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7/14/2009 5:01:47 PM
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5/22/2009 12:32:30 PM
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UCREFRP
UCREFRP Catalog Number
9336
Author
Douglas, M. E., M. R. Douglas, J. M. Lynch and D. M. McElroy
Title
Use of Geometric Morphometrics to Differentiate
USFW Year
2001
Copyright Material
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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 />
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