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12,346 results for “derivatives”

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zenodo40/100

Occurrence data on brominated phenols and their derivatives provided to EFSA

<p><span>The file contains the raw occurrence dataset on brominated phenols and their derivatives in food as extracted from EFSA DWH on 1 of December 2022&nbsp;and presented in the EFSA opinion on the update of the risk assessment of brominated phenols and their derivatives in food. This dataset is compliant with EFSA SSD2 data model and contains two additional columns documenting issues identified in the cleaning process (column: issue) and the outcome of the action taken (column: outcome) to address the issue (e.g. delete record or update values in specific fields). The link to the catalogues of controlled terminologies for the updated textual description of fields values can be found under "Related works, supplemented by&rdquo;.</span></p>

opencc-by-4.0Oct 2024View details →
zenodo40/100

A Submesoscale Eddy Identification Dataset Derived from GOCI I Chlorophyll–a Data based on Deep Learning

<p>This is an observational dataset on submesoscale eddies, which obtains from high&ndash;resolution chlorophyll&ndash;a distribution images from GOCI I. We employed a combination of digital image processing, filtering, YOLOv7&ndash;X, and small object detection techniques, along with specific chlorophyll image enhancement processing, to extract information on submesoscale eddies, including their time, polarity, geographical coordinates of the eddy center, eddy radius, coordinates of the upper left and lower right corners of the prediction box, area of the eddy's inner ellipse, and confidence score, which covers eight daily periods between 00:00 and 08:00 (UTC) from April 1, 2011, to March 31, 2021. We identified a total of 19,136 anticyclonic eddies and 93,897 cyclonic eddies at a confidence threshold of 0.2. The mean radius of anticyclonic eddies is 24.44 km (range 2.5 km to 44.25 km), while that of cyclonic eddies is 12.34 km (range 1.75 km to 44 km). The unprecedented hourly resolution dataset on submesoscale eddies provides information on their distribution, morphology, and energy dissipation, making it a significant contribution to understanding marine environments and ecosystems, as well as improving climate model predictions. The article doi associated with this dataset is https://doi.org/10.5194/essd-2024-188.</p>

opencc-by-4.0Mar 2023View details →
zenodo40/100

Dinitrogen Reduction and Functionalization by a Siloxide Supported Thulium-Potassium Complex for the Formation of Ammonia or Hydrazine Derivatives

<p>The dinitrogen (N2) chemistry of lanthanides remainsless developed compared to the d-block metals and lanthanide-promoted N2 functionalization chemistry in well-defined lanthanidecomplexes remains elusive. Here we report the synthesis andcharacterization (SQUID, EPR, DFT, X-Ray) of the siloxidesupported heterobimetallic (Tm/K) complexes[{KTm(OSi(OtBu)3)3}2(&mu;-&eta;2:&eta;2-N2)] (1) and [K3{Tm(OSi(OtBu)3)3}2(&mu;-&eta;2:&eta;2-N2)] (2). Complex 2 provides a rare example of a metalcomplex of the triply reduced N23- radical. The structure of 2 differsfrom the few previously reported N23- complexes as it presents twoTm and three K cations binding the N23- radical, facilitating N2functionalization. Notably, the K3Tm2-bound N23- moiety reacts withexcess H+ to form NH4Cl in 18% yield, and with MeOTf at roomtemperature to yield the dimethyl hydrazido complex[K2{Tm(OSi(OtBu)3)3}2(&mu;-(CH3)NN(CH3))] (3). Protonolysis of 3yields MeHN-NMeH&middot;2HCl in 18 % yield.</p>

opencc-by-4.0Oct 2024View details →
zenodo40/100

The first 10-m China's national-scale sandy beach map in 2022 derived from Sentinel-2 imagery

<p>This is the first 10-meter national scale beach map dataset of China. Based on the cloudless Sentinel-2 images for the whole year of 2022, we use the image classification method to draw a 10-meter beach map of China. The projection coordinate system of this data is WGS_1984_UTM_Zone_51N and the geographic coordinate system is GCS_WGS_1984.<br>The "Shape_Leng" field in the data set represents the circumference of the beach, the "Shape_Area" field represents the area of the beach, and the "Province" field represents the province of each independent beach.</p>

opencc-by-4.0Nov 2024View details →
zenodo40/100

Conformance Assessment of Architectural Design Decisions on API Endpoint Designs Derived from Domain Models: Dataset and Code

<p>This is the dataset and related code artifact for the article &quot;Conformance Assessment of Architectural Design Decisions on API Endpoint Designs Derived from Domain Models&quot;.</p> <p><strong>Abstract of the article:</strong></p> <p>Domain-driven design (DDD) is commonly used, especially in enterprise systems, to design microservices. A crucial aspects of microservice design is API design, which includes the design of API endpoints. In particular, we studied link mapping, API operation design, and resource segregation as &nbsp;API endpoint design issues that are linked to domain model design. Based on Architectural Design Decisions (ADD) studied in a prior empirical study on the interrelation of DDD and APIs, we suggest a new approach for the automated assessment of conformance to ADD options. This approach aims to support the continuous analysis of API endpoint designs. The approach suggests automated detectors to detect ADD options selected in a given API endpoint design, as well as an assessment scoring scheme based on our empirical results. For evaluation of our results, we first manually created a ground truth for 12 cases in a multi-case study, and then compared the results of our automated detectors to the ground truth for each of those cases.</p>

opencc-by-4.0Jun 2021View details →
dryad40/100

Functional beta diversity of New Zealand fishes: characterising morphological turnover along depth and latitude gradients, with derivation of functional bioregions

<p>Changes in the functional structures of communities are rarely examined along multiple large-scale environmental gradients. Here, we describe patterns in functional beta diversity for New Zealand marine fishes <i>vs</i> depth and latitude, including broad-scale delineation of functional bioregions. We derived eight functional traits related to food acquisition and locomotion and calculated complementary indices of functional beta diversity for 144 species of marine ray-finned fishes occurring along large-scale depth (50 - 1200 m) and latitudinal gradients (29° - 51° S) in the New Zealand Exclusive Economic Zone. We focused on a suite of morphological traits calculated directly from <i>in situ</i> Baited Remote Underwater Stereo-Video (stereo-BRUV) footage and museum specimens. We found that functional changes were primarily structured by depth followed by latitude, and that latitudinal functional turnover decreased with increasing depth. Functional turnover among cells increased with increasing depth distance, but this relationship plateaued for greater depth distances (&gt; 750 m). In contrast, functional turnover did not change significantly with increasing latitudinal distance at 700 - 1200 m depths. Shallow functional bioregions (50 - 100 m) were distinct at different latitudes, whereas deeper bioregions extended across broad latitudinal ranges. Fishes in shallow depths had a body shape conducive to efficient propulsion, while fishes in deeper depths were more elongated, enabling slow, energy-efficient locomotion, and had large eyes to enhance vision. Environmental filtering may be a primary driver of broad-scale patterns of functional beta diversity in the deep sea. Greater environmental homogeneity may lead to greater functional homogeneity across latitudinal gradients at deeper depths (700 - 1200 m). We suggest that communities living at depth may follow a 'functional village hypothesis', whereby similar key functional niches in fish communities may be maintained over large spatial scales.</p>

opencc-zeroJun 2021View details →
zenodo40/100

Using GECKO-A to derive mechanistic understanding of SOA formation from the ubiquitous but understudied camphene

<p>This data repository contains the simulation outputs of GECKO-A model used in the manuscript:&nbsp;<br> &quot;Using GECKO-A to derive mechanistic understanding of secondary organic aerosol formation from the ubiquitous but understudied camphene&quot;<br> by Afreh et al., 2021 in ACP</p> <p>The original ACP article should be properly cited when these data are used in a publication.</p>

opencc-by-4.0Jul 2021View details →
zenodo40/100

Advanced Glycation End-products are Retained in Decellularized Muscle Matrix Derived from Aged Skeletal Muscle

<p>Advanced glycation end-products (AGEs) accrue on skeletal muscle collagen in old age, stiffening the matrix and increasing inflammation. Whether decellularized biomaterials derived from aged muscle would suffer from increased AGE cross-links is unknown. We hypothesized that DMM from old muscle would have increased collagen, collagen cross-linking, stiffness, and AGEs. We isolated, decellularized, and characterized gastrocnemii of 1-month, 2-month, and 20-month old C57BlJ6 mice to determine age-dependent changes to collagen in muscle and decellularized muscle matrix (DMM). Total hydroxyproline and soluble hydroxyproline after proteinase K digestion were measured to assay collagen levels and cross-linking, respectively. Muscle fiber and DMM stiffness was determined using atomic force microscopy (AFM).&nbsp; AGE ELISAs were used to test AGE levels, and the effect of AGE cross-link breaker ALT-711 on DMM was tested. We determined age-dependent increases in collagen amount, cross-linking, and general stiffness are retained on DMM. DMM from old muscle was stiffer compared to younger groups according to shifts in AFM modulus distribution. We measured an increase in AGE-specific cross-links with old age in whole muscle and observed that these changes are countered in DMM by AGE cross-link breaker ALT-711. Future study investigating and countering the biological effects of old age on DMM is warranted.</p>

opencc-by-4.0Jun 2021View details →
zenodo40/100

Figure 6. A Bayesian consensus tree derived from 4,001 in A Heron (Aves: Ardeidae) from the Early Miocene St Bathans Fauna of Southern New Zealand

Figure 6. A Bayesian consensus tree derived from 4,001 trees sampled: Run 1 (mean = –546.302, s.d. = 0.099, Effective Sample Size = 3208.424); Run 2 (–546.223, 0.113, 2388.97). Support values are shown above the corresponding node.

opencc-by-4.0May 2010View details →
zenodo40/100

Global dataset of co-incident TLS-derived and harvested tree biomass

<p>This dataset was used to producee the figures and statistics of the publication &quot;Estimating forest aboveground biomass with terrestrial laser scanning: current status and future directions&quot;.</p> <p>This dataset contains 391 entries. Each entry is a tree that was terrestrial laser scanned and consecutively harvested to assess its aboveground biomass (AGB). AGB was also obtained from allometric scaling equations. Several ancillary tree properties such as stem diameter, foliage conditions,... and scan metadata (type of scanner, pattern) are included. We refer to the tab &#39;headers&#39; for an explanation and units of the respective columns. Elaborate method descriptions can be found in the publication or in the following original publications:</p> <ul> <li>Burt, A., Boni Vicari, M., da Costa, A. C. L., Coughlin, I., Meir, P., Rowland, L., et al. (2021). New insights into large tropical tree mass and structure from direct harvest and terrestrial lidar. Royal Society Open Science 8, 201458. doi:10.1098/rsos.201458</li> <li>Calders, K., Newnham, G., Burt, A., Murphy, S., Raumonen, P., Herold, M., et al. (2015). Nondestructive estimates of above-ground biomass using terrestrial laser scanning. Methods in Ecology and Evolution 6, 198&ndash;208. doi:10.1111/2041-210X.12301</li> <li>Demol, M., Calders, K., Krishna Moorthy, S. M., Van den Bulcke, J., Verbeeck, H., and Gielen, B. (2021). Consequences of vertical basic wood density variation on the estimation of aboveground biomass with terrestrial laser scanning. Trees 35, 671&ndash;684. doi:10.1007/s00468-020-02067-7</li> <li>Gonzalez de Tanago, J., Lau, A., Bartholomeus, H., Herold, M., Avitabile, V., Raumonen, P., et al. (2018). Estimation of above-ground biomass of large tropical trees with terrestrial LiDAR. Methods in Ecology and Evolution 9, 223&ndash;234. doi:10.1111/2041-210X.12904</li> <li>Hackenberg, J., Wassenberg, M., Spiecker, H., and Sun, D. (2015). Non destructive method for biomass prediction combining TLS derived tree volume and wood density. Forests 6, 1274&ndash;1300. doi:10.3390/ f6041274</li> <li>K&uuml;kenbrink, D., Gardi, O., Morsdorf, F., Th&uuml;rig, E., Schellenberger, A., and Mathys, L. (2021). Aboveground biomass references for urban trees from terrestrial laser scanning data. Annals of Botany, 1&ndash;16doi:10.1093/aob/mcab002</li> <li>Lau, A., Calders, K., Bartholomeus, H., Martius, C., Raumonen, P., Herold, M., et al. (2019). Tree Biomass Equations from Terrestrial LiDAR: A Case Study in Guyana. Forests 10, 527. doi:10.3390/f10060527</li> <li>Momo Takoudjou, S., Ploton, P., Sonke, B., Hackenberg, J., Griffon, S., Coligny, F., et al. (2018). Using terrestrial laser scanning data to estimate large tropical trees biomass and calibrate allometric models: A comparison with traditional destructive approach. Methods in Ecology and Evolution 9, 905&ndash;916.<br> &nbsp;doi:10.1111/2041-210X.12933</li> <li>Stovall, A. E., Vorster, A. G., Anderson, R. S., Evangelista, P. H., and Shugart, H. H. (2017). Non-destructive aboveground biomass estimation of coniferous trees using terrestrial LiDAR. Remote Sensing of Environment 200, 31&ndash;42. doi:10.1016/j.rse.2017.08.013<br> &nbsp;</li> </ul> <p><br> &nbsp;</p>

opencc-by-4.0Dec 2020View details →
zenodo40/100

FIG. 5 in A highly derived docodont from the Patagonian Late Cretaceous: evolutionary implications for Gondwanan mammals

FIG. 5. — Molar evolution and cusp homologies in lower right molars of morganucodontids, docodontids, and reigitheriids. Posterior (left) and occlusal (right) views (anterior to the left; lingual below); A, Morganucodon; B, hypothetical Early or Middle Jurassic docodont; C, Docodon from the Late Jurassic Morrison Formation; D, hypothetical Late Jurassic or Early Cretaceous reigitheriid; E, Reigitherium bunodontum from the Campanian-?Maastrichtian La Colonia Formation, Patagonia. In the occlusal views (right), anteri- or is to the right, and lingual face is toward the bottom of the page. Abbreviations: "a", cusp a; a.a.l.c., anterior additional lower cusp; "c", cusp c; cr, crenelation; i.a.l.c., intermedium additional lower cusp; m.i.c.c., main internal cungulum cusp; p.c.c., posteri- or cingulum cusp; p.i.c.c., postero-internal cingulum cusp; p.a.l.c., posterior additional lower cusp; prd, protoconid; s, sulcus. Cusps nomenclature follows Jenkins (1969), except a.a.l.c., i.a.l.c. and p.a.l.c., that are new cusps and only known in Reigitherium bonodontum. Drawings are not to scale.

opencc-zeroDec 2000View details →
zenodo40/100

FIG. 3 in A highly derived docodont from the Patagonian Late Cretaceous: evolutionary implications for Gondwanan mammals

FIG. 3. — Reigitherium bunodontum Bonaparte, 1996, specimen MEF 606; SEM stereopairs in occlusal view. Scale bar: 1 mm.

opencc-zeroDec 2000View details →
zenodo40/100

FIG. 4 in A highly derived docodont from the Patagonian Late Cretaceous: evolutionary implications for Gondwanan mammals

FIG. 4.— Left pm4-m2 series of specimen MEF 606 of Reigitherium bunodontum Bonaparte, 1990; A, external view; B, internal view; C, occlusal view. Abbreviations: c, crenulations; s, sculus. Scale bar: 2 mm.

opencc-zeroDec 2000View details →
zenodo40/100

FIG. 1 in A highly derived docodont from the Patagonian Late Cretaceous: evolutionary implications for Gondwanan mammals

FIG. 1. — Generalized stratigraphic section of La Colonia Formation in Arroyo Mirasol Chico creek, Bajada Moreno area, Chubut Province, Argentina.

opencc-zeroDec 2000View details →
zenodo40/100

FIG. 2 in A highly derived docodont from the Patagonian Late Cretaceous: evolutionary implications for Gondwanan mammals

FIG. 2.— Reigitherium bunodontum Bonaparte, 1996, specimen MEF 606; A, B, fragment of left dentary with pm4-m2; A, external view; B, internal view; C, posterior view of the dentary section behind the m2; D, occlusal view of pm4-m2; E, posterior view of m2. Abbreviations: c, crenulations; s, sculus. Scale bars: 1 mm.

opencc-zeroDec 2000View details →
zenodo40/100

Text-fig. 10. Dorsal view of endocranium of a ca. 53 mm Tachyglossus aculeatus. Derivatives of the teniform cartilages blue. con: orbitonasal commissure; tn: tectum nasi. (Modified from Kuhn 1971.) in Cartilago Teniformis And Its Derivatives: Additional Information On The Basic Composition And Evolution Of The Skull

Text-fig. 10. Dorsal view of endocranium of a ca. 53 mm Tachyglossus aculeatus. Derivatives of the teniform cartilages blue. con: orbitonasal commissure; tn: tectum nasi. (Modified from Kuhn 1971.)

opencc-by-4.0Aug 2016View details →
zenodo40/100

Text-fig. 9. Tachyglossus aculeatus. Transverse section through the orbital region of the head of a juvenile specimen. ms: sphenobturatory membrane; plb: palatine bone; psw: primary endocranial sidewall; sll: secondary lateral lamella of Kuhn (1971); this endocranial process (blue) is here interpreted as a derivative of the cartilago teniformis. (From Kuhn and Zeller 1987.) in Cartilago Teniformis And Its Derivatives: Additional Information On The Basic Composition And Evolution Of The Skull

Text-fig. 9. Tachyglossus aculeatus. Transverse section through the orbital region of the head of a juvenile specimen. ms: sphenobturatory membrane; plb: palatine bone; psw: primary endocranial sidewall; sll: secondary lateral lamella of Kuhn (1971); this endocranial process (blue) is here interpreted as a derivative of the cartilago teniformis. (From Kuhn and Zeller 1987.)

opencc-by-4.0Aug 2016View details →
zenodo40/100

Text-fig. 7. Tachyglossus aculeatus. Ventrolateral view of the head endoskeleton of a specimen shortly after it had left the pouch. fp: foramen prooticum; lpc: limbus praecapsularis (blue); ls: supracapsular lamina. (Modified from Gaupp 1913.) in Cartilago Teniformis And Its Derivatives: Additional Information On The Basic Composition And Evolution Of The Skull

Text-fig. 7. Tachyglossus aculeatus. Ventrolateral view of the head endoskeleton of a specimen shortly after it had left the pouch. fp: foramen prooticum; lpc: limbus praecapsularis (blue); ls: supracapsular lamina. (Modified from Gaupp 1913.)

opencc-by-4.0Aug 2016View details →
zenodo40/100

Text-fig. 6. Ornithorhynchus anatinus. Transverse section through the otic region of the head of a 180-mm specimen. ls: supracapsular lamina; lsc: lateral semicircular canal; mt: musculus temporalis; opa: parietal bone; opl: pluteal bone; ppe: parietal process of endocranium (blue). (Modified from Zeller 1989.) in Cartilago Teniformis And Its Derivatives: Additional Information On The Basic Composition And Evolution Of The Skull

Text-fig. 6. Ornithorhynchus anatinus. Transverse section through the otic region of the head of a 180-mm specimen. ls: supracapsular lamina; lsc: lateral semicircular canal; mt: musculus temporalis; opa: parietal bone; opl: pluteal bone; ppe: parietal process of endocranium (blue). (Modified from Zeller 1989.)

opencc-by-4.0Aug 2016View details →
zenodo40/100

Text-fig. 8. Tachyglossus aculeatus. Transverse section through the temporal region of the adult head. Membranous parts blue, autostoses brown and allostoses purple. gg: ganglion gasseri; lop: lamina obturatoria periotici; ms: sphenobturatory membrane; mt: musculus temporalis; oo: os obturans; opa: parietal bone. (Modified from Kuhn and Zeller 1987.) in Cartilago Teniformis And Its Derivatives: Additional Information On The Basic Composition And Evolution Of The Skull

Text-fig. 8. Tachyglossus aculeatus. Transverse section through the temporal region of the adult head. Membranous parts blue, autostoses brown and allostoses purple. gg: ganglion gasseri; lop: lamina obturatoria periotici; ms: sphenobturatory membrane; mt: musculus temporalis; oo: os obturans; opa: parietal bone. (Modified from Kuhn and Zeller 1987.)

opencc-by-4.0Aug 2016View details →

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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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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