Olivier J. Hardy

Dr. Olivier J. Hardy

orcid

Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

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

Representative Publications

View All Publications

16 January 2004 in Molecular Ecology
Verified
Journal Article
Closed access
PDF file
XVX. Vekemans
X. Vekemans
OHOlivier J. Hardy
Olivier J. Hardy

30 October 2019 in New Phytologist
Verified
Journal Article
Open access
PDF file
EKErik J. M. Koenen
Erik J. M. Koenen
DODario I. Ojeda
Dario I. Ojeda
RSRoyce Steeves
Royce Steeves
JMJérémy Migliore
Jérémy Migliore
FBFreek T. Bakker
Freek T. Bakker
CHColin E. Hughes
Colin E. Hughes
Summary: Phylogenomics is increasingly used to infer deep‐branching relationships while revealing the complexity of evolutionary processes such as incomplete lineage sorting, hybridization/introgression and polyploidization. We investigate the deep‐branching relationships among subfamilies of the Leguminosae (or Fabaceae), the third largest angiosperm family. Despite their ecological and economic importance, a robust phylogenetic framework for legumes based on genome‐scale sequence data is lacking. We generated alignments of 72 chloroplast genes and 7621 homologous nuclear‐encoded proteins, for 157 and 76 taxa, respectively. We analysed these with maximum likelihood, Bayesian inference, and a multispecies coalescent summary method, and evaluated support for alternative topologies across gene trees. We resolve the deepest divergences in the legume phylogeny despite lack of phylogenetic signal across all chloroplast genes and the majority of nuclear genes. Strongly supported conflict in the remainder of nuclear genes is suggestive of incomplete lineage sorting. All six subfamilies originated nearly simultaneously, suggesting that the prevailing view of some subfamilies as ‘basal’ or ‘early‐diverging’ with respect to others should be abandoned, which has important implications for understanding the evolution of legume diversity and traits. Our study highlights the limits of phylogenetic resolution in relation to rapid successive speciation.

20 March 2012 in Biological Reviews
Verified
Journal Article
Closed access
PDF file
NMNicolas Mouquet
Nicolas Mouquet
VDVincent Devictor
Vincent Devictor
CMChristine N. Meynard
Christine N. Meynard
FMFrançois Munoz
François Munoz
LBLouis-Félix Bersier
Louis-Félix Bersier
WTWilfried Thuiller
Wilfried Thuiller

2 February 2010 in Conservation Genetics
Verified
Journal Article
Closed access
PDF file
GSGernot Segelbacher
Gernot Segelbacher
SCSamuel A. Cushman
Samuel A. Cushman
BEBryan K. Epperson
Bryan K. Epperson
MFMarie-Josée Fortin
Marie-Josée Fortin
OFOlivier François
Olivier François
SMStéphanie Manel
Stéphanie Manel

1 April 2003 in Genetics
Verified
Journal Article
Open access
PDF file
OHOlivier J. Hardy
Olivier J. Hardy
NCNathalie Charbonnel
Nathalie Charbonnel
HFHélène Fréville
Hélène Fréville
MHMyriam Heuertz
Myriam Heuertz
The mutation process at microsatellite loci typically occurs at high rates and with stepwise changes in allele sizes, features that may introduce bias when using classical measures of population differentiation based on allele identity (e.g., FST, Nei’s Ds genetic distance). Allele size-based measures of differentiation, assuming a stepwise mutation process [e.g., Slatkin’s RST, Goldstein et al.’s (δμ)2], may better reflect differentiation at microsatellite loci, but they suffer high sampling variance. The relative efficiency of allele size- vs. allele identity-based statistics depends on the relative contributions of mutations vs. drift to population differentiation. We present a simple test based on a randomization procedure of allele sizes to determine whether stepwise-like mutations contributed to genetic differentiation. This test can be applied to any microsatellite data set designed to assess population differentiation and can be interpreted as testing whether FST = RST. Computer simulations show that the test efficiently identifies which of FST or RST estimates has the lowest mean square error. A significant test, implying that RST performs better than FST, is obtained when the mutation rate, μ, for a stepwise mutation process is (a) ≥ m in an island model (m being the migration rate among populations) or (b) ≥ 1/t in the case of isolated populations (t being the number of generations since population divergence). The test also informs on the efficiency of other statistics used in phylogenetical reconstruction [e.g., Ds and (δμ)2], a nonsignificant test meaning that allele identity-based statistics perform better than allele size-based ones. This test can also provide insights into the evolutionary history of populations, revealing, for example, phylogeographic patterns, as illustrated by applying it on three published data sets.