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Figure 9 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 9 - Holotype of Lophoturus molloyensis sp. n. A The arrangement of sensilla on the 7th antennal article: A conical sensillum (c), a long thick sensillum located posteriorly (Tp) and a short thick sensillum located anteriorly (Ta) with a setiform sensillum (s) located between these sensilla B Sensilla on the 6th antennal article: a conical sensillum (c), a medium length thick sensillum located posteriorly (Tp) and a long thick sensillum located intermediately (Ti) followed the short thick sensillum (Ta) C The left antenna with eight articles and the arrangement of sensilla on the 6th and 7th articles.
Figure 7 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 7 - SEM images of Lophoturus boondallus sp. n. A Mouth part showed setose labrum (l) with typical two linguiform processes (lp) and sensilla from the gnathochilarium (g) B Simple claw with lateral dorsal denticles (ldd), claw (c), small denticle (smd) and basal denticle (bd) C Male caudal bundle showed an ornamental trichome sockets (a, b and c) and the uniform caudal bundle trichome sockets (cbts); D Female caudal bundle structure displaying ornamental trichome sockets and two main parts: caudal bundle trichome sockets dorsally (cbts) and two nest trichome sockets (nts) ventrally.
Figure 6 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 6 - SEM (Scanning Electron Microscopy) images of Lophoturus boondallus sp. n. A A dorsal view of whole body showing the body trichome arrangements and the caudal bundle B A ventral view of whole body showed 13 pairs of legs C A head capsule displaying two posterior vertex trichome groups (pv), a collum (col) and tergite 2 (t2) D Trichobothria a (a), b (b) and c (c) showing different sizes in trichobothrium sockets E and F Antennal articles 6 and 7 with sensilla (Ta: thick sensillum located anteriorly, Ti: intermediated thick sensillum, Tp: posterior thick sensillum, setiform sensillum (s) and a conical sensillum (c)).
Figure 8 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 8 - Holotype of Lophoturus molloyensis sp. n. A Head capsule, absence of ommatidia indicated, two posterior vertex trichome sockets (pv) and trichobothria a, b and c with the sockets only B the collum (col) and two lateral protuberances (Lp) C Tergite 2 (t2) and D The last tergite 10 (t10), showing the arrangement of trichome sockets F Trichobothria: a (the medium base socket located posteriorly) and b (the largest base socket located laterally) are typical thin sensory hairs, c with with a claviform funicle (the smallest base socket located anteriorly) G The male, right gnathochilarium showing numerous sensilla (ranged 56 – 58 sensilla in male) E Labrum showing a pair of linguiform processes (lp) and setose surface.
Figure 3 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 3 - The depiction of holotype of Lophoturus boondallus sp. n. A A head capsule showed the posterior vertex trichome sockets (pv) and trichobothria B, C, D Collum (col) with the lateral protuberances (Lp), tergite 2 (t2) and tergite 10 (t10), with trichome socket patterns E Trichobothria: Trichobothrium a (located posteriorly with medium socket), trichobothrium b (located laterally with largest socket) are typical thin sensory hairs and trichobothrium c with a claviform funicle (located anteriorly with smallest socket) F Gnathochilaria of male and G Gnathochilaria from female (paratype) H Labrum displayed two linguiform processes (lp) and setose surface.
Figure 2 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Figure 2 Myriapoda species assessement by the current Brazilian Red List. Myriapoda threatened species according to the 2014 Brazilian Red List, which follows IUCN classification categories (CR = Critically endangered, EN = Endangered, VU = Vulnerable, NT = Near threatened, LC = Least concern, DD = Data deficient). Dashed red line indicates threatened categories.
Figure 11 from: Jiang X, Guo X, Chen H, Xie Z (2018) Four new species of the Glyphiulus javanicus group (Diplopoda, Spirostreptida, Cambalopsidae) from Southern China. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 155-179. https://doi.org/10.3897/zookeys.741.23223
Figure 11 Glyphiulus calceus sp. n., holotype. A anterior gonopods, caudal view B posterior gonopods, caudal view. Abbreviations: C = coxosternum; CMP = coxosternal mesal process; F = flagellum; L = lamelliform lobe; T = telopodite. Scale bars: A, B 0.2 mm.
Figure 9 from: Reip HS, Wesener T (2018) Intraspecific variation and phylogeography of the millipede model organism, the Black Pill Millipede Glomeris marginata (Villers, 1789) (Diplopoda, Glomerida, Glomeridae). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 93-131. https://doi.org/10.3897/zookeys.741.21917
Figure 9 Maximum likelihood tree based on the mtDNA COI gene of 97 Glomeris marginata. Midpoint rooted. Roman numerals: Haplotype lineages I–V. Colour morphs of G. marginata: Common black = none; G = grey; R = red border; P = perplexa-markings. Scale bar = 1 % genetic ML distance.
Figure 5 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 5 - Holotype of Lophoturus boondallus sp. n. A The second left leg showing a penis (p), seven leg segments (co coxa, pf pre-femur, f femur, pof: post-femur, ti tibia, T1 tarsus 1, T2 tarsus 2 and a spine), a claw and its chaetotaxy (setae on the leg segments) B a pubescent oval seta C a spine on tarsus 2 D A simple claw structure with two latero-dorsal denticles (ldd), claw (c), a basal denticle (bd) and small denticle (smd) E The ornamental trichome sockets, located dorsally on the caudal bundle structure, with six trichomes a, one trichome b and two trichomes c (c1 and c3).
Figure 4 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 4 - Antennal articles of the holotype Lophoturus boondallus sp. n. A Antenna with eight articles and the arrangement of sensilla on the 6th and 7th articles; articles 7th and 8th were equal in length; the arrangement of sensilla on the 6th and 7th antennal articles B Sensilla on the 7th antennal article; a conical sensillum (c), a long thick sensillum located posteriorly (Tp) and a short thick sensillum located anteriorly (Ta) with a setiform sensillum (s) located between these sensilla C Sensilla on the 6th antennal article; a conical sensillum (c), a medium length thick sensillum (Tp), a long thick sensillum (Ti) and the short thick sensillum (Ta).
Figure 1 from: Karam-Gemael M, Izzo T, Chagas-Jr A (2018) Why be red listed? Threatened Myriapoda species in Brazil with implications for their conservation. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 255-269. https://doi.org/10.3897/zookeys.741.21971
Figure 1 Myriapoda in the IUCN and Brazilian red lists. Timeline of Myriapoda species included in the IUCN Red Lists of Threatened Species (above the red line), and in the Brazilian Red Lists of Threatened Species (below the red line), highlighting the first myriapods listed and the current number of species listed.
Figure 14 from: Jiang X, Guo X, Chen H, Xie Z (2018) Four new species of the Glyphiulus javanicus group (Diplopoda, Spirostreptida, Cambalopsidae) from Southern China. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 155-179. https://doi.org/10.3897/zookeys.741.23223
Figure 14 Glyphiulus guangnanensis sp. n., holotype. A anterior gonopods, caudal view B posterior gonopods, caudal view.
Figure 11 from: Nefediev PS, Farzalieva GS, Tuf IH, Nedoev KK, Niyazov ST (2018) Millipede and centipede assemblages on the northern and southern slopes of the lowland Altais, southwestern Siberia, Russia (Diplopoda, Chilopoda). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 219-254. https://doi.org/10.3897/zookeys.741.21936
Figure 11 RDA ordination biplot of the distribution patterns of centipedes in soil samples on the study slopes. Environmental variables significantly contributing to the prediction are in bold. The whole model is statistically significant (F = 4.12, p = 0.002) and explains 15.2 % of variability of species data, the X-axis explains 10.3 %.
Figures 2-5 from: Nefediev PS, Farzalieva GS, Tuf IH, Nedoev KK, Niyazov ST (2018) Millipede and centipede assemblages on the northern and southern slopes of the lowland Altais, southwestern Siberia, Russia (Diplopoda, Chilopoda). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 219-254. https://doi.org/10.3897/zookeys.741.21936
Figures 2-5 Two types of study habitats. 2–3 rocky xeromorphic steppe with bushes on the southern slope 4–5 rocky forested sites on the northern slope (2–3 taken in mid-July 2017, 5 taken at the end of May 2016; all by P.N.).
Figure 10 from: Jiang X, Guo X, Chen H, Xie Z (2018) Four new species of the Glyphiulus javanicus group (Diplopoda, Spirostreptida, Cambalopsidae) from Southern China. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 155-179. https://doi.org/10.3897/zookeys.741.23223
Figure 10 Glyphiulus calceus sp. n., paratype. A anterior gonopods, caudal view B posterior gonopods, caudal view C flagellum of posterior gonopods D microsetae at lateral margin of posterior gonopods. Scale bars: A 0.2 mm B 0.15 mm C 0.025 mm D 0.03 mm.
Figure 6-7 from: Nefediev PS, Farzalieva GS, Tuf IH, Nedoev KK, Niyazov ST (2018) Millipede and centipede assemblages on the northern and southern slopes of the lowland Altais, southwestern Siberia, Russia (Diplopoda, Chilopoda). In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 219-254. https://doi.org/10.3897/zookeys.741.21936
Figure 6-7 Range limits of some millipede species in the study area. 6 Distribution of Leptoiulus tigirek (diamond) 7 Distribution of Sibiriulus latisupremus (triangle). The new localities are shown in red.
Figure 2 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 2 - Three Lophoturus species were found in state of Queensland, Australia. A L. queenslandicus Verhoeff, 1924 B L. boondallus sp. n. and C L. molloyensis sp. n. These Lophoturus species showed differences in body lengths and colour.
Figure 12 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 12 - The molecular phylogenetic analysis by maximum likelihood method. A A consensus tree of sequences from 18S marker generated by the bootstrap test (1000 replications and the support values >50% shown on the nodes) yielded a strongly supported phylogenetic tree B The maximum likelihood test of sequences from COI marker provided the molecular phylogenetic tree of evolutionary history between each species. Again, this tree supported all Lophoturus species in the same clade as in the result of 18S.
Figure 10 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 10 - Holotype of Lophoturus molloyensis sp. n. A The second right leg with a penis (p), seven leg segments (c coxa, pf pre-femur, f femur, pof post-femur, ti tibia, T1 tarsus 1, T2 tarsus 2 and a spine), a claw and its chaetotaxy (setae on the leg segments) B A pubescent oval seta C A spine on tarsus 2 D A simple claw structure showing two latero-dorsal denticles (ldd), claw (c), a basal denticle (bd) and a small denticle (smd) E The ornamental trichome sockets, which located dorsally above the caudal bundle structure, with six trichomes a, one trichome b and two trichomes c (c1 and c3).
Figure 11 from: Huynh C, Veenstra AA (2018) Two new Lophoturus species (Diplopoda, Polyxenida, Lophoproctidae) from Queensland, Australia. In: Stoev P, Edgecombe GD (Eds) Proceedings of the 17th International Congress of Myriapodology, Krabi, Thailand. ZooKeys 741: 133-154. https://doi.org/10.3897/zookeys.741.21814
Figure 11 - SEM images of Lophoturus molloyensis sp. n. A A dorsal view of whole body showing the body trichome arrangements and the caudal bundle B A ventral view of whole body showing 13 pairs of legs C A head capsule displaying two posterior vertex trichome groups (pv), a collum (col) and tergite 2 (T2) D The trichobothria: a, b and c, showing different sizes in trichobothrium sockets E Antennal articles 6 and 7 with their sensilla (Ta: thick sensillum located anteriorly, Ti: intermediate thick sensillum, Tp: posterior thick sensillum, setiform sensillum (s) and a conical sensillum (c) F Mouth parts with setose labrum (l) with typical two linguiform processes (lp) and the gnathochilarium (g).
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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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