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Figure 9 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 9 Distribution of the family Xystodesmidae, genus Riukiaria in mainland China. Red lines show the transect Muli – Kangding – Jiuzhaigou – Xi'an – Jiangle – Hangzhou, along which the elevations are crudely indicated below. 1R. belousovi2R. kabaki3R. spatuliformis4R. davidiani5R. korolevi6R. martensi7R. capaca8R. chinensis9R. tianmu.
Supplementary material 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
Polydesmus angustus, head capsule and tentorium with associated musculature
Figure 2 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 2 A Overall depth distribution of centipede individuals and species B values of Shannon's diversity index and Pielou's evenness index, calculated for centipedes, at each of the study sites C mean values of Shannon's diversity index (±SD) calculated for centipedes, at each depth of the gradient (summarised data from all localities) D overall depth distribution of millipede individuals and species E values of Shannon's diversity index and Pielou's evenness index, calculated for millipedes, at each of the study sites F mean values of Shannon's diversity index (±SD) calculated for millipedes, at each depth of the gradient.
Figure 6 from: Vujić V, Lučić L, Pavković-Lučić S, Ilić B, Jovanović Z, Makarov S, Dudić B (2020) Sexual size and shape dimorphism in Brachydesmus troglobius Daday, 1889 (Diplopoda, Polydesmida). In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 75-88. https://doi.org/10.3897/zookeys.930.48285
Figure 6 Intersexual differences of head shape in B. troglobius illustrated using Canonical Variate Analysis (CVA). Position and size of the vectors' influence on a thin-plate spline deformation grid and illustration of the pattern of intersexual differences of head shape (white bars indicate females; grey bars indicate males).
Figure 3 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 3 Polydesmus angustus, histological sections from anterior (A) to posterior (D) A articulation of tentorial transverse bar to head capsule B tentorial transverse bar and epipharyngeal bar C tentorial hypopharyngeal bar and posterior process D articulation of tentorium to "Nebententorium". Abbreviations: a2 = medial antennal muscle, a3 = lateral antennal muscle, a4 = anterior antennal muscle, asd = duct of anterior salivary gland, asg = anterior salivary gland, co = collum, eb = epipharyngeal bar of tentorium, gl = mandibular gnathal lobe, gls = gnathal lobe sclerite, hb = hypopharyngeal bar of tentorium, m1 = gnathal lobe sclerite muscle, m4 = anterior mandibular cardo muscle, m5 = posterior mandibular cardo muscle, mc = mandibular cardo, mes = median septum, mg = mandibular gnathal lobe, ms = mandibular stipes, nt = 'Nebententorium', pc = preoral chamber, ph = pharynx, po = 'Presshöcker', t1 = anterior tentorial muscle, t2 = dorsal tentorial muscle, tb = transverse bar of tentorium. Scale bars: 200 µm.
Supplementary material 1 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
Worlwide Myriapoda assessments
Figure 5 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 5 Vertical distribution of myriapods along the depth gradient in different fixative solutions (data recalculated for the same number of traps). Trend line: dashed = formaldehyde, dotted = ethylene glycol. A Vertical distribution of Chilopoda specimens along the depth gradient (5–95 cm) at five scree slopes in different fixative solutions B vertical distribution of centipede species along the depth gradient at five scree slopes in different fixative solutions C vertical distribution of Diplopoda specimens along the depth gradient (5–95 cm) at five scree slopes in different fixative solutions D vertical distribution of millipede species along the depth gradient at five scree slopes in different fixative solutions.
Figure 3 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 3 Generalised Additive Models of depth distribution pattern of A centipedes and B millipedes. Only species with significant pattern are illustrated. (F-values, * p < 0.05, ** p < 0.01): ALamyctes emarginatus (13.1**), Lithobius forficatus (17.2**), Lithobius lucifugus (5.0*), Lithobius nodulipes (9.7**) BArchiboreoiulus pallidus (22.7**), Cylindroiulus nitidus (5.4*), Glomeris connexa (5.4*), Hylebainosoma tatranum (5.4*), Leptoiulus proximus (7.3*), Mastigona bosniensis (10.5**), Megaphyllum projectum (5.4*), Melogona transsylvanica (15.2**), Polydesmus complanatus (13.1**), Trachysphaera acutula (5.4*), Unciger foetidus (4.9*).
Figure 7 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 7 Distribution of the family Polydesmidae, genus Pacidesmus in mainland China. Red lines show the transect Qujing – Wenshan – Dafang – Fengshan – Huanjiang – Guilin, along which the elevations are crudely indicated below. 1P. uncatus2P. trilobatus3P. martensi4P. sinensis5P. whitteni6P. bifidus7P. superdraco8P. tiani9P. bedosae10P. armatus11P. trifidus.
Figure 8 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 8 Distribution of the family Polydesmidae, genus Glenniea in mainland China. Red lines show the transect Beichuan – Longzhuan – Tongjiang, along which the elevations are crudely indicated below. 1G. lagredae2G. prima3G. blanca.
Figure 6 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 6 Distribution of the family Polydesmidae, genus Epanerchodus in mainland China. Red lines show the transect Shangrila – Dali – Xingyi – Beichuan – Zhengxiong – Tongren – Xi'an – Wushan – Fuchuan – Lianhua – Hangzhou – Changbaishan, along which the elevations are crudely indicated below. 1E. potanini2E. typicus3E. fuscus4E. yunnanensis5E. belousovi6E. schawalleri7E. stylotarseus8E. lipsae9E. varius10E. frater11E. soror12E. draco13E. coniger14E. gladiatus15E. chutou16E. parvus17E. jaegeri18E. martensi19E. tujiaphiulus20E. latus21E. orientalis22E. jiangxiensis23E. enrycornutus24E. sphaerisetosus25E. koreanus.
Figure 5 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 5 Distribution of the family Megalotylidae, genus Nepalella in mainland China. Red lines show the transect Baoshan – Xinlong – Beichuan – Shuicheng – Guiyang – Jinfoshan, along which the elevations are crudely indicated below. 1N. kavanaughi2N. pianma3N. magna4N. griswoldi5N. marmorata6N. lobata7N. grandoides8N. grandis9N. caeca10N. troglodytes11N. jinfoshan12N. wangi.
Figure 9 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 9 Map of Abkhazia showing the distributions of some endemic or subendemic species. Designations: red triangle (Brachychaetosoma turbanovi), blue square (Caucaseuma kelasuri), orange star (Archileucogeorgia abchasica), pink star (Omobrachyiulus implicitus), orange square (Cylindroiulus olgainna), blue ring (Paranotosoma subrotundatum), yellow star (Julus lindholmi), green star (Leucogeorgia rediviva), green ring (Dentatosoma magnum), pink ring (Heterocaucaseuma deprofundum), orange diamond (Metamastigophorophyllon giljarovi), white ring (Kubaniulus gracilis), blue star (Metamastigophorophyllon hamatum), red ring (Pseudoflagellophorella mirabilis), red diamond (Megaphyllum dioscoriadis), yellow square (Nopoiulus brevipilosus), yellow triangle (Archileucogeorgia satunini), orange ball (Heterocaucaseuma longicorne), red ball (Omobrachyiulus hortensis), blue ball (Brachydesmus furcatus), green ball (Brachydesmus simplex), yellow ball (Polydesmus lignaui), green square (Heterocaucaseuma mauriesi).
Figure 4 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 4 Distribution of the family Julidae, genus Nepalmatoiulus in mainland China. Red lines show the transect Linzhi – Kangding – Suining – Jiujiang – Meizhou, along which the elevations are crudely indicated below. 1N. tibetanus2N. brachymeritus3N. rhaphimeritus4N. polyakis5N. fraterdraconis6N. eulobos. Nepalmatoiulus yunnanensis is not mapped because no exact locality in Yunnan is known.
Figure 4 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 4 Map of central Georgia with its transect (light blue), Roki Tunnel – Tskhinvali – Tbilisi – Tsalka Reservoir – Ninotsminda – Javakheti National Park, and its macro relief (bottom).
Figure 7 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 7 Map of western Georgia (= Colchis) showing the distributions of some endemic or subendemic species. Designations: orange ball (Hyleoglomeris awchasica), red ball (Nopoiulus golovatchi), green triangle (Cylindroiulus pterophylacum), red ring (Cylindroiulus ruber), white ball (Polydesmus abchasius), blue ball (Trachysphaera fragilis), green star (Trachysphaera radiosa), pink ring (Cylindroiulus schestoperovi), yellow ring (Hirudicryptus abchasicus).
Figure 2 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 2 Map of Georgia with three transects (light blue), one each in the western, central and eastern parts of the country, to crudely show both horizontal and vertical distributions of millipedes endemic or subendemic to the country.
Figure 2 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 2 Distribution of the family Glomeridae, genus Hyleoglomeris in mainland China. Red lines show the transect Baoshan – Kangding – Honghe – Chongqing – Libo – Du'an – Tongren – Guilin – Linwu – Hong Kong – Nanjing, along which the elevations are crudely indicated below. 1H. albicorporis2H. sinensis3H. reducta4H. maculata5H. heshang6H. gudu7H. rhinceros8H. nigu9H. getuhensis10H. aschnae11H. yinshi12H. grandis13H. eusulcata14H. xueju15H. wuse16H. qiyi17H. curtisulcata18H. mulunensis19H. kunnan20H. mashanorum21H. baxian22H. variabilis23H. multistriata24H. generalis25H. rukouqu26H. xuxiakei27H. lii28H. xia29H. youhao30H. tiani31H. bicolor, 32H. emarginata.
Figure 14 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 14 Distribution of the family Cambalopsidae, genus Glyphiulus in mainland China. Red lines show the transect Xinlong – Liangshan – Honghe – Chengdu – Guiyang – Hechi – Longshan – Guilin – Hong Kong – Qingyuan, along which the elevations are crudely indicated below. 1G. basalis2G. liangshanensis3G. beroni4G. paragranulatus5G. semigranulatus6G. subobliteratus7G. subgranulatus8G. obliteratus9G. latus10G. intermedius11G. zorzini12G. guangnanensis13G. foetidus14G. sinensis15G. pergranulatus16G. quadrohamatus17G. paracostulifer18G. latellai19G. obliteratoides20G. rayrouchi21G. difficilis22G. impletus23G. granulatus24G. basazsi25G. calceus26G. parobliteratus27G. pulcher28G. echinoides29G. acutus30G. mulunensis31G. proximus32G. tiani33G. paramulunensis34G. speobius35G. deharvengi36G. melanoporus37G. septentrionalis38G. adeloglyphus39G. maocun40G. formosus41G. recticulus; G. anophthalmus and G. lipsorum are not mapped because their exact type localities remain unknown, whereas G. granulatus is mapped, but it is pantropical.
Figure 11 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 11 Map of central Georgia showing the distributions of some endemic or subendemic species. Designations: blue ring (Brachydesmus kalischewskyi), yellow ring (Caucaseuma variable), green Ring (Catamicrophyllum caucasicum), red ball (Cylindroiulus crassiphylacum), orange ring (Cylindroiulus pterophylacum), white ring (Grusiniulus redikorzevi), yellow ball (Herculina oligosagittae), blue ball (Herculina polysagittae), pink star (Leptoiulus hastatus), red diamond (Metamastigophorophyllon martensi), yellow star (Omobrachyiulus macrourus (= O. m. abchasicus)), white star (Syrioiulus georgicus).
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
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International Brain Laboratory public data
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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.