In practice, when gardeners wish to produce an abnormal condition in a tree or plant, they will, if they wish to dwarf it, graft it on a species or variety of diminished root power, and contrariwise, if they wish to increase its growth, will graft it upon a stock of strong root power. But in neither case can the graft be said to be diseased by the action of the roots of the stock.

When this root power is so far diminished as to produce complete albinism, the shoots from such roots appear to partake of this diminished power, and to lose the power of making roots, and thus become very difficult to propagate. It is sometimes said that albino cuttings cannot be rooted at all, but this is a mistake, for I have succeeded in striking such cuttings from the variegated leaved Hydrangea. It required much care to do it; they did not, however, retain their albino character after they rooted and started into growth.

Albinism and white variegation in leaves appear to be due to the chlorophyl in such leaves being able to resist the action of the three (red, yellow, and blue) rays of light. What we call color in any substance or thing is due to its reflecting these different rays in various proportions of combination and absorbing the rest of them, the various proportions giving the various shades of color. White is due to the reflection of all of them, and black to the absorption of them. In some plants with variegated foliage we have the curious fact that the cells containing chlorophyl reflecting one color produce cells which reflect an entirely different color. In the coleus "Lady Burrill," for instance, the lower half of the leaf is of a deep violet-crimson color, and the upper half is golden yellow. In other varieties of coleus, in Perilla nankiensis, and other plants, we have foliage without a particle of green in it, and yet they are perfectly healthy. This shows that green leaves are not absolutely necessary to the health of a plant.

As a proof of leaf variegation being a disease, the speaker alluded to cited a case in which a green leaved abutilon, upon which a variegated leaved variety had been grafted, threw out a variegated leaved shoot below the graft. This can easily be explained. The growth of the trunk or stem of all exogenous plants, or those which increase in size on the outside of the stem, is brought about by the descent of certain formative tissue called cambium, elaborated by the leaves and descending between the old wood and the bark, where it is formed into alburnum or woody matter. Some think that it is also formed by the roots and ascends from them as well as descending from the leaves. Be this as it may, there is no doubt about its descent. In such comparatively soft-wooded, free growing plants as the abutilon the descent of the cambium is very free and in considerable quantity, so that the stock would soon be inclosed in a layer of it descending from the graft. When being converted into woody matter it also forms adventitious buds which under certain favorable circumstances will emit shoots of the same character as the graft from which it was derived. The graft is such cases may be said to inclose the stock in a tube of its own substance, leaving the stock unaffected otherwise. The variegated shoot in this case was in reality derived from the downward growth of the graft and not from the original stock, which was not therefore contaminated by the graft. In cases where the stock is of much slower growth than the graft, or the graft is inserted upon a stock of some other species, the descending cambium does not inclose the stock, but makes layers of wood on the stem of the graft, which thus, as is frequently seen, overgrows the stock, sometimes to such an extent as to make it unsightly. Nobody ever saw an apple shoot from a crab stock, a pear from a quince stock, or a peach shoot from a plum stock. This is one of the arguments in favor of the view that cambium also rises from the roots.

Again, to show that the stock is not affected by the graft, or the graft by the stock, except as to root power, let any person graft a white beet upon a red beet, or contrariwise, when about the size of a goosequill, and when they have attained their full growth, by dividing the beet lengthwise he will find the line of demarkation between the colors perfectly distinct, neither of them running into the other.

The theory that leaf variegation is a disease has been held by many distinguished botanists and is in nowise new. But this theory has been controverted, and we think successfully, by other botanists, and it is not now accepted by the more advanced vegetable physiologists. There are now so many acute and industrious students and observers in every department of science, and the accumulation of facts is so rapid and so great, that very many of the older theories are being set aside as not in accord with the newly discovered facts. A student brought up in institutions where the old theories are inculcated has afterward to spend half his time in unlearning what he had been previously taught, and the other half in studying the new facts brought to his notice and testing the theories promulgated by men of science. Botanical science does not wholly consist in the classification and nomenclature of plants, but largely consists in a knowledge of vegetable anatomy and physiology, and these require much study and some knowledge of other sciences, such as chemistry, meteorology, geology, etc. Without such general knowledge it is difficult to form a harmonious theory in regard to any of the phenomena of plant life.


Vanilla, Cinnamon, Cocoanut.

The following interesting facts concerning the cultivation of the above products in the island of Ceylon, were given in Mr. H. B. Brady's recent address before the British Pharmaceutical Conference at Swansea: