As has been previously indicated, the advance of spring in the northern interior is much more rapid than in the Mississippi Valley and on the Gulf coast. In other words, in the North, spring comes with a rush, and during the height of the migration season in Saskatchewan the temperature in the southern part of the Mackenzie Valley just about equals that in the Lake Superior area, which is 700 miles farther south. Such conditions, coupled with the diagonal course of the birds across this region of fast-moving spring, exert a great influence on migration and are the chief factors in the acceleration of speed of travel.
Variations in speed of migration in different parts of the country are illustrated also by the movements of the cliff swallow ([fig. 5]), which breeds from Mexico to Alaska and winters in Brazil and Argentina. It would be expected in spring to appear in the United States first in Florida and Texas, then in the southern Rocky Mountain region, and finally on the Pacific coast. As a matter of fact, however, the earliest spring records come from north-central California, where the bird usually is common before the first arrivals are observed in Texas or Florida. The route taken, for many years a migration problem, was solved when it was found that these swallows went around the Gulf of Mexico rather than across it. The isochronal lines on the map show the more rapid advance along the Pacific coast. By March 20, when the vanguard has not quite reached the lower Rio Grande in Texas, the species is already north of San Francisco in California.
ALTITUDES AT WHICH BIRDS TRAVEL
At one time students of bird migration held firmly to the theory that normal migration takes place at heights above 15,000 feet, reasoning (somewhat uncertainly) that flying becomes easier as altitude is gained. Since the development of the airplane, however, and with it man's exploration of the upper regions of the air, it has become common knowledge that rarefied atmosphere adds greatly to the difficulties of flight. This is due not only to the reduction in oxygen (whether for gasoline engine or the lungs of a bird) but also to the lack of buoyancy of rarefied air. Such birds as vultures, pelicans, cranes, and some of the hawks feel this the least, since compared with body weight the supporting surface of their wings is very great, but for the smaller and shorter winged birds lack of buoyancy at high altitudes presents a difficult obstacle in flight. Even when flying close to the earth, small birds have to keep their wings in rapid motion.
Another postulate favoring the high-altitude flying theory was that the wonderful vision of birds was their sole guidance during migratory flights; and to keep landmarks in view the birds were obliged to fly high, particularly when crossing wide areas of water. This will be considered in greater detail under Orientation ([p. 23]), so here it will be sufficient to say that birds rely only in part upon vision to guide them on migration. Also, it is to be remembered that there are definite physical limitations to the range of visibility even under perfect atmospheric conditions. Chief of these is the curvature of the earth's surface. Thus, if birds flew over the Gulf of Mexico to Louisiana and Florida at a height of 5 miles, they would still be unable to see a third of the way across. And yet this trip is made twice each year by thousands of thrushes, warblers, and others.
Actual knowledge of the altitude of migratory flight is scanty, though estimates obtained by means of the telescope, and still more accurate data resulting from altimeter observation from airplanes, are slowly accumulating. It is, of course, obvious that some birds that cross mountain ranges during migration must attain a great altitude. Observers at an altitude of 14,000 feet in the Himalayas have recorded storks and cranes flying so high that they could be seen only through field glasses. Being beyond the range of unaided vision they must have been at least 6,000 feet above the observers, or at an actual altitude of 20,000 feet above sea level. Such cases, however, are exceptional, as aviators have reported that they rarely meet birds above an altitude of 5,000 feet.
It is now known that migration in general is performed below an altitude of 3,000 feet. Some proof of this statement is available. Observations made from lighthouses and other points of vantage indicate that migrants commonly travel at altitudes of a very few feet to a few hundred feet above sea or land. Sandpipers, sanderlings (Crocethia alba), and northern phalaropes (Lobipes lobatus), observed in migration on the Pacific oceanic route, have been noted to fly so low that they were visible only as they topped a wave. Observers stationed at lighthouses and lightships off the English coast have similarly recorded the passage of land birds, which sometimes flew just above the surface of the water, and rarely above 200 feet. During the World War broad areas in the air were under constant close surveillance, and among the airplane pilots and observers many took more than a casual interest in birds. Of the several hundred records resulting from their observations only 36 were of birds flying above 5,000 feet, and only 7 above 8,500 feet. Cranes were once recorded at an altitude of 15,000 feet, while the lapwing (Vanellus vanellus) was the bird most frequently seen at high levels, 8,500 feet being its greatest recorded altitude.
These observations naturally relate only to daytime travelers, but there is no reason to believe that nocturnal migration is performed at higher altitudes. The fact that many birds are killed each year by striking the lanterns at lighthouses, or other man-made obstructions, does not, however, furnish conclusive proof that low altitudes are generally used during nocturnal flight, for it should be recalled that these accidents occur chiefly in foggy or unsettled weather, and also, that powerful lights have a great attraction for many species of birds. The altitude at which birds travel is affected by other weather conditions also. For example, flight at the higher elevations is facilitated on clear, warm days by the currents of warm air that ascend from broad areas.
ORIENTATION
There probably is no single aspect of the entire subject of bird migration that challenges our admiration for birds so much as the unerring certainty with which they 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 of birds marked with numbered bands afford 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.