Our knowledge of plant anatomy, and of those laws of growth which govern certain classes of plants to-day and in past time, has been very materially widened and extended by the facts revealed to us by the detailed study of Coal-Measure species. The modern science of Plant Biology, refounded by Charles Darwin, has thrown considerable light on the laws of plant life, and it enables us to correlate structural characteristics with physiological conditions of growth. Applying the knowledge gained from living plants to the study of such extinct types as permit of close microscopic examination, we may obtain a glimpse into the secrets of the botanical binomics of Palaeozoic times. The wider questions of climatic conditions depend very largely upon the evidence of fossil botany for a rational solution. As an instance of the best authenticated and most striking alternation in climatic conditions in comparatively recent times, we may cite the glacial period or Ice-Age. The existence of Arctic conditions has been proved by purely geological evidence, but it receives additional confirmation, and derives a wider importance from the testimony of fossil plants. In rocks deposited before the spread of ice from high northern latitudes, we find indubitable proofs of a widely distributed subtropical flora in Central and Northern Europe. Passing from these rocks to more recent beds there are found indications of a fall in temperature, and such northern plants as the dwarf Birch, the Arctic Willow and others reveal the southern extension of Arctic cold to our own latitudes.

The distribution of plants in time, that is the range of classes, families, genera and species of plants through the series of strata which make up the crust of the earth, is a matter of primary importance from a botanical as well as from a geological point of view.

Among the earlier writers, Brongniart recognised the marked differences between the earlier and later floras, and attempted to correlate the periods of maximum development of certain classes of plants with definite epochs of geological history. He gives the following classification in which are represented the general outlines of plant development from Palaeozoic to Tertiary times[41].

I. Reign of Acrogens

1.

Carboniferous epoch

2.

Permian epoch.
II. Reign of Gymnosperms

3.

Triassic epoch.

4.

Jurassic epoch (including the Wealden).
III. Reign of Angiosperms

5.

Cretaceous epoch.

6.

Tertiary epoch.

Since Brongniart’s time this method of classification has been extended to many of the smaller subdivisions of the geological epochs, and species of fossil plants are often of the greatest value in questions of correlation. In recent years the systematic treatment of Coal-Measure and other plants in the hands of various Continental and English writers has clearly demonstrated their capabilities for the purpose of subdividing a series of strata into stages and zones[42]. The more complete becomes our knowledge of any flora, the greater possibility there is of making use of the plants as indices of geological age[43].

FOSSIL PLANTS AND PHYLOGENY.

Not only is it possible to derive valuable aid in the correlation of strata from the facts of plant distribution, but we may often follow the various stages in the history of a particular genus as we trace the records of its occurrence through the geologic series. In studying the march of plant life through past ages, the botanist may sometimes follow the progress of a genus from its first appearance, through the time of maximum development, to its decline or extinction. In the Palaeozoic forests there was perhaps no more conspicuous or common tree than the genus long known under the name of Calamites. This plant attained a height of fifty or a hundred feet, with a proportionate girth, and increased in thickness in a manner precisely similar to that in which our forest trees grow in diameter. The exceptionally favourable conditions under which specimens of calamitean plants have been preserved, have enabled us to become almost as familiar with the minute structure of their stems and roots, as well as with their spore-producing organs, as with those of a living species. In short, it is thoroughly established that Calamites agrees in most essential respects with our well known Equisetum, and must be included in the same order, or at least sub-class, as the recent genus of Equisetaceae. As we ascend the geologic series from the Coal-Measures, a marked numerical decline of Calamites is obvious in the Permian period, and in the red sandstones of the Vosges, which belong to the same series of rocks as the Triassic strata of the Cheshire plain, the true Calamites is replaced by a large Equisetum apparently identical in external appearance and habit of growth with the species living to-day. In the more recent strata the Horse-tails are still represented, but the size of the Tertiary species agrees more closely with the comparatively small forms which have such a wide geographical distribution at the present time. Thus we are able to trace out the history of a recent genus of Vascular Cryptogams, and to follow a particular type of organisation from the time of its maximum development, through its gradual transition to those structural characters which are represented in the living descendants of the arborescent Calamites of the coal-period forests. The pages of such a history are frequently imperfect and occasionally missing, but others, again, are written in characters as clear as those which we decipher by a microscopical examination of the tissues of a recent plant.

As one of the most striking instances in which the microscopic study of fossil plants has shown the way to a satisfactory solution of the problems of development, we may mention such extinct genera as Lyginodendron, Myeloxylon and others. Each of these genera will be dealt with at some length in the systematic part of the book, and we shall afterwards discuss the importance of such types, from the point of view of plant evolution.

The botanist who would trace out the phylogeny of any existing class or family, makes it his chief aim to discover points of contact between the particular type of structure which he is investigating, and that of other more or less closely related classes or families.

Confining himself to recent forms, he may discover, here and there, certain anatomical or embryological facts, which suggest promising lines of inquiry in the quest after such affinities as point to a common descent. Without recourse to the evidence afforded by the plants of past ages, we must always admit that our existing classification of the vegetable kingdom is an expression of real gaps which separate the several classes of plants from one another. On the other hand our recently acquired and more accurate knowledge of such genera as have been alluded to, has made us acquainted with types of plant structure which enable us to fill in some of the lacunae in our existing classification. In certain instances we find merged in a single species morphological characteristics which, in the case of recent plants, are regarded as distinctive features of different subdivisions. It has been clearly demonstrated that in Lyginodendron, we have anatomical peculiarities typical of recent cycads, combined with structural characteristics always associated with existing ferns. In rare cases, it happens that the remarkably perfect fossilisation of the tissues of fossil plants, enables us not only to give a complete description of the histology of extinct forms, but also to speak with confidence as to some of those physiological processes which governed their life.