as separate teeth owing to the breaking down of the unthickened cell-walls. The numerous spores which have been developed in the spore sac can thus only escape from the pendulous capsule through narrow slits between the teeth, and these are closed in damp air. The unicellular spores when supplied with moisture germinate (fig. 12) and give rise to the sexual generation. A filamentous protonema is first developed, some of the branches of which are exposed to the light and contain abundant chlorophyll, while others penetrate the substratum as brown or colourless rhizoids. The moss-plants arise from single projecting cells, and numerous plants may spring from the protonema developed from a single spore.
 Fig. 12.—Funaria hygrometrica. (After Goebel.) |
| A, Germinating spores. s, Wall of spore; v, vacuole; w, rhizoid.
B, Part of a developed protonema. h, Creeping filament with brown walls from which the filaments of chlorophyll-containing cells (b) arise; k, young moss-plant; w, its first rhizoid. |
The majority of the mosses belong to the same great group as Funaria, the Bryales. The other two subdivisions of the Musci are each represented by a single genus. In the Andreaeales the columella does not extend to the upper end of the capsule, and the latter opens by a number of lateral slits. The Sphagnales also have a dome-shaped spore-sac continued over the columella, and, though their capsule opens by an operculum, they differ widely from other mosses in the development of the sporogonium as well as in the characters of the sexual generation. The three groups are described separately below, but some more general features of the mosses may be considered here.
On the whole mosses grow in drier situations than the liverworts, and the arrangements they present for the conduction of water in the plant are also more complete and suggest in some cases comparisons with the higher plants. In spite of this, however, they are in great part dependent on the absorption of water through the general surface of the shoot, and the power of rapid imbibition possessed by their cell-walls, the crowded position of the small leaves on the stem, and special adaptations for the retention of water on the surface, have the same significance as in the foliose liverworts. The different appearance of exposed mosses in dry weather and after a shower illustrates this relation to the water supply. The protonema is always a well-marked stage in the life-history. Not only does a moss-plant never arise directly from the spore, but in all cases of vegetative reproduction, apart from the separation of branches by decay of older regions of the plant, a protonema is found. Usually the protonema is filamentous and ceases to be evident after the plants have developed. But in some small mosses (e.g. Ephemerum) it plays the chief part in assimilation and lives on from year to year. In Sphagnum, Andreaea and some genera of the Bryales the protonema or some of its branches have the form of flat plates or masses of cells. The formation of the moss-plant on the protonema is always from a single cell and is similar in all mosses. The first three walls in this cell intersect one another, and define the three-sided pyramidal apical cell by means of which the shoot continues to grow. In Fissidens and a few other mosses the apical cell is two-sided. The leaves formed by the successive segments gradually attain their normal size and structure. Each segment of the initial cell gives rise to a leaf and a portion of the stem; the branches arise from the lower portion of a segment and stand immediately below a leaf. The leaves may form three vertical rows, but usually their arrangement, owing to the direction of the segment walls at the apex, becomes more complicated. Their growth proceeds by means of a two-sided apical cell, and the midrib does not become more than one cell thick until later. In addition to the leaves the stem often bears hair-like structures of different kinds, some of which correspond to modified branches of protonema. The branched filamentous rhizoids which spring from the lower region of the stem also correspond to protonemal branches. The structure of both stem and leaf reaches a high grade of organization in some mosses. Not only are thick-walled sclerenchymatous cells developed to give rigidity to the periphery of the stem and the midrib of the leaf, but in many cases a special water-conducting tissue, consisting of elongated cells, the end walls of which are thin and oblique, forms a definite central strand in the stem. In the forms in which it is most highly developed (Polytrichaceae) this tissue, which is comparable with the xylem of higher plants, is surrounded by a zone of tissue physiologically comparable to phloem, and in the rhizome may be limited by an endodermis. The conducting strands in the leaves show the same tissues as in the central strand of the stem, and in the Polytrichaceae and some other mosses are in continuity with it. The independent origin of this conducting system is of great interest for comparison with the vascular system of the sporophyte of the higher plants.
The sexual organs, with the exception of the antheridia of Sphagnum, are borne at the apices of the main shoot or of branches. Their general similarity to the mature antheridia and archegonia of liverworts and the main difference in their development have been referred to. The antheridia open by means of a cap cell or groups of cells with mucilaginous contents. The details of construction of the sporogonium are referred to below. In all cases (except Archidium) a columella is present, and all the cells derived from the archesporium produce spores, no elaters being formed. In a few cases the germination of the spore commences within the capsule. The development of the sporogonium proceeds in all cases (except in Sphagnum) by means of an apical cell cutting off two rows of segments. The first periclinal division in the region forming the capsule separates an inner group of cells (the endothecium) form the peripheral layer (amphithecium). In Sphagnum, as in Anthoceros, the archesporium is derived from the amphithecium; in all other mosses it is the outermost layer of the endothecium.
Vegetative propagation is widely spread in the mosses, and, as mentioned above, a protonema is always formed in the development of the new plant. The social growth of the plants characteristic of many mosses is a result of the formation of numerous plants on the original protonema and on developments from the rhizoids. Besides this, gemmae may be formed on the protonema, on the leaves or at the apex, and some mosses have specialized shoots for their better protection or distribution. Thus in Georgia the stalked, multicellular gemmae are borne at the ends of shoots surrounded by a rosette of larger leaves, and in Aulacomnium androgynum they are raised on an elongated leafless region of the shoot. In other cases detached leaves or shoots may give rise to new plants, and when a moss is artificially divided almost any fragment may serve for reproduction.
Even in those rare cases in which the sexual generation can be developed without the intervention of spore production from the tissues of the sporogonium, a protonema is formed from cut pieces of the seta or in some cases from intact sporogonia still attached to the plant. This phenomenon of apospory was first discovered in mosses, but is now also known in a number of ferns (see Pteridophyta).
A. Longitudinal section of apex of a bud bearing archegonia (ar), enclosed by the large leaves (y); ch, small perichaetial leaves.
B. Longitudinal section of the sporogonium borne on the pseudopodium (ps); c, calyptra; ar, neck of archegonium; sg′, foot; sg, capsule.
C. S. squarrosum. Ripe sporogonium raised on the pseudopodium (qs) above the enclosing leaves (ch); c, the ruptured calyptra; sg, capsule; d, operculum.
Sphagnales.—The single genus Sphagnum occupies a very distinct and isolated position among mosses. The numerous species, which are familiar as the bog-mosses, are so similar that minute structural characters have to be relied on in their identification. The plants occur in large patches of a pale green or reddish colour on moors, and, when filling up small lakes or pools, may attain a length of some feet. Their growth has played a large part in the formation of peat. The species are distributed in temperate and arctic climates, but in the tropics only occur at high levels. The protonema forms a flat, lobed, thalloid structure attached to the soil by rhizoids, and the plants arise from marginal cells. The main shoot bears numerous branches which appear to stand in whorls; some of them bend down and become applied to the surface of the main axis. The structure of the stem and leaves is peculiar. The former shows on cross-section a thin-walled central tissue surrounded by a zone of thick-walled cells. Outside this come one to five layers of large clear cells, which when mature are dead and empty; their walls are strengthened with a spiral thickening and perforated with round pores. They serve to absorb and conduct water by capillarity. The leaves have no midrib and similar empty cells occur regularly among the narrow chlorophyll-containing cells, which thus appear as a green network. The antheridia are globular and have long stalks. They stand by the side of leaves of special club-shaped branches. The archegonial groups occupy the apices of short branches (fig. 13, A.). The mature sporogonium consists of a wide foot separated by a constriction from the globular capsule (B). There is no distinct seta, but the capsule is raised on a leafless outgrowth of the end of the branch called a pseudopodium (C, qs). The capsule, the wall of which bears rudimentary stomata, has a small operculum but no peristome. There is a short, wide columella, over which the dome-shaped spore-sac extends, and no air-space is present between the spore-sac and the wall. In the embryo a number of tiers of cells are first formed. The lower tiers
