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Key to families | Table of families and genera
Indexes to all accepted names and synonyms:
| A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z |
Annual, perennial herb, often rhizomed or stoloned, often of wet open places; roots fibrous; monoecious, dioecious, or flowers bisexual. Stem: generally 3-sided, generally solid. Leaf: generally 3-ranked; base sheathing, sheath generally closed, ligule generally 0; blade (0 or) linear, parallel-veined. Inflorescence: spikelets generally arranged in head-, spike-, raceme-, or panicle-like inflorescences; flower generally sessile in axil of flower bract, enclosed in a sac-like structure (perigynium) or generally not. Flower: unisexual or bisexual, small, generally wind-pollinated; perianth 0 or generally bristle like; stamens generally 3, anthers attached at base, 4 chambered; ovary superior, chamber 1, ovule 1, style 2–3-branched. Fruit: achene, 2–3 sided.
± 100 genera, 5000 species: especially temperate. [Gilmour et al. 2013 Kew Bull 68:85–105] Difficult; taxa differ in technical characters of inflorescence, fruit. In Carex and Kobresia, what appear to be individual pistillate flowers in fact are highly reduced inflorescences (whether or not the same applies to staminate flowers is still under debate). In some other works (e.g., FNANM) these are called spikelets, and they are treated as being arranged in spikes. Here and in TJM (1993), what appear to be individual pistillate flowers are called pistillate flowers in Carex (and they are treated as being arranged in spikelets), but spikelets in Kobresia (and they are treated as being arranged into spikes). Though internally inconsistent, the approach here is consistent with traditional usage, and reflects a preference for character states that may be determined in the field. Molecular, morphological, and embryological evidence indicates that Eriophorum crinigerum is to be segregated to a new genus, as Calliscirpus criniger (A. Gray) C.N. Gilmour et al., along with a second, newly described species, Calliscirpus brachythrix C.N. Gilmour et al. (Gilmour et al. 2013); key to genera modified by Peter W. Ball to include Calliscirpus. —Scientific Editors: S. Galen Smith, Thomas J. Rosatti, Bruce G. Baldwin.
Unabridged references: [Ball et al. 2002 FNANM 23:1–608; Bruhl 1995 Australian Syst Bot 8:125–305; Tucker 1987 J Arnold Arbor 68:361–445;]
Key to Cyperaceae
Annual, perennial herb, generally forming mats, glabrous, internal air cavities evident; caudex generally 0; rhizomes generally evident, long, scaly, bulb or tuber at tip generally 0. Stem: simple, generally erect, smooth, generally not hollow; tip generally not rooting. Leaf: 2, basal, blades 0 or tooth-like, <= 1 mm. Inflorescence: inflorescence bracts 0; spikelet terminal, 1, generally ovate, not ± flat [(± flat)], generally not forming plantlets, flowers 3–100+; flower bracts spiraled [(2-ranked)], each with 1 flower in axil, generally ovate, generally brown, generally membranous, smooth, tip generally acute to obtuse, notch 0; basal flower bract generally encircling stem, generally < 1/2 spikelet, flower generally 0. Flower: bisexual; perianth parts reduced to bristles, 0–8, generally ± <= fruit, barbs generally recurved; stamens generally 3; style 1, thread-like, base enlarged, generally persistent on fruit as tubercle. Fruit: generally obovate, generally brown; tubercle (0 or) generally distinct, generally pyramidal.Key to Eleocharis
± 200 species: tropics to boreal. (Greek: marsh-dwelling grace) [Smith et al. 2002 FNANM 23:60–120] Eleocharis lanceolata Fernald, Eleocharis equisetoides Torr. not in California.
Unabridged etymology: (Greek heleios, dwelling in a marsh, and Charis, grace)
Perennial herb 4–40 cm, stem-tuft base not swollen, without bulbs or 2-veined scales; rhizome 0.5–1.5 mm diam, weak, tip with bud 10 mm, 2–5 mm wide, elliptic; caudex present, hard. Stem: erect, 0.5–1.2 mm wide, cylindric to ± flat. Leaf: distal sheath firm, persistent, tip subtruncate to obtuse. Inflorescence: spikelets 5–10 mm, 2–4 mm wide, often 0; flower bracts 8–12, 3.5–5 mm, basal generally >= 1/2 spikelet. Flower: anthers 1.6–3.5 mm; stigmas 3. Fruit: 2–2.7 mm, 0.7–1.3 mm wide, 3-sided, smooth or fine-longitudinal-ridged or -net-like, tip narrowed, beak-like; tubercle often merging with fruit; perianth bristles 6, longest = fruit to exceeding tubercle.
Often subdominant but local. Wet meadows, fens, springs; < 3400 m. Northwestern California, High Cascade Range, Sierra Nevada, San Francisco Bay Area, Transverse Ranges, Desert Mountains; to British Columbia, northwestern Montana, Colorado. Herbarium specimens often confused with Eleocharis rostellata. Summer [Online Interchange]
Unabridged note: Lowest elev is Point Reyes, Marin Co.
Previous taxon: Eleocharis rostellata
Next taxon: Eleocharis tenuis var. tenuis
Citation for the whole project: Jepson Flora Project (eds.) 2013. Jepson eFlora, http://ucjeps.berkeley.edu/IJM.html, accessed on Oct 9 2015
Citation for this treatment: [Author of taxon treatment] 2013. Eleocharis, in Jepson Flora Project (eds.) Jepson eFlora, http://ucjeps.berkeley.edu/cgi-bin/get_IJM.pl?tid=24007, accessed on Oct 9 2015
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|Geographic subdivisions indicated for the distribution of Eleocharis suksdorfiana|| Markers link to CCH specimen records. If the markers are obscured, reload the page [or change window size and reload]. Yellow markers indicate records that may provide evidence for eFlora range revision or may have georeferencing or identification issues.
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(Note: any qualifiers in the taxon distribution description, such as 'northern', 'southern', 'adjacent' etc., are not reflected in the map above, and in some cases indication of a taxon in a subdivision is based on a single collection or author-verified occurence).
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