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5,145 results for “CO₂”

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zenodo32/100

Co-benefits of forest carbon projects in Southeast Asia

<p>This dataset contains the output rasters produced to determine the climate mitigation potential, crop pollination service for pollinator-dependent agriculture, quantity of nitrogen retained and Key Biodiversity Areas conserved at the various carbon price points, namely USD 1, 2, 3, 4, 5, 10, 15, 20, 25, 50 and 100 t<sup>-1</sup> CO<sub>2</sub>e across Southeast Asia. All data are masked to forest areas determined across the region at 1 km resolution, based on a cylindrical equal area projection.</p> <p>We also determined locations across the region where forest protections would deliver multiple benefits through a spatial overlay. Areas identified to contribute any level of co-benefit were coded 1 to 3, indicating the number of co-benefits that could be attained in addition to climate mitigation from avoided forest loss, assessed for each price point.</p> <p>Further details of the datasets can be found in Sarira et. al.&nbsp;</p> <p>For further questions or issues with the datasets, please contact Tasya Vadya Sarira at <a href="mailto:tasya.sarira@adelaide.edu.au">tasya.sarira@adelaide.edu.au</a>.</p>

opencc-by-4.0Oct 2021View details →
dryad32/100

Highly porous Co-doped NiO nanorods: Facile hydrothermal synthesis and electrocatalytic oxygen evolution properties

<p>Highly porous 3d transition metal oxide nanostructures are opening up the exciting area of oxygen evolution reaction (OER) catalysts in alkaline medium thanks to their good thermal and chemical stability, excellent physiochemical properties, high specific surface area and abundant nanopores. In this paper, highly porous Co-doped NiO nanorods were successfully synthesized by a simple hydrothermal method. The porous rod-like nanostructures were preserved with the added cobalt dopant ranging from 1 to 5 at% but were broken into aggregated nanoparticles at higher concentrations of additional cobalt. The catalytic activity of Co-doped NiO nanostructures for OER in an alkaline medium was assayed. The 5%Co-NiO sample showed a drastically enhanced activity. This result could originate from the combination of advantageous characteristics of highly porous NiO nanorods such as large surface area and high porosity as well as the important role of Co dopant that could provide more catalytic active sites, leading to an enhanced catalytic activity of the nanocatalyst.</p>

opencc-zeroOct 2021View details →
zenodo32/100

"The prolactin receptor scaffolds Janus kinase 2 via co-structure formation with phosphoinositide-4,5-bisphosphate" -- MD Trajectories

<p>MD trajectories and related files for the simulations related to the work:&nbsp;&quot;The prolactin receptor scaffolds Janus kinase 2 via co-structure formation with phosphoinositide-4,5-bisphosphate&quot; by Araya-Secchi R., Bugge K. and Seiffert et al.&nbsp;</p> <p>This dataset contains:</p> <p>1)&nbsp;Trajectories of CG-MD simulations of PRLR-LID1&nbsp;in lipid&nbsp;bilayers with POPC on the upper leaflet and two compositions&nbsp;on the lower leaflet: POPC:POPS:PIP2 80:10:10 and 90:5:5. These simulations were performed using the&nbsp;open beta version of the Martini 3 (3.b3.2) force field&nbsp;modified to increase the strength of Protein-water interactions by 10% (m3pws10).</p> <p>2) Trajectory of the all-atom simulation of the JAK2-FERM-SH2 + PRLR-LID1 complex in solution.</p> <p>3) Trajectories of CG-MD simulations of the&nbsp;JAK2-FERM-SH2 + PRLR-LID1 complex near a POPC:POPS (70:30) bilayer (8 initial conformations) performed using the Martini2 forcefield.</p> <p>4) Trajectories of CG-MD simulations of the&nbsp;JAK2-FERM-SH2 + PRLR-LID1 complex near a POPC:POPS:PIP2 (80:10:10) bilayer (16 initial conformations) performed using the Martini2 forcefield.</p>

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

Raw data for the paper "Cobalamin co-limits phytoplankton and bacterial biomass and activity in Eastern Mediterranean coastal waters"

<p>Raw data for the paper &quot;Cobalamin co-limits phytoplankton and bacterial biomass and activity in Eastern Mediterranean coastal waters&quot;.</p> <p>&nbsp;</p>

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

Table S6.44,270 pairs of co-expression relationships Between 612 lncRNAs and 2,742 mRNAs

<p>The file includes information about 44270 lncRNA-mRNA pairs related to lncRNA.ensembl,lncRNA.symbol,gene.ensembl,gene.symbol,r,FDR, as well as information about 612 lncRNAs and 2742 mRNAs associated with 44274 co-expressed gene pairs. Where, r denotes differential gene significance coefficient; p-value was corrected by Benjamini-Hochberg algorithm to obtain FDR value.</p>

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

PAsCAL WP6 Pilot 3 Autonomous Bus Line with Co-Road Users Video

<p>A summary video documenting and introducing the activities of pilot 3 of the PAsCAL real-world pilots. This pilot took place on the campus of the UAM University in Madrid, Spain. The autonomous shuttle is fully automated and has a steward on-board only for the case of incidences or passenger support but this person does not intervene with the usual function of the bus. It is important to highlight that the bus is one of the only busses operating in open traffic in Europe to date. Therefore, an important part of the pilot consisted also in involving road co-users to capture their acceptance of the vehicle.</p>

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

Planning Co-creation: PRODUCES+ (Infographic)

<p>Stages of planning co-creation (PRODICES+) &nbsp;in an infographic.</p>

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

FIGURE 4 in Munidopsis geyeri and M. exuta (Crustacea: Munidopsidae): A study of two deepsea, amphi-Atlantic species that co-occur in the southern Gulf of Mexico

FIGURE 4. Morphological comparison between Munidopsis exuta and Munidopsis geyeri juveniles. CL = carapace length.

opennotspecifiedNov 2022View details →
zenodo32/100

FIGURE 3 in Munidopsis geyeri and M. exuta (Crustacea: Munidopsidae): A study of two deepsea, amphi-Atlantic species that co-occur in the southern Gulf of Mexico

FIGURE 3. Munidopsis exuta Macpherson &amp; Segonzac, 2005. A, male, from Chapopote Knoll (CNCR 24857 = ULLZ 8861); B, ovigerous female, Chapopote Knoll (CNCR 24846 = ULLZ 8792); C, ovigerous female, Mid-Atlantic Ridge (CEAB CRU 2004-03); D, juvenile female and E, juvenile male, Florida Escarpment (CEAB CRU 2004-05); F, juvenile female, and G, ovigerous female, Bay of Biscay (CEAB CRU 2004-01). Scale bar = 10 mm in A, B, C, G; 5 mm in D, E, F.

opennotspecifiedNov 2022View details →
zenodo32/100

FIGURE 6 in Munidopsis geyeri and M. exuta (Crustacea: Munidopsidae): A study of two deepsea, amphi-Atlantic species that co-occur in the southern Gulf of Mexico

FIGURE 6. Munidopsis geyeri Pequegnat &amp; Pequegnat, 1970. Specimens from A, Regab Pockmark site (Gulf of Guinea; CEAB CRU 2004-07) and B. Chapopote Knoll (Gulf of Mexico; CNCR 24856). C, lateral and D, dorsal view. Morphological features: E, distal part of cephalothorax, antennal spine; F, shape of rostrum; G, antennular peduncle, distolateral and distodorsal spines; H, anntenal peduncle; I, third maxilliped; J, thoracic sternite; K, carpus of cheliped; L, ischium of cheliped, dorsolateral spine; M, dactylus, strongly curved at the end of extensor margin, number of teeth on flexor margin; N, telson; O, gonopod 1 (G1); P, gonopod 2 (G2).

opennotspecifiedNov 2022View details →
zenodo32/100

FIGURE 2 in Munidopsis geyeri and M. exuta (Crustacea: Munidopsidae): A study of two deepsea, amphi-Atlantic species that co-occur in the southern Gulf of Mexico

FIGURE 2. Relationships of analyzed Munidopsis species inferred using the Neighbor-Joining method and uncorrected "p" genetic distances. A, involved nucleotide sequences of combined fragment genes (COI, 12S and 16S) (same group of data used for histogram on Fig. 1B including Shinkaia crosnieri); and B, with nucleotide sequences of cytochrome c oxidase subunit 1 (COI) (same group of data used for histogram on Fig. 1A excluding Shinkaia crosnieri). The percentage of the bootstrap is indicated in each node.

opennotspecifiedNov 2022View details →
zenodo32/100

FIGURE 5 in Munidopsis geyeri and M. exuta (Crustacea: Munidopsidae): A study of two deepsea, amphi-Atlantic species that co-occur in the southern Gulf of Mexico

FIGURE 5. Geographic distribution of A, Munidopsis exuta and B, M. geyeri. Numbers with circles represent specimens analyzed in this study, letters with triangles represent populations not examined on this study. See Table 1. Base map from UNINMAR (2020).

opennotspecifiedNov 2022View details →
zenodo32/100

FIGURE. Results of discriminant function analysis (DFA) for C. arenaria (ar), C. colchica (co) and C. praecox (pr). Characters abbreviated as in Table 2. A. Reproductive characters. Loadings for the first axis (only absolute values>0.50 are given): LW = -0.53, LN = -1.53, WN = 2.40, LN/WN = 2.13. Loadings for the second axis: LN = -0.56. B. Vegetative characters. Loadings for the first axis (only absolute values>0.50 are given): IL = 0.62. Loadings for the second axis: CW = 0.86, CLL = 0.78, CLW = -0.65. in Carex section Ammoglochin (Cyperaceae) in Poland

FIGURE. Results of discriminant function analysis (DFA) for C. arenaria (ar), C. colchica (co) and C. praecox (pr). Characters abbreviated as in Table 2. A. Reproductive characters. Loadings for the first axis (only absolute values&gt;0.50 are given): LW = -0.53, LN = -1.53, WN = 2.40, LN/WN = 2.13. Loadings for the second axis: LN = -0.56. B. Vegetative characters. Loadings for the first axis (only absolute values&gt;0.50 are given): IL = 0.62. Loadings for the second axis: CW = 0.86, CLL = 0.78, CLW = -0.65.

opennotspecifiedDec 2022View details →
zenodo32/100

FIGURE. Results of discriminant function analysis (DFA) for the reproductive characters of the Ammoglochin taxa. A—along axes DF1 and DF2; B—along axes DF1 and DF3. Characters abbreviated as in Table 2). Loadings for the first axis (only absolute values>0.50 are given: LN = 1.09, WN = -1.57, LN/WN = -1.59, FGL = 0.74. Loadings for the second axis: UL/UW = 0.57, LW = 0.71, WW = 0.52. Loadings for the third axis: UL = -0.73, UW = 1.56, UL/UW = 0.92, LN = -2.76, WN = 2.53, LN/WN = 2.14. ar—C. arenaria, br—C. brizoides, co—C. colchica, cu—C. curvata, pr—C. praecox, ps—C. pseudobrizoides. in Carex section Ammoglochin (Cyperaceae) in Poland

FIGURE. Results of discriminant function analysis (DFA) for the reproductive characters of the Ammoglochin taxa. A—along axes DF1 and DF2; B—along axes DF1 and DF3. Characters abbreviated as in Table 2). Loadings for the first axis (only absolute values&gt;0.50 are given: LN = 1.09, WN = -1.57, LN/WN = -1.59, FGL = 0.74. Loadings for the second axis: UL/UW = 0.57, LW = 0.71, WW = 0.52. Loadings for the third axis: UL = -0.73, UW = 1.56, UL/UW = 0.92, LN = -2.76, WN = 2.53, LN/WN = 2.14. ar—C. arenaria, br—C. brizoides, co—C. colchica, cu—C. curvata, pr—C. praecox, ps—C. pseudobrizoides.

opennotspecifiedDec 2022View details →
zenodo32/100

FIGURE. Results of discriminant function analysis (DFA) for the vegetative characters of the Ammoglochin taxa. A—along axes DF1 and DF2; B—along axes DF1 and DF3. Characters abbreviated as in Table 2. Loadings for the first axis (only absolute values>0.50 are given): SN = 0.57. Loadings for the second axis: CL = -0.91, IL = 0.54. Loadings for the third axis: CW = 0.62, CLL = -0.52, CLW = -0.89, IL = 0.51. ar—C. arenaria, br—C. brizoides, co—C. colchica, cu—C. curvata, pr—C. praecox, ps—C. pseudobrizoides, re—C. repens. in Carex section Ammoglochin (Cyperaceae) in Poland

FIGURE. Results of discriminant function analysis (DFA) for the vegetative characters of the Ammoglochin taxa. A—along axes DF1 and DF2; B—along axes DF1 and DF3. Characters abbreviated as in Table 2. Loadings for the first axis (only absolute values&gt;0.50 are given): SN = 0.57. Loadings for the second axis: CL = -0.91, IL = 0.54. Loadings for the third axis: CW = 0.62, CLL = -0.52, CLW = -0.89, IL = 0.51. ar—C. arenaria, br—C. brizoides, co—C. colchica, cu—C. curvata, pr—C. praecox, ps—C. pseudobrizoides, re—C. repens.

opennotspecifiedDec 2022View details →
zenodo32/100

Dataset for "Co-alignment of Laboratory and In-Situ Reflectance Spectra of Chang'e-5 Lunar Soil"

<p>This dataset&nbsp;provides&nbsp;the reflectance data measured in the laboratory for the &lt;45-&mu;m, 45-355-&mu;m fractions, and bulk soil sample, respectively.</p>

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

The supplementary materials of the article"Construction of myocardial patch with mesenchymal stem cells and poly (CL-co-TOSUO)/collagen scaffolds for myocardial infarction repair by coaxial electrospinning"

<p>The supplementary materials of &quot;Construction of myocardial patch with mesenchymal stem cells and poly (CL-co-TOSUO)/collagen scaffolds for myocardial infarction repair by coaxial electrospinning&quot; consist of three figures: Figure S1: The structure and the molecular characteristics of the elastic PCT from gel permeation chromatography; Figure S2: Time series photographs of the rats&rsquo; back skin following the subcutaneous transplantation of coaxial electrospun fibrous PCT/collagen scaffolds. Figure S3: Representative histopathological images of the rats&#39; skin following the transplantation of PCT/collagen coaxial nanofibers scaffolds.</p>

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

Supplementary information files: Gene co-expression network and differential expression analyses of subcutaneous white adipose tissue reveal novel insights into the pathological mechanisms underlying ketosis in dairy cows

<p>Supplementary information files: Gene co-expression network and differential expression analyses of subcutaneous white adipose tissue reveal novel insights into the pathological mechanisms underlying ketosis in dairy cows</p>

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

Single-cell heterogeneity of EGFR and CKD4 co-amplification is linked to immune infiltration in glioblastoma

<p>This upload contains RDS objects of preprocessed&nbsp;publicly available scRNAseq data, required to run scRNAseq analyses in the manuscript &quot;Single cell heterogeneity of EGFR and CDK4 co-amplification is linked to immune infiltration in glioblastoma&quot;. The corresponding GitHub repo&nbsp;<a href="https://github.com/Michorlab/GBM_OR_immune">https://github.com/Michorlab/GBM_OR_immune</a>&nbsp;contains code to analyze the data here, as well as&nbsp;plots and tables generated on the basis of this data.</p>

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

Data for: Proximity to oilseed rape fields affects plant pollination and pollinator-mediated selection on a co-flowering plant on the Tibetan Plateau

<p><span>The ecological effects of mass-flowering crops on pollinator abundance and species richness of neighboring habitats are well established, yet the potential evolutionary consequences remain unclear. We studied effects of proximity to a mass-flowering crop on the pollination of local co-flowering plants, and on patterns of natural selection on a pollination-generalized plant on the Tibetan Plateau. We recorded pollinator visitation rates and community composition at different distances (near vs. far) to oilseed rape (Brassica napus) fields in two habitat types, and quantified pollinator-mediated selection on attractive traits of Trollius ranunculoides. The proximity to oilseed rape increased pollinator visitation in neighboring alpine meadows and changed pollinator composition in neighboring shrub meadows. Trollius ranunculoides in the alpine meadow near oilseed rape received three times more pollinator visits (mainly bees), and consequently had a 16.5% increase in seed set, but also received slightly more heterospecific pollen per stigma. In contrast, pollinator visitation to T. ranunculoides in the shrub meadow near oilseed rape was three times lower (mainly flies), leading to 10.7% lower seed despite no effect on pollen deposition. The proximity to the oilseed rape field intensified pollinator-mediated selection on flower size and weakened selection on flower height of T. ranunculoides in the alpine meadow but did not affect phenotypic selection on either trait in the shrub meadow. Our study highlights context-dependent variation in plant-pollinator interactions close to mass-flowering oilseed rape, suggesting potential effects on the evolution of flower traits of native plants through altered pollinator-mediated selection. However, context dependence may make these effects difficult to predict.</span></p>

opencc-zeroFeb 2023View 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