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292 results for “rabbit”
Mangrove leaf physiological response to local climate at Key Largo, Watson River Chickee, Taylor Slough, and Little Rabbit Key, South Florida (FCE) from July 2001 to August 2001
Determine the red mangrove leaf physiological response to the local climate to understand the local controls on plant physiology. Data were collected in the Key Largo Ranger Station, Watson River Chickee and Taylor Slough research Sites, South Florida.
Rubisco limited photosynthesis rates of Red mangrove leaves at Key Largo, Watson River Chickee, Taylor Slough, and Little Rabbit Key, South Florida (FCE) from July 2001 to August 2001
Determine the Rubisco limited carboxylation rates of red mangrove ( species Rhizophora mangle) leaves. This information will be used to model carbon sequestration by Red mangroves.
Light limited carboxylation rates of Red mangrove leaves at Key Largo, Watson River Chickee, Taylor Slough, and Little Rabbit Key, South Florida (FCE) from July 2001 to August 2001
Our goal is to determine light limited carboxylation rates of red mangrove (specie sRhizophora mangle) leaves. This information will be used to model carbon sequestration by Red mangroves.
Gastropod Biomass and Densities found at Rabbit Key Basin, Florida Bay (FCE) from March 2000 to April 2001
Grazing gastropod biomass and shell morphology were measured from 1 m2 plots within Thalassia seagrass meadow in Rabbit Key Basin, Florida Bay, Everglades National Park.
Seagrass Epiphyte Accumulation: Epiphyte Loads on Thalassia testudinum in Rabbit Key Basin, Florida Bay (FCE) from March 2000 to April 2001
Total epiphyte and epiphyte chlorophyll-a loads and leaf nutrients were measured on Thalassia seagrass short-shoots from Rabbit Key Basin, Florida Bay.
Thalassia leaf morphology and productivity measurements from arbitrary plots located in a Thalassia seagrass meadow in Rabbit Key Basin, Florida Bay (FCE) from March 2000 to April 2001
Thalassia leaf morphology and productivity were measured from six arbitrary 200 cm2 plots within a Thalassia seagrass meadow in Rabbit Key Basin, Florida Bay.
Rabbit feces counts on 1m x 1m plots from the long-term Small Mammal Exclosure Study (SMES) at Jornada Basin LTER, 1995-2020
This data package contains rabbit feces count data from plots with various levels of herbivore exclusion on Jornada Experimental Range (JER) and Chihuahuan Desert Rangeland Research Center (CDRRC) lands. Study sites were established in 1995; one in black grama grassland and the other in creosotebush shrubland to compare the impact of herbivores on ecosystem processes between these vegetation types. Parallel studies were established at the Sevilleta LTER site (New Mexico, USA) and Mapimi Biosphere Reserve (Durango, Mexico). Each study site is 1 km by 0.5 km in area. Four replicate experimental blocks were randomly located at the grassland study site to measure vegetation responses using exclusion treatments including a) all mammalian herbivores, including cattle, lagomorphs, and rodents, b) lagomorphs and cattle only, c) cattle only, and d) control accessible to all herbivores. Because grazing cattle are excluded from the entire creosote site, only three replicate experimental blocks were randomly located there including a) all mammalian herbivores, including lagomorphs, and rodents, b) lagomorphs only, and c) control accessible to all herbivores. Thirty-six sampling points were positioned at 5.8-meter intervals on a systematically located 6 by 6 point grid within each plot. A permanent one-meter by one-meter vegetation measurement quadrat is located at each of the 36 points. Each year in spring and fall from 1995-2005, the total number of rabbit feces were counted within each quadrat. After 2005, sampling frequency channged to every 5 years and data collected record only presence or absence of feces. This study is ongoing.
Rabbit survey data on creosotebush and grassland routes from the long-term Small Mammal Exclusion Study at Jornada Basin LTER, 1996-ongoing
This data package contains rabbit survey data from grassland and creosote shrubland habitats on Jornada Experimental Range (JER) and Chihuahuan Desert Rangeland Research Center (CDRRC) lands. Two survey routes were established along Jornada Basin roads in 1996; one in black grama grassland and the other in creosotebush shrubland. Quarterly surveys are conducted on these roads at or near the full moon to measure the density of rabbits in the two vegetation types. Each route is about 6 miles long. Parallel studies were established at the Sevilleta LTER site (New Mexico, USA) and Mapimi Biosphere Reserve (Durango, Mexico). Data collection began in April 1996 and includes date and time lagomorphs are spotted, species identification, habitat type, distance/direction from vehicle, and comments on the weather, moon, and anything unusual. This study is ongoing with new data collected quarterly.
SGS-LTER Long-term Monitoring Project: Spotlight Rabbit Count on the Central Plains Experimental Range, Nunn, Colorado, USA 1994-2006, ARS Study Number 98 (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/136/17. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Additional information and referenced materials can be found: http://hdl.handle.net/10217/83448. Rabbits are the most important small-mammal herbivores in shortgrass steppe, and may significant influence the physiognomy and population dynamics of herbaceous plants and woody shrubs. Rabbits also are the most important prey of mammalian carnivores such as coyotes and large raptors such as golden eagles and great horned owls. Two hares (Lepus californicus, L. townsendii) and one cottontail rabbit (Sylvilagus audubonii) occur in shortgrass steppe. In 1994, we initiated long-term studies to track changes in relative abundance of rabbits on the Central Plains Experimental Range (CPER). On four nights each year (one night each season, usually on new moon nights in January, April, July, October), we drove a 32-km route consisting of pasture two-track and gravel roads on the CPER. This wa
Rabbit Population Dynamics in Chihuahuan Desert Grasslands and Shrublands at the Sevilleta National Wildlife Refuge, New Mexico (1992-present) (Reformatted to the ecocomDP Design Pattern)
This data package is formatted as an ecocomDP (Ecological Community Data Pattern). For more information on ecocomDP see https://github.com/EDIorg/ecocomDP. This Level 1 data package was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sev/23/121705. The abstract below was extracted from the Level 0 data package and is included for context: This study explores the population dynamics of black-tail jackrabbits (Lepus californicus) and desert cottontail rabbits (Sylvilagus auduboni) in the grasslands and creosote shrublands of McKenzie Flats, Sevilleta National Wildlife Refuge. The study was initiated in January 1992, and continues quarterly each year. Rabbits are sampled via night-time spotlight transect sampling along the roads of McKenzie Flats once during winter, spring, summer, and fall. The route is 21.5 miles long. Measurements of perpendicular distance of each rabbit from the center of the road are used to estimate densities (number of rabbits per square kilometer) via Program DISTANCE. Results from January 1992 to May 2004 indicated that spring was the period of peak density period, with generally steady declines through the rest of the year until the following spring. Evidence of a long-term "cycle" (e.g., the 11-year-cycle reported for rabbits in the Great Basin Desert) does not appear in the Sevilleta rabbit populations.
Dataset of Impact of pre-breeding feeding practices on rabbit mammary gland development at mid-pregnancy
<p>The dataset includes search results used in article “Impact of pre-breeding feeding practices on rabbit mammary gland development at mid-pregnancy” biorXiv, 2022.01.17.476562, ver. 3 peer-reviewed and recommended by Peer Community in Animal Science. <a href="https://doi.org/10.1101/2022.01.17.476562">https://doi.org/10.1101/2022.01.17.476562</a></p> <p> </p> <p>Search Results Description: Please use Figure 1 from paper to trace the data made available and experimental group.</p> <p>The excel “raw data 2022-06-24” file contains the following data</p> <ol> <li>Body weight of each rabbit on a weekly basis</li> <li>Analysis of breeding parameters at mid-pregnancy</li> <li>Histological areas of each mammry tissue measured</li> <li>Optical density values obtained for biochemical leptin concentration determination</li> <li>Optical density values obtained for biochemical triglyceride concentration determination</li> <li>Optical density values obtained for biochemical glucose concentration determination</li> <li>Optical density values obtained for biochemical cholesterol concentration determination</li> <li>RT-qPCR results (Ct) from QuantStudio export for milk protein analysis</li> <li>RT-qPCR results (Ct) from QuantStudio export for lipid metabolism analysisen</li> </ol> <p>“Statistical analysis.doc” contained the description of the statistics used in Excel and the description of the linear mixed model analysis , the reference of the script available by the CRAN project is also include.The R scipt file for using the linear mixed model in R added with the "data-croissance-analysis" file.</p>
SGS-LTER Long-term Monitoring Project: Spotlight Rabbit Count on the Central Plains Experimental Range, Nunn, Colorado, USA 1994-2006, ARS Study Number 98 (Reformatted to a Darwin Core Archive)
This data package is formatted as a Darwin Core Archive (DwC-A, event core). For more information on Darwin Core see https://www.tdwg.org/standards/dwc/. This Level 2 data package was derived from the Level 1 data package found here: https://pasta.lternet.edu/package/metadata/eml/edi/327/2, which was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sgs/136/17. The abstract below was extracted from the Level 0 data package and is included for context: This data package was produced by researchers working on the Shortgrass Steppe Long Term Ecological Research (SGS-LTER) Project, administered at Colorado State University. Long-term datasets and background information (proposals, reports, photographs, etc.) on the SGS-LTER project are contained in a comprehensive project collection within the Digital Collections of Colorado (http://digitool.library.colostate.edu/R/?func=collections&collection_id=3429). The data table and associated metadata document, which is generated in Ecological Metadata Language, may be available through other repositories serving the ecological research community and represent components of the larger SGS-LTER project collection. Additional information and referenced materials can be found: http://hdl.handle.net/10217/83448. Rabbits are the most important small-mammal herbivores in shortgrass steppe, and may significant influence the physiognomy and population dynamics of herbaceous plants and woody shrubs. Rabbits also are the most important prey of mammalian carnivores such as coyotes and large raptors such as golden eagles and great horned owls. Two hares (Lepus californicus, L. townsendii) and one cottontail rabbit (Sylvilagus audubonii) occur in shortgrass steppe. In 1994, we initiated long-term studies to track changes in relative abundance of rabbits on the Central Plains Experimental Range (CPER). On four nights each year (one night each season, usually on new moon nights in January,
Rabbit Population Dynamics in Chihuahuan Desert Grasslands and Shrublands at the Sevilleta National Wildlife Refuge, New Mexico (1992-present) (Reformatted to a Darwin Core Archive)
This data package is formatted as a Darwin Core Archive (DwC-A, event core). For more information on Darwin Core see https://www.tdwg.org/standards/dwc/. This Level 2 data package was derived from the Level 1 data package found here: https://pasta.lternet.edu/package/metadata/eml/edi/334/2, which was derived from the Level 0 data package found here: https://pasta.lternet.edu/package/metadata/eml/knb-lter-sev/23/121705. The abstract below was extracted from the Level 0 data package and is included for context: This study explores the population dynamics of black-tail jackrabbits (Lepus californicus) and desert cottontail rabbits (Sylvilagus auduboni) in the grasslands and creosote shrublands of McKenzie Flats, Sevilleta National Wildlife Refuge. The study was initiated in January 1992, and continues quarterly each year. Rabbits are sampled via night-time spotlight transect sampling along the roads of McKenzie Flats once during winter, spring, summer, and fall. The route is 21.5 miles long. Measurements of perpendicular distance of each rabbit from the center of the road are used to estimate densities (number of rabbits per square kilometer) via Program DISTANCE. Results from January 1992 to May 2004 indicated that spring was the period of peak density period, with generally steady declines through the rest of the year until the following spring. Evidence of a long-term "cycle" (e.g., the 11-year-cycle reported for rabbits in the Great Basin Desert) does not appear in the Sevilleta rabbit populations.
Adaptive changes in the genomes of wild rabbits after 16 years of viral epidemics
<p>Since its introduction to control overabundant alien rabbits (Oryctolagus cuniculus), the highly virulent Rabbit Haemorrhagic Disease Virus (RHDV) has caused regular annual disease outbreaks in Australian rabbit populations. Although initially reducing rabbit abundance by 60%, continent-wide, experimental evidence has since indicated increased genetic resistance in wild rabbits that have experienced RHDV-driven selection. To identify genetic adaptations, which explain the increased resistance to this biocontrol virus, we investigated genome-wide SNP (single nucleotide polymorphism) allele frequency changes in a South Australian rabbit population that was sampled in 1996 (pre-RHD genomes) and after 16 years of RHDV outbreaks. We identified several SNPs with changed allele frequencies within or in proximity of genes that have roles potentially important for increased RHD resistance. Many of the identified genes are known to be involved in virus infections or immunity, or had previously been identified as being differentially expressed in healthy vs. acutely RHDV-infected rabbits. Furthermore, we show in a simulation study that the allele/genotype frequency changes cannot be explained by drift alone, and that several candidate genes had also been identified as being associated with surviving RHD in a different Australian rabbit population. Our unique dataset allowed us to identify candidate genes for RHDV resistance that have evolved under natural conditions, and over a time span that would not have been feasible to study in an experimental setting. Moreover, it provides a rare example of host genetic adaptations to virus-driven selection in response to a suddenly emerging infectious disease.</p>
A volumetric model of rabbit heart and torso including ECG data and ventricular activation sequence
<p>Data generated and analyzed of our work titled "A computational model of rabbit geometry and ECG: Optimizing ventricular activation sequence and APD distribution". Please see the respective publication for more context.</p> <p> </p> <ul> <li>BSPM_filtered.dat <ul> <li>Contains the filtered ECG Data</li> </ul> </li> <li>BSPM_original.bdf <ul> <li>Contains the originally recorded signal.<br> Information on the file format itself can be found here: <a href="https://www.biosemi.com/faq/file_format.htm">https://www.biosemi.com/faq/file_format.htm</a><br> Links to various toolboxes to open the file can be found here: <a href="https://www.biosemi.com/download.htm">https://www.biosemi.com/download.htm</a></li> </ul> </li> <li>CT_DataDCM.zip <ul> <li>Contains the recorded CT images of heart and torso in DCM file format</li> </ul> </li> <li>ECG_NodeIndices.txt <ul> <li>Contains the the node IDs of the torso mesh corresponding to the electrode positions of the ECG Vest</li> </ul> </li> <li>Endocardial_Surface_Papillary.stl <ul> <li>Segmented endocardial surface including papillary muscles</li> </ul> </li> <li>Mat_LeadField.dat <ul> <li>Contains the calculated lead field matrix to be used in combination with the provided Mesh_Ven.vtu. Make sure to keep the node order</li> <li> <pre><code class="language-python"># Python example of usage # Define a read_vm_vec function which reads your calculated data beforehand import numpy as np t_begin = 0 t_end = 400 LF_mat = np.loadtxt('Mat_LeadField.dat') times = np.linspace(t_begin, t_end, t_end-t_begin) result = np.zeros((len(times), 31)) for i,t in enumerate(times): vm_vec = read_vm_vec(t) result[i, :] = LF_mat.dot(vm_vec)[0:31] result = np.insert(result, 0, times, axis=1) np.savetxt('BSPM.dat', result)</code></pre> <p> </p> </li> </ul> </li> <li>Mesh_PurkinjeTree.vtp <ul> <li>The resulting optimized Purkinje Node tree. We recommend using <a href="https://www.paraview.org/">ParaView</a> for visualization</li> </ul> </li> <li>Mesh_StimPoints.vtp <ul> <li>The resulting points of stimulation.</li> </ul> </li> <li>Stim_IndexTime.dat <ul> <li>Contains the stimulation pattern in terms the node index of Mesh_Ven.vtu and the respective stimulation time</li> </ul> </li> <li>Mesh_Ven.vtu <ul> <li>Contains the ventricular mesh as well as the repective lead field matrix values for each surface node.</li> <li>Material:<br> Right Ventricle 30<br> Left Ventricle 31</li> </ul> </li> <li>Mesh_Torso.vtu <ul> <li>Contains the whole torso mesh.</li> <li>Material:<br> Fat 2<br> Bones 3<br> Blood 9<br> Cartilage 14<br> Liver 20<br> Lungs 17<br> Right Ventricle 30<br> Left Ventricle 31<br> Right Atrium 32<br> Left Atrium 33<br> Aorta 60<br> Pulmonary artery 61<br> Left Vena Jugularis 62<br> Right Vena Jugularis 62<br> Post Vena Cava 62</li> </ul> </li> </ul> <p> </p>
Fig. 8 Urine miRNA profile analysis among different groups. a in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 8 Urine miRNA profile analysis among different groups. a The volcano plot shows the individual statistically significant miRNA between acutely infected rabbits and control rabbits. In this plot, the x-axis is log2 fold-change, which shows the direction of the change (negative scale is decrease and positive scale is increase) in the levels of miRNA expression, while the y-axis is the –log10 FDR, which shows the significance of the change. b The volcano plot shows the individual statistically significant miRNA between chronically infected rabbits and control rabbits. c The volcano plot shows the individual statistically significant miRNA between acutely infected rabbits and chronically infected rabbits. d Venn diagram shows number of differentially expressed miRNA among different comparison pairs
Fig. 10 in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 10 Venn diagrams showing the common and unique DE miRNAs (a) and DE piRNAs (b) in both serum and urine between the acutely and chronically infected rabbits versus uninfected rabbits
Fig. 5 in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 5 Global view of temporal sRNA expression profiles in rabbit urine during T. gondii infection. a The sRNA correlation heatmap of sample clustering. b Principal component analysis of all identified urine sRNAs. c Unsupervised hierarchical clustering of sRNA profiling data. sRNA intensity is normalized so that blue represents low intensity and yellow represents high intensity. Columns were hierarchically clustered based on a complete linkage using Pearson correlation coefficients as the distance measure. Sample groups are acutely infected rabbits, chronically infected rabbits and uninfected control rabbits, which are labeled as AI, CI and Con, respectively
Fig. 4 in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 4 First nucleotide bias of obtained small RNA in urine samples of rabbits. a First nucleotide bias of known miRNAs in rabbit urine. b First nucleotide bias of predicted miRNAs in rabbit urine. c First nucleotide bias of predicted piRNAs in rabbit urine
Fig. 1 in A combined miRNA-piRNA signature in the serum and urine of rabbits infected with ToxoplaSMa gondii oocysts
Fig. 1 Histological features of spleen section from healthy control rabbits and rabbits experimentally infected with Toxoplasma gondii. Images showing the H&E-stained spleen section at 100× (a, b). a Spleen section from healthy, uninfected rabbit. The structures of white pulp (WP) and red pulp (RP) were clearly identified with normal cell density. b Spleen section from a rabbit with acute T. gondii infection. The number and dimension of splenic nodule are increased, and more plasma cells are observed in the splenic cord (black triangle) of red pulp. Note that granulomas are present (big black arrow). Hemosiderin deposition (small black arrow) indicated red blood cell destruction. CA central arteriole. Scale bar = 100 μm
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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.