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pampas grass, silver pampas grass, Uruguayan pampas grass

Habit Plants usually dioecious, sometimes monoecious. Plants usually perennial, sometimes annual; when perennial, cespitose, rhizomatous, or stoloniferous.
Culms

2-4 m, usually 2-4 times as long as the panicles.

usually solid, rarely hollow.

Leaves

primarily basal;

sheaths mostly glabrous, with a dense tuft of hairs at the collars;

ligules 1-2 mm;

blades to 2 m long, 3-8 cm wide, mostly flat, cauline, ascending, arching, bluish-green, abaxial surfaces glabrous basally.

distichous;

sheaths usually open;

abaxial ligules usually absent;

auricles usually absent;

adaxial ligules of hairs or membranous and ciliate;

blades not pseudopetiolate;

mesophyll non-radiate;

adaxial palisade layer absent;

fusoid cells absent;

arm cells absent;

kranz anatomy absent;

midrib simple, usually with 1 vascular bundle (an arc of bundles in Cortaderia);

adaxial bulliform cells present or not;

stomata usually with dome-shaped or parallel-sided subsidiary cells (rarely slightly triangular or high dome-shaped);

bicellular microhairs usually present, distal cell long, narrow;

papillae usually absent.

Panicles

30-130 cm, only slightly, if at all, elevated above the foliage, whitish or pinkish when young.

Inflorescences

ebracteate (subtending leaf somewhat spatheate in Urochlaena Nees), usually paniculate, sometimes racemose or spicate, occasionally a single spikelet;

disarticulation usually above the glumes and between the florets, sometimes below the glumes or in the culms.

Spikelets

15-17 mm;

calluses to 1 mm, with hairs to 2 mm;

lemmas long-attenuate to an awn, awns 2.5-5 mm;

paleas to 4 mm;

stigmas exerted.

bisexual (sometimes with unisexual florets) or unisexual, with 1-7(20) bisexual or pistillate florets, distal florets in the bisexual spikelets often sterile or staminate;

rachilla extension present.

Glumes

2, usually equal, (1)3-7-veined, usually exceeding the distal florets;

florets laterally compressed;

lemmas firmly membranous to coriaceous, 3-9-veined, rounded across the back, glabrous or with non-uncinate hairs, these sometimes in tufts or fringes, lemma apices shortly to deeply bilobed, lobes often setaceous, midveins often extended as awns, awns usually geniculate, basal segment often flat and twisted;

paleas well-developed, sometimes short relative to the lemmas;

lodicules 2, usually free, usually fleshy, rarely with a membranous apical flap, glabrous or ciliate, often with microhairs, sometimes heavily vascularized;

anthers 3;

ovaries usually glabrous, rarely with apical hairs;

haustorial synergids present, sometimes weakly developed;

styles 2, bases usually widely separated.

Caryopses

and florets not separating easily from the rachilla.

separate from the lemmas and paleas;

hila punctate or long-linear;

embryos large or small relative to the caryopses;

endosperm hard;

starch grains usually compound;

epiblasts absent;

scutellar cleft present;

mesocotyl internode elongated;

embryonic leaf margins usually meeting, sometimes overlapping, x = 6,7, 9.

2n

= 72.

Cortaderia selloana

Poaceae subfam. danthonioideae

Distribution
from FNA
AL; CA; GA; LA; NJ; OR; SC; TN; TX; UT; VA; WA
[WildflowerSearch map]
[BONAP county map]
Discussion

Cortaderia selloana is native to central South America. It is cultivated as an ornamental in the warmer parts of North America. It was thought that it would not become a weed problem because most plants sold as ornamentals are unisexual, but it is now considered an aggressive weed in California and Bendigo, Australia. The weedy Australian plants are bisexual (Walsh 1994).

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

The Danthonioideae include only one tribe, the Danthonieae, which used to be included in the Arundinoideae. Conert (1987) placed Cortaderia in a tribe of its own, but its traditional inclusion in the Danthonieae is supported by more recent work (Hilu and Esen 1990; Hsiao et al. 1998; Barker et al. 2000; Grass Phylogeny Working Group 2001). The combination of haustorial synergids, ciliate ligules, elongated embryo mesocotyls, and C3 photosynthesis distinguishes the Danthonioideae from other subfamilies of the Poaceae.

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

Source FNA vol. 25, p. 299. FNA vol. 25, p. 297. Author: Grass Phylogeny Working Group;.
Parent taxa Poaceae > subfam. Danthonioideae > tribe Danthonieae > Cortaderia Poaceae
Sibling taxa
C. jubata
Subordinate taxa
Synonyms Gynerium argenteum, C. dioica
Name authority (Schult. & Schult. f.) Asch. & Graebn. N.P. Barker & H.P. Under
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