Schleinitzia Warb.

First published in J.C.Willis, Dict. Fl. Pl., ed. 4: 594 (1919)
This genus is accepted
The native range of this genus is Philippines to Pacific.

Descriptions

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

Habit
Trees and shrubs
Ecology
Tropical secondary rain forest, woodland, wooded grassland, coastal plains and beaches
Distribution
Malesia and Papuasia (Philippines [1 sp.], Papua New Guinea, Moluccas, Solomon Isls., N Vanuatu [1 sp.]); SW & SC Pacific (S Vanuatu, E to Society Isls., New Caledonia, Fiji, Tonga, Niue and Cook Isls. [1 sp.]); NW Pacific (SE Guam and adjacent Marianas [1 sp.])
Note
In a well supported clade with Kanaloa and Desmanthus (Luckow et al., 2003; Hughes et al., 2003), this clade is sister to Leucaena, in the Leucaena group

The tribe Mimoseae (sensu Bentham, 1875) is retained here simply as a matter of convenience. All recent phylogenetic analyses indicate that Ingeae and Acacieae are derived from within Mimoseae (Chappill & Maslin, 1995; Käss & Wink, 1996; Luckow et al., 2000; Bruneau et al., 2001; Luckow et al., 2003; Herendeen et al., 2003a), making it a paraphyletic group at best. The most recent studies indicate that it may not even be monophyletic with respect to the Caesalpinioideae (Luckow et al., 2000; Bruneau et al., 2001; Luckow et al., 2003).

Although the outline of a new tribal classification of the mimosoids is emerging, we await better-supported phylogenies (based on more extensive data) before formalising new stable and useful groups. Some parts of the classification proposed here are better supported than others. Notably, the basal branches in Fig. 24 are poorly supported in most analyses and the relationships among the groups are likely to change as we acquire more data. As presently indicated (Luckow et al., 2003), the type genus Mimosa falls within the derived Piptadenia group which is in turn sister, and basally branching, to elements of Acacia and Ingeae (Fig. 24). A more narrowly circumscribed Mimoseae sens. strict. will thus leave the bulk of Mimoseae sens. lat. (i.e., as treated here) in need of new tribal allocation. The most conspicuous difference between the classification presented here and that of Lewis & Elias (1981) is the inclusion of tribe Parkieae within Mimoseae. The former was circumscribed based on imbricate aestivation of the calyx, and was considered the basal tribe within the Mimosoideae (Elias, 1981a). Recent phylogenetic analyses (Chappill & Maslin, 1995; Luckow et al., 2000; Bruneau et al., 2001; Luckow et al., 2003; Herendeen et al., 2003a), indicate that the two genera in the Parkieae, Parkia and Pentaclethra, are not sister taxa (Fig. 24). Pentaclethra is nested within Mimoseae in Luckow et al. (2000), but is either sister to caesalpinioid taxa in Bruneau et al. (2001) and Herendeen et al. (2003a), or part of a basal polytomy with Mimoseae and caesalpinioid taxa (Luckow et al., 2003). Both Parkia and Pentaclethra are included in the tribe Mimoseae pending additional data and tribal recircumscription.

Recent work (Luckow et al., submitted a) also indicates that the monospecific tribe Mimozygantheae should be subsumed in the Mimoseae near Piptadeniopsis and Prosopidastrum, currently in the Prosopis group. Otherwise, the informal groups within the Mimoseae recognised by Lewis & Elias (1981) are relatively well-supported by current phylogenies and only a few departures have been made from their system. Where relationships are either poorly supported or unresolved, the classification of Lewis & Elias (1981) is retained. The Xylia group is dismantled and the Adenanthera group recircumscribed to include Calpocalyx and Xylia . Desmanthus has been removed from the Dichrostachys group, as has Neptunia, in agreement with recent molecular and morphological phylogenetic studies (Harris et al., 1994; Hughes, 1998; Luckow, 1995, 1997). A new group is erected to accommodate Piptadeniastrum which is well separated from Newtonia in the most recent phylogeny (Luckow et al., 2000; 2003), and another to accommodate Cylicodiscus, which is more closely related to the clade containing the Prosopis, Leucaena, Dichrostachys, and Piptadenia groups than it is to the Newtonia group. Neptunia is well supported as sister to Prosopidastrum in recent analyses (Luckow et al., 2003) and is included in the Prosopis group here. Relationships of genera in the Prosopis group are not resolved, but the group is retained here as there is no evidence that it is not monophyletic. Genera newly described since 1981 include Alantsilodendron, Calliandropsis, Kanaloa, and Lemurodendron. Alantsilodendron and Calliandropsis are placed in the Dichrostachys group, and Kanaloa in the Leucaena group based on phylogenetic analyses (Hughes, 1998; Luckow, 1997; Luckow et al., 2000). Lemurodendron is tentatively included in the Newtonia group as suggested by Villiers & Guinet (1989). As treated here the Mimoseae comprises 40 genera and from (859)– 869–(879) species.

[LOWO]

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

Distribution
A genus of four species with a Pacific-centred distribution, from the Philippines to Guam and Tahiti; one species in New Guinea: Schleinitzia novoguineensis (Warb.) Verdc.
Morphology General Habit
Shrub or tree to 20 m tall, unarmed. Stipules filiform, persistent
Morphology Leaves
Leaves bipinnate, sensitive to touch, glands present on leaf rachis and pinnae rachises, leaflets opposite
Morphology Reproductive morphology Inflorescences
Inflorescences in upper axils, consisting of pedunculate glomerules aggregated into clusters, each glomerule subtended by a ring of bracts
Morphology Reproductive morphology Flowers
Flowers bisexual or occasionally male, uniform, 5-merous; calyx funnel-shaped, shortly lobed at apex; petals free, longer than calyx; stamens (8–)10, free, filaments sometimes coherent at base, anthers with a stipitate gland at apex; ovary shortly stipitate
Morphology Reproductive morphology Fruits
Fruit membranous, oblong, more or less straight, indehiscent or tardily dehiscent. Seeds oblong, biconvex.
Ecology
Found in primary and secondary forests and disturbed habitats, but especially along beach edges and in coastal habitats, on calcareous soils; from sea level to 1800 m.
Recognition
Schleinitzia is morphologically close to Leucaena but differs in the anthers with stipitate glands at the apex, and the pods which are indehiscent (or very tardily dehiscent, splitting around margins but not beyond), and seeds held transversely; the flowers are recorded as being pink to violet (sometimes greenish) with light purple stamen filaments.
[TONG]

Uses

Use
Used for wood (ceremonial firewood for cremations, fishnet frames and handicrafts), medicine (from the bark) and soil improvement
[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