Miguel Angel Bedoya Perez

Dr. Miguel Angel Bedoya Perez

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 August 2013 in Behavioral Ecology and Sociobiology
Verified
Journal Article
Closed access
PDF file
MPMiguel Angel Bedoya Perez
Miguel Angel Bedoya Perez
ACAlexandra J. R. Carthey
Alexandra J. R. Carthey
VMValentina Mella
Valentina Mella
CMClare McArthur
Clare McArthur
PBPeter B. Banks
Peter B. Banks

12 October 2013 in Oecologia
Verified
Journal Article
Closed access
PDF file
MPMiguel Angel Bedoya Perez
Miguel Angel Bedoya Perez
IIIdo Isler
Ido Isler
PBPeter B. Banks
Peter B. Banks
CMClare McArthur
Clare McArthur

8 May 2019 in Frontiers in Ecology and Evolution
Verified
Journal Article
Open access
PDF file
MPMiguel Angel Bedoya Perez
Miguel Angel Bedoya Perez
KSKristie Leigh Smith
Kristie Leigh Smith
RKRichard C. Kevin
Richard C. Kevin
JLJia Lin Luo
Jia Lin Luo
Mathew S. CrowtherMathew S. Crowther
Mathew S. Crowther
IMIain S. McGregor
Iain S. McGregor
The strong innate fear response shown by laboratory rodents to predator cues could provide powerful and innovative tools for pest management. Predator cues are routinely used to induce fear and anxiety in laboratory rodents for pharmacological studies. However, research on the fear response induced by predator cues in different species of rodents in the wild has been inconclusive with results often contradictory to laboratory experiments. Potential explanations for this inconsistency include the prey's: (i) physiological state; (ii) parasite load; (iii) differential intensity of perceived threats; (iv) fear learning and habituation; and (v) information gathering. In this review, we first explore current knowledge on the sensory mechanisms and capabilities of rodents, followed by the discussion of each of these explanations within the context of their implications for the use of antipredator response as a pest rodent management tool. Finally, we make recommendations on potential solutions and strategies to resolve issues in rodent management related to these hypotheses.

21 June 2021 in Scientific Reports
Verified
Journal Article
Open access
PDF file
MPMiguel Angel Bedoya Perez
Miguel Angel Bedoya Perez
MWMichael Ward
Michael Ward
Max William LoomesMax William Loomes
Max William Loomes
IMIain S. McGregor
Iain S. McGregor
Mathew S. CrowtherMathew S. Crowther
Mathew S. Crowther
Shortly after the enactment of restrictions aimed at limiting the spread of COVID-19, various local government and public health authorities around the world reported an increased sighting of rats. Such reports have yet to be empirically validated. Here we combined data from multi-catch rodent stations (providing data on rodent captures), rodent bait stations (providing data on rodent activity) and residents’ complaints to explore the effects of a six week lockdown period on rodent populations within the City of Sydney, Australia. The sampling interval encompassed October 2019 to July 2020 with lockdown defined as the interval from April 1st to May 15th, 2020. Rodent captures and activity (visits to bait stations) were stable prior to lockdown. Captures showed a rapid increase and then decline during the lockdown, while rodent visits to bait stations declined throughout this period. There were no changes in the frequency of complaints during lockdown relative to before and after lockdown. There was a non-directional change in the geographical distribution of indices of rodent abundance suggesting that rodents redistributed in response to resource scarcity. We hypothesize that lockdown measures initially resulted in increased rodent captures due to sudden shortage of human-derived food resources. Rodent visits to bait stations might not show this pattern due to the nature of the binary data collected, namely the presence or absence of a visit. Relocation of bait stations driven by pest management goals may also have affected the detection of any directional spatial effect. We conclude that the onset of COVID-19 may have disrupted commensal rodent populations, with possible implications for the future management of these ubiquitous urban indicator species.

13 June 2014 in Oecologia
Verified
Journal Article
Closed access
PDF file
MPMiguel Angel Bedoya Perez
Miguel Angel Bedoya Perez
DIDaniel D. Issa
Daniel D. Issa
PBPeter B. Banks
Peter B. Banks
CMClare McArthur
Clare McArthur

26 May 2021 in Behavioral Ecology
Verified
Journal Article
Open access
PDF file
MPMiguel Angel Bedoya Perez
Miguel Angel Bedoya Perez
ALAnna Le
Anna Le
IMIain S McGregor
Iain S McGregor
Mathew S. CrowtherMathew S. Crowther
Mathew S. Crowther
Sensitivity to predator-related cues and performance of antipredator behaviors are universal among prey species. Rodents exhibit a diverse suite of antipredator behaviors that have been examined in both field and laboratory studies. However, the results from the laboratory have not always translated to the field. While laboratory studies consistently indicate strong fear-inducing effects of cat fur/skin odors, it is unclear whether this occurs in the field with wild rats. To address this issue, we tested the antipredator responses of wild brown rats (Rattus norvegicus) to predatory (domestic cat fur) and nonpredatory (common brushtail possum fur) odor cues in a semi-natural experimental paradigm. Rats were housed in open air enclosures containing two feeding stations. Following several nights of acclimatization, the feeding stations were paired with cat fur, possum fur, or no fur. Rats spent less time at a feeding station that was paired with cat fur. Duration of time spent at feeding stations increased across consecutive test days and across hours within individual test nights, although the rate of increase within nights was lower for cat fur paired stations. This overall increase might reflect habituation of antipredator behaviors, increasing hunger, or loss of cue potency over time. We suggest that wild brown rats recognize and respond to cat fur odor cues, but their behavioral response is highly adaptable and finely tuned to the trade-off between predation risk and starvation that occurs across short temporal scales.