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Fig. 3 in Wide geographic distribution of overlooked parasites: Rare Microsporidia in Gammarus balcanicus, a species complex with a high rate of endemism
Fig. 3. Geographic distribution of the main rare Microsporidia infecting Gammarus balcanicus, showing their occurrence in other gammarid species over Europe. Each map (A–H) refers to the parasite taxa presented in the bottom-right inset. The host and geographic range of the Microsporidia based on this study and 1) literature data: Terry et al. (2004); Wattier et al. (2007); Krebes et al. (2010); Ovcharenko et al. (2010); Bacela-Spychalska et al. (2012); Rode et al. (2013); Grabner et al., 2014; 2015; 2017; Bojko et al. (2015); 2017; 2018; Weigand et al. (2016); Quiles et al. (2019); 2) Gen Bank sequences: MT645708 (Chen,Y. and Jiang, H. direct submission); KP699690 (Bacela-Spychalska, K. direct submission) and 3) Bacela and Ovcharenko, unpublished data.
Figs 15-22 in A new species of rake-legged mite Neocaeculus (Acari, Caeculidae) from Brazilian semiarid and new data on distribution of Andocaeculus caioi
Figs 15-22. Neocaeculus setecidades sp. nov.: 15, 17, 19, 21, trochanter, basifemur, femur and genu, respectively Legs I, II, III, IV, dorso-prolateral view; 16, 18, 20, 22, tibia and tarsus, respectively Legs I, II, III, IV, prolateral view (bt, tarsal bothridium; sol, solenidion; ts, tarsal solenidion). Scale bar: 250 μm. Dotted circles indicate solenidia and eupathidia at retrolateral positions.
Fig. 2 in The importance of considering small-scale variability in macrobenthic distribution: spatial segregation between two fiddler crab species (genus Leptuca) (Decapoda, Ocypodidae)
Fig. 2. NMDS ordination (stress = 0.16) of sites based on similarity of group composition. Leptuca leptodactyla (Rathbun in Rankin, 1898): JLM (juvenile males), JLF (juvenile females), ALM (adult males) and ALF (adult females). Leptuca uruguayensis (Nobili, 1901): JUM (juvenile males), JUF (juvenile females), AUM (adult males) and AUF (adult females).
Figs 1-5 in A new species of rake-legged mite Neocaeculus (Acari, Caeculidae) from Brazilian semiarid and new data on distribution of Andocaeculus caioi
Figs 1-5. Neocaeculus setecidades sp. nov., paratype ♀: 1, dorsal view; 2, ventral view; 3, lateral view; 4, anterior portion of aspidosomal sclerite, dorsal view; 5, tarsi of legs I, dorso-anterior view. Scales bars: 1, 2, 3, 1000 μm; 4, 250 μm; 5, 100 μm
Figs 39-42 in A new species of rake-legged mite Neocaeculus (Acari, Caeculidae) from Brazilian semiarid and new data on distribution of Andocaeculus caioi
Figs 39-42. Neocaeculus setecidades sp. nov. habitats in the Parque Nacional Sete Cidades, Piracuruca, Piauí, Brazil. 39, 40, grasslands; 41, 42, dry semideciduous Forest.
Figs 31-38 in A new species of rake-legged mite Neocaeculus (Acari, Caeculidae) from Brazilian semiarid and new data on distribution of Andocaeculus caioi
Figs 31-38. Neocaeculus setecidades sp. nov., paratype ♂, scanning electron microscope images: 31, 32, Leg II; 33-36, Leg III; 37, 38, Leg IV. Fig. 31, tarsus, dorso-prolateral view; 32, tibial solenidion, dorso-retrolateral view; 33, tarsus, retrolateral view (arrow: tarsal bothridium); 34, tarsal bothridium, dorso-retrolateral view; 35, tibial solenidion, retrolateral view; 36, tarsal claws, retrolatertal view (arrow: foliar seta); 37, tarsus, retrolateral view (arrow: tarsal bothridium); 38, tarsal bothridium base, dorso-retrolateral view. Scale bars: 31, 50 μm; 32, 34, 36, 38, 10 μm; 33, 37, 100 μm; 35, 5 μm.
Figs 6-9 in A new species of rake-legged mite Neocaeculus (Acari, Caeculidae) from Brazilian semiarid and new data on distribution of Andocaeculus caioi
Figs 6-9. Neocaeculus setecidades sp. nov., holotype ♂, cleared: 6, 8, dorsal view; 7, 9, ventral view. Scale bars: 500 μm.
Fig. 1 in The importance of considering small-scale variability in macrobenthic distribution: spatial segregation between two fiddler crab species (genus Leptuca) (Decapoda, Ocypodidae)
Fig. 1. Schematic representation of the sampling design, with subarea separation and the six random replicates. (Area=10 m²).
Figs 23-30 in A new species of rake-legged mite Neocaeculus (Acari, Caeculidae) from Brazilian semiarid and new data on distribution of Andocaeculus caioi
Figs 23-30. Neocaeculus setecidades sp. nov., paratype ♂, scanning electron microscope images, Leg I: 23, tarsus, dorso-retrolateral view; 24, tarsal claws, dorsal view (arrows: foliar setae); 25, same, retrolateral view (arrow: foliar seta); 26, tarsal distal eupathidium, ventral view; 27, tarsal medial eupathidium elevated base, lateral view (arrow: eupathidium); 28, tibial solenidion, retrolateral view; 29, tarsus, prolateral view (arrow: tarsal solenidion); 30, same, solenidion detail. Scale bars: 23, 100 μm; 24, 25, 27, 28, 30, 10 μm; 26, 5 μm; 29, 50 μm.
Figs 10-14 in A new species of rake-legged mite Neocaeculus (Acari, Caeculidae) from Brazilian semiarid and new data on distribution of Andocaeculus caioi
Figs 10-14. Neocaeculus setecidades sp. nov., holotype ♂: 10, anterior portion of tarsus of leg I, prolateral view; 11, anterior portion of aspidosomal sclerite, dorsal view; 12, palp, dorsal view; 13, palp, ventral view; 14, internal genital sclerite, ventral view (bo, bothridium; eu, eupathidium; fs, foliar seta; Po, naso seta; sol, solenidion; ts, tarsal solenidion). Scale bars: 10, 12, 13, 50 μm; 11, 250 μm; 14, 100 μm.
Fig.2 in Distribution, feeding and ecomorphology of four species of Auchenipteridae (Teleostei: Siluriformes) in Eastern Amazonia, Brazil
Fig.2. Ordination diagram of the first two PCA axes for the 15 ecomorphological attributes of four auchenipterid species: (●) Auchenipterichthys longimanus (Günther, 1864), (■) Auchenipterus nuchalis (Spix & Agassiz, 1829), (○) Tatia intermedia (Steindachner, 1877) and (□) Trachelyopterus galeatus (Linnaeus, 1766). The attributes that most influenced this distribution are shown: RMW, relative mouth width; RHL, relative head length; ARPF, aspect ratio of the pectoral fin; RHM, relative height of mouth.
Fig. 1 in Distribution, feeding and ecomorphology of four species of Auchenipteridae (Teleostei: Siluriformes) in Eastern Amazonia, Brazil
Fig. 1. Location of the Caxiuanã National Forest, municipalities of Melgaço and Portel, State of Pará, showing the ichthYofauna sampling sites.
Рис. 1–2. ВиΔы роΔа Coprophilus Latreille, 1829. 1 – C. (Zonyptilus) pseudopiceus Gildenkov, 2015, самец, гоΛотип; 2 – C. (Zonyptilus) schubertii (Motschulsky, 1860), самец (Россия, ВоΛгограΔская обΛасть). Figs 1–2. Species of the genus Coprophilus Latreille, 1829. 1 – C. (Zonyptilus) pseudopiceus Gildenkov, 2015, male, holotype; 2 – C. (Zonyptilus) schubertii (Motschulsky, 1860), male (Russia, Volgograd Region). in New data on distribution of Coprophilus Latreille, 1829 (Coleoptera: Staphylinidae: Oxytelinae) in the south of European part of Russia, in the Caucasus and Turkey
Рис. 1–2. ВиΔы роΔа Coprophilus Latreille, 1829. 1 – C. (Zonyptilus) pseudopiceus Gildenkov, 2015, самец, гоΛотип; 2 – C. (Zonyptilus) schubertii (Motschulsky, 1860), самец (Россия, ВоΛгограΔская обΛасть). Figs 1–2. Species of the genus Coprophilus Latreille, 1829. 1 – C. (Zonyptilus) pseudopiceus Gildenkov, 2015, male, holotype; 2 – C. (Zonyptilus) schubertii (Motschulsky, 1860), male (Russia, Volgograd Region).
Fig. 1. Medauromorpha gen. nov. spp., distribution maps. A, M in The new stick insect genus Medauromorpha gen. nov. with one new species from Vietnam and notes on Medauroidea Zompro, 2000 (Phasmida: Phasmatidae: Clitumninae)
Fig. 1. Medauromorpha gen. nov. spp., distribution maps. A, M. baviensis sp. nov. and M. regina (Brunner von Wattenwyl, 1907) comb. nov. B, M. foedata (Brunner von Wattenwyl, 1907) comb. nov.
Fig. 10 in Patterns of spatio-temporal distribution as criteria for the separation of planktic foraminiferal species across the Danian-Selandian transition in Spain
Fig. 10. Lower/higher (L/H) latitude taxa ratio and quantitative stratigraphic distribution of planktic foraminiferal genera across the Danian–Selandian transition at Caravaca. Asterisks indicate climate warming events identified here.
Fig. 9 in Patterns of spatio-temporal distribution as criteria for the separation of planktic foraminiferal species across the Danian-Selandian transition in Spain
Fig. 9. Cluster analyses based on Morisita's index for relative abundance data of species from Caravaca in the Acarinina uncinata Zone (4a) and in the Morozovella cf. albeari Zone (4b); l1 = Simpson's diversity index in sample j; l2 = Simpson's diversity index in sample k; xij = percentage of species i in sample j; xik = percentage of species i in sample k.
Fig. 2 in Patterns of spatio-temporal distribution as criteria for the separation of planktic foraminiferal species across the Danian-Selandian transition in Spain
Fig. 2. Comparison of some planktic foraminiferal zonations proposed for the D–S transition in low and middle latitudes. Correlation with the chronostratigraphic and magnetostratigraphic scales based on data from the Zumaia stratotype. (*) Probable biostratigraphic position of the base of the Igorina pusilla Zone by Toumarkine and Luterbacher (1985), and Canudo and Molina (1992), based on data from Zumaia. (**) Biostratigraphic position of the P3a/P3b boundary by Berggren and Pearson (2005), assuming that their species concept of I. albeari includes Morozovella crosswicksensis by Blow (1979) and Arenillas and Molina (1997) and/or M. cf. albeari by Arenillas et al. (2008). FOD, first occurrence data; L/H, lower/higher latitude, LOD, last occurence data.
Fig. 3 in Patterns of spatio-temporal distribution as criteria for the separation of planktic foraminiferal species across the Danian-Selandian transition in Spain
Fig. 3. Quantitative stratigraphic distribution of planktic foraminiferal species across the Danian–Selandian transition at Caravaca. The shown stratigraphic interval does not include the lower part of the A. uncinata Zone, where Globoconusa species were found (see Arenillas and Molina 1997).
Fig. 1 in From wildlife to humans: The global distribution of Trichinella species and genotypes in wildlife and wildlife-associated human trichinellosis
Fig. 1. Sylvatic life cycle and potential transmission routes of Trichinella spp. Created with BioRender.com.
Fig. 3 in From wildlife to humans: The global distribution of Trichinella species and genotypes in wildlife and wildlife-associated human trichinellosis
Fig. 3. Global distribution of sylvatic Trichinella species and genotypes adapted from Pozio (2016); Gottstein et al. (2009).
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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.