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<br />393 <br /> <br />DOUGLAS ET AL.-GlLA GEOMETRIC MORPHOMETRICS <br /> <br />CV2 <br /> <br />TABLE 2. CLASSIFICATION RESULTS FOR Gila cypha <br />FROM A CANONICAL ANAL'tSIS OF SHAPE COORDINATES. <br />Numbers in parentheses are classification results from t[)'C\ <br />truss analysis of McElroy and Douglas (1995). Key to V::.:::I <br />sample codes is given in Table 1. <br /> <br /> <br />DC <br /> <br />LC <br /> <br />ww <br /> <br />YR <br /> <br />BR <br /> <br />CC <br /> <br />BR <br />CC <br />DC <br />LC <br />WW <br />YR <br /> <br />24 (24) 0 (0) 0 (0) 0 (0) 1 (1) 0 (0) <br />0(0) 11 (11) 0 (0) 0 (0) 0 (0) 0 (0) <br />o (0) 0 (0) 22 (22) 0 (0) 0 (0) 0 (0) <br />o (0) 0 (0) 0 (0) 28 (28) 0 (0) 0 (0) <br />3 (1) 0 (0) 0 (0) 0 (1) 54 (55) 0 (0) <br />o (0) 0 (0) 0 (0) 0 (0) 0 (0) 5 (5) <br /> <br /> <br />97.3% of the specimens being correctly allocat- <br />ed to their collection site (Table 2). This value <br />is significantly different from that obtained <br />from 100 randomized canonical variate analyses <br />(mean of 65.5%; u = 3.50; P < 0.01). Speci- <br />mens from Westwater and Black Rocks, the two <br />sites with smallest D2 values, also group closest <br />to one another in canonical space (Fig. 2). <br /> <br /> <br />Body size and shape variation in Gila TOUusta.- <br />Roundtail chub from Rifle and Debeque can- <br />yons were significantly larger than those from <br />the other five populations but were indistin- <br />guishable from one another (Student-Neuman- <br />Keuls test; F6.20B = 9.34; P < 0.0001). As with G. <br />CYPha, all shape coordinate pairs differed signif- <br />icantly among populations (all P < 0.0001), and <br />a significant MANOVA resulted (Wilks' A = <br />0.002; X2288 = 1154.9; P < 0.0001). Here, vari- <br />ation in peduncle and head characteristics is <br />emphasized. Specimens from Cataract Canyon <br />(Appendix 2B) have a relatively shorter pedun- <br />cles that (again) taper in depth from anterior <br />to posterior, whereas those from Desolation <br />Canyon (Appendix 2C) are noticeably longer <br />and of uniform depth. Debeque (Appendix 2F) <br />and Rifle (not shown) Canyons have relatively <br />smaller heads. Indeed, the latter two popula- <br />tions are characterized by having all landmarks <br />of the head (with the exception of LMs 11, 13 <br />and 25; Fig. 1) placed relatively more anteriorly <br />when compared to other populations. Addition- <br />al aspects of shape variation are found in rela- <br />tionships of body depth to fin placement. For <br />example, Debequeand Rifle populations have <br />deepest bodies yet shortest distances between <br />pectoral and pelvic fins, whereas Westwater Can- <br />yon specimens seemingly have shallowest body <br />depths. The development of a nuchal hump is <br />slight in all G. TOUusta populations. <br />Three (of six) statistically significant canoni- <br />cal variates accounted for 85.3% of among- <br />group variation (Fig. 3). As with G. CYPha, all <br /> <br />8 <br /> <br />2 <br /> <br />@ <br /> <br />@) <br /> <br />2 <br /> <br />CV1 <br /> <br />e@ @ <br /> <br />Fig. 3. Shape variation among seven Gila robusta <br />populations based on the first two variates derived <br />from a canonical analysis of shape coordinates. Pop- <br />ulation abbreviations follow Table 1. Circles represent <br />95% confidence intervals for the group mean. <br /> <br />Mahalanobis distances (and therefore all <br />arnong-group comparisons) were significant (P <br />< 0.0001). Mahalanobis D2 values varied greatly. <br />The lowest [i.e., 11.9 sdu (= standard deviation <br />units)] occurred between Westwater and Black <br />Rocks specimens, which were closest together in <br />CV-space (Fig. 3). The highest value (76.5 sdu) <br />occurred between Cataract and Rifle Canyons. <br />Populations from Cataract and Desolation Can- <br />yons were well removed from the other five, <br />with 96.3% of all specimens correctly allocated <br />to site of origin (Table 3). This value is signifi- <br />cantly different from that obtained from 100 <br />randomized analyses (54.9%; u = 3.42; P < <br />0.01). <br /> <br />Body size and shape variation among all samples,- <br />As might be expected from the above, body size <br />(as measured by centroid size), varied among <br />all 13 samples. Two groups were detected (F12,350 <br />= 7.94; P< 0.0001): One consisted of G. TObusta <br />from Rifle and Debeque Canyons and G. CYPha <br />from the Little Colorado; the second consisted <br />of all other populations. <br />Relative warp analysis clearly separated pop- <br />ulations of G. cypha from those ofG. rOUusta, <br />except for Desolation and Caratact Canyons <br />(Fig. 4). Body shapes of G. CYPha at the latter <br />two locations were more rOUusta-like. Of all cy- <br />Pha-like forms, those from the Little Colorado <br />River were most distinct, paralleling the results <br />of the CVA of shape coordinates (Fig. 2). <br />Operational Taxonomic Units with low values <br />on the first relative warp (RWl) clearly have a <br />cypha-like morphology (i.e., deeper body with <br />pronounced nuchal hump; smaller head; lon- <br />ger, narrower peduncle; Fig. 5A), whereas those <br /> <br />!:. - <br /> <br /> <br />i <br /> <br />