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Fig. 1 in Taxonomy, systematics and biology of the Australian halotolerant wolf spider genus Tetralycosa (Araneae: Lycosidae: Artoriinae)
Fig. 1. Typical habitats and live images of Tetralycosa Roewer, 1960. A. Salt lake (southern Lake Lefroy, Western Australia), where T. alteripa (McKay, 1976) and T. baudinettei sp. nov. can be found. B. T. alteripa (McKay, 1976), burrow on Lake Lefroy. C. T. alteripa (McKay, 1976), ♀ from Lake Lefroy. D. Sea shore (Cottesloe Beach, Western Australia), where T. oraria (L. Koch, 1876) can be found. E. T. oraria (L. Koch, 1876), ♂ from Cottesloe Beach (WAM T65606). F. T. oraria (L. Koch, 1876), ♂ from Safety Beach (Western Australia) (WAM T65111).
Fig. 24 in Taxonomy, systematics and biology of the Australian halotolerant wolf spider genus Tetralycosa (Araneae: Lycosidae: Artoriinae)
Fig. 24. Tetralycosa eyrei (Hickman, 1944), ♂ (SAM NN21737) and ♀ (SAM NN13814). A–B. Left male pedipalp, ventral and retrolateral view. C. Left male pedipalp, palea section of bulbus, ventral view. D–E. Female epigyne, ventral and dorsal views. Scale bar: A–B = 1.89 mm; C = 1.23 mm; D–E = 1.26 mm.
Fig. 7 in Taxonomy, systematics and biology of the Australian halotolerant wolf spider genus Tetralycosa (Araneae: Lycosidae: Artoriinae)
Fig. 7. Tetralycosa arabanae (Framenau, Gotch & Austin, 2006), ♂, paratype (SAM NN13887) and ♀ (WAM T47297, T47296). A–B. Left male pedipalp, ventral and retrolateral view. C. Left male pedipalp, palea section of bulbus, ventral view. D. Female epigyne, ventral view (WAM T47297). E. Female epigyne, dorsal view (WAM T47296). Scale bar: A–B = 1.02 mm; C = 0.32 mm; D–E = 1.00.
Fig. 23 in Taxonomy, systematics and biology of the Australian halotolerant wolf spider genus Tetralycosa (Araneae: Lycosidae: Artoriinae)
Fig. 23. Tetralycosa adarca sp. nov. A–B. Left male pedipalp, ventral and retrolateral view (holotype SAM NN21882). C. Left male pedipalp, palea section of bulbus, ventral view (SAM NN21888). D–E. Female epigyne, ventral and dorsal view (paratype SAM NN21732). Scale bar: A–B = 2.34 mm; C = 1.37 mm; D–E = 1.82.
Fig. 4 in Taxonomy, systematics and biology of the Australian halotolerant wolf spider genus Tetralycosa (Araneae: Lycosidae: Artoriinae)
Fig. 4. Phylogenetic hypothesis of Tetralycosa Roewer, 1960 based on 31 morphological and one ecological characters. A. Basal branches including outgroups. B. Terminal salt lake clade (L = 71, Ci = 61, Ri = 80). Bremer support values> 1 are indicated by numbers in squares below the respective node.
Fig. 9 in Taxonomy, systematics and biology of the Australian halotolerant wolf spider genus Tetralycosa (Araneae: Lycosidae: Artoriinae)
Fig. 9. Tetralycosa oraria (L. Koch, 1876), T. arabanae (Framenau, Gotch & Austin, 1976) and T. caudex sp. nov., distribution records in Australia.
Fig. 5 in Phylogenetic analysis and systematic position of two new species of the ant genus Crematogaster (Hymenoptera, Formicidae) from Southeast Asia
Fig. 5. Phylogeny and distribution of the Crematogaster borneensis-group, C. khmerensisi sp. nov., C. fruhstorferi, C. ssAUS5, C. mjobergi and the C. tetracantha-group. Closed circle indicates C. khmerensis sp. nov., closed square indicates C. pfeifferi sp. nov. It is noted that C. pfeifferi sp. nov. is not represented in the phylogeny.
Fig. 4. A–D in Phylogenetic analysis and systematic position of two new species of the ant genus Crematogaster (Hymenoptera, Formicidae) from Southeast Asia
Fig. 4. A–D. Crematogaster khmerensis sp. nov., worker. A. Body in lateral view. B. Full-face view of head. C. Dorsal view of mesosoma. D. Petiole and postpetiole in dorsal view. — E–H. — Crematogaster pfeifferi sp. nov., worker. E. Body in lateral view. F. Full-face view of head. G. Dorsal view of mesosoma. H. Petiole and postpetiole in dorsal view.
Fig. 3 in Phylogenetic analysis and systematic position of two new species of the ant genus Crematogaster (Hymenoptera, Formicidae) from Southeast Asia
Fig. 3. Posterior estimates of divergence time of 24 taxa on the phylogenetic tree. Blue bars depict the 95% highest posterior density (HPD). Estimations were performed with MCMCTree using the independent rate model.
Fig. 1. Bayesian majority rule consensus tree reconstructed for 90 in Phylogenetic analysis and systematic position of two new species of the ant genus Crematogaster (Hymenoptera, Formicidae) from Southeast Asia
Fig. 1. Bayesian majority rule consensus tree reconstructed for 90 taxa using five genes (ArgK, CAD, LWRh, Top1, Wg) in a MrBayes analysis. Above node numbers indicate posterior probability. Data were partitioned by PartitionFinder v.1.1.1 and analyzed using a best fit model for each gene and codon position, with 10 million generations and a burn-in of 25 %. Area enclosed by dashed lines is enlarged on Fig. 2.
Fig. 3 in Systematic revision and palaeobiology of Rosenfeldia triasica and Rogeryon oppeli gen. et comb. nov. (Eucrustacea, Polychelida)
Fig. 3. Reconstruction of the dorsal aspect of Rosenfeldia triasica Garassino, Teruzzi & Dalla Vecchia, 1996. Please note that due to the preservation conditions of specimens, the precise outline of the carapace and shape of grooves are difficult to assess. Image hand-drawn by D. Audo.
Fig. 2 in Systematic revision and palaeobiology of Rosenfeldia triasica and Rogeryon oppeli gen. et comb. nov. (Eucrustacea, Polychelida)
Fig. 2. Comparison of the general outline of carapaces (right sides omitted, adapted from Audo 2016 and Audo et al. 2017) of the type species of each genus of fossil Polychelida. A. Adamanteryon fourneti Audo, Schweigert, Saint Martin & Charbonnier, 2014. B. Antarcticheles antarcticus Aguirre-Urreta, Buatois, Chernoglasov & Medina 1990. C. Coleia antiqua Broderip, 1835. D. Cycleryon propinquus (Schlotheim, 1822). E. Eryon cuvieri Desmarest, 1817. F. Gabaleryon coquelae Audo, Williams, Charbonnier & Schweigert, 2017. G. Hellerocaris falloti (Van Straelen, 1923). H. Knebelia bilobata (Münster, 1839). I. Palaeopentacheles roettenbacheri (Münster, 1839). J. Palaeopolycheles longipes (Fraas, 1855). K. Proeryon hartmanni (Meyer, 1836). L. Pseudocoleia mazzolenii Garassino & Teruzzi, 1993. M. Rogeryon oppeli (Woodward, 1866) gen. et comb. nov. N. Rosenfeldia triasica Garassino, Teruzzi & Dalla Vecchia, 1996. O. Soleryon amicalis Audo, Charbonnier, Schweigert & Saint Martin, 2014. P. Tethyseryon campanicus Bravi, Garassino, Bartiromo, Audo, Charbonnier, Schweigert, Thévenard & Longobardi, 2014. Q. Tetrachela raiblana (Bronn, 1858). R. Tonneleryon schweigerti Audo, 2016. S. Tropifer laevis Gould, 1857. T. Voulteryon parvulus Audo, Schweigert, Saint Martin & Charbonnier, 2014. U. Willemoesiocaris ovalis (Van Straelen, 1923). V. Wrangelleryon perates Feldmann, Schweitzer & Haggart, 2013. Illustrations not to scale.
Fig. 6 in Systematic revision and palaeobiology of Rosenfeldia triasica and Rogeryon oppeli gen. et comb. nov. (Eucrustacea, Polychelida)
Fig. 6. Reconstruction of Rogeryon oppeli (Woodward, 1866). A. Dorsal aspect. B. Known parts of the ventral aspect, thoracic appendages omitted on the right side. Please note that due to the softness of the carapace, its precise outline is uncertain. Image hand-drawn by D. Audo.
Fig. 1 in Systematic revision and palaeobiology of Rosenfeldia triasica and Rogeryon oppeli gen. et comb. nov. (Eucrustacea, Polychelida)
Fig. 1. Rosenfeldia triasica Garassino, Teruzzi & Dalla Vecchia, 1996 from the Upper Triassic (Norian) of Mount Auda, Italy. A–B. Holotype, MFSNgp 16178, dorsal view, cross-polarized light (A) and interpretative line-drawing (B). C–D. Specimen MFSNgp 40312, ventral view, cross-polarized view (C) and interpretative line-drawing (D). Abbreviations: a2 = antenna; ba = uropodal basipodite; bc = branchial carina; c = postcervical groove; ci = postcervical incision; e1e = cervical groove; en = uropodal endopod; ei = cervical incision; ex = uropodal exopod; md = mandible; mo = mandibular molar process; mxp3 = third maxilliped; o = ocular incision; P1–P5 = pereiopods 1 to 5; P? = indeterminate pereiopod; pc = postcervical carina; pla = posterolateral angle; s1–s6 = pleonites 1 to 6; t = telson. Scale bars: A–B = 10 mm; C–D = 20 mm. Photographs: D. Audo, © MFSNgp.
Fig. 5 in Systematic revision and palaeobiology of Rosenfeldia triasica and Rogeryon oppeli gen. et comb. nov. (Eucrustacea, Polychelida)
Fig. 5. Rogeryon oppeli (Woodward, 1866) gen. et comb. nov. from the Upper Jurassic (Tithonian) of Germany. A–C. Specimen SMNS 66004 (Sappenfeld), dorsal view, natural light (A), interpretative linedrawing (P1-P3 on one side were restored and are therefore drawn as outline (B) and green fluorescence (C). D. Specimen SMNS 65545 (Eichstätt), ventral view, natural light. E. Specimen SMNS 66004/2 (Langenaltheim), ventral view, natural light. F. Specimen without number (Mörnsheim, K. and H. Schumacher coll.), ventral view, UV light. Abbreviations: a1 = antenna; ba = uropodal basipodite; en = uropodal endopod; ex = uropodal exopod; o = eye; pe = petasma; P1–P5 = pereiopods 1 to 5; pla = posterolateral angle; s1–s6 = pleonites 1 to 6; sm = submarginal carina; t = telson. Scale bars: 20 mm. Photographs: G. Schweigert (A, D–F), J.T. Haug (C).
Fig. 4 in Systematic revision and palaeobiology of Rosenfeldia triasica and Rogeryon oppeli gen. et comb. nov. (Eucrustacea, Polychelida)
Fig. 4. Rogeryon oppeli (Woodward, 1866) gen. et comb. nov. from the Upper Jurassic (Tithonian) of Germany. A–B. Holotype NHMUK 44886 (Solnhofen area), dorsal view, UV-fluorescence (A) and interpretative line drawing (B). C. Specimen JMS 118 (Langenaltheim, Udo Resch coll.), dorsal view, natural light. D. Specimen SMNS 70102 (Solnhofen), dorsal view, cross-polarized light. Abbreviations: a1 = antennula; a2 = antenna; ala = anterolateral angle; ba = uropodal basipodite; c = postcervical groove; cd = carapace deformation; ci = postcervical incision; e1e = cervical groove; en = uropodal endopod; ei = cervical incision; ex = uropodal exopod; o = ocular incision; P1–P5 = pereiopods 1 to 5; pla = posterolateral angle; s1–s6 = pleonites 1 to 6; t = telson. Scale bars: 20 mm. Photographs: D. Audo, © NHMUK (A) and G. Schweigert (C–D).
Bibliography of the Systematic Literature Review of the IPBES Global Assessment, Chapter 4
<p>Bibliographies from the systematic literature review in Chapter 4 of the IPBES Global Assessment</p> <p>DOI: 10.5281/zenodo.3553579</p>
Data to Richter et al. 2020 Comparative analysis of worker head anatomy of Formica and Brachyponera (Hymenoptera: Formicidae) in Arthropod Systematics & Phylogeny
<p>This dataset contains the ant head µCT-Sanning Datasets used for the article "Comparative analysis of worker head anatomy of <em>Formica</em> and <em>Brachyponera</em> (Hymenoptera: Formicidae)" by Richter et al. published in <em>Arthropod Systematics & Phylogeny </em>2020. In addition, the image plates from that article (in highest resolution as TIF files) and a series of supplementary 3D-volume render video files are deposited.</p> <p>The datasets for CASENT0709409, CASENT0709411 and CASENT0790267 are deposited as they were used in this study (with transformation to adjust the orientation of the ant head to the global axes and cropped to reduce file size) while CASENT0709419 is deposited as the original scanning result as it was not modified for the work in this article.</p> <p>Scanning details can be found in the materials and methods section of the article. Scanning parameters were as follows:</p> <p>Power (W): 3W all specimens</p> <p>Voltage (kV): 40kV all specimens</p> <p>Voxel Size: CASENT0709409: 1,1557 µm<sup>3</sup>; CASENT0709419: 1,2244 µm<sup>3</sup>; CASENT0709411: 2,5527µm<sup>3 </sup>; CASENT0790267: 2,8337 µm<sup>3</sup> </p> <p>Exposure Time (s): CASENT0709409: 25 s; CASENT0709419: 15 s; CASENT0709411: 7 s<sup> </sup>; CASENT0790267: 5 s</p> <p>Source Distance (mm): CASENT0709409: -9,5038 mm; CASENT0709419: -9,5321 mm; CASENT0709411: 10,038 mm<sup> </sup>; CASENT0790267: 13,0037 mm</p> <p>Detector Distance (mm): CASENT0709409: 46 mm; CASENT0709419: 43,0166 mm; CASENT0709411: 16,5043 mm<sup> </sup>; CASENT0790267: 18,0015 mm</p>
Secondary studies in the academic context: A systematic mapping and survey
<p>An online version of the survey executed in the paper "Secondary studies in the academic context: A systematic mapping and survey".</p>
Figure 2 in The contribution of molecular data to our understanding of cephalopod evolution and systematics: a review
Figure 2. Polyploidy scenario suggested by and reproduced from Bonnaud et al. (2004). Updated diploid chromosome numbers (see Table 2) for the various branches are now Nautiloidea 52; Octopoda 56–60; Sepiolida 74; Sepiida 48–112; Myopsida 86–92 (?22-?172).
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.