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Fig. 8. Siphonodictyon mucosum Bergquist, 1965 in New Records and Range Extensions of Some Marine Sponges (Porifera: Demospongiae and Homoscleromorpha) from the Andaman Islands, India; Part of the Indo-Burma Biodiversity Hotspot.
Fig. 8. Siphonodictyon mucosum Bergquist, 1965. (A) Specimen after preservation. (B) Oxea. (C) Longitudinal section. (D) Longitudinal section. (E) Transverse section. (F) Transverse section.
Fig. 2 in New Records and Range Extensions of Some Marine Sponges (Porifera: Demospongiae and Homoscleromorpha) from the Andaman Islands, India; Part of the Indo-Burma Biodiversity Hotspot.
Fig. 2. Spheciospongia globularis (Dendy, 1922). (A) Specimen in situ. (B) Specimen after preservation. (C1) Large sized Tylostyles. (C2) Medium sized Tylostyles. (C3) Small sized Tylostyles. (C4) Spiraster. (D) Longitudinal section. (E) Longitudinal section. (F) Transverse section.
Fig. 14. Plakortis communis Muricy, 2011 in New Records and Range Extensions of Some Marine Sponges (Porifera: Demospongiae and Homoscleromorpha) from the Andaman Islands, India; Part of the Indo-Burma Biodiversity Hotspot.
Fig. 14. Plakortis communis Muricy, 2011. (A) Specimen after preservation. (B1) Diods. (B2) Y-shaped triods. (C) Longitudinal section. (D) Longitudinal section. (E) Transverse section. (F) Transverse section.
Fig. 12 in New Records and Range Extensions of Some Marine Sponges (Porifera: Demospongiae and Homoscleromorpha) from the Andaman Islands, India; Part of the Indo-Burma Biodiversity Hotspot.
Fig. 12. Axinyssa mertoni (Hentschel, 1912). (A) Specimen after preservation. (B) Close view of fistular structure. (C) Oxea. (D) Longitudinal section. (E) Longitudinal section. (F) Transverse section. (G) Transverse section.
Fig. 4 in New Records and Range Extensions of Some Marine Sponges (Porifera: Demospongiae and Homoscleromorpha) from the Andaman Islands, India; Part of the Indo-Burma Biodiversity Hotspot.
Fig. 4. Cliothosa aurivilli (Lindgren, 1897). (A) in situ specimen. (B) Papillar connection with the inside body mass of sponge. (C) Space inside the dead coral bored by the sponges. (D1) Thick Tyalostyles. (D2) Thin Tyalostyles. (D3) Amphiaster. (E) Longitudinal section. (F) Transverse section.
Fig. 4 in Lungworm seroprevalence in free-ranging harbour seals and molecular characterisation of marine mammal MSP
Fig. 4. Phylogenetic tree from maximum likelihood analysis of MSP nucleotide sequences of marine and terrestrial mammal parasitic nematodes including GenBank accession numbers. The percentage of replicate trees in which the associated species clustered together in the bootstrap test (1000 replicates) is shown next to the branches.
Fig. 5 in Lungworm seroprevalence in free-ranging harbour seals and molecular characterisation of marine mammal MSP
Fig. 5. Phylogenetic tree from maximum likelihood analysis of MSP amino acid sequences of marine and terrestrial mammal parasitic nematodes including GenBank accession numbers. The percentage of replicate trees in which the associated species clustered together in the bootstrap test (1000 replicates) is shown next to the branches. *amino acid sequence translated from EST sequences.
Fig. 3 in Lungworm seroprevalence in free-ranging harbour seals and molecular characterisation of marine mammal MSP
Fig. 3. Alignment of MSP amino acid sequences of marine and terrestrial mammal parasitic nematodes using the Clustal W method.
Fig. 2 in Lungworm seroprevalence in free-ranging harbour seals and molecular characterisation of marine mammal MSP
Fig. 2. Alignment of MSP nucleotide sequences of marine and terrestrial mammal parasitic nematodes using the Clustal W method.
Fig. 1 in Lungworm seroprevalence in free-ranging harbour seals and molecular characterisation of marine mammal MSP
Fig. 1. Anthelmintic treatment pattern, blood sampling time points and corresponding OD values of harbour seals in rehabilitation. Harbour seals (n = 6) were treated twice with ivermectin at arrival (day 1) at the Seal Rehabilitation and Research Centre, Pieterburen, The Netherlands, and 21 days later and once with mebendazole between day 2 and 6. OD values in grey boxes show lungworm-ELISA positive serum samples, those highlighted in blue lungworm-ELISA negative samples. Harbour seal individuals highlighted in dark grey coughed up lungworms one day after arrival. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fig. 2 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates
Fig. 2. Individual infection status by parasite by year. Strength and thickness of lines are scaled to the number of individuals that took a given infection trajectory from one year to the next. Two diagonal lines span 2012‾2014 because those individuals were not sampled in 2013. The + symbols represent every infection or non-infection found across all individuals in the study.
Fig. 3 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates
Fig. 3. Parasite species richness by species, age class and sex. Colors represent females (black) and males (gray).
Fig. 1 in Temporal and demographic blood parasite dynamics in two free-ranging neotropical primates
Fig. 1. Annual prevalence of single- and co-infections by species. Prevalence indicated for each parasite (dark gray), and each pairwise combination of parasites (light gray). Numbers near the top of each bar show the exact prevalence; black lines indicate 95% confidence intervals; dots indicate expected levels of co-infection (refer to Section 3.2). M-D is co-occurrence of M. mariae and Dipetalonema spp., D-T is Dipetalonema spp. and T. minasense, and M-T is M. mariae and T. minasense.
Fig. 1 in Gastrointestinal parasites in captive and free-ranging Cebus albifrons in the Western Amazon, Ecuador
Fig. 1. From left to right in each row: Hymenolepis sp., Capillaria sp., Strongyloides sp., Prosthenorchis elegans, Strongyle (unidentified), Entamoeba histolytica/dispar/moskovskii/ nuttalli. (40x).
Figs. 13–16 in Drasteria scolopax (Alphéraky, 1892) (Lepidoptera: Erebidae): New data on its range and ecology with description of a new subspecies
Figs. 13–16. Genitalia of Drasteria scolopax (Alphéraky, 1892): 13 — D. scolopax scolopax, lectotype, male, Gumansu; 14 — D. scolopax gilmanovi, paratype, male, Kaltabulak, 19.07.2023; 15 — D. scolopax scolopax, paralectotype, female, Gumansu; 16 — D. scolopax gilmanovi, holotype, female, Kaltabulak, 19.07.2023. Photos 14, 16 — by S. K. Korb, 13, 15 — by A. Yu. Matov Рис. 13–16. ГенитаΛии Drasteria scolopax (Alphéraky, 1892): 13 — D. scolopax scolopax, Λектотип, самец, Гумансу; 14 — D. scolopax gilmanovi, паратип, самец, КаΛтабуΛак, 19.07.2023; 15 — D. scolopax scolopax, параΛектотип, самка, Гумансу; 16 — D. scolopax gilmanovi, гоΛотип, самка, КаΛтабуΛак, 19.07.2023. Фото: 14, 16 — С. К. Корб, 13, 15 — А. Ю. Матов
Figs. 1–12 in Drasteria scolopax (Alphéraky, 1892) (Lepidoptera: Erebidae): New data on its range and ecology with description of a new subspecies
Figs. 1–12. Drasteria scolopax (Alphéraky, 1892), habitus: 1–2 — D. scolopax gilmanovi, holotype, female, Kaltabulak, 19.07.2023; 3–4 — D. scolopax gilmanovi, paratype, female, Kaltabulak, 19.07.2023; 5–6 — D. scolopax gilmanovi, paratype, male, Kaltabulak, 19.07.2023; 7–9 — D. scolopax scolopax, lectotype, male, Gumansu; 10 — D. scolopax scolopax, paralectotype, female, Gumansu; 11–12 — D. scolopax scolopax, males, Altyntag. Photos 1–6 — by S. K. Korb, 7–12 — by A. Yu. Matov Рис. 1–12. Drasteria scolopax (Alphéraky, 1892), габитус: 1–2 — D. scolopax gilmanovi, гоΛотип, самка, КаΛтабуΛак, 19.07.2023; 3–4 — D. scolopax gilmanovi, паратип, самка, КаΛтабуΛак, 19.07.2023; 5–6 — D. scolopax gilmanovi, паратип, самец, КаΛтабуΛак, 19.07.2023; 7–9 — D. scolopax scolopax, Λектотип, самец, Гумансу; 10 — D. scolopax scolopax, параΛектотип, самка, Гумансу; 11–12 — D. scolopax scolopax, самцы, АΛтынтаг. Фотографии 1–6 — С. К. Корб; 7–12 — А. Ю. Матов
Figs. 17–18 in Drasteria scolopax (Alphéraky, 1892) (Lepidoptera: Erebidae): New data on its range and ecology with description of a new subspecies
Figs. 17–18. Drasteria scolopax (Alphéraky, 1892), habitats: 17 — Transalai Mts., Kaltabulak stream; 18 — Alai Mts., Koksu River valley. Photos by P. Y. Gorbunov Рис. 17–18. Drasteria scolopax (Alphéraky, 1892), местообитания: 17 — ЗааΛайский хребет, ручей КаΛтабуΛак; 18 — АΛайский хребет, ΔоΛина реки Коксу. Фотографии П. Ю. Горбунова
Рис. 2. Некоторые преΑставитеΛи роΑа Calliteara (Lymantriidae) из Верхнебуреинского района Хабаровского края. Имаго, общий виΑ: A — C. axutha, самец, Буреинский хребет, 10 км Ю устья р. Серегекта, 27–28.06.2023; B — C. axutha, самка, там же, 3–4.07.2023; C — C. abietis, самец, р. Бурея, окоΛо устья р. Серегекта, 5–6.07.2023; D — C. abietis, самка, р. Бурея, Буреинский заповеΑник, корΑон «СтреΛка», 6–7.07.2023. ГенитаΛии самцов: E — C. axutha, F — C. abietis Fig. 2. Some Calliteara species (Lymantriidae) from Verkhnebureinsky district (Khabarovsk Kray). Adults, habitus: A — C. axutha, male, Bureinsky Range, 10 km S of the mouth of Seregekta River, 27–28 June 2023; B — C. axutha, female, at the same place, 3–4 July 2023; C — C. abietis, male, Bureya River, near the mouth of Seregekta River, 5–6 July 2023; D — C. abietis, female, Bureya River, Bureinsky Nature Reserve, ranger station 'Strelka', 6–7 July 2023. Male genitalia: E — C. axutha, F — C. abietis in Findings of Zaranga tukuringra Streltzov et Yakovlev, 2007, Calliteara axutha (Collenette, 1934) and other species of Macrolepidoptera in the northern part of the Bureinsky Range (Russia, Khabarovsk Krai)
Рис. 2. Некоторые преΑставитеΛи роΑа Calliteara (Lymantriidae) из Верхнебуреинского района Хабаровского края. Имаго, общий виΑ: A — C. axutha, самец, Буреинский хребет, 10 км Ю устья р. Серегекта, 27–28.06.2023; B — C. axutha, самка, там же, 3–4.07.2023; C — C. abietis, самец, р. Бурея, окоΛо устья р. Серегекта, 5–6.07.2023; D — C. abietis, самка, р. Бурея, Буреинский заповеΑник, корΑон «СтреΛка», 6–7.07.2023. ГенитаΛии самцов: E — C. axutha, F — C. abietis Fig. 2. Some Calliteara species (Lymantriidae) from Verkhnebureinsky district (Khabarovsk Kray). Adults, habitus: A — C. axutha, male, Bureinsky Range, 10 km S of the mouth of Seregekta River, 27–28 June 2023; B — C. axutha, female, at the same place, 3–4 July 2023; C — C. abietis, male, Bureya River, near the mouth of Seregekta River, 5–6 July 2023; D — C. abietis, female, Bureya River, Bureinsky Nature Reserve, ranger station 'Strelka', 6–7 July 2023. Male genitalia: E — C. axutha, F — C. abietis
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
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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.