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Pueraria is a genus of 15–20 species of native to south, east, and southeast and to New Guinea and northern Australia. The best known member is , also called Japanese arrowroot. The genus is named after 19th century Swiss botanist Marc Nicolas Puerari.

Plants in the genus are , shrubs, or climbing herbs, usually with large tuberous roots. Typical habitats include seasonally-dry tropical and subtropical forest, rain forest, forest margins, and scrub vegetation, often on limestone outcrops and in rocky areas.

The genus, as traditionally circumscribed, is , with different species being more related to other species in the tribe . Current research, reproduced below, splits the genus into five , one of which defines the current monophyletic genus.


Species
The genus Pueraria is highly polyphyletic; the below list is divided by clade following the result of A.N.Egan & B.Pan (2016). Earlier version, 2013 MSc thesis. In 2015, the authors validly published their proposal in . , Kew Plants of the World Online database accepts these names.


Pueraria sensu stricto
Pueraria includes the vast majority of species in the genus. They fall into a single clade sister to or containing .

  • P. alopecuroides Craib
  • P. calycina Franch.
  • P. candollei Benth.
  • Pamp.
  • P. imbricata Maesen
  • Craib
  • P. mirifica Airy Shaw & Suvat. (= P. candollei var. mirifica in Egan)
  • (Lour.) Merr. – US invasive population comes from a hybrid of more than one of the subspecies.
    • Pueraria montana var. chinensis (Ohwi) Sanjappa & Pradeep (= P. chinensis, although ILDS and the plant list instead consider P. thomsonii the synonym)
    • Pueraria montana var. lobata (Willd.) Sanjappa & Pradeep (= P. lobata)
    • Pueraria montana var. thomsonii (Benth.) Wiersema ex D.B. Ward (= P. thomsonii, missing in ILDS)
  • P. pulcherrima (Koord.) Koord.-Schum.
  • P. sikkimensis Prain
  • P. tuberosa (Roxb.ex Willd.) DC. – type species


Provisionally retained
The following are not included in the 2016 study due to insufficient material for sequencing. They are accepted by POWO.
  • Prain: conflicting proposals assigning either to the main clade or to (morphology).
  • P. bouffordii H. Ohashi: presumably in the main clade (morphology).
  • P. grandiflora Bo Pan & Bing Liu: presumably in the main clade (morphology).
  • H. Ohashi & Iokawa: presumably in the main clade (morphology).

The following are not included in Egan et al. 2016 for other reasons, but are accepted by Kew POWO:

  • P. garhwalensis L.R.Dangwal & D.S.Rawat: excluded per van der Maesen (2002)
  • P. neocaledonica Harms: not mentioned


Former members
The rest of the genus fall into four clades, sorted by distance from the main clade:

  • Benth. – sister to
    • P. phaseoloides () N. phaseoloides (Roxb.) Benth.

      P. edulis, P. montana, and N. phaseoloides make up what is known as . The morphological differences between these species are subtle.

      • N. phaseoloides var. javanicus (= P. javanica (Benth.) Benth.)
      • N. phaseoloides var. phaseoloides
      • N. phaseoloides var. subspicatus
  • A.N.Egan & B.Pan – sister to
    • P. peduncularis Grah.T. peduncularis
    • P. yunnanensis Franchet.T. yunnanensis
  • A.N.Egan & B.Pan – notably lies out of Glycininae near Kennediinae; known for a long time to be misplaced
    • P. wallichii DC.H. wallichii

The following names are not accepted even before Egan 2016 but have seen valid publication:

  • P. omeiensis Wang et TangP. montana: unaccepted name after .
  • P. stracheyi Baker (Wall.) Benth. ex Baker.
  • P. maclurei (F. P. Metcalf) F. J. Herm.Sinodolichos lagopus – still accepted by WFO

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