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Chaenactis thompsonii

Thompson's pincushion

santolina chaenactis, santolina pincushion

Habit Perennials, 10–30 cm (not or scarcely cespitose, not matted); proximal indument thinning with age, grayish, arachnoid-sericeous to thinly lanuginose. Perennials, 10–25(–35) cm (cespitose or ± matted); proximal indument thinning with age, whitish to grayish, lanuginose.
Stems

mostly 5–15+, ascending to erect.

mostly 5–15+, erect to ± spreading.

Leaves

mostly cauline, 2–5 cm;

largest blades ± elliptic, ± plane, 1-pinnately lobed;

lobes mostly 2–5 pairs, remote, ± plane.

basal, (1–)3–11 cm;

largest blades linear-cylindric to ± fusiform, 3-dimensional, 1–2-pinnately lobed;

primary lobes (7–)10–18+ pairs, ± imbricate, ultimate lobes ± involute, twisted.

Peduncles

ascending to erect, 2–5 cm.

mostly ascending to erect, mostly 8–25 cm.

Involucres

± obconic.

obconic to ± cylindric.

Corollas

7–9 mm.

5–7 mm.

Phyllaries

longest (10–)12–15 mm;

outer closely lanuginose, not stipitate-glandular, apices erect, ± rigid.

longest 8–13 mm;

outer evidently stipitate-glandular and, sometimes, ± arachnoid, apices erect, ± rigid.

Heads

mostly 1–3 per stem.

1(–3) per stem.

Cypselae

7–9 mm (eglandular);

pappi: longest scales 3.5–5 mm.

4–6 mm;

pappi: longest scales 3–4.5 mm.

2n

= 12.

Chaenactis thompsonii

Chaenactis santolinoides

Phenology Flowering Jun–Aug. Flowering (Mar–)May–Jul.
Habitat Rocky or gravelly serpentine slopes, scree, talus, openings in or above conifer forests Exposed sandy to rocky summits, ridges, scree, talus, openings in or above conifer forests, sometimes road cuts or other recent disturbances
Elevation (900–)1200–2200 m [(3000–)3900–7200 ft] (1100–)1500–2800 m [(3600–)4900–9200 ft]
Distribution
map from FNA
WA
[WildflowerSearch map]
[BONAP county map]
map from FNA
CA
[WildflowerSearch map]
[BONAP county map]
Discussion

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.)

Of conservation concern.

Chaenactis santolinoides is known from the southern Sierra Nevada and Transverse Ranges. It is sometimes cultivated in rock gardens and may be found beyond its native range. It may be relatively recently derived from an isolated segment of C. douglasii var. alpina. The morphology of C. panamintensis (here assigned to C. douglasii var. alpina) suggests past convergence toward, or genetic influence from, C. santolinoides.

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

Parent taxa Asteraceae > tribe Heliantheae > subtribe Chaenactidinae > Chaenactis > sect. Macrocarphus Asteraceae > tribe Heliantheae > subtribe Chaenactidinae > Chaenactis > sect. Macrocarphus
Sibling taxa
C. alpigena, C. artemisiifolia, C. carphoclinia, C. cusickii, C. douglasii, C. evermannii, C. fremontii, C. glabriuscula, C. macrantha, C. nevadensis, C. nevii, C. parishii, C. santolinoides, C. stevioides, C. suffrutescens, C. xantiana
C. alpigena, C. artemisiifolia, C. carphoclinia, C. cusickii, C. douglasii, C. evermannii, C. fremontii, C. glabriuscula, C. macrantha, C. nevadensis, C. nevii, C. parishii, C. stevioides, C. suffrutescens, C. thompsonii, C. xantiana
Name authority Cronquist: in C. L. Hitchcock et al., Vasc. Pl. Pacif. N.W. 5: 123, fig. [p. 125]. (1955) Greene: Bull. Torrey Bot. Club 9: 17. (1882)
Source FNA vol. 21, p. 407. Treatment author: James D. Morefield. FNA vol. 21, p. 407. Treatment author: James D. Morefield.
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