Cathormion (Benth.) Hassk.

First published in Retzia 1: 231 (1855)
This genus is accepted
The native range of this genus is Tropical Asia to N. Australia.

Descriptions

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

Distribution
A genus now considered monospecific, Cathormion umbellatum (Vahl.) Kosterm., distributed from Sumatra to New Guinea and northern Australia. Other species formerly in this genus have now been transferred to Albizia or Samanea.
Morphology General Habit
Shrub or tree to 22 m tall, often multi-stemmed and suckering
Morphology Leaves Stipules
Stipules rigid when young, becoming spinescent. Leaves bipinnate, glands present on leaf rachis and pinnae rachises, leaflets opposite and sessile
Morphology Reproductive morphology Inflorescences
Inflorescences axillary or on short lateral branches, in umbelliform corymbs, pedunculate, after fruiting becoming spinose
Morphology Reproductive morphology Flowers
Flowers bisexual, 5-merous, dimorphic. Marginal flowers on slender pedicel, with cupular calyx, lobed for ⅓ to ½ its length, corolla funnel-shaped or campanulate, staminal tube usually longer than corolla Central flowers on stout pedicel, with tubular calyx, lobed for less than ⅓ of its length, staminal tube usually shorter than corolla; ovary sessile
Morphology Reproductive morphology Fruits
Fruit indehiscent, straight or curved, lomentaceous, breaking into rounded, 1-seeded segments, mesocarp corky to woody.
Ecology
In New Guinea, Cathormion occurs in gallery woodland, beach vegetation, along the edges of swamps and the landward edge of mangroves from sea level to 150 m.
Recognition
The genus can be recognised by its suckering habit, the stipules which are rigid when young and become spinescent, the umbelliform inflorescences with slightly different marginal and central flowers, and the fruit breaking up into sub-circular 1-seeded segments.
[TONG]

Leguminosae, J.P.M. Brenan. Flora Zambesiaca 3:1. 1970

Morphology General Habit
Trees or shrubs, unarmed, at least the mature shoots.
Morphology Leaves
Leaves bipinnate, pinnae each with several to many pairs of leaflets; gland on upper side of petiole present or absent, glands often also present at insertion of the pinnae and on the upper part of the pinna-rhachis.
Morphology Reproductive morphology Inflorescences
Inflorescences of round heads which in the African species are pedunculate and mostly solitary or paired (sometimes in threes) in the axils.
Morphology Reproductive morphology Flowers
Flowers hermaphrodite, or said to be rarely male and hermaphrodite; 1 to several central flowers in each head often modified and different in form from the others, and sometimes at least hermaphrodite.
Morphology Reproductive morphology Flowers Calyx
Calyx gamosepalous, shortly (4)5-dentate.
Morphology Reproductive morphology Flowers Corolla
Corolla gamopetalous, infundibuliform, (4)5-lobed.
Morphology Reproductive morphology Flowers Androecium Stamens
Stamens numerous (c. 16-22), fertile, their filaments united in their lower part into a slender tube not or scarcely projecting from the corolla (or very shortly so in the modified central flowers).
Morphology Reproductive morphology Fruits
Pod oblong, ± falcate or spirally curved, compressed, with the margins lobed, ± constricted between the seeds, at maturity breaking up into coriaceous or hard 1-seeded joints, or sometimes apparently indehiscent; mesocarp only slightly developed, septate.
Morphology Reproductive morphology Seeds
Seeds ± compressed, exarillate.
[FZ]

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

Morphology General Habit
Trees or shrubs, unarmed
Morphology Leaves
Leaves bipinnate, pinnae each with several to many pairs of leaflets; gland on upper side of petiole present or absent; glands also often present at insertion of pinnae and on upper part of pinnarhachis
Morphology Reproductive morphology Inflorescences
Inflorescences of round heads which in the African species are pedunculate and mostly solitary or paired (sometimes in threes) in axils
Morphology Reproductive morphology Flowers
Flowers hermaphrodite, or said to be rarely ♂ and ♀; 1 to several central flowers in each head often modified and different in form from the others, and sometimes at least hermaphrodite
Morphology Reproductive morphology Flowers Calyx
Calyx gamosepalous, shortly (4–)5-dentate
Morphology Reproductive morphology Flowers Corolla
Corolla gamosepalous, infundibuliform, (4–)5-lobed
Morphology Reproductive morphology Flowers Androecium Stamens
Stamens numerous (about 16–22), fertile, their filaments united in their lower part into a slender tube not or scarcely projecting from the corolla (or very shortly so in the modified central flowers)
Morphology Reproductive morphology Fruits
Pods oblong, ± falcate or spirally curved, compressed, with their margins straight or lobed, ± constricted between the seeds, at maturity breaking up into coriaceous or hard 1-seeded joints
Morphology Reproductive morphology Seeds
Seeds ± compressed.
[FTEA]

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.

Eleven African and American species formerly included in Cathormion are now referred directly or in comment (Nielsen, 1992; Barneby & Grimes, 1996) to Albizia, Chloroleucon and Hydrochorea; Cathormion is sister to Chloroleucon in the analysis of Luckow et al., 2003
Habit
Shrubs
Ecology
Tropical riverine forest (and mangrove), seasonally dry woodland and wooded grassland
Distribution
S Asia (India and Sri Lanka), Indo-China, Malesia, Papuasia and N Australia
[LOWO]

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
  • 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