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a USDA-ARS, Coastal Plains Soil, Water, and Plant Research Center, 2611 W. Lucas St., Florence, SC 29501-1242
b Clemson Univ., Pee Dee Research and Education Center, Florence, SC
* Corresponding author (bauer{at}florence.ars.usda.gov)
| ABSTRACT |
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| INTRODUCTION |
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The value of cotton for yarn and textile manufacture is determined by the length, tensile strength, and fineness of the fibers. These fiber properties are determined by the genetic potential of the cultivar and the environmental conditions existing during the development of the boll that allow expression of that genetic potential (Ramey, 1986). Cotton bolls are initiated over a long period of time during the season, and fiber properties of bolls on the same plants can differ because of different environmental conditions during boll growth and development. Bennett et al. (1967) found substantial differences in fiber quality among bolls due to the week during the season that flowering occurred. Also, Meredith and Bridge (1973) hand-harvested all open bolls weekly and found fiber properties differed among the weekly harvested samples.
Fiber quality can also vary across fields. Johnson et al. (2002) reported considerable variation for fiber micronaire and fiber length in a 0.5-ha portion of a field in South Carolina. They found significant correlations between several fiber properties and soil pH, soil P, and soil organic matter. Emphasis has been placed lately on reducing the amount of fiber property variability within a cotton crop (May, 2002), as processing techniques require a more uniform fiber to increase throughput and yarn production. A greater understanding of the amount and causes of fiber quality variation may lead to better management practices for improved fiber quality.
We hypothesized that soil management practices influence fiber properties of bolls when measured at specific fruiting positions. We tested this hypothesis on two soil types that differ in soil water holding capacity and historical yield potential. Our objective was to determine whether soil management practices affect canopy position specific fiber properties on two soils.
| MATERIALS AND METHODS |
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The crop management treatments were winter cover (rye or none) and tillage (disk or conservation tillage). A randomized complete block experimental design was used. There were three replicates of each crop management treatment combination. The experiment was arranged in the field so that both soil types occurred within each plot. Each plot was twelve 1-m-wide cotton rows that ranged from 122 to 213 m in length. Plot lengths varied because all plots ended at the field edge which was irregular and the variation in length allowed for both soils to be included in each plot. Each plot was divided into 13.7-m-long subsections. Soil type was assigned to each subsection from the USDA-NRCS soil map and from inspection in the field.
In the rye winter cover plots, 134 kg ha–1 of Gurley Grazer rye seed was planted directly into the previous crop residues with a no-tillage grain drill on 17 Oct. 1996, 12 Nov. 1997, and 12 Nov. 1998. Each year in the spring, lime, P, K, and Mn were broadcast applied to the entire experimental area at rates based on soil test analysis. The fertilizer application also included 22.4 kg S ha–1 and 2.24 kg B ha–1. Rye and the winter weeds in all conservation tillage plots were sprayed with paraquat dichloride (1-1'dimethyl-4-4'-bipyridinium dichloride) (0.17 kg a.i. ha–1) on 30 April in 1997 and with glyphosate [N-(phosphonomethyl)glycine)] (1.12 kg a.i. ha–1) on 27 April 1998 and 15 April 1999. At this time, the disk tillage plots were disked twice (to a depth of 15 cm) and then smoothed with an S-tined harrow. A six-legged paratill was used (to a depth of 40 cm) to alleviate subsoil compaction in all plots. The paratill was used just before planting cotton on 2 May 1997 and on 11 May 1999. For the cotton grown in 1998, the paratill was used in the fall before planting rye on 10 November 1997.
Cotton was planted with a four-row planter equipped with wavy coulters on 7 May 1997, 18 May 1998, and 12 May 1999. DPL Acala 90 was planted in 1997 and 1998 and DPL 675 was planted in 1999. Seeding rate each year was approximately 10 seeds m–1 of row. Weeds were controlled using herbicides and handweeding, and for the conventional tillage plots, a cultivator was used at least once each year. Insects were regularly scouted and controlled with insecticides as needed. Fertilizer N was applied to the cotton in a split-application of NH4NO3 each year. Within one week of planting, 45 kg N ha–1 was applied each year using a four-row applicator equipped with fertilizer coulters with rear knives. A subsequent application of 45 kg N ha–1 was made with the same applicator on 20 June 1997, 18 June 1998, and 18 June 1999.
In the fall of each year, bolls were hand-harvested by canopy position from one subsection of the Norfolk soil and one subsection of the Bonneau soil within each plot. Three canopy positions were evaluated by harvesting bolls at the first node on two adjacent fruiting branches (sympodial branches). These canopy positions were Mainstem Nodes 6 and 7, Mainstem Nodes 9 and 10, and Mainstem Nodes 12 and 13. Boquet and Moser (2003) reported little difference in boll weight among first position bolls at adjacent sympodia. Because there is an approximate three-day difference in age between bolls on adjacent sympodia at the first fruiting position (Mauney, 1986), these fruiting sites were chosen since first position bolls at these three canopy positions roughly correspond to anthesis dates during the first, second, and third week of flowering. Bolls were bulk harvested from 3 m of row in 1997, 6 m of row in 1998, and 12 m of row in 1999. Each canopy position was harvested at separate times, except in 1999 when the two upper canopy positions were harvested at the same time. Hand harvests were made in September and early October each year.
The cotton in the plots was chemically defoliated with thidiazuron (N-phenyl-N'-1,2,3-thiadazol-5-ylurea), S,S,S-tributyl phosphorotithioate, and bolls were opened with ethephon [(2-chloroethyl) phosphonic acid] at the recommended rates each year. Two rows from each subplot not used for hand harvesting were harvested with a spindle picker on 30 Oct. 1997, 26 Oct. 1998, and 12 Nov. 1999. After weighing the bags of seedcotton, samples were taken from the harvest bags for determination of lint percentage and fiber property analysis. Cotton hand-harvested by canopy position and the machine-harvested samples from the harvest bags were ginned in a 10-saw laboratory gin. Samples of the fibers were sent to Starlab, Inc. (Knoxville, TN) for high volume instrumentation analysis of fiber properties.
Precipitation and temperature were measured with a weather station located within 2 km of the field. Square initiation dates for each of the three canopy positions were estimated using the findings of Constable (1991) on plant morphological development to heat unit accumulations. To evaluate the weather effects on the three canopy positions, the square initiation date for the canopy positions was set to midpoint in heat units between the two mainstem node positions that were harvested together at each canopy position.
Data were analyzed by year because the cultivar used in 1999 was different from the first two years. For the lint yield and whole-crop fiber property data from the machine harvest, data were analyzed as a split-plot design. Soil types were considered main plots and subplots were the cover crop and tillage combinations. The position-specific fiber property data from the hand-harvested samples were analyzed as a split-split plot design. Main plots were soil type, subplots were the crop management treatments and sub-subplots were the canopy positions. Because the soils were in fixed positions in the field, testing of the main effect of soil type is irrelevant, but subplot main effects and interactions involving soil types are valid (Cochran and Cox, 1957). Tests for homogeneous variance were conducted between the two soil types for all variables in each year to determine if subplot error variance could be used to compare crop management and canopy position combinations within a soil type. None of the tests indicated heterogeneous variance, so all mean comparisons were made using the pooled error variance. Sources of variation were considered significant when probability of greater F values were
0.05. Means were separated by calculating a least significant difference (LSD) when sources of variation were significant (P = 0.05).
| RESULTS AND DISCUSSION |
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Cover crop had only a small influence on yield and fiber properties of the whole crop in this study (data not shown). There were no significant interactions between cover crop and soil type or tillage for lint yield in any year. Averaged over both soil types and both tillage systems, cotton lint yield was 933 kg ha–1 following fallow and 803 kg ha–1 following rye in 1997 (P > F = 0.02), but there were no differences between rye and fallow for yield in 1998 (722 kg ha–1 following fallow and 733 kg ha–1 following rye) or in 1999 (369 kg ha–1 following fallow and 365 kg ha–1 following rye). Winter cover influenced fiber length only in 1997 when a significant cover crop x tillage interaction occurred. In that year, fiber length of cotton grown following rye was 0.2 mm longer than cotton grown following winter fallow when conservation tillage was used, but with disk tillage, fiber length following rye was 0.5 mm shorter than following winter fallow (LSD 0.05 = 0.2 mm). A significant cover crop x tillage interaction occurred for fiber length uniformity in both 1997 and 1998, but the nature of the interaction differed between years. In 1997, fiber length uniformity of cotton grown following rye with disk tillage was approximately 0.7% less than the other three tillage-winter cover combinations (rye with conservation tillage, disk tillage with both rye and fallow) while in 1998, cotton grown following rye with conservation tillage was approximately 0.9% higher than the other three tillage-winter cover treatment combinations. Micronaire and fiber strength were not affected by cover crop treatment in any year of the study.
Canopy Position Specific Fiber Properties
Rye, either as a winter cover crop in the conservation tillage system or as a green manure in the conventional tillage system, did not influence the canopy position specific fiber property response in any of the 3 yr of this study. No interactions that included both rye and canopy position were significant for any fiber property in any year (data not shown).
The influence of tillage on fiber length at each canopy position is shown in Table 3. The response of fiber length to tillage was similar for both soil types. Averaged over soil types, the canopy position specific response of fiber length to tillage was quite different for the 3 yr. In 1997, fiber length did not differ between tillage systems at any canopy position (Table 3). In both 1998 and 1999, significant tillage x canopy position interactions occurred for fiber length, but the nature of the interactions was different for the two years. With conservation tillage, fibers were 1 mm longer than fibers from cotton grown with disk tillage at Mainstem Nodes 6 to 7 in 1998, but there was no difference between the two tillage systems at the other two canopy positions. Conversely, in 1999 fibers from cotton grown with conservation tillage averaged 1 mm longer than fibers grown with disk tillage at Position 12 to 13 with no differences between tillage systems at the other two canopy positions.
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In 1999, when yield was lowest of the 3 yr (Table 1), rainfall was low during the fiber elongation phase for all canopy positions. Although a different cultivar was grown in 1999 than in the other two years, it is likely that the lack of rainfall in 1999 was the main factor causing the substantially shorter fibers in that year compared with the other two years (Fig. 1c). Better capture and/or retention of the rainfall that did occur was again likely the reason for conservation tillage having higher fiber length than conventional tillage at Position 12 to 13 (Table 2). The reason for conservation tillage having higher fiber length than disk tillage at that canopy position in 1999 but not 1997 (where bolls were also subjected to water-deficit stress) is likely at least partially due to 1999 being a much dryer year than 1997. Although canopy light interception was not measured in this study, we suspect that canopy closure did not occur by the time this canopy position flowered and began fiber elongation in 1999, so the benefits of conservation tillage on soil water supply were still present at this relatively late time in the season. In 1997, ample early precipitation resulted in a vigorously growing crop with early canopy closure and therefore there may have been little benefit of conservation tillage practices on soil water content when flowering occurred at Position 12 to 13 in that year.
The effect of tillage on fiber length uniformity mirrored the results for fiber length (Table 3). Conservation tillage had higher fiber length uniformity than disk tillage at canopy Position 6-7 in 1998 and Position 12 to 13 in 1999, and there were no differences between tillage systems at any other canopy position in any year.
Somewhat overlapping with the fiber elongation phase of development, fiber secondary wall deposition occurs from about 15 to 45 d after anthesis (Stewart, 1986). Micronaire is an estimate of the amount of secondary wall deposition. Fiber micronaire was greater for conservation tillage than for disk tillage at canopy Position 6 to 7 in 1997 and at Positions 6 to 7 and 9 to 10 in 1998 (Table 4). There were no differences between tillage systems at the other canopy positions in those years or at any canopy position in the very dry year of 1999. It is not apparent why conservation tillage had higher micronaire than disk tillage at the lowest canopy position in 1997. Lint yields were similar between the two tillage systems in that year and the micronaire of the entire crop was slightly lower in conservation tillage than in disk tillage (Table 1). Fiber length values at that canopy position were similar for the two tillage systems (Table 4) suggesting that soil water supply, at least early in the development of micronaire for these bolls, did not differ between the two tillage systems. Higher fiber micronaire at Positions 6 to 7 and 9 to 10 with disk tillage than with conservation tillage in 1998 (Table 4) may have been due to the better soil water conditions with conservation tillage (conservation tillage also had longer fibers than disk tillage at canopy Position 6–7). Bauer and Roof (2004) found highest micronaire in cotton grown in the driest of a 3-yr study.
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Cotton fiber strength was least affected by tillage in this study. Tillage had no influence on cotton fiber strength of the entire crop (Table 1) and there were no differences between disk tillage and conservation tillage at any canopy position in any year (Table 4). In contrast to the results for the other fiber properties, there was a consistent canopy position response for fiber strength across years. Bolls from Position 12 to 13 had lower fiber strength than bolls at the two other canopy positions each year.
The canopy position specific responses for fiber length and strength (Table 5) and fiber length uniformity (not shown) were generally similar for the two soil types within each year of this study. Genetic determination of these fiber properties is quite high (compared with environmental determination) (Meredith, 1984). Thus, it is not particularly surprising that the direction and magnitude of differences between canopy positions on these two soils were similar each year. On the other hand, environment plays a relatively larger role in determining micronaire compared with fiber length and strength (Meredith, 1984). Although the direction of response with canopy position for micronaire was similar for the two soils each year, the magnitude of difference between the highest and lowest value within each soil each year was much greater for the Bonneau soil than for the Norfolk soil (Table 5). These results expand the findings of Johnson et al. (2002) who found there are spatial relationships with soils for individual fiber properties. This study suggests that the amount of within canopy fiber property variability, at least for micronaire, may also be soil specific.
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Received for publication February 19, 2004.
| REFERENCES |
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