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219 results for “Albania”
FIGURES 96. Ditsributional maps —96 in New and little – known stoneflies (Plecoptera) from Albania and the neighbouring countries
FIGURES 96. Ditsributional maps —96: Leuctra metsovonica, L. balcanica and L. quadrimaculata in the Balkans and the adjacent territories
FIGURES 12–17 in New and little – known stoneflies (Plecoptera) from Albania and the neighbouring countries
FIGURES 12–17. Imago of Leuctra malcor sp. n. – 12: male terminalia, dorsal view; 13: male terminalia, lateral view; 14: male terminalia, ventral view; 15: male paraprocts, caudal view; 16: female terminalia, ventral view; 17: female terminalia, lateral view – scale 0.5 mm, Fig 15 not to scale
FIGURES 100–102. Ditsributional maps —100 in New and little – known stoneflies (Plecoptera) from Albania and the neighbouring countries
FIGURES 100–102. Ditsributional maps —100: Nemoura peristeri group; 101: Nemoura vinconi sp. n. and N. zwicki; 102: Siphonoperla graeca stat. n., S. neglecta and S. burmeisteri in the Balkans
FIGURES 29–34 in New and little – known stoneflies (Plecoptera) from Albania and the neighbouring countries
FIGURES 29–34. Male of Nemoura asceta sp. n. – 29: terminalia, ventral view; 30: terminalia, dorsal view; 31: terminalia, lateral view; 32: epiproct, apical view; 33: epiproct, left side dorsal, right side ventral view; 34: pilosity of cercus, ventro–caudal view – scale 0.5 mm, Figs 32–34 not to scale.
FIGURES 61–64 in New and little – known stoneflies (Plecoptera) from Albania and the neighbouring countries
FIGURES 61–64. Females of Nemoura anas sp. n. and N. peristeri Aubert —61–62: Nemoura anas sp. n.; 63–64: N. peristeri Aubert; 61, 63: terminalia, ventral view; 62, 64: vaginal complex —scale 0.5 mm, Figs 62, 64 not to scale.
FIGURES 56–60 in New and little – known stoneflies (Plecoptera) from Albania and the neighbouring countries
FIGURES 56–60. Male of Nemoura anas sp. n. —56: terminalia, ventral view; 57: terminalia, dorsal view; 58: terminalia, lateral view; 59: paraproct tip, ventral view; 60: epiproct, upside dorsal, downside ventral view —scale 0.5 mm, Figs 59–60 not to scale.
FIGURES 48–49 in New and little – known stoneflies (Plecoptera) from Albania and the neighbouring countries
FIGURES 48–49. Female of Nemoura vinconi sp. n. —48: female terminalia, ventral view; 49: vaginal complex – scale 0.5 mm, Fig 49 not to scale
FIGURE 1–5 in Endogean and cavernicolous beetles of the Balkans. XVI. A new, anophthalmous species of Neuraphes Thomson, 1859 (Coleoptera: Staphylinidae: Scydmaeninae) from Albania
FIGURE 1–5. Neuraphes (Pararaphes) anophthalmus sp. nov. (male). 1. Habitus, dorsal view. Scale 0.5 mm; 2. Aedeagus, dorsal view. Scale 0.1 mm; 3. Aedeagus, lateral view. Scale 0.1 mm; 4. Habitat; 5. Finding place.
Supporting data for: "Heritage of Tethyan oceanic transform faults within Alpine orogens: Paleomagnetic evidence from the Shkoder-Peja transverse zone (Northern Albania)"
<p>Paleomagnetic data from the Shkoder-Peja transverse zone, collected in the Krasta-Cukali and Albanian Alps tectonic units (Northern Albania).</p> <p>To open and navigate with Remasoft software (https://www.agico.com/text/software/remasoft/remasoft.php).</p>
National Checklists: Albania Species List
Data from: GBIF.org (23 January 2025) GBIF Occurrence Download <a href="https://doi.org/10.15468/dl.vd2ajk" target="_blank" rel="noopener">https://doi.org/10.15468/dl.vd2ajk</a>
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.
Distribution. SE Europe from Albania and Greece (including Crete) N to S Ukraine and S Russia, the Caucasus, Turkey, and N Iran, and through C Asia to W Mongolia, N, E & C China (including Hainan), and the Himalayas; isolated populations in S Croatia and Korea. Specimens collected from SW Syria may representjuvenile Geoffroy's Myotis (M. emarginatus) or a different form, and are not mapped here. in Vespertilionidae
Distribution. SE Europe from Albania and Greece (including Crete) N to S Ukraine and S Russia, the Caucasus, Turkey, and N Iran, and through C Asia to W Mongolia, N, E & C China (including Hainan), and the Himalayas; isolated populations in S Croatia and Korea. Specimens collected from SW Syria may representjuvenile Geoffroy's Myotis (M. emarginatus) or a different form, and are not mapped here.
Subspecies and Distribution. R.r.rupicapraLinnaeus,1758—Germany,Switzerland,Liechtenstein,Austria,France,[taly,Slovenia,andNWCroatia. R.r.balcanicaBolkay,1925—BosniaandHerzegovina,Serbia,Montenegro,Albania,Kosovo,Macedonia,Bulgaria,andGreece. R.r.cartusianaCouturier,1938—EFranceonWedgeofFrenchAlps. R. r. tatrica Blahout, 1972 — Tatras Mts in S Poland and N Slovakia. Subspecies rupicapra introduced into Czech Republic, Slovakia, Bulgaria, Argentina, and New Zealand. in Bovidae
Subspecies and Distribution. R.r.rupicapraLinnaeus,1758—Germany,Switzerland,Liechtenstein,Austria,France,[taly,Slovenia,andNWCroatia. R.r.balcanicaBolkay,1925—BosniaandHerzegovina,Serbia,Montenegro,Albania,Kosovo,Macedonia,Bulgaria,andGreece. R.r.cartusianaCouturier,1938—EFranceonWedgeofFrenchAlps. R. r. tatrica Blahout, 1972 — Tatras Mts in S Poland and N Slovakia. Subspecies rupicapra introduced into Czech Republic, Slovakia, Bulgaria, Argentina, and New Zealand.
Subspecies and Distribution. M.t.thomas:Barrett-Hamilton,1903—majorityofspecies'rangeinSBosniaandHerzegovina,Montenegro,Albania,andGreeceasSasPeloponnese(exceptEuboeaIandAttica). M. t. atticus G. S. Miller, 1910 — Euboea I and Attica region (SE Greece). in Cricetidae
Subspecies and Distribution. M.t.thomas:Barrett-Hamilton,1903—majorityofspecies'rangeinSBosniaandHerzegovina,Montenegro,Albania,andGreeceasSasPeloponnese(exceptEuboeaIandAttica). M. t. atticus G. S. Miller, 1910 — Euboea I and Attica region (SE Greece).
FIGURE 4 in Limonium ksamilum (Plumbaginaceae), a new species from Albania
FIGURE 4. Diagnostic features of Limonium himariense. A. Habit. B. Inflorescence. C. Detail of inflorescence. D. Spikelet. E. Inner bract, dorsal view. F. Inner bracts, lateral view. G. Outer bracts. H. Middle bracts. I. Calyces. J. Calyx lobes. K. Leaves. Illustration by S. Brullo based on living material coming from the type locality (CAT!).
FIGURE 3 in Limonium ksamilum (Plumbaginaceae), a new species from Albania
FIGURE 3. Geographical distribution of Limonium ksamilum (orange dot), L. arcuatum (blue dots), L. himariense (red dots) and L. dictyophorum (green dots).
FIGURE 2. Limonium ksamilum A. Habitat. B in Limonium ksamilum (Plumbaginaceae), a new species from Albania
FIGURE 2. Limonium ksamilum A. Habitat. B. Detail of the inflorescence. C. Habit. D. Detail of the inflorescence of Limonium himariense.
FIGURE 1 in Limonium ksamilum (Plumbaginaceae), a new species from Albania
FIGURE 1. Diagnostic features of Limonium ksamilum. A. Habit. B. Inflorescence. C. Spikelet. D. Inner bracts, dorsal view. E. Inner bract, lateral view. F. Outer bracts. G. Middle bracts. H. Calyces. I. Calyx lobes. J. Leaves. Illustration by S. Brullo based on living material coming from the type locality (CAT!).
Subspecies and Distribution. T:s.stankoviciV.Martino&E.Martino,1931—WMacedoniaandadjacentNWGreeceMts. T. s. montenegrina Krystufek, 1994 — restricted to coastal lowlands of S Montenegro and adjacent Albania. Also present in C & S Albania and W Greece as far S as N Peloponnese, also on Corfu I in the Ionian Sea, but subspecies involved not known. in Talpidae
Subspecies and Distribution. T:s.stankoviciV.Martino&E.Martino,1931—WMacedoniaandadjacentNWGreeceMts. T. s. montenegrina Krystufek, 1994 — restricted to coastal lowlands of S Montenegro and adjacent Albania. Also present in C & S Albania and W Greece as far S as N Peloponnese, also on Corfu I in the Ionian Sea, but subspecies involved not known.
Distribution. Disjunct range, W fragment encompasses the Western Alps (Switzerland, NW Italy, and SE France) and the Apennine Mts of Italy as far S as Sila Massif; in the Balkans, E portion covers topographically broken landscape in SE Bosnia and Herzegovina, adjacent Dalmatia (Croatia), Montenegro, Kosovo, W Macedonia, Albania, and W Greece. in Talpidae
Distribution. Disjunct range, W fragment encompasses the Western Alps (Switzerland, NW Italy, and SE France) and the Apennine Mts of Italy as far S as Sila Massif; in the Balkans, E portion covers topographically broken landscape in SE Bosnia and Herzegovina, adjacent Dalmatia (Croatia), Montenegro, Kosovo, W Macedonia, Albania, and W Greece.
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