Typha latifolia |
Typha angustifolia |
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broad-leaf cat-tail, common bulrush, common cattail, quenouille à feuilles larges, tule espedilla |
lesser cattail, narrow-leaf cat-tail, quenouille à feuilles étroites |
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Erect shoots | 150–300 cm; flowering shoots 1–2 cm thick in middle, stems 3–7 mm thick near inflorescence. |
150–300 cm, not glaucous; flowering shoots 5–12 mm thick in middle; stems 2–3 mm thick near inflorescence. |
Leaves | usually glaucous when fresh; sheath sides papery or membranous, margins narrowly clear, summit tapered into blade to distinctly shouldered, or rarely with firm, papery auricles; mucilage glands at sheath-blade transition usually colorless, obscure, absent from sheath center and blade; widest blades on shoot 10–23(–29) mm wide when fresh, 5–20 mm when dry, distal blades about equaling inflorescence. |
sheath sides membranous, margin broadly clear, summit with membranous auricles which often disintegrate late in season; mucilage glands at sheath-blade transition brown, absent from blade and usually from sheath center near summit; widest blades on shoot 4–12 mm wide when fresh, 3–8 mm when dry; distal blade usually markedly exceeding inflorescence. |
Inflorescences | staminate spikes contiguous with pistillate or in some clones separated by to 4(–8) cm of naked axis, about as long as pistillate, ca. 1–2 cm thick at anthesis; staminate scales colorless to straw-colored, filiform, simple, ca. 4 × 0.05 mm; pistillate spikes in flower pale green drying brownish, later blackish brown or reddish brown, in fruit often mottled with whitish patches of pistil-hair tips, 5–25 cm × 5–8 mm in flower, 24–36 mm thick in fruit; compound pedicels in fruit bristle-like, variable in same spike, 1.5–3.5 mm; pistillate bracteoles absent. |
staminate spikes separated from pistillate by 1–8(–12) cm of naked axis, ca. as long as pistillate, 1 cm thick in anthesis; staminate scales variable in same spike, straw-colored to medium brown, filiform, simple to bifid or sometimes cuneate and irregularly branched, to 6 × 0.1 mm; pistillate spikes in flower when fresh dark brown with whitish stigmas (drying brown), later medium brown, in fruit when fresh as stigmas wear off often greenish due to green carpodia, (4–)6–20 cm × 5–6 mm in flower, 13–22 mm in fruit; compound pedicels in fruit peg-like, 0.5–0.7 mm; pistillate bracteole blades forming spike surface before flowering, later exceeded by stigmas and about equaling or slightly exceeded by pistil hairs, very dark to medium brown, much darker than (or sometimes as dark as) stigmas, irregularly spatulate, 0.6 × 0.1–0.2 mm, wider than or about as wide as stigmas, apex rounded (to acute). |
Staminate flowers | 5–12 mm; anthers 1–3 mm, thecae yellow, apex dark brown; pollen in tetrads. |
4–6 mm; anthers 1.5–2 mm, thecae yellow, apex dark brown; pollen in monads or some in irregular clusters. |
Pistillate flowers | 2–3 mm in flower, 10–15 mm in fruit; pistil-hair tips colorless, whitish in mass, not enlarged; stigmas persistent, forming solid layer on spike surface, pale green in flower, drying brownish, then reddish brown or usually distally blackish, spatulate, ovate to ovate-lanceolate, 0.6–1 × 0.2–0.25 mm; carpodia exceeded by and hidden among pistil hairs, straw-colored, apex rounded. |
2 mm in flower, 5–7 mm in fruit; pistil-hair tips medium brown, distinctly swollen at 10–20X; stigmas sometimes deciduous in fruit, in flower erect, elongating, bending to form surface mat, white in flower, drying brownish, later medium brown, narrowly linear-lanceolate, 0.6–1.4 × 0.1 mm; carpodia slightly exceeded by and visible among pistil hairs at mature spike surface, green when young and fresh, straw-colored with orange-brown spots when dry, apex nearly truncate. |
Seeds | numerous. |
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2n | = 30. |
= 30. |
Typha latifolia |
Typha angustifolia |
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Phenology | Flowering late spring–summer in north, spring–early summer in south. | Flowering late spring–summer. |
Habitat | Fresh to slightly brackish water or wet soil | Often somewhat brackish or subsaline water or wet soil |
Elevation | 0–2300 m [0–7500 ft] | 0–1900 m [0–6200 ft] |
Distribution |
AK; AL; AR; AZ; CA; CO; CT; DE; FL; GA; IA; ID; IL; IN; KS; KY; LA; MA; MD; ME; MI; MN; MO; MS; MT; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; SD; TN; TX; UT; VA; VT; WA; WI; WV; WY; AB; BC; MB; NB; NF; NS; NT; ON; PE; QC; SK; YT; Mexico; Central America; South America; Eurasia; Africa [Introduced, Australia (Tasmania (introduced))]
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AR; CA; CO; CT; DE; IA; IL; IN; KS; KY; MA; MD; ME; MI; MN; MO; NC; ND; NE; NH; NJ; NM; NV; NY; OH; OK; OR; PA; RI; SC; SD; TN; VA; VT; WA; WI; WV; WY; BC; MB; NB; NS; ON; PE; QC; SK; [Mont]; Eurasia
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Discussion | The erect shoots of Typha latifolia are more fanlike when young than in other North American species because the proximal leaves (dying by mid season) spread more widely. Undoubtedly native throughout its North American range, where it is often a codominant or minor component of marshes, wet meadows, fens, and other communities. In many places it is apparently being replaced by T. angustifolia and T. angustifolia × T. latifolia (T. ×glauca) at least partly due to human disturbance of habitats. There is a specimen of T. xglauca from Anticosti Island, Quebec. Locally in California and perhaps elsewhere where hybrids are common, the pollen grains of some T. latifolia plants separate slightly and may be shed partly as mixtures of triads, dyads, and monads, perhaps due to introgression ([S. G. Smith, unpublisheddeletion.). Ph.D. thesis]. See also hybrids in key and genus. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Prior to N. Hotchkiss and H. L. Dozier (1949), Typha domingensis was generally included within T. angustifolia in North America. Because of many misidentified specimens, range expansion in recent years, and undercollecting, the distribution on the margins of the main range is somewhat uncertain. Many literature reports are based on misidentified specimens. Some workers suggested T. angustifolia was early introduced from Europe into Atlantic Coastal North America and migrated westward (R. L. Stuckey and D. P. Salamon 1987). In recent decades it has expanded its range in many regions and become much more abundant, especially in roadside ditches and other highly disturbed habitats. For example, although it was known only from one Wisconsin station in 1929 (N. C. Fassett 1930) and was very local in Iowa in 1939 (A. Hayden 1939), it is now common and widespread in both states. As it often out-competes many native marsh species to produce very dense, pure stands, and hybridizes with T. latifolia to form the probably even more competitive T. ×glauca, T. angustifolia and T. ×glauca should perhaps be classified as noxious weeds in parts of North America. Beyond the main range of T. angustifolia, there are specimens of T. ×glauca from north-central Montana (Phillips County.), west-central Manitoba (La Pas), and Anticosti Island, Quebec. There are m Many erroneous reports have come from outside of Europe and North America. For hybrids see also genus and key. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 22, p. 282. | FNA vol. 22, p. 283. |
Parent taxa | ||
Sibling taxa | ||
Name authority | Linnaeus: Sp. Pl. 2: 971. (1753) | Linnaeus: Sp. Pl. 2: 971. (1753) |
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