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a Agriculture and Agri-Food Canada, Soils and Crop Research and Development Centre, 2560 Hochelaga Blvd., Ste-Foy, PQ, Canada, G1V 2J3
b Agriculture and Agri-Food Canada, Soils and Crop Research and Development Centre, 2560 Hochelaga Blvd., Ste-Foy, PQ, Canada, G1V 2J3
c Centre de Recherche en Horticulture, Faculté des Sciences de l'Agriculture et de l'Alimentation, Université Laval, Québec, Canada, G1K 7P4
chantignym{at}em.agr.ca
| ABSTRACT |
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| INTRODUCTION |
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Physical fractionation of organic matter based on either particle size or density has proven useful to determine the fate and decomposition of crop residues in soil (Christensen, 1992). It has been found that the light fraction of crop residues rapidly decomposes (Shields and Paul, 1973), and that residue particle size decreases with a large proportion of the residual material becoming heavier because of close association with the clay- and silt-size fractions (Christensen, 1992; Aita et al., 1997). DPS is mainly composed of short wood fibers and kaolin clays used during paper-making processes, and inks and chemicals used for paper recycling purposes. Further, freshly milled DPS readily forms millimeter-size clusters of low density. Therefore, it was hypothesized that particulate and light fraction assessments would be useful to characterize the fate and decomposition pattern of DPS in agricultural soils.
Microorganisms first colonize the surface of the substrate and process the easily available C fraction at a relatively rapid rate during the initial phase of decomposition of a particulate organic substrate (Ladd et al., 1996). This initial flush of activity may lead to extracellular polysaccharide production and the binding of soil particles (Golchin et al., 1997; Ladd et al., 1996). As a result, new aggregates are formed with particulate organic matter as the central core. It is also believed that particulate organic matter occluded within soil aggregates is physically protected against decomposition (Golchin et al., 1997; Angers and Chenu, 1997).
Few studies have dealt with the use of DPS as an organic amendment or soil conditioner. Fierro et al. (1999b) studied the decomposition of DPS in a degraded sandy soil and found that the decaying substrate progressively densified but without significant fragmentation into particles <53 µm. Using similar material, Trépanier et al. (1996) found an increase in soil aggregate stability when adding 18 Mg DPS ha-1 to a silty loam cultivated to potato (Solanum tuberosum L.). However, it was found that loading rates up to 18 Mg DPS ha-1 only had a transient effect and had to be renewed each year to sustain soil stability. The fate of DPS after burial in agricultural soils, and the mechanisms by which DPS may improve soil aggregation are unknown. Further, DPS application rates larger than 18 Mg ha-1 have not been tested as a means to produce larger and prolonged improvement in soil aggregate stability. The aims of this study were (i) to determine the impact of one large addition of DPS on soil organic matter and water-stable aggregation, and (ii) to determine the physical transformations undergone by DPS as characterized by its particle size and density fractions.
| Materials and methods |
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DPS was obtained from the Daishowa, Inc., paper mill company located at Québec City, and was similar to the material used and described by Trépanier et al. (1996) and Fierro et al. (1999b). Briefly, the sludge used was generated mostly from the recycling of newspaper, which was made of black spruce [Picea mariana (Mill) BSP] fibers. Before its use, to ensure uniform mixing with the soil, DPS was pulverized to obtain a fluffy granular material <6 mm. At the time of application, the sludge had a bulk density of 0.224 Mg m-3 and a water content of 0.52 kg kg-1. Selected properties of DPS and soils are reported in Table 1 . De-inking paper sludge was applied at rates of 0 (control), 50, and 100 Mg ha-1 (dry basis) in autumn 1994 to plots of 5 by 7 m in size. The material was uniformly spread on the soil surface and buried by rototilling to obtain a worked surface layer of 20 cm thick. In the spring of 1995, the worked soil layer had settled to 15 cm and did not significantly change thereafter. Alfalfa (Medicago sativa L.), cv. Saranac, red clover (Trifolium pratense L.), cv. Florex, and bromegrass (Bromus inermis L.), cv. Baylor, were established in pure stands, and grown for the first two growing seasons of the experiment (1995 and 1996). Each spring, the soils were fertilized with P and K according to crop requirements and soil analyses (CPVQ, 1994). In the spring of 1995, an additional 0.23 kg P was added to each Mg DPS incorporated to counteract P immobilization (Fierro et al., 1999c). In the autumn of 1996 (Day 741 of the study), soils were plowed under to a depth of 20 cm and sweet corn (Zea mays L.), cv. Delectable, was grown on all plots in the growing season of 1997, and fertilized with 120 kg N ha-1. The experiment was laid out as a split-plot replicated four times on each soil type with DPS application rates as the main plots and crop species as the sub-plots.
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Whole soil C was determined by dry combustion (LECO CNS-1000, Leco Corp., St. Joseph, MI) on soil samples ground to pass a 0.5-mm sieve. There were no carbonates in the soils used. Furthermore, less than 3% of total DPS-C was present as carbonates, which was likely lost soon after application to our acid soils. Therefore, whole soil C measurements were considered to represent organic C contents.
The light fraction was determined on the basis of the method proposed by Gregorich and Ellert (1993) with some modifications dictated by the particular nature of DPS. Ten grams of air-dried soil (<6 mm) were placed in 100-mL polypropylene tubes with 40 mL of sodium polytungstate solution. Preliminary results showed that the proportion of fresh DPS recovered as light material increased with increasing density of polytungstate solution from 1.2 to 1.8 Mg m-3. A solution of 1.8 Mg m-3 was used since >95% of fresh DPS was recovered as light material with no significant gain at higher solution density. Tubes were agitated for 60 min on a reciprocal shaker. The internal side of each tube was then washed with a small quantity of sodium polytungstate solution, and tubes were centrifuged at 1000 g for 15 min. The floating material was recovered and filtered on a 0.45-µm filter membrane, and then transferred to another 100-mL tube and shaken for 30 min with 50 mL of 0.01 M CaCl2 solution. Preliminary tests indicated that this "washing-shaking" step was necessary to remove polytungstate salts retained by DPS materials, and reduced the error in estimating the weight of material recovered to <2%. Tubes were centrifuged and the floating material was recovered on a filter membrane as described above. The material remaining on the membrane was rinsed with 50 mL of deionized water and dried at 65°C until constant weight. Carbon present in the light fraction (LFC) was determined as described for whole soil C.
Particulate organic carbon (POC) was assessed according to Feller (1979) with some modifications. Briefly, 25 g of air-dried soil (<6 mm) were shaken (reciprocal shaker) for 16 h in a 250-mL plastic centrifuge bottle with 100 mL deionized water and 10 glass beads (6-mm diam.). The material was then passed on a 53-µm sieve to separate particulate (>53 µm) from fine organic matter. We tested this procedure with fresh DPS and found that 90 ± 2% of initial material was recovered as >53-µm particles. Carbon content of the fine fraction was determined as described above, and POC was calculated as the difference between whole soil C and fine fraction C (Cambardella and Elliott, 1992).
At the end of each growing season, water-stable aggregation was measured by wet sieving with slaking (Angers and Mehuys, 1993). Only soil samples collected in alfalfa plots were analyzed by this procedure. One hundred grams of air-dried soil (<6 mm) were put on the top of a nest of sieves with decreasing openings (1000 and 250 µm). The sieves were totally immersed in water for 10 min with an apparatus similar to that described by Bourget and Kemp (1957). The water containing material <250 µm was then poured onto a 53-µm sieve to yield 53- to 250-µm and <53-µm fractions. Soil fraction recovered on each sieve was weighed, corrected for sand content (Kemper and Rosenau, 1986), and expressed as a percentage of total dry soil. Soil passing the 53-µm sieve was recovered by centrifugation (15 min at 1000 g). Size classes obtained were >1 mm, 250 to 1000 µm, 53 to 250 µm, and <53 µm.
Water-stable aggregates were also observed by stereomicroscopy (Model M8, Wild Heerbrugg, Switzerland). Ten 4- to 5-mm aggregates were collected from each wet-sieved sample, and air dried. The surface of intact aggregates was first observed (80x magnification), and the aggregates were then broken apart to expose the interior and observed again (100x magnification).
Statistical Analyses
Analyses of variance were performed separately for each site and each sampling date by the GLM procedure of SAS (SAS Institute, 1989). There was no consistent crop effect on any measured soil parameters except for LFC measurements. However, since the mean square fraction attributed to the crop effect on LFC was always very small compared with the fraction attributed to the DPS effect, only the DPS effects are presented in the present paper. Contrast analyses were performed to assess for the linear or quadratic response of measured parameters to DPS loading rates. When significant (P < 0.05), the response of studied parameters to DPS amendment were always linear, and therefore, this is not further mentioned in the text.
| Results |
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Particulate Organic Carbon
Addition of DPS increased POC content of both soils (Fig. 2)
, and the effect was significant (P < 0.01) until Day 726. At the first sampling date and compared with the control soil, adding 100 Mg DPS ha-1 increased POC by 41 g kg-1 in the silty clay loam, and 38 g kg-1 in the clay loam. These values were 16 g kg-1 in both soils amended with 50 Mg DPS ha-1. As for whole soil C, POC content decreased rapidly from Day 271 to 342 and more slowly from Day 596 to 726. A large decrease in POC was also found between Day 726 to 973 subsequent to soil tillage. More than 70 to 90% of the C attributed to DPS was recovered as POC until Day 726 (Table 2)
. This proportion decreased following soil tillage in fall 1996.
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| Discussion |
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At the end of the first growing season (Day 370), the residual DPS constituted a recalcitrant C pool which decomposed slowly with a mean residence time of >15 yr (Fierro et al., 1999a). Therefore, in our study, the sudden decreases in whole soil C, POC, and LFC found from Day 726 to 973 were mostly attributable to the effect of soil tillage performed at Day 741. The residual C was located in the top 15 cm of soil and was plowed under to 20-cm depth so that some dilution occurred. Part of the effect could also be due to stimulation of decomposition induced by tillage. An effect of N fertilization in spring 1997 is to be discarded since this was performed after Day 973.
At the first sampling date (Day 271), only 50 to 70% of C attributed to DPS was accounted for by LFC in both soils. Since >95% of fresh DPS was comprised of light material, part of fresh DPS became heavier than 1.8 Mg m-3 shortly after incorporation into the soil. Furthermore, the proportion of residual DPS accounted for by light fraction decreased with time. In other words, as DPS decomposed, an increasing proportion of the remaining material had a density >1.8 Mg m-3, indicating progressive densification. Fierro et al. (1999b) reported that the density of DPS increased in a sandy soil (<5% clay), and argued that clays present in fresh DPS were mainly responsible for this phenomenon. In our case, light fraction losses appeared to be faster than in Fierro's study, indicating that encrustation with soil clays might have increased the densification rate of DPS.
The close relationship between whole soil C and POC dynamics in DPS-amended soils indicated that DPS decomposition was mostly linked to transformations in the particulate material present in fresh sludge. Furthermore, the rather constant proportion of whole soil C accounted for by POC during the first 2 yr of the study, indicated that decaying DPS remained mostly particulate (>53 µm) and that POC losses were more due to C mineralization than to a transfer to the fine (<53 µm) C fraction. This finding is different from what is generally reported on crop residue decomposition. During crop residue decomposition, particulate material is generally rapidly broken down into smaller-size fragments, resulting in increased clay- and silt-size C particles (<50 µm) at the expense of the sand-size fraction (Christensen, 1992; Aita et al., 1997). Encrustation with mineral particles such as observed in our study, would provide a physical protection to particulate organic matter against decomposition (Golchin et al., 1997; Ladd et al., 1996; Angers and Chenu, 1997), and partly explains our finding that there were no net fragmentation of the decaying DPS into particles <53 µm during decomposition. Fresh DPS is composed of short wood fibers partly embedded with clays, which also provides intrinsic physical recalcitrance to this material (Fierro et al., 1999b). Finally, the relatively high lignin content of the DPS we used (about 50%; unpublished data) renders it recalcitrant to most organisms unable to decompose lignin. Therefore, both the physical and chemical nature of DPS would explain that its decomposition pattern was different than what is commonly observed with crop residues.
Aggregate Formation and Stabilization
The improvement in soil aggregation found within 1 yr in DPS-amended soils was greater than what is reported on perennial cropping systems in eastern Canada (Angers, 1992; Carter et al., 1994; Chantigny et al., 1997). In our study, we found a positive cropping effect on soil aggregation as reflected by the increase in water-stable aggregation between Day 370 and 726 in control soils. By comparison, improvement in soil aggregation due to DPS was 1.3 to 3.5 times larger than this cropping effect.
When wet-sieving air-dried DPS, we found that >90% of this material remained on the 1-mm sieve. Hence, part of the increase in the proportion of aggregates >1 mm was due directly to the mass of water-stable DPS clusters. This effect can be roughly estimated by calculating the ratio of DPS mass remaining on the 1-mm sieve to the total soil mass (corrected for the control) recovered on the same sieve. For example, soils amended with 100 Mg DPS ha-1 received an equivalent of 116 g DPS kg-1. Assuming that 90% of the material would remain on the 1-mm sieve, 104 g DPS kg-1 would be recovered on this sieve. In the silty clay loam amended with 100 Mg DPS ha-1, the total soil mass recovered on the 1-mm sieve at Day 370 was 457 g kg-1 larger than the control soil. If we assume that the sludge used lost 50% of its initial weight during the first year (Fierro et al., 1999a), the direct mass effect of DPS would account for less than 12% of the total increase in soil aggregates >1 mm. In the clay loam, this effect would not exceed 8%. Therefore, the direct mass effect of DPS was likely minor and about 90% of the increase in the proportion of aggregates >1 mm was due to the aggregation of soil particles from smaller size fractions, and especially the 53- to 250-µm fraction.
Trépanier et al. (1996) also found a positive effect of DPS on aggregation of a silty loam, but this effect was only small and transient, and disappeared within 1 yr following DPS amendment. In our case, the DPS effect on soil aggregation decreased with time, but was still significant 3 yr after DPS application. Seemingly, the lower amounts of DPS (18 Mg DPS ha-1) used by Trépanier et al. (1996) only induced a brief effect on soil aggregation. Hence, larger loading rates provide larger and longer-lasting improvement in soil physical properties. Because of the large C-to-N ratio of this material, high loading rates might be appropriate for instance when cropping to legumes in which case early N immobilization has no consequences on crop growth (Allahdadi et al., 1998).
Visual inspection of water-stable aggregates confirmed that DPS was directly involved in soil aggregation, acting as the central core of many macroaggregates. De-inking paper sludge was already associated with soil particles shortly after the rapid decomposition phase had started, confirming LFC data showing that the light fraction of fresh DPS underwent a rapid densification due to encrustation with mineral particles. The increasing encrustation visually noticed between Day 271 and 1075 also confirmed light fraction data pointing to a progressive densification of DPS during decomposition.
A large increase in microbial biomass and activities is found when adding DPS to the soil (Tardif, 1996). In the present study, we noted visually that surface wood fibers disappeared more rapidly than internal wood fibers. We suggest that soil microbes rapidly colonized the surface of DPS clusters, and degraded exposed wood fibers to produce polysaccharides or other polymers which bound soil particles (Ladd et al., 1996). As a result, new aggregates were formed with particulate DPS as the central core. Golchin et al. (1997) proposed a model for soils in which organic matter plays a major role in aggregate formation and stabilization. In this model, encrustation of free particulate organic matter with mineral particles leads to the formation of macroaggregates with organic matter as a central core. The stability of those macroaggregates would only be transient as their organic core decomposes rapidly, and microaggregates are soon formed from the breakdown of these macroaggregates. Golchin et al. (1997) also proposed that microaggregates derived from broken down macroaggregates are more stable because their organic core is better protected against decomposition. On a longer-term period, however, the organic core slowly decomposes and the microaggregates become unstable. Considering the LFC and POC data and the images presented here, we suggest that macroaggregate formation and stabilization in DPS-amended soils occurred as proposed by Golchin et al. (1997). However, in our study, the DPS effect on stable macroaggregates was not transient and lasted for up to 3 yr.
Although soil fauna was present in our soils, its influence on DPS decomposition and soil aggregation was not studied. However, the decrease in the amounts of aggregates >1 mm between Day 370 and 1075 of the study, and the associated increase in the 250- to 1000- and 53- to 250-µm size classes might have been partly caused by faunal activity and/or organic core decomposition, which progressively reduced the size of macroaggregates and DPS clusters.
| Conclusion |
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| ACKNOWLEDGMENTS |
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| REFERENCES |
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