The green links below add additional plants to the comparison table. Blue links lead to other Web sites.
enable glossary links

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

New Mexican cliff fern, New Mexico cliff fern

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 mostly 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.

4–30 × 1.5–6 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.

linear to lanceolate, usually pinnate-pinnatifid proximally, glabrescent to sparsely glandular, never viscid;

glandular hairs with thin stalks and slightly expanded tips;

rachis with scattered glandular hairs and rare, 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 3–7 pairs of closely spaced pinnules;

abaxial and adaxial surfaces glabrescent to sparsely 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, filamentous segments, these uniseriate for most of length, composed of ± isodiametric cells, usually surpassing mature sporangia.

Spores

averaging 39–46 µm. 2n = 82.

averaging 44–52 µm. 2n = 152.

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, with 1–2-celled translucent projections on teeth.

Vein

tips frequently enlarged to form whitish hydathodes visible adaxially.

tips occasionally enlarged to form whitish hydathodes visible adaxially.

Woodsia ilvensis

Woodsia neomexicana

Phenology Sporulating summer–early fall. Sporulating summer–fall.
Habitat Cliffs and rocky slopes, found on variety of substrates including serpentine Cliffs and rocky slopes, usually on sandstone or igneous substrates
Elevation 0–1500 m (0–4900 ft) 300–3500 m (1000–11500 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; CO; NM; OK; SD; TX
[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 neomexicana traditionally has been identified as W. mexicana. Both taxa are tetraploid and may share one parent (M. D. Windham 1993); W. neomexicana is separated from typical W. mexicana by its completely filamentous indusial segments, reduced glandularity, and more northerly distribution. Isozyme data suggest that W. neomexicana is an allotetraploid hybrid between W. phillipsii and the diploid progenitor of W. oregana subsp. cathcartiana (M. D. Windham 1993). As with all allopolyploids, W. neomexicana can vary in the direction of either parent, and some plants (especially those resembling W. phillipsii) can be difficult to identify. All characters except those controlled directly by ploidy level show this tendency, and spore size remains the most dependable character for distinguishing W. phillipsii and W. neomexicana. This species hybridizes with W. oregana subsp. cathcartiana and W. phillipsii to produce sterile tetraploids and triploids, respectively.

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

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. obtusa, W. oregana, W. phillipsii, W. plummerae, W. scopulina
Synonyms Acrostichum ilvense
Name authority (Linnaeus) R. Brown: Trans. Linn. Soc. London, Bot. 11: 173. (1813) Windham: Contr. Univ. Michigan Herb. 19: 52. (1993)
Web links