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oblong woodsia, rusty cliff fern, rusty woodsia, woodsie de l'île d'elbe

cliff fern, Oregon cliff-fern, Oregon woodsia, western cliff fern, woodsie de l'Oregon

Stems

compact, erect to ascending, with abundant persistent petiole bases of ± equal length;

scales uniformly brown, lanceolate.

compact, erect to ascending, with few to many persistent petiole bases of unequal lengths;

scales often uniformly brown but at least some bicolored with dark central stripe and pale brown margins, narrowly lanceolate.

Leaves

4.5–25 × 1.2–3.5 cm.

4–25 × 1–4 cm.

Petiole

usually brown or dark purple when mature, articulate above base at swollen node, relatively brittle and easily shattered.

reddish brown to dark purple proximally when mature, not articulate above base, somewhat pliable and resistant to shattering.

Blade

narrowly lanceolate, usually 2-pinnate proximally, lacking glands, never viscid;

rachis usually with abundant hairs and scales.

linear-lanceolate to narrowly ovate, pinnate-pinnatifid or 2-pinnate proximally, sparsely to moderately glandular, never viscid;

glandular hairs with thin stalks and slightly expanded tips;

rachis with scattered glandular hairs and occasional hairlike scales.

Pinnae

ovate-lanceolate to deltate, longer than wide, abruptly tapered to a rounded or broadly acute apex;

largest pinnae with 4–9 pairs of pinnules;

abaxial surface with mixture of hairs and linear-lanceolate scales, adaxial surface with multicellular hairs concentrated along midrib.

ovate-deltate to elliptic, longer than wide, abruptly tapered to a rounded or broadly acute apex;

largest pinnae with 3–9 pairs of pinnules;

abaxial and adaxial surfaces glabrescent to moderately glandular, lacking nonglandular hairs or scales.

Indusia

of narrow, hairlike segments, these uniseriate throughout, composed of cells many times longer than wide, usually surpassing mature sporangia.

of narrow, usually filamentous segments, these uniseriate for most of length, composed of ± isodiametric cells, concealed by or slightly surpassing mature sporangia.

Spores

averaging 39–46 µm. 2n = 82.

averaging 39–50 µm.

Pinnules

entire or crenate, rarely shallowly lobed;

margins nonlustrous, thin, ciliate with multicellular hairs, lacking translucent projections.

dentate, often shallowly lobed;

margins nonlustrous, thin, with occasional glands, lacking cilia, rarely with 1–2-celled translucent projections.

Vein

tips frequently enlarged to form whitish hydathodes visible adaxially.

tips slightly (if at all) enlarged, barely visible adaxially.

Woodsia ilvensis

Woodsia oregana

Phenology Sporulating summer–early fall.
Habitat Cliffs and rocky slopes, found on variety of substrates including serpentine
Elevation 0–1500 m (0–4900 ft)
Distribution
from FNA
AK; CT; IA; IL; MA; MD; ME; MI; MN; NC; NH; NJ; NY; OH; PA; RI; VA; VT; WI; WV; AB; BC; MB; NB; NF; NS; NT; ON; QC; SK; YT; Greenland; n Eurasia
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CA; CO; IA; ID; KS; MI; MN; MT; ND; NE; NM; NV; NY; OK; OR; SD; UT; WA; WI; WY; AB; BC; MB; ON; QC; SK; only in the flora
[WildflowerSearch map]
[BONAP county map]
Discussion

Although generally separable by the characters given in the key, shade forms of Woodsia ilvensis with a reduced number of scales and hairs are occasionally misidentified as W. alpina. The morphologic distinctions between these species are further blurred by natural hybridization, which produces the intermediate triploid known as W. × gracilis. Some of the best characters for distinguishing these taxa are spore size and morphology. Spores average less than 46 µm in W. ilvensis, more than 46 µm in W. alpina, and are malformed and abortive in W. × gracilis. Woodsia ilvensis also hybridizes with W. oregana subsp. cathcartiana to form the sterile triploid W. × abbeae (F. S. Wagner 1987).

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

The variability and promiscuity of Woodsia oregana have been major sources of taxonomic difficulties in Woodsia, and more work will be necessary before relationships in this complex are fully resolved. As defined here, W. oregana comprises two subspecies that are chromosomally and biochemically distinct. In addition, the two taxa are nearly allopatric, with the diploid (subsp. oregana) confined to the Pacific Northwest and the tetraploid (subsp. cathcartiana) extending from the southwestern United States to eastern Canada. Isozyme studies indicate that subsp. cathcartiana is not an autotetraploid derived from known diploid populations of subsp. oregana, as was hypothesized by D. F. M. Brown (1964), and it may be more appropriate to recognize these taxa as distinct species. The morphologic features that distinguish these subspecies are very subtle, however, and they are associated primarily with differences in chromosome number. Until further systematic analyses are undertaken, these cytotypes should be maintained as subspecies of W. oregana.

Subspecies 2.

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

Key
1. Spores averaging 39-45 µm; cells on pinnule margins regular in shape, margins appearing entire; adaxial epidermal cells averaging less than 120 µm.
subsp. oregana
1. Spores averaging 45-50 µm; cells on pinnule margins irregular in shape, margins usually minutely dentate and appearing ragged; adaxial epidermal cells averaging more than 120 µm.
subsp. cathcartiana
Source FNA vol. 2. FNA vol. 2.
Parent taxa Dryopteridaceae > Woodsia Dryopteridaceae > Woodsia
Sibling taxa
W. alpina, W. cochisensis, W. glabella, W. neomexicana, W. obtusa, W. oregana, W. phillipsii, W. plummerae, W. scopulina
W. alpina, W. cochisensis, W. glabella, W. ilvensis, W. neomexicana, W. obtusa, W. phillipsii, W. plummerae, W. scopulina
Subordinate taxa
W. oregana subsp. cathcartiana, W. oregana subsp. oregana
Synonyms Acrostichum ilvense
Name authority (Linnaeus) R. Brown: Trans. Linn. Soc. London, Bot. 11: 173. (1813) D. C. Eaton: Canad. Naturalist & Quart. J. Sci. n. s. 2: 90. (1865)
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