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Robert G. Striegl

Publications and source records attributed to Robert G. Striegl.

At least 91 records · Page 5Linked to original sources

Quantification of surface water and groundwater flows to open‐ and closed‐basin lakes in a headwaters watershed using a descriptive oxygen stable isotope model

Accurate quantification of hydrologic fluxes in lakes is important to resource management and for placing hydrologic solute flux in an appropriate biogeochemical context. Water stable isotopes can be used to describe water movements, but they are typically only effective in lakes with long water residence times. We developed a descriptive time series model of lake surface water oxygen‐18 stable isotope signature ( δL ) that was equally useful in open‐ and closed‐basin lakes with very different hydrologic residence times. The model was applied to six lakes, including two closed‐basin lakes and four lakes arranged in a chain connected by a river, located in a headwaters watershed. Groundwater discharge was calculated by manual optimization, and other hydrologic flows were constrained by measured values including precipitation, evaporation, and streamflow at several stream gages. Modeled and observed δL were highly correlated in all lakes ( r = 0.84–0.98), suggesting that the model adequately described δL in these lakes. Average modeled stream discharge at two points along the river, 16,000 and 11,800 m 3 d −1 , compares favorably with synoptic measurement of stream discharge at these sites, 17,600 and 13,700 m 3 d −1 , respectively. Water yields in this watershed were much higher, 0.23–0.45 m, than water yields calculated from gaged streamflow in regional rivers, approximately 0.10 m, suggesting that regional groundwater discharge supports water flux through these headwaters lakes. Sensitivity and robustness analyses also emphasized the importance of considering hydrologic residence time when designing a sampling protocol for stable isotope use in lake hydrology studies.

Water Resources Research

Public review draft: A method for assessing carbon stocks, carbon sequestration, and greenhouse-gas fluxes in ecosystems of the United States under present conditions and future scenarios

The Energy Independence and Security Act of 2007 (EISA), Section 712, authorizes the U.S. Department of the Interior to develop a methodology and conduct an assessment of the Nation's ecosystems focusing on carbon stocks, carbon sequestration, and emissions of three greenhouse gases (GHGs): carbon dioxide, methane, and nitrous oxide. The major requirements include (1) an assessment of all ecosystems (terrestrial systems, such as forests, croplands, wetlands, shrub and grasslands; and aquatic ecosystems, such as rivers, lakes, and estuaries), (2) an estimation of annual potential capacities of ecosystems to increase carbon sequestration and reduce net GHG emissions in the context of mitigation strategies (including management and restoration activities), and (3) an evaluation of the effects of controlling processes, such as climate change, land use and land cover, and wildlfires. The purpose of this draft methodology for public review is to propose a technical plan to conduct the assessment. Within the methodology, the concepts of ecosystems, carbon pools, and GHG fluxes used for the assessment follow conventional definitions in use by major national and international assessment or inventory efforts. In order to estimate current ecosystem carbon stocks and GHG fluxes and to understand the potential capacity and effects of mitigation strategies, the method will use two time periods for the assessment: 2001 through 2010, which establishes a current ecosystem GHG baseline and will be used to validate the models; and 2011 through 2050, which will be used to assess future potential conditions based on a set of projected scenarios. The scenario framework is constructed using storylines of the Intergovernmental Panel on Climate Change (IPCC) Special Report Emission Scenarios (SRES), along with initial reference land-use and land-cover (LULC) and land-management scenarios. An additional three LULC and land-management mitigation scenarios will be constructed for each storyline to enhance carbon sequestration and reduce GHG fluxes in ecosystems. Input from regional experts and stakeholders will be solicited to construct realistic and meaningful scenarios. The methods for mapping the current LULC and ecosystem disturbances will require the extensive use of both remote-sensing data and in-situ (for example, forest inventory data) to capture and characterize landscape-change events. For future potential LULC and ecosystem disturbances, key drivers such as socioeconomic, policy, and climate assumptions will be used in addition to biophysical data. The product of these analyses will be a series of maps for each future year for each scenario. These annual maps will form the basis for estimating carbon storage and GHG emissions. For terrestrial ecosystems, carbon storage, carbon-sequestration capacities, and GHG emissions under the current and projected future conditions will be assessed using the LULC and ecosystem-disturbance estimates in map format with a spatially explicit biogeochemical ensemble modeling system that incorporates properties of management activities (such as tillage or harvesting) and properties of individual ecosystems (such as elevation, vegetation characteristics, and soil attributes). For aquatic ecosystems, carbon burial in sediments and GHG fluxes are functions of the current and projected future stream flow and sediment transports, and therefore will be assessed using empirical modeling methods. Validation and uncertainty analysis methods described in the methodology will follow established guidelines to assess the quality of the assessment results. The U.S. Environmental Protection Agency's Level II ecoregions map (which delineates 24 ecoregions for the Nation) will be the practical instrument for developing and delivering assessment results. Consequently, the ecoregion will be the reporting unit of the assessment because the mitigation scenarios, assessment results, validation, and uncertainty analysis will be

Open-File Report

A method for assessing carbon stocks, carbon sequestration, and greenhouse-gas fluxes in ecosystems of the United States under present conditions and future scenarios

he Energy Independence and Security Act of 2007 (EISA), Section 712, mandates the U.S. Department of the Interior to develop a methodology and conduct an assessment of the Nation’s ecosystems, focusing on carbon stocks, carbon sequestration, and emissions of three greenhouse gases (GHGs): carbon dioxide, methane, and nitrous oxide. The major requirements include (1) an assessment of all ecosystems (terrestrial systems, such as forests, croplands, wetlands, grasslands/shrublands; and aquatic ecosystems, such as rivers, lakes, and estuaries); (2) an estimate of the annual potential capacities of ecosystems to increase carbon sequestration and reduce net GHG emissions in the context of mitigation strategies (including management and restoration activities); and (3) an evaluation of the effects of controlling processes, such as climate change, land-use and land-cover change, and disturbances such as wildfires. The concepts of ecosystems, carbon pools, and GHG fluxes follow conventional definitions in use by major national and international assessment or inventory efforts. In order to estimate current ecosystem carbon stocks and GHG fluxes and to understand the potential capacity and effects of mitigation strategies, the method will use two time periods for the assessment: 2001 through 2010, which establishes a current ecosystem carbon and GHG baseline and will be used to validate the models; and 2011 through 2050, which will be used to assess potential capacities based on a set of scenarios. The scenario framework will be constructed using storylines of the Intergovernmental Panel on Climate Change (IPCC) Special Report on Emission Scenarios (SRES), along with both reference and enhanced land-use and land-cover (LULC) and land-management parameters. Additional LULC and land-management mitigation scenarios will be constructed for each storyline to increase carbon sequestration and reduce GHG fluxes in ecosystems. Input from regional experts and stakeholders will be solicited to construct these scenarios. The methods for mapping the current LULC and ecosystem disturbances will require the extensive use of both remote-sensing data and field-survey data (for example, forest inventories) to capture and characterize landscape-changing events. For potential LULC changes and ecosystem disturbances, key drivers such as socioeconomic and climate changes will be used in addition to the biophysical data. The result of these analyses will be a series of maps for each future year for each scenario. These annual maps will form the basis for estimating carbon storage and GHG emissions. For terrestrial ecosystems, carbon storage, carbon-sequestration capacities, and GHG emissions under the present conditions and future scenarios will be assessed using the LULC-change and ecosystem-disturbance estimates in map format with a spatially explicit biogeochemical ensemble modeling system that incorporates properties of management activities (such as tillage or harvesting) and properties of individual ecosystems (such as energy exchange, vegetation characteristics, hydrological cycling, and soil attributes). For aquatic ecosystems, carbon burial in sediments and fluxes of GHG are functions of the present and future potential stream flow and sediment transport and will be assessed using empirical hydrological modeling methods. Validation and uncertainty analysis methods described in the methodology will follow established guidelines to assess the quality of the assessment results. The U.S. Environmental Protection Agency’s Level II ecoregions map will be the practical instrument for developing and delivering assessment results. Consequently, the ecoregion (there are 22 modified ecoregions) will be the reporting unit of the assessment because the scenarios, assessment results, validation, and uncertainty analysis will be produced at that scale. The implementation of these methods will require collaborations among various Federal agencies, State agencies, nongovernmental organizations, and the science community. Using the method described in this document, the assessment can be completed in approximately 3 to 4 years. The primary deliverables will be assessment reports containing tables, charts, and maps that will present the estimated GHG parameters annually for 2001 through 2050 by ecosystem, pool, and scenario. The results will permit the evaluation of a range of policies, mitigation options, and research topics, such as the demographic, LULC-change, or climate-change effects on carbon stocks, carbon sequestration, and GHG fluxes in ecosystems.

Scientific Investigations Report

Suspended sediment and carbonate transport in the Yukon River Basin, Alaska: Fluxes and potential future responses to climate change

Loads and yields of suspended sediment and carbonate were measured and modeled at three locations on the Yukon, Tanana, and Porcupine Rivers in Alaska during water years 2001–2005 (1 October 2000 to 30 September 2005). Annual export of suspended sediment and carbonate upstream from the Yukon Delta averaged 68 Mt a −1 and 387 Gg a −1 , respectively, with 50% of the suspended sediment load originating in the Tanana River Basin and 88% of the carbonate load originating in the White River Basin. About half the annual suspended sediment export occurred during spring, and half occurred during summer‐autumn, with very little export in winter. On average, a minimum of 11 Mt a −1 of suspended sediment is deposited in floodplains between Eagle, Alaska, and Pilot Station, Alaska, on an annual basis, mostly in the Yukon Flats. There is about a 27% loss in the carbonate load between Eagle and Yukon River near Stevens Village, with an additional loss of about 29% between Stevens Village and Pilot Station, owing to a combination of deposition and dissolution. Comparison of current and historical suspended sediment loads for Tanana River suggests a possible link between suspended sediment yield and the Pacific decadal oscillation.

Water Resources Research

Utilizing chromophoric dissolved organic matter measurements to derive export and reactivity of dissolved organic carbon exported to the Arctic Ocean: A case study of the Yukon River, Alaska

[1] The quality and quantity of dissolved organic matter (DOM) exported by Arctic rivers is known to vary with hydrology and this exported material plays a fundamental role in the biogeochemical cycling of carbon at high latitudes. We highlight the potential of optical measurements to examine DOM quality across the hydrograph in Arctic rivers. Furthermore, we establish chromophoric DOM (CDOM) relationships to dissolved organic carbon (DOC) and lignin phenols in the Yukon River and model DOC and lignin loads from CDOM measurements, the former in excellent agreement with long‐term DOC monitoring data. Intensive sampling across the historically under‐sampled spring flush period highlights the importance of this time for total export of DOC and particularly lignin. Calculated riverine DOC loads to the Arctic Ocean show an increase from previous estimates, especially when new higher discharge data are incorporated. Increased DOC loads indicate decreased residence times for terrigenous DOM in the Arctic Ocean with important implications for the reactivity and export of this material to the Atlantic Ocean.

Geophysical Research Letters

Hydrologic support of carbon dioxide flux revealed by whole-lake carbon budgets

Freshwater lakes are an important component of the global carbon cycle through both organic carbon (OC) sequestration and carbon dioxide (CO 2 ) emission. Most lakes have a net annual loss of CO 2 to the atmosphere and substantial current evidence suggests that biologic mineralization of allochthonous OC maintains this flux. Because net CO 2 flux to the atmosphere implies net mineralization of OC within the lake ecosystem, it is also commonly assumed that net annual CO 2 emission indicates negative net ecosystem production (NEP). We explored the relationship between atmospheric CO 2 emission and NEP in two lakes known to have contrasting hydrologie characteristics and net CO 2 emission. We calculated NEP for calendar year 2004 using whole-lake OC and inorganic carbon (IC) budgets, NEP oc and NEP IC , respectively, and compared the resulting values to measured annual CO 2 flux from the lakes. In both lakes, NEP Ic and NEP Ic were positive, indicating net autotrophy. Therefore CO 2 emission from these lakes was apparently not supported by mineralization of allochthonous organic material. In both lakes, hydrologie CO 2 inputs, as well as CO 2 evolved from netcalcite precipitation, could account for the net CO 2 emission. NEP calculated from diel CO 2 measurements was also affected by hydrologie inputs of CO 2 . These results indicate that CO 2 emission and positive NEP may coincide in lakes, especially in carbonate terrain, and that all potential geologic, biogeochemical, and hydrologie sources of CO 2 need to be accounted for when using CO 2 concentrations to infer lake NEP. Copyright 2009 by the American Geophysical Union.

Journal of Geophysical Research G: Biogeosciences

Soil CO 2 Flux in the Amargosa Desert, Nevada, during El Nino 1998 and La Nina 1999

Mean annual soil CO2 fluxes from normally bare mineral soil in the Amargosa Desert in southern Nevada, United States, measured with clear and opaque soil CO2-flux chambers (autochambers) were small - <5 millimoles per square meter per day - during both El Nino 1998 and La Nina 1999. The 1998 opaque-chamber flux exceeded 1999 opaque-chamber flux by an order of magnitude, whereas the 1998 clear-chamber flux exceeded 1999 clear-chamber flux by less than a factor of two. These data suggest that above-normal soil moisture stimulated increased metabolic activity, but that much of the extra CO2 produced was recaptured by plants. Fluxes from warm moist soil were the largest sustained fluxes measured, and their hourly pattern is consistent with enhanced soil metabolic activity at some depth in the soil and photosynthetic uptake of a substantial portion of the CO2 released. Flux from cool moist soil was smaller than flux from warm moist soil. Flux from hot dry soil was intermediate between warm-moist and cool-moist fluxes, and clear-chamber flux was more than double the opaque-chamber flux, apparently due to a chamber artifact stemming from a thermally controlled CO2 reservoir near the soil surface. There was no demonstrable metabolic contribution to the very small flux from cool dry soil, which was dominated by diffusive up-flux of CO2 from the water table and temperature-controlled CO2-reservoir up- and down-fluxes. These flux patterns suggest that transfer of CO2 across the land surface is a complex process that is difficult to accurately measure.

Scientific Investigations Report

Sediment organic carbon burial in agriculturally eutrophic impoundments over the last century

We estimated organic carbon (OC) burial over the past century in 40 impoundments in one of the most intensively agricultural regions of the world. The volume of sediment deposited per unit time varied as a function of lake and watershed size, but smaller impoundments had greater deposition and accumulation rates per unit area. Annual water storage losses varied from 0.1-20% and were negatively correlated with impoundment size. Estimated sediment OC content was greatest in lakes with low ratios of watershed to impoundment area. Sediment OC burial rates were higher than those assumed for fertile impoundments by previous studies and were much higher than those measured in natural lakes. OC burial ranged from a high of 17,000 g C m-2 a-1 to a low of 148 g C m-2 a-1 and was significantly greater in small impoundments than large ones. The OC buried in these lakes originates in both autochthonous and allochthonous production. These analyses suggest that OC sequestration in moderate to large impoundments may be double the rate assumed in previous analyses. Extrapolation suggests that they may bury 4 times as much carbon (C) as the world's oceans. The world's farm ponds alone may bury more OC than the oceans and 33% as much as the world's rivers deliver to the sea. Copyright 2008 by the American Geophysical Union.

Global Biogeochemical Cycles

Transport of elemental mercury in the unsaturated zone from a waste disposal site in an arid region

Mercury contained in buried landfill waste may be released via upward emission to the atmosphere or downward leaching to groundwater. Data from the US Geological Survey’s Amargosa Desert Research Site (ADRS) in arid southwestern Nevada reveal another potential pathway of Hg release: long-distance (10 2 m) lateral migration of elemental Hg (Hg 0 ) through the unsaturated zone. Gas collected from multiple depths from two instrumented boreholes that sample the entire 110-m unsaturated zone thickness and are located 100 and 160 m away from the closest waste burial trench exhibit gaseous Hg concentrations of up to 33 and 11 ng m −3 , respectively. The vertical distribution of gaseous Hg in the borehole closest to the disposal site shows distinct subsurface peaks in concentration at depths of 1.5 and 24 m that cannot be explained by radial diffusive transport through a heterogeneous layered unsaturated zone. The inability of current models to explain gaseous Hg distribution at the ADRS highlights the need to advance the understanding of gas-phase contaminant transport in unsaturated zones to attain a comprehensive model of landfill Hg release.

Applied Geochemistry

Nutrient (N, P) loads and yields at multiple scales and subbasin types in the Yukon River basin, Alaska

Loads and yields of dissolved and particulate nitrogen (N) and phosphorus (P) were measured and modeled at three locations on the Yukon River (YR) and on the Tanana and Porcupine Rivers in Alaska during 2001-2005. Total export of N and P upstream of Yukon Delta averaged 120 Gg N a-1 and 56 Gg P a-1, respectively, with 43.5% of total N (TN) as dissolved organic N, and 98% of total P (TP) as particulate phosphorus. Approximately half of the annual export of TN and TP occurred during spring. Hydrologic yields ofTN (5.6-13.3 mmol N m-2 a-1) and TP (0.8-9.0 mmol P m-2 a-1) were least in the Porcupine basin and greatest in the Tanana basin and were proportional to water yield. Comparison of current and historical dissolved organic matter (DOM) export from the basin indicates decreased DON export with respect to total water discharge during summer and autumn in recent decades. Any possible climate-related change in annual water discharge will result in proportional changes in N and P export.

Journal of Geophysical Research G: Biogeosciences

Flux and age of dissolved organic carbon exported to the Arctic Ocean: A carbon isotopic study of the five largest arctic rivers

The export and Δ 14 C-age of dissolved organic carbon (DOC) was determined for the Yenisey, Lena, Ob', Mackenzie, and Yukon rivers for 2004–2005. Concentrations of DOC elevate significantly with increasing discharge in these rivers, causing approximately 60% of the annual export to occur during a 2-month period following spring ice breakup. We present a total annual flux from the five rivers of ∼16 teragrams (Tg), and conservatively estimate that the total input of DOC to the Arctic Ocean is 25–36 Tg, which is ∼5–20% greater than previous fluxes. These fluxes are also ∼2.5× greater than temperate rivers with similar watershed sizes and water discharge. Δ 14 C-DOC shows a clear relationship with hydrology. A small pool of DOC slightly depleted in Δ 14 C is exported with base flow. The large pool exported with spring thaw is enriched in Δ 14 C with respect to current-day atmospheric Δ 14 C-CO 2 values. A simple model predicts that ∼50% of DOC exported during the arctic spring thaw is 1–5 years old, ∼25% is 6–10 years in age, and 15% is 11–20 years old. The dominant spring melt period, a historically undersampled period, exports a large amount of young and presumably semilabile DOC to the Arctic Ocean.

Global Biogeochemical Cycles

Increased groundwater to stream discharge from permafrost thawing in the Yukon River basin: Potential impacts on lateral export of carbon and nitrogen

Arctic and subarctic watersheds are undergoing climate warming, permafrost thawing, and thermokarst formation resulting in quantitative shifts in surface water - groundwater interaction at the basin scale. Groundwater currently comprises almost one fourth of Yukon River water discharged to the Bering Sea and contributes 5-10% of the dissolved organic carbon (DOC) and nitrogen (DON) and 35-45% of the dissolved inorganic carbon (DIC) and nitrogen (DIN) loads. Long-term strearnflow records (>30 yrs) of the Yukon River basin indicate a general upward trend in groundwater contribution to streamflow of 0.7-0.9%/yr and no pervasive change in annual flow. We propose that the increases in groundwater contributions were caused predominately by climate warming and permafrost thawing that enhances infiltration and supports deeper flowpaths. The increased groundwater fraction may result in decreased DOC and DON and increased DIC and DIN export when annual flow remains unchanged.

Geophysical Research Letters

Carbon export and cycling by the Yukon, Tanana, and Porcupine rivers, Alaska, 2001-2005

Loads and yields of dissolved and particulate organic and inorganic carbon (DOC, POC, DIC, PIC) were measured and modeled at three locations on the Yukon River (YR) and on the Tanana and Porcupine rivers (TR, PR) in Alaska during 2001–2005. Total YR carbon export averaged 7.8 Tg C yr −1 , 30% as OC and 70% as IC. Total C yields (0.39–1.03 mol C m −2 yr −1 ) were proportional to water yields (139–356 mm yr −1 ; r 2 = 0.84) at all locations. Summer DOC had an aged component (fraction modern (FM) = 0.94–0.97), except in the permafrost wetland‐dominated PR, where DOC was modern. POC had FM = 0.63–0.70. DOC had high concentration, high aromaticity, and high hydrophobic content in spring and low concentration, low aromaticity, and high hydrophilic content in winter. About half of annual DOC export occurred during spring. DIC concentration and isotopic composition were strongly affected by dissolution of suspended carbonates in glacial meltwater during summer.

Water Resources Research

The global abundance and size distribution of lakes, ponds, and impoundments

One of the major impediments to the integration of lentic ecosystems into global environmental analyses has been fragmentary data on the extent and size distribution of lakes, ponds, and impoundments. We use new data sources, enhanced spatial resolution, and new analytical approaches to provide new estimates of the global abundance of surface-water bodies. A global model based on the Pareto distribution shows that the global extent of natural lakes is twice as large as previously known (304 million lakes; 4.2 million km 2 in area) and is dominated in area by millions of water bodies smaller than 1 km2. Similar analyses of impoundments based on inventories of large, engineered dams show that impounded waters cover approximately 0.26 million km2. However, construction of low-tech farm impoundments is estimated to be between 0.1 % and 6% of farm area worldwide, dependent upon precipitation, and represents >77,000 km 2 globally, at present. Overall, about 4.6 million km2 of the earth's continental "land" surface (>3%) is covered by water. These analyses underscore the importance of explicitly considering lakes, ponds, and impoundments, especially small ones, in global analyses of rates and processes. ?? 2006, by the American Society of Limnology and Oceanography, Inc.

Limnology and Oceanography

Effects of permafrost melting on CO2 and CH4 exchange of a poorly drained black spruce lowland

[1] Permafrost melting is occurring in areas of the boreal forest region where large amounts of carbon (C) are stored in organic soils. We measured soil respiration, net CO 2 flux, and net CH 4 flux during May–September 2003 and March 2004 in a black spruce lowland in interior Alaska to better understand how permafrost thaw in poorly drained landscapes affects land‐atmosphere CO 2 and CH 4 exchange. Sites included peat soils underlain by permafrost at ∼0.4 m depth (permafrost plateau, PP), four thermokarst wetlands (TW) having no permafrost in the upper 2.2 m, and peat soils bordering the thermokarst wetlands having permafrost at ∼0.5 m depth (thermokarst edges, TE). Soil respiration rates were not significantly different among the sites, and 5‐cm soil temperature explained 50–91% of the seasonal variability in soil respiration within the sites. Groundcover vegetation photosynthesis (calculated as net CO 2 minus soil respiration) was significantly different among the sites (TW > TE > PP), which can be partly attributed to the difference in photosynthetically active radiation reaching the ground at each site type. Methane emission rates were 15 to 28 times greater from TW than from TE and PP. We modeled annual soil respiration and groundcover vegetation photosynthesis using soil temperature and radiation data, and CH 4 flux by linear interpolation. We estimated all sites as net C gas sources to the atmosphere (not including tree CO 2 uptake at PP and TE), although the ranges in estimates when accounting for errors were large enough that TE and TW may have been net C sinks.

Journal of Geophysical Research G: Biogeosciences

A decrease in discharge-normalized DOC export by the Yukon River during summer through autumn

Climate warming is having a dramatic effect on the vegetation distribution and carbon cycling of terrestrial subarctic and arctic ecosystems. Here, we present hydrologic evidence that warming is also affecting the export of dissolved organic carbon and bicarbonate (DOC and HCO 3 − ) at the large basin scale. In the 831,400 km 2 Yukon River basin, water discharge (Q) corrected DOC export significantly decreased during the growing season from 1978–80 to 2001–03, indicating a major shift in terrestrial to aquatic C transfer. We conclude that decreased DOC export, relative to total summer through autumn Q, results from increased flow path, residence time, and microbial mineralization of DOC in the soil active layer and groundwater. Counter to current predictions, we argue that continued warming could result in decreased DOC export to the Bering Sea and Arctic Ocean by major subarctic and arctic rivers, due to increased respiration of organic C on land.

Geophysical Research Letters

CO2 dynamics in the Amargosa Desert: Fluxes and isotopic speciation in a deep unsaturated zone

Natural unsaturated-zone gas profiles at the U.S. Geological Survey's Amargosa Desert Research Site, near Beatty, Nevada, reveal the presence of two physically and isotopically distinct CO 2 sources, one shallow and one deep. The shallow source derives from seasonally variable autotrophic and heterotrophic respiration in the root zone. Scanning electron micrograph results indicate that at least part of the deep CO 2 source is associated with calcite precipitation at the 110-m-deep water table. We use a geochemical gas-diffusion model to explore processes of CO 2 production and behavior in the unsaturated zone. The individual isotopic species 12 CO 2 , 13 CO 2 , and 14 CO 2 are treated as separate chemical components that diffuse and react independently. Steady state model solutions, constrained by the measured δ 13 C (in CO 2 ), and δ 14 C (in CO 2 ) profiles, indicate that the shallow CO 2 source from root and microbial respiration composes ∼97% of the annual average total CO 2 production at this arid site. Despite the small contribution from deep CO 2 production amounting to ∼0.1 mol m −2 yr −1 , upward diffusion from depth strongly influences the distribution of CO 2 and carbon isotopes in the deep unsaturated zone. In addition to diffusion from deep CO 2 production, 14 C exchange with a sorbed CO 2 phase is indicated by the modeled δ 14 C profiles, confirming previous work. The new model of carbon-isotopic profiles provides a quantitative approach for evaluating fluxes of carbon under natural conditions in deep unsaturated zones.

Water Resources Research

Response to comment on "A reservoir of nitrate beneath desert soils"

We appreciate the comment by Jackson et al. ( 1 ), which underscores two points made in our recent paper ( 2 ): (i) that desert subsoil nitrate (NO – 3 ) inventories are spatially highly variable, and thereby warrant substantial measurement efforts to reduce uncertainty in global extrapolations, and (ii) that Chihuahuan Desert subsoil NO – 3 inventories tend to be much smaller than inventories in other western U.S. deserts.

Science