Adjusting cotton planting density under the climatic conditions of Henan Province, China
Authors:
Liyuan Liu aff001; Chuanzong Li aff001; Yingchun Han aff001; Zhanbiao Wang aff001; Lu Feng aff001; Xiaoyu Zhi aff001; Beifang Yang aff001; Yaping Lei aff001; Wenli Du aff001; Yabing Li aff001
Authors place of work:
Institute of Cotton Research of Chinese Academy of Agricultural Sciences, Anyang, Henan, China
aff001; State Key Laboratory of Cotton Biology, Anyang, Henan, China
aff002
Published in the journal:
PLoS ONE 14(9)
Category:
Research Article
doi:
https://doi.org/10.1371/journal.pone.0222395
Summary
The growth and development of cotton are closely related to climatic variables such as temperature and solar radiation. Adjusting planting density is one of the most effective measures for maximizing cotton yield under certain climatic conditions. The objectives of this study were (1) to determine the optimum planting density and the corresponding leaf area index (LAI) and yield under the climatic conditions of Henan Province, China, and (2) to learn how climatic conditions influence cotton growth, yield, and yield components. A three-year (2013–2015) field experiment was conducted in Anyang, Henan Province, using cultivar SCRC28 across six planting density treatments: 15,000, 33,000, 51,000, 69,000, 87,000, and 105,000 plants ha−1. The data showed that the yield attributes, including seed cotton yield, lint yield, dry matter accumulation, and the LAI, increased as planting density increased. Consequently, the treatment of the maximum density with 105,000 plants ha-1 was the highest-yielding over three years, with the LAIs averaged across the three years being 0.37 at the bud stage, 2.36 at the flower and boll-forming stage, and 1.37 at the boll-opening stage. Furthermore, the correlation between the cotton yield attributes and meteorological conditions indicated that light interception (LI) and the diurnal temperature range were the climatic factors that most strongly influenced cotton seed yield. Moreover, the influence of the number of growing degree days (GDD) on cotton was different at different growth stages. These observations will be useful for determining best management practices for cotton production under the climatic conditions of Henan Province, China.
Keywords:
Leaves – Seasons – Seeds – Flowering plants – Cotton – Flowers – Planting – Buds
Introduction
As the world population grows, worldwide demand for cotton is increasing and becoming increasingly urgent [1–2]. China is the largest cotton-producing country in the world. Moreover, Henan Province is one of the major cotton growing provinces of China, with more than 400 thousand ha planted [3]. The climate of Henan Province is semiwet during the cotton growing season from April to October. Temperatures are low in the early stage of the growing season, while in the middle and later stages, temperatures are high. Approximately 4500 growing degree days (GDD) (°C) above 10°C and over 1300 hours of incipient radiation are accumulated over the growing season. Moreover, there are approximately 600 mm of precipitation, which is concentrated in July and early August [4–6].
Determining the optimum planting density is regarded as one of the most effective agronomic practices to promote maximum yield [7–10]. Numerous studies have shown that different climatic conditions and planting densities have a great influence on crop growth and population structure [11–15]. The planting density of cotton in China varies depending upon climatic conditions, particularly solar radiation and temperature. For instance, the planting density of cotton in the Yellow River Basin is approximately 3,000 to 5,000 plants ha-1, while the planting density in Xinjiang can reach 10,000 to 20,000 plants ha-1, which is mainly due to the low annual precipitation, long duration of insolation, and short frost-free period of Xinjiang Province. Therefore, determining the optimum planting density under different climatic conditions would be helpful for cotton production in China and other countries around the world.
Extensive research has demonstrated that proper planting density is the most critical factor for establishing an optimal canopy structure consisting of a good LAI and porosity, which is an important parameter to describe the light transmission capacity of the canopy [16–19]. Researchers have sought for many years to elucidate how planting density is related to the LAI and cotton production [20–24]. They found that the LAI increases with increasing planting density; however, canopy shading occurs when the LAI is excessively high, resulting in reduced cotton production [25–26]. Studies have also shown that the LAI and yield both increase gradually as the planting density increases [27]. Consequently, the relationship between planting density, the LAI and cotton production is still confusing. Therefore, determining the precise LAI at the optimum planting density is of great significance for improving light use efficiency, which is crucial for yield. Moreover, planting density can also affect light interception (LI) and the light extinction coefficient (k), influenced by the crop structure, e.g., the LAI and the orientation of the leaf, which is an important indicator that reflects a crop's ability to intercept light within the crop canopy [28–33]. The study of Xu in 2017 proposed the “optimum planting density” as the one that produced the highest yield. The corresponding k value and LAI were the “optimum k value” and “optimum LAI”, respectively [27].
We conducted a field experiment to determine the optimum planting density, with test densities ranging from 15,000 to 105,000 plants ha-1, and the corresponding LAI and yield under the climatic conditions of Henan Province, China and to learn how these climatic conditions influence cotton growth, yield components and yield.
Materials and methods
Experimental design
Field experiments were conducted from 2013 to 2015 at an experimental field of the Institute of Cotton Research of the Chinese Academy of Agricultural Sciences in Anyang, Henan, China (longitude 36°06 N and latitude 114°21 E). Table 1 shows the climatic conditions during the cotton growing season from April to October in each year, which were obtained from the nearest meteorological station to the experimental site.
The study site was a medium loam soil that contained nitrogen, phosphorus, and potassium concentrations of 0.65, 0.01 and 0.15 g kg−1 soil, respectively. The experiment was designed randomly with cotton cultivar SCRC28 which was planted at six densities (15,000, 33,000, 51,000, 69,000, 87,000, and 105,000 plants ha-1) with 3 replicates. Each plot was 8.0 m wide and 8.0 m long and covered an area of 64.0 m2 with a 0.8 m row spacing. The sowing dates were April 17th, 2013, April 29th, 2014, and April 24th, 2015. Crop management of all the plots, including sowing, irrigation and fertilization, were the same. In addition, weeds, diseases, and pests were controlled in the cotton growing season to obtain the highest possible yields.
Sampling and measurements
PAR interception (IPAR) was calculated by measuring the incident transmitted PAR (TPAR) and the reflected PAR (RPAR). TPAR and RPAR were measured using the spatial grid method at stable positions in six population-density plots with a portable 1.0-meter-line light quantum sensor (LA-191SA, LI-COR, Lincoln, NE, USA) and datalogger (LI-1400, LI-COR) every ten days after planting each year (Zhi et al. 2014). Then, the transmitted PAR rate (tPAR), reflected PAR rate (rPAR), and intercepted PAR rate (iPAR) were calculated using the following formulas:
The LI of the canopy was computed as follows, according to the Simpson 3/8 integration rules.
The LAI and dry matter mass were obtained on the same day that the PAR data were acquired. Two plants were randomly uprooted from each test plot, except from the two edge rows, and then they were divided into roots, stems, leaves and reproductive organs. A scanner (Phantom 9800xl, MiCROTEK, Shanghai, China) was used to take photos of the leaves, and leaf areas were determined using Image-Pro Plus 7.0 (Media Cybernetics, Rockville, MD, USA). The LAI was calculated as the total plant leaf area per unit area of land. The dry mass of roots, stems, leaves and reproductive organs was determined by drying at 80°C to a constant weight.
The k value and the optimum leaf area index (LAI) were calculated according to the following formula, which was reported by Xu [27].
Statistical analysis
Correlation analysis was conducted to test the relationship between climatic factors and yield attributes. Means were compared using least significant difference tests at the p < 0.05 level of significance.
Results
Yield and yield components
There was no significant difference in seed cotton yield between the treatments with 105,000, 87,000 or 69,000 plants ha-1 in 2013 and 2015. However, in 2014, there was a significant difference between the treatments with 105,000 and 69,000 plants ha-1. This trend was also observed for lint yield, and the maximum values were obtained at the density of 105,000 plants ha-1 each year. The effects of planting density on boll weight and boll density were due to the indeterminate growth of cotton. As shown in Table 2, the boll weight decreased as the planting density increased. The opposite trend was observed for boll density. For example, as shown in Table 2, the maximum boll weight and minimum boll density appeared at a density of 15,000 plants ha-1. The lint percentage remained stable at approximately 43% in 2015. A significantly lower lint percentage was observed for a density of 105,000 plants ha-1 in 2013 and 2014.
Comparing the same planting density treatments between years, seed cotton and lint cotton yields were higher in 2015 than in other years, except for the 87,000 plants ha-1 treatment in 2014. The maximum boll weights were 6.04 g in 2013, 6.36 g in 2014, and 6.56 g in 2015. The minimum boll weights were 5.72 g in 2013, 5.77 g in 2014, and 6.07 g in 2015. The boll density, which increased by 37.6% from 2014 to 2015 in the lowest-density treatment, was significantly different between 2014 and the other two years, as shown in Table 2. The effect of planting density on yield and yield components was significantly influenced by the differing climatic conditions of each year.
Dry matter and harvest index
For a detailed analysis of the dry matter production (DM) for single plants and populations under different planting density treatments, five growth stages were studied, as shown in Table 3. There were no significant differences in DM, which was roughly equal to 1 g in all treatments, of single plants at the seedling stage except for the treatment of 105,000 plants ha-1 in 2013 and 2015. Because individual plant mass was so low, there was virtually no competition between plants at any planting density. However, the difference in DM between individual plants became more obvious in later stages, especially at the flower and boll-forming stage and boll-opening stage. Table 3 shows that the DM of single plants was highest in the lowest-density treatment: nearly three times higher for the 15,000 plants ha-1 treatment than for the 10500 plants ha-1 treatment at the boll-forming stage.
The population DM at the seedling stage increased significantly as planting density increased from 15,000 to 105,000 plants ha-1. However, there was no significant difference between the treatments of 51,000 and 69,000 plants ha-1. A similar trend was observed at the bud, preflower and boll-forming stages, but the difference became increasingly insignificant as the planting density increased. Differences in DM by population among all treatments between 51,000 and 105,000 plants ha-1 were insignificant during the boll-opening stage. Comparing the same planting density treatments across three years, the DM of single plants and populations at the seedling stage and bud stage were highest in 2013. However, the DM at later growth stages was highest in 2015.
The harvest index (HI) decreased significantly as planting density increased (Table 3). In 2014, the HI ranged from 0.52 to 0.38, with an average of 0.40 across all planting density treatments. In comparison, in 2015, the HI ranged from 0.55 to 0.34, with an average of 0.3.
Planting density and LAI
The LAI at the bud stage, flower and boll-forming stage and boll-opening stage were compared under different planting density treatments as Fig 1 shows. At the bud stage, the LAI, which was over five times higher for the 10500 plants ha-1 treatment than for the 15,000 plants ha-1 treatment in both 2014 and 2015, increased linearly as the planting density increased. The LAI increased with the growth of cotton and peaked at the flower and boll-forming stages. In the highest-density treatment, the LAI reached 2.39 in 2013, 2.25 in 2014, and 2.51 in 2015. In comparison, the LAI only reached 0.63 in 2013, 0.73 in 2014, and 0.70 in 2015 in the lowest-density treatment. With the advancement of the growth period, the LAI decreased significantly at the boll-opening stage as leaves fell at this point in the growing season. As shown in Fig 1, the LAI in the highest-density treatment decreased to 0.87 in 2013, 0.88 in 2014, and 0.7 in 2015. Comparison of LAI values for the same planting density treatments across years showed that the LAI was highest in 2014 at the bud stage. At the flower and boll-forming stage and boll-opening stage, the LAI was highest in 2015, except for the planting density treatments with 15,000 and 33,000 plants ha-1 at the flower and boll-forming stage.
As stated above, we defined the optimum LAI as the averaged LAI from 2013 to 2015 under the highest-density treatment with the highest cotton production. We calculated this as 2.39 at the flower and boll-forming stage. The average LAI values for the other treatments were 0.72, 1.24, 1.63, 2.06, and 2.26 from the lowest- to the highest-density treatments, respectively. The corresponding k values were calculated according to Formula (1). The average solar radiation intensity during the cotton growing season was 10×104 lx in Henan Province. According to Formula (2) and the value of k, we calculated parameter A for the site. By following the steps above, we modified Formula (2) as follows: LAI opt = 0.24 × (−k /1 × lnE). The values of A were 0.12, 0.10, 0.13, 0.13, 0.14, and 0.19 from the lowest- to highest-density treatments, respectively. The results of the calculations indicated that parameter A was positively related to the planting density.
Relationships between climatic conditions and the seed yield
Table 4 shows the climatic conditions of Henan Province from the sowing date to the boll-opening stage. Correlation analysis was conducted to determine the influence of climatic factors on seed cotton yield attributes (i.e., yield, yield components, DM, and LAI) at the optimum planting density (Table 5). The daily mean temperature was positively correlated with every yield attribute except boll density at the bud stage and flower and boll-forming stage, as shown in Table 5. The number of growing days was positively correlated with the seed cotton yield at the bud stage. However, during both the flower and boll-forming stage and boll-opening stage, the number of growing days was significantly negatively correlated with seed cotton yield, lint yield, DM, and boll weight. The diurnal temperature range was positively correlated with all yield attributes except for the boll density at all stages and with the LAI at the bud stage. The accumulated LI rate was significantly positively correlated with the yield attributes, especially DM. However, the accumulated LI rate was negatively correlated with boll density.
Discussion
Yield, dry matter, and harvest index
Close planting is regarded as one key management technique to improve crop yield [34–36]. However, yield does not always increase as planting density increases, although other factors may be ideal [37]. Moreover, crop yields sometimes vary between areas with different climatic conditions, even with the same planting density and optimal management [27]. In this study, yields were greatest at a density of 105,000 plants ha-1, which was regarded as the optimum planting density for Anyang, Henan Province based on the range of the experimental data.
Cotton yield was affected by planting density in terms of the yield components, including boll weight and boll density. In this study, boll weight and boll density decreased with increasing planting density, which has also been noted in previous studies [16]. In addition, many studies have verified that high biomass is the foundation of high seed yield [38–40]. Therefore, improving DM accumulation during the growing season is necessary to increase seed yield [41]. In the present study, DM production increased gradually with the advancement of the growth period under all planting densities. Additionally, DM accumulation was positively correlated with cotton yield with a certain range of planting densities, as was previously observed by Dai [42]. In this study, DM increased as planting density increased, although the differences were not significant between higher-density treatments. The highest and lowest HI was observed at densities of 15,000 plants ha-1 and 105,000 plants ha-1, respectively, supporting previous research that indicated that the HI decreased with increasing planting density [38]. However, there were small differences in the HI between years under the same planting density treatments. Therefore, we suggest that DM production played a more important role in achieving a high yield compared with the HI. These results are consistent with previous research performed on other crops [43–44].
The optimum LAI and the LI
The LAI is an important factor that is closely related to LI, which influences the DM production of cotton [13]. Moreover, the LAI is the main physiological determinant of crop yield and can be used to reflect the crop production status to some degree. Therefore, maintaining the optimum LAI is the standard strategy for increasing light utilization efficiency and obtaining high seed cotton yield, especially at the flower and boll-forming stages [27]. In this study, the optimum LAI was calculated using a modified Monsi-formula. The optimum LAI was 2.36 at a density of 105,000 plants ha-1, while the highest cotton production and the optimal LAIs in the other treatments were 0.69, 1.16, 1.61, 1.99, and 2.22, respectively. In this study, high yield was accompanied by a high LAI, as was previously observed [45–46]. We obtained Formula (2), LAI opt = 0.24 × (−k /1 × lnE), for cotton in Henan Province at the flower and boll-forming stage. In addition, the values of parameter A were 0.12, 0.10, 0.13, 0.13, 0.14, and 0.19 from the lowest- to highest-planting density treatments, respectively. The results of the calculations indicated that parameter A was positively related to planting density.
The relationship of climate to cotton yield, dry matter and the leaf area index
China has large and diverse cotton-producing areas with different climatic conditions. The optimum planting density changes significantly between different landscapes and different climates [47]. In this study, six different densities were established in Henan, which has more than 400 ha planted in cotton. The cotton yield, DM production, and LAI differed significantly under different planting densities. For example, the cotton seed yield in the lowest-density treatment was 25% lower than that in the 105,000 plants ha-1 treatment. Furthermore, the yield and yield components at the same planting density differed significantly between years. For example, cotton seed yields in the lowest-density treatments were 3909.99, 2932.82 and 3724.21 kg ha-1, respectively. These differences in yield can be attributed to the small differences in the climatic conditions between the three years.
The growth and development of cotton was significantly influenced by climatic conditions, including temperature, precipitation and solar radiation. Among the three factors, temperature has been proven to be the most important factor that influences crop growth [16]. In this study, the daily mean temperature was positively correlated with all of the yield attributes except for the boll density at the bud stage and flower and boll-forming stage. Moreover, LI was highly correlated with cotton production in a previous study [13]. Similarly, the accumulated LI rate was significantly positively correlated with all of the yield attributes at all growth stages, except for the boll density in our research, which indicates that the cotton yield will increase with increasing LI in the absence of other environmental stresses.
Conclusion
The growth and development of cotton were influenced by climatic factors to a certain degree. In this study, the accumulated LI and diurnal temperature range were significantly positively. correlated with cotton production throughout the entire growing season. The number of growing days was positively correlated with seed cotton yield at the bud stage. However, during both the flower and boll-forming stage and boll-opening stage, the number of growing days was significantly negatively correlated with the yield and yield components. The optimum LAIs for Anyang, Henan were obtained at a planting density of 105,000 plants ha-1 and averaged 0.37 at the bud stage, 2.36 at the flower and boll-forming stage, and 1.37 at the boll-opening stage across three years. There were also differences in yield and yield components among the three years because of the differences in climatic conditions each year. This research provides guidance for managing cotton planting in Henan Province, China.
Zdroje
1. McConnell JS, Mozaffari M. Yield, Petiole Nitrate, and Node Development Responses of Cotton to Early Season Nitrogen Fertilization. Journal of Plant Nutrition. 2005;27(7):1183–97. doi: 10.1081/pln-120038543
2. Yang G-z, Zhou M-y. Multi-Location Investigation of Optimum Planting Density and Boll Distribution of High-Yielding Cotton (G. hirsutum L.) in Hubei Province, China. Agricultural Sciences in China. 2010;9(12):1749–57. doi: 10.1016/s1671-2927(09)60273-x
3. Zhang H, Tian W, Zhao J, Jin L, Yang J, Liu C, et al. Diverse genetic basis of field-evolved resistance to Bt cotton in cotton bollworm from China. Proc Natl Acad Sci U S A. 2012;109(26):10275–80. Epub 2012/06/13. doi: 10.1073/pnas.1200156109 22689968; PubMed Central PMCID: PMC3387040.
4. Tian B, Zhou Z, Du FK, He C, Xin P, Ma H. The Tanaka Line shaped the phylogeographic pattern of the cotton tree (Bombax ceiba) in southwest China. Biochemical Systematics and Ecology. 2015;60:150–7. doi: 10.1016/j.bse.2015.04.014
5. Yang Y, Yang Y, Han S, Macadam I, Liu DL. Prediction of cotton yield and water demand under climate change and future adaptation measures. Agricultural Water Management. 2014;144:42–53. doi: 10.1016/j.agwat.2014.06.001
6. Bednarz CW, Nichols RL; Brown SM. Plant Density Modifies Within-Canopy Cotton Fiber Quality. Crop Science. 2006;46(2): 950–956.
7. Yang G-z, Luo X-j, Nie Y-c, Zhang X-l. Effects of Plant Density on Yield and Canopy Micro Environment in Hybrid Cotton. Journal of Integrative Agriculture. 2014;13(10):2154–63. https://doi.org/10.1016/S2095-3119(13)60727-3.
8. Bednarz CW., Shurley WD, Anthony WS, Nichols RL. Yield, quality, and profitability of cotton produced at varying plant densities. Agronomy Journal; 2005 97 (1): 235–240. doi: 10.1051/agro:2004062
9. Boroomandan P, Khoramivafa M, Haghi Y, Ebrahimi. The effects of nitrogen starter fertilizer and plant density on yield, yield components and oil and protein content of soybean (Glycine max L. Merr). Pakistan journal of biological sciences. 2009; 12(24): 378–382. doi: 10.3923/pjbs.2009.378.382 19579973
10. Liu Y-E., Hou P, Xie R-Z, Hao W-P, Li S-K, Mei XR. Spatial variation and improving measures of the utilization efficiency of accumulated temperature. Crop Science 2015;55(4), 1806–1817. doi: 10.2135/cropsci2014.10.0735
11. Iizumi T, Ramankutty N. How do weather and climate influence cropping area and intensity? Global Food Security. 2015;4:46–50. doi: 10.1016/j.gfs.2014.11.003
12. Xue H, Han Y, Li Y, Wang G, Feng L, Fan Z, et al. Spatial distribution of light interception by different plant population densities and its relationship with yield. Field Crops Research. 2015;184:17–27. doi: 10.1016/j.fcr.2015.09.004
13. Tsimba R, Edmeades GO, Millner JP, Kemp PD. The effect of planting date on maize grain yields and yield components. Field Crops Research. 2013;150:135–44. doi: 10.1016/j.fcr.2013.05.028
14. Wang C, Wang D, Li M, Ruan M, S. Canopy Structure and Radiation Interception of Cotton Grown under High Density Condition in Northern Xinjiang. Cotton Science, 2006;18(4):223–227. doi: 10.3969/j.issn.1002-7807.2006.04.007
15. Dong H, Li W, Tang W, Li Z, Zhang D, Niu Y. Yield, quality and leaf senescence of cotton grown at varying planting dates and plant densities in the Yellow River Valley of China. Field Crops Research. 2006;98(2–3):106–15. doi: 10.1016/j.fcr.2005.12.008
16. Kaggwa-Asiimwe R, Andrade-Sanchez P, Wang G. Plant architecture influences growth and yield response of upland cotton to population density. Field Crops Research. 2013;145:52–9. doi: 10.1016/j.fcr.2013.02.005
17. Giuliani R, Magnanini E, Fragassa C, Nerozzi F. Ground monitoring the light–shadow windows of a tree canopy to yield canopy light interception and morphological traits. Plant, Cell and Environment. 2000; 23: 783–796. doi: 10.1046/j.1365-3040.2000.00600.x
18. Mariscal M, Orgaz F, Villalobos F. Modelling and measurement of radiation interception by olive canopies. Agricultural and Forest Meteorology. 2000;100:183–197. doi: 10.1016/s0168-1923(99)00137-9
19. Galanopoulou-Sendouka S, Sficas A, Fotiadis N, Gagianas A., Gerakis P. Effect of population density, planting date, and genotype on plant growth and development of cotton. Agronomy Journal.1980; 72(2):347. doi: 10.2134/agronj1980.00021962007200020022x
20. Tetio-Kagho F, Gardner F. Responses of maize to plant population density. I. Canopy development, light relationships, and vegetative growth. 1988; 80(6):930. doi: 10.2134/agronj1988.00021962008000060018x
21. Begna S, Hamilton R, Dwver L., Stewart D, Smith D. Effects of population density and planting pattern on the yield and yield components of leafy reduced-stature maize in a short-season area. Agronomy & Crop Science 1997;179: 9–17. doi: 10.1111/j.1439-037X.1997.tb01142.x
22. Sarlikioti V, de Visser PH, Marcelis LF. Exploring the spatial distribution of light interception and photosynthesis of canopies by means of a functional-structural plant model. Ann Bot. 2011;107(5):875–83. Epub 2011/03/01. doi: 10.1093/aob/mcr006 21355008; PubMed Central PMCID: PMC3077986.
23. Mao L, Zhang L, Zhao X, Liu S, van der Werf W, Zhang S, et al. Crop growth, light utilization and yield of relay intercropped cotton as affected by plant density and a plant growth regulator. Field Crops Research. 2014;155:67–76. doi: 10.1016/j.fcr.2013.09.021
24. Liu T, Gu L, Dong S, Zhang J, Liu P, Zhao B. Optimum leaf removal increases canopy apparent photosynthesis, 13C-photosynthate distribution and grain yield of maize crops grown at high density. Field Crops Research. 2015;170:32–9. doi: 10.1016/j.fcr.2014.09.015
25. Srinivasan V, Kumar P, Long SP. Decreasing, not increasing, leaf area will raise crop yields under global atmospheric change. Glob Chang Biol. 2017;23(4):1626–35. Epub 2016/11/20. doi: 10.1111/gcb.13526 27860122; PubMed Central PMCID: PMC5347850.
26. Xu W, Liu C, Wang K, Xie R, Ming B, Wang Y, et al. Adjusting maize plant density to different climatic conditions across a large longitudinal distance in China. Field Crops Research. 2017;212:126–34. doi: 10.1016/j.fcr.2017.05.006
27. Flans F, Kiniry J, Board J, Westagte M, Reicosky D. Row spacing effects on light extinction coefficients of corn, sorghum, soybean and sunflower. Agronomy Journal, 1996; 88(2). 185. doi: 10.2134/agronj1996.00021962008800020011x
28. Maddonni G, Otegui M, Cirilo A. Plant population density: row spacing and hybrid effects on maize canopy architecture and light attenuation.Field Crops Research, 2001;71(3):183–193 doi: 10.1016/s0378-4290(01)00158-7
29. Chenu K, Franck N, Dauzat J, Barczi J, Rey H., Lecoeur J. Integrated responses of rosette organogenesis, morphogenesis and architecture to reduced incident light in Arabidopsis thaliana results in higher efficiency of light interception. Functional Plant Biology. 2005; 32(12): 1123–1134. doi: 10.1071/FP05091
30. Escobar-Gutiérrez AJ, Combes D, Rakocevic M, de Berranger C, Eprinchard-Ciesla A, Sinoquet H, et al. Functional relationships to estimate Morphogenetically Active Radiation (MAR) from PAR and solar broadband irradiance measurements: The case of a sorghum crop. Agricultural and Forest Meteorology. 2009;149(8):1244–53. doi: 10.1016/j.agrformet.2009.02.011
31. Clover GRG, Jaggard KW, Smith HG, Azam-Ali SN. The use of radiation interception and transpiration to predict the yield of healthy, droughted and virus-infected sugar beet. The Journal of Agricultural Science. 2001;136(2):169–78. doi: 10.1017/s002185960100853x
32. Wiechers D, Kahlen K, Stützel H. Evaluation of a radiosity based light model for greenhouse cucumber canopies. Agricultural and Forest Meteorology. 2011;151(7):906–15. doi: 10.1016/j.agrformet.2011.02.016
33. Duvrick D, Cassman K. Post-green revolution trends in yield potential of temperate maize in north-central United States. Crop Science. 1999;39(6):1622–1630. doi: 10.2135/cropsci1999.3961622x
34. Chen G, Gao J, Zhao M, Dong S, Li K., Yang Q, et al. Distribution, yield structure, and key cultural techniques of maize superhigh yield plots in recent years. Acta Agronomica Sinica. 2012; 38(1):80–85. doi: 10.3724/SP.J.1006.2012.00080
35. van Ittersum MK, Cassman KG. Yield gap analysis—Rationale, methods and applications—Introduction to the Special Issue. Field Crops Research. 2013;143:1–3. doi: 10.1016/j.fcr.2012.12.012
36. Zhi X, Han Y, Li Y, Wang G, Du W, Li X, et al. Effects of plant density on cotton yield components and quality. Journal of Integrative Agriculture. 2016;15(7):1469–79. doi: 10.1016/s2095-3119(15)61174-1
37. Gerardeaux E, Jordan-Meille L, Pellerin S. Radiation interception and conversion to biomass in two potassium-deficient cotton crops in South Benin. The Journal of Agricultural Science. 2009;147(2):155–68. doi: 10.1017/s0021859608008381
38. Tiwari R, Picchioni G, Steiner L, Jones D, Hughs S, Zhang J. Genetic variation in salt tolerance at the seedling stage in an interspecific backcross inbred line population of cultivated tetraploid cotton. Euphytica. 2013;194(1), 1–11. doi: 10.1007/s10681-013-0927-x
39. Boquet D. Cotton in ultra-narrow row spacing: Plant density and nitrogen fertilizer rates. Agronomy Journal, 2005;97(1): 279–287. doi: 10.2134/agronj2005.0279
40. Jones M, Wells R. Dry matter allocation and fruiting patterns of cotton grown at two divergent plant populations. Crop Science. 1997; 37(3): 797–802. doi: 10.2135/cropsci1997.0011183X003700030017x
41. Dai J, Li W, Tang W, Zhang D, Li Z, Lu H, et al. Manipulation of dry matter accumulation and partitioning with plant density in relation to yield stability of cotton under intensive management. Field Crops Research. 2015;180:207–15. doi: 10.1016/j.fcr.2015.06.008
42. Jones MA, Wells R. Dry matter allocation and fruiting patterns of cotton grown at two divergent plant populations. Crop Science. 1997;37:797–802. doi: 10.2135/cropsci1997.0011183X003700030017x
43. Evans L, Fischer R. Yield potential: its definition, measurement, and significance. Crop Science. 1999;39(6):1544–1551. doi: 10.2135/cropsci1999.3961544x
44. Peng S, Huang J, Sheehy J, Laza R, Visperas R, Zhong X, et al. Rice yields decline with higher night temperature from global warming. 2004;101(27):9971–9975. doi: 10.1073/pnas.0403720101 15226500
45. Echarte L, Luque S, Andrade F, Sadras V, Cirilo A, Otegui M,et al. Response of maize kernel number to plant density in Argentinean hybrids released between 1965 and 1993. Field Crops Research. 2000;68:1–8. doi: 10.1016/S0378-4290(00)00101-5
46. Hecht VL, Temperton VM, Nagel KA, Rascher U, Pude R, Postma JA. Plant density modifies root system architecture in spring barley (Hordeum vulgare L.) through a change in nodal root number. Plant and Soil. 2018;439(1–2):179–200. doi: 10.1007/s11104-018-3764-9
47. Zhi X, Han Y, Mao S, Wang G, Feng L, Yang B, et al. Light spatial distribution in the canopy and crop development in cotton. PLoS One. 2014;9(11):e113409. Epub 2014/11/20. doi: 10.1371/journal.pone.0113409 25409026; PubMed Central PMCID: PMC4237451.
Článek vyšel v časopise
PLOS One
2019 Číslo 9
- Pomohou nám s detekcí karcinomu plic i včely?
- Duševní onemocnění se u teenagerů přenáší v rámci školní třídy
- Od kostiček k lidské kůži. Jak si postavit 3D biotiskárnu?
- Řekněte mi, co jíte, a já vám řeknu, jaká je úroveň vaší kognice
- Umělá inteligence v mozkovém implantátu pomáhá muži po mrtvici s dvojjazyčnou konverzací
Nejčtenější v tomto čísle
- Graviola (Annona muricata) attenuates behavioural alterations and testicular oxidative stress induced by streptozotocin in diabetic rats
- CH(II), a cerebroprotein hydrolysate, exhibits potential neuro-protective effect on Alzheimer’s disease
- Comparison between Aptima Assays (Hologic) and the Allplex STI Essential Assay (Seegene) for the diagnosis of Sexually transmitted infections
- Assessment of glucose-6-phosphate dehydrogenase activity using CareStart G6PD rapid diagnostic test and associated genetic variants in Plasmodium vivax malaria endemic setting in Mauritania