EMERGENCE, GROWTH, AND PRODUCTION OF COLORED COTTON SUBJECTED TO SALT STRESS AND ORGANIC FERTILIZATION¹

EMERGÊNCIA, CRESCIMENTO E PRODUÇÃO DO ALGODOEIRO COLORIDO SUBMETIDO AO ESTRESSE SALINO E ADUBAÇÃO ORGÂNICA

ABSTRACT

The semi-arid region of Northeast Brazil is vulnerable to problems of water scarcity and salinity, resulting in low-quality irrigation water and the need to adopt cultivation strategies that make the production system viable. Given the above, this study aimed to evaluate emergence, growth, and production of colored cotton subjected to increasing levels of irrigation water salinity and organic matter doses. The experiment was carried out in a eutrophic Regolithic Neosol with a sandy loam texture in a greenhouse in the municipality of Campina Grande - PB, Brazil. A randomized block design was used in a 4 x 4 factorial scheme with three replicates, and the treatments corresponded to four levels of electrical conductivity of water - ECw (1.7, 3.4, 5.1, and 6.8 dS m^-1) and four doses of organic matter - OM (0, 2.5, 3.5, and 4.5% based on soil volume). Increasing irrigation water salinity with ECw values above 1.7 dS m^-1 reduced emergence, growth, and production of colored cotton, and the cotton seed weight was the variable most affected by salinity. Organic matter addition led to increased cotton growth and production, especially in terms of seed weight. Increasing doses of organic matter attenuated the effect of irrigation water salinity on the number of bolls in ‘BRS Jady’ cotton.

Keywords:
Gossypium hirsutum L; Salinity; Bovine manure.

RESUMO

A região semiárida do Nordeste Brasileiro é vulnerável aos problemas de escassez hídrica e salinidade, o que faz com que a maioria das águas utilizadas para irrigação nem sempre apresente boa qualidade, sendo necessária a adoção de estratégias de cultivo que viabilizem o sistema de produção. Diante do exposto, objetivou-se avaliar a emergência, o crescimento e a produção do algodoeiro de fibra colorida submetido a níveis crescentes de salinidade da água de irrigação e doses de matéria orgânica. O experimento foi conduzido em um Neossolo Regolítico Eutrófico de textura franco-arenosa em casa de vegetação no município de Campina Grande - PB. Utilizaram-se o delineamento experimental de blocos casualizados, em esquema fatorial 4 x 4, com três repetições, sendo os tratamentos compostos de quatro níveis de condutividade elétrica da água - CEa (1,7; 3,4; 5,1 e 6,8 dS m^-1) e quatro doses de matéria orgânica - MO (0; 2,5; 3,5 e 4,5% em base do volume de solo).O aumento da salinidade da água de irrigação com CEa superior a 1,7 dS m^-1 reduziu a emergência, o crescimento e a produção do algodoeiro colorido, sendo a massa de algodão em caroço a variável mais afetada. A adição de matéria orgânica promoveu acréscimos no crescimento e produção do algodoeiro, especialmente na massa de algodão em caroço. Doses crescentes de matéria orgânica atenuaram o efeito da salinidade da água de irrigação sobre o número de capulhos do algodoeiro ‘BRS Jady’.

Palavras-chaves:
Gossypium hirsutum L.; Salinidade; Esterco bovino.

INTRODUCTION

Colored cotton cultivation has aroused the interest of producers and consumers in Brazil and worldwide and has become an expanding market with a great socioeconomic potential to generate jobs and provide raw material for the textile industry (DANIEL et al., 2011; SILVA et al., 2014). Cotton with naturally colored fiber also has a great environmental importance in terms of eliminating the dyeing stage in the industry (CARDOSO et al., 2010).

Despite being common in the northeastern region of the country, this crop has the lowest yields in this area, where the shortage of good-quality water has become a fundamental problem for the development of agriculture. Water sources with high concentrations of salts, especially sodium, are common (NEVES et al., 2009; JIANG et al., 2012).

When in excess, salts can cause osmotic stress in plants, reducing water availability, resulting in stomatal closure and, consequently, reduced carbon dioxide availability, potentially damaging the photosynthetic apparatus (ALVES et al., 2011; SÁ et al., 2015). This may induce ionic toxicity, leading to membrane disorganization, the production or reactive oxygen species, and nutritional imbalance (AREF; RAD, 2012; MGUIS et al., 2012).

Organic fertilization is essential for crop development in low-fertility soils, especially in a commercial production, due to the need to improve the product’s quality and to meet the consumers’ demands (ABREU et al., 2005); in addition, it mitigates the deleterious effects of salts on plants due to the positive impacts on physical characteristics of soil and the plant root environment. Humic substances released by the decomposition of organic sources stimulate the absorption of water and nutrients by plants in saline environments (MAHMOUD; MOHAMED, 2008; ASIK et al., 2009).

Studies conducted with other crops, such as sweet passion fruit (DAMATTO JÚNIOR; LEONEL; PEDROSO, 2005), watermelon (CAVALCANTE et al., 2010), sugar apple (CAVALCANTE et al., 2012), guava Oliveira et al. (2014), melon (RIBEIRO et al., 2014), and cashew (MELO FILHO et al., 2015), have already reported the beneficial effects of the application of organic fertilizers on plant growth and development. It is therefore crucial to conduct further studies that provide information on the adequate organic matter content to meet the nutritional requirements of the cotton crop under semi-arid conditions in Northeast Brazil.

In this context, this study aimed to evaluate the emergence, growth, and production of the colored fiber cotton cv. BRS Jady, subjected to irrigation with increasing levels of water salinity and to different doses of organic matter amendment.

MATERIAL AND METHODS

The experiment was carried out from October 2016 to January 2017 in a greenhouse at the Center of Sciences, Technology and Natural Resources (CTRN) of the Federal University of Campina Grande (UFCG), located in the municipality of Campina Grande, Paraíba, Brazil, at the geographic coordinates 7°15’18’’ S, 35°52’28’’ W and 550 m above sea level.

The experimental design consisted of randomized blocks in a 4 x 4 factorial scheme, corresponding to four levels of irrigation water salinity - ECw (1.7, 3.4, 5.1, and 6.8 dS m^-1) and four doses of organic matter - OM (0, 2.5, 3.5, and 4.5% based on soil volume). Combined, the factors resulted in 16 treatments, with 3 replicates and 1 plant per plot, totaling 48 plants.

The plants were grown in 20-L plastic pots, which were perforated at the bottom and connected by drains to containers to collect drained water, allowing to monitor the drained volume and the crop water consumption. During the filling, the pots received a 250-g layer of crushed stones, covering the bottom of the lysimeter, and 22 kg of a non-saline, non-sodic, eutrophic Regolithic Neosol with sandy loam texture, obtained from the municipality of Esperança, Paraíba, from the 0-30 cm layer (A horizon); the chemical and physical-hydraulic characteristics of the soil are presented in Table 1.

Table 1
Chemical and physical characteristics of the eutrophic Regolithic Neosol used in the experiment, before applying the treatments.

		Chemical	characteristics
pHps	O.M	P	K+	Na+	Ca2+	Mg2+	Al3+	H+
	(dag kg-1)	(mg kg-1)			(cmolc kg-1)
5.63	1.83	18.2	0.21	0.17	3.49	2.99	0.00	5.81
		Physical	characteristics
Size fraction (g kg-1)			Textural	Water content (kPa)			Total	Density
Sand	Silt	Clay	class	33.42	1519.5	AW	porosity	(kg dm-3)
					dag kg-1		m3m-3
572.3	100.8	326.9	SL	12.68	4.98	7.70	0.57	1.31

• O.M. - Organic matter: Walkley-Black wet digestion; Ca²⁺and Mg²⁺extracted with 1 mol L^-1KCl at pH 7.0; Na⁺ and K⁺ extracted with 1 mol L^-1NH₄OAc at pH 7.0; ECse - Electrical conductivity of the saturation extract; SL - Sandy loam; AW - Available water.

The different levels of bovine manure were aged and applied as basal fertilization; the amounts were determined considering the organic matter content in the manure as equal to 45%. Top-dressing fertilization was performed using a formulation based on nitrogen (N), phosphorus (P), and potassium (K), according to the recommendation for pot experiments by Novais, Neves and Barros (1991), applying 100, 300, and 150 mg kg^-1 of soil of N, P₂O₅, and K₂O, respectively, in the form of urea, monoammonium phosphate, and potassium chloride. Fertilization was split into two top-dressing applications and applied via the irrigation water at 22 and 38 days after sowing (DAS). The pots were arranged in single rows with a spacing of 1 m and 0.6 m between the plants in the row.

Different saline solutions were prepared using the empirical relationship between the concentration of salts and the EC, as suggested by Richards (1954) (10*mmol_c L^-1 = 1 dS m^-1). Soil moisture was brought to a level corresponding to field capacity using water of the different salinity levels; subsequently, sowing was performed by planting eight seeds in each lysimeter equidistantly at a depth of 1.5 cm. The first thinning was performed at 20 DAS, leaving only the five most vigorous plants per pot. Thinning was performed again at 26 and 30 DAS, eliminating two plants from each pot.

The plants were irrigated daily; each lysimeter received a water volume necessary to maintain the field capacity of the soil. The volume applied in each irrigation event was determined according to the plant water requirement, estimated by water balance: applied water volume minus volume drained in the previous irrigation plus a leaching fraction of 0.10.

As phytosanitary control, plants were sprayed with the insecticide dimethoate at a concentration of 1.5 mL L^-1 to control white fly, as recommended by the manufacturer. Plants were sprayed always at 05:00 p.m. to minimize negative impacts on insect pollinators.

The effects of the different treatments were evaluated in the period between emergence and production of the cotton cv. BRS Jady, based on the variables emergence speed index (ESI), plant height (PH; cm), stem diameter (SD; mm), and leaf area (LA; cm²) at 40 and 60 DAS. The number of days to flower bud opening (NDFBO) and the flower abortion rate (FAR) were determined at 80 DAS, while the total number of bolls (TNB) and seed cotton weight (SCW) were determined at 114 DAS.

Cotton emergence was assessed by daily recording, until 7 DAS, the number of emerged plants, adopting as criterion the appearance of the epicotyl on the soil surface, which allowed the determination of emergence percentage - E% (number of emerged seedlings in relation to the number of seeds sown). Emergence speed index (ESI) was estimated at 7 DAS, using the methodology described by Vieira and Carvalho (1994), according to Eq.1:

$ESI\left(seedlings{day}^{-1}\right)=\frac{{Ʃ}_1}{{\mathrm{N}}_1}+\frac{{Ʃ}_2}{{\mathrm{N}}_2}\dots +\frac{{Ʃ}_n}{{\mathrm{\Sigma }}_n}$ (1)

Where Σ₁, Σ₂, ... Σ_n represent the number of emerged seedlings, at first, second, and last counts, while N₁, N₂,... N_n are the number of days from sowing to the first, second, and last counts, respectively.

The PH was determined by measuring the distance between root flare and the youngest leaf insertion point; SD was determined using a digital caliper 5 cm above the soil level. In the LA estimation, measurements of the midrib length of each leaf (cm) were taken, considering only leaves with a minimum length of 1.5 cm and a photosynthetically active area of at least 50%. Total leaf area was obtained according to the methodology described by Grimes and Carter (1969), using Eq.2:

$Y=\sum 0.4322x^{2.3002}$ (2)

where: Y= leaf area per leaf, cm²; x= midrib length of cotton leaves, cm.

The variable NDFBO was estimated by daily monitoring flower bud opening, whereas the flower abortion rate was determined based on the relationship between the number of open flower buds and the total number of bolls, in percentage. Bolls were harvested per plant, as they reached the harvesting point, and seed cotton weight was determined by weighing on a precision scale (0.001 g accuracy).

Data were subjected to analysis of variance (ANOVA), using the F test. In cases of significance, linear and quadratic polynomial regression analyses were applied, using the statistical software SISVAR version 5.3 (FERREIRA, 2011).

RESULTS AND DISCUSSION

According to the results of the ANOVA (Table 2), irrigation water salinity and organic matter doses had significant effects on emergence speed index, stem diameter, plant height, and leaf area, in all studied periods. The interaction between water salinity and organic matter doses had an effect only on stem diameter at 60 DAS.

Table 2
Summary of analysis of variance for emergence speed index (ESI), stem diameter (SD), plant height (PH) and leaf area (LA) at 40 and 60 days after sowing in the cotton cv. BRS Jady irrigated with saline water and under different doses of organic matter.

					Mean	squares
		ESI	SD		PH		LA
Source of variation	DF		Days after sowing
			40	60	40	60	40	60
Saline levels (SL)	3	0.12**	0.33**	2.60**	112.94**	507.96**	6366.26*	671561.75**
Linear regression	1	0.11**	0.92**	7.42**	328.77**	1520.06**	184732.31**	194289.88**
Quadratic regression	1	0.23**	0.04ns	0.0001ns	9.10ns	2.16ns	6093.68ns	78294.00ns
Organic matter (OM)	3	0.16**	14.32**	13.14**	1050.87**	1681.02**	390369.12**	1426656.81**
Linear regression	1	0.04**	32.43**	25.64**	1735.05**	3343.57**	948412.82**	3763409.46**
Quadratic regression	1	0.23**	9.69**	11.54**	1364.26**	1536.80**	190329.34**	513536.15*
Interaction (SL x OM)	9	0.15ns	0.25ns	0.37**	17.83ns	30.46ns	13578.14ns	77856.94ns
Blocks	2	0.01ns	0.06ns	0.02ns	54.88*	99.44*	11452.35ns	69149.16ns
Residual		5.44	5.75	4.67	10.06	9.79	33.56	32.11

• ns, **, *respectively, not significant, significant at p < 0.01 and p < 0.05.

The increment in irrigation water electrical conductivity led to a reduction in ESI and, according to the regression equations (Figure 1A), there was a linear effect with the reduction of 0.37% per unit increase; i.e., plants irrigated at the highest salinity level (6.8 dS m^-1) showed losses of 1.92% compared with those under ECw of 1.7 dS m^-1. The reduction in ESI caused by the increment in the concentration of soluble salts in the soil occurs due to the decrease in water absorption capacity, which has a direct influence on processes such as cell division and differentiation, enzymatic activity, and nutrient uptake and distribution, possibly leading to a delay in seedling emergence and the mobilization of reserves or even a decrease in seed viability (VOIGT et al., 2009). Lopes and Silva (2010), studying the effects of different saline concentrations (0, 2, 4, 6, and 8 g L^-1) on the germination of the cotton cv. BRS Rubi, reported a linear reduction in ESI, which reached values lower than 64.45% at concentrations higher than 4 g of NaCl L^-1 (7.5 mS cm^-1) in the irrigation solution.

According to Figure 1B, the emergence speed index fitted best to a quadratic regression model, as OM increased and its highest value, corresponding to 1.64 seedling day^-1, was obtained in plants fertilized with an OM dose of 1.7%. According to Clemente et al. (2012), ESI is influenced by the increase in soil organic matter, which leads to an increment in cation exchange capacity, contributing to the improvement of structure and, consequently, resulting in higher water infiltration and retention and increased aeration and soil microbial activity and diversity.

Figure 1
Emergence speed index - ESI of the cotton cv. BRS Jady, as a function of irrigation water electrical conductivity - ECw (A) and organic matter doses (B).

The increase in irrigation water salinity caused a reduction in stem diameter at 40 DAS (Figure 2 A ), equal to 1.68% per unit increase in ECw; i.e., plants irrigated with an ECw of 6.8 dS m^-1 showed reductions of 8.58% (0.38 mm) in comparison to those irrigated with 1.7 dS m^-1. Hence, the reduction in stem diameter observed in plants grown under high water salinity conditions possibly results from the decrease in the soil solution osmotic potential, which impedes water absorption by the roots, causing the plant to reduce stomatal opening as a first mechanism to reduce water loss, directly affecting water and nutrient absorption, cell division and elongation, and inhibiting plant growth. Santos et al. (2016), studying the impacts of different levels of irrigation water salinity (0.7 to 8.7 dS m^-1) on the colored cotton BRS Topázio, also observed significant effects of ECw on stem diameter, with reductions of 0.32 and 0.71 mm per unit increase in ECw at 70 and 90 days after sowing.

Figure 2
Stem diameter of the cotton cv. BRS Jady, as a function of irrigation water salinity - ECw (A) and organic matter doses (B), at 40 days after sowing (DAS) and interaction between ECw levels and organic matter doses (C), at 60 DAS.

According to the regression equation for stem diameter of the cotton cv. BRS Jady at 40 DAS (Figure 2 B ), increments in organic matter doses led to a gain of 20.28% per unit increase in OM, i.e., cotton plants grown in soil fertilized with an OM dose of 4.5% showed a 2.45 mm greater stem diameter in SD compared with those that did not receive organic matter (0%). Such an increase in SD due to the increment in organic matter doses may be related to the beneficial effects of organic matter on soil physical and chemical characteristics, thereby promoting a greater capacity of water storage and soil aeration and providing adequate conditions for the development of microorganisms beneficial to the soil and the plants, leading to favorable conditions for plant development (MESQUITA et al., 2012).

The application of organic matter in the form of bovine manure led to a reduction in SD at 60 DAS, but the intensification of the effects depended on the irrigation water salinity level (Figure 2 C ). Based on the regression analysis, an OM dose of 2.5%, associated with 1.7 dS m^-1 water salinity, resulted in a higher SD (6.68 mm). However, at the highest salinity level (6.8 dS m^-1), stem diameter decreased by 30.26, 17.00, and 11.20% in plants fertilized with 0, 2.5, and 3.5% of OM, respectively, in comparison to the lowest salinity level (1.7 dS m^-1). Despite the reductions observed with the increment in salinity levels, salt stress was attenuated in plants subjected to doses of 2.5 and 3.5%. These beneficial effects are possibly related to the capacity of the bovine manure to stimulate the release of humic substances into the soil, which results in greater root and shoot growth (CAVALCANTE et al., 2007; NASCIMENTO et al., 2011).

Considering the effect of salinity on plant height (PH) in BRS Jady cotton at 40 and 60 DAS (Figure 3 A ), the increment in water salinity led to linear reductions of 3.54 and 4.85% with per unit increase in ECw; i.e., reductions of 7.01 cm (18.07%) and 15.09 cm (24.74%) in the PH of cotton plants subjected to the highest salinity level (6.8 dS m^-1) in comparison to those irrigated with 1.7 dS m^-1 water, respectively. According to the results for SD (Figure 2 A ), as the evaluation period increased, the effects of salt stress were intensified. Hence, the reduction in PH due to the ECw levels must be associated with the increase in soil solution salt concentration, which causes a reduction in the osmotic potential and leads to a higher water retention capacity in the soil, affecting water absorption and decreasing the growth of cultivated plants (GARCIA et al., 2010). In addition, for the maintenance of osmotic and ionic homeostasis, plants allocate a certain amount of energy to the accumulation of sugars, organic acids, and ions in the vacuole, energy that could be used for growth (SANTOS et al., 2012). Higbie et al. (2010), working with a variety of cotton cultivars (DP 33B, SG 747, Acala Phy 72, Acala 1517-88, JinR 422, and Pima57-4) irrigated with two levels of water salinity (0.57 and 20 dS m^-1), observed that the height of the cultivars was inhibited when plants were irrigated with an ECw of 20 dS m^-1.

Figure 3
Plant height of the cotton cv. BRS Jady, as a function of irrigation water salinity - ECw (A) and organic matter doses (B), at 40 and 60 days after sowing (DAS).

The organic matter doses had a quadratic effect on plant height at 40 and 60 DAS (Figure 3 B ) and, according to the regression equations, maximum height values of 38.86 and 55.78 cm were obtained in plants subjected to doses of 3.3 and 3.8%, respectively. Dias et al. (2016), working with four levels of organic matter (from 0 to 15%) in BRS Topázio cotton, observed increments of 25.86 and 23.70% in height when the plants were subjected to the level of 15% organic matter, in comparison to plants that did not receive OM at 55 and 75 DAS, respectively.

Increasing irrigation water salinity also significantly reduced leaf area (LA) in BRS Jady cotton at 40 and 60 DAS (Figure 4 A ), with reductions of 6.40 and 8.28% per unit increase in ECw, which correspond to decreases of 166.46 and 537.27 cm² in LA between plants subjected to 1.7 dS m^-1 irrigation water salinity and those at the highest salinity level (6.8 dS m^-1). The reduction in leaf area, i.e., in the photosynthetic apparatus, contributes to a decrease in the production of organic photoassimilates and results in plant growth inhibition (SANTOS et al., 2013). In addition, such decrease in leaf area probably results from the reduction in cell volume; a reduction in the transpiring surface leads to the minimization of water loss through stomatal flow, thus contributing to the maintenance of a high water potential in the plant (NASCIMENTO et al., 2011). In a study with the cotton cultivar BRS Topázio, Santos et al. (2016) also found that saline water irrigation (ECw values from 0.7 to 8.7 dS m^-1) led to a reduction in leaf area equal to 5,024.72 cm² (67.11%) in plants under an ECw of 8.7 dS m^-1 in comparison to those under an ECw of 0.7 dS m^-1.

Increasing doses of organic matter had positive and significant effects (p < 0.01) on leaf area at 40 and 60 DAS (Figure 4 B ), causing increments of 69.77 and 49.72% in LA per unit increase in OM doses, respectively, at 40 and 60 DAS; i.e., plants subjected to an OM dose of 4.5% showed increments of 524.75 and 1,150.10 cm² at 40 and 60 DAS, in comparison to those that did not receive OM. Hence, increasing doses of organic matter, applied as basal fertilization, possibly promoted the proliferation of microorganisms contained in the organic material added to the soil, which may increase the level of nutrient availability to plants, leading to a greater leaf area in the cotton cv. BRS Jady (RAJENDRAN; DEVARA, 2004).

Figure 4
Leaf area of the cotton cv. BRS Jady, as a function of irrigation water salinity - ECw (A) and organic matter doses (B), at 40 and 60 days after sowing (DAS).

Based on the summary of analysis of variance (Table 3), irrigation water salinity and organic matter doses had significant effects on flower abortion rate and seed cotton weight in the cultivar BRS Jady. For the number of days to flower bud opening, only the organic matter doses had significant effects. The interaction between factors (irrigation water salinity and organic matter doses) had a significant effect on the total number of bolls (Table 3).

Table 3
Analysis of variance summary for the number of days to flower bud opening (NDFBO) and flower abortion rate (FAR) at 80 days after sowing (DAS), total number of bolls per plant (TNB) and seed cotton weight (SCW) at 114 DAS, in the cotton cv. BRS Jady irrigated with saline water and under different doses of organic matter.

Source of variation	DF			Mean squares
		NDFBO	FAR	TNB	SCW
Saline levels (SL)	3	27.74ns	11.55*	57.36**	1625.49**
Linear regression	1	53.20ns	1.06ns	160.06**	4653.26**
Quadratic regression	1	28.52ns	33.33**	12.00**	213.44**
Organic matter (OM)	3	300.74**	107.88**	47.47**	1553.22**
Linear regression	1	573.50**	248.06**	123.26**	4453.95**
Quadratic regression	1	315.18**	75.01**	2.08**	205.01**
Interaction (SL x OM)	9	13.90ns	3.55ns	2.82**	43.86ns
Blocks	2	73.39ns	31.08*	1.31	5.69ns
Residual		11.23	29.50	11.26	19.11

• ns, **, *respectively, not significant, significant at p < 0.01 and p < 0.05.

For the number of days to flower bud opening as a function of organic matter doses in the soil (Figure 5), with increasing OM doses, NDFBO decreased, with a maximum value (51 days) at an OM dose of 0%; however, the lowest value (42 days) was obtained at the OM dose of 3.3%. The early crop cycle observed in the present study can therefore be considered as an important characteristic, since the Brazilian programs of genetic improvement seek to select increasingly precocious cotton genotypes, aiming at maximum yields within shorter cultivation periods (LIMA et al., 2017). Likewise, Araújo et al. (2001), evaluating the application of increasing doses of organic matter in the form of pig manure in the snap bean crop, also found an advance in the flowering stage, resulting in earlier harvest.

Figure 5
Number of days to flower bud opening (NDFBO) in the cotton cv. BRS Jady, as a function of organic matter doses at 80 days after sowing (DAS).

For the flower abortion rate (FAR), the regression equation (Figure 6 A ) indicates that BRS Jady cotton plants subjected to saline stress in the flowering stage (80 DAS) exhibited an increase in FAR up to the ECw level of 4.1 dS m^-1 (7.62%), decreasing from this point on to the lowest value (5.54%), obtained in plants grown under the highest ECw value (6.8 dS m^-1). Torabi et al. (2013) reported that, among the deleterious effects of salinity, the reduction in plant fecundity stands out, which leads to higher flower abortion rates, followed by alterations in metabolic reactions in order to attenuate the damages caused by salt stress. Furtado et al. (2014), in a study carried out with a cowpea crop under saline conditions (ECw = 0.9 to 4.5 dS m^-1), also observed that increasing water salinity caused a proportional increment in flower abortion rate.

Figure 6
Flower abortion rate - FAR in the cotton cv. BRS Jady, as a function of irrigation water salinity - ECw (A) and organic matter doses (B), and total number of bolls - TNB (C), as a function of the interaction between the factors ECw levels and organic matter doses, at 80 days after sowing (DAS).

Increasing organic matter doses had a quadratic effect on FAR at 80 DAS and, according to the regression equation (Figure 6 B ), its maximum value (8.58%) was obtained in plants subjected to an OM dose of 4.4%. According to Silva et al. (2011), leaves and reproductive structures compete among themselves for assimilates, especially when plants are still in the growth stage, possibly because OM promotes favorable conditions for an equilibrated balance between vegetative and reproductive growth in cotton plants.

According to the regression equations presented in Figure 6 C , the total number of bolls (TNB) exhibited a quadratic response in plants fertilized with OM doses of 0 and 3.5%, and maximum TNB values of 7.49 and 9.67 bolls plant^-1 were obtained under irrigation with 1.7 dS m^-1 water. In addition, OM doses of 2.5 and 4.5% led to linear reductions of 49.05 and 46.83% in the TNB of plants irrigated with an ECw of 6.8 dS m^-1 in comparison to the ECw of 1.7dS m^-1. However, increasing organic matter doses, even under irrigation with the highest salinity level (6.8 dS m^-1), resulted in increases of 2.17, 2.49, and 3.66 bolls in the TNB at OM doses of 2.5, 3.5, and 4.5%, respectively, in comparison to plants without organic fertilization. Although the increase in flower abortion rate occurred due to the different doses of organic matter, it did not reflect in the total number of bolls. Thus, these levels of organic fertilization may have been sufficient to nourish the plant with the necessary nutrients. Probably, during plant growth and development, the supplied doses of organic matter, along with the nutrients contained in the soil, has efficiently met the nutritional requirements of the crop, mitigating the deleterious effects of irrigation water salinity and leading to gains in crop production (CAVALCANTE et al., 2010; SILVA et al., 2012).

Seed cotton weight data (Figure 7 A ) fitted to a quadratic model, and the maximum SCW (43.29 g) was obtained in plants under an ECw of 1.7 dS m^-1. In addition, increasing water salinity caused a reduction of 61.03% in this variable up to the highest salinity level (6.8 dS m^-1) in comparison to the ECw of 1.7 dS m^-1. The reduction observed in seed cotton weight (Figure 7 A ) results from the accentuated decrease in the growth of cotton plants, evidenced by SD, PH, and LA, caused by the reduction in the soil solution osmotic potential due to the high saline concentration. This situation imposes a higher expenditure of energy on the plants for water absorption and maintenance of metabolic activity, besides the synthesis of organic solutes for osmoregulation and/or protection of macromolecules. As a consequence, plant growth is reduced, which results in lower production (LEONARDO et al., 2007). Jácome et al. (2003), working with different cotton genotypes under irrigation water salinity levels ranging from 2.0 to 10.0 dS m^-1, also found losses in the production components in response to water salinity.

Figure 7
Seed cotton weight - SCW in the cotton cv. BRS Jady, as a function of irrigation water salinity - ECw (A) and organic matter doses (B) at 114 days after sowing (DAS).

Seed cotton weight was significantly and linearly influenced by the fertilization with increasing doses of organic matter, and its highest value (38.97 g plant^-1) was obtained in cotton plants grown at an OM dose of 4.5% (Figure 7 B ), which is equivalent to an increment of 26.39 g compared with plants cultivated with no addition of organic matter. This result reinforces the importance of using organic matter for the growth and production of crops. Similar results were also found by Pereira et al. (2012), who evaluated the effect of six doses of bovine manure (0, 2.5, 5, 10, 20, and 40 Mg ha^-1) on agronomic and fiber characteristics of the colored cotton BRS Rubi and also observed that the dose of 28 Mg ha^-1 promoted maximum yield, corresponding to 1,111.19 kg ha^-1 of seed cotton.

CONCLUSIONS

Increasing irrigation water salinity reduces emergence, growth, and production in the colored cotton cv. BRS Jady, and seed cotton weight is the variable most affected by salinity. Organic matter addition promotes increased cotton growth and production, especially in terms of seed cotton weight. Increasing doses of organic matter attenuate the effect of irrigation water salinity on the number of bolls in the cotton cv. BRS Jady.

ACKNOWLEDGMENTS

To the National Program of Post-Doctorate (PNPD/CAPES/UFCG), for granting the scholarship to the second author and to the National Institute of Science and Technology in Salinity - INCTSal, for funding the project.

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• 1
  Paper extracted from the postdoctoral research of the second author.

Publication Dates

• Publication in this collection
  Jul-Sep 2018

History

• Received
  26 Mar 2017
• Accepted
  23 Oct 2017