Geological setting and site description

were detected and attributed to the disseminated metallic content of the waste. In the past 5 years, much research has been carried out in relation to the spectral IP method and the identification of organic pollutants. This Ž . follows the work published by Olhoeft 1985 where the author discusses how different inter- facial processes such as the oxidation–reduction process and the clay–organic interactions may be differentiated on the basis of the observed phase spectra. Most of the work published re- cently relates to spectral IP laboratory studies ŽVanhala et al., 1992; Boerner et al., 1993; . Vanhala and Soininen, 1995 where the authors use clay or sandstone samples to examine the effect of different contaminants on the complex conductivity. Field applications are reported by Ž . Ž . Boerner et al. 1996 and Vanhala 1997 where the authors discuss the application of the spec- Ž . tral IP method in a detecting organic pollu- tants in soils with both low and high clay Ž . particle content, and b in estimating the hy- draulic conductivity of the aquifer. Following the above examples in the litera- ture, our research concentrated on the applica- tion of both the DC resistivity and IP methods in areas where groundwater contamination prob- lems existed and were associated with landfill waste. As the geology of the study area con- sisted of sand and clay layers, it was felt that the IP method could be a suitable method in our investigations. In addition, we were interested in investigating whether the organic contamination detected in the area through high concentrations Ž . of chemical oxygen demand COD and total Ž . organic carbon TOC would show any effect on the IP response. Ž . The specific objectives of our study were a the characterisation of the landfill waste in terms Ž . of both resistivity and chargeability, b the Ž . determination of the base of the landfill, c the geophysical identification of contamination in the underlying geological strata due to leachate Ž . movement, d the geophysical identification of clay layers in areas where these are shown to Ž . exist from other sources e.g., from boreholes ; the identification of these layers is important as clay layers act as natural barriers to the down- ward movement of leachate. In addition to the above objectives, we attempted to estimate aquifer properties such as porosity and hy- draulic conductivity by combining existing mea- surements of fluid electrical conductivity with the geophysical inversion results.

2. Geological setting and site description

Our area of investigation lies in East Anglia, UK, where the geological setting consists of alternating layers of clay and sand of variable thickness. The sediments within the depth of interest are of Quaternary marine and glacial origin, overlying the London clay, which occurs at approximately 70 m depth. At greater depths, the London clay is believed to overlie a Chalk formation. Past geological studies show that the aquifer system consists of a sequence of three Ž . sand aquifers top, middle, and bottom , with intervening semi-pervious clay aquitards Ž . Richardson, 1996 . A map of the area together with the boreholes of interest and the up-gradi- ent geophysical control line is shown in Fig. 1. The plan view of the landfill with its lagoons and trenches can also be seen in this figure. The detailed individual borehole logs are shown in Fig. 2. From these, it is observed that the thick- ness of both the top and middle aquifers is variable throughout our study area. From the log of borehole MP32, the first sand aquifer lies at a depth between 7 and ; 16.4 m, while the first semi-pervious silty sandrclay aquitard ap- pears between 16.4 and ; 18.0 m. For borehole MP14r15r16r17, the first aquitard appears at ; 20 m depth with the top aquifer lying be- tween 5.5 and 20 m. For borehole MP43, there seems to be no aquitard in the first ; 29 m and Ž top and middle aquifers Corton and Cromerian . sands appear as one unit. In all cases, there is a Ž . thick top layer overburden of boulder clay whose thickness also varies from location to Ž . location, ranging between 5.5 borehole MP 32 Ž . and 11.0 m borehole MP 37 . There are no logs for boreholes MP4r5 and MP 6r7. A schematic of a vertical cross-section along the central part of the landfill, from south to north, is given in Fig. 3. The site forms a small hill with its highest region approximately 7 m Ž above surrounding ground level ; 25 m above . ordnance datum, OD and with a flat region at the top approximately 150 m long. The water level is approximately ; 23.5 m below the top Ž flat region of the landfill equivalent to ; 1.5 m . above OD . The natural clay base of the landfill in the northern part of the site is ; 14 m from Ž . the top ; 11 m above OD while the base of the excavated trenches and lagoons in the south- Ž ern site was ; 17 m from the top ; 8 m above Fig. 4. The main geophysical lines in relation to the landfill. . OD . The landfill was set in operation in the 1950s after the closure of a clay pit used for brick making. Initially, the waste deposited was of domestic nature and it was placed in the south-western part of the present site. However, in the early 1970s, the deposition of liquid waste began lasting up to 1989 when the opera- tion of the site was terminated. The site re- ceived both oily and non-oily waste with two of its lagoons, B1r2 and B3 in Fig. 1, receiving the liquid waste. These lagoons had a natural Ž . clay base, while lagoon A also Fig. 1 and the existing trenches had no clay base at all, but were excavated straight into the underlying sand layer. From the limited information available on the type of waste deposited, it appears that 65–80 of the waste was agrochemical with solvents, ammonia, and heavy metals being de- posited in small but consistent quantities. There was also regular disposal of mercury and cop- per, as well as of a number of volatile organic carbons and phenolic compounds. As indicated in the vertical cross-section in Fig. 3, the liquid waste was disposed in the southern part of the site. However, 2 years before the closure of the site, a co-disposal operation was set-up with solid waste being deposited in both the southern and northern parts of the site. An inclined natural clay base Ž was left in the northern part ; 11 m above . OD so that any accumulation of leachate would naturally drain into the lagoons in the southern part. The main reason for introducing solid waste to the site was to effect a reduction of a hy- draulic mound that developed underneath the landfill, due to the deposition of the liquid waste. This hydraulic mound affected the local groundwater flow movement and resulted in its reversal. Hydrogeological studies carried out since the closure of the site in 1989 indicate the elimination of this hydraulic mound and the local groundwater flow direction following the Ž . regional one Bartlett and Dottridge, 1996 . A substantial amount of water quality infor- mation data exists from the boreholes dis- tributed around the site with clear indications of contamination of both the top and middle aquifers in the eastern part of the site. Water samples have been taken on a quarterly basis for a number of years by the landfill operators and have been analysed for both organic contamina- Ž . tion parameters COD, TOC and inorganic pa- Ž rameters chlorides, sulphates, ammoniacal ni- Ž .. trogen NH –N as well as heavy metals and 3 Table 2 Summary of geophysical surveys Survey Date System used Parameter Survey line measured characteristics L1, L2 and L3 August 1997 ABEM SAS300B Apparent Dipole–dipole array with a s 5 m; Ž . manually operated resistivity length of line L1 s 140 m; only length of line L2 s 140 m; length of line L3 s 110 m W1 March 1998 ABEM SAS4000 Apparent Wenner array Ž . fully automated system resistivity smallest electrode separation s 4.0 m; only total length of line s 320.0 m A, B and C May 1998 HUNTEC Transmitter Apparent Dipole–dipole array with a s 15.0 m; SCINTREX IPR12 resistivity and length of line A s 240 m; receiver chargeability length of line B s 150.0 m; length of line C s 210.0 m Soundings S1 May 1998 HUNTEC Transmitter Apparent Schlumberger array and S2 SCINTREX IPR12 resistivity and total length of sounding s 150.0 m receiver chargeability electrical conductivity. The borehole log infor- mation together with the water level and fluid conductivity measurements at these locations are used in the interpretation of the geophysical results. An example of the concentration values of the most important parameters measured at the different monitoring points in August 1997 is given in Table 1a. As can be seen high concentrations of chlorides, sulphates, NH –N 3 and sodium ions as well as of COD and TOC are recorded at boreholes MP32, MP43 and MP44 being indicative of contamination in both the top and middle aquifers. Similar contamina- tion levels are observed in April 1998 as shown Table 3 Geophysical lines with water levels at the associated boreholes Note: Water level measured relative to ground level. Survey Geophysical Borehole Water Geological unit where date line monitoring level monitoring point is Ž . Ž . point MP m placed in Ž . August 1997 L1 32 30 18.2 Corton sands Ž . 1st aquifer Ž . August 1997 L1 32 50 18.2 Cromerian sands Ž . 2nd aquifer August 1997 L2 14 17.5 Cromerian sands Ž . 2nd aquifer August 1997 L2 15 17.5 Crag sands Ž . 3rd aquifer August 1997 L2 16 17.5 Shelly sands August 1997 L2 17 17.5 Corton sands Ž . 1st aquifer August 1997 L3 26 11.3 Crag sands Ž . 3rd aquifer August 1997 L3 27 11.3 Cromerian sands Ž . 2nd aquifer May 1998 A 4 18.2 Cromerian Ž . 2nd aquifer May 1998 A 5 18.2 Crag Ž . 3rd aquifer March 1998 W1 6 18.3 Corton sands Ž . 1st aquifer March 1998 W1 7 18.3 Crag clay March 1998, W1 and A 43 18.4 Corton sands and May 1998 Cromerian till Ž . 1st and 2nd aquifers March 1998, W1 and A 44 18.4 Cromerian sands Ž . May 1998 2nd aquifer March 1998, W1 and A 45 18.4 Crag sands Ž . May 1998 3rd aquifer Ž . May 1998 C 37 30 19.2 Corton sands Ž . 1st aquifer Ž . May 1998 C 37 50 19.2 Cromerian sands Ž . 2nd aquifer May 1998 Sounding 32 18.2 Corton and Cromerian sands Ž . S1 1st and 2nd aquifer May 1998 Sounding 43 and 44 18.4 Corton and Cromerian sands Ž . S2 1st and 2nd aquifers in Table 1b, with the exception of MP32. This, according to site operators, is most likely due to high dilution effects in an unreliable borehole. Borehole MP44 also shows a considerable con- trast between the two surveys dates.

3. Geophysical data acquisition

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