Find research datasets worth reusing

Figure 1 in Long forsaken species diversity in the Middle American lizard Holcosus undulatus (Teiidae)

Figure 1. Geographical distribution of the formerly recognized subspecies of H. undulatus in Mexico (reproduced from Smith & Laufe, 1946); and sampling localities for H. undulatus. Numbers at dots refer to specific sample numbers of H. undulatus specimens used in this study. Locality data for these specimens are given in Table S1.

Figure 4 in Long forsaken species diversity in the Middle American lizard Holcosus undulatus (Teiidae)

Figure 4. Bayesian MCC species tree of H. undulatus inferred by simultaneous gene tree and species tree analysis of the mitochondrial and nuclear genes with *BEAST. Numbers above the branches are posterior probabilities.

Figure 3 in Long forsaken species diversity in the Middle American lizard Holcosus undulatus (Teiidae)

Figure 3. Geographical distribution of the six major, significantly supported haplotype clades identified in the Bayesian and ML phylogenetic analyses of the mitochondrial genes.

Figure 2 in Long forsaken species diversity in the Middle American lizard Holcosus undulatus (Teiidae)

Figure 2. Bayesian MCC tree of H. undulatus based on a partitioned analysis of the mitochondrial dataset. Outgroups are not shown. Numbers next to branches indicate posterior probability/bootstrap support values.

opennotspecifiedSep 2013View details →

Fig. 1 in Relationship between Oviposition Site Selection and Mandibular Asymmetry in Two Species of Lizard Beetles,Anadastus Pulchelloides Nakane and Doubledaya bucculentaLewis (Coleoptera: Erotylidae: Languriinae)

Fig. 1. Female adults, head morphology, host plants, inner wall of host internodes, and oviposition marks of Doubledaya bucculenta and Anadastus pulchelloides. A) D. bucculenta; B) head of D. bucculenta; C) Pleioblastus simonii, a host plant of D. bucculenta; D) completed oviposition mark by D. bucculenta; E) incomplete oviposition mark by D. bucculenta; F) inner wall of internode of P. simonii harboring a D. bucculenta adult; G) inner wall of internode of P. simonii with- out D. bucculenta; arrows indicate pith tissue. H) A. pulchelloides; I) head of A. pulchelloides; J) Arundinella hirta, a host plant of A. pulchelloides; K) completed oviposition mark of A. pulchelloides. Scale = 5 mm for A, 1 mm for B, D, E, F G and H, and 0.2 mm for I and K.

opennotspecifiedNov 2022View details →

Fig. 2 in Reproductive effort of unisexual and bisexual rock lizards (genus Darevskia)

Fig. 2. Stages of egg deposition and hatching of individuals of D. armeniaca individual at laboratory.

opennotspecifiedNov 2022View details →

Fig. 1 in Reproductive effort of unisexual and bisexual rock lizards (genus Darevskia)

Fig. 1. Interdependence among the components of life history. Reproductive effort increases te number and/or survival of offspring per season but decreases the potential number of reproductive seasons. Increase of an egg size positively affects offspring survival, but negatively - the number of eggs per reproductive season. Egg number and offspring survival both positively affect fitness. Red arrows show negative effects. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

opennotspecifiedNov 2022View details →

Fig. 3. A–G in Reproductive effort of unisexual and bisexual rock lizards (genus Darevskia)

Fig. 3. A–G. Gravid female individuals of five species on X - axis with body lengths (A), body weight before (FMB) (B), body weight after (FMA) (C), number of eggs (EN) (D), clutch weight (CLM) between small and large – bodies species (E), Reproductive effort (RE) (F), Relative egg weight (REM) (G) on Y - axis with 95% confidence Interval.

Fig. 3 in Allometry and morphological integration shape the chemical detection system in Liolaemus lizards (Squamata, Iguania)

Fig. 3. Allometry relationships of log10 SVL size with the palatal opening. Below, shapes reconstruction associated.

Fig. 4 in Allometry and morphological integration shape the chemical detection system in Liolaemus lizards (Squamata, Iguania)

Fig. 4. Phylomorphospace reconstruction showing in the X axis the first principal components (PC) scores and in the Y axis those second PC scores of: A-vomeronasal organ, B- palatal opening and C- tongue shape. In blue, those species belong to Argentinean group, and in red, those belong to Chilean group. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 5 in Allometry and morphological integration shape the chemical detection system in Liolaemus lizards (Squamata, Iguania)

Fig. 5. Integration patterns among vomeronasal organ (brown), palatal opening (black), tongue (cream) and the number of precloacal epidermal glands (orange). The number above indicates the coefficient of correlation, whereas black bars indicate those significant associations. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 2 in Allometry and morphological integration shape the chemical detection system in Liolaemus lizards (Squamata, Iguania)

Fig. 2. Phylogenetic relationships of Liolaemus lizards based on Esquerr´e et al. (2019), showing the relationships among studied species. In blue, those species belong to Argentinean group, and in red, those belong to Chilean group. Columns at the right show shapes symmetrized reconstruction of vomeronasal organ, palatal opening and tongue by each species. The size of the black circle represents the number of precloacal epidermal glands per studied species, whereas the black bars represent the size of snout-vent length. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 6 in Allometry and morphological integration shape the chemical detection system in Liolaemus lizards (Squamata, Iguania)

Fig. 6. Two block analyses showing the integration patterns of tongue (cream) with: A-palatal opening (black) and B– VNO (brown). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Fig. 1 in Allometry and morphological integration shape the chemical detection system in Liolaemus lizards (Squamata, Iguania)

Fig. 1. Drawing of Liolaemus cuyanus showing A-vomeronasal organ, B- palatal opening and. C- tongue. Yellow points correspond to landmarks set, and green points correspond to those landmarks used to reach symmetry and posteriorly were removed. Red points correspond to semi-landmarks. All were set on the right side; scale below corresponds to 1 mm. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

FIGURE 5 in Taxonomy, distribution, and conservation status of a rare arboreal lizard, Bronchocela celebensis Gray, 1845 (Reptilia: Agamidae) endemic to Sulawesi, Indonesia

FIGURE 5. Bronchocela celebensis in life (adult female, not collected) from Pangana Village, Central Sulawesi, Indonesia (Photo © J.A. McGuire).

FIGURE 3 in Taxonomy, distribution, and conservation status of a rare arboreal lizard, Bronchocela celebensis Gray, 1845 (Reptilia: Agamidae) endemic to Sulawesi, Indonesia

FIGURE 3. Principal Component Analysis (PCA) biplot of morphometric variation between Bronchocela celebensis (red), B. cristatella sensu stricto from Java (green) and sensu lato from adjacent islands of southern Sulawesi (blue), with (A1) combined sexes showing the morphological distinctiveness of B. celebensis; (A2) the same base biplots with vectors associated with species clusters. Each point represents an individual specimen, and the relative distance between two points is equivalent to the amount of dissimilarity.

FIGURE 2 in Taxonomy, distribution, and conservation status of a rare arboreal lizard, Bronchocela celebensis Gray, 1845 (Reptilia: Agamidae) endemic to Sulawesi, Indonesia

FIGURE 2. Boxplots of (A) head length, (B) snout–vent length, and (C) tail length of Bronchocela celebensis, B. cristatella sensu stricto from Java, and sensu lato from adjacent islands of southern Sulawesi; top, middle and bottom lines of the boxes indicate 75th percentile, median and 25th percentile, respectively.

FIGURE 1 in Taxonomy, distribution, and conservation status of a rare arboreal lizard, Bronchocela celebensis Gray, 1845 (Reptilia: Agamidae) endemic to Sulawesi, Indonesia

FIGURE 1. Current distribution map showing the collection/observation localities of Bronchocela celebensis (red) and its allopatric congener, B. cristatella sensu lato (blue) on adjacent islands of southern Sulawesi.

FIGURE 4 in Taxonomy, distribution, and conservation status of a rare arboreal lizard, Bronchocela celebensis Gray, 1845 (Reptilia: Agamidae) endemic to Sulawesi, Indonesia

FIGURE 4. Bronchocela celebensis holotype (NHMUK 1946.8.11.48, adult female) from Sulawesi, Indonesia: (A) lateral view of the anterior body, (B) dorsal head, (C) lateral head, (D) ventral head.

FIGURE 3 in A new species of lava lizard (Iguanidae: Tropidurinae: Microlophus) from the Galápagos

FIGURE 3. Male holotype (CAS 9428; SVL = 86 mm) of Microlophus slevini sp. nov. in dorsal (top), lateral (middle) and ventral (bottom) views. Photographs by Erica Ely. Scale bar: 10 mm.