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1,084 results for “substrate”

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zenodo32/100

FIGURE 1 in Podocoryna loyola, n. sp. (Hydrozoa, Hydractiniidae): a probably introduced species on artificial substrate from southern Brazil

FIGURE 1. Baía de Paranaguá and the State of Paraná in Brazil. Location of the Paranaguá Yacht Club inside the Baía de Paranaguá (where Podocoryna loyola n. sp. was found on polyethylene plates).

opennotspecifiedDec 2014View details →
zenodo32/100

FIGURE 1 in Melvicalathis, a new brachiopod genus (Terebratulida: Chlidonophoridae) from deep sea volcanic substrates, and the biogeographic significance of the mid­ocean ridge system *

FIGURE 1. The mid­ocean ridge systems and geographic distributions of Melvicalathis macroctena (Zezina, 1981), and species of the related chlidonophorid brachiopod, Bathynanus (star symbols). Note the concentration along areas of probable hard rock substrates. The two stations of "Academic Kurchatov" (type locality) are adjacent to and on the Nazca Ridge. Key to symbols: "Academic Kurchatov", RV " Melville", FS "SONNE", "Eltanin" Cruise.

opennotspecifiedDec 2008View details →
zenodo32/100

FIGURE 4 in Melvicalathis, a new brachiopod genus (Terebratulida: Chlidonophoridae) from deep sea volcanic substrates, and the biogeographic significance of the mid­ocean ridge system *

FIGURE 4. Melvicalathis macroctena (Zezina, 1981) from the Galapagos Spreading Centre. A. Interior of dorsal valve of ZMB Bra 2014 showing descending branches of crura with incomplete transverse band, and internal ridges corresponding to external costal troughs. B. Close­up of previous photograph to show details of descending branches and incomplete loop. C. Spicular skeleton after dissolution of soft tissue. D. Close­up of triangular costae showing numerous closely spaced growth lines. E. Close­up of a valve of Eucalathis to show typical beaded tuberculate costae for comparison with D.

opennotspecifiedDec 2008View details →
zenodo32/100

FIGURE 5. A–B in Melvicalathis, a new brachiopod genus (Terebratulida: Chlidonophoridae) from deep sea volcanic substrates, and the biogeographic significance of the mid­ocean ridge system *

FIGURE 5. A–B. Line drawings of Melvicalathis macroctena (Zezina, 1981) from the type locality, south east Pacific. A. View of lophophore from the ventral side. B. View of lophophore from the dorsal side. C. Schematic illustration of the cryptic habit of Melvicalathis macroctena around the walls of small tabular voids immediately beneath basalt flow surfaces. The tubes with the brachiopods were found in larger boulders of fresh, glassy basalt at RV Melville Stn #116, Southeast Indian Ridge. D. Sketch of attachment of Melvicalathis on hard substrate and probable current system around lophophore. Key. 1, place where the lophophore was removed from the mantle and the dorsal body wall—internal details are seen through the transparent ventral wall of the lophophore; 2, mouth; 3, lip; 4, transparent (soft) dorsal wall of the

opennotspecifiedDec 2008View details →
zenodo32/100

FIGURE 3 in Melvicalathis, a new brachiopod genus (Terebratulida: Chlidonophoridae) from deep sea volcanic substrates, and the biogeographic significance of the mid­ocean ridge system *

FIGURE 3. Melvicalathis macroctena (Zezina, 1981) from the Southeast Indian Ridge. A. Interior of AU B320 showing small cardinal process, internal view of costae, and correspondence between costae and scalloped margin. B. Lateral view of AU B320 showing slightly biconvex valves and strongly attrite beak. C. Posterior view of AU B320 to show hypothyrid foramen and costae. D. Close­up of C, showing pedicle collar, teeth and punctae. E. Close­up of ventral valve of AU B321 showing pedicle collar, teeth, and very narrow deltidial plates. F. Close­up of dorsal valve of AU B321 showing retracted dried pedicle, sockets and socket ridges, proximal end of crura, and part of dried lophophore. G. Lateral view of AU B321 to show rounded, ventrally­directed crural processes and dried lophophore.

opennotspecifiedDec 2008View details →
zenodo32/100

FIGURE 6 in Melvicalathis, a new brachiopod genus (Terebratulida: Chlidonophoridae) from deep sea volcanic substrates, and the biogeographic significance of the mid­ocean ridge system *

FIGURE 6. Melvicalathis macroctena (Zezina, 1981) from the Southeast Indian Ridge A. Close­up of AU B320 to show detail of angular costae, triangular in cross section, numerous closely spaced growth lines, and small, evenly spaced punctae. B. Close­up of costae showing quincunx arrangement of punctae. C. Interior of valve margin to show shell fibres, punctae and slightly tuberculate margin.

opennotspecifiedDec 2008View details →
zenodo32/100

Supporting data for Relative increases in CH4 and CO2 emissions from wetlands under global warming dependent on soil carbon substrates

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opencc-by-4.0Oct 2023View details →
zenodo32/100

Exploring the ligand binding and conformational dynamics of the substrate binding domain 1 of the ABC transporter GlnPQ

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opencc-by-4.0Nov 2023View details →
dryad32/100

Evolution of the Sabulina verna group (Caryophyllaceae) in Europe: A deep split, followed by secondary contacts, multiple allopolyploidization and colonization of challenging substrates

<p>One of the major goals of contemporary evolutionary biology is to elucidate the relative roles of allopatric and ecological differentiation and polyploidy in speciation. In this study, we address the taxonomically intricate <em>Sabulina verna</em> group, which has a disjunct Arctic–alpine postglacial range in Europe and occupies a broad range of ecological niches, including substrates toxic to plants. Using genome-wide ddRAD sequencing combined with morphometric analyses based on extensive sampling of 111 natural populations, we aimed to disentangle internal evolutionary relationships and examine their correspondence with the pronounced edaphic and ploidy diversity within the group. We identified two spatially distinct groups of diploids: a widespread Arctic–alpine group and a spatially restricted yet diverse Balkan group. Most tetraploids exhibited a considerably admixed ancestry derived from both these groups, suggesting their allopolyploid origin. Four genetic clusters in congruence with geography and mostly supported by morphological traits were recognized in the diploid Arctic–alpine group. Tetraploids are split into two distinct and geographically vicariant groups, indicating their repeated polytopic origin. Furthermore, our results also revealed at least five-fold parallel colonization of toxic substrates (serpentine and metalliferous), altogether demonstrating a complex interaction between geography, challenging substrates, and polyploidy in the evolution of the group. Finally, we propose a new taxonomic treatment of this intricate complex.</p>

opencc-zeroNov 2023View details →
zenodo32/100

Data supplement for "Drops of volatile binary mixtures on brush-covered substrates"

<p>This dataset contains supplementary data for the following publication:</p> <p>Diekmann, J. &amp; Thiele, U.<br>Drops of volatile binary mixtures on brush-covered substrates<br>EPJ-ST: Vol. 233, p. 1615-1624, 2024<br>doi: 10.1140/epjs/s11734-024-01169-4</p> <p>&nbsp;</p> <p>We provide the data and sources necessary to generate figure 2.</p>

opencc-by-4.0Feb 2024View details →
zenodo32/100

Tailoring the adhesion of electrophoretic chitosan/bioactive glass coatings by the combined surface pre-treatments of Ti substrates

<p>This record contains all files generated in the preparation process of the following publication:&nbsp;</p> <p>Agnieszka Kowalczyk, Agata Sotniczuk, Donata Kuczyńska-Zemła, Jarosław Pura, Zhiyan Xu, Aldo R. Boccaccini, Halina Garbacz,<br>"Tailoring the adhesion of electrophoretic chitosan/bioactive glass coatings by the combined surface pre-treatments of Ti substrates", submitted to Surface and Coatings Technology.</p> <p>Designations:&nbsp;<br>Ti_G2 - Titanium Grade 2&nbsp;<br>G - sample grinded on #600 grit abrasive paper<br>SP - sample shot-peened with 90-150 &micro;m shots, under pressure of 0.5 MPa<br>E - sample etched&nbsp;<br>SP+E_HF - sample shot-peened with 90-150 &micro;m shots, under the pressure of 0.5 MPa and etched in the hydrofluoric solution&nbsp;<br>SP+E_NaOH - &nbsp;sample shot-peened with 90-150 &micro;m shots, under the pressure of 0.5 MPa and etched in the sodium hydroxide solution<br>SP+E_HF_NaOH - sample shot-peened with 90-150 &micro;m shots, under the pressure of 0.5 MPa and etched first in the hydrofluoric solution and then in sodium hydroxide&nbsp;<br>EPD - samples coated with chitosan/bioglass coating<br>ADH - samples coated with chitosan/bioglass coating after conducted adhesion test<br>SBF - samples after bioactivity test in Simulated Body Fluid (SBF) solution<br>SEM - Scaning Electron Microscopy&nbsp;<br>EDS - Energy Dispersive Spectroscopy</p> <p>Folders content:</p> <ul> <li>Corrosion - contains files with data of corrosion resistance, obtained during electrochemical tests</li> <li>FTIR - contains files obtained from Fourier Transform Infrared Spectroscopy analysis of chitosan/bioglass coating</li> <li>Roughness - contains files from topography analysis obtained using optical profilometer for various scan areas</li> <li>SEM - contains folders with images of samples surfaces from Scanning Electron Microscopes. Subfolders: <ul> <li>Adhesion - contains SEM images of samples coated with chitosan/bioglass coatings after tape test</li> <li>Bioactivity test - contains SEM images and EDS analysis of samples coated with chitosan/bioglass coatings after bioactivity test in SBF</li> <li>Coatings - contains SEM images of chitosan/bioactive glass coatings deposited on different substrates</li> <li>Substrate - contains SEM images of titanium substrate after various surface modifications</li> </ul> </li> <li>Wettability - contains files with data obtained from wettability tests</li> <li>XRD - contains files with data obtained from X-ray spectroscopy analysis</li> </ul> <p>This research was supported financially by the National Science Centre, Poland under the grant OPUS 23 [2022/45/B/ST5/03398].</p> <p>&nbsp;</p>

opencc-by-4.0Mar 2024View details →
zenodo32/100

Modelling the growth of biofilms on soft substrates

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opencc-by-4.0Nov 2024View details →
zenodo32/100

Supplementary material S7: An alternative view of Varroa jolting behaviour on the brood-comb substrate.

<p>A short video to demonstrate a few instances of jolting behaviour where the mite appears to push its body in an up and down motion by flexing its legs, rather than the more commonly seen side to side motion. Each instance is of the same mite individual during the same filming session, after it has been edited to remove periods of time where this behaviour is not seen.</p>

opencc-by-4.0Oct 2021View details →
zenodo32/100

Single-molecule analysis of specificity and multivalency in binding of short linear substrate motifs to the APC/C

<p>Robust regulatory signals in the cell often depend on interactions between short linear motifs (SLiMs) and globular proteins. Many of these interactions are poorly characterized because the binding proteins cannot be produced in the amounts needed for traditional methods. To address this problem, we developed a single-molecule off-rate (SMOR) assay based on microscopy of fluorescent ligand binding to immobilized protein partners. We used it to characterize substrate binding to the Anaphase-Promoting Complex/Cyclosome (APC/C), a ubiquitin ligase that triggers chromosome segregation. We find that SLiMs in APC/C substrates (the D box and KEN box) display distinct affinities and specificities for the substrate-binding subunits of the APC/C, and we show that multiple SLiMs in a substrate generate a high-affinity multivalent interaction. The remarkably adaptable substrate-binding mechanisms of the APC/C have the potential to govern the order of substrate destruction in mitosis.</p>

opencc-by-4.0Nov 2021View details →
zenodo32/100

Selective area epitaxy of PbTe-Pb hybrid nanowires on a lattice-matched substrate

<p>This repository contains the raw data corresponding to the paper &quot;Selective area epitaxy of PbTe-Pb hybrid nanowires on a lattice-matched substrate&quot; (arXiv: 2110.13642)</p>

opencc-by-4.0Feb 2022View details →
zenodo32/100

Gradient-dynamics model for liquid drops on elastic substrates

<p>Data sets corresponding to the results shown in &quot;Gradient-dynamics model for liquid drops on elastic substrates&quot;.<br> Additionally, the scripts the plots were produced with.</p>

opencc-by-4.0Oct 2021View details →
zenodo32/100

Data for "Functional Dynamics of Substrate Recognition in TEM Beta-Lactamase"

<p>Molecular dynamics data associated with the publication: &quot;Functional Dynamics of Substrate Recognition in TEM Beta-Lactamase&quot;</p> <p>Trajectores were generated in GROMACS, and the carbon alpha coordinates were extracted and&nbsp;aligned with the JEDi analysis software. Details of the simulations and analysis are given in the publication.</p> <p>Data in apo.zip contains trajectories for 32 total trajectories of&nbsp;TEM-1, TEM-2, TEM-10, and TEM-52 beta-lactamase, each starting form different 8 crystal structures</p> <p>Data in holo.zip contains 16 trajectories of TEM-1, TEM-2, TEM-10, and TEM-52 beta-lactamase in complex with ampicillin, amoxicillin, cefotaxime, and ceftazidime each.</p> <p>Trajectories files are in comma delimited format, with rows representing degrees for freedom (789 total), and columns representing samples (10000 per trajectory file).</p> <p>Supervised Projective Learning for Orthogonal Completeness (SPLOC)&nbsp;software for analysis as performed in the publication can be found at:&nbsp;https://github.com/BioMolecularPhysicsGroup-UNCC/MachineLearning/tree/master/SPLOC&nbsp;</p>

opencc-by-4.0May 2022View details →
zenodo32/100

Simulations of Sec61 with a substrate-selective inhibitor, conformation 1

<p>Simulations for an alternative conformation of KZR-8445 bound to Sec61. Data for the conformation used in Rehan <em>et al.</em>, Nature Chemical Biology&nbsp;19, pages 1054&ndash;1062 (2023) are available at&nbsp;<a href="https://zenodo.org/record/7303653">https://zenodo.org/record/7303653</a></p>

opencc-by-4.0Jun 2022View details →
dryad32/100

Lichen speciation is sparked by a substrate requirement shift and reproduction mode differentiation

<p>We show that obligate lignicoles in lichenized Micarea are predominately asexual whereas most facultative lignicoles reproduce sexually.AQ1 Our phylogenetic analyses (ITS, mtSSU, Mcm7) together with ancestral state reconstruction show that the shift in reproduction mode has evolved independently several times within the group and that facultative and obligate lignicoles are sister species. The analyses support the assumption that the ancestor of these species was a facultative lignicole. We hypothezise that a shift in substrate requirement from bark to wood leads to differentiation in reproduction mode and becomes a driver of speciation. This is the first example of lichenized fungi where reproduction mode is connected to substrate requirement. This is also the first example where such an association is demonstrated to spark lichen speciation. Our main hypothesis is that obligate species on dead wood need to colonize new suitable substrata relatively fast and asexual reproduction is more effective a strategy for successful colonization.</p>

opencc-zeroJun 2022View details →
dryad32/100

Data from: Premating isolation is determined by larval rearing substrates in cactophilic Drosophila mojavensis. X. Age-specific dynamics of adult epicuticular hyrdocarbon expression in response to different host plants

Analysis of sexual selection and sexual isolation in Drosophila mojavensis and its relatives has revealed a pervasive role of rearing substrates on adult courtship behavior when flies were reared on fermenting cactus in preadult stages. Here, we assessed expression of contact pheromones comprised of epicuticular hydrocarbons (CHCs) from eclosion to 28 days of age in adults from two populations reared on fermenting tissues of two host cacti over the entire life cycle. Flies were never exposed to laboratory food and showed significant reductions in average CHC amounts consistent with CHCs of wild-caught flies. Overall, total hydrocarbon amounts increased from eclosion to 14–18 days, well past age at sexual maturity, and then declined in older flies. Most flies did not survive past 4 weeks. Baja California and mainland populations showed significantly different age-specific CHC profiles where Baja adults showed far less age-specific changes in CHC expression. Adults from populations reared on the host cactus typically used in nature expressed more CHCs than on the alternate host. MANCOVA with age as the covariate for the first six CHC principal components showed extensive differences in CHC composition due to age, population, cactus, sex, and age × population, age × sex, and age × cactus interactions. Thus, understanding variation in CHC composition as adult D. mojavensis age requires information about population and host plant differences, with potential influences on patterns of mate choice, sexual selection, and sexual isolation, and ultimately how these pheromones are expressed in natural populations. Studies of drosophilid aging in the wild are badly needed.

opencc-zeroDec 2013View details →

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Allen Brain Atlas

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

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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