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Geochemical data from ancient marine sediments are crucial for studying palaeo-environments, palaeo-climates, and elemental cycles. With increased accessibility to geochemical data, many databases have emerged. However, there remains a need for a more comprehensive database that focuses on deep-time marine sediment records. Here, we introduce the Deep-Time Marine Sedimentary Element Database (DM-SED). The DM-SED has been built upon the Sedimentary Geochemistry and Paleoenvironments Project (SGP) database with a new compilation of 34 874 data entries from 433 studies, totalling 63 627 entries. The DM-SED contains 2 522 255 discrete marine sedimentary data points, including major and trace elements and some stable isotopes. It includes 9207 entries from the Precambrian and 54 420 entries from the Phanerozoic, thus providing significant references for reconstructing deep-time Earth system evolution. The data files described in this paper are available at https://doi.org/10.5281/zenodo.14771859 (Lai et al., 2025). 

The largest mass extinction event is associated with changes in degassing style of the Siberian Traps volcanism. 

Abstract The development of large pore single‐crystalline covalently linked organic frameworks is critical in revealing the detailed structure‐property relationship with substrates. One emergent approach is to photo‐crosslink hydrogen‐bonded molecular crystals. Introducing complementary hydrogen‐bonded carboxylic acid building blocks is promising to construct large pore networks, but these molecules often form interpenetrated networks or non‐porous solids. Herein, we introduced heteromeric carboxylic acid dimers to construct a non‐interpenetrated molecular crystal. Crosslinking this crystal precursor with dithiols afforded a large pore single‐crystalline hydrogen‐bonded crosslinked organic framework H_COF‐101. X‐ray diffraction analysis revealed H_COF‐101 as an interlayer connected hexagonal network, which possesses flexible linkages and large porous channels to host a hydrazone photoswitch. Multicycle Z/E‐isomerization of the hydrazone took place reversibly within H_COF‐101, showcasing the potential use of H_COF‐101 for optical information storage.