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55 results for “Asia Minor”
Figure 15 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 15. Lateral aspect of the neotype minor worker of Camponotus piceus.
Figure 14 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 14. Head of the neotype minor worker of Camponotus piceus.
Figure 4 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 4. Major worker of C. anatolicus in lateral view.
Figure 10 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 10. Minor worker of C. honaziensis from the holotype nest in lateral view.
Figure 8 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 8. Paratype minor worker of C. anatolicus from the holotype nest in dorsal view.
Figure 18 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 18. Lateral aspect of large minor worker of Camponotus heidrunvogtae n.sp., holotype.
Figure 19 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 19. Dorsal aspect of large minor worker of Camponotus heidrunvogtae n.sp., holotype.
Figure 11 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 11. Minor worker of C. honaziensis from the holotype nest in dorsal view.
Figure 7 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 7. Paratype minor worker of C. anatolicus from the holotype nest in lateral view.
Figure 5 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 5. Major worker of C. anatolicus in dorsal view.
Figure 3 in A taxonomic revision of the members of the Camponotus lateralis species group (Hymenoptera: Formicidae) from Europe, Asia Minor and Caucasia
Figure 3. Head of major worker of C. anatolicus.
Data from: Asymmetric contributions of seed and pollen to gene dispersal in the marsh orchid Dactylorhiza umbrosa in Asia Minor
<p>Orchids differ from other plants in their extremely small and partly air-filled seeds that can be transported long distances by wind. Seed dispersal in orchids is expected to contribute strongly to overall gene flow, and orchids generally express low levels of genetic differentiation between populations and low pollen to seed flow ratios. However, studies in orchids distributed in northern Europe have often found a poor geographic structuring of genetic variation. Here, we studied geographic differentiation in the marsh orchid <i>Dactylorhiza umbrosa</i>, which is widely distributed in upland regions from Asia Minor to Central Asia. These areas were less affected by Pleistocene ice ages than northern Europe and the orchid should have been able to survive the last ice age in local refugia. In the plastid genome, which is dispersed by seeds, populations at close distance were clearly divergent, but the differentiation still increased with geographic distance, and a significant phylogeographic structure had developed. In the nuclear genome, which is dispersed by both seeds and pollen, populations showed an even stronger correlation between genetic and geographic distance, but average levels of differentiation were lower than in the plastid genome, and no phylogeographic structure was evident. Combining plastid and nuclear data, we found that the ratio of pollen to seed dispersal (<i>mp/ms</i>) decreases with physical distance. Comparison with orchids that grow in parts of Europe that were glaciated during the last ice suggests that a balanced structure of genetic diversity develops only slowly in many terrestrial orchids, despite of efficient seed dispersal.</p>
FIGURES 1–12 in Taxonomic review of Drilus Olivier, 1790 (Elateridae: Agrypninae: Drilini) from Asia Minor, with descriptions of seven new species and comments on the female antennal morphology in Drilini
FIGURES 1–12. Habitus images of Drilus species. 1, Drilus akbesianus (Fairmaire, 1895); 2, D. badius sp. nov.; 3, D. huijbregtsi sp. nov.; 4, D. latithorax Pic, 1902; 5, D. mertliki sp. nov.; 6, D. obscuricornis Pic, 1899; 7, D. rectus Schaufuss, 1867; 8, D. robustus sp. nov.; 9, D. sanliurfensis sp. nov.; 10, D. teunisseni sp. nov.; 11, D. turcicus sp. nov.; 12, D. iranicus Wittmer, 1967. Scale bars = 2.0 mm.
FIGURES 46–50 in Taxonomic review of Drilus Olivier, 1790 (Elateridae: Agrypninae: Drilini) from Asia Minor, with descriptions of seven new species and comments on the female antennal morphology in Drilini
FIGURES 46–50. Drilus robustus sp. nov., female. 46, habitus; 47, genitalia; 48, antenna. Larval cerci. 49, D. robustus sp. nov.; 50, Drilus sp. (Turkey, Muğla Prov., Knidos). Scale bars = 2.0 mm (Fig. 46), 1.0 mm (Figs 47, 49–50), 0.5 mm (Fig. 48).
FIGURES 34–45 in Taxonomic review of Drilus Olivier, 1790 (Elateridae: Agrypninae: Drilini) from Asia Minor, with descriptions of seven new species and comments on the female antennal morphology in Drilini
FIGURES 34–45. Male genitalia of Drilus species. 34, Drilus badius sp. nov.; 35, D. huijbregtsi sp. nov.; 36, D. latithorax Pic, 1902; 37, D. mertliki sp. nov.; 38, D. obscuricornis Pic, 1899; 39, D. rectus Schaufuss, 1867 (Turkey, Adana Prov.); 40, D. robustus sp. nov.; 41, D. sanliurfensis sp. nov.; 42, D. teunisseni sp. nov.; 43, D. turcicus sp. nov.; 44, D. iranicus Wittmer, 1967; 45, Drilus sp. (Abkhazia). Scale bars = 0.25 mm.
FIGURES 51–54 in Taxonomic review of Drilus Olivier, 1790 (Elateridae: Agrypninae: Drilini) from Asia Minor, with descriptions of seven new species and comments on the female antennal morphology in Drilini
FIGURES 51–54. Drilus robustus sp. nov. 51, larva; 52, mating couple; 53, the type locality (Turkey, Kemer env.); 54, larval skins inside the shells of Rumina decollata (Linnaeus, 1758).
FIGURES 22–33 in Taxonomic review of Drilus Olivier, 1790 (Elateridae: Agrypninae: Drilini) from Asia Minor, with descriptions of seven new species and comments on the female antennal morphology in Drilini
FIGURES 22–33. Antennae of Drilus species. 22, Drilus badius sp. nov.; 23, D. huijbregtsi sp. nov.; 24, D. latithorax Pic, 1902; 25, D. mertliki sp. nov.; 26, D. obscuricornis Pic, 1899; 27, D. rectus Schaufuss, 1867; 28, D. robustus sp. nov.; 29, D. sanliurfensis sp. nov.; 30, D. teunisseni sp. nov.; 31, D. turcicus sp. nov. Drilus robustus sp. nov., male. 32, leg; 33, last abdominal segments. Scale bars = 0.5 mm.
FIGURES 13–21 in Taxonomic review of Drilus Olivier, 1790 (Elateridae: Agrypninae: Drilini) from Asia Minor, with descriptions of seven new species and comments on the female antennal morphology in Drilini
FIGURES 13–21. Pronota of Drilus species. 13, Drilus badius sp. nov.; 14, D. huijbregtsi sp. nov.; 15, D. latithorax Pic, 1902; 16, D. mertliki sp. nov.; 17, D. obscuricornis Pic, 1899; 18, D. robustus sp. nov.; 19, D. sanliurfensis sp. nov.; 20, D. teunisseni sp. nov.; 21, D. turcicus sp. nov. Scale bars = 0.5 mm.
Distribution. SC & S Europe (including Sicily, Cyprus, Crete, and smaller Mediterranean Is), SW Asia from Asia Minor, the Caucasus region, Palestine, and N Jordan to Kashmir, the Altai Mts, Nepal, N India, and N & C China. in Vespertilionidae
Distribution. SC & S Europe (including Sicily, Cyprus, Crete, and smaller Mediterranean Is), SW Asia from Asia Minor, the Caucasus region, Palestine, and N Jordan to Kashmir, the Altai Mts, Nepal, N India, and N & C China.
On following pages: 211. Alpine Chamois (Rupicapra rupicapra); 212. Carpathian Chamois (Rupicapra carpatica); 213 Gray Goral (Nemorhaedus bedford); 216. Chinese Goral (Nemorhaedus griseus); 217. Burmese Goral (Nemorhaedus. Asia Minor Chamois (Rupicapra asiatica); 214. Himalayan Brown Goral (Nemorhaedus goral); 215. Himalayan evansi); 218. Long-tailed Goral (Nemorhaedus caudatus); 219. Red Goral (Nemorhaedus baileyi). in Bovidae
On following pages: 211. Alpine Chamois (Rupicapra rupicapra); 212. Carpathian Chamois (Rupicapra carpatica); 213 Gray Goral (Nemorhaedus bedford); 216. Chinese Goral (Nemorhaedus griseus); 217. Burmese Goral (Nemorhaedus. Asia Minor Chamois (Rupicapra asiatica); 214. Himalayan Brown Goral (Nemorhaedus goral); 215. Himalayan evansi); 218. Long-tailed Goral (Nemorhaedus caudatus); 219. Red Goral (Nemorhaedus baileyi).
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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DANDI Archive for NWB datasets
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International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.