@article {5695, title = {Molecular phylogenetic support for a broader delimitation of Uvaria (Annonaceae), inclusive of Anomianthus, Cyathostemma, Ellipeia, Ellipeiopsis and Rauwenhoffia}, journal = {Systematics and BiodiversitySystematics and Biodiversity}, volume = {7}, number = {3}, year = {2009}, note = {494YKTimes Cited:0Cited References Count:59}, month = {Sep}, pages = {249-258}, abstract = {Uvaria (Annonaceae), a large palaeotropical genus of woody climbers, closely resembles several other smaller genera, including Anomianthus, Cyathostemma, Ellipeia, Ellipeiopsis and Rauwenhoffia. A molecular phylogenetic analysis of this group was undertaken using maximum parsimony, maximum likelihood and Bayesian methods based on four chloroplast DNA regions (matK, psbA-trnH spacer, rbcL and trnL-F). The resultant trees were moderately well resolved with significant statistical support for most nodes. Uvaria is shown unequivocally to be paraphyletic, with all representatives of the other five genera nested within it. The distinguishing morphological characteristics of the related genera are re-evaluated, and interpreted as no more than specialised adaptations of the basic Uvari structure. The generic names Anomianthus, Cyathostemma, Ellipeia, Ellipeiopsis and Rauwenhoffia are accordingly reduced to synonymy with Uvaria, necessitating 11 new nomenclatural combinations and four replacement names.}, keywords = {age, amplification, Annonaceae, anomianthus, chloroplast DNA, cyathostemma, ellipeia, ellipeiopsis, lowland dipterocarp forest, malaysia, melodorum, nomenclature, phylogeny, pollination, rauwenhoffia, regions, sarawak, SYSTEMATICS, taxonomy, uvaria}, isbn = {1477-2000}, author = {Zhou, L. and Su, Y. C. F. and Saunders, R. M. K.} } @article {5621, title = {Two new species of Xylopia (Annonaceae) from Borneo}, journal = {Harvard Papers in BotanyHarvard Papers in Botany}, volume = {14}, year = {2009}, note = {206}, pages = {129-135}, author = {Turner, I. M. and D. M. Johnson} } @article {5614, title = {Novelties in Fissistigma (Annonaceae) from Borneo}, journal = {Nordic Journal of BotanyNordic Journal of Botany}, volume = {27}, year = {2009}, note = {066}, pages = {362-369}, author = {Turner, I. M.} } @article {5615, title = {A new species and a new combination in Friesodielsia (Annonaceae) of Borneo}, journal = {Edinburgh Journal of BotanyEdinburgh Journal of Botany}, volume = {66}, year = {2009}, note = {069}, pages = {365-370}, author = {Turner, I. M.} } @article {5616, title = {New species and nomenclatural combinations in Polyalthia, Meiogyne and Mitrella (Annonaceae) from Borneo}, journal = {Malayan Nature JournalMalayan Nature Journal}, volume = {61}, number = {4}, year = {2009}, note = {105, 112, 148}, pages = {267-276}, author = {Turner, I. M.} } @article {5617, title = {(1877) Proposal to conserve the name Dasymaschalon against Pelticalyx (Annonaceae)}, journal = {TaxonTaxon}, volume = {58}, year = {2009}, note = {043, 140}, pages = {301-302}, author = {Turner, I. M.} } @article {5591, title = {Evolutionary divergence times in the Annonaceae: evidence of a Late Miocene origin of Pseuduvaria in Sundaland with subsequent diversification in New Guinea}, journal = {BMC Evolutionary BiologyBMC Evolutionary Biology}, volume = {9}, number = {1}, year = {2009}, pages = {153}, abstract = {BACKGROUND:Phylogenetic analyses of the Annonaceae consistently identify four clades: a basal clade consisting of Anaxagorea, and a small {\textquoteright}ambavioid{\textquoteright} clade that is sister to two main clades, the {\textquoteright}long branch clade{\textquoteright} (LBC) and {\textquoteright}short branch clade{\textquoteright} (SBC). Divergence times in the family have previously been estimated using non-parametric rate smoothing (NPRS) and penalized likelihood (PL). Here we use an uncorrelated lognormal (UCLD) relaxed molecular clock in BEAST to estimate diversification times of the main clades within the family with a focus on the Asian genus Pseuduvaria within the SBC. Two fossil calibration points are applied, including the first use of the recently discovered Annonaceae fossil Futabanthus. The taxonomy and morphology of Pseuduvaria have been well documented, although no previous dating or biogeographical studies have been undertaken. Ancestral areas at internal nodes within Pseuduvaria are determined using dispersal-vicariance analysis (DIVA) and weighted ancestral area analysis (WAAA).RESULTS:The divergence times of the main clades within the Annonaceae were found to deviate slightly from previous estimates that used different calibration points and dating methods. In particular, our estimate for the SBC crown (55.2-26.9 Mya) is much younger than previous estimates (62.5-53.1 +/- 3.6 Mya and ca. 58.76 Mya). Early diversification of Pseuduvaria was estimated to have occurred 15-8 Mya, possibly associated with the {\textquoteright}mid-Miocene climatic optimum.{\textquoteright} Pseuduvaria is inferred to have originated in Sundaland in the late Miocene, ca. 8 Mya; subsequent migration events were predominantly eastwards towards New Guinea and Australia, although several migratory reversals are also postulated. Speciation of Pseuduvaria within New Guinea may have occurred after ca. 6.5 Mya, possibly coinciding with the formation of the Central Range orogeny from ca. 8 Mya.CONCLUSION:Our divergence time estimates within the Annonaceae are likely to be more precise as we used a UCLD clock model and calibrated the phylogeny using new fossil evidence. Pseuduvaria is shown to have dispersed from Sundaland after the late Miocene. The present-day paleotropical distribution of Pseuduvaria may have been achieved by long-distance dispersal, and speciation events might be explained by global climatic oscillations, sea level fluctuations, and tectonic activity.}, isbn = {1471-2148}, author = {Su, Yvonne and Saunders, Richard} } @article {5531, title = {(1878) Proposal to conserve the name Goniothalamus against Richella (Annonaceae)}, journal = {TaxonTaxon}, volume = {58}, year = {2009}, note = {074, 166}, pages = {302-303}, author = {Saunders, R. M. K.} } @article {5381, title = {Molecular phylogenetic and morphological evidence for the congeneric status of Goniothalamus and Richella (Annonaceae)}, journal = {TaxonTaxon}, volume = {58}, number = {1}, year = {2009}, note = {Nakkuntod, Maliwan Su, Yvonne C. F. Seelanan, Tosak Saunders, Richard M. K.}, month = {Feb}, pages = {127-132}, abstract = {Maximum parsimony, maximum likelihood and Bayesian phylogenetic analyses of selected Goniothalamus and Richella species (Annonaceae) are presented, based on sequences of three chloroplast markers (matK, psbA-trnH intergenic spacer, and trnL-trnF intergenic spacer). The two genera are shown to be congeneric, and the nomenclatural consequences of this are discussed. Morphological synapomorphies for individual clades are evaluated, although a detailed interpretation of morphological evolution will require more extensive species sampling.}, isbn = {0040-0262}, author = {Nakkuntod, M. and Su, Y. C. F. and Seelanan, T. and Saunders, R. M. K.} } @article {4984, title = {Molecular and morphological characterization of a new monotypic genus of Annonaceae, Mwasumbia, from Tanzania}, journal = {Systematic BotanySystematic Botany}, volume = {34}, number = {2}, year = {2009}, pages = {266-276}, author = {Couvreur, T.L.P and Van der Ham, R. W. J. M. and Mbele, Y.M. and Mbago, F. M. and Johnson, D. M.} } @article {4976, title = {Monograph of the syncarpous African genera Isolona and Monodora (Annonaceae)}, journal = {Systematic Botany MonographsSystematic Botany Monographs}, volume = {87}, year = {2009}, pages = {1-150}, author = {Couvreur, T.L.P} } @article {4937, title = {New species from two unknown and highly threatened mountainous areas in northwestern Madagascar: the Galoka and Kalabenono massifs}, journal = {CandolleaCandollea}, volume = {64}, year = {2009}, note = {206}, pages = {179-202}, author = {Callmander, M.W. and Rakotovao, C. and Razafitsalama, J. and Phillipson, P.B. and Buerki, S. and Hong-Wa, C. and Rakotoarivelo, N. and Andriambololonera, S. and Koopman, M.M. and Johnson, D. M. and Deroin, T. and Andriamandranto, R. and Solo, S. and Labat, J.-N. and Lowry II, P.P.} } @article {4892, title = {An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG III}, journal = {Botanical Journal of the Linnean SocietyBotanical Journal of the Linnean Society}, volume = {161}, number = {2}, year = {2009}, note = {***}, pages = {105-121}, publisher = {Blackwell Publishing Ltd}, abstract = {

A revised and updated classification for the families of flowering plants is provided. Many recent studies have yielded increasingly detailed evidence for the positions of formerly unplaced families, resulting in a number of newly adopted orders, including Amborellales, Berberidopsidales, Bruniales, Buxales, Chloranthales, Escalloniales, Huerteales, Nymphaeales, Paracryphiales, Petrosaviales, Picramniales, Trochodendrales, Vitales and Zygophyllales. A number of previously unplaced genera and families are included here in orders, greatly reducing the number of unplaced taxa; these include Hydatellaceae (Nymphaeales), Haptanthaceae (Buxales), Peridiscaceae (Saxifragales), Huaceae (Oxalidales), Centroplacaceae and Rafflesiaceae (both Malpighiales), Aphloiaceae, Geissolomataceae and Strasburgeriaceae (all Crossosomatales), Picramniaceae (Picramniales), Dipentodontaceae and Gerrardinaceae (both Huerteales), Cytinaceae (Malvales), Balanophoraceae (Santalales), Mitrastemonaceae (Ericales) and Boraginaceae (now at least known to be a member of lamiid clade). Newly segregated families for genera previously understood to be in other APG-recognized families include Petermanniaceae (Liliales), Calophyllaceae (Malpighiales), Capparaceae and Cleomaceae (both Brassicales), Schoepfiaceae (Santalales), Anacampserotaceae, Limeaceae, Lophiocarpaceae, Montiaceae and Talinaceae (all Caryophyllales) and Linderniaceae and Thomandersiaceae (both Lamiales). Use of bracketed families is abandoned because of its unpopularity, and in most cases the broader circumscriptions are retained; these include Amaryllidaceae, Asparagaceace and Xanthorrheaceae (all Asparagales), Passifloraceae (Malpighiales), Primulaceae (Ericales) and several other smaller families. Separate papers in this same volume deal with a new linear order for APG, subfamilial names that can be used for more accurate communication in Amaryllidaceae s.l., Asparagaceace s.l. and Xanthorrheaceae s.l. (all Asparagales) and a formal supraordinal classification for the flowering plants.\ \© 2009 The Linnean Society of London, Botanical Journal of the Linnean Society, 2009, 161, 105\–121.

}, keywords = {angiosperm classification, APG system, classification system, DNA phylogenetics, phylogenetic classification}, isbn = {1095-8339}, author = {APGIII} } @article {606, title = {From Africa via Europe to South America: migrational route of a species-rich genus of Neotropical lowland rain forest trees (Guatteria, Annonaceae)}, journal = {Journal of Biogeography}, volume = {36}, number = {12}, year = {2009}, note = {10.1111/j.1365-2699.2009.02162.x}, pages = {2338-2352}, isbn = {1365-2699}, url = {http://dx.doi.org/10.1111/j.1365-2699.2009.02162.x}, author = {Erkens, Roy H. J. and Jan. W. Maas and Couvreur, Thomas L.P.} } @article {110, title = {Molecular phylogenetic support for a broader delimitation of Uvaria (Annonaceae), inclusive of Anomianthus, Cyathostemma, Ellipeia, Ellipeiopsis and Rauwenhoffia}, journal = {Systematics and Biodiversity}, volume = {7}, number = {3}, year = {2009}, note = {494YKTimes Cited:0Cited References Count:59}, month = {Sep}, pages = {249-258}, abstract = {Uvaria (Annonaceae), a large palaeotropical genus of woody climbers, closely resembles several other smaller genera, including Anomianthus, Cyathostemma, Ellipeia, Ellipeiopsis and Rauwenhoffia. A molecular phylogenetic analysis of this group was undertaken using maximum parsimony, maximum likelihood and Bayesian methods based on four chloroplast DNA regions (matK, psbA-trnH spacer, rbcL and trnL-F). The resultant trees were moderately well resolved with significant statistical support for most nodes. Uvaria is shown unequivocally to be paraphyletic, with all representatives of the other five genera nested within it. The distinguishing morphological characteristics of the related genera are re-evaluated, and interpreted as no more than specialised adaptations of the basic Uvari structure. The generic names Anomianthus, Cyathostemma, Ellipeia, Ellipeiopsis and Rauwenhoffia are accordingly reduced to synonymy with Uvaria, necessitating 11 new nomenclatural combinations and four replacement names.}, keywords = {age, amplification, Annonaceae, anomianthus, chloroplast DNA, cyathostemma, ellipeia, ellipeiopsis, lowland dipterocarp forest, malaysia, melodorum, nomenclature, phylogeny, pollination, rauwenhoffia, regions, sarawak, SYSTEMATICS, taxonomy, uvaria}, isbn = {1477-2000}, url = {://000269855600002}, author = {Zhou, L. L. and Su, Y.C.F. and Saunders, R.M.K.} } @article {56, title = {Molecular and morphological characterization of a new monotypic genus of Annonaceae, Mwasumbia, from Tanzania}, journal = {Systematic Botany}, volume = {34}, number = {2}, year = {2009}, pages = {266-276}, author = {Couvreur, T.L.P. and Van der Ham, R. W. J. M. and Mbele, Y.M. and Mbago, F. M. and Johnson, D. M.} } @article {50, title = {Monograph of the syncarpous African genera Isolona and Monodora (Annonaceae)}, journal = {Systematic Botany Monographs}, volume = {87}, year = {2009}, pages = {1-150}, author = {Couvreur, T.L.P.} }