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variable in frequencies among populations being fixed for one of <br />the other of two alleles or having differing combinations of <br />homo- and heterozygotes. EST-2, which in some respects, has <br />problematic results (see discussion below), has a range of <br />frequencies which nevertheless show some semblance of geographic <br />trends (Fig. 6) with some populations fixed homozygous for the <br />111" allele (e.g., Sabino Canyon, Fossil Cr., E. Verde R.), or for <br />112" (e.g., Verde R., W. Clear Cr.), with the majority polymorphic <br />as were the two Bill Williams system samples; the 111" allele <br />occurs with greater frequency in most samples with the exception <br />of those from the upper Verde system.. At GPI-1 (Fig. 7), <br />frequencies vary widely with a 112" allele most common (homozygous <br />in several populations) relative to a 113". Again, there are <br />geographic trends in that the 113" allele occurs in samples from <br />the upper Gila and upper Verde systems with little or no <br />occurrence in the intervening area. A somewhat similar pattern <br />emerges in the Gila Basin with respect to the MPI-2 locus (Fig. <br />10) with respect to the "5" allele which is present at low to <br />moderate frequencies; that allele is prevalent in the two Bill <br />Williams samples. On the other hand, while varying widely in <br />frequencies, both alleles at the PGM locus are pervasive of the <br />entire basin with most samples polymorphic but one (Cienega Cr.) <br />fixed homozygous for the 112" allele and two samples (Fossil Spg., <br />Blue R.) homozygous for "1"; 112" occurs at greater frequencies in <br />most population samples but 111" is locally prevalent in the upper <br />Verde system samples. <br />Some loci, while being monomorphic over much of the Gila- <br />Bill Williams portion of the lower Colorado Basin, have some <br />relatively localized polymorphisms within that region. The AK-1 <br />locus (Fig. 2) has a disjunct occurrence of the 116" allele, <br />otherwise known only to the north of the Gila and Bill Williams <br />systems and possibly one Mexican sample, in the Sheehy Spring <br />sample from the extreme upper Santa Cruz portion of the Gila <br />Basin. Based on its extreme isolation, this may represent a <br />separate mutation from upper basin samples. The bGAL locus (Fig. <br />3) has some possible rare occurrences of allele 112" (otherwise <br />known in the upper basin and some Mexican samples) in samples- <br />from the upper Verde and Tonto Creek. CBP-1 (Fig. 4) again has <br />localized occurrence of a 112" allele in the upper Verde otherwise <br />mostly known from the upper basin. IDHP-2 (Fig. 8) shows a <br />similar pattern with regard to the "1" allele, which is however <br />common in the sample from the adjacent but independant Williamson <br />Valley; the remoteness of these samples from upper basin samples <br />raises a question of homology for the 111" allele in the two <br />regions. The LDH-B locus (Fig. 9) has a 111" allele unique to <br />samples from an area centered on the upper Gila Basin exclusive <br />of the Salt system, being most prevalent in those from the <br />southerly Santa Cruz (homozygous in Cienega Cr.) and San Pedro <br />systems, with the possible exception of occurrence in the San <br />Bernadino sample from the extreme northern Yaqui drainage. At <br />CK-A (Fig. 5), the 112" allele, otherwise known from population <br />12