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41 results for “Common lizard”
FIGURE 5 in Taxonomy and distribution of a common arboreal lizard, Bronchocela jubata Duméril & Bibron, 1837 (Reptilia: Agamidae), with designation of its lectotype from Java, Indonesia
FIGURE 5. Bronchocela jubata (A) in life (adult male, not collected) from Cibinong near Bogor, West Java.
FIGURE 4 in Taxonomy and distribution of a common arboreal lizard, Bronchocela jubata Duméril & Bibron, 1837 (Reptilia: Agamidae), with designation of its lectotype from Java, Indonesia
FIGURE 4. Bronchocela jubata lectotype (MNHN-RA 2542, adult male) from Java: (A) lateral view of the full body, (B) dorsal head, (C) lateral head, (D) ventral head.
FIGURE 3 in Taxonomy and distribution of a common arboreal lizard, Bronchocela jubata Duméril & Bibron, 1837 (Reptilia: Agamidae), with designation of its lectotype from Java, Indonesia
FIGURE 3. Principal Component Analysis (PCA): (A) biplot of morphometric variation in combined sexes between Bronchocela jubata (red) and B. cristatella (blue) in Java, Indonesia; (B) 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 1 in Taxonomy and distribution of a common arboreal lizard, Bronchocela jubata Duméril & Bibron, 1837 (Reptilia: Agamidae), with designation of its lectotype from Java, Indonesia
FIGURE 1. Current distribution map showing the collection/observation localities of Bronchocela jubata (red) and its sympatric congener, B. cristatella sensu lato (blue) on Java and Bali Islands; sympatric localities filled partially; for the distribution of B. jubata on Sumatra Island, see Amarasinghe et al. 2022.
FIGURE 2 in Taxonomy and distribution of a common arboreal lizard, Bronchocela jubata Duméril & Bibron, 1837 (Reptilia: Agamidae), with designation of its lectotype from Java, Indonesia
FIGURE 2. Boxplots of (A) head length, (B) snout–vent length, and (C) tail length indicating differences between Bronchocela jubata and B. cristatella in Java, Indonesia (note that both sexes were mixed); top, middle and bottom lines of the boxes indicate 75th percentile, median and 25th percentile, respectively.
Data for: Contextual behavioral interactions of common side-blotched lizards (Uta stansburiana)
<p>These datasets are a summary of all interactions between Common Side-blotched Lizards (Uta stansburiana) and other species. The first (AdultUtaInteractions) contains rows that result from individual replicate interactions during focal-animal observations in two different years. Data include date of observation, time of focal's start, ID of Common Side-blotched Lizard observerd, its sex, and body size as well as the identification of the species with which this individual interacted and its sex. Following this the are the characteristics of the focal animal during 5 min. periods before (pre) and during/following (post) an interaction for the focal animal's perch (height and diameter), movement, and displays (headbobs) as their sum during those 5-min. periods and as the difference (post less pre). Following this are interaction intensity scores (0=no interaction, 5=most intense interaction), intensity scores with initiation coded by sign (positive values as initiated by focal animal, negative as by other individual). Next are display body postures recoded during the interaction (used post-interaction only) scored as N=none or identifying the species performing the posture. These are repeated as effect codes (0=no posture, 1=posture used during interaction). Finally, a notes column indicates any noted details of the interaction.</p> <p>The other dataset (DailyInteractionsSums&Rates) contains a summary of each day's data collection during this study over the two years of study (JD=days since Jan. 1). Decimal min. contains the total time of focal observations performed on that day. Following this are columns containing the count of intrasexual and intersexual interactions as well as the count of intraspecific and interspecific interactions observed on that day. There are then two columns containing the count of events occurring between Uta stansburiana (U.s.) and Sceloporus occidentalis (S.o.) and between Uta and Sceloporus graciosus (S.g.). Next time is calculated as a decimal hours basis before the count of interactions per hour are calculated for each of the previous categories of counts.</p>
Highly variable (no clear pattern). All portions of the dorsal views were equally used. In head images the area around the eye, the top of the head, the snout and the throat were all used in similar proportions. P. carbonelli Variable for both views. Snout and middle of the dorsum used in dorsal view. Top of the head most frequently (but not strictly) used in lateral view. P. guadarramae Whole body used for dorsal view (but variable); either throat (most common) or ear region used in head lateral views. P. hispanicus Variable. Anterior portion of snout used more frequently than in other species for both dorsal and head lateral views. P. liolepis Highly variable. Whole body used in most dorsal images, area around the eye and throat used in head lateral views, but other patterns common. P. lusitanicus Highly variable. All parts of the dorsum used (but frequently the most posterior part); area around the ear frequently used in head lateral images. P. tunesiacus Highly variable. Dorsal area near the insertion of the posterior limbs used more frequently than in other species; different regions of the head used, often simultaneously. P. Ʋaucheri Highly variable. Different regions of dorsum (from head to the posterior region) used in dorsal images, all portions of the head, but most frequently the throat, used in lateral images. P. Ʋirescens Highly variable. All parts of both images used. Head and anterior part of the dorsum more used than in other species. in Identification of morphologically cryptic species with computer vision models: wall lizards (Squamata: Lacertidae: Podarcis) as a case study
Highly variable (no clear pattern). All portions of the dorsal views were equally used. In head images the area around the eye, the top of the head, the snout and the throat were all used in similar proportions. P. carbonelli Variable for both views. Snout and middle of the dorsum used in dorsal view. Top of the head most frequently (but not strictly) used in lateral view. P. guadarramae Whole body used for dorsal view (but variable); either throat (most common) or ear region used in head lateral views. P. hispanicus Variable. Anterior portion of snout used more frequently than in other species for both dorsal and head lateral views. P. liolepis Highly variable. Whole body used in most dorsal images, area around the eye and throat used in head lateral views, but other patterns common. P. lusitanicus Highly variable. All parts of the dorsum used (but frequently the most posterior part); area around the ear frequently used in head lateral images. P. tunesiacus Highly variable. Dorsal area near the insertion of the posterior limbs used more frequently than in other species; different regions of the head used, often simultaneously. P. Ʋaucheri Highly variable. Different regions of dorsum (from head to the posterior region) used in dorsal images, all portions of the head, but most frequently the throat, used in lateral images. P. Ʋirescens Highly variable. All parts of both images used. Head and anterior part of the dorsum more used than in other species.
Data from: Anthropogenic impact or anthropogenic accommodation? Distribution range expansion of the common wall lizard (Podarcis muralis) by means of artificial habitats in the north-eastern limits of its distribution range
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Data from: Microhabitat selection in the common lizard: implications of biotic interactions, age, sex, local processes, and model transferability among populations
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Data from: Context-dependent expression of sexual dimorphism in island populations of the common wall lizard (Podarcis muralis)
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Data from: Hybridization could be a common phenomenon within the highly diverse lizard genus Liolaemus
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Data for: Contextual behavioral interactions of common side-blotched lizards (Uta stansburiana)
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Data from: Hierarchical distance sampling to estimate population sizes of common lizards across a desert ecoregion
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Data from: Comparison of reproductive investment in native and non-native populations of common wall lizards reveals sex differences in adaptive potential.
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Don't judge a lizard by its colour: no evidence for differential socio-sexual behaviour and space use in the colour morphs of the European common wall lizard (Podarcis muralis)
Explaining the evolutionary origin and maintenance of colour polymorphisms is a major challenge in evolutionary biology. Such polymorphisms are commonly thought to reflect the existence of alternative behavioural or life-history strategies under negative frequency-dependent selection. The European common wall lizard Podarcis muralis exhibits a striking ventral colour polymorphism that has been intensely studied and is often assumed to reflect alternative reproductive strategies, similar to the iconic "rock-paper-scissors" system described in the North American lizard Uta stansburiana. However, available studies so far have ignored central aspects in the behavioural ecology of this species that are crucial to assess the existence of alternative reproductive strategies. Here we try to fill this gap by studying the social behaviour, space use, and reproductive performance of lizards showing different colour morphs, both in a free-ranging population from the eastern Pyrenees and in ten experimental mesocosm enclosures. In the natural population, we found no differences between morphs in site-fidelity, space use or male-female spatial overlap. Likewise, colour morph was irrelevant to socio-sexual behaviour, space use, and reproductive success within experimental enclosures. Our results contradict the commonly held hypothesis that P. muralis morphs reflect alternative behavioural strategies, and suggest that we should instead turn our attention to alternative functional explanations.
Data from: Distinct telomere differences within a reproductively bimodal common lizard population
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Climate dependent heating efficiency in the common lizard
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Data from: Iridophores and not carotenoids account for chromatic variation of carotenoid-based coloration in common lizards (Lacerta vivipara)
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Don’t judge a lizard by its colour: no evidence for differential socio-sexual behaviour and space use in the colour morphs of the European common wall lizard (Podarcis muralis)
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Data from: Climate shapes the geographic distribution and introgressive spread of colour ornamentation in common wall lizards
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