The situation at Tampico has been dealt with at length because, among all the locations for which data are available, it is the one that most strongly supports the topographical hypothesis. In none of the other cases have I been able to find a definite relation between the direction of migration and the features of the terrain. Studies of data from some of these stations disclose directional patterns that vary from night to night only slightly more than does the flight at Tampico. In three nights of observation at Lawrence, Kansas, marked by very high densities, the directional trend was north by north-northeast with a variation of less than 8°, yet Lawrence is so situated that there seems to be no feature of the landscape locally or in the whole of eastern Kansas or of western Missouri that coincides with this heading. At Mansfield, Louisiana, in twelve nights of observation, the strong east by northeast trend varied less than 15°, but again there appears to be no correlation over a wide area between this direction and any landmarks. And, at Progreso, Yucatán, where the vector resultants were 21° and 27° on successive nights, most of the birds seen had left the land and were beginning their flight northward over the trackless waters of the Gulf of Mexico. Furthermore, as I have elsewhere pointed out (1946: 205), the whole northern part of the Yucatán Peninsula itself is a flat terrain, unmarked by rivers, mountains, or any other strong physiographic features that conceivably might be followed by birds. [Illustration: FIG. 33. The nightly net trend of migrations at three stations in 1948. Each arrow is the vector resultant for a particular night, its length expressing the nightly density as a percentage of the total station density for the nights represented. Thus, the various station diagrams are not to the same scale.] In Figure 33 I have shown the directional patterns at certain stations where, unlike the cases noted above, there is considerable change on successive nights. Each vector shown is the vector resultant for one particular night. The lengths of the vectors have been determined by their respective percentages of the total computed density, or total station magnitude, for all the nights in question. In other words, the lengths of the individual vectors denote the percentile rôle that each night played in the total density. From the directional spread at these stations it becomes apparent that if most of the birds were traveling along a certain topographic feature on one night, they could not have been traveling along the same feature on other nights.