Pararchidendron I.C.Nielsen

First published in Bull. Mus. Natl. Hist. Nat., B, Adansonia 5: 327 (1983)
This genus is accepted
The native range of this genus is Central & S. Malesia to New Guinea, E. Australia.

Descriptions

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

Habit
Tree or shrub
Ecology
Tropical hilly to montane rain forest (Malesia), seasonally dry forest, and coastal scrub (Australia), 0-2250 m
Distribution
Malesia (Java) to NE Australia (Queensland, N New South Wales)
Note
'Genus C' of the Ingeae in Nielsen (1981a)

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.

[LOWO]

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

Distribution
A monospecific genus, distributed from Java to northern Australia: Pararchidendron pruinosum (Benth.) I.C. Nielsen, with an endemic variety in New Guinea, P. pruinosum var. novoguineense I.C.Nielsen. Pararchidendron occurs in primary and secondary submontane forests (in New Guinea), between 1300–2250 m.
Morphology General Habit
Shrub or tree to 30 m tall, spines absent
Morphology Leaves
Leaves bipinnate, glands present on petiole, leaf rachis, and pinnae rachises, leaflets alternate, sessile
Morphology Reproductive morphology Inflorescences
Inflorescences usually in upper axils, pedunculate, umbelliform, racemose or spicate, sometimes aggregated into panicles
Morphology Reproductive morphology Flowers
Flowers bisexual, 5-merous, uniform; calyx lobed for <½ its length, lobes valvate; corolla tubular in the lower half, lobes valvate; stamens numerous, fused into a tube at the base; ovary slightly stipitate. Fruit chartaceous, flattened, curved or contorted, dehiscent, not segmented between seeds, reddish inside
Morphology Reproductive morphology Seeds
Seeds with a pleurogram, testa black.
Recognition
The genus can be recognised by the alternate leaflets, umbelliform inflorescences, numerous stamens which are fused at the base, and the curved fruit with a reddish inside.
[TONG]

Uses

Use
Pararchidendron pruinosum (Benth.) I.C.Nielsen (snow wood, tulip siris, stinkwood) is used as an ornamental and street tree
[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