The evolutionary forces causing chromosomal speciation and adaptation are still enigmatic. Here we tested the Israeli evolutionary model of positive assciation of diloid chromosome number (2n) and genetic diversity with aridity stress in subterranean mde rats, on a 30-times-larger scale in Asia Minor. We analyzed both karyotype and allozyme diversity across Turkey, based on 37 allozymic loci in 20 localities of the Spalx kucodon and 4 localities of the Spaax ehrenbergi superspecies. We foumd extensive chromosomal speciation in S. leucodon (2n = 38, 40, 50, 54, 60, and 62) Speciation and adaptation, the major twin processes of evolution, are yet largely mysterious, notwithstanding the great past achievements and the present molecular biological revolution. The unresolved issues involve the relative importance of the relevant evolutionary forces, origin, genetics, mechanisms, modes, dynamics, and abiotic/biotic environmental correlates (1-6). This is true for most catalogued species, which are only a small fraction of the unknown number of living species (7). Likewise, the significance of karyotypic evolution has been extensively debated (6,(8)(9)(10)(11)(12)(13)(14)(15)(16)(17)(18)(19). Highlighting these extremely complex problems calls for multidisciplinary studies involving molecular, genetic, chromosomal, organismal, and ecological insights (e.g., ref. 1). Here we explore two major unresolved problems of evolutionary biology in mole rats: (i) What is the role of diploid chromosome number (2 n) values and allozymes in evolution, primarily in speciation and adaptation? and (ii) Is the evolutionary process in Spalax oriented primarily by stochastic, nonselective, and neutral factors, or, by contrast, is it driven by selective factors? In short, is the origin of species and adaptation chaotic or ordered (20), reflecting adaptive environmental patterns?The evolutionary model of subterranean mole rats of the Spalax ehrenbergi superspecies in Israel (1) supports the environmental theory of genic and chromosomal diversity in both speciation and adaptation. The four chromosomal species (2n = 52, 54, 58, and 60), previously considered one species, represent four biological sibling species at progressive stages of speciation (1) We show that in Turkish Spalax, speciation and adapta-