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599 results for “hungary”
Figure 3 from: Kokhia MS, Golovatch SI (2020) Diversity and distribution of the millipedes (Diplopoda) of Georgia, Caucasus. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 199-219. https://doi.org/10.3897/zookeys.930.47490
Figure 3 Map of western Georgia with its transect (light blue), Pitsunda – Arabika Plateau – Khaishi – Bagdati – Batumi, and macro relief (bottom).
Figure 15 from: Golovatch SI, Liu W (2020) Diversity, distribution patterns, and fauno-genesis of the millipedes (Diplopoda) of mainland China. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 153-198. https://doi.org/10.3897/zookeys.930.47513
Figure 15 Distribution of the family Haplodesmidae, genus Eutrichodesmus in mainland China. Red lines show the transect Mengla – Hekou – Beichuan – Guiyang – Huanjiang – Guilin – Yichang – Qingyuan – Guidong – Fenyi – Wuyishan – Hangzhou, along which the elevations are crudely indicated below. 1E. dorsiangulatus2E. monodentus3E. arcicollaris4E. triangularis5E. tenuis6E. latellai7E. obliteratus8E. incisus9E. latus10E. soesilae11E. triglobius12E. distinctus13E. trontelji14E. planatus15E. similis16E. sketi17E. lipsae18E. jianjia19E. apicalis20E. digitatus21E. spinatus22E. simplex23E. anisodentus24E. pectinatidentis.
Figure 3 from: Golovatch SI, Liu W (2020) Diversity, distribution patterns, and fauno-genesis of the millipedes (Diplopoda) of mainland China. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 153-198. https://doi.org/10.3897/zookeys.930.47513
Figure 3 Distribution of the family Paracortinidae, genus Paracortina in mainland China. Red lines show the transect Batang – Shangrila – Yajiang – Zhenxiong – Baise, along which the elevations are crudely indicated below. 1P. viriosa2P. serrata3P. thallina4P. carrinata5P. leptoclada6P. stimula7P. voluta8P. chinensis9P. yinae10P. zhangi.
Figure 1 from: Mesibov R (2020) A second remarkable case of parapatry in a Tasmanian millipede genus (Diplopoda, Polydesmida, Dalodesmidae). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 89-101. https://doi.org/10.3897/zookeys.930.38031
Figure 1 Adult males of Tasmaniosoma armatum Verhoeff, 1936 (top, QVM:2018:23:0093) and T. orientale Mesibov, 2010 (bottom, QVM:2018:23:0089). g indicates gonopods. The two males are from the Hop Pole Creek area (see Results section) and were collected at sites ca 0.5 km apart on the same day, 6 August 2018. Scale bar: 5 mm.
Figure 13 from: Golovatch SI, Liu W (2020) Diversity, distribution patterns, and fauno-genesis of the millipedes (Diplopoda) of mainland China. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 153-198. https://doi.org/10.3897/zookeys.930.47513
Figure 13 Distribution of the family Paradoxosomatidae, genus Tylopus in mainland China. Red lines show the transect Shangrila – Dali – Mengzi – Jinyunshan – Du'an, along which the elevations are crudely indicated below. 1T. reductus2T. kabaki3T. similis4T. schawalleri5T. sinensis6T. nigromarginatus7T. deharvengi.
Figure 10 from: Golovatch SI, Liu W (2020) Diversity, distribution patterns, and fauno-genesis of the millipedes (Diplopoda) of mainland China. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 153-198. https://doi.org/10.3897/zookeys.930.47513
Figure 10 Distribution of the family Paradoxosomatidae, genus Hedinomorpha in mainland China. Red lines show the transect Shangrila – Ganzi – Liangshan – Xining – Lanzhou – Jiuzhaigou – Xi'an, along which the elevations are crudely indicated below. 1H. montana2H. yunnanensis3H. proxima4H. crassiterga5H. bifida6H. subnigra7H. reducta8H. martensi9H. circofera10H. affinis11H. nigra12H. altiterga13H. flavobulbus14H. biramipedicula15H. jeekeli; neither H. circularis nor H. hummelii is mapped because their exact type localities remain unknown.
Figure 11 from: Golovatch SI, Liu W (2020) Diversity, distribution patterns, and fauno-genesis of the millipedes (Diplopoda) of mainland China. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 153-198. https://doi.org/10.3897/zookeys.930.47513
Figure 11 Distribution of the family Paradoxosomatidae, genus Sigipinius in mainland China. Red lines show the transect Aksu – Shangrila – Lijiang – Kangding – Jiuzhaigou, along which the elevations are crudely indicated below. 1S. kabaki2S. montana3S. spiniger4S. dentiger5S. campanuliformis6S. complex7S. simplex8S. pinnifer9S. grahami.
Figure 12 from: Golovatch SI, Liu W (2020) Diversity, distribution patterns, and fauno-genesis of the millipedes (Diplopoda) of mainland China. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 153-198. https://doi.org/10.3897/zookeys.930.47513
Figure 12 Distribution of the family Paradoxosomatidae, genus Hylomus in mainland China. Red lines show the transect Tianlin – Ziyun – Du'an – Huanjiang – Guilin – Linwu – Qingyuan – Jiujiang, along which the elevations are crudely indicated below. 1H. minutuberculus2H. getuhensis3H. phasmoides4H. variabilis5H. parvulus6H. scolopendroides7H. nodulosus8H. scutigeroides9H. spinitergus10H. lui11H. yuani12H. cornutus13H. lingulatus14H. spinissimus15H. eupterygotus16H. laticollis17H. simplipodus18H. similis19H. draco; H. longispinus is not mapped because its exact type locality remains unknown.
Figure 6 from: Mesibov R (2020) A second remarkable case of parapatry in a Tasmanian millipede genus (Diplopoda, Polydesmida, Dalodesmidae). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 89-101. https://doi.org/10.3897/zookeys.930.38031
Figure 6 Known localities for Tasmaniosoma armatum Verhoeff, 1936 (red squares) and T. orientale Mesibov, 2010 (blue squares) at the northern end of the Old Coach Road as of 3 July 2019. A Topographic map with named features B Aerial photograph taken 25 February 2010. Circled black cross in A marks locality of Tasmaniosoma male with "anomalous" gonopods (QVM:2017:23:0173).
Figure 7 from: Mesibov R (2020) A second remarkable case of parapatry in a Tasmanian millipede genus (Diplopoda, Polydesmida, Dalodesmidae). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 89-101. https://doi.org/10.3897/zookeys.930.38031
Figure 7 Known localities for Tasmaniosoma armatum Verhoeff, 1936 (red squares) and T. orientale Mesibov, 2010 (blue squares) near the West Swan River/Swan River junction as of 3 July 2019. A Topographic map with named features B Aerial photograph taken 1 December 2006. Circled black cross in A marks locality of Tasmaniosoma male with "anomalous" gonopods (QVM:23:54570).
Figure 5 from: Kokhia MS, Golovatch SI (2020) Diversity and distribution of the millipedes (Diplopoda) of Georgia, Caucasus. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 199-219. https://doi.org/10.3897/zookeys.930.47490
Figure 5 Map of eastern Georgia with its transect (light blue), Omalo – Tianeti – Akhmeta – Shilda – Kvareli – Lagodekhi – Tamariani, and its macro relief (bottom).
FIGURE 20. L in Explanation of the European Lepidocyrtus pallidus – serbicus group (Collembola, Entomobryidae), with description of new species from Hungary
FIGURE 20. L. tomosvaryi sp.nov.: dens with small dental tubercle (Photo: D. Winkler).
FIGURE 1–2. L in A new species of Lepidocyrtus (Collembola, Entomobryidae) from the Börzsöny Mountains, Hungary
FIGURE 1–2. L. traseri sp. nov. 1, habitus; 2, habitus with intense pigmentation
FIGURE 1 in New Lepidocyrtus Bourlet, 1839 from riverine woodland in Hungary (Collembola, Entomobryidae)
FIGURE 1. Lepidocyrtus isabelleae sp. nov. 1, habitus.
Management impacts on three reptile species (Vipera ursinii, Lacerta agilis, Lacerta viridis) in sandy grasslands in Hungary: Mowing should be avoided
<p>Understanding the factors that determine the abundance of populations is of key importance in conservation biology, ecology, and biogeography. For grassland‐associated species, such as the Hungarian meadow viper (<i>Vipera ursinii rakosiensis</i>), habitat management is particularly important. We aimed to study the effects of the three most common types of grassland management (grazing, mowing, and mowing + grazing) on the abundance of reptile species in meadow viper habitats in Kiskunság National Park, in Hungary. We surveyed grasslands repeatedly (<i>n</i> = 15 occasions) for reptiles in one autumn and one spring season in three 1‐ha quadrates per grassland management type. We recorded all reptiles and their activity related to operative temperatures and analyzed data by n‐mixture models. All reptile species known to occur in the habitats were observed during the surveys, but only the green lizard, sand lizard, and Hungarian meadow viper reached the minimum number of observations required for detailed analyses. Grazing had a strong positive effect on the abundance of Hungarian meadow vipers and sand lizards, while both mowing and mowing + grazing rotation had a negative effect. None of the grassland management types affected green lizard abundance. Our results suggest that grazing is the ideal type of grassland management for the endangered Hungarian meadow viper and the sand lizard. Mowing and mowing + grazing should be replaced by grazing to ensure the effectiveness of habitat management for conservation and to maintain healthy populations of grassland‐associated reptile species.</p>
Supplementary material 8 from: Bíró T, Duleba M, Földi A, Kiss KT, Orgoványi P, Trábert Z, Vadkerti E, Wetzel CE, Ács É (2022) Metabarcoding as an effective complement of microscopic studies in revealing the composition of the diatom community – a case study of an oxbow lake of Tisza River (Hungary) with the description of a new Mayamaea species. Metabarcoding and Metagenomics 6: e87497. https://doi.org/10.3897/mbmg.6.87497
Alignment S2
Supplementary material 2 from: Bíró T, Duleba M, Földi A, Kiss KT, Orgoványi P, Trábert Z, Vadkerti E, Wetzel CE, Ács É (2022) Metabarcoding as an effective complement of microscopic studies in revealing the composition of the diatom community – a case study of an oxbow lake of Tisza River (Hungary) with the description of a new Mayamaea species. Metabarcoding and Metagenomics 6: e87497. https://doi.org/10.3897/mbmg.6.87497
Table S2
Supplementary material 3 from: Bíró T, Duleba M, Földi A, Kiss KT, Orgoványi P, Trábert Z, Vadkerti E, Wetzel CE, Ács É (2022) Metabarcoding as an effective complement of microscopic studies in revealing the composition of the diatom community – a case study of an oxbow lake of Tisza River (Hungary) with the description of a new Mayamaea species. Metabarcoding and Metagenomics 6: e87497. https://doi.org/10.3897/mbmg.6.87497
Table S3
Supplementary material 1 from: Bíró T, Duleba M, Földi A, Kiss KT, Orgoványi P, Trábert Z, Vadkerti E, Wetzel CE, Ács É (2022) Metabarcoding as an effective complement of microscopic studies in revealing the composition of the diatom community – a case study of an oxbow lake of Tisza River (Hungary) with the description of a new Mayamaea species. Metabarcoding and Metagenomics 6: e87497. https://doi.org/10.3897/mbmg.6.87497
Table S1
FIGURE 1 in A new species of the vitismin cockroach genus Perspicuus Koubová, 2020 from the Late Cretaceous (Santonian) of Hungary
FIGURE 1. Map of Ajka (a) and the Ajka coal seams (b). After Szabó et al. (2022d) — modified.
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Allen Brain Atlas
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International Brain Laboratory public data
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OpenNeuro
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