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Figure 9 in Description of two new species of Neotachidius Shen & Tai, 1963 (Copepoda, Harpacticoida, Tachidiidae) from Korean brackish waters and proposal of a new genus for Tachidius (Tachidius) vicinospinalis Shen & Tai, 1964
Figure 9. Neotachidius coreanus sp. nov. (♀) A, maxilla (insets showing armature of syncoxal endites; endopod disarticulated); B, P4, anterior; C, P5-bearing and genital double-somite, lateral (P5 omitted).
Figure 5 in Description of two new species of Neotachidius Shen & Tai, 1963 (Copepoda, Harpacticoida, Tachidiidae) from Korean brackish waters and proposal of a new genus for Tachidius (Tachidius) vicinospinalis Shen & Tai, 1964
Figure 5. SEM micrographs. Neotachidius coreanus sp. nov. (♀) A, rostrum, frontal; B, maxillary endopod, posterior; C, oral area (L., labrum; P., paragnath); E, endopod of maxilliped, showing vestigial setation elements. N. parvus sp. nov. (♀) D, mandibular palp (spinular row on anterior surface of endopod arrowed).
Figure 7 in Description of two new species of Neotachidius Shen & Tai, 1963 (Copepoda, Harpacticoida, Tachidiidae) from Korean brackish waters and proposal of a new genus for Tachidius (Tachidius) vicinospinalis Shen & Tai, 1964
Figure 7. Neotachidius coreanus sp. nov. A, P2 ♀, anterior; B, P2 endopod ♂, anterior; C, detail of P2 enp-3 ♂, anterior; D, P5 ♀, anterior.
Figure 6 in Description of two new species of Neotachidius Shen & Tai, 1963 (Copepoda, Harpacticoida, Tachidiidae) from Korean brackish waters and proposal of a new genus for Tachidius (Tachidius) vicinospinalis Shen & Tai, 1964
Figure 6. Neotachidius coreanus sp. nov. A, P1 ♀, anterior; B, maxillule ♀, anterior (endopod disarticulated); C, praecoxal arthrite of maxillule ♀, posterior; D, urosome ♂, lateral.
Figure 4 in Description of two new species of Neotachidius Shen & Tai, 1963 (Copepoda, Harpacticoida, Tachidiidae) from Korean brackish waters and proposal of a new genus for Tachidius (Tachidius) vicinospinalis Shen & Tai, 1964
Figure 4. Neotachidius coreanus sp. nov. (♀) A, antennule, dorsal; B, rostrum, dorsal; C, antenna, outer lateral; D, free endopodal margin of antenna, inner lateral; E, maxilliped.
Figure 3 in Description of two new species of Neotachidius Shen & Tai, 1963 (Copepoda, Harpacticoida, Tachidiidae) from Korean brackish waters and proposal of a new genus for Tachidius (Tachidius) vicinospinalis Shen & Tai, 1964
Figure 3. Neotachidius coreanus sp. nov. (♀) A, habitus, lateral (arrow indicating rudimentary tergite of P1-bearing somite); B, detail of area between cephalosome and P2-bearing somite, lateral (tergite of P1-bearing somite arrowed); C, mandible, anterior; D, detail of mandibular gnathobase.
Figure 2 in Description of two new species of Neotachidius Shen & Tai, 1963 (Copepoda, Harpacticoida, Tachidiidae) from Korean brackish waters and proposal of a new genus for Tachidius (Tachidius) vicinospinalis Shen & Tai, 1964
Figure 2. Neotachidius coreanus sp. nov. (♀) SEM micrographs: A, prosome, dorsal (arrow indicating rudimentary tergite of P1-bearing somite); B, area between cephalosome and P2-bearing somite, showing position of intersomitic membrane and rudimentary tergite of P1-bearing somite; C, genital field, ventral (inset c: pore anterior to genital slit, arrowed).
Figure 1 in Description of two new species of Neotachidius Shen & Tai, 1963 (Copepoda, Harpacticoida, Tachidiidae) from Korean brackish waters and proposal of a new genus for Tachidius (Tachidius) vicinospinalis Shen & Tai, 1964
Figure 1. Neotachidius coreanus sp. nov. (♀). A, habitus, dorsal; B, urosome (excluding P5-bearing somite), ventral.
Fig. 1. A in Reinstatement of the Lancelet Name Asymmetron lucayanum, Recently Proposed as a Junior Synonym of Branchiostoma pelagicum (Cephalochordata)
Fig. 1. A: Holotype of Branchiostoma pelagicum, 10 mm long, reproduced from Günther (1889, pl. V, fig. B); B: A preserved 6 mm-long larva of Asymmetron lucayanum collected from the Bahamas, reproduced from Andrews (1893, pl. XIII, fig. 5), laterally inverted for comparison with A. Arrow indicates urostyloid process.
Fig. 3 in The First Record of a Species of Clausiidae (Copepoda: Cyclopoida) from Japanese Waters, with the Proposal of a New Genus
Fig. 3. Coloration of live specimen of Oshoroclausia shibazakii n. g. n. sp., holotype, adult female, NSMT–Cr 24117. A, habitus straight, dorsal; B, habitus curved, ventrolateral. Scale bar: 500 µm.
Fig. 1. Oshoroclausia shibazakii n. g. n in The First Record of a Species of Clausiidae (Copepoda: Cyclopoida) from Japanese Waters, with the Proposal of a New Genus
Fig. 1. Oshoroclausia shibazakii n. g. n. sp., holotype, adult female, NSMT–Cr 24117. A, habitus, dorsal; B, habitus, lateral; C, anterior part of cephalothorax, dorsal; D, anterior part of cephalothorax, ventral; E, left caudal ramus, ventral; F, left antennule, anterior; G, right antenna, anterior; H, terminal segment of right antenna, posterior; I, distal part of right antenna, posterior. Scale bars: A, B, 1000 µm; C, 100 µm; D–F, 50 µm; G, 30 µm; H, 20 µm; I, 10 µm.
Figure 4 Arcochthonius roynortoni n in A new species of Brachychthoniidae (Acari: Oribatida) from the Eastern Central Alps (Austria, Tyrol), with the proposal of a new genus
Figure 4 Arcochthonius roynortoni n. sp. adult: ventral view. A – subcapitulum. B – right chelicera, antiaxial view. C – right palp, antiaxial view. D – frontal view. Arrow indicates scale with possible internal ocellus (see remark #2). E – variations of frontal rostral apex. F – posterior view. Scale bar 1 Figs A, B, C 20 µm. Scale bar 2 Figs D, E, F 50 µm.
Figure 2 Arcochthonius roynortoni n in A new species of Brachychthoniidae (Acari: Oribatida) from the Eastern Central Alps (Austria, Tyrol), with the proposal of a new genus
Figure 2 Arcochthonius roynortoni n. sp. adult: ventral view (lyrifissures and legs not shown). Scale bar 50 µm.
Databases of one-way slabs under concentrated loads: parameter analyses and validation of the proposed approach
<p>This database includes information about loading, geometry, failure loads, and failure modes of slabs under concentrated loads under different support conditions. Different datasets were organized for (i) identifying the relation between specific parameters on the governing failure mechanism of the tested slabs and (ii) for validating a proposed approach to predict the shear and punching capacity of slabs under concentrated loads using the ACI 318-19 code expressions.</p>
Figures of Smart Contract Design via Modeling Environment: A proposal based on DasContract DSL
<p>Figures of "Smart Contract Design via Modeling Environment: A proposal based on DasContract DSL".</p>
Text-fig. 3. Geology of the Cheringoma Plateau, Mozambique. Sections and geological map adapted from Tinley (1977). The star symbols close to Mhengere Hill represent fossil wood and stem sites. Note that the fault relationships proposed in the northernmost Inhaminga section require re-examination. The Nguere Hills were called Gadjiua by Tinley (1977). in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 3. Geology of the Cheringoma Plateau, Mozambique. Sections and geological map adapted from Tinley (1977). The star symbols close to Mhengere Hill represent fossil wood and stem sites. Note that the fault relationships proposed in the northernmost Inhaminga section require re-examination. The Nguere Hills were called Gadjiua by Tinley (1977).
Text-fig. 4. Correlations of the strata in the Urema Graben, the Cheringoma Plateau and other parts of Mozambique proposed by various authors. The positions of fossiliferous units such as the Grudja and Cheringoma formations have been reasonably stable, whereas correlations of other rock units, especially the Mazamba Formation and the volcanics, have varied a great deal. The time scale is from Gradstein et al. (2020). in Stratigraphy, Chronology And Palaeontology Of The Tertiary Rocks Of The Cheringoma Plateau, Mozambique
Text-fig. 4. Correlations of the strata in the Urema Graben, the Cheringoma Plateau and other parts of Mozambique proposed by various authors. The positions of fossiliferous units such as the Grudja and Cheringoma formations have been reasonably stable, whereas correlations of other rock units, especially the Mazamba Formation and the volcanics, have varied a great deal. The time scale is from Gradstein et al. (2020).
Figure 4. Portal Logical Architecture-A Proposed Data Driven Architecture for Cardiology Network Application
<p>The applications that are based on a SOA environment can be configured to work both<br> as services exchanging data in point to point protocol and as a communication channel<br> between two entities that call a service provided by an entity that has the role of mediator or<br> broker. The letter can be seen as intermediary level that represents an “enterprise service bus”<br> (ESB) between service producers and consumers, offering messaging exchange services.</p>
Figure 2. System General View-A Proposed Data Driven Architecture for Cardiology Network Application
<p>Figure 2 presents a general schematic overview of the medical informational system,<br> underlying the main roles in the system together with their interactions. From an architectural<br> point of view one can identify the following main components:<br> • Host systems, named local (medical data) production systems<br> • General Practitioner system<br> • Analysis Laboratory system<br> • Hospital system<br> • Client system (interface to remote devices)<br> • Local portal (regional, national) for medical assistance, and long term data storage<br> Host systems consist of database servers connected through access points with<br> fixed/mobile medical devices. The portal will supply the functionality necessary to collect<br> information from the local interconnected systems into a centralized repository. Medical<br> services will be provided at portal level using specialized web-services that will allow access<br> to data stored in the repository.</p>
Figure 1. Schema for a data-integration solution-A Proposed Data Driven Architecture for Cardiology Network Application
<p>Data integration has favored loosening the coupling between data. This may involve<br> providing a uniform query interface over a mediated schema (see figure 1), thus transforming<br> a query into specialized queries over the original databases. One can also term this process<br> "view-based query-answering" because each of the data sources functions as a view over the<br> (nonexistent) mediated schema.</p>
ScienceDex guides
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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.