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2016

Assessing the Potential to Decrease the Gulf of

Mexico Hypoxic Zone with Midwest US Perennial

Cellulosic Feedstock Production

Andy VanLoocke

Iowa State University, [email protected]

Tracy E. Twine

University of Minnesota - Twin Cities

Christopher J. Kucharik

University of Wisconsin-Madison

Carl J. Bernacchi

University of Illinois at Urbana-Champaign

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Assessing the potential to decrease the Gulf of Mexico

hypoxic zone with Midwest US perennial cellulosic

feedstock production

A N D Y V A N L O O C K E1 ,* , T R A C Y E . T W I N E2, C H R I S T O P H E R J . K U C H A R I K3 , 4 , 5 and C A R L J . B E R N A C C H I6 , 7

1Department of Atmospheric Sciences, University of Illinois, 105 South Gregory St, Urbana, IL 61801, USA,2Department of

Soil, Water, and Climate, University of Minnesota, 1991 Upper Buford Circle, 439 Borlaug Hall, St Paul, MN 55108, USA,

3

Department of Agronomy, University of Wisconsin– Madison, 1575 Linden Drive, Madison, WI 53706, USA,4Center for Sustainability and the Global Environment, 1710 University Ave, Madison, WI 53726, USA,5Department of Energy Great Lakes Bioenergy Research Center, University of Wisconsin-Madison, Madison, WI, USA,6Department of Plant Biology, University of Illinois, 505 South Goodwin Ave, Urbana, IL 61801, USA,7USDA-ARS Global Change and Photosynthesis Research Unit, 1201 West Gregory Dr, Urbana, IL 61801, USA

Abstract

The goal of this research was to determine the changes in streamflow, dissolved inorganic nitrogen (DIN) leaching and export to the Gulf of Mexico associated with a range of large-scale dedicated perennial cellulosic bioenergy production scenarios within in the Mississippi–Atchafalaya River Basin (MARB). To achieve this goal, we used Agro-IBIS, a vegetation model capable of simulating the biogeochemistry of row crops, miscanthus and switchgrass, coupled with THMB, a hydrology model capable of simulating streamflow and DIN export. Simula-tions were conducted at varying fertilizer application rates (0–200 kg N ha 1) and fractional replacement

(5–25%) of current row crops with miscanthus or switchgrass across the MARB. The analysis also includes two scenarios where miscanthus and switchgrass (MRX and MRS, respectively) each replace the ca. 40% of maize production currently devoted to ethanol. Across the scenarios, there were minor reductions in runoff and streamflow throughout the MARB, with the largest differences (ca. 6%) occurring for miscanthus at the highest fractional replacement scenarios in drier portions of the region. However, differences in total MARB discharge at the basin outlet were less than 1.5% even in the MRX scenario. Reductions in DIN export were much larger on a percentage basis than reductions in runoff, with the highest replacement scenarios decreasing long-term mean DIN export by ca. 15% and 20% for switchgrass and miscanthus, respectively. Fertilization scenarios show that significant reductions in DIN leaching are possible even with application rates of 100 and 150 kg N ha 1 for switchgrass and miscanthus, respectively. These results indicate that, given targeted management strategies, there is potential for miscanthus and switchgrass to provide key ecosystem services by reducing the export of DIN, while avoiding hydrologic impacts of reduced streamflow.

Keywords: Agro-IBIS, hydrology, land use change, miscanthus, nitrate, perennial, stream flow, switchgrass

Received 19 April 2016; accepted 26 May 2016

Introduction

To meet the cellulosic targets set in place by the US 2007 Energy Independence and Security Act (EISA), the Mis-sissippi–Atchafalaya River Basins (MARB) may require significant land use change. Production of the current dominant ethanol feedstock in the United States, maize grain, is capped at 15 billion gallons per year by the

Renewable Fuels Standard 2 (RFS2; EPA, 2010) and is at maximum capacity, with ca. 40% of maize production devoted to ethanol (Wallander et al., 2011; https:// www.extension.iastate.edu/agdm/crops/outlook/corn balancesheet.pdf). Numerous studies implementing a wide range of statistical, empirical and numerical tech-niques have indicated that the leaching of excess nitrogen (N) fertilizer in the form of dissolved inorganic nitrogen (DIN) under current row crop production is a major dri-ver of the Gulf of Mexico hypoxic zone or ‘dead zone’ (Rabalais et al., 1996; Goolsby et al., 2000, 2001; Donner et al., 2004a; Royer et al., 2006; Alexander et al., 2008; David et al., 2010; Turner et al., 2012; Deb et al., 2015).

*Present address: Department of Agronomy, Iowa State University, 3027 Agronomy Hall, Ames, IA 50011, USA

Correspondence: Carl J. Bernacchi, tel. 217-333-8048, fax 1-217-244-7246,

e-mail: [email protected]

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In 2008, the Mississippi Basin/Gulf of Mexico Task Force set in place a goal to reduce the size of the hypoxic zone from ~20 000 to <5000 km2 by the year 2015 (Mississippi River/Gulf of Mexico Watershed Nutrient Task Force 2008). However, that goal was not met and the target has now been extended to the year 2035 (Mississippi River/Gulf of Mexico Watershed Nutrient Task Force, 2015). It is predicted that annual DIN export would have to decrease by 30–55% to meet this goal (Donner & Scavia, 2007; Scavia & Donnelly, 2007). It has been suggested that reducing N fertilizer application by~10% over the MARB could reduce DIN export by ~30%, approaching the EPA target (McIsaac et al., 2001); however, it is uncertain how this change in management might affect maize yields. Increasing maize production beyond current levels to meet cellu-losic ethanol production mandates is predicted to increase in DIN leaching and the size of the hypoxic zone (Donner & Kucharik, 2008; Secchi et al., 2011). A potential option to meet the mandated cellulosic pro-duction without increasing nutrient inputs while reduc-ing the size of the hypoxic zone is to convert a portion of the land in the MARB to produce dedicated perennial cellulosic feedstocks such as switchgrass and miscant-hus (Heaton et al., 2008; Somerville et al., 2010; Deb et al., 2015; Hudiburg et al., 2016).

The benefit of incorporating cellulosic plant material into the energy sector is to decrease the demand for fos-sil fuels and the pollution they cause, especially with respect to carbon dioxide, a key greenhouse gas (Inter-governmental Panel on Climate Change; IPCC, 2007; Davis et al., 2010; RFS2; Hudiburg et al., 2016). How-ever, it is important to evaluate the production of cellulosic feedstock in the context of environmental trade-offs that may occur, particularly those related to the hydrologic cycle (Rowe et al., 2009; Bagley et al., 2014; Bernacchi & VanLoocke, 2015). It has been shown that miscanthus and switchgrass remove more carbon (C) from the atmosphere (Davis et al., 2010; Zeri et al., 2011, 2013; Anderson-Teixeira et al., 2013), require less nutrient application (Christian et al., 1997; Heaton et al., 2004, 2010) and leach less DIN (Beale & Long, 1997; McIsaac et al., 2010; Smith et al., 2013) relative to annual crops and may present opportunities for additional ecosystem services (Costello et al., 2009; McIsaac et al., 2010; Ng et al., 2010; Davis et al., 2012). These previous findings and ecosystem model simulations show that incorporating perennials, including miscanthus or switchgrass, on land that is currently under maize pro-duction for ethanol could reduce significantly DIN leaching and greenhouse gas (GHGs) emissions on a land surface basis (Davis et al., 2012; Iqbal et al., 2015). However, experiments also show that potential cellu-losic feedstocks use more water (Hickman et al., 2010;

McIsaac et al., 2010; VanLoocke et al., 2010, 2012) than current vegetation that may result in reductions in streamflow (McIsaac et al., 2010). Historic shifts in land use associated with agricultural production have been shown to alter the hydrologic cycle at the basin scale in the MARB, with the transition from perennial grasslands in forests to annual croplands resulting in less ET and greater runoff and streamflow (Twine et al., 2004; Zhang & Schilling, 2006). Conversely, if the hydrologic cycle is altered by an increase in rates of ET associated with mis-canthus and switchgrass, less water flowing though streams and rivers could potentially inhibit river trans-portation of goods and result in higher concentrations of riverine pollutants thereby degrading water quality.

Current research focusing on water quantity and quality changes associated with cellulosic feedstocks fits into three primary categories: (1) plot-scale measure-ments of nitrate movement within the soil profile (McIsaac et al., 2010; Behnke et al., 2012; Smith et al., 2013), (2) watershed-scale models that do not include mechanistic growth and physiology modules for mis-canthus and switchgrass (Costello et al., 2009; Ng et al., 2010; Wu et al., 2012; Deb et al., 2015; Housh et al., 2015), and (3) basin-scale studies that simulate changes in leaching but do not include the routing of DIN and runoff through the MARB to the Gulf of Mexico (Davis et al., 2012). At the plot scale, miscanthus and switch-grass were shown to have significantly lower DIN leaching relative to the maize/soy rotation in central Illinois, with fertilized (57 kg N ha 1) plots of

switch-grass showing little or no leaching after reaching matu-rity (Smith et al., 2013). This reduction in leaching is attributed to extended periods of crop growth, the effi-cient internal recycling of nutrients and low fertilizer requirements associated with perennial species resulting in relatively small losses of N to the subsoil (Amougou et al., 2012; Cadoux et al., 2012; Smith et al., 2013). At the watershed scale, cellulosic feedstock production is predicted to decrease DIN export (Ng et al., 2010; Deb et al., 2015). At the basin scale, it has been shown that cellulosic production could, depending on type of feed-stock and management practice employed, reduce total MARB leaching by up to 22% if maize production for ethanol was displaced by cellulosic feedstocks (Davis et al., 2012).

While these previous studies provided evidence for the potential ecosystem services of transitioning to cel-lulosic production, it is yet to be estimated what the total change to DIN export and stream flow from the MARB would be under such scenarios. Hydrologic pro-cesses are, tightly coupled to the N cycle (Castellano et al., 2010, 2013), key drivers of DIN transport in the MARB (Donner et al., 2002) and sensitive to land use change (Twine et al., 2004). Therefore, it is crucial to

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implement a model framework explicitly validated to simulate the hydrology of miscanthus and switchgrass and that is capable of simulating DIN leaching across the entire basin.

The goal of this study was to quantify the change in streamflow and DIN export for the MARB under a range of large-scale cellulosic feedstock production sce-narios. To accomplish this goal, a series of coupled sim-ulations are conducted using the Integrated Biosphere Simulator – Agricultural version (Agro-IBIS; Kucharik, 2003) and the Terrestrial Hydrology Model with Biogeo-chemistry (THMB; Coe, 1998, 2000; Donner et al., 2002) to produce output for a range of scenarios aimed at addressing the scale of cellulosic feedstock production necessary to meet the RFS2 mandate (Table 1). The sce-narios are only intended to be hypothetical and consist of various fractions of existing crops replaced with mis-canthus or switchgrass over a range of fertilizer applica-tion rates including two scenarios where miscanthus (MRX) or switchgrass (MRS) replace the ca. 40% of maize grain currently going to ethanol. We anticipate that introducing the production of cellulosic feedstocks will (1) result in a reduction in streamflow proportional to the increase in ET through a decrease in runoff, and (2) result in a reduction in the export of DIN to the Gulf of Mexico proportional to the decrease in DIN leaching associated with the various production scenarios. If the change in DIN leaching is relatively greater than the change in runoff, we also anticipate that (3) the reduc-tion in DIN export will be greater than the reducreduc-tion in discharge within a given production scenario. Because DIN leaching is greater in the more humid (i.e., greater drainage) portions of the Midwest (Burkart & James, 1999; Goolsby et al., 2000; Donner et al., 2004a,b; Don-ner & Kucharik, 2008), we also anticipate that (4) the reduction in DIN export will be greater per unit area when miscanthus or switchgrass replace corn/soy in more humid regions relative to dry regions. Finally, because maize typically has the highest rates of ET and DIN leaching (Donner et al., 2004a,b) relative to the other major crops in MARB, we anticipate that (5) the MRX and MRS scenarios will have minimal impacts on streamflow while maximizing reductions in DIN export.

Materials and methods Model procedure description

The model procedure used in this study builds off of previous implementations of Agro-IBIS and THMB to study effects of land use change on streamflow and biogeochemistry (e.g., Donner et al., 2002; Costa et al., 2003; Donner & Kucharik, 2008; Coe et al., 2011). Agro-IBIS and THMB were run in a semicou-pled (Fig. S1) set of simulations (Table 1). The THMB

simulations were run at 5 min9 5 min (~7 km 9 9 km)

spa-tial resolution and were driven by using simulated monthly mean surface runoff, subsurface drainage and leached DIN from a corresponding 0.5° 9 0.5° IBIS grid cell. An Agro-IBIS spin-up simulation was performed with natural vegetation to allow soil carbon and nitrogen pools to reach a near equilib-rium (VanLoocke et al., 2010). A 1-year spin-up was conducted for the THMB simulations to allow mass transport to reach a quasi-steady state. Simulations in both models were run for a domain that encapsulated the MARB (50.75° N to 28.75° N; 75.75° W to 115.25° W). This procedure has been evaluated pre-viously for the simulation of streamflow and DIN export in the MARB (Donner et al., 2002; Donner & Kucharik, 2003, 2008). A description of the previous evaluations of THMB and Agro-IBIS against observations in literature is provided in the respec-tive model descriptions sections below.

A total of 54 simulations were conducted (Table 1). Simula-tions included a baseline scenario for model evaluation pur-poses with current land use and historic fertilizer application rates. A current land use scenario with approximations of cur-rent fertilizer application rates provided the control by which comparisons were made for the cellulosic feedstock scenarios. Experimental scenarios included five fraction coverage scenar-ios, where land currently in row crop (i.e., maize, soybean and/or wheat) production is converted to miscanthus or switchgrass, at five fertilizer application rates (25 simulations per feedstock). Finally, two simulations were conducted whereby miscanthus (MRX) or switchgrass (MRS) replace the ca. 40% of land currently under maize production that is being used for ethanol production.

Table 1 The fertilizer application rate and fraction of current

cropland replaced for the varying cellulosic feedstock produc-tion scenarios simulated

Fraction coverage scenario Percentage of cropland replaced % N-Fertilizer kg N ha 1

Baseline NA Historic rates*

Control NA Current rates†

5‡ 5 0, 50, 100, 150 and 200 10‡ 10 0, 50, 100, 150 and 200 15‡ 15 0, 50, 100, 150 and 200 20‡ 20 0, 50, 100, 150 and 200 25‡ 25 0, 50, 100, 150 and 200 MRX 40% of maize 0 MRS 40% of maize 50

*Historic rates are input for each crop (maize, soybean, wheat) based on the USDA state-level agricultural chemical use sur-veys (www.ers.usda.gov/Data/FertilizerUse).

Current rates are 2001–2005 average.

The 5, 10, 15, 20 and 25 Fraction coverage scenarios were sim-ulated independently for both miscanthus and switchgrass at each of the fertilizer application rates. Five replacement levels each with five fertilizer levels produces 25 scenarios per feed-stock, yielding 50 scenarios.

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Agro-IBIS description

Agro-IBIS is a dynamic global vegetation model that has been adapted from the original IBIS model (Foley et al., 1996; Kucharik et al., 2000) to simulate the biogeochemical cycles and biophysical processes associated with the production and management of most major US crops (Kucharik & Brye, 2003). Carbon and water exchange are simulated on an hourly time step based on a bio-physical/biochemical approach that includes the C3 and C4 pho-tosynthetic pathways and leaf physiology (Farquhar et al., 1980; Collatz et al., 1991) and canopy scaling (Thompson & Pollard, 1995a,b). Total evapotranspiration is calculated hourly by sum-ming the fluxes of water vapor from transpiration and direct evaporation from puddle, soil and leaf surfaces.

Fluxes and pools of C and nitrogen in soil and plant matter are calculated daily. Soil N pools include soil organic N and DIN. The primary belowground N dynamics represented in Agro-IBIS includes mineralization and immobilization. Plant uptake of N from soil pools to roots is determined by the size of N pools and the transpiration rate. Plant uptake of N is par-titioned into the various biomass pools (leaf, stem and root), and the portion that is not removed in harvest is recycled in lit-ter. Limitations are imposed on photosynthesis through modi-fying carboxylation capacity when the availability of N is suboptimal (Donner & Kucharik, 2003; Kucharik & Brye, 2003). The rate of DIN leaching is dependent on the concentration of DIN and the rate of subsurface drainage (Donner & Kucharik, 2003; Kucharik & Brye, 2003).

For the current analysis, an algorithm was developed and calibrated based on measured data (Himken et al., 1997; Heaton et al., 2009; Dohleman et al., 2012; Wilson et al., 2013; Boersma et al., 2015) to simulate the movement of C and N between aboveground (i.e., shoots) and belowground (i.e., roots and rhi-zome) pools. Miscanthus and switchgrass each have their own algorithm that is based on the mass balance and tissue-specific N concentration data (Dohleman et al., 2012). Starting on the day of emergence, the algorithm allows for translocation (i.e., the transfer of belowground biomass and N to shoots) to initi-ate canopy development (Fig. S2). As with annual crops, canopy leaf area is updated daily based on the mass of C allo-cated to leaves and the specific leaf area, which varies among crop types (Kucharik, 2003). Phenology and C allocation are dynamics throughout the growing season and are dictated by the accumulation of growing degree days or temperature thresholds. At senescence, each algorithm drives translocation of aboveground C and N to belowground storage, which has a low turnover rate over the winter (Dohleman et al., 2012).

Agro-IBIS requires hourly values of air temperature, humid-ity, solar radiation and wind speed to drive physical processes. These data were derived from a procedure that combined cli-mate data sets from University of East Anglia Clicli-mate Research Unit (New et al., 1999; Mitchell & Jones, 2005) and the National Centers for Environmental Prediction–National Center for Atmo-spheric Research reanalysis data (Kalnay et al., 1996; Kistler et al., 2001). Based on these data, hourly values were generated using a statistical procedure that accounts for diurnal patterns and relationships of atmospheric variables (Campbell & Nor-man, 1998). Soil texture in Agro-IBIS is prescribed for 11 layers of varying thickness to a depth of 2.5 m based on the CONUS

soil data set (Miller & White, 1998). Further description of Agro-IBIS and its predecessor Agro-IBIS, including its development and implementation, have been presented in detail elsewhere (Foley et al., 1996; Delire & Foley, 1999; Kucharik et al., 2000; Lenters et al., 2000; Kucharik, 2003; Donner et al., 2004a,b; Kucharik & Twine, 2007; Twine & Kucharik, 2009; Sacks & Kucharik, 2011).

The Agro-IBIS evaluation for the growth and function of cur-rent major crops (corn, soy, wheat; Kucharik, 2003; Kucharik & Twine, 2007; Twine & Kucharik, 2008; Twine et al., 2013) as well as for miscanthus and switchgrass (VanLoocke et al., 2010, 2012) has been described previously. Specific evaluations rele-vant to this work include comparisons to numerous field-based measurements of key N fluxes and pools for both aboveground and belowground dynamics (Kucharik & Brye, 2003). Agro-IBIS simulated maize yields have been compared to US Department of Agriculture yield observations across the Corn Belt (Kucharik, 2003). Simulated maize and soybean canopy fluxes and leaf area have been evaluated against flux observations over numerous growing seasons (Kucharik & Twine, 2007). Agro-IBIS simulation of miscanthus and switchgrass hydrology was evaluated against observations of ET over multiple years using two independent methods and showed strong agreement (VanLoocke et al., 2010, 2012).

THMB description

Terrestrial Hydrology Model with Biogeochemistry simulates the storage, transport and removal of water and N on an hourly time step, based on Agro-IBIS inputs of DIN leaching, surface runoff, subsurface drainage, precipitation and

evapora-tion from surface waters at a 5 min9 5 min spatial resolution

(Coe, 1998; Donner et al., 2002). Surface waters in THMB include rivers, wetlands, lakes and anthropogenic reservoirs. In THMB, the transport of input water and N depends on local topography as well as inputs from upstream grid cells.

Dis-solved inorganic N includes NOxand NH3, because NOx

repre-sents >95% of DIN reaching the Gulf of Mexico (Aulenbach

et al., 2007). THMB transports all DIN together. A portion of leached DIN is lost in the THMB surface waters due to

denitri-fication through the reduction of NO3 to N2O and N2 and is

dependent on river bed morphology, solute concentration and water temperature (Donner et al., 2004b).

The ability of THMB and its predecessors, surface water area model (i.e., SWAM) and hydrologic routing algorithm (i.e., HYDRA), to simulate streamflow (discharge) and nutrient export has been tested in numerous studies, covering a wide range of scales and locations. Evaluations include comparison of simulations against annual mean discharge and lake area for major global basins and lakes (Coe, 1998) and the accuracy of the surface hydrology in general circulation models (Coe,

2000). At the continental scale, discharge and DIN export (NO3

yield) for internal sub-basins within the MARB for ca. 30 total US observation stations from the Geological Survey, National Water Service (USGS) and Global Monthly River Discharge Data Set (Donner et al., 2002) showed good agreement with model simulations for discharge. Evaluations of an updated version of the model for the Upper Mississippi River Basin showed stronger correlation of discharge and DIN export to

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USGS observation in the basin (Donner & Kucharik, 2003; Donner et al., 2004a,b) and showed strong agreement with USGS observed DIN export at near the outlet of the MARB (Donner & Kucharik, 2008).

Land use

The fraction crop coverage in each 5 min9 5 min grid cell is

aggregated based an integration of a satellite-based data set of total area in crop production with the USDA county-level data (www.nass.usda.gov) for the area planted in major crops including maize, soybeans, spring and winter wheat (Raman-kutty et al., 2008; for a full description, see Donner & Kucharik, 2008). The distribution of natural vegetation in the model domain was determined using vegetation maps (Ramankutty & Foley, 1998) and the International Geosphere Biosphere Pro-grammes’s 1-km DISCover land cover data (Loveland & Bel-ward, 1997). There is significant uncertainty surrounding the future locations and intensity of production of cellulosic feed-stocks. Therefore, a series of simulations were conducted at varying fraction coverages for miscanthus and switchgrass (Table 1). These scenarios include even coverage across the land currently in production of maize, soy, spring and winter wheat in the MARB domain (Fig. S3a), as well as targeted replacement of existing maize/soy production, with the intent of simulating the displacement of current grain ethanol with dedicated perennial cellulosic ethanol (Fig. S3b).

Management

In the baseline scenario, each of the current crops was fertilized at historic rates, and in the control simulation, the 2001–2005 average application rates were used (Table 1; Donner & Kucharik, 2008). The fertilizer input data are based on the USDA state-level agricultural chemical use surveys (http:// www.ers.usda.gov/Data/FertilizerUse/; Donner & Kucharik, 2008). Modern rather than historic fertilizer inputs were chosen for the control run to represent the changes in the system that would occur if perennials are to replace annuals moving for-ward, rather than the changes that would have occurred over the last 30 years. Further detail on the distribution of fertilizer application and the response of the model to fertilizer input was evaluated previously by Donner et al. (2004a). With respect to the management of perennial feedstocks, there is significant uncertainty surrounding the most likely application rates of fertilizer in the management of switchgrass and miscanthus, a series of simulations were conducted at varying fertilizer levels (Table 1). This range includes the various recommendations made based on study sites for switchgrass and miscanthus (Adler et al., 2007; Miguez et al., 2008; Schmer et al., 2008; Varvel et al., 2008; Cadoux et al., 2012). Following the recom-mended practices of Smith et al. (2013), the MRX and MRS

scenarios were fertilized at 0 and 50 kg N ha 1, respectively.

Model evaluation

Simulated annual mean streamflow and DIN export from the control scenario were compared to USGS observations

(Aulenbach et al., 2007) near the outlet of the MARB. Output from the nearest corresponding THMB grid cell was compared to the USGS observations for the Mississppi River at Tambert Landing, MS, Old River Outflow, and the Atchafalaya River at Simmersport, LA. Simulated and observed values from 1980 to 2001 were summed from each of the respective observation points to produce the total MARB DIN export (Fig. 1a) and streamflow at the outlet (i.e., discharge; Fig. 1b).

Results

Comparison of streamflow and DIN export in baseline simulation to observations

The baseline simulation (Table 1) reproduces the observed interannual variability and long-term mean in

Fig. 1 Observed (US Geological Survey Open-File Report

2007-1080) and simulated (baseline scenario) dissolved inor-ganic nitrogen (DIN) export (a) and total annual discharge (b) to the Gulf of Mexico for the 22-year period spanning 1980– 2001 and the mean over that period. Values are the sum of DIN export of the Mississppi River at St. Francisville LA and the Atchafalaya River at Melville LA.

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discharge and DIN export from the MARB (Fig. 1). Sim-ulated annual mean DIN export corresponds well to the observations (model= 0.84 obs + 0.10; r2= 0.91), with the overall simulated mean within 5% of the observed value (Fig. 1a). Simulated annual mean discharge cap-tures the majority of observed interannual variability (r2= 0.93) with a slight bias (model = 1.01 obs + 2722) and the overall simulated mean is ca. 11% greater than the observed mean (Fig. 1b).

Comparison of runoff in control simulation to replacement scenarios

The Agro-IBIS simulated total annual mean runoff (sur-face+ subsurface) varies significantly across the MARB for the control simulation, with values<50 mm yr 1in the driest and western-most portions of the domain and >650 mm yr 1

near the Gulf of Mexico outlet (Fig. 2a). The pattern of total annual runoff is similar to annual mean precipitation across the Basin (data not shown), showing a general increase following the gradient in

precipitation from north to south as well as west to east. In the cellulosic replacement scenarios (Table 1), runoff is similar for all the fertilizer application rates (data not shown) but varies widely between the various fraction replacement scenarios (Fig. 3).

At the 5% replacement level, there is less than a 2% decrease in runoff (per grid cell) for switchgrass and a 2–4% decrease for miscanthus runoff relative to control (Fig. 3a, e). Differences in runoff are larger at greater replacement levels, with switchgrass decreases ranging from 2% to 8% (Fig. 3e–h) and miscanthus from 4% to 10% (Fig. 3a–d) lower than control for the 15% and 25% replacement scenarios, respectively. Compared to con-trol, throughout the Corn Belt (Iowa, Illinois, Indiana and Ohio), the MRS scenario shows less than a 4% decrease in runoff, while the MRX scenario shows a 4–6% decrease in runoff in the eastern portions and up to 10% in the western portions of the Corn Belt in total runoff.

Neither the MRX nor the MRS scenarios show any differences >2% in total runoff relative to control in the southern portions of the domain near the Lower Missis-sippi (Fig. 3d, h). Miscanthus and switchgrass both show smaller changes in total runoff under the MRX and MRS scenarios compared to control than under the respective 25% replacement scenarios (Fig. 3c–h). For all scenarios, on a percentage basis, the changes in runoff relative to control were largest in the drier western portions of the domain (Fig. 3), where the absolute values of runoff in the control simulation tended to be the lowest (Fig. 2a).

Comparison of DIN leaching in control simulation to replacement scenarios

Simulated annual mean DIN leaching also varies highly across the domain for the control simulation, with val-ues less than 5 kg N ha 1yr 1throughout most of the

unmanaged portions of the domain, and values exceed-ing 50 kg N ha 1yr 1 in eastern portions of the Corn Belt (Fig. 2b). Portions of the domain dominated by maize production have the highest leaching rates, with portions where wheat or soybean are dominant having generally lower leaching rates. Leaching rates increase with runoff within regions of similar crop production (e.g., the Corn Belt), with leaching rates 25–50% greater in the transect stretching from Eastern Illinois to Wes-tern Ohio relative to the EasWes-tern Nebraska and Iowa region (Fig. 2).

In the cellulosic replacement scenarios, DIN leaching varies with the fraction of land replaced. There is little variability across the domain for differences in DIN leaching relative to control within a given cellulosic replacement level; however, there are large differences

Fig. 2 Simulated annual mean total runoff (surface+

subsur-face) (a) and total annual mean dissolved inorganic nitrate

leaching (DIN) (b) in the Mississippi–Atchafalaya River Basin

for the control simulation over the 33-year period spanning 1970–2002.

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Fig. 3 Simulated mean annual percent difference (scenario– control) in total runoff in the Mississippi–Atchafalaya River Basin for

the miscanthus (a–d) and switchgrass (e–h) scenarios at 5% (a, e), 15% (b, f) and 25% (c, g) replacement at the 0 kg N ha 1

fertilizer rate as well as the MRX (d), and MRS (h) cellulosic for maize scenarios for the 33-year period spanning 1970–2002.

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among scenarios, with the largest differences occurring at the highest replacement levels (Fig. 4). At the 5% replacement level, neither miscanthus nor switchgrass shows reductions in mean DIN leaching exceeding 5% compared to control (Fig. 4a, e); however, as replace-ment increases to 15%, both show decreases in DIN leaching over 10% (Fig. 4b, f), and at the 25% replace-ment level, there are portions of the domain showing decreases over 20% (Fig. 4c, g). The largest differences relative to control in mean DIN leaching for both mis-canthus and switchgrass occur in the MRX and MRS scenarios, showing over 25% and 20% reductions, respectively, across the majority of the Corn Belt (Fig. 4d, h). As with runoff, miscanthus has a larger decrease in DIN relative to switchgrass throughout the MARB (Fig. 4).

Comparison of streamflow in control simulation to replacement scenarios

The THMB-simulated mean streamflow for the various rivers in the MARB network shows a range of flow rates spanning four orders of magnitude, with the fourth-and third-order rivers/streams generally less than 500 m3s 1, the second-order rivers (e.g., Missouri, Ohio and Arkansas) in the 500–5000 m3

s 1 range and the lower Mississippi and Atchafalaya ranging 5000–30 000 m3

s 1 (Fig. 5a). Similar to the results for runoff, there is little variability in streamflow for the cel-lulosic replacement scenarios with fertilizer application rate (data not shown). However, there are notable dif-ferences in streamflow between the various replacement levels relative to the control. In the cellulosic replace-ment scenarios, mean streamflow is reduced by <3% relative to control across the domain at the lowest replacement level for both miscanthus and switchgrass (Fig. 6a, e). At the 15% replacement level, switchgrass reductions in mean streamflow relative to control are still <3% throughout the domain, with miscanthus showing 3–6% reductions relative to control in portions of the upper Missouri and surrounding tributaries (Fig. 6b, f). At the 25% level, there are still very few riv-ers showing over 3% reductions in mean streamflow for switchgrass compared to control; however, reductions of up to 6% in portions of the Missouri and Upper Mis-sissippi rivers and surrounding tributaries are simu-lated (Fig. 6c, g). Similar to the pattern for runoff, the differences relative to control in streamflow are smaller in the MRX and MRS scenarios compared to the respec-tive 25% replacement scenarios (Fig. 6c–h). The MRX scenario shows a small number of rivers with 3% decreases in streamflow compared to control, while the MRS scenario differences in streamflow are <3% throughout the domain. Overall decreases in mean

streamflow relative to control are greater for miscanthus than for switchgrass, with the largest reductions occur-ring in second- and third-order rivers and correspond-ing to the areas of greatest decreases in runoff (Figs 5a and 6); however, reductions never exceeded 7% in any scenario.

Comparison of DIN export in control simulation to replacement scenarios

Simulated mean DIN export follows a pattern similar to streamflow for the control simulation across the MARB (Fig. 5). As with streamflow, the DIN export spans sev-eral orders of magnitude across all rivers, with third-and fourth-order rivers averaging between 500 third-and 5000 metric tons yr 1and second-order rivers an order of magnitude larger, and the Lower Mississippi River averaging up to 500 000 metric tons yr 1 (Fig. 5b). As with DIN leaching, only the 0 kg N ha 1 fertilizer application scenarios are shown and discussion of the dependence of DIN export on fertilizer application rate is presented only at the basin outlet.

Unlike the patterns for percent changes in streamflow for the cellulosic scenarios (Fig. 6), differences in mean DIN export relative to control are more evenly dis-tributed across the domain (Fig. 7). At the 5% replace-ment level, both miscanthus and switchgrass show an even distribution of 1–5% reductions in mean DIN export relative to the control (Fig. 7a, e). The higher replacement levels show greater decreases in mean DIN export compared to control, with the 15% replacement scenario showing reductions of 5–15% (Fig. 7b, f) and the 25% replacement showing most rivers with at least 5% reductions, and up to 15% for miscanthus, through-out the MARB (Fig. 7c, g). Following the pattern in mean DIN leaching, the largest differences in mean DIN export occurs in the MRX and MRS scenarios, with the majority of the domain showing reductions >5% and rivers in the northern portions of the MARB showing over 15% reductions relative to control (Fig. 7d, h). Overall, the percent reductions in DIN export compared to control are ca. three times greater than that for streamflow for the majority of the MARB (Figs 6 and 7).

The dependence of DIN leaching on fertilizer application rate

At the 25% fraction replacement level, there is a decrease in DIN leaching for scenarios relative to con-trol across the entire domain for the 0, 50 and 100 kg N ha 1fertilizer rate scenarios for both miscant-hus (Fig. 8a–c) and switchgrass (Fig. 8f–h). The areas in the domain with the largest cellulosic species-based decreases in DIN leaching correspond to where the

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Fig. 4 Simulated mean annual percent difference (scenario– control) in DIN leaching in the Mississippi–Atchafalaya River Basin for the miscanthus (a–d) and switchgrass (e–h) scenarios at 5% (a, e), 15% (b, f) and 25% (c, g) replacement as well as the MRX (d), and MRS (h) cellulosic for maize scenarios for the 33-year period spanning 1970–2002.

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control simulations had the highest leaching rates (Fig. 2b). The majority of the Corn Belt has decreased DIN leaching for miscanthus relative to the control for the 150 kg N ha 1fertilizer scenario relative to the con-trol (Fig. 8d) but at the 200 kg N ha 1 rate, large areas of increased DIN leaching occur for miscanthus (Fig. 8e). On the other hand, switchgrass has minimal decreases in DIN leaching in the Corn Belt for the 150 kg N ha 1and increases in DIN leaching relative to

the control for the 200 kg N ha 1 scenario across the

entire domain (Fig. 8i, j). Smaller fraction replacement scenarios have a similar pattern to the 25% level but with smaller magnitudes of differences (data not shown).

Comparison of monthly mean streamflow and DIN export at the MARB outlet

At the monthly time scale, there is no appreciable shift in the pattern of total discharge at the outlet of the MARB for either miscanthus or switchgrass across any of the scenarios (Fig. 9a, c respectively). For both mis-canthus and switchgrass, the largest differences relative to control in mean discharge are in the 25% replacement

scenario, although they are only 1–2% lower for mis-canthus (Fig. 9a) and <1% lower for switchgrass (Fig. 9c). The differences in mean DIN export are much larger than discharge for both species and for the respective scenarios (Fig. 9a, c and b, d); however, there is no appreciable shift in the pattern of monthly mean DIN export at the outlet of the MARB (Fig. 9b, d). The largest differences compared to control occur in May and June and the smallest in September through November for both species, with the MRX and MRS sce-narios showing the greatest reductions in mean DIN export for miscanthus and switchgrass (Fig. 9).

Comparison of annual mean streamflow and DIN export at the MARB outlet

At an annual time scale, differences relative to control in mean discharge at the outlet of the MARB are small relative to mean DIN export for both miscanthus and switchgrass for the various scenarios (Fig. 10). In the miscanthus scenarios, the largest decrease relative to control in mean discharge is in the 25% replacement scenario with a ca 1.5% reduction (Fig. 10a). Switchgrass shows a similar pattern; however, the mean difference compared to control for the 25% replacement scenario is <1% (Fig. 10c). Neither miscanthus nor switchgrass shows appreciable differences in discharge between the 0 and 100 kg N ha 1scenarios (Fig. 10a, c).

There are, however, large differences between the control and the replacement scenarios for mean DIN export at the outlet of the MARB. Differences in mean DIN export relative to control increase with higher replacement scenarios, with the MRX and MRS scenar-ios showing the largest reductions at ca. 20% and 16% for miscanthus and switchgrass, respectively (Fig. 10b, d). Mean DIN export was slightly higher for the 100 kg N ha 1 fertilizer scenarios relative to the

unfertilized simulations; however, the 95% confidence intervals overlap for the two scenarios for both miscant-hus and switchgrass (Fig. 10b, d, respectively). The sce-narios with rates above 100 kg N ha 1, however, have significantly more DIN export relative to control, with larger increases for switchgrass than miscanthus (data not shown).Only the MRS scenario shows no overlap in the 95% confidence interval between the control and switchgrass simulations (Fig. 10d) while both the 25% and MRX scenarios show no overlap in the 95% confi-dence interval for DIN export in the miscanthus scenar-ios (Fig. 10b).

Discussion

The goal of this study was to quantify the change in streamflow and DIN export for a range of basin-scale

Fig. 5 Simulated mean streamflow (a) and annual mean DIN

export (b) for the Mississippi–Atchafalaya River Basin for the

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Fig. 6 Simulated mean annual percent difference (scenario– control) in streamflow in the Mississippi–Atchafalaya River Basin for the miscanthus (a–d) and switchgrass (e–h) scenarios at 5% (a, e), 15% (b, f) and 25% (c, g) replacement as well as the MRX (d), and MRS (h) cellulosic for maize scenarios for the 33-year period spanning 1970–2002.

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Fig. 7 Simulated mean annual percent difference (scenario– control) in DIN export in the Mississippi–Atchafalaya River Basin for

the miscanthus (a–d) and switchgrass (e–h) scenarios at 5% (a, e), 15% (b, f) and 25% (c, g) replacement at 0 kg N ha 1as well as the

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Fig. 8 Simulated mean annual difference (scenario– control) in DIN leaching for miscanthus (a–e) and switchgrass (f–j) for fertilizer

application rates of 0 kg N ha-1(a, f), 50 kg N ha-1(b, g), 100 kg N ha-1(c, h), 150 kg N ha-1(d, i) and 200 kg N ha-1(e, j) at the 25%

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cellulosic feedstock production scenarios for the MARB, a region that is likely to undergo large-scale shifts in feedstock production to meet the goals of the RFS2 (EPA 2010). The results presented here support anticipa-tions 1 and 2 by showing that increasing the production of the cellulosic feedstocks miscanthus and switchgrass will reduce both the runoff of water and leaching of DIN, with proportional reductions in streamflow and the export of DIN in the MARB. The model indicated that the reduction in DIN leaching was much larger rel-ative to the reduction in runoff, supporting anticipation 3. The relative differences in runoff and DIN leaching varied between the simulated scenarios, with higher fer-tilizer application rates resulting in smaller reductions in DIN export (Fig. 10). On a percent basis, simulated changes in DIN leaching were similar across the domain for both miscanthus and switchgrass for the unfertilized scenario (Fig. 4). However, because the DIN leaching rates are larger in the more humid, eastern and south-ern areas (Fig. 2b), the change in the mass of leached DIN was greatest in these regions, supporting

anticipation 4. The MRX and MRS scenarios had the lowest mean DIN export of all the scenarios, and the change in mean discharge relative to control was slightly less than the 20 and 25% replacement scenarios (Fig. 10), which supports anticipation 5.

The baseline scenario simulation agreed well with observations (Fig. 1). The magnitude and spatial pat-terns of DIN leaching across the MARB in the control simulation were similar to modeling studies (Donner et al., 2002, 2004a), which were consistent with observa-tions in the basin (Goolsby et al., 2000). Our simulaobserva-tions show ca. 15 and 20% reductions in long-term mean DIN export and<2% reductions in total discharge, relative to control, for the MRS and MRX scenarios, respectively (Fig. 10). Similar to the findings presented here, Davis et al. (2012) showed that replacing land currently under maize production for ethanol in the Midwest United States with cellulosic feedstocks could reduce N leach-ing by ca. 20% while providleach-ing almost double the bio-mass for ethanol production without impacting food production. This corresponds to our MRX and MRS

Fig. 9 Simulated monthly mean total discharge (a, c) and DIN export (b, d) from the outlets of the Mississippi–Atchafalaya River

Basin over the 33-year period spanning 1970–2002 for the control as well as the miscanthus (a, b) and switchgrass (c, d) replacement scenarios.

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scenarios, which both assumed an even distribution of maize replacement. However, our results suggest replacing current crops in key areas could maximize the reductions in DIN export from the MARB, while mini-mizing impacts on streamflow. For example, relatively high DIN leaching coupled with low maize productivity in the portions of the domain with highest precipitation suggests that in these areas, transitioning to cellulosic production may have the greatest potential to improve water quality with minimal impacts on water quantity. While changes in total discharge were small relative to DIN export at the outlet of the MARB, there were areas in the western, drier portions of the basin where differ-ences in runoff and streamflow were notable, especially in the higher fraction replacement scenarios for miscant-hus (Figs 3 and 6). Our results show that switchgrass has similar water use to maize in these regions; there-fore, replacing maize with switchgrass rather than mis-canthus in these areas could minimize changes to streamflow (Fig. 6).

The simulations indicated no significant change in DIN export across the 0–100 kg N ha 1

fertilization

scenarios for miscanthus and switchgrass, but changes did occur at and above 150 kg N ha 1. The model simu-lations indicated that most of applied N is being taken up during the growing season and translocated to the rhizome during senescence or removed with biomass at harvest. These simulations agree with measurements made in Central Illinois, where miscanthus and switch-grass averaged peak N content values of ca. 340 and 170 kg N ha 1during the growing season and declined to ca. 200 and 60 kg N ha 1by December, respectively, in aboveground biomass (Dohleman et al., 2012). The decrease in aboveground N is largely accounted for by the process of remobilization or translocation to the roots and rhizomes where N is stored. The remaining N is lost through litter fall (Dohleman et al., 2012). The remaining aboveground N would be removed from the agro-ecosystems N cycle during harvest (Heaton et al., 2009; Dohleman et al., 2012) and would not be available for leaching and export by the riverine waters. How-ever, the relatively prolonged period of rigorous growth for perennials, especially miscanthus, compared to annual row crops such as maize and soybean, should

Fig. 10 Simulated annual mean and percent change relative to control with a 95% confidence interval for discharge (a, b) and DIN

export (b, d) at the outlet of the Mississippi–Atchafalaya River Basin over the 33-year period spanning 1970–2002 for the control, 0

and 100 kg N ha 1fertilizer scenarios for the miscanthus (a, b) and switchgrass (c, d) replacement scenarios. The dashed lines

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reduce losses of DIN that occur during times of drai-nage prior to and after annual crop growth when the soil is not frozen.

The simulations showing efficient uptake of N that results in low leaching rates are supported by numerous studies for miscanthus and switchgrass (Christian & Riche, 1998; McIsaac et al., 2010; Smith et al., 2013). How-ever, nutrient leaching in miscanthus and switchgrass is dependent on factors including soil type (Behnke et al., 2012), stand maturity (Christian et al., 1997) and success-ful establishment (Smith et al., 2013; Lesur-Dumoulin et al., 2016). In cases of poor establishment, leaching rates for miscanthus have been shown to be similar to nearby plots in the maize/soy rotation (Smith et al., 2013; Lesur et al., 2014). Variation of reported leaching rates under miscanthus and switchgrass has generally been small, which can be attributed to similar manage-ment and soil conditions for the research plots (e.g., McIsaac et al., 2010; Smith et al., 2013). However, one study has indicated significant increases in DIN leaching with increasing fertilizer application rate, which could be attributed to the sandy loam capped soils in that particular field site (Behnke et al., 2012).

This research is the first representation of altered land use to accommodate bioenergy feedstocks that explicitly simulates streamflow and DIN export for the entire MARB. We have focused on major hypothetical scenarios associated with the possibility of large-scale land use change related to percentage fraction of land use conversion (5–25%), nutrient applications rates (0–200 kg N ha 1), biofuel feedstock (miscanthus and

switchgrass) and type of current vegetation replaced (existing major croplands in relative proportions or just replacing maize). These scenarios, however, are very general and hypothetical and will need to be refined as the biofuel industry matures. Updates to these scenarios could change the results but are likely to fall within the range and patterns shown for the hypothetical scenarios. Given the long-term and large-scale focus of this study, factors that may increase the DIN leaching such as poor establishment and immaturity of the stand (e.g., Smith et al., 2013) were not considered. The timing of harvest and stand age may also have a significant effect on the N concentrations of biomass (Heaton et al., 2009) and the mass of N removed at harvest (Boersma et al., 2015). In this study, a constant harvest date for miscanthus and switchgrass was used; therefore, the influence of timing of harvest was not accounted for. There are also numer-ous socioeconomic, agronomic, logistical and policy fac-tors that will influence the selection and management of crops grown in a given area that are not directly consid-ered in the current study. Given the large range of vari-ous factors that determine the ultimate fate of maize grain from an area, we made the simplifying assumption

that the maize grain used for ethanol comes from an even distribution of land under maize production. Finally, the coupled model does not account for the potential for a feedback to occur between the biosphere and atmosphere whereby changes in surface hydrology associated with increased ET could affect local to regio-nal climate (Georgescu et al., 2011). Due to the nascent nature of the cellulosic industry, each of these factors was considered beyond the scope of this analysis.

Our results indicated a significant potential to reduce DIN export from the MARB under various production scenarios, at the scale required to meet RFS2, for cellu-losic feedstocks while having a relatively minor impact on total discharge. However, even the scenarios that simulate total replacement of current maize ethanol with miscanthus or switchgrass, DIN export was reduced to the EPA target levels every year. This sug-gests that targeted production of cellulosic feedstocks within particularly sensitive portions of the MARB is essential for maximizing the ecosystem services (Blesh & Drinkwater, 2013). Therefore, cellulosic feedstocks can be an important strategy for reducing the Gulf of Mexico ‘dead zone’ while potentially providing a range of additional ecosystem services.

Acknowledgements

We thank Simon Donner for his assistance in designing and executing this experiment. Steve Long, Steve Nesbitt, Nuria Gomez-Casanovas, Jesse Miller, Michael Castellano, Nic Boersma, Emily Heaton and Kelsie Ferin helped to improve this manuscript. This study was funded by the Energy Bio-sciences Institute, University of Illinois at Urbana-Champaign, the Illinois Water Resources Center and the USDA National Institute of Food and Agriculture.

References

Adler PR, Del Grosso SJ, Parton WJ (2007) Life-cycle assessment of net greenhouse-gas flux for bioenergy cropping systems. Ecological Applications, 17, 675–691. Alexander RB, Smith RA, Schwarz GE, Boyer EW, Nolan JV, Brakebill JW (2008)

Dif-ferences in phosphorus and nitrogen delivery to the Gulf of Mexico from the Mis-sissippi River Basin. Environmental Science & Technology, 42, 822–830.

Amougou N, Bertrand I, Cadoux S, Recous S (2012) Miscanthus9 giganteus leaf senescence, decomposition and C and N inputs to soil. Global Change Biology– Bioenergy, 4, 698–707.

Anderson-Teixeira KJ, Masters MD, Black CK, Zeri M, Hussain MZ, Bernacchi CJ, DeLucia EH (2013) Altered belowground carbon cycling following land-use change to perennial bioenergy crops. Ecosystems, 16, 508–520.

Aulenbach BT, Buxton HT, Battaglin WA, Coupe RH (2007) Streamflow and Nutri-ent Fluxes of the Mississippi-Atchafalaya River Basin and Subbasins for the Per-iod of Record Through 2005 (USGS Open-File Report 2007-1080).

Bagley JE, Davis SC, Georgescu M et al. (2014) The biophysical link between climate, water, and vegetation in bioenergy agro-ecosystems. Biomass and Bioenergy, 31, 187–201. Beale CV, Long SP (1997) Seasonal dynamics of nutrient accumulation and

partition-ing in the perennial C4-grasses Miscanthus9 giganteus and Spartina cynosuroides.

Biomass and Bioenergy, 12, 419–428.

Behnke GD, David MB, Voigt TB (2012) Greenhouse gas emissions, nitrate leaching, and biomass yields from production of Miscanthus9 giganteus in Illinois USA. Bioenergy Research, 5, 801–813.

(18)

Bernacchi CJ, VanLoocke A (2015) Terrestrial ecosystems in a changing environment: a dominant role for water. Annual Review of Plant Biology, 29, 599–622. Blesh J, Drinkwater LE (2013) The impact of nitrogen source and crop rotation on the

mass balances in the Mississippi River Basin. Ecological Applications, 23, 1017–1035. Boersma NN, Dohleman FG, Miguez FE, Heaton EA (2015) Autumnal leaf senes-cence in Miscanthus9 giganteus and leaf [N] differ by stand age. Journal of Experi-mental Botany, 66, 4395–4401.

Burkart MR, James DE (1999) Agricultural-nitrogen contributions to hypoxia in the Gulf of Mexico. Journal of Environmental Quality, 28, 850–859.

Cadoux S, Riche A, Yate NE, Machet JM (2012) Nutrient requirements of Miscanthus 9 giganteus: conclusions from a review of published studies. Biomass and Bioen-ergy, 13, 14–22.

Campbell GS, Norman JM (1998) An Introduction to Environmental Biophysics (2nd edn). Springer-Verlag, New York, NY.

Castellano MJ, Schmidt JP, Kaye JP, Walker C, Graham CB, Lin H, Dell CJ (2010) Hydrological and biogeochemical controls on the timing and magnitude of nitrous oxide flux across an agricultural landscape. Global Change Biology, 16, 2711–2720.

Castellano MJ, Lews DB, Kaye JP (2013) Response of soil nitrogen retention to the interactive effects of soil texture, hydrology and organic matter. Journal of Geo-physical Research Biogeosciences, 118, 280–290.

Christian DG, Riche AB (1998) Nitrate leaching loss under Miscanthus grass planted on a silty clay loam soil. Soil Use and Management, 14, 131–135.

Christian DG, Poulton PR, Riche AB, Yates NE (1997) The recovery of15N-labelled

fertilizer applied to Miscanthus9 giganteus. Biomass and Bioenergy, 12, 21–24. Coe MT (1998) A linked global model of terrestrial hydrologic processes: simulation

of modern rivers, lakes, and wetlands. Journal of Geophysical Research-Atmospheres, 103, 8885–8899.

Coe MT (2000) Modeling terrestrial hydrological systems at the continental scale: testing the accuracy of an atmospheric GCM. Journal of Climate, 13, 686–704. Coe MT, Latrubesse EM, Ferreira ME, Amsler ML (2011) The effects of deforestation

and climate variability on the streamflow of the Araguaia River, Brail. Biogeochem-istry, 105, 119–131.

Collatz GJ, Ball JT, Grivet C, Berry JA (1991) Physiological and environmental-regula-tion of stomatal conductance, photosynthesis and transpiraenvironmental-regula-tion– a model that includes a laminar boundary-layer. Agricultural and Forest Meteorology, 54, 107–136. Costa MH, Botta A, Cardille JA (2003) Effects of large-scale changes in land cover on the discharge of the Tocantins River, Southeastern Amazonia. Journal of Hydrol-ogy, 283, 206–217.

Costello C, Griffin WM, Landis EL, Matthews HS (2009) Impact of biofuel crop pro-duction on the formation of hypoxia in the Gulf of Mexico. Environmental Science & Technology, 43, 7985–7991.

David MB, Drinkwater LE, McIsaac GF (2010) Sources of nitrate yields in the Missis-sippi River basin. Journal of Environmental Quality, 39, 657–1667.

Davis SC, Parton WJ, Dohleman FG, Smith CM, Del Grosso SD, Kent AD, DeLucia EH (2010) Comparative biogeochemical cycles of bioenergy crops reveal nitrogen-fixation and low greenhouse gas emissions in a Miscanthus9 giganteus agro-eco-system. Ecosystems, 13, 144–156.

Davis SC, Parton WJ, Del Grosso JS, Keough C, Marx E, Adler PR, DeLucia EH (2012) Impact of second-generation biofuel agriculture on greenhouse-gas emis-sions in the corn-growing regions of the US. Frontiers in Ecology and the Environ-ment, 10, 69–74.

Deb D, Tuppad P, Daggupati P, Srinivasan R, Varma D (2015) Spatio-temporal impacts of biofuel production and climate variability on water quantity and qual-ity in Upper Mississippi River Basin. Water, 7, 3283–3305.

Delire C, Foley JA (1999) Evaluating the performance of a land surface/ecosystem model with biophysical measurements from contrasting environments. Journal of Geophysical Research, 104, 16895–16909.

Dohleman FG, Heaton EA, Arundale RA, Long SP (2012) Seasonal dynamcis of above- and below-ground biomass and nitrogen partitioning in Miscanthus9 giganteus and Panicum virgatum across three growing seasons. Global Change Biol-ogy– Bioenergy, 4, 534–544.

Donner SD, Kucharik CJ (2003) Evaluating the impacts of land management and cli-mate variability on crop production and nitrate export across the Upper Missis-sippi Basin. Global Biogeochemical Cycles, 17, 1–10.

Donner SD, Kucharik CJ (2008) Corn-based ethanol production compromises goal of reducing nitrogen export by the Mississippi River. Proceedings of the National Academy of Sciences of the United States of America, 102, 4513–5418.

Donner SD, Scavia D (2007) How climate controls the flux of nitrogen by the Missis-sippi River and the development of hypoxia in the Gulf of Mexico. Limnology and Oceanography, 52, 856–861.

Donner SD, Coe MT, Lenters JD, Twine TE, Foley JA (2002) Modeling the impact of hydrological changes on nitrate transport in the Mississippi River Basin from 1955–1994. Global Biogeochemical Cycles, 16, 1–19.

Donner SD, Kucharik CJ, Foley JA (2004a) Impact of changing land use practices on nitrate export by the Mississippi River. Global Biogeochemical Cycles, 18, GB1028. Donner SD, Kucharik CJ, Oppenheimer M (2004b) The influence of climate on

in-stream removal of nitrogen. Geophysical Research Letters, 31, L20509.

EPA (2010) Renewable Fuel Standard Program (RFS2) Regulatory Impact Analysis. US Environmental Protection Agency, Washington, DC.

Farquhar GD, Caemmerer SV, Berry JA (1980) A biochemical model of photosyn-thetic CO2assimilation in leaves of C-3 species. Planta, 149, 78–90.

Foley JA, Prentice IC, Ramankutty N, Levis S, Pollard D, Sitch S, Haxeltine A (1996) An integrated biosphere model of land surface processes, terrestrial carbon bal-ance, and vegetation dynamics. Global Biogeochemical Cycles, 10, 603–628. Georgescu M, Lobell DB, Field CB (2011) Direct climate effects of perennial

bioen-ergy crops in the United States. Proceedings of the National Academy of Sciences of the United States of America, 108, 4307–4312.

Goolsby DA, Battaglin WA, Aulenbach BT, Hooper RP (2000) Nitrogen flux and sources in the Mississippi River Basin. The Science of the Total Environment, 248, 75–86. Goolsby DA, Battaglin WA, Aulenbach BT, Hooper RP (2001) Nitrogen input to the

Gulf of Mexico. Journal of Environmental Quality, 30, 329–336.

Heaton E, Voigt T, Long SP (2004) A quantitative review comparing the yields of two candidate C-4 perennial biomass crops in relation to nitrogen, temperature and water. Biomass and Bioenergy, 27, 21–30.

Heaton EA, Dohleman FG, Long SP (2008) Meeting US biofuel goals with less land: the potential of miscanthus. Global Change Biology, 14, 2000–2014.

Heaton EA, Dohleman FG, Long SP (2009) Seasonal nitrogen dynamics of Miscant-hus x giganteus and Panicum virgatum. Global Change Biology– Bioenerergy, 1, 297–307.

Heaton EA, Dohleman FG, Miguez FE et al. (2010) Miscanthus: a promising biomass crop. Advances in Botanical Research, 56, 75–137.

Hickman GC, VanLoocke A, Dohleman FG, Bernacchi CJ (2010) A comparison of canopy evapotranspiration for maize and two perennial grasses identified as potential bioenergy crops. Global Change Biology– Bioenergy, 2, 157–168. Himken M, Lammel J, Neukirchen D, Czypionka-Krause U, Olfs HW (1997)

Cultivation of Miscanthus under West European conditions: seasonal changes in dry matter production, nutrient uptake and remobilization. Plant and Soil, 189, 117–126.

Housh M, Yaeger MA, Cai X (2015) Managing multiple mandates: a system of sys-tems model to analyze strategies for producing cellulosic ethanol and reducing riverine nitrate loads in the upper Mississippi River Basin. Environmental Science & Technology, 49, 11932–11940.

Hudiburg TW, Wang W, Khanna M (2016) Impacts of a 32-billion-gallon bioenergy landscape on land and fossil fuel use in the US. Nature Energy, 1, 1–7. IPCC (2007) Climate change 2007: synthesis report. In: Contribution of Working Groups

I, II and II to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change (eds Core Writing Team, Pachauri PK, Reisinger A), p. 104. IPCC, Geneva, Switzerland.

Iqbal J, Parkin TB, Helmers HJ, Zhou X, Castellano MJ (2015) Denitrification and nitrous oxide emissions in annual croplands, perennial grass buffers and restored perennial grasslands. Soil Science Society of America Journal, 79, 239–250. Kalnay E, Kanamitsu M, Kistler R et al. (1996) The NCEP/NCAR 40-year reanalysis

project. Bulletin of the American Meteorological Society, 77, 437–471.

Kistler R, Kalnay E, Collins W et al. (2001) The NCEP-NCAR 50-year reanalysis: monthly means CD-ROM and documentation. Bulletin of the American Meteorologi-cal Society, 82, 247–268.

Kucharik CJ (2003) Evaluation of a process-based Agro-Ecosystem Model (Agro-IBIS) across the US Corn Belt: simulations of the interannual variability in maize yield. Earth Interactions, 7, 1–33.

Kucharik CJ, Brye KR (2003) Integrated biosphere simulator (IBIS) yield and nitrate loss predictions for Wisconsin maize receiving varied amounts of nitrogen fertil-izer. Journal of Enviromental Quality, 32, 247–268.

Kucharik CJ, Twine TE (2007) Residue, respiration, and residuals: evaluation of a dynamic agroecosystem model using eddy flux measurements and biometric data. Agricultural and Forest Meteorology, 146, 134–158.

Kucharik CJ, Foley JA, Delire C et al. (2000) Testing the performance of a dynamic global ecosystem model: water balance, carbon balance, and vegetation structure. Global Biogeochemical Cycles, 14, 795–825.

Lenters JD, Coe MT, Foley JA (2000) Surface water balance of the continental United States, 1963-1995: regional evaluation of a terrestrial biosphere model and the NCEP/NCAR reanalysis. Journal of Geophysical Research, 10, 22393–22425.

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Lesur C, Bazot M, Bio-Beri F, Mary B, Jeuffroy MH, Loyce C (2014) Assessing nitrate leaching during the three-first years of Miscanthus9 giganteus from on-farm measurements and modeling. Global Change Biology– Bioenergy, 6, 439–49. Lesur-Dumoulin C, Lorin M, Bazot M, Jeuffroy MH, Loyce C (2016) Analysis of

young Miscanthus9 giganteus yield variability: a survey of farmers’ fields in east central France. Global Change Biology– Bioenergy, 8, 122–135.

Loveland TR, Belward AS (1997) The IGBP-DIS global 1 km land cover data set, DIS-cover: first results. International Journal of Remote Sensing, 18, 3291–3295. McIsaac GF, David MB, Gertner GZ, Goolsby DA (2001) Eutrophication: nitrate flux

in the Mississippi River. Nature, 414, 166–167.

McIsaac GF, David MB, Mitchell CA (2010) Miscanthus and switchgrass production in central Illinois: impacts on hydrology and inorganic nitrogen leaching. Journal of Environmental Quality, 39, 1790–1799.

Miguez FE, Villamil BM, Long SP, Bollero GA (2008) Meta-analysis of the effects of management factors on Miscanthus9 giganteus growth and biomass production. Agricultural and Forest Meteorology, 148, 1280–1292.

Miller DA, White RA (1998) A conterminous United States multilayer soil characteris-tics dataset for regional climate and hydrology modeling. Earth Interactions, 2, 1–26. Mississippi River/Gulf of Mexico Watershed Nutrient Task Force (2008) Gulf of Hypoxia Action Plan 2008. U.S. Environmental Protection Agency, Washington, DC. Available at: http://www.epa.gov/ms-htf/gulf-hypoxia-action-plan-2008. (accessed 21 March 2016).

Mississippi River/Gulf of Mexico Watershed Nutrient Task Force (2015) Hypoxia Task Force 2015 Report to Congress. U.S. Environmental Protection Agency, Wash-ington, DC. Available at: http://www.epa.gov/ms-htf/htf-2015-report-congress. (accessed 21 March 2016).

Mitchell TD, Jones PD (2005) An improved method of constructing a database of monthly climate observations and associated high-resolution grids. International Journal of Climatology, 25, 693–712.

New M, Hulme M, Jones P (1999) Representing twentieth century space-time climate variability. Part I: development of a 1961-90 mean monthly terrestrial climatology. Journal of Climate, 12, 829–856.

Ng LT, Eheart WJ, Cai X, Miguez F (2010) Modeling miscanthus in the soil and water assessment tool (SWAT) to simulate its water quality effects as a bioenergy crop. Environmental Science & Technology, 44, 7138–7144.

Rabalais NN, Turner RE, Justic D, Dortch Q, Wiseman W Jr, Sen Gupta BK (1996) Nutrient changes in the Mississippi River and system responses on the adjacent continental shelf. Estuaries, 19, 366–407.

Ramankutty N, Foley JA (1998) Characterizing patterns of global land use: an analy-sis of global croplands data. Global Biogeochemical Cycles, 12, 667–685.

Ramankutty N, Evan AT, Monfeda C, Foley JA (2008) Geographic distribution of global agricultural lands in the year 2000. Global Biogeochemical Cycles, 22, GB1003. Rowe RL, Street NR, Taylor G (2009) Identifying potential environmental impacts of large scale deployment of dedicated bioenergy crops in the UK. Renewable Sus-tainable Energy Reviews, 13, 260–279.

Royer TV, David MB, Gentry LE (2006) Timing of riverine export of nitrate and phosphorus from agricultural watersheds in Illinois: implications for reducing nutrient loading to the Mississippi River. Environmental Science & Technology, 40, 4126–4131.

Sacks WJ, Kucharik CJ (2011) Crop management and phenology trends in the US Corn Belt: impacts on yields, evapotranspiration and energy balance. Agricultural and Forest Meteorology, 151, 882–894.

Scavia D, Donnelly KA (2007) Reassessing hypoxia forecasts for the Gulf of Mexico. Environmental Science & Technology, 41, 8111–8117.

Schmer MR, Vogel KP, Mitchel RB, Perrin KR (2008) Net energy of cellulosic ethanol from switchgrass. Proceedings of the National Academy of Sciences of the United States of America, 105, 464–469.

Secchi S, Gassman PW, Jha M, Kurkalova L, Kling CL (2011) Potential water quality changes due to corn expansion in the Upper Mississippi River Basin. Ecological Applications, 21, 1068–1084.

Smith CM, David MB, Mitchell CA, Masters MD, Anderson-Teixeira KJ, Bernacchi CJ, DeLucia EH (2013) Reduced nitrogen losses following conversion of row crop agriculture to perennial biofuel crops. Journal of Environmental Quality, 42, 219–228. Somerville C, Youngs H, Taylor C, Davis SC, Long SP (2010) Feedstocks for

lignocel-lulosic biofuels. Science, 329, 790–792.

Thompson SL, Pollard D (1995a) A global climate model (Genesis) with a Land-Sur-face Transfer Scheme (Lsx).1. Present climate simulation. Journal of Climate, 8, 732–761.

Thompson SL, Pollard D (1995b) A global climate model (Genesis) with a Land-Sur-face Transfer Scheme (Lsx) 2. CO2sensitivity. Journal of Climate, 8, 1104–1121.

Turner RE, Rabalais NN, Justic D (2012) Predicting summer hypoxia in the northern Gulf of Mexico: redux. Marine Pollution Bulletin, 64, 319–324.

Twine TE, Kucharik CJ (2008) Evaluating a terrestrial ecosystem model with satellite information of greenness. Journal of Geophysical Research: Biogeosciences, 113, G03027. Twine TE, Kucharik CJ (2009) Climate impacts on net primary productivity trends

in natural and managed ecosystems of the central and eastern United States. Agri-cultural and Forest Meteorology, 149, 2143–2161.

Twine TE, Kucharik CJ, Foley JA (2004) Effects of land cover change on the energy and water balance of the Mississippi River basin. Journal of Hydrometeorology, 5, 640–655. Twine TE, Bryant JJ, Richter KT, Bernacchi CJ, McConnaughay KD, Morris SJ, Lea-key AD (2013) Impacts of elevated CO2concentration on the productivity and

surface energy budget of the soybean and maize agroecosystem in the Midwest USA. Global Change Biology, 19, 2838–2852.

VanLoocke A, Bernacchi CJ, Twine TE (2010) The impacts of Miscanthus x giganteus production on the Midwest US hydrologic cycle. Global Change Biology– Bioen-ergy, 2, 180–191.

VanLoocke A, Twine TE, Zeri M, Bernacchi CJ (2012) A regional comparison of water-use-efficiency for miscanthus, switchgrass and maize. Agricultural and For-est Meteorology, 164, 82–95.

Varvel GE, Vogel KP, Mitchell RB, Follett RF, Kimble JM (2008) Comparison of corn and switchgrass on marginal soils for bioenergy. Biomass and Bioenergy, 32, 18–21. Wallander S, Claassen R, Nickerson C (2011) The Ethanol Decade: An Expansion of U.S. Corn Production, 2000-09, EIB-79, U.S. Department of Agriculture, Economic Research Service.

Wilson DM, Dalluge DL, Rover M, Heaton EA, Brown RC (2013) Crop management impacts on biofuel quality: influence of switchgrass harvest time on yield, nitro-gen and ash of fast pyrolysis products. BioEnergy Research, 6, 103–113. Wu Y, Liu S, Li Z (2012) Identifying potential areas for biofuel production and

eval-uating the environmental effects: a case study of the James River Basin in the Midwestern United States. Global Change Biology– Bioenergy, 4, 875–888. Zeri M, Anderson-Teixeira KJ, Hickman GC, Masters M, DeLucia EH, Bernacchi CJ

(2011) Carbon exchange by establishing biofuel crops in Central Illinois. Agricul-ture Ecosystem and Environment, 144, 319–329.

Zeri M, Hussain ZM, Anderson-Teixeira KJ, DeLucia E, Bernacchi CJ (2013) Water use efficiency of perennial and annual bioenergy crops in central Illinois. Journal of Geophysical Research: Biogeosciences, 118, 581–589.

Zhang YK, Schilling KE (2006) Increasing streamflow and baseflow in the Missis-sippi River since the 1940s: effect of land use change. Journal of Hydrology, 324, 412–422.

Supporting Information

Additional Supporting Information may be found online in the supporting information tab for this article:

Fig. S1.Schematic representing the semicoupled Integrated

Biosphere Simulator– agricultural version (Agro-IBIS) and

Terrestrial Hydrology Model with Biogeochemistry

(THMB) process representation and workflow structure. Schematic presented here with permission from Simon Donner.

Fig. S2.Simulated mean nitrogen (N) mass in shoots (white

symbols), roots and rhizomes (gray symbols) and the total plant (black symbols) for miscanthus (a) and switchgrass (b) for the grid cell representing the site used to calibrate the translocation algorithm based on data primarily from Dohleman et al. (2012).

Fig. S3.Fraction of each 5 min9 5 min THMB grid cell in

cellulosic feedstock production throughout the Mississippi–

Atchafalaya River Basin (thick black outline) for the 25% replacement of croplands (fraction coverage scenario 5; Table 1) (a) and 40% replacement of land currently under maize production (MRX and MRS scenarios) (b).

References

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