Phylogeny and classification of Rosaceae

By D. Potter, T. Eriksson, Rodger C. Evans, Sang-Hun Oh, J. Smedmark, D. Morgan, M. Kerr, K. R. Robertson, Matthew P. Arsenault, T. A. Dickinson and 1 more. Plant Systematics and Evolution, 2007

864 citations recorded by the source corpus.

Subfields: Ecology, Evolution, Behavior and Systematics, Plant Science

View Paper: https://www.semanticscholar.org/paper/c99b4d85ed8b8fd7979d393a7630dda7451c3a60

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Ecology, Evolution, Behavior and Systematics

In Plant Science

Citations in the corpus

The high-quality draft genome of peach (Prunus persica) identifies unique patterns of genetic diversity, domestication and genome evolution (2013, neutral): “‘Texas’ x ‘Earligold’ (T x E) 18 909* (56) 223.”
Prunus microsatellite marker transferability across rosaceous crops (2010, background): “…been developed in many other Rosaceae, including other members of the subfamily Spiraeoideae tribe Amygdaleae (formerly subfamily Prunoideae; see Potter et al. 2007 and Shulaev et al. 2008), such as almond (Mnejja et al. 2005), apricot (Hagen et al. 2004), Japanese plum (Mnejja et al. 2004),…”
An R2R3 MYB transcription factor associated with regulation of the anthocyanin biosynthetic pathway in Rosaceae (2010, methodology): “Botanical classification of the Rosaceae has recently been undertaken using 88 species analysed for a combination of phenotypic and molecular marker [74].”
Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, neutral): “The Pyrinae subtribe forms a wide and iverse lineage of the Rosaceae family (Potter et al. 2007), including ;1000 species belonging to 30 different genera, with a pome-type fruit and a base chromosome number of x1⁄417 s the main distinctive ch racteristics.”
Phylogenetic inferences in Prunus (Rosaceae) using chloroplast ndhF and nuclear ribosomal ITS sequences (2008, neutral): “Recently, Potter et al. (2007) proposed a new classification of Rosaceae based on molecular phylogenetic analyses, in which they ——————————— Received: 11 April 2008 Accepted: 25 April 2008 * E-mail: <wenj@si.edu>.”
Comparative analysis of rosaceous genomes and the reconstruction of a putative ancestral genome for the family (2011, background): “It has been postulated that the poor phylogenetic resolution along the backbone of the Rosaceae phylogenetic tree suggests a rapid evolutionary radiation of lineages within the family, corresponding to a relatively recent divergence of the genera [2].”
Polyploidy, reproductive biology, and Rosaceae: understanding evolution and making classifications (2007, background): “In the classification by Potter et al. (2007) three genera are unplaced, Rosa L., Rubus L., and Filipendula Miller.”
The Dynamic Nature of Apomixis in the Angiosperms (2008, background): “Recent phylogenetic results (Potter et al. 2007) reveal that Rubus, which contains a number of apomicts, diverged early in the evolutionary history of subfamily Rosoideae.”
Variation of first‐order root traits across climatic gradients and evolutionary trends in geological time (2013, neutral): “, 2009) and APweb (Stevens, 2001 onwards) and added specific phylogeny studies (Chanderbali et al., 2001; Li & Conran, 2003; Potter et al., 2007).”
Interspecific variation in functional traits, not climatic differences among species ranges, determines demographic rates across 44 temperate and Mediterranean tree species (2010, background): “As this tree was not fully resolved, genus- and species-level polytomies were resolved by obtaining additional phylogenetic information from (i) the user-supplied data repository in Phylomatic for the Pinaceae (Rydin 2002), Rosaceae (Potter 2007) and Betulaceae (Chen 1999) and (ii) from searches of ”
ROS generation, oxidative burst and dynamic expression profiles of ROS-scavenging enzymes of superoxide dismutase (SOD), catalase (CAT) and ascorbate peroxidase (APX) in response to Erwinia amylovora in pear (Pyrus communis L) (2017, background): “, apple, pear, and quince) and ornamentals belonging to the family Rosaceae (Moradi et al. 2012; Potter et al. 2007), is a gram-negative bacterium belongs to the family Enterobacteriaceae, that utilizes a type III secretion system in host pathogenesis(C.”
Intercontinental disjunctions between eastern Asia and western North America in vascular plants highlight the biogeographic importance of the Bering land bridge from late Cretaceous to Neogene (2016, background): “It is related to but separate from Potentilla, from which it differs by lacking an epicalyx, and possessing only five stamens (Eriksson et al., 1998, 2003; Potter et al., 2007).”
The genome of the domesticated apple (Malus × domestica Borkh.) (2010, methodology): “When the genomic Wx gene sequences were integrated in the phylogenetic analysis based on sequences present in the Rosaceae databas”
Origins of Plant Diversity in the California Floristic Province (2014, background): “…tree endemic to the Channel Islands but known from mainland fossils in California, Oregon, and Nevada from as early as the Miocene, was resolved as sister to all other genera of subfamily Spiraeoideae (Potter et al. 2007) and is now treated as the sole genus of tribe Lyonothamneae (Brouillet 2008).”
The genome of woodland strawberry (Fragaria vesca) (2010, positive): “Our data support these same broad structural relationships, providing extensive evidence for the reconstruction of an ancestral genome for Rosaceae with a haploid chromosome number ( x ) of nine, consistent with the base haploid chromosome number of the largest group within the modern Rosaceae, the ”