A literature review was conducted in order to identify unique weaknesses in the physiology or metabolism of pigs that could be targeted with specific chemicals (i.e. an 'Achilles' heel' search). A promising weakness identified was the species' susceptibility to methaemoglobin-forming compounds, most likely related to their uniquely low levels of methaemoglobin reductase. Further examination revealed that sodium nitrite is a cost-effective, readily available methaemoglobin-forming compound that is highly toxic to domestic pigs, which has caused numerous accidental poisonings. Pen trials on pigs showed that sodium nitrite delivered by gavage (>90 mg kg À1 ) and freely consumed in bait (>400 mg kg À1 ) caused rapid and lethal rises in methaemoglobin. Sodium nitrite appeared to be more humane than currently used toxins, with deaths following bait consumption being considerably quicker and with fewer symptoms (within 80 min of clinical signs beginning; clinical signs including infrequent vomiting, lethargy, ataxia and dyspnoea). The review also identified a second deficiency in the metabolism of pigs, namely high sensitivity to selective inhibition of cytochrome P450 liver enzymes. This leads to potentially lethal interactions between various drugs, such as two antibiotics, monensin and tiamulin. A pen trial confirmed that the antibiotic combination in a single gavage dose was reliably and rapidly lethal to pigs. However, its utility as a pig toxin is low, because it was unpalatable to pigs when delivered in bait and appeared to cause pain and suffering (leading to the early termination of pen trials). The findings presented here demonstrate the potential of sodium nitrite as an additional feral pig toxin.1. High toxicity. 2. Acceptability to the target population. 3. Commercially and appropriately available. 4. Appropriate degradation. 5. The toxin must remain at the site of application. 6. Acceptable operator hazard.
Choosing the appropriate method to detect and monitor wildlife species is difficult if the species is rare or cryptic in appearance or behaviour. We evaluated the effectiveness of the following four methods for detecting red foxes (Vulpes vulpes) on the basis of equivalent person hours in a rural landscape in temperate Australia: camera traps, hair traps (using morphology and DNA from hair follicles), scats from bait stations (using DNA derived from the scats) and spotlighting. We also evaluated whether individual foxes could be identified using remote collection of their tissues. Genetic analysis of hair samples was the least efficient method of detection among the methods employed because of the paucity of samples obtained and the lack of follicles on sampled hairs. Scat detection was somewhat more efficient. Scats were deposited at 17% of bait stations and 80% of scats were amplified with a fox-specific marker, although only 31% of confirmed fox scats could be fully genotyped at all six microsatellite loci. Camera trapping and spotlighting were the most efficient methods of detecting fox presence in the landscape. Spotlighting success varied seasonally, with fox detections peaking in autumn (80% of spotlighting transects) and being lowest in winter (29% of transects). Cameras detected foxes at 51% of stations; however, there was limited seasonality in detection, and success rates varied with camera design. Log-linear models confirmed these trends. Our results showed that the appropriate technique for detecting foxes varies depending on the time of the year. It is suggested that wildlife managers should consider both seasonal effects and species biology when attempting to detect rare or elusive species.
Few studies have evaluated oral delivery systems of pharmaceuticals (e.g., vaccines, fertility control agents, and toxicants) to feral swine (Sus scrofa) in the United States. Our objective was to assess, through a field trial, the percentage of feral swine and nontarget animals that remove and consume baits intended to transport pharmaceuticals to feral swine in southern Texas, USA. We hand‐placed 1,178 iophenoxic acid (IA)—marked baits distributed over 1,721 ha (68 baits/km2) in April 2005 and monitored species‐specific bait removal and consumption using track stations, automated camera systems, and serum IA values from captured animals. Ninety percent of baits were removed after 72 hours. For baits for which we determined the species that “definitely” or “likely” removed bait using track stations and cameras, 51% were taken by raccoons (Procyon lotor), 22% were taken by feral swine, and 20% were taken by collared peccaries (Tayassu tajacu). We found elevated serum IA values in 74% of trapped feral swine, 89% of raccoons, and 43% of opossums (Didelphis virginiana). Our oral delivery system was successful in marking a substantial proportion of feral swine. However, our observed removal rates suggest that the majority of the baits were taken by nontarget species and, therefore, unsuitable for most pharmaceutical applications in their current form.
The lack of variance estimates constrain the utility of abundance indices calculated from camera‐trap data. We adapted a General Index model, which allows variance estimation, to analyze camera‐trap observations of feral pigs (Sus scrofa) for population monitoring in a tropical rainforest. We tested whether the index would respond to population manipulation, and found that it decreased by 57% following removal of 24 pigs and remained low in the following period. Our method is useful for monitoring other large animals in difficult landscapes, and the model can be used to enhance the value of existing data sets. © 2011 The Wildlife Society.
Substantial efforts have been made to identify the most effective practices for the control and management of invasive vertebrate pest species, such as the feral pig (Sus scrofa). We investigated the demographics, abundance, and molecular ecology of a persecuted feral pig population that was subjected to control. We then applied methodologies to determine if we could retrospectively quantify any changes in the population structure or dynamics of these pigs. Feral pig demographic and abundance parameters indicated that in this population of feral pigs, there were very few detectable changes between the two aerial culling years. We observed this despite environmental conditions being optimal for control. Genetic results indicated that pigs culled in the latter 2004 cull were genetically identical to those pigs that inhabited the area a year earlier. The genetic population was geographically larger than the sample area. These findings indicate that the recovery in feral pig density witnessed in the controlled area was not a result of reinvasion from a separate, genetically distinct population, but rather, it was the result of reinvasion from feral pigs outside the study area but within the same genetic population. Importantly, we were unable to detect any recent genetic bottlenecks. This approach has considerable potential for auditing the effectiveness of control programs of pest species and assessing the feasibility of impacting upon or locally eradicating many other free‐ranging pest species.
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