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1993 Proceedings of the Midwest Oak Savanna Conferences1993 Proceedings of the Midwest Oak Savanna Conferences

 

USE OF SOIL COLOR TO ASSESS THE ABSENCE OF WATER TABLE CHANGES WITHIN NATIVE WOODED ECOSYSTEMS SINCE SETTLEMENT

Richard Hootman and Patrick Kelsey
The Morton Arboretum
Route 53, Lisle, Illinois 60532
Tel: (312) 968-0074

 

Water tables in the soil can be measured directly using observation wells, or, in the absence of the water table, by using soil color. In the glacially derived soils of northeast Illinois, the yellowish and brownish colors result from iron from the soil parent materials. When soils with temperatures above 5oC are saturated for prolonged periods, iron becomes reduced. Because the reduced form of iron is more soluble, it is more easily leached from the soil profile. The resultant loss of iron leaves gray soil colors which reflect historic saturation elevations within the soil profile. Water table elevations (a reflection of soil saturation) were measured weekly in wooded ecosystems at the Morton Arboretum (1990-1992) and West Chicago Prairie (1991-1992) in northeastern Illinois. Observation wells set 1.5 m deep were established along soil catenas within topographic and vegetation gradients. The soil at each well site was examined and soil colors were recorded. Soil colors were compared with existing high water table elevation data to determine the degree of water table change since settlement of the area in the early 19th century. Seasonal high water tables were measured at or above elevations of gray soil colors associated with saturation, indicating that soil water tables are at levels at which they have been historically. Thus, precipitation infiltration and subsequent percolation through the soil have not changed since settlement.

INTRODUCTION

Most northeastern Illinois soils are derived from 12,000 to 14,000 year-old glacial deposits (Willman, 1971). Since that time, this region has experienced climatic fluctuations and associated shifting of plant communities reflecting the "forest-prairie tension zone" of the Prairie Peninsula (Davis, 1977; Geis and Boggess, 1968; King, 1981; Transeau, 1935). Such shifts complicate interpretation of soil development, historical vegetation change, and the definition of presettlement plant communities. Land surveys of the early to mid-nineteenth century recorded only one generation of the presettlement vegetation scenario in Illinois.

Soils provide a wealth of information for interpreting conditions prior to settlement. Historic drainage conditions and dominant vegetation cover can be determined from relict conditions within the modern soil profile. The use of soils information, therefore, is becoming more commonplace in understanding presettlement and modern ecological conditions in the Midwest (Kelsey and Hootman, 1992; Steiger, 1981; Whitney and Steiger, 1985).

One of the most important uses of soil color is for interpreting drainage class, which reflects many chemical, physical, and biological soil factors. Oxidized or ferric iron (Fe III) minerals provide the red, brown, and yellow coloration in subsoil horizons. Individual sand, silt, and clay particles in soil are coated with these abundant oxides; without the coatings, the soil particles would be gray. During periods of saturation, ferric iron is chemically reduced to ferrous iron (Fe II). Ferrous iron is more soluble than Fe III and more mobile. It moves easily with soil water and can be leached from the soil profile. Removal of iron through this process leaves the soil with gray colors called redoximorphic (redox) features (Soil Survey Staff, 1992). 

Soil color variables (hue, value, and chroma) are measured using a Munsell color chart (Soil Survey Staff, 1975). For example, with the color 10YR 5/2, 10YR is the hue, 5 is the value, and 2 is the chroma. The oxidation state of iron is expressed most strongly in the chroma color, therefore, reducing conditions are most typically measured with chroma colors. To reflect reducing conditions, gray redoximorphic features must have a color value of 4 or more and a color chroma of 2 or less (Soil Survey Staff, 1992). Color values less than 4 have likely been influenced by the addition of organic matter.

The abundance of redoximorphic features is related to the duration of reducing conditions (Vepraskas, 1992). The 2-chroma colors may dominate the soil matrix or may appear as mottles within the matrix. Greater coverage of 2-chroma redox features within a soil horizon indicates longerperiods of reduction.

Soil temperatures must be above 5oC for reducing conditions to exist. Above 5oC, the anaerobic bacteria essential in the reduction process are most active (Soil Survey Staff, 1975). This temperature also corresponds roughly to the start and end of the growing season.

Elevations of redox features within the soil profile correspond well to measured water table elevations within the same profile (Evans and Franzmeier, 1986; Franzmeier et al., 1983; Simonson and Boersma, 1972; Zobeck and Ritchie, 1984). Periods of seasonal high water table elevations, therefore, reflect the highest levels of soil saturation and, during the growing season, the maximum elevation at which reducing conditions occur. In the absence of a water table at the time of sampling a soil, redox features with a chroma of 2 or less can be used to verify the elevation of the seasonal high water table, and can reflect historic saturation and drainage characteristics within the soil.

Our study on woodlands at the Morton Arboretum and on the West Chicago Prairie was established to 1) classify soils in these two ecosystems and identify elevations of historic or relict redoximorphic features within them, 2) define extant seasonal high water table (soil saturation) levels in these wooded ecosystems, 3) correlate the redoximorphic features with existing high water table elevations, and 4) determine the extent of soil disturbance imposed since settlement and whether this has impacted surface and subsurface soil water movement.

STUDY AREAS

The 607 ha Morton Arboretum in DuPage County, Illinois, approximately 40 km west of Chicago, contains more than 250 ha of native woodland communities. The three Arboretum sites presented in this study represent a soil catena within a Quercus alba and Q. rubra closed canopy woodland. Soils developed in approximately 50 cm of loess over silty clay loam glacial till. The Typic Hapludalf in the study area is moderately well drained and the Aquic Hapludalf is somewhat poorly drained. Each is an Alfisol or forest-derived soil. The Typic Epiaquoll is a poorly drained Mollisol or prairie-derived soil located along a drainageway within the woodland. Local relief in the study area is 3.35 m.

The 120 ha West Chicago Prairie Forest Preserve, 50 km west of Chicago near West Chicago, Illinois, is managed by the Forest Preserve District of DuPage County. The study area within West Chicago Prairie presented in this paper is an oak savanna - predominantly Quercus macrocarpa and Q. velutina in the overstory - which developed on 50 to 100 cm of silty materials over sand and gravel glacial outwash. Three of the seven water table monitoring sites established on the savanna are presented in this study. These sites represent three Alfisols: a Typic Hapludalf (moderately well drained), a Mollic Endoaqualf (somewhat poorly drained), and a Typic Endoaqualf (somewhat poorly drained) (Soil Survey Staff, 1992). Local relief in the study area is 1.04 m. 

METHODS

Water table monitoring wells were established to a depth of 1.5 m at each site. The wells consisted of 3 cm-diameter solid wall PVC pipe. Water tables were measured weekly from spring thaw until winter freeze-up in 1990-1992 at the Arboretum and 1991-1992 at West Chicago Prairie.

Soils were described at each study site to a depth of 1.5 m and classified using Keys to Soil Taxonomy (Soil Survey Staff, 1992). Soil color variables (hue, value, and chroma) were determined using Munsell color charts.

RESULTS AND DISCUSSION

Precipitation levels in northeast Illinois in 1990 were above normal throughout the year. Spring and summer of 1991 were very dry, but autumn was wetter than average. Spring drought occurred again in 1992, but rainfall returned to near average by July. Water tables are a response to precipitation, and water tables were higher throughout 1990 compared to growing seasons of the other study years at the Arboretum (Fig. 1). At depths of 50 cm and higher, soil temperatures above 5oC were reached on April 18 in 1990, April 9 in 1991, and April 8 in 1992 (Morton Arboretum, unpublished data) allowing reducing conditions to develop in saturated soils for those years. After November 6, 1990 and 1991, and November 12, 1992, soil temperatures fell below 5oC at some depth above 50 cm (Morton Arboretum, unpublished data), curtailing reducing conditions.

Soils at both study areas have been relatively undisturbed physically and chemically. Grazing likely occurred on a portion of each site. Nevertheless, surface soil structure was normal within each profile examined suggesting that if grazing occurred, it did not create a lasting impact on the soil (Tables 1 and 2). No significant sheet or rill erosion has been noted in the study areas. Soil pH was 5.5 to 6.5 in the upper 55 cm at the West Chicago sites and 4.5 to 6.0 above 60 cm within the Arboretum Alfisols, implying long-term development beneath a forest canopy without prairie, and no anthropogenic chemical alteration (Tables 1 and 2). The Mollisol in the study also appeared undisturbed.

Depths of 2-chroma redox features and measured water table elevations in soils at the Morton Arboretum are presented (Fig. 1 and Table 1) and those at West Chicago Prairie (Fig. 2 and Table 2) indicate that the highest water tables occurred from late autumn until mid- to late spring. The Typic Hapludalfs at both study areas had water table elevations well above the 2-chroma elevations for several weeks early in each of the growing seasons (Figures 1 and 2). Franzmeier et al. (1983), Simonson and Boersma (1972), and Zobeck and Ritchie (1984) noted water tables often were above levels of 2-chroma redox features. Reasons for this may be interpreted from Franzmeier et al. (1983) who found that 3-chroma colors represented saturated soils with lesser periods of reduction in Indiana, often within Hapludalfs. The same appears true in this study. The 3-chroma colors on the Arboretum Typic Hapludalf occur at a depth of 20 cm (233.48 m elevation) and on West Chicago they occur at a depth of 23 cm (231.45 m elevation), elevations that are higher than the 2-chroma elevations and correspond much better to the seasonal high water tables (Figs. 1 and 2). Evans and Franzmeier (1986) and Franzmeier et al. (1983) indicate that reduction is virtually nonexistent until soil temperatures rise above 10oC. Indeed, soil temperatures rise above 10oC around May 1 in northern Illinois (Morton Arboretum, unpublished data), about which time water tables drop below 2-chroma features in the Typic Hapludalf of each study site. 

The two Endoaqualfs at West Chicago show a good correlation to 2-chroma redox features (Fig. 2). The Mollic Endoaqualf water table was at or above the 2-chroma elevation for one to two weeks early each growing season. The Typic Endoaqualf water table was at or above the 2-chroma elevation, and the soil surface, for several weeks each season. Redox features may exist within the A horizon of this soil, but the dark surface color may mask them.

This same trend is noted in the more poorly drained Arboretum woodland soils (Fig. 1). Most of the high water tables measured within these soils occurred above the zone of redox features. The color of the E horizon of the Aquic Hapludalf and the black A horizon of the Typic Epiaquoll probably mask redox features higher in these profiles.

Wilhelm (1991) suggests the soils of Arboretum woodlands are eroding because of excessive runoff and the inability of the soils to absorb and "hold" moisture. Subsequent lack of rainfall infiltration and percolation within the soils is resulting in a concomitant lowering of the water table (Wilhelm, 1991). These suggested changes are blamed on modification of the vegetation, primarily removal of the herbaceous cover. On the contrary, water table data collected on these study sites show existing high water tables to be as high as what redox features indicate existed within these soils historically. The abundance of redox features within the soils studied appears to adequately reflect the amounts of saturation and reduction now occurring within them. Soils with longer periods ofreduction during the growing season had more abundant redox features.

Although spring drought was significant in 1991 and 1992, water table elevations in the Morton Arboretum woodlands were as high or higher than those in 1990. West Chicago Prairie data also show high water tables during the spring droughts. This is an indication of these soils' ability to maintain moisture levels, and that water table depletion within the soil is a reflection of uptake by plants during the growing season and not water loss due to surface runoff. Whether or not the woody or herbaceous cover has changed over the last 150 years, the existing canopy during the growing season and litter layer during winter have maintained the hydrological, physical, and chemical integrity of these soils.

Acknowledgements

We would like to acknowledge Wayne Lampa and the Forest Preserve District of DuPage County for establishing the monitoring wells at West Chicago Prairie Forest Preserve and allowing us to collect soil and water table information, and Christopher Whelan and Marlin Bowles of the Arboretum for reviewing this manuscript.

LITERATURE CITED

Davis, A.M. 1977. The prairie-deciduous forest ecotone in the upper middle west. Annals Assoc. Amer. Geog. 67:204-213.

Evans, C.V. and D.P. Franzmeier. 1986. Saturation, aeration, and color patterns in a toposequence of soils in north-central Indiana. Soil Sci. Soc. Am. J. 50:975-980.

Franzmeier, D.P., J.E. Yahner, G.C. Steinhardt, and H.R. Sinclair, Jr. 1983. Color patterns and water table levels in some Indiana soils. Soil Sci. Soc. Am. J. 47:1196-1202.

Geis, J.W. and W.R. Boggess. 1968. The Prairie Peninsula: its origin and significance in the vegetational history of central Illinois. pp. 89-95. In: Robert E. Bergstrom (ed.) The Quaternary of Illinois: A Symposium in Observance of the Centennial of the University of Illinois.

Kelsey, P.D. and R.G. Hootman. 1992. Relationships between water tables, plant communities, and hydric soils: West Chicago Prairie, West Chicago, Illinois. Soil Surv. Horiz. 33:53-58.

King, J.E. 1981. Late Quaternary vegetational history of Illinois. Ecol. Monog. 51:43-62.

Simonson, G.H. and L. Boersma. 1972. Soil morphology and water table relations: II. Correlation between annual water table fluctuations and profile features. Soil Sci. Soc. Am. Proc. 36:649-653.

Soil Survey Staff. 1975. Soil taxonomy: A basic system of soil classification for making and interpreting soil surveys. USDA-SCS Agric. Handb. 436. U.S. Gov. Print. Office, Washington, DC.

Soil Survey Staff. 1992. Keys to soil taxonomy. Soil Management Support Services Tech. Monog. No. 19. Pocahontas Press, Inc., Blacksburg, VA.

Steiger, J.R. 1981. Soils of the prairies in western Ohio. Ohio Biol. Surv. Biol. Notes No. 15:101-107.

Transeau, E.N. 1935. The Prairie Peninsula. Ecology 16:423-437.

Vepraskas, M.J. 1992. Redoximorphic features for identifying aquic conditions. North Carolina Agric. Res. Service Tech. Bull. 301. North Carolina State University, Raleigh. 33 pp.

Whitney, G.G. and J.R. Steiger. 1985. Site-factor determinants of the presettlement prairie-forest border areas of north-central Ohio. Bot. Gaz. 146:421-430.

Wilhelm, G.S. 1991. Implications of changes in floristic composition of the Morton Arboretum's east woods. pp. 31-54. In: Proceedings of the Oak Woods Management Workshop. Eastern Illinois University, Charleston.

Willman, H.B. 1971. Summary of the geology of the Chicago area. Illinois State Geological Survey Circular 460, Urbana. 77 pp.

Zobeck, T.M. and A. Ritchie. 1984. Analysis of long-term water table depth records from a hydrosequence of soils in central Ohio. Soil Sci. Soc. Am. J. 48:119-125.

Table 1. Soil horizons and profile descriptions for the Morton Arboretum

Typic Hapludalf
  • A 0-10 cm; very dark grayish brown (10YR 3/2) silt loam; weak medium granular structure; friable; slightly acid (pH 6.1-6.5). 
  • E10-20 cm; grayish brown (10YR 5/2) silt loam; very dark grayish brown (10YR 3/2) root channels; weak, fine platy structure; friable; strongly acid (pH 5.1-5.5).
  • Bt1 20-40 cm; dark yellowish brown (10YR 4/4) silty clay loam; dark brown (10YR 4/3) clay coatings on peds; very dark grayish brown (10YR 3/2) organic matter coatings on peds; moderate, fine angular blocky structure; firm; strongly acid (pH 5.1-5.5).
  • Bt240-58 cm; dark yellowish brown (10YR 4/4) silty clay with dark brown (10YR 4/3) clay coatings; strong, medium angular blocky structure; very firm; strongly acid (pH 5.1-5.5).
  • 2Bt358-74 cm; dark brown (10YR 4/3) silty clay loam; few, fine, faint yellowish brown (10YR 5/6) mottles; discontinuous grayish brown (10YR 5/2) coatings on peds; strong, medium, subangular blocky structure; strongly acid (pH 5.1-5.5).
  • 2C74-150 cm; mixed dark brown (10YR 4/3), grayish brown (10YR 5/2), and olive brown (2.5Y 4/3) silt loam; weak, medium subangular blocky structure grading to massive; very firm; neutral (pH 7.0-7.3).
Aquic Hapludalf
  • A0-10 cm; very dark grayish brown (10YR 3/2) silt loam; weak fine granular structure; friable; neutral (pH 7.0-7.3).
  • E10-20 cm; dark grayish brown (10YR 4/2) silt loam; weak fine platy structure; few fine faint yellowish brown (10YR 5/6) mottles; friable; strongly acid (pH 5.1-5.5).
  • BE20-33 cm; dark brown (10YR 4/3) silty clay loam; weak fine subangular blocky structure; few fine faint grayish brown (10YR 5/2) and yellowish brown (10YR 5/6) mottles; firm; very strongly acid (pH 5.1-5.5).
  • Bt133-51 cm; dark yellowish brown (10YR 4/4) silty clay; weak medium angular blocky structure; dark brown (10YR 4/3) clay coatings; few fine faint gray (10YR 5/1) and common fine distinct yellowish brown (10YR 5/6) mottles; few fine faint black (10YR 2/1) manganese concretions; firm; very strongly acid (pH 4.5-5.0).
  • 2Bt251-63 cm; dark yellowish brown (10YR 4/4) silty clay loam; weak medium subangular blocky structure; dark brown (10YR 4/3) clay coatings; few fine faint gray (10YR 5/1) and common fine distinct yellowish brown (10YR 5/6) mottles; black (10YR 2/1) root channels; firm; medium acid (pH 5.6-6.0).
  • 2BC63-81 cm; dark yellowish brown (10YR 4/4) silty clay loam; weak fine subangular blocky structure; common medium distinct grayish brown (10YR 5/2) and yellowish brown (10YR 5/6) mottles; black (10YR 2/1) root channels; firm; slightly acid (pH 6.1-6.5).
  • 2C81-150 cm; brown (10YR 5/3) clay loam; weak fine subangular blocky structure; common medium distinct grayish brown (2.5Y 5/2) and brownish yellow (10YR 6/8) mottles; black (10YR 2/1) root channels; firm; moderately alkaline (pH 7.9-8.2).
Typic Epiaquoll
  • A0-25 cm; black (N 2/0) silty clay loam; few, fine, faint light olive brown (2.5Y 5/4) mottles; weak, fine, subangular blocky structure; friable; neutral (pH 7.0-7.3).
  • Bg125-41 cm; dark grayish brown (2.5Y 4/2) silty clay loam; common, medium, distinct yellowish brown (10YR 5/6) mottles; discontinuous olive gray (5Y 4/2 and 5/2) ped coatings; weak, medium subangular blocky structure; firm; medium acid (pH 5.6-6.0).
  • 2Bg241-51 cm; dark grayish brown (2.5Y 4/2) silty clay loam; common, medium, distinct yellowish brown (10YR 5/6) mottles; moderate, fine subangular blocky structure; very firm; medium acid (pH 5.6-6.0).
  • 2Cg 51-150 cm; mixed olive gray (5Y 5/2), light olive brown (2.5Y 5/6), and brownish yellow (10YR 6/8) silty clay loam; moderate, medium subangular blocky structure grading to massive; very firm; neutral (pH 7.0-7.3). 

Table 2. Soil horizons and profile descriptions for the Morton Arboretum

Typic Hapludalf 
  • A0-13 cm; black (10YR 2/1) silt loam; moderate medium granular structure; friable; neutral (pH 7.0-7.3).
  • E13-23 cm; brown (10YR 4/3) silt loam; moderate medium subangular blocky structure; friable; slightly acid (pH 6.1-6.5).
  • BE23-36 cm; brown (10YR 4/3) silty clay loam; strong medium subangular blocky structure; firm; medium acid (pH5.6-6.0).
  • Bt136-56 cm; dark yellowish brown (10YR 4/4) silty clay loam; strong medium angular blocky structure; brown (10YR 4/3) and dark brown (10YR 3/3) continuous clay coatings; very dark grayish brown and (10YR 3/2) and black (10YR 2/1) krotovinas; firm; medium acid (pH 5.6-6.0).
  • Bt256-71 cm; dark yellowish brown (10YR 4/4) clay loam; weak medium subangular blocky structure; brown (10YR 4/3) continuous clay coatings; firm; slightly acid (pH 6.1-6.5).
  • 2BC71-102 cm; dark grayish brown (2.5Y 4/2), brown (10YR 4/3), and yellowish brown (10YR 5/6) gravelly clay loam; weak coarse subangular blocky structure grading to massive; firm; neutral (pH 7.0-7.3).
  • 2C102-150 cm; olive brown (2.5Y 4/4), yellowish brown (10YR 5/6), and grayish brown (2.5Y 5/2) sandy loam; massive; firm; moderately alkaline (pH 7.9-8.2). 
Mollic Endoaqualf 
  • A0-23 cm; black (10YR 2/1) silt loam; moderate fine granular structure; friable; medium acid.
  • BE23-38 cm; dark grayish brown (10YR 4/2) silty clay loam; moderate medium subangular blocky structure; black (10YR 2/1) organic matter coatings; friable; medium acid (pH 5.6-6.1)

  • .
  • Bt138-58 cm; brown (10YR 4/3) silty clay loam; strong medium subangular blocky structure; dark grayish brown (10YR 4/2) continuous clay coatings; few fine distinct grayish brown (10YR 5/2) and yellowish brown (10YR 5/6) mottles; very firm; slightly acid (pH 6.1-6.5).
  • Bt258-79 cm; brown (10YR 5/3) silty clay loam; moderate medium prismatic structure parting to moderate mediumangular blocky structure; dark grayish brown (10YR 4/2) continuous clay coatings; black (10YR 2/1) organic matter coatings; common fine distinct light grayish brown (10YR 6/2) and gray (10YR 5/1) mottles; firm; neutral (pH 7.0-7.3).
  • 2BC79-102 cm; light brownish gray (2.5Y 6/2) light silty clay loam; weak medium prismatic structure; grayish brown (2.5Y 5/2) discontinuous clay coatings; common fine distinct yellowish brown (10YR 5/6) mottles; firm; mildly alkaline (pH 7.4-7.8).
  • 2C102-150 cm; light brownish gray (2.5Y 6/2) and brown (10YR 5/3) stratified sandy loam and silt loam; single grain and massive; common fine distinct yellowish brown (10YR 5/6) mottles; moderately alkaline (pH 7.9-8.2). 
Typic Endoqualf 
  • A0-10 cm; very dark grayish brown (10YR 3/2) silt loam; weak medium granular structure; friable; neutral (pH 7.0-7.3). 
  • EB10-20 cm; grayish brown (10YR 5/2) silt loam; weak fine platy structure; very dark grayish brown (10YR 3/2) organic matter coatings; friable; medium acid (pH 5.6-6.0).
  • BE20-28 cm; grayish brown (10YR 5/2) silt loam; weak, medium subangular blocky structure; grayish brown (10YR 3/2) clay coatings; few fine distinct yellowish brown (10YR 5/6) mottles; firm; medium acid (pH 5.6-6.0). 
  • Btg128-41 cm; dark grayish brown (2.5Y 4/2) silty clay loam; strong very fine subangular blocky structure; grayish brown (10YR 5/2) continuous clay coatings; few fine distinct yellowish brown (10YR 5/6) mottles; firm; medium acid (pH 5.6-6.0). 
  • Btg241-51 cm; dark grayish brown (2.5Y 4/2) silty clay; moderate medium subangular blocky structure; grayish brown (10YR 5/2) clay coatings; common fine medium and distinct yellowish brown (10YR 5/6) mottles; firm; medium acid (pH 5.6-6.0). 
  • Btg351-81 cm; olive gray (5Y 4/2) silty clay loam; moderate coarse subangular blocky structure; dark grayish brown (2.5Y 4/2) clay coatings; common medium distinct yellowish brown (10YR 5/6) and strong brown (7.5YR 4/6) mottles; black (10YR 2/1) manganese concretions;reddish brown (5YR 5/4) iron concretions; firm; neutral (pH 7.0-7.3). 
  • 2Cg181-122 cm; olive gray (5Y 4/2) and dark grayish brown (2.5Y 4/2) clay loam; massive; common medium distinct yellowish brown (10YR 5/6) and strong brown (7.5YR 4/6) mottles; black (10YR 2/1) manganese concretions; reddish brown (5YR 5/4) iron concretions; neutral (pH 7.0-7.3). 
  • 2Cg2122-150 cm; reddish yellow (7.5YR 6/6) and yellowish brown (10YR 5/6) sand; single grain; neutral (pH 7.0-7.3). 

 

 

 
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