Difference between revisions of "Chaenactis sect. Macrocarphus"
Fl. N. Amer. 2: 371. 1842.
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− | |basionyms={{Treatment/ID/ | + | |basionyms={{Treatment/ID/Basionym |
|name=Undefined sect. Macrocarphus | |name=Undefined sect. Macrocarphus | ||
|authority=Nuttall | |authority=Nuttall | ||
+ | |rank=section | ||
+ | |publication_title=Trans. Amer. Philos. Soc., n. s. | ||
+ | |publication_place=7: 376. 1841 | ||
}} | }} | ||
|synonyms= | |synonyms= | ||
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|distribution=w North America;nw Mexico. | |distribution=w North America;nw Mexico. | ||
|discussion=<p>Species 8 (8 in the flora).</p><!-- | |discussion=<p>Species 8 (8 in the flora).</p><!-- | ||
− | --><p>Species of sect. Macrocarphus occur mainly in montane to alpine habitats; all except Chaenactis douglasii are narrowly distributed. With C. douglasii here broadly defined, all the species of sect. Macrocarphus are sharply distinct.</p> | + | --><p>Species of sect. Macrocarphus occur mainly in montane to alpine habitats; all except <i>Chaenactis douglasii</i> are narrowly distributed. With <i>C. douglasii</i> here broadly defined, all the species of sect. Macrocarphus are sharply distinct.</p> |
|tables= | |tables= | ||
|references= | |references= | ||
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-->{{#Taxon: | -->{{#Taxon: | ||
name=Chaenactis sect. Macrocarphus | name=Chaenactis sect. Macrocarphus | ||
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|authority=(Nuttall) Torrey & A. Gray | |authority=(Nuttall) Torrey & A. Gray | ||
|rank=section | |rank=section | ||
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|publication year=1842 | |publication year=1842 | ||
|special status= | |special status= | ||
− | |source xml=https:// | + | |source xml=https://bitbucket.org/aafc-mbb/fna-data-curation/src/2e0870ddd59836b60bcf96646a41e87ea5a5943a/coarse_grained_fna_xml/V19-20-21/V21_1015.xml |
|tribe=Asteraceae tribe Heliantheae | |tribe=Asteraceae tribe Heliantheae | ||
|subtribe=Asteraceae (tribe Heliantheae) subtribe Chaenactidinae | |subtribe=Asteraceae (tribe Heliantheae) subtribe Chaenactidinae |
Latest revision as of 20:07, 5 November 2020
Biennials, perennials, or subshrubs (rarely flowering first year); proximal indument predominantly arachnoid, lanuginose, or pannose (rarely glabrescent), not farinose. Stems 1–25+, prostrate to erect; branches mainly proximal. Leaves: largest blades deltate, elliptic, linear, or ovate, (0–)1–2-pinnately or -subpalmately lobed, gland-dotted beneath indument. Heads discoid. Peduncles prostrate to erect. Phyllaries: outer ± blunt. Corollas white to pinkish or cream, actinomorphic, ± equal. Cypselae ± terete; pappi of (8–)10–20 scales in 2–4 equal or gradually unequal series. x = 6.
Distribution
w North America, nw Mexico.
Discussion
Species 8 (8 in the flora).
Species of sect. Macrocarphus occur mainly in montane to alpine habitats; all except Chaenactis douglasii are narrowly distributed. With C. douglasii here broadly defined, all the species of sect. Macrocarphus are sharply distinct.
Selected References
None.
Lower Taxa
Key
1 | Leaves ± cauline and, often, basal; plants not or scarcely cespitose, not matted; heads (1–)2–25+ per stem | > 2 |
1 | Leaves ± basal; plants cespitose or ± matted; heads 1(–3) per stem | > 5 |
2 | Subshrubs (usually); proximal indument (especially stems) persistent, whitish, densely lanuginose or pannose; largest leaf blades deltate to ovate, ± plane (California) | > 3 |
2 | Biennials or perennials (rarely slightly woody or flowering first year); proximal indument ± thinning with age, grayish, arachnoid to ± lanuginose; largest leaf blades ± elliptic or lanceolate to ovate, plane or ± 3-dimensional | > 4 |
3 | Phyllaries: longest 10–13 mm, outer predominantly arachnoid to closely lanuginose (sparsely, if at all, stipitate-glandular) | Chaenactis parishii |
3 | Phyllaries: longest 14–18 mm, outer predominantly stipitate-glandular (other indument none or sparse) | Chaenactis suffrutescens |
4 | Outer phyllaries usually densely, sometimes sparsely or obscurely, stipitate-glandular and, often, arachnoid, lanuginose, and/or villous; largest leaf blades ± 3-dimensional, usually 2-pinnately lobed, primary lobes ± congested, ultimate lobes ± involute and/or twisted | Chaenactis douglasii |
4 | Outer phyllaries closely lanuginose, not stipitate-glandular; largest leaf blades ± plane, 1-pinnately lobed, lobes remote, ± plane (Washington) | Chaenactis thompsonii |
5 | Outer phyllaries predominantly arachnoid, sericeous, or ± lanuginose (sparsely, if at all, stipitate-glandular) | > 6 |
5 | Outer phyllaries predominantly or evidently stipitate-glandular (other indument none, sparse, or ± arachnoid) | > 8 |
6 | Cypselae sparsely glandular amidst other indument; largest leaf blades 2-pinnately lobed (± 3-dimensional, primary lobes 4–12 pairs, peduncles mostly ascending to erect) | Chaenactis douglasii |
6 | Cypselae eglandular; largest leaf blades (0–)1(–2)-pinnately or -subpalmately lobed (± plane, and/or primary lobes 0–4 pairs, and/or peduncles mostly prostrate) | > 7 |
7 | Longest pappus scales 2.5–4.5 mm (lengths 0.4–0.8 times corollas); leaf blades ± plane; peduncles mostly ascending to erect; Idaho | Chaenactis evermannii |
7 | Longest pappus scales 5–8 mm (lengths 0.9–1 times corollas); leaf blades ± plane or 3-dimensional; peduncles mostly prostrate; California, Nevada | Chaenactis alpigena |
8 | Largest leaf blades deltate to ovate, ± plane, ultimate lobes ± plane | > 9 |
8 | Largest leaf blades linear-cylindric to ± elliptic or slightly ovate, ± 3-dimensional, ultimate lobes ± involute and/or twisted | > 10 |
9 | Plants 2–10(–12) cm; leaves 2.5–5 cm; longest phyllaries 9–12(–14) mm; corol-las 5.5–8 mm; longest pappus scales 3–5 mm | Chaenactis nevadensis |
9 | Plants (10–)25–45(–60) cm; leaves 5–10 cm; longest phyllaries 14–18 mm; corollas 8.5–10 mm; longest pappus scales 7–9 mm | Chaenactis suffrutescens |
10 | Largest leaf blades ± elliptic to slightly ovate, primary lobes (4–)5–9(–12) pairs, ± congested, scarcely imbricate; not s California | Chaenactis douglasii |
10 | Largest leaf blades linear-cylindric to ± fusiform, primary lobes (7–)10–18+ pairs, ± imbricate; s California | Chaenactis santolinoides |