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Streams in the southeastern United States Coastal Plains serve as an essential source of energy and nutrients for important estuarine ecosystems, and dissolved organic matter (DOM) exported from these streams can have profound impacts on the biogeochemical and ecological functions of fluvial networks. Here, we examined hydrological and temperature controls of DOM during low-flow periods from a forested stream located within the Coastal Plain physiographic region of Alabama, USA. We analyzed DOM via combining dissolved organic carbon (DOC) analysis, fluorescence excitation–emission matrix combined with parallel factor analysis (EEM-PARAFAC), and microbial degradation experiments. Four fluorescence components were identified: terrestrial humic-like DOM, microbial humic-like DOM, tyrosine-like DOM, and tryptophan-like DOM. Humic-like DOM accounted for ~70% of total fluorescence, and biodegradation experiments showed that it was less bioreactive than protein-like DOM that accounted for ~30% of total fluorescence. This observation indicates fluorescent DOM (FDOM) was controlled primarily by soil inputs and not substantially influenced by instream production and processing, suggesting that the bulk of FDOM in these streams is transported to downstream environments with limited in situ modification. Linear regression and redundancy analysis models identified that the seasonal variations in DOM were dictated primarily by hydrology and temperature. Overall, high discharge and shallow flow paths led to the enrichment of less-degraded DOM with higher percentages of microbial humic-like and tyrosine-like compounds, whereas high temperatures favored the accumulation of high-aromaticity, high-molecular-weight, terrestrial, humic-like compounds in stream water. The flux of DOC and four fluorescence components was driven primarily by water discharge. Thus, the instantaneous exports of both refractory humic-like DOM and reactive protein-like DOM were higher in wetter seasons (winter and spring). As high temperatures and severe precipitation are projected to become more prominent in the southeastern U.S. due to climate change, our findings have important implications for future changes in the amount, source, and composition of DOM in Coastal Plain streams and the associated impacts on downstream carbon and nutrient supplies and water quality.
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This content will become publicly available on April 1, 2026
Behavior of compounds leached from tire tread particles under simulated sunlight exposure
Tire tread particles are microplastics (< 5 mm) and leach organic chemicals into aquatic environments. It is important to understand the behavior of tire wear compounds in sunlight-exposed waters in terms of their persistence, removal, and transformation. Therefore, we conducted photolysis experiments with leachates from laboratory-generated tire tread particles (TTP) over 72 h in a solar simulator to evaluate the behavior of leached compounds and fluorescent components over time. Compared to initial leachates, simulated sunlight exposure resulted in ~12 % decrease in dissolved organic carbon, 11 % reduction in the total fluorescence of leachates, and ~30 % removal of the 213 chromatographic features detected by nontargeted analysis (NTA) using comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry. A decrease in total chemical abundance determined by NTA was observed, with normalized peak areas decreasing by 36.4% in the 72 h photoirradiated samples and by 13.6% in the dark samples. Fifty-three compounds were tentatively identifiable based on mass spectral matching and among them, 12 compounds were confirmed with authentic standards. Among the 53 compounds, 19 compounds were photo-labile, 27 were photo-resistant, and 7 were photo-transformation products. NTA also identified compounds previously unreported as tire-related compounds. Parallel factor analysis (PARAFAC) modeling of three-dimensional excitation-emission-matrix (EEM) data identified five fluorescent components. PARAFAC component C4 (excitation/emission peak at 285/445 nm) was found to be a fluorescent analog for 6PPD. Rapid double exponential decay kinetics were observed for the 6PPD-like component during photoirradiation. Similarly, the peak fluorescence of commercially available 6PPD exposed to simulated sunlight was reduced by >90 % in the first 0.5 h of photoirradiation. 6PPD photodegradation resulted in the production of a fluorescent transformation product resembling PARAFAC Component C2 (with emission at 360 nm). These results prove that EEM fluorescence analyses can serve as a rapid method for kinetics analysis of 6PPD, and may be combined with NTA compound tentative identification to track the behavior of other TTP-derived compounds in experimental studies.
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- Award ID(s):
- 2327008
- PAR ID:
- 10600617
- Publisher / Repository:
- Elsevier
- Date Published:
- Journal Name:
- Water Research
- Volume:
- 274
- Issue:
- C
- ISSN:
- 0043-1354
- Page Range / eLocation ID:
- 123060
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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