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Supplementary material 3 from: Diagne C, Turbelin AJ, Moodley D, Novoa A, Leroy B, Angulo E, Adamjy T, Dia CA.K.M, Taheri A, Tambo J, Dobigny G, Courchamp F (2021) The economic costs of biological invasions in Africa: a growing but neglected threat? In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 11-51. https://doi.org/10.3897/neobiota.67.59132
Summary of the descriptive columns of the database used in this study (from Diagne et al. 2020c)
Supplementary material 6 from: Diagne C, Turbelin AJ, Moodley D, Novoa A, Leroy B, Angulo E, Adamjy T, Dia CA.K.M, Taheri A, Tambo J, Dobigny G, Courchamp F (2021) The economic costs of biological invasions in Africa: a growing but neglected threat? In: Zenni RD, McDermott S, García-Berthou E, Essl F (Eds) The economic costs of biological invasions around the world. NeoBiota 67: 11-51. https://doi.org/10.3897/neobiota.67.59132
Categorization of recorded cost data into "damage" costs
FIGURE 3. G in C-heterochromatin variation in the karyotype reflects species level distinction between Erinaceus roumanicus and E. concolor (Eulipotyphla: Erinaceidae) in Turkey
FIGURE 3. G-banded karyotype of Erinaceus concolor (female from Konya in central Anatolia).
Figure 2 from: Piña Páez C, Healy RA, Guevara G, Orijel RG, Castellano MA, Cázares E, Trappe JM (2021) Greetings from belowground: two new species of truffles in the genus Pachyphlodes (Pezizaceae, Pezizales) from México. MycoKeys 82: 159-171. https://doi.org/10.3897/mycokeys.82.67685
Figure 2 Pachyphlodes brunnea (Holotype: ITCV 896) a ascoma dried b gleba in cross-section c peridium in cross-section, showing a wart composed of isodiametric cells d light microscopy of asci and spores e, fSEM microscopy of spores in surface view. Scale bars: 3 mm (a, b), 20 µm (c, d), 5 µm (e, f).
Figure 1 from: Piña Páez C, Healy RA, Guevara G, Orijel RG, Castellano MA, Cázares E, Trappe JM (2021) Greetings from belowground: two new species of truffles in the genus Pachyphlodes (Pezizaceae, Pezizales) from México. MycoKeys 82: 159-171. https://doi.org/10.3897/mycokeys.82.67685
Figure 1 The most likely tree generated from RAxML analysis of the ITS sequences of 18 Pachyphlodes species, rooted with Amylascus. Thickened branches denote >70% bootstrap support (left of slash) and >0.95 posterior probability (right of slash) from Bayesian analysis. New species are in shaded boxes, and Marronina clade demarcated. Terminals contain GenBank accession number, herbarium number, and country/state of collection. Asterisks denote sequences from holotypes.
Figure 3 from: Piña Páez C, Healy RA, Guevara G, Orijel RG, Castellano MA, Cázares E, Trappe JM (2021) Greetings from belowground: two new species of truffles in the genus Pachyphlodes (Pezizaceae, Pezizales) from México. MycoKeys 82: 159-171. https://doi.org/10.3897/mycokeys.82.67685
Figure 3 Pachyphlodes coalescens (Holotype: MEXU 26842) a ascoma fresh b gleba in cross-section c peridium in cross-section, showing a wart composed of isodiametric cells d light microscopy of asci and spores e, fSEM microscopy of spores in surface view. Scale bars: 5 mm (a, b), 100 µm (c), 10 µm (d, e), 5 µm (f).
Text-fig. 5. Fossils of some mammalian taxa from Gánovce-Hrádok Neanderthal site. a) Castor fiber – mandible dext. et sin. with incisors and p4 – m3 in lateral (mandible) and occlusal (cheek teeth) views (OF 6664–6665); b) Ursus ex gr. spelaeus – right mandible fragment with m1 – m3 in lateral view (P-unnumbered); c) Coelodonta antiquitatis – p2 sin. in buccal view (OF 7188); d) Equus sp. I (cf. taubachensis) – P3 – M3 dext. in travertine, buccal view (P-14302); e) Equus sp. II (cf. germanicus) – Mt sin. fragment in anterior view (OF unnumbered); f) Alces alces – left maxilla fragment with M1 – M3 in occlusal view (P-14303); g) Mammuthus primigenius – m2 sin. in occlusal view (P-14312); h) Palaeoloxodon antiquus – palate fragment with M3 dext. et sin. in occlusal view (P-14281). 50 mm scale is for a–c, 100 mm scale is for d–h. in Revised Floral And Faunal Assemblages From Late Pleistocene Deposits Of The Gánovce-Hrádok Neanderthal Site -Biostratigraphic And Palaeoecological Implications
Text-fig. 5. Fossils of some mammalian taxa from Gánovce-Hrádok Neanderthal site. a) Castor fiber – mandible dext. et sin. with incisors and p4 – m3 in lateral (mandible) and occlusal (cheek teeth) views (OF 6664–6665); b) Ursus ex gr. spelaeus – right mandible fragment with m1 – m3 in lateral view (P-unnumbered); c) Coelodonta antiquitatis – p2 sin. in buccal view (OF 7188); d) Equus sp. I (cf. taubachensis) – P3 – M3 dext. in travertine, buccal view (P-14302); e) Equus sp. II (cf. germanicus) – Mt sin. fragment in anterior view (OF unnumbered); f) Alces alces – left maxilla fragment with M1 – M3 in occlusal view (P-14303); g) Mammuthus primigenius – m2 sin. in occlusal view (P-14312); h) Palaeoloxodon antiquus – palate fragment with M3 dext. et sin. in occlusal view (P-14281). 50 mm scale is for a–c, 100 mm scale is for d–h.
FIGURE 131. Orchestina spp., male palps. A–C. O . cristinae. D–F. O. valquiria. G–I. O . platnicki. A, D, G. Prolateral. B, E, H. Dorsal. C, F, I in Taxonomic Revision Of The Jumping Goblin Spiders Of The Genus Orchestina Simon, 1882, In The Americas (Araneae: Oonopidae)
FIGURE 131. Orchestina spp., male palps. A–C. O . cristinae. D–F. O. valquiria. G–I. O . platnicki. A, D, G. Prolateral. B, E, H. Dorsal. C, F, I. Retrolateral. Scale bars: 0.2 mm. (PBI_OON 10935, 40482, 30270).
Figure 6. Acanthocyrtus lineatus Womersley. A, habitus. B, interocular setae. C, dorsal body chaetotaxy. D, hind claw. E, dental spines. F, mucro. G, I, body scales. H in Revision of Acanthocyrtus (Collembola: Entomobryidae), with description of a new genus from eastern Asia
Figure 6. Acanthocyrtus lineatus Womersley. A, habitus. B, interocular setae. C, dorsal body chaetotaxy. D, hind claw. E, dental spines. F, mucro. G, I, body scales. H, scales on dens. Scale bars: A and C = 0.5 mm; B, D–I = 25 Mm.
Figure 71. Steatoda bipunctata. A–F, male. A–C, palp. A, mesial. B, ventral. C, ectal. D–G, prosoma. D, profile. E in Morphological phylogeny of cobweb spiders and their relatives (Araneae, Araneoidea, Theridiidae)
Figure 71. Steatoda bipunctata. A–F, male. A–C, palp. A, mesial. B, ventral. C, ectal. D–G, prosoma. D, profile. E, details of setae; note raised bases (123-1). F, posterior tip with stridulatory ridges (128-1) in two clearly separate patches (129-0). G, female with inconspicuous stridulatory ridges. Scale bars: 100 Mm.
Figure 41. Coleosoma floridanum. A, B, male palp. A, ventral. B, ectal. C, chelicera. D, prolateral cheliceral teeth. E, abdominal SPR. F, prosomal stridulatory ridges. G in Morphological phylogeny of cobweb spiders and their relatives (Araneae, Araneoidea, Theridiidae)
Figure 41. Coleosoma floridanum. A, B, male palp. A, ventral. B, ectal. C, chelicera. D, prolateral cheliceral teeth. E, abdominal SPR. F, prosomal stridulatory ridges. G, epigynum. Scale bars: A, B, E–G, 50 Mm; C, 100 Mm; D, 20 Mm.
Figure 15. Metabus conacyt. A, female habitus. C, epigynum ventral view. C, caudal view. D, ventral view cleared. E, dorsal view cleared. F–G, male pedipalp. F, ectal view. G, ventral view. H, mesal view. Scale bars 0.2 in Systematics of the spider genus Metabus O. P.-Cambridge, 1899 (Araneoidea: Tetragnathidae) with additions to the tetragnathid fauna of Chile and comments on the phylogeny of Tetragnathidae
Figure 15. Metabus conacyt. A, female habitus. C, epigynum ventral view. C, caudal view. D, ventral view cleared. E, dorsal view cleared. F–G, male pedipalp. F, ectal view. G, ventral view. H, mesal view. Scale bars 0.2 mm, except in habitus 1 mm.
Figure 3 from: Deans A, Seltmann K, Yoder M, Miko I, Forshage M, Bertone M, Agosti D, Austin A, Balhoff J, Borowiec M, Brady S, Broad G, Brothers D, Burks R, Buffington M, Campbell H, Dew K, Ernst A, Fernandez-Triana J, Gates M, Gibson G, Jennings J, Johnson N, Karlsson D, Kawada R, Krogmann L, Kula R, Ohl M, Rasmussen C, Ronquist F, Schulmeister S, Sharkey M, Talamas E, Tucker E, Vilhelmsen L, Ward P, Wharton R (2012) A hymenopterists' guide to the Hymenoptera Anatomy Ontology: utility, clarification, and future directions. Journal of Hymenoptera Research 27: 67-88. https://doi.org/10.3897/jhr.27.2961
Figure 3 - The detailed breakdown report from an analyzer report. See Using the "analyzer" tool for explanation.
Figure 2 from: Deans A, Seltmann K, Yoder M, Miko I, Forshage M, Bertone M, Agosti D, Austin A, Balhoff J, Borowiec M, Brady S, Broad G, Brothers D, Burks R, Buffington M, Campbell H, Dew K, Ernst A, Fernandez-Triana J, Gates M, Gibson G, Jennings J, Johnson N, Karlsson D, Kawada R, Krogmann L, Kula R, Ohl M, Rasmussen C, Ronquist F, Schulmeister S, Sharkey M, Talamas E, Tucker E, Vilhelmsen L, Ward P, Wharton R (2012) A hymenopterists' guide to the Hymenoptera Anatomy Ontology: utility, clarification, and future directions. Journal of Hymenoptera Research 27: 67-88. https://doi.org/10.3897/jhr.27.2961
Figure 2 - Using and interpreting results from the analyzer. See Using the "analyzer" tool for explanation. A Help link B Input field C CAPTCHA test D Result table E Download link; and F Detailed breakdown link.
Figure 6 from: Barrantes G, Triana E, Shaw S, Jones G (2011) Characteristics of the cocoon and natural history of the gregarious Meteorus restionis sp. n. (Hymenoptera, Braconidae, Meteorinae) from Costa Rica. Journal of Hymenoptera Research 20: 9-21. https://doi.org/10.3897/jhr.29.867
Figure 6 - Details of the threads and resin-like clog. A A pair of relatively thick threads, possibly produced by a single larva, glued together B The threads consist of a large number of fibrils C Clog of a resin-like substance. Clogs bind together threads along the cable.
Figure 4 from: Barrantes G, Triana E, Shaw S, Jones G (2011) Characteristics of the cocoon and natural history of the gregarious Meteorus restionis sp. n. (Hymenoptera, Braconidae, Meteorinae) from Costa Rica. Journal of Hymenoptera Research 20: 9-21. https://doi.org/10.3897/jhr.29.867
Figure 4 - Cocoons attached by the posterior end to the cable. A A circle of relatively thick threads secure the cocoon to the cable B Cocoon attached to the cable.
Figure 1 from: Barrantes G, Triana E, Shaw S, Jones G (2011) Characteristics of the cocoon and natural history of the gregarious Meteorus restionis sp. n. (Hymenoptera, Braconidae, Meteorinae) from Costa Rica. Journal of Hymenoptera Research 20: 9-21. https://doi.org/10.3897/jhr.29.867
Figure 1 - Meteorus restionis sp. n., lateral view. A Detail of head and anterior mesosoma B Detail of mesosoma showing mesopleuron and sternaulus sculpture C Middle and hind coxa sculpture D Apex of antennal flagellum E Hind tarsal claw with basal lobe; part of ovipositor sheath on left.
Figure 3 from: Barrantes G, Triana E, Shaw S, Jones G (2011) Characteristics of the cocoon and natural history of the gregarious Meteorus restionis sp. n. (Hymenoptera, Braconidae, Meteorinae) from Costa Rica. Journal of Hymenoptera Research 20: 9-21. https://doi.org/10.3897/jhr.29.867
Figure 3 - Group and shape of cocoons of Meteorus restionis. A Distal section of a hanging cable showing 20 of the 49 cocoons in the group. Note the nearly perpendicular position of the cocoons relative to the cable B Individual cocoon; note the lack of the nipple-like anterior end typical in cocoons of other species C Detail of the anterior end showing its shape and the very fine cut produced for the wasp inside prior to its emergence.
Figure 5 from: Barrantes G, Triana E, Shaw S, Jones G (2011) Characteristics of the cocoon and natural history of the gregarious Meteorus restionis sp. n. (Hymenoptera, Braconidae, Meteorinae) from Costa Rica. Journal of Hymenoptera Research 20: 9-21. https://doi.org/10.3897/jhr.29.867
Figure 5 - Cap of the cocoon and pupating wasp. A The cap finely cut by the wasp hangs from a few threads to the rest of the cocoon. The bottom of the cap is covered by a soft yellowish pad B Position of the pupating wasp inside the cocoon; the top of the wasp's head rests on the pad.
Figure 3 from: Tepe E, Rodríguez-Castañeda G, Glassmire A, Dyer L (2014) Piper kelleyi, a hotspot of ecological interactions and a new species from Ecuador and Peru. PhytoKeys 34: 19-32. https://doi.org/10.3897/phytokeys.34.6376
Figure 3 - Distribution of Piper kelleyi. A Distribution of known localities based on collections (open diamonds) and study plots used to gather natural history data (blue circles) B Predicted distribution based on analysis of habitat parameters using the maximum entropy method. Areas in red are the most likely to have suitable habitat for Piper kelleyi (probability = 0.75–0.87), and areas in blue (0.02–0.08) or unlabeled (< 0.02) are the least likely.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.