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Figures 5-8 from: Golovatch SI (2015) Cave Diplopoda of southern China with reference to millipede diversity in Southeast Asia. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 79-94. https://doi.org/10.3897/zookeys.510.8640
Figures 5-8 - Habitus photos of Pacidesmus armatus Golovatch, Geoffroy & Mauriès, 2010, Desmoxytes scolopendroides Golovatch, Geoffroy & Mauriès, 2010, Eutrichodesmus filisetiger Golovatch, Geoffroy, Mauriès & VandenSpiegel, 2009, and Eutrichodesmus aster Golovatch, Geoffroy, Mauriès & VandenSpiegel, 2009, all presumed trogloionts from Guangxi, Guangxi, Vietnam, and Vietnam, respectively. After Golovatch et al. (2009c, 2010a, 2010b). Photos courtesy L. Deharveng & A. Bedos.
Figure 3 from: Oeyen JP, Wesener T (2015) Steps towards a phylogeny of the pill millipedes: non-monophyly of the family Protoglomeridae, with an integrative redescription of Eupeyerimhoffia archimedis (Diplopoda, Glomerida). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 49-64. https://doi.org/10.3897/zookeys.510.8675
Figure 3 - Eupeyerimhoffia archimedis (Strasser, 1965) male, SEM. A Head, frontal view B Head, ventral view C Head, detail of lateral area D Antenna, posterior viewE Antenna, antennomere 6 and 7 F Antenna, apical edge of antennomere 3 G Mandible, mesal view H Gnathochilarium, ventral view I Endochilarium, dorsal view J Gnathochilarium, lateral and inner palpi, dorsal view K Endochilarium, detail of median area, dorsal view. Abbreviations: 1-7 = Antennal segments number 1-7; 4iT = 4-combed inner tooth; AC = Apical cone; AF = Antennal fossa; Ca = Cardine; Co = Condylus; cP = Central pads; CT = Central tooth; eT = External tooth; fS = fringed seam; Gu = Gula; iA = Intermediate area; iL = Incisura lateralis; iP = Inner palpi; L = Labrum; LL = Lamella linguales; LP = Lateral palpi; M = Mentum; MP = Molar plate; O = Ocellaria; O1-O4 = Ocelli 1-4; pL = Pectinate lamellae; pmL = paramedian lobe; TO = Organ of Tömösváry; SC = Sensory clusters; St = Stipites. Arrows mark sensilla basiconica. Scale bar: 400 μm (A, B); 200 μm (C); 150 μm (D); 25 μm (E); 10 μm (F); 100 μm (G); 250 μm (H, I); 40 μm (J); 50 μm (K).
Figure 2 from: Oeyen JP, Wesener T (2015) Steps towards a phylogeny of the pill millipedes: non-monophyly of the family Protoglomeridae, with an integrative redescription of Eupeyerimhoffia archimedis (Diplopoda, Glomerida). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 49-64. https://doi.org/10.3897/zookeys.510.8675
Figure 2 - Maximum likelihood bootstrap consensus tree. Members of the family Protoglomeridae are marked in bold.
Figure 2 from: Stoev P, Akkari N, Komerički A, Edgecombe GD, Bonato L (2015) At the end of the rope: Geophilus hadesi sp. n. – the world's deepest cave-dwelling centipede (Chilopoda, Geophilomorpha, Geophilidae). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 95-114. https://doi.org/10.3897/zookeys.510.9614
Figure 2 - Geophilus hadesi sp. n. Habitus of male specimen (CBSS: CHP515). Photo taken in situ in the Lukina jama – Trojama cave system, at -980 m below the surface (Fig. 22), 1–3 August 2011. Photo credit: J. Bedek.
Figure 2 from: Edgecombe GD, Vahtera V, Giribet G, Kaunisto P (2015) Species limits and phylogeography of Newportia (Scolopendromorpha) and implications for widespread morphospecies. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 65-77. https://doi.org/10.3897/zookeys.510.8573
Figure 2 - Strict consensus of two optimal cladograms for Newportia under parameter set 111 for parsimony (POY) analysis. Abbreviations: BRA, Brazil; COL, Colombia; CR, Costa Rica; DR, Dominican Republic; ECU, Ecuador; FRG, French Guiana; GUA, Guatemala; HON, Honduras; MEX, Mexico.
Figure 1 from: Oeyen JP, Wesener T (2015) Steps towards a phylogeny of the pill millipedes: non-monophyly of the family Protoglomeridae, with an integrative redescription of Eupeyerimhoffia archimedis (Diplopoda, Glomerida). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 49-64. https://doi.org/10.3897/zookeys.510.8675
Figure 1 - Eupeyerimhoffia archimedis (Strasser, 1965) female in situ and habitat. A Eupeyerimhoffia archimedis female rolled up, in situ B Eupeyerimhoffia archimedis female in situ C Habitat of Eupeyerimhoffia archimedis, close to the type locality Ferla.
Figure 4 from: Del Latte L, Bortolin F, Rota-Stabelli O, Fusco G, Bonato L (2015) Molecular-based estimate of species number, phylogenetic relationships and divergence times for the genus Stenotaenia (Chilopoda, Geophilomorpha) in the Italian region. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 31-47. https://doi.org/10.3897/zookeys.510.8808
Figure 4 - Dated phylogeny. Estimates of divergence time, calculated using 28S sequences and two priors (age of the root and substitution rate) in the package BEAST v1.7.2 (see text). 95% High Posterior Density intervals are represented by coloured bars for the most robust nodes, emphasized by a circle. Greek letters refer to the species tentatively recognised (see Fig. 1). The tree has the same topology of the concatenated ML tree of Fig. 3, but for the position of Tuoba sydneyensis and the relationships within the group formed by species β, ε, γ and the specimen from Iran. The specimen from Volpago (species δ) is absent because its 28S sequence was not obtained. Time scale is different in the two intervals 0–100 and 100–200 Ma.
Figure 3 from: Del Latte L, Bortolin F, Rota-Stabelli O, Fusco G, Bonato L (2015) Molecular-based estimate of species number, phylogenetic relationships and divergence times for the genus Stenotaenia (Chilopoda, Geophilomorpha) in the Italian region. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 31-47. https://doi.org/10.3897/zookeys.510.8808
Figure 3 - Maximum likelihood phylogeny. ML tree obtained from concatenated COI and 28S sequences, by the GTR+I+G model, and manually rooted. The following support values are indicated at the nodes (only for those present in the topology obtained from the concatenated sequences): ML bootstrap for the analysis of concatenated genes (upper left); Bayesian posterior probabilities (upper right, in italics); ML bootstrap for the analysis of COI sequences (lower left); ML bootstrap for the analysis of 28S sequences (lower right). Bootstrap values < 50% and posterior probabilities < 0.50 are not shown. Circles indicate ingroup nodes that are highly supported in the tree based on concatenated sequences. Terminal node groupings indicated by Greek letters refer to the species tentatively recognized (see text and Fig. 1). The specimen from Volpago (species δ) is absent because its 28S sequence was not obtained.
Figure 1 from: David J-F, Coulis M (2015) Millipedes faced with drought: the life cycle of a Mediterranean population of Ommatoiulus sabulosus (Linnaeus) (Diplopoda, Julida, Julidae). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 115-124. https://doi.org/10.3897/zookeys.510.8838
Figure 1 - Phenology of Ommatoiulus sabulosus in Provence (October 2013–April 2014). Stadia are indicated on the horizontal axis and those of three identifiable generations (G 2011 without any individuals, G 2012 and G 2013) are grouped together. White bars = undifferentiated juveniles and females; grey bars = immature and intercalary males; black bars = adult males. Abundant (+) or very abundant (++) juveniles of stadia II and III were not included in the calculation of percentages.
Figure 1 from: Del Latte L, Bortolin F, Rota-Stabelli O, Fusco G, Bonato L (2015) Molecular-based estimate of species number, phylogenetic relationships and divergence times for the genus Stenotaenia (Chilopoda, Geophilomorpha) in the Italian region. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 31-47. https://doi.org/10.3897/zookeys.510.8808
Figure 1 - Sampling localities of Stenotaenia in the Italian region. Greek letters refer to the species tentatively recognized after the analyses (see text).
Figure 1 from: Wesener T, Voigtländer K, Decker P, Oeyen JF, Spelda J, Lindner N (2015) First results of the German Barcode of Life (GBOL) – Myriapoda project: Cryptic lineages in German Stenotaenia linearis (Koch, 1835) (Chilopoda, Geophilomorpha). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 15-29. https://doi.org/10.3897/zookeys.510.8852
Figure 1 - Maximum likelihood tree, 1000 bootstrap replicates. L1–L3 = Stenotaenia linearis lineages 1–3; NRW = North Rhine-Westphalia; Baden-W = Baden-Württemberg. Stenotaenia 'sorrentina' comes from GenBank and might refer to Stenotaenia forficularis. For exact locality data, see Table 1.
Figure 3 from: Wesener T, Voigtländer K, Decker P, Oeyen JF, Spelda J, Lindner N (2015) First results of the German Barcode of Life (GBOL) – Myriapoda project: Cryptic lineages in German Stenotaenia linearis (Koch, 1835) (Chilopoda, Geophilomorpha). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 15-29. https://doi.org/10.3897/zookeys.510.8852
Figure 3 - Map of Stenotaenia linearis samples studied during GBOL (large dots), as well as other Stenotaenia linearis records from Edaphobase, the ZSM and ZFMK collection (small dots, status 10.2014). Yellow = Stenotaenia linearis L1; Blue = Stenotaenia linearis L2; Green = Stenotaenia linearis L3. (A) Stenotaenia linearis in the field, photo: J. Spelda, specimen from Stuttgart-Hofen, Zuckerberg.
Figure 2 from: Wesener T, Voigtländer K, Decker P, Oeyen JF, Spelda J, Lindner N (2015) First results of the German Barcode of Life (GBOL) – Myriapoda project: Cryptic lineages in German Stenotaenia linearis (Koch, 1835) (Chilopoda, Geophilomorpha). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 15-29. https://doi.org/10.3897/zookeys.510.8852
Figure 2 - Frequency distribution of pairwise intraspecific (blue) and interspecific (red) distances. Blue circle = intraspecific distances of Geophilus alpinus and among Stenotaenia linearis L3; Red circle = interspecific distances and distances between Stenotaenia linearis lineages. Basic table see Suppl. material 1.
Figure 2 from: Tajovský K, Tuf IH (2015) Introduction for Proceedings volume of 16th International Congress of Myriapodology. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 1-4. https://doi.org/10.3897/zookeys.510.10176
Figure 2 - Legend of Fig. 1. 1 Boyan Vagalinski 2 Oliver Macek 3 Lucio Bonato 4 Hsueh-Wen Chang 5 Norman Lindner 6 Laura Del Latte 7 Irina Semenyuk 8 Michaela Bodner 9 Fieng-Lan Sun 10 Chao-chun Chen 11 Piyatida Pimvichai 12 Warut Siriwut 13 Natdanai Likhitrakarn 14 Małgorzata Leśniewska 15 Jolanta Wytwer 16 Michaela Kratochvílová 17 Christian Kronmüller 18 Cuong Huynh 19 Nattarin Wongthamwanich 20 João Paulo Pena-Barbosa 21 Julian Bueno-Villegas 22 Varpu Vahtera 23 Peter Decker 24 Barbara Jäschke 25 Julia Nefedieva 26 Roghaieh Zarei 27 Leszek Jendryszik 28 Ivan H. Tuf 29 Karel Tajovský 30 Sergei Ilyich Golovatch 31 Günther Raspotnig 32 Hans S. Reip 33 Darina Bachvarova 34 Elena Valentinovna Mikhaljova 35 Michalina Kszuk-Jendrysik 36 Pavel Stoev 37 Somsak Panha 38 Nesrine Akkari 39 Pavel Nefediev 40 Jean-Jacques Geoffroy 41 Giuseppe Fusco 42 Karin Voigtländer 43 Jean-Francois David 44 Bjarne Meidell 45 Amazonas Chagas-Jr. 46 Manoela Karam Gemael 47 Carsten H. G. Müller 48 Ivan Kos 49 Blanka Ravnjak 50 Maja Kastelic 51 Branka Vode 52 Megan Short 53 Hilke Ruhberg 54 Pavel Kocourek 55 Timotej Mock 56 Grzegorz Antoni Kania 57 John Lewis 58 Greg Edgecombe 59 Joseph Hannibal 60 Vladimír Šustr 61 Michal Rendoš 62 Andrej Mock 63 László Dányi 64 Ansgar Poloczek 65 Stylianos Simasiakis 66 Andy Sombke 67 Eivind Andreas Baste Undheim 68 Pavel Saska 69 Aleksandr Evsiukov 70 Willi Xylander 71 Bruce A. Snyder 72 Jan Philip Oeyen 73 Petr Dolejš 74 Henrik Enghoff 75 Ana Komerički 76 Markus Koch 77 Jörg Rosenberg 78 Iurii Diachkov 79 Daniela Bartel 80 Nikolaus U. Szucsich 81 Zoltán Korsós 82 Thomas Wesener 83 David Bogyo 84 Per Djursvoll. Aleksandar Doichinov, Elisavet Georgopoulou, Eszter Lazányi, Gabriella Papastefanou and Irina Zenkova are missing.
Figure 10 from: Golovatch SI (2015) Cave Diplopoda of southern China with reference to millipede diversity in Southeast Asia. In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 79-94. https://doi.org/10.3897/zookeys.510.8640
Figure 10 - Habitus of Glyphiulus difficilis Golovatch, Geoffroy, Mauriès & VandenSpiegel, 2011, a presumed troglobiont from Guangxi. Scale bar: 1.5 mm. After Golovatch et al. (2011b). SEM micrograph courtesy D. VandenSpiegel.
Figure 6 from: Papastefanou G, Panayiotou E, Mylonas M, Simaiakis SM (2015) Centipede assemblages along an urbanization gradient in the city of Heraklion, Crete (Greece). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 163-179. https://doi.org/10.3897/zookeys.510.8414
Figure 6 - Total and average abundance of all four generalist species as well as average abundance of each generalist species along the urban-rural gradient, Eupolybothrus litoralis (♦), Lithobius nigripalpis (▲), Scolopendra cretica (■), Scutigera coleoptrata (●). White columns show total abundance, grey columns show average abundance with bars with standard deviation.
Figure 1 from: Nefedieva JS, Nefediev PS, Sakhnevich MB, Dyachkov YV (2015) Distribution of millipedes along an altitudinal gradient in the south of Lake Teletskoye, Altai Mts, Russia (Diplopoda). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 141-161. https://doi.org/10.3897/zookeys.510.8855
Figure 1 - Neighbour-joining tree of similarity / dissimilarity of studied sites on species diversity.
Figure 3 from: Leśniewska M, Jastrzębski P, Stańska M, Hajdamowicz I (2015) Centipede (Chilopoda) richness and diversity in the Bug River valley (Eastern Poland). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 125-139. https://doi.org/10.3897/zookeys.510.8763
Figure 3 - Dendrogram of the similarities of centipede composition in different habitats (distance/similarity measure – Bray and Curtis, cluster method –nearest neighbor) For designations see Table 1.
Figures 15-19 from: Stoev P, Akkari N, Komerički A, Edgecombe GD, Bonato L (2015) At the end of the rope: Geophilus hadesi sp. n. – the world's deepest cave-dwelling centipede (Chilopoda, Geophilomorpha, Geophilidae). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 95-114. https://doi.org/10.3897/zookeys.510.9614
Figures 15-19 - Geophilus hadesi sp. n. 15 close up of metasternite of leg-bearing segment 26, ventral 16 left leg 8, anterio-lateral 17 close up of the tip of the right ultimate leg, external view 18 postpedal segments, ventral 19 close up of pretarsus and tarsus of midbody leg, lateral. SEM micrographs taken from female paratype NHMW8363 from cave Muda labudova. Abbreviations: tarsus 2 (t2), pretarsus (pt), isolated coxal pore (icxp), anal valve (av), first genital pleurosternite (fgp), gonopods (g).
Figure 2 from: Leśniewska M, Jastrzębski P, Stańska M, Hajdamowicz I (2015) Centipede (Chilopoda) richness and diversity in the Bug River valley (Eastern Poland). In: Tuf IH, Tajovský K (Eds) Proceedings of the 16th International Congress of Myriapodology, Olomouc, Czech Republic. ZooKeys 510: 125-139. https://doi.org/10.3897/zookeys.510.8763
Figure 2 - Similarity of species (distance/similarity measure Bray and Curtis; cluster method: nearest neighbor). Species nomenclature in Table 1.
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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
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