Pellaea ternifolia |
Pellaea atropurpurea |
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trans-Pecos cliffbrake |
pelléade à stipe pourpre, purple cliff-brake, purple-stem cliff-brake |
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Stems | compact, ascending, stout, 5–10 mm diam.; scales bicolored, linear-subulate, 0.1–0.3 mm wide, centers black, thick, margins brown, thin, erose-dentate. |
compact, ascending, stout, 5–10 mm diam.; scales uniformly reddish brown (or tan), linear-subulate, 0.1–0.3 mm wide, thin, margins entire to denticulate. |
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Leaves | monomorphic, clustered on stem, 10–50 cm; croziers sparsely to densely villous. |
somewhat dimorphic, sterile leaves shorter and less divided than fertile leaves, clustered on stems, 5–50 cm; croziers villous. |
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Petiole | black or dark purple, lustrous, rounded or slightly flattened adaxially, without prominent articulation lines. |
reddish purple to nearly black, lustrous, rounded adaxially, without prominent articulation lines. |
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Blade | linear to ovate, deeply pinnate-pinnatifid proximally, 2.5–8 cm wide; rachis black or purple throughout, straight, often flattened adaxially, glabrous or villous. |
elongate-deltate, usually 2-pinnate proximally, 2–18 cm wide; rachis reddish purple throughout, straight, rounded adaxially, densely pubescent adaxially with short, curly, appressed hairs. |
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Ultimate segments | linear-oblong, 10–40 mm, leathery, glabrous to sparsely villous abaxially on midrib; margins recurved on fertile segments, rarely covering more than 1/2 abaxial surface, borders whitish, entire; apex mucronate. |
linear-oblong, 10–75 mm, leathery, sparsely villous abaxially near midrib; margins weakly recurved to plane on fertile segments, usually covering less than 1/2 abaxial surface, borders whitish, crenulate; apex obtuse to slightly mucronate. |
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Pinnae | perpendicular to rachis or slightly ascending, not decurrent on rachis, ternate at base of leaf; costae absent. |
perpendicular to rachis or ascending, not decurrent on rachis, usually with 3–15 ultimate segments; costae straight, 10–100 mm, often longer than ultimate segments. |
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Veins | of ultimate segments obscure. |
of ultimate segments obscure. |
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Sporangia | long-stalked, containing 64 spores, not intermixed with farina-producing glands. |
long-stalked, containing 32 spores, not intermixed with farina-producing glands. |
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n | = 2n = 87, apogamous. |
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Pellaea ternifolia |
Pellaea atropurpurea |
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Phenology | Sporulating summer–fall. | |||||||||
Habitat | Calcareous cliffs and rocky slopes, usually on limestone | |||||||||
Elevation | 100–2500 m (300–8200 ft) | |||||||||
Distribution |
AZ; TX; Mexico; Central America; South America; Pacific Islands in Hawaii
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AL; AR; AZ; CO; CT; DC; FL; GA; IA; IL; IN; KS; KY; LA; MA; MD; MI; MN; MO; MS; NC; NE; NJ; NM; NV; NY; OH; OK; PA; RI; SC; SD; TN; TX; UT; VA; VT; WI; WV; WY; ON; QC; Mexico; Central America in Guatemala
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Discussion | Subspecies 3 (3 in the flora). Pellaea ternifolia is represented in the flora by three morphologically and chromosomally distinct taxa. These discrete genetic entities also show a tendency toward geographic isolation and are treated here as subspecies. Diploid populations referred to P. ternifolia subsp. ternifolia are scattered from Texas through Mexico to South America. The pubescent tetraploid (P. ternifolia subsp. villosa) follows the Sierra Madre Oriental from Puebla, Mexico, north to Texas; the glabrous tetraploid (P. ternifolia subsp. arizonica) occurs in Arizona, Texas, and northern Mexico. Isozyme and chromosome studies suggest that both tetraploids are segmental allopolyploids produced by hybridization between subsp. ternifolia and other (as yet unidentified) diploid elements within P. ternifolia. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Contrary to D. B. Lellinger's (1985) hypothesis, isozyme data indicate that neither Pellaea glabella nor P. ternifolia was involved in the origin of this apogamous triploid. Instead, it appears that P. atropurpurea is an autopolyploid derivative of a single diploid taxon that has not yet been located. A thorough survey of spore number per sporangium in this species should be undertaken to determine whether the diploid progenitor is still extant. Collections from western Canada identified as P. atropurpurea actually represent P. gastonyi, an apogamous tetraploid produced by hybridization between P. atropurpurea and diploid populations of P. glabella. Pellaea atropurpurea has also hybridized with P. wrightiana; the hybrid is a rare apogamous pentaploid known only from western Oklahoma. Pellaea lyngholmii is the apogamous tetraploid hybrid between P. atropurpurea and P. truncata. Pellaea atropurpurea is distinguished from all these hybrids by having rachises that are densely pubescent adaxially, larger ultimate segments, and spores averaging less than 62 µm in diameter. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 2, p. 180. | FNA vol. 2. | ||||||||
Parent taxa | Pteridaceae > Pellaea | Pteridaceae > Pellaea | ||||||||
Sibling taxa | ||||||||||
Subordinate taxa | ||||||||||
Synonyms | Pteris ternifolia | Pteris atropurpurea, P. atropurpurea var. cristata | ||||||||
Name authority | (Cavanilles) Link: Fil. Spec. 59. (1841) | (Linnaeus) Link: Fil. Spec. 59. (1841) | ||||||||
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