Abstract The biogeochemistry of rapidly retreating Andean glaciers is poorly understood, and Ecuadorian glacier dissolved organic matter (DOM) composition is unknown. This study examined molecular composition and carbon isotopes of DOM from supraglacial and outflow streams (n = 5 and 14, respectively) across five ice capped volcanoes in Ecuador. Compositional metrics were paired with streamwater isotope analyses (δ18O) to assess if outflow DOM composition was associated with regional precipitation gradients and thus an atmospheric origin of glacier DOM. Ecuadorian glacier outflows exported ancient, biolabile dissolved organic carbon (DOC), and DOM contained a high relative abundance (RA) of aliphatic and peptide‐like compounds (≥27%RA). Outflows were consistently more depleted in Δ14C‐DOC (i.e., older) compared to supraglacial streams (mean −195.2 and −61.3‰ respectively), perhaps due to integration of spatially heterogenous and variably aged DOM pools across the supraglacial environment, or incorporation of aged subglacial OM as runoff was routed to the outflow. Across Ecuador, Δ14C‐DOC enrichment was associated with decreased aromaticity of DOM, due to increased contributions of organic matter (OM) from microbial processes or atmospheric deposition of recently fixed and subsequently degraded OM (e.g., biomass burning byproducts). There was a regional gradient between glacier outflow DOM composition and streamwater δ18O, suggesting covariation between regional precipitation gradients and the DOM exported from glacier outflows. Ultimately, this highlights that atmospheric deposition may exert a control on glacier outflow DOM composition, suggesting regional air circulation patterns and precipitation sources in part determine the origins and quality of OM exported from glacier environments.
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Dust deposition drives microbial metabolism in a remote, high-elevation catchment
In barren alpine catchments of the Colorado Rocky Mountains, microorganisms are typically carbon (C)-limited, and C-limitation can influence critical heterotrophic processes, such as denitrification. In these remote locations, organic matter deposited during dust intrusion events and other forms of aerosol deposition may be an important C source for heterotrophs; however, little is known regarding the biodegradability of atmospherically deposited organic matter. This study evaluated the extent to which organic matter in Holocene dust and other types of atmospheric deposition in the Colorado Rocky Mountains could support metabolic activity and be biodegraded by alpine bacteria. Microplate bioassays revealed that all atmospheric deposition samples were able to activate microbial metabolism. Decreases in dissolved organic carbon (DOC) concentrations over time in biodegradability incubations reflect the presence of two pools of dissolved organic matter (DOM), a rapidly decaying pool with rate constants in the range of 0.0130–0.039 d–1and a slowly decaying pool with rate constants in the range of 0.0008–0.009 d–1. Changes in the fluorescence excitation-emission matrix of solutions evaluated over time indicated a transformation of organic matter by bacteria resulting in a more humic-like fluorescence signature. Fluorescence spectroscopic analyses, therefore, suggest that the degradation of non-fluorescent DOM in glutamate and dust-derived C sources by bacteria results in the production of fluorescent DOM.
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- Award ID(s):
- 1637686
- PAR ID:
- 10545814
- Publisher / Repository:
- SAGE Publications
- Date Published:
- Journal Name:
- The Holocene
- Volume:
- 30
- Issue:
- 4
- ISSN:
- 0959-6836
- Format(s):
- Medium: X Size: p. 589-596
- Size(s):
- p. 589-596
- Sponsoring Org:
- National Science Foundation
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Abstract A comprehensive cross‐biome assessment of major nitrogen (N) species that includes dissolved organic N (DON) is central to understanding interactions between inorganic nutrients and organic matter in running waters. Here, we synthesize stream water N chemistry across biomes and find that the composition of the dissolved N pool shifts from highly heterogeneous to primarily comprised of inorganic N, in tandem with dissolved organic matter (DOM) becoming more N‐rich, in response to nutrient enrichment from human disturbances. We identify two critical thresholds of total dissolved N (TDN) concentrations where the proportions of organic and inorganic N shift. With low TDN concentrations (0–1.3 mg/L N), the dominant form of N is highly variable, and DON ranges from 0% to 100% of TDN. At TDN concentrations above 2.8 mg/L, inorganic N dominates the N pool and DON rarely exceeds 25% of TDN. This transition to inorganic N dominance coincides with a shift in the stoichiometry of the DOM pool, where DOM becomes progressively enriched in N and DON concentrations are less tightly associated with concentrations of dissolved organic carbon (DOC). This shift in DOM stoichiometry (defined as DOC:DON ratios) suggests that fundamental changes in the biogeochemical cycles of C and N in freshwater ecosystems are occurring across the globe as human activity alters inorganic N and DOM sources and availability. Alterations to DOM stoichiometry are likely to have important implications for both the fate of DOM and its role as a source of N as it is transported downstream to the coastal ocean.more » « less
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