Superregnum: Eukaryota
Regnum: Plantae
Divisio: Tracheophyta
Divisio: Pinophyta
Classis: Pinopsida
Ordo: Pinales
Familia: Taxaceae
Genera: Amentotaxus – Austrotaxus – Cephalotaxus – Pseudotaxus – Taxus – Torreya
Paleogenera: †Diploporus – †Mataoraphyllum – †Vesquia
Name
Taxaceae Gray, Nat. Arr. Brit. Pl. 2: 222, 226 (1822), nom. cons. ['Taxideæ'].
type genus: Taxus L. Sp. Pl. 2: 1040. (1753)
Synonyms
Heterotypic
Amentotaxaceae Kudô & Yamam. J. Soc. Trop. Agric. 3: 110. (1931)
Austrotaxaceae Nakai Tyosen Sanrin Kaiho 158: 14. (1938)
Cephalotaxaceae Neger, Nadelhölzer 23, 30 (1907)
Torreyaceae Nakai Tyosen Sanrin Kaiho 158: 14,–23. (1938)
References
S.F.Gray 1822. A natural arrangement of British plants 2: 222, 226.
Anderson, E. & Owens, J. N. 2003. Analysing the reproductive biology of Taxus: should it be included in Coniferales? Acta Hort. 615: 233–234.
Christenhusz, M.J.M., Reveal, J.L., Farjon, A., Gardner, M.F., Mill, R.R. & Chase, M.W. 2011. A new classification and linear sequence of extant gymnosperms. Phytotaxa 19: 55–70. DOI: 10.11646/phytotaxa.19.1.3 Open access Reference page.
Govaerts, R. et al. 2014. Taxaceae in World Checklist of Selected Plant Families. The Board of Trustees of the Royal Botanic Gardens, Kew. Published online. Accessed: 2014 Feb. 2. Reference page.
Price, R. A. 2003. Generic and familial relationships of the Taxaceae from rbcL and matK sequence comparisons. Acta Hort. 615: 235–237.
Pole, M., & Moore, P. R. 2011. A late Miocene leaf assemblage from Coromandel Peninsula, New Zealand, and its climatic implications. Alcheringa 35 (1): 103–121. DOI: 10.1080/03115518.2010.481829
Tropicos.org 2014. Taxaceae. Missouri Botanical Garden. Published online. Accessed: 2 Feb. 2014.
Vernacular names
беларуская: Цісавыя
English: Yew
suomi: Marjakuusikasvit
日本語: イチイ科
македонски: Тиси
português: Taxácea
Türkçe: Porsukgiller
中文: 三尖杉科
Taxaceae (/tækˈseɪsii/), commonly called the yew family, is a coniferous family which includes six extant and two extinct genera, and about 30 species of plants, or in older interpretations three genera and 7 to 12 species.
They are many-branched, small trees and shrubs. The leaves are evergreen, spirally arranged, often twisted at the base to appear 2-ranked. They are linear to lanceolate, and have pale green or white stomatal bands on the undersides. The plants are dioecious, rarely monoecious. The male cones are 2–5 millimetres (0.079–0.197 in) long, and shed pollen in the early spring. The female 'cones' are highly reduced to a single seed. As the seed matures, a fleshy aril partly encloses it. The developmental origin of the aril is unclear, but it may represent a fused pair of swollen leaves.[1] The mature aril is brightly coloured, soft, juicy and sweet, and is eaten by birds which then disperse the hard seed undamaged in their droppings. However, the seeds are highly poisonous to humans, containing the poisons taxine and taxol.[2]
Classification
Taxaceae is now generally included with all other conifers in the order Pinales, as DNA analysis has shown that the yews are phylogenetically nested in the Pinales,[3] a conclusion supported by micromorphology studies.[4] Formerly they were often treated as distinct from other conifers by placing them in a separate order Taxales. Ernest Henry Wilson referred to Taxaceae as "taxads" in his 1916 book.[5] Taxaceae is thought to be the sister group to Cupressaceae, from which it diverged during the early-mid Triassic. The clade comprising both is sister to Sciadopityaceae, which diverged from them during the early-mid Permian.[6]
The broadly defined Taxaceae (including Cephalotaxus) comprises six extant genera and about 30 species overall. Cephalotaxus is now included in Taxaceae, rather than being recognized as the core of its own family, Cephalotaxaceae. Phylogenetic evidence strongly supports a very close relationship between Cephalotaxus and other members of Taxaceae,[7][8][9] and morphological differences between them are not substantial. Previous recognition of two distinct families, Taxaceae and Cephalotaxaceae (e.g.,[10]), was based on relatively minor morphological details: Taxaceae (excluding Cephalotaxus) has smaller mature seeds growing to 5–8 millimetres (0.20–0.31 in) in 6–8 months, that are not fully enclosed by the aril; in contrast, Cephalotaxus seeds have a longer maturation period (from 18–20 months), and larger mature seeds (12–40 millimetres (0.47–1.57 in)) fully enclosed by the aril. However, there are also very clear morphological connections between Cephalotaxus and other members of Taxaceae,[11][12] and considered in tandem with the phylogenetic evidence, there is no compelling need to recognize Cephalotaxus (or other genera in Taxaceae) as a distinct family,.[7][8]
Extant genera
Genus | Species | Image |
---|---|---|
Amentotaxus Pilg. – Catkin-yew |
|
|
Amentotaxus argotaenia
|
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Austrotaxus Compton – New Caledonia yew |
|
|
Austrotaxus spicata
|
||
Cephalotaxus Siebold & Zucc. ex Endl. – Plum yew |
|
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Cephalotaxus sinensis
|
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Pseudotaxus W.C.Cheng – White-berry yew |
|
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Taxus L. – Common yew |
|
|
Taxus brevifolia
|
||
Torreya Arn. – Nutmeg yew |
|
Torreya californica
|
Footnotes
Dörken, Veit Martin; Nimsch, Hubertus; Rudall, Paula J (2018-08-22). "Origin of the Taxaceae aril: evolutionary implications of seed-cone teratologies in Pseudotaxus chienii". Annals of Botany. Oxford University Press (OUP). 123 (1): 133–143. doi:10.1093/aob/mcy150. ISSN 0305-7364. PMC 6344100. PMID 30137225.
Yew Poisoning: MedLine Plus Medical Encyclopedia
Chase, M. W.; Soltis, D. E.; et al. (1993). "Phylogenetics of Seed Plants: An Analysis of Nucleotide Sequences from the Plastid Gene rbcL" (PDF). Annals of the Missouri Botanical Garden. JSTOR. 80 (3): 528. doi:10.2307/2399846. hdl:1969.1/179875. ISSN 0026-6493. JSTOR 2399846.
Anderson, E.; Owens, J.N. (2003). "Analyzing the Reproductive Biology of Taxus: Should It be Included in Coniferales?". Acta Horticulturae. International Society for Horticultural Science (ISHS) (615): 233–234. doi:10.17660/actahortic.2003.615.22. ISSN 0567-7572.
Wilson, Ernest Henry (1916). The conifers and taxads of Japan. Issued December 30, 1916. Cambridge: University Press. doi:10.5962/bhl.title.17457.
Stull, Gregory W.; Qu, Xiao-Jian; Parins-Fukuchi, Caroline; Yang, Ying-Ying; Yang, Jun-Bo; Yang, Zhi-Yun; Hu, Yi; Ma, Hong; Soltis, Pamela S.; Soltis, Douglas E.; Li, De-Zhu (July 19, 2021). "Gene duplications and phylogenomic conflict underlie major pulses of phenotypic evolution in gymnosperms". Nature Plants. 7 (8): 1015–1025. doi:10.1038/s41477-021-00964-4. ISSN 2055-0278.
Quinn, C. J.; Price, R. A.; Gadek, P. A. (2002). "Familial Concepts and Relationships in the Conifer Based on rbcL and matK Sequence Comparisons". Kew Bulletin. JSTOR. 57 (3): 513. doi:10.2307/4110984. ISSN 0075-5974. JSTOR 4110984. S2CID 83816639.
Rai, Hardeep S.; Reeves, Patrick A.; Peakall, Rod; Olmstead, Richard G.; Graham, Sean W. (2008). "Inference of higher-order conifer relationships from a multi-locus plastid data set". Botany. Canadian Science Publishing. 86 (7): 658–669. doi:10.1139/b08-062. ISSN 1916-2790. S2CID 14007221.
One Thousand Plant Transcriptomes Initiative (2019). "One thousand plant transcriptomes and the phylogenomics of green plants". Nature. Springer Science and Business Media LLC. 574 (7780): 679–685. doi:10.1038/s41586-019-1693-2. ISSN 0028-0836. PMC 6872490. PMID 31645766.
Hart, Jeffrey A. (1987). "A cladistic analysis of conifers: preliminary results". Journal of the Arnold Arboretum. 68 (3): 269–307. ISSN 0004-2625. JSTOR 43782212.
Doyle, James A. (1998). "Phylogeny of Vascular Plants". Annual Review of Ecology and Systematics. Annual Reviews. 29 (1): 567–599. doi:10.1146/annurev.ecolsys.29.1.567. ISSN 0066-4162. S2CID 85631751.
Stützel, Thomas; Röwekamp, Iris (1999). "Female reproductive structures in Taxales". Flora. Elsevier BV. 194 (2): 145–157. doi:10.1016/s0367-2530(17)30893-9. ISSN 0367-2530.
Manchester, S.R. (1994). "Fruits and Seeds of the Middle Eocene Nut Beds Flora, Clarno Formation, Oregon". Palaeontographica Americana. 58: 30–31.
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