Geology topics

John J. Johnston

Publications and source records attributed to John J. Johnston.

5 recordsLinked to original sources

USGS2012

Assessment of toxicity and potential risk of the anticoagulant rodenticide diphacinone using Eastern screech-owls (Megascops asio)

In the United States, new regulatory restrictions have been placed on the use of some second-generation anticoagulant rodenticides. This action may be offset by expanded use of first-generation compounds (e.g., diphacinone; DPN). Single-day acute oral exposure of adult Eastern screech-owls (Megascops asio) to DPN evoked overt signs of intoxication, coagulopathy, histopathological lesions (e.g., hemorrhage, hepatocellular vacuolation), and/ or lethality at doses as low as 130 mg/kg body weight, although there was no dose-response relation. However, this single-day exposure protocol does not mimic the multiple-day field exposures required to cause mortality in rodent pest species and non-target birds and mammals. In 7-day feeding trials, similar toxic effects were observed in owls fed diets containing 2.15, 9.55 or 22.6 ppm DPN, but at a small fraction (<5%) of the acute oral dose. In the dietary trial, the average lowest-observed-adverse-effect-level for prolonged clotting time was 1.68 mg DPN/kg owl/week (0.24 mg/kg owl/day; 0.049 mg/owl/day) and the lowest lethal dose was 5.75 mg DPN/kg owl/week (0.82 mg/kg owl/day). In this feeding trial, DPN concentration in liver ranged from 0.473 to 2.21 μg/g wet weight, and was directly related to the daily and cumulative dose consumed by each owl. A probabilistic risk assessment indicated that daily exposure to as little as 3-5 g of liver from DPN-poisoned rodents for 7 days could result in prolonged clotting time in the endangered Hawaiian shorteared owl (Asio flammeus sandwichensis) and Hawaiian hawk (Buteo solitarius), and daily exposure to greater quantities (9-13 g of liver) could result in low-level mortality. These findings can assist natural resource managers in weighing the costs and benefits of anticoagulant rodenticide use in pest control and eradication programs.

Ecotoxicology↗

USGS2011

Acute toxicity, histopathology, and coagulopathy in American kestrels (Falco sparverius) following administration of the rodenticie diphacinone

The acute oral toxicity of the anticoagulant rodenticide diphacinone was found to be over 20 times greater in American kestrels (Falco sparverius; median lethal dose 96.8 mg/kg body weight) compared with Northern bobwhite (Colinus virginianus) and mallards (Anas platyrhynchos). Modest evidence of internal bleeding was observed at necropsy, although histological examination of heart, liver, kidney, lung, intestine, and skeletal muscle revealed hemorrhage over a wide range of doses (35.1-675 mg/kg). Residue analysis suggests that the half-life of diphacinone in the liver of kestrels that survived was relatively short, with the majority of the dose cleared within 7 d of exposure. Several precise and sensitive clotting assays (prothrombin time, Russell's viper venom time, thrombin clotting time) were adapted for use in this species, and oral administration of diphacinone at 50 mg/kg increased prothrombin time and Russell?s viper venom time at 48 and 96 h postdose compared with controls. Prolongation of in vitro clotting time reflects impaired coagulation complex activity, and generally corresponded with the onset of overt signs of toxicity and lethality. In view of the toxicity and risk evaluation data derived from American kestrels, the involvement of diphacinone in some raptor mortality events, and the paucity of threshold effects data following short-term dietary exposure for birds of prey, additional feeding trials with captive raptors are warranted to characterize more fully the risk of secondary poisoning.

Environmental Toxicology and Chemistry↗

USGS2010

Acute toxicity of diphacinone in Northern bobwhite: Effects on survival and blood clotting

The anticoagulant rodenticide diphacinone was slightly toxic (acute oral LD 50 2014 mg/kg) to Northern bobwhite ( Colinus virginianus ) in a 14-day acute toxicity trial. Precise and sensitive assays of blood clotting (prothrombin time, Russell’s Viper venom time, and thrombin clotting time) were adapted for use in quail, and this combination of assays is recommended to measure the effects of anticoagulant rodenticides. A single oral sublethal dose of diphacinone (434 mg/kg body weight) prolonged clotting time at 48 h post-dose compared to controls. At 783 mg/kg (approximate LD 02 ), clotting time was prolonged at both 24 and 48 h post-dose. Prolongation of in vitro clotting time reflects impaired coagulation complex activity, and was detected before overt signs of toxicity were apparent at the greatest dosages (2868 and 3666 mg/kg) in the acute toxicity trial. These clotting time assays and toxicity data will assist in the development of a pharmacodynamic model to predict toxicity, and also facilitate rodenticide hazard and risk assessments in avian species.

Ecotoxicology and Environmental Safety↗

USGS2010

Comparative toxicity of diphacinone to northern bobwhite (Colinus virginianus) and American kestrels (Falco sparverius)

The acute oral toxicity of the anticoagulant rodenticide diphacinone was found to be about 20 times greater to American kestrels (LD 50 =97 mg/kg) than to northern bobwhite (LD 50 =2,014 mg/kg). Several precise and sensitive clotting assays (prothrombin time, Russell's Viper venom time, thrombin clotting time) were adapted for use in these species, and this combination of assays is recommended to detect effects of diphacinone and other rodenticides on coagulation. Oral administration of diphacinone over a range of doses (sublethal to the extrapolated LD 15 ) prolonged prothrombin time and Russell's Viper venom time within 24 to 48 hrs post-exposure. Prolongation of in vitro clotting time reflects impaired coagulation complex activity and was detected before or at the onset of overt signs of toxicity and lethality. These data will assist in the development of a pharmacodynamic model to assess and predict rodenticide toxicity to non-target avian species.

Proceedings of the 24th Vertebrate Pest Conference↗

USGS2003

Nontarget bird exposure to DRC-1339 during fall in North Dakota and spring in South Dakota

Blackbirds frequently use ripening sunflower ( Heltantbus annuus ) as a food source in the northern Great Plains. In 1999 and 2000, the avicide DRC-1339 (3-chloro-4-methylaniline hydrochloride) was used experimentally on fall-ripening sunflower fields in North Dakota so researchers could evaluate its effectiveness for reducing crop depredations by blackbirds. DRC-1339 was applied to rice and broadcast on the ground in a confined area within ripening sunflower fields. One objective of this study was to determine whether nontarget birds, birds other than blackbirds, were eating rice and were exposed to the DRC-1339. In 1999, 8 of 11 (73%) sparrows collected by shotgun in sunflower fields treated with DRe-1339 had rice in their gastrointestinal (GI) tracts. In 2000, 5 mourning doves ( Zenaida macroura ) and 3 sparrows were collected by shotgun in sunflower fields treated with DRC-1339. Three doves had rice in their GI tracts, 4 doves and all 3 sparrows had measurable DRC1339 concentrations in their GI tracts, and 3 mourning doves and 1 savannah sparrow ( Passerculus sanduncbensis ) exhibited histopathological signs of kidney damage. In April 2002, untreated rice was applied to corn stubble plots in South Dakota to determine which bird species ate rice. In 2002, 3 of 3 song sparrows ( Melospiza melodia ) collected by shotgun had rice in their GI tracts. Our results demonstrate that the use of DRC-1339 to control blackbirds in the northern Great Plains will likely expose nontarget birds to the DRC-1339 bait.

North Dakota, South Dakota↗