Polypodium virginianum |
Polypodium hesperium |
|
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common polypody, polypode de virginie, rock polypody, tripes-de-roches |
western polypody, western polypody fern |
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Stems | often whitish pruinose, slender, to 6 mm diam., acrid-tasting; scales weakly bicolored, lanceolate, contorted distally, base and margins light brown, sometimes with dark central stripe, margins denticulate. |
occasionally whitish pruinose, slender to moderately stout, to 6 mm diam., acrid- to sweet-tasting: scales concolored, brown or slightly mottled, often darker near point of attachment, lanceolate, usually symmetric, margins entire to denticulate. |
Leaves | to 40 cm. |
to 35 cm. |
Petiole | slender, to 2 mm diam. |
slender, to 1.5 mm diam. |
Blade | oblong to narrowly lanceolate, pinnatifid, usually widest near middle, occasionally at or near base, to 7 cm wide, somewhat leathery; rachis sparsely scaly to glabrescent abaxially, glabrous adaxially; scales lanceolate-ovate, usually more than 6 cells wide. |
oblong to lanceolate-ovate, occasionally deltate, pinnatifid, usually widest at or near middle, to 7 cm wide, herbaceous to somewhat leathery; rachis sparsely scaly to glabrescent abaxially, glabrous adaxially; scales linear-lanceolate, usually less than 6 cells wide. |
Segments | oblong, less than 8 mm wide; margins entire to crenulate; apex rounded to broadly acute; midrib glabrous adaxially. |
oblong to linear-lanceolate, less than 12 mm wide; margins entire to crenulate or obscurely serrate; apex obtuse to acute; midrib glabrous adaxially. |
Sori | midway between margin and midrib to nearly marginal, less than 3 mm diam., circular when immature. |
midway between margin and midrib, less than 3 mm diam., oval when immature. |
Spores | more than 52 µm, tuberculate, surface projections more than 3 µm tall. |
more than 58 µm, rugose to verrucose or tuberculate, surface projections commonly less than 3 µm. 2n = 148. |
Venation | free. |
free. |
Sporangiasters | present, usually less than 40 per sorus, heads covered with glandular hairs. |
absent. |
2n | = 148. |
|
Polypodium virginianum |
Polypodium hesperium |
|
Phenology | Sporulating summer–fall. | Sporulating summer–fall. |
Habitat | Cliffs and rocky slopes, on a variety of substrates | Cracks and ledges on cliffs, on a variety of noncalcareous substrates, rarely on limestone |
Elevation | 0–1800 m (0–5900 ft) | 300–3500 m. (1000–11500 ft.) |
Distribution |
AL; AR; CT; DC; DE; GA; IA; IL; IN; KY; MA; MD; ME; MI; MN; MO; NC; NH; NJ; NY; OH; PA; RI; SC; SD; TN; VA; VT; WI; WV; AB; MB; NB; NF; NS; NT; ON; PE; QC; SK; SPM
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AZ; CA; CO; ID; MT; NM; NV; OR; UT; WA; BC; Mexico in Chihuahua; Baja California
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Discussion | Traditionally, two cytotypes have been recognized within Polypodium virginianum (I. Manton and M. Shivas 1953). Recent research has demonstrated that the tetraploid cytotype, which properly bears the name P. virginianum (R. Cranfill and D. M. Britton 1983), is an allopolyploid produced by hybridization between the diploid cytotype (here called P. appalachianum) and P. sibiricum (C. H. Haufler and M. D. Windham 1991; C. H. Haufler and Wang Z. R. 1991). Although sometimes similar to its diploid parents in overall leaf morphology, P. virginianum has consistently larger spores, typically more than 52 µm (see additional comments under P. appalachianum and P. sibiricum). Frequent hybridizations between P. virginianum and P. appalachianum form morphologically intermediate, triploid individuals with misshapen spores. Sterile triploids also result from hybridization between P. virginianum and P. sibiricum. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Using morphologic and chromosomal data, F. A. Lang (1971) proposed that Polypodium hesperium originated through allotetraploidy involving P. glycyrrhiza and P. amorphum, a hypothesis recently supported by electrophoretic studies (C. H. Haufler, M. D. Windham, and E. W. Rabe, unpublished). Variations in spore surface morphology and banding patterns observed in isozyme studies indicate that P. hesperium may have originated more than once from different individuals of the same species. Some collections of P. hesperium can be mistaken for P. glycyrrhiza, but the latter species is easily distinguished by its pubescent rachises, linear blade scales, and smaller spores (less than 58 µm). Although P. amorphum has sporangiasters and P. hesperium lacks them, misshapen sporangia in P. hesperium can mimic these distinctive soral structures. Therefore, it is often necessary to use a combination of soral, stem scale, and blade scale features (discussed in the key) to separate P. hesperium from P. amorphum. Hybridization occurs between P. hesperium and each of its progenitor diploids to form triploid individuals with misshapen spores (F. A. Lang 1971). Rare, sterile, tetraploid hybrids with P. saximontanum have also been detected (M. D. Windham, unpublished). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 2. | FNA vol. 2. |
Parent taxa | Polypodiaceae > Polypodium | Polypodiaceae > Polypodium |
Sibling taxa | ||
Synonyms | P. vinlandicum, P. vulgare var. americanum, P. vulgare var. virginianum | P. prolongilobum, P. vulgare subsp. columbianum, P. vulgare var. columbianum, P. vulgare var. hesperium |
Name authority | Linnaeus: Sp. Pl. 2: 1085. (1753) | Maxon: Proc. Biol. Soc. Wash. 13: 200. (1900) |
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