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Mark Dornblaser

Publications and source records attributed to Mark Dornblaser.

8 recordsLinked to original sources

Dissolved carbon export by large river systems is influenced by source area heterogeneity

Rivers and streams export inorganic and organic carbon derived from contributing landscapes and so downstream carbon fluxes are important quantitative indicators of change in ecosystem function and for the full accounting of terrestrial carbon budgets. Carbon concentration-discharge ( C-Q ) relationships in rivers provide important information about carbon source and behavior in watersheds and are useful for estimating carbon export. However, C-Q relationships are complex in large river systems because of spatial and temporal heterogeneity in carbon dynamics across the watershed and river networks. We quantified dissolved organic carbon (DOC) and dissolved inorganic carbon (DIC) fluxes in the Upper Mississippi River basin and investigated their relationships with land cover and hydrology. The magnitude of dissolved carbon yields ranged widely among stations, 0.6–5.7 g DOC m −2 yr −1 and 2.9–11.8 g DIC m −2 yr −1 . Spatial patterns in carbon fluxes were strongly related to land cover, with agricultural sites having high DIC/low DOC exports and forested and wetland areas having the opposite. DIC was always negatively related to discharge ( Q ), while the DOC- Q relationship varied with land cover. Differential behavior of carbon across the basin resulted in Q having a weak relationship with DOC and DIC at the basin outlet. Hence, there is a need to improve understanding of headwater terrestrial-to-aquatic carbon connections in order to improve basin-to-continental-scale carbon export estimates. Our results demonstrate that quantitative understanding of carbon export by large rivers can be improved by incorporating stream network information, such as the timing, location, and source of constituent flux, rather than relying solely upon relationships between constituent behavior and seasonality or discharge at the basin outlet.

Minnesota, Wisconsin

Hydrologic and landscape controls on dissolved organic matter composition across western North American Arctic lakes

Northern high-latitude lakes are hotspots for cycling dissolved organic carbon (DOC) inputs from allochthonous sources to the atmosphere. However, the spatial distribution of lake dissolved organic matter (DOM) is largely unknown across Arctic-boreal regions with respect to the surrounding landscape. We expand on regional studies of northern high-latitude DOM composition by integrating DOC concentrations, optical properties, and molecular-level characterization from lakes spanning the Canadian Taiga to the Alaskan Tundra. Lakes were sampled during the summer from July to early September to capture the growing season. DOM became more optically processed and molecular-level aromaticity increased northward across the Canadian Shield to the southern Arctic and from interior Alaska to the Tundra, suggesting relatively greater DOM incorporation from allochthonous sources. Using water isotopes (δ 18 O-H 2 O), we report a weak overall trend of increasing DOC and decreasing aromaticity in lakes that were hydrologically isolated from the landscape and enriched in δ 18 O-H 2 O, while within-region trends were stronger and varied depending on the landscape. Finally, DOC correlated weakly with chromophoric dissolved organic matter (CDOM) across the study sites, suggesting that autochthonous and photobleached DOM were a major component of the DOC in these regions; however, some of the northernmost and wetland-dominated lakes followed pan-Arctic riverine DOC-CDOM relationships, indicating strong contributions from allochthonous inputs. As many lakes across the North American Arctic are experiencing changes in temperature and precipitation, we expect the proportions of allochthonous and autochthonous DOM to respond with aquatic optical browning with greater landscape connectivity and more internally produced DOM in hydrologically isolated lakes.

Global Biogeochemical Cycles

The importance of lake emergent aquatic vegetation for estimating Arctic-boreal methane emissions

Areas of lakes that support emergent aquatic vegetation emit disproportionately more methane than open water but are under-represented in upscaled estimates of lake greenhouse gas emissions. These shallow areas are typically less than ∼1.5 m deep and can be detected with synthetic aperture radar (SAR). To assess the importance of lake emergent vegetation (LEV) zones to landscape-scale methane emissions, we combine airborne SAR mapping with field measurements of vegetated and open-water methane flux. First, we use Uninhabited Aerial Vehicle SAR data from the NASA Arctic-Boreal Vulnerability Experiment to map LEV in 4,572 lakes across four Arctic-boreal study areas and find it comprises ∼16% of lake area, exceeding previous estimates, and exhibiting strong regional differences (averaging 59 [50–68]%, 22 [20–25]%, 1.0 [0.8–1.2]%, and 7.0 [5.0–12]% of lake areas in the Peace-Athabasca Delta, Yukon Flats, and northern and southern Canadian Shield, respectively). Next, we account for these vegetated areas through a simple upscaling exercise using paired methane fluxes from regions of open water and LEV. After excluding vegetated areas that could be accounted for as wetlands, we find that inclusion of LEV increases overall lake emissions by 21 [18–25]% relative to estimates that do not differentiate lake zones. While LEV zones are proportionately greater in small lakes, this relationship is weak and varies regionally, underscoring the need for methane-relevant remote sensing measurements of lake zones and a consistent criterion for distinguishing wetlands. Finally, Arctic-boreal lake methane upscaling estimates can be improved with more measurements from all lake zones.

Journal of Geophysical Research: Biogeosciences

Anthropogenic landcover impacts fluvial dissolved organic matter composition in the Upper Mississippi River Basin

Landcover changes have altered the natural carbon cycle; however, most landcover studies focus on either forest conversion to agriculture or urban, rarely both. We present differences in dissolved organic carbon (DOC) concentrations and dissolved organic matter (DOM) molecular composition within Upper Mississippi River Basin low order streams and rivers draining one of three dominant landcovers (forest, agriculture, and urban). Streams draining forest and urban landcovers have greater DOC concentrations, likely driven by differences in carbon sourcing, microbial processing, and soil disturbance. Using Fourier transform-ion cyclotron resonance mass spectrometry, 24% of assigned molecular formulae are common across all landcovers. Relative abundances of N-,S- heteroatomic formulae (CHON, CHOS, CHONS) are higher for agricultural and urban streams, with agricultural stream DOM having more N-containing formulae compared to urban stream DOM, which has more S-containing formulae. Higher N-,S- heteroatomic formulae abundance, along with enrichment in aliphatic, N-aliphatic, and highly unsaturated and phenolic (low O/C) compound categories within agricultural and urban stream DOM are likely to result from increased anthropogenic inputs, autochthonous production, and microbial processing associated with agricultural and urban impacts. Reduced N-,S- heteroatomic formulae abundances in forested stream DOM, along with enrichments in condensed aromatics, polyphenolics, and highly unsaturated phenolic (high O/C) compound categories, likely reflect greater contributions from surrounding organic-rich forest soil and vegetation. Overall, landcover change from forested to agriculture lowers DOC concentrations and changes from forested to agriculture or urban increases autochthonous, and presumably more biolabile, DOM contributions with ramifications for stream biogeochemical cycling.

Iowa, Minnesota, Wisconsin

Spatiotemporal dynamics of CO2 gas exchange from headwater mountain streams

Mountain streams play an important role in the global carbon cycle by transporting, metabolizing, and exchanging carbon they receive from the terrestrial environment. The rates at which these processes occur remain highly uncertain because of a paucity of observations and the difficulty of measuring gas exchange rates in steep, turbulent mountain streams. This uncertainty is compounded by large temporal and spatial variability in stream carbon dioxide (CO 2 ) concentrations in mountain environments. In this study, we measured diel, seasonal, and annual variations in CO 2 partial pressure ( p CO 2 ) in seven headwater streams and a groundwater spring in the Colorado Rocky Mountains to determine how CO 2 exchange fluxes ( ) vary with time, annual precipitation, and landscape characteristics. Our results show that temporal variability in p CO 2 and in mountain streams is large and is strongly influenced by solar radiation, the accumulation and melting of seasonal snowpacks, and interannual variations in precipitation. Spatial variations in p CO 2 and were related to landscape characteristics, with soil organic matter, wetlands, and likely groundwater discharge zones having a positive influence. Periglacial features, such as ice and rock glaciers, had a negative influence on stream p CO 2 and . Estimated from streams in an alpine/subalpine region of Colorado was 3.4 kg C m −2 yr −1 normalized to stream surface area (95% CI: 2.1–5.0 kg C m −2 yr −1 ), consistent with recent work on CO 2 exchange from mountain streams in the Swiss Alps. Our results highlight the importance of mountain streams as substantial contributors in the global carbon cycle.

Colorado

Storm-scale and seasonal dynamics of carbon export from a nested subarctic watershed underlain by permafrost

Subarctic catchments underlain by permafrost sequester a major stock of frozen organic carbon (C), which may be mobilized as the Arctic warms. Warming can impact C export from thawing soils by altering the depth and timing of runoff related to changing storm and fire regimes and altered soil thaw depths. We investigated C export in a first order headwater stream (West Twin Creek) and its receiving third order river (Beaver Creek) in interior Alaska using discrete sampling of dissolved organic and inorganic C (DOC and DIC) and 15-min collection of specific conductance (SC), fluorescent dissolved organic matter (fDOM) and water discharge (Q). Storm SC-Q relationships displayed negative slopes, indicating solute limitation and limited influence of seasonal soil thaw on storm runoff chemistry. Concurrently, fDOM-Q displayed positive slopes that decreased over the summer, indicating flushing of a limited fDOM pool. Baseflow DIC increased over the season concurrent with soil thaw, with higher DIC at the larger scale indicating greater influence of deeper, mineral-rich flow paths. Storm and seasonal trends were generally similar at both scales. The biggest difference was in fDOM, which displayed higher concentrations and slower depletion in the first order stream. Improved process understanding from this study can be used to better predict carbon export and cycling by stream networks as northern forests and arctic regions continue to warm.

Alaska

USGS permafrost research determines the risks of permafrost thaw to biologic and hydrologic resources

The U.S. Geological Survey (USGS), in collaboration with university, Federal, Tribal, and independent partners, conducts fundamental research on the distribution, vulnerability, and importance of permafrost in arctic and boreal ecosystems. Scientists, land managers, and policy makers use USGS data to help make decisions for development, wildlife habitat, and other needs. Native villages and cities can forecast landscape change and where soils are vulnerable to thaw with more certainty. The scientific community can use USGS data to develop scenarios of future permafrost change.

Alaska

Mercury export from the Yukon River Basin and potential response to a changing climate

We measured mercury (Hg) concentrations and calculated export and yield from the Yukon River Basin (YRB) to quantify Hg flux from a large, permafrost-dominated, high-latitude watershed. Exports of Hg averaged 4400 kg Hg yr -1 . The average annual yield for the YRB during the study period was 5.17 &mu;g m -2 yr -1 , which is 3&ndash;32 times more than Hg yields reported for 8 other major northern hemisphere river basins. The vast majority (90%) of Hg export is associated with particulates. Half of the annual export of Hg occurred during the spring with about 80% of 34 samples exceeding the U.S. EPA Hg standard for adverse chronic effects to biota. Dissolved and particulate organic carbon exports explained 81% and 50%, respectively, of the variance in Hg exports, and both were significantly ( p < 0.001) correlated with water discharge. Recent measurements indicate that permafrost contains a substantial reservoir of Hg. Consequently, climate warming will likely accelerate the mobilization of Hg from thawing permafrost increasing the export of organic carbon associated Hg and thus potentially exacerbating the production of bioavailable methylmercury from permafrost-dominated northern river basins.

Alaska