Sophoreae

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Sophoreae
Kowhai flowers.jpg
Sophora tetraptera
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Clade: Rosids
Order: Fabales
Family: Fabaceae
Subfamily: Faboideae
Clade: Meso-Papilionoideae
Clade: Genistoids
Clade: Core Genistoids
Tribe: Sophoreae
(Spreng. ex DC. 1825) Cardoso et al. 2013 [1] [2]
Genera

See text

Synonyms [2]
  • Euchresteae (Nakai) H.Ohashi 1973
  • Sophora group sensu Polhill 1994
  • Sophoreae sensu stricto
  • Sophoreae sensu Polhill 1981pro parte 7
  • Thermopsideae Yakovlev 1972

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. [2] [3] [4] Various morphological [5] [6] [7] [8] and molecular [9] [10] [11] [12] [13] analyses indicated that Sophoreae as traditionally circumscribed was polyphyletic. [14] This led to a re-circumscription of Sophoreae, which resulted in the transfer of many genera to other tribes (Amburaneae, Angylocalyceae, Baphieae, Camoensieae, the Cladrastis clade, Exostyleae, Leptolobieae, Ormosieae, Podalyrieae, and the Vataireoids). [2] This also necessitated the inclusion of two former tribes, Euchresteae and Thermopsideae, in the new definition of Sophoreae. [2] [15] [16] [17] [18] Tribe Sophoreae, as currently circumscribed, consistently forms a monophyletic clade in molecular phylogenetic analyses. [2] [12] [17] [19] [20] [21] [22] The Sophoreae arose 40.8 ± 2.4 million years ago (in the Eocene). [8] [23]

Contents

Description of morphological synapomorphies has yet to be undertaken, but members of this tribe can be distinguished by the relatively simple flowers, unspecialized pinnate leaves, accumulation of quinolizidine alkaloids, [24] and the presence of free stamens. [2] The tribe does have a node-based definition: the crown clade originating from the most recent common ancestor of Bolusanthus speciosus (Bolus) Harms and Sophora davidii (Franch.) Pavol.. [23]

Genera

Sophoreae comprises the following genera: [2]

Notes

  1. ↑ Often included in Sophora , rather than treated as a segregate genus.

Related Research Articles

<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">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.

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.

<i>Luetzelburgia</i> Genus of legumes

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.

<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">Podalyrieae</span> Tribe of legumes

The tribe Podalyrieae is one of the subdivisions of the plant family Fabaceae.

<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> 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.

<i>Cladrastis</i> clade Clade of legumes

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 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.

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.

<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.

References

  1. ↑ Wojciechowski MF (2013). "Towards a new classification of Leguminosae: Naming clades using non-Linnaean phylogenetic nomenclature". S Afr J Bot . 89: 85–93. doi: 10.1016/j.sajb.2013.06.017 .
  2. 1 2 3 4 5 6 7 8 Cardoso D, Pennington RT, de Queiroz LP, Boatwright JS, Van Wyk B-E, Wojciechowski 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 .
  3. ↑ Polhill RM (1981). "Sophoreae". In Polhill RM, Raven PH (eds.). Advances in Legume Systematics, Parts 1 and 2. Royal Botanic Gardens, Kew. pp. 213–230. ISBN   9780855212247.
  4. ↑ Polhill RM (1994). "Classification of the Leguminosae". In Bisby FA, Buckingham J, Harborne JB (eds.). Phytochemical Dictionary of the Leguminosae, Plants and Their Constituents, Volume 1. Chapman and Hall/CRC Press, London. pp. xxv–xlvii. ISBN   9780412397707.
  5. ↑ Chappill JA (1995). "Cladistic analysis of the Leguminosae: the development of an explicit hypothesis". In Crisp MD, Doyle JJ (eds.). Advances in Legume Systematics, Part 7: Phylogeny. Royal Botanic Gardens, Kew. pp. 1–9. ISBN   978-0947643799.
  6. ↑ Herendeen PS (1995). "Phylogenetic relationships of the tribe Swartzieae". In Crisp MD, Doyle JJ (eds.). Advances in Legume Systematics, Part 7: Phylogeny. Royal Botanic Gardens, Kew. pp. 123–132. ISBN   978-0947643799.
  7. ↑ Ferguson IK, Schrire BD, Shepperton R (1994). "Pollen morphology of the tribe Sophoreae and relationships between subfamilies Caesalpinioideae and Papilionoideae". In Ferguson IK, Tucker SC (eds.). Advances in Legume Systematics, Part 6: Structural Botany. Royal Botanic Gardens, Kew. pp. 53–96. ISBN   978-0947643782.
  8. 1 2 Crepet WL, Herendeen PS (1992). "Papilionoid flowers from the early Eocene of southeastern North America". In Herendeen PS, Dilcher DL (eds.). Advances in Legume Systematics, Part 4: The Fossil Record. Royal Botanic Gardens, Kew. pp. 43–55. ISBN   978-0947643409.
  9. ↑ Käss E, Wink M (1996). "Molecular evolution of the Leguminosae: Phylogeny of the three subfamilies based on rbcL-sequences". Biochem Syst Ecol . 24 (5): 365–378. doi:10.1016/0305-1978(96)00032-4.
  10. ↑ Doyle JJ, Doyle JL, Ballenger JA, Palmer JD (1996). "The distribution and phylogenetic significance of a 50-Kb chloroplast DNA inversion in the flowering plant family Leguminosae". Mol Phylogenet Evol . 5 (2): 429–438. doi: 10.1006/mpev.1996.0038 . PMID   8728401.
  11. ↑ Doyle JJ, Doyle JL, Ballenger JA, Dickson EE, Kajita T, Ohashi H (1997). "A phylogeny of the chloroplast gene rbcL in the Leguminosae: taxonomic correlations and insights into the evolution of nodulation". Am J Bot . 84 (4): 541–554. doi: 10.2307/2446030 . JSTOR   2446030. PMID   21708606.
  12. 1 2 Pennington RT, Lavin M, Ireland H, Klitgaard B, Preston J, Hu J-M (2001). "Phylogenetic relationships of basal papilionoid legumes based upon sequences of the chloroplast trnL intron". Syst Bot . 55 (5): 818–836. doi:10.1043/0363-6445-26.3.537 (inactive 31 January 2024). JSTOR   3093980.{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)
  13. ↑ Pennington RT, Klitgaard BB, Ireland H, Lavin M (2000). "New insights into floral evolution of basal Papilionoideae from molecular phylogenies". In Herendeen PS, Bruneau A (eds.). Advances in Legume Systematics, Part 9. Royal Botanic Gardens, Kew. pp. 233–248. ISBN   978-1842460177.
  14. ↑ Pennington RT, Stirton CH, Schrire BD (2005). "Tribe Sophoreae". In Lewis G, Schrire B, Mackinder B, Lock M (eds.). Legumes of the World. Royal Botanic Gardens, Kew. pp. 227–249. ISBN   978-1900347808.
  15. ↑ Lock JM (2005). "Tribe Thermopsideae". In Lewis G, Schrire B, Mackinder B, Lock M (eds.). Legumes of the World. Royal Botanic Gardens, Kew. pp. 263–265. ISBN   978-1900347808.
  16. ↑ Ohashi H. (2005). "Tribe Euchresteae". In Lewis G, Schrire B, Mackinder B, Lock M (eds.). Legumes of the World. Royal Botanic Gardens, Kew. pp. 260–261. ISBN   978-1900347808.
  17. 1 2 LPWG [Legume Phylogeny Working Group] (2013). "Legume phylogeny and classification in the 21st century: progress, prospects and lessons for other species-rich clades" (PDF). Taxon . 62 (2): 217–248. doi:10.12705/622.8. hdl:10566/3455.
  18. ↑ Wang HC, Sun H, Compton JA, Yang JB (2006). "A phylogeny of Thermopsideae (Leguminosae: Papilionoideae) inferred from nuclear ribosomal internal transcribed spacer (ITS) sequences". Bot J Linn Soc . 151 (3): 365–373. doi: 10.1111/j.1095-8339.2006.00512.x .
  19. ↑ Hu J-M, Lavin M, Wojciechowski MF, Sanderson MJ (2002). "Phylogenetic analysis of nuclear ribosomal ITS/5.85 sequences in the tribe Millettieae (Fabaceae): Poecilanthe–Cyclolobium, the core Millettieae, and the Callerya group". Syst Bot . 27 (4): 722–733. doi:10.1043/0363-6445-27.4.722 (inactive 31 January 2024).{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)
  20. ↑ Cardoso D, de Queiroz LP, Pennington RT, de Lima HC, Fonty É, Wojciechowski MF, Lavin M (2012). "Revisiting the phylogeny of papilionoid legumes: new insights from comprehensively sampled early-branching lineages". Am J Bot . 99 (12): 1991–2013. doi:10.3732/ajb.1200380. PMID   23221500.
  21. ↑ Wojciechowski MF, Lavin M, Sanderson MJ (2004). "A phylogeny of legumes (Leguminosae) based on analysis of the plastid matK gene resolves many well-supported subclades within the family". Am J Bot . 91 (11): 1846–1862. doi: 10.3732/ajb.91.11.1846 . PMID   21652332.
  22. ↑ Kajita T, Ohashi H, Takeishi Y, Bailey CD, Doyle JJ (2001). "RbcL and legume phylogeny, with particular reference to Phaseoleae, Millettieae, and allies". Syst Bot . 26 (3): 515–536. doi:10.1043/0363-6445-26.3.515 (inactive 31 January 2024).{{cite journal}}: CS1 maint: DOI inactive as of January 2024 (link)
  23. 1 2 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.
  24. ↑ Wink M, Mohamed GIA (2003). "Evolution of chemical defense traits in the Leguminosae: mapping of distribution patterns of secondary metabolites on a molecular phylogeny inferred from nucleotide sequences of the rbcL gene". Biochem Syst Ecol . 31 (8): 897–917. doi:10.1016/S0305-1978(03)00085-1.
  25. ↑ Edwards D, Hawkins JA (2007). "Are Cape floral clades the same age? Contemporaneous origins of two lineages in the genistoids s.l. (Fabaceae)". Mol Phylogenet Evol . 45 (3): 952–70. doi:10.1016/j.ympev.2007.09.014. PMID   17980626.
  26. ↑ Uysal T, Ertuğrul K, Bozkurt M (2014). "A new genus segregated from Thermopsis (Fabaceae: Papilionoideae): Vuralia". Plant Systematics and Evolution . 300 (7): 1627–1637. doi:10.1007/s00606-014-0988-x. S2CID   15019593.
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