Section-Cutting—Staining No method of examination can equal, for general applicability and usefulness, that of section-work. The relations of the parts to each other being preserved, it is possible to draw conclusions as to their actual relations which no other mode allows of, and we shall devote this concluding chapter to some account of the methods to be employed to this end. The apparatus required is not necessarily complicated. Reduced to its elements, it consists essentially only of a razor to cut the sections and a dish to receive them. It but seldom happens, however, that the relations of the parts in sufficiently thin sections can be preserved by such a rough-and-ready method, and frequently the object to be cut is of such small dimensions as to render it impossible to deal with it in this way. It is therefore necessary to “imbed” it, so as to obtain a handle by which to hold it, in such a way that it shall be equally supported in all directions. Moreover, since the human hand can only in exceptional cases be brought to such a pitch of skill Let us deal with the imbedding first. If it be desired to imbed a tissue which has merely been fixed with formalin, the block should be immersed in strong gum (made by saturating water with picked gum arabic, white and clean) for several days. It is then taken out and, without draining, transferred to the plate of a freezing microtome, and the sections cut from the frozen block, and mounted in glycerine at once. This plan is of limited usefulness, since it allows of very little differentiation of the tissue elements, and that only optical. To get the best results, some plan of staining must be adopted. Perhaps the simplest, and certainly a very excellent one, is as follows. After the tissue has been passed from the hardening, or fixing, fluid into the successive alcohols, as described, it is placed in the following solution. Take about forty grains of carmine and eighty grains of borax, dissolve in about an ounce of water, add to the mixture an ounce of methylated spirit, and let it A mixture of wax and almond oil, in proportions varying with the heat of the weather, usually about equal ones, is prepared. The piece of tissue is freed from superfluous spirit by being placed on a bit of blotting-paper for a minute or two, and is then immersed in a quantity of the wax-and-oil mixture contained in a little box of paper or lead-foil. The tissue is held on the point of a needle, and lifted up and down until it is coated with the mixture, and, before solidification of the mass sets in, is lowered into the box and left to cool. The block now furnishes a handle, and this should be wrapped round with paper, the sections cut with the keenest The simple method above detailed will answer most ordinary purposes, provided that a few precautions be attended to. The chief are as follows. The outside of the block of tissue must be sufficiently dry for the wax-and-oil to adhere to it. The razor must be extremely sharp, and must be kept so by application to a Turkey stone during the section-cutting. The blade must be drawn across the tissue from heel to point, and kept wetted with spirit the whole time, so as to prevent any dragging of the section. The transference of the section to the slide must be effected by means of a section-lifter, which may be made by beating out a piece of stout copper wire to a thin flat blade; or a small palette-knife, or German-silver lifter, may be purchased The question of staining sections is a very large one, and is becoming of daily increasing complexity. We cannot go into it here, further than to say that most sections cut from unstained tissue will yield excellent results if stained first with Delafield’s logwood solution (to be obtained at Baker’s) to a very slight extent, and then with a solution of safranin. The sections should be washed with tap-water after the logwood stain, and should be of a pale violet colour. If over-stained, the colour may to a great extent be removed by washing with a very weak solution of hydrochloric acid, about two drops of acid to each ounce of water, and repeated washing in tap-water to remove the acid, and restore the violet. The safranin stain should be weak, and should be allowed to act for some time. From this last the sections are transferred to strong spirit, the latter being renewed until the sections cease to give up the red dye; and they may then be mounted as described. The results with most Further information must be sought in the book already mentioned. Let us, in closing, warn the beginner of two things which are of general application in practical microscopy. The first is, not to be discouraged by failures. The manipulations are in many cases very delicate, and premiums must be paid to experience for insurance against failure in every one of the processes. The second is, that the most scrupulous cleanliness will hardly suffice to prevent contamination of preparation by the all-pervasive dust which, invisible to the eye, assumes colossal proportions under the microscope, and the particles of which have an unpleasant habit of collecting on the most interesting or most beautiful portion of the preparation. This can only be guarded against by careful filtration of all fluids, and constant watchfulness. A preparation properly made is a thing of beauty, and a joy for ever,—or if not for ever, at any rate for many years; and one such will repay an infinitude of pains taken in its production. |