how much Na has been added to the mixed  to zero, then substituting the values from Table 3.8
                 groundwater sample by cation exchange, equation  into equation 3.25:
                 3.23 can be re-written as:

                  Cation exchange in the Lower Mersey Basin Permo-Triassic sandstone         BO X
                  aquifer, England                                                           3.7


                  The Lower Mersey Basin Permo-Triassic sandstone aquifer of north-
                  west England demonstrates the effect of very long-term natural
                  flushing of a saline aquifer. The aquifer comprises two main units:
                  the Permian Collyhurst Sandstone Formation and the Triassic
                  Sherwood Sandstone Formation that dip southwards at about 5°
                  and are up to 500 m thick. To the south, the aquifer unit is overlain
                  by the Triassic Mercia Mudstone Group, a formation which contains
                  evaporites. Underlying the aquifer is a Permian sequence, the upper
                  formations of which are of low permeability that rest uncon-
                  formably on Carboniferous mudstones. The sequence is extensively
                  faulted with throws frequently in excess of 100 m. Overlying the
                  older formations are highly heterogeneous, vertically variable
                  Quaternary deposits dominated by glacial till. Pumping of the
                  aquifer system has caused a decline in water levels such that much
                  of the sandstone aquifer is no longer confined by the till.
                    Typical compositions of the sandstones are quartz 60–70%,
                  feldspar 3–6%, lithic clasts 8%, calcite 0–10% and clays (including
                  smectite) <15%. Haematite imparts a red colour to most of the
                  sequence. The sandstones contain thin mudstone beds often less
                  than 10 cm in thickness. Cation exchange capacities are of the
                                 −1
                  order of 1 meq (100 g) . Underlying the fresh groundwaters pre-
                                                    −
                  sent in the area are saline groundwaters attaining a Cl concentra-
                               −1
                  tion of up to 100 g L , which appear to be derived from dissolution
                  of evaporites in the overlying Mercia Mudstone Group (Tellam
                  1995). This saline water is present within 50 m of ground level
                  immediately up-flow of the Warburton Fault Block and along the
                  Mersey Valley but the freshwater–saline water interface is found
                  deeper both to the north and south (Tellam et al. 1986).
                    A hydrochemical survey of around 180 boreholes across the
                  Lower Mersey Basin was conducted in the period 1979–1980. The
                  results were presented by Tellam (1994) and five water types were
                                                      −1
                  identified (Table 1, Fig. 1). Salinities ranged from 100 mg L up to
                  brackish water concentrations. Ion proportions varied widely, with
                  Ca-HCO , Ca-SO and Na-HCO being dominant water types in var-
                                     3
                       3
                            4
                  ious locations. The large storativity of the aquifer means that the
                  groundwater chemistry does not substantially change seasonally.
                  The spatial distribution of water types is shown in Fig. 2. In general,
                  the hydrochemical distribution of water types correlates with the
                  broad pattern of groundwater flow in the aquifer. Type 1 water is  Fig. 1 The central area of a Piper diagram showing the
                  found in areas of recent groundwater recharge, in contrast to older  distribution of hydrochemical water types in the Lower Mersey
                  fresh groundwaters (Types 4 and 5) and saline groundwater   Basin Permo-Triassic sandstone aquifer. After Tellam (1994).
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