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Research and Development Institute for the Agri-Environment (IRDA), 2700 Einstein, Complexe scientifique, D.1.110, Sainte-Foy, QC, Canada G1P 3W8
* Corresponding author (adrien.ndaye{at}irda.qc.ca)
Received for publication December 16, 2005.
| ABSTRACT |
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Abbreviations: ANR, apparent N recovery MWD, mean weight diameter of aggregates PMS, mixed paper mill sludges SOM, soil organic matter
| INTRODUCTION |
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Before 1995, only primary sludges were produced by paper mills. These wastes were used mainly for degraded site reclamation. Primary sludges have high C/N ratios (>200) and they induced N immobilization, which reduced plant growth (Fierro et al., 2000). Since 1997, new environmental technologies in the paper mill industry have resulted in the production of secondary sludges enriched in N, P and K (N'Dayegamiye et al., 2003). Primary and secondary sludges are then mixed, making this waste more attractive for agricultural use. Currently, PMS are generally comprised of 60% primary sludges and 40% secondary sludges. Few mills produce de-inking paper sludges with higher C/N ratios (3060) that are also applied to agricultural land (Lalande et al., 2003).
The form of N present in organic residues determines its availability to crop. Manure N availability to crop in the first yr after application is mostly determined by its inorganic N content (Beauchamp, 1986). However, the inorganic N (NH4N and NO3N) content in PMS represents between only 5 to 21% of total N (Simard, 2001; Arfaoui et al., 2001; N'Dayegamiye et al., 2003). Thus, most of N in PMS is in organic form and must be mineralized to complete crop N needs. High N mineralization and N availability occurs from decomposing organic residues with N content above 2% as for PMS, and immobilization occurs below that N concentration (Palm and Sanchez, 1991).
Crop response to organic residues (manure, green manure or PMS) cannot be attributed solely to nutrient supply. When added to the soil, organic residues such as cattle manure (Magdoff and Amadon, 1980) and green manure (Wagger et al., 1998; N'Dayegamiye and Tran, 2001) improved crop yields beyond what could be attributed to the sole effect of supplied N. Other beneficial effects may be related to the improvement of physical, chemical and biological properties. For example, improving soil structure promotes better root growth and plant nutrient absorption, increases soil moisture and improves soil microbial activities for better nutrient mineralization (Kirchner et al., 1993; Wagger et al., 1998).
It has been demonstrated that the nature of organic residues determines its influence on microbial activity and soil aggregation (Lynch and Bragg, 1985). Microbial biomass and activity in soil is an indicator of C turnover and availability from organic residues (Tian et al., 1992). De-inking paper sludges have higher C/N ratios than PMS (Fierro et al., 2000), and organic residues with high C/N ratios and high lignin content decompose slowly in soil, and their influence on soil microbial activity and aggregation is low (N'Dayegamiye and Angers, 1993; Fierro et al., 2000). The PMS that have high labile C content and low C/N ratios (N'Dayegamiye and Watt, 2000) could stimulate microbial growth, enzymatic activity, nutrient availability and promote soil aggregation.
Knowing the agronomic benefits of PMS will facilitate their use as source of nutrients and soil conditioner. The objectives of this 3-yr study were to: (i) determine corn yields, apparent N recoveries in year of application and in subsequent year; and (ii) assess changes in soil properties following 3 yr of annual PMS applications.
| MATERIALS AND METHODS |
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A completely randomized block experiment included three PMS rates (20, 40, and 60 Mg ha1 on a wet basis) applied alone or with N fertilizer (90 and 135 kg1, for PMS rates of 40 and 20 Mg ha1 respectively). Treatments also included a control without PMS or N fertilizer, and a mineral N fertilizer (180 kg ha1) as recommended for corn cropping in the area of experiment. No N fertilizer was applied to 60 Mg ha1 plots. To ensure that P and K availability were not a limiting factor to crop growth, all treatments including the control received P and K fertilizers at the rates recommended for corn, depending on soil analysis (15 kg P and 85 kg K ha1). The experimental plots were 10 m wide by 12 m long with 12 rows of corn planted on 0.76-m row spacing.
In the first (1997) and third yr (1999) of the experiment, PMS and N fertilizer were applied to the entire surface of plots. In the second yr (1998) of the experiment, the plots were split to study annual vs. biennial PMS and N fertilizer applications on corn yields and N nutrition. The subplots were 5 m wide by 12 m long. The same treatments described above were applied to half of each plot and no N fertilizer or PMS were applied on the second half of the plot to evaluate residual PMS and N fertilizer effects.
The PMS and fertilizers were applied in late April of each year and immediately incorporated by disking in the 0- to 10-cm soil layer. Corn hybrid (Dekalb 3432550 corn heat units, CHU) was seeded at 76 100 plants ha1 every year. Corn grain yields were determined by harvesting 12-m of the center two rows of each plot with a combine. To determine aboveground corn N content, whole plants were cut at the soil surface, chopped, weighed, and a 600-g to 800-g subsample was dried at 65°C and weighed again for dry matter calculations. Grain specific gravity was determined on a 500-g grain sample.
Analytical Methods
The PMS subsamples were collected the day of their application, and were kept at 4°C until analyzed. Samples were dried at 70°C, weighed to determine dry matter content, and ground to pass through a 2-mm sieve before analysis. The PMS pH was measured on the dried sample in a PMS/water mixture (1:1). Organic C and N content was determined by dry combustion using a LECO C-N-S 1000 analyzer (LECO Corp., St. Joseph, MI). Mineral N as NH4N and NO3N was analyzed on wet samples, extracted using 2 M KCl (Bremner and Mulvaney, 1982) and measured with a Technicon Autonalyzer. Total N content in plant samples, and P, K, Ca, and Mg contents of PMS were extracted by digestion in H2SO4 and H2SeO3 with the addition of H2SO4 for 1 h at 400°C (Isaac and Johnson 1980). The PMS contents of B, Cu, Fe, Mn, and Zn were obtained after dry-ashing at 450°C for 3 h, and extraction in 2 M HCl (Richards, 1993). Total N content in plant samples was determined on an Automated Technicon Autoanalyzer, and mineral elements in PMS by inductively coupled plasma optical emission spectrometer (PerkinElmer 4300 DV, Boston, MA).
Composite soil samples made from 12 cores were collected from the top (020 cm) soil layer in April 1997 at the initiation of the study. Samples were air-dried and sieved to pass a 2-mm sieve. A portion was kept to determine soil pH, soil texture and mineral element contents. Another portion was ground to pass through a 0.25-mm screen for organic C and total N analysis. Organic C was determined by the WalkleyBlack method (Allison et al., 1965), and total N by Kjeldahl digestion (Bremner and Mulvaney, 1982). As usually recommended for Quebec soils, extractable P, K, Ca and Mg were extracted in a Mehlich III solution (Mehlich, 1984). Total N levels were measured on an Automated Technicon Autoanalyzer and mineral elements (P, K, Ca, and Mg) on inductively coupled plasma optical emission spectrometer (PerkinElmer 4300 DV, Boston, MA). Particle size analysis was performed on air-dried soils by the pipette method after the destruction of organic matter with H2O2 and dispersion with sodium hexametaphosphate (Gee and Bauder, 1986). Soil pH was measured in 1:1 soil/water solution.
At the end of the experiment in October 1999, six soil cores (5-cm diam.) were collected to a depth of 20 cm to determine changes in physical and biological properties and the content of soil C and N. Soil samples were obtained only from plots receiving annual PMS and N fertilizer treatments, and the control. The soil cores were pooled to make one composite soil per plot, sieved in the field to pass a 6-mm sieve and then stored at 4°C until analysis. A portion of the moist soil samples was used to determine soil structure and aggregation, microbial biomass C, urease and phosphatase activities, and N mineralization. Subsamples of the moist soil were air-dried and ground at <0.5 mm to determine the soil C and N contents and soil organic matter (SOM) density fractions.
To separate SOM density fractions, 20 g of finely ground soil (<0.5 mm) was suspended in 100 mL of NaI solution with a specific gravity of 1.59 g cm3 (Janzen, 1987; N'Dayegamiye et al., 1997). This suspension was stirred and centrifuged at 5600 x g for 30 min. The supernatant solution was decanted onto a 0.45-µm filter under suction; this procedure was repeated three times to ensure complete recovery of the light fraction (LF). The material remaining on the filter was considered as the LF and the remaining soil as the heavy fraction (HF). The LF and HF fractions of SOM were dried at 65°C, weighed and determined for their organic C and total N contents. Total N and organic C content of soil and density fractions of SOM was determined on a LECO C-N-S 1000 analyzer (LECO Corp., St. Joseph, MI).
Water-stable aggregation was determined by the wet sieving method. Forty grams of air-dried soil (>6 mm) were put on the top of a series of sieves (5, 2, 1, and <0.25 mm) and the sieves were immersed in water and shaken for 10 min. The soil fractions recovered on each sieve were dried at 65°C for 24 h, weighed, corrected for sand and expressed as a percentage of total dry soil (Kemper and Rosenau, 1986). Aggregate MWD was calculated according to Haynes and Beare (1997).
Acid and alkaline phosphatase activities were determined using p-nitrophenol phosphate at pH 6.5 and pH 11 respectively, according to Tabatabai (1982). Duplicate field-moist soil samples (1 g) were incubated at 37°C for 1 h, and the p-nitrophenol released by the enzymes was measured by spectrophotometry (Hitachi U-1000) at 420 nm. Urease activity was determined on duplicate field-moist soil samples (2.5 g) incubated at 37°C for 2 h (Tabatabai, 1982). The NH4N produced was determined by spectrophotometry at 636 µm using indophenol blue.
Soil microbial biomass C was determined using the chloroform fumigation extraction method (Vance et al., 1987). Duplicate field-moist soil subsamples (50 g) were fumigated in closed vessels with chloroform (CHCl3) for 24 h. The soluble C content of fumigated and unfumigated (control) soils were exctracted with 0.5 M K2SO4. The C in the extracts was analyzed using persulfate oxidation on a carbon autoanalyzer (Dohrmann DC-180, Santa Clara, CA). An extraction efficiency coefficient of 0.38 was used to convert soluble C into biomass C (Vance et al., 1987).
The soil mineralization potential was measured by incubating field-moist soil samples (150 g) at 25°C for 20 d at field capacity. The nitrates were extracted with 2 M KCl (Bremner and Mulvaney, 1982) before and after the period of incubation and determined on Technicon analysis system. The N mineralization potential represents the difference between the nitrate contents at the beginning and the end of the incubation.
Calculations
Data obtained on corn N uptake in 1997 and 1998 were used to determine apparent N recoveries and efficiency for N fertilizer and PMS. Apparent N recovery was calculated by the difference method using mineral fertilizer or PMS treatments and the unfertilized and unamended control. Apparent N recovery in the year of PMS application (1997) and ANR in residual year (1998), was calculated as follows:
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Statistical Methods
For corn yields, grain specific gravity and N uptake in the first yr (1997), data were analyzed with an analysis of variance with single-degree of freedom contrasts to determine treatment differences. In the second and third yr, a two-way analysis of variance for split-plot design and contrasts were used with PMS and N fertilizer treatments as main plot and application frequency (annual vs. biennial) as subplot. The soil physical and biological properties measured in 1999 in plots with annual PMS and N fertilizer applications only were subjected to an analysis of variance and means of treatments were compared using the least significant difference after a significant ANOVA test at P
0.05. Analyses were conducted using the SAS GLM procedure (SAS Institute, 1989).
| RESULTS AND DISCUSSION |
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Corn grain specific gravity was not influenced by N fertilizer or PMS applications, compared to the unfertilized control. Corn N uptake was increased by PMS applications in all years. This PMS effect was quadratic suggesting important soil contribution on corn N nutrition. Corn N uptake was lower with biennial than annual incorporation of PMS (Table 3).
The data obtained indicate that corn yields and N uptake were strongly increased by PMS applications. Most of N in PMS is in organic form and must be mineralized to complete crop N needs. For that, synchronization between N mineralization and N uptake is an important factor controlling N availability to subsequent crops. Our results are consistent with other published studies that demonstrated that crop response to PMS applications depends on the length of growing season for a particular crop; corn, being a long season crop utilizes PMS nutrients well. This is in agreement with previous studies reporting that paper mill sludges, applied on different soil types and under various climatic conditions, significantly increased the yield of winter cabbage (Brassica oleracea var capitata L. Bartolo), sweet and grain corn (Simard, 2001; N'Dayegamiye et al., 2003), and mixed grass alfalfa stand (Medicago sativa L.) and timothy (Phleum pratense L.) (Arfaoui et al., 2001).
Results on corn N uptake indicate that PMS applications provided significant amounts of available N in the first yr of application and in subsequent year resulting in high corn yields. Corn N recovery from PMS and N fertilizer were calculated and are presented in Table 4. For N fertilizer treatment (180 kg ha1), the ANR was 49% in 1997 and 13% in the residual year (1998). The ANR from PMS rates providing 163 to 489 kg N ha1 ranged from 17 to 21% in the year of application and from 15 to 21% in the residual year. The ANR in the year of application decreased with increasing PMS rates and total inputs (Table 4). On a Baudette soil series (fine-silty over clayey, mixed, non acid, mesic, Typic Humaquept), N'Dayegamiye et al. (2003) also obtained lower ANR for corn with applied PMS at high rates (6090 Mg ha1). The ANR values measured in PMS-treated soils in the year of application were generally half of those obtained with mineral N fertilizer (Table 4). This is likely because PMS N was mostly in the organic form (9095%. Table 1), and therefore must be mineralized before being available to crop. The PMS ANR in the residual year (1998) were generally higher than those of mineral N fertilizer.
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The yield response obtained with PMS in this study may have been due to more then N additions. Enhanced corn yields may also be attributed to more favorable physical, chemical and biological conditions in soils amended with PMS, as was also observed for green manures applied to soils under similar climatic conditions (Abdallahi and N'Dayegamiye, 2000). For example, yield increases ranging from 5 to 25% have been attributed to manure improvement of soil properties (Magdoff and Amadon, 1980).
Soil Properties
Changes in soil physical and biological properties and in C content of soil and density fractions of SOM after three PMS applications are presented in Tables 5
to 7. The PMS applications alone or with N fertilizer significantly increased the proportion of water-stable aggregates >5 mm and the MWD of aggregates, as compared to N fertilizer treatment and the control (Table 5). Moreover, the proportion of soil macro-aggregates >5 mm were increased three to four times in soil that received PMS, in comparison with N fertilizer and the control. Results indicate that repeated PMS applications even at low rates (20 Mg ha1) have influenced soil macro-aggregation. Three PMS applications at 40 to 60 Mg ha1 yr1 significantly reduced the soil bulk density in 0- to 10-cm soil layer (Table 5), due probably to their significant effect on the improvement of soil structure.
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The effects of PMS on the soil aggregation also could be related to the transitory components in decomposing PMS (polysaccharides) and to the growth of soil microorganisms (fungi, bacteria), that are known to participate in soil aggregation (Oades and Waters, 1991). During aggregate formation, micro-aggregates are bound together by polysaccharides and hyphae to form stable macro-aggregates (Oades, 1984). However, they are considered only temporary binding agents as they persist for about a year. Unless they are replaced annually, the binding effects disappear and the amount of water-stable aggregates declines (Oades, 1984). This suggests that labile components (polysaccharides) in decomposing PMS and the soil microbial biomass can rapidly induce soil aggregation, but this effect may be transient and disappear after a short time as measured in two cycles of a wheat (Triticum aestivum L.) and field pea (Poa pratensis L.) rotation (Chan and Heenan, 1999). Results of this study indicate that repeated PMS applications even at a low rate (20 Mg ha1) have sustained soil aggregation and increased water-stable aggregates.
Increasing the abundance of soil macro-aggregates and reducing bulk density provides a microenvironment that supports increased biological activity and soil mineralization potential, a key component of soil fertility. Reducing bulk density positively impacts many soil properties including increased soil water holding capacity, greater pore space, and higher water infiltration rates. The application of PMS increased soil microbial biomass C and alkaline phosphatase activity compared to the control and N fertilizer treatments (Table 6). Urease activity and mineralized N were increased only for the two higher PMS rates (40 and 60 Mg ha1). The increase of soil microbial biomass and enzymatic activity is a reflection of PMS C turnover and availability to microflora as was also demonstrated by Tian et al. (1992). The PMS application significantly increased alkaline phosphatase and urease activities (Table 6), which are related to soil microbial biomass (Frankenberger and Dick, 1983). These data indicated that PMS applications increased soil microbial biomass and consequently influenced extracellular polysaccharide production (Tisdall and Oades, 1982) implied in the binding of soil micro-aggregates into macro-aggregates, as indicated earlier by Tardif (1996) and Golchin et al. (1997).
Changes in C and N contents of the soil and the density fractions of SOM are shown in Table 7. The PMS additions at 40 to 60 Mg ha1 increased the soil C content by 22 and 26%, and 18 and 22%, compared to the control and N fertilizer, respectively. The PMS applications also increased the C and N concentrations in the LF of SOM, but had no effects on the HF. The highest C and N concentrations occurred were about 10 times as great in the LF fraction, as compared to the whole soil and the HF. The increases in C and N contents of the LF of SOM is probably due to the abundance of labile C in these wastes, and also due to the stimulation of soil biomass growth (Table 6). The LF of SOM is strongly related to soil microbial biomass, soil enzyme and carbohydrate contents (Janzen et al., 1992). Golchin et al. (1994) indicated that the soil LF is constituted of microbial biomass and metabolites, and decomposing OM originating from plant debris and organic wastes. Organic matter included in LF would also be involved in soil aggregation (Oades, 1984; Golchin et al., 1994), which could explain the significant increases of soil macro-aggregates (>5 mm) following PMS application (Table 5), although significant correlations were not obtained among those parameters.
When further decomposed, the SOM present in LF is adsorbed on clay minerals, becomes HF, and is then stabilized against further decomposition (Golchin et al., 1994). Surprisingly three consecutive applications of PMS had no significant effect on the C content of HF as also observed by N'Dayegamiye and Tran (2001), following two incorporations of five species of green manures into soil. Increases in C content of HF could be measured only after long-term application of PMS as was demonstrated after 20 yr of annual application of dairy manure at 20 Mg ha1 (N'Dayegamiye et al., 1997). The significant increase of soil organic C after only three PMS applications was unexpected. This increase is probably due to amorphous SOM from decomposing PMS and microbial products, which constitute the LF of SOM (Golchin et al., 1994). As this labile SOM could gradually be decomposed, this suggests that periodic PMS applications are necessary to maintain optimal SOM levels and to sustain microbial activity and aggregation. Results obtained in this study indicate that three applications of PMS with low C/N ratios stimulated soil microorganism growth and activity, increased the SOM as well as soil macro-aggregates (Tables 5
7), and therefore could have influenced corn growth, yields and N nutrition.
| CONCLUSIONS |
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| ACKNOWLEDGMENTS |
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| REFERENCES |
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