David C. Podgorski

The effect of extraction methods on detecting hydrocarbon oxidation products (HOPs) in groundwater remains unclear. HOPs are polar, water-soluble byproducts of petroleum biodegradation. Our previous work showed that liquid-liquid extraction (LLE), a method commonly used in regulatory monitoring, has a significantly lower extraction efficiency for HOPs compared to solid-phase extraction (SPE). In this study, we evaluate the analytical limitations and compositional selectivity of LLE and SPE using groundwater samples from the Bemidji, MN, crude oil spill site. Optical properties were characterized using excitation-emission matrix spectroscopy (EEMs), and a three-component PARAFAC model was validated, showing consistent trends across both extracts and whole water samples. Ultrahigh-resolution mass spectrometry (UHR-MS) revealed that LLE selectively recovered aliphatic-like compounds but underrepresented more polar oxygenated HOPs. In contrast, SPE methods were more effective at isolating highly oxidized compound classes. These differences were consistent across a gradient of contamination. Overall, the LLE was less precise and less representative of polar HOPs, introducing bias in the characterization of HOPs. This study is the first to quantitatively demonstrate the compositional selectivity and analytical bias of LLE versus SPE for HOPs using combined EEM-PARAFAC and UHR-MS techniques, with implications for long-term monitoring and site assessment protocols.

Ballast water released from ships into coastal environments has been identified as a mechanism that introduces contaminants of concern into coastal ecosystems.

Plastics are accumulating on Earth, including at sea. The photodegradation of microplastics floating in seawater produces dissolved organic matter (DOM), indicating that sunlight can photodissolve microplastics at the sea surface. To characterize the chemistry of DOM produced as microplastics photodissolve, three microplastics that occur in surface waters, polyethylene (PE), polypropylene (PP), and expanded polystyrene (EPS), were incubated floating on seawater in both the light and the dark. We present the molecular signatures of the DOM produced during these incubations, as determined via ultrahigh-resolution mass spectrometry. Zero to 12 products were identified in the dark, whereas 319-705 photoproducts were identified in the light. Photoproduced DOM included oxygen atoms, indicating that soluble, oxygen-containing organics were formed as plastics photodegrade. PP and PE plastics have hydrogen-to-carbon (H/C) ratios of 2 and generated DOM with average H/C values of 1.7 ± 0.1 to 1.8 ± 0.1, whereas EPS, which has an H/C of 1, generated DOM with an average H/C of 0.9 ± 0.2, indicating the stoichiometry of photoproduced DOM was related to the stoichiometry of the photodegrading polymer. The photodissolution of plastics produced hundreds of photoproducts with varying elemental stoichiometries, indicating that a single abiotic process (photochemistry) can generate hundreds of different chemicals from stoichiometrically monotonous polymers.

Hydrocarbon oxidation products (HOPs) formed from crude oil and diesel were generated from laboratory simulated spills at four different periods (1, 4, 7, and 10 days) under environmental conditions that mimicked those in Cook Inlet, Alaska.

Arctic lakes store, modify, and transport large quantities of carbon from terrestrial environments to the atmosphere; however, the spatial and temporal relationships between quantity and composition of dissolved organic matter (DOM) have not been well characterized across broad arctic regions. Moreover, most arctic lake DOM compositions have been examined during the ice‐free summer, whereas DOM cycling between the ice‐covered winter months and summer have not been addressed. To resolve these spatial and seasonal uncertainties in DOM cycling, we sampled a series of arctic lakes from the North Slope of Alaska across a latitudinal gradient in the winter and summer over 3 years. Samples were analyzed for dissolved organic carbon concentration and DOM composition was characterized using optical and fluorescence properties combined with molecular‐level analysis using Fourier transform‐ion cyclotron resonance mass spectrometry. Tundra lake DOM properties including aromaticity and molecular stoichiometries were similar to other northern high‐latitude lakes, but optical parameters related to aromaticity and molecular weight were greater in major arctic rivers and in coastal lakes in the North Slope region. DOM composition was highly seasonal, with ice exclusion concentrating microbially processed DOM in the winter water columns, potentially influencing DOM cycling the following summer. However, the greatest variations in DOM composition were related to lake depth and likely other physical features including morphology and bathymetry. As the Arctic warms, we expect changes in hydrology and ice cover to enhance under‐ice microbial DOM processing, early summer photodegradation, and ultimately carbon fluxes to the atmosphere after ice‐out.