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68 results for “myriapod”
Supplementary material 1 from: Sammet K, Ivask M, Kurina O (2018) A synopsis of Estonian myriapod fauna (Myriapoda: Chilopoda, Diplopoda, Symphyla and Pauropoda). ZooKeys 793: 63-96. https://doi.org/10.3897/zookeys.793.28050
Full collecting details for one finding from each locality. The locality numbers correspond to those in Table 1 and Figure 1. :
Figure 1 in Why are there so few "far southern" myriapods?
Figure 1. The far southern hemisphere showing Antarctica and the principal island groups listed in the text.
Data from: A new dimension in documenting new species: high-detail imaging for myriapod taxonomy and first 3D cybertype of a new millipede species (Diplopoda, Julida, Julidae)
Open the record for dataset details and reuse information.
Figure 3 in Terrestrial isopods and myriapods in a forested scree slope: subterranean biodiversity, depth gradient and annual dynamics
Figure 3. Activity dynamics of isopod Ligidium germanicum (LIGE); diplopods Mecogonopodium carpathicum (MECA), Polydesmus denticulatus (PODE), Trachysphaera acutula (TRAC); and centipedes Harpolithobius anodus (HAAN), Lithobius forficatus (LIFO), during the period November 2008– November 2009.
Figure 2 in Terrestrial isopods and myriapods in a forested scree slope: subterranean biodiversity, depth gradient and annual dynamics
Figure 2. The non-metric multidimensional scaling ordination analysis (NMS) diagram of Isopoda and Myriapoda collected during both sampling periods; variance explained by axes 1 and 2 as 87.0% and 8.7%, respectively (triangles – depths, dots – species). Abbreviations: i – Isopoda: LIGE – Ligidium germanicum, MEGR – Mesoniscus graniger, TRCA – Trichoniscus carpaticus; d – Diplopoda: JUCU – Julus curvicornis, LEMA – Leptoiulus mariae, LETR – L. trilobatus, MECA – Mecogonopodium carpathicum, POCO – Polydesmus complanatus, PODE – Polydesmus denticulatus, TRAC – Trachysphaera acutula, STST – Strongylosoma stigmatosum; c – Chilopoda: HAAN – Harpolithobius anodus, LI - Lithobius sp. juv., LIFO – Lithobius forficatus, LILU – Lithobius lucifugus; STAC – Strigamia acuminata, STTR – Strigamia transsilvanica.
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 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.).
Supplementary material 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
Table S2
Figure 1 from: Horňák O, Mock A, Šarapatka B, Tuf IH (2020) Character of woodland fragments affects distribution of myriapod assemblages in agricultural landscape. In: Korsós Z, Dányi L (Eds) Proceedings of the 18th International Congress of Myriapodology, Budapest, Hungary. ZooKeys 930: 139-151. https://doi.org/10.3897/zookeys.930.48586
Figure 1 GAM plots evaluating effect of selected measured environmental factors to communities of centipedes and millipedes a relationship between size of wood fragments and number of centipedes' species trapped b relationship between thickness of leaf litter and number of centipedes trapped c relationship between species richness of trees in sites and number of centipedes trapped d relationship between thickness of leaf litter and number of millipedes trapped. Circles on diagram represent individual fragments of woodland.
Figure 4 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 4 Graphical presentation of myriapod community characteristics in different fixative solutions (N = number of individuals). A Formaldehyde to ethylene glycol ratio of sampled centipede species from all study sites, where both fixating solutions were used B formaldehyde to ethylene glycol ratio of sampled millipede species from all study sites, where both fixating solutions were used.
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 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 1 from: Parra-Gómez A, Pérez-Schultheiss J, Fernández LD (2024) Redescription of the enigmatic myriapod Hanseniella chilensis (Hansen, 1903) (Symphyla, Scutigerellidae) based on scanning electron microscope images of Chilean specimens. ZooKeys 1198: 1-15. https://doi.org/10.3897/zookeys.1198.119723
Figure 1 APG-17-a Male, dorsal view A head, first tergite and part of the second tergite (dfs-distinct frontal seta, ms-macroseta) B tergites 2–5 (am-anterolateral macrochaeta, hm-hind macrochaeta, pm-posterolateral macrochaeta) C tergites 11–13 D last tergite and cerci (hm-hind macrochaeta (abraded), hs-hind seta). Scale bars: 200.0 µm (A–C); 100.0 µm (D).
Figure 4 from: Parra-Gómez A, Pérez-Schultheiss J, Fernández LD (2024) Redescription of the enigmatic myriapod Hanseniella chilensis (Hansen, 1903) (Symphyla, Scutigerellidae) based on scanning electron microscope images of Chilean specimens. ZooKeys 1198: 1-15. https://doi.org/10.3897/zookeys.1198.119723
Figure 4 Illustrations showing some relevant structures of the species A antennomere 20 of a male B apical antennomere (sensory organs not as detailed as described due to their small size, smallest one not visible on this angle) C distal end of the first pair of legs D distal end of the last pair of legs (frontal seta abraded) E styli. Scale bar: 50 µm.
Figure 3 from: Parra-Gómez A, Pérez-Schultheiss J, Fernández LD (2024) Redescription of the enigmatic myriapod Hanseniella chilensis (Hansen, 1903) (Symphyla, Scutigerellidae) based on scanning electron microscope images of Chilean specimens. ZooKeys 1198: 1-15. https://doi.org/10.3897/zookeys.1198.119723
Figure 3 PG-71-L-a Female, ventral view A head and first pair of legs B ventral surface details proximal to left leg of pair 8 and its 2 first podomeres, podomere 4 and 5 of pair 7 partially show (lm-laminar needles, sc-scale-like cuticle, slm-"scales" with laminar needles) C coxal sac near leg pair 4 D last pair of legs and cerci (ap-apical seta, ls-large seta, os-outer seta). Scale bars: 100.0 µm (A, D); 50.0 µm (B); 20.0 µm (C).
Figure 2 from: Parra-Gómez A, Pérez-Schultheiss J, Fernández LD (2024) Redescription of the enigmatic myriapod Hanseniella chilensis (Hansen, 1903) (Symphyla, Scutigerellidae) based on scanning electron microscope images of Chilean specimens. ZooKeys 1198: 1-15. https://doi.org/10.3897/zookeys.1198.119723
Figure 2 Details of some relevant structures of APG-17-a Male (A, B) and PG-71-L-a Female (C, D) A central rod and triangular sulcus from the top of the head (hs-hind seta, oe-ovoid end, ss-short seta, ts-triangular sulcus) B tergal surface of tergite 3 (cr-cuticular rim) C Tömösváry organ and proximal surface (km-knob with microseta, lp-linguiform protuberance) D apical zone of the last antennomere (sb-sensilla basiconica, so-sensory organ). Scale bars: 50.0 µm (A, B); 10.0 µm (C, D).
Figure 5 from: Parra-Gómez A, Pérez-Schultheiss J, Fernández LD (2024) Redescription of the enigmatic myriapod Hanseniella chilensis (Hansen, 1903) (Symphyla, Scutigerellidae) based on scanning electron microscope images of Chilean specimens. ZooKeys 1198: 1-15. https://doi.org/10.3897/zookeys.1198.119723
Figure 5 All known records of Hanseniella chilensis (Hansen, 1903). Diamond = uncertain records from the literature, Star = new record herein, Circle = literature records.
Figure 7 from: Sammet K, Ivask M, Kurina O (2018) A synopsis of Estonian myriapod fauna (Myriapoda: Chilopoda, Diplopoda, Symphyla and Pauropoda). ZooKeys 793: 63-96. https://doi.org/10.3897/zookeys.793.28050
Figure 7 Habitat preferences of common Estonian Diplopoda. For explanation of the vertical axis and numbers denoting different habitats on the horizontal axis see Fig. 6.
Figure 6 from: Sammet K, Ivask M, Kurina O (2018) A synopsis of Estonian myriapod fauna (Myriapoda: Chilopoda, Diplopoda, Symphyla and Pauropoda). ZooKeys 793: 63-96. https://doi.org/10.3897/zookeys.793.28050
Figure 6 Proportion of samples from different habitats and habitat preferences of common Estonian Chilopoda. Vertical axis: relative abundances (numbers of findings divided by proportion of sampling effort). Horizontal axis numbers represent habitat types as follows: 1 Coastal meadows and alvars 2 Broad-leaved (nemoral) forests 3 Boreo-nemoral deciduous forests 4 Dry heathland forests 5 Drier boreo-nemoral mixed forests 6 Mesophilic boreal forests 7 Hillock forests 8 Carrs and swamp forests 9 Bogs 10 Fens and waterlogged meadows 11 Inland mesophilic grasslands 12 Rural gardens 13 Urban parks and graveyards 14 Arable fields. For detailed description of habitats see Material and methods.
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