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sugarcane plumegrass

Habit Plants rhizomatous. Plants annual or perennial; synoecious, monoecious, or dioecious; primarily herbaceous, habit varied.
Culms

1-2.5 m;

nodes sericeous, hairs to 5 mm.

annual, usually solid, sometimes somewhat woody, sometimes decumbent, often branched above the base.

Sheaths

glabrate or glabrous;

auricles absent;

ligules 2-6 mm;

blades usually 35-70 cm long, 8-30 mm wide, adaxial surfaces glabrous or pilose.

Leaves

distichous;

sheaths usually open;

auricles usually absent;

abaxial ligules usually absent, occasionally present as a line of hairs;

adaxial ligules membranous, sometimes also ciliate, or of hairs, sometimes absent;

blades sometimes pseudopetiolate;

mesophyll radiate or non-radiate;

adaxial palisade layer absent;

fusoid cells usually absent;

arm cells usually absent;

kranz anatomy absent or present;

midribs usually simple, rarely complex;

adaxial bulliform cells present;

stomata with triangular or dome-shaped subsidiary cells;

bicellular microhairs usually present, with a long, narrow distal cell;

papillae absent or present.

Inflorescences

ebracteate (Paniceae) or bracteate (most Andropogoneae) panicles, racemes, spikes, or complex arrangements of rames (in the Andropogoneae), usually bisexual, sometimes unisexual;

disarticulation usually below the glumes, frequently in the secondary and higher order axes of the inflorescences.

Peduncles

40-80 cm, pilose;

panicles 6-15 cm wide, oblong or lanceolate;

rachises 15-30 cm, pilose;

lowest nodes densely pilose;

primary branches 2-13 cm, ascending or appressed to the rachises;

rame internodes 2-5.5 mm, pilose.

Spikelets

bisexual or unisexual, frequently paired or in triplets, the members of each unit usually with pedicels of different lengths or 1 spikelet sessile.

Glumes

usually 2, equal or unequal, shorter or longer than the adjacent florets, sometimes exceeding the distal florets;

florets 2(-4), usually dorsally compressed, sometimes terete or laterally compressed;

lower florets sterile or staminate, frequently reduced to a lemma;

upper florets usually bisexual;

lemmas hyaline to coriaceous, lacking uncinate hairs, often terminally awned;

awns single;

paleas of bisexual florets well-developed, reduced, or absent;

lodicules usually 2, sometimes absent, cuneate, free, fleshy, usually glabrous;

anthers 1-3;

ovaries usually glabrous;

haustorial synergids absent;

style branches 2, free and close or fused at the base.

Caryopses

hila usually punctate;

endosperm hard, without lipid;

starch grains simple;

embryos large in relation to the caryopses, usually waisted;

epiblasts usually absent;

scutellar cleft present;

mesocotyl internode elongated;

embryonic leaf margins usually overlapping, rarely just meeting, x = 5, (7), 9, 10, (12), (14).

Pedicels

2.5-5 mm, pilose.

Sessile

spikelets 4.2-6 mm long, 0.8-1.1 mm wide, straw-colored.

Callus

hairs (7)15-20(25) mm, longer than the spikelets, straw-colored or brown;

glumes usually glabrous;

lower glumes smooth, indistinctly 5-veined;

lower lemmas 3-5 mm, without veins;

upper lemmas 2.5-3.5 mm, 1-veined, entire;

awns 12-26 mm, straight or curved, terete basally;

lodicule veins sometimes extending into hairlike projections;

anthers 2.

Pedicellate

spikelets similar to the sessile spikelets, except frequently pilose.

2n

= 30, 60, 90.

Saccharum giganteum

Poaceae subfam. panicoideae

Distribution
from FNA
AL; AR; DC; DE; FL; GA; IL; KY; LA; MD; MO; MS; NC; NJ; NY; OK; PA; SC; TN; TX; VA
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Discussion

Saccharum giganteum grows in wet soils of bogs, swales, and swamps. Its range extends from the eastern and southeastern United States to Central America. It is a polymorphic, primarily chasmogamous species that intergrades morphologically with the primarily cleistogamous S. trinii (Hack.) Renvoize in Central America. The combination of long callus hairs and straight awns distinguishes it from all other species of Saccharum in the Flora region.

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

The subfamily Panicoideae is most abundant in tropical and subtropical regions, particularly mesic portions of such regions, but several species grow in temperate regions of the world. Within the Flora region, the Panicoideae are represented by 59 genera and 364 species. They are most abundant in the eastern United States (Barkworth and Capels 2000). Photosynthesis may be either C3 or C4. All three pathways are found in the subfamily, but the PCK and NAD-ME variants appear to have evolved only once, while the NADP-ME pathways seems to have evolved several different times (Giussani et al. 2001).

The Panicoideae were first recognized as a distinct unit by Brown (1814), earlier than any of the other subfamilial taxa of the Poaceae. Its early recognition is undoubtedly attributable to its distinctive spikelets. Recognition of the tribe Gynerieae is recent (Sanchez-Ken and Clark 2001) and its placement in the Panicoideae, rather than the Centothecoideae, should be regarded as tentative.

Spikelets with two florets are found in many other subfamilies, but rarely do they follow the pattern of the lower floret being sterile or staminate and the upper floret bisexual. Development of unisexual florets within the Panicoideae appears to be consistent across the subfamily (LeRoux and Kellogg 1999), but differs from that in the Ehrhartoideae (Zaitcheck et al. 2000).

The Paniceae and Andropogoneae have their conventional interpretation in this Flora, so far as the North American taxa are concerned. Molecular studies, however, while strongly supporting the monophyly of the Andropogoneae, show the Paniceae to be paraphyletic, with two distinct clades. In one of these clades, most taxa have a chromosome base number of x = 9, but some have x = 10, and the taxa are pan-tropical in origin. The taxa in the other clade, with one exception, have a chromosome base number of x = 10 and are American in origin. This latter clade is sister to the Andropogoneae, which also have a chromosome base number of x = 10 (Gomez-Martinez and Culham 2000; Giussanni et al. 2001; Barber et al. 2002).

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

Key
1. Blades of leaves on the lower 1/2 of the culms disarticulating from the sheaths; plants 2-15 m tall, unisexual, without axillary inflorescences; blades with midribs 5-15 mm wide
Gynerieae
1. Blades of most or all cauline leaves remaining attached to the sheaths; plants 0.05-6 m tall, usually bisexual, sometimes with unisexual inflorescences, often with axillary inflorescences; blades with midribs 0.2-5 mm wide.
→ 2
2. Glumes usually conspicuously unequal; lower glumes usually greatly exceeded by the upper florets; upper glumes from subequal to longer than the distal florets; lemmas of the upper florets usually coriaceous to indurate; disarticulation usually beneath the glumes, not in the axes of the inflorescence branches
Paniceae
2. Glumes usually subequal, usually exceeding and concealing the florets; lemmas of the upper florets hyaline to membranous; disarticulation frequently in the axes of the inflorescence branches
Andropogoneae
Source FNA vol. 25, p. 611. FNA vol. 25, p. 351. Author: Grass Phylogeny Working Group;.
Parent taxa Poaceae > subfam. Panicoideae > tribe Andropogoneae > Saccharum Poaceae
Sibling taxa
S. alopecuroides, S. baldwinii, S. bengalense, S. brevibarbe, S. coarctatum, S. officinarum, S. ravennae, S. spontaneum
Synonyms Erianthus giganteus
Name authority (Walter) Pers. Link
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