Dimorphandra Schott, Syst. Veg. [Sprengel] 4(2): 404. 1827.
publication ID |
https://dx.doi.org/10.3897/phytokeys.240.101716 |
persistent identifier |
https://treatment.plazi.org/id/33BA03C3-06EF-FCCF-CD4C-59C4653420B8 |
treatment provided by |
|
scientific name |
Dimorphandra Schott, Syst. Veg. [Sprengel] 4(2): 404. 1827. |
status |
|
Dimorphandra Schott, Syst. Veg. [Sprengel] 4(2): 404. 1827. View in CoL
Figs 88 View Figure 88 , 89 View Figure 89 , 90 View Figure 90
Type.
Dimorphandra exaltata Schott
Description.
Unarmed small or medium trees 3-5 (7) m, to canopy trees 40 (50) m; trunk buttressed or not; brachyblasts absent; usually pubescent in all parts with reddish to dark or light brown hairs. Stipules present or absent, caducous. Leaves bipinnate, rachis 5-90 cm long; pinnae 1-40 or more pairs; leaflets 1-50 pairs, opposite or alternate, commonly glabrous above and pubescent below, venation brochidodromous. Inflorescences short or elongated spiciform racemes, often arranged in paniculate or corymbose synflorescences; bracteoles caducous or absent. Flowers small, pale yellow to cream or dark orange to reddish, fragrant, 5-merous, diplostemonous; calyx cupuliform, tubular or campanulate; petals obovate, oblong or spatulate, glabrous or pilose; fertile stamens 5, filaments thin, with oblong, dorsifixed anthers, anther glands absent; staminodes 5, spatulate, free or connate forming a dome, with or without a rudimentary anther at the apex, usually deciduous at anthesis; pollen tricolpate monads; ovary sessile, subsessile, or stipitate, multi-ovulate, glabrous or densely hairy, style short to absent, stigma conical, terminal. Fruit dehiscent or indehiscent legumes, linear-oblong, curved or suborbicular, flat, valves leathery or woody. Seeds orbicular, flat, cylindrical or oblong.
Chromosome number.
2 n = 28 ( Muniz et al. 2020).
Included species and geographic distribution.
26 species, including four subspecies ( Silva 1986; Silva 2019), restricted to the Neotropics, occurring mostly in Brazil (23 species) and also in Bolivia, Colombia, Guyana, Peru and Venezuela (Fig. 90 View Figure 90 ).
Ecology.
Predominates in tropical rainforests, including both terra firme and seasonally flooded ( igapó) forests, white-sand forests (campinarana), savannas, and less often in seasonally dry forests. Fruits of D. mollis Benth. are important food resources for tapirs ( Bizerril et al. 2005).
Etymology.
Dimorphandra refers to the androecium that has five stamens alternating with five staminodes, that is, two morphological forms of the stamens.
Human uses.
Dimorphandra species have the ability to fix nitrogen ( Fonseca et al. 2012) and are therefore important for improving soil fertility. Fruits are used in traditional medicine ( Féres et al. 2006). Extracts from D. gardneriana Tul. and D. mollis fruits containing the bioflavonoids rutin and quercetin are used by cosmetic and pharmaceutical industries, sometimes causing decline in natural populations ( Filizola 2013).
Notes.
The genus is classified into three subgenera: Dimorphandra (11 species), Phaneropsia Tul. (5 species) and Pocillum Tul. (10 species), which can be differentiated by leaf morphology, inflorescence architecture and fruit shape ( Silva 1986; Silva 2019). Dimorphandra seeds are dispersed by authocory, hydrochory or zoochory ( Silva 1986). Dimorphandra is not recovered as monophyletic in recent phylogenomic analyses (Fig. 87 View Figure 87 ) in which representatives of subgenera Phaneropsia and Pocillum ( D. davisii Sprague & Sandwith and D. macrostachya Benth., respectively) form a clade independent from subgenus Dimorphandra Dimorphandra ( D. gardneriana ). Other studies with increased taxonomic sampling found similar results, but relationships were uncertain because of phylogenetic conflict ( Rocha et al. 2024). Future studies with an expanded taxonomic sample and robust topology are required for a new circumscription of the genus.
Taxonomic references.
Bentham (1840); Ducke (1925); Ragonese (1973); Silva (2019); Silva and Hopkins (2018); Silva (1981, 1986); Taubert (1894).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
Kingdom |
|
Phylum |
|
Class |
|
Order |
|
Family |