Monocot fossils suitable for molecular dating analyses
WJD Iles, SY Smith, MA Gandolfo… - Botanical Journal of the …, 2015 - academic.oup.com
Recent re-examinations and new fossil findings have added significantly to the data
available for evaluating the evolutionary history of the monocotyledons. Integrating data from …
available for evaluating the evolutionary history of the monocotyledons. Integrating data from …
MADS about the evolution of orchid flowers
M Mondragón-Palomino, G Theißen - Trends in plant science, 2008 - cell.com
Orchids have unique flowers involving three types of perianth organs: outer tepals, lateral
inner tepals, and a lip. Expression studies indicate that the identity of these organs is …
inner tepals, and a lip. Expression studies indicate that the identity of these organs is …
Plastid phylogenomic analysis of green plants: a billion years of evolutionary history
Premise of the Study For the past one billion years, green plants (Viridiplantae) have
dominated global ecosystems, yet many key branches in their evolutionary history remain …
dominated global ecosystems, yet many key branches in their evolutionary history remain …
Monocot plastid phylogenomics, timeline, net rates of species diversification, the power of multi‐gene analyses, and a functional model for the origin of monocots
Premise of the Study We present the first plastome phylogeny encompassing all 77 monocot
families, estimate branch support, and infer monocot‐wide divergence times and rates of …
families, estimate branch support, and infer monocot‐wide divergence times and rates of …
Angiosperm phylogeny: 17 genes, 640 taxa
• Premise of the study: Recent analyses employing up to five genes have provided
numerous insights into angiosperm phylogeny, but many relationships have remained …
numerous insights into angiosperm phylogeny, but many relationships have remained …
[图书][B] Flowering plants
A Takhtajan - 2009 - Springer
Friedman WE, RC Moore, and MD Purugganan. 2004. The evolution of plant development.
Am. J. Bot. 91: 1726–1741. Friis EM, PR Crane, and KP Pedersen. 1997. Fossil history of …
Am. J. Bot. 91: 1726–1741. Friis EM, PR Crane, and KP Pedersen. 1997. Fossil history of …
Phylogeny, adaptive radiation, and historical biogeography in Bromeliaceae: insights from an eight‐locus plastid phylogeny
TJ Givnish, MHJ Barfuss, B Van Ee… - American journal of …, 2011 - Wiley Online Library
• Premise: Bromeliaceae form a large, ecologically diverse family of angiosperms native to
the New World. We use a bromeliad phylogeny based on eight plastid regions to analyze …
the New World. We use a bromeliad phylogeny based on eight plastid regions to analyze …
[图书][B] Phylogeny and Evolution of the Angiosperms
Although they are relative latecomers on the evolutionary scene, having emerged only 135?
170 million years ago, angiosperms—or flowering plants—are the most diverse and species …
170 million years ago, angiosperms—or flowering plants—are the most diverse and species …
[HTML][HTML] A 250 plastome phylogeny of the grass family (Poaceae): topological support under different data partitions
The systematics of grasses has advanced through applications of plastome phylogenomics,
although studies have been largely limited to subfamilies or other subgroups of Poaceae …
although studies have been largely limited to subfamilies or other subgroups of Poaceae …
[HTML][HTML] Dynamics and evolution of the inverted repeat-large single copy junctions in the chloroplast genomes of monocots
RJ Wang, CL Cheng, CC Chang, CL Wu, TM Su… - BMC evolutionary …, 2008 - Springer
Background Various expansions or contractions of inverted repeats (IRs) in chloroplast
genomes led to fluxes in the IR-LSC (large single copy) junctions. Previous studies revealed …
genomes led to fluxes in the IR-LSC (large single copy) junctions. Previous studies revealed …