skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Assessing the prevalence, products, and pathways of dissolved organic matter partial photo-oxidation in arctic surface waters
In sunlit waters, photodegradation of dissolved organic matter (DOM) yields completely oxidized carbon ( i.e. , CO 2 ) as well as a suite of partially oxidized compounds formed from oxygen incorporation ( i.e. , partial photo-oxidation). Of these two groups of DOM photo-products, more studies focus on CO 2 (a greenhouse gas) than on partially oxidized DOM, which is likely a diverse group of compounds with poorly constrained roles in aquatic carbon cycling or biogeochemistry. The objective of this study is to address knowledge gaps on the prevalence, products, and pathways of DOM partial photo-oxidation. Here we traced the photochemical incorporation of isotopically labelled 18 O 2 into DOM isolated from Alaskan Arctic surface waters using high-resolution mass spectrometry. Complete and partial photo-oxidation of DOM was also quantified as CO 2 production and O 2 consumption. The majority of 18 O-containing partial oxidation photo-products were classified as carboxylic rich alicyclic molecules (CRAM) and overlapped in composition with previously reported photo-products known to result from the oxidation of DOM by singlet oxygen. These results support a previously proposed hypothesis that photo-oxidation by singlet oxygen may contribute to the formation of CRAM, a compound class of DOM ubiquitously observed in surface waters. The novel application of an isotopic tracer for oxygen incorporation with a mass balance approach to quantify complete and partial photo-oxidation of DOM revealed that less than one mol of O 2 is required to produce one mol of CO 2 . A sensitivity analysis based on this new knowledge demonstrated that the magnitude of DOM partial photo-oxidation may be underestimated by up to four-fold. Consequently, partial photo-oxidation likely plays a more prominent role in shaping DOM composition in sunlit waters of the Arctic than previously understood. Therefore, partial photo-oxidation should be increasingly incorporated into the experimental framework of studies focused on DOM composition in surface waters.  more » « less
Award ID(s):
1637459 1936769 1753731
PAR ID:
10314427
Author(s) / Creator(s):
;
Date Published:
Journal Name:
Environmental Science: Processes & Impacts
Volume:
22
Issue:
5
ISSN:
2050-7887
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract The thawing of ancient organic carbon stored in arctic permafrost soils, and its oxidation to carbon dioxide (CO2, a greenhouse gas), is predicted to amplify global warming. However, the extent to which organic carbon in thawing permafrost soils will be released as CO2is uncertain. A critical unknown is the extent to which dissolved organic carbon (DOC) from thawing permafrost soils is respired to CO2by microbes upon export of freshly thawed DOC to both dark bottom waters and sunlit surface waters. In this study, we quantified the radiocarbon age and13C composition of CO2produced by microbial respiration of DOC that was leached from permafrost soils and either kept in the dark or exposed to ultraviolet and visible wavelengths of light. We show that permafrost DOC most labile to microbial respiration was as old or older (ages 4,000–11,000 a BP) and more13C‐depleted than the bulk DOC in both dark and light‐exposed treatments, likely indicating respiration of old,13C‐depleted lignin and lipid fractions of the permafrost DOC pool. Light exposure either increased, decreased, or had no effect on the magnitude of microbial respiration of old permafrost DOC relative to respiration in the dark, depending on both the extent of DOC oxidation during exposure to light and the wavelength of light. Together, these findings suggest that photochemical changes affecting the lability of permafrost DOC during sunlight exposure are an important control on the magnitude of microbial respiration of permafrost DOC in arctic surface waters. 
    more » « less
  2. Abstract Dissolved organic matter (DOM) is an intermediate between organic carbon formed by primary producers and carbon dioxide (CO2) produced through respiration, making it a key component of the carbon cycle in aquatic ecosystems. Its composition influences the routes of mineralization. Here, we evaluate DOM composition as a function of time and depth in Lake Mendota, a highly productive eutrophic lake that stratifies in warm months and is located in Madison, Wisconsin, USA. Dissolved organic carbon concentrations and optical properties are presented for 73 samples collected at a single location at varying depths within the water column from June to November. A subset of samples is analyzed by Fourier transform‐ion cyclotron resonance mass spectrometry (FT‐ICR MS) to investigate DOM composition at the molecular level. Temporally, increases in more oxidized formulas are observed in both the epilimnion and hypolimnion. At the surface, correlations between DOM formulas and both chlorophyll concentrations and light intensity show that photochemical reactions contribute to DOM oxidation. In the hypolimnion, redox conditions and interactions with sediments likely influence temporal compositional change. Our results show DOM composition varies with depth with more highly oxidized formulas identified deeper in the water column. However, DOM composition varies more temporally than by location within the water column. This work has implications for climate change as DOM photooxidation in lakes represents an understudied flux of CO2to the atmosphere. Additionally, lake eutrophication is increasing due to warming temperatures and this data set yields detailed molecular information about DOM composition and processing in such lakes. 
    more » « less
  3. Dissolved natural organic matter (DOM) is a complex matrix of organic matter that is ubiquitous in natural aquatic environments. So far, substantial research has been conducted on the DOM adsorption on Mn oxides as well as the reduction processes of Mn oxides by DOM. However, little is known about the oxidative roles of DOM in oxidizing Mn2+(aq) to Mn(III/IV) oxide solids. Sunlight-driven processes can initiate the degradation of DOM accompanied by the formation of photochemically produced reactive intermediates, including excited triplet state DOM (3DOM*), hydroxyl radical (•OH), superoxide radical (O2•−), hydrogen peroxide (H2O2), and singlet oxygen (1O2). Further, in the presence of halide ions, reactive halogen species can be generated by reactions between 3DOM* and halide ions, and by reactions between •OH and halide ions. In this study, we found that the solution pH controlled the oxidation of Mn2+(aq) to Mn oxide solids during photolysis of DOM. Among the reactive oxygen species, Mn2+(aq) was found to be oxidized to Mn oxide solids mainly by O2•−. The DOM with different quantities of aromatic functional groups affected its oxidative capability. With the addition of bromide ions (Br−), Mn2+(aq) oxidation was promoted further by formation Br radicals, which can also oxidize Mn2+(aq) to Mn oxide solids. These findings can help us better understand the oxidative role of DOM in the formation of Mn oxide solids in organic-rich surface water. In addition, this study assists in comprehending the impacts of the photolytic reactions between DOM and halide ions and their resulting reactive oxygen and halogen species on the oxidation and reduction processes of other transition metal oxides in the environment. 
    more » « less
  4. Doi, Hideyuki (Ed.)
    A large volume of freshwater is incorporated in the relatively fresh (salinity ~32–33) Pacific Ocean waters that are transported north through the Bering Strait relative to deep Atlantic salinity in the Arctic Ocean (salinity ~34.8). These freshened waters help maintain the halocline that separates cold Arctic surface waters from warmer Arctic Ocean waters at depth. The stable oxygen isotope composition of the Bering Sea contribution to the upper Arctic Ocean halocline was established as early as the late 1980’s as having a δ 18 O V - SMOW value of approximately -1.1‰. More recent data indicates a shift to an isotopic composition that is more depleted in 18 O (mean δ 18 O value ~-1.5‰). This shift is supported by a data synthesis of >1400 water samples (salinity from 32.5 to 33.5) from the northern Bering and Chukchi seas, from the years 1987–2020, which show significant year-to-year, seasonal and regional variability. This change in the oxygen isotope composition of water in the upper halocline is consistent with observations of added freshwater in the Canada Basin, and mooring-based estimates of increased freshwater inflows through Bering Strait. Here, we use this isotopic time-series as an independent means of estimating freshwater flux changes through the Bering Strait. We employed a simple end-member mixing model that requires that the volume of freshwater (including runoff and other meteoric water, but not sea ice melt) flowing through Bering Strait has increased by ~40% over the past two decades to account for a change in the isotopic composition of the 33.1 salinity water from a δ 18 O value of approximately -1.1‰ to a mean of -1.5‰. This freshwater flux change is comparable with independent published measurements made from mooring arrays in the Bering Strait (freshwater fluxes rising from 2000–2500 km 3 in 2001 to 3000–3500 km 3 in 2011). 
    more » « less
  5. Manganese (Mn) oxide solids widely exist in nature, serving as both electron donors and acceptors for a variety of redox reactions. Previous studies have highlighted the adsorption of dissolved organic matter (DOM) on Mn oxides, as well as the reduction of Mn oxides by DOM. Here, we show the underappreciated roles of photolytic reactions of DOM in Mn2+(aq) oxidation and its consequential formation of Mn oxide solids. During the photolysis of DOM, reactive intermediates including excited triplet state DOM (3DOM*), hydroxyl radical (•OH), superoxide radical (O2•−), hydrogen peroxide (H2O2), and singlet oxygen (1O2) can be generated. Among them, we found that O2•− was responsible for Mn oxidation. In addition, in the presence of bromide ions (Br−), the photolytic reactions between DOM and Br− formed reactive bromide radicals and facilitated the oxidation of Mn2+(aq) to Mn oxide solids. Moreover, the composition of DOM affected its oxidative capability. When DOM contained more aromatic functional groups, we observed more oxidation of Mn2+ to Mn oxides. These new findings advance our knowledge of natural Mn2+ oxidation and Mn(III/IV) oxide formation, as well as the hitherto overlooked oxidative role of DOM in the oxidation of metal ions in surface water under sunlight illumination. 
    more » « less