Flora of North America species comparison

Hybrids between Gymnocarpium jessoense subsp. parvulum and G. dryopteris (G. × intermedium Sarvela) are usually found wherever these two taxa occur together (Finland; Manitoba, Northwest Territories, Ontario, Quebec, Saskatchewan, Yukon; Alaska, Michigan, Minnesota, Wisconsin), and they are particularly abundant in the Great Lakes region. These hybrids have sometimes been referred to as G. × heterosporum, a name that is, however, correctly restricted to unique hybrids between G. robertianum and G. appalachianum (see discussion under G. robertianum; K. M. Pryer 1992). Gymnocarpium × intermedium is intermediate between the two parental species in its leaf morphology and glandularity, and it can be readily distinguished by its small, blackish, malformed, abortive spores, as well as large, brown, round spores that may allow this taxon to reproduce apogamously. Of the Gymnocarpium sterile hybrids, G. × intermedium is the easiest to distinguish morphologically.

(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.)