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599 results for “hungary”
Data from: Phylogeny of Mycoplasma bovis isolates from Hungary based on multi locus sequence typing and multiple-locus variable-number tandem repeat analysis
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Collared pratincole nest success in Hungary
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Data from: Appraisal of the fossil record of Homarus (nephropid lobster), with description of a new species from the upper Oligocene of Hungary and remarks on the status of Hoploparia
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Data from: Genotyping of Coxiella burnetii from domestic ruminants and human in Hungary: indication of various genotypes
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Antimicrobial resistance monitoring results complementing the EU Overview Summary Report on AMR in zoonotic and indicator bacteria from humans, animals and food in 2017/2018 - Hungary
<p>This dataset contains AMR monitoring results in animals and food at the isolate level pursuant to Article 9 of Directive 2003/99/EC and to Annex, part B, of Commission implementing Decision 2013/652/EU. In addition, the dataset includes any other results from isolates than the ones mentioned in the Commission implementing Decision 2013/652/EU. The quantitative minimum inhibitory concentration (MIC) data from dilution methods are included. REPORTING AUTHORITIES CONTRIBUTING TO EACH DATA COLLECTION: AMR_2018_HU_20200204: >> National Food Chain Safety Office</p>
Figures 15-17 in The first lowland species of the Holarctic alpine ground spider genus Parasyrisca (Araneae, Gnaphosidae) from Hungary
Figures 15-17. Seasonal vegetation changes on the habitat of Parasyrisca arrabonica: 15 summer vegetation dominated by the late-coming pink (Dianthus serotinus) 16 winter vegetation of the habitat 17 spring vegetation characterized by different feather grasses (Stipa capillata, S. borysthenica).
Figures 10-11 in The first lowland species of the Holarctic alpine ground spider genus Parasyrisca (Araneae, Gnaphosidae) from Hungary
Figures 10-11. Parasyrisca arrabonica Szinetár & Eichardt, sp. n. male bulb, close-ups: 10 male pedipalp, ventral view, close-up 11 bulbus, prolateral view, conductor removed (c – conductor, e – embolus, ta – terminal apophysis), showing the long embolus and base of the terminal apophysis.
Figure 3 in Three new species and a new record of tenuipalpid mites (Acari: Tenuipalpidae) from Hungary
Figure 3. Tenuipalpus budensis sp. nov. Female. (A) Dorsal view. (B) Ventral view. (C) Spermatheca. (D) Palp. (E) Right leg I. (F) Right leg III. (G) Right leg IV.
Figure 2 in Three new species and a new record of tenuipalpid mites (Acari: Tenuipalpidae) from Hungary
Figure 2. Cenopalpus adventicius sp. nov. (A) Dorsal view – female. (B) Dorsal seta sc2 – female. (C) Dorsal seta h1 – female. (D) Ventral view – female. (E) Spermatheca. (F) Gnathosoma – female. (G) Palp – female. (H) Right leg I – female. (I) Right leg III – female. (J) Right leg IV – female. (K) Dorsal view – male. (L) Ventral view – male. (M) Dorsal view – deutonymph. (N) Right leg I – deutonymph. (O)Right leg III – deutonymph. (P) Right leg IV – deutonymph.
Figure 1 in Three new species and a new record of tenuipalpid mites (Acari: Tenuipalpidae) from Hungary
Figure 1. Cenopalpus cumanicus sp. nov. (A) Dorsal view – female. (B) Dorsal seta sc2 – female. (C) Dorsal seta c1 – female. (D) Dorsal seta e1 – female. (E) Ventral view – female. (F) Spermatheca. (G) Gnathosoma – female. (H) Left leg I – female. (I) Right leg III – female. (J) Right leg IV – female. (K) Dorsal view – deutonymph. (L) Right leg I – deutonymph. (M) Right leg III – deutonymph. (N) Right leg IV – deutonymph.
Data from: Does morphology reflect osteohistology-based ontogeny? A case study of Late Cretaceous pterosaur jaw symphyses from Hungary reveals hidden taxonomic diversity
With a single complete mandible and 56 mandibular symphyseal fragments of various sizes, the Late Cretaceous Hungarian azhdarchid material has been considered one of the most extensive monospecific pterosaur assemblages in the world. Representing a broad size range, these elements have been thought to demonstrate a developmental series of Bakonydraco galaczi. As such, they were ideal to test whether absolute size and/or morphology reliably indicate relative ontogenetic stages in this pterosaur. Forty-five specimens were selected for multivariate morphometrics and classified into four size classes. After acquiring the morphometric data set, we thin-sectioned eight symphyses representing all size groups and classified them into relative ontogenetic stages based on qualitative microstructural inspection prior to quantitative histological analyses. Microstructural characters suggestive of developmental state were then quantified for intra- and interindividual uni- and multivariate analyses to test the correspondence among the results of qualitative and quantitative analyses. In contrast to our expectations, histological features identified the smallest specimen as an adult and not an early juvenile. The substantial size difference between this specimen and other adults, along with its distinct microanatomical and histological features, implies the presence of at least two pterosaur taxa in this symphysis assemblage. This hypothesis is further supported by multivariate morphometrics, which separate the smallest symphyses from all other specimens that form one continuous group. Although the latter group also shows considerable size variability in corresponding ontogenetic stages, this suggests developmental plasticity rather than the presence of even more taxa, and indicates that symphysis size and morphology are poor indicators of skeletal maturity in these animals. Hence, bone histology is an important independent test of the assessment of ontogenetic stage using size and morphology.
Figure 4 from: VandenSpiegel D, Shelley RM, Golovatch SI (2020) The millipede genus Globanus Attems, 1914, endemic to São Tomé and Príncipe, with the description of a new species (Diplopoda, Spirostreptida, Spirostreptidae). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 61-74. https://doi.org/10.3897/zookeys.930.49236
Figure 4 Globanus marginescaber (Karsch, 1884), ♂ topotype from Príncipe Island. A habitus, lateral view B left coxite, posterior view C, D right telopodite, posterior and mesal views, respectively. Abbreviations: atp = antetorsal process, lap = latero-apical process, , map = mesapical metaplical process, mp = metaplica, pp = proplica, ps = proplica spine, px = paracoxite. Scale bars: 5 mm (A); 200 µm (B, C, D).
Figure 5 from: VandenSpiegel D, Shelley RM, Golovatch SI (2020) The millipede genus Globanus Attems, 1914, endemic to São Tomé and Príncipe, with the description of a new species (Diplopoda, Spirostreptida, Spirostreptidae). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 61-74. https://doi.org/10.3897/zookeys.930.49236
Figure 5 Globanus integer (Karsch, 1884), ♂ topotype. A habitus, lateral view B right gonopod, posterior view C left coxite, posterior view D right telopodite, posterior view. Abbreviations: atp = antetorsal process, bs = basomere, lap = latero-apical process, map = meso-apical metaplical process, mp = metaplica, pp = proplica, ps = proplica spine, px = paracoxite. Scale bars: 5 mm (A); 200 µm (B–D).
Figure 3 from: VandenSpiegel D, Shelley RM, Golovatch SI (2020) The millipede genus Globanus Attems, 1914, endemic to São Tomé and Príncipe, with the description of a new species (Diplopoda, Spirostreptida, Spirostreptidae). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 61-74. https://doi.org/10.3897/zookeys.930.49236
Figure 3 Globanus drewesi sp. nov. ♂ paratype. A, B left coxite, oral and caudal views, respectively C tip of left coxite, caudal view D, E left telopodite detached, anterior and posterior views, respectively F tip of left telopodite, posterior view. Abbreviations: atp = antetorsal process, bs = basomere, fb = flattened blade, lap = latero-apical process, map = meso-apical metaplical process, mp = metaplica, pp = proplica, ps = proplica spine, px = paracoxite, sp = subtriangular projection. Scale bars: 200 µm (A, B, D, E); 100 µm (C, F).
Supplementary material 1 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Table S1
Figure 3 from: Karam-Gemael M, Decker P, Stoev P, Marques MI, Chagas Jr A (2020) Conservation of terrestrial invertebrates: a review of IUCN and regional Red Lists for Myriapoda. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 221-229. https://doi.org/10.3897/zookeys.930.48943
Figure 3 Proportion of extinction risk categories of the Worldwide Myriapoda Red List presented here. Includes data from regional Red Lists from eleven countries and from IUCN Red List of Threatened Species. Threatened categories are within dashed red lines.
Figure 1 from: VandenSpiegel D, Shelley RM, Golovatch SI (2020) The millipede genus Globanus Attems, 1914, endemic to São Tomé and Príncipe, with the description of a new species (Diplopoda, Spirostreptida, Spirostreptidae). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 61-74. https://doi.org/10.3897/zookeys.930.49236
Figure 1 Lobogonus trilobatus Demange, 1971, ♂ syntype. A habitus, lateral view B transverse section of midbody segment C right gonopod, posterior view D left telopodite, anterior view E tip of telopodite. Abbreviations: atp = antetorsal process, bs = basomere, lap = latero-apical process, map = meso-apical metaplical process, mp = metaplica, pp = proplica, sb = seminal branch. Scale bars: 10 mm (A); 1 mm (C); 500 µm (D, E).
Figure 1 from: Haľková B, Tuf IH, Tajovský K, Mock A (2020) Subterranean biodiversity and depth distribution of myriapods in forested scree slopes of Central Europe. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 117-137. https://doi.org/10.3897/zookeys.930.48914
Figure 1 Location of the study sites. 1 Doline next to Silická ľadnica Ice Cave 2 Vysoká Hill (both sites in Slovak Karst National Park) 3 Drienok Valley (Revúcka Highlands) 4 Belinské skaly (Cerová vrchovina Highlands) 5 Okopanec Hill (Malé Karpaty Mts.) 6–8 Three localities near the Zbrašov Aragonite Caves and Hůrka u Hranic (Moravian-Silesian Foothills) 9–11 Three localities in Chrudim region (Iron Mts.).
Figure 2 from: Moritz L, Koch M (2020) No Tömösváry organ in flat backed millipedes (Diplopoda, Polydesmida). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 103-115. https://doi.org/10.3897/zookeys.930.48438
Figure 2 Articulation of the tentorial transverse bar to the head capsule in the PolydesmidaA–C head in lateral view (anterior is left), volume rendering D–F head, sagittal section through tentorial transverse bar, volume rendering A, D, GOxidus gracilisB, E, HCoromus vittatusC, F, ITymbodesmus sp. JPolydesmus angustusG–J optical cross sections K, L the Tömösváry organ in Eurydesmus laxus after Hennings (1906): K cross-section, modified from Hennings (1906, plate XXXI, fig. 11) L head in lateral view, modified from Hennings (1906, plate XXXI, fig. 9). Abbreviations: at = antenna, co = collum, gls = gnathal lobe sclerite, hc = head capsule, la = labrum, mc = mandibular cardo, ms = mandibular stipes, tb = transverse bar of tentorium, pp = posterior process of tentorium. Asterisk (*) indicates the structure previously interpreted by Hennings (1906) as Tömösváry organ. In the volume renderings the tentorium is marked with a red dotted line. Arrows indicate the flexible connection of transverse bar and head capsule. Scale bars: 100 µm (G–J).
Figure 1 from: Moritz L, Koch M (2020) No Tömösváry organ in flat backed millipedes (Diplopoda, Polydesmida). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 103-115. https://doi.org/10.3897/zookeys.930.48438
Figure 1 Polydesmus angustus, head A–D volume rendering based on micro-CT data: A Frontal view B cross-section, posterior view, plane indicated in C C lateral view D sagittal view, cutting plane indicated in A E–G details of connection of tentorial transverse bar to head capsule at incisura lateralis, plane as indicated in D: E histological section (Paraffin, Azan-staining) F histological section (Araldite, Toluidine blue) G optical section of micro-CT scan. Abbreviations: at = antenna, co = collum, eb = epipharyngeal bar of tentorium, gc = gnathochilarium, gls = gnathal lobe sclerite, hc = head capsule, il = incisura lateralis, la = labrum, mc = mandibular cardo, mg = mandibular gnathal lobe, ms = mandibular stipes, pp = posterior process of tentorium, tb = transverse bar of tentorium. Asterisk (*) indicates structure previously interpreted by Hennings (1906) as the Tömösváry organ in the Polydesmida. In the volume renderings the tentorium is marked with a red dotted line. Scale bar: 100 µm (E–G).
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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.