Nature

Sup 5. Open with ImageJ. Sup 6. Open with ImageJ. Sup 7. Open with ImageJ. Sup 8. Open with ImageJ. Sup 9. Open with ImageJ. Sup 10. Open with ImageJ. Sup 11. Open with ImageJ. Sup 12. Open with ImageJ (lif files) and Vevo (the rest of the files). Sup 13. Open with ImageJ. Sup 14. Open with ImageJ. Sup 15. Open with ImageJ. Sup 16. Open with ImageJ. Sup 17. Open with ImageJ.

7z archive files of NMR and mass spectra of each compound.

Supporting research data

Dataset for publication https://doi.org/10.1038/s41586-023-06907-7, "Altermagnetic lifting of Kramers spin degeneracy", Nature volume 626, pages 517–522 (2024). Dataset include input and potential files for calculation on SPR-KKR package 8.6. Detailed descriptions are in the README text documents in subdirectories.

This repository (mirrored from https://github.com/LisaHuelsmann/latitudinalCNDD) contains the code to reproduce the analyses by Hülsmann et al., which uses repeated census data from 23 large forest sites from the ForestGEO network to analyze latitudinal patterns in stabilizing conspecific negative density dependence (CNDD). The repository holds the folders code (all Rscripts), data_prep (input and derived output data to run the analyses) and reproducibility_exports (CNDD estimates to reproduce the main meta-regressions). Moreover, when running the analysis pipeline, a folder out will be created with the results of mortality models, meta-regressions, and tables for the Extended Data. Because tree data from most ForestGEO sites cannot be made freely available, we generated 'fake sites' based on small samples of the dataset from Barro Colorado Island (BCI, Panama) available here. These fake sites were artificially aligned along a latitudinal gradient to be able to run the full analysis pipeline. Methodology We used repeated census data from 23 large forest sites around the globe to analyze latitudinal patterns in stabilizing conspecific negative density dependence (CNDD) following a three-step approach: First, we fitted species-site-specific mortality models from repeated observations of individual trees. Second, we used these models to quantify CNDD for each species and site using an estimator designed to maximize robustness, comparability, and relevance for fitness and stabilization. Third, we used meta-regressions to explore three distinct latitudinal patterns in CNDD derived from the hypothesis that CNDD is more influential for maintaining local tree species diversity in the tropics. Robustness of the analysis pipeline was validated by model diagnostics and randomization. This approach is based on recently developed best-practice statistical methods for estimating CNDD. Crucially, the use of dynamic mortality data allowed us to avoid the statistical pitfalls of previous CNDD studies, in particular analyses of the static relationship of number of saplings to number of adults, where the null hypothesis is a positive linear relationship but regression dilution flattens this relationship and thus biases analyses towards finding CNDD, especially for rare species. By fitting mortality models where the null hypothesis is no relationship between survival and number of conspecific neighbors, we ensure that any regression dilution has a conservative effect by reducing CNDD estimates. We also addressed other recently identified limitations of CNDD analyses, namely non-linear and saturating CNDD, the comparability of CNDD among species and sites, and the extent to which CNDD estimates are meaningful for stabilization and species coexistence. System and R Packages All analyses were conducted in R version 4.2.1 on Ubuntu 20.04.4 LTS, but the code has also been tested on macOS Monterey 12.6. Major steps of the analyses were carried out with the following R packages: mgcv (Version 1.8-40) metafor (Version 3.4-0) DHARMa (Version 0.4.6) The expected runtime for the demo dataset on a normal computer is approx. a few minutes for the data preparation, approx. 24h for the mortality models (the grid search is computationally quite expensive), 20min for the meta-regressions, and a few seconds for the tables. Runtime can be reduced when using more cores for the mortality models and meta-regressions. Contact Lisa Hülsmann, EASI lab, University of Bayreuth, lisa.huelsmann@uni-bayreuth.de

Research objective: determine whether DNA loop-extruding SMC complexes can bypass CTCFType of research: Single-molecule in vitro reconstitution of DNA loop extrusion using purified proteinsMethod of data collection: HiLO microscopyType of data: Images (.tif). Due to the large size of the raw data, pointers to the data location are included in this dataset

Research objective: determine whether DNA loop-extruding SMC complexes can bypass CTCFType of research: Single-molecule in vitro reconstitution of DNA loop extrusion using purified proteinsMethod of data collection: HiLO microscopyType of data: Images (.tif). Due to the large size of the raw data, pointers to the data location are included in this dataset

The repository contains raw data, processing scripts, simulation files, and GDS files for the manuscript "Room-temperature quantum optomechanics using an ultra-low noise cavity." For detailed usage instructions, please take a look at the ReadMe.txt files.

Model of cGAS ubiquitylation.

This file contains the raw data of main Figures and extended data figures of the manuscript