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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.

 

Estuaries function as important transporters, transformers, and producers of organic matter (OM). Along the freshwater to saltwater gradient, the composition of OM is influenced by physical and biogeochemical processes that change spatially and temporally, making it difficult to constrain OM in these ecosystems. In addition, many of the environmental parameters (temperature, precipitation, riverine discharge) controlling OM are expected to change due to climate change. To better understand the environmental drivers of OM quantity (concentration) and quality (absorbance, fluorescence), we assessed both dissolved OM (DOM) and particulate OM (POM) spatially, along the freshwater to saltwater gradient and temporally, for a full year. We found seasonal differences in salinity throughout the estuary due to elevated riverine discharge during the late fall to early spring, with corresponding changes to OM quantity and quality. Using redundancy analysis, we found DOM covaried with salinity (adjusted r2 = 0.35, 0.41 for surface and bottom), indicating terrestrial sources of DOM in riverine discharge were the dominant DOM sources throughout the estuary, while POM covaried with environmental indictors of terrestrial sources (turbidity, adjusted r2 = 0.16, 0.23 for surface and bottom) as well as phytoplankton biomass (chlorophyll-a, adjusted r2 = 0.25, 0.14 for surface and bottom). Responses in OM quantity and quality observed during the period of elevated discharge were similar to studies assessing OM quality following extreme storm events suggesting that regional changes in precipitation, as predicted by climate change, will be as important in changing the estuarine OM pool as episodic storm events in the future. 

Abstract. The net ecosystem productivity (NEP) of two seagrassmeadows within one of the largest seagrass ecosystems in the world, FloridaBay, was assessed using direct measurements over consecutive diel cyclesduring a short study in the fall of 2018. We report significant differencesbetween NEP determined by dissolved inorganic carbon (NEPDIC) and bydissolved oxygen (NEPDO), likely driven by differences in air–water gasexchange and contrasting responses to variations in light intensity. We alsoacknowledge the impact of advective exchange on metabolic calculations ofNEP and net ecosystem calcification (NEC) using the “open-water” approachand attempt to quantify this effect. In this first direct determination ofNEPDIC in seagrass, we found that both seagrass ecosystems were netheterotrophic, on average, despite large differences in seagrass netabove-ground primary productivity. NEC was also negative, indicating thatboth sites were net dissolving carbonate minerals. We suggest that acombination of carbonate dissolution and respiration in sediments exceededseagrass primary production and calcification, supporting our negative NEPand NEC measurements. However, given the limited spatial (two sites) andtemporal (8 d) extent of this study, our results may not berepresentative of Florida Bay as a whole and may be season-specific. Theresults of this study highlight the need for better temporal resolution,accurate carbonate chemistry accounting, and an improved understanding ofphysical mixing processes in future seagrass metabolism studies. 

Estuaries regulate transport of dissolved organic carbon (DOC) from land to ocean. Export of terrestrial DOC from coastal watersheds is exacerbated by increasing major rainfall and storm events and human activities, leading to pulses of DOC that are shunted through rivers downstream to estuaries. Despite an upward trend of extreme events, the fate of the pulsed terrestrial DOC in estuaries remains unclear. We analyzed the effects of seven major tropical cyclones (TC) from 1999 to 2017 on the quantity and fate of DOC in the Neuse River Estuary (NC, USA). Significant TC‐induced increases in DOC were observed throughout the estuary; the increase lasting from around 50 d at head‐of‐tide to over 6 months in lower estuary. Our results suggest that pulsed terrestrial DOC associated with TCs temporarily overwhelms the estuarine filter's abiotic and biotic degradation capacity under such high flow events, enhancing the shunt of terrestrial carbon to the coastal ocean.

 

To assess climate‐mediated terrestrial‐aquatic linkages in Arctic lakes and potential impacts on light attenuation and carbon cycling, we evaluated lake responses to climate drivers in two areas of west Greenland with differing climate patterns. We selected four lakes in a warmer, drier area to compare with four lakes from a cooler, wetter area proximal to the Greenland Ice Sheet. In June from 2013–2018, we measured epilimnetic water temperature, 1% depth of photosynthetically active radiation (PAR), dissolved organic carbon (DOC), specific ultraviolet absorbance (SUVA₂₅₄), DOC‐normalized absorbance at 380 nm (a*₃₈₀), and chlorophylla. Interannual coherence of 1% PAR and DOC was particularly high for lakes within the warmer, drier area. This coherence suggests forcing of Arctic lake features by a large‐scale driver, likely climate. Redundancy analysis showed that monthly average precipitation, winter North Atlantic Oscillation (NAO) index (NAO_W), spring average air temperature, and spring average precipitation influenced the lake variables (p= 0.003, adj.R²= 0.58). In particular, monthly average precipitation contributed to increases in soil‐derived DOC quality metrics and chlorophyllaand decreased 1% PAR. Interannual changes in lake responses to climate drivers were more apparent in the warmer, drier area than the cooler, wetter area. The interannual lake responses within and between areas, associated with climate trends, suggest that with ongoing rapid climate change in the Arctic, there could be widespread impacts on key lake responses important for light attenuation and carbon cycling.

 

Prediction of high latitude response to climate change is hampered by poor understanding of the role of nonlinear changes in ecosystem forcing and response. While the effects of nonlinear climate change are often delayed or dampened by internal ecosystem dynamics, recent warming events in the Arctic have driven rapid environmental response, raising questions of how terrestrial and freshwater systems in this region may shift in response to abrupt climate change. We quantified environmental responses to recent abrupt climate change in West Greenland using long-term monitoring and paleoecological reconstructions. Using >40 years of weather data, we found that after 1994, mean June air temperatures shifted 2.2 °C higher and mean winter precipitation doubled from 21 to 40 mm; since 2006, mean July air temperatures shifted 1.1 °C higher. Nonlinear environmental responses occurred with or shortly after these abrupt climate shifts, including increasing ice sheet discharge, increasing dust, advancing plant phenology, and in lakes, earlier ice out and greater diversity of algal functional traits. Our analyses reveal rapid environmental responses to nonlinear climate shifts, underscoring the highly responsive nature of Arctic ecosystems to abrupt transitions.