Decalobanthus discoidespermus (Donn.Sm.) Staples, 2022

Staples, G., 2022, A synoptic revision of the golden glories, genus Decalobanthus (Convolvulaceae), Blumea 67 (1), pp. 37-70 : 49-50

publication ID

https://doi.org/10.3767/blumea.2022.67.01.08

persistent identifier

https://treatment.plazi.org/id/03CAC652-504E-FFCF-E142-FB5DFA70FDE7

treatment provided by

Felipe

scientific name

Decalobanthus discoidespermus (Donn.Sm.) Staples
status

comb. nov.

8. Decalobanthus discoidespermus (Donn.Sm.) Staples View in CoL , comb. nov. — Fig. 5 View Fig ; Map 6 View Map 6

Ipomoea discoidesperma Donn.Sm., Bot. Gaz. View in CoL 14 (1889) 27. — Operculina discoidesperma (Donn.Sm.) House (1909) View in CoL 68. — Merremia discoidesperma (Donn.Sm.) C.A. O’Donnell (1941) View in CoL 495. — Lectotype (first step designated by Standley & Williams(1970) 73,second step designated here;see Typification): Von Türckheim 744 (lecto US [ US 00111388]; isolecto US [ US 00111389]*), Guatemala, Alta Verapaz, Pansamalá.

Operculina populifolia Hallier f. ex Urb. (1912) View in CoL 342. — Lectotype (designated by Staples et al. (2020) 131): Wright 3083 (lecto MO [MO-150302]), Cuba.

Stems and branches not lenticellate. Leaves basally attached, broadly ovate to suborbicular, 6–14 by 3.5–12 cm, bases rounded to emarginate; secondary veins 5–7 on either side of the midvein. Inflorescences cymose or flowers solitary; bracts caducous. Flower sepals equal, ovate, 20–26 by 10–16 mm, apically rounded to acute; corollas tubular-funnelform, 4.8–6 cm long, bright yellow, glabrous, limb 3–3.5 cm diam, entire or 5-sided; stamens unequal, included, filaments hairy above insertion point, anthers 3–5 mm long; pistil included, equalling or slightly exceeding stamens. Fruiting calyx accrescent, woody, blackish, deciduous. Fruit a utricle, globose, 3–4 cm diam, chartaceous, pale brown, tardily breaking irregularly. Seed 1, quatrefoil, flattened spheroidal, 1.8–2.5 cm diam, bearing a circular hilum on one side and an impressed cross on the reverse, black, velutinous at first, later glabrous and shiny.

Previously published illustrations — Gunn (1977: f. 6, 7). An excellent series of detailed colour photos taken in the field by Reinaldo Aguilar (https://flic.kr/p/2mdpYGA vouchered by Aguilar 17796 in CR) is available online.

Distribution — Pacific and Atlantic coasts of Middle America (southern Mexico, Guatemala, Nicaragua, Costa Rica), and the Greater Antilles ( Cuba, Dominican Republic, Haiti) in the Caribbean. Absent from Belize, El Salvador, and Honduras, whether from low collecting density or lack of suitable habitats is unknown. Reports for Panamá are based solely on drift seeds found on beaches as pointed out by Gunn (1977); the species was not included in the ‘Flora of Panama Convolvulaceae’ ( Austin 1975, 1978).

Habitat & Ecology — A species seemingly always found in forested habitats such as selva alta perennifolia (primaria) (tall evergreen primary forest), lower montane rain forest, cloud forest (broadleaf), and wet somewhat degraded rainforest. Soil types recorded include a limestone fissured ridge and deep laterite (on eruptive). Elevations range from 100–900(–1650) m .

Vernacular names — Cuba: Almorrana ( Alain 1957), terciopelo (Eggers 4981), tomate de mar ( Alain 1957). Guatemala: Boton de terciopelo (Von Türckheim 744), quiebra-cajete ( Standley & Williams 1970). Mexico: Ppak i kaknab (Mayan; Gunn 1977: 237), quiebraplato amarillo (Spanish; Dugés s.n.). Nicaragua: Contra-venano (E.P. Alexander s.n.). English name for the seed: Mary’s-bean ( Gunn 1977).

Uses — The seeds are well documented to drift thousands of kilometres via ocean currents ( Gunn & Dennis 1976, Gunn 1977) in both the North Atlantic and North Pacific. Several ethnobotanical uses are known in places where these seeds wash ashore ( Gunn & Dennis 1976, Gunn 1977).

Typification — John Donnell Smith (1889) did not desig- nate a holotype per se and cited two different specimens, Von Türckheim 744 and S. Watson 412, in the protologue, both of which, under the modern ICN (Turland et al. 2018), are to be considered syntypes. Standley & Williams (1970: 73) made an indirect first step lectotype choice when they stated the ‘type’ was ‘from Pansamalá, Türckheim 744’. Later mentions of the ‘holotype’ by Gunn (1977: 250) and ‘lectotype’ by McDonald (1993: 65) reiterated this choice. However, there are two sheets of Von Türckheim 744 in the US and I have here made a second step lectotypification by choosing the sheet with bar code US 00111388 as the lectotype.

Note — The vegetative and floral morphology of this Neotropical species is congruent with the genus concept for Decalobanthus as proposed here. However molecular sequences extracted from herbarium vouchers proved ambiguous and so the species has not been placed in any molecular phylogenetic arrangement published to date. When conclusive molecular data is available, I fully expect this species will be placed in the Decalobanthus clade. Nevertheless, on a morphological basis alone I am confident that this species belongs in Decalobanthus .

A

Harvard University - Arnold Arboretum

Kingdom

Plantae

Phylum

Tracheophyta

Class

Magnoliopsida

Order

Solanales

Family

Convolvulaceae

Genus

Decalobanthus

Loc

Decalobanthus discoidespermus (Donn.Sm.) Staples

Staples, G. 2022
2022
Loc

Merremia discoidesperma (Donn.Sm.) C.A. O’Donnell (1941)

C. A. O'Donnell 1941
1941
Loc

Operculina populifolia Hallier f. ex

Urb. 1912
1912
Loc

Operculina discoidesperma (Donn.Sm.)

House 1909
1909
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