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65 results for “Eremias”
Рис. 1. Ооцисты криптоспориΔий моΔифицированные, световая микроскопия по метоΔу ЦиΛя — НиΛьсена (Henriksen, Pohlenz 1981) (размеры увеΛичены в 1000 раз, 1 ΔеΛение равно 10 мкм): A — ооцисты изоΛированные из Testudo graeca из Апшеронской попуΛяции; B — ооцисты изоΛированные из Paralaudakia caucasia из Гобустанской попуΛяции; С — ооцисты изоΛированные из Eremias arguta; D — ооцисты изоΛированные из Natrix tessellata из Апшеронской попуΛяции. Автор: С. О. МамеΔова Fig. 1. Cryptosporidium oocysts stained with carbol-fucsin (Henriksen, Pohlenz 1981) (Magnification 1000 x, each segment corresponds to 10 μm): A — oocysts found in Testudo graeca from Absheron population; B — oocysts found in Paralaudakia caucasia from Gobustan population; C — oocysts found in Eremias argute; D — oocysts found in Natrix tessellata from Absheron population. Author: S. O. Mamedova in Intestinal coccidia (Apicomplexa: Coccidia) in reptiles of Azerbaijan and anthropogenic influences on their prevalence
Рис. 1. Ооцисты криптоспориΔий моΔифицированные, световая микроскопия по метоΔу ЦиΛя — НиΛьсена (Henriksen, Pohlenz 1981) (размеры увеΛичены в 1000 раз, 1 ΔеΛение равно 10 мкм): A — ооцисты изоΛированные из Testudo graeca из Апшеронской попуΛяции; B — ооцисты изоΛированные из Paralaudakia caucasia из Гобустанской попуΛяции; С — ооцисты изоΛированные из Eremias arguta; D — ооцисты изоΛированные из Natrix tessellata из Апшеронской попуΛяции. Автор: С. О. МамеΔова Fig. 1. Cryptosporidium oocysts stained with carbol-fucsin (Henriksen, Pohlenz 1981) (Magnification 1000 x, each segment corresponds to 10 μm): A — oocysts found in Testudo graeca from Absheron population; B — oocysts found in Paralaudakia caucasia from Gobustan population; C — oocysts found in Eremias argute; D — oocysts found in Natrix tessellata from Absheron population. Author: S. O. Mamedova
Figure 2 in Age structure and body size of the Strauch's racerunner, Eremias strauchi strauchi Kessler, 1878
Figure 2. Age frequency distributions for males and females of an Eremias strauchi strauchi sample population.
Figure 1 in The first record of age structure and body size of the Suphan Racerunner, Eremias suphani Başoğlu & Hellmich, 1968
Figure 1. Cross-section (18 µm thick) at the diaphysis level of a phalanx of male E. suphani, 60.52 mm SVL, 7 years old. Six LAGs were observed in the periosteal bone. The first LAG was destroyed by endosteal resorption and endosteal bone was present. Periphery was not regarded as a LAG. Arrows indicate endosteal resorption and periphery, and arrowheads indicate LAGs. e.b. = endosteal bone, m.c. = marrow cavity, r.l. = reversal line, p = periphery.
Figure 2 in A new record of Eremias montanus Rastegar-Pouyani & Rastegar-Pouyani, 2001 (Sauria: Lacertidae) from Kurdistan Province, Western Iran
Figure 2. The natural habitat of Eremias (Eremias) montanus (new record) in Badr and Parishan highlands, at about 2466 m elevation.
Figure 1 in A new record of Eremias montanus Rastegar-Pouyani & Rastegar-Pouyani, 2001 (Sauria: Lacertidae) from Kurdistan Province, Western Iran
Figure 1. The red square is the location of the newly-collected specimen of E. (Eremias) montanus in Kurdistan province.
Figure 3 in Habitat associations and conservation of Eremias acutirostris (Boulenger, 1887) in the Sistan region, Zabol, Iran
Figure 3. Habitat of Eremias acutirostris along the road from Bonjar to Doost Mohammad, Sistan region, Iran.
Figure 2 in Habitat associations and conservation of Eremias acutirostris (Boulenger, 1887) in the Sistan region, Zabol, Iran
Figure 2. Map of Iran and the location of limited population (A) of Eremias acutirostris in east of Iran.
Female lizards (Eremias argus) reverse Bergmann's rule across altitude
<p><span>The evolution of body size within and among species is predicted to be influenced by multifarious environmental factors. However, the specific drivers of body size variation have remained difficult to understand because of the wide range of proximate factors that covary with ectotherm body sizes across populations with varying local environmental conditions. Here, </span><span>we used female </span><span><em>Eremias</em> <em>argus</em></span> <span>lizards collected from different populations across their wide range in China and </span><span>constructed linear mixed models to assess how climatic conditions and/or available resources at different altitudes shape the geographical patterns of lizard body size across </span><span>altitude. Lizard populations showed significant differences in body size across altitudes. Furthermore, w</span><span>e found that climatic and seasonal changes along the altitudinal gradient also explained variations in body size among populations. Specifically, body size decreased with colder and drier environmental conditions at high altitudes, reversing Bergmann's rule. Limited resources at high altitudes, measured by the low vegetative index, may also constrain body size.</span><span> </span><span>Therefore, our study demonstrates that </span><span>multifarious</span><span> environmental factors could strongly influence the intraspecific variation in organisms' body size.</span></p>
Female lizards (Eremias argus) reverse Bergmann’s rule across altitude
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Figure 2 in The first record of age structure and body size of the Suphan Racerunner, Eremias suphani Başoğlu & Hellmich, 1968
Figure 2. Age structure of the population of Suphan Racerunner E. suphani from eastern Turkey.
Figure 1 in Habitat associations and conservation of Eremias acutirostris (Boulenger, 1887) in the Sistan region, Zabol, Iran
Figure 1. Adult male Eremias acutirostris from the Zabol region, Iran.
FIGURE 6 in Fahimi's racerunner, a new species of the genus Eremias Fitzinger, 1834 (Sauria: Lacertidae) from Iran
FIGURE 6. Differences in shape and size of parietals, interparietal and frontoparietals between E. fahimii sp. nov. (A) and E. papenfussi (B).
FIGURE 2 in Fahimi's racerunner, a new species of the genus Eremias Fitzinger, 1834 (Sauria: Lacertidae) from Iran
FIGURE 2. The phylogenetic tree of ten species of Eremias with the combined genes (Cyt b and 12S). The topology of BI and ML trees is the same, therefore only ML tree is shown and values above and below branches indicate bootstrap supports for ML and posterior probabilities for the Bayesian analyses, respectively.
FIGURE 2 in A new species of Eremias (Squamata: Lacertidae) from the arid mountains of Pakistan
FIGURE 2. The holotype of Eremias kakari sp. nov. PMNH 842: A—dorsal view; B—ventral view; C—dorsal head view; D—lateral head view.
FIGURE 5 in A new species of Eremias (Squamata: Lacertidae) from the arid mountains of Pakistan
FIGURE 5. Paratypes of Eremias kakari sp. nov. PMNH 840, 842–846 showing the dorsal and lateral head view. Note the variations in arrangement of frontal, supraoculars, infranasal and rostal.
FIGURE 4 in A new species of Eremias (Squamata: Lacertidae) from the arid mountains of Pakistan
FIGURE 4. Paratypes of Eremias kakari sp. nov. PMNH 4048, 4092–4097 dorsal (above) and ventral (below) view.
FIGURE 1 in A new species of Eremias (Squamata: Lacertidae) from the arid mountains of Pakistan
FIGURE 1. The type localities of the members of the subgenus Rhabderemias including the new species, Eremias kakari sp. nov.
FIGURE 3 in A new species of Eremias (Squamata: Lacertidae) from the arid mountains of Pakistan
FIGURE 3. Paratypes of Eremias kakari sp. nov. PMNH 840, 843–846 dorsal (above) and ventral (below) view.
FIGURE 10 in MtDNA differentiation and taxonomy of Central Asian racerunners of Eremias multiocellata - E. przewalskii species complex (Squamata, Lacertidae)
FIGURE 10. Type locality of Eremias dzungarica sp. nov. in vicinity of Uyench Sum, Khovd Aimaq, western Mongolia: rock outcrops, typical habitat of Eremias dzungarica sp. nov. (the "rock form") (A); sand dunes, typical habitat of the "sand form" of E. multiocellata (B).
FIGURE 11 in MtDNA differentiation and taxonomy of Central Asian racerunners of Eremias multiocellata - E. przewalskii species complex (Squamata, Lacertidae)
FIGURE 11. Dorsal patterns of Eremias multiocellata—E. przewalskii complex members (in scale): A—E. multiocellata; sand form A (ZMMU R-12841); B—E. multiocellata; sand form B (ZMMU R-13215); C—E. multiocellata; sand form B (ZMMU R-13206); D—E. szczerbaki (ZMBPI R-000657; 635; 655); E—E. stummeri (ZMMU R–14335); F—Eremias sp. 1 (ZMMU R- 14330); G—E. yarkandensis (types BMNH 1917.3.6.28; 1917.3.6.29); H—E. buechneri (ZISP-9131); I—E. yarkandensis (ZMMU R-14344); J—E. dzungarica sp. nov. (ZMMU R–12846); K—E. cf. reticulata (ZMMU R-12855); L—E. przewalskii (ZMMU R-13214); M—E. przewalskii (ZMMU R-13209).
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