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FIGURES 27–31. Lasioseius spp., dorsoventral habitus. 27. L in On some blattisociid mites (Acari: Mesostigmata: Lasioseius, Cheiroseius) from Slovakia, with notes on the genus Hyattella sensu Krantz, 1962
FIGURES 27–31. Lasioseius spp., dorsoventral habitus. 27. L. cheiroseioides sp. nov. (female); 28. L. epicrioides (female); 29. L. diffindatus (female); 30. L. lacunosus (male); 31. L. lacunosus (female). Scale bar: 300 µm.
FIGURES 23–26. Lasioseius spp., females. 23. L in On some blattisociid mites (Acari: Mesostigmata: Lasioseius, Cheiroseius) from Slovakia, with notes on the genus Hyattella sensu Krantz, 1962
FIGURES 23–26. Lasioseius spp., females. 23. L. lacunosus, ventral shields; 24. L. cheiroseioides sp. nov., dorsal shield sculpture of hexagonal area; 25. L. lacunosus, dorsal shield sculpture of hexagonal area; 26. L. epicrioides, dorsal shield sculpture of posteromedial area. Scale bars: 50 µm (Fig. 23), 25 µm (Figs 24‒26).
FIGURE 18–22. Lasioseius lacunosus. 18 in On some blattisociid mites (Acari: Mesostigmata: Lasioseius, Cheiroseius) from Slovakia, with notes on the genus Hyattella sensu Krantz, 1962
FIGURE 18–22. Lasioseius lacunosus. 18. Chelicera (male), lateral view; 19. Epistome (male); 20. Chelicera (female), lateral view; 21. Femur II (male), ventral view; 22. Tarsus II (male), ventral view. Scale bars: 25 µm (Figs 18‒20), 50 µm (Figs 21, 22).
FIGURES 15–17. Lasioseius spp., females. 15. L in On some blattisociid mites (Acari: Mesostigmata: Lasioseius, Cheiroseius) from Slovakia, with notes on the genus Hyattella sensu Krantz, 1962
FIGURES 15–17. Lasioseius spp., females. 15. L. cheiroseioides sp. nov., sperm-reception structures, lateral view; 16. L. lacunosus, dorsal idiosoma; 17. L. lacunosus, ventral gnathosoma. Scale bars: 25 µm (Fig. 17), 50 µm (Fig. 15), 100 µm (Fig. 16).
FIGURES 8‒11 in On some blattisociid mites (Acari: Mesostigmata: Lasioseius, Cheiroseius) from Slovakia, with notes on the genus Hyattella sensu Krantz, 1962
FIGURES 8‒11. Lasioseius cheiroseioides sp. nov., female. 8. Ventral gnathosoma; 9. Epistome; 10. Chelicera, dorsal view, with chelicera of Lasioseius epicrioides for comparison (on the left); 11. fixed digit of chelicera, dorsal view. Scale bars: 25 µm.
FIGURES 12‒14 in On some blattisociid mites (Acari: Mesostigmata: Lasioseius, Cheiroseius) from Slovakia, with notes on the genus Hyattella sensu Krantz, 1962
FIGURES 12‒14. Lasioseius cheiroseioides sp. nov., female. 12. Ventral shields; 13. Sternal and metasternal shields, with anterior part of epigynal shield; 14. Detail of posterolateral dorsal setae. Scale bars: 50 µm (Figs 12, 13), 25 µm (Fig. 14).
FIGURES 1–6 in On some blattisociid mites (Acari: Mesostigmata: Lasioseius, Cheiroseius) from Slovakia, with notes on the genus Hyattella sensu Krantz, 1962
FIGURES 1–6. Lasioseius cheiroseioides sp. nov., female. 1. Dorsal idiosoma; 2. Ventral idiosoma; 3. Tarsus II, dorsal view; 4. Tarsus III, dorsal view; 5. Tarsus IV, dorsal view; 6. Cheliceral digits, lateral view. Scale bars: 100 µm (Figs 1‒5), 25 µm (Fig. 6).
Supplementary material 3 from: Macko P, Derka T, Šamulková M, Novikmec M, Svitok M (2023) Checklist, distribution, diversity, and rarity of mayflies (Ephemeroptera) in Slovakia. ZooKeys 1183: 39-64. https://doi.org/10.3897/zookeys.1183.109819
Number of mayfly species in five frequency classes, and their altitudinal and geographical distributions
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.
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.
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.
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. S.b.betulinaPallas,1779—C&EEuropeEthroughEuropeanRussiaandSWSiberiatoNEAltaiMts;rangeextendsNabovetheArcticCircle(above68°N). S.b.montanaMéhely,1913—Alps(Switzerland,SGermany,andAustria),BohemianForest(CzechRepublic),andCarpathians(Slovakia,SPoland,SUkraine,andRomania). S.b.norvegicaChaworth-Musters,1927—Scandinavia. S. b. taigica Stroganov & Potapkina, 1950 — S Siberian uplands in S Russia between NE Altai Mts E to NE Lake Baikal in Irkutsk and Buryatia. in Sminthidae
Subspecies and Distribution. S.b.betulinaPallas,1779—C&EEuropeEthroughEuropeanRussiaandSWSiberiatoNEAltaiMts;rangeextendsNabovetheArcticCircle(above68°N). S.b.montanaMéhely,1913—Alps(Switzerland,SGermany,andAustria),BohemianForest(CzechRepublic),andCarpathians(Slovakia,SPoland,SUkraine,andRomania). S.b.norvegicaChaworth-Musters,1927—Scandinavia. S. b. taigica Stroganov & Potapkina, 1950 — S Siberian uplands in S Russia between NE Altai Mts E to NE Lake Baikal in Irkutsk and Buryatia.
Subspecies and Distribution. n. nivalis Martins, 1842 — Alps. OONDno. abulensis Morales, 1936 — Iberian Peninsula.. aleco Paspalev, V. Martino & Pesheyv, 1952 — E Balkan Peninsula. 9. appenninicus Dal Piaz, 1929 — Italian Peninsula.. cedrorum Spitzenberger, 1973 — Taurus Mts and SW Anatolia, Turkey. 3. dementievi Heptner, 1939 — S Turkmenistan and NE Iran.. hermonis G. S. Miller, 1908 — Lebanon, W & S Syria, and extreme N Israel. OADSs. malyi Bolkay, 1925 — W Balkan Peninsula.. mirhanreini Schafer, 1935 — Tatra Mts in S Poland and Slovakia.. olympus Neuhauser, 1936 — NW Anatolia, N Turkey. 83 £. pontius G. S. Miller, 1908 — NE Anatolia, NE Turkey. n. trialeticus Shidlovsky, 1919 — Caucasus. C. n. ulpius G. S. Miller, 1908 — E & S Carpathian Mts in SW Ukraine and Romania. Also present in S France, S Turkey (Hatay Province), and NW Iran, but subspecies involved not known. in Cricetidae
Subspecies and Distribution. n. nivalis Martins, 1842 — Alps. OONDno. abulensis Morales, 1936 — Iberian Peninsula.. aleco Paspalev, V. Martino & Pesheyv, 1952 — E Balkan Peninsula. 9. appenninicus Dal Piaz, 1929 — Italian Peninsula.. cedrorum Spitzenberger, 1973 — Taurus Mts and SW Anatolia, Turkey. 3. dementievi Heptner, 1939 — S Turkmenistan and NE Iran.. hermonis G. S. Miller, 1908 — Lebanon, W & S Syria, and extreme N Israel. OADSs. malyi Bolkay, 1925 — W Balkan Peninsula.. mirhanreini Schafer, 1935 — Tatra Mts in S Poland and Slovakia.. olympus Neuhauser, 1936 — NW Anatolia, N Turkey. 83 £. pontius G. S. Miller, 1908 — NE Anatolia, NE Turkey. n. trialeticus Shidlovsky, 1919 — Caucasus. C. n. ulpius G. S. Miller, 1908 — E & S Carpathian Mts in SW Ukraine and Romania. Also present in S France, S Turkey (Hatay Province), and NW Iran, but subspecies involved not known.
Subspecies and Distribution. M. m. marmota Linnaeus, 1758 — Alps in Germany, Austria, Switzerland, France, and Italy. M. m. latirostris Kratochvil, 1961 — High Tatra Mts of Slovakia and Poland. Nominate subspecies reintroduced to Romania (Carpathian Mts) and Slovenia (Julian Alps), and introduced into the Black Forest (Germany), the Massif Central, Jura, and Vosgues (France), the Pyrenees (France, Spain, and Andorra), E Austria, Apennine Mts (Italy), N Serbia, Montenegro. in Sciuridae
Subspecies and Distribution. M. m. marmota Linnaeus, 1758 — Alps in Germany, Austria, Switzerland, France, and Italy. M. m. latirostris Kratochvil, 1961 — High Tatra Mts of Slovakia and Poland. Nominate subspecies reintroduced to Romania (Carpathian Mts) and Slovenia (Julian Alps), and introduced into the Black Forest (Germany), the Massif Central, Jura, and Vosgues (France), the Pyrenees (France, Spain, and Andorra), E Austria, Apennine Mts (Italy), N Serbia, Montenegro.
Subspecies and Distribution. S.a.alpinusSchinz,1837—SEFrance,Switzerland,NItaly,C&SGermany,SWCzechRepublic,Austria,Slovenia,NWHungary,Croatia,BosniaandHerzegovina,Serbia,Montenegro,andNAlbania. S.a.hercynicusG.S.Miller,1909—NGermany(Harz);possiblyextinct. S. a. tatricus Kratochvil & Rosicky, 1952 — N & E Czech Republic, Slovakia, S Poland, W Ukraine, NE Hungary, and Romania. in Soricidae
Subspecies and Distribution. S.a.alpinusSchinz,1837—SEFrance,Switzerland,NItaly,C&SGermany,SWCzechRepublic,Austria,Slovenia,NWHungary,Croatia,BosniaandHerzegovina,Serbia,Montenegro,andNAlbania. S.a.hercynicusG.S.Miller,1909—NGermany(Harz);possiblyextinct. S. a. tatricus Kratochvil & Rosicky, 1952 — N & E Czech Republic, Slovakia, S Poland, W Ukraine, NE Hungary, and Romania.
Distribution. Endemic to SE Europe (Austria, Slovakia, Hungary, Croatia, Bosnia and Herzegovina, Serbia, Montenegro, Albania, Greece, Romania, Bulgaria, Moldova, Ukraine, and Russia). in Muridae
Distribution. Endemic to SE Europe (Austria, Slovakia, Hungary, Croatia, Bosnia and Herzegovina, Serbia, Montenegro, Albania, Greece, Romania, Bulgaria, Moldova, Ukraine, and Russia).
St. Joseph sculpture (Nitra, Slovakia)
Source: Objaverse 1.0 / Sketchfab
Supplementary material 1 from: Zach P, Panigaj Ľ, Honěk A, Nedvěd O, Kulfan J, Martinková Z, Selyemová D, Viglášová S, Roy H (2014) The invasion history, distribution and colour pattern forms of the harlequin ladybird beetle Harmonia axyridis (Pall.) (Coleoptera, Coccinellidae) in Slovakia, Central Europe. ZooKeys 412: 89-102. https://doi.org/10.3897/zookeys.412.6587
Records of Harmonia axyridis in Slovakia: Explanation note: There are records from 2008 to 2012; years 2008 and 2009 marked in bold. The localities (sites of collection) are arranged in alphabetical order. Indicated are the numeric code of the mapping square (see Fig. 1), year of the first record and name of observer. Data on absence of the species are indicated by subsequent records of the species in the same squares or near squares from which it had not previously been recorded (e.g. 2008 – no record, 2009 – first record).
Supplementary material 1 from: Mikula P, Csanády A, Hromada M (2018) A critical evaluation of the exotic bird collection of the Šariš Museum in Bardejov, Slovakia. ZooKeys 776: 139-152. https://doi.org/10.3897/zookeys.776.24462
Table S1 : Explanation note: Exotic bird specimens held by the Šaris Museum in Bardejov, Slovakia, including their updated identification, previous identification provided by museum, family and order of bird specimen, conservation status according IUCN, country / region of specimen origin, locality of collection, acquisition number and year, inventory and notebook number, date of collection, and whether specimen is located in public exhibition or scientific collection. ? – information on locality and / or date was not found but we added this information for some specimens based on our knowledge of when and where Weisz collected specimens (for more details see method section).
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