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947 results for “Balkans”
Figure 8 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 8. Cyphophthalmus paragamiani sp. nov. (holotype except B, D – female paratype). A, male dorsum; B, female dorsum (partially damaged); C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 18 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 18. Cyphophthalmus kratochvili sp. nov. (holotype except B – paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 29 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 29. Cyphophthalmus corfuanus (Kratochvíl) (male 1.70 mm from Corfu). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 12 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 12. Cyphophthalmus minutus (Kratochvíl) (neotype except B, F – topotype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 11 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 11. Cyphophthalmus minutus (Kratochvíl) (neotype except C – topotype). A, spermatopositor, dorsal view; B, male ventral prosomal complex; C, female ventral prosomal complex; D, basitarsus and telotarsus of leg I; E, basitarsus and telotarsus of leg IV; F, tibia and tarsus of pedipalp; G, chelicera; H, adenostyle. Scale bars: A, H = 100 Mm; B–G = 400 Mm.
Figure 14 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 14. Cyphophthalmus gordani sp. nov. (holotype except B, F – female paratype). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 35. A in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 35. A, geographical distribution of the three phylogenetic lines of the genus Cyphophthalmus (signs often cover more than one locality); B, distribution of presented species in south-eastern part of the Balkan Peninsula.
Figure 34 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 34. Cyphophthalmus hlavaci sp. nov. (paratypes from Bast). A, male dorsum; B, female dorsum; C, dorsum granulation (fifth to ninth tergite); D, detail of granulation (convex tubercles) at the border of eighth to ninth tergite; E, terminal posterior part of the male dorsum with pores of anal glands; F, dorsum, frontal view.
Figure 6 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 6. Detail of integument ornamentation of the third opisthosomal segment, dorsal. A, Cyphophthalmus corfuanus (Kratochvíl); B, Cyphophthalmus zetae sp. nov.; C, Cyphophthalmus martensi sp. nov.; D, Cyphophthalmus beschkovi (Mitov); E, Cyphophthalmus sp. (Cave, Mt. Biokovo, Dalmatia); F, Cyphophthalmus noctiphilus (Kratochvíl).
Figure 5 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 5. Distal portion of ovipositor (left terminal lobe excluded), ventral view. A, Cyphophthalmus minutus (Kratochvíl) topotype; B, Cyphophthalmus gordani sp. nov.; C, Cyphophthalmus neretvanus sp. nov.; D, Cyphophthalmus trebinjanus sp. nov.; E, Cyphophthalmus ognjenovici sp. nov.; F, Cyphophthalmus rumijae sp. nov.; G, Cyphophthalmus martensi sp. nov. Circles represent insertion of ventral setae; x represent insertion of dorsal setae. Scale bar = 100 Mm.
Figure 4 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 4. Distal portion of ovipositor (left terminal lobe excluded), ventral view. A, Cyphophthalmus gjorgjevici (Hadži), (Rašće, Macedonia); B, Cyphophthalmus paragamiani sp. nov.; C, Cyphophthalmus thracicus sp. nov.; D, Cyphophthalmus cf. thracicus (Evros, Greece); E, Cyphophthalmus corfuanus (Kratochvíl) (Corfu); F, Cyphophthalmus zetae sp. nov.; G, Cyphophthalmus hlavaci sp. nov. Circles represent insertion of ventral setae; x represent insertion of dorsal setae. Scale bar = 100 Mm.
Figure 7 in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 7. Cyphophthalmus paragamiani sp. nov. (holotype). A, spermatopositor (dorsal view); B, ventral prosomal complex; C, basitarsus and telotarsus of leg I; D, basitarsus and telotarsus of leg IV; E, tibia and tarsus of pedipalp; F, chelicera; G, adenostyle. Scale bars: A, G = 100 Mm; B–F = 400 Mm.
Figure 3. Male anal regions. A–B in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 3. Male anal regions. A–B, Cyphophthalmus corfuanus (Kratochvíl); C, Cyphophthalmus serbicus (Hadži); D, Cyphophthalmus ere Karaman; E, Cyphophthalmus ognjenovici sp. nov.; F, Cyphophthalmus duricorius Joseph.
Figure 1. A, C in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 1. A, C, Siro exilis Hoffman, 1963 (West Virginia, Summers County). A, spermatopositor, dorsal view; C, ventral prosomal complex. B, D, Cyphophthalmus teyrovskyi (Kratochvíl, 1938). B, spermatopositor, dorsal view; D, ventral prosomal complex. Not to scale.
Figure 2. A–B, spiracles. A in The taxonomical status and diversity of Balkan sironids (Opiliones, Cyphophthalmi) with descriptions of twelve new species
Figure 2. A–B, spiracles. A, Siro exilis Hoffman (West Virginia, Summers County), light micoscopy microphotograph; B, Cyphophthalmus hlavaci sp. nov., scanning electron micrograph. C–D, outlet ducts and pores of anal glands. C, S. exilis Hoffman (West Virginia, Summers County); D, Cyphophthalmus serbicus (Hadži). E–F, spermatopositor movable fingers (digiti mobiles). E, Cyphophthalmus cf. zetae sp. nov. (Manastir Morača, Montenegro); F, Cyphophthalmus gordani sp. nov. Not to scale.
Key triggers of adaptive genetic variability of sessile oak [Q. petraea (Matt.) Liebl.] from the Balkan refugia: outlier detection and association of SNP loci from ddRAD-seq data
<p>Knowledge on the genetic composition of <em>Quercus petraea</em> in south-eastern Europe is limited despite the species' significant role in the re-colonisation of Europe during the Holocene, and the diverse climate and physical geography of the region. Therefore, it is imperative to conduct research on adaptation in sessile oak to better understand its ecological significance in the region. While large sets of SNPs have been developed for the species, there is a continued need for smaller sets of SNPs that are highly informative about the possible adaptation to this varied landscape. By using double digest restriction site associated DNA sequencing data from our previous study, we mapped RAD-tag sequences to the <em>Quercus robur</em> reference genome and identified a set of SNPs putatively related to drought stress-response. A total of 179 individuals from eighteen natural populations at sites covering heterogeneous climatic conditions in the southeastern natural distribution range of <em>Q. petraea</em> were genotyped. The detected highly polymorphic variant sites revealed three genetic clusters with a generally low level of genetic differentiation and balanced diversity among them but showed a north–southeast gradient. Selection tests showed nine outlier SNPs positioned in different functional regions. Genotype-environment association analysis of these markers yielded a total of 53 significant associations, explaining 2.4–16.6% of the total genetic variation. Our work exemplifies that adaptation to drought may be under natural selection in the examined <em>Q. petraea</em> populations.</p>
Figure 7. a in Genus Chersotis Boisduval, 1840 (Lepidoptera: Noctuidae) in Croatia with some notes on the other Balkan countries: DNA barcoding, distribution and new records
Figure 7. a) Ch. margaritacea, female. Albania, Korca County, above Zvezdë, 1088m, N40°43'59"; E020°52'49", 23.IX.2016, S. Beshkov, A. Vaso & A. Nahirnić leg., b) Ch. margaritacea female. AL, Mali i Thatë (=Galičica Mts), above Bregas Village, 1485m, N40°48'34"; E020°50'05", 20.VIII.2017, S. Beshkov & A. Nahirnić leg., c) Ch. multangula, male. AL, Korca County, Krusheve, 11.VII.2018., d) Ch.multangula, male. Al, Lure Mts, 1687m, 9.VII.2019, e) Ch. multangula, male genitalia with everted vesica. AL, Mali i Thatë (=Galičica Mts), above Bregas Village, 1485m, N40°48'34"; E020°50'05", 20.VIII.2017, S. Beshkov & A. Nahirnić leg. Gen. prep. 8./14.II.2018, S. Beshkov, f) Ch. multangula, female genitalia. SW Bulgaria, Maleshevska Planina Mts, below Alaborun top, 980m, 10.VIII.2000, S. Beshkov leg.
Figure 6. a in Genus Chersotis Boisduval, 1840 (Lepidoptera: Noctuidae) in Croatia with some notes on the other Balkan countries: DNA barcoding, distribution and new records
Figure 6. a) Ch. laeta leonhardi. Croatia, Mt. Biokovo, below Sv. Jure, 43°20'26.2"N 17°03'08.0"E, 1620 m a.s.l.,30.VIII.2018, T. Koren leg. b) Ch. laeta leonhardi. Albania, Tirana County, Dajt Mt, Shkallë Village, 893m, N41°19'49"; E019°57'55", 29.VI.2017, S. Beshkov & A. Nahirnić leg. c) Ch. laeta leonhardi. AL, Tomorr Mts, below Abaz Ali Top, 1730m, N40.6111, E020.1885, 13.VII.2018, S. Beshkov & A. Nahirnić leg., d) Ch. laeta leonhardi. AL, Bjeshkët e Nemuna Mts (=Prokletije Mts), Radohima Mt., between Qafa e Thorës pass and Theth village, south-east of Shtegu peak, 1657m, N42.3854, E019.7502, 19.VII.2018, S. Beshkov & A. Nahirnić leg., e) Ch. laeta leonhardi, male genitalia with everted vesica. Gen. prep. 3./21.XII.2020, S. Beshkov. AL, Bjeshkët e Nemuna Mts (=Prokletije Mts), Radohima Mt., between Qafa e Thorës pass and Theth village, south-east of Shtegu peak, 1657m, N42.3854, E019.7502, 19.VII.2018, S. Beshkov & A. Nahirnić leg., f) Ch. laeta leonhardi, male genitalia with everted vesica. Gen. prep. 2./22.XII.2020, S. Beshkov. AL, Korca County, above Drenovë Village, 1050m, N40°35'18"; E020°48'23", 7.VII.2016, S. Beshkov & A. Nahirnić leg.
Figure 4. a in Genus Chersotis Boisduval, 1840 (Lepidoptera: Noctuidae) in Croatia with some notes on the other Balkan countries: DNA barcoding, distribution and new records
Figure 4. a) Ch. fimbriola thurneri, female. Albania, Korca County, above Boboshticë Village, 1225m, N40°32'26"; E020°47'31", 08.VII.2016, S. Beshkov & A. Nahirnić leg., b) Ch. fimbriola thurneri, male genitalia with everted vesica. Gen. prep. 4./22.XII.2020, S. Beshkov. AL, Korca County, above Boboshticë, 1225m, N40°32'26"; E020°47'31", 08.VII.2016, S. Beshkov & A. Nahirnić leg. c.) Ch. fimbriola ssp., male genitalia with everted vesica. Gen. prep. 6./22.XII.2020, S. Beshkov. North Macedonia, above Demir Kapija Town, 244m, N41°22'58"; E022°11'45", 10.VI.2018, S. Beshkov & A. Nahirnić leg. d) Ch. fimbriola thurneri, male genitalia with everted vesica. Gen. prep. 5./22.XII.2020, S. Beshkov. AL, Korca County, above Drenovë Village, 1050m, N40°35'18"; E020°48'23", 7.VII.2016, S. Beshkov & A. Nahirnić leg. e) Ch. fimbriola ssp.female genitalia. Gen. prep. 1./22.XI.1999, S. Beshkov. SW Bulgaria, Pirin Mts, Yane Sandansky Chaler, 1200 m alt., 29.VII.1969, det. and in coll. of Al. Slivov in IBER (Sofia).
Figure 3. a in Genus Chersotis Boisduval, 1840 (Lepidoptera: Noctuidae) in Croatia with some notes on the other Balkan countries: DNA barcoding, distribution and new records
Figure 3. a) Ch. anatolica, male. Albania, Tomorr Mts, Abaz Ali Top, 2379m, N40.6361, E020.1615, 14.VII.2018, S. Beshkov & A. Nahirnić leg.; b) Ch. elegans, male. AL, Korca County, west from Pepellash Village, 1318m, N40°28'55"; E020°41'27", 22.VIII. 2017, S. Beshkov & A. Nahirnić leg.; c) Ch. anatolica, male genitalia with everted vesica. Gen. prep. 1./04.III.2019, S. Beshkov. AL, Tomorr Mts, Abaz Ali Top, 2379m, N40.6361, E020.1615, 11.VIII.2018, S. Beshkov, A. Nahirnić & C. Plant leg.; d) Ch. elegans, male genitalia with everted vesica. Gen. prep. 1./03.III.2019, S. Beshkov. AL, Mt. Tomorr, Abaz Aliu Top below to south, 2026 m, N40°37'19", E020°10'42", 10.VIII.2018, S. Beshkov, A. Nahirnić & C. Plant leg., e) Ch. elegans, female genitalia. Gen. prep. 9./14.II.2018, S. Beshkov. AL, Mali i Thatë (=Galičica Mts), above Bregas Village, 1485m, N40°48'34"; E020°50'05", 20.VIII.2017, S. Beshkov & A. Nahirnić leg., f) & g) Ch. elegans, everted vesica, Gen. prep. 2./22.III.2017, S. Beshkov. Serbia, Slivovicki Vis, N43°08'29", E022°23'12", 03.IX.2016, S. Beshkov, A. Nahirnić leg.
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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.