NITROGEN AND POTASSIUM IN SAFFLOWER: CHLOROPHYLL INDEX, BIOMETRIC CHARACTERISTICS AND WATER USE EFFICIENCY

NITROGÊNIO E POTÁSSIO EM CÁRTAMO: ÍNDICE DE CLOROFILA, CARACTERÍSTICAS BIOMÉTRICAS E USO DA ÁGUA

ABSTRACT

Safflower crops is usually intended for production of seeds to oil extraction. The objective of this work was to evaluate the chlorophyll index, biometric characteristics and water use efficiency of safflower plants grown under different nitrogen and potassium rates and controlled soil water tension. The experiment was conducted in a greenhouse, in pots containing 8 dm³ of a Oxisol. A complete randomized block experimental design in a 5x5 factorial arrangement was used, with four replications, consisting of five nitrogen rates (0, 60, 120, 180 and 240 mg dm^-3) and five potassium rates (0, 50, 100, 150 and 200 mg dm^-3). The safflower number of leaves, stem diameter, chlorophyll index, number of capitula, shoot, root and total dry weights, water consumption and water use efficiency were evaluated. Data were subjected to analysis of variance (F test) at 5% of probability and to polynomial regression. The nitrogen and potassium fertilization, as independent factors, affected the safflower plants. The chlorophyll index, biometric characteristics and water use efficiency of safflower showed better responses under nitrogen rates of 82 to 168 mg dm^-3. The responses of chlorophyll index, biometric characteristics and water use efficiency of safflower increased 10 to 60% with potassium fertilization.

Keywords:
Carthamus tinctorius L.; Fertilization; Plant production

RESUMO

O cártamo destina-se à produção de grãos para a obtenção de óleo vegetal. Objetivou-se avaliar o índice de clorofila, as características biométricas e a eficiência no uso da água de plantas de cártamo sob doses de nitrogênio e potássio. O experimento foi conduzido em casa de vegetação, em vasos contendo 8 dm³ de um Latossolo Vermelho. O delineamento experimental foi blocos casualizados, com esquema fatorial 5x5 correspondente a cinco doses de nitrogênio (0, 60, 120, 180 e 240 mg dm^-3) e cinco doses de potássio (0, 50, 100, 150 e 200 mg dm^-3), com quatro repetições. Avaliou-se o número de folhas, diâmetro de caule, índice de clorofila, número de capítulos, massa seca da parte aérea, massa seca de raízes, massa seca total, consumo de água e eficiência no uso da água. Os dados foram submetidos a 5% de probabilidade de erro a análise de variância pelo teste F e regressão polinomial. O índice de clorofila, as características biométricas e a eficiência no uso da água das plantas de cártamo apresentaram melhores respostas nas doses de nitrogênio entre 82 a 168 mg dm^-3. A adubação potássica nas plantas de cártamo proporcionou respostas crescentes com incrementos de 10 a 60% para o índice de clorofila, nas características biométricas e na eficiência de uso da água. As respostas a adubação com nitrogênio e potássio no cártamo ocorrem com efeito isolado.

Palavras-chave:
Carthamus tinctorius L.; Adubação; Produção vegetal

INTRODUCTION

Safflower (Carthamus tinctorius L.) crops is usually intended for production of seeds to oil extraction, which has high quality as human food and potential for biofuel production (DORDAS; SIOULAS, 2008; SHAHROKHNIA; SEPASKHAH, 2016).

Safflower is an herbaceous plant with good adaptability to hot and dry climate conditions due to its deep root system, thus, it is an alternative for crop rotation in Brazil (ANICÉSIO et al., 2015; BONFIM-SILVA et al., 2015).

However, the expansion of safflower crops depends on studies on soil fertilization for recommendation of adequate fertilizer rates for the nutritional balance of this species, increasing its yield, technical efficiency and economic return of the initial investment (WENDLING et al., 2008).

Nitrogen is one of the most required nutrients by plants, since it is part of proteins, enzymes, chlorophyll, nucleic acids, and contribute to hormone synthesis (TAIZ; ZEIGER, 2013).

Potassium is the most concentrated cation in plants, with important physiological and metabolic functions, such as enzymatic activation, photosynthesis and translocation of assimilates, thus, it can be a limiting factor for crop yields (TAIZ; ZEIGER, 2013).

Potassium is the most common nutrient interacting with nitrogen in crops. Growth stimulation by nitrogen fertilization requires adequate potassium fertilization; otherwise, deficiency of this nutrient may occur due to dilution (CANTARELLA, 2007).

Nitrogen excess increases protein content of plants, to the detriment of carbohydrates, resulting in excessive development of the plant shoot in relation to its root system, thus, it may increase lodging (MARSCHNER, 1986). On the other hand, potassium increases resistance to plant lodging, probably by contributing to increase the stem diameter and acceleration of lignification of sclerenchyma cells (PRETTY, 1982).

These nutrients are directly related to the water use efficient of crops. Adequate nitrogen fertilization increases the root system depth, resulting in a higher volume of soil used, reducing the effects of water deficit (DORDAS; SIOULAS, 2008). Potassium maintains the plant maximum photosynthetic capacity with the lowest water loss possible through osmotic control and opening and closing of stomata (FARQUHAR; SHARKEY, 1982).

An appropriate nitrogen and potassium fertilization can also increase the chlorophyll index of leaves, which is related positively to nutritional and production characteristics of plants, increasing photosynthesis and production of assimilates retained by biometric structures (TAIZ; ZEIGER, 2013).

According to Bonfim-Silva et al. (2015), nitrogen fertilization increases chlorophyll index and biometric characteristics of safflower crops. Shahrokhnia and Sepaskhah (2016) found increases in productive components and greater water use efficiency in safflower crops with greater availability of nitrogen.

Abbadi, Gerendas and Sattelmacher (2008), Hussien and Wuhaib (2010) and Palizdar, Delkhosh and Shirani Rad (2011) observed increases in biometric characteristics and higher yields in safflower crops with greater availability of potassium. However, studies evaluating the interaction of nitrogen with potassium on safflower growth are still scarce in the literature.

Thus, the objective of this work was to evaluate the chlorophyll index, biometric characteristics and water use efficiency of safflower plants grown in a Oxisol under different nitrogen and potassium rates and controlled soil water tension.

MATERIAL AND METHODS

The experiment was conducted in a greenhouse of the Institute of Agricultural Sciences and Technology of the Federal University of Mato Grosso, Rondonópolis, State of Mato Grosso, Brazil (16º27’49”S, 50º34’47”W and altitude of 284 m), from July to September, 2014. A complete randomized block experimental design in a 5x5 factorial arrangement was used, with four replications, consisting of five nitrogen rates (0, 60, 120, 180 and 240 mg dm^-3) and five potassium rates (0, 50, 100, 150 and 200 mg dm^-3).

The soil used was a Oxisol (EMBRAPA, 2013), collected from the layer 0.0-0.2 m of an area with Cerrado vegetation. The soil was sieved in a 2-mm mesh sieve (EMBRAPA, 2011) for chemical and granulometry analysis, which showed pH (CaCl₂)=4.1, P=2.4 mg dm^-3, K=28 mg dm^-3, Ca=0.3 cmol_c dm^-3, Mg=0.2 cmol_c dm^-3, Al=1.1 cmol_c dm^-3, H=4.2 cmol_c dm^-3, organic matter=22.7 g dm^-3, sum of bases=0.6 cmol_c dm^-3, cation exchange capacity=5.9 cmol_c dm^-3, base saturation=9.8%, sand=549 g kg^-1, silt=84 g kg^-1 and clay=367 g kg^-1.

The experiment was conducted in pots containing 8 dm³ of soil sieved in a 4 mm. Liming was performed after soil homogenization, using dolomitic limestone (TNP=80.3), to increase the base saturation to 60%. Subsequently, the soil irrigated to 60% of the water retention capacity, sealed in plastic bags and incubated for 30 days.

Planting fertilization with phosphorus and micronutrients was carried out with the recommended rates, using single superphosphate (150 mg P₂O₅ dm^-3), 1 mg dm^-3 of B (boric acid) and Cu (chloride copper), 3 mg dm^-3 of Mn (manganese chloride) and Zn (zinc sulfate) and 0.2 mg dm^-3 of Mo (sodium molybdate).

Potassium fertilization (0, 50, 100, 150 and 200 mg dm^-3) was divided into two applications, at planting and 10 days after emergence (DAE), using pure potassium chloride. Nitrogen fertilization (0, 60, 120, 180 and 240 mg dm^-3) was carried out at 10, 20 and 30 DAE, using urea. Four safflower plants were used per pot, using the cultivar IMA-0213.

Irrigation was carried out by a subsurface self-irrigation system as described by Bonfim-Silva, Monteiro and Silva (2007), consisting of a porous ceramic capsule (height of 9 cm, diameter of 5 cm and wall thickness of 0.5 cm) connected to a reservoir (Mariotte bottle) by a transparent flexible microtube (Figure 1).

Figure 1
Self-irrigating system. Porous capsule (A), transparent microtube (B), water column height (C), graduated water reservoir (Mariotte bottle) (D) and system implemented (E).

The self-irrigating system continuously supplied the amount of water lost by the evapotranspiration of the soil-plant system. The reservoir was graded with a numerical scale to determine the water consumption of the experimental unit (Figure 1 D ).

The control of soil water tension was defined by the height of the water column (Figure 1 C ). Changes in soil water tension during the experiment were carried out according to the crop requirement, maintaining it at 3 (0-20 DAE), 4 (20-45 DAE) and 2 (45-74 DAE) kPa.

Number of leaves, stem diameter and chlorophyll index were evaluated at 55 and 74 DAE. The number of capitula and shoot, root and total dry weight, water consumption and water use efficiency were evaluated at 74 DAE.

The stem diameter was measured at 2 cm from the soil surface using an analog caliper. Chlorophyll index were assessed using a Minolta SPAD-502 chlorophyll meter in five random leaves of the middle third of the plants.

The plants were removed from the soil and their shoots were separated to evaluate the number of capitula and shoot dry weight (sum of the leaves, stems and capitula dry weights). The roots were washed under a 4 mm sieve. The root and shoot dry weights were measured in a semi-analytical balance after the plant parts were dried in a forced-air circulation oven at 65 ºC for 72 hours.

The scale of the reservoir level (cm) was based on the reservoir diameter, converted into volume (dm³). This scale was used to quantify the water consumption, considering the water content of the reservoir before and after its replenishing. The amount of water consumed from planting to 74 DAE were summed to obtain the total water consumption.

The water use efficiency (g dm^-3) of the plants as a function of nitrogen and potassium rates (Equation 1) was calculated from the relation between the plant total dry weight (g pot^-1) and total water consumption (dm³ pot^-1).

$\mathrm{W}\mathrm{a}\mathrm{t}\mathrm{e}\mathrm{r}\mathrm{}\mathrm{u}\mathrm{s}\mathrm{e}\mathrm{}\mathrm{e}\mathrm{f}\mathrm{f}\mathrm{i}\mathrm{c}\mathrm{i}\mathrm{e}\mathrm{n}\mathrm{c}\mathrm{e}\mathrm{}=\mathrm{}\frac{\mathrm{T}\mathrm{o}\mathrm{t}\mathrm{a}\mathrm{l}\mathrm{}\mathrm{d}\mathrm{r}\mathrm{y}\mathrm{}\mathrm{w}\mathrm{e}\mathrm{i}\mathrm{g}\mathrm{h}\mathrm{t}}{\mathrm{W}\mathrm{a}\mathrm{t}\mathrm{e}\mathrm{r}\mathrm{}\mathrm{c}\mathrm{o}\mathrm{n}\mathrm{s}\mathrm{u}\mathrm{m}\mathrm{p}\mathrm{t}\mathrm{i}\mathrm{o}\mathrm{n}}$ (Equation 1)

The variables were subjected to a response surface study, using the Statistical Analysis System (SAS INSTITUTE, 2002). The combinations of nitrogen and potassium rates were subjected to analysis of variance and significant means by the F test were subjected to the response surface study, using the RSREG command. Non-significant results of the interaction between nitrogen and potassium rates were subjected to the study of independent factors by polynomial regression, using the GLM command. The analyses were performed with significance level of 5%.

RESULTS AND DISCUSSION

The chlorophyll index of the treatments were significantly affected only by the nitrogen rates, described by a quadratic model, showing the highest index (60.5) with the nitrogen rate of 168 mg dm^-3 at 55 DAE. The chlorophyll index increased due to the nitrogen rates at 74 DAE, described by a linear equation (Figure 2).

Figure 2
Chlorophyll index (CI) of safflower plants grown in a Oxisol, at 55 and 74 days after emergence (DAE), as a function of nitrogen rates. ***= significant at 0.1% and **= significant at 1%.

Nitrogen is part of the chlorophyll molecule, thus, its adequate rate increases plant photosynthesis and growth (TAIZ; ZEIGER, 2013). Dordas and Sioulas (2008) found higher rates of photosynthesis with increasing chlorophyll index in safflower plants. Thus, within certain limits, the chlorophyll index of the leaves is positively related to the plant production, due to the accumulation of photoassimilates. The decreasing chlorophyll index over time found in the present work was probably due to the process of nitrogen redistribution in the plant, since the plant flowering occurred in the second evaluation, and part of the nitrogen was translocated to the capitula through the source-drain relation.

The nitrogen and potassium rates, as independent factors, affected the number of leaves. The data of the treatments with nitrogen rates were fitted to a quadratic equation, showing the highest number of leaves with the rates of 123 (55 DAE) and 128 (74 DAE) mg dm^-3 (Figure 3 A ).

Figure 3
Number of leaves (NL) of safflower plants grown in a Oxisol, at 55 and 74 days after emergence (DAE), as a function of nitrogen (A) and potassium (B) rates, ***= significant at 0.1% and *= significant at 5%.

These results were similar to those found by Bonfim-Silva et al. (2015), who found increases in number of leaves of safflower due to nitrogen fertilization, reporting the highest number of leaves with rates of 118 (25 DAE), 132 (45 DAE) and 162 (65 DAE) mg dm^-3. Increases in number of leaves due to nitrogen fertilization usually increase leaf area, thus promoting a greater area of incidence of solar radiation, carbon assimilation and plant growth and production (CRUZ et al., 2007).

The number of leaves of treatments with potassium rates were fitted to a linear equation, the treatment with the highest rate (200 mg dm^-3) showing an increase of 21 (55 DAE) and 26% (74 DAE) compared with the treatment without potassium fertilization (Figure 3 B ). Potassium fertilization increases the number of leaves due to its contribution to several biochemical processes, such as carbohydrate metabolism, photosynthesis, respiration and enzymatic activation (COELHO et al., 2007).

The nitrogen and potassium rates, as independent factors, significantly affected the stem diameter in both evaluations (Figure 4). The stem diameter data of the treatments with nitrogen fertilization were fitted to a quadratic equation, with the highest SD found with nitrogen rates of 106 mg dm^-3, at 55 DAE (6.6 mm) and 87 mg dm^-3, at 74 DAE (6.21 mm) (Figure 4 A ).

Figure 4
Stem diameter (SD) of safflower plants grown in a Oxisol, at 55 and 74 days after emergence (DAE), as a function of nitrogen (A) and potassium (B) rates. ***= significant at 0.1%, **= significant at 1% and *= significant at 5%.

The stem diameter was lower in the second evaluation (Figure 4 A ) because the plants were at the end of the flowering stage, beginning the process of translocation of carbohydrate reserves from the stem to the capitula. According to Dordas and Sioulas (2009), stem reserves can be used for grain filling.

The stem diameter data of the treatments with potassium rates were fitted to a linear equation at 55 DAE, and to a quadratic equation at 74 DAE, with maximum stem diameter of 6.37 mm (167 mg dm^-3), showing an increase of 17.6%, compared with the treatment without potassium fertilization (Figure 4 B ). These results show the importance of nutritional balance for these plants, since excess nitrogen reduced the stem diameter and the potassium fertilization favored this variable, even at higher rates. The stem diameter of safflower is important for crop management, since a high stem diameter reduce plant lodging, facilitating cultural practices and harvesting (BISCARO et al., 2008).

The nitrogen and potassium rates, as independent factors, affected the number of capitula, whose data showed a linear response to nitrogen and a quadratic response to potassium fertilization (Figure 5). The highest number of capitula (22) was found under nitrogen fertilization of 137 mg dm^-3 (Figure 5 A ).

Figure 5
Number of capitula (NC) of safflower plants grown in a Oxisol, at 74 days after emergence (DAE), as a function of nitrogen (A) and potassium (B) rates. ***= significant at 0.1%, **= significant at 1% and *= significant at 5%.

Number of capitula per plant is an important yield component due to its direct relation with the final crop yield. Nitrogen increases vegetative growth, leading to a better fruiting. The results of the present work confirm those found by Gilbert and Tucker (1967) and Jones and Tucker (1968), who reported increases in yield components of safflower, especially number of capitula and seed weight per plant, as a function of nitrogen fertilization.

The higher potassium rate used (200 mg dm^-3) increased the number of capitula in 26.35%, compared with the treatment without potassium fertilization (Figure 5 B ). This result is similar to those reported by Palizdar, Delkhosh and Shirani Rad (2011), who found greater number of capitula with potassium rate of 150 kg ha^-1 in a safflower crop, with an increase of 40%, compared with plants without potassium fertilization.

The nitrogen and potassium rates, as independent factors, significantly affected the shoot dry weight (Figure 6), whose data were fitted to a quadratic equation, with the highest yield (52.33 g pot^-1) found with the nitrogen rate of 106 mg dm^-3 (Figure 6 A ). This result was similar to that found by Bonfim-Silva et al. (2015), who found increases in shoot dry weight with nitrogen rates of up to 177.02 mg dm^-3.

Figure 6
Shoot dry weight (SDW) of safflower plants grown in a Oxisol, at 74 days after emergence (DAE), as a function of nitrogen (A) and potassium (B) rates. ***= significant at 0.1%, **= significant at 1% and *= significant at 5%.

The shoot dry weight data had a linear response to the potassium rates, with an increase of 35%, comparing the treatment with the highest rate (200 mg dm^-3) with the treatment without potassium fertilization (Figure 6 B ).

The potassium rates, as an independent factor, significantly affected the root dry weight, whose data were fitted to a linear equation, with an increase of 33%, comparing the treatment with the higher potassium rate with the treatment without potassium fertilization (Figure 7).

Figure 7
Root dry weight (RDW) of safflower plants grown in a Oxisol, at 74 days after emergence (DAE), as a function of potassium rates. ***= significant at 0.1%.

The root dry weight was lower in treatments without potassium fertilization, denoting the effect of the nutritional status of the plants, especially regarding potassium, on root growth (ESHEL; WAISEL, 1996). Potassium contributes to transport of nitrate to the plant shoot and photoassimilates by the phloem, enzymatic activation and osmotic regulation, favoring the root growth (MALAVOLTA; VITTI; OLIVEIRA, 1997) and consequently, the shoot growth.

Hussien and Wuhaib (2010) found similar results evaluating safflower growth under potassium rates (0, 45, 90, 135 and 180 kg ha^-1 of K₂SO₄), with higher root dry weight with 180 kg ha^-1.

The nitrogen and potassium rates, as independent factors, significantly affected the total dry weight, whose data were fitted to quadratic (nitrogen) and linear (potassium) equations (Figures 8 A and 8B). The maximum total dry weight (60 g pot^-1) was found with the nitrogen rate of 102 mg dm^-3.

Figure 8
Total dry weight (TDW) of safflower plants grown in a Oxisol, at 74 days after emergence (DAE), as a function of nitrogen (A) and potassium (B) rates. ***= significant at 0.1%, **= significant at 1% and *= significant at 5%.

Aiyelaagbe, Fagbayide and Makinde (2005), Dordas and Sioulas (2009) and Ebrahimian and Soleymani (2013) found similar results, with significant response of total dry weight of safflower plants to nitrogen fertilization.

Nitrogen fertilization affected positively the total dry weight of safflower plants, since this nutrient is part of all amino acids, amides, proteins, nucleic acids, nucleotides, polyamines, plant hormones and several other types of metabolic components (EPSTEIN; BLOOM, 2006).

The highest total dry weight under potassium fertilization was found with the rate of 200 mg dm^-3, with an increase of 35%, compared with the treatment without potassium fertilization (Figure 8 B ), showing the positive effect of potassium fertilization on the total dry weight of safflower plants. Similar results were found by Abbadi, Gerendas and Sattelmacher (2008), evaluating safflower plants in greenhouse conditions (28 and 15 ºC) on substrates with different potassium rates, with maximum total dry weight under the potassium rate of 90 mg dm^-3.

The potassium rates, as an independent factor, significantly affected the water consumption. The water consumption data were fitted to a linear equation, showing an increase of 10%, compared with the treatment without potassium fertilization (Figure 9).

Figure 9
Water consumption (WC) of safflower plants grown in a Oxisol, at 74 days after emergence (DAE), as a function of potassium rates. *= significant at 5%.

According to Reichardt (1978), the evapotranspiration of plants with good establishment and development is mainly affected by the transpiration rate, which becomes higher than the evaporation rate. Therefore, plants with higher dry weight present higher water consumption.

The nitrogen and potassium rates, as independent factors, affected the water use efficiency, whose data were fitted to quadratic (nitrogen) and linear (potassium) equations (Figure 10). The maximum water use efficiency (2.23 g dm^-3) was found with nitrogen fertilization of 82 mg dm^-3 (Figure 10 A ).

Figure 10
Water use efficiency (WUE) of safflower plants grown in a Oxisol, at 74 days after emergence (DAE), as a function of nitrogen (A) and potassium (B) rates. ***= significant at 0.1 % and *= significant at 5%.

Adequate rates of nitrogen increase the plant’s ability of use the water intake for dry weight production. Dordas and Sioula (2008) reported an increase of 60% in water use efficiency by safflower plants due to nitrogen (200 kg ha^-1), compared with plants without nitrogen fertilization. Shahrokhnia and Sepaskhah (2016) also found higher water use efficiency in safflower crops with the nitrogen rate of 200 kg ha^-1. These authors emphasized the importance of this variable in regions of low water availability.

The water use efficiency showed an increasing linear response to potassium rates, with maximum water use efficiency (2.47 g dm^-3) with 200 mg dm^-3 (Figure 10 B ). According to these results, the increasing potassium rates increased the WUE of safflower plants, which better use of the available water in the soil for dry weight production.

Water use efficiency is related to control of stomatal opening and closure, which is dependent on potassium, maintaining a minimum water loss during the absorption of CO₂ for photosynthesis (PIMENTEL, 2004), resulting in reduced transpiration rates and larger leaf area per dry weight of the plant (IGBAL et al., 2011).

CONCLUSION

The nitrogen and potassium fertilization, as independent factors, affected the safflower plants.

The chlorophyll index, biometric characteristics and water use efficiency of safflower plants showed better responses with nitrogen rates of 82 to 168 mg dm^-3.

The responses of chlorophyll index, biometric characteristics and water use efficiency of safflower increased 10 to 60% with potassium fertilization.

ACKNOWLEDGEMENTS

We thank the CAPES, CNPq e IMAmt(Instituto Mato-grossense do Algodão).

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• Paper extracted from the dissertation masters of the first author.

Publication Dates

• Publication in this collection
  Apr-Jun 2018

History

• Received
  14 Aug 2016
• Accepted
  03 May 2017