Parochetus communis | |
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Scientific classification | |
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Subtribe: | Parochetinae Chaudhary & Sanjappa |
Genus: | Parochetus |
Species: | P. communis |
Binomial name | |
Parochetus communis Buch.-Ham. ex D. Don | |
Synonyms [3] [4] [5] | |
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Parochetus communis, known in English as shamrock pea or blue oxalis, [1] is a species of legume, and the only species in the genus Parochetus and in the subtribe Parochetinae. [6] It is a low-growing plant with blue papilionaceous flowers and clover-like leaves. It is found in the mountains of Asia and tropical Africa, and has been introduced to New Zealand.
Parochetus communis is a prostrate herb, growing up to 10–20 centimetres (3.9–7.9 in) tall. [2] Its leaves are trifoliate (three-parted, like a clover leaf), with each leaflet being 8–20 mm (0.3–0.8 in) long and similarly wide (exceptionally up to 40 mm or 1.6 in). [2] [7] The leaflets are cuneate (wedge-shaped) at the base, and notched at the tip, with margins that may be smooth or have minute teeth. [2] [7] The stipules at the base of each leaf-stalk are 4–5 mm (0.16–0.20 in) long and entire (untoothed and undivided). [2]
The flowers of P. communis are borne singly or in clusters of up to three flowers on stalks that are typically 8–15 cm (3.1–5.9 in) long, but can be 1.5–25 cm (0.6–9.8 in) long. [2] [7] The flowers are generally blue, but occasionally white or purple; the standard (the large upper petal) is 12–20 mm (0.5–0.8 in) long, notched at the tip, and narrowed at the base. [2] [7] The wings (lateral petals) are around 13 mm (0.5 in) long, and the keel is 20–25 mm (0.8–1.0 in) long and 3–4 mm (0.1–0.2 in) wide. [2]
The seeds of P. communis form inside pods; each pod is 15–25 mm (0.6–1.0 in) long and 4–5 mm (0.16–0.20 in) wide and contains 8–12 seeds, with each seed being around 2 mm (0.08 in) long and slightly kidney-shaped, somewhat narrower than long. [2] [7]
Parochetus communis is native to the Himalaya and other Asian mountain systems as far south as Java, and also the Afrotropical mountains. [8] In Africa, it is found in Burundi, central Ethiopia, eastern parts of the Democratic Republic of the Congo, Kenya, Rwanda, Tanzania and western parts of Uganda, and grows in damp, shady places on the forest floor or along the banks of streams and rivers at altitudes of 1,500–2,000 metres (4,900–6,600 ft). [7] In China, it grows at altitudes of 1,800–3,000 m (5,900–9,800 ft). [2] Parochetus communis has been introduced to New Zealand, where it was first recorded in 1944. [9]
Because of its wide distribution and the absence of any threats to the species, Parochetus communis is classified as Least Concern on the IUCN Red List. [1]
The genus Parochetus was established by David Don (based on unpublished manuscripts by Francis Hamilton) in Hamilton's Prodromus Floræ Nepalensis ("Introduction to the Flora of Nepal") of 1825 [10] for the two species P. communis and P. major, which were separated on the basis of their leaf margins. [4] In 1835, John Forbes Royle described a third species, P. oxalidifolia, again based on leaf margin differences. It was later realised that intergradations between all three leaf forms were seen, and so the three taxa were merged into a single species. [4] In 1871, Parochetus was collected from Africa for the first time, as part of David Livingstone's Zambezi Expedition, from Mount Chiradzulu in southern Malawi. [11] A new species, Parochetus africanus, was erected for specimens from Africa in 1991 by Roger Marcus Polhill, but this was reduced to a subspecies of P. communis in 1998 because of a perceived lack of differentiating characters. [4]
Parochetus is traditionally classified in the tribe Trifolieae of the family Leguminosae (Fabaceae), although its inclusion in that tribe has also been considered doubtful. [12] Because Parochetus could not be comfortably accommodated in either of the existing subtribes of the Trifolieae, a new subtribe, Parochetinae, was erected in 1998 to accommodate Parochetus alone. [13]
Parochetus has been grown in Europe since the early 19th century, [11] but is considered "tender" in the United Kingdom, and will only survive outdoors in warm and sheltered areas. [14] Plants from Asian stock may be hardier than those from Africa. [11]
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The Fabaceae or Leguminosae, commonly known as the legume, pea, or bean family, are a large and economically important family of flowering plants. It includes trees, shrubs, and perennial or annual herbaceous plants, which are easily recognized by their fruit (legume) and their compound, stipulate leaves. Many legumes have characteristic flowers and fruits. The family is widely distributed, and is the third-largest land plant family in number of species, behind only the Orchidaceae and Asteraceae, with about 765 genera and nearly 20,000 known species.
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Medicago arborea is a flowering plant species in the pea and bean family Fabaceae. Common names include moon trefoil, shrub medick, alfalfa arborea, and tree medick. It is found throughout Europe and especially in the Mediterranean basin, primarily on rocky shores among shrubby vegetation. It forms a symbiotic relationship with the bacterium Sinorhizobium meliloti, which is capable of nitrogen fixation. It is the only member of the genus Medicago which is used as an ornamental. M. arborea is sometimes misidentified as Cytisus, which it resembles.
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Barbieria is a genus of flowering plants in the legume family, Fabaceae.
Cyathostegia is a genus of flowering plants in the legume family, Fabaceae. It belongs to the subfamily Faboideae. It is often considered to be a monotypic genus containing only Cyathostegia mathewsii. Some sources include Cyathostegia weberbaueri.
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The tribe Sophoreae is one of the subdivisions of the plant family Fabaceae. Traditionally this tribe has been used as a wastebasket taxon to accommodate genera of Faboideae which exhibit actinomorphic, rather than zygomorphic floral symmetry and/or incompletely differentiated petals and free stamens. Various morphological and molecular analyses indicated that Sophoreae as traditionally circumscribed was polyphyletic. This led to a re-circumscription of Sophoreae, which resulted in the transfer of many genera to other tribes. This also necessitated the inclusion of two former tribes, Euchresteae and Thermopsideae, in the new definition of Sophoreae. Tribe Sophoreae, as currently circumscribed, consistently forms a monophyletic clade in molecular phylogenetic analyses. The Sophoreae arose 40.8 ± 2.4 million years ago.
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The Andira clade is a predominantly Neotropical, monophyletic clade of the flowering plant subfamily Faboideae. The members of this clade were formerly included in tribe Dalbergieae, but this placement was questioned due to differences in wood anatomy and fruit, seed, seedling, floral, and vegetative characters. Recent molecular phylogenetic evidence has shown that they belong to a unique evolutionary lineage. It is predicted to have diverged from the other legume lineages in the late Eocene).
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