Chaenactis thompsonii
Chaenactis
Thompson's pincushion
chaenactis, dusty-maidens, false-yarrow, pincushion
mostly 5–15+, ascending to erect.
erect to prostrate, usually branched.
mostly cauline, 2–5 cm;
largest blades ± elliptic, ± plane, 1-pinnately lobed;
lobes mostly 2–5 pairs, remote, ± plane.
basal and/or cauline (smaller and sparser distally except in C. cusickii); alternate; usually petiolate;
blades deltate, elliptic, linear, oblanceolate, or ovate (plane or ± 3-dimensional), (0–)1–4-pinnately (rarely -subpalmately) lobed, ultimate margins entire, faces glabrous or hairy, often stipitate-glandular or gland-dotted.
ascending to erect, 2–5 cm.
± obconic.
hemispheric to obconic or broadly cylindric, (3–)5–15[–25] mm diam.
convex to ± flat, pitted and/or knobby, usually epaleate (paleae 3–10+ in C. carphoclinia).
0 (sometimes simulated by enlarged peripheral disc corollas).
8–70+, bisexual, fertile (diurnal with anthers exserted except in C. macrantha);
corollas white, pinkish, cream, or yellow, tubes shorter than cylindric or funnelform throats, lobes 5, deltate to ± lanceolate (sometimes enlarged, unequal; style-branch appendages blunt, obscure).
7–9 mm.
longest (10–)12–15 mm;
outer closely lanuginose, not stipitate-glandular, apices erect, ± rigid.
5–21+ in 1–2(–3) series (subequal to unequal).
mostly 1–3 per stem.
discoid or ± radiant, borne singly or in (terminal) ± cymiform arrays (erect in bud except C. macrantha).
7–9 mm (eglandular);
pappi: longest scales 3.5–5 mm.
clavate to ± cylindric or compressed, obscurely 8–20-angled, faces scabrous and strigose to densely sericeous (usually eglandular);
pappi usually persistent, of (1–)4–20, distinct, ± erose scales in 1–4 series (equal or unequal, outer then shorter, scales usually fewer and/or shorter on peripheral cypselae, midnerves obscure), sometimes 0 or coroniform.
= ? (n = 6, 8, plus polyploids and dysploid numbers).
Chaenactis thompsonii
Chaenactis
Of conservation concern.
Chaenactis thompsonii appears to be sister to C. evermannii; it is known from the mountains of central and northwestern Washington. The similar habits of C. thompsonii and C. ramosa (= C. douglasii var. douglasii) appear to result from convergent evolution in the distinctive habitat of their type localities (Wenatchee Mountains), not from a close genetic relationship as suggested by Cronquist.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
Species 18 (17 in the flora).
Chaenactis species grow in arid to alpine or Mediterranean climates, usually in open, unstable or early seral habitats (loose sand, scree, talus, shrink-swell clay, fire-adapted vegetation, recent disturbances). Some annual species have been grown in gardens in the eastern United States.
Differences in induments are key to distinguishing some Chaenactis species. Unless otherwise noted in descriptions and key leads, assume for any given plant that indument of proximal leaves and adjacent proximal portions of stems (“proximal indument”) is similar; indument of distal leaves is, likewise, similar to indument of stem portions from which they arise; peduncle indument is denser distally than proximally; and distal peduncle indument is similar to proximal phyllary indument. Unless otherwise noted, phyllary traits apply to the outer series only. Pappus scales may be equal, subequal, or unequal; unequal scales may intergrade (here said to be in gradually unequal series) or may form two, more or less uniform, shorter and longer series (here said to be in abruptly unequal series); subequal scales are said to be in subequal series. Excellent illustrations of most Chaenactis species appeared in L. Abrams and R. S. Ferris (1923–1960, vol. 4) and A. Cronquist (1955).
Section Acarphaea is distinctive by its farinose indument and base chromosome number of 8, among other traits; it could prove to be a separate, convergent genus. Natural and artificial hybrids have been documented among some members of sect. Chaenactis (see further discussion there). Reports of hybrids among species of the other two sections are few and doubtful. Chaenactis appears to be most closely related to the monotypic Dimeresia and Orochaenactis, which B. G. Baldwin et al. (2002) treated together as a narrowly circumscribed tribe, Chaenactideae.
(Discussion copyrighted by Flora of North America; reprinted with permission.)
1. Annuals; proximal indument predominantly ± farinose, not arachnoid; largest leaf blades (2–)3–4-pinnately lobed | sect. Acarphaea |
1. Annuals, biennials, perennials, or subshrubs; proximal indument predominantly arachnoid, lanuginose, pannose, stipitate-glandular, or glabrescent, not farinose; largest leaf blades (0–)1–2-pinnately or -subpalmately lobed | → 2 |
2. Biennials, perennials, or subshrubs (rarely flowering first year); pappi of (8–)10–20 scales in 2–4 equal or gradually unequal series; leaf blades gland-dotted beneath indument | sect. Macrocarphus |
2. Annuals; pappi usually of (1–)4–8(–14) scales in 1, 2 abruptly unequal, or 2–3 gradually unequal series, sometimes 0 or coroniform; leaf blades not gland-dotted (except C. macrantha) | sect. Chaenactis |
WA
Flora NW
PNW Herbaria
WildflowerSearch
iNaturalist
USDA Plants Database
CA
OR
