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We conducted research to develop a safe and effective toxic bait to control the small Indian mongoose (Urva auropunctata), an invasive vertebrate predator impacting the survival of native species in Hawai'i and in other parts of the world. A preserved fish-based bait product was found to be highly palatable to mongooses in cage trials and subsequent formulations with diphacinone (0.005%) showed promise as an efficacious toxic bait for mongooses. This product is intended for future use to control mongooses in conservation and urban areas, and as a biosecurity tool at ports of entry to address accidental introductions into mongoose-free areas. Anticipated delivery of this toxic bait is in tamper-proof bait stations. We designed three prototype bait stations constructed with polyvinyl chloride (PVC) drainage pipes and evaluated their performance in enclosure trials with wild-caught mongooses and in field trials with free-ranging mongooses. A commercially available tamper-resistant rodenticide bait station was also used for comparison to the prototypes in our trials. The goal was to develop a bait station that is readily used by mongooses, allows for bait consumption in place, prevents removal of bait, and restricts access to nontarget animals. We used a non-toxic formulation of the fish-based bait product and monitored bait station use, visitation rates, bait uptake, and spillage. All four bait station types were used by mongooses in the laboratory, and one PVC bait station design and the commercial bait station exhibited multiple mongoose visitations with minimal bait spillage in the field. We did not record any significant nontarget species interactions with the bait during the field trials. The PVC bait station design and commercial bait station are approved methods of bait delivery in the subsequent field efficacy trials under an Experimental Use Permit for the upcoming registration of "Fish-based Bait for Mongooses" with the Environmental Protection Agency. [ABSTRACT FROM AUTHOR]

A specific and sensitive liquid chromatography-tandem mass spectrometry method was developed and validated for the determination of the anticoagulant rodenticide diphacinone (DPN) in mouse and rat liver. Tissue samples were extracted with a mixture of water and acetonitrile containing ammonium hydroxide. The extracted sample was cleaned up with a combination of liquid-liquid partitioning and dispersive solid phase extraction. Chromatographic separation was achieved using a Waters X-Bridge BEH C-18 LC column (50 mm, 2.1 mm ID, 2.5 μm particle size) with detection on a triple quadrupole mass spectrometer in multiple reaction monitoring (MRM) mode. The monitored transition for DPN was m/z 339.0 → 167.0 for quantitation and 339.0 → 172.0 and 339.0 → 116.0 for confirmation. The linear range was 0.5 to 375 ng/mL. The average precision of DPN, represented by the relative standard deviation of the observed concentrations, was 7.2% (range = 0.97% - 20.4%) and the average accuracy, represented by the relative error, was 5.8% (range = 1.06% - 14.7%). The recovery of DPN fortified at 3 different levels averaged 106% in rat liver and 101% in mouse liver. The established method was successfully used to determine DPN residue levels in Polynesian rats (Rattus exulans) and mice (Mus musculus) fed two different formulated baits containing DPN. The observed residue levels were consistent with values observed in other rodent studies. However, the amount of bait consumed was lower for the novel baits evaluated in this study. [ABSTRACT FROM AUTHOR]