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828 COMA, 1991, NO. 3 <br />V IATE ANALYSIS OF STANDA RDIZED PCA SC ORES OF MEASUREMENTS AND STANDARD- <br />TABLE 4. CANONICAL AR <br />s are the results of an <br />f CVA loadin alyses with dorsal-fin rays included and <br />IZED COUNTS. The two <br />omitted. g <br />sets o <br />The same set of standardized PCA scores w as used for each analysis. <br /> Canonical vector loadings <br /> First analysis Second analysis <br />Character <br />1 <br />2 <br />1 <br />2 <br />PCA axis 1 0.13175 -0.02654 0.29673 0.04392 <br />43603 <br />-0 <br />PCA axis 2 0.80062 -1.02306 1.46241 <br />23940 <br />1 . <br />0.73585 <br />PCA axis 3 0.62336 <br />52598 <br />0 -1.27442 <br />-0.39820 . <br />0.92915 -0.97829 <br />PCA axis 4 <br />PCA axis 5 . <br />0.08375 -0.38383 0.24055 0.49310 <br />PCA axis 6 -0.09881 0.49592 -0.38436 <br />35367 <br />0 -0.41492 <br />0.39593 <br />Lateral-line scales 0.21902 -0.41333 . <br />omitted <br />Dorsal-fin rays -2.45691 -0.91952 <br />08175 <br />0 0.00905 -0.16599 <br />Anal-fin rays 0.03886 <br />03276 <br />-0 . <br />0.21546 -0.18225 -0.12537 <br />Pectoral-fin rays . <br />01176 <br />-0 0.08675 -0.07120 -0.05523 <br />Pelvic-fin rays . <br />00342 <br />-0 0.12206 -0.05297 -0.19980 <br />Gill rakers . <br />species, being 32.11 ± 2.40 in P. oregonensis and <br />37.27 ± 2.89 in P. umpquae, indicating slight <br />overlap. In general, if only the differences in <br />proportions had been used to distinguish these <br />species, such differences could be viewed as spu- <br />rious, resulting from allometric differences in <br />the individuals sampled. However, the methods <br />used to choose the interorbital width character <br />should ensure that the difference is real. To <br />ascertain the usefulness of this character over <br />the range of size, a linear regression of inter- <br />orbital width and standard length for P. oregon- <br />ensis and P. umpquae was performed, the sample <br />prediction intervals were distinct (Fig. 4), with <br />little overlap. For this regression, five very large <br />individuals of P. oregonensis were eliminated to <br />provide a more readable plot. If the large in- <br />dividuals had been included, the entire plot for <br />P. umpquae would have been compressed into <br />the left quarter of the graph. In all, the inter- <br />orbital width/prepectoral length proportion <br />represented the best single proportion available <br />for confident identification of these two species. <br />Apparent from the regression scatterplot is a <br />polymorphism in morphology between the two <br />samples of P. umpquae from the Umpqua River. <br />The two samples were taken from different <br />streams in the Umpqua drainage, and they were <br />also taken five years apart. Both populations <br />had a nearly perfect linear relationship between <br />the two measurements, clearly separable from <br />P. oregonensis, but the sample of large individ- <br />uals (UCLA W86-4) had a different linear re- <br />lationship than the sample of small individuals <br />(UCLA W81-15). Although there was no rec- <br />ognizable difference in counts or other mor- <br />phological features, these populations deserve <br />further study to evaluate the origin of this vari- <br />ation. <br />Phylogenetic relationships.-Gap-coding of six <br />meristics and 45 proportional measures (Table <br />5) yielded 38 multistate characters. Statistical <br />evaluation of variation between ingroup and <br />outgroup taxa supported the recognition of all <br />six counts, 17 of 18 head proportions, and 15 <br />of 27 body proportions as multistate characters. <br />These characters produced a single Wagner tree <br />(Fig. 5) with a consistency index (CI) of 0.868. <br />General consistency of the different groups of <br />characters demonstrated that counts had a CI <br />of 0.778, head proportions a CI of 0.857, and <br />body proportions a CI of 0.920. We note that <br />those features most easily quantified (meristics) <br />had the lowest CI. Although only a subset of <br />the body proportions contributed useful mul- <br />tistate characters, those that did yielded char- <br />acters of high consistency. A homoplasy matrix <br />for this analysis (Table 6) indicated that most <br />(20 of 28 homoplastic steps) were associated with <br />P. Lucius with nearly half of these between P. <br />Lucius and M. conocephalus. This tree supported <br />the monophyly of the genus Ptychocheilus, and <br />lineages within the genus were supported by <br />multiple synapomorphies (Table 7). These re- <br />sults confirmed the sister-group relationship of