Caesalpinioideae

Last updated

Caesalpinioideae
Temporal range: Middle Paleocene - recent [1]
RoyalPoinciana.jpg
Royal poinciana, Delonix regia
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Fabales
Family: Fabaceae
Subfamily: Caesalpinioideae
DC. 1825
Type genus
Caesalpinia
L.
Clades

See text

Synonyms
  • Cercidoideae Burmeist. 1837
  • GCM Clade Marazzi et al. 2012 [2]
  • MCC Clade Doyle 2011 [3] [4]
  • Mimosoideae DC. 1825
Chamaecrista absus Chamaecrista absus W2 IMG 3465.jpg
Chamaecrista absus

Caesalpinioideae is a botanical name at the rank of subfamily, placed in the large family Fabaceae or Leguminosae. Its name is formed from the generic name Caesalpinia . It is known also as the peacock flower subfamily. [5] The Caesalpinioideae are mainly trees distributed in the moist tropics, but include such temperate species as the honeylocust ( Gleditsia triacanthos ) and Kentucky coffeetree ( Gymnocladus dioicus ). It has the following clade-based definition:

Contents

The most inclusive crown clade containing Arcoa gonavensis Urb. and Mimosa pudica L., but not Bobgunnia fistuloides (Harms) J. H. Kirkbr. & Wiersema, Duparquetia orchidacea Baill., or Poeppigia procera C.Presl [6]

In some classifications, for example the Cronquist system, the group is recognized at the rank of family, Caesalpiniaceae.

Characteristics

Taxonomy

Phylogenetics

Caesalpinioideae, as it was traditionally circumscribed, was paraphyletic. Several molecular phylogenies in the early 2000s showed that the other two subfamilies of Fabaceae (Faboideae and Mimosoideae) were both nested within Caesalpinioideae. [7] [8] [9] [10] Consequently, the subfamilies of Fabaceae were reorganized to make them monophyletic. [6] Caesalpinioideae, as currently defined, contains the following subclades: [8]

Fabales

Faboideae (outgroup)

Caesalpinioideae

Umtiza clade

Dimorphandra group A

Tachigali clade

Peltophorum clade

Dimorphandra group B (with the mimosoid clade nested within)

Related Research Articles

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

The Mimosoideae are a traditional subfamily of trees, herbs, lianas, and shrubs in the pea family (Fabaceae) that mostly grow in tropical and subtropical climates. They are typically characterized by having radially symmetric flowers, with petals that are twice divided (valvate) in bud and with numerous showy, prominent stamens.

<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.

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

The subfamily Detarioideae is one of the subdivisions of the plant family Fabaceae (legumes). This subfamily includes many tropical trees, some of which are used for timber or have ecological importance. The subfamily consists of 84 genera, most of which are native to Africa and Asia. Pride of Burma and tamarind are two of the most notable species in Detarioideae. It has the following clade-based definition:

The most inclusive crown clade containing Goniorrhachis marginataTaub. and Aphanocalyx cynometroidesOliv., but not Cercis canadensisL., Duparquetia orchidaceaBaill., or Bobgunnia fistuloides(Harms) J. H. Kirkbr. & Wiersema.

<i>Parkia</i> Genus of plants

Parkia is a genus of flowering plants in the family Fabaceae. It belongs to the mimosoid clade of the subfamily Caesalpinioideae. Several species are known as African locust bean.

<i>Dimorphandra</i> Genus of legumes

Dimorphandra is a genus of legume in the family Fabaceae, subfamily Caesalpinioideae. It includes 26 species native to northern South America, ranging from Colombia and Venezuela to Bolivia, Paraguay, and southeastern Brazil.

<i>Macrosamanea</i> Genus of legumes

Macrosamanea is a genus of flowering plant in the legume family, Fabaceae. It includes 11 species of trees and shrubs native to northern South America. The genus is most diverse and numerous in the Amazon Basin, extending into the Orinoco basin and the Guianas. Typical habitat is tropical rain forest, mostly riparian and seasonally-flooded. Two species are native to seasonally-inundated wooded grassland (savanna) on sandy soils. The genus belongs to the mimosoid clade of the subfamily Caesalpinioideae.

<i>Stryphnodendron</i> Genus of legumes

Stryphnodendron is a genus of flowering plant in the legume family, Fabaceae. It includes 28 species of trees and suffrutices native to the tropical Americas, ranging from Nicaragua to Bolivia, Paraguay, and southern Brazil. Typical habitats include tropical rain forest and riparian forest, seasonally dry forest, cerrado, and caatinga. It belongs to the mimosoid clade of the subfamily Caesalpinioideae.

<i>Tachigali</i> Genus of legumes

Tachigali is a flowering plant genus in the legume family (Fabaceae). It includes 74 species of trees native to the tropical Americas, ranging from Nicaragua to Bolivia, Paraguay, and southern Brazil. Typical habitats include tropical rain forest, lower montane forest, seasonally-flooded and non-flooded evergreen lowland forest and woodland, gallery and riparian forest, sometimes on white sands, cerrado and other dry woodland, and rocky grassland.

<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.

<i>Lysiphyllum</i> Genus of legumes

Lysiphyllum is a genus of flowering plants in the legume family, Fabaceae. It includes nine species of trees, semi-scandent shrubs, and lianas which range from India through Southeast Asia to Australasia. Typical habitats include seasonally-dry tropical forest and woodland, vine thickets, Brigalow and Gidgee scrubland, floodplains, alluvial flats, tidal forest, mangroves, river and stream banks, and occasionally dunes and coral islets. They can grow on diverse soils including calcareous, granitic, and basaltic.

<i>Paloue</i> Genus of legumes

Paloue is a genus of flowering plants in the family Fabaceae. It belongs to the subfamily Detarioideae. The genera was first created with the description of Paloue guianensis by Aublet in 1775.

<i>Pentaclethra</i> Genus of legumes

Pentaclethra is a small genus of trees from the tropics. They are flowering plants in the family Fabaceae. They belong to the mimosoid clade of the subfamily Caesalpinioideae.

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

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.

<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">Caesalpinieae</span> Tribe of legumes

The tribe Caesalpinieae is one of the subdivisions of the plant family Fabaceae: subfamily Caesalpinioideae.

<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.

<i>Mezoneuron</i> Genus of legumes

Mezoneuron is a genus of flowering plants in the legume family, Fabaceae. It belongs to the subfamily Caesalpinioideae and the tribe Caesalpinieae.

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

The subfamily Dialioideae is one of the subdivisions of the plant family Fabaceae (legumes). This subfamily includes many tropical trees and shrubs. The subfamily consists of 17 genera, which are widespread throughout the tropics. It has the following clade-based definition:

The most inclusive crown clade containing Poeppigia proceraC.Presland Dialium guianense(Aubl.) Sandwith, but not Cercis canadensisL., Duparquetia orchidaceaBaill., or Bobgunnia fistuloides(Harms) J. H. Kirkbr. & Wiersema

References

  1. "Fabales". www.mobot.org. Retrieved 2023-06-16.
  2. Marazzi B, Ané C, Simon MF, Delgado-Salinas A, Luckow M, Sanderson MJ (2012). "Locating evolutionary precursors on a phylogenetic tree". Evolution . 66 (12): 3918–3930. doi:10.1111/j.1558-5646.2012.01720.x. PMID   23206146. S2CID   8336248.
  3. Doyle JJ (2011). "Phylogenetic perspectives on the origins of nodulation". Molecular Plant-Microbe Interactions. 24 (11): 1289–1295. doi: 10.1094/MPMI-05-11-0114 . PMID   21995796.
  4. Doyle JJ (2012). "Polyploidy in legumes". In Soltis PS, Soltis DE (eds.). Polyploidy and genome evolution. Berlin, Heidelberg: Springer. pp. 147–180. doi:10.1007/978-3-642-31442-1_9. ISBN   978-3-642-31441-4.
  5. "Flowers in Singapore".
  6. 1 2 The Legume Phylogeny Working Group (LPWG). (2017). "A new subfamily classification of the Leguminosae based on a taxonomically comprehensive phylogeny". Taxon . 66 (1): 44–77. doi: 10.12705/661.3 . hdl: 10568/90658 .
  7. Bruneau A, Forest F, Herendeen PS, Klitgaard BB, Lewis GP (2001). "Phylogenetic Relationships in the Caesalpinioideae (Leguminosae) as Inferred from Chloroplast trnL Intron Sequences". Syst Bot . 26 (3): 487–514. doi:10.1043/0363-6445-26.3.487 (inactive 31 January 2024).{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)
  8. 1 2 Bruneau A, Mercure M, Lewis GP, Herendeen PS (2008). "Phylogenetic patterns and diversification in the caesalpinioid legumes". Botany. 86 (7): 697–718. doi:10.1139/B08-058.
  9. Manzanilla V, Bruneau A (2012). "Phylogeny reconstruction in the Caesalpinieae grade (Leguminosae) based on duplicated copies of the sucrose synthase gene and plastid markers". Molecular Phylogenetics and Evolution . 65 (1): 149–162. doi:10.1016/j.ympev.2012.05.035. PMID   22699157.
  10. Cardoso D, Pennington RT, de Queiroz LP, Boatwright JS, Van Wykd B-E, Wojciechowskie MF, Lavin M (2013). "Reconstructing the deep-branching relationships of the papilionoid legumes". S. Afr. J. Bot. 89: 58–75. doi: 10.1016/j.sajb.2013.05.001 .