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128 results for “Bosnia and Herzegovina”
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 1 in Checklist of the earthworm fauna of Bosnia & Herzegovina (Oligochaeta: Lumbricidae)
FIGURE 1. Collecting sites in Bosnia & Herzegovina (circle: literature data; triangle: author's data). The figure with the collecting sites was displayed using Google Maps.
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.
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).
FIGURES 32–33 in Description of the larvae of Drusus radovanovici septentrionis Marinković- Gospodnetić, 1976 and Drusus croaticus Marinković-Gospodnetić, 1971 (Trichoptera: Limnephilidae) from Bosnia and Herzegovina, and Croatia
FIGURES 32–33. Gill diagrams: position of filaments on abdominal segments I–VIII; —gills always present; ☺— gills not present always. 32, Drusus radovanovici septentrionis Marinković-Gospodnetić, 1976; 33, Drusus croaticus Marinković-Gospodnetić, 1971.
FIGURES 25–31 in Description of the larvae of Drusus radovanovici septentrionis Marinković- Gospodnetić, 1976 and Drusus croaticus Marinković-Gospodnetić, 1971 (Trichoptera: Limnephilidae) from Bosnia and Herzegovina, and Croatia
FIGURES 25–31. Drusus croaticus Marinković-Gospodnetić, 1971. 25, pronotum, mesonotum, lateral view; 26, pronotum, mesonotum and metanotum, dorsal view; 27, forelegs, lateral view; 28, mid-legs, lateral view; 29, hind-legs, lateral view; 30, abdominal segment IX, dorsal view; 31, anal proleg, lateral view.
FIGURES 2–9 in Description of the larvae of Drusus radovanovici septentrionis Marinković- Gospodnetić, 1976 and Drusus croaticus Marinković-Gospodnetić, 1971 (Trichoptera: Limnephilidae) from Bosnia and Herzegovina, and Croatia
FIGURES 2–9. Drusus radovanovici septentrionis Marinković-Gospodnetić, 1976. 2, larva in its case, dorsal view; 3, larva, lateral view; 4, head and pronotum, lateral view; 5, head and pronotum, dorsolateral view; 6, head capsule, lateral view, 7, spinules; 8, head capsule, frontal view; 9 mandibles, dorsal view.
FIGURE 1 in Description of the larvae of Drusus radovanovici septentrionis Marinković- Gospodnetić, 1976 and Drusus croaticus Marinković-Gospodnetić, 1971 (Trichoptera: Limnephilidae) from Bosnia and Herzegovina, and Croatia
FIGURE 1. Distribution of Drusus croaticus Marinković-Gospodnetić, 1971, Drusus radovanovici radovanovici Marinković-Gospodnetić, 1970, D. radovanovici septentrionis Marinković-Gospodnetić, 1976 and area of Drusus species from bosnicus group; 1, Livno, 2, Plitvice Lakes National Park, 3, the Kostelka River spring, 4, the Čabranka River spring.
FIGURES 18–24 in Description of the larvae of Drusus radovanovici septentrionis Marinković- Gospodnetić, 1976 and Drusus croaticus Marinković-Gospodnetić, 1971 (Trichoptera: Limnephilidae) from Bosnia and Herzegovina, and Croatia
FIGURES 18–24. Drusus croaticus Marinković-Gospodnetić, 1971. 18, larva in its case, lateral view; 19, larva, lateral view; 20, head and pronotum, dorsolateral view; 21, head lateral view; 22, head capsule, frontal view; 23, mandibles, dorsal view; 24, head capsule, ventral view.
FIGURES 10–17 in Description of the larvae of Drusus radovanovici septentrionis Marinković- Gospodnetić, 1976 and Drusus croaticus Marinković-Gospodnetić, 1971 (Trichoptera: Limnephilidae) from Bosnia and Herzegovina, and Croatia
FIGURES 10–17. Drusus radovanovici septentrionis Marinković-Gospodnetić, 1976. 10, head capsule, ventral view; 11, pronotum, mesonotum, lateral view; 12, pronotum, mesonotum and metanotum, dorsal view; 13, forelegs, lateral view; 14, mid-legs, lateral view; 15, hind-legs, lateral view; 16, abdominal segment IX, dorsal view; 17, anal proleg, lateral view.
Open Science stakeholders in Albania, Armenia, Bosnia and Herzegovina, Bulgaria, Croatia, Cyprus, Georgia, Greece, Hungary, Moldova, Montenegro, North Macedonia, Romania, Serbia and Slovenia [updated, February 2023]
<p>The dataset contains tabular information about 1118 stakeholders (1079 unique entities) in 15 countries of Southeastern Europe that have been identified as Open Science stakeholders within the framework of the project NI4OS-Europe, funded by the European Commission under the INFRAEOSC-5b call.</p> <p>It was collected between November 2022 and the end of January 2023 based on the information provided by project partners from Albania, Armenia, Bosnia and Herzegovina, Bulgaria, Croatia, Cyprus, Georgia, Greece, Hungary, Moldova, Montenegro, North Macedonia, Romania, Serbia and Slovenia. It builds upon the dataset collected in 2019 as part of the NI4OS-Europe landscaping activity (Kosanović, Biljana, Ševkušić, Milica, & Otašević, Vladimir. (2020). Open Science stakeholders in Albania, Armenia, Bosnia and Herzegovina, Bulgaria, Croatia, Cyprus, Georgia, Greece, Hungary, Moldova, Montenegro, North Macedonia, Romania, Serbia and Slovenia [Data set]. Zenodo. <a href="https://doi.org/10.5281/zenodo.3766125">https://doi.org/10.5281/zenodo.3766125</a>). In November 2022, the project partners were invited to review and update this original dataset.</p> <p>The stakeholders are classified into five groups based on their role in the research ecosystem: FUND (research funders and policymakers), CREATE (universities, research institutes, etc.), SUPPORT (libraries, repositories, research infrastructures, etc.), CONSUME (organizations using research results in their work, e.g. SMEs) and FACILITATE (individuals and organizations involved in promoting the principles off open science).<br> The dataset contains the following information for each entry: country, stakeholder category/role, official/legal name of the organization, city, Zipcode, addresses (street name and number), URL of the institutional website, geographic coordinates (latitude and longitude).</p> <p>****Dataset contents****<br> NI4OS_Stakeholder_Map_20230222.csv, data file, comma-separated values<br> NI4OS_Stakeholder_Map_20230222-README.txt, metadata, text format</p> <p>****Column headers and field types***<br> Country (text)<br> StakeHoldersRole (text, ItemList{fund,create,facilitate,consume,support})<br> InstitutionName (text)<br> City (text)<br> Zipcode (text)<br> Address (text)<br> URL (text-web address)<br> Latitude (number.decimal(2,7))<br> Longitude (number.decimal(2,7))</p> <p>Data from this dataset have been quality-checked by the NI4OS-Europe project team. We recommend these data for further use.<br> <br> The dataset was used to generate an interactive map: https://ni4os.eu/os-stakeholders-map//</p> <p>****Dataset license****<br> The dataset is made available under the Creative Commons Attribution 4.0 International License (CC BY 4.0), <a href="https://creativecommons.org/licenses/by/4.0">https://creativecommons.org/licenses/by/4.0</a></p>
Population-based Age-stratified Seroepidemiological Investigation Protocol for Coronavirus 2019 (COVID-19) Infection in the Federation of Bosnia and Herzegovina
ClinicalTrials.gov study NCT05124535. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
Molecular variability of Field Maple populations (Acer campestre L.) in Bosnia and Herzegovina
Measures to preserve forest trees should focus on the preservation of intra-species genetic variability, which reflects a species' adaptive evolutionary potential enabling it to survive unfavourable conditions. Altogether 25 populations of Field Maple from Bosnia and Herzegovina were studied at ten nuclear microsatellite loci. A high level of genetic variability was identified as a result of the eco-geographical pattern, while ecological distance is a better predictor of genetic variability in the populations than geographical distance. The average genetic differentiation of the populations is low with the exception of sub-Mediterranean populations, above all the most southerly population (Trebinje). This indicates the fragmented distribution of the sub-Mediterranean populations, resulting in spatial isolation and the resultant increase in genetic divergence of these populations. Since the Trebinje population alone has not experienced a genetic bottleneck in the recent past (in one mutation model), the assumption is that this is a refugial population displaying a specific genetic structure. Three typical sub-Mediterranean populations (Trebinje, Ljubuški and Mostar) derive from a single source gene pool, suggesting a potential gene flow between populations over time. The results of the study may prove useful for the preservation of the species and its genetic diversity, particularly by means of in situ and ex situ conservation of the southernmost (peripheral) populations. The results obtained may also serve as a basis for further studies in other parts of the species' range, with a view to determining the interaction of ecological, geographical, climatic and migratory factors with the overall genetic variability.
Figure 5 from: Hofman S, Rysiewska A, Osikowski A, Falniowski A (2020) A new species of Kerkia Radoman, 1978 (Caenogastropoda, Hydrobiidae) from Bosnia and Herzegovina. ZooKeys 973: 17-33. https://doi.org/10.3897/zookeys.973.52788
Figure 5 Shell variability of Kerkia briani, labels the same as in the molecular trees. Scale bar: 0.5 mm.
Figure 6 from: Hofman S, Rysiewska A, Osikowski A, Falniowski A (2020) A new species of Kerkia Radoman, 1978 (Caenogastropoda, Hydrobiidae) from Bosnia and Herzegovina. ZooKeys 973: 17-33. https://doi.org/10.3897/zookeys.973.52788
Figure 6 Renal and pallial section of the female reproductive organs of Kerkia briani: A the loop of oviduct in its normal position and the loop of the rectum B the loop of oviduct moved to show the receptaculum seminis and duct of bursa. Abbreviations: bc – bursa copulatrix, cbc – duct of bursa, ga – albuminoid gland, gn – nidamental gland, gp – gonoporus, ov – oviduct, ovl – loop of renal oviduct, rec – rectum, rs – receptaculum seminis. Scale bars: 1 mm.
Figure 2 from: Hofman S, Rysiewska A, Osikowski A, Falniowski A (2020) A new species of Kerkia Radoman, 1978 (Caenogastropoda, Hydrobiidae) from Bosnia and Herzegovina. ZooKeys 973: 17-33. https://doi.org/10.3897/zookeys.973.52788
Figure 2 Type locality of Kerkia briani sp. nov.: A, B River Trebišnjica with the spring Polički Studenac Vrelo at its right bank C the spring from where interstitial snails were pumped.
Figure 8 from: Hofman S, Rysiewska A, Osikowski A, Falniowski A (2020) A new species of Kerkia Radoman, 1978 (Caenogastropoda, Hydrobiidae) from Bosnia and Herzegovina. ZooKeys 973: 17-33. https://doi.org/10.3897/zookeys.973.52788
Figure 8 Maximum Likelihood tree inferred from mitochondrial COI. Bootstrap supports above 60% with corresponding Bayesian probabilities are given.
Figure 1 from: Ćurčić S, Vesović N, Vrbica M, Popović S, Radovanović Ž, Ćurčić NB, Rađa T (2021) A new species of Leonhardia Reitter, 1901 (Coleoptera, Leiodidae, Leptodirini) from Bosnia and Herzegovina, with a key to species of the genus. Subterranean Biology 41: 69-85. https://doi.org/10.3897/subtbiol.41.75613
Figure 1 Map of Bosnia and Herzegovina showing locality records for all taxa of Leonhardia. The grey pattern indicates karst terrain L. reitteri reitteri (blue circles), L. reitteri mersa (blue cross), L. reitteri zariquieyi (blue rhombuses), L. delminiumica (green squares), L. jajcensis (lime deltoid), L. hilfi hilfi (orange star), L. hilfi robusta (orange sun), L. sebesicensis (pink pentagon), L. droveniki (red hexagon), L. solaki sp. nov. (yellow triangle). Scale bar: 50 km.
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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
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
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
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.