Tellima

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Tellima
Tellima grandiflora 11202.JPG
Status TNC G5.svg
Secure  (NatureServe) [1]
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Angiosperms
Clade: Eudicots
Order: Saxifragales
Family: Saxifragaceae
Genus: Tellima
R.Br. (1823)
Species:
T. grandiflora
Binomial name
Tellima grandiflora
(Pursh) Dougl. ex Lindl. (1828)
Synonyms [2]
  • Mitella acerifoliaSchltdl. (1844)
  • Mitella grandifloraPursh (1813) (basionym)
  • Tellima brevifloraRydb. (1905)
  • Tellima grandiflora var. virescensRegel (1867)
  • Tellima nudicaulisGreene (1891)
  • Tellima odorataHowell (1898)
  • Tiarella alternifoliaFisch. ex Ser. (1830), not validly publ.

Tellima grandiflora, the bigflower tellima [3] or fringecups, is a herbaceous perennial flowering plant in the family Saxifragaceae. It is the only species in the genus Tellima. [4] [5]

Contents

Description

It has rounded stalked leaves mostly growing from the base emerging from a rootstock and bluntly toothed reaching heights of 30 cm. [6] It is evergreen in mild winters. Flowers are borne in spring and early summer, on spikes, terminal racemes, up to 60 cm high. The green calyx is 6–8 mm long; the five flower petals are greenish-white to purple, pinnately divided and spreading. The petals are deeply fringed. It has 10 stamens and 2 styles. [6]

Distribution

The plant is a native of moist forests in western North America, from Alaska and British Columbia to northern California. [7] It can be a garden escape and become naturalised in some other areas, e.g. Ireland and Great Britain. Although it is secure in the western portions of its range, Tellima grandiflora is listed as vulnerable in Idaho and Montana, and as critically imperiled in Alberta. [8]

Tellima grandiflora 4967f.JPG

Uses

It is widely grown in gardens. Different strains have been developed. It seeds itself freely in suitable climates.

This plant, crushed and made into an infusion, was used by the Skagit to aid people in sicknesses such as loss of appetite. [9] Ellagitannins are chemical compounds that have potential antiviral activity. [10] Tellimagrandin II, the first of the ellagitannins, formed from pentagalloyl glucose, is laccase-catalyzed dimerised to cornusiin E in T. grandiflora. [11]

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<span class="mw-page-title-main">Tellimagrandin II</span> Chemical compound

Tellimagrandin II is the first of the ellagitannins formed from 1,2,3,4,6-pentagalloyl-glucose. It can be found in Geum japonicum and Syzygium aromaticum (clove).

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<span class="mw-page-title-main">Cornusiin E</span> Chemical compound

Cornusiin E is a dimeric derivative of tellimagrandin II found in Tellima grandiflora.

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References

  1. "tellima grandiflora". NatureServe Explorer. NatureServe. Retrieved 2018-04-13.
  2. Tellima grandiflora (Pursh) Douglas ex Lindl. Plants of the World Online . Retrieved 14 April 2024.
  3. USDA, NRCS (n.d.). "Tellima grandiflora". The PLANTS Database (plants.usda.gov). Greensboro, North Carolina: National Plant Data Team. Retrieved 8 December 2015.
  4. Charles Leo Hitchcock & Arthur Cronquist (1973). Flora of the Pacific Northwest: an Illustrated Manual . Seattle: University of Washington Press. ISBN   978-0-295-95273-4.
  5. Mark Turner & Phyllis Gustafson (2006). Wildflowers of the Pacific Northwest . Portland, OR: Timber Press. ISBN   978-0-88192-745-0.
  6. 1 2 Parnell, J. and Curtis, T. 2012. Webb's An Irish Flora. Cork University Press. ISBN   978-185918-4783
  7. "Tellima grandiflora". WTU Herbarium Image Collection. Burke Museum of Natural History and Culture . Retrieved April 26, 2011.
  8. "Comprehensive Report Species -". explorer.natureserve.org. Retrieved 2018-04-14.
  9. Jim Pojar & Andy MacKinnon (2004). Plants of the Pacific Northwest Coast. Edmonton: Lone Pine Publishing. ISBN   978-1-55105-530-5.
  10. Stéphane Quideau; Tatiana Varadinova; Diana Karagiozova; Michael Jourdes; Patrick Pardon; Christian Baudry; Petia Genova; Theodore Diakov & Rozalina Petrova (February 2004). "Main structural and stereochemical aspects of the antiherpetic activity of nonahydroxyterphenoyl-containing C-glycosidic ellagitannins". Chemistry & Biodiversity . 1 (2): 247–258. doi:10.1002/cbdv.200490021. PMID   17191843. S2CID   21637300.
  11. Ruth Niemetz & Georg G. Gross (2003). "Ellagitannin biosynthesis: laccase-catalyzed dimerization of tellimagrandin II to cornusiin E in Tellima grandiflora". Phytochemistry . 64 (7): 1197–1201. Bibcode:2003PChem..64.1197N. doi:10.1016/j.phytochem.2003.08.013. PMID   14599517.