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figure 6 in Deceptive conservatism of claws: distinct phyletic lineages concealed within Isohypsibioidea (Eutardigrada) revealed by molecular and morphological evidence
figure 6 Cuticular surface of various members of Isohypsibioidea (SEM): A–B – Fractonotus verrucosus (Isohypsibiidae), obtuse tubercles and plaques; C – Dianea sattleri comb. nov. (Isohypsibiidae), small wrinkled gibbosities; D – Ursulinius pappi comb. nov. (Isohypsibiidae), large reticulated gibbosities; E – Ursulinius elegans (Binda & Pilato, 1971) comb. nov. (Isohypsibiidae), large ornamented gibbosities; F – Doryphoribius dawkinsi (Doryphoribiidae fam. nov.), large sculptured gibbosities; G – Grevenius granulifer comb. nov. (Doryphoribiidae fam. nov.), irregularDownloaded small tubercles from; BrillH.– com Grevenius 12/12/2023 pushkini02:59:51PM (Tumanov, 2003) comb. nov. via (Open Doryphoribiidae Access. This fam. isnovan.), open cuticular accesswrinkles article. Scale distributed bars in under micrometresthe terms of the prevailing CC-BY license at the time of publication. http://creativecommons.org/licenses/by-nc/4.0
figure 5 in Deceptive conservatism of claws: distinct phyletic lineages concealed within Isohypsibioidea (Eutardigrada) revealed by molecular and morphological evidence
figure 5 Peribuccal structures of various members of Isohypsibioidea (SEM): A – Isohypsibius coulsoni Kaczmarek et al., 2012 (Isohypsibiidae); B – Ursulinius pappi comb. nov. (Isohypsibiidae); C – Fractonotus verrucosus (Isohypsibiidae); D – Halobiotus crispae (Halobiotidae fam. nov.); E – Doryphoribius dawkinsi (Doryphoribiidae fam. nov.); F – Apodibius confusus (Doryphoribiidae fam. nov.); G – Thulinius ruffoi (Bertolani, 1981) (Doryphoribiidae fam. nov.); H – Pseudobiotus megalonyx (Doryphoribiidae fam. nov.); I – Grevenius granulifer comb. nov. (Doryphoribiidae fam. nov.); J – Hexapodibius micronyx (Hexapodibiidae). Incised arrowheads indicate the first row of Downloadedteeth, from emptyBrill. incised com 12/12/ arrowheads2023 – 02: the 59:51PM second row of teeth, arrowheadsvia Open – fused Access. peribuccal This is an lamellaeopen, empty access article arrowheads – distributed peribuccalunderwrin-the terms of the prevailing CC-BY license at the time of publication. kles, and the asterisk points the peribuccal chemosensory http organ://. Scale bars creativecommons= 1 µm.org/licenses/by-nc/4.0
Figure 9 in Deep - water hypoxic meiobenthic Protozoa and Metazoa taxa of the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 9. Proportion of soft-shelled foraminifera inhabiting different sediment layers along the depth gradient.
Figure 8 in Deep - water hypoxic meiobenthic Protozoa and Metazoa taxa of the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 8. Proportion of hard-shelled foraminifera inhabiting different sediment layers along the depth gradient.
Figure 7 in Deep - water hypoxic meiobenthic Protozoa and Metazoa taxa of the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 7. Distribution of the Foraminifera (hard-shelled and soft-shelled) abundance (N) along depth gradient at the Bosporus outlet area of the Black Sea.
Figure 6 in Deep - water hypoxic meiobenthic Protozoa and Metazoa taxa of the Istanbul Strait's (Bosporus) outlet area of the Black Sea
Figure 6. Proportion of the Ciliophora inhabiting different sediment layers along the depth gradient at the Bosporus outlet area of the Black Sea.
Figure 1 in Mitochondrial genomes of four pierid butterfly species (Lepidoptera: Pieridae) with assessments about Pieridae phylogeny upon multiple mitogenomic datasets
Figure 1. Circular map of Baltia butleri, Talbotia naganum, Pontia callidice, Pontia daplidice mitochondrial genome. COI, COII, and COIII refer to the cytochrome oxidase subunits; CytB refers to cytochrome B; ATP6 and ATP8 refer to subunits 6 and 8 of F0 ATPase; ND1-6 refers to the components of NADH dehydrogenase. The tRNAs locations are marked by the color blocks and labeled by the IUPAC-IUB single letter amino acid code. L1, L2, S1, and S2 denote tRNALeu (CUN), tRNALeu (UUR), tRNASer (AGN), and tRNASer (UCN), respectively. The non-underlined genes are transcribed on the majority strand whereas the underlined genes are transcribed on the minority strand.
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.
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.
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.
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.
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.
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.
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.
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.
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!).
Figure 16 in Mitochondrial genomes of four pierid butterfly species (Lepidoptera: Pieridae) with assessments about Pieridae phylogeny upon multiple mitogenomic datasets
Figure 16. Bayesian inference (BI) and Maximum likehood (ML) phylogenetic trees inferred from mitochondrial genomes of pierid family based on 22tRNA genes.
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).
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.
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.
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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.