Robinioids

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Robinioids
Robinia Pseudoacacia flower.JPG
Robinia pseudoacacia
Scientific classification
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Robinioids
Tribes

The robinioids are one of the four major clades (along with the genisitoids, dalbergioids and millettioids) in subfamily Faboideae of the plant family Fabaceae (Leguminosae). It is composed of the traditional tribes Loteae, Sesbanieae and Robinieae. It is a large and important clade that is distributed in mostly temperate areas. Species in this clade share a unique determinate root nodule structure. The clade is predicted to have diverged from the other legume lineages 48.3±1.0 million years ago (in the Eocene). [1]

Contents

History

Only two tribes (Loteae and Robinieae) were traditionally included in clade robinioids. Lavin & Schrire later included Sesbanieae into clade robinioids. [2] Tribe Robinieae is primarily in tropical and arid temperate areas, containing mostly trees and shrubs of New World. Tribe Loteae are herbaceous and small shrubby legumes closely related with Old World tribe Galegeae. [3]

Loteae was originally a smaller group of legumes until later in 1994 Polhill merged Loteae and tribe Coronilleae and greatly expanded Loteae. [4] Sesbanieae is a tribe with single genus Sesbania, which was originally placed under tribe Robinieae.

Systematics

Loteae and Robinieae are traditionally grouped under clade robinioids: these two major groups are primarily found in Europe, North America, and South America. [1] [4] Sesbanieae was a group included in 2005. [1]

Monophyly:

Monophyly of tribe Loteae: molecular data have shown support for monophyly with the exception for New World Lotus. Monophyly of Old World Lotus is moderately supported whereas New World Lotus is considered as paraphyletic. [5]

Monophyly of tribe Robinieae and Sesbanieae is strongly supported. Sesbanieae only has one genus Sesbania.

Intratribal relationship: Sesbanieae is either sister to Loteae, or sister to the rest of clade robinioids. [6] [7]

Related Research Articles

<span class="mw-page-title-main">Fabaceae</span> Family of legume flowering plants

The Fabaceae or Leguminosae, commonly known as the legume, pea, or bean family, are a large and agriculturally 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. 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.

<i>Camoensia</i> (plant) Genus of legumes

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.

<span class="mw-page-title-main">Galegeae</span> Tribe of leguminous plants

Galegeae is a tribe in the flowering plant family Fabaceae, subfamily Faboideae. The tribe is found mostly in the northern hemisphere, but can also be found in Australia, Africa, and South America. Recent molecular phylogenetic work has determined that tribe Galegeae is paraphyletic, and that its members are scattered throughout the IR-lacking clade.

<span class="mw-page-title-main">Crotalarieae</span> Tribe of legumes

Crotalarieae is a tribe of flowering plants belonging to the family Fabaceae. It includes rooibos (Aspalathus linearis), harvested for sale as a tisane.

<span class="mw-page-title-main">Cercidoideae</span> Subfamily of legumes

Cercidoideae is a subfamily in the pea family, Fabaceae. Well-known members include Cercis (redbuds), including species widely cultivated as ornamental trees in the United States and Europe, Bauhinia, widely cultivated as an ornamental tree in tropical Asia, and Tylosema, a semi-woody genus of Africa. The subfamily occupies a basal position within the Fabaceae and is supported as monophyletic in many molecular phylogenies. At the 6th International Legume Conference, the Legume Phylogeny Working Group proposed elevating the tribe Cercidae to the level of subfamily within the Leguminosae (Fabaceae). The consensus agreed to the change, which was fully implemented in 2017. It has the following clade-based definition:

The most inclusive crown clade containing Cercis canadensisL. and Bauhinia divaricataL. but not Poeppigia proceraC.Presl, Duparquetia orchidaceaBaill., or Bobgunnia fistuloides(Harms) J.H.Kirkbr. & Wiersema.

<span class="mw-page-title-main">Brongniartieae</span> Tribe of legumes

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."

<span class="mw-page-title-main">Indigofereae</span> Tribe of legumes

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.

<span class="mw-page-title-main">Sophoreae</span> Tribe of legumes

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.

<span class="mw-page-title-main">Swartzieae</span> Clade of legumes

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.

<span class="mw-page-title-main">Vataireoids</span> Clade of legumes

The vataireoids are an early-branching monophyletic clade of the flowering plant subfamily Faboideae that are mostly found in northern South America, primarily Brazil.

<span class="mw-page-title-main">Inverted repeat-lacking clade</span>

The inverted repeat-lacking clade(IRLC) is a monophyletic clade of the flowering plant subfamily Faboideae. Faboideae includes the majority of agriculturally-cultivated legumes. It 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 AstragalusL., HedysarumL., MedicagoL., OxytropisDC., SwainsonaSalisb., and TrifoliumL..

<span class="mw-page-title-main">ADA clade</span> Clade of flowering plants

The ADA clade is the earliest-branching monophyletic clade of the flowering plant subfamily Faboideae. Evidence for this clade was sparse until recent molecular phylogenies that included basal faboid genera that previously had been poorly sampled.

<span class="mw-page-title-main">Exostyleae</span> Clade of legumes

The tribe Exostyleae is an early-branching monophyletic clade of the flowering plant subfamily Faboideae that are mostly found in Neotropical rainforests.

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 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.

<span class="mw-page-title-main">Genistoids</span> Clade of legumes

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.

<span class="mw-page-title-main">Dalbergioids</span> Clade of legumes

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.

<span class="mw-page-title-main">Baphieae</span> Tribe of legumes

The tribe Baphieae is one of the subdivisions of the plant family Fabaceae. The Baphieae tribe arose 55.3 ± 0.4 million years ago.

<span class="mw-page-title-main">Mirbelioids</span> Group of legumes

The Mirbelioids are an informal subdivision of the plant family Fabaceae that includes the former tribes Bossiaeeae and Mirbelieae. They are consistently recovered as a monophyletic clade in molecular phylogenies. The Mirbelioids arose 48.4 ± 1.3 million years ago. Members of this clade are mostly ericoid (sclerophyllous) shrubs with yellow and red flowers found in Australia, Tasmania, and Papua-New Guinea. 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. Members of this clade exhibit unusual embryology compared to other legumes, either enlarged antipodal cells in the embryo sac or the production of multiple embryo sacs. There has been a shift from bee pollination to bird pollination several times in this clade. Mirbelioids produce quinolizidine alkaloids, but unlike most papilionoids, they do not produce isoflavones. Many of the Mirbelioids have pseudoraceme inflorescences.

Gwilym Peter Lewis is a British botanist, a curator at the Royal Botanic Gardens, Kew, and a leading expert on neotropical Leguminosae.

References

  1. 1 2 3 Lavin M, Herendeen PS, Wojciechowski MF (2005). "Evolutionary rates analysis of Leguminosae implicates a rapid diversification of lineages during the tertiary". Syst Biol . 54 (4): 575–94. doi: 10.1080/10635150590947131 . PMID   16085576.
  2. Lewis G, Lavin M, Schrire BD (2005). Legumes of the World. Royal Botanic Gardens, Kew. pp. 452–453. ISBN   978-1-900347-80-8.
  3. Dormer, 1945
  4. 1 2 Polhill, 1994
  5. Allan et al., 2003
  6. Wojciechowski et al., 2000
  7. Lavin et al., 2003

Bibliography

  • Polhill, R. M. (1994). Classification of the Leguminosae. Pages xxxv–xlviii in Phytochemical Dictionary of the Leguminosae (F. A. Bisby, J. Buckingham, and J. B. Harborne, eds.). Chapman and Hall, New York, NY.
  • Lavin M. and Schrire B. D. (2005). Sesbanieae. Pages 452-453 in Legumes of the world (Lewis et al., eds.). Royal Botanic Gardens, Kew, UK.
  • Lavin M. and Schrire B. D. (2005). Robinieae. Pages 467-473 in Legumes of the world (Lewis et al., eds.). Royal Botanic Gardens, Kew, UK.
  • Allan G. J., Zimmer E. A., Wagner W. L. and Sokoloff D. D.. (2003). Molecular phylogenetic analyses of tribe Loteae (Leguminosae): implications for classification and biogeography. Pages 371-393 in Advances in legume systematics, part 10: higher level systematics (B.B. Klitgaard and A. Bruneau, eds.). Royal Botanic Gardens, Kew, UK.
  • Wojciechowski M. F., Sanderson M. J., Steele K. P. and Liston A. (2000). Molecular phylogeny of the “temperate herbaceous tribes” of papilionoid legumes: a supertree approach. Pages 277-298 in Advances in Legume Systematics, part 9 (P. S. Herendeen and A. Bruneau, eds.). Royal Botanic Gardens, Kew, UK.
  • Dormer, K.J. (1945). An investigation of the taxonomic value of shoot structure in angiosperms with especial reference to Leguminosae. Ann. Bot., n.s. 9: 141-153.