Skip to main content

ORIGINAL RESEARCH article

Front. Plant Sci., 03 August 2018
Sec. Agroecology

\r\nXinyue ZhangXinyue Zhang1Hongkun YangHongkun Yang1John L. SniderJohn L. Snider2Rizwan ZahoorRizwan Zahoor1Babar IqbalBabar Iqbal1Binglin ChenBinglin Chen1Yali MengYali Meng1Zhiguo Zhou*Zhiguo Zhou1*
  • 1College of Agriculture, Nanjing Agricultural University, Nanjing, China
  • 2Department of Crop and Soil Sciences, University of Georgia, Tifton, GA, United States

In order to increase cotton productivity and optimize fiber quality on limited arable land, an integrated crop management system (ICMS), which combined with some optimal management practices, is projected to replace the conventional crop management system (CCMS) for cotton production in the Yangtze River valley. The seedcotton yield and fiber quality with respect to fruiting position under ICMS and CCMS were investigated in 2012 and 2013 in two fields differing in soil fertility. Reduced bolls on fruiting branches 1–10 (FB1−10) and at fruiting position 1–2 (FP1−2) on FB11−15 could not be fully compensated by increased bolls on FB16+ under CCMS, resulting in more seedcotton yield under ICMS relative to that under CCMS. Fiber at majority fruiting positions under CCMS were longer and stronger than those under ICMS, but CCMS increased the contribution of bolls on FB11+ to the cotton yield, which overall resulted in no significant change in fiber length and strength by management system at field level. The number of bolls at FP1−2 on FB1−5 under CCMS while the number of bolls on FB1−5 and at FP1−2 on FB1−5 were not significantly changed by soil fertility, resulting in diminished yield difference in soil fertility among ICMS relative to that of CCMS. The high soil fertility significantly increased seedcotton yield relative to low soil fertility, which was attributed to more number of bolls on FB11+ and higher seedcotton weight per boll at all fruiting positions. High soil fertility field not only recorded superior fiber quality on FB11+, but also increased the contribution of these bolls to the cotton yield relative to those in the low soil fertility field, resulting in no significant change in overall fiber quality among soil fertility. These findings demonstrate that by combining optimal management practices on infertile soils ICMS could minimize the yield differences due to soil fertility without sacrificing fiber quality.

Introduction

Cotton (Gossypium hirsutum L.) is an important cash crop and provides raw material for producing textiles. However, with increasing population and greater demand for food in China, a large area of fertile land previously cultivated to cotton has been occupied by food crops (Zhao and Tisdell, 2009). Thus, cotton production has moved to low soil fertility fields (Dong et al., 2012). Low soil fertility has a negative impact on cotton production (Das et al., 2006; Singh and Ahlawat, 2014; Kintché et al., 2015), and this coupled with poor field management have imposed substantial challenges to cotton production (Dong et al., 2009). Therefore, it is essential to optimize management practices to improve seedcotton yield and fiber quality in the low soil fertility fields.

Numerous studies showed that agronomic management practices such as plant density (Bednarz et al., 2000; Ghader et al., 2012; Feng et al., 2014) and nitrogen management (Reddy et al., 2004; Saleem et al., 2010; Yang et al., 2011) have a profound effect on seedcotton yield and fiber quality. Moreover, high crop yields and quality are difficult to achieve by altering single management practices in isolation (Robertson et al., 2000; Ladha et al., 2003), and interactions exist among agronomic practices since yield is determined by the most limiting factor (Dai et al., 2017). An integrated approach that optimizes nutrients and other agronomic management practices would allow the maximization of crop yield (Wang et al., 2017). In order to increase yield, some progressive farmers generally integrate optimized management practices into their conventional crop management system (CCMS); this has been referred to as an integrated crop management system (ICMS) or “best management” system. Several recent reports have indicated that the productivity of rice (Balasubramanian et al., 2005; Cao and Yin, 2015), wheat (Gupta and Seth, 2007) and maize (Jin et al., 2012) are effectively enhanced by adopting ICMS. Whether ICMS can also improve cotton yield and fiber quality requires further study.

Soil fertility is an important factor governing agricultural practices (Sawan et al., 2006). Soil fertility includes levels of organic matter, total nitrogen, available nitrogen, phosphorus, and potassium (Xiong et al., 2003; Zingore et al., 2007). The soil fertility level of a given field can greatly influence crop response to different management practices (CRI, 2013). Dong et al. (2010) found that increased plant density and/or nitrogen rate significantly increased cotton yield in low soil fertility situations but not under high soil fertility. Moreover, soil fertility has different effects on the productivity of cropping systems. Improved soil fertility could increase the yield of long-season cotton or cotton in a double-cropping system, but the yield of short-season cotton or cotton grown in monoculture may not be affected by soil fertility (Feng et al., 2017; Lu et al., 2017). While a number of studies have addressed the impact of management systems or individual management practices on cotton productivity, studies evaluating integrated management practices under contrasting soil fertility levels are limited. This information will be extremely important for producers attempting to make management decisions specifically tailored to their production scenarios.

Cotton produces bolls that vary in size and fruiting position depending on soil quality and other environmental conditions, resulting in different boll distribution patterns and within-canopy fiber quality (Mauney, 1986). Boll distribution patterns and within-canopy fiber quality can be used to explain differences in productivity and to evaluate the effects of crop management (Kerby and Buxton, 1981). Therefore, the objectives of this study were to determine (i) the differences in seedcotton yield and fiber quality with respect to fruiting position under CCMS and ICMS; and (ii) the differential yield responses of CCMS and ICMS to soil fertility; and (iii) how soil fertility influences the seedcotton yield and fiber quality with respect to fruiting position.

Materials and Methods

Experimental Site and Plant Material

A 2-year field study was conducted during 2012 and 2013 under two different soil fertility levels (low and high soil fertility fields, 200 m apart) at Dafeng, Jiangsu, China (33°19′N, 120°45′E). The soil at the experimental site was typical sandy loam, and two soil fertility levels were identified based on the soil nutrient status (Table 1; Yang et al., 2016). Siza 3, a widely planted cotton cultivar in the Yangtze River Valley was used as plant material. Weather data, i.e. mean daily temperature, mean daily solar radiation and total rainfall during boll development with respect to fruiting position were obtained from a weather station (Campbell AG800, Genetics, USA) located near the experimental site.

TABLE 1
www.frontiersin.org

Table 1. Soil fertility status of the two experimental fields studied in 2012 (n = 5).

Experimental Design

A CCMS and an ICMS was applied to two fields with different soil fertility levels in a 2 × 2 factorial design, with three replicates of the four treatments. CCMS followed a longstanding management practice which is utilized by the majority of farmers in the Yangtze River valley (Yang et al., 2017). The ICMS is based on CCMS but incorporates practices aimed at improving productivity, including optimal plant density, growth-driven fertilizer schedule, simplified seedling rising technology. Notably, the integration of the economic N application rate, number of N splits, and optimum plant density were based on our previous single-factor experiments (Chen et al., 2015, 2016; Meng et al., 2016), and the simplified seedling rising technology for ICMS was aimed to reduce labor cost using mechanized transplantation.

A detailed explanation of each system was provided in Table 2. Nitrogen of CCMS was applied at a rate of 300 kg ha−1, with 40% as basal dose and the remaining 60% was applied at the initial flowering stage, whereas nitrogen of ICMS was applied at an economic rate of 375 kg ha−1 (calculated according to Baker et al., 2004) in 4 splits, 20% as basal, 25% at the initial flowering stage, 40% at full-bloom stage and the remaining 15% at the end of the flowering stage, which was timed to coincide with growth-driven nitrogen demand of cotton plants. CCMS adopted a labor-intensive traditional seedling rising method (Dong et al., 2007) and seedlings were transplanted manually at a lower density of 18,000 plant ha−1, whereas ICMS adopted a simplified seedling rising technology (Dai et al., 2017) and seedlings were transplanted mechanically at an optimal density of 30,000 plants ha−1. The cottonseed used in the nursery was treated with fungicides: 8% tolclofos-methyl, 12% thiram, and 6% carbendazim. Seedlings were transplanted in the fields on May 15 when they had 3–4 true leaves. Each plot size was 220 m2 with 20 rows, having 1.1 m distance between rows and 0.5 m between plants in the row for CCMS and 0.3 m between plants in the row for ICMS.

TABLE 2
www.frontiersin.org

Table 2. Nutrients management, plant density, and seedling rising method of CCMS and ICMS in 2012 and 2013.

Sampling and Processing

Agronomic Traits and Boll Distribution

Vertically, plants were divided into four primary zones, i.e., FB1−5 (fruiting branches 1 through 5), FB6−10 (fruiting branches 6 through 10), FB11−15 (fruiting branches 11 through 15) and FB16+ (the 16th and upper fruiting branches). Similarly, plants were divided horizontally into two primary zones, the first and second fruiting positions closest to the main stem (FP1−2) and the third and greater fruiting positions (FP3+). Fifteen successive plants from three central rows in each replicate plot of two management systems in the low and high soil fertility fields were randomly tagged at maturity to determine the number of fruiting branches and positions, and the number of mature bolls (>2 cm in diameter) on the eight primary zones per unit area.

Fiber Quality

Bolls from FB3, FB8, FB13 were chosen as representative samples for zones FB1−5, FB6−10, FB11−15, respectively. Bolls from FB18 and FB16 were chosen to represent FB16+ of CCMS and ICMS, respectively. White blooms in each position were tagged with a jeweler tag, labeling the flowering and boll opening date, which encompasses the entire boll development period. All tagged, open bolls from each primary zone were harvested by hand. The seedcotton was ginned, and fiber was sent to the Cotton Quality Supervision, Inspection, and Testing Center of the China Ministry of Agriculture for quality analysis. Fiber qualities including fiber length, strength, and micronaire of each lint sample were measured with the Uster HVI MF100 cotton fiber quality analyzer (USTER®, Uster, Zurich, Switzerland).

Net Photosynthetic Rate of the Main Stem Leaves on Different Fruiting Branches

Net photosynthetic rate was measured on main stem leaves of representative fruiting branches on July 15, August 15 and September 15 in 2012 and 2013 in each field. Measurements were made using a Li-6400XT portable photosynthetic system (Li-COR, Lincoln, NE, USA) under 1,500 μmol m−2 s−1 light intensity, 65 ± 5% relative humidity, 32 ± 2°C leaf temperature and 380 ± 5 ppm CO2 between 9:30 and 11:00 a.m. on cloudless days.

Statistical Analyses

The effects of year (Y), soil fertility (S), management system (M) and their interactions on environmental conditions, morphological indices and net photosynthetic rates were analyzed using a full factorial three-way ANOVA. While, The effects of year (Y), soil fertility (S), management system (M), fruiting positions (FP) and their interactions on seedcotton yield, yield components, and fiber quality with respect to fruiting positions were analyzed using a full factorial four-way ANOVA. All statistical analyses in our study were performed using IBM SPSS Statistics 20.0 (SPSS Inc. Chicago, Illinois, USA).

Results

Environmental Conditions for Flowering and Boll Maturation

The flowering date, time required for boll maturation and the mean daily temperature of bolls with respect to fruiting position varied significantly across years, but they were not affected by the interactions between year and any of other factors (Table 5). The flowering date, time required for boll maturation, and environmental conditions during flowering and boll maturation within a given soil fertility and management system were consistent across years (Table 5).

The flowering date, duration of boll development, and environmental conditions experienced by bolls at different fruiting positions were significantly affected by year and management system, but only the flowering date and time required for boll maturation were significantly affected by soil fertility (Table 5). Among management systems, the average flowering date of bolls with respect to fruiting position under ICMS was delayed 6d and the average time for boll maturation with respect to fruiting position under ICMS was 6d longer relative to bolls under CCMS (Table 3), which resulted in different climate conditions experienced during boll growth and development despite the fact that the bolls were at the same fruiting position for CCMS and ICMS (Table 4). Compared with ICMS, the mean daily temperature during growth and development of bolls under CCMS was elevated by 1.6°C (Table 4A). Among soil fertility levels, low soil fertility delayed the flowering date 4d but shortened the time required for boll maturation by 3d compared with the high soil fertility level. Therefore, there was no significant difference in the mean daily temperature during growth and development of bolls at the same fruiting position between the low and high soil fertility fields (Table 4A).

TABLE 3
www.frontiersin.org

Table 3. Flowering date and time for boll maturation of bolls with respect to fruiting position (FP) under CCMS and ICMS in the low and high soil fertility fields in 2012 and 2013 (n = 45).

TABLE 4
www.frontiersin.org

Table 4. Mean daily temperature (A), mean daily solar radiation (B), and total rainfall (C) during the period between anthesis and boll open of bolls with respect to fruiting position (FP) under CCMS and ICMS in the low and high soil fertility fields in 2012 and 2013 (n = 45).

TABLE 5
www.frontiersin.org

Table 5. Results of ANOVA on the effects of year (Y), soil fertility (S), management system (M), and their interactions on time for boll maturation, mean daily temperature, mean daily solar radiation, and total rainfall during the period between anthesis and boll open of bolls with respect to fruiting position.

Morphological Indices of Cotton

All the morphological indices of cotton measured in the present study varied significantly across years, but there was no interaction between year and any other effects (Table 6). The variations in morphological indices with soil fertility and management system were consistent across years (Table 6).

TABLE 6
www.frontiersin.org

Table 6. Effects of management system on morphological indices in the low and high soil fertility fields in 2012 and 2013 (n = 45).

The morphological indices of cotton were significantly affected by soil fertility and management system but no S × M interaction was observed (Table 6). Among management systems, the number of fruiting branches, and fruiting positions per plant, the ratio of fruiting positions to fruiting branches, and boll retention under ICMS were significantly lower than those under CCMS. Conversely, the number of fruiting branches and fruiting positions per hectare under ICMS were higher than those of CCMS due to different plant densities in the contrasting management systems. Whether assessed on a per plant or per hectare basis, among soil fertility levels, the number of fruiting branches, fruiting positions, and the ratio of fruiting positions to fruiting branches under the two management systems in the low soil fertility field were lower than those in the high soil fertility field; however, boll retention exhibited an inverse trend.

Seedcotton Yield and Yield Component Distribution Within the Canopy

Seedcotton yield, boll number and seedcotton weight per boll with respect to fruiting position varied significantly across years, but no interactions between year and any other effect were observed (Table 8). The variations in seedcotton yield and yield components with respect to fruiting position, soil fertility, and management system were consistent across years (Table 8).

The seedcotton yield, boll number and seedcotton weight per boll at a given fruiting position were significantly affected by soil fertility, management system (except seedcotton weight per boll), and M × FP interaction, but not by S × M and S × FP interactions (Table 8). Among management systems, ICMS produced more bolls on FB1−10 and at FP1−2 on FB11−15 than CCMS. In contrast, the number of bolls on FB16+ under ICMS was significantly lower than for the CCMS treatment (Table 7A). Interestingly, a differential response of boll distribution to fertility levels was observed under management systems. Compared with the management systems in the high soil fertility field, the number of bolls at FP1−2 on FB1−5 under CCMS was not significantly changed by decreased soil fertility, while the number of bolls on FB1−5 and at FP1−2 on FB6−10 under ICMS were not significantly changed by decreased soil fertility. With respect to soil fertility, the number of bolls on FB11+ in the low soil fertility field was significantly reduced relative to that in the high soil fertility field. Similar results were found in seedcotton yield with respect to fruiting position (Table 7C), and seedcotton weight per boll at all fruiting positions was decreased in the low soil fertility field relative to that in the high soil fertility field (Table 7B).

TABLE 7
www.frontiersin.org

Table 7. Effects of management system on boll number (A), seedcotton weight per boll (B), seedcotton yield (C), and contribution rate to yield (D) of boll with respect to fruiting position (FP) in the low and high soil fertility fields in 2012 and 2013 (n = 45).

The contributions of bolls at different fruiting positions to yield was significantly affected by S × FP and M × FP interactions (Table 8). Bolls on upper fruiting branches (FB11+) were more important contributors to overall yield production under CCMS and/or in the high soil fertility field than those of ICMS and/or in the low soil fertility field. The average contribution of the bolls on FB11+ to the total yield under CCMS was 11.13% higher than that under ICMS and the average contribution of the bolls on FB11+ to the total yield in the high soil fertility field was 3.48% higher than that in the low soil fertility field (Table 7D).

TABLE 8
www.frontiersin.org

Table 8. Results of ANOVA on the effects of year (Y), soil fertility (S), management system (M), fruiting position (FP) and their interactions on boll number, seedcotton weight per boll, seedcotton yield, and contribution rate to yield of boll with respect to fruiting position.

Fiber Quality Distribution Within the Canopy

The fiber quality parameters length, strength and micronaire were significantly affected by year, soil fertility, management system, and fruiting position (Table 10).

Fiber length and strength were also significantly affected by Y × M, M × FP, and Y × M × FP interactions (Table 10). The effects of management system on fiber length and strength differed in different years and fruiting branches (Table 10). In 2012, the fiber of bolls at FP1−2 on FB1−5 under ICMS was longer and stronger than that under CCMS, and an inverse trend was detected at all other fruiting positions in either field. While, in 2013, the fiber of bolls at FP1−2 on FB1−5 under ICMS was longer and stronger than fiber produced under CCMS; however, an inverse trend was only detected at FP3+ on FB6−10 and on FB11+ in either field (Tables 9A,B). By comparison, the micronaire was not significantly affected by Y × M, M × FP, and Y × M × FP interactions (Table 10). Fiber micronaire at all fruiting positions under ICMS was consistently lower than under CCMS in 2012 and 2013 in either field (Table 9C).

TABLE 9
www.frontiersin.org

Table 9. Effects of management system on fiber length (A), strength (B), and micronaire (C) of boll with respect to fruiting position in the low and high soil fertility fields in 2012 and 2013 (n = 18).

TABLE 10
www.frontiersin.org

Table 10. Results of ANOVA on the effects of year (Y), soil fertility (S), management system (M), fruiting position (FP) and their interactions on fiber length, strength, and micronaire of boll with respect to fruiting position.

Fiber length, strength, and micronaire were also significantly affected by S × FP interaction (Table 10). Among soil fertility, there was no significant difference in fiber quality on FB1−10 between the low and high soil fertility fields, but fiber length, strength, and micronaire on FB11+ in the low soil fertility field were lower than those in the high soil fertility field (Table 9).

Net Photosynthetic Rate of the Main Stem Leaves on Different Fruiting Branches

On August 15, the net photosynthetic rate of leaves on FB1−5, FB6−10, and FB11−15 was significantly affected by year, soil fertility, and management system, but only the net photosynthetic rate of leaves on FB1−5 was significantly affected by S × M interaction (Table 11).

TABLE 11
www.frontiersin.org

Table 11. Effects of management system on net photosynthetic rate of the main stem leaves on different fruiting branches (FB) in the low and high soil fertility fields in 2012 and 2013 (n = 27).

The net photosynthetic rate of leaves on FB6−15 under the two management systems in the low soil fertility field was lower than that in the high soil fertility field. But there was no significant difference under ICMS between the low and high soil fertility fields, while the net photosynthetic rate of leaves on FB1−5 under CCMS in the low soil fertility field was lower than in the high soil fertility field (Table 11).

On September 15, the net photosynthetic rate of leaves on FB1−5, FB6−10, FB11−15, and FB16+ was significantly affected by year (except FB1−5 and FB6−10), soil fertility, and management system, but only the net photosynthetic rate of leaves on FB1−5 and FB6−10 was significantly affected by S × M interaction (Table 11).

The net photosynthetic rate of leaves on FB11+ under the two management systems in the low soil fertility field was lower than that in the high soil fertility field. However, there was no significant difference in the net photosynthetic rate of leaves on FB6−10 under ICMS between the low and high soil fertility fields, and the net photosynthetic rate of leaves on FB6−10 under CCMS in the low soil fertility field was lower than that in the high soil fertility field. Moreover, the net photosynthetic rate of leaves on FB1−5 under ICMS in the low soil fertility field was higher than that in the high soil fertility field and there was no significant difference in the net photosynthetic rate of leaves on FB1−5 under CCMS between the low and high soil fertility fields (Table 11).

Discussion

Seedcotton Yield and Fiber Quality of Boll With Respect to Fruiting Position Under CCMS and ICMS

The fruiting habit of the cotton plant is altered by nitrogen rate and plant density, where plants produced more bolls on upper branches and produce more horizontal fruiting sites along longer fruiting branches as plant density is decreased (Bednarz et al., 2000) and nitrogen rate is increased (Boquet et al., 1994). In our study, despite having lower nitrogen rates and split applications, CCMS allowed the plants to set more apical fruiting branches and distal fruiting positions than did the plants under ICMS, which had a higher plant density (Table 6). Reduced plant density in cotton allowed for yield compensation by increasing boll production on upper branches (Bednarz et al., 2000). In our study, the seedcotton yield of bolls on FB16+ played a compensating role in yield production under CCMS. Boll reduction on FB1−10 and at FP1−2 on FB11−15 under CCMS was not compensated for by bolls formed at FP3+ on FB11−15. Moreover, this loss could not be fully compensated for by increased bolls on FB16+ and led to more total bolls produced under ICMS relative to CCMS in either field (Table 7A). This resulted in yield differences between CCMS and ICMS that were mainly associated with plant density differences between the two management systems.

Fiber length, strength and micronaire were significantly affected by management system. Fiber micronaire at all fruiting positions under ICMS were consistently higher than those under CCMS, which was in agreement with the previous research that micronaire was increased with increasing levels of nitrogen application under high temperature and reduced by increased nitrogen application under low temperature (Boman et al., 1997). Fiber length and strength were significantly affected by management system × fruiting position interaction (Table 10). The fiber at FP1−2 on FB1−5 under ICMS was longer and stronger than that of CCMS in either field due to the fact that more nitrogen fertilizer was applied at the initial flowering stage under CCMS (Tables 9A,B). This result is in agreement with (Zhao et al., 2012), where high temperature during the boll development period along with a high nitrogen rate was not conducive to fiber quality formation. 23~25°C was the optimal temperature for fiber quality formation (Reddy et al., 1999) and supplemented nitrogen fertilizer could mitigate the negative influence of low temperature on fiber quality in the later flowering season (Reddy et al., 2004; Zhao et al., 2012). However, in our study, although the ICMS applied nitrogen at the end of the flowering stage, the fiber on upper fruiting branches under ICMS was shorter and weaker than those of CCMS. Lower temperature decreased sucrose export in cotton leaves (Liu et al., 2013) and less photosynthate was transferred to fiber, which resulted in inferior fiber quality (Liu et al., 2015a,b). This may be due to the temperature during boll growth under ICMS, which was 1~2°C lower than for CCMS (Table 4A), and the positive effect of nitrogen application was likely masked by the temperature difference. These results indicated that fiber length, strength and micronaire, was not just a function of management but also depended on the climatic conditions prevailing during boll development. Interestingly, there was no significant difference in fiber length and strength between CCMS and ICMS at the field level, regardless of year and soil fertility (data not shown). Though fiber length and strength at many fruiting positions under CCMS were superior to ICMS, the seedcotton yield of bolls on upper fruiting branches supported a higher percentage of the total seedcotton yield under CCMS. In comparison, the bolls on upper fruiting branches had inferior fiber quality to those on the lower fruiting branches (Table 9), in agreement with previous studies (Knight et al., 1988; Crawley et al., 1996). Hence, there was no significant difference in fiber length and strength between CCMS and ICMS at the field level in either field. These results indicated that we could achieve higher seedcotton yield without limiting fiber quality by applying integrated crop management practices by enhancing the number of bolls on the fruiting branches and positions where fiber quality is generally superior.

Climatic extremes such as drought and/or elevated temperature become more frequent with climate change (Gilgen and Feller, 2013; Mittal et al., 2014), which potentially negatively affect nutrient availability and plant growth (Aragon and De Datta, 1982; Feller and Vaseva, 2014; He and Dijkstra, 2014). Drought reduced available soil nitrogen and then reduced the number of bolls on upper fruiting branches (Wang et al., 2016). The cotton yield loss of a drought-stressed cotton crop could be compensated for by optimizing nitrogen rate and postponing part of nitrogen fertilization through enhancing water use efficiency (Li et al., 2017; Shi et al., 2018). The ICMS utilized in the current study utilized a growth stage-driven fertilizer schedule which ensured and adequate nitrogen supply for plant growth, which may mitigate the impact of drought on seedcotton yield compared with CCMS. Elevated temperature also adversely affects fiber quality on lower fruiting branches under CCMS but it improves fiber quality on upper fruiting branches under ICMS, which may result in superior fiber quality for ICMS relative to CCMS in extreme high-temperature events. Therefore, maybe ICMS has a greater capacity to tolerate extreme climate events than CCMS.

The Differential Yield Response of CCMS and ICMS to Soil Fertility

The boll number per hectare under ICMS and CCMS in the low soil fertility field were 8.0 and 11.7% less than those in the high soil fertility field, respectively (Table 7A), which resulted in reduced seedcotton yield difference in soil fertility among ICMS relative to that of CCMS.

Plant growth was adversely affected by low soil fertility and both CCMS and ICMS exhibited fewer upper fruiting branches and number of nodes per fruiting branch in the low soil fertility field than in the high soil fertility field (Table 6). However, there was a differential response of the boll number and seedcotton yield to decreased soil fertility in response to management system (Tables 7A,C). The plants under CCMS with a low plant density had larger inter-plant space to exploit (Eaton, 1955), and less organic and inorganic nutrients supplied in the low soil fertility field that reduced the net photosynthetic rate of the leaves (Table 11), thus resulting in reduced source strength and capacity to retain bolls at FP3+ on FB1−5 and on FB6+ under CCMS in the low soil fertility field relative to the high soil fertility field. However, the plants under ICMS with a high plant density had less inter-plant space for growth, and the increased leaf area index expected by improving soil fertility would reduce the efficiency of photosynthetic photon flux density interception (Heitholt, 1994) and decrease net photosynthetic rate of leaves on lower fruiting branches (FB1−10) (Table 11). Decreased soil fertility reduced the net photosynthetic rate of the leaves on FB11+ but increased soil fertility enhanced the net photosynthetic rate of the leaves on FB1−10 under ICMS. Therefore, more assimilate production of leaves on lower fruiting branches due to increased net photosynthetic rate of leaves on FB1−10 (Buxton et al., 1977) in the low soil fertility field led to more boll retention on lower fruiting branches under ICMS relative to the high soil fertility field. Finally, the number of bolls on FB1−5 and at FP1−2 on FB6−10 under ICMS was not significantly changed by decreased soil fertility. Our results indicate that the yield difference due to soil fertility was lower for ICMS because it combined some optimal management practices relative to those of CCMS; so ICMS could mitigate the impact of cotton production on low fertility soils.

Seedcotton Yield and Fiber Quality of Boll With Respect to Fruiting Position in the Low and High Soil Fertility Fields

The nutrient status of the high soil fertility field contributed to a greater number of bolls (Table 7A) and higher seedcotton weight per boll (Table 7B), which was consistent with prior reports (Feng et al., 2017). Furthermore, the results suggested that low soil fertility would decrease the number of bolls on upper fruiting branches and seedcotton weight per boll at all fruiting positions, resulting in lower yield of the low soil fertility field relative to those in the high soil fertility field.

There was no significant difference in fiber length, strength and micronaire between the low and high soil fertility fields at the field level; similar results were observed by Blaise et al. (2005), who reported that fiber length, strength and micronaire were not significantly affected by the application of farmyard manure. However, we found that fiber length, strength, and micronaire of the bolls on the upper fruiting branches in the low soil fertility field were inferior to those in the high soil fertility field. This is because the high soil fertility field could maintain a constant supply of soil nutrients and maintain net photosynthetic rate of leaves on upper fruiting branches, thereby supporting a greater boll load and improving fiber quality (Pettigrew, 1995). In addition, a greater percentage of the total yield was attributed to upper fruiting branches in the high soil fertility field, where fiber quality is generally inferior (Table 9). Thus, the net effect was no measurable gain in overall fiber length, strength and micronaire between the low and high soil fertility fields.

Conclusions

In our study, we evaluated the responses of seedcotton yield and fiber quality as a function of fruiting positions, management systems, and soil fertility levels. Our results clearly demonstrated that:

(i) The boll reduction on FB1−10 and at FP1−2 on FB11−15 under CCMS could not be fully compensated for by increased bolls on FB16+, resulting in lower overall seedcotton yield under CCMS relative to that under ICMS.

(ii) The number of bolls at FP1−2 on FB1−5 under CCMS while the number of bolls on FB1−5 and at FP1−2 on FB6−10 under ICMS were not significantly changed by soil fertility, resulting in diminished yield differences in soil fertility among ICMS relative to that of CCMS.

(iii) High soil fertility enhanced seedcotton yield by increasing the number of bolls on upper fruiting branches (FB11+) and the seedcotton weight per boll at all fruiting positions.

(iv) Fiber length and strength at the majority of fruiting positions under CCMS was superior to those under ICMS. However, there was no significant difference in fiber length and strength between CCMS and ICMS at the field level, which was attributed to the elevated contribution of bolls on lower fruiting branches (FB1−10) to the total yield.

(v) High soil fertility increased not only fiber length, strength, and micronaire, but also the contribution of bolls on upper fruiting branches (FB11+) to the total yield. Thus, fiber length, strength and micronaire were not changed by soil fertility at the field level.

(vi) ICMS maybe have a greater capacity to tolerate extreme climate events than CCMS, but this needs to be further verified in the future.

Author Contributions

ZZ, YM, and BC conceived the idea and led the study design. XZ carried out the experiment, performed analysis and wrote the paper. HY assisted in plant sampling and laboratory analysis. RZ, JS and BI assisted manuscript writing and editing. All authors reviewed the manuscript.

Funding

We are grateful for financial support from the Special Fund for Agro-scientific Research in public interest (201303002, 201503136), National Natural Science Foundation of China (31371583, 31401327), China Agriculture Research System (CARS-18-14), Jiangsu Collaborative Innovation Centre for Modern Crop production (JCIC-MCP).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We really appreciate all members in Nanjing Agricultural University, Dafeng Experimental Station for their helps on cotton management.

References

Aragon, E., and De Datta, S. (1982). Drought response of rice at different nitrogen levels using line source. Irrigat. Sci. 3, 63–73. doi: 10.1007/BF00264850

CrossRef Full Text | Google Scholar

Baker, D. A., Young, D. L., Huggins, D. R., and Pan, W. L. (2004). Economically optimal nitrogen fertilization for yield and protein in hard red spring wheat. Agron. J. 96, 116–123. doi: 10.2134/agronj2004.0116

CrossRef Full Text | Google Scholar

Balasubramanian, V., Rajendran, R., Ravi, V., Chellaiah, N., Castro, E., Chandrasekaran, B., et al. (2005). Integrated crop management for enhancing yield, factor productivity and profitability in Asian rice farms. IRC Newsl. 54, 63–73.

Bednarz, C. W., Bridges, D. C., and Brown, S. M. (2000). Analysis of cotton yield stability across population densities. Agron. J. 92, 128–135. doi: 10.2134/agronj2000.921128x

CrossRef Full Text | Google Scholar

Blaise, D., Singh, J., Bonde, A., Tekale, K., and Mayee, C. (2005). Effects of farmyard manure and fertilizers on yield, fibre quality and nutrient balance of rainfed cotton (Gossypium hirsutum). Bioresour. Technol. 96, 345–349. doi: 10.1016/j.biortech.2004.03.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Boman, R., Raun, W., Westerman, R., and Banks, J. (1997). Long-term nitrogen fertilization in short-season cotton: interpretation of agronomic characteristics using stability analysis. J. Produc. Agric. 10, 580–585. doi: 10.2134/jpa1997.0580

CrossRef Full Text | Google Scholar

Boquet, D. J., Moser, E. B., and Breitenbeck, G. A. (1994). Boll weight and within-plant yield distribution in field-grown cotton given different levels of nitrogen. Agron. J. 86, 20–26. doi: 10.2134/agronj1994.00021962008600010005x

CrossRef Full Text | Google Scholar

Buxton, D., Briggs, R., Patterson, L., and Watkins, S. (1977). Canopy characteristics of narrow-row cotton as influenced by plant density. Agron. J. 69, 929–933. doi: 10.2134/agronj1977.00021962006900060009x

CrossRef Full Text | Google Scholar

Cao, Y., and Yin, B. (2015). Effects of integrated high-efficiency practice versus conventional practice on rice yield and N fate. Agric. Ecosyst. Environ. 202, 1–7. doi: 10.1016/j.agee.2015.01.001

CrossRef Full Text | Google Scholar

Chen, B., Yang, H., Song, W., Liu, C., Xu, J., Zhao, W., et al. (2016). Effect of N fertilization rate on soil alkali-hydrolyzable N, subtending leaf N concentration, fiber yield, and quality of cotton. Crop J. 4, 323–330. doi: 10.1016/j.cj.2016.03.006

CrossRef Full Text | Google Scholar

Chen, M., Zhao, W., Meng, Y., Chen, B., Wang, Y., Zhou, Z., et al. (2015). A model for simulating the cotton (Gossypium hirsutum l.) embryo oil and protein accumulation under varying environmental conditions. Field Crops Res. 183, 79–91. doi: 10.1016/j.fcr.2015.07.011

CrossRef Full Text | Google Scholar

Crawley, S. R., Jenkins, J. N., and McCarty, J. C. (1996). “Comparison of fiber properties by fruiting positions of two cultivars,” in Proceedings of Beltwide Cotton Production Conference, (Nashville, TN).

Google Scholar

CRI (2013). Cultivation of Cotton in China. Shanghai: Shanghai Science and Technology Press.

Dai, J., Kong, X., Zhang, D., Li, W., and Dong, H. (2017). Technologies and theoretical basis of light and simplified cotton cultivation in China. Field Crops Res. 214, 142–148. doi: 10.1016/j.fcr.2017.09.005

CrossRef Full Text | Google Scholar

Das, A., Prasad, M., Gautam, R., and Shivay, Y. (2006). Productivity of cotton (Gossypium hirsutum) as influenced by organic and inorganic sources of nitrogen. Indian J. Agri. Sci. 76, 354–357.

Dong, H., Kong, X., Li, W., Tang, W., and Zhang, D. (2010). Effects of plant density and nitrogen and potassium fertilization on cotton yield and uptake of major nutrients in two fields with varying fertility. Field Crops Res. 119, 106–113. doi: 10.1016/j.fcr.2010.06.019

CrossRef Full Text | Google Scholar

Dong, H., Li, W., Eneji, A. E., and Zhang, D. (2012). Nitrogen rate and plant density effects on yield and late-season leaf senescence of cotton raised on a saline field. Field Crops Res. 126, 137–144. doi: 10.1016/j.fcr.2011.10.005

CrossRef Full Text | Google Scholar

Dong, H., Li, W., Tang, W., Li, Z., and Zhang, D. (2007). Enhanced plant growth, development and fiber yield of Bt transgenic cotton by an integration of plastic mulching and seedling transplanting. Ind. Crop Prod. 26, 298–306. doi: 10.1016/j.indcrop.2007.03.008

CrossRef Full Text | Google Scholar

Dong, H., Li, W., Tang, W., and Zhang, D. (2009). Early plastic mulching increases stand establishment and lint yield of cotton in saline fields. Field Crops Res. 111, 269–275. doi: 10.1016/j.fcr.2009.01.001

CrossRef Full Text | Google Scholar

Eaton, F. M. (1955). Physiology of the cotton plant. Ann. Rev. Plant Physiol. 6, 299–328. doi: 10.1146/annurev.pp.06.060155.001503

CrossRef Full Text | Google Scholar

Feller, U., and Vaseva, I. I. (2014). Extreme climatic events: impacts of drought and high temperature on physiological processes in agronomically important plants. Front. Environ. Sci. 2:39. doi: 10.3389/fenvs.2014.00039

CrossRef Full Text | Google Scholar

Feng, L., Mathis, G., Ritchie, G., and Han, Y. (2014). Optimizing irrigation and plant density for improved cotton yield and fiber quality. Agron. J. 106, 1111–1118. doi: 10.2134/agronj13.0503

CrossRef Full Text | Google Scholar

Feng, L., Wang, G., Han, Y., Li, Y., Zhu, Y., Zhou, Z., et al. (2017). Effects of planting pattern on growth and yield and economic benefits of cotton in a wheat-cotton double cropping system versus monoculture cotton. Field Crops Res. 213, 100–108. doi: 10.1016/j.fcr.2017.07.003

CrossRef Full Text | Google Scholar

Ghader, F. F., Aali, M. S. M., Cancholi, O., Yousefidaz, M., and Miri, A. A. (2012). Yield and Fiber Quality Comparison of Cotton Planted in Ultra-narrow Row and Conventional Row. 75–91.

Google Scholar

Gilgen, A. K., and Feller, U. (2013). Drought stress alters solute allocation in broadleaf dock (Rumex obtusifolius). Weed Sci. 61, 104–108. doi: 10.1614/WS-D-12-00074.1

CrossRef Full Text | Google Scholar

Gupta, R., and Seth, A. (2007). A review of resource conserving technologies for sustainable management of the rice–wheat cropping systems of the Indo-Gangetic plains (IGP). Crop Prot. 26, 436–447. doi: 10.1016/j.cropro.2006.04.030

CrossRef Full Text | Google Scholar

He, M., and Dijkstra, F. A. (2014). Drought effect on plant nitrogen and phosphorus: a meta-analysis. New Phytologist. 204, 924–931. doi: 10.1111/nph.12952

PubMed Abstract | CrossRef Full Text | Google Scholar

Heitholt, J. J. (1994). Canopy characteristics associated with deficient and excessive cotton plant population densities. Crop Sci. 34, 1291–1297. doi: 10.2135/cropsci1994.0011183X003400050028x

CrossRef Full Text | Google Scholar

Jin, L., Cui, H., Li, B., Zhang, J., Dong, S., and Liu, P. (2012). Effects of integrated agronomic management practices on yield and nitrogen efficiency of summer maize in North China. Field Crops Res. 134, 30–35. doi: 10.1016/j.fcr.2012.04.008

CrossRef Full Text | Google Scholar

Kerby, T., and Buxton, D. (1981). Competition between adjacent fruiting forms in cotton. Agron. J. 73, 867–871. doi: 10.2134/agronj1981.00021962007300050028x

CrossRef Full Text | Google Scholar

Kintché, K., Guibert, H., Sogbedji, J., Levêque, J., Bonfoh, B., and Tittonell, P. (2015). Long-term mineral fertiliser use and maize residue incorporation do not compensate for carbon and nutrient losses from a Ferralsol under continuous maize–cotton cropping. Field Crops Res. 184, 192–200. doi: 10.1016/j.fcr.2015.04.019

CrossRef Full Text | Google Scholar

Knight, B., Jenkins, J. N., and McCarty, J. C. (1988). “Effects of fruiting position on field and fiber quality in commercial cotton,” in Proceedings of Beltwide Cotton Production Conference, (New Orleans, LA).

Google Scholar

Ladha, J. K., Hill, J. E., Duxbury, J. M., Gupta, R. K., and Buresh, R. J. (2003). Improving the Productivity and Sustainability of Rice-Wheat Systems: Issues and Impacts. American Society of Agronomy-Crop Science Society of America-Soil Science Society of America, Madison, WI.

Li, W., Li, Y., and Feng, S. (2017). Regulation of root-sourced ABA to growth and water use efficiency of cottonseedling and their response to different nitrogen levels and distribution ratios. Acta Eco. Sin. 37, 6712–6723 (In Chinese, with English abstract).

Liu, J., Ma, Y., Lü, F., Chen, J., Zhou, Z., Wang, Y. Oosterhuis, D. M., et al. (2013). Changes of sucrose metabolism in leaf subtending to cotton boll under cool temperature due to late planting. Field Crops Res. 144, 200–211. doi: 10.1016/j.fcr.2013.02.003

CrossRef Full Text | Google Scholar

Liu, J., Meng, Y., Chen, J., Lü, F., Ma, Y., Chen, B., Oosterhuis, D. M., et al. (2015a). Effect of late planting and shading on cotton yield and fiber quality formation. Field Crops Res. 183, 1–13. doi: 10.1016/j.fcr.2015.07.008

CrossRef Full Text | Google Scholar

Liu, J., Meng, Y., Lü, F., Chen, J., Ma, Y., Wang, Y., et al. (2015b). Photosynthetic characteristics of the subtending leaf of cotton boll at different fruiting branch nodes and their relationships with lint yield and fiber quality. Front. Plant Sci. 6:747. doi: 10.3389/fpls.2015.00747

PubMed Abstract | CrossRef Full Text | Google Scholar

Lu, H., Dai, J., Li, W., Tang, W., Zhang, D., Eneji, A. E., et al. (2017). Yield and economic benefits of late planted short-season cotton versus full-season cotton relayed with garlic. Field Crops Res. 200, 80–87. doi: 10.1016/j.fcr.2016.10.006

CrossRef Full Text | Google Scholar

Mauney, J. R. (1986). “Vegetative growth and development of fruiting sites,” in Cotton Physiology, eds J. R. Mauney and J. M. Stewart (Memphis, TN: The Cotton Foundation), 11–28.

Google Scholar

Meng, Y., Lv, F., Zhao, W., Chen, J., Zhu, L., Wang, Y., et al. (2016). Plant density influences fiber sucrose metabolism in relation to cotton fiber quality. Acta physiol. Plant. 38:112. doi: 10.1007/s11738-016-2129-3

CrossRef Full Text | Google Scholar

Mittal, N., Mishra, A., Singh, R., and Kumar, P. (2014). Assessing future changes in seasonal climatic extremes in the Ganges river basin using an ensemble of regional climate models. Clim. Change 123, 273–286. doi: 10.1007/s10584-014-1056-9

CrossRef Full Text | Google Scholar

Pettigrew, W. T. (1995). Source-to-sink manipulation effects on cotton fiber quality. Agron. J. 87, 947–952. doi: 10.2134/agronj1995.00021962008700050029x

CrossRef Full Text | Google Scholar

Reddy, K. R., Davidonis, G. H., Johnson, A. S., and Vinyard, B. T. (1999). Temperature regime and carbon dioxide enrichment alter cotton boll development and fiber properties. Agron. J. 91, 851–858. doi: 10.2134/agronj1999.915851x

CrossRef Full Text | Google Scholar

Reddy, K. R., Koti, S., Davidonis, G. H., and Reddy, V. R. (2004). Interactive effects of carbon dioxide and nitrogen nutrition on cotton growth, development, yield, and fiber quality. Agron. J. 96, 1148–1157. doi: 10.2134/agronj2004.1148

CrossRef Full Text | Google Scholar

Robertson, G. P., Paul, E. A., and Harwood, R. R. (2000). Greenhouse gases in intensive agriculture: contributions of individual gases to the radiative forcing of the atmosphere. Science. 289, 1922–1925. doi: 10.1126/science.289.5486.1922

PubMed Abstract | CrossRef Full Text | Google Scholar

Saleem, M., Maqsood, M., Javaid, A., Hassan, M., and Khaliq, T. (2010). Optimum irrigation and integrated nutrition improves the crop growth and net assimilation rate of cotton (Gossipium hirsutum L.). Pak. J. Bot. 42, 3659–3669.

Google Scholar

Sawan, Z., Mahmoud, M., and El-Guibali, A. H. (2006). Response of yield, yield components, and fiber properties of Egyptian cotton (Gossypium barbadense L.) to nitrogen fertilization and foliar-applied potassium and mepiquat chloride. J. Cotton Sci. 10, 224–234.

Google Scholar

Shi, H., Zhang, J., Yan, Q., Li, C., and Li, J. (2018). Compensation effects of nitrogen fertilizer on yield and quality cotton under insufficient irrigation. J. Plant Nutr. Fertilizers. 24, 134–145 (In Chinese, with English abstract). doi: 10.11674/zwyf.17090

CrossRef Full Text

Singh, R. J., and Ahlawat, I. (2014). Effects of transgenic cotton-based cropping systems and their fertility levels on succeeding wheat crop. Commun. Soil Sci. Plant. 45, 2385–2396. doi: 10.1080/00103624.2014.912291

CrossRef Full Text | Google Scholar

Wang, D., Huang, J., Nie, L., Wang, F., Ling, X., Cui, K., et al. (2017). Integrated crop management practices for maximizing grain yield of double-season rice crop. Sci. Rep. 7:8982. doi: 10.1038/srep38982

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, R., Ji, S., Zhang, P., Meng, Y., Wang, Y., Chen, B., et al. (2016). Drought effects on cotton yield and fiber quality on different fruiting branches. Crop Sci. 56, 1265–1276. doi: 10.2135/cropsci2015.08.0477

CrossRef Full Text | Google Scholar

Xiong, H., Tang, Y., Ren, D., Li, X., Cheng, K., Yao, W., et al. (2003). Studies on relationships between different soil types and climate condition and grains yield of rice. Southwest China, J. Agric. Sci. 17, 305–309 (In Chinese, with English abstract). doi: 10.3969/j.issn.10014829.2004.04.009

CrossRef Full Text

Yang, G., Tang, H., Nie, Y., and Zhang, X. (2011). Responses of cotton growth, yield, and biomass to nitrogen split application ratio. Eur. J. Agron. 35, 164–170. doi: 10.1016/j.eja.2011.06.001

CrossRef Full Text | Google Scholar

Yang, H., Meng, Y., Chen, B., Zhang, X., Wang, Y., Zhao, W., et al. (2016). How integrated management strategies promote protein quality of cotton embryos: high levels of soil available N, N assimilation and protein accumulation rate. Front. Plant Sci. 7:1118. doi: 10.3389/fpls.2016.01118

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, H., Zhang, X., Chen, B., Meng, Y., Wang, Y., Zhao, W., et al. (2017). Integrated management strategies increase cottonseed, oil and protein poduction: the key role of carbohydrate metabolism. Front Plant Sci. 8:48. doi: 10.3389/fpls.2017.00048

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, W., Wang, Y., Zhou, Z., Meng, Y., Chen, B., and Oosterhuis, D. M. (2012). Effect of nitrogen rates and flowering dates on fiber quality of cotton (Gossypium hirsutum L.). Am. J. Exp. Agr. 2:133. doi: 10.9734/AJEA/2012/954

CrossRef Full Text | Google Scholar

Zhao, X., and Tisdell, C. (2009). The sustainability of cotton production in china and in Australia: comparative economic and environment issues. Clement Allan Tisdell. 19, 265–289.

Zingore, S., Murwira, H. K., Delve, R. J., and Giller, K. E. (2007). Influence of nutrient management strategies on variability of soil fertility, crop yields and nutrient balances on smallholder farms in Zimbabwe. Agr. Ecosyst. Environ. 119, 112–126. doi: 10.1016/j.agee.2006.06.019

CrossRef Full Text | Google Scholar

Keywords: cotton (Gossypium hirsutum L.), management system, soil fertility, seedcotton yield, fiber quality, fruiting position

Citation: Zhang X, Yang H, Snider JL, Zahoor R, Iqbal B, Chen B, Meng Y and Zhou Z (2018) A Comparative Study of Integrated Crop Management System vs. Conventional Crop Management System for Cotton Yield and Fiber Quality With Respect to Fruiting Position Under Different Soil Fertility Levels. Front. Plant Sci. 9:958. doi: 10.3389/fpls.2018.00958

Received: 22 December 2017; Accepted: 14 June 2018;
Published: 03 August 2018.

Edited by:

Urs Feller, Universität Bern, Switzerland

Reviewed by:

Francisco Sánchez-Bayo, University of Sydney, Australia
Fernando José Cebola Lidon, Universidade Nova de Lisboa, Portugal

Copyright © 2018 Zhang, Yang, Snider, Zahoor, Iqbal, Chen, Meng and Zhou. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Zhiguo Zhou, Z2lzY290dEBuamF1LmVkdS5jbg==

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.