Dialioideae

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Dialioideae
Dialium schlechteri00.jpg
Dialium schlechteri Harms
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Fabales
Family: Fabaceae
Subfamily: Dialioideae
Legume Phylogeny Working Group [1]
Type genus
Dialium
L.
Genera

See text

Synonyms
  • Dialiinae H.S.Irwin & Barneby 1981
  • Dialiinae Clade [2]
  • Labicheinae H.S.Irwin & Barneby 1981

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:

Contents

The most inclusive crown clade containing Poeppigia procera C.Presland Dialium guianense (Aubl.) Sandwith, but not Cercis canadensis L., Duparquetia orchidacea Baill., or Bobgunnia fistuloides (Harms) J. H. Kirkbr. & Wiersema [1]

Members of the family also share the following morphological characteristics: the presence of cymose inflorescences, the absence of vestured pits in the xylem, and a high degree of organ loss. [2] [3]

Taxonomy

Dialioideae comprises the following genera: [1]

Phylogenetics

Dialioideae exhibits the following phylogenetic relationships: [4] (compare [2] [5] [6] [7] )

Fabales

outgroup

Dialioideae

Poeppigia

Eligmocarpus

Baudouinia

Uittienia

Zenia

Distemonanthus

Apuleia

Koompassia

Martiodendron

Mendoravia

Storckiella

Kalappia

Petalostylis

Labichea

Dialium (including Dicorynia and Androcalymma )

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">Caesalpinioideae</span> Subfamily of legumes

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. The Caesalpinioideae are mainly trees distributed in the moist tropics, but include such temperate species as the honeylocust and Kentucky coffeetree. It has the following clade-based definition:

The most inclusive crown clade containing Arcoa gonavensisUrb. and Mimosa pudicaL., but not Bobgunnia fistuloides(Harms) J. H. Kirkbr. & Wiersema, Duparquetia orchidaceaBaill., or Poeppigia proceraC.Presl

<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.

<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 Myanmar and Thailand to Peninsular Malaysia, Borneo, the Philippines, Java, the Lesser Sunda Islands, New Guinea, the Bismarck Archipelago, and Australia. 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.

<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">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">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.

<i>Lysiphyllum hookeri</i> Species of legume

Lysiphyllum hookeri is a species of small tree endemic to Queensland, Australia, of the legume plant family Fabaceae. These trees are known by a variety of common names, including pegunny, alibangbang, Hooker's bauhinia, white bauhinia, mountain ebony and Queensland ebony.

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

The robinioids are one of the four major clades 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.

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

The inverted repeat-lacking clade(IRLC) is a monophyletic clade of the flowering plant subfamily Faboideae (or Papilionaceae). 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 (in the Eocene). It includes several large, temperate genera such as AstragalusL., HedysarumL., MedicagoL., OxytropisDC., SwainsonaSalisb., and TrifoliumL..

<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.

<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">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.

References

  1. 1 2 3 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 .
  2. 1 2 3 Herendeen PS, Bruneau A, Lewis GP (2003). "Phylogenetic relationships in Caesalpinioid legumes: A preliminary analysis based on morphological and molecular data". In Klitgaard BB, Bruneau A (eds.). Advances in Legume Systematics, Part 10: Higher Level Systematics. Royal Botanic Gardens, Kew. pp. 37–62. ISBN   9781842460542.
  3. Zimmerman E, Prenner G, Bruneau A (2013). "Floral ontogeny in Dialiinae (Caesalpinioideae: Cassieae), a study in organ loss and instability". South African Journal of Botany. 89: 188–209. doi: 10.1016/j.sajb.2013.06.020 .
  4. Zimmerman E. (2014). Systematics and floral evolution of the Dialiinae (Caesalpinioideae), a diverse lineage of tropical legumes (Ph.D). Papyrus: Institutional Repository, Université de Montréal. hdl:1866/11208.
  5. 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)
  6. 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.
  7. 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.