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artemisia leaf chaenactis, white pincushion

Parish chaenactis, Parish's chaenactis

Habit Plants (15–)25–90(–200) cm. Subshrubs, (10–)20–40(–60) cm (not cespitose or matted); proximal indument (especially of stems) persistent, whitish, densely lanuginose or pannose.
Stems

mostly 5–15+, erect.

Leaves

basal (withering) and cauline, 3–15(–20) cm;

largest blades ± plane, not succulent;

primary lobes mostly 5–10 pairs, ultimate lobes ± crowded, antrorse, lanceolate to elliptic, plane.

mostly cauline, (1–)2–5 cm;

largest blades lance-ovate or deltate, ± plane, 1-pinnately lobed;

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

Peduncles

1.5–6 cm.

ascending to erect, 2–8(–20) cm.

Involucres

± hemispheric, mostly 10–15 mm diam.

± obconic.

Receptacles

paleae 0.

Corollas

5–7 mm.

7–8.5 mm.

Phyllaries

longest 7–10(–12) mm, ± densely villous, not or sparsely glandular;

apices (all) erect, ± green, acute or scarcely acuminate, not aristate, ± plane.

longest 10–13 mm;

outer predominantly arachnoid to closely lanuginose (sparsely, if at all, stipitate-glandular), apices ± squarrose, pliant.

Heads

mostly 1–3 per stem.

Cypselae

compressed, 4–7 mm;

pappi 0 or coroniform (of ± 10 scales, longest 0.1–0.5 mm).

4–7 mm;

pappi: longest scales 6–8 mm.

2n

= 16.

= 12.

Chaenactis artemisiifolia

Chaenactis parishii

Phenology Flowering Apr–early Jul. Flowering May–Jul.
Habitat Dry canyons, open slopes, often over granitoid rocks, locally abundant in chaparral burns or other recovering disturbances Open rocky to sandy soils in low montane chaparral
Elevation 80–1600 m (300–5200 ft) 1300–2500 m (4300–8200 ft)
Distribution
from FNA
CA; Mexico (Baja California)
[WildflowerSearch map]
[BONAP county map]
from FNA
CA; Mexico (Baja California)
[BONAP county map]
Discussion

In the flora area, Chaenactis artemisiifolia is known from the Transverse and Peninsular ranges and seaward valleys of southwestern California. It is fire-adapted; its germination is significantly enhanced by exposure to biomass smoke (J. E. Keeley and C. J. Fotheringham 1998).

Chaenactis lacera Greene, the eighteenth species of the genus, is known from coastal portions (including islands) of the western Vizcaíno Desert in Baja California and Baja California Sur, Mexico. Forms of C. artemisiifolia sometimes resemble C. lacera in coastal southern California (P. Stockwell 1940), where C. lacera could eventually be introduced. Besides the key characteristics above, C. lacera differs from C. artemisiifolia by its largest leaf blades broadly ± elliptic, 2–3-pinnately lobed, ultimate lobes remote, recurved to retrorse, ± linear, involute (leaf blades appearing ± skeletal).

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

Of conservation concern.

Chaenactis parishii is sometimes cultivated in rock gardens. It is known from small, isolated populations in the higher Peninsular Ranges of Riverside and San Diego counties and adjacent Baja California. Chaenactis parishii and C. suffrutescens form a species pair well marked by the (usually) subshrubby habit, proximal indument persistent, white, felty, heads relatively large, and largest leaf blades lance-ovate to deltate.

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

Source FNA vol. 21, p. 402. FNA vol. 21, p. 404.
Parent taxa Asteraceae > tribe Heliantheae > subtribe Chaenactidinae > Chaenactis > sect. Acarphaea Asteraceae > tribe Heliantheae > subtribe Chaenactidinae > Chaenactis > sect. Macrocarphus
Sibling taxa
C. alpigena, 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. thompsonii, 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. santolinoides, C. stevioides, C. suffrutescens, C. thompsonii, C. xantiana
Synonyms Acarphaea artemisiifolia
Name authority (Harvey & A. Gray) A. Gray: Proc. Amer. Acad. Arts 10: 74. (1874) A. Gray: Proc. Amer. Acad. Arts 20: 299. (1885)
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