1. Family: Fabaceae Lindl.
    1. Peltophorum (Vogel) Benth.

      1. This genus is accepted, and is native to Asia-Tropical, Africa, Southern America, Northern Territory and Asia-Temperate..

    [FTEA]

    Leguminosae, J. B. Gillett, R. M. Polhill & B. Verdcourt. Flora of Tropical East Africa. 1971

    Habit
     is a genus of trees rather closely related to Bussea (p. 25), with similar yellow flowers and a peltate stigma, but with a flattened indehiscent pod winged along both sutures.
    [LOWO]

    Legumes of the World. Edited by G. Lewis, B. Schrire, B. MacKinder & M. Lock. Royal Botanic Gardens, Kew. (2005)

    Habit
    Trees
    Ecology
    Seasonally dry tropical and evergreen (mainly lowland) forest, beaches and mangrove forest, coastal monsoon vine thicket, flood plains and tidal flats, bushveld and woodland
    Distribution
    pantropical (into the subtropics) with 2 native to the Neotropics (1 in E Brazil, N Uruguay, NE Argentina, Paraguay, Bolivia and the Caribbean, the other restricted to Venezuela, although this probably conspecific with the first), 1 native to southern Africa, 1 in Malesia (Sabah, Sarawak, Kalimantan), and 2 widespread in Asia (Thailand, Cambodia, Laos, Vietnam, and Peninsula Malaysia, 1 extending to Sumatra and Java, the other to Sri Lanka, the Philippines, and N Australia); many species widely cultivated
    Note
    Polhill & Vidal (1981) and Polhill (1994) included the genus in the Peltophorum group of tribe Caesalpinieae, a placement confirmed by the molecular analysis of Haston et al. (2003) in which Peltophorum is sister to Bussea. Peltophorum venezuelense L.Cárdenas, Rodr.-Rodr. & Varela probably best treated as conspecific with P. dubium (Spreng.) Taub., thus limiting the Neotropics to a single indigenous species

    Polhill & Vidal (1981) divided the Caesalpinieae into 8 informal generic groups: the Gleditsia group (2 genera), the Acrocarpus group (monogeneric), the Sclerolobium group (3 genera), the Peltophorum group (13 genera), the Caesalpinia group (16 genera), the Poeppigia and Pterogyne groups (both monogeneric) and the Dimorphandra group (10 genera). They commented that the tribe is “a remarkable mixture of relics and complexes of relatively recent speciation, providing many pitfalls for formal systematics and biogeographical interpretations”. Polhill (1994) added a ninth informal group, the monogeneric Orphanodendron group, and placed Cordeauxia as a synonym of Stuhlmannia (both genera recognised in the present treatment) so that the total of 47 genera in the tribe remained unchanged. Within the tribe, Parkinsonia (including Cercidium), Conzattia and Lemuropisum were moved from the Caesalpinia group to the Peltophorum group (Polhill, 1994) in agreement with the subsequently published works of Lewis & Schrire (1995) and Du Puy et al. (1995b).

    Since 1994 several studies have cast new light on intergeneric relationships within the Caesalpinieae, necessitating the restructuring of some of the nine informal generic groups presented by Polhill (1994). As pointed out in the introduction to tribe Cassieae, the genus Ceratonia has been removed from that tribe to the Caesalpinieae, and Poeppigia has been removed from the Caesalpinieae to the Cassieae (for further detail see discussion under each genus). In the rbcL phylogeny of Doyle et al. (1997) the Caesalpinieae, as traditionally circumscribed, was shown to be paraphyletic with members scattered throughout a clade which also included genera of the Cassieae and one mimosoid genus. The molecular analysis of Kajita et al. (2001) also found the Caesalpinieae to be non-monophyletic. In the molecular analysis of Bruneau et al. (2001) some of the informal generic groups of Polhill (1994) were supported as monophyletic but the tribe as a whole was clearly demonstrated to be paraphyletic. With regard to intergeneric relationships, Pterogyne resolved as sister to a Caesalpinia group clade; Batesia and Vouacapoua fell outside a core- Peltophorum group, and the Dimorphandra group was clearly shown to be a diverse assemblage of genera, many of which share certain characteristics with the Mimosoideae, specifically with members of tribe Mimoseae (Bruneau et al., 2001). Erythrophleum was sister to a clade that comprised the majority of the Mimosoideae sampled, and Pachyelasma was sister to the two mimosoid genera Pentaclethra and Calpocalyx. Herendeen et al. (2003a) in a combined molecular-morphological analysis which expanded on the study of Bruneau et al. (2001), presented an ‘Umtiza clade’ containing Gymnocladus and Gleditsia (the two members of Polhill and Vidal’s Gleditsia Group), Umtiza (traditionally included in tribe Detarieae), Tetrapterocarpon (from the Dimorphandra Group), Acrocarpus (the sole genus of the Acrocarpus Group), and Ceratonia (from subtribe Ceratoniinae in tribe Cassieae). This new generic grouping raises some fascinating phytogeographical questions (see Schrire et al., pages 21–54, this volume). Pterogyne resolved as sister to a Chamaecrista-Senna clade (of tribe Cassieae) a relationship worthy of further study; Batesia and Vouacapoua again fell outside the core-Peltophorum group; Dimorphandra grouped with Mora as sister to all Mimosoideae, and Pachyelasma grouped with Erythrophleum as sister to the Dimorphandra-Mimosoideae clade. In the phylogenetic investigation of Haston et al. (2003), the Peltophorum group of Polhill (1994) was non-monophyletic but there was support for a core-Peltophorum group comprising Peltophorum, Parkinsonia, Schizolobium, Conzattia, Delonix, Lemuropisum, Colvillea and Bussea. Pterogyne resolved as sister to a clade containing Haematoxylum and Cordeauxia (both of the Caesalpinia group), thus supporting the earlier findings of Bruneau et al. (2001) rather than those of Herendeen et al. (2003a). Haston et al. (submitted) have further refined the relationships of the non core-Peltophorum group genera. They place Arapatiella and Jacqueshuberia with Tachigali in a newly defined Tachigali group and find strong molecular support for associating Batesia with Recordoxylon and Melanoxylon in a new Batesia group. Moldenhawera is placed in its own monogeneric group sister to a Tachigali group–core-Peltophorum group–Dimorphandra group–Mimosoideae clade. In an analysis testing the monophyly of the Umtiza clade (Herendeen et al., 2003b), Arcoa (traditionally of the Dimorphandra group) from the Dominican Republic was added to the group of genera in that clade.

    Without doubt, the genus with the greatest taxonomic and nomenclatural complexity within the Caesalpinieae is the type genus Caesalpinia, which in its broadest sense comprises c. 140 spp. and contains 25 generic names in synonymy. Of these 140 species, 12–15 predominantly Asian taxa have still to be included in molecular studies and cannot yet be assigned to any generic segregate recognised in this treatment (see notes under Caesalpinia L.). Studies by Lewis & Schrire (1995), Simpson & Miao (1997), Lewis (1998), Simpson (1998, 1999), Simpson & Lewis (2003) and Simpson et al. (2003), have clearly demonstrated that Caesalpinia, as traditionally circumscribed, is polyphyletic. In this treatment Hoffmannseggia is recognised as distinct following Simpson & Miao (1997), Simpson (1999) and Ulibarri (1979, 1996); Pomaria is also segregated from Caesalpinia sens. lat. following Simpson (1998) and Simpson & Lewis (2003). The genera Coulteria, Erythrostemon, Guilandina, Libidibia, Mezoneuron, Poincianella and Tara are also reinstated following the findings of Lewis & Schrire (1995), Lewis (1998), Simpson et al. (2003), Lewis & Bruneau (unpublished), Lewis & Lavin (unpublished) and Sotoyo (unpublished). Caesalpinia sens. strict. is, in consequence, reduced to a genus of 25 species.

    The Caesalpinieae as presented here contains 56 genera and (423)–436–(448) species (Fig. 23). Thirty two of the genera contain 3 or fewer species each, with 23 monospecific (a second species of Orphanodendron has apparently been discovered in Colombia, but is, as yet, undescribed [Cogollo Pacheco, pers. comm., 2002]). A new genus, tentatively named as Heteroflorum by Sousa & Delgado (1993), but not yet formally published, is a monospecific Mexican endemic closely related to Conzattia. It is not dealt with here. The informal generic groups of tribe Caesalpinieae presented by Polhill & Vidal (1981) and Polhill (1994) are retained in part in Fig. 23 which accompanies this treatment, but there are some noteworthy exceptions. The Gleditsia and Acrocarpus groups are both subsumed into the ‘Umtiza clade’; Diptychandra is rejected from the Sclerolobium group which now becomes the Tachigali group and includes Arapatiella and Jacqueshuberia; Poeppigia is moved to the Cassieae; several genera are removed from the Peltophorum group leaving a core of nine related genera (if Heteroflorum is included); Batesia, together with Recordoxylon and Melanoxylon constitutes a new Batesia group based on the work of Haston et al. (submitted). Moldenhawera is placed in its own group as its generic relationships are currently unclear (Haston et al., submitted). The Caesalpinia group increases in size from 12 to 21 genera. Five genera are currently too poorly known for them to be placed with confidence: Campsiandra, Chidlowia, Diptychandra, Orphanodendron and Vouacapoua.

    [FZ]

    Leguminosae, R.K. Brummitt, A.C. Chikuni, J.M. Lock & R.M. Polhill. Flora Zambesiaca 3:2. 2007

    Habit
    Small to medium trees, unarmed.
    General
    Young shoots and inflorescences covered with brown indumentum and sometimes scattered stalked, swollen-headed glands.
    Leaves
    Leaves alternate, bipinnate, without specialised glands; pinnae up to 21 pairs; leaflets up to 32 pairs per pinna, usually oblong; stipules caducous.
    Flowers
    Flowers in terminal and lateral racemes often aggregated to form a pseudopanicle; bracts usually linear-lanceolate, caducous.
    Receptacle
    Receptacle comprising a lower narrow part simulating the pedicel and an upper broad shallow disc.
    Calyx
    Sepals appearing separate but actually joined by a very short tube [see note], imbricate with scarious margins, usually reflexed in flower.
    Corolla
    Petals somewhat unequal, the upper one shorter than the others, all ± spathulate with brown pubescence on the outside of the claw and extending up the middle of the blade.
    Stamens
    Stamens 10, not exceeding the petals; filaments glabrous in the upper part but the broader basal part conspicuously brown-villous; anthers dorsifixed, dehiscing by longitudinal slits.
    Pistil
    Ovary subsessile, brown-pubescent or -tomentose; style pubescent in lower part, gradually becoming glabrous distally; stigma peltate.
    Fruits
    Pods 4–12 cm long, oblong to narrowly elliptic, not conspicuously pubescent, strongly compressed, with distinct wings 3–6 mm broad along each margin, indehiscent; seeds 1 to few, oblong or discoid, strongly compressed, elongated longitudinally within the pod.
    [LOWO]
    Use
    Widely cultivated for ornament and shade; some species used for carpentry, planking, furniture and fuelwood; leaves used for livestock fodder; some medicinal uses and dyes

    Images

    Distribution

    Native to:

    Angola, Argentina Northeast, Bahamas, Bismarck Archipelago, Bolivia, Borneo, Botswana, Brazil North, Brazil Northeast, Brazil South, Brazil Southeast, Brazil West-Central, Cambodia, Caprivi Strip, China Southeast, Cuba, Dominican Republic, Guyana, Hainan, Haiti, Jawa, KwaZulu-Natal, Laos, Malawi, Malaya, Mozambique, Namibia, New Guinea, Northern Provinces, Northern Territory, Paraguay, Philippines, Sri Lanka, Sulawesi, Sumatera, Swaziland, Thailand, Uruguay, Venezuela, Vietnam, Zambia, Zaïre, Zimbabwe

    Introduced into:

    Andaman Is., Assam, Bangladesh, Burkina, Burundi, California, China South-Central, East Himalaya, Fiji, Florida, French Guiana, Gabon, Gambia, Ghana, Guinea, Gulf of Guinea Is., Hawaii, Honduras, India, Ivory Coast, Kenya, Laccadive Is., Leeward Is., Lesser Sunda Is., Liberia, Madagascar, Maldives, Mexico Southwest, Nicobar Is., Nigeria, Pakistan, Panamá, Puerto Rico, Queensland, Sierra Leone, Sudan, Suriname, Tanzania, Togo, Trinidad-Tobago, Uganda, West Himalaya, Western Australia, Windward Is.

    Peltophorum (Vogel) Benth. appears in other Kew resources:

    Date Reference Identified As Barcode Type Status
    Bamps, P. [5016], São Paulo K000849296

    First published in J. Bot. (Hooker) 2: 75 (1840)

    Literature

    Flora Zambesiaca
    • in Hooker’s J. Bot. Kew Gard. Misc. 2: 75 (1840) nom. conserv.
    Flora of Tropical East Africa

    Sources

    Flora Zambesiaca
    Flora Zambesiaca
    http://creativecommons.org/licenses/by-nc-sa/3.0

    Flora of Tropical East Africa
    Flora of Tropical East Africa
    http://creativecommons.org/licenses/by-nc-sa/3.0

    Herbarium Catalogue Specimens
    'The Herbarium Catalogue, Royal Botanic Gardens, Kew. Published on the Internet http://www.kew.org/herbcat [accessed on Day Month Year]'. Please enter the date on which you consulted the system.
    Digital Image © Board of Trustees, RBG Kew http://creativecommons.org/licenses/by/3.0/

    Kew Backbone Distributions
    The International Plant Names Index and World Checklist of Selected Plant Families 2018. Published on the Internet at http://www.ipni.org and http://apps.kew.org/wcsp/
    © Copyright 2017 World Checklist of Selected Plant Families. http://creativecommons.org/licenses/by/3.0

    Kew Names and Taxonomic Backbone
    The International Plant Names Index and World Checklist of Selected Plant Families 2018. Published on the Internet at http://www.ipni.org and http://apps.kew.org/wcsp/
    © Copyright 2017 International Plant Names Index and World Checklist of Selected Plant Families. http://creativecommons.org/licenses/by/3.0

    Legumes of the World Online
    http://creativecommons.org/licenses/by-nc-sa/3.0