Daniel Potter

Dr. Daniel Potter

Department of Plant Sciences, University of California Davis, Davis, CA 95616, USA
orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

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

Representative Publications

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28 June 2007 in Plant Systematics and Evolution
Verified
Journal Article
Closed access
PDF file
Daniel PotterDaniel Potter
Daniel Potter
TET. Eriksson
T. Eriksson
RER. C. Evans
R. C. Evans
SOS. Oh
S. Oh
JSJ. E. E. Smedmark
J. E. E. Smedmark
CCC. S. Campbell
C. S. Campbell

6 February 2007 in Tree Genetics & Genomes
Verified
Journal Article
Closed access
PDF file
MAMallikarjuna K. Aradhya
Mallikarjuna K. Aradhya
Daniel PotterDaniel Potter
Daniel Potter
FGFangyou Gao
Fangyou Gao
CSCharles J. Simon
Charles J. Simon

9 May 2006 in Plant Systematics and Evolution
Verified
Journal Article
Closed access
PDF file
EBE. Bortiri
E. Bortiri
BHB. Vanden Heuvel
B. Vanden Heuvel
Daniel PotterDaniel Potter
Daniel Potter

1 February 1998 in Protist
Verified
Journal Article
Closed access
RARobert A. Andersen
Robert A. Andersen
RBRobyn W. Brett
Robyn W. Brett
Daniel PotterDaniel Potter
Daniel Potter
JSJulianne P. Sexton
Julianne P. Sexton

1 April 2000 in Systematic Botany
Verified
Journal Article
Closed access
Daniel PotterDaniel Potter
Daniel Potter
JLJames J. Luby
James J. Luby
RHRichard E. Harrison
Richard E. Harrison

1 January 2005 in American Journal of Botany
Verified
Journal Article
Open access
PDF file
SOSang‐Hun Oh
Sang‐Hun Oh
Daniel PotterDaniel Potter
Daniel Potter
A phylogeny of the tribe Neillieae (Rosaceae), which comprises Neillia, Stephanandra, and Physocarpus, was reconstructed based on nucleotide sequences of several regions of cpDNA, the ITS and ETS regions of rDNA, and the second intron of LEAFY, to elucidate relationships among genera and species in Neillieae and to assess the historical biogeography of the tribe. Phylogenetic analyses indicated that Physocarpus and Neillia‐Stephanandra were strongly supported as monophyletic and suggested that Stephanandra may have originated by hybridization between two lineages of Neillia. Dispersal‐vicariance analyses suggested that the most recent common ancestor of Neillieae may have occupied eastern Asia and western North America and that Physocarpus and Neillia‐Stephanandra may have been split by an intercontinental vicariance event in the early Miocene. The biogeographic analyses also suggested that species of Neillia and Stephanandra diversified in eastern Asia, whereas in Physocarpus one dispersal event from western North America to eastern Asia occurred. Two divergent types of LEAFY sequences were found in the eastern North American species, P. opulifolius, but only one type was present in each plant. The two types of sequences may represent homeologous genes that originated by hybridization between P. capitatus and P. monogynus, both western North American species.