Bauhinia Plum. ex L.

George R. Proctor (2012). Flora of the Cayman Isands (Second Edition). Royal Botanic Gardens, Kew

Morphology General Habit

Trees or shrubs, erect or climbing, with or without spines or tendrils; leaves simple, of 2 united leaflets more or less parted at the apex, or rarely completely 2-foliolate; stipules small and soon falling

Morphology Reproductive morphology Flowers

Flowers solitary or in racemes, these simple and terminal or axillary, or paniculate; calyx with a short elongate tube, the limb more or less spathe-like, before anthesis either closed and entire, or else contracted at the apex and 5-toothed, after anthesis remaining entire or variously splitting.

Morphology Reproductive morphology Flowers Corolla

Petals 5, slightly unequal-Perfect stamens 10 or less, some or most often being reduced to staminodia or lacking; anthers attached at the middle and opening longitudinally

Morphology Reproductive morphology Flowers Gynoecium Ovary

Ovary stalked or subsessile, with 2–many ovules; style various, the stigma small or often dilated and peltate

Morphology Reproductive morphology Fruits

Pods oblong or linear, compressed, 2-valved with elastic valves, or indehiscent; seeds roundish, compressed, and with endosperm; cotyledons flat, more or less fleshy.

Distribution

A pantropical genus of more than 200 species, several often cultivated for ornament.

Leguminosae, R.K. Brummitt, A.C. Chikuni, J.M. Lock & R.M. Polhill. Flora Zambesiaca 3:2. 2007

Morphology General Habit

Trees or shrubs, seldom scandent or climbing, without tendrils, but branch tips sometimes coiling.

Morphology Leaves

Leaves bilobed or occasionally divided to the base, palmately nerved; stipules deciduous.

Morphology Reproductive morphology Flowers

Flowers in racemes or solitary, usually large and showy, bisexual, zygomorphic.

Morphology Reproductive morphology Flowers Calyx

Calyx spathaceous (the sepals ± cohering after the calyx has opened) above a variably developed hypanthium.

Morphology Reproductive morphology Flowers Corolla

Petals 5(6), free.

Morphology Reproductive morphology Flowers Androecium

Stamens 1–10, sometimes accompanied by staminodes, free; anthers opening by longitudinal slits.

Morphology Reproductive morphology Flowers Gynoecium Pistil

Ovary usually stipitate; style elongate; stigma capitate or small, sometimes unilateral.

Morphology Reproductive morphology Fruits

Pods linear-oblong to strap-shaped or broadened upwards, ± woody, dehiscent or elsewhere occasionally indehiscent, few- to many-seeded.

Morphology Reproductive morphology Seeds

Seeds ± compressed; hilum circular or crescent-shaped, with a U-shaped to hairpin-shaped scar of 2 aril lobes developed from the funicle.

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

Vernacular

camel`s-foot

Habit

Trees and shrubs (sometimes semi-scandent)

Ecology

Seasonally dry tropical bushland, woodland, wooded grassland (savanna and cerrado), thorn scrub (including caatinga) and coastal forest; several on sand or limestone; less than 20 spp. in wet habitats, infrequently in evergreen humid forest and rain forest; c. 15 in montane and submontane areas with B. brachycarpa being reported at elevations of up to 3200m in China. Bauhinia ungulata (Ramirez et al., 1984), B. pauletia (Heithaus et al., 1974, Hokche & Ramirez, 1990) & B. multinervia (Hokche & Ramirez, 1990) have all been shown to be pollinated by bats.

Distribution

A pantropical genus. Sect. Pauletia c. 78 species in tropical America; sect. Bauhinia c. 20 from Mexico to Northeast Brazil; sect. Amaria 18 from N South America to Mexico; sect. Alvesia c. 7 in southern Africa, S Asia, S China and Malesia; sect. Micralvesia 9 in Africa, S Asia, S China and Malesia; sect. Telestria 5 in S Asia, S China and Malesia; sect. Pseudophanera 1 in S Asia and Malesia; sect. Afrobauhinia c. 20 in southern Africa and Madagascar; sect Semla 2 in S Asia; sect Pseudobauhinia 1 in China; sect Benthamia 2 from Brazil to Argentina. In the neotropics, Brazil Southwest is the most diverse region (37 taxa). In Asia and Australasia, the most taxon rich country is Thailand, in Africa Madagascar, both accommodating 16 taxa.

Note

Bauhinia in its broadest sense has been divided by various authors into as many as 26 segregate genera (Wunderlin, 1976). Wunderlin et al. (1981, 1987) took a broad view of the genus and placed in synonymy all of the segregate genera recognised by De Wit (1956). Most recent African Floras have adopted a less inclusive approach, which is followed here. Bauhinia subgenus Bauhinia was divided into 9 sections, 2 subsections and 19 series by Wunderlin et al. (1987), but section Gigasiphon is here considered as a separate genus. Phylogenetic analysis of the plastid trnL-trnF region by Sinou et al. (2009) indicated that of the 8 sections of Bauhinia described by Wunderlin et al. (1987) only Amaria, Bauhinia & Alvesia are monophyletic. The analysis also indicated that sect. Pseudobauhinia is nested within Bauhinia s.s. rather than Phanera, where it was placed by Wunderlin et al. (1987). We here follow this arrangement, as B. bohniana, the single species in sect. Pseudophanera, is a shrub without tendrils whereas species within Phanera are lianas with tendrils. We have also included section Semla here rather than within Lasiobema on the same morphological grounds. Palynological studies by Banks et al. (2014) indicate that sections Pseudobauhinia, Afrobauhinia, Alvesia & Amaria each have a single distinct pollen type, whereas in each of the sections Pauletia, Telestria and Bauhinia there are 2 distinct pollen types. Some of the neotropical taxa included here in Bauhinia s.s. may later be proven to belong to segregate genera, but we await further evidence in the form of a comprehensive phylogenetic analysis of the whole genus to complement the numerous regional morphological studies.

Tribe Cercideae is basally branching in the Leguminosae (Bruneau et al., 2001; Herendeen et al., 2003a), as predicted by Wunderlin et al. (1981), and Cercis is the most basally branching genus in the tribe. While much taxonomic work has been carried out on the tribe in the past thirty years (e.g., Larsen et al., 1980, 1984; Wunderlin, 1976, 1979; Wunderlin et al., 1981, 1987; Zhang, 1995; Vaz, 2003; Vaz & Tozzi, 2003), few species have been included in phylogenetic analyses and inter- and intra-generic relationships are still largely unresolved with the exception of Cercis (Hao et al., 2001; Davis et al., 2002b).

Wunderlin (1979) and Wunderlin et al. (1981) divided the tribe into two subtribes, Cercidinae and Bauhiniinae, based on seed, floral and fruit characters. Walpers (1842) had already down-ranked Bauhinieae Benth. (1840) to subtribal status, thus the combination Bauhiniinae (Benth.) Wunderlin (1979) is superfluous. Polhill (1994) kept the Cercideae unchanged with two subtribes and five genera. While the Cercidinae contains three small distinct genera, Cercis, Griffonia and Adenolobus, the Bauhiniinae houses the monospecific Madagascan genus Brenierea and the large, diverse pantropical genus Bauhinia sens. lat. which has been segregated into as many as twenty-six genera by various authors (Wunderlin, 1976).

While many of the Bauhinia segregates are based on minor morphological differences, others are distinguished morphologically by a suite of characters. Britton and Rose (1930), in their account of the Caesalpiniaceae for the North American Flora, divided Bauhinia into several segregate genera, including Schnella Raddi which here is treated as a synonym of Phanera, but might prove to be distinct as indicated in recent molecular analyses by Forest (unpublished data). Britton and Killip (1936) recognised Schnella as distinct from Bauhinia in Colombia. De Wit (1956), treating ‘Malaysian Bauhinieae’, recognised Bracteolanthus, Lysiphyllum, Gigasiphon, Piliostigma, Lasiobema and Phanera as separate genera and this was largely followed by subsequent flora writers in Africa and New Guinea (e.g., Brenan, 1967; Coetzer & Ross in Ross, 1977; Verdcourt, 1979). Others have retained a more inclusive Bauhinia proposed by Wunderlin et al. (1981, 1987), e.g., Macbride (1943: 207–220) for Peru; Larsen et al. (1980) for the Flora of Cambodia, Laos and Vietnam; Larsen et al. (1984) for the Flora of Thailand; Chen (1988) for China, and Larsen & Larsen in Hou et al. (1996) in Flora Malesiana. Zhang (1995) published a morphological cladistic analysis of the series of Bauhinia sens. lat., but few species of Bauhinia have been included in molecular studies. It remains equivocal as to whether Bauhinia sens. lat. is monophyletic, but preliminary molecular results indicate that some elements should be reinstated as distinct genera (Bruneau et al., in prep.; Forest, unpubl.). This runs contrary to the findings of Larsen & Larsen in Hou et al. (1996) who concluded “that Bauhinia in the sense of Linnaeus, Bentham, De Candolle, Taubert and Hutchinson is an evolutionary unit and a very natural genus”. Larsen and Larsen also noted that Bauhinia sens. lat. presents a reticulate pattern of variation across its pantropical range (this apparently conflicting somewhat with its status as a “natural genus”). While this is undoubtedly true if the genus is considered as all-inclusive, recent studies of legume distributions in general (Schrire et al., this volume and 2005) have revealed repeated patterns of generic distribution which appear to be duplicated by at least some of the segregates of Bauhinia. If these segregates are recognised as distinct genera (as several are in this treatment) then the reticulate pattern of variation of Bauhinia is far less pronounced. More sampling at the species level in molecular analyses and more morphological studies are needed across the full pantropical range of Bauhinia sens. lat. before inter- and intra-generic relationships are clearly resolved. In the current account genera that have been recognised as distinct from Bauhinia in at least one flora treatment that post-dates De Wit (1956) have been treated as separate genera, especially where these are supported by the preliminary results from a chloroplast trnL (intron and spacer) sequence analysis (Forest, unpubl.). The reader’s attention is also alerted to the detailed infra-generic division of Bauhinia by Wunderlin et al. (1987) in their reorganisation of the Cercideae which also forms a sound basis for sampling in future studies.

Palynological studies of Bauhinia (Larsen, 1975; Schmitz, 1977; Ferguson & Pearce, 1986) have all stressed the considerable variation in pollen morphology within the genus sens. lat. and there are clear correlations between pollen exine ornamentation, floral morphology and pollination. It remains to be seen just how closely these correspond to evolutionary relationships of species. Nevertheless, Schmitz (1977) made several new combinations in segregate genera of Bauhinia based on palynological type. These included new names in Lasiobema, Lysiphyllum, Pauletia, Perlebia and Phanera (Pauletia and Perlebia here considered as synonyms of Bauhinia). Zhang (1995), who analysed morphologically the series of Bauhinia proposed by Wunderlin et al. (1987), concluded that while some supraspecific segregates of the genus were supported, none of the subgenera appeared to be monophyletic. Several realignments were proposed.

The Cercideae as presented here includes 12 genera and (322)–335–(348) species. This treatment differs from Wunderlin et al. (1981, 1987) and Polhill (1994) in that Barklya, Gigasiphon, Lasiobema, Lysiphyllum, Phanera, Piliostigma and Tylosema are considered distinct from Bauhinia. While some of these may well be reincluded in Bauhinia after further study, yet other genera may be reinstated from within Bauhinia. Bracteolanthus, treated as distinct by De Wit (1956), is here included in Lysiphyllum following Wunderlin et al. (1987), while Barklya, considered congeneric with Bauhinia by Wunderlin (1979) and Wunderlin et al. (1981, 1987) is considered distinct following George (1998b) and Forest (unpublished data). The reinstatement of Lasiobema appears least well supported (Forest, unpubl.).

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

Morphology General Habit

Shrubs or small trees

Morphology Leaves

Leaves simple, conspicuously bilobed, or rarely divided to base

Morphology Reproductive morphology Flowers

Flowers usually large and showy, bisexual, in short racemes or solitary

Morphology Reproductive morphology Flowers Calyx

Calyx spathaceous (sepals ± cohering after calyx has opened)

Morphology Reproductive morphology Flowers Corolla

Petals 5

Morphology Reproductive morphology Flowers Androecium Stamens

Fertile stamens 1–10, sometimes accompanied by staminodes; filaments glabrous or hairy

Morphology Reproductive morphology Flowers Gynoecium Style

Style elongate; stigma capitate or small

Morphology Reproductive morphology Fruits

Pods oblong to linear, few–many-seeded, usually woody, dehiscent (in Flora area).

Distribution

Some 200 species, pantropical, often treated in a broader sense to include such genera as Piliostigma and Tylosema, see e. g. Wunderlin, Larsen & Larsen in Adv. Leg. Syst.: 107–116 (1981).

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

Distribution

A pantropical genus of approximately 160 species when treated in a strict sense; Gigasiphon here recognised as a distinct genus, and the tendrilled climbers in Phanera are not included in this treatment of trees (see Mackinder & Clark 2014 for further details). The genus, in this strict sense, is probably not indigenous to New Guinea but is represented by at least five cultivated species.

Morphology General Habit

Shrubs or small trees to 10 m (in New Guinea)

Morphology Leaves Stipules

Stipules small, caducous

Morphology Leaves

Leaves simple, bilobed or entire; primary veins 3–15, midvein ending with a mucro (free, small point)

Morphology Reproductive morphology Inflorescences

Inflorescences terminal or axillary, racemes, panicles, or corymbs or flowers solitary. Flowers bisexual or unisexual (plants monoecious, andromonoecious, or androdioecious); hypanthium cupular, campanulate, or tubular; calyx spathaceous at anthesis; petals 5, subequal to strongly differentiated, subsessile or prominently clawed, white, yellowish orange, pink, or purplish red; fertile stamens 1–10; anthers dorsifixed, longitudinally dehiscent; ovary 1- to many ovuled, sessile or with a stalk; stigma small or prominent, variously shaped. Fruit flat, elliptic, oblong, obovoid, or linear, woody or thinly valved, dehiscent or indehiscent

Morphology Reproductive morphology Seeds

Seeds few to many; endosperm present or not.

Recognition

Members of the genus are cultivated in gardens, but it is possible that they are to be encountered as naturalised plants in lowland areas near human habitation. Bauhinia in the strict sense can be recognised by the tree or shrub habit, the lack of tendrils, the simple leaves which are usually bilobed, the spathaceous calyx, and the flowers with 1–10 fertile stamens.