Abstract Dissolved organic and inorganic carbon (DOC and DIC) influence water quality, ecosystem health, and carbon cycling. Dissolved carbon species are produced by biogeochemical reactions and laterally exported to streams via distinct shallow and deep subsurface flow paths. These processes are arduous to measure and challenge the quantification of global carbon cycles. Here we ask: when, where, and how much is dissolved carbon produced in and laterally exported from the subsurface to streams? We used a catchment‐scale reactive transport model, BioRT‐HBV, with hydrometeorology and stream carbon data to illuminate the “invisible” subsurface processes at Sleepers River, a carbonate‐based catchment in Vermont, United States. Results depict a conceptual model where DOC is produced mostly in shallow soils (3.7 ± 0.6 g/m2/yr) and in summer at peak root and microbial respiration. DOC is flushed from soils to the stream (1.0 ± 0.2 g/m2/yr) especially during snowmelt and storms. A large fraction of DOC (2.5 ± 0.2 g/m2/yr) percolates to the deeper subsurface, fueling deep respiration to generate DIC. DIC is exported predominantly from the deeper subsurface (7.1 ± 0.4 g/m2/yr, compared to 1.3 ± 0.3 g/m2/yr from shallow soils). Deep respiration reduces DOC and increases DIC concentrations at depth, leading to commonly observed DOC flushing (increasing concentrations with discharge) and DIC dilution patterns (decreasing concentrations with discharge). Surprisingly, respiration processes generate more DIC than weathering in this carbonate‐based catchment. These findings underscore the importance of vertical connectivity between the shallow and deep subsurface, highlighting the overlooked role of deep carbon processing and export.
more »
« less
Young Versus Old: Does Forest Age Regulate Water and Dissolved Carbon Processes Belowground?
Abstract Forest plantations are widespread globally. Young forest plantations (hereafter young forests) differ from natural old‐growth forests (hereafter old forests) in above‐ and below‐ground structures, shaping water and carbon cycling processes. While above‐ground differences are well studied, below‐ground hydrology and biogeochemical processes remain poorly understood. Here we asked:How do hydrological flow paths and dissolved carbon processes belowground differ between young and old forests?Using a process‐based hydro‐biogeochemical model (BioRT‐HBV) constrained by streamflow and dissolved organic and inorganic carbon (DOC and DIC) data, we analyzed three pairs of young‐old forests at the H.J. Andrews Experimental Forest, Oregon, USA. Detailed simulations for a 57‐year‐old plantation (WS01) and a naturally regenerated ∼500‐year‐old forest (WS02) showed that the young forest had lower streamflow and smaller deep groundwater contributions (20%) than the old forest (30%). DOC was mainly produced in shallow soil but diverged with depth: transformed into DIC in the young forest and further produced in the old forest, yielding contrasting export patterns of flushing (DOC increases with discharge) and dilution (DOC decreases with discharge). These differences likely stem from variations in subsurface structures, supported by deeper, denser roots in old forest. Extending the analysis to two additional pairs showed (a) higher DOC and DIC concentrations in all old forests; (b) consistent DIC dilution patterns but variable DOC patterns. Numerical experiments indicate that these diverse DOC behaviors result from interactions among forest age, geology, and hydrological connectivity, and other factors, highlighting the overlooked role of forest development in subsurface carbon cycling.
more »
« less
- Award ID(s):
- 2034232
- PAR ID:
- 10675150
- Publisher / Repository:
- American Geophysical Union
- Date Published:
- Journal Name:
- Water Resources Research
- Volume:
- 62
- Issue:
- 1
- ISSN:
- 0043-1397
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
High elevation mountain watersheds are undergoing rapid warming and declining snow fractions worldwide, causing earlier and quicker snowmelt. Understanding how this hydrologic shift affects subsurface flow paths, biogeochemical reactions, and solute export has been challenging due to the entanglement of hydrological and biogeochemical processes. Coal Creek, a high-elevation catchment (2,700 3,700 m, 53 km2) in Colorado, is experiencing a higher rate of warming than surrounding low-lying areas. This warming corresponds with dynamic and increased responses from biogenic solutes and dissolved organic carbon (DOC), whereas the behavior of geogenic solutes and dissolved inorganic carbon (DIC) has remained relatively unchanged. DOC has experienced the largest concentration increase (>3x), with annual average flow weighted concentrations positively correlated to average annual temperature. This suggests temperature is the main driver of increasing DOC levels. Although DOC and DIC response to warming is influenced by many drivers, the relative contribution of each remains unknown. DOC and DIC were analyzed to incorporate both carbon component products of soil respiration (DOC and CO2) and to represent high solute concentrations transported by shallow (DOC) versus deep (DIC) subsurface flow. The contrasting behavior of these carbon solutes indicates climate change and warming are driving changes in organic matter decomposition and soil respiration. Modeling results from the process-based model HBV-BioRT show increased temperatures cause earlier snowmelt and streamflow generation and lower peak discharge. As stream flow generation occurs earlier, so do DOC flushing and DIC dilution events. Additionally, post-snowmelt periods show greater DOC production and concentrations under warming scenarios. Results indicated increased production of DOC in post-snowmelt periods. DOC is then flushed out by earlier snowmelt partitioned through the shallow soil zone. Most process-based studies lack a watershed-scale understanding of carbon transformation and flow path alterations. This work demonstrates complex hydrologic and biogeochemical coupling at the watershed scale to illustrate how water flow paths and chemistry are responding to a changing climate in highelevation mountain watersheds.more » « less
-
Abstract Terrestrial production and export of dissolved organic and inorganic carbon (DOC and DIC) to streams depends on water flow and biogeochemical processes in and beneath soils. Yet, understanding of these processes in a rapidly changing climate is limited. Using the watershed‐scale reactive‐transport model BioRT‐HBV and stream data from a snow‐dominated catchment in the Rockies, we show deeper groundwater flow averaged about 20% of annual discharge, rising to ∼35% in drier years. DOC and DIC production and export peaked during snowmelt and wet years, driven more by hydrology than temperature. DOC was primarily produced in shallow soils (1.94 ± 1.45 gC/m2/year), stored via sorption, and flushed out during snowmelt. Some DOC was recharged to and further consumed in the deeper subsurface via respiration (−0.27 ± 0.02 gC/m2/year), therefore reducing concentrations in deeper groundwater and stream DOC concentrations at low discharge. Consequently, DOC was primarily exported from the shallow zone (1.62 ± 0.96 gC/m2/year, compared to 0.12 ± 0.02 gC/m2/year from the deeper zone). DIC was produced in both zones but at higher rates in shallow soils (1.34 ± 1.00 gC/m2/year) than in the deep subsurface (0.36 ± 0.02 gC/m2/year). Deep respiration elevated DIC concentrations in the deep zone and stream DIC concentrations at low discharge. In other words, deep respiration is responsible for the commonly‐observed increasing DOC concentrations (flushing) and decreasing DIC concentrations (dilution) with increasing discharge. DIC export from the shallow zone was ~66% of annual export but can drop to ∼53% in drier years. Numerical experiments suggest lower carbon production and export in a warmer, drier future, and a higher proportion from deeper flow and respiration processes. These results underscore the often‐overlooked but growing importance of deeper processes in a warming climate.more » « less
-
Abstract Despite much interest in relationships among carbon and water in forests, few studies assess how carbon accumulation scales with water use in forested watersheds with varied histories. This study quantified tree growth, water use efficiency, and carbon‐water tradeoffs of young versus mature/old‐growth forest in three small (13–22 ha) watersheds in the H.J. Andrews Experimental Forest, Oregon, USA. To quantify and scale carbon‐water tradeoffs from trees to watersheds, tree‐ring records and greenness and wetness indices from remote sensing were combined with long‐term vegetation, climate, and streamflow data from young forest watersheds (trees ∼45 years of age) and from a mature/old‐growth forest watershed (trees 150–500 years of age). Biomass production was closely related to water use; water use efficiency (basal area increment per unit of evapotranspiration) was lower; and carbon‐water tradeoffs were steeper in young forest plantations compared with old‐growth forest for which the tree growth record begins in the 1850s. Greenness and wetness indices from Landsat imagery were not significant predictors of streamflow or tree growth over the period 1984 to 2017, and soil C and N did not differ significantly among watersheds. Multiple lines of evidence show that mature and old‐growth forest watersheds store and accumulate more carbon, are more drought resistant, and better sustain water availability compared to young forests. These results provide a basis for reconstructions and predictions that are potentially broadly applicable, because first‐order watersheds occupy 80%–90% of large river basins and study watersheds are representative of forest history in the Pacific Northwest region.more » « less
-
Key Points Mackenzie River biogeochemical discharge decreases the southeastern Beaufort Sea carbon sink Terrestrial dissolved inorganic carbon (DIC) is the primary driver of outgassing events in the SBS, followed by terrestrial DOC Interannual variability in river discharge modulates localized air‐sea CO 2 fluxmore » « less
An official website of the United States government

