Of the thallus, whatever its external form, by branched, continuous or septate, coenocytic tubes (Siphoneae and Fungi), or by simple or branched cell-threads (Red and many Green Algae), in both cases growing mainly or entirely at the apex of each branch, is almost universal in.
The Mosses and Liverworts include forms with a more or less leaf-like thallus, such as many of the liverworts, and forms in which the plant shows a differentiation into a stem bearing remarkably simple leaves, as in the true mosses.
The thallus in all cases consists of a branched filament of cells placed end to end, as in many of the Green Algae.
Or the thallus may have a leaf-like form, the branches from the central threads which form the midrib growing out mainly in one plane and forming a lamina, extended right and left of the midrib.
In the bulky forms colorless branches frequently grow out from some of the cortical cells, and, pushing among the already-formed threads in a longitudinal direction, serve to strengthen the thallus by weaving its original threads together.
Many of the lower forms of Brown Seaweeds (Phoeophyceae) have a thallus consisting of simple or branched cell threads, as in the green and red forms. The lateral union of the branches to form a solid thallus is not, however, so common, nor is it carried to so high a pitch of elaboration as in the Rhodophyceae.
A meristematic (cell-dividing) region occupying the whole of a certain transverse zone of the thallus, and cutting off new cells to add to the permanent tissue on both sides.
In the Fucaceae, on the other hand, there is a single prismatic apical cell situated at the bottom of a groove at the growing apex of the thallus, which cuts off cells from its sides to add to the peripheral, and from its base to add to the central permanent cells.
In many Laminariaceae the thallus also grows regularly in thickness by division of its surface layer, adding to the subjacent permanent tissue and thus forming a secondary meristem.
In the Bryophytes water is still absorbed, not only from the soil but also largely from rain, dew, &c., through the general surface of the subaerial body (thallus), or in the more differentiated forms through the leaves.
The plant-body (thallus) is always small and normally lives in very damp air, so that the demands of terrestrial life are at a minimum.
A sufficient description of the thallus of the liverworts will be found in the article BRYOIHYTA.
We may note the universal Li occurrence on the lower surface of the thallus of fixing ver and absorbing rhizoids in accordance with the terrestrial Worts.
The frondose (thalloid) Jungermanniales show no such differentiation of an assimilating tissue, though the upper cells of the thallus usually have more chlorophyll than the rest.
They serve to conduct water through the thallus, the assimilating parts of which are in these forms often raised above the soil and are comparatively remote from the rhizoid-bearing (water-absorbing) region.
Gonium largely independent of the supply of elaborated organic food from the thallus of the mother plant (the gametophyte).
In the liverworts we find fixation of the thallus by water-absorbing rhizoids; in certain forms with a localized region of water-absorption the development of a primitive hydrom or water-conducting system; and in others with rather a massive type of thallus the differentiation of a special assimilative and transpiring system.
The gametophyte, which bears the sexual organs, is either a free-living thallus corresponding in degree of differentiation with the lower liverworts, or it is a mass of cells which always remains enclosed in a spore and is parasitic upon the sporophyte.
From the primitive uniform Systems. mass of undifferentiated assimilating cells, which we may conceive of as the starting-point of differentiation, though such an undifferentiated body is only actually realized in the thallus of the lower Algae, there is, (1) on the one hand, a specialization of a surface layer regulating the immediate relations of the plant with its surroundings.
The remaining tissue of the plant-body, a tissue that we must regard phylogenetically as the remnant of the undifferentiated tissu~ of the primitive thallus, but which often undergoes further different,iation of its own, the better to fulfil its characteristically vital functions for the whole plant, is known, from its peripheral position in relation to the primitively central conducting tissue, as (3) the cortex.
The algal cells are never known to form spores while part of the lichen-thallus, but they may do so when separated from it and growing free.
The green (or blue-green) cells were termed gonidia by Wallroth, who looked upon them as asexual reproductive cells, but when it was later realized that they were not reproductive elements they were considered as mere outgrowths of the hyphae of the thallus which had developed chlorophyll.
Rees in 1871 produced the sterile thallus of a Collema from its constituents; later Stahl did the same for three species.
The thallus or body of the lichen is of very different form in different genera.
We can distinguish this class of forms as lichens with a homoiomerous thallus, i.e.
The majority of the lichens, however, possess a stratified thallus in which the gonidia are found as a definite layer or layers embedded in a pseudoparenchymatous mass of fungal hyphae, i.e.
In external form the heteromerous thallus presents the following modifications.
(a) The foliaceous (leaf-like) thallus, which may be either peltate, i.e.
(c) The crustaceous thallus, which is the most common of all, forms a mere crust on the substratum, varying in thickness, and may be squamose (in Squamaria), radiate (in Placodium), areolate, granulose or pulverulent (in various Lecanorae and Lecideae).
(d) The hypophloeodal thallus is often concealed beneath the bark of trees (as in some Verrucariae and Arthoniae), or enters into the fibres of wood (as in Xylographa and After Bonnier, from v.
I, Germinating ascospore (sp) 2, Thallus in process of formawith branching germ-tube tion.
In 1865 De Bary suggested the possibility that such lichens as Collema, Ephebe, &c., arose as a result of the attack of parasitic Ascomycetes upon the algae, Nostoc, Chroococcus, &c. In 1867 the observations of Famintzin and Baranetzky showed that the gonidia, in certain cases, were able to live outside the lichen-thallus, and in the case of Physcia, Evernia and Cladonia were able to form zoospores.
In colour also the thallus externally is very variable.
In the moist state of the thallus these colours are much less apparent, as the textures then become more or less translucent, and the thallus usually prevents the greenish colour of the gonidia (e.g.
The thallus may be free upon the surface of the substratum (e.g.
These may penetrate but slightly into the substratum, but the connexion established may be so close that it is impossible to remove the thallus from the substratum without injury (e.g.
The typical heteromerous thallus shows on section a peripheral, thin and therefore transparent, layer, the cortical layer, and centrally a mass of denser tissue the so-called medullary layer, between these two layers is the algal zone or gonidial layer (figs.
The surface of the thallus often exhibits outgrowths in the form of warts, hairs, &c. The medullary layer, which usually forms the main part of the thallus, is distinguished from the cortical layer by its looser consistence and the presence in it of numerous, large, air-containing spaces.
500 times.) A branched filiform thallus of Stigonema with the hyphae of the fungus growing through its gelatinous membranes.
Extremity of a branch of the thallus with a young lateral branch a; h, hyphae; g, cells of the alga; gs, the apex of the thallus.
- Section of Homoiomerous Thallus of Collema conglomeratum, with Nostoc threads scattered among the hyphae.
- In about 100 species of lichens peculiar growths are developed in the interior of the thallus which cause a slight projection of the upper or lower surface.