Plant diversity and grassland productivity

Meta-analyses have pointed to a positive relationship between plant species diversity (most often expressed as species richness) and phytomass productionReference Cardinale, Wright, Cadotte, Carroll, Hector, Srivastava, Loreau and Weis¹³ or have shown no clear relationshipReference Adler, Seabloom, Borer, Hillebrand, Hautier, Hector, Harpole, O'Halloran, Grace, Anderson, Bakker, Biederman, Brown, Buckley, Calabrese, Chu, Cleland, Collins, Cottingham, Crawley, Damschen, Davies, DeCrappeo, Fay, Firn, Frater, Gasarch, Gruner, Hagenah, Lambers, Humphries, Jin, Kay, Kirkman, Klein, Knops, La Pierre, Lambrinos, Li, MacDougall, McCulley, Melbourne, Mitchell, Moore, Morgan, Mortensen, Orrock, Prober, Pyke, Risch, Schutz, Smith, Stevens, Sullivan, Wang, Wragg, Wright and Yang¹⁴. A positive diversity–productivity relationship would have obvious practical application in managed grasslands. In that regard, agricultural scientists have begun to explore the relationship in an agronomic contextReference Wiegelt, Weisser, Buchmann and Scherer-Lorenzen¹⁵.

Greater herbage production from diverse mixtures of forage species compared with monocultures or bicultures (grass–legume) has been demonstrated in multiple experiments at different scales in the USReference Tracy and Sanderson^16–Reference Picasso, Brummer, Liebman, Dixon and Wilsey¹⁹ and EuropeReference Bullock, Pywell and Walker^20–Reference Nyfeler, Huguenin-Elie, Suter, Frossard and Lüscher²². Economic analyses have also pointed to greater economic returns and reduced production risk compared with grass monocultures or grass–legume biculturesReference Sanderson, Corson, Rotz and Soder^23, Reference Deak, Hall, Sanderson, Corson and Rotz²⁴. In several instances, the productivity benefit of complex mixtures stemmed from the inclusion of key species (e.g., highly productive or drought tolerant species), which supports the concept that functional traits rather than number of species govern outputs of ecosystem servicesReference Mouillot, Villéger, Scherer-Lorenzen and Mason²⁵. The latter point emphasizes the need for more information on functional traits of forages to formulate rational combinations of plants to achieve specific functions in managed grasslandsReference Comas, Goslee, Skinner and Sanderson²⁶.

In pasture-based livestock production systems, greater herbage production and nutritive value are not realized unless the grazing animal efficiently consumes and utilizes the herbage. Grazing trials with livestock have demonstrated variable results for beef cattle gain on forage mixtures versus monoculturesReference Tracy and Faulkner²⁷ and no differences in milk production or herbage intake of dairy cowsReference Soder, Sanderson, Stack and Muller²⁸. Very few grazing trials have been conducted to determine the livestock productivity response to plant diversity in pastures. Greater plant diversity may provide other benefits to grazing livestock including detoxification servicesReference Villalba, Provenza, Clemensen, Larsen and Juhnke²⁹ and enhanced mineral nutritionReference Pirhofer-Walzl, Søegaard, Høgh-Jensen, Eriksen, Sanderson, Rasmussen and Rasmussen³⁰.

Plant diversity and soil carbon

Managed grasslands generally have greater soil C levels than annual cropland (Fig. 2). For example, managed grasslands in Kansas had 43 Mg ha⁻¹ greater soil C in the surface 1 m than annual croplandReference Glover, Culman, Tianna DuPont, Broussard, Young, Mangan, Mai, Crews, DeHaan, Buckley, Ferris, Turner, Reynolds and Wyse³². There are few, if any, studies on plant diversity effects on C sequestration in forage and pastureland. Research on restored native grasslands at the Cedar Creek, MN site indicated greater soil C storage with greater plant diversityReference DeDyn, Shiel, Ostle, McNamara, Oakley, Young, Freeman, Fenner, Quirk and Bardgett³³. Grassland restoration practices increased soil C mainly because of the inclusion of the temperate legume red clover (Trifolium pratense L.) and not due to increased plant species richness generated by fertilizer reduction or seed additionReference DeDyn, Shiel, Ostle, McNamara, Oakley, Young, Freeman, Fenner, Quirk and Bardgett³³. Inclusion of red clover may have enhanced nutrient cycling through food webs and improved soil structure leading to increased soil CReference van Eekeren, van Liere, de Vries, Rutgers, de Goode and Brussard³⁴. Similarly, adding alfalfa (Medicago sativa L.) to annual cropping sequences for small grains increased soil C through greater belowground C input and soil biological activityReference Sainju and Lenssen³⁵. Thus, the inclusion of species with key functional traits (e.g., N₂ fixation through a legume) in managed grasslands may be more important than greater richness or diversity. Carbon sequestration in grasslands depends on maintaining C accumulation rates, avoidance of C loss via disturbance and restoring functionality of degraded grasslandReference Havstad, Peters, Skaggs, Brown, Bestelmeyer, Fredrickson, Herrick and Wright³⁶.

Figure 2.

Soil organic matter levels (to a 10-cm depth) in four cropping systems implemented for 36 years in the Netherlands. Permanent grass was perennial ryegrass–white clover mixture. Temporary grassland alternated between 3 years of grass for grazing with 3 years of cropped forage for mechanical harvest. The temporary arable system alternated between 3 years of grass with 3 years of maize. The permanent arable system was in maize. Adapted from van Eekeren et al.Reference van Eekeren, Bommele, Bloem, Schouten, Rutgers, de Goode, Rehaul and Brussard³¹

Invasion resistance

Invasion resistance of managed grasslands could be improved by formulating unique functional combinations of forage speciesReference Drewnovsky and James³⁷. Research conducted at several scales in a variety of managed grasslands has indicated that species-rich forage mixtures can reduce weed invasionReference Sanderson, Soder, Muller, Klement, Skinner and Goslee^17–Reference Picasso, Brummer, Liebman, Dixon and Wilsey^19, Reference Kirwan, Luscher, Sebastia, Finn, Collins, Porqueddu, Helgadottir, Baadshaug, Brophy, Coran, Dalmannsdottir, Delgado, Elgersma, Fothergill, Frankow-Lindberg, Golinski, Grieu, Gustavsson, Hoglind, Huguenin-Elie, Iliadis, Jorgensen, Kadziuliene, Karyotis, Lunnan, Malengier, Maltoni, Meyer, Nyfeler, Nykenen-Kurki, Parente, Smit, Thumm and Connolly^21, Reference Dodd, Barker and Wedderburn^38–Reference Frankow-Linberg, Brophy, Collins and Connolly⁴⁰. Combining forage species into functional mixtures has been successful in reducing the establishment of invasive plants in rangelandsReference Sheley and Carpinelli⁴¹. Mixed-species pastures may be more resistant to invasion by weeds because of (i) more competition created by greater use of resources or (ii) the inclusion of a few dominant productive species that preclude invasionReference Kennedy, Naeem, Howe, Knops, Tilman and Reich⁴².

Weed abundance was inversely related to the evenness (evenness is a measure of the relative distribution or proportion of plant species in a community) of forage species in clipped plots and on-farm surveys of plant species diversity in pasturesReference Tracy and Sanderson^16, Reference Tracy and Sanderson⁴³. In research designed to control for species evenness, however, there was no evidence that evenness of grass–legume mixtures affected weed invasionReference Sanderson, Brink and Stout⁴⁴. Species composition of the mixtures, however, had a strong effect on invasion, indicating that selecting the appropriate species in mixtures to achieve a specific function is more important than evenness of the species in the mixture.

Management tools needed for diverse mixtures

Few, if any studies, have addressed management issues associated with the use of complex mixtures of forages or other crop plants. Tools are needed to aid the selection of specific mixtures for managed grasslands and to guide the spatial distribution or arrangement of species and mixtures across the various site-types on a farm to achieve specific functions. This includes defining the functional traits of plants so that a rational functional diversity approach can be followed, designing agricultural plant communities to achieve specific functions or combinations of functions rather than simply ‘piling on’ species to achieve diversity in numbers onlyReference Cadotte, Carscadden and Mirotchnick⁴⁵. Management of highly diverse grasslands to deliver multiple ecosystem services (e.g., soil C storage, biodiversity conservation and enhanced nutrient cycling) in addition to herbage production will likely require trade-off among services and well-designed economic incentives for farmer adoptionReference Klimek, Richter gen., Steinmann, Freese and Isselstein⁴⁶.

Crop selection and sequencing

Crop selection and sequencing can serve as a critical component in conservation of agricultural systems. Among the many options available to select and sequence crops, a fixed-sequence system, whereby crops are sequenced in a consistent, unchanging pattern, is the most simple. Fixed-sequence systems, however, can contribute to the development of pest and disease infestationsReference Krupinsky, Bailey, McMullen, Gossen and Turkington^51, Reference Anderson⁵², be less responsive to external stressors (e.g., weather)Reference Farahani, Peterson and Westfall⁵³ and may limit opportunities to take advantage of market conditions and/or government programsReference Karlen, Varvel, Bullock and Cruse⁴⁷. Accordingly, fixed sequences can suffer from significant drawbacks that limit their sustainability over the long term, particularly in the context of challenges associated with anticipated climate change⁵⁴.

To increase cropping system responsiveness to externalities, opportunity/flex crop sequences have been developed to allow for adjustments in cropping intensity and/or diversity using critical information at planting, such as soil water statusReference Farahani, Peterson and Westfall^53, Reference Peterson, Westfall, Peairs, Sherrod, Poss, Gangloff, Larson, Thompson, Ahuja, Koch and Walker⁵⁵. Even greater flexibility in annual crop sequencing may be realized through the application of a dynamic cropping system concept, where crop sequence decisions are made annually to optimize production, economic and resource conservation goalsReference Tanaka, Krupinsky, Liebig, Merrill, Ries, Hendrickson, Johnson and Hanson⁵⁶. Dynamic cropping systems are location specific, with unique crop portfolios (i.e., adapted crop species) within an ecoregion, and require a thorough understanding of short-term (one to three years) crop sequencing effects on relevant agronomic and environmental response variablesReference Krupinsky, Tanaka, Merrill, Liebig and Hanson⁵⁷. Successful application of the dynamic cropping system concept can increase adaptability to high-risk conditions, and may therefore be more economically and environmentally sustainable than other crop selection and sequencing approaches.

The application of dynamic cropping systems has increased crop yield and decreased yield variability in the northern Great PlainsReference Tanaka, Krupinsky, Merrill, Liebig and Hanson⁵⁸. Strategic inclusion of dry pea (Pisum sativum L.) in a dynamic cropping system increased subsequent spring wheat (Triticum aestivum L.) grain yield by 30% compared with monoculture spring wheat because of improvements in precipitation-use efficiencyReference Tanaka, Liebig, Krupinsky and Merrill⁵⁰. Analysis of long-term data revealed that spring wheat grain yield varied least in a dynamic cropping system compared with other less diverse crop-sequencing approachesReference Tanaka, Liebig, Krupinsky and Merrill⁵⁰ (Fig. 3). Moreover, grain yield in the dynamic system was 17–20% greater than 3- and 5-year rotations containing spring wheat (Fig. 3). Such outcomes suggest an inherent resilience of dynamic cropping systems to achieve greater production consistently within a variable environment.

Figure 3.

Minimum, maximum and mean spring wheat yield within five cropping systems differing in diversity near Mandan, North Dakota. C-F, Spring wheat–fallow; Continuous, continuous spring wheat; 3-yr system, three-year crop rotation; 5-yr system, five-year crop rotation; Dynamic, dynamic cropping system.

Cover crops

Use of cover crops in annual cropping systems is consistent with the principles of conservation agriculture from the standpoint of maximizing soil cover, stimulating biological activity and increasing diversity. Although cover crops are often categorized by type (e.g., grasses, legumes and brassicasReference Clark⁵⁹), their use in addressing specific agronomic and/or natural resource issues underscores the value of functional categorization, such as increasing surface cover, assimilating plant nutrients, improving soil–water relations, and decreasing pests and diseasesReference Thorup-Kristensen^60, Reference Snapp, Swinton, Labarta, Mutch, Black, Leep, Nyiraneza and O'Neil⁶¹. In this regard, numerous reviews have documented the functional value of cover crops to improve ecosystem services, environmental quality and farm profitability across a wide range of growing conditionsReference Clark^59, Reference Russelle, Hargrove and Follett^62–Reference Dabney, Delgado, Meisinger, Schomberg, Liebig, Kasper, Mitchell, Reeves, Delgado and Follett⁶⁵. Among these outcomes, cover crops can reduce soil erosion by protecting soil from raindrop impact, improving soil structure and increasing infiltrationReference Langdale, Blevins, Karlen, McCool, Nearing, Skidmore, Thomas, Tyler, Williams and Hargrove^66, Reference Kaspar, Radke and Laflen⁶⁷. Cover crops can enhance soil biological abundance and activityReference Six, Frey, Thiet and Batten⁶⁸, thereby contributing to increased N mineralization rates and N supplying potential of soilReference Grant, Peterson and Campbell^69, Reference Wienhold and Halvorson⁷⁰.

Emerging use of cover crop cocktails (i.e., complex mixtures of functionally diverse cover crops planted concurrently) offers the potential to exploit previously untapped spatial and temporal niches in diverse cropping systems to improve ecosystem services. Unfortunately, generalizations regarding their effectiveness are currently limited by a lack of published findings.

Bioenergy cropping systems

Before the 20th century, significant pasture and hayland areas were required for grazing animals to maintain draft power for rural farms and urban transportationReference McShane, Tarr and Mohl⁷¹. The transition from draft power to the internal combustion engine in US agriculture contributed to the decline in land dedicated to perennial systems, increased reliance on fossil fuels to produce food and led to single enterprise systems (Fig. 1). Concerns about energy security and increased greenhouse gas emissions from fossil fuels have boosted efforts to develop sustainable energy and transportation fuels from biomass. A greater reliance on biofuels may improve or worsen the long-term sustainability of arable cropland, biodiversity and human health, depending on the feedstock source and management practices implemented.

Maize (Zea mays L.) grain ethanol is currently the dominant biofuel feedstock in the US and had contributed to annual crop expansion into existing grasslands to meet the demands for food, feed and biofuelsReference Fargione, Cooper, Flaspohler, Hill, Lehman, Tilman, McCoy, McLeod, Nelson and Oberhauser⁷². Large-scale conversion of grasslands to maize production can have potentially large effects on biodiversity, water quality, wildlife habitat and other ecosystem services (Fig. 4). Agricultural residues, such as maize stover, are expected to provide substantial amounts of biomass for conversion into biofuels, but excessive maize stover removal can lead to increased soil erosion and decreased soil organic CReference Blanco-Canqui and Lal⁷³. Further, grazing of maize stover after harvest is a simple and economical way of integrating crop–livestock systemsReference Klopfenstein, Roth, Rivera and Lewis⁷⁸.

Figure 4.

(a) Star diagram showing degree of ecosystem services associated with maize grain ethanol system. The length of each spoke shows the relative magnitude of each ecosystem service provided by the system relative to the highest provision of that service across all systems. (b) Star diagram showing degree of ecosystem services associated with switchgrass bioenergy system. (c) Star diagram showing degree of ecosystem services associated with low-input high-diversity bioenergy system. Source of information based on interpretation of information in selected referencesReference Fargione, Cooper, Flaspohler, Hill, Lehman, Tilman, McCoy, McLeod, Nelson and Oberhauser^72–Reference Anand, Archer, Bergtold, Canales, Braun, Karlen and Johnson⁷⁷.

If crop residues become a significant source of biomass feedstock, there will be a critical need for timely and accurate data on residue cover to ensure sustainability; however, no government program exists to objectively monitor residue cover across large areasReference Nowak^79–Reference Aguilar, Evans and Daughtry⁸¹. The Conservation Technology Information Center (CTIC) holds the most extensive and up-to-date information on residue cover of the US Midwest, but these data are based on ‘windshield observation’ estimates⁸². Coupled with a strong scientific foundation and proven algorithms, remotely sensed data offer objective and fast measurement of crop residue cover over large areas. Moreover, accessibility to some satellite images is becoming easier as key government agencies offer these data to the public at no cost⁸³.

Herbaceous perennial bioenergy crop systems are perceived to be more sustainable and provide more ecosystem services than maize grain ethanol or agricultural residuesReference Jordan, Boody, Broussard, Glover, Keeney, McCown, McIsaac, Mueller, Murray, Neal, Pansing, Turner, Warner and Wyse⁷⁴ (Fig. 4). Environmental, societal and economic trade-offs need to be considered when transitioning back to the use of perennial feedstocks to meet rural and urban energy demands. Perennial energy crop systems will probably be planted on marginal cropland or conservation grasslandsReference Walsh, De la Torre Ugarte, Shapouri and Slinsky⁸⁴. Converting annual cropland production to perennial systems will probably reduce soil erosion, increase soil C sequestration, reduce farm-level fossil fuel requirements and increase wildlife habitatReference Farrell, Plevin, Turner, Jones, O'Hare and Kammen^75, Reference McLaughlin, De la Torre Ugarte, Garten, Lynd, Sanderson, Tolbert and Wolf⁷⁶. However, converting idle, pasture, or conservation land to perennial energy crops may lead to wildlife habitat loss, a decline in plant community diversity and a shift in livestock production from pastures to confinement feeding depending on the region, feedstock used and management practices implemented. Perennial bioenergy cropping systems could also be used as a dual-purpose crop, in which a grazing or forage harvest is implemented in addition to a bioenergy harvestReference Guretzky, Biermacher, Cook, Kering and Mosali⁸⁵. Rotational systems may be developed in specific climates to incorporate grazing livestock and bioenergy harvests. Integrating a livestock component within herbaceous bioenergy cropping systems further adds management complexity but may offer reduced enterprise risk.

Use of low-input high diversity prairie mixtures (up to 16 species) has been proposed as a sustainable way to produce bioenergy on degraded landsReference Tilman, Hill and Lehman⁸⁶ (Fig. 4). Some research demonstrated greater biomass yields with greater numbers of perennial species in mixturesReference DeHaan, Weisberg, Tilman and Fornara⁸⁷. In other research, however, two-species grass–legume mixtures or N-fertilized switchgrass monocultures produced similar or greater biomass yields than low-input high-diversity mixturesReference Schmer, Vogel, Mitchell and Perrin^88, Reference Mangan, Sheaffer, Wyse, Ehlke and Reich⁸⁹. Monocultures of warm-season grasses produced more biomass less expensively than polyculturesReference Griffith, Epplin, Fuhlendorf and Gillen⁹⁰. Observational research on conservation grasslands in the northeastern USA indicated a negative relationship between plant species diversity on biomass production and biochemical composition conversionReference Adler, Sanderson, Weimer and Vogel⁹¹. An environmental trade-off exists between maximizing diversity within plant communities grown for bioenergy purposes and having meaningful biomass supplies to meet societal energy demands. However, it should be recognized that native, perennial monocultures or simple polyculture systems provide more ecosystem services such as C sequestration, wildlife habitat, landscape heterogeneity and nutrient regulation than the existing annual cropping systemsReference Camill, McKone, Sturges, Severud, Ellis, Limmer, Martin, Navratil, Purdie, Sandel, Talukder and Trout⁹².

Fixing nitrogen to reduce external inputs

Legumes contribute N to cropping systems through symbiotic N fixation. Accordingly, legumes play an important role in diverse cropping systems through their effects on plant available NReference Grant, Peterson and Campbell⁶⁹. Agronomic outcomes from the inclusion of legumes in cropping systems, however, depend on their use either as cover or grain crops, as most N in annual legumes is contained in seed. When harvested for seed, N contributions to the soil from annual legumes are negligible or slightly positiveReference Stevenson and van Kessel^107, Reference Miller, Gan, McConkey and McDonald¹⁰⁸. Conversely, when annual legumes are used as green manure, significant N can be made available to soil for subsequent crop uptakeReference Grant, Peterson and Campbell^69, Reference Power¹⁰⁹.

Legumes can have additional positive crop sequence effects on subsequent crops. Underlying mechanisms contributing to yield responses are highly complex, and are probably the interaction of legume effects on soil water status, N availability and disruption of pest cyclesReference Anderson^52, Reference Miller, McConkey, Clayton, Brandt, Staricka, Johnston, Lafond, Schatz, Baltensperger and Neill^110, Reference Merrill, Tanaka, Krupinsky and Ries¹¹¹. Accordingly, association of N contributions from annual legumes with increased crop yield is not always consistentReference Krupinsky, Bailey, McMullen, Gossen and Turkington^51, Reference Miller, McConkey, Clayton, Brandt, Staricka, Johnston, Lafond, Schatz, Baltensperger and Neill¹¹⁰. Conversely, perennial legumes, such as alfalfa, can provide significant short-term (3–5 years) N additions to soilReference Kelner, Vessey and Entz¹¹² and subsequent yield increases in grain crops following forage stand terminationReference Hoyt^113, Reference Entz, Baron, Carr, Meyer, Smith and McCaughey¹¹⁴. Such yield benefits from perennial legumes, however, are not reproducible across all management systems. In regions where limited precipitation seriously limits crop productivity, perennial legumes can create a ‘forage-induced drought’, resulting in depressed crop yields following stand terminationReference Entz, Baron, Carr, Meyer, Smith and McCaughey¹¹⁴.

Carbon sequestration

Adoption of complex cropping systems can enhance soil C sequestration and improve soil quality. The magnitude and rate of soil C sequestration depends on crop selection and sequence, site history, and edaphic and climatic factors that directly affect biomass productivity and C retention in soilReference Karlen, Varvel, Bullock and Cruse^47, Reference Brady and Weil¹¹⁵. Crop sequences that include perennial phases are most effective at increasing soil C due to below-ground C input from root biomass and rhizodeposition and decreases in soil C loss from erosionReference Zan, Fyles, Girouard and Samson^116, Reference Dabney, Shields, Temple and Langendoen¹¹⁷. Crop sequences with frequent inclusion of easily decomposable, low residue producing crops (e.g., annual legumes) are least likely to increase soil CReference Varvel¹¹⁸.

It is important to note that while certain cropping systems can lead to soil C accrual, their effects on global warming potential can be variable based on N₂O flux, resulting in either enhanced (e.g., increased soil C and decreased N₂O emission) or negated (e.g., increased soil C and increased N₂O emission) climate mitigation potential (Fig. 5). Such variable responses emphasize the importance of inclusive greenhouse gas evaluations to clearly determine trade-offs associated with management.

Figure 5.

Conceptual diagram documenting potential climate mitigation outcomes associated with soil C accrual and nitrous oxide flux.

Increased soil C in diverse cropping systems has been linked to changes in soil physical, chemical and biological properties that affect ecosystem functions, such as nutrient cycling, filtering and buffering capacity, and regulation of hydrological attributesReference Andrews, Karlen and Cambardella^119, Reference Hudson¹²⁰. Carbon-induced improvements in soil attributes and related functions can positively affect crop yield and environmental qualityReference Wienhold, Pikul, Liebig, Mikha, Varvel, Doran and Andrews¹²¹. Accordingly, management decisions leading to increased soil C in diverse cropping systems contribute to increased agroecosystem resilience under anticipated climate changeReference Delgado, Groffman, Nearing, Goddard, Reicosky, Lal, Kitchen, Rice, Towery and Salon^122, Reference Lal, Delgado, Groffman, Millar, Dell and Rotz¹²³.

Enhancing soil biology to improve soil function

Arbuscular mycorrhizal (AM) fungi are critical to the formation of economically and environmentally sustainable grasslands and livestock agricultural systems by closing water and nutrient cyclesReference Allen, Swenson, Querejeta, Egerton-Warburton and Treseder^124, Reference Smith and Read¹²⁵. These fungi are obligate root symbiotes of about 90% of all vascular plantsReference Carlile and Watkinson¹²⁶ and are ubiquitous in most soilsReference Carlile and Watkinson^126–Reference Wright and Upadhyaya¹²⁸. In this relationship, plants allocate photosynthetic C to the fungus to stimulate the acquisition of nutrients from the soil via the fungal hyphaeReference Allen, Swenson, Querejeta, Egerton-Warburton and Treseder^124, Reference Wright and Upadhyaya¹²⁸. Plants also benefit through greater absorption of water; stimulation of growth hormones; protection against pathogens; and soil structural improvement for better porosity, water infiltration and root penetrationReference Allen, Swenson, Querejeta, Egerton-Warburton and Treseder^124, Reference Miller and Jastrow^129–Reference Purin and Rillig¹³².

AM fungal hyphae are also responsible for macroaggregate (>0.25 mm) formation by providing the framework upon which organic matter collectsReference Miller and Jastrow¹²⁹. AM fungi produce glomalin, a glycoprotein found in abundance in both native and agricultural soilsReference Wright and Upadhyaya^128, Reference Wright and Upadhyaya¹³⁰. Glomalin is located in the fungal hyphal cell wall and may protect it from pathogen attack and nutrient and water lossReference Nichols, Wright, Magdoff and Weil^131–Reference Borowicz¹³³. As the hyphae decompose, glomalin sloughs off and may ‘glue’ and stabilize soil aggregatesReference Wright and Upadhyaya^128, Reference Wright and Upadhyaya¹³⁰.

In agricultural systems, mycorrhizal fungi are vulnerable to excess fertilization or pesticide useReference Nichols, Wright, Magdoff and Weil^131, Reference Rillig and Allen^134, Reference Ryan and Graham¹³⁵, physical destruction by tillageReference Beare, Hu, Coleman and Hendrix¹³⁶ and absence of host plants, resulting in reductions in C allocation to the rhizosphereReference Rillig and Allen^134, Reference Treseder and Turner¹³⁷ and weakened relationship with newer crop varietiesReference Hamel and Plenchette^138, Reference Sawers, Gutjahr and Paszkowski¹³⁹. Excess fertilization may cause plant roots to reject AM colonization, preventing the fungus from obtaining the C it needs to live and grow. Fungicides may reduce mycorrhizal populations directly or indirectly by affecting soil organisms responsible for breaking down organic matter and minerals into the plant nutrients that AM fungi access in exchange for C. Tillage fragments fungal hyphae, making the fungus more susceptible to decomposition and reducing its ability to survive until the next growing season. Use of non-mycorrhizal crops, or crops with a weak relationship with mycorrhizal fungi, limits the amount of C the fungus receives, therefore affecting growth and activity.

Health of the grassland AM fungi relationship depends on plant diversity and community structure, and the level of plant dependence on AM fungi. As grazing intensity increases, mycorrhizal growth and activity decrease through reduction in living roots and activityReference Klumpp, Fontaine, Attard, Le Roux, Gleixner and Soussana¹⁴⁰. Under heavy grazing or no grazing, invasive species tend to dominate, which reduces plant diversity and may reduce mycorrhizal number and diversityReference Callaway, Thelen, Rodriguez and Holben^141, Reference Mummey and Rillig¹⁴². Warm-season plants are more dependent on mycorrhizal fungi than cool-season plantsReference Bentivenga and Hetrick^143, Reference Hetrick, Wilson and Schwab¹⁴⁴.

Economics

Diversification in agricultural production has economic benefits related to risk management and economy of scope. Economy of scope refers to situations where the cost of producing multiple outputs is lower for a single-integrated firm than for multiple specialized firmsReference Panzar and Willig¹⁴⁵. This can occur with complementarities in production, such as in producing crops and livestock, where grain or forages from crop production are used for animal feed, and livestock manure is used for fertilizer, reducing the cost for both. As another example, growing crops in rotation increases yields or reduces inputs relative to growing individual crops continuously in monoculture. Research has shown that the economy of scope in agriculture can be significant. Crops and livestock were produced at a much lower cost for integrated farms in Wisconsin than in specialized farmsReference Chavas and Aliber¹⁴⁶. The cost of joint crop and livestock production for Missouri farmers was on average 14% less than the cost of specialized crop or livestock productionReference Wu and Prato¹⁴⁷. Integrated farms, however, were less efficient than specialized farms at adjusting the mix of inputs used in production to minimize costs. As a result, total cost efficiency tended to be lower for integrated farmsReference Wu and Prato¹⁴⁷. Diversification can include off-farm income sources as well as different farm enterprises. Off-farm income can be critical for small farms to remain competitive with larger farmsReference Nehring, Fernandez-Cornejo and Banker¹⁴⁸. Fernandez-Cornejo et al.Reference Fernandez-Cornejo, Mishra, Nehring, Hendricks, Southern and Gregory¹⁴⁹ showed a 24% cost saving for corn and soybean producers with off-farm income compared with those without.

Both the WisconsinReference Chavas and Aliber¹⁴⁶ and MissouriReference Wu and Prato¹⁴⁷ studies showed that the economy of scope tended to decline with the size of the enterprise, so that larger farms would find it beneficial to specialize. This is also probably related to economy of scale. Economy of scale occurs when cost of production decreases with increasing farm size. In developed countries, research indicates that costs tend to decline for small farms and reach a stable lower level for intermediate to large farm sizesReference Chavas¹⁵⁰. Economy of scale is often associated with specialization, because management of larger farms becomes more complex with more enterprises, and management of more specialized systems is easier and improves production control and efficiencyReference Chavas and Barham^151, Reference Chavas and Holt¹⁵². Specialization in larger farms may also contribute to economy of scale by spreading capital costs over more units of production (although this might not be the case if the same equipment/facilities could be spread over multiple enterprises) and the ability to obtain volume discounts on input purchases. However, the trend toward greater specialization with farm size is not universal. Morrison Paul et al.Reference Morrison Paul, Nehring, Banker and Somwaru¹⁵³ indicated greater benefits to diversification with larger farm size for US farms. Skolrud et al.Reference Skolrud, O'Donoghue, Shumway and Melhim¹⁵⁴ showed that the relationship is industry-specific for Washington farms, with trends toward greater diversification with increasing farm size for wheat, beef and apple farms, but greater specialization with increasing farm size for dairies.

Risk management can be an additional driver for diversification. Farmers are generally risk averse, i.e., they are made worse off by being exposed to risk and may be willing to forgo some income for a reduction in risk. Diversification can reduce risk exposure by including income from a range of enterprises that are influenced in different ways by varying weather and market conditions. Incomes from these different enterprises are typically not perfectly correlated, so the overall variation in income is reduced. While risk management concerns may provide an incentive for agricultural diversification, some have noted that diversification to off-farm investments may be a more effective diversification strategyReference Young and Barry¹⁵⁵. Other risk management tools including crop insurance and government programs, and marketing tools such as forward contracting and futures and options markets, may have important interactions with diversification. Availability of crop insurance and government programs has been observed to reduce incentives for diversification at the farm level for a South Dakota case farmReference Archer, Pikul, Riedell, Hanson and Krupinsky¹⁵⁶. Others, however, found a general positive relationship between farm diversification and government payments and crop insurance for US farmsReference Mishra, El-Osta and Sandretto¹⁵⁷. Other factors may be more important drivers of diversificationReference Pannell, Malcolm and Kingwell¹⁵⁸. In addition to risk and economies of scope, other key drivers of diversification include non-uniformity of resource quality (e.g., different soil types might be better suited to different types of production) and resource constraints (e.g., time and equipment constraints), and that the ‘main issue raised by variability of price and production is how to respond tactically and dynamically to unfolding opportunities or threats to generate additional income or to avoid losses.’Reference Pannell, Malcolm and Kingwell¹⁵⁸ This indicates the need for development of dynamic agricultural systems and tools for managing these systems. This would build on the dynamic cropping systems approach discussed earlier, and expand the approach to other agricultural systems.

Economy of scope may also play an important role in producers’ willingness to supply non-marketed ecosystem services. From an economic perspective, the willingness of producers to supply ecosystem services depends on whether provision of these services increases profits or reduces risks at the farm level. Many ecosystem services do not have an effect on profits or risks at the farm level, because many effects are driven by processes at a larger spatial scale than the farm level, occur primarily off-farm and (or) may be public goods where markets do not fully capture the value of these servicesReference Randall^159–Reference Lant, Kraft, Beaulieu, Bennett, Loftus and Nicklow¹⁶¹. For example, the spatial pattern of land cover across broad geographic regions can have a large effect on the population and distribution of wildlife species. In the absence of a market for wildlife services, the wildlife produces no income for a farm situated within the landscape. Furthermore, even if a market existed for the wildlife services, the provision of these services would depend on coordinating the pattern of land use among the various farms within the landscape. These services, however, are produced jointly with marketed agricultural products. In cases where the non-marketed ecosystem services are complementary with marketed goods (economy of scope between non-marketed ecosystem services and agricultural products) producers may not need additional incentive to achieve the non-marketed servicesReference Wossink and Swinton¹⁶². This can occur for ecosystem services that provide productivity or input reduction benefits. Examples include practices that enhance pollinator habitat, soil N fixation, or enhance soil quality through increased soil organic carbon (SOC) storage and reduced erosion, and these enhancements can produce benefits beyond the farm level.

Trade-offs

Not all ecosystem services may be realized at once, hence a critical challenge is to identify and accurately assess trade-offs among desired services. In addition, achieving ecosystem service goals may produce economic and social trade-offs. For example, maintaining acceptable wildlife habitat on grassland farms may compromise the quantity and quality of forage needed for livestock production, and this has economic consequences for the livestock producer. In this instance, trade-offs among wildlife habitat, livestock production and economic return at the farm level must be decided and the trade-off assessment encumbered by practical and ethical considerationsReference Brauman, Daily, Ka'eo and Mooney¹⁶³. The value of an ecosystem service must be assessed within the context of the service, and includes both social and economic values. A grassland farmer may value grassland for its provisioning services (quantity and quality of forage), whereas a grassland conservationist may value attributes such as appropriate plant diversity and vegetation structure that support bird populations. Identifying trade-offs among the various dimensions of sustainability for alternative production systems provide a transparent mechanism for decision makers to determine an appropriate balance among competing goalsReference Weersink, Jeffrey and Pannell¹⁶⁴. Trade-offs can be strongly influenced by spatial variation in resourcesReference Antle and Capalbo^165, Reference Antle and Stoorvogel¹⁶⁶, as well as dynamics over time.

Increasing bioenergy production from agricultural land may require trade-offs in land use. In the USA, projections of expanded ethanol and biodiesel production suggest large reductions in pasturelandReference De La Torre Ugarte, English and Jensen¹⁶⁷. A global analysis of bioenergy production suggested that shifting livestock production from pasture to confinement feeding would reduce land needs for agricultureReference Taheripour, Hertel and Tyner¹⁶⁸. If these changes in land use are realized, there may be pressure to intensify inputs and management on remaining hay, forage and pastureland in the future¹⁶⁹. The expanding need for biomass production would probably force forage and grazing livestock production on to more marginal lands with potential trade-offs in soil and water quality.

Monitoring changes in land use, especially in grassland, and in cropping diversity presents a significant challenge. The cropland data layer of the National Agricultural Statistics Service is by far the most extensive spatial dataset depicting the major crop-specific land cover on the entire conterminous USA. But even the cropland data layer generalized grassland into broad categories such as pasture/grass and other hays. Broad categorizations of some of these land uses possess inaccuracy in quantifying ecosystem services and mapping essential resourcesReference Naidoo, Balmford, Costanza, Fisher, Green, Lehner, Malcolm and Ricketts¹⁷⁰. A more specific baseline data for monitoring grassland and pastureland would pave the way for better resource management, reliable detection and intervention of land use conversion and accurate assessment of ecosystem services.

An alternative for increasing bioenergy production without shifting land use is utilizing crop residues as feedstocks. A field-level case study analysis of the potential for harvesting corn stover for bioenergy production showed soil organic C losses with corn stover harvest using a traditional tillage system. However, by switching from conventional tillage to no-till, soil organic C could be increased while harvesting biomass and increasing farm profitsReference Anand, Archer, Bergtold, Canales, Braun, Karlen and Johnson⁷⁷.

Similar cases have been identified where economic returns and provision of ecosystem services may be both improved. For example, in irrigated crop production, research showed opportunities to reduce net greenhouse gas emission and increase economic returns by avoiding excess application of N fertilizer and by switching from conventionally tilled continuous corn to a no-till corn–bean rotationReference Archer and Halvorson¹⁷¹. However, achieving further reductions in net greenhouse gas would reduce farm profitability. This is a common observation where market forces lead producers to maximize profitability, and the economic optimum and environmental optimum typically do not coincide. As a result, achieving increases in ecosystem services often comes at a cost to farm profitability.

This trade-off between ecosystem services and economic returns could be reduced if ecosystem services provided an economic benefit to the farmer. This may occur if markets are developed where farmers would be compensated for the value of ecosystem services they provided. Also, as indicated earlier, this may occur when the ecosystem services provide input-reducing or productivity benefits. Diverse integrated agricultural systems, where inputs from one enterprise come from products of another enterprise, and which rely on well-functioning ecosystem services such as disease and pest suppression, and nutrient and water cycling, are likely to realize these input-reducing and productivity benefits. Diverse integrated systems can reduce the trade-offs, and in some cases provide win–win opportunities for simultaneously increasing agricultural profitability and ecosystem services.