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o <br /> On December 19, 1991, 80 liters of Treatek's microbial inoculant were applied to the sod The <br /> inoculant contained Arthrobacter species microorganisms with a culture population of 1 x 1013 <br /> cells/ml The inoculant was applied at a dilution rate of approximately 30 liters per 150 gallons of <br /> water utilizing a high pressure spray applicator Once applied, the soil bed was tilled to provide <br /> for complete mixing of the inocula Water was applied to the bed to provide a uniform moisture <br /> content of not less than 10% and the bed was recovered with plastic <br /> ' In conjunction with the application of the inocula, various sod samples were collected from the <br /> treatment bed's soils for lar head space screening The jar head space screening consisted of the <br /> collection of approximately one-half full stainless steel tubes of soils from the locations shown on <br /> ' Figure 4 and capping the tubes with aluminum foil The tubes were then allowed to sit for <br /> approximately 5 minutes after which an organic vapor analyzer's (OVA) (Foxborough Model 108A) <br /> detector tube was inserted through the aluminum foil to measure the volatile organic compound <br /> ' concentrations in the vacant portion of the tube Table 1 is a listing of the OVA readings collected <br /> from the locations shown on Figure 4 <br /> On December 23, 1991, the first of the bi-weekly treatment bed tilling operations was conducted <br /> Onsite tilling log sheets were maintained by TreaTek personnel and these log sheets are included <br /> in Appendix B Upon completion of the tilling, jar head space reading were again collected from <br /> the approximate locations shown on Figure 4 These readings, along with other lar head space <br /> ' readings collected periodically during the course of the remedial program, are shown on Table 2 <br /> Once the site activities were completed, the bed was recovered <br /> ' The bed was tilled on a bi-weekly basis for a six week period which ended with the last tilling <br /> conducted on January 28, 1992 Due to the seasonal rains, the bed was not uncoverd and several <br /> tilling periods were not completed in order to maintain a constant moisture level of the bed <br /> Four weeks into the projected six week remedial program (January 16, 1990), two preliminary <br /> confirmation composite soil samples were collected from four locations in each half of the bed The <br /> results from these two samples indicated that no Benzene, Toluene, Xylene or Ethylbenzene <br /> ' (BTX&E) compounds were present and that only the bed's north half composite sample exhibited <br /> detectable concentrations of TPH-G (18 mg/kg) The analytical data report for these two soil <br /> samples is enclosed as Appendix C This confirmation sampling was conducted to provide TreaTek <br /> with an indication as to the on-going effectiveness of the remedial process <br /> Based on these preliminary results, it was decided to conduct the confirmation soil sampling, as <br /> discussed in the remedial work plan, on January 30, 1992 which ended the six week projected <br /> ' remedial program duration <br /> The confirmation sod sampling consisted of the collection of one composite sod sample from each <br /> ' 50 cuyds of soil in the treatment bed The treatment bed was visually divided into twelve separate <br /> segments as shown on Figure 5 From each segment, a composite sample was collected from four <br /> distinct locations <br /> ' Each composite sample was collected by filling a stainless steel sample collection tube (2'x 60) one <br /> quarter full from soils at a depth of at least 16 inches beneath the bed surface from each of the four <br /> composite collection locations within the sample collection segment of the treatment bed Between <br /> each sample collection location, aluminum foil was placed over the tube ends to prevent compound <br /> volatilization Once the tube was filled, both ends were capped with aluminum foil and plastic end <br /> caps and secured with elastic tape The tubes were them labeled and placed in Ziplocke plastic <br /> bags and stored on ice for shipment to the analytical laboratory <br /> 6 <br />