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947 results for “Balkans”

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zenodo44/100

Dataset and Code: Lability in Balkan Slavic

<p>This is a dataset for the article: Makartsev, Maxim; Wahlstr&ouml;m, Max and Anastasia Escher. 2025. "Lability in Balkan Slavic,"&nbsp;<em>Studies in Language 49</em> [Special issue: &ldquo;Areal Effects in Argument-Coding Patterns&rdquo;]</p> <p><span>Abstract: The article assesses claims made in the previous studies regarding the increase in the number of identical transitive and intransitive verbs with patient-like arguments, that is, patientively labile (P-labile) verbs, in Macedonian in comparison with the other South Slavic languages. Based on an extensive sample of 130 varieties from different parts of the South Slavic dialectal continuum, this study confirms the observations regarding increased lability in Western and some Southeastern Macedonian dialects. Additionally, outside the labile hotbed, lability remains low with relatively homogenous patterning.</span></p> <p><span>Keywords: lability, </span>causativity<span>, Balkan linguistics, South Slavic dialectology, language contact.</span></p>

opencc-by-4.0Nov 2024View details →
zenodo44/100

Emissions for individual housing in the Western Balkans

<p>Emissions for individual housing in the Western Balkans<br>-----------------------------------------------------------------<br>Version: Open data version 1<br>Date: 2024-10-09<br>Spatial reference system: ETRS89 / ETRS-LAEA (EPSG:3035)<br>Grid resolution: 500x500 m<br>DOI: 10.5281/zenodo.13906810</p> <p>Files<br>-------------------<br>emission_sector-C2_wb6_500m_2019_NOx.tif &nbsp; &nbsp;Gridded emissions for NOx<br>emission_sector-C2_wb6_500m_2019_PM10.tif &nbsp; Gridded emissions for PM10<br>emission_sector-C2_wb6_500m_2019_PM25.tif &nbsp; Gridded emissions for PM2.5<br>emission_sector-C2_wb6_500m_2019_SOx.tif &nbsp; &nbsp;Gridded emissions for SOx<br>readme.txt &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;This readme-file</p> <p>Sector<br>-------------------<br>SNAP: 020200<br>GNFR: C2 (residential stationary combustion)<br>NFR: 1.A.4.b.i (Residential plants)</p> <p>Substances<br>-------------------<br>NOx: Nitrogen oxides as NO2<br>PM10: Particulate matter up to 10 &micro;m size<br>PM2.5: Particulate matter up to 2.5 &micro;m size<br>SOx: Sulphuric oxides (as SO2)</p> <p><br>Years<br>-------------------<br>2019</p> <p><br>Units<br>-------------------<br>ton/year</p> <p>Fileformat<br>-------------------<br>geotiff</p>

opencc-by-4.0Oct 2024View details →
zenodo40/100

Figure 2. Summer core area delineation. The straight line with a in Demographic characteristics, seasonal range and habitat topography of Balkan chamois population in its southernmost limit of its distribution (Giona mountain, Greece)

Figure 2. Summer core area delineation. The straight line with a slope of –1 represents the random use of space within the population seasonal range. The curve that sags below the line of random use represents the clumped use of space. The summer core area can be defined at the point whose tangent has slope –1, e.g. 85%, that is, whose tangent is parallel to the line of random use. This is also the point of the curve that is furthest from the line of random use.

opencc-by-4.0Jan 2014View details →
zenodo40/100

FIGURES 14 – 16 in The larvae of Micropterna coiffaiti Décamps 1963, Micropterna taurica Martynov 1917, and Potamophylax goulandriorum Malicky 1974 (Trichoptera: Limnephilidae), including a key to the hitherto known Stenophylacini larvae of the Hellenic western Balkan region

FIGURES 14 – 16. Micropterna coiffaiti Décamps 1963, 5 th instar larva. 14, Dorsa of abdominal segments VIII and IX, dorsal (pds = posterodorsal setae). 15, Tip of abdomen, right lateral (black arrow: posterolateral seta). 16, Larval case, right lateral. Scale bars: 1 mm. FIGURES 17 – 18. Micropterna taurica Martynov, 1917, 5 th instar larva. 17, Head, dorsal, with whitish sediment particles attached to large-scale microspinule areas. 18, Head, right lateral, detail of large-scale microspinule areas at frontoclypeus and parietalia (black arrows). Scale bars: 1 mm (except 18: 0.5 mm).

opencc-zeroDec 2016View details →
zenodo40/100

FIGURES 7 – 13 in The larvae of Micropterna coiffaiti Décamps 1963, Micropterna taurica Martynov 1917, and Potamophylax goulandriorum Malicky 1974 (Trichoptera: Limnephilidae), including a key to the hitherto known Stenophylacini larvae of the Hellenic western Balkan region

FIGURES 7 – 13. Micropterna coiffaiti Décamps 1963, 5 th instar larva. 7, Metanotum and abdominal segment I, dorsal (sa 1 – sa 3: setal areas 1 – 3). 8, Right foreleg, anterior face. 9, Right midleg, anterior face (black arrow: proximodorsal seta; white arrows: additional face setae). 10, Right hind leg, anterior face. 11, Detail of left midleg trochanter, ventral (black arrows: additional setae on proximal section of trochanter). 12, Metathorax and anterior abdominal segments, right lateral (black arrow: no posterior sclerite on lateral protuberance). 13, Sternum of abdominal segment I, ventral. Scale bars: 1 mm.

opencc-zeroDec 2016View details →
zenodo40/100

FIGURES 1 – 6 in The larvae of Micropterna coiffaiti Décamps 1963, Micropterna taurica Martynov 1917, and Potamophylax goulandriorum Malicky 1974 (Trichoptera: Limnephilidae), including a key to the hitherto known Stenophylacini larvae of the Hellenic western Balkan region

FIGURES 1 – 6. Micropterna coiffaiti Décamps 1963, 5 th instar larva. 1, Head, dorsal (small white and black numbers: setal positions # 1 – 17, x, and y on frontoclypeus and right parietal; # 17: only setal base visible, seta missing; white arrow: antenna). 2, Head, right lateral (dotted oval: spinule area). 3, Head, ventral (small white number: position of base of seta # 18; seta missing). 4, Head and pronotum, right lateral (a: prosternal horn; b: pronotal transverse groove; d: intermediate pale setae; e: long dark setae). 5, Pro- and mesonota, dorsal (c: short, pale setae; sa 1 – sa 3: setal areas 1 – 3). 6, Prosternum. Scale bars: 1 mm (except 5: 0.5 mm).

opencc-zeroDec 2016View details →
zenodo40/100

Digitalization indicators and date on FDI for CEE and Balkan countries

<p>The data representing digitalization indicators and data for the foreign direct investment for the CEE and Balkan countries.&nbsp;</p>

opencc-by-4.0Oct 2023View details →
zenodo40/100

Digitalization in Balkan Countries

<p>This data was collected based on primary sources like IMF,WB, and secondary sources like ITU about the Balkan countries, represented by Serbia, Montenegro, North Macedonia, Bosna a Hercegovina &nbsp;, Kosovo, and Albania, where the expansion is described. The data is described between the period 2018 to 2022, where it is possible to obtain a general, comprehensive overview about digitalization in Balkan countries .</p>

opencc-by-4.0Nov 2023View details →
zenodo40/100

Figure 17 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 17. Distribution of some xeromontane Noctuidae species at the Balkan Peninsula. Legend:♦ Rhyacia helvetina schepleri;□ Dichagyris celsicola goateri;● Chersotis capnistis schnacki;ORhyacia psammia stavroitiacus.

opencc-by-4.0Oct 2014View details →
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Figure 14 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 14. Distribution ofErebia ottomana in Europa and on the Balkan peninsula. Legend: o – E. ottomana ottomana (Ulu dagh), b – E. ottomana balcanica, bu – E. ottomana bureschi, d – E. ottomana drenovskii, be – E. ottomana benacensis, t – E. ottomana tardenota.

opencc-by-4.0Oct 2014View details →
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Figure 12 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 12. Distribution of arctic­alpine species in the Carpathians and on the Balkan peninsula. Legend: ◊ Zygaena exulans, O Erebia pandrose, ♦ Glacies coracina, □ Grammia quenselii, ● Anarta melanopa rupestralis, O Agrotis fatidica.

opencc-by-4.0Oct 2014View details →
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Figure 15 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 15. Distribution ofErebia rhodopensis and related species. Legend: rh – E. rhodopensis, ae – E. aethiopella, g – E. gorgone.

opencc-by-4.0Oct 2014View details →
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Figure 9 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 9. Distribution of Boloria pales on the Balkan peninsula and in the Carpathians. The western Balkanic populations are connected with the Eastern Alpine nominotypic subspecies. The Southern Carpathian populations (B. pales carpathomeridionalis) are related to the Eastern BalkanicB. pales rilaensis.

opencc-by-4.0Oct 2014View details →
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Figure 11 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 11. Distribution of Euphydryas cynthia in Europe. c – Euphydryas cynthia cynthia; a – Euphydryas cynthia alpicola; l – Euphydryas cynthia leonhardi; d – Euphydryas cynthia drenovskyi. The population of the Rila Mts shows some parallel characters (e.g. reddish submarginal spots in males, less dichrous females) with the nominotypic subspecies. The population of the Pirin Mts is characterised by whitish submarginal spots in males and more dichrous colouration in females, as in the subspeciesE. cynthia alpicola.

opencc-by-4.0Oct 2014View details →
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Figure 10 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 10. Distribution ofErebia manto(black circles) undE. cassioides(open circles) in the high mountain systems of southeastern Europe. E. manto is widely distributed in the Carpathians, partly as the nominotypic subspecies (N­NE Carpathians), partly as E. manto trajanus (E and S Carpathians). It occurs as E. manto osmana only in some high mountains of Bosnia. E cassioides occurs in the western Balkan Peninsula as E. cassioides illyrica (Crna Gora) and illyromacedonica (FYR Makedonia and Greek Macedonia), and as E. cassioides kinoshitai (Stara Planina) and E. cassioides macedonica(Rila, Pirin) in the eastern high mountains of the peninsula.

opencc-by-4.0Oct 2014View details →
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Figure 8 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 8. Allo­ and parapatric distribution of Erebia tyndarus­ group in Europa. The Balkanic populations (Durmitor, Maglić, Volujak:R. cassioides illyrica; Šar planina, Korab: E.cassioides illyromacedonica; Stara Planina:E. cassioides kinoshitai; Rila, Pirin: E. cassioides macedonica) are allied to the Southern Carpathian E. cassioides neleus. Further abbreviations:c E. cassioides cassioides,caE. calcaria,a E. arvernensis,niE. nivalis,hE. hispania.

opencc-by-4.0Oct 2014View details →
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Figure 13 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 13. Distribution ofBoloria graeca. Legend: Balcan peninsula southern part:B. graeca graeca; Balcan peninsula NW and E part:B. graeca balcanica; SW Alps:B. graeca tendensis.B. graeca graecaandB. graeca balcanicaare only slightly differentiated (probably as a geographical cline!).

opencc-by-4.0Oct 2014View details →
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Figure 4 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 4. Distribution of Erebia melas on the Balkan peninsula and in the Carpathians. Legend: 1 – Erebia melas leonhardi; 2–3 – E. melas acoris(2) andE. melas nanos(3); 4 – E. melasof the Rtanj Planina (probably extinct); 5 – E. melas melas; 6 – E. melas koenigiella(instable altitudinal form ofE. m. melas); 7–9 – E. melas carpathicola(7, 8) and E. melas runcensis (9). Legend of the inlayed map: white sector – reddish coloration, black sector – black wing coloration; left side of the circle: male upper­ and underside, right side of the circle: female upper­ and underside (Hungarian Natural History Museum, Zoological State Collection Munich and coll. Varga, Debrecen).

opencc-by-4.0Oct 2014View details →
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Figure 7 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 7. Vertical distribution of the alpine and Balkanic oreal species in the Pirin Mts. Legend: Horizontal lines 1 – upper limit of grassy vegetation (Vihren, 2915 m), 2­ upper limit of Pinus montana (isolated scrubs) ~ 2600 m, 3 – upper limit of Pinus montana/Juniperus nana zone ~ 2400 m, 4 – lower limit of Arctic­Alpine cusheon plants and dwarf scrubs ~ 2300 m, 5 – upper limit ofPinus heldreichii stands. Vertical lines: 1 – Boloria graeca, 2 – Erebia melas, 3 – E. ottomana, 4 – E. orientalis, 5 – E. rhodopensis, 6 – Boloria pales, 7 – Euphydryas cynthia, 8 – Erebia cassioides, 9 – E. gorge, 10 – Glacies coracina.

opencc-by-4.0Oct 2014View details →
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Figure 5 in Biogeography of the high mountain Lepidoptera in the Balkan Peninsula

Figure 5. Vertical distribution of the Boloria pales­ group in European high mountains. The niche overlap is between the synpatric species is mostly insignificant.

opencc-by-4.0Oct 2014View details →

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Allen Brain Atlas

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allen-brain-atlas
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DANDI Archive for NWB datasets

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dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record