Archidendropsis I.C.Nielsen

First published in Fl. Nouv.-Calédonie 12: 66 (1983)
This genus is accepted
The native range of this genus is Papuasia to New Caledonia.

Descriptions

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

Note

Nielsen (1981a) recognised 21 genera in Ingeae (Table 7), although 4 were not given generic names, but were referred to as ‘Gen. A’ to ‘Gen. D’. He recognised the genus Marmaroxylon, although without a generic number, so that the tribe, to the casual observer, appeared to contain only 20 genera. The genus Punjuba appended by Nielsen (1981a) under “genera and species of unknown affinity” is here treated as a synonym of Abarema, following Barneby & Grimes (1996), although we suggest that this may be reinstated as a good genus in the future. Nielsen (1981a) also included Pithecellobium incuriale (Vell.) Benth. as a “species of unknown affinity” but this is now placed in Leucochloron Barneby & Grimes (1996).

Polhill (1994) increased the number of genera of Ingeae to 25 (Table 7). He recognised Nielsen’s ‘Gen. A’ as Paraserianthes I.C.Nielsen, ‘Gen. B’ as Archidendropsis I.C.Nielsen, ‘Gen. C’ as Pararchidendron I.C.Nielsen, and ‘Gen. D’ as Macrosamanea Britton & Rose ex Britton & Killip. He placed Faidherbia in Ingeae for the first time, reinstated Cathormion, Samanea and Chloroleucon, and recognised the monospecific Obolinga Barneby (subsequently subsumed into Cojoba by Barneby & Grimes, 1997). Zapoteca, a segregate of Calliandra described by Hernández (1986), was also added by Polhill (1994). Klugiodendron, recognised by Nielsen (1981a), was considered a synonym of Abarema by Polhill (1994), and Affonsea was placed as a synonym of Inga, a position later confirmed by Pennington (1997).

The present treatment of Ingeae recognises 36 genera (24 of which are New World endemics) and (935)–951–(966) species (Fig. 27). We follow Barneby & Grimes (1997) in placing Obolinga as a synonym of Cojoba. Eight genera: Blanchetiodendron, Ebenopsis, Hesperalbizia, Hydrochorea, Leucochloron, Painteria, Pseudosamanea, and Sphinga, have either been reinstated or described as new since 1994 (Barneby & Grimes, 1996). Paraserianthes section Falcataria was raised to generic status as Falcataria (I.C.Nielsen) Barneby & Grimes (1996). Balizia Barneby & Grimes (1996) is considered a synonym of Albizia following Rico Arce (1999). Guinetia L.Rico & M.Sousa was described as new (Rico Arce et al., 1999, publ. 2000), and Viguieranthus Villiers in 2002.

Clarification of generic relationships within tribe Ingeae still suffers from a paucity of molecular data, partly due to a lack of appropriate material for DNA extraction of the recently described and reinstated genera. Luckow et al. (2000) included four ingoid genera in their analysis of the basal genera of Mimosoideae. These formed a group together with Faidherbia (then still considered a member of tribe Acacieae, although moved to Ingeae by Polhill (1994)). Barneby & Grimes (1996) concentrating on neotropical taxa, divided American ingoids into five informal alliances: the Abarema-, Samanea-, Chloroleucon-, Pithecellobium- and Inga- alliances. Genera of uncertain position within their system included Albizia, Enterolobium and Cedrelinga. Lysiloma was considered as intermediate between tribes Ingeae and Acacieae. Luckow et al. (2003) carried out a phylogenetic analysis of the Mimosoideae using chloroplast DNA sequence data. They treated sixteen of the 36 ingoid genera recognised in this account, including Faidherbia, but concluded that relationships within the Ingeae are generally unresolved and that, with only a few exceptions, clades within the ingoid part of their topology were not strongly supported. Albizia proved to be polyphyletic, supporting the findings of Grimes (1999).

Any new classification of the Ingeae will require sampling of all the genera not included by Luckow et al. (2003) and more extensive sampling of the larger and putatively non-monophyletic genera. Relationships between ingoid genera and the various elements of a polyphyletic Acacia have still to be resolved, although Luckow et al. (2003) have an Acacia subgenus Phyllodineae clade nested within the Ingeae, suggesting that at least part of Acacia sens. lat. (the Australian phyllodinous acacias) might be included within the Ingeae in the future, or that the Ingeae, as currently circumscribed, may have to be broken up into several distinct suprageneric taxa. Such suggestions are premature as 20 ingoid genera, including Abarema, Archidendron, Pithecellobium, Zygia and the largely Madagascan Viguieranthus have not yet been included in molecular analyses.

'Genus B' of the Ingeae in Nielsen (1981a)
Vernacular
salmon bean, red lancewood, dead finish
Habit
Trees and shrubs
Ecology
Tropical mostly lowland rain forest, but 2 of the Australian species in drier eucalypt woodland, vine thicket and acacia shrubland
Distribution
SW Pacific (8 spp., New Caledonia), Australia (3 spp., Queensland,), Papuasia (3 spp., New Guinea-New Britain-Solomon Islands)
[LOWO]

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

Morphology General Habit
Trees and shrubs to 42 m tall, spines absent
Morphology Leaves Stipules
Stipules filiform or auriculate, usually caducous
Morphology Leaves
Leave bipinnate, glands usually present on leaf rachis and often on pinnae rachises, leaflets opposite or alternate
Morphology Reproductive morphology Inflorescences
Inflorescences spikes or racemes, rarely glomerules. Flowers bisexual, 3- or 5-merous, uniform; sepals fused at the base, valvate in bud; petals fused at the base, valvate in bud; stamens numerous, fused into a tube at the base; ovary with 1 carpel (in New Guinea)
Morphology Reproductive morphology Fruits
Immature fruit thickened at margins, mature fruit not known in New Guinea, elsewhere usually chartaceous, flattened, straight or curved, dehiscent along sutures, not internally divided between seeds
Morphology Reproductive morphology Seeds
Seeds flattened, sometimes narrowly winged, testa thin, without pleurogram.
Distribution
The two species in New Guinea both have a restricted range, A. sepikensis is from West Sepik province, Papua New Guinea, whilst A. spicata is from Umboi Island, New Britain; they have been recorded from lowland rain forest between 15–350 m. A genus of 14 species, from New Guinea, the Solomon Islands, Queensland and New Caledonia. Two endemic species in New Guinea: Archidendropsis sepikensis (Verdc.) I.C.Nielsen and A. spicata (Verdc.) I.C.Nielsen. In Verdcourt (1979), the former was treated under Albizia, whilst the latter was placed within Archidendron.
Recognition
Both Archidendropsis species in New Guinea have opposite leaflets (cf. alternate leaflets in Serianthes), the inflorescence unit is a raceme or spike, but the inflorescences are not cauliflorous (cf. Archidendron), and there is a single ovary per flower.
[TONG]

Uses

Use
Various species ( salmon bean, red lancewood, dead finish ) used for timber (cabinet making and turnery), whips and as ornamentals
[LOWO]

Sources

  • 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

    • 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