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Figure 13 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 13. Pheggomisetes globiceps globiceps from the Dushnika Cave, village of Iskrets (near Sofia), Mt. Ponor Planina, Western Bulgaria. A, topotype male, aedeagus (lateral view). B, topotype male, aedeagus (dorsal view). C, topotype male, abdominal sternite IX (urite). D, topotype female, gonocoxites IX and gonosubcoxites IX. Scales = 0.1 mm.
Figure 12 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 12. Pheggomisetes globiceps globiceps from the Dushnika Cave, village of Iskrets (near Sofia), Mt. Ponor Planina, Western Bulgaria. Topotype male, habitus (dorsal view). Scale = 5.0 mm.
Figure 11 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 11. Pheggomisetes globiceps ilandjievi from the Golyama Balabanova Dupka Cave, village of Komshtitsa (near Sofia), Stara Planina Mts., Western Bulgaria. A, topotype male, aedeagus (lateral view). B, topotype male, aedeagus (dorsal view). C, topotype male, abdominal sternite IX (urite). D, topotype female, gonocoxites IX and gonosubcoxites IX. Scales = 0.1 mm.
Figure 9 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 9. Pheggomisetes globiceps ninae comb. & stat. nov. from the Hodžina Dupka Pit, village of PetrlaŠ (near Dimitrovgrad), Stara Planina Mts., Southeast Serbia. Bright-field (A–D) and TPEF (E–H) microscopy images. A, E, topotype male, aedeagus (lateral view). B, F, topotype male, aedeagus (dorsal view). C, G, topotype male, abdominal sternite IX (urite). D, H, topotype female, gonocoxites IX and gonosubcoxites IX. Scales = 0.1 mm.
Figure 16 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 16. TPEF microscopy images of the aedeagus of P. globiceps ninae comb. & stat. nov. A, lateral view with longitudinal section plane (red square). B, lateral view with cross-sectional plane (red line). C, a corresponding longitudinal section. D, a corresponding cross section. Scales = 0.10 mm (A–C) and 0.05 mm (D).
Figure 14 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 14. Distribution of Pheggomisetes taxa in Serbia and the immediate surroundings. Scale = 10 km.
Figure 6 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 6. Pheggomisetes globiceps ciniglavcensis subsp. nov. from the Propas Pit, village of Činiglavci (near Pirot), Stara Planina Mts., Southeast Serbia. Holotype male, habitus (dorsal view). Scale = 5.0 mm.
Figure 5 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 5. Pheggomisetes serbicus belensis subsp. nov. from the Suva Dupka Cave, village of Bela (near Pirot), Stara Planina Mts., Southeast Serbia. Bright-field (A–D) and TPEF (E–H) microscopy images. A, E, holotype male, aedeagus (lateral view). B, F, holotype male, aedeagus (dorsal view). C, G, holotype male, abdominal sternite IX (urite). D, H, paratype female, gonocoxites IX and gonosubcoxites IX. Scales = 0.1 mm.
Figure 4 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 4. Pheggomisetes serbicus belensis subsp. nov. from the Suva Dupka Cave, village of Bela (near Pirot), Stara Planina Mts., Southeast Serbia. Holotype male, habitus (dorsal view). Scale = 5.0 mm.
Figure 3 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 3. Shape of the shoulders in the Pheggomisetes subspecies analysed. A, P. serbicus serbicus subsp. nov. B, P. globiceps ciniglavcensis subsp. nov. C, P. globiceps ilandjievi. D, P. serbicus belensis subsp. nov. E, P. globiceps ninae comb. & stat. nov. F, P. globiceps globiceps. Scales = 0.5 mm.
Figure 7 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 7. Pheggomisetes globiceps ciniglavcensis subsp. nov. from the Propas Pit, village of Činiglavci (near Pirot), Stara Planina Mts., Southeast Serbia. Bright-field (A–D) and TPEF (E–H) microscopy images. A, E, holotype male, aedeagus (lateral view). B, F, holotype male, aedeagus (dorsal view). C, G, holotype male, abdominal sternite IX (urite). D, H, paratype female, gonocoxites IX and gonosubcoxites IX. Scales = 0.1 mm.
Figure 1 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 1. Pheggomisetes serbicus sp. nov. from the Pež Dupka Cave, village of Dojkinci (near Pirot), Stara Planina Mts., Southeast Serbia. Holotype male, habitus (dorsal view). Scale = 5.0 mm.
Figure 2 in The genus Pheggomisetes Knirsch, 1923 (Coleoptera: Carabidae: Trechinae) in Serbia: taxonomy, morphology and molecular phylogeny
Figure 2. Pheggomisetes serbicus sp. nov. from the Pež Dupka Cave, village of Dojkinci (near Pirot), Stara Planina Mts., Southeast Serbia. Bright-field (A–D) and TPEF (E–H) microscopy images. A, E, holotype male, aedeagus (lateral view). B, F, holotype male, aedeagus (dorsal view). C, G, holotype male, abdominal sternite IX (urite). D, H, paratype female, gonocoxites IX and gonosubcoxites IX. Scales = 0.1 mm.
Subspecies and Distribution. V. p. peregusna Giildenstadt, 1770 — Russia. V. p. alpherakii Birula, 1910 — Afghanistan, Iran, Pakistan, Tajikistan, Turkmenistan, and Uzbekistan. V. p. euxina Pocock, 1936 — Bulgaria, Greece, Macedonia, Montenegro, Romania, Serbia, Turkey, and Ukraine. V. p. negans G. S. Miller, 1910 — NC & W China and S Mongolia. V.p. pallidior Stroganov, 1948 — Kazakhstan. V. p. syriaca Pocock, 1936 — Armenia, Azerbaidjan, Egypt, Georgia, Iraq, Israel, Lebanon, and Syria. in Mustelidae
Subspecies and Distribution. V. p. peregusna Giildenstadt, 1770 — Russia. V. p. alpherakii Birula, 1910 — Afghanistan, Iran, Pakistan, Tajikistan, Turkmenistan, and Uzbekistan. V. p. euxina Pocock, 1936 — Bulgaria, Greece, Macedonia, Montenegro, Romania, Serbia, Turkey, and Ukraine. V. p. negans G. S. Miller, 1910 — NC & W China and S Mongolia. V.p. pallidior Stroganov, 1948 — Kazakhstan. V. p. syriaca Pocock, 1936 — Armenia, Azerbaidjan, Egypt, Georgia, Iraq, Israel, Lebanon, and Syria.
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.
Supplementary material 1 from: Anđelković AA, Pavlović DM, Marisavljević DP, Živković MM, Novković MZ, Popović SS, Cvijanović DL, Radulović SB (2022) Plant invasions in riparian areas of the Middle Danube Basin in Serbia. NeoBiota 71: 23-48. https://doi.org/10.3897/neobiota.71.69716
List of the studied rivers/canal sections and their catchment area affiliation (and code in the analysis)
Figs 1–5 in First record of Cylindrotoma distinctissima (Meigen, 1818) from Serbia and new data on the occurrence of Cylindrotomidae (Diptera) in Bulgaria and Romania
Figs 1–5. Cylindrotoma distinctissima distinctissima (Meigen, 1818) from Kopaonik Mountains (Serbia); 1 – dorsal view of male hypopygium, 2 – habitus, 3 – dorsal view of the head (antennae removed), 4 – lateral view of the head, 5 – wing. Photos by L.-P. Kolcsár.
Figs 7 & 8. 7 in First record of Cylindrotoma distinctissima (Meigen, 1818) from Serbia and new data on the occurrence of Cylindrotomidae (Diptera) in Bulgaria and Romania
Figs 7 & 8. 7 – Occurrence of Cylindrotoma distinctissima distinctissima) in Bulgaria, Romania and Serbia; white cirlces – literature data, grey circles – new records. 8 – Occurrence of Diogma glabrata (triangles) and Triogma trisulcata (squares) in Romania; white and gray color applies respectively to literature data and new records.
Subspecies and Distribution. N. p. procyonoides Gray, 1834 — W & SW China and N Indochina. N. p. albus Hornaday, 1904 — Japan (Hokkaido). N. p. koreensis Mori, 1922 — Korean Peninsula. N. p. orestes Thomas, 1923 — C & S China. N. p. ussuriensis Matschie, 1907 — NE China, E Mongolia, and SE Russia. N. p. viverrinus Temminck, 1839 — Japan. Introduced (ussuriensis) to the Baltic states, Belarus, Bulgaria, Czech Republic, Finland, Germany, Hungary, Moldova, Poland, Romania, W Russia, Serbia, Slovakia, Sweden, and Ukraine, occasionally seen in Austria, Bosnia, Denmark, France, the Netherlands, Norway, Slovenia, and Switzerland. in Canidae
Subspecies and Distribution. N. p. procyonoides Gray, 1834 — W & SW China and N Indochina. N. p. albus Hornaday, 1904 — Japan (Hokkaido). N. p. koreensis Mori, 1922 — Korean Peninsula. N. p. orestes Thomas, 1923 — C & S China. N. p. ussuriensis Matschie, 1907 — NE China, E Mongolia, and SE Russia. N. p. viverrinus Temminck, 1839 — Japan. Introduced (ussuriensis) to the Baltic states, Belarus, Bulgaria, Czech Republic, Finland, Germany, Hungary, Moldova, Poland, Romania, W Russia, Serbia, Slovakia, Sweden, and Ukraine, occasionally seen in Austria, Bosnia, Denmark, France, the Netherlands, Norway, Slovenia, and Switzerland.
FIGURE 6 in Potamophylax idliri sp. nov. (Trichoptera: Limnephilidae), a new species from the Jastrebac Mountains in Serbia, with molecular and ecological notes
FIGURE 6. Lateral profiles of male genitalia of four species of the Potamophylax winneguthi Species Cluster: 6A, P. coronavirus Ibrahimi, Bilalli & Vitecek 2021 (in Ibrahimi et al. 2021); 6B, P. juliani Kumanski 1999; 6C, P. winneguthi (Klapálek 1902); 6D, P. idliri sp. nov. Scale bars = 0.25 mm.
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Allen Brain Atlas
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OpenNeuro
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