Andira clade | |
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Scientific classification | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Clade: | Angiosperms |
Clade: | Eudicots |
Clade: | Rosids |
Order: | Fabales |
Family: | Fabaceae |
Subfamily: | Faboideae |
Clade: | Meso-Papilionoideae |
Clade: | Andira clade Cardoso et al. 2012 [1] [2] |
Genera | |
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The Andira clade is a predominantly Neotropical, monophyletic clade of the flowering plant subfamily Faboideae (or Papilionaceae). [1] [2] The members of this clade were formerly included in tribe Dalbergieae, [4] but this placement was questioned due to differences in wood anatomy and fruit, seed, seedling, floral, and vegetative characters. [5] [6] [7] [8] Recent molecular phylogenetic evidence has shown that they belong to a unique evolutionary lineage. [1] [2] [9] [10] [11] [12] It is predicted to have diverged from the other legume lineages in the late Eocene). [13]
The name of this clade is informal and is not assumed to have any particular taxonomic rank like the names authorized by the ICBN or the ICPN. [14] The clade does not currently have a node-based definition, but several morphological synapomorphies have been identified: "mostly fascicled leaves and densely flowered paniculate inflorescences at distal branch ends, [...] truly papilionate flowers involving petal differentiation and stamen connation", and "divergent fruit morphologies" (drupaceous in Andira and laterally compressed samaras in Hymenolobium ). [1] [2] [7] [8]
Andira is a genus of flowering plants in the legume family, Fabaceae. It is distributed in the tropical Americas, except for A. inermis, which also occurs in Africa. It was formerly assigned to the tribe Dalbergieae, but molecular phylogenetic studies in 2012 and 2013 placed it in a unique clade within subfamily Faboideae named the Andira clade.
Airyantha is a small genus of flowering plants in the legume family, Fabaceae. It belongs to the subfamily Faboideae. It was named after the botanist Herbert Kenneth Airy Shaw. It was traditionally assigned to the tribe Sophoreae; however, recent molecular phylogenetic analyses reassigned Airyantha into the Baphieae tribe.
Hymenolobium is a genus of flowering plants in the legume family, Fabaceae. It includes 14 species of trees native to Central America and northern South America, ranging from Honduras to Bolivia and southeastern Brazil. Most species are native to Brazil, the Guianas, and Venezuela, with one extending into Peru, another into Ecuador, and one native to Central America. Trees are typically very tall and emergent in tropical humid lowland rain forest.
Leucomphalos is a genus of flowering plants in the legume family, Fabaceae. It contains a single species, Leucomphalos capparideus, a climbing perennial shrub native to the Guineo-Congolian forest of Nigeria, Cameroon, Equatorial Guinea, Gabon, and the Gulf of Guinea Islands. It belongs to the subfamily Faboideae. Leucomphalos was traditionally assigned to the tribe Sophoreae; however, recent molecular phylogenetic analyses reassigned Leucomphalos to the Baphieae tribe.
Luetzelburgia is a genus of flowering plants in the legume family, Fabaceae. It includes 14 species of trees and shrubs native to Brazil, Bolivia, and Colombia. Typical habitat is seasonally-dry tropical lowland woodland and wooded grassland, and occasionally lowland rain forests. The genus belongs to the subfamily Faboideae. It was traditionally assigned to the tribe Sophoreae, mainly on the basis of flower morphology; recent molecular phylogenetic analyses assigned Luetzelburgia into an informal, monophyletic clade called the "vataireoids". Keys for the different species of Luetzelburgia have been published.
The tribe Amorpheae is an early-branching clade within the flowering plant subfamily Faboideae or Papilionaceae. It is found from Mexico to Argentina. It was recently found to belong in a larger clade known informally as the dalbergioids sensu lato. This tribe is consistently resolved as monophyletic in molecular phylogenetic analyses. It is estimated to have arisen 36.9 ± 3.0 million years ago. A node-based definition for Amorpheae is: "the MRCA of Psorothamnus arborescens and Eysenhardtia orthocarpa." The tribe exhibits the following morphological synapomorphies: "epidermal glands throughout the plant body; dry, indehiscent fruits that are single-seeded; and terminal inflorescences."
The tribe Brongniartieae is one of the subdivisions of the plant family Fabaceae, primarily found in tropical regions of the Americas and in Australia The members of this tribe consistently form a monophyletic clade in molecular phylogenetic analyses. The tribe does not currently have a node-based definition, but morphological synapomorphies have been identified:
"stamens united by filaments in an adaxially open tube; anthers alternately long and basifixed, short and versatile; anther connective inconspicuous; septa present between seeds in pods; aril lateral lobe present and fitting into heel of funicle; fine red glandular processes present in axils; and pollen tricolporate with opercula and no definite endoaperture."
The tribe Dalbergieae is an early-branching clade within the flowering plant subfamily Faboideae. Within that subfamily, it belongs to an unranked clade called the dalbergioids. It was recently revised to include many genera formerly placed in tribes Adesmieae and Aeschynomeneae and to be included in a monophyletic group informally known as the dalbergioids sensu lato. The members of this tribe have a distinctive root nodule morphology, often referred to as an "aeschynomenoid" or "dalbergioid" nodule.
The tribe Dipterygeae is one of the subdivisions of the plant family Fabaceae. It was recently recircumscribed to include the following genera:
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.
The tribe Swartzieae is an early-branching monophyletic clade of the flowering plant subfamily Faboideae or Papilionaceae. 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. It was recently revised and most of its genera were redistributed to other tribes. Under its new circumscription, this clade is consistently resolved in molecular phylogenies. Members of this tribe possess "non-papilionate swartzioid flowers[…]largely characterized by a tendency to lack petals combined with a profusion and elaboration of free stamens" and a "lack of unidirectional order in the initiation of the stamens". They also have "complete or near complete fusion of sepals resulting from intercalary growth early in development, relatively numerous stamens, and a single or no petal, with other petals not at all apparent in development." The tribe is predicted to have diverged from the other legume lineages 48.9±2.8 million years ago.
The vataireoids are an early-branching monophyletic clade of the flowering plant subfamily Faboideae that are mostly found in northern South America, primarily Brazil.
The inverted repeat-lacking clade (IRLC) is a monophyletic clade of the flowering plant subfamily Faboideae. Faboideae includes the majority of agriculturally-cultivated legumes. The name of this clade is informal and is not assumed to have any particular taxonomic rank like the names authorized by the ICBN or the ICPN. The clade is characterized by the loss of one of the two 25-kb inverted repeats in the plastid genome that are found in most land plants. It is consistently resolved in molecular phylogenies. The clade is predicted to have diverged from the other legume lineages 39.0±2.4 million years ago. It includes several large, temperate genera such as Astragalus, Hedysarum, Medicago, Oxytropis, Swainsona, and Trifolium.
The non-protein amino acid-accumulating clade, also known as the Canavanine-accumulating clade is a clade of the flowering plant subfamily Faboideae that includes the majority of agriculturally-cultivated legumes. It is characterized by the accumulation of the non-proteinogenic amino acid canavanine in the seeds—a deterrent against herbivory. This phylogenetic trait was first recognized in the early 1980s. This clade is consistently resolved in molecular phylogenies. It contains many economically important genera, including Cicer, Glycine, Medicago, Phaseolus, Trifolium, Vicia, and Vigna.
The tribe Exostyleae is an early-branching monophyletic clade of the flowering plant subfamily Faboideae that are mostly found in Neotropical rainforests.
The Cladrastis clade is a monophyletic clade of the flowering plant subfamily Faboideae that is found in eastern Asia and southern North America. It is consistently resolved in molecular phylogenies and is sister to the Meso-Papilionoideae. Evidence for the existence of this clade was first proposed based on morphological (floral), cytological, and biochemical evidence. It is predicted to have diverged from the other legume lineages 47.4±2.6 million years ago.
The tribe Ormosieae is one of the subdivisions of the plant family Fabaceae, primarily found in tropical regions of the Americas, but also in southeast Asia and northern Australia. The members of this tribe were formerly included in tribe Sophoreae, but were recently circumscribed into a new tribe. The members of this tribe consistently form a monophyletic clade in molecular phylogenetic analyses. The tribe does not currently have a node-based definition, but morphological synapomorphies have been tentatively identified: "mostly dehiscent pods with woody valves" and "tufts of minute colleter-like glands in the axils of bract and bracteoles". Like other genistoids, members of tribe Ormosieae are known to produce quinolizidine alkaloids.
The Genistoids are one of the major radiations in the plant family Fabaceae. Members of this phylogenetic clade are primarily found in the Southern hemisphere. Some genera are pollinated by birds. The genistoid clade is consistently resolved as monophyletic in molecular phylogenetic analyses. It is estimated to have arisen 56.4 ± 0.2 million years ago. A node-based definition for the genistoids is: "the MRCA of Poecilanthe parviflora and Lupinus argenteus." One morphological synapomorphy has been tentatively identified: production of quinolizidine alkaloids. Some genera also accumulate pyrrolizidine. A new genus, to be segregated from Clathrotropis, has also been proposed to occupy an undetermined position within the genistoid clade.
The dalbergioids are an early-branching monophyletic clade of the flowering plant subfamily Faboideae or Papilionaceae. They are pantropical, particularly being found in the neotropics and sub-Saharan Africa. This clade is consistently resolved as monophyletic in molecular phylogenetic analyses. It is estimated to have arisen 55.3 ± 0.5 million years ago. A node-based definition for the dalbergioids is: "The least inclusive crown clade that contains Amorpha fruticosaL. 1753 and Dalbergia sissooRoxb. ex DC. 1825." Indehiscent pods may be a morphological synapomorphy for the clade.
Meso-Papilionoideae is a monophyletic clade of the flowering plant subfamily Faboideae that includes the majority of papilionoid legumes. This clade is consistently resolved in molecular phylogenies. It contains many agronomically important genera, including Arachis (peanut), Cicer (chickpea), Glycine (soybean), Medicago (alfalfa), Phaseolus, Trifolium (clover), Vicia (vetch), and Vigna.
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