Jepson Interchange (more information)
Print edition is available from the University of California Press
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This page is based on the 1993 Jepson Manual.
Please see the Jepson eFlora for up-to-date information about California vascular plants. |
| Jepson Flora Project: Jepson Interchange |
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TREATMENT FROM THE JEPSON MANUAL |
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Jepson Interchange (more information) |
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©Copyright 1993 by the Regents of the University of California
Print edition is available from the University of California Press |
| The second edition of The Jepson Manual (2012) is available from the University of California Press | |
| See also the Jepson eFlora, which parallels the Second Edition |
Annual to bamboo-like; roots generally fibrous
Stem generally round, hollow; nodes swollen, solid
Leaves alternate, 2-ranked, generally linear; sheath generally open; ligule membranous or hairy, at blade base
Inflorescence various (of generally many spikelets)
Spikelet: glumes generally 2; florets (lemma, palea, flower) 1–many; lemma generally membranous, sometimes glume-like; palea generally ± transparent, ± enclosed by lemma
Flower generally bisexual, minute; stamens generally 3; stigmas generally 2, generally plumose
Fruit: achene-like grain
Genera in family: 650–900 genera; ± 10,000 species: worldwide; greatest economic importance of any family (wheat, rice, maize, millet, sorghum, sugar cane, forage crops, ornamental, weeds; thatching, weaving, building materials).[Hitchcock 1951 Manual grasses US, USDA Misc Publ 200; Clayton & Renvoise 1986 Kew Bull Add Series 13] See Glossary p. 26 for illustrations of general family characteristics. Generally wind-pollinated.
Perennial, generally cespitose, generally ± glabrous; bisexual, dioecious in F. kingii
Stem erect
Leaves ± basal; sheath generally persisting; collar generally glabrous; ligule generally < 1 mm, membranous, truncate, minutely fringed; blade flat or rolled, basal lobes generally 0
Inflorescence panicle-like; branches dense and appressed to open and spreading
Spikelet: glumes < lowest floret, unequal, lower 1–3-veined, upper 3–5-veined; axis breaking above glumes and between florets, florets 2–10, generally bisexual; lemma base generally glabrous, 5-veined (rarely 3- or 7-veined), not converging at tip; awn generally terminal, straight, glabrous; palea ± = lemma; stamens 3
Fruit free from palea, generally beakless
Etymology: (Latin: ancient name)
Reference: [Frederiksen 1982 Nord J Bot 2:525–536]
| Native |
Stems 3–10 dm, generally densely clumped; nodes visible
Leaf: sheath clearly persistent; ligule < 0.5 mm; blade 5–35 cm, < 2 mm wide, rolled, scabrous, ± stiff
Inflorescence 6–20 cm; branches ± appressed, scabrous
Spikelet 7–17 mm; lower glume ± 2.5–6 mm, upper 4–8 mm; axis generally visible, generally zigzag; florets 3–9; lemma ± 6–10 mm, scabrous near tip, awn 1–6 mm; anthers 3–4.5 mm; ovary tip glabrous
Chromosomes: 2n=28
Ecology: Dry, open or shady places
Elevation: generally < 1800 m.
Bioregional distribution: Northwestern California, Cascade Range, n&c Sierra Nevada, n&c Central Western California, Modoc Plateau
Distribution outside California: to Canada, ColoradoHorticultural information: DRN, IRR: 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24; CVS; also STBL.
| YOU CAN HELP US make sure that our distributional information is correct and current. If you know that a plant occurs in a wild, reproducing state in a Jepson bioregion NOT highlighted on the map, please contact us with that information. Please realize that we cannot incorporate range extensions without access to a voucher specimen, which should (ultimately) be deposited in an herbarium. You can send the pressed, dried collection (with complete locality information indicated) to us (e-mail us for details) or refer us to an accessioned herbarium specimen. Non-occurrence of a plant in an indicated area is difficult to document, but we will especially value your input on those types of possible errors (see automatic conversion of distribution data to maps). |
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