(1), Sarcostoma Blume (5), Stolzia Schltr. From a biological point of view, such an association also helps to understand the biogeography of Epidendreae as a whole. (2001a). The originally monospecific genus Vietorchis Aver. In Phalaenopsis are included Grussia M.Wolff, Hygrochilus Pfitzer, Lesliea Seidenf., Nothodoritis Z.H.Tsi, Ornithochilus (Lindl.) This, too, seems reasonable, but, for the present, we retain past circumscriptions of Caladenia (as in Hopper & Brown, 2004). (Orchidaceae), Generic recircumscriptions of Oncidiinae (Orchidaceae: Cymbidieae) based on maximum likelihood analysis of combined DNA datasets, New combinations in subtribe Eriinae (Epidendroideae: Podochileae), Taxonomic changes in Goodyerinae (Orchidaceae: Orchidoideae), Orchidaceous additions to the floras of China and Myanmar, Studies in Neotropical Goodyerinae (Orchidaceae) 5, Toward a phylogenetic subfamilial classification for the Compositae (Asteraceae), Proceedings of the Biological Society of Washington, Sistemática filogenética e biologia floral de Pogoniinae sul-americanas, e revisão taxonômica e análise das ceras epicuticulares do gênero. and Calanthe densiflora Lindl., apart from most other species of Calanthe, to which Gastrochis is sister. Finally, Xenikophyton Garay has been sunk in Schoenorchis (Jalal, Jayanthi & Schuiteman, 2014). (58), Aeranthes Lindl. Five is a reasonable number of subfamilies and is easily remembered by everyone, but, in other large families, the number of subfamilies has been greatly increased as a result of molecular studies and a tendency to split in order to maintain some long-recognized subfamilies, making these systems much more difficult for students and non-specialists to use. (8), Sphyrarhynchus Mansf. (6), Luisia Gaudich. (16), Soterosanthus F.Lehm. (47), Microtis R.Br. (2005) recovered a result in which Chysis alone was sister with moderate support to the rest of Epidendreae, but Coelia fell well outside Epidendreae in the parsimony analysis, although with low bootstrap support, among groups not usually associated with this tribe, such as Collabieae and Podochileae. Górniak et al. (2001) recognized a large number of genera segregated from Caladenia, we prefer to maintain the broader concept of this large, mostly Australian genus (as per Hopper & Brown, 2004). (6), Ponera Lindl. data), which is morphologically better treated in a subgenus of Cattleya. The Atlas of Florida Plants provides a source of information for the distribution of plants within the state and taxonomic information. A prominent example in which such splitting of a genus was eventually accepted is that of Cypripedium, which had been the sole genus of that subfamily (or even family). Orchidaceae are one of the two largest families of flowering plants, and are perhaps second only to Asteraceae (The Plant List, 2014). Phylogenetic relationships within Orchidaceae based on a low-copy nuclear coding gene, Phylogenetics of tribe Orchideae (Orchidaceae: Orchidoideae) based on combined DNA matrices: inferences regarding timing of diversification and evolution of pollination syndromes, Molecular systematics of subtribe Orchidinae and Asian taxa of Habenariinae (Orchideae, Orchidaceae) based on plastid, Nomenclatural notes arising from studies into the tribe Diurideae (Orchidaceae), New combinations in Aeridinae (Orchidaceae), New combinations and description of two new species in, Icones pleurothallidinarum XXVIII. (1), Changnienia S.S.Chien (1), Coelia† Lindl. (7), Triphora Nutt. In subtribe Orchidinae, further phylogenetic work has resulted in a number of changes in the generic circumscription. Aeridinae have presented a large number of problems throughout their history, and several major shifts have occurred. A quick look at the many polytomies in Figure 1 demonstrates that more work is needed to sort out subtribal relationships within many tribes (e.g. (323), Oberonioides* Szlach. The Orchidaceae is divided into two sub-families: Sub-family I. Diandroideae: Stamens 2 belonging to the lateral members of the inner whorl, the 3rd of the same is modified to a staminode placed above the anthers; the members of the outer whorl of androecium are either suppressed or … ex Blume(9), Cymbidium Sw. (71), Grammatophyllum Blume (12), Porphyroglottis Ridl. (34), Stalkya Garay (1), Stenorrhynchos Rich. Pachyphyllum Kunth and Raycadenco Dodson are now included in Fernandezia Ruiz & Pav. (1), Platylepis A.Rich. [i.e. (1). However, the generic boundaries are unclear, and phylogenetic studies show that many genera are paraphyletic or even polyphyletic,[22] so a clear assignment of genera to subtribes is currently not possible. Subtree links. Finally, Chiron, Guiard & van den Berg (2012) discovered that two species (one first described in Phloeophila Hoehne & Schltr., the other then unnamed) formed a small isolated clade within Pleurothallidinae, and Chiron (2012) named this Sansonia. Neolindleya has recently been included in Galearis (Jin et al., 2014). is a synonym of Taeniophyllum; they differ chiefly in the former having leaves and the latter not. A new monospecific genus, Schuitemania, was described by Ormerod (2002). (22). In Orchidoideae, no study published thus far has resolved with internal support relationships of the four tribes recognized in this classification. (3), Chamorchis Rich. (36), Centrostigma Schltr. (2), Psilochilus Barb.Rodr. When we look back at Chase et al. (11), Sudamerlycaste* Archila (42), Teuscheria Garay (7), Xylobium Lindl. Orchidaceae. The initial scheme of 1981 was modified in 1986, twice in 1990, and then again in 1993. (2), Systeloglossum Schltr. Idaho Species . The family presents more than 25,000 species, distributed around the world, but showing greatest diversity in tropical regions. Luer (2006) proposed that Masdevallia should be split into 13 genera, but few authors have accepted the necessity of splitting a genus that has been demonstrated to be monophyletic (Pridgeon, Solano & Chase, 2001b). In analyses of multiple DNA loci, Thaia was found to be sister to a large clade comprising the epidendroid genera with well-developed pollinia (Xiang et al., 2012) and, because of its phylogenetic placement and divergent morphological traits, it was described as a new tribe, a rank that we follow here. M. A. Clements (pers. (5), Chytroglossa Rchb.f. (2003). We present below, in a rough phylogenetic sequence, a description of the changes in each subfamily, tribe and subtribe; at the end, in the  Appendix, is a list of the genera with the number of species indicated (from the Monocot Checklist, Govaerts, 2014); this also includes authors for all genera. (2003), rather than into two subtribes as in Chase et al. In morphological terms, Bromheadia is highly dissimilar to Adrorhizon and Sirhookera. (110). 2015. Des Plantes 2: 68, July – Aug. 1763.. Orchidaceae Juss. would be morphologically undiagnosable. (2), Bulleyia Schltr. It may well be that, in the longer term, recognition of such segregates will prevail, but more discussion is required before a consensus to make such changes is reached. Guanchezia was included in the analysis of Whitten et al. Search for other works by this author on: Novas combinações, novas ocorrências e notas sobre espécies pouco conhecidas, para as orquídeas do Bresil, Molecular phylogenetics and morphological reappraisal of the, Molecular phylogenetics of the species-rich genus, Phylogenetic placement, taxonomic revision and a new species of, An overview of the phylogenetic relationships within Epidendroideae inferred from multiple DNA regions and recircumscription of Epidendreae and Arethuseae (Orchidaceae), A phylogenetic study of Laeliinae (Orchidaceae) based on combined nuclear and plastid DNA sequences, Generic realignments in Maxillariinae (Orchidaceae), Phylogenetic position and floral morphology of the Brazilian endemic, monospecific genus, A molecular phylogeny for the large African orchid genus, The phylogenetic position of the enigmatic orchid genus, Leave it to the leaves: a molecular phylogenetic study of Malaxideae (Epidendroideae, Orchidaceae), On the value of nuclear and mitochondrial gene sequences for reconstructing the phylogeny of vanilloid orchids (Vanilloideae, Orchidaceae), Vanilla orchids: natural history and cultivation, Proceedings of the Fifth Monocot Conference, Phylogenetic relationships of Pogoniinae (Vanilloideae, Orchidaceae): an herbaceous example of the eastern North America–eastern Asia phytogeographic disjunction, Molecular phylogeny of Vandeae (Orchidaceae) and the evolution of leaflessness, DNA data and Orchidaceae systematics: a new phylogenetic classification, Taxonomic transfers in Oncidiinae to accord with, Oncidiinae nomenclature: generic changes in, Phylogenetic analysis of the subtribe Chloraeinae (Orchidaceae): a preliminary approach based on three chloroplast markers, Un nouveau genre brésilien dans la sous-tribu Pleurothallidinae (Orchidaceae), avec une nouvelle espéce, Quatre nouvelles espèces d'Orchidaceae du Brésil, Phylogenetic analysis of Chloraeinae (Orchidaceae) based on plastid and nuclear DNA sequences, Genera orchidacearum, Vol. 6 genera with about 115 species, mostly terrestrials or lithophytes: This is the largest subfamily, comprising more than 10,000 species in about 90 to 100 genera. 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