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cattail, cumbungi, southern cat-tail

cat-tail family

Habit Herbs, perennial, of fresh to slightly brackish wetlands, often emergent, rhizomatous, caulescent in flower, smooth, glabrous.
Erect shoots

150–400 cm, not glaucous; flowering shoots 1–2 cm thick in middle;

stems 3–4 mm thick near spike.

Leaves

sheath sides membranous, margin broadly clear, summit tapered to blade or with persistent, membranous auricles;

mucilage glands at sheath-blade transition orange-brown, numerous on entire sheath and proximal 1–10 cm of blade;

widest blades on shoot 6–18 mm wide when fresh, 5–15 mm when dry;

distal blade about equaling inflorescence.

basal and cauline, 2-ranked, mostly ascending;

sheaths open, margins overlapping, clear, summit tapered into blade or auriculate;

blades twisted into loose helix, narrowly linear-attenuate, apex acute, aerenchyma prominent.

Inflorescences

staminate spike separated from pistillate by (0–)1–8 cm of naked axis, ca. 1.4 X longer than pistillate, 1 cm thick at anthesis; staminate scales straw-colored to mostly bright orange-brown, variable in same spike, linear to cuneate, often laciniate distally, to 3–4 × 0.3 mm; pistillate spikes in flower when fresh bright cinnamon-brown with whitish stigmas (drying brownish), later orange- (to medium) brown, in fruit generally paler as stigmas and often bracteole blades wear off, ca. 6–35 cm × 5–6 mm in flower, 15–25 mm in fruit;

compound pedicels in fruit peg-like, ca. 0.6–0.9 mm; pistillate bracteole blades forming spike surface before flowering, later slightly exceeded by stigmas and slightly exceeding pistil hairs, straw-colored to bright orange-brown, much paler than to nearly same color as stigmas, irregularly narrowly to broadly spatulate or lanceolate, 0.8 × 0.1–0.3 mm, mostly wider than stigmas, apex variable in same inflorescence or different plants, acute or acuminate.

1, terminal, erect, equaled or exceeded by cauline leaves, cylindric, spikelike (hereafter "spikes"); staminate spike flowers deciduous but axis generally persistent; staminate spike distal to pistillate spike;

young spikes subtended by early-deciduous bracts resembling reduced foliage leaves, 1 bract subtending pistillate spike, 1 bract subtending and several within staminate spike;

,staminate spike flowers deciduous but axis generally persistent; staminate axis with numerous simple or branched scales arising among flowers; pistillate axis with numerous projections ("compound pedicels"), evident on denuded fruiting spike, each bearing several flowers; in some species flowers subtended by slender bracteoles.

Flowers

unisexual, staminate and pistillate on same plants, numerous, densely packed in unisexual spikes, minute, wind-pollinated (stigmas receptive several days before pollen is shed);

perianth probably represented by staminate scales and by hairs on stipes of pistillate flowers.

Staminate flowers

5 mm;

anthers 2–2.5 mm, thecae yellow, apex bright orange-brown;

pollen in single grains.

stipitate;

stamens 1–several, filaments connate;

anthers basifixed, connective distally extended.

Pistillate flowers

2 mm in flower, 8–9 mm in fruit;

pistil-hair tips straw-colored to orange-brown in mass, usually with 1 subapical bright orange-brown, generally enlarged cell;

stigmas often deciduous in fruit, in flower erect, elongating, bending to form surface mat, white in flower when fresh, later bright orange-brown, narrowly linear-lanceolate, ca. 1 × 0.1 mm;

carpodia slightly exceeded by pistil hairs, usually evident at fruiting spike surface, straw-colored, orange-spotted, apex broadly rounded.

hypogynous, stipitate (stipe bearing numerous straight hairs, developing after flowering, acting in wind dispersal of fruits);

pistils 1, 1-carpellate;

ovariesy 1-locular;

placentation apical;

ovules 1;

styles 1, unbranched;

stigmas 1, whitish or green, drying brown, 1-sided, smooth; agamous flowers numerous (ovaries modified after flowering as carpodia).

Fruits

follicles, fusiform;

pericarp clear, hyalinetransparent, splitting longitudinally in water to release seed.

Seeds

endosperm starchy, oily;

embryo cylindric.

2n

= 30.

Typha domingensis

Typhaceae

Phenology Flowering spring–summer.
Habitat Often in brackish water or wet soil
Elevation 0–2000 m (0–6600 ft)
Distribution
from FNA
AL; AR; AZ; CA; CO; DE; FL; GA; IL; KS; KY; LA; MD; MO; MS; NC; NE; NM; NV; OK; SC; TX; UT; VA; WY; Mexico; Central America; South America; West Indies; West Indies; Eurasia; Africa; Pacific Islands (New Zealand); Australia
[WildflowerSearch map]
[BONAP county map]
Boreal to tropical regions worldwide
[BONAP county map]
Discussion

Typha domingensis aggressively invades and forms nearly pure stands in brackish or nutrient-enriched wetlands in the Florida Everglades and elsewhere. It is established but does not mature fruits on the cold coast of northern California. There are specimens of putative hybrids with T. angustifolia beyond the main range of T. domingensis, in southeastern and northwestern Nebraska and southeastern Kentucky, and with T. latifolia in southeastern Nebraska. Vegetative T. domingensis or hybrids occur on the Atlantic Coast north as far as Delaware. (S. G. Smith, unpublished). The northern Illinois locality is a power plant cooling pond. The Wyoming record is from a hot spring and may be a hybrid with T. latifolia. Typha domingensis probably should be treated as a highly variable pantropic and warm temperate species, occurring to 40º E north and south latitude worldwide, and needing study to determine infraspecific taxa and delimitation from related species (B. G. Briggs and L. A. S. Johnson and B. G. Briggs 1968; S. G. Smith 1987). For hybrids see also genus and key.

Other References (plus corrections and additions) missing from this file. Have added and corrected these data with Bob’s 2d blue-line.

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

The extensive literature on morphology and taxonomy of Typhaceae has been recently reviewed by (U. Müller-Doblies and D. Müller-Doblies (1977); R. M. T. Dahlgren and H. T. Clifford (1982); R. M. T. Dahlgren et al. (19853); and J. W. Thieret and J. O. Luken (1996). The inflorescence is probably reduced from a compound structure.

Sparganium and Typha are very similar and perhaps should be placed in one family, as summarized by J. W. Thieret and J. O. Luken (1996): T (J. W. Thieret and J. O. Luken 1996). Other authors (e.g., D. Müller-Doblies 1970; U. Müller-Doblies and D. Müller-Doblies 1977; W. Schultze-Motel 1980) placed Sparganium in the Typhaceae.

Pre-Englerian [authors] ... placed Typha and Sparganium together in a single family, the Typhaceae. [H. G. A.] Engler (1886) put these genera in separate families, thus starting a tradition that has been followed by almost all subsequent authors until recently, when [D.] Müller-Doblies (1970) re-examined the relationships of the genera and concluded that "the five different characters by which Engler justified the family Sparganiaceae are wrong or, in two cases, without any significance... The few remaining but very obvious differences may be explained to a large extend [sic] by an adaptation of Typha to anemochory [wind-dispersal of propagules]...."

The phylogenetic relationships of the Typhales with other families remain controversial, and it seems best to treat the taxon as an isolated order of uncertain relationships pending further research. Various authors have placed the Typhales close to or within the Pandanales, Arales, Poales, Liliales, Pontederiales, or Philydrales or in the Commeliniflorae generally close to the Cyperales and Juncales (J. W. Thieret and J. O. Luken 1996).

Genus Genera 1, species ca. 8–13 (3 in the flora).

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

Source FNA vol. 22. FNA vol. 22, p. 278. Author: S. Galen Smith.
Parent taxa Typhaceae > Typha
Sibling taxa
T. angustifolia, T. latifolia
Subordinate taxa
Name authority Persoon: Syn. Pl. 2: 532. (1807) A. L. Jussieu
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