Caesalpinioideae Explained
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.[1] 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:
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
In some classifications, for example the
Cronquist system, the group is recognized at the rank of family, Caesalpiniaceae.
Characteristics
- Specialised extrafloral nectaries often present on the petiole and / or on the primary and secondary rachises, usually between pinnae or leaflet pairs
- Leaves commonly bipinnate
- Inflorescences globose, spicate
- Aestivation valvate
- Anthers often with a stipitate or sessile apical gland
- Pollen commonly in tetrads, bitetrads or polyads
- Seeds usually with an open or closed pleurogram on both faces
- Root nodules variably present and indeterminate
- 10 Stamens, aside from various core mimosoid genera bearing a few factors more
Taxonomy
See main article: Caesalpinieae.
- Cassieae Clade
- Dimorphandra Group A
- Dimorphandra Group B
- Peltophorum Clade
-
- Tachigali Clade
- Umtiza Clade
- Unassigned
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.[2] [3] [4] [5] Consequently, the subfamilies of Fabaceae were reorganized to make them monophyletic.[6] Caesalpinioideae, as currently defined, contains the following subclades:[3]
Notes and References
- Web site: Flowers in Singapore.
- Bruneau A, Forest F, Herendeen PS, Klitgaard BB, Lewis GP . 2001 . Phylogenetic Relationships in the Caesalpinioideae (Leguminosae) as Inferred from Chloroplast trnL Intron Sequences . . 26 . 3 . 487–514 . 10.1043/0363-6445-26.3.487. 31 January 2024 .
- Bruneau A, Mercure M, Lewis GP, Herendeen PS . 2008 . Phylogenetic patterns and diversification in the caesalpinioid legumes . Botany . 86 . 7 . 697–718 . 10.1139/B08-058.
- Manzanilla V, Bruneau A . 2012 . Phylogeny reconstruction in the Caesalpinieae grade (Leguminosae) based on duplicated copies of the sucrose synthase gene and plastid markers . . 65 . 1 . 149–162 . 10.1016/j.ympev.2012.05.035. 22699157 .
- 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 . 10.1016/j.sajb.2013.05.001. free . 10566/3193 . free .
- The Legume Phylogeny Working Group (LPWG). . 2017 . A new subfamily classification of the Leguminosae based on a taxonomically comprehensive phylogeny . . 66 . 1 . 44–77 . 10.12705/661.3. free . 10568/90658 . free .