Geology Reports⌕ Search

USGS · 70042388

Multi-scale measurements and modeling of denitrification in streams with varying flow and nitrate concentration in the upper Mississippi River basin, USA

Abstract

Denitrification is an important net sink for NO 3 − in streams, but direct measurements are limited and in situ controlling factors are not well known. We measured denitrification at multiple scales over a range of flow conditions and NO 3 − concentrations in streams draining agricultural land in the upper Mississippi River basin. Comparisons of reach-scale measurements (in-stream mass transport and tracer tests) with local-scale in situ measurements (pore-water profiles, benthic chambers) and laboratory data (sediment core microcosms) gave evidence for heterogeneity in factors affecting benthic denitrification both temporally (e.g., seasonal variation in NO 3 − concentrations and loads, flood-related disruption and re-growth of benthic communities and organic deposits) and spatially (e.g., local stream morphology and sediment characteristics). When expressed as vertical denitrification flux per unit area of streambed ( U denit , in μmol N m −2 h −1 ), results of different methods for a given set of conditions commonly were in agreement within a factor of 2–3. At approximately constant temperature (~20 ± 4°C) and with minimal benthic disturbance, our aggregated data indicated an overall positive relation between U denit (~0–4,000 μmol N m −2 h −1 ) and stream NO 3 − concentration (~20–1,100 μmol L −1 ) representing seasonal variation from spring high flow (high NO 3 − ) to late summer low flow (low NO 3 − ). The temporal dependence of U denit on NO 3 − was less than first-order and could be described about equally well with power-law or saturation equations (e.g., for the unweighted dataset, U denit ≈26 * [NO 3 − ] 0.44 or U denit ≈640 * [NO 3 − ]/[180 + NO 3 − ]; for a partially weighted dataset, U denit ≈14 * [NO 3 − ] 0.54 or U denit ≈700 * [NO 3 − ]/[320 + NO 3 − ]). Similar parameters were derived from a recent spatial comparison of stream denitrification extending to lower NO 3 − concentrations (LINX2), and from the combined dataset from both studies over 3 orders of magnitude in NO 3 − concentration. Hypothetical models based on our results illustrate: (1) U denit was inversely related to denitrification rate constant ( k 1 denit , in day −1 ) and vertical transfer velocity ( v f,denit , in m day −1 ) at seasonal and possibly event time scales; (2) although k 1 denit was relatively large at low flow (low NO 3 − ), its impact on annual loads was relatively small because higher concentrations and loads at high flow were not fully compensated by increases in U denit ; and (3) although NO 3 − assimilation and denitrification were linked through production of organic reactants, rates of NO 3 − loss by these processes may have been partially decoupled by changes in flow and sediment transport. Whereas k 1 denit and v f,denit are linked implicitly with stream depth, NO 3 − concentration, and(or) NO 3 − load, estimates of U denit may be related more directly to field factors (including NO 3 − concentration) affecting denitrification rates in benthic sediments. Regional regressions and simulations of benthic denitrification in stream networks might be improved by including a non-linear relation between U denit and stream NO 3 − concentration and accounting for temporal variation.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J.K. Bohlke, Ronald C. Antweiler, Judson W. Harvey, Andrew E. Laursen, Lesley K. Smith, Richard L. Smith, Mary A. Voytek. 2009-01-13. Multi-scale measurements and modeling of denitrification in streams with varying flow and nitrate concentration in the upper Mississippi River basin, USA. https://doi.org/10.1007/s10533-008-9282-8

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

Water table rise sustains carbon release from soils in wetland-dominated landscapes: An intact soil core study

Wetland-dominated landscapes influence carbon cycling through their potential to act as both carbon sinks and sources. Wetlands in low-relief landscapes have dynamic terrestrial-aquatic interfaces that change seasonally with variable surface water and groundwater levels. However, few studies have directly quantified dissolved organic matter (DOM) release and greenhouse gas (CO 2 , CH 4 ) fluxes from wetland soils along terrestrial-aquatic interfaces as they are seasonally re-saturated by groundwater. To estimate groundwater-mediated soil DOM and gas fluxes, we performed laboratory simulations of vertical groundwater rise on intact soil cores collected from four Delmarva bay wetlands located in the Mid-Atlantic United States. At each wetland, one core was collected from within the wetland basin and the other from the transitional zone at the basin edge. Cores were re-saturated with groundwater over 15 days and then kept fully saturated for an additional 25 days. Source groundwater, soil porewater, and exfiltrated surface water samples were collected and analyzed for pH, ORP, DOM concentration, and DOM optical indices. In both the wetland and transition zone cores, porewater DOM concentrations increased over the wet up and were sustained during prolonged saturation. Optical indices shifted from recently produced, microbial-like signatures towards aromatic, terrestrial-like signatures. Fluxes of CO 2 decreased as the duration of soil saturation increased and soil cores switched from CH 4 sinks to sources upon full soil core saturation. Results indicate that groundwater rise sustains carbon mobilization from soils in wetland-dominated landscapes, emphasizing the need to understand how climate-driven changes to groundwater dynamics may affect carbon fluxes along terrestrial-aquatic interfaces.

Delaware, Maryland↗

Seasonal synchronicity and multi-decadal stability of headwater biogeochemistry in the northern temperate zone

Temporal patterns in chemistry of headwater streams reflect responses of water and elemental cycles to perturbations occurring at local to global scales. We evaluated multi-scale temporal patterns in up to 32 y of monthly observations of stream chemistry (ammonium, calcium, dissolved organic carbon, nitrate, total dissolved phosphorus, and sulfate) in 22 reference catchments within the northern temperate zone of North America. Multivariate autoregressive state-space (MARSS) models were applied to quantify patterns at multi-decadal, seasonal, and shorter intervals during a period that encompassed warming climate, seasonal changes in precipitation, and regional declines in atmospheric deposition. Significant long-term trends in solute concentrations within a subset of the catchments were consistent with recovery from atmospheric deposition (e.g., calcium, nitrate, sulfate) and increased precipitation (e.g., dissolved organic carbon). Lack of evidence for multi-decadal trends in most catchments suggests resilience of northern temperate ecosystems or that subtle net effects of simultaneous changes in climate and disturbance regimes do not result in directional trends. Synchronous seasonal oscillations of solute concentrations occurred across many catchments, reflecting shared climate and biotic drivers of seasonality within the northern temperate zone. Despite shared patterns among catchments at a seasonal scale, multi-scale temporal patterns were statistically distinct among even adjacent headwater catchments, implying that local attributes of headwater catchments modify the signals imparted by atmospheric phenomena and regional disturbances. To effectively characterize hydrologic and biogeochemical responses to changing climate and disturbance regimes, catchment monitoring programs could include multiple streams with contributing areas that encompass regional heterogeneity in vegetation, topography, and elevation. Overall, detection of long-term patterns and trends requires monitoring multiple catchments at a frequency that captures periodic variation (e.g., seasonality) and a duration encompassing the perturbations of interest.

Biogeochemistry↗

Rare earth element and phosphorus mobility depend on adsorption to Al-, Fe-, and Mn-oxyhydroxides in a headwater stream in Vermont, USA

We evaluated base cations, Al, Fe, Mn, REEs, DOC, anions, and P mobilization during three discharge events (E-1, E-2, E-3) at the headwater catchment W-9, Sleepers River, Vermont, USA. Peak discharge ranged from 3.696 (E-1) to 0.073 (E-3) mm h −1 . Eight samples from each event were speciated for total (unfiltered-acidified) and dissolved (0.45 µm filtered-acidified). During E-1, total Al, Fe, and Mn increased to maxima of 376 (1790X), 161 (194X), and 38 (45X) µmol L −1 , respectively. Concurrently, total La, Ce, Pr, and Nd increased to maxima of 87 (590X), 114 (671X), 15 (375X), and 53 (408X) nmol L −1 , respectively, greatly exceeding the dissolved fraction. Totals for Er > Yb > Tm > Lu reached comparable enrichments near or at maximum discharge. Discharge ranged from 0.41 to 0.94 mm h −1 during E-2, a snowmelt event. Total Al was comparatively stable; total Fe and Mn increased 15X and 79X, remaining less than total Al. Total La, Ce, Pr, and Nd peaked with total Fe and Mn. E-3, a late summer rain, resembled E-1 but had much lower maxima for all REEs, P, Al, Fe, and Mn. Particulate, total, and dissolved REEs and P correlated with DOC and with total Al, Fe, and Mn over all discharges, with molar Al > Fe > Mn (most samples) for E-1 and E-3. Maximum total and dissolved P declined from 15.4 and 0.89 (E-1) to 0.98 and 0.27 µmol L −1 (E-3), respectively. Particulate REEs correlated strongly (R 2 = 0.95–0.96) with Al, Fe, and Mn particulates eroded from the stream bed and continuously precipitated during and after high discharge of groundwater.

Vermont↗