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INTRODUCTION <br /> Title 22, Article 3, Section 66261.24 (6) of the California Cade of Regulations (CCR) establishes <br /> the criteria for the identification of hazardous and extremely hazardous waste. The Department of Health <br /> Services (DOHS) compiles and evaluates analytical data for compliance with the toxicity criteria for <br /> potentially hazardous waste. <br /> l <br /> 'These analytical data have been derived from water and environmental samples submitted to <br /> laboratories certified by the DOHS for analysis. The California DOHS 96-Hour Acute Aquatic Toxicity <br /> testing assures CCR compliance and minimizes risk to the environment orthreat to public health. <br /> Laboratory certification by the DOHS standardized the toxicity testing program by requiring <br /> certification of testing laboratories and by utilizing the procedures set forth by Dr. James Polisini, <br /> Department of Fish and Game, Water Pollution Control Laboratory (Polisini 1988). Following this <br /> methodology, a waste can be evaluated for potential hazardous waste declassification. <br /> Currently; CCR, Title 22, Section 66261.24, Article 6 requires wastes to pass the 96-hour aquatic <br /> toxicity screen testing with greater than 50% survival at the 500 mg/I concentration. In addition to this <br /> regulation, the DOHS protocol requires wastes to pass the 96-hour aquatic toxicity screen testing with <br /> greater than 50% survival at the 500 mg/t concentration and a minimum of 60%survival at the 750 mg/l <br /> concentration for compliance. When these screening criteria are not achieved, the DOHS test protocol <br /> requires additional definitive serial dilution toxicity testing with a minimum of five test concentrations <br /> prior to making a hazardous waste compliance determination, <br /> Toxicity testing conducted by MBC for this report is a static non-renewal acute toxicity screen <br /> test following Standard Methods and the procedures of Dr. James Polisini. Death is the effect measured <br /> and toxicity is reported as percent survivorship at 250 mgA, 500 mg/I and 750 mg/I concentrations and a <br /> LCw calculated from these data. Original data worksheets will remain on file at MBC. <br /> MATERIALS AND METHODS <br /> Facilities <br /> The toxicity tests are conducted in a laboratory located away from disturbances of non-laboratory <br /> personnel or other laboratory or heavy equipment. The laboratory, measuring approximately 20 x 20 ft, is <br /> Insulated to protect it from rapid temperature changes. Shelves and water tables are provided which <br /> allow a capacity of 200 or more 5-gallon aquaria, as well as bench space for laboratory equipment and <br /> instruments. <br /> Lighting is provided by five evenly spaced two lamp 4-foot cool white fluorescent fixtures that are <br /> regulated by a 24-hour timer. The lighting remains on for 16 hours and is off for 8 hours. <br /> The temperature of the toxicity testing laboratory is maintained by a commercial climate <br /> controlled unit controlled by wall-mounted thermostat which provide accuracy to±2 0C. <br /> A Rustrak Madel 2066 continuous recording thermograph monitored the laboratory's temperature <br /> 24 hours per day. The Rustrak is calibrated annually by the manufacturer to insure accuracy. Maximum- <br /> minimum thermometers are maintained within the laboratory to provide "back-up"temperature variation <br />