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87 results for “Canis lupus”

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zenodo44/100

Dataset for the Diet of the grey wolf Canis lupus in Roztocze and Solska Forest, south-east Poland

<p>The dataset for the article: Mysłajek R.W., Stachyra P., Figura M., Nędzyńska-Stygar M., Stefański R., Korga M., Kwiatkowska I., Stępniak K.M., Tołkacz K., Nowak S. 2022. Diet of the grey wolf <em>Canis lupus</em> in Roztocze and Solska Forest, south-east Poland. Journal of Vertebrate Biology 71: 22040. DOI: <a href="https://doi.org/10.25225/jvb.22040">10.25225/jvb.22040</a></p>

opencc-by-4.0Aug 2023View details →
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Fig. 1 in Taeniid species of the Iberian wolf (Canis lupus signatus) in Portugal with special focus on Echinococcus spp.

Fig. 1. Sampling areas in the North of Portugal. (a) In the northern area (1) 57 fecal samples were collected and in Leomilde, the southern area (2), 11 samples; (b) Approximate location of samples in the northern area, named according to the corresponding wolf pack territories [(1) Boulhosa (n = 1), (2) Vez (n = 20), (3) Castro Laboreiro (n = 1), (4) Soajo (n = 7), (5) Pitões (n = 4), (6) Amarela (n = 10), (7) Vila Verde (n = 1) and (8) Gerês (n = 13)].

opencc-by-4.0Dec 2013View details →
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Figure 2 in Status Survey of Indian Grey Wolf (Canis lupus pallipes) in West Bengal and some part of Jharkhand

Figure 2. Forest cover map of study area. Showing the different forest types across the two states i.e. West Bengal and Jharkhand. Forest cover map has been classified in to open-forest, moderate-dense forest, very dense forest, Scrubland, no forest and water bodies. (Source: Forest Survey of India 2013).

opencc-by-4.0Dec 2019View details →
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Figure 3 in Status Survey of Indian Grey Wolf (Canis lupus pallipes) in West Bengal and some part of Jharkhand

Figure 3. Direct sighting and indirect evidences for wolf presence in the study area. A and B showing the direct sighting of Wolf from study districts of west Bengal, while C and D are the footprints of wolf.

opencc-by-4.0Dec 2019View details →
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Figure 1 in Status Survey of Indian Grey Wolf (Canis lupus pallipes) in West Bengal and some part of Jharkhand

Figure 1. Elevation map of study area. Showing the different elevation profiles of the study area ranging up to 3474 m. The colour ramp signifies the ranging from high to low elevation across the landscape, where red colour indicates the high elevation ranges and green showing the lower elevation ranges.

opencc-by-4.0Dec 2019View details →
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Figure 2. A in On tooth anomalies and the loss of Canis lupus (Mammalia: Carnivora) in Turkey*

Figure 2. A- Root fusion of the premolars (Skull No: 17), Balveols of the root fusion (Skull No: 17), C- root fusion (Skull No: 29), D- premolar tended to be 3-rooted (2 roots could not be seperated) (Skull No: 29), E- alveol of the root fusion (Skull No: 29), and F- root fusion anomaly in the lower jaw (Skull No: 29).

opencc-by-4.0Aug 2019View details →
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Figure 4. A in On tooth anomalies and the loss of Canis lupus (Mammalia: Carnivora) in Turkey*

Figure 4. A- Premolar loss (Skull No: 6), B- premolar loss (Skull No: 10), C- premolar loss (Skull No: 16), D- premolar loss (Skull No: 20), E- premolar loss (Skull No: 20), and F- molar loss (Skull No: 27).

opencc-by-4.0Aug 2019View details →
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Figure 7. A in On tooth anomalies and the loss of Canis lupus (Mammalia: Carnivora) in Turkey*

Figure 7. A- Carnassial remnant (Skull No: 3), B- premolar remnant (Skull No: 10), C- premolar remnant (Skull No: 19), and D- premolar remnant (Skull No: 27).

opencc-by-4.0Aug 2019View details →
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Figure 6. A in On tooth anomalies and the loss of Canis lupus (Mammalia: Carnivora) in Turkey*

Figure 6. A- Incisor fracture (Skull No: 9), B- incisor fracture (Skull No: 10), C- canine fracture (Skull No:12), D- premolar fracture (Skull No: 14), E- incisor fracture (Skull No: 16), Fmultiple fractures (Skull No: 18), G- multiple fractures (Skull No: 18), and H- incisor fracture (Skull No: 29).

opencc-by-4.0Aug 2019View details →
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Figure 3. A in On tooth anomalies and the loss of Canis lupus (Mammalia: Carnivora) in Turkey*

Figure 3. A- Premolar additional root bilaterally (Skull No: 11), B- additional root anomaly of the lower premolars overlapped the upper third premolars (Skull No: 11), and C- 3-rooted tooth (Skull No: 11).

opencc-by-4.0Aug 2019View details →
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Fig. 5 in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada

Fig. 5. On the left, whole mounted Cryptocotyle lingua adult trematode stained with borax carmine (credit: Brent Wagner). On the right, distribution of foxes (Vulpes vulpes) infected with C. lingua in the Subarctic (samples (n) collected along James Bay and the St Lawrence estuary) and Humid Continental climate collected during winter 2016–2017 by trappers from Qu´ebec, Canada. Arrows indicate major waterways.

opencc-by-4.0Dec 2021View details →
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Fig. 2. A in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada

Fig. 2. A) Parasite genus richness in foxes (Vulpes vulpes, blue), coyotes (Canis latrans, orange), and wolves (Canis lupus, gray) from Qu´ebec, Canada, determined by gross examination and fecal flotation combined (N = 250). Fewer foxes were uninfected than coyotes (p = 0.006). More foxes were infected by two parasite genera than coyotes (p = 0.004). B) Parasite genus richness between Subarctic (yellow) and Humid Continental climate (green) in foxes from Qu´ebec, Canada, determined by gross examination and fecal flotation combined (N = 155). No significant difference in parasite genera was seen in foxes between Subarctic and Humid Continental climate regions. Parasites counted in both histograms were: diphyllobothriids (likely Dibothriocephalus spp.), Echinococcus spp., Taenia spp., Capillaria spp., Toxascaris sp., Toxocara sp., Trichuris sp., Uncinaria sp., Alaria sp., Cryptocotyle sp., and Metorchis sp. Parasites observed in both fecal and gross examination were only counted once. Bars represent 95% confidence intervals. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Dec 2021View details →
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Fig. 6 in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada

Fig. 6. Distribution of foxes (Vulpes vulpes), coyotes (Canis latrans), and wolves (Canis lupus) infected with Toxascaris leonina (left, N = 55) and Toxocara canis (right, N = 19) in the Subarctic and Humid Continental climate collected during winter 2016–2017 by hunters and trappers from Qu´ebec, Canada.

opencc-by-4.0Dec 2021View details →
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Fig. 1. K in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada

Fig. 1. K¨oppen climate regions and sampling distribution of foxes (Vulpes vulpes, N = 176), coyotes (Canis latrans, N = 77), and wolves (Canis lupus, N = 23) collected during winter 2016–2017 by hunters and trappers from Qu´ebec, Canada. Arrows indicate major waterways.

opencc-by-4.0Dec 2021View details →
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Fig. 4 in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada

Fig. 4. Mixed taeniid infections in the Humid Continental climate in coyotes (Canis latrans) and wolves (Canis lupus) from Qu´ebec, Canada, following molecular analyses. Abbreviations on x-axis: E. can, Echinococcus canadensis; T. hyd, Taenia hydatigena; T. twi, T. twitchelli; T. kra, T. krabbei; T. pis, T. pisiformis-"like"; T. cra, T. crassiceps.

opencc-by-4.0Dec 2021View details →
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Fig. 3 in Host and geographic differences in prevalence and diversity of gastrointestinal helminths of foxes (Vulpes vulpes), coyotes (Canis latrans) and wolves (Canis lupus) in Quebec´, Canada

Fig. 3. Neighbour-joining tree of Jukes-Cantor distances among sequences of CO1 (alignment 450 bp using all sites) from Alaria available on GenBank as of 7 July 2021. Data from Alaria americana, including data from the present study, indicated by darker shaded cluster and white font. Sequences from A. alata are HM022221-3, KF751233-4, KP123416-20, KP123422-5, KX962374, KX962392, KX962395, KX962397-8, KX962402, KX962406, KX962415, KX962421, KX962433, KX962437, KX962454-5, KX962471-2, KX962481, KX962491, KY012317, MT103215-31; from Alaria sp. in Argentina KF572949, MH892076, MT328804-6; from Alaria sp. in Wisconsin, USA KT223036; from A. americana MZ605217-33 (present study) and MH536507 (indicated with an asterisk).

opencc-by-4.0Dec 2021View details →
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Fig. 6 in Angiostrongylus vasorum in foxes (Vulpes vulpes) and wolves (Canis lupus italicus) from Abruzzo region, Italy

Fig. 6. Lung of red fox: adult nematode within a pulmonary artery (A). Lung of wolf: nematode larvae were observed in alveolar spaces causing a thickening of connective tissue and a fibrotic response (B). Two nematode larvae were visible in the mediastinal lymph node of a red fox (C). Lymphocytic and eosinophilic infiltrates were present in brain tissue of a red fox infected with A. vasorum (D). Hematoxylin and Eosin (H&amp;E) stain. Final magnification: × 100 (A–B), ×200 (C), × 400 (D). Scale bar: 200 μm (A–B), 100 μm (C), 50 μm (D). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

opencc-by-4.0Aug 2021View details →
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Fig. 4 in Angiostrongylus vasorum in foxes (Vulpes vulpes) and wolves (Canis lupus italicus) from Abruzzo region, Italy

Fig. 4. Angiostrongylus vasorum: scanning electron micrographies (SEM). A higher magnification of A) anterior end of adult worm, enface view showing the oral orifice; B) anterior end of adult worm, lateral view; C) posterior end of adult male, enface view showing copulatory bursa and spicules; D) detail of posterior end of adult male at higher magnification; E) posterior end of adult male, showing lateral rays of copulatory bursa.

opencc-by-4.0Aug 2021View details →
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Fig. 3 in Angiostrongylus vasorum in foxes (Vulpes vulpes) and wolves (Canis lupus italicus) from Abruzzo region, Italy

Fig. 3. Province of Chieti, showing the municipalities of origin in which tested wolves resulted positive for Angiostrongylus vasorum.

opencc-by-4.0Aug 2021View details →
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Fig. 2 in Angiostrongylus vasorum in foxes (Vulpes vulpes) and wolves (Canis lupus italicus) from Abruzzo region, Italy

Fig. 2. Province of Chieti, showing the municipalities of origin in which tested foxes resulted positive for Angiostrongylus vasorum.

opencc-by-4.0Aug 2021View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record