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erect boerhavia, erect spiderling

red spiderling, spreading hogweed

Habit Herbs, annual [slightly woody at base]; taproot tapered, soft or ± woody. Herbs, perennial [rarely appearing annual], sometimes slightly woody at base; taproot fusiform, woody.
Stems

usually erect, sometimes decumbent, profusely branched primarily distally, 2–12 dm, minutely puberulent with bent hairs basally, usually glabrous, rarely sparsely puberulent distally.

decumbent, ascending, or erect, usually profusely branched throughout, 3–10 dm, glabrous or minutely pubescent basally, glabrous or sparsely pubescent distally.

Leaves

mostly in basal 1/2 of plant;

larger leaves with petiole 6–40(–55) mm, blade broadly rhombic-ovate, triangular-ovate, ovate, oval, or lanceolate, 20–50(–80) × 10–45 mm (distal leaves smaller, proportionately narrower), adaxial surface usually glabrous, sometimes minutely puberulent, usually minutely punctate, abaxial surface slightly paler than adaxial, usually glabrous, sometimes minutely puberulent, usually punctate with small patches of small brown cells, base obtuse to round, margins entire or sinuate, apex usually acute, less often obtuse or rounded.

mostly in basal 1/2 of plant;

larger leaves with petiole 10–30 mm, blade broadly lanceolate, ovate, or broadly ovate, occasionally ± round, 20–60 × 15–50 mm (distal leaves smaller, often proportionally narrower), base truncate, broadly cuneate, round, or shallowly cordate, often oblique, margins sinuate, apex obtuse to round, abaxial surface paler than adaxial, glabrous or minutely puberulent, sometimes glandular, usually with few large multicellular hairs on veins, adaxial surface glabrous, rarely sparsely puberulent, neither surface punctate.

Inflorescences

terminal, forked ca. 4–6 times ± evenly, diffuse, usually with sticky internodal bands;

branches strongly ascending, terminating in irregular umbellate or subracemose clusters of flowers, not all pedicels attaching at same point (flowers occasionally borne singly).

terminal, forked ca. 3–6 times ± equally, diffuse, occasionally with sticky internodal bands;

branches divergent, terminating in compact subumbellate or capitate, 2–5-flowered clusters.

Flowers

pedicel (0–)0.3–2.5(–5) mm;

bracts at base of perianth deciduous, usually 2, narrowly to broadly lanceolate, 0.5–1 mm, apex often acuminate;

perianth whitish, usually tinged with pink or purple [bright pink] between lobes and in tube, campanulate beyond constriction, 1–1.5 mm;

stamens 2–4, slightly exserted.

pedicel shorter than 0.5 mm;

bract at base of perianth quickly deciduous, 1, lanceolate, 0.8–1 mm;

perianth purplish red to reddish pink or nearly white, campanulate beyond constriction, 1–1.5 mm;

stamens 2–3, included or barely exserted.

Fruits

1–11 per cluster, pale greenish to straw colored or tan, narrowly obconic, (2.7–)3–3.5[–4] × 1.2–1.5 mm (l/w: (2–)2.3–3.2), apex truncate or broadly low conic, glabrous;

ribs 5, acute, slightly rugose adjacent to sulci;

sulci 0.5–1 times as wide as base of ribs, slightly to prominently coarsely transverse rugose, not papillate.

(1–)2–5(–9) per cluster, gray-brown to brown, obpyramidal, (3–)3.5–4.5 × 1–1.2 mm (l/w: 2.8–4.1), apex broadly conic, with sparse or moderately dense stipitate-glandular hairs on ribs, less densely pubescent or glabrous in sulci [rarely entirely glabrous];

ribs 5, round, smooth;

sulci ± 2–2.5 times as wide as base of ribs, not rugose, not papillate.

2n

= 26, 52, 54, 116.

Boerhavia erecta

Boerhavia diffusa

Phenology Flowering early summer-mid fall. Flowering mid winter–early fall [year-round].
Habitat Disturbed areas, gardens, road and railroad rights-of-way, stream beds Disturbed areas, waste places, roadsides, dry pinelands, among scrub on tropical reefs
Elevation 0-1700 m [probably much higher in tropics] (0-5600 ft [probably much higher in tropics]) 0-50[-1800] m (0-200[-5900] ft)
Distribution
from FNA
AL; AR; AZ; FL; GA; LA; MD; MO; MS; NC; NM; OK; SC; TN; TX; Mexico; Central America; South America; West Indies [Widely introduced throughout the tropics and warm-temperate regions]
[WildflowerSearch map]
[BONAP county map]
from FNA
FL; GA; SC; Mexico; Central America; South America; West Indies; Asia; Africa; Indian Ocean Islands; Pacific Islands; Australia
[WildflowerSearch map]
[BONAP county map]
Discussion

Boerhavia erecta occasionally forms mixed populations with B. intermedia without apparent intergradation. Rarely, some specimens seem to combine features of either species, particularly with regard to inflorescence structure. This is especially so in Sonora, Mexico, and in parts of the Sonoran Desert in Arizona. The two species bloom simultaneously and are visited by small insects. Given the presumed close relationship and weedy habitats of each, hybridization seems possible. Usually, the two species can be distinguished by the differences in fruit length, the appearance of a crownlike apex of the nearly mature fruits of B. erecta (apex of ridges slightly expanded, apex of fruit slightly conic), and the more precisely constructed terminal umbels of B. intermedia. Both species, particularly B. intermedia, may produce entire inflorescences with branches terminating in single flowers. R. E. Woodson Jr. and H. J. Kidd (1961) suggested that B. erecta hybridizes with the perennial B. diffusa.

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

Boerhavia diffusa belongs to a pantropical complex whose distribution, because of differing taxonomic treatments, is not precisely discernable. In North America, the West Indies, and elsewhere, the complex has been treated as having one (e.g., R. W. Long and O. Lakela 1971; R. P. Wunderlin 1998) or two species (E. A. Kellogg 1988; J. K. Small 1913c; P. C. Standley 1918; C. Whitehouse 1996). In the latter situation various binomials have been used. The abrupt bend in the ribs near the fruit apex, making a broadly conic apex, seems to be a useful character for distinguishing most B. diffusa. The shape of the apex, the sparse pubescence of the fruit, the few fruits in individual terminal clusters, and the open, ± leafless inflorescence may have led R. E. Woodson Jr. and H. J. Kidd (1961) to suspect hybridization of this complex with the annual B. erecta. Hybridization is plausible (R. Spellenberg 2000), but clearly intermediate plants are not known.

The leaves are sometimes used as a vegetable (C. Whitehouse 1996). Extracts from roots are used to prepare an expectorant, a diuretic, and a laxative, and in treating asthma (S. P. Ambasta 1986).

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

Source FNA vol. 4, p. 22. FNA vol. 4, p. 19.
Parent taxa Nyctaginaceae > Boerhavia Nyctaginaceae > Boerhavia
Sibling taxa
B. anisophylla, B. ciliata, B. coccinea, B. coulteri, B. diffusa, B. gracillima, B. intermedia, B. linearifolia, B. megaptera, B. pterocarpa, B. purpurascens, B. spicata, B. torreyana, B. triquetra, B. wrightii
B. anisophylla, B. ciliata, B. coccinea, B. coulteri, B. erecta, B. gracillima, B. intermedia, B. linearifolia, B. megaptera, B. pterocarpa, B. purpurascens, B. spicata, B. torreyana, B. triquetra, B. wrightii
Name authority Linnaeus: Sp. Pl. 1: 3. (1753) Linnaeus: Sp. Pl. 1: 3. (1753)
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