Chaenactis thompsonii |
Chaenactis santolinoides |
|
|---|---|---|
|
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 |
WA
|
CA
|
| 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 | ||
| Sibling taxa | ||
| 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. | FNA vol. 21, p. 407. |
| Web links | ||