Millettia Wight & Arn.

First published in Prodr. Fl. Ind. Orient. 1: 263 (1834)
This genus is accepted
The native range of this genus is Tropical & Subtropical Old World.

Descriptions

Timothy M. A. Utteridge and Laura V. S. Jennings (2022). Trees of New Guinea. Kew Publishing. Royal Botanic Gardens, Kew

Distribution
About 150 species (although the genus is not a natural group and likely to be divided in the future): subtropical and tropical Africa, Asia, and Australia; two species in New Guinea, including Millettia pinnata (L.) Panigrahi which was previously treated under the genus Pongamia in Verdcourt (1979).
Morphology General Habit
Shrubs, lianas or trees to 35 m (in New Guinea)
Morphology Leaves Stipules
Stipules present, persistent or caducous
Morphology Leaves
Leaves imparipinnate, leaflet blades opposite or rarely subalternate; stipels present or absent. Inflorescences axillary, racemose, unbranched, rachis with lateral flowering branchlets reduced to knobs at each node
Morphology Reproductive morphology Flowers
Flowers in clusters of 2–5; bracts and bracteoles present; calyx tube broad, cup-shaped or shortly 5-toothed; adaxial 2 teeth ±connate; standard petal large (up to 2 cm long), with or without basal calluses; upper stamen sometimes free in bud and becoming adherent to other 9 when flower mature; ovary linear; style straight or inflexed
Morphology Reproductive morphology Fruits
Fruit 2-valved, flat, sometimes cylindric or inflated only around ellipsoid seeds, tardily dehiscent, not winged or with 2 wings perpendicular to abaxial or both sutures
Morphology Reproductive morphology Seeds
Seeds 1–2(–3) (in New Guinea), kidney-shaped.
Ecology
Found in primary and secondary lowland habitats including rain forest, coastal vegetation, and the edges of mangrove and swamp forest; sea level to 1200 m.
Recognition
Millettia pinnata (commonly cultivated) can be identified by the imparipinnate leaves with 5–7 opposite leaflets, axillary unbranched racemes, the cup-like calyx without distinct teeth, the laterally compressed, oblong-ellipsoid fruit, usually with only 1–2 seeds.
[TONG]

M. Thulin et al. Flora of Somalia, Vol. 1-4 [updated 2008] https://plants.jstor.org/collection/FLOS

Morphology General Habit
Trees, shrubs or lianes
Morphology Leaves
Leaves imparipinnate; leaflets opposite, rarely subalternate
Morphology Reproductive morphology Inflorescences
Flowers large, in panicles often contracted to pseudoracemes
Morphology Reproductive morphology Flowers Corolla
Corolla white, pink or violet; standard usually silky outside
Morphology Reproductive morphology Flowers Androecium Stamens Filaments
Vexillary stamen free at first, but usually becoming adherent in the mature flower
Morphology Reproductive morphology Flowers Disc
Disc often present between stamens and ovary
Morphology Reproductive morphology Flowers Gynoecium Ovary
Ovary pubescent; ovules 3–11, ± evenly distributed throughout the ovary
Morphology Reproductive morphology Fruits
Pod dehiscent, usually flat, 2- or more-seeded.
Distribution
Some 200 species in tropical and subtropical Africa, Asia and Australasia.
[FSOM]

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

Morphology General Habit
Trees, shrubs or lianes, or rarely semi-herbaceous plants with a woody rootstock
Morphology Leaves
Leaves imparipinnate, the leaflets entire, usually opposite; stipellae usually present; a pulvinus present at the base of the rhachis
Morphology Reproductive morphology Inflorescences
Inflorescence paniculate, but often pseudoracemose by the contraction of the floriferous branches to mere knobs
Morphology Reproductive morphology Flowers Calyx
Calyx almost truncate or divided for up to two-thirds of its length, the upper pair of teeth united for most of their length
Morphology Reproductive morphology Flowers Corolla
Corolla rarely under 1 cm. long, white, pink, blue or violet, not speckled, silky or glabrous outside; keel-petals lightly united, somewhat pouched but not spurred, their claws and the usually rather longer claws of the wings often ± attached near the base to the filament-sheath
Morphology Reproductive morphology Flowers Androecium Stamens
Vexillary stamen usually free in the young bud and remaining so at its base in the mature flower, but usually becoming adherent to its neighbours above; 5 of the 9 united stamens rather longer than the others; anthers all alike, dorsifixed below the middle; filaments not widened at the tip
Morphology Reproductive morphology Flowers Disc
Disc between stamens and ovary tubular, annular or lobed or flat and undeveloped
Morphology Reproductive morphology Flowers Gynoecium Pistil
Ovary pubescent, sessile or shortly stipitate, with (2–)3–ll ovules; style usually pubescent near the base, glabrous above, ± circular in cross-section, straight or incurved at the tip; stigma small, terminal, discoid or capitate
Morphology Reproductive morphology Fruits
Pod dehiscent, usually flat, rarely subcylindrical, 2- or more seeded; funicle often with a pulpy swelling at the proximal side (towards the pedicel)
Morphology Reproductive morphology Seeds
Seeds usually well separated from one another, sometimes “longitudinal” (long axis parallel to that of pod), more often “transverse” or “obliquely transverse”, usually rather flat, usually having around the hilum a short ring-like white or yellow aril prolonged at one side into a strap-shaped process clasping the funicle.
[FTEA]

Flora Zambesiaca Leguminosae subfamily Papillionoideae by B. Verdcourt*

Morphology General Habit
Trees, shrubs or lianes, or rarely semi-herbaceous plants with a woody rootstock. Trees, shrubs or lianes, or rarely semi-herbaceous plants with a woody rootstock.
Morphology Leaves
Leaves imparipinnate, the leaflets entire, usually opposite; stipels usually present but absent in 2 cultivated species in the Flora area; a pulvinus present at the base of the peduncle. Leaves imparipinnate, the leaflets entire, usually opposite; stipels usually present but absent in 2 cultivated species in the Flora area; a pulvinus present at the base of the peduncle.
Morphology Reproductive morphology Inflorescences
Inflorescence paniculate, but often pseudoracemose by the contraction of the floriferous branches to mere knobs. Inflorescence paniculate, but often pseudoracemose by the contraction of the floriferous branches to mere knobs.
Morphology Reproductive morphology Flowers Calyx
Calyx almost truncate or divided for up to ? of its length, the upper pair of teeth united for most of their length. Calyx almost truncate or divided for up to ⅔ of its length, the upper pair of teeth united for most of their length.
Morphology Reproductive morphology Flowers Corolla
Corolla rarely under 1 cm long, white, pink, blue or violet, not speckled, silky or glabrous outside; keel petals lightly united, somewhat pouched but not spurred, their claws and the usually rather longer claws of the wings often ± attached near the base to the filament sheath. Corolla rarely under 1 cm long, white, pink, blue or violet, not speckled, silky or glabrous outside; keel petals lightly united, somewhat pouched but not spurred, their claws and the usually rather longer claws of the wings often ± attached near the base to the filament sheath.
Morphology Reproductive morphology Flowers Androecium Stamens
Upper stamen usually free in the young bud and remaining so at its base in the mature flower, but usually becoming adherent to its neighbours above; 5 of the 9 united stamens rather longer than the others; anthers uniform, dorsifixed below the middle; filaments not widened at the tip. Upper stamen usually free in the young bud and remaining so at its base in the mature flower, but usually becoming adherent to its neighbours above; 5 of the 9 united stamens rather longer than the others; anthers uniform, dorsifixed below the middle; filaments not widened at the tip.
Morphology Reproductive morphology Flowers Disc
Disk between stamens and ovary tubular, annular or lobed or flat and undeveloped. Disk between stamens and ovary tubular, annular or lobed or flat and undeveloped.
Morphology Reproductive morphology Flowers Gynoecium Ovary
Ovary pubescent, sessile or shortly stipitate, with (2)3–11 ovules; style usually pubescent near the base, glabrous above, ± circular in cross-section, straight or incurved at the tip; stigma small, terminal, discoid or capitate.
Morphology Reproductive morphology Flowers Gynoecium Pistil
Ovary pubescent, sessile or shortly stipitate, with (2)3–11 ovules; style usually pubescent near the base, glabrous above, ± circular in cross-section, straight or incurved at the tip; stigma small, terminal, discoid or capitate.
Morphology Reproductive morphology Fruits
Pod dehiscent, usually flat, rarely subcylindrical, 2- or more seeded; funicle often with a pulpy swelling at the proximal side (towards the pedicel). Pod dehiscent, usually flat, rarely subcylindrical, 2- or more seeded; funicle often with a pulpy swelling at the proximal side (towards the pedicel).
Morphology Reproductive morphology Seeds
Seeds usually well separated from one another, sometimes “longitudinal” (long axis parallel to that of pod), more often “transverse” or “obliquely transverse”, usually rather flat, usually having around the hilum a short ring-like white or yellow aril prolonged at one side into a strap-shaped process clasping the funicle. Seeds usually well separated from one another, sometimes “longitudinal” (long axis parallel to that of pod), more often “transverse” or “obliquely transverse”, usually rather flat, usually having around the hilum a short ring-like white or yellow aril prolonged at one side into a strap-shaped process clasping the funicle.
[FZ]

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

Note

Relationships among genera of Millettieae have been notoriously difficult to unravel based on traditional morphological evidence and this is exemplified by the alphabetical arrangement of genera in the tribal treatments of Geesink (1981; 1984) and Polhill (1994). Geesink (1981) recognised 44 genera and c. 870 species in tribe Millettieae (as ‘Tephrosieae’) while 43 genera were accounted for in Geesink (1984) and Polhill (1994). The genera recognised, however, varied considerably with only 33 genera in common to both treatments of Geesink, while the list of Polhill (1994) combined elements of Geesink (1981, 1984) with new data accumulated since then. Tephrosia has traditionally comprised some 400 species but this is re-estimated at c. 350 species here.

The traditional circumscription of the predominantly pantropical and subtropical tribe Millettieae is followed here (Fig. 45), with 45 genera and (904)–909–(914) species being recognised, (i.e. excluding the two genera and 11 species transferred to Brongniartieae, see Table 8), although the concept of what comprises Millettieae sens. strict. is changing rapidly based on evidence from molecular phylogenies. Sequence data for millettioid genera comes from the plastid rbcL gene (Doyle et al., 1997; 2000; Kajita et al., 2001; Hu & Chang, 2003), phytochrome nucleotide genes (Lavin et al., 1998), the plastid trnK-matK region (Hu et al., 2000) and the nuclear ITS region (Hu, 2000; Hu et al., 2002). Molecular data, together with reinterpreted evidence based on chemistry (Evans et al., 1985) and wood anatomy (Gasson et al., 2004), have been the basis for recognising a number of informal suprageneric groupings and for transferring Cyclolobium and Poecilanthe to tribe Brongniartieae (Table 8; Fig. 45).

 The most far-reaching result of the above molecular analyses was that a substantial part of the traditionally circumscribed tribe Phaseoleae is more closely allied to the core-Millettieae than to the Phaseoleae sens. lat. clade (see page 393). Circumscription of a revised tribe Millettieae is not possible at present until genera are more comprehensively sampled; however, a Millettioid sens. strict. group might be expected to include some genera in the basal millettioid and phaseoloid group, Phaseoleae subtribes Diocleinae, Ophrestiinae and in small part the Erythrininae, tribe Abreae and the core-Millettieae (Fig. 45). The basal millettioid and phaseoloid group comprises 17 genera (94 species) that may belong either in the Millettioids sens. strict. or Phaseoleae sens. lat., or to a clade sister to both these groups (e.g., Kajita et al., 2001). The core-Millettieae clade comprises c. 22 genera and c. 777 spp., with some additional generic segregates being necessary within the ‘canavanine group’ (Evans et al., 1985), to accommodate species of Millettia sens. lat. and Fordia sens. lat., which on the basis of molecular and chemical evidence are excluded from Millettia and Fordia sens. strict.

Relationships between the major groups of genera centred on Lonchocarpus, Derris, Millettia and Tephrosia remain obscure, and still reflect a geographical bias in segregating them, i.e. distributions are limited largely to the New World in the Lonchocarpus group, and the Old World in the other groups. The suggestion that the Andean South American genus Apurimacia might be sister to the largely Old World Tephrosia rather than to Lonchocarpus (e.g., Kajita et al., 2001) is possibly indicative of other Old World–New World sister groups yet to be found. Further molecular evidence will probably result in an overall reduction in the number of genera recognised, particularly in the Tephrosia and Lonchocarpus groups where various small or monotypic ‘one-organ’ genera may be better placed within larger genera. Ptycholobium, Requienia and Paratephrosia, for example, are difficult to distinguish from Tephrosia, but for the emphasis traditionally placed on their atypical pods.

This genus is in need of major revision since recent molecular evidence (Hu et al., 2000; Kajita et al., 2001; Hu et al., 2002) has shown Millettia to be polyphyletic; estimates of the number of species vary from 90-200 and the total given above is based on a review of current literature and herbarium collections
Habit
Trees, shrubs or lianas
Ecology
Tropical rain forest and seasonally dry lowland to upland forest and forest margins, woodland, thicket and wooded grassland, and secondary vegetation types
Distribution
c. 90-100 spp. in Africa and Madagascar (in Africa c. 65 spp. occur in WC regions; 14 spp. Zanzibar-Inhambane; 6 spp. Zambezian; c. 4 spp. Somalia-Masai; c. 2 spp. Sudanian; c. 1 sp. Afromontane; 8 spp. endemic to Madagascar); to China, the Indian subcontinent, Indo-China and Malesia
[LOWO]

Uses

Use
Used as fish poisons, insecticides, timber (e.g., M. laurentii De Wild. [wenge] ; M. stuhlmannii Taub. [panga panga, mpande] , for flooring, furniture, cabinet work, construction, veneers, joinery and agricultural implements); as nitrogen fixers in agroforestry (soil rehabilitation), fuelwood, ornamentals and for medicine
[LOWO]

Sources

  • Flora Zambesiaca

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

    • Flora of Somalia
    • 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

  • Kew Names and Taxonomic Backbone

    • The International Plant Names Index and World Checklist of Vascular Plants 2024. Published on the Internet at http://www.ipni.org and https://powo.science.kew.org/
    • © Copyright 2023 International Plant Names Index and World Checklist of Vascular Plants. http://creativecommons.org/licenses/by/3.0
  • Legumes of the World Online

    • Digital Image © Board of Trustees, RBG Kew http://creativecommons.org/licenses/by-nc-sa/3.0/
    • http://creativecommons.org/licenses/by-nc-sa/3.0
  • Trees of New Guinea

    • Trees of New Guinea
    • http://creativecommons.org/licenses/by-nc-sa/3.0
  • World Checklist of Vascular plants (WCVP)

    • The International Plant Names Index and World Checklist of Vascular Plants 2024. Published on the Internet at http://www.ipni.org and https://powo.science.kew.org/
    • © Copyright 2023 World Checklist of Vascular Plants. http://creativecommons.org/licenses/by/3.0