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Journal ArticleDOI

Phylogenetic relationships in family Magnoliaceae inferred from ndhF sequences.

TL;DR: The molecular data strongly suggest that a taxonomic realignment of infrafamilial delimitations and compositions should be considered in the Magnoliaceae.
Abstract: The ndhF sequences of 99 taxa, representing all sections in extant Magnoliaceae, were analyzed to address phylogenetic questions in the family. Magnolia macrophylla and M. dealbata, North American species of Magnolia section Rytidospermum, are placed at the base in the subfamily Magnolioideae although its supporting value is low. In the remaining taxa, several distinctive lineages are recognized: (1) Magnolia, the biggest genus in the family, is not monophyletic; (2) Michelia, including section Maingola of Magnolia subgenus Magnolia, is closely related with Elmerrillia and sections Alcimandra and Aromadendron of Magnolia subgenus Magnolia; (3) the associates of Michelia are grouped with Magnolia subgenus Yulania and section Gynopodium of Magnolia subgenus Magnolia; (4) Pachylarnax forms a clade with sections Manglietiastrum and Gynopodium of Magnolia; (5) a well-supported Manglietia clade is recognized; (6) Caribbean species of section Theorhodon of Magnolia subgenus Magnolia, which are section Splendentes sensu Vazquez-Garcia, are closely allied with New World members of Magnolia subgenus Talauma; and (7) section Rytidospermum of Magnolia subgenus Magnolia and subgenus Talauma are polyphyletic. The separated clades in the molecular tree are considerably different from traditional taxonomic dispositions in the family. The molecular data strongly suggest that a taxonomic realignment of infrafamilial delimitations and compositions should be considered.
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Book ChapterDOI
TL;DR: Molecular studies suggest that divergence times for transatlantic Tertiary relict disjuncts generally fall between 10 and 40 Ma, even though most geological evidence shows that the North Atlantic Land Bridge (NALB) was severed around 50 Ma, which raises the issue of whether a partial NALB allowed migration of floras between Eurasia and North America throughout much of the Tertiaries.
Abstract: Tertiary relict floras contain survivors from plant communities that were distributed throughout a large part of the Northern Hemisphere during much of the Tertiary (i.e. 65 – 15 million years ago (Ma)). They are now mainly restricted to warm humid areas (refugia) in southeastern and western North America, East Asia and southwest Eurasia. Recent molecular phylogenetic studies show that within East Asia the Tertiary relict flora is best divided into two distinct refugial groups, with geographical distributions centred on the Japan/Korea/northeast China and southeast China/Himalayas regions respectively. Recognition of this division leads to a significant improvement in our understanding of the origins and evolution of Tertiary relict floras in East Asia and elsewhere. Molecular studies also indicate two putative clusters of divergence times for East Asian-North American Tertiary relict disjuncts occurring at 5 and 10 Ma. These clusters might reflect a break in the continuity of the Tertiary flora between East Asia and North America across Beringia during a cold period 6–8 Ma, i.e. before the Bering Land Bridge was severed approximately 5 Ma. In addition, there is some evidence that evergreen disjuncts diverged earlier than their deciduous counterparts, possibly due to the high latitude of Beringia. Molecular studies further suggest that divergence times for transatlantic Tertiary relict disjuncts generally fall between 10 and 40 Ma, even though most geological evidence shows that the North Atlantic Land Bridge (NALB), which connected the floras of Europe and North America, was severed around 50 Ma. This raises the issue of whether a partial NALB allowed migration of floras between Eurasia and North America throughout much of the Tertiary. Tertiary relict floras are notable for exhibiting slow morphological evolution (stasis). This might result from large-scale allopatric speciation, together with stabilising selection.

326 citations


Cites background from "Phylogenetic relationships in famil..."

  • ...Furthermore, many such groups are paraphyletic (Shi et al., 1998; Kim and Kim, 1999; Wen, 1999, 2000, 2001; Hileman et al., 2001; Kim et al., 2001)....

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  • ...There is no clear Japan–China divide within Magnolia (Kim et al., 2001), Acer (Hasebe et al....

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  • ...Maingola (Kim et al., 2001)....

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Journal ArticleDOI
TL;DR: This work evaluates early floral evolution in angiosperms by parsimony optimization of morphological characters on phylogenetic trees derived from morphological and molecular data and indicates that the simple flowers of the newly recognized basal groups are reduced rather than primitively simple.
Abstract: Increasingly robust understanding of angiosperm phylogeny allows more secure reconstruction of the flower in the most recent common ancestor of extant angiosperms and its early evolution. The surprising emergence of several extant and fossil taxa with simple flowers near the base of the angiosperms-Chloranthaceae, Ceratophyllum, Hydatellaceae, and the Early Cretaceous fossil Archaefructus (the last three are water plants)-has brought a new twist to this problem. We evaluate early floral evolution in angiosperms by parsimony optimization of morphological characters on phylogenetic trees derived from morphological and molecular data. Our analyses imply that Ceratophyllum may be related to Chloranthaceae, and Archaefructus to either Hydatellaceae or Ceratophyllum. Inferred ancestral features include more than two whorls (or series) of tepals and stamens, stamens with protruding adaxial or lateral pollen sacs, several free, ascidiate carpels closed by secretion, extended stigma, extragynoecial compitum, and one or several ventral pendent ovule(s). The ancestral state in other characters is equivocal: e.g., bisexual vs. unisexual flowers, whorled vs. spiral floral phyllotaxis, presence vs. absence of tepal differentiation, anatropous vs. orthotropous ovules. Our results indicate that the simple flowers of the newly recognized basal groups are reduced rather than primitively simple.

293 citations

Journal ArticleDOI
TL;DR: A molecular phylogenetic analysis of the Magnoliaceae, a former boreotropical element that currently contains both tropical and temperate disjuncts, indicates the tropical American section Talauma branched first, followed by the tropical Asian clade and the West Indies clade.
Abstract: The boreotropical flora concept suggests that relictual tropical disjunctions between Asia and the Americas are a result of the expansion of the circumboreal tropical flora from the middle to the close of the Eocene. Subsequently, temperate species diverged at high latitudes and migrated to other continents. To test this concept, we conducted a molecular phylogenetic analysis (using cpDNA) of the Magnoliaceae, a former boreotropical element that currently contains both tropical and temperate disjuncts. Divergence times of the clades were estimated using sequences of matK and two intergenic regions consisting of psbA-trnH and atpB-rbcL. Results indicate the tropical American section Talauma branched first, followed by the tropical Asian clade and the West Indies clade. Within the remaining taxa, two temperate disjunctions were formed. Assuming the temperate disjunction of Magnolia acuminata and Asian relatives occurred 25 mya (late Oligocene; based on seed fossil records), section Talauma diverged 42 mya (mid-Eocene), and tropical Asian and the West Indies clades 36 mya (late Eocene). These events correlate with cooling temperatures during the middle to late Eocene and probably caused the tropical disjunctions.

200 citations

Journal ArticleDOI
TL;DR: The earliest angiosperms may have been biochemically flexible in their B function and "tinkered" with floral organ identity and well before the oldest angiosperm fossils.
Abstract: B-function MADS-box genes play crucial roles in floral development in model angiosperms. We reconstructed the structural and functional implications of B-function gene phylogeny in the earliest extant flowering plants based on analyses that include 25 new AP3 and PI sequences representing critical lineages of the basalmost angiosperms: Amborella, Nuphar (Nymphaeaceae), and Illicium (Austrobaileyales). The ancestral size of exon 5 in PI-homologues is 42 bp, typical of exon 5 in other plant MADS-box genes. This 42-bp length is found in PI-homologues from Amborella and Nymphaeaceae, successive sisters to all other angiosperms. Following these basalmost branches, a deletion occurred in exon 5, yielding a length of 30 bp, a condition that unites all other angiosperms. Several shared amino acid strings, including a prominent "DEAER" motif, are present in the AP3- and PI-homologues of Amborella. These may be ancestral motifs that were present before the duplication that yielded the AP3 and PI lineages and subsequently were modified after the divergence of Amborella. Other structural features were identified, including a motif that unites the previously described TM6 clade and a deletion in AP3-homologues that unites all Magnoliales. Phylogenetic analyses of AP3- and PI-homologues yielded gene trees that generally track organismal phylogeny as inferred by multigene data sets. With both AP3 and PI amino acid sequences, Amborella and Nymphaeaceae are sister to all other angiosperms. Using nonparametric rate smoothing (NPRS), we estimated that the duplication that produced the AP3 and PI lineages occurred approximately 260 mya (231-290). This places the duplication after the split between extant gymnosperms and angiosperms, but well before the oldest angiosperm fossils. A striking similarity in the multimer-signalling C domains of the Amborella proteins suggests the potential for the formation of unique transcription-factor complexes. The earliest angiosperms may have been biochemically flexible in their B function and "tinkered" with floral organ identity.

198 citations

Journal ArticleDOI
TL;DR: Polyploidy is now viewed not as a mere side branch of evolution, but as a major mechanism of evolution and diversification.
Abstract: Throughout the past century, hybridization and polyploidization have variously been viewed as drivers of biodiversity (e.g. Arnold, 1997) or evolutionary noise, unimportant to the main processes of evolution (e.g. Stebbins, 1950; Wagner, 1970). Wagner (1970) argued that while polyploids have always existed, they have never diversified or played a major role in the evolution of plants, and that the study of polyploidy (as well as inbreeding, apomixis, and hybridization) has led researchers to be ‘carried away with side branches and blind alleys that go nowhere’. However, the use of molecular tools revolutionized the study of polyploidy, revealing that a given polyploid species often forms multiple times (reviewed in Soltis & Soltis, 1993, 1999, 2000, 2009). The realization that recurrent polyploidization from genetically differentiated parents is the rule that shattered the earlier perceptions of polyploids as genetically depauperate (Stebbins, 1950; Wagner, 1970). Because of multiple origins, polyploid species can maintain high levels of segregating genetic variation through the incorporation of genetic diversity from multiple populations of their diploid progenitors (e.g. Soltis & Soltis, 1993, 1999, 2000; Tate et al., 2005). Numerous studies have also shown that polyploid genomes are highly dynamic, with enormous potential for generating novel genetic variation (e.g. Gaeta et al., 2007; Doyle et al., 2008; Leitch & Leitch, 2008; Flagel & Wendel, 2009; Hawkins et al., 2009; Chester et al., 2012; Hao et al., 2013; Roulin et al., 2013). Furthermore, genomic studies have also revealed numerous ancient polyploidy events across the angiosperms (e.g. Vision et al., 2000; Bowers et al., 2003; Blanc &Wolfe, 2004; Paterson et al., 2004; Schlueter et al., 2004; Van de Peer & Meyer, 2005; Cannon et al., 2006; Cui et al., 2006; Tuskan et al., 2006; Jaillon et al., 2007; Barker et al., 2008, 2009; Lyons et al., 2008; Ming et al., 2008; Shi et al., 2010; Van de Peer, 2011; Jiao et al., 2012; McKain et al., 2012; Tayale & Parisod, 2013; reviewed in Soltis et al., 2009); all angiosperms have undergone at least one round of polyploidy (e.g. Jiao et al., 2011; Amborella Genome Consortium, 2013). Polyploidy is now viewed not as a mere side branch of evolution, but as a major mechanism of evolution and diversification.

153 citations


Cites background from "Phylogenetic relationships in famil..."

  • ...However, if Magnolia had been included in Mayrose et al. (2011), and the phylogeny of Kim et al. (2001) employed, the genus would have been incorrectly considered primarily diploid, giving rise to a few polyploids....

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References
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Journal ArticleDOI
TL;DR: A new method for determining nucleotide sequences in DNA is described, which makes use of the 2',3'-dideoxy and arabinon nucleoside analogues of the normal deoxynucleoside triphosphates, which act as specific chain-terminating inhibitors of DNA polymerase.
Abstract: A new method for determining nucleotide sequences in DNA is described. It is similar to the “plus and minus” method [Sanger, F. & Coulson, A. R. (1975) J. Mol. Biol. 94, 441-448] but makes use of the 2′,3′-dideoxy and arabinonucleoside analogues of the normal deoxynucleoside triphosphates, which act as specific chain-terminating inhibitors of DNA polymerase. The technique has been applied to the DNA of bacteriophage ϕX174 and is more rapid and more accurate than either the plus or the minus method.

62,728 citations

Journal ArticleDOI
TL;DR: ClUSTAL X is a new windows interface for the widely-used progressive multiple sequence alignment program CLUSTAL W, providing an integrated system for performing multiple sequence and profile alignments and analysing the results.
Abstract: CLUSTAL X is a new windows interface for the widely-used progressive multiple sequence alignment program CLUSTAL W. The new system is easy to use, providing an integrated system for performing multiple sequence and profile alignments and analysing the results. CLUSTAL X displays the sequence alignment in a window on the screen. A versatile sequence colouring scheme allows the user to highlight conserved features in the alignment. Pull-down menus provide all the options required for traditional multiple sequence and profile alignment. New features include: the ability to cut-and-paste sequences to change the order of the alignment, selection of a subset of the sequences to be realigned, and selection of a sub-range of the alignment to be realigned and inserted back into the original alignment. Alignment quality analysis can be performed and low-scoring segments or exceptional residues can be highlighted. Quality analysis and realignment of selected residue ranges provide the user with a powerful tool to improve and refine difficult alignments and to trap errors in input sequences. CLUSTAL X has been compiled on SUN Solaris, IRIX5.3 on Silicon Graphics, Digital UNIX on DECstations, Microsoft Windows (32 bit) for PCs, Linux ELF for x86 PCs, and Macintosh PowerMac.

38,522 citations

Journal ArticleDOI
TL;DR: Some examples were worked out using reported globin sequences to show that synonymous substitutions occur at much higher rates than amino acid-altering substitutions in evolution.
Abstract: Some simple formulae were obtained which enable us to estimate evolutionary distances in terms of the number of nucleotide substitutions (and, also, the evolutionary rates when the divergence times are known). In comparing a pair of nucleotide sequences, we distinguish two types of differences; if homologous sites are occupied by different nucleotide bases but both are purines or both pyrimidines, the difference is called type I (or “transition” type), while, if one of the two is a purine and the other is a pyrimidine, the difference is called type II (or “transversion” type). Letting P and Q be respectively the fractions of nucleotide sites showing type I and type II differences between two sequences compared, then the evolutionary distance per site is K = — (1/2) ln {(1 — 2P — Q) }. The evolutionary rate per year is then given by k = K/(2T), where T is the time since the divergence of the two sequences. If only the third codon positions are compared, the synonymous component of the evolutionary base substitutions per site is estimated by K'S = — (1/2) ln (1 — 2P — Q). Also, formulae for standard errors were obtained. Some examples were worked out using reported globin sequences to show that synonymous substitutions occur at much higher rates than amino acid-altering substitutions in evolution.

26,016 citations

Journal ArticleDOI
TL;DR: From the kinetic data, it becomes evident that the reductive amination reaction is highly adaptive to the ammonium environment.

14,480 citations