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William S. Alverson - One of the best experts on this subject based on the ideXlab platform.
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structure and evolution of the androecium in the malvatheca clade malvaceae s l and implications for malvaceae and Malvales
Plant Systematics and Evolution, 2006Co-Authors: Maria Von Balthazar, Hansthomas Janka, William S. Alverson, Jürg Schönenberger, Clemens Bayer, David A. BaumAbstract:Androecial development and structure as well as floral vasculature of six selected species of Bombacoideae and of several smaller lineages of the Malvatheca clade (Malvaceae s.l.) were studied. All studied taxa share a similar pattern of androecial development: initially, five antepetalous/antetepalous and five alternipetalous/alternitepalous primary androecial primordia develop on a ring wall. Two elongate secondary androecial primordia form on each antepetalous/antetepalous sector. At anthesis the androecium consists of an androecial tube crowned by five androecial lobes. Each of these lobes is the developmental product of an alternipetalous/alternitepalous primary androecial primordium and its two neighbouring antepetalous/antetepalous secondary androecial primordia. The elongate, sessile androecial units are positioned along the lateral margins of the androecial lobes and in the distal part of the androecial tube. Seen in the light of the most recent studies of floral development and phylogeny of the Malvaceae and the Malvales as a whole, our data indicate that i) elongate, sessile androecial units are ancestral in the Malvatheca clade, that ii) an obdiplostemonous floral ground plan is a synapomorphy for the Malvaceae, and that iii) diplostemony is most likely ancestral in the Malvales.
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Phylogeny of the core Malvales: evidence from ndhF sequence data.
American journal of botany, 1999Co-Authors: William S. Alverson, Clemens Bayer, Barbara A Whitlock, Reto Nyffeler, David A. BaumAbstract:The monophyly of the group comprising the core malvalean families, Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae, was recently confirmed by molecular studies, but the internal structure of this clade is poorly understood. In this study, we examined sequences of the chloroplast ndhF gene (aligned length 2226 bp) from 70 exemplars representing 35 of the 39 putative tribes of core Malvales. The monophyly of one traditional family, the Malvaceae, was supported in the trees resulting from these data, but the other three families, as traditionally circumscribed, are nonmonophyletic. In addition, the following relationships were well supported: (1) a clade, /Malvatheca, consisting of traditional Malvaceae and Bombacaceae (except some members of tribe Durioneae), plus Fremontodendronand Chiranthodendron, which are usually treated as Sterculiaceae; (2) a clade, /Malvadendrina, supported by a unique 21-bp (base pair) deletion and consisting of /Malvatheca, plus five additional subclades, including representatives of Sterculiaceae and Tiliaceae, and Durionieae; (3) a clade, /Byttneriina, with genera traditionally assigned to several tribes of Tiliaceae, plus exemplars of tribes Byttnerieae, Hermannieae, and Lasiopetaleae of Sterculiaceae. The most striking departures from traditional classifications are the following: Durio and relatives appear to be more closely related to Helicteres and Reevesia (Sterculiaceae) than to Bombacaceae; several genera traditionally considered as Bombacaceae (Camptostemon, Matisia, Phragmotheca, and Quararibea) or Sterculiaceae (Chiranthodendron and Fremontodendron) appear as sister lineages to the traditional Malvaceae; the traditional tribe Helictereae (Sterculiaceae) is polyphyletic; and Sterculiaceae and Tiliaceae, as traditionally circumscribed, represent polyphyletic groups that cannot sensibly be maintained with their traditional limits for purposes of classification. We discuss morphological characters and conclude that there has been extensive homoplasy in characters previously used to delineate major taxonomic groups in core Malvales. The topologies here also suggest that /Malvatheca do not have as a synapormophy monothecate anthers, as has been previously supposed but, instead, may be united by dithecate, transversely septate (polysporangiate) anthers, as found in basal members of both /Bombacoideae and /Malvoideae. Thus, ‘‘monothecate’’ anthers may have been derived at least twice, independently, within the /Bombacoideae (core Bombacaceae) and /Malvoideae (traditional Malvaceae).
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support for an expanded family concept of malvaceae within a recircumscribed order Malvales a combined analysis of plastid atpb and rbcl dna sequences
Botanical Journal of the Linnean Society, 1999Co-Authors: Clemens Bayer, William S. Alverson, Klaus Kubitzki, Michael F Fay, Anette Y De Bruijn, Vincent Savolainen, Cynthia M Morton, Mark W ChaseAbstract:Abstract Sequence analyses of the plastid genes atp B and rbc L support an expanded order Malvales. Within this alliance, core Malvales are clearly supported and comprise most genera that have previously been included in Sterculiaceae, Tiliaceae, Bombacaceae, and Malvaceae. Additional well supported malvalean alliances include the bixalean clade (Bixaceae, Diegodendraceae, and Cochlospermaceae), the cistalean clade (Cistaceae, Dipterocarpaceae, and Sarcolaenaceae) and Thymelaeaceae (including Gonystyloideae and Aquilarioideae). Our results indicate sister-group relationships between (1) Neuradaceae and the cistalean clade; (2) Sphaerosepalaceae and Thymelaeaceae; (3) these two clades (1 and 2); and (4) all these and an alliance comprising the bixalean clade and core Malvales, but this pattern is weakly supported by the bootstrap. The affinities of Muntingiaceae and Petenaea are especially ambiguous, although almost certainly they are Malvales s.l. The traditional delimitation of families within core Malvales is untenable. Instead, we propose to merge Sterculiaceae, Tiliaceae and Bombacaceae with Malvaceae and subdivide this enlarged family Malvaceae into nine subfamilies based on molecular, morphological, and biogeographical data: (1) Byttnerioideae, including tribes Byttnerieae, Lasiopetaleae and Theobromeae (all of which have cucullate petals) and Hermannieae; (2) Grewioideae, including most genera of former Tiliaceae; (3) Tilioideae, monogeneric in our analysis; (4) Helicteroideae, comprising most of the taxa previously included in Helictereae, plus Mansonia , Triplochiton (indicating that apocarpy evolved at least twice within Malvaceae) and possibly Durioneae; (5) Sterculioideae, defined by apetalous, apocarpous, usually unisexual flowers with androgynophores; (6) Brownlowioideae, circumscribed as in previous classifications; (7) Dombeyoideae, expanded to include Burretiodendron , Eriolaena , Pterospermum , and Schoutenia ; (8) Bombacoideae, corresponding to former Bombacaceae (without Durioneae) but including Fremontodendreae and Pentaplaris ; (9) Malvoideae, monophyletic but difficult to delimit from Bombacoideae, which with more data and taxon sampling than here might prove to be paraphyletic without Malvoideae.
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circumscription of the Malvales and relationships to other rosidae evidence from rbcl sequence data
American Journal of Botany, 1998Co-Authors: William S. Alverson, David A. Baum, Mark W Chase, Kenneth G Karol, Susan M Swensen, Richard M Mccourt, Kenneth J SytsmaAbstract:The order Malvales remains poorly circumscribed, despite its seemingly indisputable core constituents: Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae. We conducted a two-step parsimony analysis on 125 rbcL sequences to clarify the composition of Malvales, to determine the relationships of some controversial families, and to identify the placement of the Malvales within Rosidae. We sampled taxa that have been previously suggested to be within, or close to, Malvales (83 sequences), plus additional rosids (26 sequences) and nonrosid eudicots (16 sequences) to provide a broader framework for the analysis. The resulting trees strongly support the monophyly of the core malvalean families, listed above. In addition, these data serve to identify a broader group of taxa that are closely associated with the core families. This expanded malvalean clade is composed of four major subclades: (1) the core families (Bombacaceae, Malvaceae, Sterculiaceae, Tiliaceae); (2) Bixaceae, Cochlospermaceae, and Sphaerosepalaceae (Rhopalocarpaceae); (3) Thymelaeaceae sensu lato (s.l.); and (4) Cistaceae, Dipterocarpaceae s.l., Sarcolaenaceae (Chlaenaceae), and Muntingia. In addition, Neurada (Neuradaceae or Rosaceae) falls in the expanded malvalean clade but not clearly within any of the four major subclades. This expanded malvalean clade is sister to either the expanded capparalean clade of Rodman et al. or the sapindalean clade of Gadek et al. Members of Elaeocarpaceae, hypothesized by most authors as a sister group to the four core malvalean families, are shown to not fall close to these taxa. Also excluded as members of, or sister groups to, the expanded malvalean clade were the families Aextoxicaceae, Barbeyaceae, Cannabinaceae, Cecropiaceae, Dichapetalaceae, Elaeagnaceae, Euphorbiaceae s.l., Huaceae, Lecythidaceae, Moraceae s.l., Pandaceae, Plagiopteraceae, Rhamnaceae, Scytopetalaceae, Ulmaceae, and Urticaceae. The order Malvales, as traditionally circumscribed, includes four core families, Bombacaceae (;250 spp.), Malvaceae (1500 spp.), Sterculiaceae (1000 spp.), and Tiliaceae (400 spp.), plus from one to eight other families depending upon author (Takhtajan, 1987, 1997; Cronquist, 1988; Dahlgren, 1989; Thorne, 1992). Considering only the core four families, the order comprises predominantly woody and tropical trees, including several economically important genera such as cotton (Gossypium
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Circumscription of the Malvales and relationships to other Rosidae: evidence from rbcL sequence data.
American journal of botany, 1998Co-Authors: William S. Alverson, David A. Baum, Mark W Chase, Kenneth G Karol, Susan M Swensen, Richard M Mccourt, Kenneth J SytsmaAbstract:The order Malvales remains poorly circumscribed, despite its seemingly indisputable core constituents: Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae. We conducted a two-step parsimony analysis on 125 rbcL sequences to clarify the composition of Malvales, to determine the relationships of some controversial families, and to identify the placement of the Malvales within Rosidae. We sampled taxa that have been previously suggested to be within, or close to, Malvales (83 sequences), plus additional rosids (26 sequences) and nonrosid eudicots (16 sequences) to provide a broader framework for the analysis. The resulting trees strongly support the monophyly of the core malvalean families, listed above. In addition, these data serve to identify a broader group of taxa that are closely associated with the core families. This expanded malvalean clade is composed of four major subclades: (1) the core families (Bombacaceae, Malvaceae, Sterculiaceae, Tiliaceae); (2) Bixaceae, Cochlospermaceae, and Sphaerosepalaceae (Rhopalocarpaceae); (3) Thymelaeaceae sensu lato (s.l.); and (4) Cistaceae, Dipterocarpaceae s.l., Sarcolaenaceae (Chlaenaceae), and Muntingia. In addition, Neurada (Neuradaceae or Rosaceae) falls in the expanded malvalean clade but not clearly within any of the four major subclades. This expanded malvalean clade is sister to either the expanded capparalean clade of Rodman et al. or the sapindalean clade of Gadek et al. Members of Elaeocarpaceae, hypothesized by most authors as a sister group to the four core malvalean families, are shown to not fall close to these taxa. Also excluded as members of, or sister groups to, the expanded malvalean clade were the families Aextoxicaceae, Barbeyaceae, Cannabinaceae, Cecropiaceae, Dichapetalaceae, Elaeagnaceae, Euphorbiaceae s.l., Huaceae, Lecythidaceae, Moraceae s.l., Pandaceae, Plagiopteraceae, Rhamnaceae, Scytopetalaceae, Ulmaceae, and Urticaceae.
Mark W Chase - One of the best experts on this subject based on the ideXlab platform.
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support for an expanded family concept of malvaceae within a recircumscribed order Malvales a combined analysis of plastid atpb and rbcl dna sequences
Botanical Journal of the Linnean Society, 1999Co-Authors: Clemens Bayer, William S. Alverson, Klaus Kubitzki, Michael F Fay, Anette Y De Bruijn, Vincent Savolainen, Cynthia M Morton, Mark W ChaseAbstract:Abstract Sequence analyses of the plastid genes atp B and rbc L support an expanded order Malvales. Within this alliance, core Malvales are clearly supported and comprise most genera that have previously been included in Sterculiaceae, Tiliaceae, Bombacaceae, and Malvaceae. Additional well supported malvalean alliances include the bixalean clade (Bixaceae, Diegodendraceae, and Cochlospermaceae), the cistalean clade (Cistaceae, Dipterocarpaceae, and Sarcolaenaceae) and Thymelaeaceae (including Gonystyloideae and Aquilarioideae). Our results indicate sister-group relationships between (1) Neuradaceae and the cistalean clade; (2) Sphaerosepalaceae and Thymelaeaceae; (3) these two clades (1 and 2); and (4) all these and an alliance comprising the bixalean clade and core Malvales, but this pattern is weakly supported by the bootstrap. The affinities of Muntingiaceae and Petenaea are especially ambiguous, although almost certainly they are Malvales s.l. The traditional delimitation of families within core Malvales is untenable. Instead, we propose to merge Sterculiaceae, Tiliaceae and Bombacaceae with Malvaceae and subdivide this enlarged family Malvaceae into nine subfamilies based on molecular, morphological, and biogeographical data: (1) Byttnerioideae, including tribes Byttnerieae, Lasiopetaleae and Theobromeae (all of which have cucullate petals) and Hermannieae; (2) Grewioideae, including most genera of former Tiliaceae; (3) Tilioideae, monogeneric in our analysis; (4) Helicteroideae, comprising most of the taxa previously included in Helictereae, plus Mansonia , Triplochiton (indicating that apocarpy evolved at least twice within Malvaceae) and possibly Durioneae; (5) Sterculioideae, defined by apetalous, apocarpous, usually unisexual flowers with androgynophores; (6) Brownlowioideae, circumscribed as in previous classifications; (7) Dombeyoideae, expanded to include Burretiodendron , Eriolaena , Pterospermum , and Schoutenia ; (8) Bombacoideae, corresponding to former Bombacaceae (without Durioneae) but including Fremontodendreae and Pentaplaris ; (9) Malvoideae, monophyletic but difficult to delimit from Bombacoideae, which with more data and taxon sampling than here might prove to be paraphyletic without Malvoideae.
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circumscription of the Malvales and relationships to other rosidae evidence from rbcl sequence data
American Journal of Botany, 1998Co-Authors: William S. Alverson, David A. Baum, Mark W Chase, Kenneth G Karol, Susan M Swensen, Richard M Mccourt, Kenneth J SytsmaAbstract:The order Malvales remains poorly circumscribed, despite its seemingly indisputable core constituents: Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae. We conducted a two-step parsimony analysis on 125 rbcL sequences to clarify the composition of Malvales, to determine the relationships of some controversial families, and to identify the placement of the Malvales within Rosidae. We sampled taxa that have been previously suggested to be within, or close to, Malvales (83 sequences), plus additional rosids (26 sequences) and nonrosid eudicots (16 sequences) to provide a broader framework for the analysis. The resulting trees strongly support the monophyly of the core malvalean families, listed above. In addition, these data serve to identify a broader group of taxa that are closely associated with the core families. This expanded malvalean clade is composed of four major subclades: (1) the core families (Bombacaceae, Malvaceae, Sterculiaceae, Tiliaceae); (2) Bixaceae, Cochlospermaceae, and Sphaerosepalaceae (Rhopalocarpaceae); (3) Thymelaeaceae sensu lato (s.l.); and (4) Cistaceae, Dipterocarpaceae s.l., Sarcolaenaceae (Chlaenaceae), and Muntingia. In addition, Neurada (Neuradaceae or Rosaceae) falls in the expanded malvalean clade but not clearly within any of the four major subclades. This expanded malvalean clade is sister to either the expanded capparalean clade of Rodman et al. or the sapindalean clade of Gadek et al. Members of Elaeocarpaceae, hypothesized by most authors as a sister group to the four core malvalean families, are shown to not fall close to these taxa. Also excluded as members of, or sister groups to, the expanded malvalean clade were the families Aextoxicaceae, Barbeyaceae, Cannabinaceae, Cecropiaceae, Dichapetalaceae, Elaeagnaceae, Euphorbiaceae s.l., Huaceae, Lecythidaceae, Moraceae s.l., Pandaceae, Plagiopteraceae, Rhamnaceae, Scytopetalaceae, Ulmaceae, and Urticaceae. The order Malvales, as traditionally circumscribed, includes four core families, Bombacaceae (;250 spp.), Malvaceae (1500 spp.), Sterculiaceae (1000 spp.), and Tiliaceae (400 spp.), plus from one to eight other families depending upon author (Takhtajan, 1987, 1997; Cronquist, 1988; Dahlgren, 1989; Thorne, 1992). Considering only the core four families, the order comprises predominantly woody and tropical trees, including several economically important genera such as cotton (Gossypium
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Circumscription of the Malvales and relationships to other Rosidae: evidence from rbcL sequence data.
American journal of botany, 1998Co-Authors: William S. Alverson, David A. Baum, Mark W Chase, Kenneth G Karol, Susan M Swensen, Richard M Mccourt, Kenneth J SytsmaAbstract:The order Malvales remains poorly circumscribed, despite its seemingly indisputable core constituents: Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae. We conducted a two-step parsimony analysis on 125 rbcL sequences to clarify the composition of Malvales, to determine the relationships of some controversial families, and to identify the placement of the Malvales within Rosidae. We sampled taxa that have been previously suggested to be within, or close to, Malvales (83 sequences), plus additional rosids (26 sequences) and nonrosid eudicots (16 sequences) to provide a broader framework for the analysis. The resulting trees strongly support the monophyly of the core malvalean families, listed above. In addition, these data serve to identify a broader group of taxa that are closely associated with the core families. This expanded malvalean clade is composed of four major subclades: (1) the core families (Bombacaceae, Malvaceae, Sterculiaceae, Tiliaceae); (2) Bixaceae, Cochlospermaceae, and Sphaerosepalaceae (Rhopalocarpaceae); (3) Thymelaeaceae sensu lato (s.l.); and (4) Cistaceae, Dipterocarpaceae s.l., Sarcolaenaceae (Chlaenaceae), and Muntingia. In addition, Neurada (Neuradaceae or Rosaceae) falls in the expanded malvalean clade but not clearly within any of the four major subclades. This expanded malvalean clade is sister to either the expanded capparalean clade of Rodman et al. or the sapindalean clade of Gadek et al. Members of Elaeocarpaceae, hypothesized by most authors as a sister group to the four core malvalean families, are shown to not fall close to these taxa. Also excluded as members of, or sister groups to, the expanded malvalean clade were the families Aextoxicaceae, Barbeyaceae, Cannabinaceae, Cecropiaceae, Dichapetalaceae, Elaeagnaceae, Euphorbiaceae s.l., Huaceae, Lecythidaceae, Moraceae s.l., Pandaceae, Plagiopteraceae, Rhamnaceae, Scytopetalaceae, Ulmaceae, and Urticaceae.
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Muntingiaceae, a new family of dicotyledons with malvalean affinities
TAXON, 1998Co-Authors: Clemens Bayer, Mark W Chase, Michael F FayAbstract:The family Muntingiaceae, here described, includes the Neotropical, monotypic genera Muntingia and Dicraspidia, and probably Neotessmannia, which have previously been included in Elaeocarpaceae, Tiliaceae, or Flacourtiaceae. Morphological data discussed here and molecular data published elsewhere indicate that none of these families can be regarded as closely related to these genera. Muntingiaceae belong to a clade that comprises core Malvales (Sterculiaceae, Tiliaceae, Bombacaceae, and Malvaceae) and several other families. Within this alliance, relationships are presently unresolved.
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Plastid rbc L sequence data indicate a close affinity between Diegodendron and Bixa
TAXON, 1998Co-Authors: Michael F Fay, William S. Alverson, Clemens Bayer, Anette Y De Bruijn, Mark W ChaseAbstract:Summary Diegodendron humbertii Capuron (Diegodendraceae Capuron) is endemic to Madagascar. The family is monospecific, and whereas various affinities have been suggested, its phylo- genetic position has remained unclear. Analysis of rbcL sequence data indicates a close re- lationship to Bixa. Together these taxa form a monophyletic group with a somewhat more distant relationship to other groups of Malvales s.l. including Cochlospermaceae. Cochlo- spermaceae (Cochlospermum and Amoreuxia) should be maintained as a family distinct from Bixaceae but if Bixaceae are expanded to include Cochlospermaceae they should also include Diegodendron. DNA extraction from herbarium specimens, involving modifications to the standard extraction and amplification techniques, is described.
David A. Baum - One of the best experts on this subject based on the ideXlab platform.
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phylogenetic relationships and floral evolution of the byttnerioideae sterculiaceae or malvaceae s l based on sequences of the chloroplast gene ndhf
Systematic Botany, 2009Co-Authors: Barbara A Whitlock, Clemens Bayer, David A. BaumAbstract:Abstract Previous studies of the Malvales have shown that the Sterculiaceae are not monophyletic. However, members of four traditionally recognized tribes of Sterculiaceae (Byttnerieae, Theobromeae, Hermannieae, Lasiopetaleae) appear to constitute a clade named Byttnerioideae. Here we analyze sequences of the chloroplast gene ndhF for 37 species of Byttnerioideae. The monophyly of this diverse group of plants is supported with the inclusion of Kleinhovia from a fifth tribe of Sterculiaceae (Helictereae). The Hermannieae is the only tribe that appears to be monophyletic as traditionally circumscribed. Rulingia and Commersonia, two genera formerly placed in the Byttnerieae, are in a clade with all members of the Lasiopetaleae. The remaining Byttnerieae, Theobromeae, and Kleinhovia form two clades at the base of the Byttnerioideae. These results imply that the unusual hooded petals of many Byttnerioideae (e.g., Theobroma cacao) are plesiomorphic for the clade, with subsequent transitions to large, flat petal...
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structure and evolution of the androecium in the malvatheca clade malvaceae s l and implications for malvaceae and Malvales
Plant Systematics and Evolution, 2006Co-Authors: Maria Von Balthazar, Hansthomas Janka, William S. Alverson, Jürg Schönenberger, Clemens Bayer, David A. BaumAbstract:Androecial development and structure as well as floral vasculature of six selected species of Bombacoideae and of several smaller lineages of the Malvatheca clade (Malvaceae s.l.) were studied. All studied taxa share a similar pattern of androecial development: initially, five antepetalous/antetepalous and five alternipetalous/alternitepalous primary androecial primordia develop on a ring wall. Two elongate secondary androecial primordia form on each antepetalous/antetepalous sector. At anthesis the androecium consists of an androecial tube crowned by five androecial lobes. Each of these lobes is the developmental product of an alternipetalous/alternitepalous primary androecial primordium and its two neighbouring antepetalous/antetepalous secondary androecial primordia. The elongate, sessile androecial units are positioned along the lateral margins of the androecial lobes and in the distal part of the androecial tube. Seen in the light of the most recent studies of floral development and phylogeny of the Malvaceae and the Malvales as a whole, our data indicate that i) elongate, sessile androecial units are ancestral in the Malvatheca clade, that ii) an obdiplostemonous floral ground plan is a synapomorphy for the Malvaceae, and that iii) diplostemony is most likely ancestral in the Malvales.
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Phylogeny of the core Malvales: evidence from ndhF sequence data.
American journal of botany, 1999Co-Authors: William S. Alverson, Clemens Bayer, Barbara A Whitlock, Reto Nyffeler, David A. BaumAbstract:The monophyly of the group comprising the core malvalean families, Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae, was recently confirmed by molecular studies, but the internal structure of this clade is poorly understood. In this study, we examined sequences of the chloroplast ndhF gene (aligned length 2226 bp) from 70 exemplars representing 35 of the 39 putative tribes of core Malvales. The monophyly of one traditional family, the Malvaceae, was supported in the trees resulting from these data, but the other three families, as traditionally circumscribed, are nonmonophyletic. In addition, the following relationships were well supported: (1) a clade, /Malvatheca, consisting of traditional Malvaceae and Bombacaceae (except some members of tribe Durioneae), plus Fremontodendronand Chiranthodendron, which are usually treated as Sterculiaceae; (2) a clade, /Malvadendrina, supported by a unique 21-bp (base pair) deletion and consisting of /Malvatheca, plus five additional subclades, including representatives of Sterculiaceae and Tiliaceae, and Durionieae; (3) a clade, /Byttneriina, with genera traditionally assigned to several tribes of Tiliaceae, plus exemplars of tribes Byttnerieae, Hermannieae, and Lasiopetaleae of Sterculiaceae. The most striking departures from traditional classifications are the following: Durio and relatives appear to be more closely related to Helicteres and Reevesia (Sterculiaceae) than to Bombacaceae; several genera traditionally considered as Bombacaceae (Camptostemon, Matisia, Phragmotheca, and Quararibea) or Sterculiaceae (Chiranthodendron and Fremontodendron) appear as sister lineages to the traditional Malvaceae; the traditional tribe Helictereae (Sterculiaceae) is polyphyletic; and Sterculiaceae and Tiliaceae, as traditionally circumscribed, represent polyphyletic groups that cannot sensibly be maintained with their traditional limits for purposes of classification. We discuss morphological characters and conclude that there has been extensive homoplasy in characters previously used to delineate major taxonomic groups in core Malvales. The topologies here also suggest that /Malvatheca do not have as a synapormophy monothecate anthers, as has been previously supposed but, instead, may be united by dithecate, transversely septate (polysporangiate) anthers, as found in basal members of both /Bombacoideae and /Malvoideae. Thus, ‘‘monothecate’’ anthers may have been derived at least twice, independently, within the /Bombacoideae (core Bombacaceae) and /Malvoideae (traditional Malvaceae).
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circumscription of the Malvales and relationships to other rosidae evidence from rbcl sequence data
American Journal of Botany, 1998Co-Authors: William S. Alverson, David A. Baum, Mark W Chase, Kenneth G Karol, Susan M Swensen, Richard M Mccourt, Kenneth J SytsmaAbstract:The order Malvales remains poorly circumscribed, despite its seemingly indisputable core constituents: Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae. We conducted a two-step parsimony analysis on 125 rbcL sequences to clarify the composition of Malvales, to determine the relationships of some controversial families, and to identify the placement of the Malvales within Rosidae. We sampled taxa that have been previously suggested to be within, or close to, Malvales (83 sequences), plus additional rosids (26 sequences) and nonrosid eudicots (16 sequences) to provide a broader framework for the analysis. The resulting trees strongly support the monophyly of the core malvalean families, listed above. In addition, these data serve to identify a broader group of taxa that are closely associated with the core families. This expanded malvalean clade is composed of four major subclades: (1) the core families (Bombacaceae, Malvaceae, Sterculiaceae, Tiliaceae); (2) Bixaceae, Cochlospermaceae, and Sphaerosepalaceae (Rhopalocarpaceae); (3) Thymelaeaceae sensu lato (s.l.); and (4) Cistaceae, Dipterocarpaceae s.l., Sarcolaenaceae (Chlaenaceae), and Muntingia. In addition, Neurada (Neuradaceae or Rosaceae) falls in the expanded malvalean clade but not clearly within any of the four major subclades. This expanded malvalean clade is sister to either the expanded capparalean clade of Rodman et al. or the sapindalean clade of Gadek et al. Members of Elaeocarpaceae, hypothesized by most authors as a sister group to the four core malvalean families, are shown to not fall close to these taxa. Also excluded as members of, or sister groups to, the expanded malvalean clade were the families Aextoxicaceae, Barbeyaceae, Cannabinaceae, Cecropiaceae, Dichapetalaceae, Elaeagnaceae, Euphorbiaceae s.l., Huaceae, Lecythidaceae, Moraceae s.l., Pandaceae, Plagiopteraceae, Rhamnaceae, Scytopetalaceae, Ulmaceae, and Urticaceae. The order Malvales, as traditionally circumscribed, includes four core families, Bombacaceae (;250 spp.), Malvaceae (1500 spp.), Sterculiaceae (1000 spp.), and Tiliaceae (400 spp.), plus from one to eight other families depending upon author (Takhtajan, 1987, 1997; Cronquist, 1988; Dahlgren, 1989; Thorne, 1992). Considering only the core four families, the order comprises predominantly woody and tropical trees, including several economically important genera such as cotton (Gossypium
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Circumscription of the Malvales and relationships to other Rosidae: evidence from rbcL sequence data.
American journal of botany, 1998Co-Authors: William S. Alverson, David A. Baum, Mark W Chase, Kenneth G Karol, Susan M Swensen, Richard M Mccourt, Kenneth J SytsmaAbstract:The order Malvales remains poorly circumscribed, despite its seemingly indisputable core constituents: Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae. We conducted a two-step parsimony analysis on 125 rbcL sequences to clarify the composition of Malvales, to determine the relationships of some controversial families, and to identify the placement of the Malvales within Rosidae. We sampled taxa that have been previously suggested to be within, or close to, Malvales (83 sequences), plus additional rosids (26 sequences) and nonrosid eudicots (16 sequences) to provide a broader framework for the analysis. The resulting trees strongly support the monophyly of the core malvalean families, listed above. In addition, these data serve to identify a broader group of taxa that are closely associated with the core families. This expanded malvalean clade is composed of four major subclades: (1) the core families (Bombacaceae, Malvaceae, Sterculiaceae, Tiliaceae); (2) Bixaceae, Cochlospermaceae, and Sphaerosepalaceae (Rhopalocarpaceae); (3) Thymelaeaceae sensu lato (s.l.); and (4) Cistaceae, Dipterocarpaceae s.l., Sarcolaenaceae (Chlaenaceae), and Muntingia. In addition, Neurada (Neuradaceae or Rosaceae) falls in the expanded malvalean clade but not clearly within any of the four major subclades. This expanded malvalean clade is sister to either the expanded capparalean clade of Rodman et al. or the sapindalean clade of Gadek et al. Members of Elaeocarpaceae, hypothesized by most authors as a sister group to the four core malvalean families, are shown to not fall close to these taxa. Also excluded as members of, or sister groups to, the expanded malvalean clade were the families Aextoxicaceae, Barbeyaceae, Cannabinaceae, Cecropiaceae, Dichapetalaceae, Elaeagnaceae, Euphorbiaceae s.l., Huaceae, Lecythidaceae, Moraceae s.l., Pandaceae, Plagiopteraceae, Rhamnaceae, Scytopetalaceae, Ulmaceae, and Urticaceae.
Kenneth J Sytsma - One of the best experts on this subject based on the ideXlab platform.
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circumscription of the Malvales and relationships to other rosidae evidence from rbcl sequence data
American Journal of Botany, 1998Co-Authors: William S. Alverson, David A. Baum, Mark W Chase, Kenneth G Karol, Susan M Swensen, Richard M Mccourt, Kenneth J SytsmaAbstract:The order Malvales remains poorly circumscribed, despite its seemingly indisputable core constituents: Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae. We conducted a two-step parsimony analysis on 125 rbcL sequences to clarify the composition of Malvales, to determine the relationships of some controversial families, and to identify the placement of the Malvales within Rosidae. We sampled taxa that have been previously suggested to be within, or close to, Malvales (83 sequences), plus additional rosids (26 sequences) and nonrosid eudicots (16 sequences) to provide a broader framework for the analysis. The resulting trees strongly support the monophyly of the core malvalean families, listed above. In addition, these data serve to identify a broader group of taxa that are closely associated with the core families. This expanded malvalean clade is composed of four major subclades: (1) the core families (Bombacaceae, Malvaceae, Sterculiaceae, Tiliaceae); (2) Bixaceae, Cochlospermaceae, and Sphaerosepalaceae (Rhopalocarpaceae); (3) Thymelaeaceae sensu lato (s.l.); and (4) Cistaceae, Dipterocarpaceae s.l., Sarcolaenaceae (Chlaenaceae), and Muntingia. In addition, Neurada (Neuradaceae or Rosaceae) falls in the expanded malvalean clade but not clearly within any of the four major subclades. This expanded malvalean clade is sister to either the expanded capparalean clade of Rodman et al. or the sapindalean clade of Gadek et al. Members of Elaeocarpaceae, hypothesized by most authors as a sister group to the four core malvalean families, are shown to not fall close to these taxa. Also excluded as members of, or sister groups to, the expanded malvalean clade were the families Aextoxicaceae, Barbeyaceae, Cannabinaceae, Cecropiaceae, Dichapetalaceae, Elaeagnaceae, Euphorbiaceae s.l., Huaceae, Lecythidaceae, Moraceae s.l., Pandaceae, Plagiopteraceae, Rhamnaceae, Scytopetalaceae, Ulmaceae, and Urticaceae. The order Malvales, as traditionally circumscribed, includes four core families, Bombacaceae (;250 spp.), Malvaceae (1500 spp.), Sterculiaceae (1000 spp.), and Tiliaceae (400 spp.), plus from one to eight other families depending upon author (Takhtajan, 1987, 1997; Cronquist, 1988; Dahlgren, 1989; Thorne, 1992). Considering only the core four families, the order comprises predominantly woody and tropical trees, including several economically important genera such as cotton (Gossypium
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Circumscription of the Malvales and relationships to other Rosidae: evidence from rbcL sequence data.
American journal of botany, 1998Co-Authors: William S. Alverson, David A. Baum, Mark W Chase, Kenneth G Karol, Susan M Swensen, Richard M Mccourt, Kenneth J SytsmaAbstract:The order Malvales remains poorly circumscribed, despite its seemingly indisputable core constituents: Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae. We conducted a two-step parsimony analysis on 125 rbcL sequences to clarify the composition of Malvales, to determine the relationships of some controversial families, and to identify the placement of the Malvales within Rosidae. We sampled taxa that have been previously suggested to be within, or close to, Malvales (83 sequences), plus additional rosids (26 sequences) and nonrosid eudicots (16 sequences) to provide a broader framework for the analysis. The resulting trees strongly support the monophyly of the core malvalean families, listed above. In addition, these data serve to identify a broader group of taxa that are closely associated with the core families. This expanded malvalean clade is composed of four major subclades: (1) the core families (Bombacaceae, Malvaceae, Sterculiaceae, Tiliaceae); (2) Bixaceae, Cochlospermaceae, and Sphaerosepalaceae (Rhopalocarpaceae); (3) Thymelaeaceae sensu lato (s.l.); and (4) Cistaceae, Dipterocarpaceae s.l., Sarcolaenaceae (Chlaenaceae), and Muntingia. In addition, Neurada (Neuradaceae or Rosaceae) falls in the expanded malvalean clade but not clearly within any of the four major subclades. This expanded malvalean clade is sister to either the expanded capparalean clade of Rodman et al. or the sapindalean clade of Gadek et al. Members of Elaeocarpaceae, hypothesized by most authors as a sister group to the four core malvalean families, are shown to not fall close to these taxa. Also excluded as members of, or sister groups to, the expanded malvalean clade were the families Aextoxicaceae, Barbeyaceae, Cannabinaceae, Cecropiaceae, Dichapetalaceae, Elaeagnaceae, Euphorbiaceae s.l., Huaceae, Lecythidaceae, Moraceae s.l., Pandaceae, Plagiopteraceae, Rhamnaceae, Scytopetalaceae, Ulmaceae, and Urticaceae.
Clemens Bayer - One of the best experts on this subject based on the ideXlab platform.
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phylogenetic relationships and floral evolution of the byttnerioideae sterculiaceae or malvaceae s l based on sequences of the chloroplast gene ndhf
Systematic Botany, 2009Co-Authors: Barbara A Whitlock, Clemens Bayer, David A. BaumAbstract:Abstract Previous studies of the Malvales have shown that the Sterculiaceae are not monophyletic. However, members of four traditionally recognized tribes of Sterculiaceae (Byttnerieae, Theobromeae, Hermannieae, Lasiopetaleae) appear to constitute a clade named Byttnerioideae. Here we analyze sequences of the chloroplast gene ndhF for 37 species of Byttnerioideae. The monophyly of this diverse group of plants is supported with the inclusion of Kleinhovia from a fifth tribe of Sterculiaceae (Helictereae). The Hermannieae is the only tribe that appears to be monophyletic as traditionally circumscribed. Rulingia and Commersonia, two genera formerly placed in the Byttnerieae, are in a clade with all members of the Lasiopetaleae. The remaining Byttnerieae, Theobromeae, and Kleinhovia form two clades at the base of the Byttnerioideae. These results imply that the unusual hooded petals of many Byttnerioideae (e.g., Theobroma cacao) are plesiomorphic for the clade, with subsequent transitions to large, flat petal...
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structure and evolution of the androecium in the malvatheca clade malvaceae s l and implications for malvaceae and Malvales
Plant Systematics and Evolution, 2006Co-Authors: Maria Von Balthazar, Hansthomas Janka, William S. Alverson, Jürg Schönenberger, Clemens Bayer, David A. BaumAbstract:Androecial development and structure as well as floral vasculature of six selected species of Bombacoideae and of several smaller lineages of the Malvatheca clade (Malvaceae s.l.) were studied. All studied taxa share a similar pattern of androecial development: initially, five antepetalous/antetepalous and five alternipetalous/alternitepalous primary androecial primordia develop on a ring wall. Two elongate secondary androecial primordia form on each antepetalous/antetepalous sector. At anthesis the androecium consists of an androecial tube crowned by five androecial lobes. Each of these lobes is the developmental product of an alternipetalous/alternitepalous primary androecial primordium and its two neighbouring antepetalous/antetepalous secondary androecial primordia. The elongate, sessile androecial units are positioned along the lateral margins of the androecial lobes and in the distal part of the androecial tube. Seen in the light of the most recent studies of floral development and phylogeny of the Malvaceae and the Malvales as a whole, our data indicate that i) elongate, sessile androecial units are ancestral in the Malvatheca clade, that ii) an obdiplostemonous floral ground plan is a synapomorphy for the Malvaceae, and that iii) diplostemony is most likely ancestral in the Malvales.
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flowering plants dicotyledons Malvales capparales and non betalain caryophyllales
2003Co-Authors: Klaus Kubitzki, Clemens BayerAbstract:to Expanded Caryophyllales.- Conspectus of Families of Expanded Caryophyllales.- to Capparales.- Conspectus of the Families of Capparales.- to Malvales.- Conspectus of the Families of Malvales.- General References.- Akaniaceae.- Ancistrocladaceae.- Asteropeiaceae.- Bataceae.- Bixaceae.- Capparaceae.- Caricaceae.- Cistaceae.- Cochlospermaceae.- Cruciferae.- Diegodendraceae.- Dioncophyllaceae.- Dipterocarpaceae.- Droseraceae.- Drosophyllaceae.- Emblingiaceae.- Frankeniaceae.- Gyrostemonaceae.- Koeberliniaceae.- Limnanthaceae.- Malvaceae.- Moringaceae.- Muntingiaceae.- Nepenthaceae.- Neuradaceae.- Pentadiplandraceae.- Physenaceae.- Resedaceae.- Rhabdodendraceae.- Salvadoraceae.- Sarcolaenaceae.- Setchellanthaceae.- Simmondsiaceae.- Sphaerosepalaceae.- Tamaricaceae.- Tapisciaceae.- Tepuianthaceae.- Thymelaeaceae.- Tovariaceae.- Tropaeolaceae.- Hydrastidaceae.- Index of Scientific Names.
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Phylogeny of the core Malvales: evidence from ndhF sequence data.
American journal of botany, 1999Co-Authors: William S. Alverson, Clemens Bayer, Barbara A Whitlock, Reto Nyffeler, David A. BaumAbstract:The monophyly of the group comprising the core malvalean families, Bombacaceae, Malvaceae, Sterculiaceae, and Tiliaceae, was recently confirmed by molecular studies, but the internal structure of this clade is poorly understood. In this study, we examined sequences of the chloroplast ndhF gene (aligned length 2226 bp) from 70 exemplars representing 35 of the 39 putative tribes of core Malvales. The monophyly of one traditional family, the Malvaceae, was supported in the trees resulting from these data, but the other three families, as traditionally circumscribed, are nonmonophyletic. In addition, the following relationships were well supported: (1) a clade, /Malvatheca, consisting of traditional Malvaceae and Bombacaceae (except some members of tribe Durioneae), plus Fremontodendronand Chiranthodendron, which are usually treated as Sterculiaceae; (2) a clade, /Malvadendrina, supported by a unique 21-bp (base pair) deletion and consisting of /Malvatheca, plus five additional subclades, including representatives of Sterculiaceae and Tiliaceae, and Durionieae; (3) a clade, /Byttneriina, with genera traditionally assigned to several tribes of Tiliaceae, plus exemplars of tribes Byttnerieae, Hermannieae, and Lasiopetaleae of Sterculiaceae. The most striking departures from traditional classifications are the following: Durio and relatives appear to be more closely related to Helicteres and Reevesia (Sterculiaceae) than to Bombacaceae; several genera traditionally considered as Bombacaceae (Camptostemon, Matisia, Phragmotheca, and Quararibea) or Sterculiaceae (Chiranthodendron and Fremontodendron) appear as sister lineages to the traditional Malvaceae; the traditional tribe Helictereae (Sterculiaceae) is polyphyletic; and Sterculiaceae and Tiliaceae, as traditionally circumscribed, represent polyphyletic groups that cannot sensibly be maintained with their traditional limits for purposes of classification. We discuss morphological characters and conclude that there has been extensive homoplasy in characters previously used to delineate major taxonomic groups in core Malvales. The topologies here also suggest that /Malvatheca do not have as a synapormophy monothecate anthers, as has been previously supposed but, instead, may be united by dithecate, transversely septate (polysporangiate) anthers, as found in basal members of both /Bombacoideae and /Malvoideae. Thus, ‘‘monothecate’’ anthers may have been derived at least twice, independently, within the /Bombacoideae (core Bombacaceae) and /Malvoideae (traditional Malvaceae).
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support for an expanded family concept of malvaceae within a recircumscribed order Malvales a combined analysis of plastid atpb and rbcl dna sequences
Botanical Journal of the Linnean Society, 1999Co-Authors: Clemens Bayer, William S. Alverson, Klaus Kubitzki, Michael F Fay, Anette Y De Bruijn, Vincent Savolainen, Cynthia M Morton, Mark W ChaseAbstract:Abstract Sequence analyses of the plastid genes atp B and rbc L support an expanded order Malvales. Within this alliance, core Malvales are clearly supported and comprise most genera that have previously been included in Sterculiaceae, Tiliaceae, Bombacaceae, and Malvaceae. Additional well supported malvalean alliances include the bixalean clade (Bixaceae, Diegodendraceae, and Cochlospermaceae), the cistalean clade (Cistaceae, Dipterocarpaceae, and Sarcolaenaceae) and Thymelaeaceae (including Gonystyloideae and Aquilarioideae). Our results indicate sister-group relationships between (1) Neuradaceae and the cistalean clade; (2) Sphaerosepalaceae and Thymelaeaceae; (3) these two clades (1 and 2); and (4) all these and an alliance comprising the bixalean clade and core Malvales, but this pattern is weakly supported by the bootstrap. The affinities of Muntingiaceae and Petenaea are especially ambiguous, although almost certainly they are Malvales s.l. The traditional delimitation of families within core Malvales is untenable. Instead, we propose to merge Sterculiaceae, Tiliaceae and Bombacaceae with Malvaceae and subdivide this enlarged family Malvaceae into nine subfamilies based on molecular, morphological, and biogeographical data: (1) Byttnerioideae, including tribes Byttnerieae, Lasiopetaleae and Theobromeae (all of which have cucullate petals) and Hermannieae; (2) Grewioideae, including most genera of former Tiliaceae; (3) Tilioideae, monogeneric in our analysis; (4) Helicteroideae, comprising most of the taxa previously included in Helictereae, plus Mansonia , Triplochiton (indicating that apocarpy evolved at least twice within Malvaceae) and possibly Durioneae; (5) Sterculioideae, defined by apetalous, apocarpous, usually unisexual flowers with androgynophores; (6) Brownlowioideae, circumscribed as in previous classifications; (7) Dombeyoideae, expanded to include Burretiodendron , Eriolaena , Pterospermum , and Schoutenia ; (8) Bombacoideae, corresponding to former Bombacaceae (without Durioneae) but including Fremontodendreae and Pentaplaris ; (9) Malvoideae, monophyletic but difficult to delimit from Bombacoideae, which with more data and taxon sampling than here might prove to be paraphyletic without Malvoideae.