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Experimental X-ray Diffraction Data for "Cooling-Induced Order-Disorder Phase Transition in CsPbBr3 Nanocrystal Superlattices"

Experimental X-ray diffraction data:  -- temperature-dependent diffraction patterns (theta:2theta, rocking curves) for C18 and C8 CsPbBr3 nanocrystal superlattice samples; -- room temperature diffraction patterns (theta:2theta, rocking curves) for C6, C8, C10, C12, and C18 CsPbBr3 nanocrystal superlattices; in all files, first column is angle in degrees and the second column is intensity.

Data for "Octahedral tilt-driven phase transitions in BaZrS3 chalcogenide perovskite"

This record contains: 1. database with data from density functional theory calculations used for training a neuroevolution potential (NEP) for the BaZrS3 chalcogenide perovskite 2. the NEP machine learning interatomic potential 3. test and training set used to construct the potential

Dataset of the publication: Tailoring spin waves in 2D transition metal phosphorus trichalcogenides via atomic-layer substitution

Dataset of the publication: Tailoring spin waves in 2D transition metal phosphorus trichalcogenides via atomic-layer substitution DOI: 10.1039/d2dt02482a A. M. Ruiz, DL. Esteras, A. Rybakov, J. J. Baldov  Dalton Trans., 54, 44, 16816-16823 (2022)

Dataset of the publication: Unlocking room-temperature bistable spin transition at the nanoscale: the synthesis of core@shell [Fe(NH2trz)3(NO3)2]@SiO2 nanoparticles

Dataset of the publication: Unlocking room-temperature bistable spin transition at the nanoscale: the synthesis of core@shell [Fe(NH2trz)3(NO3)2]@SiO2 nanoparticles DOI: 10.1039/d4dt00911h A. Regueiro, M. Marti-Carrascosa, R. Torres-Cavanillas, E. Coronado  Dalton Trans., 53, 20, 8764-8771 (2024)

opencc-by-4.0Dec 2024View details →

Dataset of the publication: Design and processing as ultrathin films of a sublimable Iron(II) spin crossover material exhibiting efficient and fast light-induced spin transition

Dataset of the publication: Design and processing as ultrathin films of a sublimable Iron(II) spin crossover material exhibiting efficient and fast light-induced spin transition DOI: 10.1021/acs.chemmater.3c01704 M. Gavara-Edo, F. J. Valverde-Muñoz, M. C. Muñoz, S. Elidrissi, F. Marques-Moros, J. Herrero-Martín, K. Znovjyak, M. Seredyuk, J. A. Real, E. Coronado  Chem. Mater., 35, 22, 9591-9602 (2023)

opengpl-3.0-or-laterJan 2024View details →

Conservation outcomes of dietary transitions across different values of nature - model outputs

Archive of output reports produced for the MAgPIE v4.8.2 paper Conservation outcomes of dietary transitions across different values of nature. Data The data contain the MAgPIE model and post-processing outputs for all assessed scenarios, including the sensitivity test across the SSP1 and SSP3 scenarios. <ul> <li>The file rev9_healthyLscps_AOH_full_report.Rds contains the outputs of our Area of Habitat (AOH) assessment for all assessed species and across all scenarios. The summary statistics shown in Figure 2 and Figure 3 have been derived from this data set. The data has also been used to create Extended Data Figures 5-7 and is shown in the Supplementary Information. However, for Extended Data Figure 7 the data was used in combination with rasterized range polygons obtained from the IUCN Red List Database (IUCN 2020).</li> <li>The file rev9_healthyLscps_pollSuff_report_all.Rds reports the global and regional cropland area (Mha) that is subject to insufficient and sufficient pollination supply. This is specified in the column ‘poll_class’, where 1 is insufficient and 2 is sufficient pollination supply. The data is shown in Figure 4, Extended Data Figure 8 and the Supplementary Information.</li> <li>The file rev9_healthyLscps_RUSLE_report_all.Rds  reports estimated global and regional soil loss in Pg per year across all modelled scenarios. The data is displayed in Figure 4, Extended Data Figure 9 and the Supplementary Information.</li> <li>The file rev9_healthyLscps_allSSP_report.rds contains regional and global output variables from the MAgPIE model used in this study. The data is shown in Figure 1 and 5, as well as in Extended Data Figures 2-4 and the Supplementary Information.</li> <li>The file rev9_healthyLscps_validation.rds contains validation data for the MAgPIE model output variables.</li> </ul>   Model code The model code of the MAgPIE and SEALS models can be accessed via: MAgPIE model code: <ul> <li><a href="https://doi.org/10.5281/zenodo.13833444">https://doi.org/10.5281/zenodo.13833444</a> and <a href="https://github.com/magpiemodel/magpie">https://github.com/magpiemodel/magpie</a></li> </ul> MAgPIE model documentation: <ul> <li><a href="https://rse.pik-potsdam.de/doc/magpie/4.3.5/">https://rse.pik-potsdam.de/doc/magpie/4.8.2/</a></li> </ul> SEALS model code: <ul> <li><a href="https://github.com/jandrewjohnson/seals_dev/releases/tag/v1.0.0">https://github.com/jandrewjohnson/seals_dev/releases/tag/v1.0.0</a></li> </ul> SEALS mode documentation: <ul> <li><a href="https://justinandrewjohnson.com/earth_economy_devstack/seals_overview.html">https://justinandrewjohnson.com/earth_economy_devstack/seals_overview.html</a></li> </ul>   Cited references IUCN. (2020). The IUCN Red List of Threatened Species. Version 2020-2. https://www.iucnredlist.org. Downloaded on 25 November 2020

dryad40/100

Data from: Evolution of dispersal, habit, and pollination in Africa pushed Apocynaceae diversification after the Eocene-Oligocene climate transition

Apocynaceae (the dogbane and milkweed family) is one of the ten largest flowering plant families, with approximately 5,350 species and diverse morphology and ecology, ranging from large trees and lianas that are emblematic of tropical rainforests, to herbs in temperate grasslands, to succulents in dry, open landscapes, and to vines in a wide variety of habitats. Despite a specialized and conservative basic floral architecture, Apocynaceae are hyperdiverse in flower size, corolla shape, and especially derived floral morphological features. These are mainly associated with the development of corolline and/or staminal coronas and a spectrum of integration of floral structures culminating with the formation of a gynostegium and pollinaria—specialized pollen dispersal units. To date, no detailed analysis has been conducted to estimate the origin and diversification of this lineage in space and time. Here, we use the most comprehensive time-calibrated phylogeny of Apocynaceae, which includes approximately 20% of the species covering all major lineages, and information on species number and distributions obtained from the most up-to-date monograph of the family to investigate the biogeographical history of the lineage and its diversification dynamics. South America, Africa, and Southeast Asia (potentially including Oceania), were recovered as the most likely ancestral area of extant Apocynaceae diversity; this tropical climatic belt in the equatorial region retained the oldest extant lineages and these three tropical regions likely represent museums of the family. Africa was confirmed as the cradle of pollinia-bearing lineages and the main source of Apocynaceae intercontinental dispersals. We detected 12 shifts toward accelerated species diversification, of which 11 were in the APSA clade (apocynoids, Periplocoideae, Secamonoideae, and Asclepiadoideae), eight of these in the pollinia-bearing lineages and six within Asclepiadoideae. Wind-dispersed comose seeds, climbing growth form, and pollinia appeared sequentially within the APSA clade and probably work synergistically in the occupation of drier and cooler habitats. Overall, we hypothesize that temporal patterns in diversification of Apocynaceae was mainly shaped by a sequence of morphological innovations that conferred higher capacity to disperse and establish in seasonal, unstable, and open habitats, which have expanded since the Eocene-Oligocene climate transition.

opencc-zeroOct 2021View details →

opencc-by-4.0Nov 2021View details →

Experimental data for "Electric field drives Chern transition in Hofstadter bands of twisted double bilayer graphene"

This experimental dataset was used in our study of "Electric field drives Chern transition in Hofstadter bands of twisted double bilayer graphene".

opencc-by-4.0Dec 2021View details →

Multistate modeling of Florida scrub-jay adult survival and breeding transitions

Metadata for data file “MS4APR2020 ALL ENTER 2 STATES.txt” for the research published in Ecosphere Article ECS21-0698 Multistate modeling of Florida scrub-jay adult survival and breeding transitions David R. Breininger1&dagger;, Geoffrey M. Carter1, Stephanie A. Legare1 William V. Payne1, Eric D. Stolen1, Daniel J. Breininger2, James E. Lyon3 1Herndon Solutions Group, LLC, NASA Environmental and Medical Contract, NEM-022, Kennedy Space Center, FL 32899, U.S.A. 2Department of Mathematics, Florida Institute of Technology, Melbourne FL, 32899 U.S.A. 3Merritt Island National Wildlife Refuge, Titusville FL 32901, U.S.A. &dagger; Corresponding author: e-mail: <a href="mailto:david.r.breininger@nasa.gov">david.r.breininger@nasa.gov</a> The data uses input file format described in the Program MARK manual (White and Burnham 1999, Cooch and White 2006).  Each record (row) starts with an adult bird’s capture history, followed by group variables (each bird belongs to only one group) and then covariates, which here are all time specific.  Time starts with 2001 and ends with 2015. Periods “.” in the capture history represented birds that were censored because the study sites were discontinued.  <table> <tbody> <tr> <td>   The first 15 columns represent states from 2001 to 2015 where “I” refers to nonbreeder, “2” refers to breeder and “0” occurs when the bird is not observed. </td> </tr> <tr> <td> Spaces occur after the capture history and between group variables and covariates. </td> </tr> <tr> <td> The first group variable identifies males if given a "1". </td> </tr> <tr> <td> The second group variable identifies females if given a :1". </td> </tr> <tr> <td> The third and final group membership identifies birds of unknown sex if given a "1". </td> </tr> <tr> <td> All following data refer to time-specific covariates except for the semicolon at the end of each individual's record. </td> </tr> <tr> <td> The first 14 covariates refer to whether a bird resided on the study site edge (0) or interior (1). </td> </tr> <tr> <td> The 2nd set of 14 covariates refer density (number of pairs/potential pairs) within the local population. </td> </tr> <tr> <td> The 3rd set of 14 covariates refer to population breeder mortality rates (number of banded breeders that died/number of banded breeders). </td> </tr> <tr> <td> The final set of 14 covariates refer to mean family group size of adults in each local population. </td> </tr> </tbody> </table>

FIG. 11. — A-C in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 11. — A-C, Bryocryptella torquata (Jullien, 1903); A, colony fragment, frontal view, POTB13: AMPG(IV) 2815a; B, colony fragment, dorsal view, POTB13: AMPG(IV) 2815b; C, detail view of zooids, FAN31: AMPG(IV) 3500a; D, Tessaradoma boreale (Busk, 1860), colony fragment, FAN28: AMPG(IV) 3613. E-F, Kionidella excelsa Koschinsky, 1885; E, colony fragment, basal view, FAN7: AMPG(IV)3570a; F, frontal view of a few zooids, FAN16: AMPG(IV) 3572. Scale bars: A, 500 µm; B, E, 200 µm; C, F, 100 µm; D, 1 mm.

FIG. 9. — A, B in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 9. — A, B, Cupuladria cf. canariensis (Busk, 1859); A, frontal view of a whole colony, KER39: AMPG(IV) 3078a; B, dorsal view of a whole colony, KER39: AMPG(IV) 3078b; C, D, Discoporella reussiana (Manzoni, 1869); C, frontal view of a whole colony, KER30: AMPG(IV) 3102; D, dorsal view of a whole colony, KER30: AMPG(IV) 3101; E, Nellia tenella (Lamarck, 1816), detail of an internode showing two zooids in frontal view, KER17: AMPG(IV) 3150a; F-H, Canda rectangulata Udin, 1964; F, dorsal view of an internode fragment, FAN35: AMPG(IV) 3506a; G, frontal view of an internode fragment, FAN35: AMPG(IV) 3506b; H, Detail of the same fragment, FAN35: AMPG(IV) 3506b. Scale bars: A-D, 1 mm; E, H, 100 µm; F-G, 200 µm.

FIG. 8. — A-C in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 8. — A-C, Crisia aculeata Hassall, 1841; A, internode, frontal view, POTB13: AMPG(IV) 2828a; B, internode, dorsal view, POTB13 2828b: AMPG(IV); C, internode with gonozooid, KAP22: AMPG(IV) 3339. D-F, Crisia denticulata (Lamarck, 1816); D, internode, frontal view, POTB13: AMPG(IV) 2829a; E, internode dorsal view, POTB13: AMPG(IV) 2829b; F, gonozooid, POTB13: AMPG(IV) 2829c. Scale bars: A, 500 µm; B-F, 200 µm.

FIG. 6 in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 6. — Theoretical zonation in a transect from coastal to upper bathyal palaeoenvironments following Pérès & Picard (1964). This bionomic depth zonation illustrates the situation on flat muddy bottoms in areas with very clear waters, like in the oligotrophic (eastern) Mediterranean Sea. The distribution of bryozoan growth-form assemblages (in average number of fragments per sample) and the average number of species in each assemblage is indicated in a grey circle (partly inspired from Moissette 2000).

FIG. 1. — A in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 1. — A, Situation map of Crete within the eastern Mediterranean; B, geological sketch map of the island of Crete (after Krijgsman et al. 1994), with location of the studied sections.

FIG. 7. — A, B in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 7. — A, B, Anguisia verrucosa Jullien, 1882; A, bifurcating branch, FAN36: AMPG(IV) 3471; B, encrusting base (left) and erect peristome of the encrusting proximal zooid of a running branch (right), FAN35: AMPG(IV) 3470; C, D, Exidmonea atlantica (Forbes in Johnston, 1847); C, fragment of a branch, frontal view (with a gonozooid on the left upper part), POTB13: AMPG(IV) 2853a; D, fragment of a branch, dorsal view, POTB13: AMPG(IV) 2853b; E-G, Ybselosoecia typica (Manzoni, 1878); E, fragment of a branch (with a large gonozooid), frontal view, POTB13: AMPG(IV) 2881a; F, detail of the ooeciostome of another gonozooid, POTB13: AMPG(IV) 2881b; G, fragment of a branch, dorsal view, POTB13: AMPG(IV) 2881c. Scale bars: A, D, 200 µm; B, G, 100 µm; C-E, 500 µm.

FIG. 2 in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 2. — Schematic sedimentary log of Potamida composite section with sample location and semi-quantitative abundances of bryozoan species.

FIG. 10. — A-C in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 10. — A-C, Scrupocellaria cf. elliptica (Reuss, 1847); A, view of some zooids showing opesia with 4 spine bases on the outer distal part and 3 spine bases + 1 scutal spine on the inner distal rim, FAN36: AMPG(IV) 3587; B, zooids with 7 spine bases and the scutum, FAN35: AMPG(IV) 3586a; C, dorsal surface of a colony fragment with small vibracularia and radicular pores, FAN35: AMPG(IV) 3586b; D, E, Scrupocellaria scrupea Busk, 1852; D, ovicellate colony fragment, FAN35: AMPG(IV) 3590a; E, detail frontal view showing opesia with five spine bases, FAN35: AMPG(IV) 3590b; F-H, Cellaria salicornioides Lamouroux, 1816; F, part of a slender internode, FAN18: AMPG(IV) 3513a; G, detail view showing denticles and endotoichal ovicells, POTB13: AMPG(IV) 2821a; H, avicularia in frontal and lateral view (arrow), POTB13: AMPG(IV) 2821b; I, Gemellipora eburnea Smitt, 1873, broken internode showing two zooids with two oval scars separated by a thin interzooidal groove, CAP032: AMPG(IV) 3426. Scale bars: A-E, G, I, 100 µm; F, H, 200 µm.

FIG. 12. — A-G in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 12. — A-G, Batopora rosula (Reuss, 1847); A, colony, basal-lateral view (arrow indicates the scar of an ovicellate zooid), FAN7: AMPG(IV) 3475a; B, colony, apical view, FAN7: AMPG(IV) 3475b; C, colony, lateral-apical view, FAN7: AMPG(IV) 3475c; D-G, juvenile forms (G, basal view), FAN18: AMPG(IV)a-d; H-I, Orbitulipora excentrica Seguenza, 1880; H, whole colony, FAN22: AMPG(IV) 3580a; I, detail view of the left part of the same colony (arrows indicate ovicellate zooids), FAN22: AMPG(IV) 3580a. Scale bars: H, 500 µm; A-C, I, 200 µm; D-G, 100 µm.

FIG. 5 in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 5. — Schematic sedimentary log of Faneromeni section with sample location and semi-quantitative abundances of bryozoan species.

FIG. 3 in Bryozoan faunas at the Tortonian-Messinian transition. A palaeoenvironmental case study from Crete Island, eastern Mediterranean

FIG. 3. — Schematic sedimentary log of Keramoutsi section with sample location and semi-quantitative abundances of bryozoan species.