Chaenactis macrantha |
Chaenactis |
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big-head dusty maidens, bighead dustymaiden, large-flower chaenactis, Mohave pincushion, Mojave pincushion, showy dustymaidens |
chaenactis, dusty-maidens, false-yarrow, pincushion |
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Habit | Plants 5–25(–35) cm; proximal indument grayish, arachnoid-sericeous to closely lanuginose (sometimes tardily glabrescent). | Annuals, biennials, perennials, or subshrubs, (2–)5–70(–200) cm (taprooted). | ||||||||
Stems | mostly 1–5; branches mainly proximal. |
erect to prostrate, usually branched. |
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Leaves | basal (withering) and cauline, 1.5–7 cm; largest blades ± elliptic to ovate, ± plane, not succulent, 1(–2)-pinnately lobed (± gland-dotted beneath indument); primary lobes mostly 2–5 pairs, ± remote, ultimate lobes ± 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. |
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Peduncles | 1.5–8 cm, arachnoid-sericeous to thinly lanuginose distally, not stipitate-glandular. |
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Involucres | ± obconic to broadly cylindric. |
hemispheric to obconic or broadly cylindric, (3–)5–15[–25] mm diam. |
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Receptacles | convex to ± flat, pitted and/or knobby, usually epaleate (paleae 3–10+ in C. carphoclinia). |
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Florets | corollas (nocturnal) white to pinkish or cream, 9–12(–15) mm (lengths 1.8–2.2 times cypselae; anthers ± included); peripheral corollas nocturnally spreading, actinomorphic, scarcely enlarged. |
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Ray florets | 0 (sometimes simulated by enlarged peripheral disc corollas). |
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Disc florets | 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). |
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Phyllaries | longest 12–18 mm; outer arachnoid-sericeous to thinly lanuginose in fruit, not stipitate-glandular, apices ± squarrose, blunt, pliant. |
5–21+ in 1–2(–3) series (subequal to unequal). |
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Heads | (± radiant, nocturnally), mostly 1–5(–7) per stem (nodding in bud). |
discoid or ± radiant, borne singly or in (terminal) ± cymiform arrays (erect in bud except C. macrantha). |
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Cypselae | 5–6(–7) mm; pappi of 8 scales in 2, abruptly unequal series, longest scales 5–7 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. |
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x | = ? (n = 6, 8, plus polyploids and dysploid numbers). |
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2n | = 12. |
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Chaenactis macrantha |
Chaenactis |
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Phenology | Flowering Mar–early Jul. | |||||||||
Habitat | Open, loose, light-colored, silty, usually calcareous or alkaline, desert soils, often covered by or mixed with gravel | |||||||||
Elevation | 600–2200 m (2000–7200 ft) | |||||||||
Distribution |
AZ; CA; ID; NV; OR; UT
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w North America; nw Mexico |
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Discussion | Though the derived floral features of Chaenactis macrantha obscure its relationships, it may represent a link between sect. Chaenactis (annuals; pappus scales in regular, often strongly reduced series) and sect. Macrocarphus (leaf blades gland-dotted). Resemblance of its heads, leaves, and indument to those of C. thompsonii and relatives is striking. It appears to form no natural hybrids, perhaps because of its nocturnal corollas. (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.) |
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Key |
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Source | FNA vol. 21, p. 410. | FNA vol. 21, p. 400. | ||||||||
Parent taxa | Asteraceae > tribe Heliantheae > subtribe Chaenactidinae > Chaenactis > sect. Chaenactis | Asteraceae > tribe Heliantheae > subtribe Chaenactidinae | ||||||||
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Subordinate taxa | ||||||||||
Name authority | D. C. Eaton: in S. Watson, Botany (Fortieth Parallel), 171, plate 18, figs. 1–5. (1871) | de Candolle: in A. P. de Candolle and A. L. P. P. de Candolle, Prodr. 5: 659. (1836) | ||||||||
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