Flora of North America species comparison

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Carex schweinitzii

Cyperaceae

carex de Schweinitz, Schweinitz's sedge

sedge family
Habit Plants extensively colonial; rhizomes long. Herbs, annual or perennial, cespitose or not, rhizomatous or not, stoloniferous or not.
Roots

fibrous, principally adventitious.
Culms

trigonous in cross section, 18–65 cm, smooth distally.

Stems

(culms) usually trigonous, occasionally terete, rarely compressed, usually solid, rarely hollow or septate.
Leaves

basal sheaths pale brown;

ligules as wide to wider than long;

blades pale to mid green, flat to W-shaped, 4–11 mm wide, glabrous.

basal and/or cauline, alternate, usually 3-ranked, rarely 2-ranked or multi-ranked, bases forming cylindric sheaths enclosing stem, margins usually fused;

junction of sheaths and blades often with adaxial flaps of tissue or fringes of hair (ligules);

blades frequently absent from some basal leaves, rarely from cauline leaves, when present divergent or ascending, flat, folded, plicate, rolled, or terete, linear, venation parallel.
Inflorescences

8–24 cm;

proximal bract 11–37 cm, exceeding inflorescence;

proximal 2–4 spikes pistillate, erect or often the proximal ascending to spreading;

terminal 1(–2) spikes staminate.

Flowers

hypogynous, bisexual in most genera, unisexual in Scleria, Carex, Cymophyllus, and Kobresia;

perianth absent or with (1–)3–6(–30) bristles and/or scales, usually falling off with fruit;

stamens usually (1–)3, rarely more, usually distinct;

anthers basifixed;

pistils 1, 2–3(–4)-carpellate, fused, locule 1;

style undivided or branches 2–3(–4);

stigma sometimes papillate.
Perigynia

ascending, 7–11-veined, narrowly elliptic, 4.2–7 × 1.3–1.8 mm, apex tapered;

beak 1.4–2.4 mm, bidentulate, smooth, teeth straight, 0.2–0.5 mm.

Fruits

achenes, usually trigonous or biconvex;

pericarps thin (except in Scleria).
Achenes

pale brown, trigonous, smooth.

Seeds

1;

testa thin, free from pericarp;

embryo basal;

endosperm abundant.
Pistillate

scales lanceolate-acuminate, 2.4–6.9 × 0.3–0.9 mm, shorter than or the proximal longer than perigynia, margins serrulate-ciliate, apex with prominent scabrous awn.

Staminate

scales acute to acuminate, smooth except at tip.

Stigmas

3.

Primary

inflorescences (spikelets) a shortened axis; glumaceous bracts (scales) 1–many, spirally arranged, sometimes 2-ranked, usually appressed or ascending;

scales usually all fertile, each subtending a single flower, sometimes proximal and/or distal scales empty;

lateral spikes often with basal, usually empty, usually 2-keeled scale (prophyll); occasionally prophyll subtending and enclosing rachilla, bearing 1 pistillate, sometimes (0–)3 staminate flowers and empty scales (Carex, Cymophyllus, and Kobresia).
Secondary

inflorescences panicles, often modified to corymb, pseudoumbel, cyme (anthela), raceme, spike, or capitulum (head), rarely single spike, usually subtended by foliaceous or, less frequently, glumaceous bracts;

secondary inflorescences sometimes simulating spikelets (Carex, Cymophyllus, and Kobresia).
x

= 5–ca. 100.

Carex schweinitzii

Cyperaceae
Phenology Fruiting Jun–Jul.
Habitat Shallow cold streams, springheads, seeps, margins of fens, and seepy stream, pond, and lakeshores in open or lightly shaded sites, in highly calcareous soils
Elevation 100–600 m (300–2000 ft)
Distribution
from FNA
CT; MA; MI; MO; NY; PA; VA; VT; WI; ON
[WildflowerSearch map]
[BONAP county map]
Worldwide
[BONAP county map]
Discussion

Carex schweinitzii is very local and uncommon but often forms large colonies where present. It hybridizes occasionally with C. hystericina. The single, old Missouri collection (G. Yatskievych 1999+) seems so far disjunct as to suggest that there may have been a label mixup.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Genera ca. 100, species ca. 5000 (27 genera, 843 species in the flora).

No consensus exists regarding the number of genera and the overall relationships of genera within Cyperaceae. The most recent account of the family (P. Goetghebeur 1998) recognized 104 genera distributed among 4 subfamilies and 14 tribes. That arrangement differs somewhat from that of J. Bruhl (1995). With one minor exception the arrangement of the family here follows that of Goetghebeur.

The family is characterized by the occurrence of a number of unusual cytological features including: (1) chromosomes with diffuse centromeres, (2) post-reductional meiosis, and (3) pollen grains formed from tetrads in which 3 of the 4 microspores fail to develop. The first two features are found in at least some Juncaceae and are unique to the two families. Juncaceae also have pollen in tetrads, but in that family all four microspores produce pollen grains. Some species in some genera of Cyperaceae (particularly Eleocharis) possess chromosomes with localized centromeres (S. S. Bir et al. 1993). The wide range of chromosome numbers found in Cyperaceae is largely because of agmatoploidy; polyploidy has been hypothesized for some genera, especially Eleocharis, although polyploidy has not been demonstrated unequivocally.

Because of morphologic similarities in vegetative and inflorescence characters, the family has commonly been associated with Poaceae. Cytological features discussed above clearly indicate that to be a superficial similarity. Data from rbcL studies also support the view that Cyperaceae and Poaceae are not closely related (M. R. Duvall et al. 1993b; G. M. Plunkett et al. 1995); they do support the concept of close relationship between Cyperaceae and Juncaceae.

For most families of flowering plants the phenological data given are flowering times. Because most Cyperaceae cannot be reliably identified when in flower, in this volume fruiting time is given for all species by season, sometimes qualified by early, mid, or late, or by months. The fruiting time has been interpreted broadly to include the period when the fruit is more or less fully formed but not yet ripe. The fruiting period provided covers the entire range of the taxon. Quite a difference between fruiting periods in different parts of the range of the species may well occur, especially for widespread species and species with extensive elevation range.

For a recent, comprehensive review of the economic importance of Cyperaceae, see D. A. Simpson and C. A. Inglis (2001).

(Discussion copyrighted by Flora of North America; reprinted with permission.)
Key
1. Flowers and achenes partially to completely enclosed in scalelike structure (perigynium); perigynium in axil of scale; flowers unisexual (see Plate 1. A, B, C).
→ 2
1. Flowers and achenes not enclosed in scalelike perigynium; flowers in axil of scale; flowers usually bisexual, sometimes some, rarely all, flowers unisexual.
→ 4
2. Perigynia open to 1 side, at least some containing 1–3 staminate flowers as well as 1 pistillate flower (see Plate 1. A).
Kobresia
2. Perigynia closed except for pore at tip through which style protrudes, always containing only 1 pistillate flower (see Plate 1. B, C).
→ 3
3. Culms usually with several blade-bearing leaves, sometimes all basal; blades flat, V-shaped, M-shaped, rarely terete or involute in cross section, commonly less than 2 cm wide, if flat with distinct midrib.
Carex
3. Culms with 1(–2) basal leaves; blades flat, usually 2–5 cm wide, without evident midrib.
Cymophyllus
4. Flowers with perianth of 1 or more hairs, bristles, scales, or bristles and scales, usually persistent on achene (see Plate 1. D, E, F; Plate 2. A).
→ 5
4. Flowers without perianth of hairs, bristles, or scales.
→ 27
5. Perianth of hairs or bristles, much exceeding subtending scales in fruit, more than 2 times as long as achene, including persistent style base, if present (see Plate 1. D).
→ 6
5. Perianth not or scarcely exceeding subtending scales in fruit, not more than 2 times as long as achene, including persistent style base, if present (see Plate 1. E, F; Plate 2. A).
→ 9
6. Perianth hairs strongly curled, tangled in fruit (woolly in appearance).
Scirpus
6. Perianth hairs ± straight, not tangled (silky in appearance).
→ 7
7. Perianth hairs (8–)10+ in each flower; spikelets (excluding hairs) 1+ cm.
Eriophorum
7. Perianth hairs mostly 6 in each flower; spikelets (excluding hairs) not more than 1 cm.
→ 8
8. Perianth hairs antrorsely barbed; leaf blades to 25 cm × 2.5–4 mm.
Eriophorum
8. Perianth hairs smooth; leaf blades less than 1 cm × 1 mm.
Trichophorum
9. Spikelets compressed laterally; scales 2-ranked at least in proximal 1/2, keeled (see Plate 2. C).
→ 10
9. Spikelets ± rounded in cross section; scales spirally arranged, not keeled (distichous in Websteria) (see Plate 2. D).
→ 13
10. Achenes biconvex; styles 2-fid.
→ 11
10. Achenes trigonous; styles 3-fid.
→ 12
11. Persistent style base of achene enlarged (see Plate 2. B).
Rhynchospora
11. Persistent style base of achene linear.
Dulichium
12. Achenes with persistent enlarged style base; culms simple with 1 spikelet; scales pale or yellow-brown to red-brown (see Plate 2. A).
Eleocharis
12. Achenes without persistent enlarged style base; culms distally branched with several spikelets; scales black or very dark purple.
Schoenus
13. Perianth consisting of scales or of 3 scales and 3 bristles (see Plate 1. E, F).
→ 14
13. Perianth consisting of hairs or bristles, bristles rarely somewhat flattened and straplike (see Plate 2. A).
→ 15
14. Perianth consisting of 3 bristles and 3 spatulate scales; leaves usually hairy, hairs sometimes confined to junction of blade and sheath (see Plate 1. E).
Fuirena
14. Perianth consisting of 1–2 scales; leaves glabrous (see Plate 2. F).
Lipocarpha
15. Culms apparently without blade-bearing leaves; leaves absent or consisting only of sheaths.
→ 16
15. Culms with blade-bearing leaves; at least distal leaves with blades 5+ mm.
→ 18
16. Spikelets consisting of 2 scales, distal scale subtending flower; culms with branches in successive false whorls, which terminate in clusters of leaves essentially indistinguishable from stems; spikelets borne singly on branches arising from among leaves.
Websteria
16. Spikelets with 4+ scales and 2+ flowers; culms unbranched except sometimes in inflorescence; either 1 terminal spikelet or several spikelets in branched inflorescence.
→ 17
17. Style base enlarged, persistent in fruit, usually clearly differentiated from achene; culms with 1 spikelet (see Plate 2. A).
Eleocharis
17. Style base not or scarcely enlarged, deciduous in fruit; culms usually with several spikelets in branched though sometimes congested inflorescence.
Schoenoplectus
18. Style base enlarged, persistent as differentiated tubercle on achene (see Plate 2. A, B).
→ 19
18. Style base not or only slightly enlarged, deciduous or small portion persistent as undifferentiated beak.
→ 20
19. Culms unbranched, with 1 spikelet; spikelets with 1 proximal scale empty.
Eleocharis
19. Culms usually distally branched, with more than 1 spikelet; spikelets usually with 2+ proximal scales empty.
Rhynchospora
20. Spikelets 2+, arranged in distichous spike.
Blysmopsis
20. Spikelets 1–500, arranged in panicle or clustered into 1 or more heads or solitary.
→ 21
21. Leaf blades and bracts with prominent midrib forming keel on abaxial surface, or blades folded along midrib; inflorescences obviously terminal (see Plate 2. F).
→ 22
21. Leaf blades and bracts various, midrib not forming prominent keel on abaxial surface, sometimes with several ribs equally prominent; proximal bract sometimes erect, as if continuation of culm; inflorescences then appearing lateral.
→ 23
22. Scales glabrous, never both notched and awned at tip; spikelets less than 3.5(–5) mm diam.; achenes 0.6–1.8 mm, mnutely papillose.
Scirpus
22. Scales puberulent on abaxial surface, often glabrescent, notched and awned at tip; spikelets mostly 4–10 mm diam.; achenes 2.3–5.5 mm, smooth.
Bolboschoenus
23. Bracts 2+, the proximal 10+ mm, exceeding spikelets by at least 3 mm; spikelets usually 2+.
→ 24
23. Bracts mostly 1–2, less than 10 mm, shorter than or exceeding spikelet by no more than 3 mm; spikelets always solitary.
→ 25
24. Proximal leaf sheaths often disintegrating into fibers; stems and leaf blades tough, wiry.
Amphiscirpus
24. Proximal leaf sheaths never disintegrating into fibers; leaf blades soft, herbaceous.
Schoenoplectus
25. Anthers 3 mm; achenes 2.5–3.5 mm.
Schoenoplectus
25. Anthers 1–2.5 mm; achenes 1.5–2.5 mm.
→ 26
26. Culms with all leaves basal; sheaths often disintegrating into fibers; perianth bristles retrorsely spinulose.
Amphiscirpus
26. Culms with bladeless sheaths or distal sheaths with blade to 5 mm; sheaths not fibrous; perianth bristles smooth or scabrous.
Trichophorum
27. Spikelets with scales arranged in 2 rows, at least proximally, commonly compressed; scales keeled (see Plate 2. C).
→ 28
27. Spikelets with scales spirally arranged or arranged in more than 2 rows, usually not compressed; scales not keeled (see Plate 2. D).
→ 32
28. Spikelets with 1–2+ proximal scales empty.
→ 29
28. Spikelets usually with all scales subtending flowers.
→ 30
29. Inflorescences of 1–5 straw-colored spikelets.
Abildgaardia
29. Inflorescences of (1–)10–25 black or dark purple spikelets.
Schoenus
30. Styles 3-fid; achenes trigonous.
Cyperus
30. Styles 2-fid; achenes flat to biconvex.
→ 31
31. Spikelets with 5–many scales; inflorescences variously arranged.
Cyperus
31. Spikelets with 1–3 scales; inflorescences with 1–4 dense spikes.
Kyllinga
32. Style base enlarged, persistent in fruit as differentiated or conic apical tubercle (see Plate 2. A, B).
→ 33
32. Style base not or scarcely enlarged, deciduous or undifferentiated portion persisting as cylindric beak.
→ 35
33. Culms with 1 spikelet, without blade-bearing leaves or with blade not exceeding 4 mm.
Eleocharis
33. Culms with inflorescences of 2+ spikelets, with 1+ blade-bearing leaves usually much exceeding 4 mm.
→ 34
34. Mouth of leaf sheaths fimbriate-ciliate; styles 3-fid; achenes trigonous.
Bulbostylis
34. Mouth of leaf sheaths glabrous; styles usually 2-fid; achenes usually biconvex.
Rhynchospora
35. Flowers unisexual; spikelets with only one pistillate flower or entirely staminate (see Plate 2. E).
Scleria
35. Flowers usually bisexual; spikelets usually with 2+ bisexual flowers.
→ 36
36. Leaves ligulate, ligules membranous or row of hairs or cilia (see Plate 2. F).
→ 37
36. Leaves not ligulate, rarely with lateral groups of hairs at junction of blade and sheath.
→ 42
37. Styles 2-fid; achenes biconvex.
→ 38
37. Styles 3-fid; achenes trigonous.
→ 39
38. Spikelets with all scales subtending flower.
Scirpus
38. Spikelets with proximal 1–2+ scales empty.
Fimbristylis
39. Culms with single terminal spikelet.
Trichophorum
39. Culms with 2+ spikelets.
→ 40
40. Leaf blades and bracts not prominently keeled on abaxial surface.
Fimbristylis
40. Leaf blades and bracts with midrib forming prominent keel on abaxial surface.
→ 41
41. Inflorescence bracts not ciliate; scales not spinose.
Scirpus
41. Inflorescence bracts ciliate proximally; scales with spinose tip.
Oxycaryum
42. Leaves with 2 lateral groups of hairs (at least some hairs 0.3 mm) at junction of blade and sheath.
Bulbostylis
42. Leaves glabrous or with only short hairs at junction of blade and sheath.
→ 43
43. Inflorescences apparently lateral; proximal bract erect, appearing to be continuation of stem (see Plate 2. G).
→ 44
43. Inflorescences evidently terminal (sometimes some axillary); bracts ascending or spreading, none appearing to be continuation of stem.
→ 46
44. Achenes faintly to prominently rugose or transversely ridged.
Schoenoplectus
44. Achenes smooth, papillose, or longitudinally ridged.
→ 45
45. Spikelets with 8–25 scales.
Isolepis
45. Spikelets with (1–)3 scales.
Lipocarpha
46. Spikelets with all scales subtending flowers.
Isolepis
46. Spikelets with 1+ proximal scales empty.
→ 47
47. Styles 2-fid; achenes biconvex.
Fimbristylis
47. Styles 3-fid; achenes trigonous or round in cross section.
→ 48
48. Plants annual, not rhizomatous; widest leaves not more than 2 mm wide; achenes usually 1.5 mm or less, reticulate-honeycombed.
Fimbristylis
48. Plants perennial, rhizomatous; widest leaves usually more than 2 mm wide; achenes 1.5–3 mm, smooth or rugose.
→ 49
49. Inflorescences terminal, capitate; culms not more than 20 cm.
Remirea
49. Inflorescences terminal or some lateral, corymbose or subcapitate; culms usually 70+ cm.
Cladium
Source FNA vol. 23, p. 509. FNA vol. 23, p. 3. Authors: Peter W. Ball, A. A. Reznicek, David F. Murray.
Parent taxa Cyperaceae > Carex > sect. Vesicariae
Sibling taxa
C. aboriginum, C. abrupta, C. abscondita, C. acidicola, C. acutiformis, C. adelostoma, C. adusta, C. aestivalis, C. aggregata, C. alata, C. albicans, C. albida, C. albolutescens, C. albonigra, C. albursina, C. alma, C. alopecoidea, C. amphibola, C. amplectens, C. amplifolia, C. angustata, C. annectens, C. anthoxanthea, C. aperta, C. appalachica, C. aquatilis, C. arapahoensis, C. arcta, C. arctata, C. arctiformis, C. arenaria, C. argyrantha, C. arkansana, C. assiniboinensis, C. atherodes, C. athrostachya, C. atlantica, C. atrata, C. atratiformis, C. atrofusca, C. atrosquama, C. aurea, C. aureolensis, C. austrina, C. austrocaroliniana, C. backii, C. baileyi, C. baltzellii, C. barbarae, C. barrattii, C. basiantha, C. bebbii, C. bella, C. bicknellii, C. bicolor, C. bigelowii, C. biltmoreana, C. blanda, C. bolanderi, C. bonanzensis, C. brainerdii, C. brevicaulis, C. brevior, C. breweri, C. bromoides, C. brunnescens, C. brysonii, C. bulbostylis, C. bullata, C. bushii, C. buxbaumii, C. calcifugens, C. californica, C. canescens, C. capillaris, C. capitata, C. careyana, C. caroliniana, C. caryophyllea, C. castanea, C. cephaloidea, C. cephalophora, C. chalciolepis, C. chapmanii, C. cherokeensis, C. chihuahuensis, C. chordorrhiza, C. circinata, C. collinsii, C. communis, C. comosa, C. complanata, C. concinna, C. concinnoides, C. congdonii, C. conjuncta, C. conoidea, C. constanceana, C. cordillerana, C. corrugata, C. crawei, C. crawfordii, C. crebriflora, C. crinita, C. cristatella, C. crus-corvi, C. cryptolepis, C. cumberlandensis, C. cumulata, C. curatorum, C. cusickii, C. dasycarpa, C. davisii, C. davyi, C. debilis, C. decomposita, C. deflexa, C. densa, C. deweyana, C. diandra, C. digitalis, C. diluta, C. disperma, C. distans, C. disticha, C. divisa, C. divulsa, C. douglasii, C. duriuscula, C. ebenea, C. eburnea, C. echinata, C. edwardsiana, C. egglestonii, C. eleusinoides, C. elliottii, C. elynoides, C. emoryi, C. endlichii, C. engelmannii, C. epapillosa, C. exilis, C. exsiccata, C. extensa, C. festucacea, C. feta, C. filifolia, C. fissa, C. fissuricola, C. flacca, C. flaccosperma, C. flava, C. floridana, C. foenea, C. folliculata, C. formosa, C. fracta, C. frankii, C. fuliginosa, C. garberi, C. geophila, C. geyeri, C. gholsonii, C. gigantea, C. glacialis, C. glareosa, C. glaucescens, C. glaucodea, C. globosa, C. gmelinii, C. godfreyi, C. gracilescens, C. gracilior, C. gracillima, C. granularis, C. gravida, C. grayi, C. grisea, C. gynandra, C. gynocrates, C. gynodynama, C. halliana, C. hallii, C. harfordii, C. hassei, C. haydeniana, C. haydenii, C. heleonastes, C. helleri, C. hendersonii, C. heteroneura, C. heterostachya, C. hirsutella, C. hirta, C. hirtifolia, C. hirtissima, C. hitchcockiana, C. holostoma, C. hoodii, C. hookeriana, C. hormathodes, C. hostiana, C. houghtoniana, C. hyalina, C. hyalinolepis, C. hystericina, C. idahoa, C. illota, C. impressinervia, C. incurviformis, C. infirminervia, C. inops, C. integra, C. interior, C. interrupta, C. intumescens, C. jamesii, C. jonesii, C. joorii, C. juniperorum, C. kobomugi, C. kraliana, C. krausei, C. lachenalii, C. lacustris, C. laeviconica, C. laeviculmis, C. laevivaginata, C. lapponica, C. lasiocarpa, C. latebracteata, C. lativena, C. laxa, C. laxiculmis, C. laxiflora, C. leavenworthii, C. lemmonii, C. lenticularis, C. leporinella, C. leptalea, C. leptonervia, C. leptopoda, C. limosa, C. livida, C. loliacea, C. lonchocarpa, C. longii, C. louisianica, C. lucorum, C. lupuliformis, C. lupulina, C. lurida, C. lutea, C. luzulifolia, C. luzulina, C. lyngbyei, C. mackenziei, C. macloviana, C. macrocephala, C. macrochaeta, C. magellanica, C. manhartii, C. marina, C. mariposana, C. maritima, C. mckittrickensis, C. meadii, C. media, C. melanostachya, C. membranacea, C. mendocinensis, C. merritt-fernaldii, C. mertensii, C. mesochorea, C. michauxiana, C. microchaeta, C. microdonta, C. microglochin, C. micropoda, C. microptera, C. misera, C. missouriensis, C. mitchelliana, C. molesta, C. molestiformis, C. muehlenbergii, C. multicaulis, C. multicostata, C. muricata, C. muriculata, C. muskingumensis, C. nardina, C. nebrascensis, C. nelsonii, C. nervina, C. neurophora, C. nigra, C. nigricans, C. nigromarginata, C. normalis, C. norvegica, C. nova, C. novae-angliae, C. nudata, C. obispoensis, C. obnupta, C. obtusata, C. occidentalis, C. oklahomensis, C. oligocarpa, C. oligosperma, C. opaca, C. oreocharis, C. ormostachya, C. oronensis, C. ouachitana, C. ovalis, C. oxylepis, C. ozarkana, C. pachystachya, C. paeninsulae, C. paleacea, C. pallescens, C. panicea, C. pansa, C. parallela, C. parryana, C. pauciflora, C. paysonis, C. peckii, C. pedunculata, C. pellita, C. pelocarpa, C. pendula, C. pensylvanica, C. perdentata, C. perglobosa, C. petasata, C. petricosa, C. phaeocephala, C. picta, C. pigra, C. pityophila, C. planispicata, C. planostachys, C. plantaginea, C. platyphylla, C. pluriflora, C. podocarpa, C. polymorpha, C. praeceptorum, C. praegracilis, C. prairea, C. prasina, C. praticola, C. preslii, C. projecta, C. proposita, C. pseudocyperus, C. pumila, C. purpurifera, C. radfordii, C. radiata, C. ramenskii, C. rariflora, C. raynoldsii, C. recta, C. reniformis, C. retroflexa, C. retrorsa, C. richardsonii, C. roanensis, C. rosea, C. rossii, C. rostrata, C. rotundata, C. rufina, C. rupestris, C. ruthii, C. sabulosa, C. salina, C. sartwelliana, C. sartwellii, C. saxatilis, C. saximontana, C. scabrata, C. scabriuscula, C. schottii, C. scirpoidea, C. scoparia, C. scopulorum, C. senta, C. seorsa, C. serpenticola, C. serratodens, C. sheldonii, C. shinnersii, C. shortiana, C. siccata, C. silicea, C. simulata, C. socialis, C. sparganioides, C. specifica, C. spectabilis, C. specuicola, C. spicata, C. spissa, C. sprengelii, C. squarrosa, C. stenoptila, C. sterilis, C. stevenii, C. stipata, C. straminea, C. straminiformis, C. striata, C. striatula, C. stricta, C. styloflexa, C. stylosa, C. subbracteata, C. suberecta, C. subfusca, C. subnigricans, C. subspathacea, C. superata, C. supina, C. swanii, C. sychnocephala, C. sylvatica, C. tahoensis, C. tenax, C. tenera, C. tenuiflora, C. tetanica, C. tetrastachya, C. texensis, C. thornei, C. thurberi, C. timida, C. tincta, C. tompkinsii, C. tonsa, C. torreyi, C. torta, C. triangularis, C. tribuloides, C. trichocarpa, C. triquetra, C. trisperma, C. tuckermanii, C. tumulicola, C. turbinata, C. turgescens, C. typhina, C. umbellata, C. unilateralis, C. ursina, C. utriculata, C. vacillans, C. vaginata, C. vallicola, C. venusta, C. vernacula, C. verrucosa, C. vesicaria, C. vestita, C. vexans, C. virescens, C. viridula, C. vulpinoidea, C. whitneyi, C. wiegandii, C. willdenowii, C. williamsii, C. woodii, C. wootonii, C. xerantica
Subordinate taxa
Abildgaardia, Amphiscirpus, Blysmopsis, Bolboschoenus, Bulbostylis, Carex, Cladium, Cymophyllus, Cyperus, Dulichium, Eleocharis, Eriophorum, Fimbristylis, Fuirena, Isolepis, Kobresia, Kyllinga, Lipocarpha, Oxycaryum, Remirea, Rhynchospora, Schoenoplectus, Schoenus, Scirpus, Scleria, Trichophorum, Websteria
Name authority Dewey ex Schweinitz: Ann. Lyceum Nat. Hist. New York 1: 71. (1824) Jussieu
Web links 
Unless otherwise noted, all data comes from the online version of the Flora of North America, who have made most of their content available via a Creative Commons license (CC BY 4.0).



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(If the plant you're looking for doesn't show up in the auto-complete list, that means it either isn't described in Flora of North America yet, or it's listed under a synonym. And please note that Flora of North America is still missing several plant families, including Apiaceae, Boraginaceae, and Polemoniaceae.)

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