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81 results for “Kosovo”
Determination of areas with release potential of snow avalanche in Sharr Mountains (Kosovo) - Appendix A
<p>Map of areas with avalanche release potential in Sharr Mountains (Kosovo) - Fuzzy Logic potential determination method</p>
Determination of areas with release potential of snow avalanche in Sharr Mountains (Kosovo) - Appendix B
<p>Map of areas with avalanche release potential in Sharr Mountains (Kosovo) - AHP potential determination method</p>
Figure 1 in New additions to the caddisfly fauna (Insecta: Trichoptera) of the Sharr Mountains in Kosovo
Figure 1. Seven sampling stations at the Opojë Region
Figure 1 in Contribution to the knowledge of fish fauna of Kosovo with a special note on some invasive species
Figure 1. Four sampling stations in Badovc Lake (B1, B2, B3, and B4).
Figure 2 in Description of the hitherto unknown female of Rhyacophila siparantum Ibrahimi, Bilalli & Kučinić, 2021 (Trichoptera: Rhyacophilidae) from Kosovo
Figure 2. Map of sampling station, Bogë Stream, Rugovë Mountain, Kosovo.
Table 1 in Description of the hitherto unknown female of Rhyacophila siparantum Ibrahimi, Bilalli & Kučinić, 2021 (Trichoptera: Rhyacophilidae) from Kosovo
<p><b>Table 1.</b> Diagnostic matrix for female genitalia of <i>Rhyacophila siparantum, R. schmidinarica</i> and <i>R. hirticornis</i>.</p><table><tbody><tr><th>Character</th><th><i>R. siparantum</i></th><th><i>R. schmidinarica</i></th><th><i>R. hirticornis</i></th></tr><tr><th>Lateral view</th></tr></tbody><tbody><tr><th>Segment VIII</th><td>Sharp acuminate apex of ventral lobe</td><td>Blunt apex of ventral lobe, nearly triangular</td><td>Blunt apex of ventral lobe, nearly triangular</td></tr><tr><th>Vaginal apparatus</th><td>Sclerotized part large, membranous part small</td><td>NA</td><td>Sclerotized part small, membranous part large</td></tr><tr><th>Ventral view</th></tr><tr><th>Segment VIII</th><td>Segment generally high, with rounded apex</td><td>Segment generally low, with straight, truncated apex</td><td>Segment generally low, with straight, truncated apex</td></tr><tr><th>Vaginal apparatus</th><td>Sclerotized dorsal part high, basally ending with two high teeth encircling small membranous ventral part</td><td>NA</td><td>Sclerotized dorsal part low, basally ending with two low teeth encircling large membranous ventral part</td></tr><tr><th>Dorsal view</th></tr><tr><th>Segment VIII</th><td>Segment generally high, apically ending with two triangular small lobes with small V shaped indentation in between</td><td>Segment generally low, apically ending with two rounded lobes with high V shaped indentation in between</td><td>Segment generally high, apically ending with two triangular small lobes with small V shaped indentation in between</td></tr></tbody></table>
Figure 7 in Rhyacophila siparantum sp. nov. (Trichoptera: Rhyacophilidae), a new species of the R. philopotamoides species group from the Republic of Kosovo with molecular and ecological notes
Figure 7. Enlarged aedeagus and parameres of Rhyacophila siparantum sp. nov.
Figure 1 in Rhyacophila siparantum sp. nov. (Trichoptera: Rhyacophilidae), a new species of the R. philopotamoides species group from the Republic of Kosovo with molecular and ecological notes
Figure 1. Male of Rhyacophila siparantum sp. nov.
Figure 6 in Rhyacophila siparantum sp. nov. (Trichoptera: Rhyacophilidae), a new species of the R. philopotamoides species group from the Republic of Kosovo with molecular and ecological notes
Figure 6. Dorsal profile of Rhyacophila siparantum sp. nov.
Figure 5 in Rhyacophila siparantum sp. nov. (Trichoptera: Rhyacophilidae), a new species of the R. philopotamoides species group from the Republic of Kosovo with molecular and ecological notes
Figure 5. Lateral profile of Rhyacophila siparantum sp. nov.
FIGURES 1–5 in Some zerconid mites (Acari: Mesostigmata: Zerconidae) from Kosovo (SerbiaMontenegro) with description of Zercon kosovina sp. nov.
FIGURES 1–5. Zercon kosovina sp. nov. 1. Dorsal idiosoma; 2. Dorsal idiosoma; 3. Opisthonotal setae I2–I6; 4. Opisthonotal setae I3 and I4; 5. Opisthonotal seta I6. Scale bar: a: 200 µm, b: 50 µm, c: 20 µm).
FIGURES 6–8 in Some zerconid mites (Acari: Mesostigmata: Zerconidae) from Kosovo (SerbiaMontenegro) with description of Zercon kosovina sp. nov.
FIGURES 6–8. Zercon kosovina sp. nov. 6. Podonotal sculpture between setae i4 and i5; 7 Opisthonotal sculpture between setae I1 and I3; 8. Ventral idiosoma. Scale bar: a: 200 µm, c: 20 µm).
FIGURE 5 in New records for the Kosovo caddisfly fauna with the description of a new species, Drusus dardanicus sp. nov. (Trichoptera: Limnephilidae)
FIGURE 5. Distributions of Drusus discophorus-Group taxa. The species inhabit the Balkan Mountains region with partly overlapping distributions.
FIGURE 3 in New records for the Kosovo caddisfly fauna with the description of a new species, Drusus dardanicus sp. nov. (Trichoptera: Limnephilidae)
FIGURE 3. Male genitalia of Drusus dardanicus sp. nov.. 3A, right lateral view; 3B, caudal view; 3C, dorsal view.
FIGURE 4 in New records for the Kosovo caddisfly fauna with the description of a new species, Drusus dardanicus sp. nov. (Trichoptera: Limnephilidae)
FIGURE 4. Results of phylogenetic inference. B/MCMCMC species tree analysis for nine Drusus species (24 terminal taxa) based on 3444-bp-long sequence from 5 loci (mtCOI5-P + mtCOI3-P + 16SmrDNA + CADH + 28S). Bold branches indicate highly supported (pp≥0.95) clades.
FIGURE 2 in New records for the Kosovo caddisfly fauna with the description of a new species, Drusus dardanicus sp. nov. (Trichoptera: Limnephilidae)
FIGURE 2. Male genitalia of Drusus dardanicus sp. nov. 2A, right lateral view; 2B, right paramere in right lateral view; 2C, ventral view, 2D, caudal view, 2E, dorsal view. Scale bar 1 mm. Drawn by Vitecek.
FIGURE 1 in New records for the Kosovo caddisfly fauna with the description of a new species, Drusus dardanicus sp. nov. (Trichoptera: Limnephilidae)
FIGURE 1. The watersheds of the Llap and Sitnica rivers with indicated main tributaries: magenta color, Sitnica River watershed; blue color, Llap River watershed.
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest. in Suidae
Subspecies and Distribution. S. s. scrofa Linnaeus, 1758 — W Europe, from Denmark, Germany, Poland, and Czech Republic to N Italy and N Iberian Peninsula; possibly also Albania. The taxonomic status of animals in Austria, Switzerland, Slovenia, and Slovakia is unclear but presumably these populations are included in scrofa, as are the populations of Sweden, Finland, and the Baltic states. However, restocking of once depleted populations, for example in Italy, has likely involved the introduction and mixing of this subspecies with other subspecies, such as attila. S. s. affinis Gray, 1847 — S India and Sri Lanka. S. s. algirus Loche, 1867 — Tunisia, Algeria, and Morocco, on the coastal side of the mountains or in the low montane areas. S. s. attila Thomas, 1912 — Hungary, Ukraine, C & S Belarus, Romania, Moldova, and S Russia towards the N flank of the Caucasus, but not including the Transcaucasian countries of Georgia, Armenia, and Azerbaijan. The range possibly extends as far S as the Mesopotamian Delta in Iraq, in which case it would likely include W & SW Iran, and possibly E Turkey and Syria, where it borders with lybicus. Such a range could not be easily reconciled with a statement by Groves that "the difference between pigs from N and S of the Caucasus is quite striking; Transcaucasian boars are certainly not attila." This subspecies may also extend into C Asia and include Kazakhstan, Uzbekistan, and Turkmenistan, but no data exist to support this. S. s. baeticus Thomas, 1912 — originally described from Coto Donana, S Spain, and later merged with meridionalis; also S Portugal. Unless evidence is found that these Italian and Iberian populations are the relics of a much larger formerly contiguous range, this subspecies should be kept as distinct. S. s. coreanus Heude, 1897 — Korean Peninsula. S. s. eristatus Wagner, 1839 — Himalayas S to C India and E to Indochina (N of the Kra Isthmus). S. s. davidi Groves, 1981 — the arid zone from E Iran to Gujarat, including Pakistan and NW India, and perhaps N to Tajikistan. S. s. leucomystax Temminck, 1842 — main Is ofJapan (Honshu, Shikoku, Kyushu, Nakadori, Hiburijima, Tojima, Kushima, and other smaller Is). S. s. lybicus Gray, 1868 — Bulgaria, Greece, Turkey, Syria, Jordan, Israel, Palestine, in the past also in Lybia, and Egypt. The former Yugoslavia was included in its range, which would suggest that now Slovenia, Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Kosovo are within the range of this subspecies, although the exact boundaries are unclear. Pigs from Albania have been assigned to S. s. scrofa. S. s. majori De Beaux & Festa, 1927 — C & S Italian Peninsula. S. s. menidionalis Forsyth Major, 1882 — Corsica and Sardinia, with the proviso that the two populations are very likely to be introduced or feral. S. s. moupinensis Milne-Edwards, 1871 — China, S to Vietnam and W to Sichuan. S. s. nigripes Blanford, 1875 — the flanks of the Tianshan mountains in Kyrgyzstan and NW China (Xinjiang). An animal photographed in NE Iran (Golestan) looked like this subspecies. S. s. nukiuanus Kuroda, 1924 — Iriomote, Ishigaki, Okinawa, Tokunoshima, Amamioshima, and Kakerome Is in the Ryukyu chain in extreme S Japan, though some of these populations have hybridized with introduced domesticates. S. s. sibiricus Staffe, 1922 — Mongolia and Transbaikal (S & E of Lake Baikal). S. s. tawvanus Swinhoe, 1863 — Taiwan. S. s. ussuricus Heude, 1888 — far E Russia and the Manchurian region (China). Korean populations were previously included in this subspecies, but based on new evidence, the Korean taxon seems more similar to moupinensis. S. s. vittatus Boie, 1828 — Malay Peninsula, S of the Isthmus of Kra, the offshore islands of Terutai and Langkawi, Sumatra, Riau Archipelago, Java, Bali, and a range of smaller islands around these, including Babi, Bakong, Batam, Bawean, Bengkalis, Bintan, Bulan, Bunguran, Cuyo, Deli, Durian, Enggano, Galang, Jambongan, Karimon (Riau Is), Kundur, Lagong, Laut, Lingga, Lingung, Mapor, Moro Kecil, North Pagai, Nias, Panaitan, Payong, Penang, Pinie, Rupat, Siantan, Siberut, Simeulue, Singkep, Sugi, Sugi Bawa, Telibon, Tinggi, Tuangku, and the Tambelan Is. This species was originally present from the British Is in the extreme W, through Eurasia from S Scandinavia to S Siberia, extending as far E as Korea and Japan, and SE into some of the Sunda Is and Taiwan. In the S the species ranged along the Nile Valley to Khartoum, and N of the Sahara in Africa, more orless following the continental coasts of S, E, and SE Asia. Within this range it was absent only from extremely dry deserts, e.g. the driest regions of Mongolia and in China W of Sichuan; and alpine zones, such as the high altitudes of Pamir and Tien Shan. In recent centuries, the range of S. scrofa has changed dramatically because of hunting and changes in available habitat. The species disappeared from the British Is in the 17" century, from Denmark in the 19" century, and was greatly reduced in range and numbers in the 20" century from areas as distant as Tunisia, Sudan, Germany, and Russia. Following these severe declines, there were some slight population recoveries in Russia, Italy, Spain, and Germany in the mid-20™ century, and natural and assisted range expansions in Denmark and Sweden. The species has also been inadvertently reintroduced in various locations in the Great Britain via escapees of mixed origin from commercial farming enterprises. Ex-S. scrofa stocks also occur as introduced feral populations in various other parts of the world, including Australia, New Zealand, the eastern Malay Archipelago, and in North, Central, and South America. In all of these areas they are now generally recognized as a major pest.
FIGURE 19 in The Rhyacophila fasciata Group in Europe: Rhyacophila macedonica Karaouzas Valladolid & Ibrahimi (n. sp.) from Greece, Kosovo, Republic of North Macedonia and Serbia (Trichoptera: Rhyacophilidae)
FIGURE 19. Spatial distribution of Rhyacophila macedonica Karaouzas, Valladolid & Ibrahimi (n. sp.), Rhyacophila kykladica Malicky & Sipahiler 1993 and Rhyacophila fasciata Hagen 1859 in Greece, Republic of North Macedonia, Kosovo and Serbia. Circle: localities of R. macedonica. Triangles: localities of R. fasciata. Diamond: localities of R. kykladica. White, orange: specimens from Greece. Green: specimens from Kosovo. Purple: specimens from Republic of North Macedonia. Brown: specimens from Serbia.
FIGURES 10, 11 in The Rhyacophila fasciata Group in Europe: Rhyacophila macedonica Karaouzas Valladolid & Ibrahimi (n. sp.) from Greece, Kosovo, Republic of North Macedonia and Serbia (Trichoptera: Rhyacophilidae)
FIGURES 10, 11. Male and female genitalia of Rhyacophila macedonica Karaouzas, Valladolid & Ibrahimi (n. sp.), respectively. 10, male: 10A, 2nd segment of left inferior appendage, left lateral; 10BV, 10BL, parameres: 10BV, parameres (p) and ventral lobe of aedeagus (phallicata) (vl), ventral; 10BL, left paramere, left lateral. 10CL, 10CD, aedeagus (phallicata) and lateroventral lobes: 10CL, aedeagus and ventral lobe, left lateral; 10CD, aedeagus and its lateroventral lobes (lvl), dorsal. 10DD, apicodorsal lobe of segment IX (al) and preanal appendages (pa); 10DV, segment X, ventral, ab= apical band, as= anal sclerites, va= nonsclerotized ventral area. 11, female segments VIII–XI: 11L, left lateral; 11D, dorsal; 11V, ventral. Scale bars: unlabelled = 1 mm; ● = 0.5 mm; * = 200 µm.
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