@article {5728, title = {A decade of uncertainty: Resolving the phylogenetic position of Diclinanona (Annonaceae), including taxonomic notes and a key to the species}, journal = {TaxonTaxon}, volume = {63}, number = {6}, year = {2014}, pages = {1244-1252}, isbn = {0040-0262}, author = {Erkens, Roy HJ and Chatrou, Lars W and Chaowasku, Tanawat and Westra, Lubbert Y Th and Maas, Jan W and Maas, Paul JM} } @article {5688, title = {Pruning the polyphyletic genus Polyalthia (Annonaceae) and resurrecting the genus Monoon}, journal = {TaxonTaxon}, volume = {61}, number = {5}, year = {2012}, pages = {1021-1039}, abstract = {The highly polyphyletic status of the species-rich genus Polyalthia (Annonaceae) remains one of the most significant impediments to revisionary and floristic taxonomic research in the family. Although Polyalthia has recently been reduced in taxonomic scope, the remaining species in the genus still form a phylogenetically disparate and morphologically heterogeneous assemblage. We use maximum parsimony, maximum likelihood and Bayesian phylogenetic reconstructions based on chloroplast DNA sequence data (matK, rbcL, trnL-F) to show that the remaining Polyalthia species segregate into three clades: a clade sister to Miliusa; a clade that also includes all Enicosanthum and Woodiellantha species sampled, sister to Neo-uvaria; and a clade that also includes all Haplostichanthus species sampled, inferred (based on previous research) to be sister to Popowia. Diagnostic morphological and anatomical characters are evaluated for the latter two clades, and diagnostic leaf and seed characters identified. Based on these results, the generic name Monoon is resurrected for the clade that includes Enicosanthum and Woodiellantha, following the transfer of 37 species from Polyalthia s.l., 18 species from Enicosanthum and the single Woodiellantha species. The generic name Haplostichanthus is furthermore synonymised with Polyalthia s.str., necessitating nine nomenclatural changes, including six new combinations and three replacement names.}, keywords = {Annonaceae, ENICOSANTHUM, HAPLOSTICHANTHUS, MOLECULAR PHYLOGENETICS, MONOON, nomenclature, POLYALTHIA, taxonomy, WOODIELLANTHA}, author = {Xue, Bine and Su, Yvonne C. F. and Thomas, Daniel C. and Saunders, Richard M. K.} } @article {5642, title = {Studies in Annonaceae. XIV. Index to generic names of Annonaceae.}, journal = {TaxonTaxon}, volume = {39}, year = {1990}, pages = {675-690}, author = {van Setten, A. K. and Maas, P.J.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 {5598, title = {Generic delimitation and historical biogeography in the early-divergent {\textquoteright}ambavioid{\textquoteright} lineage of Annonaceae: Cananga, Cyathocalyx and Drepananthus}, journal = {TaxonTaxon}, volume = {59}, year = {2010}, pages = {1721-1734}, author = {Surveswaran, S. and Wang, Rui Jiang and Su, YCF and Saunders, R.M.K.} } @article {5564, title = {Morphological and functional flower characteristics of New and Old World Annonaceae with respect to their mode of pollination}, journal = {TaxonTaxon}, volume = {52}, number = {4}, year = {2003}, pages = {701-718}, abstract = {The Annonaceae show a broader flower biological radiation than originally thought, with flowers being pollinated not only by beetles, but also by thrips, flies and even bees. The majority of species have hermaphroditic protogynous flowers. Species with white or yellowish-white, small, delicate, day-active flowers, may be pollinated either solely by thrips, or by thrips and small beetles (e.g., species of Bocageopsis, Oxandra, Xylopia). Several of these thrips-pollinated species have stamens with an elongated, tongue-like connective. Pollination by flies is not well documented for American species, notwithstanding it appears to be more common in Old World species, e.g., in the genus Pseuduvaria. The mitriform flowers exhale an unpleasant smell, produce nectar in purple-colored petal glands and have a sapromyiophilous syndrome. Flies enter the flower center through large openings between the inner petals. Beetle-pollinated Annonaceae have flowers with comparatively thick and, often, fleshy petals, which, during anthesis frequently form a pollination chamber with the petals inclining over the flower center. The stamens usually have peltate connective shields, probably a device for protection against voracious beetles. Some cantharophilous species have flowers which are day-active while others are night-active. When they are in their pistillate phase, the beetles are attracted by characteristic odor components. They enter the pollination chamber and usually remain in the interior of the flower until the flower has changed to its staminate phase, when pollen is shed and afterwards petals and stamens detach. Two lines of cantharophilous Annonaceae are recognizable on the basis of present knowledge. Species with smaller and more delicate flowers are pollinated by small beetles (Nitidulidae, Curculionidae, Chrysomelidae and Staphylinidae), whereas species with large, more robust flowers in the Neotropics are pollinated by large beetles of the family Scarabaeidae, subfamily Dynastinae. Some species of the cantharophilous Annonaceae, especially the large-flowered ones, but also some species with smaller flowers, produce heat during anthesis (thermogenesis). Food bodies, developed on the adaxial surfaces or sides of the petals, provide unique nourishment possibilities for beetles when they stay inside the flowers during the pistillate phase. In the staminate stage of the flower, after pollen is shed, beetles also feed on pollen. Apparently, no dynastid-flower relationship has evolved in Asia and Australia. Pollination by bees was discovered recently in Unonopsis guatterioides in Amazonia and Uvaria concava in North Queensland: the first by scent-collecting euglossine males and the second by pollen-collecting Meliponinae. The general trends in morphological/functional floral characteristics in the family are discussed in a presumptive phylogenetic context.}, author = {Silberbauer-Gottsberger, I and Gottsberger, G. and Webber, A.} } @article {5539, title = {Proposal to conserve the name Enicosanthum against Monoon (Annonaceae)}, journal = {TaxonTaxon}, volume = {60}, number = {1}, year = {2011}, pages = {236-237}, author = {Saunders, Richard M. K. and Xue, B.} } @article {5540, title = {(1992) Proposal to conserve the name Enicosanthum against Monoon (Annonaceae)}, journal = {TaxonTaxon}, volume = {60}, year = {2011}, note = {048, 061, 069, 099, 103, 119, 142, 148}, pages = {236-237}, author = {Saunders, R. M. K. and Xue, Bine} } @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 {5537, title = {Phylogenetic affinities of Polyalthia species (Annonaceae) with columellar-sulcate pollen: Enlarging the Madagascan endemic genus Fenerivia}, journal = {TaxonTaxon}, volume = {60}, year = {2011}, pages = {1407-1416}, author = {Saunders, Richard M. K. and Su, Y.F.C. and Xue, B.} } @article {5457, title = {Nomina nova generica et combinationes nova Spermatophytorum et Pteridophytorum}, journal = {TaxonTaxon}, volume = {31}, year = {1982}, note = {045, 205}, pages = {555}, author = {Rauschert, S.} } @article {5399, title = {Miliusa globosa, comb. nov. for M. roxburghiana}, journal = {TaxonTaxon}, volume = {33}, year = {1984}, note = {110}, pages = {713-714}, author = {Panigrahi, G. and S. C. Mishra} } @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 {5248, title = {Variations in the apertural region of Annonaceae pollen}, journal = {TaxonTaxon}, volume = {37}, number = {3}, year = {1988}, month = {Aug}, pages = {644-656}, author = {Le Thomas, A.} } @article {5224, title = {Studies in Annonaceae. XIII. The role of morphological characters in subsequent classifications of Annonaceae. A comparative survey}, journal = {TaxonTaxon}, volume = {39}, number = {1}, year = {1990}, pages = {16-32}, author = {Koek-Noorman, J. and Westra, L.Y. Th. and Maas, P.J.M.} } @article {5059, title = {Classification of a large and widespread genus of Neotropical trees, Guatteria (Annonaceae) and its three satellite genera Guatteriella, Guatteriopsis and Heteropetalum}, journal = {TaxonTaxon}, volume = {56}, number = {3}, year = {2007}, month = {Aug}, pages = {757-774}, isbn = {0040-0262}, author = {Erkens, R. H. J. and Chatrou, L. W. and Koek-Noorrnan, J. and Maas, J. W. and Maas, P. J. M.} } @article {4948, title = {Proposal to conserve the name Meiogyne against Fitzalania (Annonaceae) }, journal = {TaxonTaxon}, year = {2011}, author = {Chaowasku, Tanawat and Zijlstra, Gea and Chatrou, L. W.} } @article {4949, title = {(2029) Proposal to conserve the name Meiogyne against Fitzalania (Annonaceae)}, journal = {TaxonTaxon}, volume = {60}, number = {5}, year = {2011}, note = {067, 105}, author = {Chaowasku, Tanawat and Zijlstra, Gea and Chatrou, Lars W.} }