Abstract Dissolved organic matter (DOM) is the foundation of the microbial loop and plays an important role in estuarine water quality and ecosystem metabolism. Because estuaries are influenced by DOM with different sources and composition, changing hydrologic regimes, and diverse microbial community assemblages, the biological fate of DOM (i.e., microbial degradation) differs across spatiotemporal scales and between DOM pools. To better understand controls on DOM degradation, we characterized the biogeochemical and physical conditions of the York River Estuary (YRE), a sub-estuary of the Chesapeake Bay in southeast Virginia (USA), during October 2018 and February, April, and July 2019. We then evaluated how these conditions influenced the degradation of dissolved organic carbon (DOC) and nitrogen (DON) and chromophoric dissolved organic matter (CDOM) by conducting parallel dark incubations of surface water collected along the YRE. Compared to other sampling dates, DOC reactivity (ΔDOC (%)) was over two-fold higher in October when freshwater discharge was lower, temperatures were warmer, and autochthonous, aquatic sources of DOC dominated. ΔDOC (%) was near zero when allochthonous, terrestrial sources of DOC were more abundant and when temperatures were cooler during higher discharge periods in February when precipitation in the Chesapeake Bay region was anomalously high. DON was up to six times less reactive than DOC and was sometimes produced during the incubations whereas ΔCDOM (%) was highly variable between sampling periods. Like ΔDOC (%), spatiotemporal patterns in ΔDON (%) were controlled primarily by hydrology and DOM source and composition. Our results show that higher freshwater discharge associated with prolonged wet periods decreased estuarine flushing time and increased the delivery of allochthonous DOM derived from terrestrial sources into coastal waters, resulting in lower rates of DOM degradation especially under cool conditions. While these findings provide evidence for seasonal variation in DOM degradation, shifting environmental conditions (e.g., increasing temperatures and precipitation) due to climate change may also have interactive effects on the magnitude and composition of DOM exported to estuaries and its subsequent reactivity.
more »
« less
Composition and Bioreactivity of Dissolved Organic Matter Leachates From End Members in a Mountain to Prairie Transitional River Valley
Abstract River organic matter transformations impact the cycling of energy, carbon, and nutrients. The delivery of distinct dissolved organic matter (DOM) sources can alter aquatic DOM cycling and associated biogeochemical processes. Yet DOM source and reactivity are not well‐defined for many river systems, including in western Canada. Here, we explore DOM cycling in the mainstem of the Oldman River (stream order 6–7), a heavily regulated river network in southern Alberta (Canada). We compared seasonal river DOM content, composition, and bioavailability with nine endmember leachates from the river valley using optical properties and incubations to estimate biodegradable dissolved organic carbon (BDOC). River DOM composition was most similar to terrestrial soil leachates, followed by autochthonous DOM leachates. River DOM bioavailability was low (BDOC = 0%–16.6%, mean of 7.1%). Endmember leachate bioavailability increased from soils (BDOC = 23.9%–53.7%), to autochthonous sources (fish excretion, macrophytes, biofilm; BDOC = 49.9%–80.0%), to terrestrial vegetation (leaves, shrubs, grass; BDOC > 80%), scaling positively with protein‐like DOM content and amount of leachable dissolved organic carbon (DOC), and negatively with aromaticity. Seasonally, DOC concentrations changed little despite >15‐fold increases in discharge during spring. River DOM composition shifted modestly toward soil‐like endmembers in spring and more bioavailable autochthonous end members in autumn and winter. Low DOM bioavailability in the river mainstem and low DOC yields shown in previous work point to limited internal processing of DOM and limited bioavailable DOM delivery to downstream habitats, possibly due to upstream flow regulation. Our observations provide important insights into the functioning of western Canadian aquatic networks.
more »
« less
- Award ID(s):
- 2053048
- PAR ID:
- 10517841
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Journal of Geophysical Research: Biogeosciences
- Volume:
- 129
- Issue:
- 6
- ISSN:
- 2169-8953
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Coastal erosion mobilizes large quantities of organic matter (OM) to the Arctic Ocean where it may fuel greenhouse gas emissions and marine production. While the biodegradability of permafrost‐derived dissolved organic carbon (DOC) has been extensively studied in inland soils and freshwaters, few studies have examined dissolved OM (DOM) leached from eroding coastal permafrost in seawater. To address this knowledge gap, we sampled three horizons from bluff exposures near Drew Point, Alaska: seasonally thawed active layer soils, permafrost containing Holocene terrestrial and/or lacustrine OM, and permafrost containing late‐Pleistocene marine‐derived OM. Samples were leached in seawater to compare DOC yields, DOM composition (chromophoric DOM, Fourier transform ion cyclotron resonance mass spectrometry), and biodegradable DOC (BDOC). Holocene terrestrial permafrost leached the most DOC compared to active layer soils and Pleistocene marine permafrost. However, DOC from Pleistocene marine permafrost was the most biodegradable (33 ± 6% over 90 days), followed by DOC from active layer soils (23 ± 5%) and Holocene terrestrial permafrost (14 ± 3%). Permafrost leachates contained relatively more aliphatic and peptide‐like formulae, whereas active layer leachates contained relatively more aromatic formulae. BDOC was positively correlated with nitrogen‐containing and aliphatic formulae, and negatively correlated with polyphenolic and condensed aromatic formulae. Using estimates of eroding OM, we scale our results to estimate DOC and BDOC inputs to the Alaska Beaufort Sea. While DOC inputs from coastal erosion are relatively small compared to rivers, our results suggest that erosion may be an important source of BDOC to the Beaufort Sea when river inputs are low.more » « less
-
Abstract The West Siberian Lowland (WSL) contains some of the largest wetlands and most extensive peatlands on Earth, storing vast amounts of vulnerable carbon across permafrost‐free to continuous permafrost zones. As temperature and precipitation changes continue to alter the Siberian landscape, carbon transfer to the atmosphere and export to the Arctic Ocean will be impacted. However, the drivers of organic carbon transfer are largely unknown across this region. We characterized seasonal dissolved organic carbon (DOC) concentration and dissolved organic matter (DOM) composition of WSL rivers from the middle reaches of the Ob’ River in the permafrost‐free zone, as well as tributaries of the Taz River in the northern continuous permafrost zone. DOC and aromatic DOM properties increased from spring to autumn in the Ob’ tributaries, reflecting the seasonal transition from groundwater‐sourced to terrestrial DOM. Differences in molecular‐level signatures via ultra‐high resolution mass spectrometry revealed the influence of redox processes on DOM composition in the winter while terrestrial DOM sourcing shifted from surface litter aliphatics and highly unsaturated and phenolic high‐O/C (HUPHigh O/C) compounds in the spring to subsurface soils and HUPLow O/Ccompounds by autumn. Furthermore, aromaticity and organic N were related to landscape properties including peatlands, forest cover, and the ratio of needleleaf:broadleaf forests. Finally, the Taz River tributaries were similar to summer and autumn Ob’ tributaries, but more enriched in N and S‐containing compounds. These signatures were likely derived from thawing permafrost, which we expect to increase in northern rivers due to active layer expansion in a warming Arctic.more » « less
-
Abstract The Amazon River exports over 10% of the global riverine dissolved organic carbon (DOC) flux to the ocean. However, several downstream clearwater tributaries, such as the Tapajós River, are typically not included in these measurements, omitting a crucial part of the Amazon carbon cycle. This study investigated near‐monthly DOC and dissolved organic matter (DOM) composition via optical, fluorescence spectroscopy, and ultra‐high resolution mass spectrometry (FT‐ICR MS) of the Tapajós River for 8 years (2016–2024) to better understand patterns and drivers of potential organic carbon export to the lower Amazon River. DOM composition and DOC export were driven by the seasonal flood pulse of the Tapajós River, exporting aromatic terrestrial DOM from the watershed during high discharge and internally produced algal or microbial DOM during dry periods. On average, we report that the Tapajós River exports 1.38 Tg DOC annually to the downstream Amazon mixing zone, representing an amount of DOC exported by other major world rivers such as the Yukon or Mekong River. Furthermore, organic carbon export varied interannually with less DOC exported during dry El Niño events and more algal‐derived DOM exported during bloom periods. Finally, as grassland and cropland landcover increased over the study period, we observed an average decrease in aromatic DOM and an increase in microbially processed fluorophores. Our study suggests that temperature, precipitation, and anthropogenic land use changes in clearwater rivers will impact carbon export across the lower Amazon River network.more » « less
-
Abstract Wetland and permafrost soils contain some of Earth's largest reservoirs of organic carbon, and these stores are threatened by rapid warming across the Arctic. Nearly half of northern wetlands are affected by permafrost. As these ecosystems warm, the cycling of dissolved organic matter (DOM) and the opportunities for microbial degradation are changing. This is particularly evident as the relationship between wetland and permafrost DOM dynamics evolves, especially with the introduction of permafrost‐derived DOM into wetland environments. Thus, understanding the interplay of DOM composition and microbial communities from wetlands and permafrost is critical to predicting the impact of released carbon on global carbon cycling. As little is understood about the interactions between wetland active layer and permafrost‐derived sources as they intermingle, we conducted experimental bioincubations of mixtures of DOM and microbial communities from two fen wetland depths (shallow: 0–15 cm, and deep: 15–30 cm) and two ages of permafrost soil (Holocene and Pleistocene). We found that the source of microbial inoculum was not a significant driver of dissolved organic carbon (DOC) degradation across treatments; rather, DOM source and specifically, DOM molecular composition, controlled the rate of DOC loss over 100 days of bioincubations. DOC loss across all treatments was negatively correlated with modified aromaticity index, O/C, and the relative abundance of condensed aromatic and polyphenolic formula, and positively correlated with H/C and the relative abundance of aliphatic and peptide‐like formula. Pleistocene permafrost‐derived DOC exhibited ∼70% loss during the bioincubation driven by its initial molecular‐level composition, highlighting its high bioavailability irrespective of microbial source.more » « less
An official website of the United States government
