Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
193
datasets available to search
ShareScore release 0.7.1
Dataset results
193 results for “browsing”
Figure 4. After merging, overview is more transparent. Tens of persons were merged together into clusters in order to clarify the visualization. Firms and persons are recognized based on their icons.-Browsing Semantic Data in Slovakia
<p>The usefulness of such visualization has its key points regarding connections. Thanks to SBR browsing module, we were able to get 22 firm records for “Váhostav” query. Between any 2 companies, connections may be (and often are) not bidirectional, so, in order to navigate through connections, we have refined all 22 records. Although, even being filtered, graph is still complex. And it is possible to further navigate and search for outgoing connections, for example firm “MERLIN TRADE, a.s.” on Fig.4 contains item on “Ján Kato”, which is already included in our graph and connected to “VÁHOSTAV&SK&DEVELOPEMENT” on bottom left side and “VÁHOSTAV&SK, a.s.” in the center. Edge coloring and drawing is helpful with overlapped edges. For methods of visualization, including coloring, we refer to studies of H. Omote and K. Sugiyama (2006), and I. Herman, G. Melanon, and M. S. Marshall (2000) or our study on graph clutter filtering and connectivity distance (Mojzis & Laclavik, 2014).</p>
Figure 3. Graph created directly from the results.-Browsing Semantic Data in Slovakia
<p>Resulting graph is rather complex. There are 175 vertices and 201 edges, which were created directly, containing 158 persons and 17 companies. As we see on Figure 3, some filtering methods are required in order to create suitable overview of relations. Figure 4 thus shows the visualization of the same graph, but with tens of vertices merged. Now it contains 22 persons and 17 companies. A merging was performed for clarification and is built inside the visualization module. A simple condition says that a merging is performed if persons are unique, thus if a person is connected only to 1 firm. More formally, person vertices are merged, if their vertex degree equals 1 (each).</p>
Figure 2. Results for firm name "Váhostav" are in table. Each row defines a firm with its name, identification number and address. Then a connection is specified (whether it be a person or another firm).-Browsing Semantic Data in Slovakia
<p>We have searched for firm “Váhostav”, which is a rather big firm in Slovakia, with many press articles published about31. On Figure 2 there is a browsing window, for SBR data results, displaying tabular structure, which was refined from SBR dataset by continuous querying.</p>
Figure 1. Schema of clientside application for semantic browsing.-Browsing Semantic Data in Slovakia
<p>With the aim primary on unstructured information extraction and refining, relationship discovery and visualization, we propose our solution for SBR in the first place. The reason for this is, primary, that HTML formatted results of SBR are very jerky and uncertainty regarding the structure of information is very high. Readers can also be pointed by J. Suchal and P. Vojtek (2009), that care should be taken towards type errors. We discuss that later. In this work, we try to fill&up the gap of visualization and, somehow limited data access offered by SBR, adapting to the problems disclaimed above. We suggest a new client& side paradigm, which does not depend on a particular website like foaf.sk. Figure 1 describes the schema briefly and the key elements are parsers with other tools on the top and structured formats, for datastore, on the bottom.</p>
Data from: Recovery of silver fir (Abies alba Mill.) seedlings from ungulate browsing mirrors soil nitrogen availability
<p><em>Abies alba</em> (Mill.) has a high potential for mitigating climate change in European mountain forests, yet, its natural regeneration is severely limited by ungulate browsing. Here, we simulated browsing in a common garden experiment to study growth and physiological traits, measured from bulk needles, using a randomized block design with two levels of browsing severity and seedlings originating from 19 populations across Switzerland. Genetic factors explained most variation in growth (on average, 51.5%) and physiological traits (10.2%) under control conditions, while heavy browsing considerably reduced the genetic effects on growth (to 30%), but doubled those on physiological traits related to C storage. While browsing reduced seedling height, it also lowered seedling water use efficiency (decreased δ<sup>13</sup>C) and increased their δ<sup>15</sup>N. Different populations reacted differently to browsing stress, and for seedling height, starch concentration and δ<sup>15</sup>N population differences appeared to be the result of natural selection. First, we found that populations originating from the warmest regions recovered the fastest from browsing stress, and they did so by mobilizing starch from their needles, which suggests a genetic underpinning for a growth-storage trade-off across populations. Second, we found that seedlings originating from mountain populations growing on steep slopes had a higher δ<sup>15</sup>N in the common garden than those originating from flat areas, indicating that they have been selected to grow on N poor, potentially drained, soils. This finding was corroborated by the fact that N concentration in adult needles was lower on steep slopes than on flat ground, strongly indicating that steep slopes are the most N poor environments. These results suggest that populations adapted to these N poor environments have a genetically based high N use efficiency, which could be necessary for their recover from ungulate browsing.</p>
FIG. 7 in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 7. — Hyoid apparatus and buccal cavity of seedsnipes (here Thinocorus Eschscholtz,1829):A, lateral view of the hyoid apparatus displaced downward relative to the mandible; B, rostral part of the hyolingual apparatus; C, buccal cavity, the floor on the left, the roof on the right, a plant item present in the buccal cavity of the dissected specimen has been left in its place. Abbreviations: see text.
FIG. 5 in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 5. — Lateral views of the successive planes of the dissection of the dorsal adductors in Thinocorus Eschscholtz, 1829: A-D, deep portion of the external adductor; E, m. pseudotemporalis profundus, posterior adductor and protractors; a, b, transversal sections of the orbito-zygomatic process; e, aponeuroses of m. pseudotemporalis profundus. Abbreviations: see text.
FIG. 4 in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 4. — Cranial musculature of Attagis Geoffroy Saint-Hilaire & Lesson, 1831, successive planes of the dissection: A, general view; B, lateral view through the orbit; b, internal aponeuroses of m. pseudotemporalis superficialis; C-E, lateral views of portions of the external adductor. Abbreviations: see text.
FIG. 1 in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 1. — Particularities of seedsnipe's skull: A, Thinocorus orbignyianus Geoffroy Saint-Hilaire & Lesson, 1831; B, Attagis gayi Geoffroy Saint-Hilaire & Lesson, 1831; C-E, Thinocorus Eschscholtz, 1829; C, ventral view of the mandible and palate; D, surface of the mandibular joint with location of the contact area of the lateral and caudal condyles of the quadrate; E, caudal view of the mandibular joint. Abbreviations: see text.
FIG. 9. — A in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 9. — A, static graphical analysis of the equilibrium of forces when a food item is clamped in the bill (for more details see Dzerzhinsky 1972; Korzun et al. 2003, 2004a, b); adductors exert force A from the mandible towards the cranium and force A', superimposed, opposite and equal to A (for the clarity of the figure, A has not been represented on its point of application but directly placed at j along its axis of action); force A is decomposed into F (mandibular clamping force applied along the axis going through the clamping points of the item in the bill) and K (force of the quadrate applied on the quadrato-mandibular joint q); force K is itself decomposed into M (pressure force of the quadrate on the cranium along the axis q-x) and R (retraction force of the upper jaw along the axis of the jugal bar); in turn R is decomposed into F' (clamping force of the item by the upper jaw, opposed and equal to F) and N (pressure force of the upper jaw on the cranium at the level of the prokinetic hinge b); at the equilibrium, forces M, N and A (so A') are applied to point z where they cancel each other; a, meeting point of the three axes of 1) clamping, 2) action on the cranium via the prokinetic joint, and 3) retraction of the upper jaw along the jugal bar; j, meeting point of the axes of 1) clamping, 2) action of the adductors, and 3) action on the cranium through the mandibular joint; x, joint of the quadrate on the neurocranium; c = meeting point of the jugal bar and the maxilla.
FIG. 6. — A-D in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 6. — A-D, ventral views of the successive planes of the dissection of m. pterygoideus in Thinocorus Eschscholtz, 1829. Abbreviations: see text.
FIG. 3 in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 3. — Schema of the arrangement of the internal aponeuroses of external adductor in Thinocorus Eschscholtz, 1829 (A) and Attagis Geoffroy Saint-Hilaire & Lesson, 1831 (B). Abbreviations: see text.
FIG. 8 in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 8. — Forces in action when a fixed plant item is taken off; A, a plant item is pulled along the axis of the bill; B, a plant item is torn off by moving the head downward towards the breast. Abbreviations:F (= F' at equilibrium), clamping forces respectively exerted by the mandible and the upper jaw; Fr, resistance force of the item, labelled Fra when this item is pulled along the axis of the bill and Frb when this item is torn off by moving the head downward towards the breast (Fra = Frb); Ff, friction force which depends on the clamping forces: Ff = 2 k F (k = coefficient of friction); the lever arms of Fra and Frb are respectively indicated l and h, with l> h; so Fra has a less favourable lever arm than Frb: the action of these forces depending on their respective momentum, we have Fra × h
FIG. 2 in Adaptation of seedsnipes (Aves, Charadriiformes, Thinocoridae) to browsing: a study of their feeding apparatus
FIG. 2. — Cranial musculature of Thinocorus Eschscholtz, 1829, successive planes of the dissection: A, general view; B, lateral view through the orbit; b aponeuroses of m. pseudotemporalis superficialis; C, D, lateral views of the superficial and medial portions of the external adductor. Abbreviations: see text.
Twenty years of Salix height in response to experimental manipulation of browsing and water table, northern range of Yellowstone National Park
<p>This respository contains multiple datasets collected during a 20 year investigation of the responses of willow (<em>Salix </em>spp.) communities in Yellowstone National Park after the restoration of large carnivores. The study sought to understand whether the restoration of wolves to the food web cause a change in the state of willow communities that occured while wolves were absent. Each dataset has a corresonding file of metadata. </p>
Winter browsing by moose (Alces alces) in a forested mountainous landscape of West-Central Sweden
Open the record for dataset details and reuse information.
Twenty years of Salix height in response to experimental manipulation of browsing and water table, northern range of Yellowstone National Park
Open the record for dataset details and reuse information.
Effects of mammalian browsing on fine root processes and production in the floodplains of BCEF
The effects of browsing by moose and snowshoe hares on fine root production, mortality and decomposition in early successional forest ecosystems along the Tanana River floodplain in interior Alaska were studied over a 3 year period using minirhizotrons placed inside and outside large permanent exclosures. Fine root production and mortality varied seasonally, with greatest rates of production occurring during June each year, and greatest rates of mortality occurring in fall and over winter. Annual production and mortality during 1993, a year of unusually low precipitation, were significantly higher than during either 1992 or 1994. Aboveground herbivory significantly reduced monthly rates of fine root production, and on an annual basis, fine root production of browsed plots (311.4 - 31.7 mm tube-1 yr-1) was significantly less than that of unbrowsed plots (453.8-49.8 mm tube-1 yr-1) when averaged over 3 years. Because herbivory had less of an effect on monthly or annual rates of fine root mortality, fine root turnover was higher for browsed stands. Browsed plants had a higher percentage of annual production in surface soil layers. Production on all plots shifted to deeper soil layers as the growing season progressed; this shift occurred deeper in the profile for unbrowsed plants than for browsed plants. We used a parameter estimation program (Program MARK) to generate fine root survival and decomposition estimates from models testing the direct and interactive effects of time period, cohort, i.e., when the root first appeared, age of the root, browsing, and site on fine root longevity and decomposability. Cohort effects showed that survival of fine roots was greatest for roots that first appeared in May, and progressively declined for roots first appearing during subsequent time periods, while aged-based estimates showed a rapid decline in survival over the interval following first appearance. Survival and decomposition estimates were inversely correlated within a grow
Effects of vertebrate and invertebrate herbivory on plant cover in early successional habitat: Stem production and browsing on plants within experimental plots on the Tanana River 2012-2013
This dataset contains information on stem production and browsing on plants within experimental plots on the Tanana River. There are 6 permanent plots, each of which contains two fenced subplots and two unfenced subplots. Subplots are sprayed with either insecticide (insect-treated subplots) or water (controls) annually. This particular dataset contains the number and size of stems produced by Salix interior on unfenced study plots, and the number and size of stems browsed, during 2012-13.
Fine-scale habitat heterogeneity influences browsing damage by elephant and giraffe
Effects of large mammalian herbivores on woody vegetation tend to be heterogeneous in space and time, but the factors that drive such heterogeneity are poorly understood. We examined the influence of fine-scale habitat heterogeneity on the distribution and browsing effects of two of the largest African terrestrial mammals, the elephant and giraffe. We conducted this study within a 120-ha (500 x 2400 m) ForestGEO long-term vegetation monitoring plot located at Mpala Research Center, Kenya. The plot traverses three distinct topographic habitats ('plateau', 'steep slopes', and 'valley') with contrasting elevation, slope, soil properties, and vegetation composition. To quantify browsing damage, we focused on Acacia mellifera, a palatable tree species that occurs across the three habitat categories. Overall tree density, species richness, and diversity was highest on the steep slopes and lowest on the plateau. Acacia mellifera trees were tallest and had the lowest number of stems per tree on the steep slopes. Both elephant and giraffe avoided the steep slopes and their activity was higher during the wet season than during the dry season. Browsing damage on Acacia mellifera was lowest on the steep slopes. Elephant browsing damage was highest in the valley whereas giraffe browsing damage was highest on the plateau. Our findings suggest that fine-scale habitat heterogeneity is an important factor in predicting the distribution of large herbivores and their effects on vegetation and may interact with other drivers such as edaphic variations to influence local variation in vegetation structure and composition.
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.