Camoensia is a genus of 2 species of lianas in the family Fabaceae, subfamily Faboideae, native to the Gulf of Guinea, Africa. C. scandens is cultivated as an ornamental plant; it has one of the largest leguminous flowers, up to 20 cm across. The genus has classically been assigned to the tribe Sophoreae, but was recently assigned to its own monophyletic tribe, Camoensieae, on the basis of molecular phylogenetic evidence. Species of Camoensia are known to produce quinolizidine alkaloids, consistent with their placement in the genistoid clade.
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.
Crotalarieae is a tribe of flowering plants belonging to the family Fabaceae. It includes rooibos (Aspalathus linearis), which is harvested for sale as a tisane.
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 Indigofereae is a subdivision of the plant family Fabaceae. It is consistently recovered as a monophyletic clade in molecular phylogenies. The Indigofereae arose 30.0 ± 3.3 million years ago.
The tribe Podalyrieae is one of the subdivisions of the plant family Fabaceae.
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.
Leptolobieae is a Neotropical, early-branching monophyletic clade of the flowering plant subfamily Faboideae or Papilionaceae that are mostly found in South America.
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 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 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).
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.
