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Figure 37 in Early Palaeogene Louisinidae (Macroscelidea, Mammalia), their relationships and north European diversity
Figure 37. Illustrations of character 48 states 0–6 and their parsimonious transformations.
Figure 36 in Early Palaeogene Louisinidae (Macroscelidea, Mammalia), their relationships and north European diversity
Figure 36. Illustrations of character 36 states 0–7 and their parsimonious transformations.
Figure 35 in Early Palaeogene Louisinidae (Macroscelidea, Mammalia), their relationships and north European diversity
Figure 35. Illustrations of character 10 states 0–8 and their parsimonious transformations.
Figure 34 in Early Palaeogene Louisinidae (Macroscelidea, Mammalia), their relationships and north European diversity
Figure 34. Illustrations of character 9 states 0–5 and their parsimonious transformations.
Figure 5 in A new species of Adactylidium (Acari: Heterostigmata: Acarophenacidae) associated withPhlaeothrips sp. (Thysanoptera: Phlaeothripidae) from European Russia
Figure 5 DIC micrographs ofAdactylidium europaeumn. sp., female (holotype): A – left parts of prodorsum and tergite C, B – hysterosoma, ventral aspect.
Figure 9 in The European Tertiary Neritiliidae (Mollusca, Gastropoda, Neritopsina): indicators of tropical submarine cave environments and freshwater faunas
Figure 9. Geographic distribution of the Recent marine Neritiliidae (dotted line) and principal occurrences of the genus Pisulina (•); fossil occurrences of the marine Neritiliidae (O); occurrences of the Recent (★) and fossil (✩) freshwater Neritiliidae.
Figure 2 in First European evidence for transcontinental dispersal of Crocodylus (late Neogene of southern Italy)
Figure 2. Blind pockets, or cecal recesses, are a synapomorphy of Crocodylus and absent in the only other brevirostrine crocodylian known in the European Miocene, the extinct alligatoroid genus Diplocynodon, and in the living African crocodylid genus Osteolaemus. A, B, right maxilla of Crocodylus sp. from Monte Gargano (BSP 2004 I 1) respectively in medial and latero-dorsal views; the arrows in A show anterior depressions and area of cecal recesses; the arrow in B shows the para-sagittal groove (see text). C, detail of a blind pocket; the arrows indicate a pocket whose lateral wall is only partly preserved. D, right maxilla in medial view of Crocodylus niloticus, juvenile, NMW 533; the arrows show anterior depressions and area of cecal recesses. E, right maxilla in medial view of Osteolaemus tetraspis, BSP 1982 X 5635. F, right maxilla in medial view of Diplocynodon styriacus from the Early Miocene (MN 5; BSP 1953 II 13) of Appertshofen, Germany. Teeth have been eliminated in D and F for ease of comparison. In order better to show the presence of the shallow depressions, the maxilla in A is figured in medial–ventral view; note that the palatal lamina is broken off at its base. The polygonal cavities visible on the right side of the D. styriacus maxilla in D are due to local breakage of the palatal lamina and are not cecal recesses. Scale bar equals 10 mm.
Figure 20 in Comparative morphology, biology and phylogeny of terminal-instar larvae of the European species of Toryminae (Hym., Chalcidoidea, Torymidae) parasitoids of gall wasps (Hym. Cynipidae)
Figure 20. Bootstrap consensus tree with implied weights (constant of concavity, k = 2) and no constraints from phylogenetic analyses of larval data. Numbers below branches indicate bootstrap support values above 50%.
Figure 14 in Comparative morphology, biology and phylogeny of terminal-instar larvae of the European species of Toryminae (Hym., Chalcidoidea, Torymidae) parasitoids of gall wasps (Hym. Cynipidae)
Figure 14. Mandibles of terminal-instar larvae of Torymidae. A, Adontomerus crassipes (anterior left). B, Adontomerus crassipes (anterior right). C, Adontomerus impolitus (posterior right). D, Adontomerus impolitus (posterior left). E, Chalcimerus borcea (posterior right). F, Chalcimerus borceai (posterior left). G, Glyphomerus stigma (posterior right). H, Glyphomerus stigma (posterior left). I, Glyphomerus tibialis (posterior right). J, Glyphomerus tibialis (posterior left). K, Idiomacromerus centaureae (anterior left). L, Idiomacromerus centaureae (anterior right). M, Idiomacromerus papaveris (posterior right). N, Idiomacromerus papaveris (posterior left). O, Idiomacromerus silybi (posterior right). P, Idiomacromerus silybi (posterior left).
Figure 3 in Comparative morphology, biology and phylogeny of terminal-instar larvae of the European species of Toryminae (Hym., Chalcidoidea, Torymidae) parasitoids of gall wasps (Hym. Cynipidae)
Figure 3. Terminal-instar larva of Torymus cingulatus Nees (anterior view of head) illustrating the terminology used in the text. Letters refer to the following structures: af, antennal foramina; am, antero-medial setae of antennal region; amf, antero-medial setae of frons; an, antenna; anr, antennal area; cl, clypeus; cs, clypeal setae; fr, frons; gn, genal setae; gr, genal region; hr, hypostomal region; hs, hypostomal setae; lb, labrum; lcs, latero-clypeal setae; po, preoral cavity; val, antero-lateral setae of vertex; vam, antero-medial setae of vertex; vr, vertex region.
Figure 6 in European cave shrimp species (Decapoda: Caridea: Atyidae), redefined after a phylogenetic study; redefinition of some taxa, a new genus and four new Troglocaris species
Figure 6. Distal articles of pereopods III and V. Sp, Troglocaris (Spelaeocaris) pretneri, male from Dejanova pećina; fSp, T. (S.) pretneri female, after Matjašič (1956a,b); Ta, Troglocaris (Troglocaris) a. anophthalmus, male from Kompoljska jama; fTa, T. (T.) a. anophthalmus, female from Kompoljska jama. See the Appendix for a list of abbreviations. Scale bars: see Fig. 4: sD for mx, mxp; sF for all pp.
Figure 6 in Cranial variation in the European badger Meles meles (Carnivora, Mustelidae) in Scandinavia
Figure 6. Histograms for length between the angular process and infradentale in different forms of the European badger: 1, 'south-western Norwegian' form; 2, 'main Fennoscandian' form; 3, 'non–Fennoscandian' form.
Figure 4 in Cranial variation in the European badger Meles meles (Carnivora, Mustelidae) in Scandinavia
Figure 4. The range of the 'Fennoscandian badgers' based on posterior classification probabilities (females and males are combined): 0–0.3, 'non–Fennoscandian' badgers; 0.3–0.6, unclear classified specimens (2.2%), 0.6–1.0, 'Fennoscandian' badgers.
Figure 7 in Gliridae (Rodentia, Mammalia) with a simple dental pattern: a new genus and new species from the European Early and Middle Miocene
Figure 7. Simplomys julii (Daams, 1989) from Artesilla (Fig. 7A–H; J–L; N–O) and San Roque 3 (Fig. 7I, M) (collection MNCN). A, P4 ART-2444. B, M1 ART-3. C, M2 ART-28. D, M3 ART-21. E, P4 ART-2447. F, M1 ART-4 holotype. G, M2 ART-13. H, M3 ART-1176. I, p4 SR3-803. J, m1 ART-16. K, m2 ART-14. L, m3 ART-1036. M, p4 SR3-604. N, m1 ART-22. O, m2 ART-27. Right side specimens underlined. Holotype in italics.
Figure 4 in Gliridae (Rodentia, Mammalia) with a simple dental pattern: a new genus and new species from the European Early and Middle Miocene
Figure 4. Simplomys simplicidens (De Bruijn, 1966) from Valdemoros 3F (Fig. 4A–H) and Artesilla (Fig. 4I–P) (collection MNCN). A, P4 VA3F-27. B, M1 VA3F-39. C, M2 VA3F-52. D, M3 VA3F-62. E, p4 VA3F-342. F, m1 VA3F-73. G, m2 VA3F-76. H, m3 VA3F-95. I, P4 ART-1134. J, M1 ART-931. K, M2 ART-943. L, M3 ART-1173. M, p4 ART-2455. N, m1 ART-966. O, m2 ART-990. P, m3 ART-1186. Right side specimens underlined.
Fig. 9 in A new species of the European freshwater bryozoan fauna: Plumatella similirepens WOOD, 2001 (Bryozoa, Phylactolaemata)
Fig. 9: Plumatella similirepens. Scanning electron micrograph of the suture. Scale bar = 20 µm. Fig. 10: Plumatella similirepens. Scanning electron micrograph of the sessoblast. a) Frontal valve. Scale bar = 100 µm. b) Detail of a). Scale bar = 50 µm. Fig. 11: Scanning electron micrograph of dorsal valve. a) Plumatella repens from the same hatchery. Scale bar = 100 µm. b) Detail of a). Scale bar = 50 µm. c) Typical Plumatella repens from an Italian natural site. Scale bar = 100 µm. d) Detail of c). Scale bar = 20 µm.
Supplementary material 3 from: Aspöck H, Aspöck U, Walochnik J, Kniha E (2021) Where did the Central European populations of Ornatoraphidia flavilabris (Costa) come from? (Neuropterida, Raphidioptera, Raphidiidae). Deutsche Entomologische Zeitschrift 68(2): 249-259. https://doi.org/10.3897/dez.68.70814
Multiple sequence alignment based on cytochrome c oxidase subunit 3 (cox3) sequences
Figure 2 from: Aspöck H, Aspöck U, Walochnik J, Kniha E (2021) Where did the Central European populations of Ornatoraphidia flavilabris (Costa) come from? (Neuropterida, Raphidioptera, Raphidiidae). Deutsche Entomologische Zeitschrift 68(2): 249-259. https://doi.org/10.3897/dez.68.70814
Figure 2 Ornatoraphidia flavilabris, female. Greece, Phokis, S Pendayi, 38°34.95'N, 22°03.45'E, 960 m, 31 May 2008, H. & U. Aspöck leg., now in coll. NHMW. (Photo: P. Sehnal, NHMW). Length of forewing: 10.5 mm.
Figure 1 from: Aspöck H, Aspöck U, Walochnik J, Kniha E (2021) Where did the Central European populations of Ornatoraphidia flavilabris (Costa) come from? (Neuropterida, Raphidioptera, Raphidiidae). Deutsche Entomologische Zeitschrift 68(2): 249-259. https://doi.org/10.3897/dez.68.70814
Figure 1 Ornatoraphidia flavilabris, male. Austria, Eichkogel, 48°03.75'N, 16°17.55'E, 358 m, 10 May 2021, H. & U. Aspöck leg., now in coll. NHMW. (Photo: H. Bruckner, NHMW). Length of forewing: 8.4 mm.
Supplementary material 4 from: Aspöck H, Aspöck U, Walochnik J, Kniha E (2021) Where did the Central European populations of Ornatoraphidia flavilabris (Costa) come from? (Neuropterida, Raphidioptera, Raphidiidae). Deutsche Entomologische Zeitschrift 68(2): 249-259. https://doi.org/10.3897/dez.68.70814
Multiple sequence alignment based on 28S rRNA gene (28S) sequences
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Allen Brain Atlas
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Annotated Behaviour and Observability Dataset (ABODe)
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