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Fig. 2 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.
Fig. 2. Bruggmanniella turoguei sp. nov. (A) Male head (ventral view) (B) Male antenna (7–12 segment). (C) Female antenna (7–12 segment). (D) Male 1st tarsomere. (E) Male 5th tarsomere. (F) Female 5th tarsomere. (G) Male wing. (H) Female wing. Scale bars: A–C = 0.03 mm; D–F = 0.1 mm; G–H = 1 mm.
Fig. 1 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.
Fig. 1. Plant galls induced by Taiwanese Bruggmanniella species on Cinnamomum species. (A) Stem galls on C. insularimontanum. (B) Stem galls on C. subavenium. (C) Stem galls on C. osmophloeum. (D) Leaf galls on C. osmophloeum.
Fig. 4 in Molecular Phylogeny Revealing the Single Origin of -associated (Diptera: Cecidomyiidae) in Asia, with Descriptions of Three New and One Newly Recorded Species from Taiwan.
Fig. 4. Bruggmanniella sanlianensis sp. nov. (A) Male head (ventral view) (B) Male antenna (8–12 segment). (C) Female antenna (8–12 segment). (D) Male 1st tarsomere. (E) Male 5th tarsomere. (F) Female 5th tarsomere. (G) Male wing. (H) Female wing. Scale bars: A–C = 0.03 mm; D–F = 0.1 mm; G–H = 1 mm.
Fig. 1. A in Seasonality, richness and prevalence of intestinal parasites of three neotropical primates (Alouatta seniculus, Ateles hybridus and Cebus versicolor) in a fragmented forest in Colombia
Fig. 1. A. Trichuris sp., B. Oxyuridae, C. Ancylostomatidae, D. Strongyloides sp. (larva), E. Ascarididae, F. Gnathostomatidae, G. Trichostrongylidae, H-I. Trematodes, J. Entamoeba sp. (cyst), K. Acanthocephala, L. Balantidiidae.
Fig. 3 in New spatial records of three Odonata species from the Western Ghats, India (Coenagrionidae, Aeshnidae)
Fig. 3. Photograph of Pseudagrion spencei Fraser, 1922 taken at Satara, Maharashtra, India Рис. 3. Pseudagrion spencei Fraser, 1922, Сатаре, Махараштра, ИнΑия
Fig. 2 in New spatial records of three Odonata species from the Western Ghats, India (Coenagrionidae, Aeshnidae)
Fig. 2. Map showing the locality records of A. keralensis (AK), P. spencei (PS) and G. khasiaca (GK) in the Western Ghats, India Рис. 2. Карта с указанием местонахожΑений A. keralensis (AK), P. spencei (PS) и G. khasiaca (GK) в ЗапаΑных Гатах, ИнΑия
Рис. 2. ΔоΛговременная Αинамика весенней чисΛенности трех виΑов уток (A — трескунка; B — касатки; C — шиΛохвости) на ΑебеΑинском стационаре Хинганского заповеΑника (показаны уровень значимости и 95-процентный ΑоверитеΛьный интерваΛ) Fig. 2. Long-term spring number dynamics of three duck species at the Lebedinsky Station of Khingansky State Nature Reserve with p-values and 0.95 confidence intervals. A — Gargany; B — Falcated Duck; C — Pintail in The results of long-term observation of waterfowl spring migration in Khingan Nature Reserve, Eastern Russia
Рис. 2. ΔоΛговременная Αинамика весенней чисΛенности трех виΑов уток (A — трескунка; B — касатки; C — шиΛохвости) на ΑебеΑинском стационаре Хинганского заповеΑника (показаны уровень значимости и 95-процентный ΑоверитеΛьный интерваΛ) Fig. 2. Long-term spring number dynamics of three duck species at the Lebedinsky Station of Khingansky State Nature Reserve with p-values and 0.95 confidence intervals. A — Gargany; B — Falcated Duck; C — Pintail
Fig. 1 in Three species of Echinococcus granulosus sensu lato infect camels on the Arabian Peninsula
Fig. 1 Sequence alignment of the 9 haplotypes. Substitutions were indicated with their nucleotide code, deletions were marked by (-), and dots (.) indicate identical nucleotide at the specified position in comparison with the reference sequence AF297617 (Lee et al. 2002). *nucleotides substitution positions, based on the start of the complete cox1 gene, read vertically
Fig. 2 Phylogenetic tree showing the relation between the Saudi Arabian haplotypes with 65 in Three species of Echinococcus granulosus sensu lato infect camels on the Arabian Peninsula
Fig. 2 Phylogenetic tree showing the relation between the Saudi Arabian haplotypes with 65 reference sequences. The Saudi Arabian haplotypes (H01-09) are in bold. The reference sequences along with their accession numbers and origin of isolate were included for each. T. solium was used as an outgroup taxon. The branch to outgroup was shortened by 0.2 substitutions per site
Fig. 4 in Ticks on the move-climate change-induced range shifts of three tick species in Europe: current and future habitat suitability for Ixodes ricinus in comparison with Dermacentor reticulatus and Dermacentor marginatus
Fig. 4 Area projected as suitable or unsutable under current and future (2081–2100) climatic conditions (km2) for the three tick species in comparison. a Ixodes ricinus. b Dermacentor reticulatus. c D. marginatus. The corresponding maps are shown in Figs. 1–3 in the main document. Future suitable conditions refers to the area (km2) projected as unsuitable under current climatic conditions but suitable under future climatic conditions (i.e., potential new range). Continuing suitable conditions refers to area (km2) projected as suitable under current climatic conditions as well as under future climatic conditions (i.e., stable presence). Continuing unsuitable conditions refers to area (km 2) projected as unsuitable under current climatic conditions as well as under future climatic conditions (i.e. stable absence). Future unsuitable conditions refers to the area (km.2) projected as suitable under current climatic conditions but unsuitable under future climatic conditions (i.e., potential extinction)
Fig. 2 Projected future changes for Dermacentor reticulatus until 2080–2100. a SSP 126. b SSP 245. c SSP 370. d SSP 585 in Ticks on the move-climate change-induced range shifts of three tick species in Europe: current and future habitat suitability for Ixodes ricinus in comparison with Dermacentor reticulatus and Dermacentor marginatus
Fig. 2 Projected future changes for Dermacentor reticulatus until 2080–2100. a SSP 126. b SSP 245. c SSP 370. d SSP 585. In dark blue: area projected as suitable under current climatic conditions but unsuitable under future climatic conditions (i.e., potential extinction). In light blue: area projected as unsuitable under current climatic conditions as well as under future climatic conditions (i.e., stable absence). In orange: area projected as suitable under current climatic conditions as well as under future climatic conditions (i.e., stable range). In red: area projected as unsuitable under current climatic conditions but suitable under future climatic conditions (i.e., potential new range). AUC = 0.8333 (average over 10 replicates using cross-validation, standard deviation = 0.001113603). Threshold to transform the logistic model output: 0.3816 (10% omission rate threshold). Maps were built using ESRI ArcGIS (Release 10.7, www.esri.com). Projection: Europe Albers Equal Area Conic
Fig. 2 Projected future changes for Dermacentor reticulatus until 2080–2100. a SSP 126. b SSP 245. c SSP 370. d SSP 585 in Ticks on the move-climate change-induced range shifts of three tick species in Europe: current and future habitat suitability for Ixodes ricinus in comparison with Dermacentor reticulatus and Dermacentor marginatus
Fig. 2 Projected future changes for Dermacentor reticulatus until 2080–2100. a SSP 126. b SSP 245. c SSP 370. d SSP 585. In dark blue: area projected as suitable under current climatic conditions but unsuitable under future climatic conditions (i.e., potential extinction). In light blue: area projected as unsuitable under current climatic conditions as well as under future climatic conditions (i.e., stable absence). In orange: area projected as suitable under current climatic conditions as well as under future climatic conditions (i.e., stable
Fig. 4 in Ticks on the move-climate change-induced range shifts of three tick species in Europe: current and future habitat suitability for Ixodes ricinus in comparison with Dermacentor reticulatus and Dermacentor marginatus
Fig. 4 Area projected as suitable or unsutable under current and future (2081–2100) climatic conditions (km2) for the three tick species in comparison. a Ixodes ricinus. b Dermacentor reticulatus. c D. marginatus. The corresponding maps are shown in Figs. 1–3 in the main document. Future suitable conditions refers to the area (km2) projected as unsuitable under current climatic conditions but suitable under future climatic conditions (i.e., potential new range). Continuing suitable conditions refers to area (km2) projected as suitable under
Fig. 1 Projected future changes for Ixodes ricinus until 2081–2100. a SSP 126. b SSP 245. c SSP 370. d SSP 585 in Ticks on the move-climate change-induced range shifts of three tick species in Europe: current and future habitat suitability for Ixodes ricinus in comparison with Dermacentor reticulatus and Dermacentor marginatus
Fig. 1 Projected future changes for Ixodes ricinus until 2081–2100. a SSP 126. b SSP 245. c SSP 370. d SSP 585. In dark blue: area projected as suitable under current climatic conditions but unsuitable under future climatic conditions (i.e., potential extinction). In light blue: area projected as unsuitable under current climatic conditions as well as under future climatic conditions (i.e., stable absence). In orange: area projected as suitable under current climatic conditions as well as under future climatic conditions (i.e., stable range). In red:
Fig. 5 in Ticks on the move-climate change-induced range shifts of three tick species in Europe: current and future habitat suitability for Ixodes ricinus in comparison with Dermacentor reticulatus and Dermacentor marginatus
Fig. 5 Potential co-occurrence under current and future climatic conditions. a Under near current climatic conditions (1970–2000). b Under projected future climatic conditions (exemplarily for SSP 245) for the period 2041–2060. c Under projected future climatic conditions (SSP 245) for the period 2081–2100. Colors indicate areas where climatic suitability is projected for the respective species; for non-mentioned species ("none of them"), the area is climatically unsuitable according to the modelling results. The thresholds to transform the logistic model output (10% omission rate threshold) are as follows: 0.3368 for Ixodes ricinus, 0.3816 for Dermacentor reticulatus, and 0.4298 for D. marginatus. Maps were built using ESRI Arc-GIS (Release 10.7, www.esri.com). Projection: Europe Albers Equal Area Conic. (A hatch-based version of this figure is additionally provided in the Supplementary Material: Figure S11.)
Fig. 3 Projected future changes for Dermacentor marginatus until 2080–2100. a SSP 126. b SSP 245. c SSP 370. d SSP 585 in Ticks on the move-climate change-induced range shifts of three tick species in Europe: current and future habitat suitability for Ixodes ricinus in comparison with Dermacentor reticulatus and Dermacentor marginatus
Fig. 3 Projected future changes for Dermacentor marginatus until 2080–2100. a SSP 126. b SSP 245. c SSP 370. d SSP 585. In dark blue: area projected as suitable under current climatic conditions but unsuitable under future climatic conditions (i.e., potential extinction). In light blue: area projected as unsuitable under current climatic conditions as well as under future climatic conditions (i.e., stable absence). In orange: area projected as suitable under current climatic conditions as well as under future climatic conditions (i.e., stable range). In red: area projected as unsuitable under current climatic conditions but suitable under future climatic conditions (i.e., potential new range). AUC = 0.8229 (average over 10 replicates using cross-validation, standard deviation = 0.001121953). Threshold to transform the logistic model output: 0.4298 (10% omission rate threshold). Maps were built using ESRI ArcGIS (Release 10.7, www.esri.com). Projection: Europe Albers Equal Area Conic
Fig. 8 in New record of three oxytrichid ciliates (Ciliophora: Oxytrichidae) from South Korea
Fig. 8. Maximum likelihood (ML) phylogenetic tree inferred from 18S rDNA sequences of Oxytrichidae ciliates. The phylogenetic trees show the position of three soil ciliates of Oxytricha lithofera (arrow), Pleurotricha curdsi (arrowhead) and Sterkiella tetracirrata (double-arrowhead). New sequences are shown in bold text. Numbers at nodes indicate the bootstrap values of ML and the posterior probability of BI. Nodes designated by an asterisk (*) correspond to the supports not recovered in the estimated BI tree. The scale bar corresponds to two substitutions per 100 nucleotide positions.
Fig. 7 in New record of three oxytrichid ciliates (Ciliophora: Oxytrichidae) from South Korea
Fig. 7. Morphology of Sterkiella tetracirrata from live (A-D) and protargol-impregnated (E, F) specimens. A, B, Ventral view of typical specimen live arrow denotes contractile vacuole (arrow); C, Ventral view of typical specimen; D, Ventral view showing macronuclear nodules (arrow) and micronuclei (arrowhead); E, F, Ventral and dorsal view of typical specimen; Scale bars: 50 μm (C, E, F).
Fig. 6 in New record of three oxytrichid ciliates (Ciliophora: Oxytrichidae) from South Korea
Fig. 6. Morphology of Sterkiella tetracirrata from live (A) and protargol-impregnated (B, C) specimens. A, Ventral view of typical specimen; B, C, Ventral and dorsal view of typical specimen; AZM, adoral zone of membranelles; BC, buccal cirri; CC, caudal cirri; DM, dorsomarginal row; E, endoral membrane; FC, frontal cirri; LMR, left marginal cirral row; PTC, pretransverse cirri; RMR, right marginal cirral row; TC, transverse cirri; 1-4, dorsal kineties 1-4; Scale bars: 50 μm (A-C).
Fig. 5 in New record of three oxytrichid ciliates (Ciliophora: Oxytrichidae) from South Korea
Fig. 5. Morphology of Pleurotricha curdsi from protargol-impregnated (A-D) specimens. A, B, Ventral and dorsal view of typical specimen; C, Ventral view showing macronuclear nodules (arrow) and micronuclei (arrowhead); D, Ventral view of posterior end; AZM, adoral zone of membranelles; E, endoral membrane; FC, frontal cirri; LMR, left marginal cirral row; P, paroral membrane; PTC, pretransverse cirri; RMR, right marginal cirral row; TC, transverse cirri; Scale bars: 50 μm (A), 10 μm (C).
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.