Flora of North America species comparison

Long recognized as Cystopteris fragilis var. mackayi, C. tenuis was returned to species status by R. C. Moran (1983b). It is probably an allotetraploid originating from C. protrusa and an extinct diploid related to C. fragilis (C. H. Haufler 1985; C. H. Haufler and M. D. Windham 1991).

Cystopteris tenuis is common in eastern North America and less frequent at the northern and western perimeter of its range. In the center of its distribution (Minnesota, Iowa, Illinois, Wisconsin, Indiana, Ohio, Pennsylvania), the narrow, elliptic pinnae angled toward the blade apex and the rounded teeth make C. tenuis relatively distinct from C. fragilis and C. protrusa (although the early season, sterile leaves of C. protrusa often resemble those of C. tenuis). In the west and especially in the northeast, C. tenuis and C. fragilis are difficult to distinguish. For the most part, C. fragilis is confined to higher latitudes and elevations than C. tenuis, but the two species can be sympatric and occasionally form sterile tetraploid hybrids. Cystopteris protrusa and C. tenuis are infrequently sympatric, but where they are, sterile triploid hybrids can occur. Hybrids between C. tenuis and C. tennesseensis are recognized as C. × wagneri (R. C. Moran 1983). Hybridization between C. tenuis and C. bulbifera has also been reported (R. C. Moran 1982b). This hybrid, C. × illinoensis R. C. Moran, is known only from the type and needs to be studied further.

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

The family Dryopteridaceae has been variously circumscribed; it is here delimited in a manner similar to that of R. M. Tryon and A. F. Tryon (1982) but with the inclusion of Nephrolepis. In many works, the family has gone under the illegitimate name Aspidiaceae. Some authorities define Dryopteridaceae more narrowly, to exclude Athyrium, Deparia, Diplazium, Cystopteris, and Gymnocarpium (Athyriaceae or Woodsiaceae), Woodsia (Woodsiaceae), Lomariopsis (Lomariopsidaceae), Nephrolepis (Nephrolepidaceae or Davalliaceae), Onoclea and Matteuccia (Onocleaceae), and Ctenitis and Tectaria (Tectariaceae). Characteristics holding Dryopteridaceae (as circumscribed here) together include the bilateral, monolete spores, often broadly winged perispore, absence of needlelike hairs, scaly stem and petiole bases, abaxial (nonmarginal) sori, base chromosome number of 40 or 41 (also 38 and 39 in Woodsia, 37 in Onoclea, 42 in Cystopteris), and usually indusiate sori. Loss of indusium, dimorphism, areolate venation, and reduced blade dissection have occurred repeatedly along many evolutionary lines in Dryopteridaceae, and in general these characteristics are often not very useful in delimiting genera or assessing intergeneric relationships.

In some genera, especially Phanerophlebia and Polystichum, the blade bears very narrow scales (sometimes called microscales) that resemble uniseriate hairs. These scales may be only one or two cells wide. Every intergradation exists between these filiform microscales and more typical, wider scales, and the two types are the same color, generally tan to brownish. Microscales are probably not homologous with true hairs, which may be either unicellular or multicellular, uncolored or sometimes reddish (as in Tectaria and Ctenitis), glandular (as in Woodsia) or not. Hairs in Dryopteridaceae, if present at all, are generally readily distinguishable from the needlelike, transparent ones found in Thelypteridaceae.

Genera ca. 60, species perhaps exceeding 3000 (18 genera, 79 species in the flora).

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