Population biology of pteridophytes has attracted considerable attention over the last 20 years as documented in successive reviews by Klekowski (1969), Lloyd (1974b), Klekowski (1979), Page (1979), Haufler (1987), Klekowski (1988), and Cousens (1988). Yet much remains unknown, particularly with respect to species' specific differences in reproduction and the reflection of these differences in species' demographic and distribution patterns. Homosporous pteridophytes as a group are often considered to be equivalent to one another in their ability to disperse and migrate (Tryon, 1970, 1972, 1986) and superior to seed plants with regard to species' dispersability (Smith, 1972; Tryon, 1986). These views are based primarily upon the presumed ease of dispersal of pteridophyte spores in comparison with seeds and a potential of homosporous ferns to reproduce by single spores capable of producing self-fertile bisexual gametophytes. Indeed, some species have these capabilities; examples of longrange and recent disjunctions and of wide-ranging species are readily found among homosporous pteridophytes (Wagner, 1972; Tryon, 1970, 1972, 1986; Smith, 1972). However, to extrapolate from these species to generalizations encompassing all homosporous pteridophytes obscures significant differences among species imposed by differences in fecundity, habitat requirements, mating systems, and gametophyte ecology (Klekowski, 1969, 1972, 1979, 1988; Lloyd, 1974a, 1974b; Cousens, 1979, 1981; Cousens et al., 1985; Cousens et al., 1988; Schneller, 1975, 1979; Grime, 1985; Farrar, 1976; Farrar & Gooch, 1975; Crist & Farrar, 1983; J. Peck, 1980; C. Peck, 1985). Species-specific characteristics in combination with local habitat characteristics, in fact, determine geographic ranges of fern species that are generally comparable to those of seed plants (Wagner, 1972) and bryophytes (Anderson, 1971; Crum, 1972). In an attempt to elucidate factors differentiating species' abilities to disperse via gametophyte reproduction, we have conducted complementary field and laboratory studies on a number of co-occurring fern species in Central Iowa. For purposes of comparison, we have divided fern life history into a series of successive stages and processes (Table 1), each of which contributes in serial fashion to the species' overall reproductive potential. Most of our work has been conducted at a state preserve where sixteen pteridophyte species are
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