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249 results for “hare”
Figure 1 in Designation of a Neotype for the Dwarf Sea Hare Aplysia concava G. B. Sowerby I, 1833, and a Review of the Status of Aplysia norfolkensis G. B. Sowerby II, 1869 (Mollusca: Heterobranchia)
Figure 1. Photograph of living neotype of Aplysia concava, specimen AMS C.574820, Newcastle, NSW, Australia, collected 14 December 2016, by Stephen D. A. Smith. Photograph: M. Nimbs.
The role of sea hares as significant algal herbivores on the Southern Great Barrier Reef
<p>The data files are as follows:</p> <p>Other species - raw data on genera of algae (and some other organisms) observed in quadrats during our surveys at Heron Island</p> <p>algal.distribution.tabulated - summary data on the three most common algal genera used for chi-squared test.</p> <p>algal.dry.weights - data for trials aimed at establishing an equation to convert displacement volume of bundles of Laurencia to dry weights in grams</p> <p>algal.herbivory.trials - data from sea hare herbivory trials, including amount eaten each 24 hour trial and sea hare size.</p> <p>All data was collected by the primary researchers in the field.</p> <p>The R script to process these files is available here: https://github.com/rcrofts/SeaHareScript.git.</p> <p>These data were processed using RStudio version 1.2.5019 </p>
Fig. 2 in Allozyme Variability Of Brown Hares (Lepus Europaeus) From The Vojvodina (Serbia), Compared To Central And Southeastern European Populations
Fig. 2. Scatterplots of population-specific dimension stimulus coordinates as obtained from multidimensional scaling (three-dimensional model); A (up): plot of first and second dimensions, B (down): plot of first and third dimensions. Convex polygons encompass the 20 Austrian (black circles and light grey area) and the eight Bulgarian (white circles and dark grey area) populations, respectively. Black cross indicates the Vojvodina (VOJ) population; for acronymes of Austrian populations see
Fig. 1 in Allozyme Variability Of Brown Hares (Lepus Europaeus) From The Vojvodina (Serbia), Compared To Central And Southeastern European Populations
Fig. 1. Unrooted Wagner dendogram based on modified Roger's distances (WRIGHT 1978), representing genetic relationships among brown hares from the Vojvodina (VOJ), 20 Austrian (population acronyme – A), and eight Bulgarian (population acronyme – BL) populations. For acronymes of the Austrian populations see HARTL et al. (1993) and for Bulgarian populations see SUCHENTRUNK et
Fig. 3 in Allozyme Variability Of Brown Hares (Lepus Europaeus) From The Vojvodina (Serbia), Compared To Central And Southeastern European Populations
Fig. 3. Stepwise discriminant analysis (DA): box plots of discriminant scores for the Austrian and Bulgarian populations as well as the discriminant score of the initially unclassified Vojvodina population (cross, VOJ), as obtained from DA of stimulus coordinates from the multidimensional scaling (three-dimensional model). The stippled horizontal line indicates classification of VOJ to the Aus-
Fig. 1 in Spatial, Temporal And Individual Variability In The Autumn Diet Of European Hare (Lepus Europaeus) In Hungary
Fig. 1. Localities of the study areas. Study areas are shown as gray patches, the capital (Budapest) by striped gray area, Lake Balaton and Lake Tisza by black ones. Black lines are Hungarian rivers and
Older than 4 Fig. 1 in Comparison Of Two Age Determination Methods Of The European Hares (Lepus Europaeus Pallas, 1778) In Southwest Lithuania
Older than 4 Fig. 1. The measurements of ulna-radius of the years European hares. 3-4 year old 18 a – juvenile, b- adult; 1 - length of epiphyses ossification in ulna; 2- width of epiphysis cartilage 2-3 year old 8 in ulna; 3- high of epiphyses in in ulna-radius; 4 - width of ulna-radius at the thickest part. Juvenile (under 1 year old)
Рис. 2. НижнечеΛюстные кости из шурфа Ш-1, кв. Б-3: А — собоΛь (Martes zibellina); Б — заяц-беΛяк (Lepus timidus); В — пищухи (Ochotona sp.) Fig. 2. Mandibular bones from D-1, sq. B-3: A — sable (Martes zibellina); Б — white hare (Lepus timidus); В — pikas (Ochotona sp.) in New data on the Holocene vertebrate fauna of the Middle Lena and Aldan Rivers basins (Yakutia) based on the materials from archaeological sites Jampa, Kuznets I, II Daban-Yuryakh, and Buor-Khaya I, II, III
Рис. 2. НижнечеΛюстные кости из шурфа Ш-1, кв. Б-3: А — собоΛь (Martes zibellina); Б — заяц-беΛяк (Lepus timidus); В — пищухи (Ochotona sp.) Fig. 2. Mandibular bones from D-1, sq. B-3: A — sable (Martes zibellina); Б — white hare (Lepus timidus); В — pikas (Ochotona sp.)
The usage of phrasal verbs (emu) ye den, (emu) ye duru and (emu) ye hare in Akan Twi Asante
<p>A project done as part of the "Urbane Feldforschung" seminar in Humboldt University of Berlin in 2018. This is a project on Akan Twi Asante, a language spoken in Ghana. The subject is the usage of phrasal verbs (emu) ye den, (emu) ye duru and (emu) ye hare in the Asante dialect of Akan Twi.</p> <p>Collected data includes 6 glossed sentences in Akan on the topic mentioned above and 56 words from the Swadesh List. <br> <br> <br> <br> </p>
The usage of phrasal verbs (emu) ye den, (emu) ye duru and (emu) ye hare in Akan Twi Asante
<p>A project done as part of the "Urbane Feldforschung" seminar in Humboldt University of Berlin in 2018. This is a project on Akan Twi Asante, a language spoken in Ghana. The subject is the usage of phrasal verbs (emu) ye den, (emu) ye duru and (emu) ye hare in the Asante dialect of Akan Twi.</p> <p>Collected data includes 6 glossed sentences in Akan on the topic mentioned above and 56 words from the Swadesh List. <br> </p>
Figure 5 in The taxonomic status and geographic distribution of the European hare (Lepus europaeus Pallas, 1778) in Turkey (Mammalia: Lagomorpha)
Figure 5. The group centroids obtained from discriminant functions: 1 = Thracian specimen, 2 = Southwest Anatolian population, 3 = Central and East-Central Anatolian population, 4 = Northeast Anatolian population, 5 = Southeast Anatolian population.
Fig. 3 in Gastrointestinal parasite infestation in the alpine mountain hare (Lepus timidus varronis): Are abiotic environmental factors such as elevation, temperature and precipitation affecting prevalence of parasite species?
Fig. 3. Parasite infestation in faeces and ambient temperature. Correlation between parasite infestation in Alpine mountain hare faeces (n = 52) and average, minimal, and maximal temperature found in Vorarlberg (Austria) during the years 2014 and 2015. Count visualises the number of faecal samples. See text for details on statistics.
Fig. 2 in Gastrointestinal parasite infestation in the alpine mountain hare (Lepus timidus varronis): Are abiotic environmental factors such as elevation, temperature and precipitation affecting prevalence of parasite species?
Fig. 2. Number of parasite types per faeces and severity of parasitic infestation. Correlation between number of parasite types per Alpine mountain hare faeces and severity of parasitic infestation (n = 28) found in Vorarlberg (Austria) during the years 2014 and 2015. Count visualises the number of faecal samples. The severity of infestation is indicated by scattered ((+)), low (+), intermediate (++), and high (+++) infestation. See text for details on statistics.
Fig. 2. Hare 19 in Cysticercosis by Taenia pisiformis in Brown Hare (Lepus europaeus) in Northern Italy: Epidemiologic and pathologic features
Fig. 2. Hare 19/2015. Histological image of a hepatic cyst (T. pisiformis), visible on the left. Focal infiltrate of eosinophil granulocytes with few lymphocytes, macrophages and plasma cells on the right. H&E, Bar = 200 μm.
Fig. 1. Hare 36 in Cysticercosis by Taenia pisiformis in Brown Hare (Lepus europaeus) in Northern Italy: Epidemiologic and pathologic features
Fig. 1. Hare 36/2013, liver and stomach. Cysticercosis (T. pisiformis) in liver surface and gastric peritoneum.
Fig. 1. Recent Cape hare Lepus capensis Linnaeus, 1758 RAM R2 in Head and neck posture in sauropod dinosaurs inferred from extant animals
Fig. 1. Recent Cape hare Lepus capensis Linnaeus, 1758 RAM R2 in right lateral view, illustrating maximally extended pose (A) and ONP (B): skull, cervical vertebrae 1–7 and dorsal vertebrae 1–2. Note the very weak dorsal deflection of the base of the neck in ONP, contrasting with the much stronger deflection illustrated in a live rabbit by Vidal et al. (1986: fig. 4).
Fig. 3 in "Till death do us apart": The common destiny of brown hare and its parasite community
Fig. 3. Histological section of lungs of hares infected by Protostrongylus spp. A. Interstitial verminous bronchopneumonia with several cross and longitudinal sections of larvae on the right and the bottom of the photo. Bronchial and alveolar septa are thickened due to inflammatory cellular reaction (eosinophil granulocytes and mononuclear cells). A lymphoid nodule is visible on the left side. H&E, Bar = 100 μm. B. Interstitial verminous bronchopneumonia with scattered cross sections of adult parasites, five of them in the centre of the photo. H&E, Bar = 100 μm.
Fig. 2 in "Till death do us apart": The common destiny of brown hare and its parasite community
Fig. 2. Normal (up) and abnormal (bottom) T. retortaeformis male genital cone. In the abnormal nematode no spicula are present notwithstanding the perfectly developed gubernaculum (partially covered by the two spicules in the upper photo) and caudal bursa. Bar is 50 μm.
Fig. 2 in Identification of the tapeworm Mosgovoyia pectinata (Anoplocephalidae) in Faroese mountain hares (Lepus timidus)
Fig. 2. Bayesian inference tree of phylogenetic relationships of Mosgovoyia spp. and other anoplocephalid (s. s.) cestodes of mammals based on sequences of the mitochondrial nad1 gene. The new sequence from Lepus timidus from Faroes in bold. Posterior probabilities of the Bayesian analysis (first value) and bootstrap support of the Maximum likelihood (ML) analysis (second value) are indicated at nodes. The inclusion of Neoctenotaenia ctenoides in the "lagomorph clade" is not supported by either of the phylogenetic methods. Hymenolepis diminuta and Arostrilepis sp. (Hymenolepididae) were used as outgroups (not shown).
Fig. 1 in Identification of the tapeworm Mosgovoyia pectinata (Anoplocephalidae) in Faroese mountain hares (Lepus timidus)
Fig. 1. Geographic location of the Faroe Islands and spatial distribution of mountain hares on the islands (green colour). Tapeworms were collected from four hares, hunted in four villages: 1) Vestmanna, 2) Eiði, 3) Kollafjørður and 4) Viðareiði. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
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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.