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Debunking Human Health Risk, APPENDIX D - LBAMspray.com

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LIGHT BROWN APPLE MOTH ERADICATION PROJECT<br />

<strong>APPENDIX</strong> D<br />

DRAFT PEIR<br />

HUMAN HEALTH RISK ASSESSMENT<br />

Isomate ® -LBAM Plus (Isomate) as the three proposed pheromone formulations of primary<br />

interest for the eradication Program, as well as two microcapsule formulations CheckMate ®<br />

LBAM-F (CheckMate) and Scentry Biologicals, Inc.’s (SBI’s) NoMate ® LBAM MEC (NoMate)<br />

that are not currently proposed for use in the Program), (2) proposed use of Bacillus<br />

thuringiensis kurstaki (Btk) for ground treatment, (3) proposed use of another bacterial<br />

insecticide, spinosad, for ground treatment and (4) proposed use of permethrin with a pheromone<br />

in male attractant treatments for ground application. In addition, evaluation of the No Program<br />

Alternative examines the increased use of several of the chemicals currently registered for use by<br />

the USEPA and the California Department of Pesticide Regulation (DPR) for control or<br />

prevention of LBAM including, but not limited to, chlorpyrifos, permethrin, lambda-cyhalothrin,<br />

spinosad, and Btk.<br />

Table D1-1<br />

Condensed Summary of LBAM Eradication Alternatives Evaluated in the EIR<br />

Alternative Application Method Chemical (s)<br />

No Program<br />

As per label directions<br />

Chlorpyrifos, Permethrin, Lambda-cyhalothrin, Spinosad,<br />

Btk<br />

Mating Disruption - 1 Twist Ties Isomate (LBAM pheromones)<br />

Mating Disruption - 2 Ground Applications HERCON, SPLAT (LBAM pheromones)<br />

Mating Disruption - 3 Aerial Release HERCON, SPLAT (LBAM pheromones)<br />

Male Moth Attractant (Alternative MMA)<br />

Ground Application<br />

SPLAT (LBAM pheromones), Permethrin (inert<br />

ingredients: ethylbenzene; 1,2,4-trimethylbenzene)<br />

Organic Treatment (Alternative Bt) Ground Treatments Bacillus thuringiensis kurstaki<br />

Organic Treatment (Alternative S, spinosad) Ground Treatments Spinosad<br />

Inundative Parasite Wasp Release (Alternative Bio-P)<br />

Sterile Insect Technique (Alternative SIT)<br />

None–not considered further in this <strong>Risk</strong> Assessment<br />

None–not considered further in this <strong>Risk</strong> Assessment<br />

This Appendix D to the PEIR follows standard HHRA protocols (National Research Council<br />

[NRC] 1983, 1994; California’s Office of Environmental <strong>Health</strong> Hazard Assessment [OEHHA]<br />

2003) and addresses the four key elements of risk assessment — hazard identification,<br />

identification of chemicals of potential concern; exposure assessment; dose-response assessment;<br />

and risk characterization. This screening level assessment examines only potential toxicological<br />

impacts to hypothetical human receptor populations from the use of the chemical formulations<br />

proposed for use to eradicate LBAM. Other impact analyses are provided in the other appendices<br />

of this report, consistent with CEQA Guidelines. Findings in this Appendix D are integrated into<br />

the PEIR, in Section 8 <strong>Human</strong> <strong>Health</strong> and in other appropriate sections.<br />

This screening level risk assessment uses default parameters and assumptions to assess potential<br />

health effects of exposure to chemicals proposed for use and other chemicals previously used or<br />

available for use under No Program. No site-specific or other data attributable to actual human<br />

populations are used. The likelihood of adverse health effects resulting from programmatic<br />

activities was estimated by calculating chemical-specific intakes to each of four hypothetical<br />

receptor populations. These intakes were calculated from the estimated exposure point<br />

concentrations (EPCs) of each of the different chemicals for each <strong>com</strong>plete exposure pathway.<br />

Estimated intakes were then <strong>com</strong>pared against toxicity criteria obtained from the literature or<br />

derived in this assessment if sufficient toxicity data were available. These <strong>com</strong>parisons were<br />

used to evaluate whether any of the chemicals may pose potential hazards or risks to the receptor<br />

populations.<br />

D1-2 App D_HHRA_508.doc JULY 2009

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