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FIGURE 1–8. Fig. 1 in Endogean and cavernicolous Coleoptera of the Balkans. XVII. A new species of the genus Speluncarius Reitter, 1886 (Coleoptera, Carabidae, Harpalinae, Pterostichini) from Croatia
FIGURE 1–8. Fig. 1. Speluncarius (s.str.) biokovensis, habitus (photo Dušan Beňo); Fig. 2. Speluncarius (s.str.) anophthalmus, habitus (photo Dušan Beňo); Fig. 3. Speluncarius (s.str.) setipennis, habitus (photo Dušan Beňo); Fig. 4. Speluncarius (s.str.) setipennis, habitus in nature (photo Antonín Kůrka); Fig. 5. Speluncarius (s.str.) biokovensis, aedeagus, lateral view, scale = 0.5mm; Fig. 6. Speluncarius (s.str.) anophthalmus, aedeagus, lateral view, scale = 0.5mm; Fig. 7. Speluncarius (s.str.) setipennis, aedeagus, lateral view, scale = 0.5mm; Fig. 8. Distribution of Speluncarius (s.str.) of western Balkans (1—S. anophthalmus, 2—S. setipennis, 3—S. biokovensis, 4—S. minutulus).
FIGURE 3 in Blackflies (Diptera: Simuliidae) in Croatia: species richness, distribution and relationship to surrounding countries
FIGURE 3. Comparison of Croatian blackfly assemblage with faunas of surrounding countries. Surface area (km): Italy (301,338 km²), Slovenia (20,273 km²), Hungary (93,030 km²), SRB = Serbia (88,361 km²), Bosnia and Herzegovina (51,197 km²), Croatia (56,594 km2).
Zagreb Cathedral facade, Croatia
I shot more than 200 photos for this cathedral during my holiday. Source: Objaverse 1.0 / Sketchfab
Replication Data for Younger adolescents' perspectives on book censorship in Croatia
<p>Questionnaire and raw research data from younger adolescents’ perspectives on book censorship research. </p>
Distribution. SW Asia from Iraq and Iran to Afghanistan, Pakistan, India, Nepal, and Bhutan; also Bangladesh, Myanmar and S China (including Hainan I). Introduced to Antigua, Barbados, Beef Island, Buck Island, Carriacou, Croatia, Cuba, Fiji, French Guiana, Goat Island, Grenada, Guadeloupe, Guyana, Hawaii, Hispaniola, Jamaica, Japan, Jost Van Dyke, La Desirade, Lavango, Mafia (Tanzania), Marie Galante, Martinique, Maui, Mauritius, Molokai, Nevis, Oahu, Puerto Rico, St. Croix, St. John, St. Kitts, St. Lucia, St. Martin, St. Thomas, St. Vincent, Surinam, Tortola, Trinidad, Vieques, and Water Island. Introduction was unsuccessful in the Dominican Republic. The Small Indian Mongoose or the Javan Mongoose is said to occur on Hong Kong since the 1980s, and to have been also introduced to some Indonesian islands (particularly Ambon). in Herpestidae
Distribution. SW Asia from Iraq and Iran to Afghanistan, Pakistan, India, Nepal, and Bhutan; also Bangladesh, Myanmar and S China (including Hainan I). Introduced to Antigua, Barbados, Beef Island, Buck Island, Carriacou, Croatia, Cuba, Fiji, French Guiana, Goat Island, Grenada, Guadeloupe, Guyana, Hawaii, Hispaniola, Jamaica, Japan, Jost Van Dyke, La Desirade, Lavango, Mafia (Tanzania), Marie Galante, Martinique, Maui, Mauritius, Molokai, Nevis, Oahu, Puerto Rico, St. Croix, St. John, St. Kitts, St. Lucia, St. Martin, St. Thomas, St. Vincent, Surinam, Tortola, Trinidad, Vieques, and Water Island. Introduction was unsuccessful in the Dominican Republic. The Small Indian Mongoose or the Javan Mongoose is said to occur on Hong Kong since the 1980s, and to have been also introduced to some Indonesian islands (particularly Ambon).
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.
Sample based prevalence data complementing the European Union One Health 2020 Zoonoses Report - Croatia
<p>This dataset contains monitoring data on zoonoses and zoonotic agents under the Directive 2003/99/EC. This Directive requires Member Sates (MSs) to collect, evaluate and report data on zoonoses and zoonotic agents. MSs can also report monitoring data and information on some other pathogenic microbiological agents in foodstuffs. Relevant EU legislation: Commission Regulation (EC) No 2073/2005,Commission Regulation (EC) No 1441/2007, Commission Regulation (EU) No 1086/2011, Commission Regulation (EU) No 209/2013, Commission Regulation(EU) No 217/2014.</p>
FIGURES 21–25. Cymbella amicula stat. nov. et nom. nov. SEM external view. 21. Frustule and whole valve. 22–25 in Cymbopleura amicula stat nov. et. nom. nov. (Bacillariophyceae)-a rare diatom species from a karst river in Croatia
FIGURES 21–25. Cymbella amicula stat. nov. et nom. nov. SEM external view. 21. Frustule and whole valve. 22–25. External view of whole valves. Scale bars 5 µm (Figs 21–25).
FIGURES 2–20 in Cymbopleura amicula stat nov. et. nom. nov. (Bacillariophyceae)-a rare diatom species from a karst river in Croatia
FIGURES 2–20. Cymbella amicula stat. nov. et nom. nov. (HRNDC000026) LM, size diminution series. Scale bar = 10 µm.
FIGURES 26–31. Cymbella amicula stat. nov. et nom. nov. SEM internal view. 26–28 in Cymbopleura amicula stat nov. et. nom. nov. (Bacillariophyceae)-a rare diatom species from a karst river in Croatia
FIGURES 26–31. Cymbella amicula stat. nov. et nom. nov. SEM internal view. 26–28. View of the whole valve. 29, 30. Detailed view of the valve centre, showing the overgrowth of silica that covers the proximal raphe ends. 31. Detailed view of valve apex showing the small, knob-like helictoglossa. Scale bars in 10 µm (Figs 26 and 27), 5 µm (Fig. 28), 2 µm (Figs 29–31).
Supplementary material 1 from: Krčmar S, Kučinić M, Pezzi M, Bruvo Mađarić B (2022) DNA barcoding of the horsefly fauna (Diptera, Tabanidae) of Croatia with notes on the morphology and taxonomy of selected species from Chrysopsinae and Tabaninae. ZooKeys 1087: 141-161. https://doi.org/10.3897/zookeys.1087.78707
Morphological characteristics of females of some horseflies from subfamily Tabaninae and Chrysopsinae
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.
Distribution. India, S Nepal, S Bhutan, Bangladesh, and Sri Lanka. Chital have been introduced in Europe (Croatia, Ukraine, Moldova), Armenia, the Andaman Is, New Guinea, Australia, USA (California, Texas & Hawaii), Brazil, Uruguay, and Argentina. in Cervidae
Distribution. India, S Nepal, S Bhutan, Bangladesh, and Sri Lanka. Chital have been introduced in Europe (Croatia, Ukraine, Moldova), Armenia, the Andaman Is, New Guinea, Australia, USA (California, Texas & Hawaii), Brazil, Uruguay, and Argentina.
Distribution. Mediterranean, scattered in islands in Aegean and Ionian seas and coasts of Greece and W Turkey, NE Morocco, and NW Algeria; E Atlantic Ocean at Desertas Is (Madeira Is group) and Ras Nouadhibou (= Cabo Blanco/Cap Blanc Peninsula) on the border between Western Sahara and Mauritania; occasionally recorded in Canary Is, Mauritania (Banc d'Arguin), Tunisia (La Gallite), Libya (Cyrenaic coast), and the Adriatic coast in Croatia. in Phocidae
Distribution. Mediterranean, scattered in islands in Aegean and Ionian seas and coasts of Greece and W Turkey, NE Morocco, and NW Algeria; E Atlantic Ocean at Desertas Is (Madeira Is group) and Ras Nouadhibou (= Cabo Blanco/Cap Blanc Peninsula) on the border between Western Sahara and Mauritania; occasionally recorded in Canary Is, Mauritania (Banc d'Arguin), Tunisia (La Gallite), Libya (Cyrenaic coast), and the Adriatic coast in Croatia.
Distribution. Most of Europe, from the British Is and NW France E to W Siberia as far E as Irtysh and Ob rivers, and from S Sweden, S Finland, and S Karelia (Russia) S to N Italy and N Balkans; marginally present also in NW Kazakhstan. In E Europe and in Asia the border roughly follows the extreme extension of the taiga in the N (northernmost record is from Pechora River close to 68°N) and the steppe-forest—steppe transition in the S. Present on some Is in the Baltic Sea and around Denmark (Oland, Funen, Zeeland, Bjgrng, Tasinge, Tung, Langeland, Riigen, Usedom, and Wollin), around Great Britain (Sky, Mull, Anglesey, Wight, and Jersey), offshore W coast of France (Ouessant and Ré), and on Cres (Croatia) as the only Mediterranean I. in Talpidae
Distribution. Most of Europe, from the British Is and NW France E to W Siberia as far E as Irtysh and Ob rivers, and from S Sweden, S Finland, and S Karelia (Russia) S to N Italy and N Balkans; marginally present also in NW Kazakhstan. In E Europe and in Asia the border roughly follows the extreme extension of the taiga in the N (northernmost record is from Pechora River close to 68°N) and the steppe-forest—steppe transition in the S. Present on some Is in the Baltic Sea and around Denmark (Oland, Funen, Zeeland, Bjgrng, Tasinge, Tung, Langeland, Riigen, Usedom, and Wollin), around Great Britain (Sky, Mull, Anglesey, Wight, and Jersey), offshore W coast of France (Ouessant and Ré), and on Cres (Croatia) as the only Mediterranean I.
Distribution. Mediterranean Europe in N Spain, S France, W & S Switzerland, N Italy, S Austria, Slovenia, Hungary, Croatia, N Bosnia and Herzegovina, and NE Serbia. in Cricetidae
Distribution. Mediterranean Europe in N Spain, S France, W & S Switzerland, N Italy, S Austria, Slovenia, Hungary, Croatia, N Bosnia and Herzegovina, and NE Serbia.
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.
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. Croatia (including Adriatic islands of Korc¢ula and Mljet), S Bosnia and Herzegovina, Montenegro, S Serbia, Kosovo, Albania, Macedonia, SW Bulgaria, and Greece (including Ionian islands of Corfu, Cephalonia, Zakhyntos, and Kythera, and Aegean islands of Thasos, Alonissos, Peristera, Euboea, and Satamis). in Muridae
Distribution. Croatia (including Adriatic islands of Korc¢ula and Mljet), S Bosnia and Herzegovina, Montenegro, S Serbia, Kosovo, Albania, Macedonia, SW Bulgaria, and Greece (including Ionian islands of Corfu, Cephalonia, Zakhyntos, and Kythera, and Aegean islands of Thasos, Alonissos, Peristera, Euboea, and Satamis).
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).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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
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