Browsing by Author "Smith, AR"
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Item Open Access A classification for extant ferns(Taxon, 2006-01-01) Smith, AR; Pryer, KM; Schuettpelz, E; Korall, P; Schneider, H; Wolf, PGWe present a revised classification for extant ferns, with emphasis on ordinal and familial ranks, and a synopsis of included genera. Our classification reflects recently published phylogenetic hypotheses based on both morphological and molecular data. Within our new classification, we 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.Item Open Access A worldwide phylogeny of Adiantum (Pteridaceae) reveals remarkable convergent evolution in leaf blade architecture(Taxon, 2018-06-01) Huiet, L; Li, F; Kao, T; Prado, J; Smith, AR; Schuettpelz, E; Pryeri, KM© International Association for Plant Taxonomy (IAPT) 2018, All rights reserved. Adiantum is among the most distinctive and easily recognized leptosporangiate fern genera. Despite encompassing an astonishing range of leaf complexity, all species of Adiantum share a unique character state not observed in other ferns: sporangia borne directly on the reflexed leaf margin or “false indusium” (pseudoindusium). The over 200 species of Adiantum span six continents and are nearly all terrestrial. Here, we present one of the most comprehensive phylogenies for any large (200+ spp.) monophyletic, subcosmopolitan genus of ferns to date. We build upon previous datasets, providing new data from four plastid markers (rbcL, atpA, rpoA, chlN) for 146 taxa. All sampled taxa can be unequivocally assigned to one of nine robustly supported clades. Although some of these unite to form larger, well-supported lineages, the backbone of our phylogeny has several short branches and generally weak support, making it difficult to accurately assess deep relationships. Our maximum likelihood-based ancestral character state reconstructions of leaf blade architecture reveal remarkable convergent evolution across multiple clades for nearly all leaf forms. A single unique synapomorphy—leaves once-pinnate, usually with prolonged rooting tips—defines the philippense clade. Although a rare occurrence in Adiantum, simple leaves occur in three distinct clades (davidii, philippense, peruvianum). Most taxa have leaves that are more than once-pinnate, and only a few of these (in the formosum and pedatum clades) exhibit the distinct pseudopedate form. Distributional ranges for each of the terminal taxa show that most species (75%) are restricted to only one of six major biogeographical regions. Forty-eight of our sampled species (nearly one-third) are endemic to South America.Item Open Access Adiantumshastense, a new species of maidenhair fern from California.(PhytoKeys, 2015) Huiet, L; Lenz, M; Nelson, JK; Pryer, KM; Smith, ARA new species of Adiantum is described from California. This species is endemic to northern California and is currently known only from Shasta County. We describe its discovery after first being collected over a century ago and distinguish it from Adiantumjordanii and Adiantumcapillus-veneris. It is evergreen and is sometimes, but not always, associated with limestone. The range of Adiantumshastense Huiet & A.R.Sm., sp. nov., is similar to several other Shasta County endemics that occur in the mesic forests of the Eastern Klamath Range, close to Shasta Lake, on limestone and metasedimentary substrates.Item Open Access Are there too many fern genera?(Taxon, 2018-06-01) Schuettpelz, E; Rouhan, G; Pryer, KM; Rothfels, CJ; Prado, J; Sundue, MA; Windham, MD; Moran, RC; Smith, ARItem Open Access Evolution of vascular plant body plans: a phylogenetic perspective(Developmental genetics and plant evolution, 2002) Schneider, H; Pryer, KM; Cranfill, R; Smith, AR; Wolf, PGItem Open Access Fern classification(2008-01-01) Smith, AR; Pryer, KATHLEENM; Schuettpelz, ERIC; Korall, P; Schneider, HARALD; Wolf, PG© Cambridge University Press 2008 and Cambridge University Press 2009. Introduction and historical summary Over the past 70 years, many fern classifications, nearly all based on morphology, most explicitly or implicitly phylogenetic, have been proposed. The most complete and commonly used classifications, some intended primarily as herbarium (filing) schemes, are summarized in Table 16.1, and include: Christensen (1938), Copeland (1947), Holttum (1947, 1949), Nayar (1970), Bierhorst (1971), Crabbe et al. (1975), Pichi Sermolli (1977), Ching (1978), Tryon and Tryon (1982), Kramer (in Kubitzki, 1990), Hennipman (1996), and Stevenson and Loconte (1996). Other classifications or trees implying relationships, some with a regional focus, include Bower (1926), Ching (1940), Dickason (1946), Wagner (1969), Tagawa and Iwatsuki (1972), Holttum (1973), and M.ckel (1974). Tryon (1952) and Pichi Sermolli (1973) reviewed and reproduced many of these and still earlier classifications, and Pichi Sermolli (1970, 1981, 1982, 1986) also summarized information on family names of ferns. Smith (1996) provided a summary and discussion of recent classifications. With the advent of cladistic methods and molecular sequencing techniques, there has been an increased interest in classifications reflecting evolutionary relationships. Phylogenetic studies robustly support a basal dichotomy within vascular plants, separating the lycophytes (less than 1% of extant vascular plants) from the euphyllophytes (Figure 16.1; Raubeson and Jansen, 1992, Kenrick and Crane, 1997; Pryer et al., 2001a, 2004a, 2004b; Qiu et al., 2006). Living euphyllophytes, in turn, comprise two major clades: spermatophytes (seed plants), which are in excess of 260000 species (Thorne, 2002; Scotland and Wortley, 2003), and ferns (sensu Pryer et al. 2004b), with about 9000 species, including horsetails, whisk ferns, and all eusporangiate and leptosporangiate ferns.Item Open Access Horsetails and ferns are a monophyletic group and the closest living relatives to seed plants.(Nature, 2001-02) Pryer, KM; Schneider, H; Smith, AR; Cranfill, R; Wolf, PG; Hunt, JS; Sipes, SDMost of the 470-million-year history of plants on land belongs to bryophytes, pteridophytes and gymnosperms, which eventually yielded to the ecological dominance by angiosperms 90 Myr ago. Our knowledge of angiosperm phylogeny, particularly the branching order of the earliest lineages, has recently been increased by the concurrence of multigene sequence analyses. However, reconstructing relationships for all the main lineages of vascular plants that diverged since the Devonian period has remained a challenge. Here we report phylogenetic analyses of combined data--from morphology and from four genes--for 35 representatives from all the main lineages of land plants. We show that there are three monophyletic groups of extant vascular plants: (1) lycophytes, (2) seed plants and (3) a clade including equisetophytes (horsetails), psilotophytes (whisk ferns) and all eusporangiate and leptosporangiate ferns. Our maximum-likelihood analysis shows unambiguously that horsetails and ferns together are the closest relatives to seed plants. This refutes the prevailing view that horsetails and ferns are transitional evolutionary grades between bryophytes and seed plants, and has important implications for our understanding of the development and evolution of plants.Item Open Access Is morphology really at odds with molecules in estimating fern phylogeny?(Systematic Botany, 2009-07-01) Schneider, H; Smith, AR; Pryer, KMUsing a morphological dataset of 136 vegetative and reproductive characters, we infer the tracheophyte phylogeny with an emphasis on early divergences of ferns (monilophytes). The dataset comprises morphological, anatomical, biochemical, and some DNA structural characters for a taxon sample of 35 species, including representatives of all major lineages of vascular plants, especially ferns. Phylogenetic relationships among vascular plants are reconstructed using maximum parsimony and Bayesian inference. Both approaches yield similar relationships and provide evidence for three major lineages of extant vascular plants: lycophytes, ferns, and seed plants. Lycophytes are sister to the euphyllophyte clade, which comprises the fern and seed plant lineages. The fern lineage consists of five clades: horsetails, whisk ferns, ophioglossoids, marattioids, and leptosporangiate ferns. This lineage is supported by characters of the spore wall and has a parsimony bootstrap value of 76%, although the Bayesian posterior probability is only 0.53. Each of the five fern clades is well supported, but the relationships among them lack statistical support. Our independent phylogenetic analyses of morphological evidence recover the same deep phylogenetic relationships among tracheophytes as found in previous studies utilizing DNA sequence data, but differ in some ways within seed plants and within ferns. We discuss the extensive independent evolution of the five extant fern clades and the evidence for the placement of whisk ferns and horsetails in our morphological analyses. © 2009 by the American Society of Plant Taxonomists.Item Open Access Metaxya lanosa, a second species in the genus and fern family Metaxyaceae(Systematic Botany, 2001-10-11) Smith, AR; Tuomisto, H; Pryer, KM; Hunt, JS; Wolf, PGWe describe and illustrate Metaxya lanosa, the second known species in the genus and the fern family Metaxyaceae (Pteridophyta). It is currently known from four different watersheds in Amazonian Peru and Venezuela. It can be distinguished readily from M. rostrata by the noticeably woolly-hairy stipes and rachises (hairs red-brown or orange-brown and easily abraded), broader, more elliptic pinnae, cartilaginous and whitish pinna margins, more distinct veins abaxially, and longer pinna stalks, especially on the distal pinnae, rbcL data from a very limited sampling are ambiguous but do not reject support for the recognition of at least two species within Metaxya.Item Open Access Phylogenetic relationships and evolution of extant horsetails, Equisetum, based on chloroplast DNA sequence data (rbcL and trnL-F)(International Journal of Plant Sciences, 2003-01-01) Des Marais, DL; Smith, AR; Britton, DM; Pryer, KMEquisetum is a small and morphologically distinct genus with a rich fossil record. Two subgenera have been recognized based principally on stomatal position and stem branching: subg. Equisetum (eight species; superficial stomates; stems branched) and subg. Hippochaete (seven species; sunken stomates; stems generally unbranched). Prior attempts at understanding Equisetum systematics, phylogeny, and character evolution have been hampered by the high degree of morphological plasticity in the genus as well as by frequent hybridization among members within each subgenus. We present the first explicit phylogenetic study of Equisetum, including all 15 species and two samples of one widespread hybrid, Equisetum x ferrissii, based on a combined analysis of two chloroplast markers, rbcL and trnL-F. Our robustly supported phylogeny identifies two monophyletic clades corresponding to the two subgenera recognized by earlier workers. The phylogenetic placement of Equisetum bogotense, however, is ambiguous. In maximum likelihood analyses, it allies with subg. Hippochaete as the most basal member, while maximum parsimony places it as sister to the rest of the genus. A consensus phylogeny from the two analyses is presented as a basal trichotomy (E. bogotense, subg. Hippochaete, subg. Equisetum), and morphological character evolution is discussed. We detected rate heterogeneity in the rbcL locus between the two subgenera that can be attributed to an increased rate of nucleotide substitution (transversions) in subg. Hippochaete. We calculated molecular-based age estimates using the penalized likelihood approach, which accounts for rate heterogeneity and does not assume a molecular clock. The Equisetum crown group appears to have diversified in the early Cenozoic, whereas the Equisetaceae total group is estimated to have a Paleozoic origin. These molecular-based age estimates are in remarkable agreement with current interpretations of the fossil record.Item Open Access Phylogenetic relationships of the enigmatic fern families Hymenophyllopsidaceae and Lophosoriaceae: Evidence from rbcL nucleotide sequences(Plant Systematics and Evolution, 1999-01-01) Wolf, PG; Sipes, SD; White, MR; Martines, ML; Pryer, KM; Smith, AR; Ueda, KNucleotide sequences from rbcL were used to infer relationships of Lophosoriaceae and Hymenophyllopsidaceae. The phylogenetic positions of these two monotypic fern families have been debated, and neither group had been included in recent molecular systematic studies of ferns. Maximum parsimony analysis of our data supported a sister relationship between Lophosoria and Dicksonia, and also between Hymenophyllopsis and Cyathea. Thus, both newly-examined families appear to be part of a previously characterized and well-supported clade of tree ferns. The inferred relationships of Lophosoria are consistent with most (but not all) recent treatments. However, Hymenophyllopsis includes only small delicate plants superficially similar to filmy ferns (Hymenophyllaceae), very different from the large arborescent taxa. Nevertheless, some synapomorphic characteristics are shared with the tree fern clade. Further studies on gametophytes of Hymenophyllopsis are needed to test these hypotheses of relationship.Item Open Access Phylogeny and relationships of the neotropical Adiantum raddianum group (Pteridaceae)(Taxon, 2016-12-01) Hirai, RY; Schuettpelz, E; Huiet, L; Pryer, KM; Smith, AR; Prado, J© International Association for Plant Taxonomy (IAPT) 2016. With more than 200 species, the maidenhair fern genus Adiantum is among the top ten most diverse fern genera. Adiantum is pantropical in distribution and, due to the presence of a unique synapomorphy (sporangia borne on indusia rather than laminae), perhaps the most easily recognized fern genus. Many of its members, including numerous cultivars derived from A. raddianum, are grown as ornamentals. Because of its size, a comprehensive taxonomic study of Adiantum is difficult and the genus is perhaps better approached through a series of narrower studies. Here, we focus specifically on A. raddianum and putative allies. We find a newly defined A. raddianum group to be strongly supported as monophyletic and segregated from other maidenhair ferns on the basis of genetic as well as morphological characteristics. Bayesian inference and maximum likelihood analyses of plastid atpA, chlL, chlN, rbcL, and rpoA sequences support the A raddianum clade as sister to A poiretii and its allies. We identify round-reniform indusia to be a characteristic of the A.raddianum group (vs. lunate in the A.poiretii group). Additionally, we find species in the Apoiretii group to differ in having a unique 66 nucleotide deletion in our chlN gene alignment. The neotropical Araddianum group comprises at least 17 species (14 studied here), some widely distributed; one was recently described (A. alan-smithii).Item Open Access rbcL data reveal two monophyletic groups of filmy ferns (Filicopsida: Hymenophyllaceae).(American journal of botany, 2001-06) Pryer, KM; Smith, AR; Hunt, JS; Dubuisson, JYThe "filmy fern" family, Hymenophyllaceae, is traditionally partitioned into two principal genera, Trichomanes s.l. (sensu lato) and Hymenophyllum s.l., based upon sorus shape characters. This basic split in the family has been widely debated this past century and hence was evaluated here by using rbcL nucleotide sequence data in a phylogenetic study of 26 filmy ferns and nine outgroup taxa. Our results confirm the monophyly of the family and provide robust support for two monophyletic groups that correspond to the two classical genera. In addition, we show that some taxa of uncertain affinity, such as the monotypic genera Cardiomanes and Serpyllopsis, and at least one species of Microtrichomanes, are convincingly included within Hymenophyllum s.l. The tubular- or conical-based sorus that typifies Trichomanes s.l. and Cardiomanes, the most basal member of Hymenophyllum s.l., is a plesiomorphic character state for the family. Tubular-based sori occurring in other members of Hymenophyllum s.l. are most likely derived independently and more than one time. While rbcL data are able to provide a well-supported phylogenetic estimate within Trichomanes s.l., they are inadequate for resolving relationships within Hymenophyllum s.l., which will require data from additional sources. This disparity in resolution reflects differential rates of evolution for rbcL within Hymenophyllaceae.Item Open Access rbcL phylogeny of the fern genus Trichomanes (Hymenophyllaceae), with special reference to Neotropical taxa(International Journal of Plant Sciences, 2003-01-01) Dubuisson, JY; Hennequin, S; Douzery, EJP; Cranfill, RB; Smith, AR; Pryer, KMIn order to estimate evolutionary relationships within the filmy fern genus Trichomanes (Hymenophyllaceae), we performed a phylogenetic analysis using rbcL nucleotide data from 46 species of Trichomanes belonging to all four of C. V. Morton's subgenera: Achomanes, Didymoglossum, Pachychaetum, and Trichomanes. Outgroups included four species of Hymenophyllum in three different subgenera, plus the monotypic genus Cardiomanes, from New Zealand. We find high resolution and robust support at most nodes, regardless of the phylogenetic optimization criterion used (maximum parsimony or maximum likelihood). Two species belonging to Morton's Asiatic sections Callistopteris and Cephalomanes are in unresolved basal positions within Trichomanes s.l., suggesting that rbcL data alone are inadequate for estimating the earliest cladogenetic events. Out of the four Morton trichomanoid subgenera, only subg. Didymoglossum appears monophyletic. Other noteworthy results include the following: (1) lianescent sect. Lacostea is more closely related to sect. Davalliopsis (traditionally placed in subg. Pachychaetum) than to other members of subg. Achomanes; (2) sections Davalliopsis and Lacostea, together with species of the morphologically different subg. Achomanes, make up a strongly supported Neotropical clade; (3) all hemiepiphytes (but not true lianas) and strictly epiphytic or epipetric species (Morton's subgenera Trichomanes and Didymoglossum) group together in an ecologically definable clade that also includes the terrestrial sect. Nesopteris; and (4) sect. Lacosteopsis (sensu Morton) is polyphyletic and comprises two distantly related clades: large hemiepiphytic climbers and small strictly epiphytic/epipetric taxa. Each of these associations is somewhat unexpected but is supported by cytological, geographical, and/or ecological evidence. We conclude that many morphological characters traditionally used for delimiting groups within Trichomanes are, in part, plesiomorphic or homoplastic. Additionally, we discuss probable multiple origins of Neotropical Trichomanes.Item Open Access Rediscovery of Polypodium calirhiza (Polypodiaceae) in Mexico(Brittonia, 2014-01-01) Sigel, EM; Windham, MD; Smith, AR; Dyer, RJ; Pryer, KMThis study addresses reported discrepancies regarding the occurrence of Polypodium calirhiza in Mexico. The original paper describing this taxon cited collections from Mexico, but the species was omitted from the recent Pteridophytes of Mexico. Originally treated as a tetraploid cytotype of P. californicum, P. calirhiza now is hypothesized to have arisen through hybridization between P. glycyrrhiza and P. californicum. The tetraploid can be difficult to distinguish from either of its putative parents, but especially so from P. californicum. Our analyses show that a combination of spore length and abaxial rachis scale morphology consistently distinguishes P. calirhiza from P. californicum, and we confirm that both species occur in Mexico. Although occasionally found growing together in the United States, the two species are strongly allopatric in Mexico: P. californicum is restricted to coastal regions of the Baja California peninsula and neighboring Pacific islands, whereas P. calirhiza grows at high elevations in central and southern Mexico. The occurrence of P. calirhiza in Oaxaca, Mexico, marks the southernmost extent of the P. vulgare complex in the Western Hemisphere. © 2014 The New York Botanical Garden.Item Open Access Rediscovery of Polypodium calirhiza (Polypodiaceae) in Mexico(Brittonia, 2014) Sigel, EM; Windham, MD; Smith, AR; Dyer, RJ; Pryer, KMThis study addresses reported discrepancies regarding the occurrence of Polypodium calirhiza in Mexico. The original paper describing this taxon cited collections from Mexico, but the species was omitted from the recent Pteridophytes of Mexico. Originally treated as a tetraploid cytotype of P. californicum, P. calirhiza now is hypothesized to have arisen through hybridization between P. glycyrrhiza and P. californicum. The tetraploid can be difficult to distinguish from either of its putative parents, but especially so from P. californicum. Our analyses show that a combination of spore length and abaxial rachis scale morphology consistently distinguishes P. calirhiza from P. californicum, and we confirm that both species occur in Mexico. Although occasionally found growing together in the United States, the two species are strongly allopatric in Mexico: P. californicum is restricted to coastal regions of the Baja California peninsula and neighboring Pacific islands, whereas P. calirhiza grows at high elevations in central and southern Mexico. The occurrence of P. calirhiza in Oaxaca, Mexico, marks the southernmost extent of the P. vulgare complex in the Western Hemisphere. © 2014 The New York Botanical Garden.