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

blunt-lobe woodsia, blunt-lobed cliff fern, bluntlobe cliff fern, woodsie à lobes arrondis

Stems

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

scales uniformly brown, lanceolate.

compact to creeping, erect to horizontal, 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.

8–60 × 2.5–12 cm.

Petiole

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

light brown or straw-colored when mature, occasionally darker at very base, not articulate above base, relatively brittle and easily shattered.

Blade

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

rachis usually with abundant hairs and scales.

lanceolate to ovate, 2-pinnate to 2-pinnate-pinnatifid proximally, moderately glandular, rarely somewhat viscid;

many glandular hairs with thick stalks and distinctly bulbous tips;

rachis with glandular hairs and scattered, often 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, occasionally attenuate;

largest pinnae with 5–14 pairs of pinnules;

abaxial and adaxial surfaces 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 relatively broad, nonfilamentous segments, these multiseriate throughout, composed of ± isodiametric cells, entire or glandular along distal edge, concealed by or slightly surpassing mature sporangia.

Spores

averaging 39–46 µm. 2n = 82.

averaging 35–47 µm.

Pinnules

entire or crenate, rarely shallowly lobed;

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

dentate, sometimes deeply lobed;

margins nonlustrous, thin, with occasional glands, lacking cilia or translucent projections.

Vein

tips frequently enlarged to form whitish hydathodes visible adaxially.

tips usually enlarged to form whitish hydathodes visible adaxially.

Woodsia ilvensis

Woodsia obtusa

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
AL; AR; CT; DE; FL; GA; IA; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MS; NC; NE; NH; NJ; NY; OH; OK; PA; RI; SC; TN; TX; VA; VT; WI; WV; ON; QC; 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.)

Woodsia obtusa comprises two cytotypes that are treated here as subspecies because they show subtle morphologic and ecological distinctions and tend to have different distributions. Tetraploid populations (subsp. obtusa) are found throughout the eastern flora, commonly occurring on limestone. The diploid (subsp. occidentalis) is found near the western edge of the species range, usually on sandstone and granitic substrates. Isozyme studies suggest that subsp. obtusa may have been derived from subsp. occidentalis through autopolyploidy (M. D. Windham 1993). The westernmost collections of Woodsia obtusa (all subsp. occidentalis) come from the Wichita Mountains of Oklahoma and the Edwards Plateau of Texas. Reports of this species from the trans-Pecos region of western Texas are apparently based on misidentifications.

Subspecies 2.

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

Key
1. Spores averaging 42-47 µm; proximal pinnules of lower pinnae usually shallowly lobed or merely dentate; blades coarsely cut and evidently 2-pinnate; stems compact to short-creeping, individual branches usually 5-10 mm diam.
subsp. obtusa
1. Spores averaging 35-42 µm; proximal pinnules of lower pinnae usually deeply lobed or pinnatifid; blades finely cut, 2-pinnate-pinnatifid; stems short- to long-creeping, individual branches 3-5 mm diam.
subsp. occidentalis
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. oregana, W. phillipsii, W. plummerae, W. scopulina
Subordinate taxa
W. obtusa subsp. obtusa, W. obtusa subsp. occidentalis
Synonyms Acrostichum ilvense Aspidium obtusum, W. perriniana
Name authority (Linnaeus) R. Brown: Trans. Linn. Soc. London, Bot. 11: 173. (1813) (Swartz) Torrey: New York State, Rep. Geol. Surv. 195. (1840)
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