Woodsia oregana subsp. cathcartiana |
Woodsia |
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cliff-fern, woodsia |
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Habit | Plants usually on rock. | |||||||||||||||||||||||||||||||||||||
Stems | compact to creeping; ascending or erect (rarely horizontal), stolons absent. |
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Leaves | monomorphic, dying back over winter or sometimes persistent into the next season. |
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Petiole | 1/5–3/4 length of blade, base not conspicuously swollen; vascular bundles 2, arranged laterally, ± round or oblong in cross section. |
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Blade | linear to lanceolate or ovate, 1–2-pinnate-pinnatifid, gradually reduced distally to pinnatifid apex, herbaceous. |
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Pinnae | not articulate to rachis, segment margins entire to dentate, not spiny; proximal pinnae somewhat reduced, sessile, bases usually ± equilateral; costae often shallowly grooved adaxially, grooves ± continuous from rachis to costae; indument of glandular (occasionally nonglandular) hairs on both surfaces, rarely absent. |
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Veins | free, simple or forked. |
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Sori | in 1 row between midrib and margin on ultimate segments, round; indusia basal, dissected into several to numerous filamentous or scalelike segments encircling sorus, persistent but often obscure in mature sori. |
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Spores | brownish, cristate, rarely rugose. |
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Cells | on pinnule margins irregular in shape, margins usually minutely dentate and appearing ragged; adaxial epidermal cells averaging more than 120 µm. Spores averaging 45–50 µm. 2n = 152. |
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x | = 38, 39, 41. |
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Woodsia oregana subsp. cathcartiana |
Woodsia |
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Phenology | Sporulating summer–fall. | |||||||||||||||||||||||||||||||||||||
Habitat | Cliffs and rocky slopes, found on a variety of substrates including both granite and limestone | |||||||||||||||||||||||||||||||||||||
Elevation | 0–4000 m (0–13100 ft) | |||||||||||||||||||||||||||||||||||||
Distribution |
AZ; CA; CO; IA; ID; KS; MI; MN; MT; ND; NE; NM; NV; NY; OK; SD; UT; WI; WY; MB; ON; QC; SK |
Mostly north temperate regions and higher elevations in the tropics |
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Discussion | D. F. M. Brown (1964) believed that Woodsia oregana subsp. cathcartiana was confined to a single locality on the Minnesota-Wisconsin border. Recent chromosome counts, however, indicate that the tetraploid cytotype of Woodsia oregana is actually more widespread than the diploid subsp. oregana (M. D. Windham 1993). The inclusion of western U.S. collections within the definition of this taxon is supported by isozyme data that indicate some plants from Arizona and New Mexico are identical to those collected at the type locality of subsp. cathcartiana. In addition to crossing with subsp. oregana (see comments above), W. oregana subsp. cathcartiana hybridizes with W. neomexicana to produce sterile tetraploids of intermediate morphology. It also crosses with W. obtusa subsp. obtusa, resulting in the sterile tetraploid W. × kansana Brooks. F. S. Wagner (1987) has shown that W. oregana subsp. cathcartiana, not W. scopulina, hybridizes with W. ilvensis to form the sterile triploid W. × abbeae. Some morphologic evidence suggests that W. × maxonii may be a hybrid between subsp. cathcartiana and W. scopulina subsp. laurentiana; this hypothesis requires further testing. The difficulties involved with separating subsp. cathcartiana from certain plants of W. plummerae are discussed under that species. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Woodsia is a well-marked genus; its morphology and chromosome base number (x = 41) provide evidence of relationships to the dryopteroid ferns. Most authors consider Cystopteris to be its closest ally, and the two genera are often confused in herbarium collections. The resemblance is superficial in many ways, however, and Woodsia is easily distinguished from Cystopteris by its persistent petiole bases, multilobed indusia, and obscure veins that end in hydathodes before reaching the leaf margin. The North American species of Woodsia fall into two natural groups that might be recognized as subgenera. Woodsia ilvensis, W. glabella, and W. alpina have articulate petioles, indusial segments that are uniseriate throughout and composed of cells that are much longer than wide, entire or crenate pinnules, strictly concolored stem scales, and chromosome base numbers of 39–41. They are circumboreal in distribution and show clear affinities to species found only in Eurasia. The remainder of the North American taxa have petioles that are not articulate, indusial segments that are multiseriate at the base and composed of cells that are isodiametric or slightly longer than wide, dentate pinnules, often bicolored stem scales, and a chromosome base number of 38. All of these species are endemic to the New World and probably represent a distinct lineage within the genus. Hybridization is common within these natural groups, but intergroup hybrids are relatively rare. Species ca. 30 (10 in the flora). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 2. | FNA vol. 2. | ||||||||||||||||||||||||||||||||||||
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Synonyms | W. cathcartiana, W. oregana, W. oregana, W. oregana var. cathcartiana, W. pusilla var. cathcartiana | |||||||||||||||||||||||||||||||||||||
Name authority | (B. L. Robinson) Windham: Contr. Univ. Michigan Herb. 19: 58. (1993) | R. Brown: Prodr. 158. (1810) | ||||||||||||||||||||||||||||||||||||
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