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Abstract Seasonal phytoplankton blooms in Greenland’s coastal waters form the base of marine food webs and contribute to oceanic carbon uptake. In Qeqertarsuup Tunua, West Greenland, a secondary summertime bloom follows the Arctic spring bloom, enhancing annual primary productivity. Emerging evidence links this summer bloom to subglacial discharge from Sermeq Kujalleq, the most active glacier on the Greenland Ice Sheet. This discharge drives localized upwelling that may alleviate nutrient limitation in surface waters, yet this mechanism remains poorly quantified. Here, we employ a high-resolution biogeochemical model nested within a global state estimate to assess how discharge-driven upwelling influences primary productivity and carbon fluxes. We find that upwelling increases summer productivity by 15–40% in Qeqertarsuup Tunua, yet annual carbon dioxide uptake rises by only  ~3% due to reduced solubility in plume-upwelled waters. These findings suggest that intensifying ice sheet melt may alter Greenland’s coastal productivity and carbon cycling under future climate scenarios. 

Abstract Subglacial discharge emerging from the base of Greenland's marine‐terminating glaciers drives upwelling of nutrient‐rich bottom waters to the euphotic zone, which can fuel nitrate‐limited phytoplankton growth. Here, we use buoyant plume theory to quantify this subglacial discharge‐driven nutrient supply on a pan‐Greenland scale. The modeled nitrate fluxes were concentrated in a few critical systems, with half of the total modeled nitrate flux anomaly occurring at just 14% of marine‐terminating glaciers. Increasing subglacial discharge fluxes results in elevated nitrate fluxes, with the largest flux occurring at Jakobshavn Isbræ in Disko Bay, where subglacial discharge is largest. Subglacial discharge and nitrate flux anomaly also account for significant temporal variability in summer satellite chlorophyll a (Chl) within 50 km of Greenland's coast, particularly in some regions in central west and northwest Greenland. 

Abstract Optical polarizers encompass a class of anisotropic materials that pass-through discrete orientations of light and are found in wide-ranging technologies, from windows and glasses to cameras, digital displays and photonic devices. The wire-grids, ordered surfaces, and aligned nanomaterials used to make polarized films cannot be easily reconfigured once aligned, limiting their use to stationary cross-polarizers in, for example, liquid crystal displays. Here we describe a supramolecular material set and patterning approach where the polarization angle in stand-alone films can be precisely defined at the single pixel level and reconfigured following initial alignment. This capability enables new routes for non-binary information storage, retrieval, and intrinsic encryption, and it suggests future technologies such as photonic chips that can be reconfigured using non-contact patterning.