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The mountain beaver (Aplodontia rufa) is a fossorialrodent species endemic to the Pacific Northwest and portions of California. This herbivore inflicts millions of dollars of damage annually to forest seedling plantations. Currently, extensive trapping prior to planting is the most reliable method for reducing damage. With increasing restrictions placed on trapping, forest resource managers need alternative tools to minimize forest damage. This study assessed the potential of four toxicants registered for underground use to controlmountain beaver; zinc phosphide, diphacinone, chlorophacinone, and strychnine. Zinc phosphide and strychnine are acute toxicants, whereas diphacinone and chlorophacinone are anticoagulants. Anticoagulants prevent the recycling of vitamin K in the body, which inhibits the production of clotting factors. Efficacy varied among treatments. Zinc phosphide and strychnine were avoided by mountain beaver. Pre-baiting marginally increased acceptance of strychnine, but did not alter mountain beaver acceptance of zinc phosphide. Diphacinone and chlorophacinone were both readily consumed, but only chlorophacinone was 100% effective after a 14-day baiting regime. Subsequently, we tested the effects of diet on the efficacy of diphacinone by varying the availability of food containing vitamin K, the anticoagulant antidote. Restricting access to potential sources of vitamin K appeared to increase efficacy. We conclude that anticoagulants hold some promise as additional tools for managers to reduce mountain beaver populations with chlorophacinone showing the most promise. However, limitations to anticoagulant baits include the necessity of long-term baiting (greater than 10 days), a possible decrease in toxicity if baits contact moisture, and potential primary hazards.