Gamochaeta purpurea
Gamochaeta
purple everlasting-cudweed, spoon-leaf cudweed, spoon-leaf purple everlasting
cudweed, everlasting
erect to decumbent-ascending, densely but loosely pannose or pannose-tomentose.
1+, usually erect, sometimes decumbent-ascending.
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.
basal and cauline; alternate;
sessile;
blades mostly linear to oblanceolate or spatulate, bases cuneate to ± cordate, margins entire, sometimes sinuate, abaxial faces mostly white or gray and tomentose or pannose-tomentose, adaxial green and glabrescent or glabrous, or grayish and arachnose, loosely tomentose, or subpannose.
turbinate-cylindric, 4–4.5 mm, bases sparsely arachnose.
narrowly to broadly campanulate, 2.5–5 mm.
flat (concave in fruit), glabrous, epaleate.
bisexual 3–4; all corollas usually purplish distally.
50–130, more numerous than bisexual florets;
corollas all yellow or purplish-tipped.
2–7;
corollas all yellow or distally purplish.
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 3–7 series, unequal, mostly brownish to stramineous, sometimes purplish, hyaline, often shiny, distally chartaceous to scarious, eglandular.
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).
disciform, usually in glomerules borne in continuous or interrupted, usually spiciform, sometimes paniculiform, arrays (reduced to terminal glomerules in depauperate individuals).
(tan) 0.6–0.7 mm.
oblong, slightly flattened, faces with papilliform hairs (myxogenic, their lengths about equaling diams.);
pappi readily falling, of 12–28 barbellulate bristles in 1 series (basally connate in smooth rings, falling as units).
= 7.
= 14, 28.
Gamochaeta purpurea
Gamochaeta
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.)
Species ca. 50 (12 in the flora).
Gamochaeta comprises about 50 species (A. L. Cabrera 1961; S. E. Freire and L. Iharlegui 1997) or about 80 species (Cabrera 1977+, part 10), all native to the Americas. Most are known only from South America; some apparently are native to Mexico and the flora area (G. L. Nesom 2004b). Some species are strongly weedy and have extended non-native ranges. Because of inconsistencies in the identification of those species, it has been difficult to evaluate the overall distributions of the widespread species.
The distinctiveness of Gamochaeta was emphasized by A. L. Cabrera (1961, and in later floristic treatments of South American species) and by other botanists who have treated it as a separate genus in the last decade. The genus is distinguished by its combination of relatively small heads in spiciform arrays, concave post-fruiting receptacles, truncate collecting appendages of style branches in bisexual florets, relatively small cypselae with minute, mucilage-producing papilliform hairs on the faces, and pappus bristles basally connate in smooth rings and released as single units. It seems likely that most species are primarily autogamous, in view of the tiny, non-showy heads that barely open through flowering. The consistency of vegetative and floral features in some of the species supports this hypothesis.
In the flora area, some species have commonly been treated as variants within Gamochaeta purpurea; distinctions are evident in the field, where it is common to find as many as five species growing in proximity without intergradation. Species of Gamochaeta are distinguished by differences primarily in root form, leaf shape, nature and distribution of indument, and phyllary morphology. Chromosome counts have been reported for some species; because of the unreliability of identifications, vouchers for those counts should be restudied.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
1. Leaves bicolor (abaxial faces closely white-pannose to pannose-tomentose, indument obscuring epidermis, adaxial faces glabrous or glabrate to sparsely arachnose) | → 2 |
1. Leaves concolor or weakly bicolor (abaxial and adaxial faces ± equally greenish to gray-greenish, indument usually loosely tomentose or arachnose, sometimes subpannose, adaxial sometimes glabrescent in G. stagnalis) | → 7 |
2. Basal and proximal cauline leaves usually withering before flowering (clusters of smaller leaves usually present in cauline axils); stems erect or ascending; plants (30–)50–85 cm; apices of inner phyllaries acute-acuminate; flowering mostly Jul–Aug | G. simplicicaulis |
2. Basal and proximal cauline leaves present or not at flowering; stems erect to decumbent-ascending; plants mostly 10–50 cm; apices of inner phyllaries acute to obtuse, rounded, or blunt; flowering mostly Apr–Jun(–Jul in G. calviceps) | → 3 |
3. Adaxial leaf faces glabrous or glabrate; involucres (± purplish) 2.5–3 mm, bases glabrous; outer phyllaries elliptic-obovate to broadly ovate-elliptic, apices rounded to obtuse; bisexual florets 2–3 | G. coarctata |
3. Adaxial leaf faces sparsely arachnose (hairs persistent, evident at 10×); involucres (sometimes purplish) 3–4.5(–5) mm, bases (imbedded in tomentum) often sparsely arachnose on proximal 1/5–1/2; outer phyllaries ovate, ovate-triangular, or ovate-lanceolate, apices acute to acuminate; bisexual florets 2–6 | → 4 |
4. Stems not pannose (induments whitish, like closely appressed, polished cloth, hairs usually not individually evident); involucres 3–3.5(–4) mm; apices of inner phyllaries acute to acute-acuminate; bisexual florets 2–4 (cypselae purple) | G. chionesthes |
4. Stems usually ± pannose or pannose-tomentose (hairs individually evident, longitudinally arranged); involucres 3–4.5 mm; apices of inner phyllaries acute, obtuse, or truncate-rounded, sometimes apiculate; bisexual florets 3–6 (cypselae tan to brownish) | → 5 |
5. Blades of cauline leaves oblanceolate to spatulate (basal cells of hairs on adaxial faces persistent, expanded, glassy); involucres 4–4.5 mm; laminae of inner phyllaries triangular, apices acute (not apiculate); bisexual florets 3–4; plants fibrous-rooted or taprooted | G. purpurea |
5. Blades of cauline leaves oblanceolate to oblanceolate-oblong or oblanceolate-obovate; involucres 4.5–5 or 3–3.5 mm; laminae of inner phyllaries elliptic-oblong to oblong, apices truncate-rounded or obtuse and apiculate; bisexual florets (3–)4–6; plants usually fibrous-rooted, rarely taprooted | → 6 |
6. Arrays of heads uninterrupted (1–5 cm in early flowering) to strongly interrupted, mostly 5–18 cm × 10–12 mm (pressed); involucres 3–3.5 mm; outer phyllaries (tawny-transparent, never dark brown) ovate to ovate-lanceolate; cypselae 0.5–0.6 mm | G. argyrinea |
6. Arrays of heads usually continuous, rarely interrupted (then proximally), mostly 1–6(–8) cm × 12–18 mm (pressed); involucres 4.5–5 mm; outer phyllaries (and, often, laminae of inner, dark or greenish brown) broadly ovate-triangular (mid phyllaries ± keeled near apices); cypselae 0.7–0.8 mm | G. ustulata |
7. Leaf blades linear to narrowly oblanceolate (often folded along midveins, distally becoming arcuate, ± patent bracts surpassing the heads; basal cells of hairs on adaxial faces expanded, glassy); apices of outer phyllaries (brown) acute-acuminate (usually involute and spreading or recurving); Texas, near Mexican border | G. sphacelata |
7. Leaf blades linear or linear-oblanceolate to spatulate, narrowly lanceolate, oblong-oblanceolate, oblanceolate-obovate, or oblanceolate (folded or not; if distal leaves or bracts surpassing heads, not arcuate and ± patent); apices of outer phyllaries (sometimes brownish) sometimes acute to acute-acuminate or attenuate-apiculate (not involute, except in G. calviceps); mostly (not always) se United States. | → 8 |
8. Blades of basal and proximal cauline leaves 4–16 mm wide (bracts among heads spatulate to oblanceolate, at least the proximal surpassing the glomerules of heads) | G. pensylvanica |
8. Blades of basal and proximal cauline leaves 2–6(–10) mm wide (mid and distal cauline becoming oblanceolate to linear, bracts among heads linear, oblanceolate, or oblong-oblanceolate, surpassing glomerules or not) | → 9 |
9. Blades of mid and distal cauline leaves oblanceolate (bases subclasping; bracts among heads mostly shorter than glomerules); involucres (not purplish) 3.5–4 mm; phyl- laries in 4–5 series | G. stachydifolia |
9. Blades of mid and distal cauline leaves oblong-oblanceolate or oblanceolate to spatulate, narrowly lanceolate, linear-oblanceolate, or linear (bases not subclasping; bracts among heads shorter or longer than glomerules); involucres (sometimes purplish) 2.5–3.5 mm; phyllaries in 5–7 or 3–4(–5) series | → 10 |
10. Involucres (not purplish) 3–3.5 mm, bases sparsely arachnose or glabrous; arrays of heads interrupted (at least distally, main axes visible between heads); phyllaries in 5–7 series, outer ovate-triangular, lengths 1/3–1/2 inner, apices acute-acuminate; flowering May–Jul | G. calviceps |
10. Involucres (usually purplish, at stereome-lamina junctions of phyllaries) 2.5–3 mm, bases sparsely arachnose; arrays of heads initially capitate clusters or cylindric and uninterrupted (at least distally, main axes obscured by heads); phyllaries in 3–4(–5) series, outer ovate-lanceolate, lengths 1/2–2/3 inner, apices narrowly to broadly acute; flowering (Feb–)Mar–May (later with moisture) | → 11 |
11. Cauline leaves and bracts among heads narrowly lanceolate, linear-oblanceolate, or linear; arrays of heads initially uninterrupted cylindro- spiciform (becoming glomerulate-interrupted in late flowering) | G. antillana |
11. Cauline leaves and bracts among heads mostly oblanceolate to oblong-oblanceolate (± uniform in size and shape); arrays of heads capitate clusters or interrupted spiciform arrays (from early through late flowering) | G. stagnalis |
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