Page:EB1911 - Volume 04.djvu/726

 The power of vegetative propagation is widely spread. When artificially divided small fragments of the gametophyte are found to be capable of growing into new individuals. Apart from the separation of branches by the decay of older portions, special gemmae are found in many species. In Aneura the contents of superficial cells, after becoming surrounded by a new wall and dividing, escape as bi-cellular gemmae. Usually the gemmae arise by the outgrowth of superficial cells, and become free by breaking away from their stalk. When separated they may be single cells or consist of two or numerous cells. In Blasia and Marchantia the gemmae are formed within tubular or cup-shaped receptacles, out of which they are forced by the swelling of mucilage secreted by special hairs.

Marchantiales.—The plants of this group are most abundant in warm sunny localities, and grow for the most part on soil or rocks often in exposed situations. Nine genera are represented in Britain. Targionia is found on exposed rocks, but the other forms are less strikingly xerophytic; Marchantia polymorpha and Lunularia spread largely by the gemmae formed in the special gemma-cups on the thallus, and occur commonly in greenhouses. The large thallus of Conocephalus covers stones by the waterside, while Dumortiera is a hygrophyte confined to damp and shady situations. Among the Ricciaceae, most of which grow on soil, Ricciocarpus and Riccia natans occur floating on still water. The dorsiventral thallus is constructed on the same plan throughout the group, and shows a lower region composed of cells containing little chlorophyll and an upper stratum specialized for assimilation and transpiration. The lower region usually forms a more or less clearly marked midrib, and consists of parenchymatous cells, some of which may contain oil-bodies or be differentiated as mucilage cells or sclerenchyma fibres. Behind the apex, which has a number of initial cells, a series of amphigastria or ventral scales is formed. These consist of a single layer of cells, and their terminal appendages often fold over the apex and protect it. Usually they stand in two rows, but sometimes accessory rows occur, and in Riccia only a single median row is present. The thallus bears two sorts of rhizoids, wider ones with smooth walls which grow directly down into the soil, and longer, narrower ones, with peg-like thickenings of the wall projecting into the cell-cavity. The peg-rhizoids, which are peculiar to the group, converge under shelter of the amphigastria to the midrib, beneath which they form a wick-like strand. Through this water is conducted by capillarity as well as in the cell cavities. The upper stratum of the thallus is constructed to regulate the giving off of the water thus absorbed. It consists of a series of air-chambers (fig. 6, B) formed by certain lines of the superficial cells growing up from the surface, and as the thallus increases in area continuing to divide so as to roof in the chamber. The layer forming the roof is called the “epidermis,” and the small opening left leading into the chamber is bounded by a special ring of cells and forms the “stoma” or air-pore. In most species of Riccia the air-chambers are only narrow passages, but in the other Marchantiales they are more extended. In the simplest cases the sides and base of the chambers perform the work of assimilation (e.g. Corsinia). Usually the surface is extended by the development of partitions in the chambers (Reboulia), or by the growth from the floor of the chamber of short filaments of chlorophyllous cells (Targionia. Marchantia, fig. 6). The stomata may be simply surrounded by one or more series of narrower cells, or, as in the thallus of Marchantia and on the archegoniophores of other forms, may become barrel-shaped structures by the division of the ring of cells bounding the pore. In some cases the lowermost circle of cells can be approximated so as to close the pore. In Dumortiera the air-chambers are absent, their formation being only indicated at the apex.

The sexual organs are always situated on the morphologically upper surface of the thallus. In Riccia they are scattered singly and protected by the air-chamber layer. The scattered position of the antheridia is also found in some of the higher forms, but usually they are grouped on special antheridiophores which in Marchantia are stalked, disk-shaped branch-systems (fig. 5). The individual antheridia are sunk in depressions from which the spermatozoids are in some cases forcibly ejected. The archegonial groups in Corsinia are sunk in a depression of the upper surface, while in Targionia they are displaced to the lower side of the anterior end of a branch. In all the other forms they are borne on special archegoniophores which have the form of a disk-shaped head borne on a stalk. The archegoniophore may be an upgrowth from the dorsal surface of the thallus (e.g. Plagiochasma), or the apex of the branch may take part in its formation. When the disk, around which archegonia are developed at intervals, is simply raised on a stalk-like continuation of the branch, a single groove protecting a strand of peg-rhizoids is found on the ventral face of the stalk (Reboulia). In the highest forms (e.g. Marchantia) the archegoniophore corresponds to the repeatedly branched continuation of the thallus, and the archegonia arise in relation to the growing points which are displaced to the lower surface of the disk. In this case two grooves are found in the stalk. The archegonia are protected by being sunk in depressions of the disk or by a special two-lipped involucre. In Marchantia and Fimbriaria an additional investment termed in descriptive works the perianth, grows up around each fertilized archegonium (fig. 1, 3, d). The simple sporogonium found in the Ricciaceae (fig. 4, A) has been described above; as the spores develop, the wall of the spherical capsule is absorbed and the spores lie free in the calyptra, by the decay of which they are set free. In Corsinia the capsule has a well-developed foot, but the sterile cells found among the spore-mother-cells do not become elaters, but remain thin-walled and simply contribute to the nutrition of the spores. In all other forms elaters with spirally thickened walls are found. The seta is short, the capsule being usually raised upon the archegoniophore. Dehiscence takes place either by the upper portion of the capsule splitting into short teeth or falling away as a whole or in fragments as a sort of operculum. The spores on germination form a short germ-tube, in the terminal cell of which the apical cell is established, but the direction of growth of the young thallus is usually not in the same straight line as the germ-tube. The Marchantiales are divided into a number of groups which represent distinct lines of advance from forms like the Ricciaceae, but the details of their classification cannot be entered upon here. The general nature of the progression exhibited by the group as a whole will, however, be evident from the above account.

Jungermanniales.—This large series of liverworts, which presents great variety in the organization of the sexual generation, is divided into two main groups according to whether the formation of archegonia terminates the growth of the branch or does not utilize the apex. The latter condition is characteristic of the more primitive group of the Anacrogynous Jungermanniaceae, in which the branch continues its growth after the formation of archegonia so that they (and later the sporogonia) stand on the dorsal surface of the thallus or leafy plant. In the Acrogynous Jungermanniaceae the plant is throughout foliose, and the archegonia occupy the ends of the main shoot or of its branches. The antheridia are usually globular and long-stalked. The capsule opens by splitting into four halves.

Jungermanniaceae Anacrogynae.—The great range of form in the sexual plant is well illustrated by the nine genera of this group