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Abstract Freshwater from the Arctic participates in the globally important Atlantic Meridional Overturning Circulation (AMOC). We use high‐resolution, in situ observations of dissolved organic matter (DOM) fluorescence to trace the origins of freshwater and organic carbon in the densest component of the AMOC, namely Denmark Strait Overflow Water (DSOW). We find a distinct terrestrial DOM signal in DSOW and trace it upstream to the Siberian shelves in the Arctic Ocean. This implies a riverine origin of freshwater in DSOW. We estimate that the Siberian Shelf water contribution constitutes approximately 1% of DSOW. Ocean circulation modeling confirms the inferred pathway and highlights Denmark Strait as an important location for the entrainment of the riverine signal into DSOW. Our proposed method can be deployed on a range of observing systems to elucidate freshwater dispersion across the Arctic and subarctic, thereby contributing to the broader discussion on freshwater impacts and organic carbon sequestration in the AMOC. 

Abstract Investigations of hydrostatic pressure effects on microbial enzymatic processing are challenging but critical for understanding element cycling in the world's oceans. In this study, we developed and tested a stainless‐steel pressure cell capable of withstanding up to 110 MPa of hydrostatic pressure (equivalent to ~ 11,000 m depth), featuring three sapphire windows that enable real‐time measurements of spectral absorption and fluorescence. The temperature‐controlled system (5–50°C) can be incorporated in standard laboratory spectrofluorophotometers. The hydrostatic pressure of the 2.6 mL sample is regulated using a manually controlled spindle pump. The system was tested with fluorometric enzyme assays and used to evaluate the activity of chitinase enzymes produced by piezophilic and piezosensitive marine bacteria at a constant temperature of 10°C. Experiments on enzymes from three bacterial strains revealed distinct and reproducible differences in pressure responses. This compact system enables precise monitoring of pressure‐sensitive activity of microbial communities and extracellular enzymes and thus provides an avenue for detailed investigations on the importance of hydrostatic pressure in regulating deep‐sea biogeochemical processing. 

Abstract Analysis of lignin in seawater is essential to understanding the fate of terrestrial dissolved organic matter (DOM) in the ocean and its role in the carbon cycle. Lignin is typically quantified by gas or liquid chromatography, coupled with mass spectrometry (GC‐MS or LC‐MS). MS instrumentation can be relatively expensive to purchase and maintain. Here we present an improved approach for quantification of lignin phenols using LC and absorbance detection. The approach applies a modified version of parallel factor analysis (PARAFAC2) to 2^ndderivative absorbance chromatograms. It is capable of isolating individual elution profiles of analytes despite co‐elution and overall improves sensitivity and specificity, compared to manual integration methods. For most lignin phenols, detection limits below 5 nmol L⁻¹were achieved, which is comparable to MS detection. The reproducibility across all laboratory stages for our reference material showed a relative standard deviation between 1.47% and 16.84% for all 11 lignin phenols. Changing the amount of DOM in the reaction vessel for the oxidation (dissolved organic carbon between 22 and 367 mmol L⁻¹), did not significantly affect the final lignin phenol composition. The new method was applied to seawater samples from the Kattegat and Davis Strait. The total concentration of dissolved lignin phenols measured in the two areas was between 4.3–10.1 and 2.1–3.2 nmol L⁻¹, respectively, which is within the range found by other studies. Comparison with a different oxidation approach and detection method (GC‐MS) gave similar results and underline the potential of LC and absorbance detection for analysis of dissolved lignin with our proposed method. 

Abstract Many challenges remain before we can fully understand the multifaceted role that natural organic matter (NOM) plays in soil and aquatic systems. These challenges remain despite the considerable progress that has been made in understanding NOM’s properties and reactivity using the latest analytical techniques. For nearly 4 decades, the International Humic Substances Society (IHSS, which is a non-profit scientific society) has distributed standard substances that adhere to strict isolation protocols and reference materials that are collected in bulk and originate from clearly defined sites. These NOM standard and reference samples offer relatively uniform materials for designing experiments and developing new analytical methods. The protocols for isolating NOM, and humic and fulvic acid fractions of NOM utilize well-established preparative scale column chromatography and reverse osmosis methods. These standard and reference NOM samples are used by the international scientific community to study NOM across a range of disciplines from engineered to natural systems, thereby seeding the transfer of knowledge across research fields. Recently, powerful new analytical techniques used to characterize NOM have revealed complexities in its composition that transcend the “microbial” vs. “terrestrial” precursor paradigm. To continue to advance NOM research in the Anthropocene epoch, a workshop was convened to identify potential new sites for NOM samples that would encompass a range of sources and precursor materials and would be relevant for studying NOM’s role in mediating environmental and biogeochemical processes. We anticipate that expanding the portfolio of IHSS reference and standard NOM samples available to the research community will enable this diverse group of scientists and engineers to better understand the role that NOM plays globally under the influence of anthropogenic mediated changes.