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24 results for “Tarentola”
Figura 2 in Primera Argentina cita de Tarentola mauritanica (Squamata: Phyllodactylidae) en la provincia de Neuquén,
Figura 2. Distribución de Tarentola mauritanica en la Argentina. Los puntos azules corresponden a los registros previos a este trabajo. El punto amarillo representa el primer registro de la especie para la provincia de Neuquén.
Figura 1. Ejemplar MPCN-H-267 in Primera Argentina cita de Tarentola mauritanica (Squamata: Phyllodactylidae) en la provincia de Neuquén,
Figura 1. Ejemplar MPCN-H-267 hembra colectado en la provincia de Neuquén.
FIGURE 1 in Does The African Native Host Explain The African Origin Of The Parasite? The Maltese Geckobia Estherae N. Sp. Parasitic On Tarentola Mauritanica (Acari: Raphignathoidea: Pterygosomatidae)
FIGURE 1: Geckobia estherae n. sp., female: a – Dorsal view female; b – Ventral view; c – Infracapitulum, palp and chelicerae, ventral view; d – Anogenital area (some setae are only represented by the base).
FIGURE 2 in Does The African Native Host Explain The African Origin Of The Parasite? The Maltese Geckobia Estherae N. Sp. Parasitic On Tarentola Mauritanica (Acari: Raphignathoidea: Pterygosomatidae)
FIGURE 2: Geckobia estherae n. sp., female: a – Scutum and ocular lenses; b – distal part of left chelicera; c – Different shape of body setae: from left to right: scutal and dorsal setae, and four shapes of ventral setae, below: coxal setae; d-e – Tarsi I and II; f – Epimeral plate ventral view and leg IV.
Data from: Morphological and functional implications of sexual size dimorphism in the Moorish gecko, Tarentola mauritanica
Sexual dimorphism (SD) is a common trait in animals, appearing due to sexual selection, fecundity selection or natural selection promoting sexual niche segregation. To evaluate the relative contribution of these mechanisms in shaping phenotypic patterns, we explored morphological and functional SD in the Moorish gecko, Tarentola mauritanica (Linnaeus, 1758). This species is particularly interesting because the sex of individuals is determined by the incubation temperature of the eggs, which may pose constraints on the expression of SD. Our results indicate the existence of marked SD in T. mauritanica. Males were overall larger than females, and were able to bite harder, but we found no differences between the sexes in climbing capacities. When differences in body size were taken into account, SD became less pronounced, appearing only in relative head dimensions, relative hind limb length and bite force. Different body parts varied under the same static allometric slopes in both sexes, a pattern not very usual in lizards. Put together, our results suggest constraints in the expression of SD in the Moorish gecko, possibly due to either not particularly intense sexual selection, to counter-balancing selection in similar traits in both sexes, or to the mode of sexual determination.
FIGURE 4 in A new gecko of the genus Tarentola (Squamata: Gekkonidae) from Eastern Cuba
FIGURE 4. Habitats of Tarentola crombiei in the arid south coast of Eastern Cuba. (A) General landscape: a marine terrace in Siboney, Santiago de Cuba, covered by typical xerophytic vegetation; (B) xerophytic scrub at La Mesa de Leo Prada (type locality), surroundings of Boca del Jauco, Maisí, Guantánamo; (C) dry clumps of Agave sp., on rocky soil, one of the diurnal microhabitats of species in the type locality; (D) communal nest of T. crombiei in a dry Agave sp. (finger nail about 8 mm). Photos: A and B, by Arturo Kirkconnell; C and D, by Gerardo Begué.
FIGURE 1. Male MNHNCu 4664 in A new gecko of the genus Tarentola (Squamata: Gekkonidae) from Eastern Cuba
FIGURE 1. Male MNHNCu 4664 of Tarentola crombiei n. sp. (A), from Siboney (Reserva Ecológica Siboney-Juticí), Santiago de Cuba, (B) an adult male of T. a. americana from the same locality, and (C) an adult male of T. a. americana (MNHNCu 4653) from Cueva Ambrosio, Península de Hicacos, Matanzas province. Escale bar= 1cm.
FIGURE 2 in A new gecko of the genus Tarentola (Squamata: Gekkonidae) from Eastern Cuba
FIGURE 2. Fourth toe dorsal arrangement of scales in (A) Tarentola crombiei (paratype male MNHNCu 4646), and (B) T. americana, both from Siboney (Reserva Ecológica Siboney-Juticí), Santiago de Cuba Province. Scale bar= 1 mm.
FIGURE 3 in A new gecko of the genus Tarentola (Squamata: Gekkonidae) from Eastern Cuba
FIGURE 3. Distribution map of Tarentola crombiei and T. americana in Cuba. Numbers refer to the following localities: (1) Cabo Cruz, Granma; (2) Siboney (Reserva Ecológica Siboney-Juticí, Santiago de Cuba); (3) Reserva Ecológica de Hatibonico, Guantánamo; (4) U. S. Naval Base, Guantánamo (including four sublocalities within a range of 6 km, referred in the list of paratype specimens); (5) Puerto Escondido, Guantánamo; (6) La Mesa de Leo Prada, Maisí, Guantánamo (type locality of T. crombiei); (7) La Patana, Maisí, Guantánamo.
FIGURE 3 in Does The African Native Host Explain The African Origin Of The Parasite? The Maltese Geckobia Estherae N. Sp. Parasitic On Tarentola Mauritanica (Acari: Raphignathoidea: Pterygosomatidae)
FIGURE 3: Geckobia estherae n. sp. General and ventral view (picture from W. Pflieger)
Figure 4. Discriminant analyses for males and females previously called T in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 4. Discriminant analyses for males and females previously called T. darwini. The total contribution of each of the two Canonical Discriminant Functions (CDF1 and CDF2) to explain the total morphological variation is also given. See Material and methods for details.
Figure 2 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 2. Phylogenetic relationships of endemic Cape Verde Tarentola taxa and their relatives from the Canary Islands modified from Vasconcelos et al. (2010) based on cytochrome b and 12S rRNA genes. The tree was inferred using maximum likelihood (ML) and GTR+I+G model of sequence evolution (log likelihood = -6468.896) and was rooted using Tarentola americana. Bootstrap support values above 60% for the ML analysis are shown below nodes. Posterior probability (PP) values higher than 95% for the Bayesian analysis are represented by an asterisk (*) and are shown above nodes. Names in bold follow the new taxonomic proposal and non-bold ones the taxonomy accepted in previous recent papers (Carranza et al., 2000; Jesus et al., 2002; Vasconcelos et al., 2010). For further details see Vasconcelos et al. (2010). Characters immediately to the right of island names correspond to the 15 evolutionarily significant units (ESUs) of A, B, C, and D clades recognized in the present work and represented in split green bars. Lines of evidence (in grey): 1, mitochondrial DNA (independent cyt b parsimony networks with a connection limit of 95%; see Appendix 3); 2, nuclear DNA (absence of shared haplotypes in MC1R); 3, morphology (detection of any diagnostic morphological character or a set of a unique combination of characters). Integration approaches (in red) from the most conservative to the most inflationist: ITC stands for integration by total congruence (all lines of evidence should be congruent), IPC stands for integration by partial congruence, retained in the present study (at least two lines of evidence are necessary); IC stands for integration by cumulation (one line of evidence is sufficient). Species are represented in split red bars and subspecies in yellow.
Figure 3 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 3. Parsimony networks corresponding to the PDC, ACM4 and MC1R nDNA sequence variation in Tarentola from the Cape Verde Islands. Lines represent a mutational step, circles haplotypes and dots missing haplotypes. The size of circles is proportional to the number of haplotypes and colours to the number of individuals. The dotted circles represent the most probable ancestral haplotype. Samples from the same island are similarly coloured but with different tonalities for different taxa. For correspondences of sample and location codes see Appendix 1.
Figure 7 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 7. Photographs of the dorsal and lateral views of Tarentola of the Cape Verde Islands. A1, T. boavistensis; A2, T. bocagei; A3, T. fogoensis; A4, T. darwini; B1, T. substituta; B2, T. raziana; B3, T. caboverdiana; C, T. nicolauensis; D1, T. gigas (T. gigas brancoensis on the left and T. gigas gigas on the right); D2, T. rudis; D3, T. protogigas protogigas; D4, T. p. hartogi from Brava Island; D5, T. p. hartogi from Rombos Islets; D6, T. maioensis.
Figure 1 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 1. Map of the Cape Verde Islands showing the geographical location (latitudes and longitudes) and altitudes of the islands and the origins of the new Tarentola samples included in the genetic (circles) and morphological (diamonds) analyses (Geographic Coordinate System, Datum WGS 84). Island and taxa colours match the colours used on the network analyses. No specimens were found on Sal.
Figure 6 in An integrative taxonomic revision of the Tarentola geckos (Squamata, Phyllodactylidae) of the Cape Verde Islands
Figure 6. Typical dorsal patterns of Tarentola species of the Cape Verde Islands (adapted from Joger, 1993).
FIG. 3 in Reproductive and Morphological Characteristics of Hemidactylus turcicus (Squamata: Gekkonidae) and Tarentola annularis (Squamata: Phyllodactylidae) in Southern Egypt
FIG. 3. Monthly variation in the mean of the masses of ovary, oviduct, and liver of female Hemidactylus turcicus (A–C) and Tarentola annularis (D–F). Sample size for each monthly sample is given.
FIG. 2 in Reproductive and Morphological Characteristics of Hemidactylus turcicus (Squamata: Gekkonidae) and Tarentola annularis (Squamata: Phyllodactylidae) in Southern Egypt
FIG. 2. Mass–snout vent length relationships in Hemidactylus turcicus (A) and Tarentola annularis (B). The male regression equation is above the lines, whereas the female regression equation is below.
FIG. 1 in Reproductive and Morphological Characteristics of Hemidactylus turcicus (Squamata: Gekkonidae) and Tarentola annularis (Squamata: Phyllodactylidae) in Southern Egypt
FIG. 1. Monthly variation in the mean temperature, relative humidity, and photoperiod in Abu Rawash (A) and Izbet al Asfar (B).
FIG. 4 in Reproductive and Morphological Characteristics of Hemidactylus turcicus (Squamata: Gekkonidae) and Tarentola annularis (Squamata: Phyllodactylidae) in Southern Egypt
FIG. 4. Monthly variation in the testis mass, percent reproductive specimens for males (sperm in epididymides), and liver mass of male Hemidactylus turcicus (A–C) and male Tarentola annularis (D–F). Sample size for each monthly sample is given.
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