Research Article |
Corresponding author: Luiz Henrique M. Fonseca ( luizhmf@gmail.com ) Academic editor: Alan Paton
© 2015 Luiz Henrique M. Fonseca, Simone Miranda Cabral, Maria de Fátima Agra, Lúcia G. Lohmann.
This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Citation:
Fonseca LHM, Cabral SM, Agra MF, Lohmann LG (2015) Taxonomic updates in Dolichandra Cham. (Bignonieae, Bignoniaceae). PhytoKeys 46: 35-43. https://doi.org/10.3897/phytokeys.46.8421
|
Dolichandra is a genus of lianas found in dry and wet Neotropical forests. The genus currently includes eight species and is well characterized by molecular and morphological synapomorphies. Here, Macfadyena hispida (DC.) Seemann is removed from synonomy with Dolichandra uncata (Andrews) L.G. Lohmann based on the presence of the hispid indument, vinaceus ovary, long fruits, and winged seeds. The combination Dolichandra hispida (DC.) L.H. Fonseca & L.G. Lohmann, comb. nov. is proposed, increasing the number of accepted species of Dolichandra to nine. A taxonomic key for all species of Dolichandra is presented.
Taxonomic key, Neotropical lianas, Dolichandra hispida
Dolichandra Cham. is a genus of lianas that belongs to the tribe Bignonieae, in the plant family Bignoniaceae (
The current circumscription of Dolichandra is based on molecular phylogenetic data (
The genus is distributed in wet and dry Neotropical forests, from Mexico to northern Argentina (
Dolichandra cynanchoides (cham.) L.G.Lohmann is cultivated as ornamental in Argentina (
During phylogenic and taxonomic studies of Dolichandra, it became clear that Macfadyena hispida (DC.) Seem. is morphologically distinct from D. uncata (Andrews) L.G.Lohmann and should be recognized as a separate taxon. We here present the necessary new combination. We also provide a taxonomic key for the genus, thus facilitating the identification of the species.
This study was based on botanical collections from nine herbaria (ESA, FUEL, INPA, MBM, MO, NY, SP, SPF, and UPCB). Morphological studies were carried out under a stereomicroscope using dried and fresh specimens. Morphological terminology for leaves follows
Spathodea hispida DC., Prodr. 9: 205. 1845.
Macfadyena hispida (DC.) Seemann, J. Bot. 1: 227. 1863.
Type: Brazil. Mato Grosso: Cuiabá, 1832, A. Silva Manso 105A (holotype: G-DC [G00133604]!).
Spathodea mollis Sond., Linnaea 22: 561. 1849.
Macfadyena mollis (Sond.) Seemann, J. Bot. 1: 227. 1863.
Type: Brazil. Minas Gerais: Caldas, 1855, A.F. Regnell I-292 (lectotype, designated here: MO [2229711]!).
Macfadyena pubescens Moore, Trans. Linn. Soc. London, Bot. ser. 2, 4: 418. 1895.
Paraguay. “inter Villa Maria et Corumbá”, Dec 1891–92, S. Moore 1021 (holotype: BM image [578432]!).
Liana. Stems terete, striate, interpetiolar region with ridges and glandular fields, eglandular and glandular trichomes covering the stem surface, eglandular trichomes simple, densely distributed in a hispid indument, glandular trichomes peltate and pateliform, flaky bark absent; prophylls 1.6–3 mm long, subulate, apiculate, smooth, hispid. Leaves bifoliolate with a terminal tendril; petioles semi-terete, hispid and with peltate trichomes, 0.95–4.49 cm long; petiolules terete, hispid with simple and peltate trichomes, 0.3–2.9 cm long, with equal length; tendrils trifid and uncinate; leaflets ovate, obovate or elliptic, apex acute to short acuminate with a drip tip, base rounded, symmetric or slight asymmetric, 3.2–8.6 × 1.2–7.14 cm, margin entire, membranaceous, the abaxial surface hispid with simple trichomes more concentrated on the veins, peltate trichomes throughout and pateliform glandular trichomes concentrated at the base, the adaxial surface hispid, primary venation straight, unbranched, secondary venation brochidodromous and tertiary venation percurrent. Inflorescence an axillary 3-flowered cyme, rarely reduced to one flower; pedicels 0.5–4.3 cm long, hispid and with peltate glandular trichomes; receptacle with pateliform trichomes; bracts deciduous, floral bracts filiform, deciduous, rarely present, elliptic to obovate, 0.7–5.5 mm long, membranaceous. Calyx green, bi-lobed, spathaceous with an incurved apicule, 1.4–3.2 × 0.7–1.6 cm, membranaceous, glabrate to hispidulous, with peltate trichomes. Corolla yellow, bilabiate with the upper 2 lobes reflexed and the lower 3 lobes forward, tubular-infundibuliform, glabrate, hispidulous 5.1–9.1 cm long, 1.3–2.2 cm, 4–5.7 cm wide; lobes obcordate, 1.2–2 cm long, 1.2–2.15 cm wide, margin entire. Androecium inserted at the tube, with simple trichomes at the insertion; short filaments 1.15–1.7 cm long, longer filaments 1.74–2.4 cm long, glabrous, attached at the same height from the base of the corolla, 4.5–9.4 mm from the base; staminode 8–9 mm long; anthers pale-yellow or white, 3–3.9 mm long. Gynoecium inserted at the tube, glabrous; pistil 3.3–3.8 cm long; ovary vinaceus, linear, 7–9 × 1.4 mm long; style 2.6–3 cm long; stigma rhombic. Fruits linear, attenuate toward base and apex, 77–125.8 × 1.17–2.2 cm, smooth, with lenticels, glabrous. Seeds with hyaline wings, thin, 2.2–3.8 × 1.4–1.8 cm wide, seed body oblong to ovoid, woody, 6–9 × 8–15 mm.
A single specimen was cited by Sonder for Spathodea mollis labeled 292 in Regnell’s first series of collections from Brazil. Four specimens labeled as Regnell I-292 were located, one at K [000449792], two at BR [876279] [876378] and one at MO [2229711]. The best quality material is selected here as lectotype.
Dolichandra hispida is easily differentiated from all other species of Dolichandra by the unique hispid indument found on the vegetative and reproductive portions of this species, as well as the presence of a vinaceus ovary. Dolichandra hispida has been treated as a synonym of D. uncata since
Comparison of Dolichandra hispida and D. uncata; non-overlapping characters are shown in bold.
Characters | Dolichandra hispida | Dolichandra uncata |
---|---|---|
Leaflet form | Ovate, obovate (rare elliptic) | Elliptic (rare Ovate, obovate) |
Leaflet apex | Acute to short acuminate | Long acuminate (rare short acuminate) |
Indument | Hispid | Pubescent (rare glabrous) |
Calyx | Short apiculate (1.2–2.3 mm) | Long apiculate (1.8–3.4 mm) |
Ovary color | Vinaceus | Green |
Fruit length | 9.2–38.5 cm | 77–125.8 cm |
Seed texture | Hyaline | Corky/woody |
Dolichandra uncata occurs predominantly in riverbanks, swamps and mangroves, presenting seeds that are corky and supposedly adapted for water dispersal (
Dolichandra hispida occurs in southern, southwestern and central Brazil, Paraguay and Bolivia, whereas D. uncata has its northern limit in Mexico and southern limit in Argentina and Uruguay (Fig.
This species was collected in flower in September, October, November, December and January and in fruit in September, November, December, January and February.
Dolichandra hispida is here considered as Least Concern [LC] according to IUCN criteria (
Argentina. Misiones: Guarani, 03 Mar 2000, N. Deginani 1630 (MO); Bolivia. Santa Cruz: Estancia San Miguelito, 200 km al E de la ciudad de Santa Cruz, 02 Dez 1996, A. Fuentes 1342 (MO); Las Trancas, Lomerio, las parcelas de Bolfor, Las Trancas ‘95, 16 Nov 1994, A. Jardim 1204 (MO); Brazil. Mato Grosso: Alta Floresta, Fazenda Mogno, Ponte do 27, margem direita, mata de capoeira, solo arenoso, 18 Sep 1991, Macedo et al. 3009 (INPA); Paraná: Antonina, Rio Mergulhão, 31 Oct 1973, G. Hatschbach 29172 (MBM); Foz do Iguaçu, Parque Nacional das Cataratas do Iguaçu, 14 Oct 1962, G. Hatschbach 9378 (MBM); Guaraqueçaba, Tagaçaba de Cima, Rio Tagaçaba, orla da Floresta Atlântica, 20 Nov 2003, G. Hatschbach et al. 76720 (MBM); Irati, Riozinho, 01 Oct 1982, G. Hatschbach 45518 (MBM); Laranjeiras do Sul, Salto Santiago, 07 Mar 1991, Silva et al. 955 (UPCB, SP); Fazenda Santa Ana, 31 Oct 1985, Dias s. n. (FUEL, MO); Morretes, início da Estrada do Itupava, beira do Rio Nhumdiaquara, próximo à ponte de Morretes, 29 m elev., 25°26'1.31"S, 48° 52'26.31"W, 12 Mar 2008, L.H.M. Fonseca et al. 27 (SPF, MBM); Pinhão, Vale do Rio Iguaçu, Córrego Estreito, 22 Feb 1996, G. Hatschbach et al. 64429 (MBM); Rio Bonito do Iguaçu, Fazenda Giacomet-Marodin, Pinhal Ralo, 23 Jun 1995, Poliquesi & Cordeiro 328 (MBM, SPF); Tibagi, 696 m elev., 12 Oct 1959, G. Hatschbach 6373 (MBM); Rio Grande do Sul: Morrinhos do Sul, Morro do Forno, trepadeira em borda de Mata Atlântica de encosta, 19 Oct 1997, Jarenkow & Sobral 3204 (MBM); Santa Catarina: Apiúna, floresta ombrófila densa, 549 m elev., 27°10'27"S, 49°18'08"W, 11 Oct 2009, K. Kniess 561 (SPF); São Paulo: Iporanga, estrada entre Apiaí e Iporanga, floresta ombrófila densa, próximo ao Rio Bethary, 240 m elev., 24°32'55"S, 48°41'09"W, 23 Oct 2010, L.H.M. Fonseca & D. Tarabay 157 (SPF, SP, MBM, MO); Iporanga, estrada entre Apiaí e Iporanga, floresta ombrófila densa, próximo ao Rio Bethary, 23 Oct 2010, L.H.M. Fonseca & D. Tarabay 162 (SPF, SP, MBM, MO). Paraguay. Chaco: Bahia Negra, 13 Nov 1946, T. Rojas 13743 (MO); Itapua: Pirapo, Cerca Pirapo. Sitio de plantaciones experimentales de CEDEFO, 10 Oct 1984, D.R. Brunner & W. Buck 853 (MO); Alto Parana: Puerto Stroessner, Itaipu, Forest Reserve Noe. Pto. Puente Stroessner, 27 May 1989, A.H. Gentry 66144 (MO).
1a | Calyx 5-lobed; branchlets with flaky bark; leaflets chartaceous | 2 |
– | Calyx 2–3-lobed; branchlets without flaky bark; leaflets chartaceous or membranaceous | 3 |
2a | Floral bracts linear–lanceolate to subulate, < 1 mm wide; calyx lobes rounded and shortly mucronate, magenta, puberulent; corolla puberulent outside with peltate trichomes at the lobes; Colombia, Costa Rica, and Ecuador | D. steyermarkii |
– | Floral bracts elliptic or lanceolate, 2–3 mm wide; calyx lobes ovate–lanceolate, attenuate and mucronate, green, glabrous (except at margin); corolla glabrous outside (sometimes sparsely pubescent at apex); Brazilian Atlantic Forest | D. unguiculata |
3a | Leaflet margins toothed; seed wings woody with a narrow hyaline margin; prophylls subulate, and smooth; riverbanks of Uruguay River basin | D. dentata |
– | Leaflet margins generally entire (rarely toothed); seed wings hyaline, rarely woody but then, never with a hyaline margin; prophylls generally ovate and lanceolate, if ovate then striate, if smooth then lanceolate or subulate | 4 |
4a | Anthers and stigma exserted; corolla bilabiate with the upper 2 lobes forward and the lower 3 lobes reflexed, red; fruit elliptic and coriaceous | D. cynanchoides |
– | Anthers and stigma included; corolla bilabiate with the upper 2 lobes reflexed and the lower 3 lobes forward, yellow or purple; fruit linear, rarely elliptic, but then woody | 5 |
5a | Leaflet chartaceous; calyx 3-lobed, covering approximately 1/3 of the corolla; corolla purple | D. chodatii |
– | Leaflet membranaceous; calyx 2-lobed or truncated, covering approximately 1/4 or 1/5 of the corolla; corolla yellow | 6 |
6a | Floral bracts foliaceous; calyx with a recurved apicule; fruit an oblong-elliptic capsule | D. quadrivalvis |
– | Floral bracts filiform; calyx without an apicule, if apiculated then the apicule is incurved and never recurved; fruit a narrow, linear capsule | 7 |
7a | Calyx cupular, truncate to sinuous, without an apicule; prophylls ovate and striate | D. unguis-cati |
– | Calyx usually subspathaceously split, often with an incurved apicule; prophylls subulate-lanceolate or subulate and smooth | 8 |
8a | Indument hispidous; ovary vinaceus; fruits 77–125.8 cm long; seeds with hyaline wings; deciduous forests of northern Argentina, southern, southwestern and central Brazil, Paraguay and Bolivia | D. hispida |
– | Species glabrous to puberulous, never hispid; ovary green; fruits 9.2–38.5 cm long; seeds woody and opaque, hyaline wings absent; mangroves and swamps from Mexico to Argentina and Trinidad | D. uncata |
We thank FAPESP for a Master’s scholarship to LHMF (2009/12508-3) and a regular research grant to LGL (2011/50859-2); a collaborative Dimensions of Biodiversity Grant supported by FAPESP (2012/50260), NSF and NASA; CNPq for a Pq-1C fellowship to LGL and a Pq-2 fellowship to MFA; and, IDEA WILD for field equipment. We are also grateful to Iona Stevens for her review and comments on this manuscript; Dayane Tarabay for field assistance; Iona Stevens, Alberto Vicentini and André Olmos Simões for comments on earlier versions of the manuscript; and, the curators of the herbarium ESA, FUEL, INPA, MBM, MO, NY, SP, and UPCB for specimen loans.