Orientation
There probably is no single aspect of the entire subject of bird migration that challenges our admiration so much as the unerring certainty with which birds cover thousands of miles of land and water to come to rest in exactly the same spot where they spent the previous summer or winter. The records from birds marked with numbered bands offer abundant proof that the same individuals of many species will return again and again to their identical nesting sites. These data show also that many individuals migrate in fall over the same route, year after year, making the same stops and finally arriving at the precise thicket that served them in previous winters.
The faculty that enables these birds to point their course accurately over vast expanses of land and water may, for want of a better term, be called a "sense of direction." Man recognizes this sense in himself, though usually it is imperfect and frequently at fault. Nevertheless the facility with which experienced hunters and woodsmen locate tiny camps or other points in forested or mountainous country, frequently cloaked by darkness or fog, with all recognizable landmarks obliterated seems due to this faculty. Ability to travel with precision over unmarked trails is not limited either to birds or to man. It is likewise possessed by many other mammals as well as by some insects and fishes, the well-known migrations of the salmon and the eel being notable examples.
Ability to follow a more or less definite course to a definite goal is evidently part of an inherited faculty. Both the path and the goal must have been determined either when the habit originated or in the course of its subsequent evolution. The theory is sometimes advanced that the older and more experienced birds lead the way, showing the route to their younger companions. This explanation may be acceptable for some species, but not for those in which adults and the young migrate at different times. The young cowbird that is reared by foster parents flocks with others of its kind when grown and in many cases can hardly be said to have adult guidance in migration. An inherited migratory instinct with a definite sense of the goal to be reached and the route to be followed must be attributed to these birds.
It is well known that birds possess wonderful vision. If they also have retentive memories subsequent trips over the route may well be steered in part by recognizable landmarks. The arguments against the theory of vision and memory are chiefly that much migration takes place by night and that great stretches of the open sea are crossed without hesitation. Nevertheless, the nights are rarely so dark that all terrestrial objects are totally obscured, and such features as coastlines and rivers are just those that are most likely to be seen in the faintest light, particularly by the acute vision of the bird and from its aerial points of observation. But some birds fly unerringly through the densest fog. Members of the Biological Survey, proceeding by steamer from the island of Unalaska to Bogoslof Island in Bering Sea, through a fog that was so heavy as to make invisible every object beyond a hundred yards, recorded the fact that flocks of murres, returning to Bogoslof, after quests for food, broke through the wall of fog astern, flew by the vessel, and disappeared into the mists ahead. The ship was heading direct for the island by the use of compass and chart, but its course was no more sure than that of the birds.
Some investigators have asserted that the sense of direction has its seat in the ears or nasal passages and thus that the bird is enabled to identify air currents and other phenomena. It has been found that disturbance of the columella or the semicircular canals of the inner ear will destroy the homing instinct of the racing pigeon, but experiments in the form of delicate operations, or closing the ears with wax, prove such a serious shock to the sensitive nervous system of the bird that they cannot be considered as affording conclusive evidence. Several years ago careful studies were made of the homing instinct of the sooty and noddy terns, tropical species that in the Atlantic region reach their most northern breeding point on the Dry Tortugas Islands, off the southwest coast of Florida. They are not known to wander regularly any appreciable distance farther north. It was found that some were able to return to their nests on the Tortugas after they had been taken on board ship, confined in cages below decks, and carried northward to distances varying from 400 to 800 miles before being released. Landmarks of all kinds were entirely lacking, and the birds certainly were liberated in a region in which they had had no previous experience.
Possibly the "homing instinct" as shown by these terns, by the man-o'-war birds that are trained and used as message carriers in the Tuamotu, Gilbert, and Marshall Islands, and by the homing pigeon, is not identical with the sense of perceptive orientation that figures in the flights of migratory birds. Nevertheless, it seems closely akin and is probably caused by the same impulses, whatever they may be and however they may be received. It should be remembered, however, that while homing may involve flight from a point that the bird has never before visited, the flight is always to a known point—that is, the bird's nest—while, on the other hand, the first migratory flight is always from the region of the bird's birth to a region it has never before visited. The spring migration might, of course, be more nearly considered as true "homing."
Some students have leaned strongly toward the possible existence of a "magnetic sense" as being the important factor in the power of geographical orientation. The theory that migratory birds might be responsive to the magnetic field of the earth was conceived as early as 1855, when some experimental work was done in Russia, and nearly 60 years later in France. Recently investigations in this field have been conducted by Yeagley (1947) and by Gordon (1948) with diametrically opposite results. The idea carries with it the implication that contained in the bird's body is an organ that is sensitive to the effect of its motion through the vertical component of the magnetic field and to other related factors. In the tests by Dr. Yeagley, 20 young homing pigeons were given training flights to their home loft from distances up to 100 miles. Permanent magnets were then affixed to the under side of the manus part of the wings of half of the birds while copper plates of equivalent weight were attached to the wings of the other half. All birds were released singly at an air-line distance of about 65 miles from the loft. The results were most suggestive, as only two of the birds carrying magnets returned to the loft, whereas eight of the controls returned.
With certain minor modifications, this experiment was repeated by Gordon. In this case 60 pigeons were used and releases were made from points up to 58 miles, where the direction of flight was such that the birds had to navigate across the gradient of the magnetic field. Every bird returned to its loft on the day of release regardless of whether it carried magnets or unmagnetized bars of the same weight.
Attempts to demonstrate the effect of radio waves on the navigational ability of birds also have produced contradictory results. In some of these tests, homing pigeons released near broadcasting stations have appeared to be hopelessly confused, whereas in others, apparently conducted in the same manner, no effects could be discerned. It is obvious that before the electromagnetic theory can be accepted or rejected, much additional experimental work is necessary.
In concluding this discussion of orientation it is pertinent to point out that the migratory instinct appears to be more or less transitory, that it is not persistent over an extended period. Migratory birds may be arrested en route, either by natural conditions, such as unusual food supplies, or forcibly by the act of man, and detained until the end or nearly the end of the migratory season, and then may not attempt to finish the journey, apparently having lost the migratory impulse. In the fall and early winter of 1929, abundant food and an open season caused an unusual number of mallard ducks to arrest their migration and remain in western Montana and northern Idaho. Later, however, a heavy snowfall with subzero temperatures suddenly cut off the food supply, with the result that great numbers of the birds starved to death, when a flight of a few hours would have carried them to a region of open water and abundant food.