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An update of the Angiosperm Phylogeny Group classification for the orders and families of flowering plants: APG IV
Open accessAbstract
An update of the Angiosperm Phylogeny Group (APG) classification of the orders and families of angiosperms is presented.Several new orders are recognized: Boraginales, Dilleniales, Icacinales, Metteniusiales and Vahliales.This brings the total number of orders and families recognized in the APG system to 64 and 416, respectively.We propose two additional informal major clades, superrosids and superasterids, that each comprise the additional orders that are included in the larger clades dominated by the rosids and asterids.Families that made up potentially monofamilial orders, Dasypogonaceae and Sabiaceae, are instead referred to Arecales and Proteales, respectively.Two parasitic families formerly of uncertain positions are now placed: Cynomoriaceae in Saxifragales and Apodanthaceae in Cucurbitales.Although there is evidence that some families recognized in APG III are not monophyletic, we make no changes in Dioscoreales and Santalales relative to APG III and leave some genera in Lamiales unplaced (e.g.Peltanthera).These changes in familial circumscription and recognition have all resulted from new results published since APG III, except for some changes simply due to nomenclatural issues, which include substituting Asphodelaceae for Xanthorrhoeaceae (Asparagales) and Francoaceae for Melianthaceae (Geraniales); however, in Francoaceae we also include Bersamaceae, Ledocarpaceae, Rhynchothecaceae and Vivianiaceae.Other changes to family limits are not drastic or numerous and are mostly focused on some members of the lamiids, especially the former Icacinaceae that have long been problematic with several genera moved to the formerly monogeneric Metteniusaceae, but minor changes in circumscription include Aristolochiaceae (now including Lactoridaceae and Hydnoraceae; Aristolochiales), Maundiaceae (removed from Juncaginaceae; Alismatales), Restionaceae (now re-including Anarthriaceae and Centrolepidaceae; Poales), Buxaceae (now including Haptanthaceae; Buxales), Peraceae (split from Euphorbiaceae; Malpighiales), recognition of Petenaeaceae (Huerteales), Kewaceae, Limeaceae, Macarthuriaceae and Microteaceae (all Caryophyllales), Petiveriaceae split from Phytolaccaceae (Caryophyllales), changes to the generic composition of Ixonanthaceae and Irvingiaceae (with transfer of Allantospermum from the former to the latter; Malpighiales), transfer of Pakaraimaea (formerly Dipterocarpaceae) to Cistaceae (Malvales), transfer of Borthwickia, Forchhammeria, Stixis and Tirania (formerly all Capparaceae) to Resedaceae (Brassicales), Nyssaceae split from Cornaceae (Cornales), Pteleocarpa moved to Gelsemiaceae (Gentianales), changes to the generic composition of Gesneriaceae (Sanango moved from Loganiaceae) and Orobanchaceae (now including Lindenbergiaceae and
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Phylotranscriptomic analysis of the origin and early diversification of land plants
Wickett, N. J., Mirarab, S., Nguyen, N., Warnow, T., Carpenter, E., Matasci, N., Ayyampalayam, S., Barker, M. S., Burleigh, J. G., Gitzendanner, M. A., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323926111 · Cited by 1,252 · cited 3×
“Zeng et al. (2014) and Wickett et al. (2014) both analysed low-copy nuclear genes (59 and 852 genes, respectively), but relatively few angiosperms (60 and 37, respectively, the latter focused on all green plants), and reached similar conclusions about relationships to those found in the majority of…”
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Flowers, T. J., & Colmer, T. D. (2008) · New Phytologist · doi:10.1111/j.1469-8137.2008.02531.x · Cited by 2,789
NCBI Taxonomy: a comprehensive update on curation, resources and tools
Schoch, C. L., Ciufo, S., Domrachev, M., Hotton, C. L., Kannan, S., Khovanskaya, R., Leipe, D., Mcveigh, R., O’Neill, K., Robbertse, B., et al. (2020) · Database · doi:10.1093/database/baaa062 · Cited by 2,635
Phylotranscriptomic analysis of the origin and early diversification of land plants
Wickett, N. J., Mirarab, S., Nguyen, N., Warnow, T., Carpenter, E., Matasci, N., Ayyampalayam, S., Barker, M. S., Burleigh, J. G., Gitzendanner, M. A., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1323926111 · Cited by 1,252
A Burning Story: The Role of Fire in the History of Life
Pausas, J. G., & Keeley, J. E. (2009) · BioScience · doi:10.1525/bio.2009.59.7.10 · Cited by 1,226
Global trait–environment relationships of plant communities
Bruelheide, H., Dengler, J., Purschke, O., Lenoir, J., Jiménez-Alfaro, B., Hennekens, S. M., Botta-Dukát, Z., Chytrý, M., Field, R., Jansen, F., et al. (2018) · Nature Ecology & Evolution · doi:10.1038/s41559-018-0699-8 · Cited by 614
Metadata
- Authors
- The Angiosperm Phylogeny Group
- Venue
- Botanical Journal of the Linnean Society
- Publisher
- Oxford University Press (OUP)
- Published
- 2016-03-24
- Volume
- 181
- Issue
- 1
- Pages
- 1-20
- ISSN
- 0024-4074 (ISSN-L)
- OpenAlex
- W2166152751
- Cited by
- 9,555
- References
- 1
- FWCI
- 745.26
- Type
- journal article
- Language
- en
- Open access
- bronze
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