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A Classification for Extant Ferns Author(S): Alan R A Classification for Extant Ferns Author(s): Alan R. Smith, Kathleen M. Pryer, Eric Schuettpelz, Petra Korall, Harald Schneider and Paul G. Wolf Source: Taxon, Vol. 55, No. 3 (Aug., 2006), pp. 705-731 Published by: International Association for Plant Taxonomy (IAPT) Stable URL: http://www.jstor.org/stable/25065646 . Accessed: 11/10/2013 12:39 Your use of the JSTOR archive indicates your acceptance of the Terms & Conditions of Use, available at . http://www.jstor.org/page/info/about/policies/terms.jsp . JSTOR is a not-for-profit service that helps scholars, researchers, and students discover, use, and build upon a wide range of content in a trusted digital archive. We use information technology and tools to increase productivity and facilitate new forms of scholarship. For more information about JSTOR, please contact [email protected]. International Association for Plant Taxonomy (IAPT) is collaborating with JSTOR to digitize, preserve and extend access to Taxon. http://www.jstor.org This content downloaded from 132.198.144.248 on Fri, 11 Oct 2013 12:39:16 PM All use subject to JSTOR Terms and Conditions TAXON 55 (3) August 2006: 705-731 Smith & al. Fern classification TAXONOMY A classification for extant ferns Alan R. Smith1, Kathleen M. Pryer2, Eric Schuettpelz2, Petra Korall2'3, Harald Schneider4 & Paul G Wolf5 1 University Herbarium, 1001 Valley Life Sciences Building #2465, University of California, Berkeley, California 94720-2465, U.S.A. [email protected] (author for correspondence). 2 Department of Biology, Duke University, Durham, North Carolina 27708-0338, U.S.A. 3 Department of Phanerogamic Botany, Swedish Museum of Natural History, Box 50007, SE-104 05 Stock holm, Sweden. 4 Albrecht-von-Haller-Lnstitut f?r Pflanzenwissenschaften, Abteilung Systematische Botanik, Georg-August Universit?t, Untere Karsp?le 2, 37073 G?ttingen, Germany. 5 Department of Biology, Utah State University, Logan, Utah 84322-5305, U.S.A. We present a revised classification for extant ferns, with emphasis on ordinal and familial ranks, and a synop sis of included genera. Our classification reflects recently published phylogenetic hypotheses based on both we morphological and molecular data. Within our new classification, recognize four monophyletic classes, 11 monophyletic orders, and 37 families, 32 of which are strongly supported as monophyletic. One new family, Cibotiaceae Korall, is described. The phylogenetic affinities of a few genera in the order Polypodiales are unclear and their familial placements are therefore tentative. Alphabetical lists of accepted genera (including common synonyms), families, orders, and taxa of higher rank are provided. KEYWORDS: classification, Cibotiaceae, ferns, monilophytes, monophyletic. INTRODUCTION | Euphyllophytes Recent phylogenetic studies have revealed a basal Lycophytes Spermatophytes Monilophytes dichotomy within vascular plants, separating the lyco phytes (less than 1% of extant vascular plants) from the euphyllophytes (Fig. 1;Raubeson & Jansen, 1992; Ken rick & Crane, 1997; Pryer & al, 2001a, 2004a, b). Liv ing euphyllophytes, in turn, comprise two major clades: the spermatophytes (seed plants), which are in excess of 260,000 species (Thome, 2002; Scotland & Wortley, 2003), and the monilophytes (ferns, sensu Pryer & al., 2004b), with about 9,000 species, including horsetails, whisk ferns, and all eusporangiate and leptosporangiate ferns. Plants that are included in the lycophyte and fern 1. Consensus of clades are all spore-bearing or "seed-free", and because Fig. phylogeny depicting relationships vascular summarizes the of this common feature their members have been major plant lineages. Topology lumped results of previously published phylogenetic studies under various such as together historically terms, "pteri (e.g., Raubeson & Jansen, 1992; Kenrick & Crane, 1997; dophytes" and "ferns and fern allies"?paraphyletic Renzaglia & al., 2000; Pryer & al., 2001a, see main text for assemblages of plants. The focus of this reclassification others). Resolved nodes have received bootstrap support ?70. is exclusively on ferns (Division Tracheophyta, Sub division Euphyllophytina, Infradivision Moniliformop ses, of Kenrick & Crane, 1997), characterized by lateral ferns (Hasebe & al, 1994, 1995; Manhart, 1994, 1995 root origin in the endodermis, usually mesarch pro Pryer & al, 1995, 2001a, 2004b; Kranz & Huss, 1996 toxylem in shoots, a pseudoendospore, plasmodial tape Pahnke & al, 1996;Wolf, 1997;Wolf & al, 1998 turn, and sperm cells with 30-1000 flagellae (Renzaglia Beckert & al, 1999; Vangerow & al, 1999; Sano & al. & al., 2000; Schneider & al., 2002a). 2000a; Schneider& al, 2004c;Wikstr?m & Pryer,2005 Increasingly robust phylogenetic hypotheses for Tsutsumi & Kato, 2006; Schuettpelz & al, in press), uti 705 This content downloaded from 132.198.144.248 on Fri, 11 Oct 2013 12:39:16 PM All use subject to JSTOR Terms and Conditions Smith & al. Fern classification TAXON 55 (3) August 2006: 705-731 lizing data from morphology, seven chloroplast markers serve us best if we name only those clades that are read (rbcL, atpA, atpB, accD, rpsA, 16S rDNA, ITS), one nu ily recognizable and characterized by morphological clear gene (18S rDNA), and three mitochondrial genes synapomorphic characters, at least at family and higher (atpl, nadl, nad5) prompt us to reevaluate the classifi ranks. However, more traditional (morphology-based) cation of these vascular plants. Multiple-gene phyloge and practical classifications are sometimes incompatible netic analyses, e.g., studies by Wolf (1996), Wolf & al. with the results and classifications implied by phyloge (1998), Pryer & al. (2001a, 2004b), Schneider & al. netic studies, especially when the principle of monophy (2004c), Wikstr?m & Pryer (2005), and Schuettpelz & al. ly is used as a grouping criterion (recognizing clades, and (in press), have given rise to growing conviction in both not paraphyletic grades; APG II, 2003). When a tradi the composition and relationships of taxa at familial and tionally recognized family nests within another, complex ordinal ranks. Five recent morphological analyses of classificatory choices ensue: (1) recognition of para relationships, by Pryer & al. (1995, 2001a), Schneider phyletic families (Brummitt, 1996, 1997; Lid?n & al, (1996a), Stevenson & Loconte (1996), and Schneider & 1997; Moore, 1998; Diggs & Lipscomb, 2002; Grant, al. (in prep.) have increased support for the molecular 2003); (2) dismemberment of a recognized family into based consensus topology. For eusporangiate and basal smaller families (e.g., the disintegration of classical leptosporangiate ferns, evidence is now sufficient to al Scrophulariaceae; Olmstead & al, 2001); or (3) integra low us to circumscribe confidently most clades and as tion of the traditional family that causes the paraphyly sign ranks. However, for some more derived leptospo into the "progenitor" family. The first choice, preferred rangiate ferns, the phylogenetic evidence is still some by some, leads to recognition of unnatural (non-mono what equivocal. Consequently, declaration of phyloge phyletic) groups, which in our opinion often retards or netic positions for some taxa and the assignment of ranks obscures investigation into interesting biological, phyto (which we consider subjective and secondary), in a clas geographic, and evolutionary questions. The second so sical "Linnaean-style" hierarchy, are tentative. In this pa lution supposes that we have morphological synapomor per, we present a revised view of the classification of ex phies for nodes that lead to all of the segregate families, tant ferns, taking into account all relevant evidence. We and this is not often the case, although one hopes that focus our classification at the ranks of class, order, and eventually we shall find these synapomorphies. Until family, believing that the information at hand is most then, itmay be nearly impossible to define some segre appropriate for resolution and understanding of relation gate families in such a way that they would be both ships at these levels. Within most families, and especial keyable and circumscribable. The third solution is a "fast ly at the generic level, there is still insufficient evidence fix" to the problem, but expediency often demands that to attempt many classificatory decisions. at least some of the intrafamilial subclades also be rec In the classification proposed herein, we account for, ognized taxonomically, either at a lower rank (e.g., sub and place in a revised taxonomic framework, all names at family), or with an unranked informal name (e.g., "gram on can family and ordinal rank utilized in previous major classifi mitid ferns") until further decisions rank be made. cations directed at ferns, particularly those that have been This third option seems to us the most practicable and proposed in the last eighty years: Bower (1926), Christen practical solution toward a "first-pass" revision of fern sen (1938),Ching (1940, 1978),Dickason (1946),Cope classification. As more data are gathered and future phy land (1947),Holttum (1947, 1949, 1973),Pichi Sermolli logenetic analyses provide better resolved and better sup (1958, 1977), Mehra (1961), Wagner (1969), Nayar ported topologies, one expects further insight into identi (1970), Tagawa& Iwatsuki (1972),Mickel (1974), Try fying synapomorphies for segregate taxa, enabling even on & Tryon (1982), Kramer (in Kubitzki, 1990), Hennip tual movement toward the second option of recognizing man (1996), and Stevenson & Loconte (1996).
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