If we question the physical possibility of Landois’ explanation, an alternative is still open to us. The late Prof. Graham has applied the principle of Diffusion to the respiration of animals, and has shown how by a diffusion-process the carbonic acid produced in the remote cavities would be moved along the smaller tubes, and emptied into wider tubes, from which it could be expelled by muscular action. The carbonic acid is not merely exchanged for oxygen, but for a larger volume of oxygen (O 95 : CO2 81); and there is consequently a tendency to accumulation within the tubes, which is counteracted by the elasticity of the air vessels, as well as by special muscular contractions.[153]
Whether diffusion or injection by muscular pressure is the chief means of effecting the interchange of gases between the outer air and the inner tissues of the Insect, is a question to be dealt with by physical enquiry.
If we suppose two reservoirs of different gases at slightly different pressures to be connected by a capillary tube of moderate dimensions, such as one of the larger tracheæ of the Cockroach, transference by the molecular movements of diffusion would be small compared with that effected by the flow of the gas in mass. But if the single tube were replaced by a number of others, of the same total area, but of the fineness (say) of the pores in graphite, the flow of the gas would be stopped, and the transference would be effected by diffusion only. We may next consider tubes of intermediate fineness, say a tracheal tubule of the Cockroach at the point where the spiral thread ceases, and where the exchange of gases through the wall of the tubule becomes comparatively unobstructed. Such a tubule is about ·0001 in. diameter. If we may extend to such tubules the laws which hold good for the flow of gases in capillary tubes of much greater diameter, the quantity of air which might be transmitted in a given time by muscular pressure of known amount can be determined. Suppose the difference of pressure at the two ends of the tubule to be one-hundredth of an atmosphere, and further, that the tubule is a quarter of an inch long and ·0001 in. diameter. The tubule would then be cleared out every four seconds. Such a flow of air along innumerable tubules might well suffice for the respiratory needs of the Cockroach. Without laying too much stress upon this calculation, for which exact data are wanting, we may be satisfied that an appreciable quantity of air may be made by muscular pressure to flow along even the finer air passages of an Insect.[154]
Respiratory Movements of Insects.
By FÉLIX PLATEAU, Professor in the University of Ghent.
The respiratory movements of large Insects are in general very apparent, and many observers have said something about what they have seen in various species. It is only since the publication of Rathke’s memoir, however, that precise views have been gained as to the mechanism of these movements. This remarkable work, treating of the respiratory movements in Insects, the movable skeletal plates, and the respiratory muscles characteristic of all the principal groups, filled an important blank in our knowledge. But, notwithstanding the skill displayed in this research, many questions still remained unanswered, which required more exact methods than mere observation with the naked eye or the simple lens.
The writer, who was followed a year later by Langendorff, conceived the idea of studying, by such graphic methods as are now familiar, the respiratory movements of perfect Insects. He has made use of two modes of investigation. The first, or graphic method, in the strict sense of the term, consisted in recording upon a revolving cylinder of smoked paper the respiratory movements, transmitted by means of very light levers of Bristol board, attached to any selected part of the Insect’s exoskeleton. Unfortunately, this plan is only applicable to insects of more than average size. A second method, that of projection, consisted in introducing the Insect, carried upon a small support, into a large magic lantern fitted with a good petroleum lamp. When the amplification does not exceed 12 diameters, a sharp profile may be obtained, upon which the actual displacements may be measured, true to the fraction of a millimetre. Placing a sheet of white paper upon the lantern screen, the outlines of the profile are carefully traced in pencil so as to give two superposed figures, representing the phases of inspiration and expiration respectively. By altering the position of the Insect, so as to obtain profiles of transverse section, or of the different parts of the body, and, further, by gluing very small paper slips to parts whose movements are hard to observe, the successive positions of the slips being then drawn, complete information is at last obtained of every detail of the respiratory movements: nothing is lost.
This method, similar to that employed by the English physiologist, Hutchinson,[155] is valuable, because it enables us, with a little practice, to investigate readily the respiratory movements of very small Arthropods, such as Flies or Lady-birds. It has this advantage over all others, that it leaves no room for errors of interpretation.
Not satisfied with mere observation by such means as these, of the respiratory movements of Insects, the writer has also studied the muscles concerned, and, in common with other physiologists (Faivre, Barlow, Luchsinger, Dönhoff, and Langendorff), has examined the action of the various nervous centres upon the respiratory organs. The results at which he has arrived may be summarised as follows:—
1. There is no close relation between the character of the respiratory movements of an Insect and its position in the zoological system. Respiratory movements are similar only when the arrangement of the abdominal segments, and especially when the disposition of the attached muscles are almost identical. Thus, for example, the respiratory movements of a Cockroach are different from those of other Orthoptera, but resemble those of Hemiptera Heteroptera.