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The dataset provides Rhizostoma pulmo newly released ephyrae statoliths measurements., The data set is provided as an Excel file within a compressed folder that also includes a single README file (in text format) containing a detailed description of the data structure., [METHODOLOGY] Description of methods used for collection/generation of data: Six combinations of temperature and PCO2 (18, 24 and 30ºC with a PCO2 of 500 and 1000 ppm each) were applied during 32 days to different groups of polyps of Rhizostoma pulmo. From the released ephyrae during this period, three specimens from each treatment were randomly taken. From each ephyra, three of its eight statocysts were randomly selected and all the statoliths inside were counted and measured via inverted optical microscopy.-- Methods for processing the data: Data were analyzed using RStudio software. To obtain the variable "volume", its values were obtained using the formula for the volume of a regular hexagonal prism., This data set includes data collected from ICMAN-CSIC (Spain), consisting of measurements of the size and number of the statoliths present in newly released Rhizostoma pulmo ephirae under conditions of oceanic warming and acidification (IPCC SSP5-8.5 scenario). From each ephyra, three of its eight statocysts were randomly selected and all the statoliths inside were counted and measured., This research was funded by the Spanish Ministerio de Economía y Competitividad (grant number CTM2016-75487-R “Respuesta de medusas mediterráneas al efecto interactivo de motores climáticos de impacto: supervivencia en un Mediterráneo más cálido y ácido”, proyect MED2CA), CSIC (grant number 202330E57 “Estudio de los efectos de motores de impacto del cambio climático sobre las dinámicas poblacionales de medusas mediterráneas”) and the Project Agreement “Detección de medusas en el mar Balear y su relación con las condiciones ambientales: hacia el desarrollo de un sistema de predicción pre-operacional” among Govern des Illes Balears, SOCIB and CSIC (Disposición 15052 del BOE núm. 310 de 2020). It was also financially sustainned by a Ph.D. fellowship (FPU22/03487) from the Spanish Ministerio de Ciencia, Innovación y Universidades., Peer reviewed

STM topographs and dI/dV spectra of molecules within molecular layers, dI/dV spectra of a wide voltage range, additional DFT results, an explanation of the Green function approach used to estimate TK, and a description of the synthesis of CoTPPBr2I2., Peer reviewed

Figure S1. Phylogenetic tree of voltage-gated K+ channel protein sequences from tomato and Arabidopsis and expression of SlK5.1 and SlK5.2 in tomato plants. Figure S2. Generation of slskor KO mutants with the CRISPR-Cas system. Figure S3. Phylogenetic tree of S-type anion channel protein sequences from tomato and Arabidopsis and gene expression in tomato roots. Figure S4. slskor plants exhibited increased Na+ and Cl- content in shoots under salt stress. Figure S5. Protein sequence alignment of AtSKOR and SlSKOR. Figure S6. Phylogenetic tree of CIPK protein sequences from tomato and Arabidopsis. Figure S7. Effect of SlCIPK9+SlCBL1 and SlCIPK2+SlCBL1 on SlSKOR activity. Table S1. Primers used in this study Table S2. Fold-change values in qRT-PCR experiments. Methods S1. Selection of homolog proteins and calculation of SlSKOR functional parameters. Dataset 1. Data supporting the findings of this study, Peer reviewed

MMC S1. Details of experimental techniques and supplementary hydrogen adsorption measurements., Peer reviewed

Schemes of glass formation of supercooled liquid and Moynihan equal-area method for determining Tf, raw data of isothermal physical aging tests, precision verification of TTS, procedure for TTS of reported data from literatures, and the corresponding master curve., Peer reviewed

See the supplementary material for the convergence tests of total energy and MAE (Figs. S1–S6), the dependency between the value of the MAE and Ueff (Figs. S7–S9), and the 3d-orbital-decomposed PDOS obtained by HSE06 (Fig. S10)., Peer reviewed

Further information on the (Te, Tl)–MDEF method, the multicoverage EANN PES, and the photoinduced CO desorption dynamics., Peer reviewed

Section 1. Methods Section 2. Extended data of anisotropic transport on device S1 Section 3. Comparison between samples Section 4. Angular dependence of the second-order non-linear response Section 5. Raw data of magnetoresistance measurements Section 6. Non-linear conductivity on device S2 Section 7. Scaling law of the non-linear conductivity, Peer reviewed

Theoretical description of electromagnetic fields and forces using the multipolar decomposition of GLMT and the surface integration of the Maxwell stress tensor (Tij), description of the experimental setup detailing the wavefront phase modulation system, the imaging system of the trapping region, and the trap stiffness constant (κx/y) measurement system, and trap stiffness measurements through the PSD method: operation of the four-quadrant photodetector and Lorentzian fitting procedure of the experimental power spectrum., Peer reviewed

Soft tissue defects or pathologies frequently necessitate the use of biomaterials that provide the volume required for subsequent vascularization and tissue formation as autrografts are not always a feasible alternative. Supramolecular hydrogels represent promising candidates because of their 3D structure, which resembles the native extracellular matrix, and their capacity to entrap and sustain living cells. Guanosine-based hydrogels have emerged as prime candidates in recent years since the nucleoside self-assembles into well-ordered structures like G-quadruplexes by coordinating K+ ions and π–π stacking, ultimately forming an extensive nanofibrillar network. However, such compositions were frequently inappropriate for 3D printing due to material spreading and low shape stability over time. Thus, the present work aimed to develop a binary cell-laden hydrogel capable of ensuring cell survival while providing enough stability to ensure scaffold biointegration during soft tissue reconstruction. For that purpose, a binary hydrogel made of guanosine and guanosine 5'-monophosphate was optimized, rat mesenchymal stem cells were entrapped, and the composition was bioprinted. To further increase stability, the printed structure was coated with hyperbranched polyethylenimine. Scanning electron microscopic studies demonstrated an extensive nanofibrillar network, indicating excellent G-quadruplex formation, and rheological analysis confirmed good printing and thixotropic qualities. Additionally, diffusion tests using fluorescein isothiocyanate labeled-dextran (70, 500, and 2000 kDa) showed that nutrients of various molecular weights may diffuse through the hydrogel scaffold. Finally, cells were evenly distributed throughout the printed scaffold, cell survival was 85% after 21 days, and lipid droplet formation was observed after 7 days under adipogenic conditions, indicating successful differentiation and proper cell functioning. To conclude, such hydrogels may enable the 3D bioprinting of customized scaffolds perfectly matching the respective soft tissue defect, thereby potentially improving the outcome of the tissue reconstruction intervention., Peer reviewed