CHAPTER I
THE FERNS AND THEIR ALLIES

In its lowest forms vegetable life is a very simple affair. The minute Algæ which clothe damp surfaces with a green film show few indeed of the characteristics with which we are familiar in the higher plants. Certainly they are green, proving that the tiny cells of which they are composed contain the wonderful colouring matter—chlorophyll, by means of which they are able to assimilate carbon from the carbonic acid of the air. There is, however, in these lowly plants no sign of a stem, a leaf, or a root. As we ascend in the scale of vegetable life we begin to get an increasing number of distinctive characters. In the case of the Mosses we have plants with distinct stems and leaves. But Mosses have no true roots, neither is there any vascular (woody) tissue in their composition. Mounting yet higher in the scale we come to a very important and interesting group of plants usually referred to as the Vascular Cryptogams. In this group are included the Ferns, the Horsetails, and the Club Mosses. In passing, it may be pointed out that the term Cryptogam is a name which was originally given to the flowerless plants by Linnæus to indicate that the plan of fertilization was hidden. The name is still retained, but it has lost its meaning in this sense, in that since the introduction of high-power microscopes it is not necessarily more difficult to study the fertilization of the non-flowering plants than it is to watch the process in the kinds which bear blossoms.

A small acquaintance with the Vascular Cryptogams will show us that they approach very closely to the flowering plants, or Phanerogams, as they are called, in their general features. It is true that in the cases of the Club Mosses and Horsetails the leaves are small or very poorly developed, but with the Ferns the foliage is often of an advanced type. All the Vascular Cryptogams, apart from a few insignificant exceptions, produce real roots; and, as the name implies, in a botanical sense, evidence woody tissue in their composition. Whilst the Club Mosses and Horsetails are comparatively humble plants, the Ferns have reached a remarkable development in the arboreal species. These, of course, grow into large trees which may be fifty or more feet in height, with thick woody trunks. Our common Male Fern not infrequently forms a short trunk-like stem if it is allowed to remain in an undisturbed state for a number of years. Not all the Ferns are large or even of moderate size; many of the Filmy Ferns are so minute that they are often taken for Mosses by those who do not know any better.

All the Vascular Cryptogams show an alternation of generation; that is, in the life history of each plant there is a sexual and an asexual individual. As is fully explained later, the plant which arises from the spore of the Vascular Cryptogam is quite an insignificant body known as the prothallus. This has a comparatively short existence in most cases. It is on the prothallus, however, that the sexual organs are produced, and after fertilization the plant as we know it arises. This individual is called the sporophyte. The plant is responsible for the spores which are produced in little cases called sporangia. These are borne straight on the leaves, and are produced without anything in the way of fertilization having taken place. As far as the Ferns are concerned, the spores are all of one kind, but in certain of the Club Mosses two kinds of spores are produced.

Apart from a few exceptions the Vascular Cryptogams are mostly perennial in habit. In many cases other means of reproduction are available than the agency of spores. It is believed that the Bracken Fern is rarely reproduced by its spores. The increase of this plant seems to be very effectively carried out by means of the strong growing underground stems which shoot about in all directions. The Horsetails commonly propagate themselves in the same way, and it is this which makes them so difficult to eradicate in the garden. In the case of many Ferns a common mode of increase is that of budding off new plants on the leaf. The well-known New Zealand species, Asplenium bulbiferum, produces little buds on its fronds; these grow into small plants, so that each leaf may be responsible for dozens of new individuals. An even more singular case is the so-called Walking Fern from North America (Scolopendrium rhizophyllum), which bears long, tapering leaves something like our Hartstongue. These bend over in such a way that their tips touch the ground; on the point of the frond a bud is developed. Roots go down into the soil from the point of the frond, leaves shoot upwards, and thus a new plant is born. In some species of Club Moss the increase of the plant by spore production is supplemented by a plan which involves the bearing of bulbils on the shoots. These are vegetative processes which give rise to new individuals when they tumble to the ground.

It is of interest to consider the general characteristics of the members of the Fern tribe. As a rule the stem is either in the nature of a short underground process bearing a rosette of leaves, as in the case of the Male Fern and Hartstongue, or there is a horizontal stem more or less below the surface of the soil, such as is to be seen in the case of the Bracken Fern and the Polypody. Sometimes the stem assumes the proportions of a trunk, but these Tree Ferns only occur in the tropics. Where the stem of the Fern is upright it is properly termed a caudex, whilst in its horizontal form it is spoken of as a rhizome. There is actually some doubt as to the real nature of the frond of the Fern. Some botanists are inclined to believe that it is not really a leaf at all, but is a modified stem structure. Those who hold this view consider that the curious scaly structures so common amongst Ferns are really the leaves of the plant. Here the matter must be left on the present occasion, as it is proposed to use the terms leaf and frond as meaning the same thing.

An outstanding feature in the case of most Ferns is the remarkable manner in which the fronds are subdivided. In the case of the Male Fern it is seen that the upper part of the stalk, or rachis, as it is called, bears two rows of leaflets. These leaflets are properly referred to as pinnæ. When the leaflets are subdivided the divisions are spoken of as pinnules. These pinnules may be deeply lobed, and when this is the case each lobe is called a segment. In very large fronds the pinnules are again divided; the frond is then said to be tri-pinnate. Sometimes towards the top of the pinnæ or the frond the divisions become less pronounced; this character is designated pinnatifid. It should be noticed that the lower portion of the stalk, on which there are no pinnæ, is called a stipes. Of course in some cases, as with the Hartstongue, the leaf is quite undivided, without even any very pronounced indentations on the margin.

The unrolling of the Fern frond is a very beautiful process. Where the leaf is not divided in any way the process of expanding resembles the uncoiling of a watch-spring. Even where there are divisions the unrolling goes forward in the same manner with each subdivision, even down to the lobes. This particular mode of unfolding is called circinate. The texture of the leaves of Ferns is mostly thin and delicate, so that apart from some exceptions the foliage is not able to withstand the action of dry air. A notable feature with a large number of Ferns is the length of time which the leaves take to develop. The fronds of the Male Fern, for instance, start in the bud at least two years before they actually unfold. An examination will show that the roots of the Male Fern spring from the frond bases. It will be found that the position of the roots is the same in all Ferns.

With all Ferns the production of spores is confined to the leaves. In many instances there is no distinction between the fertile and the barren leaves. The stem does not start at once to produce leaves bearing the sporangia or spore cases. Thus, in the very young Fern the fronds are always barren; as the stem becomes older, fertile fronds are produced. In some cases the sporangia are borne on distinct leaves, as in the case of the Hard Fern, or on special parts of the leaves, in the manner to be seen in the Royal Fern. The difference in such cases is not really a very important distinction. A careful examination of the fertile portion of a Royal Fern frond will show a small amount of green tissue, or mesophyll, as it is called, at the lower portion of the pinnæ. Actually the fertile leaf, or part of a leaf, is similar to the barren portions, save that it produces a much reduced amount of green tissue or, in some cases, perhaps none at all.

In general appearance the Club Mosses bear a resemblance to the true Mosses, and hence the popular name, which is certainly rather misleading. With these plants the leaves are small and almost bristle-like, and are gathered closely round the stem. In many of the Club Mosses a large part of the stem lies closely along the ground, and from this at intervals roots are sent down into the soil and leafy shoots rise upwards. The sporangia are produced on special leaves, which are usually gathered together in the form of cones.