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Fig. 14 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 14. Additive tree (phenogram), based on Mahalanobis D2 distances (table 13), depicting meristic resemblance among nine groups of Aspidoscelis tesselata. Distances (similarities) between groups are computed by adding lengths of nodes between groups of interest. Terminal nodes represent the nine groups, and internal nodes represent horizontal distances between clusters. As an interpretation example, the resemblance between Conchas 6CE and Conchas 1CE is 7.2 + 3.2 + 2.2 + 2.8 + 5.6 = 21.0, while the resemblance between Conchas 6CE and Macho EC is 7.2 + 1.0 + 1.9 + 3.1 = 13.2.

Fig. 3 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 3. Electrophoretic phenotypes of sACOH, a monomeric enzyme, from liver homogenates of nine specimens of A. tesselata of pattern class CE from Conchas Lake State Park, New Mexico. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Lanes for individual lizards are labeled beside their patterns on the gel. Anode is to the right.

Fig. 11 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 11. Pattern of multivariate morphological variation among Aspidoscelis tesselata of pattern classes C (N = 44), E (N = 32), and New Mexico D (N = 5) from the vicinity of Sumner Lake State Park, De Baca County, New Mexico. Canonical variate scores were derived from a canonical variate analysis using meristic characters identified in table 10.

Fig. 2 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 2. Electrophoretic phenotypes of GPI, a dimeric enzyme, from erythrocyte hemolysates of six specimens of Aspidoscelis. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Note the very slight difference in migration between the products of the ballele versus callele. Lanes for individual lizards are labeled beside their patterns on the gel as follows: TESC, A. tesselata of pattern class CE from Conchas Lake State Park, New Mexico; and TESE, A. tesselata of pattern class E from Sandoval County, New Mexico. Anode is to the right.

Fig. 1 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 1. Geographic relationships among four northern collecting localities of Aspidoscelis tesselata of color pattern classes C, New Mexico D, and E and convenience classes CE and EC. Color patterns found at the four sites are (1) Conchas Lake State Park: CE and New Mexico D; (2) Sumner Lake State Park: C, New Mexico D, and E; (3) Puerto de Luna: E; and (4) Arroyo del Macho: EC.

Fig. 7 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 7. Color pattern variation in Aspidoscelis tesselata of pattern class CE from the vicinity of Conchas Lake State Park, San Miguel County, New Mexico. Morphological subgroup 6CE: A (RU 0002, 93 mm SVL); B (RU 0029, 96 mm SVL); morphological subgroup 1CE: C (RU 0013, 95 mm SVL); D (RU 0030, 89 mm SVL); E (RU 0021, 95 mm SVL); morphological subgroup 8CE: F (RU 0027, 86 mm SVL).

Fig. 4 in Congruent Patterns of Genetic and Morphological Variation in the Parthenogenetic Lizard Aspidoscelis tesselata (Squamata: Teiidae) and the Origins of Color Pattern Classes and Genotypic Clones in Eastern New Mexico

Fig. 4. Electrophoretic phenotypes of MPI, a monomeric enzyme, from liver homogenates of 11 specimens of Aspidoscelis. Letters below gel identify allozymes based on alleles present (table 3), and the genotype of each lizard is listed on the right. Lanes for individual lizards are labeled beside their patterns on the gel (with genotype) as follows: NEOTESA, B, and C, different pattern classes of the triploid A. neotesselata from Colorado; TESC and D, A. tesselata of pattern classes CE and D from Conchas Lake State Park, New Mexico; TESE, A. tesselata of pattern class EC from Arroyo del Macho, New Mexico; TESF, A. dixoni from New Mexico; TESF × PUN, triploid hybrid of A. dixoni × A. tigris punctilinealis from New Mexico; and TESG and H, A. dixoni of two pattern classes from Texas. Anode is to the right.

Figure 12 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 12. Two strophes of a less common type of song of Cettia brunnescens, West Bengal, India, May; same individual as in Figure 8; tape recording by Per Alström.

Figure 10. A cut from part II in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 10. A cut from part II and the beginning of part III of the song of Cettia brunnescens, West Bengal, India, May, different individual compared with Figures 8 and 9. Tape recording by Per Alström.

Figure 11. A in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 11. A, one song strophe of Cettia brunnescens, Uttaranchal, India, June; tape recording by Pratap Singh. B, the same recording as that shown in (A) but with the detail from part II at a higher time resolution. C, a different song strophe from the same individual. Detail from part II at a higher time resolution.

Figure 7 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 7. One song strophe of Cettia brunnescens, Arunachal Pradesh, India, June; tape recording by Pratap Singh.

Figure 9 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 9. One song strophe of Cettia brunnescens, West Bengal, India, May; tape recording by Per Alström.

Figure 8. A in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 8. A, one song strophe of Cettia brunnescens, West Bengal, India, May; tape recording by Per Alström. This is from a different individual than the song strophe shown in Figure 9. B, the same recording as that shown in (A) but with the detail from part II and the beginning of part III at a higher time resolution.

Figure 3 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 3. One song strophe of Cettia a. acanthizoides, Shaanxi, China, June; tape recording by Per Alström.

Figure 2 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 2. Plot of canonical scores from discriminant functions analysis between members of the Cettia acanthizoides group.

Figure 14. Cytochrome b in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 14. Cytochrome b tree of the three taxa in the Cettia acanthizoides complex and Cettia cetti albiventris, rooted with Phylloscopus chloronotus, estimated by Bayesian inference under the GTR + I model. Posterior probabilities (81 000 trees) are shown above nodes, and parsimony bootstrap values (1000 replicates) are shown below nodes.

Figure 5. A in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 5. A, one song strophe of Cettia a. acanthizoides, Fujian, China, May; tape recording by Per Alström. B, the same recording as that shown in (A) but with the detail from part II at a higher time resolution.

Figure 4 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 4. One song strophe of Cettia a. acanthizoides, Sichuan, China, May; tape recording by Per Alström.

Figure 13 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 13. Calls of Cettia a. acanthizoides (A: Shaanxi, China; B: Sichuan, China), Cettia a. concolor (C: Taiwan), and C. brunnescens (D: West Bengal, India). All tape recordings are by Per Alström, except for (C), which is from Liu (1995).

Figure 1 in Morphological, vocal and genetic divergence in the Cettia acanthizoides complex (Aves: Cettiidae)

Figure 1. Point map and extrapolated distributional ranges of the taxa in the Cettia acanthizoides complex. One-letter abbreviations indicate specimen localities, either studied by us or reported by museums and/or in the literature (Ludlow & Kinnear, 1944; Vaurie, 1972; Cheng, 1987; Inskipp & Inskipp, 1991; Wang et al., 1991; Rasmussen & Anderton, 2005; Spierenburg, 2005). See text for specimen locality marked 'b?'.