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Invasive Animals CRC > Publications > Scientific Papers

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Additional toxins for feral pig (Sus scrofa) control: identifying and testing Achilles' heels

Vaccination of feral pigs (Sus scrofa) using iophenoxic acid as a simulated vaccine 

Feral pig population structuring in the rangelands of eastern Australia: applications for designing adaptive management units

An assessment of the genetic diversity and structure within and among populations of wild pigs (Sus scrofa) from Australia and Papua New Guinea

Species-specific visitation and removal of baits for delivery of pharmaceuticals to feral swine

Additional toxins for feral pig (Sus scrofa) control: identifying and testing Achilles' heels

BRENDAN D. COWLED
Invasive Animals Cooperative Research Centre, University of Canberra, Canberra ACT 2601; the University of Sydney, School of Veterinary Science, Sydney NSW, 2001, Australia

STEVEN J. LAPIDGE
Invasive Animals Cooperative Research Centre, University of Canberra, Canberra ACT 2601, Australia

PETER ELSWORTH
Biosecurity Queensland, Robert Wicks Pest Animal Research Centre, Inglewood, Qld 4387, Australia

Abstract

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 ethaemoglobin-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 kg1) and freely consumed in bait (>400 mg kg1) 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.

(WILDLIFE RESEARCH 2008, 35: 651-662. CSIRO Publishing).

Vaccination of feral pigs (Sus scrofa) using iophenoxic acid as a simulated vaccine

BRENDAN D. COWLED
Invasive Animals Cooperative Research Centre, University of Canberra, Canberra ACT 2601, Australia

STEVEN J. LAPIDGE
Invasive Animals Cooperative Research Centre, University of Canberra, Canberra ACT 2601, Australia

MICHELLE SMITH
Animal Control Technologies Australia P/L, PO Box 279, Somerton VIC 3062, Australia

LINTON STAPLES

Animal Control Technologies Australia P/L, PO Box 279, Somerton VIC 3062, Australia

Abstract

Objectives
To develop an encapsulation method for delivery of vaccines to feral pigs, and quantify the effect of iophenoxic acid on captive feral pig blood iodine concentrations to assist in investigation of factors affecting vaccine uptake.
Design and methods
Feral pigs were administered iophenoxic acid by oral gavage, and consumption was assessed for different encapsulation methods in baits. Blood iodine concentrations were monitored for eight days after consumption. The relationship between dose rate, time since dosing and blood iodine concentration was assessed for gavaged and baited captive feral pigs. Wild feral pigs were baited with PIGOUT® baits containing 20 mg of encapsulated iophenoxic acid to simulate a vaccination program. Using knowledge from the pen studies, bait uptake and factors affecting bait uptake were investigated.
Results
Bait-delivered iophenoxic acid led to variable and inconsistent changes in blood iodine concentrations, in contrast to pigs receiving iophenoxic acid by gavage. This precluded accurate assessment of the quantity consumed, but still allowed a conservative determination of bait uptake. Iophenoxic acid in smaller capsules was consumed readily. Increasing baiting intensity appeared to increase bait uptake by wild feral pigs, and pigs of varying sexes, ages and weights appeared equally likely to consume baits.
Conclusions
Encapsulated liquids can be delivered to feral pigs within baits, should the need to vaccinate feral pigs for fertility or disease management arise. High baiting intensities may be required.
(AUSTRALIAN VETERINARY JOURNAL 86:1 and 2, January, February 2008).



Feral pig population structuring in the rangelands of eastern Australia: applications for designing adaptive management units

BRENDAN D. COWLED
Invasive Animals Cooperative Research Centre, University of Canberra, Canberra ACT 2601, Australia.

JACLYN ALDENHOVEN
Centre for Advanced Technologies in Animal Genetics and Reproduction (Reprogen), Faculty of Veterinary Science, University of Sydney, Sydney NSW 2006, Australia.

INAKWU O.A. ODEH
Faculty of Agriculture, Food and Natural Resources, University of Sydney, Sydney NSW 2006, Australia.

TOM GARRETT
Queensland Macropod & Wild Game Harvesters Assoc Inc., 1 Creek Street, Amby QLD 4462, Australia.

CHRIS MORAN
Centre for Advanced Technologies in Animal Genetics and Reproduction (Reprogen), Faculty of Veterinary Science, University of Sydney, Sydney NSW 2006, Australia.

STEVEN J. LAPIDGE
Invasive Animals Cooperative Research Centre, University of Canberra, Canberra ACT 2601, Australia.

Abstract

Feral pigs (Sus scrofa) are an invasive species in Australia. Their negative impact on conservation values has been demonstrated, and they are controlled in many areas in the rangelands of Australia. However, they are usually controlled over small, often ad hoc management units (MUs), and previous research has revealed that these MUs can be inadequate. Understanding feral pig population structuring can aid in the design of appropriate MUs. This study documents an approach to improving MUs for feral pig control in the rangelands of Australia. Feral pigs from a 500,000 km2 region were genotyped with 13 polymorphic markers. Genetic analyses were used to identify population structure. Identified sub-populations were then related to geographical and environmental gradients with geographical information systems, regression analysis and with canonical correspondence analysis. Five sub-populations were identified. These were moderately differentiated, with relatively high migration rates. Two sub-populations in drier, lower elevation areas overlapped, due to extensive migration, probably along the large, inland rivers and flood plains. Sub-populations in higher rainfall environments appeared less likely to migrate. Sub-population differentiation was also dependant on distance, indicating isolation by distance was present.  A case study applying an adaptive MU to a previously controlled area is presented. Generally, however, MUs for feral pig control for natural resource protection and endemic disease eradication in the rangelands should take into account geographical size, but also geographic features, especially major rivers in low-rainfall areas.
(CONSERVATION GENETICS 9: 211-224 2008) 

Measuring the Demographic and Genetic Effects of Pest Control in a Highly Persecuted Feral Pig Population

BRENDAN D. COWLED
Invasive Animal Cooperative Research Centre, Canberra, ACT 2601, Australia

STEVEN J. LAPIDGE
Invasive Animal Cooperative Research Centre, Canberra, ACT 2601, Australia

JORDAN O. HAMPTON
School of Veterinary and Biomedical Sciences, Murdoch University, Western Australia 6150, Australia

PETER B. S. SPENCER
School of Biological Sciences and Biotechnology, Murdoch University, Western Australia 6150, Australia

Abstract

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 re-invasion from a separate, genetically distinct population, but rather, it was the result of re-invasion 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. (JOURNAL OF WILDLIFE MANAGEMENT 706):16901697; 2006).

Using Baits to Deliver Pharmaceuticals to Feral Swine in Southern Texas

TYLER A. CAMPBELL
United States Department of Agriculture, Animal and Plant Health Inspection Service, Wildlife Services, National Wildlife Research Centre, Texas Field Station, Texas A&M University-Kingsville, Kingsville TX, USA

STEVEN J. LAPIDGE
Invasive Animals Cooperative Research Centre, Unley, South Australia, Australia

DAVID B. LONG

United States Department of Agriculture, Animal and Plant Health Inspection Service, Wildlife Services, National Wildlife Research Centre, Texas Field Station, Texas A&M University-Kingsville, Kingsville TX, USA

Abstract

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 non-target animals that remove and consume baits intended to transport pharmaceuticals to feral swine in southern Texas. 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 non-target species and, therefore, unsuitable for most pharmaceutical applications in their current form.
(WILDLIFE SOCIETY BULLETIN 34(4):000000; 2006)

Efficacy of manufactured PIGOUT baits for localised control of feral pigs in the semi-arid Queensland rangelands

BRENDAN D. COWLED
Pest Animal Control Cooperative Research Centre (now Invasive Animals CRC)

EDDIE GIFFORD
CSIRO Sustainable Ecosystems, GPO Box 284, Canberra ACT 2601, Australia

MICHELLE SMITH
Animal Control Technologies Australia P/L, PO Box 279, Somerton VIC 3062, Australia

LINTON STAPLES

Animal Control Technologies Australia P/L, PO Box 279, Somerton VIC 3062, Australia

STEVEN J. LAPIDGE
Invasive Animals Cooperative Research Centre, University of Canberra, ACT 2601, Australia.

Abstract

Conservative population declines of 73% were recorded in three independent feral pig populations in Welford National Park, Queensland, when PIGOUT baits containing 72 mg of sodium fluoroacetate were used in a baiting program following prefeeding. Declines were measured using a prebaiting population census with remote cameras, followed by carcass recovery. The knockdown of susceptible feral pigs may have been higher than this, since any carcasses not recovered reduced the recorded efficacy. In addition, feral pigs know to have left the baiting area after trapping and telemetry-tagging, and subsequently not exposed to toxic baits, were included in the analysis.

The use of remote cameras and carcass recovery appears to be a relatively accurate means of recording localised declines in feral pig populations. This method is applicable only when carcass recovery is possible, such as in open areas in the semi-arid rangelands.   A decline of 86% of radio-tagged feral pigs attending bait stations was also recorded. Camera observations revealed no non-target consumption of baits.  Measurement of sodium fluoroacetate contaminated tissues from feral pigs showed that residues were too low to present a significant risk to recorded scavenging animals in the area. Some feral pigs vomited before death, with vomitus containing sodium fluoroacetate poison at high concentrations. No vomitus was consumed by non-target species. Almost all feral pigs were killed relatively rapidly after ingestion of sodium fluoroacetate and the signs observed in a small number of poisoned feral pigs did not indicate a significant welfare concern.

(WILDLIFE RESEARCH 33, 427-437 2006) CSIRO Publishing www.publish.csiro.au/journals/wr

Attractiveness of a novel omnivore bait, PIGOUT, to feral pigs (Sus scrofa) and assessment of risks of bait uptake by non-target species

BRENDAN D. COWLED
Pest Animal Control Cooperative Research Centre (now Invasive Animals CRC)

STEVEN J. LAPIDGE
Invasive Animals Cooperative Research Centre, University of Canberra, ACT 2601, Australia

MICHELLE SMITH
Animal Control Technologies Australia P/L, PO Box 279, Somerton VIC 3062, Australia

LINTON STAPLES
Animal Control Technologies Australia P/L, PO Box 279, Somerton VIC 3062, Australia

Abstract

Following a bait-preference pilot study on captive feral pigs, a series of field studies assessed the attractiveness and target-specificity of a prototype manufactured feral pig bait (PIGOUT). Two promising test baits and fresh meat reference baits were biomarked with iophenoxic acid and aerially distributed in 100-km2 blocks of land infested with feral pigs in western Queensland to assess field uptake and target-specificity without prefeeding.

Uptake was assessed by measuring blood iodine levels in aerially shot feral pigs. In all, 80% of feral pigs sampled in a non-toxic PIGOUT-baited area had significantly elevated blood iodine, compared with 52% of sampled feral pigs in a meat-baited area (although slightly different baiting strategies were employed). No age or sex bias was evident in PIGOUT-consuming feral pigs.  No monitored manufactured baits were consumed by non-target species in 500 bait-nights.  Attractiveness and target-specificity trials of ground-laid, unfenced PIGOUT baits compared with reference baits were subsequently undertaken in several regions of eastern Australia. Results showed that PIGOUT was consumed readily by feral pigs at all sites, and that it offered significant improvement in target specificity when compared with unfenced wheat or meat baits. However, the baits were consumed by small numbers of macropods, birds and possums.  Available evidence indicates that the target-specificity of PIGOUT bait is highest in the rangelands, reducing slightly in temperate areas and subalpine forests, where abundance of small animals is higher.

(WILDLIFE RESEARCH 33, 651-660 2006) CSIRO Publishing www.publish.csiro.au/journals/wr

An assessment of the genetic diversity and structure within and among populations of wild pigs (Sus scrofa) from Australia and Papua New Guinea

P.B.S. SPENCER
School of Biological Sciences and Biotechnology, Murdoch University, Murdoch WA 6150, Australia

J. HAMPTON
School of Biological Sciences and Biotechnology, Murdoch University, Murdoch WA 6150, Australia

S. J. LAPIDGE
Invasive Animals Cooperative Research Centre, University of Canberra, Canberra ACT 2617, Australia

J. MITCHELL
Queensland Department of Natural Resources and Water, PO Box 187, Charters Towers QLD 4820, Australia

J. LEE
Australian Quarantine and Inspection Service, PO Box 96, Cairns International Airport, Cairns QLD 4870, Australia

Species-specific visitation and removal of baits for delivery of pharmaceuticals to feral swine

TYLER A. CAMPBELL AND   DAVID B. LONG
United States Department of Agriculture, Animal and Plant Health Inspection Service, Wildlife Services, National Wildlife Research Centre, Texas Field Station, Texas A&M University-Kingsville, Kingsville TX, USA

Abstract

Within the domestic swine industry there is growing trepidation about the role feral swine (Sus scrofa) play in the maintenance and transmission of important swine diseases. Innovative disease management tools for feral swine are needed.  We used field trials conducted in southern Texas from February to March 2006 to compare species-specific visitation and removal rates of fish-flavored and vegetable-flavored baits with and without commercially available raccoon (Procyon lotor) repellent (trial 1) and removal rates of baits deployed in a systematic and cluster arrangement (trial 2). During trial 1, 1) cumulative bait removal rates after four nights ranged from 93% to 98%; 2) bait removal rates by feral swine, raccoons, and collared peccaries (Pecari tajacu) did not differ by treatment; and 3) coyotes (Canis latrans) removed more fish-flavored baits without raccoon repellent and white-tailed deer removed more vegetable-flavored baits without raccoon repellent than expected. During trial 2, feral swine removed fish-flavored baits distributed in a cluster arrangement (eight baits within 5 m2) at a rate greater than expected.  Our observed bait removal rates illustrate bait attractiveness to feral swine. However, the diverse assemblage of omnivores in the United States compared with Australia where the baits were manufactured adds complexity to the development of a feral swine-specific baiting system for pharmaceutical delivery.