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15 results for “Testudo hermanni”
Fig. 6 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change
Fig. 6. Result of the analysis of Binomial tests (CliMond 2090 (2081–2100)): A — T. graeca; B — T. hermanni.
Fig. 3 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change
Fig. 3. Niche clustering (Geographic space, CliMond 1975 (1970–2000)) from: A — T. graeca (1. T. g. ibera, 2. T. nikolskii, 3. T. g. anamurensis, 4. T. g. floweri, 5. T. g. antakyensis, 6. T. g. pallasi, 7. T. g. armenica, 8. T. g. perses, buxtoni, 9. T. g. terrestris); B — T. hermanni (1. T. h. hermanni, 2. T. h. hervegovinensis, 3. T. h. boettgeri), red circles showing the approximate ranges of subspecies according to "Turtles…, 2017" World" (2017).
Fig. 2 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change
Fig. 2. The "Ecological envelope" — relationship bio01 "Annual mean temperature", °C & bio12 "Annual precipitation", mm (DivaGis): A — T. graeca; B — T. hermanni.
Fig. 5 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change
Fig. 5. Potential (probabilistic) model of T. hermanni world expansion built in the Maxent program based on the CliMond: A — 1975 (1970–2000); B — 2090 (2081–2100)) climatic data and GBIF data (2021). Areas of the highest habitat suitability (> 0.3–0.5) are colored in red and areas of the lowest (<0.2) — in blue (SAGA GIS).
Fig. 4 in Gis Modelling Of The Distribution Of Terrestrial Tortoise Species: Testudo Graeca And Testudo Hermanni (Testudines, Testudinidae) Of Eastern Europe In The Context Of Climate Change
Fig. 4. Potential (probabilistic) model of T. graeca expansion built in the Maxent program based on the CliMond: A — 1975 (1970–2000); B — 2090 (2081–2100)) climatic data and GBIF data (2021 a). Areas of the highest habitat suitability (> 0.3–0.5) are colored in red and areas of the lowest (<0.2) — in blue (SAGA GIS).
Fig. 1 in Scavenging behavior of an adult Hermann's Tortoise (Testudo hermanni Gmelin, 1789) (Reptilia: Testudinidae)
Fig. 1. The Common Toad found dead on a road (on the left) and the Hermann's Tortoise feeding on it at the same place about 20 days after its death.
Figure 2 in Activity patterns and habitat preference of eastern Hermann's tortoise (Testudo hermanni boettgeri) in Serbia
Figure 2. Percent of occurrence of tortoises in specific habitat types in consecutive years. For description of habitat types, see Section 2.2.
Figure 1 in Activity patterns and habitat preference of eastern Hermann's tortoise (Testudo hermanni boettgeri) in Serbia
Figure 1. The study area. The map was constructed with Google Earth. The white line borders the area where monitoring was conducted. Triangles mark the position of open habitat or grassland. Squares mark the position of human-modified habitat. Surface without symbols represents forest.
Figure 2 in Population Genetic Structure of Testudo hermanni boettgeri (Hermann's Tortoise) in Türkiye
Figure 2.UPGMA distance tree created using the Reynolds (1983) weighted model (the node values are bootstrap values estimated with 1000 permutations).
Figure 1 in Population Genetic Structure of Testudo hermanni boettgeri (Hermann's Tortoise) in Türkiye
Figure 1. Sampling localities of T. h. boettgeri (Loc 1: Malkara, Loc 2: Orhaniye, Loc 3: Hanlıyenice, Loc 4: Adasarhan, Loc 5: Balabanlı, Loc 6: İpsala, Loc 7: Hacılar, Loc 8: Şeytanderesi, Loc 9: Meriç, Loc10: Taşlısekban, Loc 11: Kırklareli, Loc 12: Çöpköy, Loc 13: Demirköy, Loc 14: Erikler, and Loc 15: Keşan; the colorations symbolize the clusters).
Figure 3 in Population Genetic Structure of Testudo hermanni boettgeri (Hermann's Tortoise) in Türkiye
Figure 3. Population assignment test performed with Structure. (A) Barplots that estimated membership coefficients of the analyzed individuals in each locality. (B) Barplot, K = 2, clusters for 8 groups in the UPGMA distance tree. (C) Graph of ∆K as a function of the number of groups K, (Evanno's method) (the numbers on the barplots symbolize the sampling localities).
Figure 4 in Population Genetic Structure of Testudo hermanni boettgeri (Hermann's Tortoise) in Türkiye
Figure 4. Maps of the population clusters (K) identified by GENELAND. (A) Map spatial distribution of each group defined, K = 2. (B) Map of the posterior probability defined, K = 2 (the numbers symbolize the sampling localities, the colors in A and B symbolize the clusters inferred in STRUCTURE).
First detection of herpesvirus and mycoplasma in free-ranging Hermann's tortoises (Testudo hermanni), and in potential pet vectors
<p>Two types of pathogens cause highly contagious upper respiratory tract diseases (URTD) in Chelonians: testudinid herpesviruses (TeHV) and a mycoplasma (<em>Mycoplasma agassizii</em>). In captivity, these infections are frequent and can provoke outbreaks. Pet trade generates international flow of tortoises, often without sanitary checking; individuals intentionally or accidentally released in the wild may spread pathogens. A better understanding of the transmission of infectious agents from captivity to wild tortoises is needed. Many exotic individuals have been introduced in populations of the endangered western Hermann’s tortoise (<em>Testudo hermanni hermanni</em>), notably spur-thighed tortoises (<em>Testudo graeca</em>). We assessed the presence of TeHV and mycoplasma in native western Hermann’s tortoises and in potential pet vectors in south-eastern France. Using a large sample (N=572 tortoises), this study revealed the worrying presence of herpesvirus in 7 free-ranging individuals (3 sub-populations). Additionally, <em>Mycoplasma agassizii</em> was detected in 15 of the 18 populations sampled with a frequency ranging from 2.5 to 25%. Exotic spur-thighed tortoises showed high frequency of <em>Mycoplasma </em>infection in captivity (18%) and in individuals (50%) found in native Hermann’s tortoise sub-populations, suggesting that this species could be a significant vector. The paucity of information of TeHV on European tortoise’ URTD in natural settings, especially in combination with mycoplasma, prompts for further studies. Indeed, sick tortoises remain concealed and may not be easily detected in the field. Our results indicate that both the prevalence and health impact of URTD are high should be scrutinized in the field.</p>
Fig. 1 in Notes on the diet of Testudo hermanni boettgeri and T. graeca ibera in south-western Bulgaria with first cases of geophagy and myrmecophagy from the country
Fig. 1. Individuals of T. hermanni feeding on figs (A), mulberries (B), and dog feces (C).
Fig. 1 in A Case of winter activity of the Hermann's Tortoise (Testudo hermanni Gmelin, 1789) (Reptilia: Testudinidae) from Bulgaria
Fig. 1. The plantation of Quercus suber and the adult female T. hermanni recorded in it.
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