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6,861 results for “Animals”
Agriculture - General: Animal Production and Health 2
<p>Original data comes from a project which takes or took place as part of the DFG priority program “Exploratories for large-scale and long-term functional biodiversity research”. The data is stored together with descriptive metadata, in combination called a dataset, in the project repository (<a href="https://www.bexis.uni-jena.de">https://www.bexis.uni-jena.de</a>). Species information was extracted from that original dataset. The second paragraph is part of the metadata of the original dataset.Trapping small mammals with live traps in all three Exploratories and all EPs, but not grasland plots with cattle. Heinze E (2016). Small mammal species list 08. Biodiversity Exploratories. Occurrence dataset <a href="https://doi.org/10.15468/pioxzy">https://doi.org/10.15468/pioxzy</a> accessed via GBIF.org</p>
Data for: Why do phylogenomic analyses of early animal evolution continue to disagree? Sites in different structural environments yield different answers
<p>Supporting data for "Why do phylogenomic analyses of early animal evolution continue to disagree? Sites in different structural environments yield different answers" submitted by A Pandey and EL Braun. File is a gzipped tarball including protein multiple sequence alignments, phylogenetic trees, and other supporting data; see included README for details.</p>
Tables and Figures complementing the European Union Summary Report on Antimicrobial Resistance in Zoonotic and Indicator Bacteria from Humans, Animals and Food in 2016
<p>All tables, figures and maps produced for the European Union Summary Report on Antimicrobial Resistance in Zoonotic and Indicator Bacteria from Humans, Animals and Food in 2016 are provided.</p>
A guide to using a multiple-matrix animal model to disentangle genetic and nongenetic causes of phenotypic variance
<p>Simulated data associated with the paper "A guide to using a multiple-matrix animal model to disentangle genetic and nongenetic causes of phenotypic variance".</p> <p>The main dataset is contained within the mermaids.csv, with columns explained within the associated README file. Epigenetic and social network information are contained within the other two datasets</p>
Tables and Figures complementing the European Union Summary Report on Antimicrobial Resistance in Zoonotic and Indicator Bacteria from Humans, Animals and Food in 2017
<p>All tables, figures and maps produced for the European Union Summary Report on Antimicrobial Resistance in Zoonotic and Indicator Bacteria from Humans, Animals and Food in 2017 are provided.</p>
Supplementary Data: Evolution of the cholesterol biosynthesis pathway in animals
<p>Cholesterol plays essential roles in animal development and disease progression. Here, we characterize the evolutionary pattern of the canonical cholesterol biosynthesis pathway (CBP) in the animal kingdom using both genome-wide analyses and functional experiments. CBP genes in the basal metazoans were inherited from their last common eukaryotic ancestor and evolutionarily conserved for cholesterol biosynthesis. The genomes of both the basal metazoans and deuterostomes retain almost the full set of CBP genes, while Cnidaria and many protostomes have independently experienced multiple massive losses of CBP genes that might be due to the geologic events during the Ediacaran period, such as the appearance of an exogenous sterol supply and the frequent perturbation of ocean oxygenation. Meanwhile, the indispensable utilization processes of cholesterol potentially strengthened the maintenance of the complete set of CBP genes in vertebrates. These results strengthen both biotic and abiotic roles in the macroevolution of a biosynthesis pathway in animals.</p>
Skeleton of Struthiomimus altus. Genotype specimen, Amer. Mus. 5339. One-tenth natural size In this panel mount the animal is placed approximately as found. The pollex is too closely appressed to the other digits, see Fig. 3. in Skeletal Adaptations of Ornitholestes, Struthiomimus, Tyrannosaurus
Skeleton of Struthiomimus altus. Genotype specimen, Amer. Mus. 5339. One-tenth natural size In this panel mount the animal is placed approximately as found. The pollex is too closely appressed to the other digits, see Fig. 3.
PULSE Project Animation
<p>Project animation explaining ultra-fast pulsed lasers and project objectives.</p>
Figure. Food preferences of Chinese mole shrew (Anourosorex squamipes) from an urban area. a, b, c, d. Mean relative consumption along six trials for each food set are shown in a, b, c, d, respectively. (see materials and methods for details on the calculation of relative consumption). in Natural animal food preference of Chinese mole shrew (Anourosorex squamipes) from an urban area: a laboratory study
Figure. Food preferences of Chinese mole shrew (Anourosorex squamipes) from an urban area. a, b, c, d. Mean relative consumption along six trials for each food set are shown in a, b, c, d, respectively. (see materials and methods for details on the calculation of relative consumption).
Fig. 1 in Cardiopulmonary nematodes of wild carnivores from Denmark: Do they serve as reservoir hosts for infections in domestic animals?
Fig. 1. Map of Denmark showing Denmark's position in Europe and a map of Denmark showing the regional division and the four major cities.
Fig. 7. Karyotype from a Central Site L. spenceri unsexed juvenile, animal 2. A representative karyotype demonstrates the L. spenceri 2n in The critically endangered species Litoria spenceri demonstrates subpopulation karyotype diversity
Fig. 7. Karyotype from a Central Site L. spenceri unsexed juvenile, animal 2. A representative karyotype demonstrates the L. spenceri 2n = 26 karyotype and DAPI negative areas in the long arms of chromosomes 9 and 11.
Fig. 6. Karyotype from a Central Site L. spenceri unsexed juvenile, animal 1. A representative karyotype demonstrates the L. spenceri 2n in The critically endangered species Litoria spenceri demonstrates subpopulation karyotype diversity
Fig. 6. Karyotype from a Central Site L. spenceri unsexed juvenile, animal 1. A representative karyotype demonstrates the L. spenceri 2n = 26 karyotype and DAPI negative areas in the long arms of chromosomes 9 and 11.
Fig. 4. Chromosomes 9 and 11 from different L. spenceri populations. Three representative chromosomes from each animal demonstrate a in The critically endangered species Litoria spenceri demonstrates subpopulation karyotype diversity
Fig. 4. Chromosomes 9 and 11 from different L. spenceri populations. Three representative chromosomes from each animal demonstrate a highly conserved DAPI negative region in the long arms of chromosome 9. A DAPI negative region is observed in the long arm of chromosome 11, but only in the Central Site juveniles and in only one matched chromosome of the Northern Site x Central Site tadpole hybrid. Arrows indicate the chromosome 11 DAPI negative region. Asterisks indicate the paired submetacentric chromosome 11 matched pair of the Northern Site x Central Site tadpole hybrid.
Fig. 2 in Toxoplasma gondii contamination at an animal agriculture facility: Environmental, agricultural animal, and wildlife contamination indicator evaluation
Fig. 2. Soil sampling and animal trapping locations at Little River Animal and Environmental Unit in Walland, Tennessee, United States.
Fig. 1 in Toxoplasma gondii contamination at an animal agriculture facility: Environmental, agricultural animal, and wildlife contamination indicator evaluation
Fig. 1. The geographic location of the study site, Little River Animal and Environmental Unit in Walland, Tennessee, United States.
Fig. 5 in The earliest known venomous animals recognized among conodonts
Fig. 5. Venom delivery structures of extant fish. A–C. Dorsal spines of Pterois volitans Linnaeus, 1758, family Scorpaenidae. A. Whole spine; ZPAL C.19/165.1. B. Distal portion of another spine, fractured to show cross−section; ZPAL C.19/165.2. C. Magnification of a fragment; ZPAL C.19/165.3. D. Anterior part of the lower jaw of Meiacanthus grammistes (Valenciennes), 1836, family Blenniidae, Indonesia; ZPAL C.19/2.1.
Fig. 4 in The earliest known venomous animals recognized among conodonts
Fig. 4. Venomous teeth of some extant vertebrates. A. Fang from the lower jaw of the fish Meiacanthus grammistes (Valenciennes, 1836), family Blenniidae, Indonesia; ZPAL C.19/153.2. B. Tooth from the lower jaw of the lizard Heloderma suspectum Cope, 1869, North America; ZPAL C.19/165.1. C. Posterior maxillary tooth of the snake Psammophis cf. shokari Forskal, 1775, family Colubridae; ZPAL C.19/155.1, in dorsal (C1) and oblique (C2) views. D, E. Fangs of the snake Trimeresurus gramineus (Shaw, 1802), family Viperidae, India.1 D. ZPAL C.19/164, Mature form in lateral view. E. ZPAL C.19/164.2, replacement fang of the same snake in oblique view.
Fig. 3 in The earliest known venomous animals recognized among conodonts
Fig. 3. Grasping apparatuses of the conodont Panderodus and fossil and extant chaetognaths. A. Partly deformed apparatus of the Silurian conodont Panderodus unicostatus Branson and Mehl, 1933, Ukraine, Podolia; ZPAL C.15/1 (same as Dzik and Drygant 1986: fig. 1, new photograph). B. Apparatus of the fossil chaetognath Phakelodus tenuis (Müller, 1959), subsurface Upper Cambrian of northern Poland; ZPAL C.4/6.2 (same as Szaniawski 1982: fig. 1, new photograph). C. Left half of the grasping spine apparatus of the extant chaetognath Sagitta sp., North Sea; ZPAL C.4/1.1. D. Head of the extant chaetognath Sagitta sp. with grasping spine apparatus in acting position, North Sea; ZPAL C.4/619.
Fig. 1 in The earliest known venomous animals recognized among conodonts
Fig. 1. Elements of venomous conodonts. A. Panderodus sulcatus (Fåhraeus, 1966), Middle Ordovician, borehole Deniski, eastern Poland; ZPAL C.19/150.1. B. Panderodus greenlandensis Armstrong, 1990, Early Silurian, Jädivere, Estonia; ZPAL C.19/145.2. C, D. Protopanderodus calceatus Bagnoli and Stouge, 1997, Middle Ordovician, borehole Pieszkowo, north−eastern Poland. C. Whole element; ZPAL C.19/156.3. D. A fragment showing cross section; ZPAL C.19/159.19. E. Panderodus sp., Middle Ordovician, borehole Stadniki, eastern Poland; ZPAL C.19/159.12. F. Dapsilodus mutatus (Branson and Mehl, 1933), Late Ordovician, borehole Stadniki, eastern Poland; ZPAL C.19/159.4. G. Decoriconus fragilis (Branson and Mehl, 1933), Middle Silurian, borehole Gołdap, northern Poland; ZPAL C.19/160.12. H. Parapanderodus sp., Early Silurian, Podolia, Ukraine; ZPAL C.15/1. I. Panderodus sp. Middle Silurian, borehole Gołdap, northern Poland; ZPAL C.19/149.2, whole element (I1), distal part of the specimen showing wear of the tip (I2). J. Panderodus greenlandensis, Early Silurian, Jädivere, Estonia; ZPAL C.19/145.1, whole specimen (J1), distal part of the same specimen showing wear of the tip (J2), a fragment of the specimen showing thin longitudinal ridges parallel to the groove and sharp edges delimiting the grooved surface (J3), basal part of the specimen showing coarse ridges (J4).
Fig. 2 in The earliest known venomous animals recognized among conodonts
Fig. 2. Cross sections of the elements of Panderodus. A. Panderodus greenlandensis Armstrong, 1990, Early Silurian, Jädivere, Estonia; ZPAL C.19/137.1. Basal part (A1) and above the basal part (A2). B. Distal part of Panderodus sp., Middle Ordovician, borehole Deniski, eastern Poland; ZPAL C.19/19.5. Abbreviations: bb, basal body; bc, basal cavity; cr, crown; gr, groove.
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.