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.
199
datasets available to search
ShareScore release 0.9.0
Dataset results
199 results for “Adaptive Systems”
Figure 3. Piercing-sucking mandibles. A–C in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 3. Piercing-sucking mandibles. A–C, Berosus patruelis Berg, 1885, first-instar larva, SEM micrograph: A, left mandible, ventral view; B, detail of mandibular teeth, ventral view; C, right mandible, dorsal view. D–F, Laccobius hammondi Gentili, 1984, third-instar larva, SEM micrograph, dorsal view: D, left mandible; E, detail of mandibular teeth; F, right mandible. G–I, Oocyclus iguazu (Oliva, 1996) third-instar larva, SEM micrograph, dorsal view; G, left mandible; H, detail of mandibular teeth; I, right mandible.
Figure 15 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 15. Phylogeny of the Hydrophiloidea with mapped evolution of tracheal system (A) and mouthparts (B, C). Two alternative ancestral state reconstructions of mouthparts, considering mouthparts of the Pelthydrus-group as: B, piercingsucking; C, chewing (only tribe Laccobiini shown). D, number of species of aquatic genera of Hydrophilidae with known larvae. Colors of branches/bars/pie-charts indicate functional morphology of mouthparts (red = piercing-sucking, blue = chewing, green = filter-feeding) and development of the tracheal system (grey = open; orange = closed).
Figure 6 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 6. Labroclypeal region of Hemiosus larvae. A, B, Hemiosus bruchi Knisch, 1924, third-instar larva, SEM micrograph, dorsal view: A, labroclypeus; B, left epistomal lobe. C–E, Hemiosus multimaculatus (Jensen-Haarup, 1910), third-instar larva, dorsal view: C, left epistomal lobe, SEM micrograph; D, detail of gFR2 serrated setae, SEM micrograph; E, left epistomal lobe, light microscope photograph. Abbreviations: EpLb, epistomal lobe; NS, nasale. Colours: light blue, frontoclypeal region; green, gFR1, group of sensilla of nasale; violet, gFR2, group of sensilla of epistomal lobe.
Figure 5 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 5. Labroclypeal region of larvae with chewing feeding system, SEM micrograph, dorsal view. A, Tropisternus acaragua Bachmann, 1969, first-instar larva. B, Hydrochara caraboides (Linnaeus, 1758), first-instar larva. C, Hydrophilus (Dibolocelus) palpalis Brullé, 1837, second-instar larva. D, Derallus paranensis Oliva, 1981, first instar larva. E, Helochares ventricosus Bruch, 1915, first-instar larva. F, Hydroglobus puncticolle Bruch, 1915, third-instar larva. G, Dactylosternum cacti (LeConte, 1855), third-instar larva. H, Cercyon quisquilius (Linnaeus, 1761), third-instar larva, white arrow indicates labroclypeal notch. Colours: light blue, frontoclypeal region; green, gFR1, group of sensilla of nasale; violet, gFR2, group of sensilla of epistomal lobe.
Figure 2 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 2. Chewing mandibles, SEM micrograph, dorsal view. A, Derallus sp., first-instar larva. B, Enochrus sp., firstinstar larva. C, Tropisternus sp., second-instar larva. D, Hydrophilus (Dibolocelus) palpalis Brullé, 1837, first-instar larva. E, Dactylosternum cacti (LeConte, 1855), third-instar larva. F, Cercyon quisquilius (Linnaeus, 1761), third-instar larva. Abbreviations: rc1, first retinaculum; rc2, second retinaculum; rc3, third retinaculum.
Figure 12 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 12. Schematic drawing of the piercing-sucking feeding mechanism: 1, sucking channel; 2, epistomal-mandibular coupling system; 3, flexible area.
Figure 11 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 11. Summary of the main structures related with piercing-sucking feeding mechanism, SEM micrograph. A, B, Berosus sp., third-instar larva: A, lobular-mandibular coupling system, dorsal view; B, detail of lobular-mandibular coupling system, ventral view. C, Laccobius (Microlaccobius) sp., third-instar larva, left epistomal lobe, dorsal view.
Figure 9 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 9. Labium of larvae with chewing (A–B) and piercing-sucking (C–D) feeding system, dorsal view. A, Enochrus sp., first-instar larva, SEM micrograph. B, Derallus sp., first-instar larva, SEM micrograph. C, Berosus sp., third-instar larva, SEM micrograph. D, Oocyclus sapphirus Short & García, 2010, first-instar larva, light microscope photograph.
Figure 14 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 14. Summary of the main structures related with apneustic respiratory system. A–C, Berosus decolor Knisch, 1924, light microscope photograph: A, habitus, first-instar larva, dorsal view; B; terminal spiracle, third-instar larva, dorsal view; C; detail of the abdominal spiracular trachea and tracheal gill, dorsal view. D, Berosus pallipes Brullé, 1841, abdominal spiracle, third-instar larva, dorsal view. E–H, Berosus sp., third-instar larva, SEM micrograph: E, spiracular chamber, ventral view; F; first abdominal segment bearing tracheal gill, dorsal view; G, detail of tracheal gill surface; H, abdominal spiracle. I, J, Hemiosus bruchi Knisch, 1924, third-instar larva, SEM micrograph: I, last abdominal segments, dorsal view; J, abdominal spiracle. K, Hemiosus multimaculatus (Jensen-Haarup, 1910), spiracular chamber, third-instar larva, ventral view.
Figure 13 in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 13. Summary of the main structures related with metapneustic respiratory system. A, Tropisternus latus (Brullé, 1837), spiracular chamber, first-instar larva, light microscope photograph, dorsal view. B, Helochares ventricosus Bruch, 1915, spiracular chamber, first-instar larva, light microscope photograph, dorsal view. C, Tropisternus latus (Brullé, 1837), spiracular chamber, first-instar larva, light microscope photograph, dorsal view. D, Helochares ventricosus Bruch, 1915, abdominal spiracle, first-instar larva, light microscope photograph, dorsal view. E–H, Tropisternus setiger Germar, 1824, SEM micrograph: E, spiracular chamber, third-instar larva, ventral view; F, detail of the terminal spiracle with dust filter, third-instar larva, ventral view; G, abdominal spiracle, first-instar larva, dorsal view; H, detail of the closed abdominal spiracles, first-instar larva, dorsal view. I, J, Oocyclus iguazu (Oliva 1996) third-instar larva, SEM micrograph: I, spiracular chamber, dorsal view; J, biforous abdominal spiracle, dorsal view. K, Laccobius kunashiricus Shatrovskiy, 1984, spiracular chamber, third-instar larva, SEM micrograph, dorsal view.
Figure 8. Labroclypeal region. A, B in REVIEW Going underwater: multiple origins and functional morphology of piercing-sucking feeding and tracheal system adaptations in water scavenger beetle larvae (Coleoptera: Hydrophiloidea)
Figure 8. Labroclypeal region. A, B, Hybogralius hartmeyeri (Régimbart, 1908), third-instar larva, light microscope photographs, dorsal view: A, labroclypeus; B, left epistomal lobe. C, D, Epimetopus mendeli Fikáček et al. 2011, first-instar larva, SEM micrograph, dorsal view: C, labroclypeus; D, right epistomal lobe. Abbreviations: EpLb, epistomal lobe; NS, nasale. Colours: light blue, frontoclypeal region; green, gFR1, group of sensilla of nasale; violet, gFR2, group of sensilla of epistomal lobe.
Microsatellites data set: Correlated population genetic structure in a three-tiered host-parasite system: the potential for coevolution and adaptive divergence
<p><span><span><span><span><span><span><span><span><span><span><span>Three subspecies of Northern Bahamian Rock Iguanas, <i>Cyclura cychlura</i>, are currently recognized: <i>C. c. cychlura,</i>restricted to Andros Island, and <i>C. c. figginsi</i> and <i>C. c. inornata,</i> native to the Exuma Island chain. Populations on Andros are genetically distinct from Exuma Island populations, yet genetic divergence among populations in the Exumas is inconsistent with the two currently recognized subspecies from those islands. The potential consequences of this discrepancy might include the recognition of a single subspecies throughout the Exumas rather than two. That inference also ignores evidence that populations of <i>C. cychlura</i> are potentially adaptively divergent. We compared patterns of population relatedness in a three-tiered host-parasite system: <i>C. cychlura</i> iguanas, their ticks (genus <i>Amblyomma</i>, preferentially parasitizing these reptiles), and <i>Rickettsia </i>spp. endosymbionts (within tick ectoparasites). Our results indicate that while <i>C. c. cychlura</i> on Andros is consistently supported as a separate clade, patterns of relatedness among populations of <i>C. c. figginsi</i> and <i>C. c. inornata</i> within the Exuma Island chain are more complex. The distribution of the hosts, different tick species, and <i>Rickettsia</i> spp., supports the evolutionary independence of <i>C. c. inornata</i>. Further, these patterns are also consistent with two independent evolutionarily significant units within <i>C. c. figginsi</i>. Our findings suggest coevolutionary relationships between the reptile hosts, their ectoparasites, and rickettsial organisms, suggesting local adaptation. This work also speaks to the limitations of using neutral molecular markers from a single focal taxon as the sole currency for recognizing evolutionary novelty in populations of endangered species.</span></span></span></span></span></span></span></span></span></span></span></p>
Supplementary Video for Hierarchical Vision Navigation System for Quadruped Robots with Foothold Adaptation Learning
<p>This file contains video of the real world experiments presented in the paper "Hierarchical Vision Navigation System for Quadruped Robots with Foothold Adaptation Learning". </p> <p>It also provides a high-level overview of the motivation and the theory developed in the paper.<br> </p>
Tocchini and Mango_An adapted MS2-MCP system to visualize endogenous cytoplasmic mRNA with live imaging in Caenorhabditis elegans_Table S1_Raw data
<p><strong>Table S1. Raw data.</strong> List of quantitation of GFP intensities of heads (<em>spc-1</em>) or pharynges (<em>dlg-1</em>) in the different figures.</p>
Dataset accompanying the submission titled "Adaptive covariance hybridization for the assimilation of SST observations within a coupled Earth system reanalysis"
<p>The dataset contains the data accompanying our submission entitled "Adaptive covariance hybridization for the assimilation of SST observations within a coupled Earth system reanalysis". It contains:</p> <ol> <li>The yearly outputs of the free run</li> <li>The observations</li> <li>The yearly outputs of the runs of the standard hybrid</li> <li>The yearly outputs of the runs of the adaptive hybrid</li> <li>The grid of the model</li> <li>The maps of the hybridization coefficients</li> <li>The python and matlab scripts used to plot the figures of the article</li> </ol>
Adaptive Restraints to Accelerate Geometry Optimizations of Large Biomolecular Systems
<p>Supplementary Dataset for above-titled manuscript. Contains input files and representative final structures for tested GFP system, diaspartic acid system, and mNeonGreen system.</p>
Data for the manuscript: Enabling Climate Change Adaptation in Coastal Systems. A Systematic Literature Review
<p>This dataset includes the list of publications, framework and dataset used for the paper "Enabling Climate Change Adaptation in Coastal Systems. A Systematic Literature Review"</p>
TEM dataset for "Simultaneous entry as an adaptation to virulence in a novel satellite-helper system infecting Streptomyces species"
<p>Dataset of thirteen transmission electron micrographs of the Flayer satellite-helper phage system. Images of MindFlayer helper virions with MiniFlayer satellite attachment were taken on a Morgagni M268 Transmission Electron Microscope and used for morphological measurements. </p>
Data for "Early planting adaptation makes the coupled food-water system more sustainable under climate change"
<p>Data for submission "Early planting adaptation makes the coupled food-water system more sustainable under climate change"</p><p>All data are in netcdf format and can be read in ncl, python, R code capacity.</p><p> </p><p><strong>geo_em.d01.conus.corn:</strong></p><p>Domain setup file for the Noah-MP crop model in the US corn belt. Lat/lon location specified by "XLAT_<i>M" and "XLONG_M</i>" variable and corn planting area specified by "CROPTYPE" variable.</p><p> </p><p>Three zip files are uploaded containing data from model simulations and county-level yield and irrigation record:</p><p><strong>Yield_data.zip:</strong></p><p>yield data from model simulations (denoted by three scenarios, CTRL, PGW, TAVE), with irrigation (irr), and from USDA NASS (NASS).</p><p><strong>Irrigation_data.zip:</strong></p><p>Irrigation amount data from three scenarios (CTRL, PGW, TAVE for early planting), and from USGS water use record (2005 and 2010).</p><p><strong>TempPrecPET.zip:</strong></p><p>temperature and precipitation and potential evapotranspiration data (PET) for the CTRL and PGW climate scenarios. </p>
EPstein-barr Virus DNA Response to Systemic Therapy for Treatment Adaptation in High Risk NPC (EP-STAR)
ClinicalTrials.gov study NCT04072107. IPD Sharing: NO. Countries: 1. Publications: 0.
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.