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247 results for “Lithobiomorpha”
Figure 18a. from: Eupolybothrus cavernicolus Komerički & Stoev sp. n. (Chilopoda: Lithobiomorpha: Lithobiidae): the first eukaryotic species description combining transcriptomic, DNA barcoding and micro-CT imaging data - Biodiversity Data Journal 1: e1013 (28 October 2013) https://doi.org/10.3897/BDJ.1.e1013
Figure 18a. - Prefemur of male leg 15. From Stoev et al. (2010). Figure 18a. Eupolybothrus caesar Figure 18b. Eupolybothrus spiniger <br> Eupolybothrus caesar
Figure 19. from: Eupolybothrus cavernicolus Komerički & Stoev sp. n. (Chilopoda: Lithobiomorpha: Lithobiidae): the first eukaryotic species description combining transcriptomic, DNA barcoding and micro-CT imaging data - Biodiversity Data Journal 1: e1013 (28 October 2013) https://doi.org/10.3897/BDJ.1.e1013
Figure 19. - Delineation of Eupolybothrus species – Neighbor joining tree K2P distances. Visualised are the clusters obtained from the reversed Statistical Parsimony (SP) method and the Automatic Barcoding Gap Discovery (ABGD) procedure. Bootstrap support for the identified lineages are given above. The intraspecific genetic variability is given for each cluster. Source data is available in Suppl. material 1.
Figure 20b. from: Eupolybothrus cavernicolus Komerički & Stoev sp. n. (Chilopoda: Lithobiomorpha: Lithobiidae): the first eukaryotic species description combining transcriptomic, DNA barcoding and micro-CT imaging data - Biodiversity Data Journal 1: e1013 (28 October 2013) https://doi.org/10.3897/BDJ.1.e1013
Figure 20b. - Gene annotation. Original data available from GigaScience GigaDB (Stoev et al. 2013). Figure 20a. E-value, identity and species distribution statistics of the sequences that can find homologs on Nr database Figure 20b. COG functional classification of the transcripts Figure 20c. GO categories of the transcripts <br> COG functional classification of the transcripts
Figure 17b. from: Eupolybothrus cavernicolus Komerički & Stoev sp. n. (Chilopoda: Lithobiomorpha: Lithobiidae): the first eukaryotic species description combining transcriptomic, DNA barcoding and micro-CT imaging data - Biodiversity Data Journal 1: e1013 (28 October 2013) https://doi.org/10.3897/BDJ.1.e1013
Figure 17b. - Prefemur of male leg 15. From Stoev et al. (2010). Figure 17a. Eupolybothrus tabularum Figure 17b. Eupolybothrus excellens <br> Eupolybothrus excellens
Fig. 1. Female 12 in New data on lithobiomorph centipedes (Chilopoda, Lithobiomorpha) from anthropogenic habitats of Siberia
Fig. 1. Female 12th tibia with a distal spinose projection (indicated by arrow) of Lamyctes africanus (Porath, 1871) from the environs of Unga village, Kemerovskaya Oblast, Russia. Scale: 0.1 mm.
Figure 1 in On some remarkable records of Chilopoda (Geophilomorpha, Lithobiomorpha) from Turkmenistan
Figure 1. Distribution of Dignathodon microcephalus (Lucas, 1846), Henia bicarinata (Meinert, 1870) (both circle), Clinopodes escherichii (Verhoeff, 1896) (triangle), and Lithobius viriatus Sseliwanoff, 1881 (square) in Turkmenistan. Abbreviations: KZ – Kazakhstan.
Figures 2–6 in On some remarkable records of Chilopoda (Geophilomorpha, Lithobiomorpha) from Turkmenistan
Figures 2–6. Dignathodon microcephalus (Lucas, 1846) (ZMMU Rc 8434): 2 – head, ventral view. Henia bicarinata (Meinert, 1870) (ZMMU Rc 7448): 3 – head, ventral view. Clinopodes escherichii (Verhoeff, 1896) (ZMMU Rc 8431: 4–5; Rc 8433: 6): 4 – front body fragment, ventral view; 5, 6 – rear body fragment, ventral view. Scale: 0.1 mm.
Figures 7–10. Lithobius viriatus Sseliwanoff, 1881 in On some remarkable records of Chilopoda (Geophilomorpha, Lithobiomorpha) from Turkmenistan
Figures 7–10. Lithobius viriatus Sseliwanoff, 1881 (female, Rc 8408): 7 – dental margin of forcipular coxosternite, ventral view; 8–10 – gonopods, mesal, dorsal, and ventral views. Scale: 0.2 mm.
Linked collectors and determiners for: A redescription of the species of Eupolybothrus Verhoeff s. str. preserved in the British Museum (Natural History) and the Hope departement of Zoology Oxford (Chilopoda Lithobiomorpha).
Natural history specimen data linked to collectors and determiners held within, "A redescription of the species of Eupolybothrus Verhoeff s. str. preserved in the British Museum (Natural History) and the Hope departement of Zoology Oxford (Chilopoda Lithobiomorpha)". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/c45d2e6e-acd9-4dc4-97e5-94d24a7a65aa">https://bionomia.net/dataset/c45d2e6e-acd9-4dc4-97e5-94d24a7a65aa</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/c45d2e6e-acd9-4dc4-97e5-94d24a7a65aa">https://gbif.org/dataset/c45d2e6e-acd9-4dc4-97e5-94d24a7a65aa</a>. Formatted as a Frictionless Data package.
Fig. 7 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 7. Area cladogram for Paralamyctes based on relationships under most congruent parameters for combined morphological and molecular data (Fig. 3, left cladogram). Stable clades are indicated (present in at least six parameter sets for the combined data).
Fig. 5 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 5. Details of the pretarsus of Henicopidae, showing characters 57 and 58 in Appendix 1. A. Paralamyctes (Thingathinga) grayi, dorsal view. B. Paralamyctes (Thingathinga) validus, anterior view. C. Paralamyctes (Haasiella) trailli, anterior view. D. Cermatobius japonicus, posterior view. E. Lamyctes emarginatus, anterior view. F. Anopsobius neozelanicus, dorsal view. All scales 10 m.
Fig. 3 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 3. Cladograms based on the combined analysis of all data (morphological + molecular). Cladogram at left is the single shortest tree of 7343 steps obtained for the most congruent parameter set (111); cladogram at right is strict consensus for all 12 parameters. Numbers on branches indicate jackknife frequencies.
Fig. 4 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 4. Graphic plots of sensitivity analyses. Black square = monophyly of indicated clade under gap cost and transversion:transition ratio shown along the axes; grey square = monophyly in some minimal length cladograms; white square = non-monophyly.
Fig. 2 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 2. Cladograms based on the combined analysis of all molecular data. Cladogram at left is the single tree at 7174 steps obtained for the most congruent parameter set (111); cladogram at right is strict consensus for all 12 parameter sets. Numbers on branches indicate jackknife frequencies.
Fig. 1 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 1. Strict consensus of 10 000 shortest cladograms based on morphological data (134 steps; CI = 0.56; RI = 0.86). Branches for the ingroup (Henicopidae) appear darker than those for the outgroup (Lithobiidae). Numbers above branches indicate jackknife frequencies; numbers below branches indicate absolute Bremer support and relative fit difference, RFD, shown as a percentage (see text for a description of these support measures). Labels on branches indicate groups recovered in all morphological analyses (Anopsobiinae, Lamyctes-Henicops Group within Henicopini, Zygethobiini) and traditional membership of Henicopinae. Paralamyctes (unresolved) is traditionally assigned to Henicopini.
Figure 21. from: Eupolybothrus cavernicolus Komerički & Stoev sp. n. (Chilopoda: Lithobiomorpha: Lithobiidae): the first eukaryotic species description combining transcriptomic, DNA barcoding and micro-CT imaging data - Biodiversity Data Journal 1: e1013 (28 October 2013) https://doi.org/10.3897/BDJ.1.e1013
Figure 21. - Eupolybothrus cavernicolus Komerički & Stoev sp. n., paratype, 3D model, volume rendering, created with CTVox, virtual rotation and dissection. Movie available at: YouTube.
Figure 22. from: Eupolybothrus cavernicolus Komerički & Stoev sp. n. (Chilopoda: Lithobiomorpha: Lithobiidae): the first eukaryotic species description combining transcriptomic, DNA barcoding and micro-CT imaging data - Biodiversity Data Journal 1: e1013 (28 October 2013) https://doi.org/10.3897/BDJ.1.e1013
Figure 22. - Movie of Eupolybothrus cavernicolus Komerički & Stoev sp. n., holotype, filmed ex-situ in a plastic container. Movie available at: YouTube.
Fig. 6 in Relationships of Henicopidae (Chilopoda: Lithobiomorpha): New molecular data, classification and biogeography
Fig. 6. Distributions of Anopsobiinae and Zygethobiini.
Figure 5. Bayesian tree for the 38 in Two new species of lithobiid centipedes and the first record of Lamyctes africanus Porath (Chilopoda: Lithobiomorpha) in China
Figure 5. Bayesian tree for the 38 sequences based on COI sequences. The Bayesian posterior probabilities from Bayesian analyses are presented above the main branches. The scale bar represents substitutions per site. Country of origin given in square brackets: AU = Australia; CH = China; GE = Germany; DK = Denmark; SA = South Africa.
Figure 4 in Two new species of lithobiid centipedes and the first record of Lamyctes africanus Porath (Chilopoda: Lithobiomorpha) in China
Figure 4. Lamyctes africanus (Porath)ı (aıe) RKZ11ı female: (a) dorsal viewı scale 1 mm; (e) ventral view of posterior segments and gonopodsı scale 100 µm; (b) RKZ3ı female: forcipular segmentı ventral viewı scale bar 500 µm; (c) RKZ11ı female: leg 12 in dorsal lateral viewı scale 500 μm; (d) RKZ13ı female: leg 15 in dorsal lateral viewı scale 500 μm.
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