the margins are glandular as in Eragrostis Willdenoviana and Eragrostis major.

The base of the leaf may be narrower, broader than, or about the same as the breadth of the leaf-sheath. It may be rounded, amplexicaul or narrowed. At the base and just above the ligular region there will always be a white distinct zone in the lamina of all grasses called the collar. This collar varies in length and breadth according to the species of grass.

Fig. 16.—Transverse section of leaf-buds.
A. Conduplicate; 1, 2 and 3. leaf-sheaths; 4 and 5. leaf-blades. B. Convolute; 1 and 2, leaf-sheaths; 3 and 4. leaf-blades.

In young shoots all the leaf-blades are usually found folded at the terminal portions. In most cases the leaf-blade is rolled up inwards from one end to the other so that one margin is inside and the other outside. This folding is termed convolute. This is the kind of folding that is found in most grasses. However, there are some grasses such as Eleusine ægyptiaca and Chloris barbata, in which the folding is different. In these grasses the laminas are folded flat on their midribs so that each half of the blade is folded flat on the other, the inner surfaces being in contact. The leaves are said to be conduplicate in this case. When the leaves are conduplicate the shoots are more or less compressed. (See fig. 16.)

CHAPTER III.
THE INFLORESCENCE AND FLOWER.

The flowers of grasses are reduced to their essential organs, the stamens and the pistil. The flowers are aggregated together on distinct shoots constituting the inflorescence of grasses. Sooner or later all the branches of a grass-plant terminate in inflorescences which usually stand far above the foliage leaves. As in other flowering plants, in grasses also different forms of inflorescence are met with. But in grasses the unit of the inflorescence is the spikelet and not the flower.

The forms of inflorescence usually met with are the spike, raceme and panicle. When the spikelets are sessile or borne directly along an elongated axis as in Enteropogon melicoides the inflorescence is a spike. If the spikelets borne by the axis are all stalked, however short the pedicels may be, it is a raceme. It must, however, be remembered that true spikes are very rare. An inflorescence may appear to be a spike, but on a close examination it will be seen to consist of spikelets more or less pedicelled. Such an inflorescence, strictly speaking, is a spiciform raceme. The branches of the inflorescence in Paspalum scrobiculatum or Panicum javanicum are racemes and the whole inflorescence is a compound raceme. The inflorescence is a panicle when the spikelets are borne on secondary, tertiary or further subdivided branches. Panicles differ very much in appearance according to the relative length and stoutness of the branches. In Eragrostis tremula the panicle is very diffuse, in Eragrostis Willdenoviana less so. The panicle in Sporobolus coromandelianus is pyramidal and the branches are all verticillate, the lower being longer than the upper. The branches of a panicle are usually loose, spreading or drooping in most grasses. But in some species of grasses such as Pennisetum Alopecuros and Setaria glauca, the paniculate inflorescences become so contracted that the pedicels and the short branches are hidden and the inflorescence appears to be a spike. Such inflorescences as these are called spiciform panicles. The inflorescences in several species of Andropogon consist of racemes so much modified as to appear exactly like a spike. What looks like a spike in these cases consists of a jointed axis and each joint bears a pair of spikelets, one sessile and the other pedicelled.

The name rachis is given to the axis of the spike, raceme and panicle, whether the axis is the main one or of the branch. The rachis of the inflorescence is usually cylindrical. In some grasses it is zigzag as in Pennisetum cenchroides. It is very much flattened in Paspalum scrobiculatum, but somewhat trigonous in Digitaria sanguinalis. In very many grasses the rachis is continuous, but in a few cases it consists of internodes or joints which disarticulate at maturity. Many species of Andropogon have such jointed rachises. Sometimes the joints become greatly thickened and the surface hollowed out, the spikelets fitting in the cavities as in Rottboellia and Manisuris.

In panicles, especially when they are diffuse, the primary branches may be disposed irregularly or in verticils on the main axis. For example in the panicle of Eragrostis Willdenoviana, the branches are irregularly disposed, whereas in Sporobolus coromandelianus the branches are verticillate. In both these grasses fleshy cushions are developed in the axils of the branches. These swellings help to spread out the branches especially at the time of anthesis. The branches at the top spread out earlier than those below.

Sometimes at the base of the rachises, main or secondary, glandular streaks are seen as in the rachises of Sporobolus coromandelianus. These glands secrete a viscid juice at the time of anthesis.

Fig. 17.—The Spikelet of Dinebra arabica.
1 and 2. Empty glumes; 3, 4, 5, and 6. flowering glumes with flowers.

The spikelet may be considered as a specialised branch consisting of a short axis, the rachilla bearing a series of modified bracts, the glumes, the lower pair being empty but the others bearing flowers in their axils. The glumes are two-ranked and imbricating. As a type for the spikelet that of an Eragrostis or Dinebra may be chosen. (See fig. 17.) In this spikelet the rachilla bears a number of glumes alternating and imbricating. The first two glumes at the base of the spikelet do not bear any flowers and so these two glumes are usually called empty glumes. This is the case in almost all the species of grasses. The third and the subsequent glumes are regularly arranged on the slender rachilla alternately in two rows. In the axils of each of these glumes there is a flower, except perhaps in the topmost glume. The flower is usually enclosed by the glume and another structure found opposite the glume and differing very much from the glume. This is the palea. It is attached to the axis of the flower and its back is towards the rachilla. Generally there are two nerves in a palea and its margins are enclosed within those of the glume. The palea is homologous with the prophyllum which it very much resembles. The prophyllum is usually found in the branches of grasses, but it is not confined to grasses alone. It occurs in the branches of some species of Commelina.

The spikelets vary very much in their structure. The spikelets in grasses of several genera consist of only four glumes. As usual the first two glumes are empty and the remaining two are flower-bearing glumes. Both these glumes may have perfect flowers as in Isachne or the terminal one may contain a perfect flower, the lower having either a staminate flower or only a palea. Very often the spikelets are unisexual and the male and female spikelets may be on the same plant as in Coix Lachryma-Jobi and Polytoca barbata, or they may be on different plants as in Spinifex squarrosus.

The glumes of a