Published online 20 May 2008
Published in Crop Sci 48:1211-1218 (2008)
© 2008 Crop Science Society of America
677 S. Segoe Rd., Madison, WI 53711 USA
Soil Compaction, Corn Yield Response, and Soil Nutrient Pool Dynamics within an Integrated Crop-Livestock System in Illinois
Benjamin F. Tracya,* and
Yan Zhangb
a Dep. of Crop, Soil and Environmental Sciences, Virginia Polytechnic Institute and State Univ., Blacksburg, VA 24061
b Dep. of Crop Sciences, Univ. of Illinois, Urbana, IL 61801
* Corresponding author (bftracy{at}vt.edu).
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ABSTRACT
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Integrated crop–livestock systems directly link crop and livestock production together to generate positive economic and environmental outcomes. Some methods used in integrated systems, like winter grazing on cropland, could negatively affect soil properties and crop productivity. We compared soil compaction, corn (Zea mays L.) yield, and soil nutrient pools between an integrated crop–livestock system and continuous corn system to address this issue. The study was conducted near Pana, IL, between 2002 and 2006. Soil compaction was evaluated indirectly by measuring soil penetration resistance (PR) and surface CO2 effluxes. Total soil C, N, and microbial biomass C, were measured from 2002 to 2005. Soil PR and CO2 effluxes showed inconsistent trends related to soil compaction and cattle presence. Corn yield from 2004 to 2006 was higher (P = 0.01) in the integrated system (11.6 Mg ha–1) compared with continuous corn (10.6 Mg ha–1). Total soil C concentration increased significantly from 2002 to 2005 within components of the integrated system but remained unchanged in continuous corn. Microbial biomass C was also higher in the integrated system but only in 2005. The study determined that integration of crops with livestock had generally positive effects on crop yield and soil organic matter despite the potential for livestock to compact soil during winter grazing.
Abbreviations: CC, continuous corn C-O-P, corn–oat–pasture CSP, cool-season grass pasture PR, penetration resistance WSP, warm-season grass pasture
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INTRODUCTION
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INTEGRATED CROP–LIVESTOCK systems involve linking crop and livestock production together to generate positive economic and environmental outcomes (Allen et al., 2007). The actual relationship between crops and livestock can vary in these systems. It may range from relatively intimate, within-farm integration of crops and livestock (e.g., grazing crop residues after grain harvest) to more indirect relationships (e.g., shared manure application among crop farms within a region). Most evidence suggests integrated crop–livestock systems are more environmentally protective, or restorative, than modern cropping systems that rely on monoculture and heavy external inputs of fertilizer and pesticide (Allen et al., 2005; Katsvairo et al., 2006; Sulc and Tracy 2007). Allen et al. (2005) found that an integrated cattle–cotton (Gossypium hirsutum L.) system with 54% of the land in permanent C4 grass pasture used 23% less irrigation water, 40% less fertilizer N, and fewer chemical inputs and was 90% more profitable than the cotton monoculture. In the northern U.S. Great Plains, diversifying cropping systems with forages was found to increase grain crop yields, reduce weed pressure, and improve soil quality (Entz et al., 2002). Integrated systems may also help reduce winter feed costs in temperate regions. Winter feed can often account for half of the annual production costs in a typical beef cow operation (Schoonmaker et al., 2003). Cost reductions are often achieved by grazing grain crop residues or cool-season annual crops after harvest to save on purchased hay or grain (Klopfenstein et al., 1987; Ward, 1978).
Some integrated systems involve grazing livestock on cropland. A concern is that livestock presence on cropland would negatively affect soil properties and subsequent crop productivity. This situation may occur when livestock trample on moist, non–sod-bearing cropland soils causing compaction and subsequent crop yield reductions though alteration of soil physical and biological properties (Krenzer et al., 1989; Mapfumo et al., 1999; Worrell et al., 1992). Soil compaction was one component addressed in an integrated crop–livestock system experiment that was initiated in 2002 at the University of Illinois, Dudley Smith Farm near Pana, IL. In this system, cash crops consisting of corn (Zea mays L.) and oat (Avena sativa L.) were grown in summer while cattle grazed adjacent perennial pastures (cool and warm-season grasses). When pastures became dormant in fall, cattle were moved to croplands where they spent late fall and winter grazing a mixture of cool-season annual cover crops and corn residues. In spring, cattle were returned to cool-season grass pastures. The objective of this study was to determine whether cattle presence on cropland would negatively affect soil quality parameters and subsequent crop yields.
To meet this objective, we compared soil compaction, soil nutrient pools, and corn yield between the integrated crop–livestock system and a continuous corn system between 2002 and 2006. Soil compaction from cattle trampling was evaluated indirectly by measuring soil penetration resistance (PR) and surface CO2 effluxes. Soil PR is a measure of soil strength and can be used as an index of soil compaction (Clark et al., 2004; Unger and Kaspar, 1994). Surface CO2 efflux is a measure of net CO2 production of a soil that includes respiration of roots and mineralization of organic matter. Soil compaction from machine traffic or cattle trampling could reduce soil respiration by reducing pore space and limiting O2 diffusion (Conlin and van den Driessche, 1996, 2000; Shestak and Busse, 2005; Torbert and Wood, 1992). Reduced soil respiration may indicate less microbial activity and anaerobic conditions, both of which could negatively affect crop yield. In this study, we used measurements of surface CO2 efflux during the growing season as an integrative variable to determine potential persistence of soil compaction from winter grazing. We hypothesized that cattle trampling on cropland would increase soil compaction and reduce corn yield relative to corn that experienced no winter grazing.
We also measured several soil nutrient pools—total soil C, N, and microbial biomass C and used them as indicators of soil quality. Total C and N closely reflect quantity of soil organic matter and microbial biomass C is an active pool of organic matter whose size and activity strongly influences nutrient availability and plant productivity (Paul, 1984, Chapin et al., 2002). Microbial biomass C is frequently used as an indicator of soil quality since it tends to be more sensitive to management than total C (Brookes, 1995; Jordan et al., 1995). Because of the presence of cattle, perennial grasses, and cover crops in the integrated system, we hypothesized that soil organic matter and soil microbial biomass would be greater compared with continuous corn.
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MATERIALS AND METHODS
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Site Description and Experimental Design
The study site is located on the Dudley Smith research farm near Pana, IL (39°23' N, 89°4' W). The farm had been in corn–soybean [Glycine max (L.) Merr.] rotation for at least 10 yr before it was converted for use in this experiment. In 2002 all 90 ha of the farm were converted to a replicated farming systems experiment that integrates cash grain crops with beef cattle produced on the same land unit. The area has mean annual temperature of 13.4°C and mean annual precipitation of 1001 mm. Weather data were taken from a nearby station (
5 km) maintained by Illinois State Climatologist and Illinois State Water Survey. Soils at the Dudley Smith farm are of the Virden series. They consist of silty, clay loams classified as fine, smectitic, mesic Vertic Argiaquolls. Before start of the experiment, 84 soil samples were taken across the farm for baseline data. Soil pH averaged 6.3, while P and K averaged 32 mg kg–1, and 152 mg kg–1, respectively at a 0- to 15-cm profile depth. Before beginning the experiment, limestone, P, and K were applied to individual treatment plots within the farming system using recommendations based on soil test results.
The integrated farming system was replicated three times across the study site. Each farming system unit consisted of four treatments (Fig. 1
) that included (i) corn–oat–pasture treatment (C-O-P) consisting of equal areas of corn and oats grown in summer and then used for winter grazing (19 ha), (ii) a continuous corn rotation (CC) that was managed exactly as corn in C-O-P plots except without winter grazing (2 ha), (iii) perennial cool-season grass pastures (CSP) (6 ha), and (iv) perennial warm-season grass pastures (WSP) (2 ha). The treatment plots differed in size because more land was needed to supply winter forage for cattle. Winter pasture cannot be grazed multiple times like summer perennial pasture in rotation and this necessitates using more land area. Details on grazing protocols are described below.

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Figure 1. Schematic diagram of integrated farming system used in the experiment showing the four treatments. The farming system is replicated three times across the study site. C-O-P, corn–oats–pasture treatment; CSP, cool-season grass pasture; WSP, warm-season grass pasture; CC, continuous corn.
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Perennial pastures were established in spring of 2002 into a clean seedbed. Within each farming system, three different cool-season pastures were planted on equal area basis. That is, three 2-ha pastures within each 6-ha area. The three pastures consisted of (i) tall fescue [Lolium arundinaceum (Schreb.) S.J. Darbyshire] sown at 22 kg ha–1, (ii) a mixture of orchardgrass (Dactylis glomerata L.) and tall fescue sown at 8.5 and 11 kg ha–1, and (iii) a mixture of perennial ryegrass (Lolium perenne L.), festulolium [X Festulolium loliaceum (Huds.) Fourn.], tall fescue, and orchardgrass sown at 2, 2, 2, and 17 kg ha–1, respectively. Red clover (Trifolium pratense L.) and white clover (Trifolium repens L.) were frost seeded into pastures in March 2003 at a rate 5 kg ha–1. Warm-season perennial pastures were planted with eastern gamagrass [Tripsacum dactyloides (L.) L.], big bluestem (Andropogon gerardii Vitman), and little bluestem [Schizachyrium scoparium (Michx.) Nash] at a rate of 4.5 kg ha–1, respectively, and kura clover (Trifolium ambiguum M. Bieb) at 2.7 kg ha–1.
Production of corn and oat started in spring 2003 and continued through 2006. For both crops, conventional tillage was used for seedbed preparation that included chisel plowing and field cultivation in spring. In the C-O-P and CC treatments, a Roundup Ready corn hybrid was planted each year in mid-late April. Corn was planted to achieve a target population of 75,000 plants ha–1 using 76-cm row spacing. Nitrogen was applied as urea both preplant and sidedress when corn was V6 stage. Nitrogen rates ranged between 150 and 190 kg N ha–1. Corn was harvested in mid-late September. Oats planted for grain were sown in early April at a rate of 59 kg ha–1 total weight with a 0.17-m row spacing. Oats were fertilized with urea at a rate of 60 kg N ha–1 at planting. Corn and oats are rotated each year between adjacent fields (Fig. 1). Corn was treated with one application of glyphosate isopropylamine salt herbicide (1.12 kg a.i. ha–1) in June to control weeds. Oats received no herbicide treatment. After oats were harvested in July, a cool-season annual mixture of oat, cereal rye (Secale cereale L.), and turnip (Brassica spp.) was sown into a clean, prepared seedbed with seeding rates at 70, 80, and 8 kg ha–1, respectively.
Grazing Management
Grazing on the three replicate farming systems began in fall 2003 and continued through 2006. Cattle grazed cool-season pasture in spring, summer, and fall at a stocking rate of 2.5 cows ha–1 (Fig. 1). In each replicate, cool-season pastures were divided into six equal-sized paddocks for rotational stocking. Warm-season grass pastures were divided into two paddocks and used to extend the rotation in midsummer. Paddock residency periods varied between 1 and 6 d during the growing season depending on forage availability. When perennial pastures become unproductive in late October, we moved cattle to croplands where they grazed cool-season annuals and corn residues (Fig. 1). Pregnant beef cows grazed each cropland area from November to March with calving occurring in February and March. Stocking rate was 1 cow ha–1 on croplands. A strip grazing method was used on cropland by moving a single strand of portable electric fence 25 m approximately every 5 to 10 d depending on forage availability. Cattle had equal access to corn residues and cool-season annuals in each strip in addition to a stationary water source. Because cattle needed access to water during the strip grazing, we could not fence them from previously grazed strips in the field. Cattle were fed hay and grain as needed when forage became limiting on cropland pastures. Hay and grain were fed in dry lot areas separate from the treatment plots so they did not influence soil properties in sampling areas. Cattle were given ad libitum access to salt blocks throughout the year.
Crop and Soil Sampling
Due to logistical difficulties of sampling the large cropland plots (19 ha), we chose to confine sampling to smaller, semipermanent sampling areas that we felt were representative of each treatment. To do this, we located one 0.5-ha sampling area in each plot such that they would be grazed at the same time during the strip grazing progression. In this way, each sampling area across the three replications would be grazed at the same time. Because the strips were not back-fenced, cattle traveled through plots multiple times to get to a water source. Our placement of sampling areas maximized the likelihood of a similar cattle exposure to all plots throughout the winter. In the perennial pastures, we choose one random paddock in each replication for sampling and established a 0.5-ha sampling area in the center. Total soil C, N, and microbial biomass C were measured from soil samples collected in each fall from 2002 to 2005. Soil PR, surface CO2 effluxes, and corn yield were measured in 2004 and 2005.
Soil PR was measured in late March 2004 and late April 2005 when soils were near or above field capacity. Twenty electronic penetrometer measurements (1-cm cone diameter, 2-cm cone length) were taken at a 90° angle to a depth of 46 cm. Measurements were recorded at 2.5 cm intervals and then averaged to obtain two values for 0- to 23-cm and 24- to 46-cm depth intervals. Because soil PR depends on soil moisture, we measured soil moisture gravimetrically from six locations in same depth increments. Soils were weighed wet then dried for 48 h at 50°C and weighed again. We suspected there might be differences between soil PR under grazed corn residues and cool-season annuals so we sampled both parts of the C-O-P treatments separately. Soil PR was measured in perennial pastures, but pastures were much drier than croplands in 2005. These differences made it difficult to make a meaningful comparison among the treatments in 2005 so data from perennial pastures will not be presented.
The yield component method was used to estimate corn grain yield in C-O-P and CC treatments (University of Illinois Extension, 2000). In each respective sampling plot, we selected 12 random areas to estimate corn yield. At each sampling point, the number of ears was counted within a 5.3-m length of row and kernel number estimated for three randomly selected ears. Those data were used to calculate grain yield. Sampling in 2004, 2005, and 2006 was done in mid to late August.
For soil variables, 18 soil cores (2.5-cm diameter) were taken from random locations within each 0.5-ha sampling area to a depth of 15 cm. Sampling was done in each October or early November after corn harvest. Subsamples were combined and dried for at least 48 h at 50°C. Roots >1-mm diameter were removed, and soil finely ground for analyses. Total C and N concentrations were analyzed using a CHN analyzer (ECS 4010, Costech Analytical Technologies Inc., Valencia, CA). The chloroform fumigation–incubation method was used for soil microbial C determination (Jenkinson and Powlson, 1976; Franzluebbers et al., 1996). For processing, 10 g of dry soil was placed in a 50-mL glass beaker. Soil moisture was brought up to
50% of soil water holding capacity. Samples then were pre-incubated in the dark for 5 d at
25°C in closed mason jars with a few milliliters of water to maintain humidity. After pre-incubation, samples were fumigated with chloroform for 24 h and then transferred to mason jars. Each jar contained a 20-mL scintillation vial containing 1-mL of 2 M NaOH to absorb the CO2. Jars were incubated in the dark at 25°C for 10 d. After incubation NaOH was titrated with 1 M HCl, soil microbial biomass C was calculated using a kC value of 0.41 for fumigated samples without subtracting an unfumigated control (Franzluebbers et al., 1999; Voroney and Paul, 1984).
Surface CO2 effluxes were measured using a portable CO2 infrared gas analyzer (LiCor 6400, LiCor Inc., Lincoln, NE) with a closed, static soil respiration chamber. Measurements were taken from three or four PVC collars (10-cm diameter x 7 cm) per plot that were inserted into soil to a depth of 2 cm. Surface CO2 effluxes were measured twice each month from May to December in 2004 and May to October in 2005. Measurements were conducted between 0900 and 1500 h with exposure time for CO2 efflux measurement averaging about 5 min per sampling point depending on soil conditions.
All variables were analyzed using analysis of variance (ANOVA) in the GLM procedure of SAS (SAS Institute, 2003). Farming system treatments included (i) C-O-P treatment, (ii) CC rotation, (iii) perennial cool-season grass pasture (CSP), and (iv) warm-season grass pasture (WSP). Subsamples for all variables were pooled within each treatment before analysis to give a sample size of n = 3. Treatment and year were used as independent variables and if significant treatment x year interactions were found (P < 0.10), years were analyzed separately. Corn grain yields were compared between continuous corn and cropland pasture (C-O-P). We did not have an ungrazed control for oat grain yield. Total C, N, microbial biomass C, and CO2 effluxes were compared among the four main treatments, C-O-P, CC, CSP, and WSP. For these variables in the C-O-P treatment, data was pooled from corn residue and cool-season annual plots. Linear regression was used to determine relationships between total C, N pools, and time over the 4-yr study period. Carbon dioxide efflux data collected over each year were analyzed using a repeated measures ANOVA. Fisher's LSD test was used to evaluate treatment differences of significant main effects (P = 0.10).
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RESULTS AND DISCUSSION
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Climatic Conditions
The majority of data in this study were collected between 2004 and 2005. In 2004, summer was cooler than long-term average data by about 2°C from June to August (Table 1
). Temperature in 2005 was closer to the long-term average. Precipitation in 2004 was generally more variable than 2005 (Table 1). Annual precipitation in 2005 was
13% below the long-term (1950–2005) average (1016 mm). The precipitation in spring and early summer (March to June) in 2005 was drier, about 60% less than long-term average in this period. Because of precipitation and freeze-thaw events, soils were often wet when cattle were present on croplands during late fall and winter. Cattle trampling during these times caused severe soil disturbance.
Soil Compaction and Corn Yield
Soil compaction is a complex function of soil texture, moisture, grazing intensity, vegetation composition, and climate (Twerdoff et al., 1999). In this study, we measured soil compaction indirectly using PR and surface CO2 effluxes. Soil compaction is best measured using both PR and bulk density, but PR should give a good indication of compaction if soil moisture is measured simultaneously. Analysis of PR showed a significant treatment x year interaction so years were analyzed separately. Soil moisture was higher in 2004 (281 g kg–1) compared with 2005 (242 g kg–1) when we measured PR. Soil under grazed corn residues tended to be drier (P = 0.13) in 2005 than in 2004, especially at the 24- to 26-cm depth (197 vs. 237 g kg–1). The drier soils likely affected soil PR measurements in 2005 and may explain the higher values under corn residues (Table 2
). Precipitation was also higher in March 2004 (13 cm) compared with April 2005 (5 cm) when PR was measured. Overall, PR measurements did not show a consistent trend, but suggested that cattle presence on grazed cropland may compact soils relative to CC plots in some years (Table 2). Although PR was measured on perennial pastures, we did not include this data because pasture soils were much drier than cropland soils in 2005. Preliminary data collected in 2004 suggested that pasture soils were no more compacted than cropland, which supports findings from other studies (Mapfumo et al., 1999).
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Table 2. Soil penetration resistance measured in spring of 2004 and 2005 to 46-cm depth. Values are means ± 1 SE.
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Soil compaction can affect surface CO2 effluxes by reducing air-filled porosity which, in turn, may restrict O2 diffusion and increase CO2 accumulation (Conlin and van den Driessche, 2000; Santruckova et al., 1993). If this situation persists, anaerobic conditions in the root zone could negatively affect crop growth (Linn and Doran, 1984). The highest mean efflux rates were reached in late spring or early summer and were close to zero in winter for both pastures and croplands (data not shown). No differences were found among treatments in 2004, but perennial pastures showed higher respiration rates (3.6 µmol CO2 m–2 s–1) compared with CC and C-O-P treatments (2.3 µmol CO2 m–2 s–1) in 2005 (P < 0.001). Greater fine root biomass and the larger soil organic C pool, which is a substrate for heterotrophic activity may have contributed to the higher soil respiration rates measured in pastures in 2005. Similarly, Wagai et al. (1998) reported a greater soil surface CO2 flux in a native prairie than no-till corn plots in spring and summer in southern Wisconsin. In forest soils, Shestak and Busse (2005) found that soil compaction in a clay loam significantly reduced soil respiration as much as 51% on severely compacted soils. They suggested reduced respiration resulted from less pore space in soils and not reduced biological activity. Torbert and Wood (1992) found similar results in a laboratory study using a loamy sand soil. In our study, surface CO2 efflux rates were similar between CC and C-O-P treatments both years suggesting that if there was soil compaction caused by cattle in winter, it may not have persisted into the growing season. Spring cultivation and tillage in our study would have likely reduced any shallow compaction that developed over the winter.
Some studies suggest presence of cattle on cropland in winter can compact soils and reduce crop yield (Krenzer et al., 1989; Mullins and Burmester, 1997; Worrell et al., 1992). Our results suggest trampling and soil disturbance from cattle presence on cropland had no negative affect on subsequent corn grain yield and may have helped increase yield over CC plots. No year x treatment interactions were found and mean corn yield from 2004 to 2006 was significantly higher (P = 0.01) on C-O-P treatments (11.6 Mg ha–1) compared with CC (10.6 Mg ha–1). Differences between CC and C-O-P corn grain yield were greater in 2005 and 2006 compared with 2004 suggesting a potential rotational effect (Fig. 2
). In a study from Iowa, Clark et al. (2004) showed that winter grazing on corn residues had a minimal effect on subsequent soybean yield. This was especially true if grazing was restricted to periods when soils were frozen or if soil was disked before soybean planting. In our study, grazing often occurred when soils were not frozen. We did, however, use conventional tillage before planting, and this may have alleviated some compaction. Moreover, we would probably expect to see greater yield effects related to compaction in a dry year when crops are under stress (Sidhu and Duiker, 2006; Unger and Kaspar, 1994). In this region, corn is especially sensitive to stress in July when pollination and grain fill occurs. Rainfall in 2004 and 2005 was above normal in July and near normal in 2006 so plants were not drought stressed during this critical period (Table 1). A review by Unger and Kaspar (1994) suggested that PR greater than 20 kg cm–2 in a dry soil will severely restrict root growth. Our PR measurements approached this threshold in relatively wet soils (Table 2) so it is possible that PR measured in this study was sufficient to restrict root growth under prolonged dry conditions.

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Figure 2. Estimated corn grain yield from 2004 to 2006 in continuous corn and cropland pasture (C-O-P) plots.
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Soil Carbon and Nitrogen Pools
Grasslands generally accumulate more soil organic matter compared with annual cropland (Bronson et al., 2004; Franzluebbers et al., 2000; Studdert et al., 1997). Microbial biomass C is an active component of organic matter, and it usually positively associated with high plant biomass production (Tracy and Frank, 1998) and dense root systems (Stone and Buttery, 1989). Groffman et al. (1995) observed that microbial biomass C was four times greater in grazed prairie compared with annual cropland, and this difference was mainly associated with total C inputs. In our study, we found no significant treatment x year interaction for total soil C or N. Total C increased in CSP and C-O-P treatments, while total C concentrations in CC treatments remained largely unchanged (Fig. 3
). Linear regression confirmed that total C concentration increased in CSP treatments from 2002 to 2005 (R2 = 0.47, P = 0.02) and in C-O-P (R2 = 0.31, P = 0.07). Total N increased only in the C-O-P treatments—from 1.1 to 1.6 g kg–1 between 2002 and 2005 (linear regression R2 = 0.47, P = 0.02). Total N concentrations in other treatments remained unchanged over the 4 yr (data not shown). Mean soil C to N ratios ranged from 12 in WSP to 13.3 in C-O-P. Microbial biomass C showed more variation than total C, and we found a significant treatment x year interaction (P < 0.001). Clear treatment differences were found for microbial biomass C only in 2005 (Table 3
). Microbial biomass concentrations were highest in CSP and C-O-P treatments and lowest in CC treatments (P < 0.001). These results suggest that CSP and C-O-P treatments may have built up a greater quantity of labile carbon relative to the other treatments by 2005. The higher annual variation in microbial biomass may reflect its sensitivity to management and environmental factors. In terms of soil compaction, it appears to have mixed effects on soil microbial biomass C with some studies showing no effect (Shestak and Busse, 2005) while others having found reductions in microbial biomass C (Jordan et al., 1999). Cattle presence on cropland appeared to have no detrimental effect on microbial biomass concentrations in this study.

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Figure 3. Trends in total soil C over the four year study period. C-O-P, corn–oats–pasture treatment; CSP, cool-season grass pasture; WSP, warm-season grass pasture; CC, continuous corn. LSD values are given for each year to compare treatments.
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Our results generally indicate that integration of cattle and pasture within a grain crop rotation increases the quantity and quality of soil organic matter compared with continuous cropping. Combining all treatments within the integrated system over 4 yr revealed that total C averaged 19.1 g kg–1 while continuous corn averaged 17.3 g kg–1. The biggest separation in total C concentration occurred in the final year (2005) where total C in the integrated system averaged 21 g kg–1 and 17.2 g kg–1 in continuous corn. Acosta-Martinez et al. (2004) compared soil quality parameters in an integrated livestock–cotton production system in Texas with continuous cotton. They found that soil organic carbon, microbial biomass C and N, enzyme activities, and protozoa populations were higher in the integrated system suggesting that the quality of soil organic matter was higher in this system compared with continuous cotton. Like our study, those improvements were largely the result of perennial pasture within the system. Hoof disturbance from cattle grazing on cropland appeared to have no negative effect on soil C or N pools relative to continuous corn. In fact, the size of soil C and N pools showed some of the greatest increases in C-O-P treatments over 4 yr of this experiment. Organic matter inputs from manure, cool-season annuals, and crop residues likely contributed to the increases in C pools we observed. Only CSP treatments showed greater increases in C pools, which we expected.
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CONCLUSIONS
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Our data indicated that cattle presence on cropland may have caused soil compaction in some years, but it had no negative effect on soil properties or corn grain yield. From a whole-farm perspective, we found significant increases in soil C pools within 5 yr of conversion from corn–soybean rotation. These results suggest a farming system integrating cattle with grain crops can build soil organic matter rapidly, and this should have many positive ramifications for system productivity overall. A critical component in this system appears to be integration of perennial pasture and annual cover crops within the system. Cover crop residues, fine root turnover, and manure inputs likely help boost soil organic matter levels and negate soil compaction that might result from cattle trampling on non–sod-bearing soils. Nevertheless, longer term evaluation of this integrated system will be required to make robust conclusions about its impact on soil quality and crop productivity. At this point though, our results suggest wintering cattle on crop residues and cropland pasture should help reduce winter feeding costs without negatively affecting crop productivity and soil quality.
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NOTES
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All rights reserved. No part of this periodical may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or any information storage and retrieval system, without permission in writing from the publisher. Permission for printing and for reprinting the material contained herein has been obtained by the publisher.
Received for publication July 16, 2007.
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REFERENCES
|
|---|
- Acosta-Martinez, V., T.M. Zobeck, and V. Allen. 2004. Soil microbial, chemical, and physical properties in continuous cotton and integrated crop-livestock systems. Soil Sci. Soc. Am. J. 68:1875–1884.[Abstract/Free Full Text]
- Allen, V.G., M.T. Baker, E. Segarra, and C.P. Brown. 2007. Integrated irrigated crop–livestock systems in dry climates. Agron. J. 99:346–360.[Abstract/Free Full Text]
- Allen, V.G., C.P. Brown, R. Kellison, E. Segarra, T. Wheeler, P.A. Dotray, J.C. Conkwright, C.J. Green, and V. Acosta-Martinez. 2005. Integrating cotton and beef production to reduce water withdrawal from the Ogallala Aquifer in the Southern High Plains. Agron. J. 97:556–567.[Abstract/Free Full Text]
- Bronson, K.F., T.M. Zobeck, T.T. Chua, V. Acosta-Martinez, R.S.V. Pelt, and J.D. Booker. 2004. Carbon and nitrogen pools of southern high plains cropland and grassland soils. Soil Sci. Soc. Am. J. 68:1695–1704.[Abstract/Free Full Text]
- Brookes, P.C. 1995. The use of microbial parameters in monitoring soil pollution by heavy metals. Biol. Fertil. Soils 19:269–279.[CrossRef]
- Chapin, F.C., H.A. Mooney, and P.A. Matson. 2002. Principles of terrestrial ecosystem ecology. Springer, New York.
- Clark, J.T., J.R. Russell, D.L. Karlen, P.L. Singleton, W.D. Busby, and B.C. Peterson. 2004. Soil surface property and soybean yield response to corn stover grazing. Agron. J. 96:1364–1371.[Abstract/Free Full Text]
- Conlin, T.S.S., and R. van den Driessche. 1996. Short term effects of soil compaction on growth of Pinus contorta seedlings. Can. J. For. Res. 26:727–739.
- Conlin, T.S.S., and R. van den Driessche. 2000. Response of soil CO2 and O-2 concentrations to forest soil compaction at the long-term soil productivity sites in central British Columbia. Can. J. Soil Sci. 80:625–632.
- Entz, M.H., V.S. Baron, P.M. Carr, D.W. Meyer, S.R. Smith Jr., and W.P. McCaughey. 2002. Potential of forages to diversify cropping systems in the Northern Great Plains. Agron. J. 94:240–250.[Abstract/Free Full Text]
- Franzluebbers, A.J., R.L. Haney, and F.M. Hons. 1999. Relationships of chloroform fumigation-incubation to soil organic pools. Soil Biol. Biochem. 31:395–405.[CrossRef]
- Franzluebbers, A.J., R.L. Haney, F.M. Hons, and D.A. Zuberer. 1996. Determination of microbial biomass and nitrogen mineralization following rewetting of dried soil. Soil Sci. Soc. Am. J. 60:1133–1139.[Abstract/Free Full Text]
- Franzluebbers, A.J., J.A. Stuedemann, H.H. Schomberg, and S.R. Wilkinson. 2000. Soil organic C and N pools under long-term pasture management in the southern Piedmont USA. Soil Biol. Biochem. 32:469–478.[CrossRef]
- Groffman, P.M., C.W. Rice, and J.M. Tiedje. 1995. Denitrification in a tallgrass prairie landscape. Ecology 74:855–862.[CrossRef]
- Jenkinson, D.S., and D.S. Powlson. 1976. The effects of biocide treatments on metabolism in soil: I. Fumigation with chloroform. Soil Biol. Biochem. 8:167–177.[CrossRef]
- Jordan, D., F. Li, F. Ponder, E.C. Berry, V.C. Hubbard, and K.Y. Kim. 1999. The effects of forest practices on earthworm populations and soil microbial biomass in a hardwood forest in Missouri. Appl. Soil Ecol. 13:31–38.[CrossRef]
- Jordan, D.R., W.A. Kremer, K. Bergfield, Y. Kim, and V.N. Cacnio. 1995. Evaluation of microbial methods as potential indicators of soil quality in historical agricultural fields. Biol. Fertil. Soils 19:297–302.[CrossRef]
- Katsvairo, T.W., D.L. Wright, J.J. Marois, D.L. Hartzog, J.R. Rich, and P.J. Wiatrak. 2006. Sod–livestock integration into the peanut–cotton rotation: A systems farming approach. Agron. J. 98:1156–1171.[Abstract/Free Full Text]
- Klopfenstein, T., L. Roth, S. Rivera, and M. Lewis. 1987. Corn residues in beef production systems. J. Anim. Sci. 65:1139–1148.[Abstract/Free Full Text]
- Krenzer, E.G., C.F. Chee, and J.F. Stone. 1989. Effects of animal traffic on soil compaction in wheat pastures. J. Prod. Agric. 2:246–249.
- Linn, D.M., and J.W. Doran. 1984. Effect of water-filled pore-space on carbon-dioxide and nitrous-oxide production in tilled and nontilled soils. Soil Sci. Soc. Am. J. 48:1267–1272.[Abstract/Free Full Text]
- Mapfumo, E., D.S. Chanasyk, M.A. Naeth, and V.S. Baron. 1999. Soil compaction under grazing of annual and perennial forages. Can. J. Soil Sci. 79:191–199.
- Mullins, G.L., and C.H. Burmester. 1997. Starter fertilizer and the method and rate of potassium fertilizer effects on cotton grown on soils with and without winter grazing by cattle. Commun. Soil Sci. Plant Anal. 28:739–746.[CrossRef][Web of Science]
- Paul, E.A. 1984. Dynamics of organic matter in soils. Plant Soil 76:275–285.[CrossRef][Web of Science]
- Santruckova, H., O. Heinemeyer, and E.A. Kaiser. 1993. The influence of soil compaction on microbial biomass and organic-carbon turnover in microaggregates and macroaggregates. Geoderma 56:587–598.[CrossRef][Web of Science]
- SAS Institute. 2003. The SAS system for windows. Version 9.1. SAS Inst., Cary, NC.
- Schoonmaker, J.P., S.C. Loerch, J.E. Rossi, and M.L. Borger. 2003. Stock-piled forage or limit-fed corn as alternatives to hay for gestating and lactating beef cows. J. Anim. Sci. 81:1099–1105.[Abstract/Free Full Text]
- Shestak, C.J., and M.D. Busse. 2005. Compaction alters physical but not biological indices of soil health. Soil Sci. Soc. Am. J. 69:236–246.[Abstract/Free Full Text]
- Sidhu, D., and S.W. Duiker. 2006. Soil compaction in conservation tillage: Crop impacts. Agron. J. 98:1257–1264.[Abstract/Free Full Text]
- Stone, J.A., and B.R. Buttery. 1989. Nine forages and the aggregation of a clay loam soil. Can. J. Soil Sci. 69:165–169.
- Studdert, G.A., H.E. Echeverria, and E.M. Casanovas. 1997. Crop-pasture rotation for sustaining quality and productivity of a Typic Argiudoll. Soil Sci. Soc. Am. J. 61:1466–1472.[Abstract/Free Full Text]
- Sulc, R.M., and B.F. Tracy. 2007. Integrated crop–livestock systems in the U.S. Corn Belt. Agron J. 99:335–345.[CrossRef]
- Torbert, H.A., and C.W. Wood. 1992. Effects of soil compaction and water-filled pore-space on soil microbial activity and N losses. Commun. Soil Sci. Plant Anal. 23:1321–1331.[Web of Science]
- Tracy, B.F., and D.A. Frank. 1998. Herbivore influence on soil microbial biomass and nitrogen mineralization in a northern grassland ecosystem: Yellowstone National Park. Oecologia 114:556–562.[CrossRef][Web of Science]
- Twerdoff, D.A., D.S. Chanasyk, E. Mapfumo, M.A. Naeth, and V.S. Baron. 1999. Impacts of forage grazing and cultivation on near-surface relative compaction. Can. J. Soil Sci. 79:465–471.
- Unger, P.W., and T.C. Kaspar. 1994. Soil compaction and root-growth: A review. Agron. J. 86:759–766.[Abstract/Free Full Text]
- University of Illinois Extension. 2000. Illinois Agronomy Handbook. University of Illinois, Urbana.
- Voroney, R.P., and E.A. Paul. 1984. Determination of kc and kn in situ for calibration of the chloroform fumigation incubation method. Soil Biol. Biochem. 16:9–14.[CrossRef]
- Wagai, R., K.R. Brye, S.T. Gower, J.M. Norman, and L.G. Bundy. 1998. Land use and environmental factors influencing soil surface CO2 flux and microbial biomass in natural and managed ecosystems in southern Wisconsin. Soil Biol. Biochem. 30:1501–1509.[CrossRef]
- Ward, J.K. 1978. Utilization of corn and grain sorghum residues in beef cow forage systems. J. Anim. Sci. 46:831–840.[Abstract/Free Full Text]
- Worrell, M.A., D.J. Undersander, and A. Khalilian. 1992. Grazing wheat to different morphological stages for effects on grain yield and soil compaction. J. Prod. Agric. 5:81–85.
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