Denise B. O'Meara

Dr. Denise B. O'Meara


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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9 March 2020 in Mammal Review
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Journal Article
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SBSamuel S. Browett
Samuel S. Browett
DODenise B. O'Meara
Denise B. O'Meara
AMAllan D. McDevitt
Allan D. McDevitt

22 June 2013 in Mammal Research
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Journal Article
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DODenise B. O'Meara
Denise B. O'Meara
ESEmma Sheehy
Emma Sheehy
PTPeter D. Turner
Peter D. Turner
DODeclan O’mAhony
Declan O’mAhony
AHAndrew P. Harrington
Andrew P. Harrington
COCatherine O’rEilly
Catherine O’rEilly

18 August 2021 in Proceedings Of The Royal Society B-Biological Sciences
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Journal Article
Open access
XHXavier A. Harrison
Xavier A. Harrison
AMAllan D. McDevitt
Allan D. McDevitt
JDJenny C. Dunn
Jenny C. Dunn
SGSarah M. Griffiths
Sarah M. Griffiths
CBChiara Benvenuto
Chiara Benvenuto
RARachael Antwis
Rachael Antwis
Interactions between hosts and their resident microbial communities are a fundamental component of fitness for both agents. Though recent research has highlighted the importance of interactions between animals and their bacterial communities, comparative evidence for fungi is lacking, especially in natural populations. Using data from 49 species, we present novel evidence of strong covariation between fungal and bacterial communities across the host phylogeny, indicative of recruitment by hosts for specific suites of microbes. Using co-occurrence networks, we demonstrate marked variation across host taxonomy in patterns of covariation between bacterial and fungal abundances. Host phylogeny drives differences in the overall richness of bacterial and fungal communities, but the effect of diet on richness was only evident in the mammalian gut microbiome. Sample type, tissue storage and DNA extraction method also affected bacterial and fungal community composition, and future studies would benefit from standardized approaches to sample processing. Collectively these data indicate fungal microbiomes may play a key role in host fitness and suggest an urgent need to study multiple agents of the animal microbiome to accurately determine the strength and ecological significance of host–microbe interactions.

5 October 2022 in Ecosphere
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Journal Article
Open access
JTJoshua P. Twining
Joshua P. Twining
CMClaire McFarlane
Claire McFarlane
DODenise B. O'Meara
Denise B. O'Meara
COCatherine O'Reilly
Catherine O'Reilly
MRMarina Reyne
Marina Reyne
BABen C. Augustine
Ben C. Augustine
Effective monitoring of wildlife populations forms the foundation of modern‐day conservation biology. Without reliable estimates of population size, it is not possible to determine population trends, a key requirement in determining species status under international legislation. Carnivores are one of the more difficult taxonomic groups to monitor due to low population densities and elusive behavior. Here, we compare conventional live trapping and two more modern, noninvasive field methods of population estimation: genetic fingerprinting from hair tube sampling and camera trapping for the pine marten (Martes martes). We apply marked spatial capture–recapture (SCR) models to the genetic and live‐trapping data where individuals were identifiable, and unmarked SCR (uSCR), camera‐trap distance sampling (CT‐DS), and random encounter models (REMs) to the camera‐trap data where individual ID was not possible. All five approaches produced plausible and relatively consistent point estimates (0.49–1.20 individuals/km2) despite differences in precision, cost, and effort being apparent. Genetic fingerprinting produced the most precise estimate out of the two approaches for marked animal populations and had the key benefit of being noninvasive but was the most expensive of all the methods. Live trapping produced the highest point estimate while being cheapest, but the most labor intensive and least precise. The camera‐trapping methods for unmarked animal populations were the most time efficient and precise except uSCR with a moderately informative prior (uSCRm), which produced the second least precise density estimate of all the methods compared. The CT‐DS produced the most precise estimate of all the methods, followed by REM and then uSCR with a strongly informative prior (uSCRs). While choice of method of density estimation depends on objectives and funding constraints, as well as the species of interest, we demonstrate the importance of usinga prioriknowledge of target species and consideration of planned statistical analysis to produce appropriate experimental designs with critical consideration required regarding trap spacing and spatial extent. Such considerations broaden the comparability and applicability of these methods and will serve to provide key reference estimates for researchers, wildlife managers, and non‐governmental organizations involved in monitoring wildlife populations.

13 June 2012 in Biological Journal of the Linnean Society
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Journal Article
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DODenise B. O'Meara
Denise B. O'Meara
CECeiridwen J. Edwards
Ceiridwen J. Edwards
DSD. Paddy Sleeman
D. Paddy Sleeman
TCTom F. Cross
Tom F. Cross
MSMark J. Statham
Mark J. Statham
JCJens Carlsson
Jens Carlsson
The present study examined the contemporary genetic composition of the Eurasian badger, Meles meles, in Ireland, Britain and Western Europe, using six

12 September 2018 in Ecology and Evolution
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Journal Article
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JGJimena Guerrero
Jimena Guerrero
Andrew ByrneAndrew Byrne
Andrew Byrne
JLJohn Lavery
John Lavery
EPEleanor Presho
Eleanor Presho
GKGavin Kelly
Gavin Kelly
AAAdrian Allen
Adrian Allen
The population genetic structure of free‐ranging species is expected to reflect landscape‐level effects. Quantifying the role of these factors and their relative contribution often has important implications for wildlife management. The population genetics of the European badger (Meles meles) have received considerable attention, not least because the species acts as a potential wildlife reservoir for bovine tuberculosis (bTB) in Britain and Ireland. Herein, we detail the most comprehensive population and landscape genetic study of the badger in Ireland to date—comprised of 454 Irish badger samples, genotyped at 14 microsatellite loci. Bayesian and multivariate clustering methods demonstrated continuous clinal variation across the island, with potentially distinct differentiation observed in Northern Ireland. Landscape genetic analyses identified geographic distance and elevation as the primary drivers of genetic differentiation, in keeping with badgers exhibiting high levels of philopatry. Other factors hypothesized to affect gene flow, including earth worm habitat suitability, land cover type, and the River Shannon, had little to no detectable effect. By providing a more accurate picture of badger population structure and the factors effecting it, these data can guide current efforts to manage the species in Ireland and to better understand its role in bTB.