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a AWMRU, USDA-ARS, 810 Hwy. 12 East, Mississippi State, MS 39762
b AWMRU, USDA-ARS, 230 Bennett Ln., Bowling Green, KY 42104
c WMFRU, USDA-ARS, 810 Hwy. 12 East, Mississippi State, MS 39762
* Corresponding author (htewolde{at}ars.usda.gov)
Received for publication August 22, 2006.
| ABSTRACT |
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Abbreviations: DAP, days after planting LnNn, litter (Mg ha1) and nitrogen as urea ammonium nitrate (kg ha1) NTPA, applied total plant available nitrogen PEE, phosphorus extraction efficiency STD, farm standard fertilization with inorganic fertilizers UAN, urea ammonium nitrate
| INTRODUCTION |
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However, mismanaged litter use and a resulting environmental damage is often a concern when using litter as a soil amendment or a fertilizer. Phosphorus is the single most important nutrient of environmental concern when litter is applied as a source of crop nutrients. This is because litter contains P in excess of the crop requirement when applied to meet the N need. Typically, the N:P ratio of broiler litter is about 2 (Collins et al., 1999). But, under optimum production, the tissue N:P ratio, which is a function of the N and P uptake, varies between 1.5 for cereal crops and 20 for oilseed and legume crops (Sadras, 2006). The N:P ratio of container-grown cotton before maturity can be as large as 6.0 (Tewolde et al., 2005). Cotton in certain parts of the southeastern region in the USA receives up to 140 kg N ha1 but only 0 to 30 kg P ha1, a 4.7 N:P ratio. Therefore, applying litter to meet the N need of cotton would result in excess P application and, over time, in the accumulation of P in the soil.
Effective management of litter to minimize or prevent the buildup of P, when litter is used as the primary cotton fertilizer in soils that historically received no litter, requires adequate knowledge of the amount of P extracted and removed by harvested crop. Limited amount of research has been conducted to generate this kind of knowledge in forage grasses (Evers, 2002; Brink et al., 2001). In a year-round forage production system, Evers (2002) determined a maximum P uptake of 36.6 kg P ha1 by annual ryegrass (Lolium multiflorum L.) and 18.6 kg P ha1 by Coastal bermudagrass [Cynodon dactylon (L.) Pers.] for a total of 55.3 kg P ha1 uptake from the same soil that received 9 Mg ha1 litter applied once in October plus 168 kg N ha1 as ammonium nitrate applied three times during the year. Brink et al. (2001) measured the P uptake by 12 temperate legume and four temperate grass species that received 9 Mg ha1 poultry litter and reported a maximum 2 yr average uptake of 23.4 kg P ha1 by annual ryegrass.
The fraction of litter P that can be extracted by cotton and the consequences of applying litter to meet the nutritional needs of cotton in part or in full on soil accumulation of P are not well investigated. There is only one recent research that reported the extraction efficiency of litter-derived P by container-grown cotton (Tewolde et al., 2005). This research which used an inert media in a greenhouse showed that cotton extracted a maximum of only 16% of applied litter P in the absence of any other source of P. To our knowledge, no other research has documented the efficiency of cotton in extracting litter P.
When supplied with conventional inorganic fertilizers, reported amount of P extracted by cotton is variable. According to Halevy (1976), irrigated cotton in Israel extracted 44 to 46 kg P ha1 with
44% of the total (1921 kg P ha1) harvested in the seed. Others reported substantially less P uptake. Bassett et al. (1970) reported an average P uptake of only 19 kg ha1 by mature irrigated cotton in California USA with only 9 to 12 kg ha1 removal of P with harvested seed. Mullins and Burmester (1990) reported total P uptake of 16.3 to 18.2 kg ha1 in Alabama USA with only 9.1 kg P ha1 removed from the field in harvested seed. More recently, Dorahy et al. (2004) reported an average extraction across 17 field experiments in Australia of 21 kg P ha1 at cut-out (defined as
5 nodes above white flower), 2/3 of which (15 kg ha1) accumulated in seed. Although the report by Halevy (1976) that cotton can extract up to 46 kg P ha1 is encouraging, the other reports suggest that use of litter on cotton can lead to accumulation of P that may not be environmentally sustainable. This research was conducted to quantify the magnitude of P extracted by cotton when fertilized with broiler litter and to determine whether supplementing litter with inorganic N improves P extraction. The research was part of a larger program with an overall goal of developing best management practices for using poultry litter as a primary fertilizer for optimum cotton production in the southeastern USA.
| MATERIALS AND METHODS |
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The 10 treatment combinations within each location were tested in a randomized complete block design with three or four replications. The plots consisted of four 119 m-long rows spaced 1.02 m apart at Cruger and eight 73 m-long rows spaced 0.97 m apart at Coffeeville. Each treatment was applied to the same plot in all 3 yr. Each year, UAN (32% N) was applied between square and first flower stage as a sidedress using a commercial liquid fertilizer applicator equipped with coulters which opened slits about 0.15 to 0.20 m away from the row center into which the UAN solution was injected to a depth of
0.10 m. Inorganic N, P, and K fertilizers were applied to the STD at the same rate as adjacent fields as practiced by the respective farm. This treatment received 135 kg N ha1 yr1 as UAN under the conventional-till at Cruger. Under the no-till at Coffeeville, the treatment received 101 kg N ha1 in 2002 and 118 kg N ha1 in 2003 and 2004 as UAN. Phosphorus was applied as triple superphosphate (0460 NP2O5K2O) to the STD at 0, 20, and 0 kg P ha1 at Cruger and 29, 20, and 0 kg P ha1 at Coffeeville in 2002, 2003, and 2004, respectively. Potassium was applied to the STD as KCl (0060 NP2O5K2O) at 140, 98, and 93 kg K ha1 at Cruger and 56, 75, and 112 kg K ha1 at Coffeeville in 2002, 2003, and 2004, respectively. All P and K fertilizers were applied to the STD as a broadcast by hand before planting.
Litter was applied 3, 1, and 10 d before planting at Cruger in 2002, 2003, and 2004, respectively. At Coffeeville it was applied 22 d before planting in 2002, 25 days after planting (DAP) in 2003, and 9 DAP in 2004. Each year, the litter was broadcast-applied with a commercial fertilizer spreader equipped with ground speed-sensing radar, an electronic scale, and a rate-control computer system (Barrons & Brothers, Inc., Gainsville, GA). Litter was soil-incorporated in the same day of application under the conventional-till at Cruger but was not incorporated under the no-till at Coffeeville. Cotton was planted on 19 Apr. 2002, 16 Apr. 2003, and 19 Apr. 2004 at Cruger; and on 21 May 2002, 2 May 2003, and 28 Apr. 2004 at Coffeeville. Additional details on soil properties, crop management, and weather are provided elsewhere (Tewolde et al., 2007).
Extracted P was determined based on aboveground whole-plant samples collected from 0.5- to 0.6-m2 center rows of each plot. Plant samples were taken four times during the 2002 and 2003 growing seasons from Cruger and during the 2002 growing season from Coffeeville. The samples from Cruger were taken 68, 97, 112, and 130 DAP in 2002, and 78, 98, 121, and 135 DAP in 2003. The samples from Coffeeville were taken 50, 71, 93, and 112 DAP in 2002. In other years, plants were sampled only at the end of the season: 134 DAP in 2004 from Cruger, and 137 DAP in 2003 and 138 DAP in 2004 from Coffeeville. Each year, cotton started flowering in late June at Cruger and in early to mid-July at Coffeeville.
Plants from both locations were cut at soil level, separated into leaves (leaf blade + petioles), stems (branches + main stem), and reproductive parts (squares + flowers + bolls). Reproductive parts were further separated into burs, seed, and lint when bolls were mature enough to make the separation feasible. The lint was separated from seed using a 10-saw gin. All other separations were accomplished by hand. All plant parts were dried in a forced-air oven at 80°C to constant weight, weighed, and ground to pass a 1-mm sieve. Seed samples were delinted with H2SO4 before grinding as linters on seed made homogenization extremely difficult.
Phosphorus concentration in plant parts was determined using an inductively coupled dual axial Argon plasma spectrophotometer (ICP, Thermo Jarrell-Ash Model 1000, Franklin, MA) (Donohue and Aho, 1992). Approximately 0.2 g of the dried and ground sample was ashed in a muffle furnace at 500°C for 4 h. The ash was digested by adding 1.0 mL 6 M HCl for 1 h and 40 mL of a double-acid solution of 0.0125 M H2SO4 and 0.05 M HCl for an additional 1 h. The digested solution was then filtered using a 2V Whatman (Maidstone, UK) filter paper and analyzed for total P concentration by the ICP. Phosphorus concentration in the litter was determined by the same method used for the plant tissues.
Accumulation of P in each plant part was calculated as the product of P concentration and dry weight of each plant part. Total P extracted by aboveground plant parts was determined as the sum of P accumulation in leaves, stems, and reproductive parts. Phosphorus concentration was not analyzed in all lint samples as the P content of lint was expected to be low. Total P accumulation in lint was therefore determined by multiplying the lint dry weight of each sample by an average lint P concentration measured on all lint samples from 1 yr-location. Each lint sample used for analysis was thoroughly cleaned by hand to remove contaminating debris. The fraction of P partitioned to a plant part was calculated as a percentage of the total P extracted by all aboveground plant parts. The efficiency of cotton in extracting applied P (PEE), which is sometimes referred to as apparent P recovery, was computed as total extracted P as a percentage of the total applied P after accounting for P extracted by untreated plants as
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Litter and supplemental UAN-N effects on P concentration in each plant part and amount of extracted P by each plant part were tested by subjecting the data to ANOVA using MIXED model analysis on SAS (Littell et al., 2002). Preliminary ANOVA was performed for a randomized complete block design with a factorial treatment structure for litter and UAN-N factors. Additional analysis was performed using a trend to describe the litter and UAN-N treatment structure as a response surface model where the full model had three slope parameters that included litter linear (LL), UAN-N linear (NL), and their interactions (LL x NL). The significance of the linear effects of litter (LL) and UAN-N (NL) were tested by omitting the LL x NL interaction term from the full model when the interaction was not significant. Regression analysis was used to test the relationship between amount of extracted P and tissue P concentration with applied total plant available N (NTPA). The NTPA was estimated by summing applied litter N and UAN-N with the assumption that 50% of the total litter N (Tewolde et al., 2007) and 100% of the UAN-N become plant available in the cotton growing season. All differences mentioned in the discussion are significant at P
0.05 unless stated otherwise.
| RESULTS AND DISCUSSION |
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Phosphorus Concentration in Plant Parts
Phosphorus concentration of bulk whole leaves (petioles + blades) on any of the sampling days in 2002 and 2003 at Cruger and in 2002 at Coffeeville ranged between 2.4 and 7.7 g kg1 (Table 1). This range is well within or above the published sufficiency range of 1.5 to 6.0, which is based on the youngest fully mature leaf blades taken between early and late flowering (Mitchell and Baker, 2000). Among all plant parts excluding lint, seeds or reproductive parts had the largest P concentration and stems had the least at any stage in the season. At maturity, seed P concentration of all treatments at either location exceeded 6.4 g kg1 and was as much as 10.6 g kg1. Lint P concentration, measured on Cruger samples taken at the end of the season in 2002 only, did not exceed 0.5 g kg1 which is even less than that of stem P concentration. The largest reported P concentration of cotton fertilized with conventional inorganic fertilizers is 7 g kg1 in seed and 3 to 5 g kg1 in leaves (Halevy, 1976). Others reported even lower leaf and seed P concentration (Bassett et al., 1970; Mullins and Burmester, 1990).
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Treatments affected leaf P concentration, with litter application affecting leaf P concentration less consistently than UAN-N application despite applying different amounts of P in litter depending on the rate. The litter-linear (LL) effect on leaf P concentration was not significant in any of the four sampling days at Cruger or Coffeeville in 2002 and in the first two sampling days in 2003 at Cruger (Table 1). The UAN-N-linear (NL) effect, on the other hand, was significant on three of the four sampling days in 2002 at Cruger and in the last two sampling days in 2003 at Cruger and in 2002 at Coffeeville. Leaf P concentration decreased with increasing UAN-N rate. Usually the untreated control (L0N0), which received no UAN-N, litter, or any other fertilization, had the largest leaf P concentration. Leaf P concentration of this treatment at the end of the season was 4.1 g kg1 in 2002 and 6.9 g kg1 in 2003 at Cruger. End-of-season leaf P concentration of the L0N0 treatment at Coffeeville in 2002 was even greater at 7.7 g kg1. Treatments that received adequate N fertilization usually had the least leaf P concentration on all days. The STD treatment, for example, which received adequate N and was among the top-yielding treatments (Tewolde et al., 2007), usually had the lowest end-of-season leaf P concentration with 3.0 g kg1 in 2002 and 2.6 g kg1 in 2003 at Cruger and 4.4 g kg1 in 2002 at Coffeeville. The L4.5N67 treatment, which also received adequate N and yielded as good as or better than the STD (Tewolde et al., 2007), had leaf P concentration similar to that of the STD (3.5 g P kg1 in 2002, 2.9 g P kg1 in 2003 at Cruger, and 4.3 g P kg1 in 2002 at Coffeeville).
The dependence of leaf P concentration on N nutrition became more apparent when leaf P concentration was regressed on NTPA, which showed that leaf P concentration measured later in the season decreased with increasing NTPA (Fig. 1 ). The response of P concentration to litter, UAN-N, or NTPA in the other plant parts was similar to the response of leaf P concentration at both locations. The cotton plant appears to continue extracting P even when applied N is inadequate regardless of the adequacy of soil P. Soil P extracted by Mehlich-3 solution (Mehlich, 1984) immediately before planting each season was 40.4 mg kg1 in 2002 and 63.2 mg kg1 in 2003 at Cruger and 8.1 mg kg1 in 2002 at Coffeeville. Inhibited plant growth due to N deficiency while plants continued to absorb P probably leads to greater P concentration in leaves and the other plant parts. Evers (2002) reported an inverse relationship between P concentration in forage grasses and the amount of N applied each year and attributed this relationship to increased forage production due to increased applied N and therefore a dilution effect on the P concentration in the forage. When P is absorbed in excess of plant metabolic needs, it is probably stored in leaf cell vacuoles as an inorganic P and as a phytate P in seeds (Marschner, 1995). Up to 77% (6.4 g kg1) of the total seed P in cotton is found in the form of phytate compared with 55% in wheat (Triticum aestivum L.), 73% in corn (Zea mays L.), and 65% in rice (Oryza sativa L.) grains (Godoy et al., 2005).
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65 DAP to 36.5 kg P ha1 at
125 DAP (Fig. 2
). The increase in total extracted P beyond
90 DAP was solely due to rapid accumulation of P in seed. Phosphorus accumulation in leaves and stems peaked at
90 DAP and gradually declined thereafter with the decline in stems being much smaller than in leaves. Amount of P accumulated in burs also declined from 11.0 kg P ha1 at
90 DAP to only 4.9 kg P ha1 at
125 DAP. The decreasing trend of P accumulation in leaves, burs, and stems and the increasing trend in seeds suggest that P is remobilized from burs, leaves, and stems to seed, although some P may have also been lost in self-defoliated senescent leaves.
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To our knowledge, the largest reported P extraction by mature cotton is 44 to 46 kg P ha1 by Halevy (1976), who grew cotton in Israel under irrigation after applying NPK fertilizers presumably from inorganic sources. Bassett et al. (1970), who used one of the two cultivars used by Halevy (1976) under irrigation and applied only N fertilizers, reported a maximum P extraction of only 19 kg P ha1 with only 9 to 12 kg P ha1 removal from the field with harvested seed. More recently, Dorahy et al. (2004) reported P uptake by cotton that received P fertilizers in eastern Australia to range between 13 and 31 kg P ha1 at cutout. This is still substantially lower than the extraction we recorded in our research, where we fertilized with broiler litter supplemented with inorganic N. This may be an indication that the cotton plant may extract P in excess of its normal metabolic need when fertilized with poultry litter supplemented with inorganic N. It seems a large fraction of this excess P is stored in the seed.
The maximum P extracted by one cotton harvest in one season recorded in our research was equivalent to the maximum P extracted by year-round forage harvested six or seven times during the year (Evers, 2002). Evers (2002) grew Coastal bermudagrass which was overseeded with annual ryegrass in the winter and measured a maximum P uptake of 18.6 kg ha1 by bermudagrass and 36.6 kg ha1 by ryegrass for a total of 55.3 kg P ha1 uptake from the same soil that received 9 Mg ha1 litter applied once in October plus 168 kg N ha1 as ammonium nitrate applied three times during the year. When harvested only once, the maximum P uptake by temperate legume and grass species was less than half that of cotton in our research (Brink et al., 2001). This shows cotton extracts as much P as or more P than forage and pasture crops to which litter has traditionally been applied.
Extracted Total Phosphorus at Coffeeville versus Cruger
Relative comparison of extracted P by certain treatments shows that plants at Coffeeville extracted as much P as plants at Cruger despite producing less lint and aboveground dry weight. For example, the L6.7N0 treatment extracted 37.5, 32.4, and 39.8 kg P ha1 at Coffeeville compared with 29.4, 36.7, and 42.5 kg P ha1 at Cruger at the end of the season in 2002, 2003, and 2004, respectively (Fig. 3). The L6.7N0 treatment produced 1269, 1405, and 1252 kg ha1 lint at Coffeeville and 1643, 1484, and 1424 kg ha1 lint at Cruger (Tewolde et al., 2007). Mehlich 3 extractable soil P (Mehlich, 1984) before planting each season at Coffeeville (19.4 mg P kg1 soil averaged across years) was also much less than at Cruger (60.7 mg P kg1 soil averaged across years). The ability of the cotton at Coffeeville in extracting P comparable to that of the cotton at Cruger, despite producing less lint and aboveground biomass, may be because lower soil pH at Coffeeville than at Cruger may have contributed to greater plant availability and extraction of P from the soil. The greater P concentration in plant parts at Coffeeville than at Cruger (Table 1) may be an indication that P was more available and extractable at Coffeeville than at Cruger. Averaged across all treatments, preplant soil pH in the top 0.15-m soil depth was 5.5, 5.7, and 5.8 at Coffeeville and 6.0, 6.1, and 6.4 at Cruger in 2002, 2003, and 2004, respectively. Cultivars may also have contributed to a greater P extraction at Coffeeville than at Cruger, but some reports indicate that cultivars may not differ in P uptake (Mullins and Burmester, 1990).
End-of-Season Phosphorus Extraction Efficiency
When averaged across all treatments that received litter, cotton at the end of the season extracted less P than applied each of the 3 yr within a location. Plants extracted an average of 38.7, 12.1, and 13.9 kg ha1 less P than applied at Cruger and an average of 40.7, 24.9, and 25.6 kg ha1 less P than applied at Coffeeville in 2002, 2003, and 2004, respectively (Table 3). The greater discrepancy between extracted and applied P in 2002 than in 2003 or 2004 is most likely due to a greater litter P concentration in 2002 (
18 g kg1) than in 2003 and 2004 (
12 g kg1) and therefore due to applying more litter P in 2002 than in the other 2 yr. Applied litter remained the same each year. The litter used for both locations in 2002 was supplied by a commercial broiler chicken producer in southern Mississippi and the litter used in 2003 and 2004 was supplied by another commercial broiler chicken producer in central Mississippi. The difference in P concentration between the two litter sources is probably indicative of the importance of P management in poultry production practices to minimize excess P in the litter.
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Phosphorus extraction efficiency, which is the efficiency by which cotton extracted litter-derived P after accounting for P supplied by the soil reserve, was as large as 46.6% at Cruger and 40.9% at Coffeeville among all treatments that received litter (Table 3). Within each level of UAN-N, PEE usually was largest with 2.2 Mg ha1 litter application and smallest with 6.7 Mg ha1 litter application. When averaged across all years and the three UAN-N levels, PEE was 23.3, 16.3, and 12.8% at Cruger and 21.3, 15.7, and 13.9% at Coffeeville when applied litter was 2.2, 4.5, and 6.7 Mg ha1, respectively. This decrease of PEE with increasing litter rate is because extracted amount of P did not proportionally increase with increasing applied litter rate and therefore with increasing litter-derived P rate. The low PEE found in this field research, to some extent, agrees with a finding by Tewolde et al. (2005) who reported a maximum of only 16% litter P extraction by immature cotton grown in an inert media in a greenhouse.
Supplementing litter with UAN-N improved PEE, although this was only occasionally significant. Phosphorus extraction efficiency averaged across all years and litter rates was 12.7, 19.8, and 26.6% at Cruger and 13.4, 15.8, and 26.6% at Coffeeville when 0, 34, and 67 kg ha1 supplemental UAN-N was applied, respectively (Table 3). The increase in PEE with increasing supplemental UAN-N rate most likely is because of increases in seed cotton yield and plant growth in proportion to the UAN-N rate. This may be one reason applying litter to meet a portion of the N need and applying inorganic N to meet the other portion of the cotton N need may be the best strategy of managing litter-derived P when litter is used as the primary cotton fertilizer in high-P soils.
Overall, our results indicate that applying the higher rates of litter will lead to accumulation of P in the soil over time. Of the three litter rates tested in this research, soil P accumulation to detrimental levels is less likely to happen when the lower rate of 2.2 Mg ha1 litter is used. However, applying 2.2 Mg ha1 litter may not be an attractive practice for a grower because this rate supplies too little (
25%) of the N need of cotton (Tewolde et al., 2007) for growers to invest and make litter use as part of their fertilization program. Litter rate of 6.7 Mg ha1 supplied
75% of the N need for cotton production in this research. But, our results show cotton extracts much less P than supplied by 6.7 Mg ha1 litter, a rate which is likely to result in accumulation of P in the soil. The intermediate rate of 4.5 Mg ha1 may be a more attractive rate because it supplies
50% of the N need of cotton, and the buildup of soil P when this rate is used is less than that of the 6.7 Mg ha1 litter rate. Further, the 4.5 Mg ha1 litter application supplemented with 67 kg ha1 UAN-N resulted in the best lint yield each of the 3 yr at both locations (Tewolde et al., 2007). If it is necessary to apply the higher rates of litter rate, another viable strategy may be to draw down accumulated soil P by stopping litter application for a few years and by fertilizing with inorganic N sources until an amount of P equivalent to that added by previous years' litter application has been removed with harvested crop after which litter fertilization may be resumed.
Partitioning of Phosphorus to Plant Parts
Phosphorus extracted by aboveground plant parts at the end of the season was recovered largely in reproductive parts including seed, lint, and bur. An average across treatments, years, and locations of 71% of the total extracted P was partitioned to reproductive parts. Seed alone contained 52.7% of the total extracted P and lint contained an additional 2.4% for a total of 55.1% that would be removed with harvested crop.
Litter and UAN-N applications significantly affected partitioning of P to plant parts mostly in 2003 at Cruger (Table 4). Increasing litter rate at this location in 2003 linearly decreased P partitioning to leaves but linearly increased P partitioning to seeds. For example, when no UAN-N was applied, partitioning of P to leaves at 0, 2.2, 4.5, and 6.7 Mg ha1 litter was 22.7, 20.2, 17.2, and 12.3%, respectively, with a corresponding partitioning to seed of 50.6, 52.2, 54.2, and 60.5%. Increasing applied UAN-N also had similar effect on P partitioning. The P partitioning to leaves of the 2.2 Mg ha1 litter treatment supplemented with 0, 34, or 67 kg ha1 UAN-N was 20.2, 13.9, and 12.0%, respectively, with a corresponding partitioning to seed of 52.2, 60.6, and 61.6%.
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| CONCLUSIONS |
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18 g kg1 P concentration but removes only about 55% of it in harvested seed and lint. Applying litter
4.5 Mg ha1 supplies P in excess of the amount that can be extracted by cotton and would result in the buildup of soil P over time. Supplementing litter with inorganic N fertilization increases P extraction but not to the extent that all of the litter-derived P is extracted. Supplemental inorganic N increases extracted litter P by increasing dry weight, not by increasing tissue P concentration. Increasing supplemental inorganic N or litter rate, to the contrary, decreases tissue P concentration. In addition to increasing total P extraction, supplementing litter with inorganic N benefits litter-P management because it seems to shift P partitioning from vegetative to reproductive parts and therefore increases the P amount removed in harvested crop. Overall, this research shows cotton extracts as much P as or more P than forage and pasture crops to which litter has traditionally been applied although cotton may not extract all of the P supplied by
4.5 Mg ha1 litter. | ACKNOWLEDGMENTS |
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| REFERENCES |
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