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Training Manual Development Of Cultivars And Seed ... - icrisat

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Stem. The pearl millet stem or culm consists of nodes and internodes. The solid stem is thick at the<br />

base. The nodes are slightly swollen, and axillary buds are present in shallow grooves at the nodes. The<br />

nodes are hairy as well as glabrous with a gradual increase in hairiness from the base to the apex. The<br />

lower internodes are largely covered by the sheaths of the leaves, while the upper internodes are only<br />

partly covered. The upper internodes are more elongated than the lower ones. The height of the stem<br />

ranges from 0.5 m to 3.0 m.<br />

Tillers. The development of tillers starts from the lower nodes of the stem 3-5 weeks after emergence.<br />

These are called primary tillers. The secondary (axillary) tillers develop from the axillary buds at the upper<br />

nodes, usually after completion of flowering on the main stem.<br />

Leaves. The leaves are arranged alternately in two vertical rows on the culm. They are linear in shape<br />

comprising of a leaf sheath and a blade. The leaf sheaths are light green or purple and envelop the stem<br />

slightly above the nodes. The leaf sheaths overlap at the base of the stem but are open in the upper<br />

portion. The leaf sheath is glabrous and grooved. Ligules are present at the junction of the leaf blade and<br />

the leaf sheath. They are membranous, hairy, 4-5 mm long, and clasp the stem.<br />

The leaf blade is lanceolate, 90-100 cm long and 5-8 cm wide, with a pointed tip. The midrib is<br />

dull green. Auricles are present at the base of the leaf blade. The upper leaf surface is scarbid and hairy,<br />

while the lower one is smooth and glabrous.<br />

The leaf area of pearl millet is calculated by measuring the length and the width (at the broadest<br />

point) as suggested by Singh et al. (1970).<br />

Reproductive System<br />

Leaf area = Leaf length (cm) x Leaf width (cm) x 0.7236<br />

The shoot apex is transformed into a reproductive apex (Fig. 4) with the formation of the panicle<br />

meristem. The panicle meristem is bulbous, with a constriction at its base. It develops tunica and corpus<br />

layers in the inflorescence axis. These cells (tunica and corpus) are eumeristematic. The different floral<br />

organs develop from the apex. The organogenesis and maturation of organs in the spikelet apex are<br />

acropetal (Gill 1991).<br />

Inflorescence. The pearl millet inflorescence is a false spike, ranging from 5 to 150 cm in length and<br />

1 to 5 cm in diameter. The panicle is terminal, varying in shape from cylindrical to candle-shaped. The<br />

spike consists of a central rachis which is closely packed with fascicles. Each fascicle consists of one<br />

or more spikelets and a whorl of 70-80 bristles. The tip of the spike has only a single spikelet. The<br />

bristles may be free or united to form an involucre. About 10-15 bristles in the upper whorls are longer<br />

than those in the lower ones. The bristles are broader at the base and narrower at the tip. They are<br />

scarbid and green or purple. An inflorescence may contain 870-3000 spikelets with an average of 1600<br />

(Khairwal et al. 1990).<br />

Spikelets. The spikelets are small, lanceolate, and acute. Each spikelet consists of two glumes, one<br />

outer and one inner. The outer glume is broad, short, membranous, and truncate. The inner glume is<br />

broad and half the size of the spikelet. Between the two glumes, there are (two) florets. The lower floret<br />

is staminate and the upper floret is hermaphrodite (Fig. 5). Spikelets are generally bifloret but can<br />

sometimes be trifloret or tetrafloret; in rare instances, more than four florets are present (Maiti and Bisen<br />

1979).<br />

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