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black swallow-wort

dompte-venin

Stems

erect to prostrate proximally, twining distally.

twining, sometimes only at tips [not twining], unarmed, minutely pilosulous with eglandular trichomes in decurrent lines from nodes to glabrate [densely pubescent or glabrous].

Leaves

petiole 0.5–1.5 cm;

blade pinnipalmately veined, lanceolate to broadly ovate, 3–12 × 1–6.5 cm, membranous, base truncate, rounded, or subcordate, with 2–8 laminar colleters, margins ciliate, apex attenuate to acuminate, surfaces pilosulous on veins abaxially, glabrous adaxially.

persistent, opposite, petiolate (sessile);

stipular colleters apparently absent;

laminar colleters present or absent.

Inflorescences

solitary at nodes, simple or compound cymes, 4–10-flowered;

peduncle 0.5–1.5 cm, pilosulous.

axillary, cymose, pedunculate.

Pedicels

5–6 mm, pilosulous.

Flowers

calyx lobes lanceolate to deltate, 1–1.5 mm, apex acute, pilosulous to glabrate, margins ciliate;

corolla very dark purple, rotate to rotate-campanulate, fleshy, lobes apically planar, deltate, 1.5–3 mm, ± as wide as long, apex acute, glabrous abaxially, pilosulous to hispidulous adaxially, gynostegial corona a thick, shallowly 5-lobed or crenulate ring exceeding style apex, reddish purple to dark purple;

style apex depressed, umbonate, green.

calycine colleters present;

corolla pinkish tan, pale reddish brown, or dark purple [cream, yellowish], campanulate to rotate, aestivation contort-dextrorse (nearly valvate);

coralline corona absent;

androecium and gynoecium united into a gynostegium adnate to corolla tube;

gynostegial corona annular or of 1 whorl of 5 thick, laminar to prismatic segments;

anthers adnate to style, locules 2;

pollen in each theca massed into a rigid, vertically oriented pollinium, pollinia lacrimiform, joined from adjacent anthers by translators to common corpusculum and together forming a pollinarium.

Fruits

follicles, solitary or paired, pendulous, narrowly lance-ovoid to fusiform, smooth, glabrous.

Seeds

7–15, brown, ovate, 6–8 × 3–4.5 mm;

coma white, 2–3 cm.

winged, not beaked, ovate or lanceolate, lenticular, comose, not arillate.

Follicles

4–8 × 0.7–1 cm, apex attenuate to acuminate.

Vines

(erect herbs), herbaceous;

latex clear.

x

= 11.

2n

= 44.

Vincetoxicum nigrum

Vincetoxicum

Phenology Flowering May–Aug(–Nov); fruiting (Jun–)Jul–Oct.
Habitat Disturbed areas, gardens, fences, old fields, pastures, roadsides, streamsides, ravines, slopes, beaches, rail­roads, limestone, igneous substrates, rocky soils, thickets, woods, grasslands.
Elevation 0–400 m. (0–1300 ft.)
Distribution
from FNA
CT; IL; IN; KS; KY; MA; MD; ME; MI; MO; NH; NJ; NY; OH; PA; RI; VT; WI; ON; QC; sw Europe (France, Italy, Portugal, Spain) [Introduced in North America]
[WildflowerSearch map]
Europe; Asia [Introduced in North America]
Discussion

Vincetoxicum nigrum is more widely known in North America by the illegitimate name Cynanchum nigrum (Linnaeus) Persoon, a later homonym of C. nigrum Cavanilles [basionym of the Mesoamerican species Gonolobus niger (Cavanilles) R. Brown ex Schultes]. It is the more frequently encountered and better established of the two Vincetoxicum species in the United States. One of the earliest and best documented escapes from cultivation occurred in Cambridge, Massachusetts, where garden plantings at Harvard University (when Asa Gray was herbarium director in the late 1800s) and elsewhere were documented as serving as invasion foci for surrounding areas. The species is still commonly encountered on fences in many places in Cambridge. In addition to the states listed above, V. nigrum is known from cultivation near Minneapolis, Minnesota, but is not yet known to have escaped in that state. Chromosome numbers of 2n = 22 and 2n = 44 have been reported from the native range in Europe, and it is unclear whether the introduced populations are exclusively tetraploid or also include diploids (A. DiTomasso et al. 2005). Unlike most species of Apocynaceae that have been studied, V. nigrum has been shown to be capable of autogamous pollination through the in situ germination of pollinia within anther thecae (DiTomasso et al.).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Species ca. 28–35 (2 in the flora).

Vincetoxicum has been treated in many regional floras in North America as a synonym of a large and polyphyletic Cynanchum; however, these genera have been shown to be rather distantly related (S. Liede and A. Täuber 2002; Liede et al. 2012). The circumscription adopted here corresponds in part to the Vincetoxicum clade of Liede et al. (2016). The later homonym Vincetoxicum Walter refers to distantly related species of Gonolobus and Matelea (subtribe Gonolobinae) and is a source of some taxonomic confusion because numerous American species of those genera were described under Vincetoxicum.

Vincetoxicum is well supported as belonging to the Tylophorinae K. Schumann (Asclepiadeae Duby). S. Liede et al. (2012, 2016) recommended uniting Vincetoxicum with Tylophora R. Brown and all other genera of Tylophorinae, except Pentatropis R. Brown ex Wight & Arnott, in order to resolve the non-monophyly of Tylophora and Vincetoxicum. This extreme proposal does not affect species in the flora area, but it seems prudent to exclude Tylophora from the synonymy of Vincetoxicum until a more considered approach to a revision of Tylophorinae is undertaken, weighing the advantages and disadvantages of broadly versus narrowly circumscribed genera.

Reports of Vincetoxicum hirundinaria Medikus [synonyms: Cynanchum medium (Decaisne) K. Schumann, not R. Brown, C. vincetoxicum, V. medium, V. officinale] are based upon plants not persisting outside cultivation or misapplication to plants of V. rossicum. Vincetoxicum hirundinaria was occasionally cultivated in the late nineteenth and early twentieth centuries at scattered sites in the northern United States and southern Canada, but none of the occurrences outside of cultivation appears to have persisted and no extant populations are known. Inconsistent recognition of the specific distinction between V. hirundinaria and V. rossicum, coupled with misapplication of the name C. medium to plants of V. rossicum in the Americas, has led to many erroneous reports of naturalized populations of V. hirundinaria in the flora area. For example, the concept of V. hirundinaria of H. A. Gleason and A. Cronquist (1991) combines attributes of both species. Vincetoxicum hirundinaria can be distinguished most readily from the two naturalized species in the flora area by the cream to yellowish cream corollas.

The two naturalized species in the region, Vincetoxicum nigrum and V. rossicum, are considered invasive and to be threats to native forest understory vegetation. Means to control these species are an active area of research (A. DiTomasso et al. 2005) and the continuing use of V. nigrum as a horticultural species should be curtailed. Monarch butterfly larvae (Danaus plexippus) do not complete development on V. nigrum or V. rossicum; however, there is equivocal evidence for monarch oviposition on Vincetoxicum (DiTomasso et al.). An unusual reproductive characteristic of many species of Vincetoxicum, shared by V. nigrum and V. rossicum, is polyembryonic seeds (DiTomasso et al.).

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Key
1. Corollas dark purple, adaxially pilosulous to hispidulous, lobes deltate, ± as long as wide, apically planar, coronas annular, shallowly lobed; peduncles 0.5–1.5 cm; seeds 6–8 mm.
V. nigrum
1. Corollas pinkish tan to reddish brown, adaxially glabrous, lobes lanceolate, 1.5–2 times longer than wide, apically twisted, coronas of 5 prismatic segments united basally; peduncles 1.5–2.5 cm; seeds 4–6.5 mm.
V. rossicum
Source FNA vol. 14. FNA vol. 14. Author: Mark Fishbein.
Parent taxa Apocynaceae > Vincetoxicum Apocynaceae
Sibling taxa
V. rossicum
Subordinate taxa
V. nigrum, V. rossicum
Synonyms Asclepias nigra, Cynanchum louiseae Antitoxicum, Cynanchum section vincetoxicum
Name authority (Linnaeus) Moench: Suppl. Meth., 313. (1802) Wolf: Gen. Pl., 130. (1776)
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