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Data collected during the quarterly soil bongs will be compiled with previous data The <br /> drilling will continue until enough data has been obtained to provide evidence for site <br /> closure <br /> The soil bonngs will be drilled to a minimum depth of 40 feet Samples will be collected at <br /> five-foot intervals from each boring All samples will be field screened using a PID. Selected <br /> samples will then be transported to a state-certified laboratory and analyzed for total <br /> petroleum hydrocarbons (TPH as gasoline) and volatile aromatics (BTE&X) in accordance <br /> with EPA methods 8015 and 8020, respectively <br /> Soil samples will also be collected and analyzed by a microbiologist for bacterial species and <br /> Inumbers No specific plate tests have been designed for the bacteria used in the inoculum <br /> Generally, bacteria must be pathogenic to have a specific test for identification, the <br /> development of bacterial identification systems is economically driven At the present time <br /> Ithere is no "economic" need to identify non-pathogens, therefore, no specific "packaged" <br /> identification systems are available <br /> IThe following identification process will be used dung the bioremediation project <br /> I1) A microbiologist will receive and perform all bacteriological assessments <br /> 2) The sample will be plated on suitable media for isolation <br /> 3) Species and strain identification will be made by using gram stain, colonial <br /> and cellular morphology, proper biochemical reactions (species dependant) <br /> and proper differential media (species dependant) The expertise of a <br /> bacteriologist will be employed <br /> I4) Bacterial numbers and different strains will be reported <br /> 5) Species present in individual samples is considered to be proprietary and <br /> confidential information is not reported <br /> It must be noted that bacterial species should not be compared to species of higher forms <br /> of life Bacteria do not sexually reproduce, bacterial species identification are based upon <br /> differential media and biochemical tests, not reproductive isolation <br /> Each bacterial species can have many different strains, these strains will differ from other <br /> strains within the same species with respect to biochemical test, reactions to differential <br /> media and metabolic activity For example, not all strains of pathogenic bacteria are <br /> pathogenic, often some can be avirulent <br /> There is much variability in bacterial species identification One example is S aureus, it is <br /> named for the golden color it exhibits However, not all S aureus are golden in color It is, <br /> Oeo1.V-1 A-61 8e.vrra I.. p <br /> i33/GM'6a-hrAt91 8 <br />