Chaenactis glabriuscula |
Chaenactis evermannii |
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common yellow chaenactis, yellow pincushion |
Evermann's pincushion |
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Habit | Plants 6–60 cm; proximal indument grayish to whitish, arachnoid to densely lanuginose, or glabrescent. | Perennials, mostly 6–12 cm (cespitose or ± matted); proximal indument thinning with age, grayish, mostly arachnoid-sericeous to thinly lanuginose. | ||||||||||||||||
Stems | mostly 1–5(–12; sometimes ± horizontal); branches proximal and, often, distal. |
mostly 5–20+, ascending to erect. |
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Leaves | basal (often withering) and cauline, 1–10 cm; largest blades linear or ± elliptic, plane to 3-dimensional, succulent or not, (0–)1–2-pinnately lobed; primary lobes 1–7 pairs, remote to ± congested, ultimate lobes ± plane, involute, twisted, and/or terete. |
basal, 1–5 cm; largest blades broadly ± elliptic, ± plane, 1-pinnately lobed; lobes 2–5 pairs, remote, ± plane. |
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Peduncles | 1–20(–30) cm, distally stipitate-glandular, ± villous, arachnoid-sericeous, lanuginose, and/or glabrescent. |
mostly ascending to erect, 5–10 cm. |
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Involucres | ± hemispheric to obconic or broadly cylindric. |
± obconic. |
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Florets | corollas bright to dark yellow, 4–8 mm (inner); peripheral corollas spreading, ± zygomorphic, enlarged. |
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Corollas | 5–6.5 mm. |
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Phyllaries | longest 4.5–10 mm; outer stipitate-glandular, ± villous, arachnoid-sericeous, lanuginose, and/or glabrescent in fruit, apices erect, blunt, ± rigid. |
longest 8–12 mm; outer predominantly closely lanuginose, sparsely, if at all, stipitate-glandular, apices erect, ± rigid. |
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Heads | (± radiant) mostly 1–20+ per stem. |
1(–3) per stem. |
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Cypselae | 3–9 mm (± terete); pappi of (1–)4 scales in 1 series, or of (5–)8 scales in 2, abruptly unequal series, longest scales (1–)2–8 mm. |
5–6.5 mm (eglandular); pappi: longest scales 2.5–4.5 mm (lengths 0.4–0.8 times corollas). |
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2n | = 12. |
= 12. |
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Chaenactis glabriuscula |
Chaenactis evermannii |
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Phenology | Flowering Jun–Aug. | |||||||||||||||||
Habitat | Subalpine, usually decomposing granitic sand or gravel slopes, ridges, scree, talus, openings in or above conifer forests | |||||||||||||||||
Elevation | 1200–3000 m (3900–9800 ft) | |||||||||||||||||
Distribution |
CA; nw Mexico
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ID |
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Discussion | Varieties 5 (5 in the flora). The diverse and intergrading forms here included in Chaenactis glabriuscula have been divided by P. Stockwell (1940) and subsequent workers into as many as four species and ten varieties. Chaenactis glabriuscula is known from the southern two-thirds of the Californian Floristic Province and adjacent desert edges. It has been reported in Massachusetts as a garden escape (variety unspecified); it is not expected to persist there outside cultivation. Complete interfertility among the taxa recognized here as Chaenactis glabriuscula vars. glabriuscula, megacephala, and lanosa was demonstrated by P. Stockwell (1940). Intraspecific crosses involving C. glabriuscula var. orcuttiana were much less successful; C. glabriuscula var. heterocarpha was not tested. As noted by W. J. Hooker and G. A. W. Arnott ([1830–]1841) and D. W. Kyhos (1965), some forms of C. glabriuscula differ from C. stevioides or C. fremontii only in corolla color, which can be lost in older or poorly preserved specimens. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Chaenactis evermannii is known from mountains of central Idaho. Reports of it from Washington and California/Nevada (P. Stockwell 1940, some as C. nevadensis var. mainsiana) were based on specimens of C. thompsonii and C. alpigena, respectively; all three species are closely related. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 21, p. 411. | FNA vol. 21, p. 408. | ||||||||||||||||
Parent taxa | Asteraceae > tribe Heliantheae > subtribe Chaenactidinae > Chaenactis > sect. Chaenactis | Asteraceae > tribe Heliantheae > subtribe Chaenactidinae > Chaenactis > sect. Macrocarphus | ||||||||||||||||
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Subordinate taxa | ||||||||||||||||||
Synonyms | C. nevadensis var. mainsiana | |||||||||||||||||
Name authority | de Candolle: in A. P. de Candolle and A. L. P. P. de Candolle, Prodr. 5: 659. (1836) | Greene: Leafl. Bot. Observ. Crit. 2: 224. (1912) | ||||||||||||||||
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