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purple everlasting-cudweed, spoon-leaf cudweed, spoon-leaf purple everlasting

desert cudweed

Habit Annuals (sometimes winter annuals), 10–40(–50) cm; fibrous-rooted or taprooted. Annuals, 2.5–20(–35) cm; usually taprooted, sometimes fibrous-rooted.
Stems

erect to decumbent-ascending, densely but loosely pannose or pannose-tomentose.

erect to decumbent-ascending, densely and loosely arachnose-tomentose.

Leaves

basal and cauline, basal and proximal cauline usually withering before flowering;

blades oblanceolate to spatulate, 1–6 cm × 5–14 mm (distal similar, at least among proximal heads, margins sometimes sinuate), faces usually bicolor, abaxial closely white-pannose, adaxial usually sparsely arachnose (basal cells of hairs persistent, expanded, glassy), sometimes glabrescent.

mostly cauline, basal usually withering before flowering, blades mostly oblanceolate to oblong-oblanceolate (± uniform in size and shape), 1–2.5(–3) cm × 2–6 mm, faces concolor or weakly bicolor, both loosely tomentose or adaxial glabrescent and greener.

Involucres

turbinate-cylindric, 4–4.5 mm, bases sparsely arachnose.

campanulate, 2.5–3 mm, bases sparsely arachnose.

Florets

bisexual 3–4; all corollas usually purplish distally.

bisexual (2–)3(–4); all corollas purplish distally.

Phyllaries

in 4–5 series, outer ovate-triangular, lengths 1/3–2/3 inner, apices acute-acuminate, inner triangular-lanceolate (usually striate), laminae purplish (in bud) to whitish or silvery (in fruit), apices acute (not apiculate).

in 3–4(–5) series, outer ovate-triangular, lengths 1/2–2/3 inner, apices broadly acute, inner oblong, laminae usually purple (immediately beyond stereome and along proximal margins), apices (whitish) rounded-obtuse.

Heads

initially in continuous spiciform arrays 1–4(–5) cm × (5–)10–15 mm, later interrupted (glomerules widely separated, bracteate, the proximal often on relatively long peduncles).

in capitate clusters (in smallest plants) ca. 1 cm or interrupted, spiciform arrays 1–3(–12) cm × 8–12 mm (pressed, sometimes branching at proximal nodes, glomerules subtended by divergent-ascending bracts similar to distal cauline leaves).

Cypselae

(tan) 0.6–0.7 mm.

(tan) 0.3–0.5 mm.

2n

= 14, 28.

Gamochaeta purpurea

Gamochaeta stagnalis

Phenology Flowering Apr–May(–Jun). Flowering (Mar–)Apr(–May).
Habitat Open, usually disturbed, commonly sandy habitats, roadsides, fields, woodland clearings and edges Sandy, often moist soils, washes, permanent streams, canyon bottoms, flower beds, riparian, desert grasslands, juniper-grasslands, creosote bush-mesquite-cholla, oak woodlands
Elevation 5–300 m (0–1000 ft) 900–1800 m (3000–5900 ft)
Distribution
from FNA
AL; AR; AZ; CT; DC; DE; FL; GA; IA; IL; IN; KS; KY; LA; MA; MD; ME; MI; MO; MS; NC; NJ; NY; OH; OK; PA; RI; SC; TN; TX; VA; WV; HI; ON; Mexico; South America; West Indies; Central America (Nicaragua)
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from FNA
AZ; NM; Mexico
[BONAP county map]
Discussion

Gamochaeta purpurea apparently is native to North America and adventive elsewhere.

Basal cells of hairs on adaxial faces of leaves are expanded and glassy (versus hairs filiform to bases in most other species) and are diagnostic for Gamochaeta purpurea. From Maryland northward, plants of G. purpurea produce relatively small basal rosettes and relatively shallow fibrous roots or a filiform taproot; southward and southwestward, the basal rosettes often are larger and the fibrous roots are denser.

Gamochaeta purpurea apparently occurs widely through the world as a weed; it is fairly clearly native to eastern North America, where it is the least weedy of the gamochaetas. Plants of G. purpurea in southern Arizona along perennial streams at the base of the Santa Catalina Mountains were first collected in 1903 (G. L. Nesom 2004) and were, perhaps, accidentally established through visitation; the same sites are heavily infested by other, more aggressive, nonnative species. Collections of G. purpurea also have been made at higher elevations in the Santa Catalina, Rincon, and Chiricahua mountains, where the species is less likely to have been introduced by human activity. It also seems unlikely that plants in scattered Mexican localities were introduced there by human activity.

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

Morphologic differences between Gamochaeta antillana and G. stagnalis are subtle but consistent; the two are distinct in geography and ecology. The previous attribution of G. falcata (Lamarck) Cabrera to Arizona (G. L. Nesom 1990f) was based on specimens of G. stagnalis. Those plants have been misidentified as G. purpurea also.

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

Source FNA vol. 19, p. 433. FNA vol. 19, p. 437.
Parent taxa Asteraceae > tribe Gnaphalieae > Gamochaeta Asteraceae > tribe Gnaphalieae > Gamochaeta
Sibling taxa
G. antillana, G. argyrinea, G. calviceps, G. chionesthes, G. coarctata, G. pensylvanica, G. simplicicaulis, G. sphacelata, G. stachydifolia, G. stagnalis, G. ustulata
G. antillana, G. argyrinea, G. calviceps, G. chionesthes, G. coarctata, G. pensylvanica, G. purpurea, G. simplicicaulis, G. sphacelata, G. stachydifolia, G. ustulata
Synonyms Gnaphalium purpureum, G. rosacea, Gnaphalium rosaceum Gnaphalium stagnale
Name authority (Linnaeus) Cabrera: Bol. Soc. Argent. Bot. 9: 377. (1961) (I. M. Johnston) Anderberg: Opera Bot. 104: 157. (1991)
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