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113 results for “Leporidae”
Fig. 6 in Three new species of Eimeria (Apicomplexa: Eimeriidae) from the Amami rabbit, Pentalagus furnessi (Mammalia: Leporidae)
Fig. 6. Line drawings of the Eimeria species detected in the Amami rabbit. (a) Eimeria furnessi. (b) Eimeria hilleri. (c) Eimeria sagentae. Scale bar = 10 μ
Fig. 4 in Three new species of Eimeria (Apicomplexa: Eimeriidae) from the Amami rabbit, Pentalagus furnessi (Mammalia: Leporidae)
Fig. 4. Nomarski interference contrast photographs of oocysts of Eimeria hilleri from the Amami rabbit stored in a potassium dichromate solution. M: micropyle; N: nucleus; OWo: outer layer of the wall; OWi: inner layer of the wall; RB: refractile body; SB: Stieda body; SR: sporocyst residuum; SSB: substieda body. Scale bars (all in the same scale) = 10 μm.
Fig. 2 in Three new species of Eimeria (Apicomplexa: Eimeriidae) from the Amami rabbit, Pentalagus furnessi (Mammalia: Leporidae)
Fig. 2. Endogenous stages of coccidian parasites found in the section of the jejunum and ileum of the Amami rabbit. HE. Scale bar = 20 μm and applies to all parts. (a) Schizont-like structures (arrows) in detached epithelial cells. (b) Immature microgamont (arrow) with basophilic small nuclei. (c) Immature macrogamont (arrow) with eosinophilic bodies. (d) Microgamont (arrow) with peripherally located basophilic nuclei. (e) Macrogamont (arrow) with peripheral arrangement of eosinophilic wall-forming bodies. (f) Unsporulated oocyst (arrow) with a central nucleus and oocyst wall. High-resolution version of these slides for use with the Virtual Microscope are available as eSlide: VM06653.
Fig. 5 in Three new species of Eimeria (Apicomplexa: Eimeriidae) from the Amami rabbit, Pentalagus furnessi (Mammalia: Leporidae)
Fig. 5. Nomarski interference contrast photographs of oocysts of Eimeria sagentae from the Amami rabbit stored in a potassium dichromate solution. M: micropyle; N: nucleus; OWo: outer layer of the wall; OWi: inner layer of the wall; RB: refractile body; SB: Stieda body; SO: sporont; SR: sporocyst residuum. Scale bars (all in the same scale) = 10 μm.
Fig. 1 in Three new species of Eimeria (Apicomplexa: Eimeriidae) from the Amami rabbit, Pentalagus furnessi (Mammalia: Leporidae)
Fig. 1. Map showing the location of the Amami-Oshima and Tokunoshima Islands. Circles indicate the sites where fecal samples of Amami rabbits were collected in the field.
Fig. 3 in Three new species of Eimeria (Apicomplexa: Eimeriidae) from the Amami rabbit, Pentalagus furnessi (Mammalia: Leporidae)
Fig. 3. Nomarski interference contrast photographs of oocysts of Eimeria furnessi from the Amami rabbit stored in a potassium dichromate solution. M: micropyle; N: nucleus; OWo: outer layer of the wall; OWi: inner layer of the wall; RB: refractile body; SB: Stieda body; SO: sporont; SR: sporocyst residuum. Scale bars (all in the same scale) = 10 μm.
Figure 8. Leporidae. A, B. Hypolagus fontinalis left p3, UCMP 41205 in The fauna and chronostratigraphy of the middle Miocene Mascall type area, John Day Basin, Oregon, USA
Figure 8. Leporidae. A, B. Hypolagus fontinalis left p3, UCMP 41205 (A),JODA 4283 (B). C, D. Hypolagus parviplicatus left p3, JODA 2328 (C); JODA 2326 (D). E. Archaeolagus sp. left M1 or M2, JODA 17386. All in occlusal view. Scale bar=1mm
Linked collectors and determiners for: Distribución potencial de las especies de Leporidae en México y las implicaciones para su conservación.
Natural history specimen data linked to collectors and determiners held within, "Distribución potencial de las especies de Leporidae en México y las implicaciones para su conservación". Claims or attributions were made on Bionomia by volunteer Scribes, <a href="https://bionomia.net/dataset/a98ae4c4-7662-4fec-be45-acb526c624b6">https://bionomia.net/dataset/a98ae4c4-7662-4fec-be45-acb526c624b6</a> using specimen data from the dataset aggregated by the Global Biodiversity Information Facility, <a href="https://gbif.org/dataset/a98ae4c4-7662-4fec-be45-acb526c624b6">https://gbif.org/dataset/a98ae4c4-7662-4fec-be45-acb526c624b6</a>. Formatted as a Frictionless Data package.
Molecular phenotyping uncovers differences in basic housekeeping functions among closely related species of hares (Lepus spp., Lagomorpha: Leporidae)
<p>Speciation is a fundamental evolutionary process, which results in genetic differentiation of populations and manifests as discrete morphological, physiological as well as behavioral differences. Each species has had its own evolutionary trajectory, formed by many types of selection pressures and random drift, making it extremely complicated to associate genetic differences between the species with the phenotypic differences. In the present study, we have used an in vitro model to analyze in depth the genetic and gene regulation differences between fibroblasts of two closely related mammals, arctic/subarctic mountain hare (Lepus timidus Linnaeus) and a temperate, steppe-like climate adapted brown hare (Lepus europaeus Pallas). We discovered the existence of a species-specific expression pattern of 1,623 genes, manifesting in differences in cell growth, respiration, and metabolism. Interspecific differences in the housekeeping functions of fibroblast cells suggest speciation acts on fundamental processes, even in these two interfertile species. Our results help to understand the molecular constituents of a species difference on a cellular level, which could contribute to the maintenance of the species boundary.</p>
Low genetic diversity and shallow population structure in the broom hare, Lepus castroviejoi (Lagomorpha:Leporidae)
<p><span class="TextRun SCXW115721130 BCX4"><span class="NormalTextRun SCXW115721130 BCX4">Microsatellite dataset of 322 hare samples from five species: 76 samples from the broom hare (</span></span><em><span class="TextRun SCXW115721130 BCX4"><span class="NormalTextRun SCXW115721130 BCX4">Lepus </span><span class="NormalTextRun SCXW115721130 BCX4">castroviejoi</span></span></em><span class="TextRun SCXW115721130 BCX4"><span class="NormalTextRun SCXW115721130 BCX4">); 81 for the European hare (<em>L. europaeus</em>); 68 for the Iberian hare (<em>L. granatensis</em>); 77 for the mountain hare (<em>L. timidus</em>); and 20 for the Italian hare (<em>L. corsicanus</em>).</span></span></p>
Low genetic diversity and shallow population structure in the broom hare, Lepus castroviejoi (Lagomorpha:Leporidae)
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Molecular phenotyping uncovers differences in basic housekeeping functions among closely related species of hares (Lepus spp., Lagomorpha: Leporidae)
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Sevilleta site, station Sevilleta, study of animal density of Leporidae in units of numberPerKilometerSquared on a quarterly timescale
The EcoTrends project was established in 2004 by Dr. Debra Peters (Jornada Basin LTER, USDA-ARS Jornada Experimental Range) and Dr. Ariel Lugo (Luquillo LTER, USDA-FS Luquillo Experimental Forest) to support the collection and analysis of long-term ecological datasets. The project is a large synthesis effort focused on improving the accessibility and use of long-term data. At present, there are ~50 state and federally funded research sites that are participating and contributing to the EcoTrends project, including all 26 Long-Term Ecological Research (LTER) sites and sites funded by the USDA Agriculture Research Service (ARS), USDA Forest Service, US Department of Energy, US Geological Survey (USGS) and numerous universities. Data from the EcoTrends project are available through an exploratory web portal (http://www.ecotrends.info). This web portal enables the continuation of data compilation and accessibility by users through an interactive web application. Ongoing data compilation is updated through both manual and automatic processing as part of the LTER Provenance Aware Synthesis Tracking Architecture (PASTA). The web portal is a collaboration between the Jornada LTER and the LTER Network Office. The following dataset from Sevilleta (SEV) contains animal density of Leporidae measurements in numberPerKilometerSquared units and were aggregated to a quarterly timescale.
Sevilleta site, station Sevilleta, study of animal density of Leporidae in units of numberPerKilometerSquared on a yearly timescale
The EcoTrends project was established in 2004 by Dr. Debra Peters (Jornada Basin LTER, USDA-ARS Jornada Experimental Range) and Dr. Ariel Lugo (Luquillo LTER, USDA-FS Luquillo Experimental Forest) to support the collection and analysis of long-term ecological datasets. The project is a large synthesis effort focused on improving the accessibility and use of long-term data. At present, there are ~50 state and federally funded research sites that are participating and contributing to the EcoTrends project, including all 26 Long-Term Ecological Research (LTER) sites and sites funded by the USDA Agriculture Research Service (ARS), USDA Forest Service, US Department of Energy, US Geological Survey (USGS) and numerous universities. Data from the EcoTrends project are available through an exploratory web portal (http://www.ecotrends.info). This web portal enables the continuation of data compilation and accessibility by users through an interactive web application. Ongoing data compilation is updated through both manual and automatic processing as part of the LTER Provenance Aware Synthesis Tracking Architecture (PASTA). The web portal is a collaboration between the Jornada LTER and the LTER Network Office. The following dataset from Sevilleta (SEV) contains animal density of Leporidae measurements in numberPerKilometerSquared units and were aggregated to a yearly timescale.
Jornada Basin LTER/Jornada Experimental Range site, station Rabbit survey route in creosote vegetation zone, study of animal abundance of Leporidae in units of numberPer10KiometerOfRoad on a yearly timescale
The EcoTrends project was established in 2004 by Dr. Debra Peters (Jornada Basin LTER, USDA-ARS Jornada Experimental Range) and Dr. Ariel Lugo (Luquillo LTER, USDA-FS Luquillo Experimental Forest) to support the collection and analysis of long-term ecological datasets. The project is a large synthesis effort focused on improving the accessibility and use of long-term data. At present, there are ~50 state and federally funded research sites that are participating and contributing to the EcoTrends project, including all 26 Long-Term Ecological Research (LTER) sites and sites funded by the USDA Agriculture Research Service (ARS), USDA Forest Service, US Department of Energy, US Geological Survey (USGS) and numerous universities. Data from the EcoTrends project are available through an exploratory web portal (http://www.ecotrends.info). This web portal enables the continuation of data compilation and accessibility by users through an interactive web application. Ongoing data compilation is updated through both manual and automatic processing as part of the LTER Provenance Aware Synthesis Tracking Architecture (PASTA). The web portal is a collaboration between the Jornada LTER and the LTER Network Office. The following dataset from Jornada Basin LTER/Jornada Experimental Range (JRN) contains animal abundance of Leporidae measurements in numberPer10KiometerOfRoad units and were aggregated to a yearly timescale.
Jornada Basin LTER/Jornada Experimental Range site, station Rabbit survey route in grassland vegetation zone, study of animal abundance of Leporidae in units of numberPer10KiometerOfRoad on a yearly timescale
The EcoTrends project was established in 2004 by Dr. Debra Peters (Jornada Basin LTER, USDA-ARS Jornada Experimental Range) and Dr. Ariel Lugo (Luquillo LTER, USDA-FS Luquillo Experimental Forest) to support the collection and analysis of long-term ecological datasets. The project is a large synthesis effort focused on improving the accessibility and use of long-term data. At present, there are ~50 state and federally funded research sites that are participating and contributing to the EcoTrends project, including all 26 Long-Term Ecological Research (LTER) sites and sites funded by the USDA Agriculture Research Service (ARS), USDA Forest Service, US Department of Energy, US Geological Survey (USGS) and numerous universities. Data from the EcoTrends project are available through an exploratory web portal (http://www.ecotrends.info). This web portal enables the continuation of data compilation and accessibility by users through an interactive web application. Ongoing data compilation is updated through both manual and automatic processing as part of the LTER Provenance Aware Synthesis Tracking Architecture (PASTA). The web portal is a collaboration between the Jornada LTER and the LTER Network Office. The following dataset from Jornada Basin LTER/Jornada Experimental Range (JRN) contains animal abundance of Leporidae measurements in numberPer10KiometerOfRoad units and were aggregated to a yearly timescale.
FIGURE 2 in Genetic evidence supports Sylvilagus mansuetus (Lagomorpha: Leporidae) as a subspecies of S. bachmani
FIGURE 2. Phylogram produced by the Bayesian analysis of concatenated genes (1,854 bp): Cyt b (800 bp), COI (654 bp), and β-fib I7 (400 bp). All specimens of the 3 subspecies of Sylvilagus bachmani, i.e. S. b. cerrosensis, S. b. mariposae, S. b. macrorhinus, and S. mansuetus were monophyletic. Nodes with solid circles have a posterior probability values of 1.0.
FIGURE 1 in Genetic evidence supports Sylvilagus mansuetus (Lagomorpha: Leporidae) as a subspecies of S. bachmani
FIGURE 1. Map of the distribution area of Sylvilagus bachmani (in grey) and examined specimens of S. mansuetus and the three different subspecies of S. bachmani: S. b. cerrosensis, S. b. mariposae, and S. b. macrorhinus, from the Baja California Peninsula, Mexico, and California, USA.
Subspecies and Distribution. L. c. californicus Gray, 1837 — SW Oregon, and NW California (W USA). L. c. altamirae Nelson, 1904 — SE Tamaulipas (NE Mexico). L. c. asellus Miller, 1899 — SE Coahuila, NE, S Nuevo Leon, E & SE Zacatecas, San Luis Potosi, Aguascalientes, NE tip ofJalisco, N Guanajuato, and NW Querétaro (NC Mexico). L. c. bennettiz Gray, 1843 — SW California (SW USA), and NW Baja California (NW Mexico). L. c. curts Hall, 1951 — Is along the coast of Tamaulipas (NE Mexico). L. c. deserticola Mearns, 1896 — SE Oregon, S Idaho, SW Montana, NE & E California, Nevada, Utah except SE, and NW, W & SW Arizona (W & SW USA), and NW Sonora and NE Baja California (NW Mexico). The population in SW Montanais isolated. L. c. eremicus J. A. Allen, 1894 — S Arizona (SW USA), N Sonora except extreme NW, NW Chihuahua (N Mexico). L. c. festinus Nelson, 1904 — S Querétaro, Hidalgo, and N State of Mexico (C Mexico). L. c. magdalenae Nelson, 1907 — Magdalena I, Baja California Sur (NW Mexico). L. c. martirensis Stowell, 1895 —Baja California except NW & NE and NE Baja California Sur (NW Mexico). L. c. melanotis Mearns, 1890 — S South Dakota, SE Wyoming, Nebraska, E Colorado, Kansas, W Missouri, NE New Mexico, Oklahoma, W Arkansas, and N Texas (C USA). An isolated population exists in E Oklahoma. L. c. merriami Mearns, 1896 — S Texas (S USA), and NE Coahuila, N Tamaulipas, and N Nuevo Leon (NE Mexico). L. c. richardsonii Bachman, 1839 — C California (SW USA). L. c. sheldoni Burt, 1933 — Isla del Carmen, Baja California Sur (NW Mexico). L. c. texianus Waterhouse, 1848 — SE Utah, SW Colorado, NE Arizona, New Mexico except the NE, and W Texas (C USA), Chihuahua except the NW, W, & SW extremes, W Coahuila, E Durango, and NW Zacatecas (NC Mexico). L. c. wallawalla Merriam, 1904 — S Washington, C & W Oregon, NE California, and NW Nevada (NW USA). L. ¢. xanti Thomas, 1898 — Baja California Sur except the NE (NW Mexico). in Leporidae
Subspecies and Distribution. L. c. californicus Gray, 1837 — SW Oregon, and NW California (W USA). L. c. altamirae Nelson, 1904 — SE Tamaulipas (NE Mexico). L. c. asellus Miller, 1899 — SE Coahuila, NE, S Nuevo Leon, E & SE Zacatecas, San Luis Potosi, Aguascalientes, NE tip ofJalisco, N Guanajuato, and NW Querétaro (NC Mexico). L. c. bennettiz Gray, 1843 — SW California (SW USA), and NW Baja California (NW Mexico). L. c. curts Hall, 1951 — Is along the coast of Tamaulipas (NE Mexico). L. c. deserticola Mearns, 1896 — SE Oregon, S Idaho, SW Montana, NE & E California, Nevada, Utah except SE, and NW, W & SW Arizona (W & SW USA), and NW Sonora and NE Baja California (NW Mexico). The population in SW Montanais isolated. L. c. eremicus J. A. Allen, 1894 — S Arizona (SW USA), N Sonora except extreme NW, NW Chihuahua (N Mexico). L. c. festinus Nelson, 1904 — S Querétaro, Hidalgo, and N State of Mexico (C Mexico). L. c. magdalenae Nelson, 1907 — Magdalena I, Baja California Sur (NW Mexico). L. c. martirensis Stowell, 1895 —Baja California except NW & NE and NE Baja California Sur (NW Mexico). L. c. melanotis Mearns, 1890 — S South Dakota, SE Wyoming, Nebraska, E Colorado, Kansas, W Missouri, NE New Mexico, Oklahoma, W Arkansas, and N Texas (C USA). An isolated population exists in E Oklahoma. L. c. merriami Mearns, 1896 — S Texas (S USA), and NE Coahuila, N Tamaulipas, and N Nuevo Leon (NE Mexico). L. c. richardsonii Bachman, 1839 — C California (SW USA). L. c. sheldoni Burt, 1933 — Isla del Carmen, Baja California Sur (NW Mexico). L. c. texianus Waterhouse, 1848 — SE Utah, SW Colorado, NE Arizona, New Mexico except the NE, and W Texas (C USA), Chihuahua except the NW, W, & SW extremes, W Coahuila, E Durango, and NW Zacatecas (NC Mexico). L. c. wallawalla Merriam, 1904 — S Washington, C & W Oregon, NE California, and NW Nevada (NW USA). L. ¢. xanti Thomas, 1898 — Baja California Sur except the NE (NW Mexico).
On following pages: 51. Tehuantepec Jackrabbit (Lepus flavigularis); 52. Iberian Hare (Lepus granatensis); 53. European Hare (Lepus europaeus); 54. Broom Hare (Lepus castroviejoi); 55. Corsican Hare (Lepus corsicanus); 56. White-tailed Jackrabbit (Lepus townsendii); 57. Arctic Hare (Lepus arcticus); 58. Alaskan Hare (Lepus othus); 59. Mountain Hare (Lepus timidus); 60. Japanese Hare (Lepus brachyurus); 61. Manchurian Hare (Lepus mandshuricus); 62. Korean Hare Lepus coreanus); 63. Chinese Hare (Lepus sinensis). in Leporidae
On following pages: 51. Tehuantepec Jackrabbit (Lepus flavigularis); 52. Iberian Hare (Lepus granatensis); 53. European Hare (Lepus europaeus); 54. Broom Hare (Lepus castroviejoi); 55. Corsican Hare (Lepus corsicanus); 56. White-tailed Jackrabbit (Lepus townsendii); 57. Arctic Hare (Lepus arcticus); 58. Alaskan Hare (Lepus othus); 59. Mountain Hare (Lepus timidus); 60. Japanese Hare (Lepus brachyurus); 61. Manchurian Hare (Lepus mandshuricus); 62. Korean Hare Lepus coreanus); 63. Chinese Hare (Lepus sinensis).
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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.