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pelléade à stipe pourpre, purple cliff-brake, purple-stem cliff-brake

coffee cliffbrake, coffee fern

Stems

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.

creeping, horizontal, slender, 2–4 mm diam.;

scales mostly bicolored, narrowly lanceolate, largest scales 0.3–0.8 mm wide, centers black, thick, margins brown, thin, irregularly dentate.

Leaves

somewhat dimorphic, sterile leaves shorter and less divided than fertile leaves, clustered on stems, 5–50 cm;

croziers villous.

monomorphic, scattered along stem, 10–60 cm;

croziers not conspicuously pubescent, densely scaly.

Petiole

reddish purple to nearly black, lustrous, rounded adaxially, without prominent articulation lines.

straw-colored, tan, or gray, not lustrous, rounded or slightly flattened adaxially, without prominent articulation lines.

Blade

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.

elongate-deltate, usually 3-pinnate proximally, 3–20 cm wide;

rachis tan throughout, straight to slightly flexuous, rounded or flattened adaxially, glabrous or pubescent.

Ultimate segments

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.

elliptic to ovate, 3–15 mm, somewhat herbaceous, glabrous to sparsely pubescent abaxially;

margins recurved on fertile segments, usually covering less than 1/2 abaxial surface, borders whitish, entire;

apex retuse to rounded.

Pinnae

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.

ascending or perpendicular to rachis, not decurrent on rachis, with 8–50 ultimate segments;

costae usually straight, 15–140 mm, longer than ultimate segments.

Veins

of ultimate segments obscure.

of ultimate segments evident.

Sporangia

long-stalked, containing 32 spores, not intermixed with farina-producing glands.

short-stalked, containing 64 or 32 spores, not intermixed with farina-producing glands.

n

= 2n = 87, apogamous.

2n

= 58;

n = 2n = 87, 116, apogamous.

Pellaea atropurpurea

Pellaea andromedifolia

Phenology Sporulating summer–fall. Sporulating late spring–summer.
Habitat Calcareous cliffs and rocky slopes, usually on limestone Rocky slopes and ledges, usually on igneous substrates
Elevation 100–2500 m (300–8200 ft) 0–1500 m (0–4900 ft)
Distribution
from FNA
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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from FNA
CA; OR; Mexico in Baja California
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Discussion

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.)

Pellaea andromedifolia comprises three cytotypes: a sexually reproducing diploid, an apogamous triploid, and an apogamous tetraploid. Isozyme studies by G. J. Gastony and L. D. Gottlieb (1985) suggested that the apogamous triploid is an autopolyploid derived from sexual diploid populations. The apogamous tetraploid apparently resulted from hybridization between diploid and triploid individuals. These cytotypes have not been formally recognized as subspecies because their ranges seem to overlap extensively and because the ploidy level of the type collection of P. andromedifolia is not known.

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

Source FNA vol. 2. FNA vol. 2.
Parent taxa Pteridaceae > Pellaea Pteridaceae > Pellaea
Sibling taxa
P. andromedifolia, P. brachyptera, P. breweri, P. bridgesii, P. cordifolia, P. gastonyi, P. glabella, P. intermedia, P. lyngholmii, P. mucronata, P. ovata, P. ternifolia, P. truncata, P. wrightiana
P. atropurpurea, P. brachyptera, P. breweri, P. bridgesii, P. cordifolia, P. gastonyi, P. glabella, P. intermedia, P. lyngholmii, P. mucronata, P. ovata, P. ternifolia, P. truncata, P. wrightiana
Synonyms Pteris atropurpurea, P. atropurpurea var. cristata Pteris andromedifolia, P. andromedifolia var. pubescens
Name authority (Linnaeus) Link: Fil. Spec. 59. (1841) (Kaulfuss) Fée
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