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Jennifer Cordova

Publications and source records attributed to Jennifer Cordova.

5 recordsLinked to original sources

Edible baits for systemic flea control, plague mitigation, and wildlife conservation: Evaluation of four active ingredients with three rodent species in western North America

The flea-borne agent of plague, Yersinia pestis , is lethal to endangered black-footed ferrets ( Mustela nigripes , BFFs) and the prairie dogs ( Cynomys spp., PDs) on which BFFs depend for habitat and prey. We developed bait pellets containing insecticides for flea control with PDs. Individual baits contained 0.46, 0.91, 1.21, or 1.52 mg fipronil, 5.40 mg afoxolaner, 50.62 mg fluralaner, or 85.20 mg spinosad. From 2023 to 2025, we tested the baits with black-tailed PDs ( C. ludovicianus , BTPDs), Gunnison's PDs ( C. gunnisoni , GPDs), and Richardson's ground squirrels ( Urocitellus richardsonii , RGSs). We sampled hosts 2810 times and detected 8825 fleas across 2 U.S. States, 1 Canadian Province, 6 sites, 9 PD colonies, and 41 sampling plots. Over ∼12 mo across 5 replicates in South Dakota, USA, bait pellets with 0.91 or 1.52 mg fipronil, applied at a rate of 125 baits/ha, were more effective in reducing the abundance of fleas on BTPDs than 0.46 mg fipronil or the 3 other active ingredients; on 2 South Dakota replicates with data from 24 mo posttreatment, the effects of fipronil pellets on flea abundance had waned after ∼24 mo. Similarly, over ∼12 mo on 2 replicates in Arizona, USA, pellets with 1.52 mg fipronil were more effective in reducing the abundance of fleas on GPDs than pellets with 0.46 mg fipronil; on 1 replicate with available data from ∼2 yr posttreatment, the effects of fipronil pellets had waned after ∼24 mo. Over ∼8-11 mo across 2 replicates in Saskatchewan, Canada, baits with 1.21 mg fipronil/pellet were more effective in suppressing the abundance of fleas on BTPDs and RGSs when applied at 250 pellets/ha than 62 pellets/ha; flea control had waned after ∼20-23 mo. When applied annually at 125-250/ha, baits with 0.84-1.52 mg fipronil (FipBits) provided an effective, efficient, and affordable tool for flea control on PD colonies.

Arizona, Saskatchewan, South Dakota

Flea control on prairie dogs (Cynomys spp.) with fipronil bait pellets: Potential plague mitigation tool for rapid field application and wildlife conservation

Sylvatic plague is a widespread, primarily flea-vectored disease in western North America. Because plague is highly lethal to endangered black-footed ferrets ( Mustela nigripes , BFFs) and the prairie dogs ( Cynomys spp., PDs) on which BFFs depend for habitat and prey, minimizing the impacts of plague is a priority at BFF reintroduction sites. We developed a new, flour-based bait pellet containing 0.84 mg of fipronil and weighing ∼1.25 g (FipBits). We measured the degree and duration of flea control on black-tailed PDs ( C. ludovicianus ) in Montana and on Gunnison's PDs ( C. gunnisoni ) in Arizona, USA from 2018–2020. FipBits were distributed on treated plots one time at a rate of 125/ha. Fleas were virtually eliminated in Montana from 1 mo posttreatment to 1 yr later and remained substantially depressed 2 yr posttreatment. With the split colony design, we probably underestimated the degree of flea control achieved with FipBits due to crossover edge effects along the arbitrary line dividing the plots. Flea control in Arizona was significant from 1 mo posttreatment to 1 yr later, but flea abundance had recovered by 2 yr posttreatment. Flea control was evaluated from 2020–2021 in South Dakota, USA on four plots treated with three concentrations of fipronil in FipBits (0.68, 0.71, and 0.83 mg/FipBit). Fleas were essentially eliminated for 10 mo on the 0.83-mg plot and were substantially reduced on the two 0.71-mg plots. Fleas were reduced on the 0.68-mg plot, but the degree of control was less than observed on other treated plots. Impacts of plague on PDs and BFFs would probably be greatly reduced by the levels of flea control observed with FipBits. Options for expanded FipBit evaluations are being pursued for what may become a highly practical, affordable, and effective plague mitigation tool.

Arizona, Montana, South Dakota

Sylvatic plague vaccine partially protects prairie dogs (Cynomys spp.) in field trials

Sylvatic plague, caused by Yersinia pestis , frequently afflicts prairie dogs ( Cynomys spp.), causing population declines and local extirpations. We tested the effectiveness of bait-delivered sylvatic plague vaccine (SPV) in prairie dog colonies on 29 paired placebo and treatment plots (1–59 ha in size; average 16.9 ha) in 7 western states from 2013 to 2015. We compared relative abundance (using catch per unit effort (CPUE) as an index) and apparent survival of prairie dogs on 26 of the 29 paired plots, 12 with confirmed or suspected plague ( Y. pestis positive carcasses or fleas). Even though plague mortality occurred in prairie dogs on vaccine plots, SPV treatment had an overall positive effect on CPUE in all three years, regardless of plague status. Odds of capturing a unique animal were 1.10 (95% confidence interval [C.I.] 1.02–1.19) times higher per trap day on vaccine-treated plots than placebo plots in 2013, 1.47 (95% C.I. 1.41–1.52) times higher in 2014 and 1.19 (95% C.I. 1.13–1.25) times higher in 2015. On pairs where plague occurred, odds of apparent survival were 1.76 (95% Bayesian credible interval [B.C.I.] 1.28–2.43) times higher on vaccine plots than placebo plots for adults and 2.41 (95% B.C.I. 1.72–3.38) times higher for juveniles. Our results provide evidence that consumption of vaccine-laden baits can protect prairie dogs against plague; however, further evaluation and refinement are needed to optimize SPV use as a management tool.

EcoHealth

The innate immune response may be important for surviving plague in wild Gunnison's prairie dogs

Prairie dogs (Cynomys spp.) are highly susceptible to Yersinia pestis, with ≥99% mortality reported from multiple studies of plague epizootics. A colony of Gunnison's prairie dogs (Cynomys gunnisoni) in the Aubrey Valley (AV) of northern Arizona appears to have survived several regional epizootics of plague, whereas nearby colonies have been severely affected by Y. pestis. To examine potential mechanisms accounting for survival in the AV colony, we conducted a laboratory Y. pestis challenge experiment on 60 wild-caught prairie dogs from AV and from a nearby, large colony with frequent past outbreaks of plague, Espee (n = 30 per colony). Test animals were challenged subcutaneously with the fully virulent Y. pestis strain CO92 at three doses: 50, 5,000, and 50,000 colony-forming units (cfu); this range is lethal in black-tailed prairie dogs (Cynomys ludovicianus). Contrary to our expectations, only 40% of the animals died. Although mortality trended higher in the Espee colony (50%) compared with AV (30%), the differences among infectious doses were not statistically significant. Only 39% of the survivors developed moderate to high antibody levels to Y. pestis, indicating that mechanisms other than humoral immunity are important in resistance to plague. The ratio of neutrophils to lymphocytes was not correlated with plague survival in this study. However, several immune proteins with roles in innate immunity (VCAM-1, CXCL-1, and vWF) were upregulated during plague infection and warrant further inquiry into their role for protection against this disease. These results suggest plague resistance exists in wild populations of the Gunnison's prairie dog and provide important directions for future studies.

Arizona

Population differences in host immune factors may influence survival of Gunnison's prairie dogs ( Cynomys Gunnisoni ) during plague outbreaks

Over the past 40 yr, epizootics of plague ( Yersinia pestis ) in northern Arizona have reduced populations of the Gunnison’s prairie dog ( Cynomys gunnisoni ), with the exception of a large population found in the Aubrey Valley (AV). To examine potential mechanisms accounting for their survival, we collected prairie dog serum samples in 2005–2006 from AV and a neighboring population near Seligman (SE), Arizona. We quantified gene expression at 58 diverse immune proteins using a multiplexed enzyme-linked immunosorbent assay panel. We found a subset of proteins important in coagulation and inflammation (tissue factor [TF], calbindin [Cal], and thrombopoietin [TPO]) and T-cell responses (CD40L and CD40) that were present in AV at levels two to eight times greater than SE. These results suggest that AV and SE animals might differ in their ability to mount an immune response.

Arizona