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Fig. 1 in Parasitic development in intestines and oocyst shedding patterns for infection by Eimeria uekii and Eimeria raichoi in Japanese rock ptarmigans, Lagopus muta japonica, protected by cages in the Southern Japanese Alps
Fig. 1. Shelter used for cage protection of Japanese rock ptarmigan broods on Mt. Kita (35̊40′N, 138̊14′E), Japan in 2019.
Fig. 1 in Temporal dynamics of species associations in the parasite community of European eels, Anguilla anguilla, from a coastal lagoon
Fig. 1. Abundance (mean number of parasites per host, including non-infected hosts) of the six most common helminth parasites of eels, Anguilla anguilla, in Comacchio Lagoons, during three sampling periods: 2005–2006 (N = 140 eels), 2010–2013 (N = 131), and 2015–2017 (N = 30). Note that some values for the time period 2015–2017 are based on very few fish; see Table 1 for actual numbers and for full species names.
Fig. 2 in Impacts of ontogenetic dietary shifts on the food-transmitted intestinal parasite communities of two lake salmonids
Fig. 2. Correlation between the mean number of parasite taxa and mean length among the different size classes of Arctic charr and brown trout with a 95% confidence interval.
Fig. 1 in Impacts of ontogenetic dietary shifts on the food-transmitted intestinal parasite communities of two lake salmonids
Fig. 1. Frequency of occurrence of prey categories in the diet of a) Arctic charr and b) brown trout throughout their ontogenesis. Prey categories not related to intestinal parasite transmission are excluded.
Fig. 1 in Apparent lack of spill-over of parasites from an invasive anuran: PCR detects Entamoeba in cane toads (Rhinella marina) but not in sympatric Australian native frogs
Fig. 1. Study site location in Australia's Northern Territory (left). Map showing the Research Station where the initial amoebiasis outbreak was observed (Shilton et al., 2018); and sample collection sites Leaning Tree Lagoon and Caravan Park (right). In 2018, cane toads and native frogs were collected at Leaning Tree Lagoon. In 2020, cane toads were collected at the Caravan Park and road-killed native frogs were collected from the highway between the Research Station and Leaning Tree Lagoon. Left-hand panel image from GoogleMaps.
Fig. 4 in Impacts of ontogenetic dietary shifts on the food-transmitted intestinal parasite communities of two lake salmonids
Fig. 4. Nonmetric multidimensional scaling (NMDS) plot on Bray-Curtis distances of a) Arctic charr and b) brown trout showing dissimilarity in parasite community composition between different size classes including 95% confidence intervals ellipses. NMDS converged on a three-dimensional solution with an acceptable stress level.
Fig. 7 in Impacts of ontogenetic dietary shifts on the food-transmitted intestinal parasite communities of two lake salmonids
Fig. 7. Canonical correspondence analysis (CCA) performed on parasite abundances as a function of presence-absence of prey types and fish length in a) Arctic charr and b) brown trout (Cre. = Crepidostomum spp., Cya. = Cyatocephalus truncatus, Eub.s. = Eubothrium salvelini, Eub.c. = Eubothrium crassum, Pro. = Proteocephalus sp., Dib. = Dibothriocephalus spp.).
Fig. 7 in Mammal parasites in arid Australia
Fig. 7. Distributions of selected endemic species of hydromyine rodents in Australia for which published helminthological studies are available. A, Distributions of the grassland melomys, Melomys burtoni, the fawn-footed melomys, M. cervinipes and the white-tailed rat, Uromys caudimaculatus; B, Distributions of the delicate mouse, Pseudomys delicatulus and the sandy inland mouse, P. hermansburgensis; C, Distributions of the eastern chestnut mouse, P. gracilicaudatus and the desert mouse, P. desertor.
Fig. 5 in Mammal parasites in arid Australia
Fig. 5. Geographical distributions of the closely related strongylid nematode species Rugopharynx australis and R. macropodis. Records based on Beveridge and Chilton (1999) and voucher specimens deposited in the South Australian Museum, Adelaide. Rugopharynx australis (represented by closed circles) occurs in the stomachs of Macropus fuliginosus, M. giganteus, Osphranter rufus and O. robustus; R. macropodis (represented by open squares) occurs in the stomachs of M. fuliginosus and M. giganteus.
Fig. 3 in Mammal parasites in arid Australia
Fig. 3. Geographical distributions of the arid adapted kangaroos, the red kangaroo (Osphranter rufus) (A) and the euro (Macropus robustus erubescens) (B) with its related sub-species, the eastern wallaroo (M. r. robustus) and the northern wallaroo (M. r. woodwardi), occurring in higher rainfall areas to the east and north of the arid zone respectively. Named localities are sites at which epidemiological studies of the parasites of these kangaroo species have been undertaken.
Fig. 2 in Mammal parasites in arid Australia
Fig. 2. Geographical distributions of the rain-forest adapted pademelons (Thylogale spp.: Macropodidae) (A) and the grey kangaroos (Macropus fuliginosus and M. giganteus (Macropodidae) (B), with ranges of the latter two species extending into the semi-arid and arid ranges of the continent. Named localities are sites at which epidemiological studies of the parasites of these kangaroo species have been undertaken.
Fig. 7 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations
Fig. 7. Distribution of the records of parasitic arthropods in relation to host species and their distribution in the sub-regions of the Antarctic region. Legend: AAP = Antarctic Peninsula (including South Shetland Islands and Palmer Archipelago), AWS = Antarctica Weddell Sea sector, AAT = Antarctica Atlantic Ocean sector (including Bouvet Island), AIW = Antarctica Indian Ocean West sector, AIE = Antarctica Indian Ocean East sector, ARS = Antarctica Ross Sea sector (including Scott and Balleny Islands), APW = Antarctica Pacific Ocean West sector, APE = Antarctica Pacific Ocean East sector (including Peter I Island), SOI = South Orkney Island, SGI = South Georgia Island, SSI = South Sandwich Islands, PEI = Prince Edward Islands, CRI = Crozet Islands, KEI = Kerguelen Islands, HMI = Heard and McDonald Islands.
Fig. 3 in Digenean parasites of deep-sea teleosts: A progress report
Fig. 3. Depth ranges of five digeneans of Coryphaenoides armatus in the NE Atlantic (adapted from Bray et al., 1999). Shaded portion shows depth range of the host, 282–5180 m, according to Froese and Pauly (2019).
Fig. 5 in Impacts of ontogenetic dietary shifts on the food-transmitted intestinal parasite communities of two lake salmonids
Fig. 5. Differences in parasite community composition between Arctic charr and brown trout using nonmetric multidimensional scaling (NMDS) plot on Bray-Curtis distances, including 95% confidence interval ellipses. NMDS converged on a three-dimensional solution with an acceptable stress level.
Fig. 2 in Apparent lack of spill-over of parasites from an invasive anuran: PCR detects Entamoeba in cane toads (Rhinella marina) but not in sympatric Australian native frogs
Fig. 2. Six of the amphibian species surveyed for Entamoeba in this study. a) Cyclorana australis, b) Litoria bicolor, c) Litoria dahlii, d) Litoria nasuta, e) Litoria rothii and f) Rhinella marina.
Fig. 3 in Impacts of ontogenetic dietary shifts on the food-transmitted intestinal parasite communities of two lake salmonids
Fig. 3. Prevalence of intestinal parasites in Arctic charr (black) and brown trout (grey) throughout their ontogenesis with 95% confidence intervals.
Fig. 4 in Mammal parasites in arid Australia
Fig. 4. Geographical distributions of species of rock wallaby (Petrogale) (Macropodidae) in eastern Australia, comparing that of the rain-forest inhabiting P. persephone, with the closely related members of the P. penicillata species complex (P. assimilis, P. inornata, P. godmani, P. mareeba, P. penicillata, P. sharmani) occurring in a parapatric pattern along the east coast, and P. purpureicollis, the most arid-adapted species.
Fig. 6 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations
Fig. 6. Distribution of host species and host-parasite-location records in the Antarctic region, excluding stragglers and contaminants. Legend: (A) avian hosts, (B) pinniped hosts, (C) chewing lice, (D) sucking lice, (E) fleas, (F) ticks, (G) nasal mites, (H) feather mites.
Fig. 4 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations
Fig. 4. Genera of fleas (Ceratophyllidae – 1, Pygiopsyllidae – 2, Rhopalopsyllidae – 3), pentastomes (Reighardiidae – 4), hard ticks (Ixodidae – 5), parasitic mites (Laelapidae – 6, Halarachnidae – 7, Rhinonyssidae – 8) and feather mites (Alloptidae – 9, Avenzoariidae – 10, Freyanidae – 11, Xolalgidae – 12) recorded infesting Antarctic birds and mammals.
Fig. 5 in Arthropod parasites of Antarctic and Subantarctic birds and pinnipeds: A review of host-parasite associations
Fig. 5. Network representation and mean and standard deviation of degrees and betweenness centrality of the host-parasite associations by host families (A) and parasite families (B), excluding stragglers and contaminants. Degrees (number of connections of a given node) may be interpreted as a measure of the host breadth of a given parasite species or the parasite diversity of a given host species; node size is drawn proportional to the number of degrees. Betweenness centrality (proportion of shortest paths between nodes that pass through a given node) may be interpreted as a measure of the potential influence a species has over the spread of vectorborne pathogens through the network.
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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.