We are, unfortunately, not taught to regard the travelling surfaces and movements of animals as correlated in any way to surrounding media, and, as a consequence, are apt to consider walking as distinct from swimming, and walking and swimming as distinct from flying, than which there can be no greater mistake. Walking, swimming, and flying are in reality only modifications of each other. Walking merges into swimming, and swimming into flying, by insensible gradations. The modifications which result in walking, swimming, and flying are necessitated by the fact that the earth affords a greater amount of support than the water, and the water than the air.

That walking, swimming, and flying represent integral parts of the same problem is proved by the fact that most quadrupeds swim as well as walk, and some even fly; while many marine animals walk as well as swim, and birds and insects walk, swim, and fly indiscriminately. When the land animals, properly so called, are in the habit of taking to the water or the air; or the inhabitants of the water are constantly taking to the land or the air; or the insects and birds which are more peculiarly organized for flight, spend much of their time on the land and in the water; their organs of locomotion must possess those peculiarities of structure which characterize, as a class, those animals which live on the land, in the water, or in the air respectively.

In this we have an explanation of the gossamer wing of the insect,—the curiously modified hand of the bat and bird,—the webbed hands and feet of the Otter, Ornithorhynchus, Seal, and Walrus,—the expanded tail of the Whale, Porpoise, Dugong, and Manatee,—the feet of the Ostrich, Apteryx, and Dodo, exclusively designed for running,—the feet of the Ducks, Gulls, and Petrels, specially adapted for swimming,—and the wings and feet of the Penguins, Auks, and Guillemots, especially designed for diving. Other and intermediate modifications occur in the Flying-fish, Flying Lizard, and Flying Squirrel; and some animals, as the Frog, Newt, and several of the aquatic insects (the Ephemera or May-fly for example[1]) which begin their career by swimming, come ultimately to walk, leap, and even fly.[2]

Every degree and variety of motion, which is peculiar to the land, and to the water- and air-navigating animals as such, is imitated by others which take to the elements in question secondarily or at intervals.

Of all animal movements, flight is indisputably the finest. It may be regarded as the poetry of motion. The fact that a creature as heavy, bulk for bulk, as many solid substances, can by the unaided movements of its wings urge itself through the air with a speed little short of a cannon-ball, fills the mind with wonder. Flight (if I may be allowed the expression) is a more unstable movement than that of walking and swimming; the instability increasing as the medium to be traversed becomes less dense. It, however, does not essentially differ from the other two, and I shall be able to show in the following pages, that the materials and forces employed in flight are literally the same as those employed in walking and swimming. This is an encouraging circumstance as far as artificial flight is concerned, as the same elements and forces employed in constructing locomotives and steamboats may, and probably will at no distant period, be successfully employed in constructing flying machines. Flight is a purely mechanical problem. It is warped in and out with the other animal movements, and forms a link of a great chain of motion which drags its weary length over the land, through the water, and, notwithstanding its weight, through the air. To understand flight, it is necessary to understand walking and swimming, and it is with a view to simplifying our conceptions of this most delightful form of locomotion that the present work is mainly written. The chapters on walking and swimming naturally lead up to those on flying.

In the animal kingdom the movements are adapted either to the land, the water, or the air; these constituting the three great highways of nature. As a result, the instruments by which locomotion is effected are specially modified. This is necessary because of the different densities and the different degrees of resistance furnished by the land, water, and air respectively. On the land the extremities of animals encounter the maximum of resistance, and occasion the minimum of displacement. In the air, the pinions experience the minimum of resistance, and effect the maximum of displacement; the water being intermediate both as regards the degree of resistance offered and the amount of displacement produced. The speed of an animal is determined by its shape, mass, power, and the density of the medium on or in which it moves. It is more difficult to walk on sand or snow than on a macadamized road. In like manner (unless the travelling surfaces are specially modified), it is more troublesome to swim than to walk, and to fly than to swim. This arises from the displacement produced, and the consequent want of support. The land supplies the fulcrum for the levers formed by the extremities or travelling surfaces of animals with terrestrial habits; the water furnishes the fulcrum for the levers formed by the tail and fins of fishes, sea mammals, etc.; and the air the fulcrum for the levers formed by the wings of insects, bats, and birds. The fulcrum supplied by the land is immovable; that supplied by the water and air movable. The mobility and immobility of the fulcrum constitute the principal difference between walking, swimming, and flying; the travelling surfaces of animals increasing in size as the medium to be traversed becomes less dense and the fulcrum more movable. Thus terrestrial animals have smaller travelling surfaces than amphibia, amphibia than fishes, and fishes than insects, bats, and birds. Another point to be studied in connexion with unyielding and yielding fulcra, is the resistance offered to forward motion. A land animal is supported by the earth, and experiences little resistance from the air through which it moves, unless the speed attained is high. Its principal friction is that occasioned by the contact of its travelling surfaces with the earth. If these are few, the speed is generally great, as in quadrupeds. A fish, or sea mammal, is of nearly the same specific gravity as the water it inhabits; in other words, it is supported with as little or less effort than a land animal. As, however, the fluid in which it moves is more dense than air, the resistance it experiences in forward motion is greater than that experienced by land animals, and by insects, bats, and birds. As a consequence fishes are for the most part elliptical in shape; this being the form calculated to cleave the water with the greatest ease. A flying animal is immensely heavier than the air. The support which it receives, and the resistance experienced by it in forward motion, are reduced to a minimum. Flight, because of the rarity of the air, is infinitely more rapid than either walking, running, or swimming. The flying animal receives support from the air by increasing the size of its travelling surfaces, which act after the manner of twisted inclined planes or kites. When an insect, a bat, or a bird is launched in space, its weight (from the tendency of all bodies to fall vertically downwards) presses upon the inclined planes or kites formed by the wings in such a manner as to become converted directly into a propelling, and indirectly into a buoying or supporting power. This can be proved by experiment, as I shall show subsequently. But for the share which the weight or mass of the flying creature takes in flight, the protracted journeys of birds of passage would be impossible. Some authorities are of opinion that birds even sleep upon the wing. Certain it is that the albatross, that prince of the feathered tribe, can sail about for a whole hour without once flapping his pinions. This can only be done in virtue of the weight of the bird acting upon the inclined planes or kites formed by the wings as stated.

The weight of the body plays an important part in walking and swimming, as well as in flying. A biped which advances by steps and not by leaps may be said to roll over its extremities,[3] the foot of the extremity which happens to be upon the ground for the time forming the centre of a circle, the radius of which is described by the trunk in forward motion. In like manner the foot which is off the ground and swinging forward pendulum fashion in space, may be said to roll or rotate upon the trunk, the head of the femur forming the centre of a circle the radius of which is described by the advancing foot. A double rolling movement is thus established, the body rolling on the extremity the one instant, the extremity rolling on the trunk the next. During these movements the body rises and falls. The double rolling movement is necessary not only to the progression of bipeds, but also to that of quadrupeds. As the body cannot advance without the extremities, so the extremities cannot advance without the body. The double rolling movement is necessary to continuity of motion. If there was only one movement there would be dead points or halts in walking and running, similar to what occur in leaping. The continuity of movement necessary to progression in some bipeds (man for instance) is further secured by a pendulum movement in the arms as well as in the legs, the right arm swinging before the body when the right leg swings behind it, and the converse. The right leg and left arm advance simultaneously, and alternate with the left leg and right arm, which likewise advance together. This gives rise to a double twisting of the body at the shoulders and loins. The legs and arms when advancing move in curves, the convexities of the curves made by the right leg and left arm, which advance together when a step is being made, being directed outwards, and forming, when placed together, a more or less symmetrical ellipse. If the curves formed by the legs and arms respectively be united, they form waved lines which intersect at every step. This arises from the fact that the curves formed by the right and left legs are found alternately on either side of a given line, the same holding true of the right and left arms. Walking is consequently to be regarded as the result of a twisting diagonal movement in the trunk and in the extremities. Without this movement, the momentum acquired by the different portions of the moving mass could not be utilized. As the momentum acquired by animals in walking, swimming, and flying forms an important factor in those movements, it is necessary that we should have a just conception of the value to be attached to weight when in motion. In the horse when walking, the stride is something like five feet, in trotting ten feet, but in galloping eighteen or more feet. The stride is in fact determined by the speed acquired by the mass of the body of the horse; the momentum at which the mass is moving carrying the limbs forward.[4]

In the swimming of the fish, the body is thrown into double or figure-of-8 curves, as in the walking of the biped. The twisting of the body, and the continuity of movement which that twisting begets, reappear. The curves formed in the swimming of the fish are never less than two, a caudal and a cephalic one. They may and do exceed this number in the long-bodied fishes. The tail of the fish is made to vibrate pendulum fashion on either side of the spine, when it is lashed to and fro in the act of swimming. It is made to rotate upon one or more of the vertebræ of the spine, the vertebra or vertebræ forming the centre of a lemniscate, which is described by the caudal fin. There is, therefore, an obvious analogy between the tail of the fish and the extremity of the biped. This is proved by the conformation and swimming of the seal,—an animal in which the posterior extremities are modified to resemble the tail of the fish. In the swimming of the seal the hind legs are applied to the water by a sculling figure-of-8 motion, in the same manner as the tail of the fish. Similar remarks might be made with regard to the swimming of the whale, dugong, manatee, and porpoise, sea mammals, which still more closely resemble the fish in shape. The double curve into which the fish throws its body in swimming, and which gives continuity of motion, also supplies the requisite degree of steadiness. When the tail is lashed from side to side there is a tendency to produce a corresponding movement in the head, which is at once corrected by the complementary curve. Nor is this all; the cephalic curve, in conjunction with the water contained within it, forms the point d’appui for the caudal curve, and vice versa. When a fish swims, the anterior and posterior portions of its body (supposing it to be a short-bodied fish) form curves, the convexities of which are directed on opposite sides of a given line, as is the case in the extremities of the biped when walking. The mass of the fish, like the mass of the biped, when once set in motion, contributes to progression by augmenting the rate of speed. The velocity acquired by certain fishes is very great. A shark can gambol around the bows of a ship in full sail; and a sword-fish (such is the momentum acquired by it) has been known to thrust its tusk through the copper sheathing of a vessel, a layer of felt, four inches of deal, and fourteen inches of oaken plank.[5]

The wing of the bird does not materially differ from the extremity of the biped or the tail of the fish. It is constructed on a similar plan, and acts on the same principle. The tail of the fish, the wing of the bird, and the extremity of the biped and quadruped, are screws structurally and functionally. In proof of this, compare the bones of the wing of a bird with the bones of the arm of a man, or those of the fore-leg of an elephant, or any other quadruped. In either case the bones are twisted upon themselves like the screw of an augur. The tail of the fish, the extremities of the biped and quadruped, and the wing of the bird, when moving, describe waved tracks. Thus the wing of the bird, when it is made to oscillate, is thrown into double or figure-of-8 curves, like the body of the fish. When, moreover, the wing ascends and descends to make the up and down strokes, it rotates within the facettes or depressions situated on the scapula and coracoid bones, precisely in the same way that the arm of a man rotates in the glenoid cavity, or the leg in the acetabular cavity in the act of walking. The ascent and descent of the wing in flying correspond to the steps made by the extremities in walking; the wing rotating upon the body of the bird during the down stroke, the body of the bird rotating on the wing during the up stroke. When the wing descends it describes a downward and forward curve, and elevates the body in an upward and forward curve. When the body descends, it describes a downward and forward curve, the wing being elevated in an upward and forward curve. The curves made by the wing and body in flight form, when united, waved lines, which intersect each other at every beat of the wing. The wing and the body act upon each other alternately (the one being active when the other is passive), and the descent of the wing is not more necessary to the elevation of the body than the descent of the body is to the elevation of the wing. It is thus that the weight of the flying animal is utilized, slip avoided, and continuity of movement secured.

As to the actual waste of tissue involved in walking, swimming, and flying, there is much discrepancy of opinion. It is commonly believed that a bird exerts quite an enormous amount of power as compared with a fish; a fish exerting a much greater power than a land animal. This, there can be no doubt, is a popular delusion. A bird can fly for a whole day, a fish can swim for a whole day, and a man can walk for a whole day. If so, the bird requires no greater power than the fish, and the fish than the man. The speed of the bird as compared with that of the fish, or the speed of the fish as compared with that of the man, is no criterion of the power exerted. The speed is only partly traceable to the power. As has just been stated, it is due in a principal measure to the shape and size of the travelling surfaces, the density of the medium traversed, the resistance experienced to forward motion, and the part performed by the mass of the animal, when moving and acting upon its travelling surfaces. It is erroneous to suppose that a bird is stronger, weight for weight, than a fish, or a fish than a man. It is equally erroneous to assume that the exertions of a flying animal are herculean as compared with those of a walking or swimming animal. Observation and experiment incline me to believe just the opposite. A flying creature, when fairly launched in space (because of the part which weight plays in flight, and the little resistance experienced in forward motion), sweeps through the air with almost no exertion.[6] This is proved by the sailing flight of the albatross, and by the fact that some insects can fly when two-thirds of their wing area have been removed. (This experiment is detailed further on.) These observations are calculated to show the grave necessity for studying the media to be traversed; the fulcra which the media furnish, and the size, shape, and movements of the travelling surfaces. The travelling surfaces of animals, as has been already explained, furnish the levers by whose instrumentality the movements of walking, swimming, and flying are effected.