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a Environmental Science Graduate Program, Ohio State Univ., 2021 Coffey Road, Columbus, OH 43210 USA
b School of Natural Resources, Ohio State Univ., 2021 Coffey Road, Columbus, OH 43210 USA
bigham.1{at}osu.edu
| ABSTRACT |
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Abbreviations: CBD, citrate-bicarbonate-dithionite DTA, differential thermal analysis FC%mass, fractional conversion factor for magnetic susceptibility TG, thermogravimetric analysis XRD, x-ray diffraction
fd, frequency-dependent magnetic susceptibility
lf, low frequency mass specific magnetic susceptibility
| INTRODUCTION |
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Whenever he saw the sea, or a fire, he fell silent, impressed by their elemental force.Paulo Coelho, The Alchemist
SMALL-SCALE RUBBER FARMERS in Sepunggur, Sumatra, Indonesia, indicated in a recent survey that fire is widely used to clear forests because it provides an easy and economical means of increasing access to the fields (Ketterings et al., 1999). Forest vegetation is slashed in the beginning of the dry season (MarchApril) and burned from June through August. If a first-time broadcast burn does not remove enough aboveground biomass, the remaining wood is piled in heaps of 200 to 400 kg and burned a second time.
Peak temperatures measured at the soil surface during broadcast and subsequent secondary burns vary widely. Intensities depend not only on the fuel load and the water content of the slashed biomass (Brown, 1988) but also on the stacking pattern, climatic conditions during the burn, and the size of the area being burned. Hartford and Frandsen (1992) measured maximum surface temperatures of 400°C in a ground (litter and duff) fire, and Sertsu and Sanchez (1978) reported temperatures >500°C in shifting cultivation fires. Similar intensities have been recorded by Wells et al. (1979) and Chandler et al. (1983), whereas burns in Senegal reportedly reached levels >700°C (Masson, 1948).
Heat transfer into the soil depends not only on the surface temperature but also on the duration of exposure, on the water content of the soil, and the soil pore distribution (Steward et al., 1990). Ghuman and Lal (1989) measured temperatures of 218°C at 1 cm below the soil surface in windrows burned after clearing a tropical rainforest. Temperatures dropped to 150, 104, and 70°C at 5-, 10-, and 20-cm depths, respectively. DeBano et al. (1979), as reported in Brown (1988), found that temperatures at the 5-cm depth did not change significantly even when surface temperatures reached 700°C.
Numerous papers have shown that low-intensity burns (<250°C) affect soil biological and chemical properties (e.g., Nye and Greenland, 1960), but the impact of burning on soil mineralogy has not been widely evaluated even though moderate (250500°C) and severe fires (>500°C) have the potential to cause mineral transformations. Kaolinite, for example, has been shown to decompose at temperatures between 500 and 700°C (Richardson, 1972). Gibbsite may be completely destroyed by heating in air at 200°C (Rooksby, 1972), and goethite is altered to hematite at
300°C (Cornell and Schwertmann, 1996). Synthetic magnetite transforms to maghemite at temperatures as low as 220°C (Sidhu, 1988), and pure maghemite may revert to hematite at temperatures around 350°C (Mullins, 1977). However, natural maghemites are often stabilized by impurities giving rise to transformation temperatures exceeding 600°C (Mullins, 1977).
Most studies of the heat stability of minerals have been performed in the laboratory with either synthetic or purified natural minerals. Under field conditions, fire has been observed to collapse some 2:1 phyllosilicates and destroy kaolinite (Ulery et al., 1996). The presence of maghemite in soils has often been attributed to the dehydroxylation of goethite or lepidocrocite by burning in the presence of organic matter (Van der Marel, 1951; Taylor and Schwertmann, 1974; Anand and Gilkes, 1987; Stanjek, 1987). Maghemite formation is of interest because of its ferrimagnetic character and the potential for using magnetic techniques to evaluate the conversion process. Magnetic susceptibility (the total magnetic force in a material divided by the strength of the magnetic field inducing magnetization) is one such method.
Besides aiding in the identification of Fe oxide transformations due to fire, magnetic susceptibility measurements may give an indication of fire intensity when results are expressed as frequency-dependent magnetic susceptibility (
fd) or as a fractional conversion factor (FC%mass). Dearing (1994) has suggested that soils with
fd between 10 and 15% are dominated by ultrafine ferrimagnetic particles that are often products of high-intensity burning. The FC%mass is calculated as the ratio of the magnetic susceptibility of a field soil to the magnetic susceptibility of the same soil after being exposed to 550°C for 8 h in an oven. High values of the fractional conversion factor indicate that Fe oxide conversion took place prior to reheating. Lower values are obtained where prior burning was either absent or of low intensity. In situations where laboratory facilities for XRD are not available, Fe concentrations are very low, field measurements are needed, or the amount of sample is limited, magnetic susceptibility may be a good tool for measuring fire intensities and fire-induced changes in Fe oxides.
We investigated the effect of heat intensity on the mineralogy of Oxisols in the Sepunggur area, Jambi Province, Sumatra, Indonesia, where slash-and-burn agriculture is still commonly used (Ketterings et al., 1999). Our objectives were to evaluate (i) the effects of burn intensity on soil mineralogy, (ii) the use of magnetic susceptibility as a tool for measuring burn intensity, and (iii) factors influencing changes in magnetic susceptibility.
| Materials and methods |
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Field Experiment I
Field Experiment I was a 12- to 15-yr-old secondary forest that was burned in July 1997. The entire field (0.75 ha) was subjected to a low-intensity broadcast burn by the farmer. Following the broadcast burn, three burn piles were established (400 kg of wood with stem diameters between 3.2 and 6.4 cm) on an area of 3 by 3 m. The piles were ignited, and temperatures were measured using heat-sensitive crayons (Cole Parmer, Vernon Hills, IL) situated directly on top of the mineral soil and beneath any existing vegetative litter. Crayons were placed in the center, at the edge, and outside each pile. A control sample was taken in a 12- to 15-yr-old secondary forest near the burned field (Table 1)
. The farmer indicated that the age of the forest surrounding the burned plot was identical to the forest that was slashed, burned, and sampled during this experiment. Therefore, the samples taken in the forest reflect the situation prior to slash-and-burn, the samples taken outside the piles reflect the situation after a low-intensity broadcast burn, and the samples taken underneath the piles reflect the effect of high-intensity secondary fires at two temperatures. All locations were sampled at depths of 0 to 5 cm (hereafter referred to as topsoil) and 5 to 15 cm (hereafter referred to as subsoil). Ash, charcoal, and unburned wood remaining on the field after the secondary burn were carefully removed prior to soil sampling. Each location was sampled before the burn and 1 d and 1, 2, 4, 8, and 12 wk after the burn. Soil water contents (105°C) were determined at each sampling time. Samples were returned to the laboratory the same day, sieved through a 2-mm sieve, and air-dried for further analysis.
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Routine Soil Analyses
Whole soil samples were analyzed for organic C according to the WalkleyBlack method (Walkley, 1947). The pH was determined electrometrically in a 1:5 mass ratio of soil/water after shaking the samples on a reciprocal shaker for 2 h. Particle-size analyses were performed using standard sieve and pipette methods (Kilmer and Alexander, 1949) following removal of organic matter with 30% (w/w) H2O2. The samples were extracted with citrate-bicarbonate-dithionite (CBD) (Mehra and Jackson, 1960) to dissolve crystalline Fe oxides, except magnetite. Final extracts were analyzed for Fe by atomic absorption spectrophotometry.
Soil Fractionation
Soil samples taken from Field Experiment II and from Field Experiment I before the second burn were treated with 1 M NaOAc-HOAc buffer (pH 5) and 30% (w/w) H2O2 to remove organic matter (Jackson, 1975). The residual materials were washed free of excess salts, dispersed in water, and separated into sand (20.05 mm), silt (0.050.002 mm), and clay (<0.002 mm) fractions using standard sieve and gravity sedimentation techniques (Jackson, 1975). The sand and silt fractions were dried at 60°C, whereas the clays were Na-saturated, quick frozen, and freeze-dried.
Magnetic Susceptibility
All whole soil samples and particle-size fractions were analyzed for magnetic susceptibility with a Bartington MS2 Susceptibility System (ASC Scientific, Carlsbad, CA). This system was equipped with a dual-frequency sensor that accepted 10-cm3 samples in standard plastic pots. Mass-specific magnetic susceptibility was calculated as the volume-specific susceptibility (
) divided by the density of the sample in the 10-cm3 pots. Low-frequency (0.46 kHz) magnetic susceptibility (
lf, units of m3 kg-1) was measured for all samples prior to exposing them to a high-frequency magnetic field (4.6 kHz). The dual-frequency measurements permitted the calculation of frequency-dependent magnetic susceptibility as:
![]() | (1) |
fd is the volume-specific frequency-dependent magnetic susceptibility in percentage,
lf is the low-frequency (0.46 kHz) volume-specific magnetic susceptibility x 10-5, and
hf is the high-frequency (4.6 kHz) volume-specific magnetic susceptibility x 10-5. The mean diamagnetic volume specific magnetic susceptibility of the standard 10-cm3 pot was -0.4 x 10-5. All volume-specific magnetic susceptibility measurements were adjusted for this value prior to calculating mass-specific susceptibility. Soils with
fd between 10 and 15% were considered to contain ultrafine (<0.035 µm) ferrimagnetic minerals as reported by Dearing (1994).
A second set of dried (60°C) samples was exposed to 550°C for 8 h and analyzed for
lf after cooling to room temperature. Fractional conversion values, which may serve as indicators of prior burning (Dearing, 1994), were calculated as:
![]() | (2) |
lf is the mass-specific low-frequency (0.46 kHz) magnetic susceptibility x 10-8 m3 kg-1, and
lf @ 550°C is the
lf of 550°C exposed soil x 10-8 m3 kg-1.
X-Ray Diffraction
The sand and silt samples were ground in a ceramic mortar and pestle to pass a 250-µm sieve and backfilled to produce randomly oriented sample mounts. Two-hundred milligrams of each clay were mixed with 15 mL of deionized water, and one drop of 0.5 M NaOH was added to enhance dispersion. The suspensions were then ultrasonically dispersed for 30 s, and 5 mL of the suspension were filtered through a 0.22-µm Millipore filter (Millipore Corp., Bedford, MA). Filtration was stopped when the deposits were almost dry. The oriented aggregates were then transferred onto glass slides for XRD analyses. The oriented clays were scanned after air drying and after heating to 550°C for 4 h. All samples were analyzed with a Philips diffractometer (Philips Elec. Inst., Mahwah, NJ) using CuK
radiation (35 kV, 20 mA) and a graphite monochromater. Measurements were made by step scanning with a fixed time of 4 s per 0.05°2
for routine work and a fixed time of 6 s per 0.01°2
for detailed analyses of Fe oxides. In most cases, the XRD patterns were obtained from 2 to 70°2
. Minerals occurring in the sand, silt, and clay fractions were identified on the basis of their diagnostic XRD peaks and their response to heating. Hydroxy-Al vermiculite was distinguished from vermiculite and chlorite by the partial collapse of the 1.4-nm peak with heating to 550°C.
Thermal Analysis
Thermal analyses of clay and silt samples were conducted to quantify kaolinite and gibbsite concentrations using a Seiko SSC 5020 instrument (Haake Inst., Paramus, NJ) that provided simultaneous thermogravimetric (TG) and differential thermal analysis (DTA). Approximately 50 mg of sample were heated from 25 to 1000°C at a rate of 20°C min-1 under a continuous flow (200 mL min-1) of dry N2 gas. Calibration of the temperature signal was achieved using the melting points of In and Sn. Calibration of the thermal balance was performed using a reference weight provided by the instrument manufacturer. Thermal events associated with dehydroxylation of kaolinite and gibbsite were assigned based on published literature (e.g., Dixon, 1966) and analyses of standard mineral samples.
Oven Experiment I: Effect of Added Carbon
Duplicate, 10-g samples of forest soil (05 and 515 cm) from the control area of Field Experiment II were mixed with 0, 20, 40, 80, 100, 150, and 200 g kg-1 air-dried, processed Indian tea (Camellia sinensis L.) or 50 and 100 g kg-1 granulated sugar. Samples were exposed to 600°C for 930 min to ensure the complete conversion of antiferromagnetic to ferrimagnetic minerals. Weight loss, water content, and magnetic susceptibility were measured after heating. The tea used in this experiment was combusted at 600°C for 8 h to determine the ash content by weight loss.
Oven Experiment II: Kinetics
Duplicate 25-g soil samples (05 and 515 cm) from the control area of Field Experiment II were placed in 2-cm-diam. glass vials and heated in a muffle furnace. Samples were exposed to 300 or 600°C for 1, 2, 4, 6, 10, 15, 30, 45, 90, 120, 240, 360, and 660 min. Weight loss, water content, and magnetic susceptibility were measured after heating. Samples were, in addition, analyzed for CBD-extractable Fe oxides. The magnetic susceptibility of the material remaining after CBD extraction was measured in order to determine the contribution of the CBD-extractable Fe oxides to the total magnetic susceptibility.
Statistical Analyses
All results of Field Experiment I were initially analyzed in a complete randomized block design in three replicates with three factors: treatment (forest, first burn estimated as 100°C exposure, 300°C exposure during second burn, and 600°C exposure during second burn), depth (05 and 515 cm), and time (0, 1, 7, 14, 28, 56, and 84 d after burning). Parameters were considered time dependent when differences over time were larger than the standard deviations of the individual treatments, the uncertainty of the means when sampling in triplicate, or the standard deviations of the forest treatment. Analyses of the 60 grid samples (05 cm depth) in the forest neighboring that of Field Experiment I showed that taking three samples to calculate a mean
would result in an uncertainty of the mean of 63.7 x 10-8 m3 kg-1 for
lf and 2.6% for
fd. Uncertainties for the subsoil (515 cm) means were less: 26.3 x 10-8 m3 kg-1 for
lf and 1.9% for
fd. Although several magnetic susceptibility parameters showed significant differences among sampling times, those differences did not follow a recognizable pattern. Nor were they larger than the standard deviations of the parameters in the forest treatment or the uncertainty of the mean estimates when taking three replicates. The time series samples of Field Experiment I were thus combined to calculate the average for each replicate per treatment per layer for further heat exposure comparisons. Because the samplings over time cannot be considered completely independent, we calculated the averages of the 18 measurements and analyzed Field Experiment I as a two-factorial experiment (fire intensity at four levels and depth of sampling at two levels) in three replicates. Analyses of variance were performed using the software package Genstat 5 for Windows, Release 3.2 (Genstat 5, 1987).
Field Experiment II did not have independent replicates due to the fact that bulk samples were taken. Each bulk sample was separated into two subsamples that were analyzed separately and in duplicate in order to assess the precision of the measurements. Results were expressed as means and standard deviations.
| Results and discussion |
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The sand fraction contributed <3% of the total soil magnetic susceptibility after all heat treatments except for the combusted topsoil, where it was responsible for 84% of the total (Table 3) . The glassy, sand-sized particles showed high spontaneous magnetization, with
lf values of 2584 x 10-8 m3 kg-1 (Table 3). The magnetic susceptibility of the subsoil sand fraction was one-half that of the overlying topsoil in areas exposed to 600°C surface temperatures. Silt in the forest soil contained quartz, gibbsite, kaolinite, goethite, anatase, and traces of hydroxy-Al-vermiculite. Once again, burning the topsoil resulted in a decrease in quartz peak intensities after exposure to 600°C (Fig. 1)
. A decrease in gibbsite concentration occurred at 300°C and was evident in both XRD (Fig. 1) and TG analyses (Table 4)
. No further reductions with heating were noted from thermal analysis, but XRD peaks for gibbsite decreased in intensity at 600°C and were absent in the combusted (>600°C) topsoil (Fig. 1). Kaolinite concentrations in the silt fraction of the topsoil were mostly unaltered by heating. In the subsoil, quartz peak intensities remained unchanged through 300°C but were lower after exposure to 600°C (data not shown). Kaolinite, gibbsite, and goethite concentrations in the subsoil silt fractions were unaltered by the surface fires. Heat exposure increased the magnetic susceptibility of silt fractions from both the topsoil and subsoil (Table 3).
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lf of the maghemite can be calculated as 53870 x 10-8 m3 kg-1 if we assume that these particles are mostly maghemite. This value corresponds well with the
lf of 54000 x 10-8 m3 kg-1 found by Graham and Scollar (1976) and is slightly higher than those previously reported for pure maghemites (Mullins, 1977; Dearing, 1994).
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lf of forest topsoil increased upon exposure to fire (600°C) by a factor of 1.2, whereas in Field Experiment II the increase was by a factor of 15.5 (compare
lf for forest with
lf at 600°C in Table 5)
. Furthermore, the magnetic susceptibility of unburned forest soil in Field Experiment I was six times (topsoil) and four times (subsoil) larger than the magnetic susceptibility of the forest soil in Field Experiment II. The FC%mass values for topsoil amounted to 20.8 and 2.3% for Field Experiments I and II, respectively. For subsoil, the FC%mass values were 56.2 and 1.7% for Field Experiment I and II, respectively. These observations suggest that the field in Field Experiment II had not been seriously impacted by prior burns; whereas, the forest soil in Field Experiment I had probably been burned previously. The topography of the field in Field Experiment I was flat, and the area was surrounded by forest. We therefore can assume that erosion did not play a major role in changing the magnetic susceptibility of the soil so that the effects of burning may be detectable for long periods of time.
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lf and
fd in the topsoil (05 cm) at both field sites (Table 5); however, the increases were more dramatic in Field Experiment II. Subsoil (515 cm) effects were absent in Field Experiment I and present but less extreme than in the 0- to 5-cm depth at Field Experiment II. These results suggest that heat transfer did not reach below 5 cm in Field Experiment I but did at Field Experiment II. The location of Field Experiment II (on top of a small hill), favorable climatic conditions, a longer period of drying after the slash, and a larger burn area might have contributed to higher fire intensities and deeper heat penetration into the soil at this site relative to Field Experiment I. An increase in
fd indicates the formation of ultrafine superparamagnetic grains upon heating (Dearing, 1994). In the combusted (>600°C) topsoil from Field Experiment II,
fd approached the upper limit of 15% (Dearing, 1994), indicating that ultrafine maghemite particles dominated the magnetic fraction.
Fractional conversion factors (FC%mass) also increased with heat intensity. Combusted topsoil (>600°C) from Field Experiment II gave a FC%mass value of
100%, indicating that maximum conversion of goethite to maghemite had taken place in the field (Table 5). The FC%mass values appear to be good indicators of fire intensity for the 0- to 5-cm depth samples. In this regard, it is surprising that the 5- to 15-cm depth samples showed higher FC%mass values for all heat intensities in Field Experiment I and for the 100 and 300°C treatments in Field Experiment II. It might be expected that the subsoil FC%mass values would be lower because there was less exposure to the high surface temperatures. However, the total organic matter contents of the 5- to 15-cm depth samples were, on average, half those of the 0- to 5-cm depth materials and may have limited the conversion of goethite to maghemite. We investigated the contribution of soil organic matter and Fe oxide concentration, as well as the kinetics of change in magnetic susceptibility at two temperatures (300 and 600°C), in two oven experiments using the forest soil from Field Experiment II (Table 1).
Contribution of Soil Organic Matter to Increases in Magnetic Susceptibility
Adding additional organic material to the unburned topsoil of Field Experiment II prior to exposing it to 600°C for 930 min caused a linear decrease in magnetic susceptibility (Fig. 5) according to the relationship:
![]() | (3) |
lf is the mass-specific magnetic susceptibility at low frequency in 10-8 m3 kg-1, and masstea is the number of grams of air-dry tea kg-1 soil. Standard errors amounted to 7.1 x 10-8 m3 kg-1 and 0.067 x 10-8 m3 g-1 for the intercept and the slope, respectively. The tea contained 61 g kg-1 ash, and this paramagnetic ash was apparently responsible for the decrease in magnetic susceptibility due to a dilution effect.
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lf up to 50% (Fig. 5). The
lf increased until 105 g kg-1 organic material were added and then reached a plateau of 2147 x10-8 m3 kg-1. Eighty-five percent of this increase was achieved with the addition of 80 g kg-1 organic material. The organic C content of the forest subsoil prior to burning was 20 g kg-1. Addition of 105 g kg-1 tea (with 61 g kg-1 ash) to the subsoil made the organic matter level similar to that of the topsoil. Apparently, 70 g kg-1 organic C was sufficient to keep this soil reduced during the burn and enabled complete conversion of goethite to maghemite.
Addition of 50 and 100 g kg-1 granulated sugar increased the
lf of the topsoil to 654 and 696 x 10-8 m3 kg-1, respectively. For subsoil the results were 1517 and 1869 x 10-8 m3 kg-1 for 50 and 100 g kg-1 sugar addition, respectively. These values deviated only slightly from the values obtained with the tea experiment.
These observations support our earlier hypothesis that the amount of organic matter controlled the conversion of goethite to maghemite in the subsoil. Similar results were obtained by Brown (1988) who observed an increase in magnetic susceptibility when flour was added to a sample before igniting it at 550°C for 1 h. The relatively high FC%mass for subsoil as compared with topsoil (Table 5) could thus be explained by insufficient organic matter to keep the environment reduced during burning. The final
lf of the subsoil material after addition of extra organic matter was higher than for topsoil with the same organic matter content, which is probably due to the higher CBD-extractable Fe oxide content of the subsoil (24 g kg-1 Fe in subsoil vs. 12 g kg-1 Fe in the forest topsoil).
Conversion Kinetics
The increase in
lf during the first 30 min of heat exposure in Oven Experiment II is shown in Fig. 6
. Also indicated in the same figure are the final levels of
lf reached after 660 min of exposure. Soil water determinations (results not shown) indicated that pore water was lost at 300 and 600°C after 10 and 1 min of exposure, respectively. The lag time in response to temperature for the 300°C curve can be explained by the initial vaporization of soil water; that is, conversion of goethite to maghemite did not take place until water in the samples had vaporized. After water vaporization,
lf increased sharply to 80% of the maximum level within 220, 115, 300, and 75 min for topsoil at 600°C, subsoil at 600°C, topsoil at 300°C, and subsoil at 300°C, respectively.
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lf obtained by heating the topsoil for an extended period of time at 600°C was
50% of that observed for the subsoil. Part or all of this difference in obtainable
lf was probably due to the fact that the forest subsoil contained 24 g kg-1 CBD-extractable Fe; whereas, the topsoil contained only 12 g kg-1 CBD-extractable Fe. The CBD-extractable Fe in the samples exposed to 600°C decreased rapidly with time of exposure. A similar decrease was observed in the combusted topsoil in Field Experiment II and was most likely due to the formation of glassy, sand-sized particles that encapsulated and protected the ultrafine maghemite particles.
Field vs. Laboratory Levels of Magnetic Susceptibility
In both field experiments, burning produced measurable changes in magnetic susceptibility, especially in the topsoil where fires lasted for a longer time (Field Experiment II). The extent of change differed significantly from those obtained in oven experiments, where temperature levels and duration of exposure were controlled. Maximum achievable
lf levels with oven experiments using forest soil from Field Experiment II were 728 (topsoil) and 1333 x 10-8 m3 kg-1 (subsoil) at 600°C and 543 (topsoil) and 1188 x 10-8 m3 kg-1 (subsoil) at 300°C (Fig. 6). The values obtained at comparable temperatures in the field were much lower. Topsoil exposed to 300°C in the oven reached field-observed levels after 12 min of exposure. For subsoil material, 3 min of oven exposure was sufficient to reach field levels. For exposure to 600°C in the oven, field-observed levels were reached after 3 min (topsoil) and 15 s (subsoil). Because field samples had a water content of
450 g kg-1 directly before the burn (much larger than the water content of the 60°C dried soil that was used in the oven experiments), an increase in time needed for evaporation of the remaining water probably accounts for the substantial increase in time of exposure required in the field.
The highest magnetic susceptibility found in Field Experiment II (combusted topsoil) was 2467 x 10-8 m3 kg-1. The FC%mass approached 100% for the combusted topsoil, indicating that this was the maximum obtainable magnetic susceptibility. The magnetic susceptibility of combusted topsoil in Field Experiment II was higher than the maximum achievable level for forest topsoil (670 x 10-8 m3 kg-1) in Oven Experiment II and also of subsoil with the addition of extra organic matter (2147 x 10-8 m3 kg-1). Because topsoil from the originally unburned forest soil used in the oven experiment contained less than one-third of the CBD-extractable Fe oxides (12 g kg-1 Fe in forest topsoil, 41 g kg-1 Fe in slashed topsoil prior to burning), a higher magnetic susceptibility for the field-combusted topsoil should be expected.
| Conclusions |
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In a recent survey in the Sepunggur area (Ketterings et al., 1999), farmers indicated that reddened soil was undesirable for crop growth, based upon their observation that it could not hold water and was not fertile. Our research showed that severe burning had drastic effects on soil texture and mineralogy. Changes in soil mineralogy also take place at lower fire intensities and are still likely to influence the soil fertility status. Further research is needed to determine how important these changes in soil mineralogy are for nutrient availability in the growing season after the burn. Magnetic susceptibility should be an excellent tool for determining the spatial variability of fire intensity for soil fertility evaluations.Genstat 5
| ACKNOWLEDGMENTS |
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Received for publication February 1, 1999.
| REFERENCES |
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