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Article

Light Intensity Modulates the Accumulation of Carbohydrates, Antioxidant Enzymes and Production of Iceberg Lettuce under Tropical Conditions

by
Eduardo Santana Aires
1,*,
Carlos Alberto Aragão
2,
Bárbara França Dantas
3,
João Domingos Rodrigues
4 and
Elizabeth Orika Ono
4
1
Department of Horticulture, School of Agronomy, São Paulo State University, Botucatu 18618-000, Brazil
2
Department of Technology and Social Sciences, Bahia State University, Juazeiro 48900-000, Brazil
3
Seeds Lab, Embrapa Semiárido, Petrolina 56302-970, Brazil
4
Department of Botany, Institute of Biosciences, São Paulo State University, Botucatu 18618-000, Brazil
*
Author to whom correspondence should be addressed.
Horticulturae 2021, 7(12), 553; https://doi.org/10.3390/horticulturae7120553
Submission received: 22 October 2021 / Revised: 24 November 2021 / Accepted: 28 November 2021 / Published: 5 December 2021
(This article belongs to the Special Issue Advances in Protected Vegetable Cultivation)
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Abstract

:
High solar radiation in tropical regions can affect the development, physiology, and biochemistry of plants. Our aim with this research was to evaluate the biochemical responses and production of iceberg lettuce cultivars under environments with different shadings. An experiment under field conditions was installed in a 4 × 4 factorial scheme. Four cultivars of iceberg lettuce (Great Lakes, Winslow, Delicia, and Balsamo) and four environments with different shadings (three types of shading screens: red, ChromatiNet®, and black; and treatment under the full sun) were evaluated. Forty-five days after transplanting, the plants were harvested, and the biomass was weighed to obtain the fresh consumable part (FCP) and the biochemical parameters: total soluble sugar (TSS), reducing sugar (RS), and the activity of SOD, CAT, and POD. We found that shading modulates biochemical and productive responses of iceberg lettuce, and the main microclimatic factor related to these responses was solar radiation. We observed a negative correlation between RS and FCP. The solar radiation between 16 and 18 MJ·m−2·day−1, observed in the environments with a black screen and ChromatiNet®, promoted the highest activity of the SOD enzyme and average levels of TSS and RS, providing higher FCP of the cultivars Delícia and Balsamo in high temperatures period.

1. Introduction

A recent study shows that not only is the temperature a limiting factor for head formation in this type of lettuce, but mainly solar radiation, with a range of 17.6 to 19.5 MJ·m−2·day−1 of solar radiation global being ideal for iceberg lettuce production at average temperatures of 27.8 °C [3]. High irradiance causes photoinhibition in this crop, as the radiation flow above the trophic limit can lead to increased transpiration through the upper leaves and possible stomatal closure [4].
Iceberg lettuce production is directly influenced by temperature since it is a species from temperate regions. Head lettuce formation is impaired at temperatures above 20 °C. High temperatures stimulate its bolting, which is accelerated as this climatic factor increases [1]. This is why the production of this vegetable in high-temperature regions, mainly semi-arid, is still not very expressive. In these regions, the weather conditions are characterized by high solar radiation (average 21.6 MJ·m−2·day−1), high temperatures (average 26 °C), low relative humidity, and reduced rainfall (average 700 mm per year) [2].
The use of shading screens reduces the solar radiation direct incidence in plants, thus causing temperature reduction, which favors crops that need lower radiant energy flow. Lower incidence of solar energy can contribute to reducing the extreme effects of radiation, especially on photorespiration, and provide better environmental conditions for increasing the yield and quality of leaves for consumption [5].
Thus, the shading screens alter the microclimatic conditions of the environments (temperature, relative humidity, and solar radiation). The light intensity is also affected, which directly affects several photoreceptors present in plants [6], causing metabolic alterations and, consequently, influencing plant growth and development. Lettuce does not require high light intensity, about 500 μmol·m−2·s−1 in summer [7]. Light intensity is an important factor for plant metabolism. The reduction of this factor causes photosynthesis not to work efficiently, leading to etiolation, but excessive light intensity can generate reactive oxygen species (ROS) and cause photoinhibition [8].
ROS cause oxidative damage to the lipids and membrane proteins. To prevent this damage, plants activate various defense mechanisms. One of the forms of defense is the activation of the enzymatic antioxidant system that includes superoxide dismutase (SOD, EC 1.15.1.1), catalase (CAT, EC 1.11.1.6), and peroxidase (POD,1.11.1.7) [9]. The activity of enzymes SOD, CAT, and POD can indicate whether the lettuce plants are under environmental stress. Studies involving the activity of antioxidant enzymes in lettuce plants under water deficit, salinity, and artificial lighting have already been reported and the activity of the enzymes SOD, CAT, and POD increase significantly under stress conditions [10,11].
Through plant breeding, cultivars that are more tolerant to high temperatures and solar radiation have been developed, and are thus adapted to tropical conditions without stimulating bolting and latex production. Allied to this, the technique of using shading screens to protect crops can increase the production of lettuce, allowing the growers to produce lettuce throughout the year, including during high temperatures or in the offseason [12]. However, there is a lack of information on the relationship between these enzymes’ activity and the levels of sugars in the leaves during formation of the head of iceberg lettuce in tropical conditions of high temperature and solar radiation.
Based on the presented arguments, our research hypothesizes that the use of shading screens can be an efficient management for the cultivation of iceberg lettuce in regions of high temperature linked to the indication of cultivars adapted to these conditions. Therefore, this study aimed to evaluate the biochemical responses: sugar levels, the activity of antioxidant enzymes; and the commercial production of iceberg lettuce cultivars under environments with different shadings.

2. Materials and Methods

The experiment was carried out in the Experimental Vegetable Production Area of the Department of Technology and Social Sciences, Juazeiro Campus, of the State University of Bahia, in Juazeiro, Brazil, located at 9°25′14″ S and 40°29′08″ W with an average altitude of 360 m above sea level. According to the Köppen classification, the region has a semi-arid climate, BSh-type, with an average temperature and precipitation of 23.6 °C and 455 mm. From October to December 2019, the following events occurred: sowing, 10 October 2019; transplanting, 5 November 2019; harvest, 20 December 2019. In the spring season, the northeast region of Brazil experienced a period of high temperatures.
A randomized block design arranged in a 4 × 4 factorial scheme with four replications was used. Four iceberg lettuce cultivars (Great Lakes, Winslow, Delícia, and Balsamo) and four environments with different shadings (without shading under the full sun (FS), shading with a red screen (RS), shading with ChromatiNet® (CS), and shading with a black screen (BS)) were evaluated. According to the manufacturer, the ChromatiNet® screen is a mesh that manipulates the spectrum of sunlight, breaking direct light by converting it to diffused light [13]. Each plot consisted of twelve plants, and the four plants in the middle of plots were used for the evaluations.
The iceberg lettuce seedlings were produced in Styrofoam trays, filled with commercial substrate Plantmax® with 4.90 g·kg−1 of N, 1.47 g·kg−1 of P, 7.0 g·kg−1 K, 12.50 g·kg−1 of Ca, 120 g·kg−1 of Mg, 1.80 g·kg−1 of S, C/N of 34/1, 285 g·kg−1 of organic matter, and pH of 6.20. The trays were placed on benches with 0.5 m height, under a protected environment covered with 50% black shading screen, and after 25 days, they were transplanted to the seedbeds with a spacing of 0.25 × 0.25 m. The shading environments had a ceiling height of 2.00 m, and the screens were fixed on eucalyptus stakes with wire at 1.50 m height.
The soil had the following chemical properties: pH = 6.42, P = 56 mg dm−3, K = 0.22 cmolc dm−3, Ca = 5.0 cmolc dm−3, Mg = 1.70 cmolc dm−3, Al = 0.0 cmolc dm−3, CTC = 7.01 cmolc dm−3, and EC = 0.77 dS.m−1. Soil preparation was carried out with plowing, harrowing, and seedbed preparation at 30 cm height. Each seedbed was 16 m long by 1.5 m wide. Each experimental plot had 0.75 × 1.50 m with twelve plants. The four plants in the middle of plot were used for the evaluations. Planting fertilization was based on the recommendation of fertilization of the state of Bahia for lettuce cultivation by applying 6.3 kg ha−1 of N and 21.3 kg of P2O5 ha−1, using urea (44% of N) and simple superphosphate (18% of P2O5). For the topdressing fertilization, we also followed the recommendation of fertilization of the state of Bahia for lettuce cultivation by applying 38.0 kg ha−1 of N and 26.0 kg ha−1 of Ca, using calcium nitrate (15% of N and 19% Ca) as a source, performed 20 days after transplanting.
The air temperature (average, maximum, and minimum), relative humidity (average, maximum, and minimum), and solar radiation from the shading treatments and full sun were monitored using meteorological sensors installed at 50 cm height. The sensors were connected to the automatic data system (Datalogger), programmed to take readings every five seconds and hourly averages.
Plants were harvested 45 days after transplanting (DAT) and were taken to the laboratory where the plants were weighed to determine the fresh consumable part (i.e., heads) (FCP), removing the external. The results are expressed in g·plant−1. Immediately after harvesting, two replications with four central leaves from two plants per plot were collected and wrapped in aluminum foil, submerged in liquid nitrogen, and stored in an ultra-freezer at −80 °C for enzymatic analysis and sugar content evaluation.
The raw extract was obtained for all analyzes by macerating 1 g of the sample in 5 mL of 0.1 M potassium phosphate buffer (pH 7.5) containing 1.0 mM of ethylenediaminetetra acetic acid (EDTA), 3.0 mM dithiothreitol (DTT), 5% polyvinylpolypyrrolidone (PVPP), and 10.0 mM ascorbic acid and centrifuged at 10,000 rpm for 10 min at 4.0 °C. The supernatant was used to determine total protein content (TP), total soluble sugars (TSS), reducing sugars (RS), and activities of the enzymes superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD).
The total protein content (TP) was obtained using the method described by [14], and was measured to determine specific enzyme activity. For the total soluble sugar (TSS) content, the anthrone method described in [15,16] was used. The content of reducing sugars (RS) was quantified by the method described by [17], using 3,5-dinitrosalicylic (DNS).
The activity of the superoxide dismutase (SOD) enzyme was determined according to [18], taking into account the enzyme’s ability to inhibit the photo-reduction of nitrotetrazolium blue chloride (NBT), expressed in UE·min−1·mgTP−1 (unit of enzyme per minute per milligram of protein). For the catalase enzyme (CAT) activity, the methodology described by [19] was used. The results are expressed as μmolH2O2·min−1·μgTP−1. POD activity was determined in a spectrophotometer by measuring the formation of purpurogallin at 430 nm [20], and the activity is expressed in UE·min−1·g−1.
The data were submitted to the Anderson Darling’s homogeneity test through the Minitab software for statistical analysis. Once the normality of the data was verified, the analysis of variance (F-test) was performed, in which the means were grouped by the Scott Knott test at 5% probability, using the AGROESTAT® software. Correlation analysis was performed among all evaluated variables.

3. Results

Among the microclimatic characteristics evaluated, global solar radiation was the most affected by shading screens (Figure 1a), which, in turn, affected plant development. The average radiation observed in the period was about 16 MJ·m−2·day−1, 18 MJ·m−2·day−1, 25 MJ·m−2·day−1, and 30 MJ·m−2·day−1 in black screen (BS), ChromatiNet® screen (CS), red screen (RS), and full sun (FS), respectively. There was a reduction of 0.5 °C in the shaded environments with BS and CS concerning the FS. The average temperature values during the period were 28.1 °C, 28.0 °C, 27.6 °C, and 27.6 °C for FS, VS, CS, and BS, respectively (Figure 1b). For the transmittance, the red, ChromatiNet®, and black shading screens presented 80%, 60%, and 55%, respectively.
Figure 2 shows the distribution of spectral radiation under the three studied covers. Among the shades, the highest infrared radiation (IR) transmittance occurred in the environment covered with a red screen (42.72%), followed by ChromatiNet® screen (28.69%), and the lowest IR in the environment with a black screen (28.39%). While the highest transmittance of ultraviolet radiation occurred on ChromatiNet® (5.91%) and the lowest on red screen (4.98%). For photosynthetically active radiation transmittance, the highest value was observed in the environment with red screen (42.72%), followed by ChromatiNet® screen (28.69%) and black screen (28.39%).
The significant interaction between cultivars and studied environments was observed for all variables analyzed (Table 1). It is noticeable that there were many cultivar × environment interactions, suggesting that cultivars responded differently to environment changes for different traits.
The accumulation of carbohydrates observed by the content of total soluble sugars (TSS) and reducing sugars (RS) was higher in the Great Lakes cultivar in the full sun (FS) environment with about 78 µmol·g−1 of commercial fresh matter (CMF) and shaded with the red screen (RS), with 6.40 µmol·g−1, respectively (Table 2).
As an indication of stress in lettuce plants, the activity of antioxidant enzymes was evaluated. In this context, the lettuce cultivars showed different responses to the enzymes SOD, CAT, and POD in the different environments studied (Table 3 and Table 4). For the enzyme SOD activity, the cultivars Delícia and Balsamo stood out in the BS and RS environments, as did the Great Lakes cultivar in RS (Table 3). The enzyme SOD had the highest activity under BS, with 16 MJ·m−2·day−1 of average solar radiation, followed by CS, which presented 18 MJ·m−2·day−1 (Figure 1a). Thus, the environments with solar radiation values higher than 25 MJ·m−2·day−1, RS and FS, inhibited the action of the SOD enzyme in the iceberg lettuce cultivars tested (Table 3).
For CAT enzyme activity, higher values, 12 µmol H2O2·min−1.µgTP−1, were observed in the plants of the cultivars Great Lakes and Balsamo under the red screen. The highest values for POD enzyme activity, about 20 UE·min−1·gTP−1, were observed in the Great Lakes cultivar in full sun and Winslow under RS. Analyzing the activity of CAT and POD enzymes, higher values of CAT enzyme activity were observed in plants grown under BS and CS, while POD activity was higher in FS. Thus, plants grown under BS and CS modulate antioxidant response via CAT, and those grown under FS modulate via POD.
All cultivars grown in full sun were less productive than the other environments (Table 4). The highest values were reached by cultivars Delícia and Balsamo in the CS environment, about 210 g·plant−1, followed by the Balsamo cultivar grown in BS. The Great Lakes cultivar did not produce lettuce head in any environments studied, and, as a result is not found in Table 4. However, even without head formation (FCP), this cultivar developed leaves, and these were used for biochemical analysis.
Analyzing the correlation between the variables (Table 5), mainly to know which of these influences commercial fresh matter, it was possible to verify a negative correlation of this variable with the RS content and POD enzyme activity and positive between FCP and SOD activity.

4. Discussion

The distribution of spectral radiation (Figure 2) under the three shades studied was not the main reason for the biochemical and productive alterations of the studied iceberg lettuce cultivars, since the difference between IR, UV, and PAR between the screens was small. However, the high incidence of solar radiation recorded during the period of the experiment caused changes in the biochemical aspects of the iceberg lettuce, reducing the photosynthetic efficiency of the plants and negatively interfering with all the characteristics evaluated in full sun (Figure 1). However, it was observed that the use of shading screens reduced the intensity of radiant energy, providing better quality and distribution of solar radiation within the protected environments, resulting in better crop performance.
High photosynthetic rates promote the synthesis of sugars that reflect greater growth and storage of carbohydrates in the physiological sinks [21]. Lettuce grown in a hydroponic system showed high contents of total sugars in the basal leaves because these leaves are functioning as the main source of photoassimilates [22]. Therefore, the cultivar Great Lakes may have shown better photosynthetic efficiency in environments with FS and RS when compared to other screens. However, these sugars were used for bolting—or inhibiting the lettuce head formation, the commercial product of lettuce—in this cultivar.
In temperate climate conditions and winter, greater solar radiation has a beneficial effect on the greater accumulation of dry matter and total soluble sugars in lettuce plants [23]. For tropical and semi-arid conditions, as in the present research, a more appropriate range of solar radiation is observed that allows greater liquid photosynthesis, increase in TSS, and head formation of iceberg lettuce. This behavior was evidenced in the Balsamo cultivar in environments with BS and CS, where greater commercial biomass production accompanied the highest TSS content (Table 2).
In a study with lettuce, maximum temperature above 25 °C caused less accumulation of carbohydrates and less growth and mass at the end of the cycle [24]. Thus, for lettuce types that do not produce head, the increase in these variables can indicate ideal cultivation conditions. On the other hand, the decline in the values of sugar and starch in lettuce leaves may be indicative of stress, caused by the restricted absorption of water and nutrients and limited photosynthesis [24], which can reduce stomatal conductance, and, consequently, photosynthesis, thus reducing productivity.
In this research, it was not possible to observe the relationship between the reducing sugars content and indicative stress due to the restriction of photosynthesis since the plants in environments with CS and BS presented lower reducing sugars and greater production (Table 2 and Table 4) when compared to the FS and RS. According to [25], global solar radiation around 20.7 MJ·m−2·day−1 favors the photosynthetic rate and greater production in lettuce experiments. Approximate values between 16 and 18 MJ·m−2·day−1 were observed for BS and CS, suggesting that this range is efficient for raising RS contents in the Balsamo cultivar and results from a better photosynthetic performance than the other cultivars studied.
A well-known consequence of high temperature in plants is a reduction in photosynthesis rate, while respiration and photorespiration rates increase considerably under high temperatures [26]. However, one must also consider the energy balance of the environment. The increase in temperature and solar radiation leads to a rise in the environment’s vapor pressure deficit, reducing photosynthesis and increasing photorespiration, forming reactive oxygen species (ROS).
When plants are subjected to some biotic or abiotic stress, the first response observed in the plant is the drastic increase in ROS production that causes oxidative damage in proteins, lipids, and nucleic acids, characterizing oxidative stress [27]. The first ROS formed is superoxide (•O−2), which gives rise to the other reactive oxygen species. The •O−2, through the enzyme SOD, is dismutated to H2O2 [28]. Radiation causes the expression of defense genes, initiating ROS generation by the enzyme nicotinamide adenine dinucleotide phosphate (NADPH) oxidase on the plasma membrane cytoplasm; these species are formed in mitochondria and chloroplasts [29]. Regulation of H2O2 levels occurs through a variety of enzymes, such as ascorbate peroxidase (APX), catalase (CAT), peroxidase (POD), glutathione S-transferase (GST), glutathione reductase (GR), and glutathione peroxidase (GPX) [30].
Considering the environments in this study, solar radiation was responsible for modulating the activity response of the antioxidant enzymes SOD, CAT, and POD in lettuce plants (Table 3 and Table 4) since the temperature and relative air humidity did not experience significant changes due to the use of shading screens (Figure 1b). The cultivars studied showed different responses, showing tolerance to high solar radiation environments for expressing genes for activating antioxidative metabolism.
Regarding the reduction in the harmful effects of H2O2, the action of the CAT enzyme is similar to that of some other enzymes, such as peroxidases. However, CAT is more effective in relatively high concentrations of H2O2 (mM) in a condition of severe stresses since CAT does not need a reducing agent, being efficient for the removal of H2O2 [31].
Solar radiation may have modulated the antioxidant system’s response, in that under higher values of this microclimatic factor, the activation of POD occurred, while with lower values, CAT activation occurred. The average temperature of the shaded environments and the full sun was higher than that recommended to cultivate iceberg lettuce (Figure 1b). This thermal stress led to an increase in ROS production, which, due to the action of the SOD enzyme, may have been converted into H2O2. In environments with higher radiation, POD acted for the conversion of H2O2 (Table 4), while in environments with less radiation, CAT was the main reason for this conversion (Table 3). CAT is more efficient for reducing the effects of H2O2; thus, cultivars under CS and BS, with less solar radiation, may have presented less damage to the cell membrane and, consequently, better responses to the formation of commercial matter (Table 4).
Weiguo et al. [11] observed that the POD enzyme action was more evident under a condition of greater light intensity when compared to CAT in lettuce plants. These same authors also observed that the excess of energy of light intensity, 600 µmol·m−2·s−1 led to the production of ROS and a relatively substantial increase in lipid peroxidation. In a second assessment, the activities of SOD, CAT, and POD increased; a certain proportion of ROS was eliminated; and lipid peroxidation decreased.
Thus, when the solar radiation is between 16 and 18 MJ·m−2·day−1, as observed in environments with BS, the enzyme SOD activity increases. There may also be a reduction in damage to the cell membrane. There was also no photoinhibition in the cultivars Balsamo, Winslow, and Delícia, leading to greater accumulation of biomass and commercial production in these environments (Table 4).
The microclimate generated by shading screens in the environments, with lower average temperature and solar radiation, provided a 241% increase in the commercial fresh matter for Delicia cultivar and 254% for the Balsamo cultivar compared to CS and FS. A higher fresh matter of iceberg lettuce was observed in a shaded environment with a 37% reduction in solar radiation when compared to the full sun. The shaded environments provide excellent light conditions in the summer production of this vegetable [32]. However, the Great Lakes cultivar did not produce lettuce head at all under any environment conditions, indicating that lettuce is not productive in tropical regions, regardless of what kind of shading method is used.
The positive relationship between the activity of the SOD enzyme and FCP can be related to the role of this enzyme in protecting plant cells from the harmful consequences of the increase in respiratory metabolism caused by the high temperature observed during this study. This enzyme is active in the first line of antioxidative defense by dismuting the superoxide radical to hydrogen peroxide and molecular oxygen [33]. Although not correlated with FCP, the CAT enzyme is considered a crucial enzyme to prevent the effects caused by stress due to its high catalytic activity, acting in the removal of hydrogen peroxide (H2O2) and, consequently, reducing lipid peroxidation and damage to cell membranes [34].
As for the negative relationship between POD activity and FCP, this effect may be related to this enzyme’s ability to reduce H2O2, which may not have been efficient enough to reduce abiotic stress and increase commercial fresh matter values of lettuce. It is known that the activity of the POD enzyme is not as efficient as CAT; for example, the authors of [35] point out that CAT is the main eliminating enzyme of this reactive oxygen species.
Thus, through the correlation analysis, it is possible to affirm that the high content of reducing sugars is used as an energy source for the bolting of iceberg lettuce, which leads to no head formation, mainly in the Great Lakes cultivar. For antioxidant enzymes, SOD has a positive relationship with FCP due to the detoxification function of ROS, which reduces stress and allows a greater accumulation of commercial fresh matter. The POD, having a lower capacity to detoxify H2O2, did not present a positive correlation with the FCP.
As for the cultivars, there was a different answer for each of them in each different environment, with this variation resulting from the adaptive capacity of the genetic material used; even though all are indicated for tropical conditions, full sun results in only 80 g.plant−1 of FCP. The cultivars Balsamo and Delícia can be indicated, as they present the highest yields when cultivated in environments covered with ChromatiNet®.
The average solar radiation in South America between the parallels 15° N and 15° S is 250 Wm−2 or 21.6 MJ·m−2·day−1 [36], above those found in this study (Figure 1a) for growing lettuce in high-temperature conditions. Solar radiation is an important meteorological component for iceberg lettuce production, and values above 20.7 MJ·m−2·day−1 reduced commercial production and the activity of antioxidant enzymes, and increased iceberg lettuce bolting in this study. The use of shading screens is a technology that must be used to make the cultivation of this vegetable feasible in certain regions.

5. Conclusions

The shading screens that we used in this research caused microclimate changes in the environments, mainly in solar radiation. This factor was predominant in the modulation of the iceberg lettuce cultivars biochemical and productive responses.
Solar radiation between 16 and 18 MJ·m−2·day−1, observed in shaded environments with a black screen and ChromatiNet® screen, promoted greater activity of the SOD enzyme and average values of TSS and RS, providing greater commercial production of Delícia and Balsamo cultivars in the period of high temperatures.
There is a negative correlation between the values of reducing sugars and the fresh consumable part (FCP). This component indicates the early bolting of the Great Lakes cultivar in the conditions of this research.
Future studies should be carried out to understand the impact of light quality on yield and post-harvest quality of iceberg lettuce in tropical conditions.

Author Contributions

Conceptualization, E.S.A., J.D.R. and E.O.O.; methodology, E.S.A. and B.F.D.; validation, C.A.A. and B.F.D.; formal analysis, C.A.A. and B.F.D.; investigation, E.S.A.; resources, B.F.D.; data curation, C.A.A. and E.S.A.; writing—original draft preparation, E.S.A.; writing—review and editing, E.O.O. and J.D.R.; visualization, B.F.D., J.D.R., and C.A.A.; supervision, C.A.A.; project administration, E.S.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We are grateful to the Research Support Foundation of Bahia (FAPESB).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Santi, A.; Carvalho, M.A.; Campos, O.R.; Silva, A.F.; Almeida, J.L.; Monteiro, S. Ação de material orgânico sobre a produção e características comerciais de cultivares de alface. Hortic. Bras. 2010, 28, 87–90. [Google Scholar] [CrossRef] [Green Version]
  2. Andrade-Lima, D. The Caatinga dominium. Rev. Bras. Botânica 1981, 4, 149–153. [Google Scholar]
  3. Aires, E.S.; Aragão, C.A.; Gomes, I.L.S.; Souza, G.N.; Andrade, I.G.V.; Oliveira, A.B.N.; Yuri, J.E. Growth and production of crisphead lettuce cultivars in protected cultivation and high temperatures. Braz. J. Agric. Sci. 2020, 15, 1–9. [Google Scholar] [CrossRef]
  4. Fu, W.; Li, P.; Wu, Y. Effects of different light intensities on chlorophyll fluorescence characteristics and yield in lettuce. Sci. Hortic. 2012, 135, 45–51. [Google Scholar] [CrossRef]
  5. Blind, A.D.; Silva Filho, D.F. Desempenho produtivo de cultivares de alface americana na estação seca da Amazônia Central. Biosci. J. 2015, 31, 404–414. [Google Scholar] [CrossRef]
  6. Folta, K.M.; Maruhnich, S.A. Green light: A signal to slow down or stop. J. Exp. Bot. 2007, 58, 3099–3111. [Google Scholar] [CrossRef] [PubMed]
  7. Hassanien, R.H.E.; Ming, L. Influences of greenhouse-integrated semi-transparent photovoltaics on microclimate and lettuce growth. Int. J. Agric. Biol. Eng. 2017, 10, 11–22. [Google Scholar] [CrossRef] [Green Version]
  8. Ruangrak, E.; Khummueng, W. Effects of artificial light sources on accumulation of phytochemical contents in hydroponic lettuce. J. Hortic. Sci. Biotechnol. 2019, 94, 378–388. [Google Scholar] [CrossRef]
  9. Molassiotis, A.; Sotiropoulos, T.; Tanou, G.; Diamantidis, G.; Therios, I. Boron-induced oxidative damage and antioxidant and nucleolytic responses in shoot tips culture of the apple rootstock EM 9 Malus domestica Borkh. Environ. Exp. Bot. 2006, 56, 54–62. [Google Scholar] [CrossRef]
  10. Muhairi, M.A.; Cheruth, A.J.; Kurup, S.S.; Rabert, G.A.; Al-Yafei, M.S. Effect of abscisic acid on biochemical constituents, enzymatic and non enzymatic antioxidant status of lettuce (Lactuca sativa L.) under varied irrigation regimes. Cogent Food Agric. 2015, 1, 1080888. [Google Scholar] [CrossRef]
  11. Weiguo, F.; Pingping, L.; Yanyou, W.; Jianjian, T. Effects of different light intensities on anti-oxidative enzyme activity, quality and biomass in lettuce. Hortic. Sci. 2012, 39, 129–134. [Google Scholar] [CrossRef] [Green Version]
  12. Ntsoane, L.L.; Soundy, P.; Jifon, J.; Sivakumar, D. Variety-specific responses of lettuce grown under the different-coloured shade nets on phytochemical quality after postharvest storage. J. Hortic. Sci. Biotechnol. 2016, 91, 520–528. [Google Scholar] [CrossRef]
  13. POLYSAC. POLYSAC Chromatinet®. 2021. Available online: https://www.ginegar.com.br/agricultura/telas/chromatinet-combinada (accessed on 15 July 2021).
  14. Bradford, M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 1976, 72, 248–254. [Google Scholar] [CrossRef]
  15. Morris, D.L. Quantitative determination of carbohydrates with Drywood’s anthrone reagent. Science 1948, 107, 254–255. [Google Scholar] [CrossRef] [PubMed]
  16. Yemm, E.W.; Willis, A.J. The estimation of carbohydrates in plants extracts by anthrone. Biochem. J. 1954, 57, 508–514. [Google Scholar] [CrossRef] [Green Version]
  17. Miller, G.L. Use of dinitrosalicylic and reagent for determination of reducing sugar. Anal. Chem. 1959, 31, 426–428. [Google Scholar] [CrossRef]
  18. Giannopolitis, C.N.; Ries, S.K. Superoxide dismutases. I. Occurrence in higher plants. Plant Physiol. 1977, 59, 309–314. [Google Scholar] [CrossRef] [PubMed]
  19. Azevedo, R.A.D.; Alas, R.M.; Smith, R.J.; Lea, P.J. Response of antioxidant enzymes to transfer from elevated carbon dioxide to air and ozone fumigation, in the leaves and roots of wild-type and a catalase-deficient mutant of barley. Physiol. Plant. 1998, 104, 280–292. [Google Scholar] [CrossRef]
  20. Teisseire, H.; Guy, V. Copper-induced changes in antioxidant enzymes activities in fronds of duckweed Lemna minor. Plant Sci. 2000, 153, 65–72. [Google Scholar] [CrossRef]
  21. Taiz, L.; Zeiger, E. Fisiologia e Desenvolvimento Vegetal, 6th ed.; Artmed: Porto Alegre, Brazil, 2018; pp. 125–126.
  22. Cometti, N.N.; Matias, G.C.S.; Zonta, E.; Mary, W.; Fernandes, M.S. Compostos nitrogenados e açúcares solúveis em tecidos de alface orgânica, hidropônica e convencional. Hortic. Bras. 2004, 22, 748–753. [Google Scholar] [CrossRef] [Green Version]
  23. Wojciechowska, R.; Długosz-Grochowska, O.; Kołton, A.; Żupnik, M. Effects of LED supplemental lighting on yield and some quality parameters of lamb’s lettuce grown in two winter cycles. Sci. Hortic. 2015, 187, 80–86. [Google Scholar] [CrossRef]
  24. Sung, J.; Cho, M.; Sonn, Y.; Yun, H.; Kang, S.; Shinogi, Y.; Oh, T. Mineral uptake and soluble carbohydrates of lettuce: Effects of air temperatures and mineral supply levels. J. Fac. Agric. 2016, 61, 41–46. [Google Scholar] [CrossRef]
  25. Jie, H.; Kong, L.S. Growth and photosynthetic responses of three aeroponically grown Lettuce cultivars (Lactuca sativa L.) to different rootzone temperatures and growth irradiances under tropical aerial conditions. J. Hortic. Sci. Biotechnol. 1998, 73, 173–180. [Google Scholar] [CrossRef]
  26. Nakamoto, H.; Hiyama, T. Heat–shock proteins and temperature stress. In Handbook of Plant and Crop Stress; Pessarakli, M., Dekker, M., Eds.; Marcel Dekker: New York, NY, USA, 1999; pp. 399–416. [Google Scholar]
  27. Barbosa, M.R.; Silva, M.M.D.A.; Willadino, L.; Ulisses, C.; Camara, T.R. Geração e desintoxicação enzimática de espécies reativas de oxigênio em plantas. Ciência Rural 2014, 44, 453–460. [Google Scholar] [CrossRef] [Green Version]
  28. Bhattacharjee, S. Sites of generation and physicochemical basis of formation of reactive oxygen species in plant cell. In Reactive Oxygen Species and Antioxidants in Higher Plants, 2nd ed.; Gupta, S.D., Ed.; Science Publishers: New York, NY, USA, 2010; pp. 80–110. [Google Scholar]
  29. Petrov, V.; Hille, J.; Mueller-Roeber, B.; Gechev, T.S. ROS-mediated abiotic stress-induced programmed cell death in plants. Front. Plant Sci. 2015, 6, 69. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  30. Lehmann, S.; Serrano, M.; L’Haridon, F.; Tjamos, S.E.; Metraux, J.P. Reactive oxygen species and plant resistance to fungal pathogens. Phytochemistry 2015, 112, 54–62. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  31. Sharma, P.; Jha, A.B.; Dubey, R.S.; Pessarakli, M. Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. J. Bot. 2012, 2012, 217037. [Google Scholar] [CrossRef] [Green Version]
  32. Ilić, S.Z.; Milenković, L.; Dimitrijević, A.; Stanojević, L.; Cvetković, D.; Kevrešan, Ž.; Mastilović, J. Light modification by color nets improve quality of lettuce from summer production. Sci. Hortic. 2017, 226, 389–397. [Google Scholar] [CrossRef]
  33. Harter, L.S.; Harter, F.S.; Deuner, C.; Meneghello, G.E.; Villela, F.A. Salinidade e desempenho fisiológico de sementes e plântulas de morango. Hortic. Bras. 2014, 32, 80–85. [Google Scholar] [CrossRef]
  34. Eyidogan, F.; Öz, M.T. Effect of salinity on antioxidant responses of chickpea seedlings. Acta Physiol. Plant. 2007, 29, 485–493. [Google Scholar] [CrossRef]
  35. Hasanuzzaman, M.; Nahar, K.; Anee, T.I.; Khan, M.I.R.; Fujita, M. Silicon-mediated regulation of antioxidant defense and glyoxalase systems confers drought stress tolerance in Brassica napus L. S. Afr. J. Bot. 2018, 115, 50–57. [Google Scholar] [CrossRef]
  36. Pinto, L.I.C.; Costa, M.H.; Diniz, L.M.F.; Sediyama, G.C.; Pruski, F.F. Product comparison of solar radiation incident surface for South America. Rev. Bras. Meteorol. 2010, 25, 469–478. [Google Scholar] [CrossRef]
Horticulturae 07 00553 g001 550
Figure 1. Global solar radiation (a), in MJ·m−2·day−1, and average temperature (b), in °C, in full sun (FS) and shaded environments with the red screen (RS), ChromatiNet® screen (CS), and black screen (BS). DAT, days after transplanting.
Figure 1. Global solar radiation (a), in MJ·m−2·day−1, and average temperature (b), in °C, in full sun (FS) and shaded environments with the red screen (RS), ChromatiNet® screen (CS), and black screen (BS). DAT, days after transplanting.
Horticulturae 07 00553 g001
Horticulturae 07 00553 g002 550
Figure 2. Spectral radiation distribution under shaded environments with the black screen (BS), ChromatiNet® screen (CS), red screen (RS) and full sun (FS). TR—transmittance, Infrared radiation (IR), ultraviolet radiation (UV) and photosynthetically active radiation (PAR).
Figure 2. Spectral radiation distribution under shaded environments with the black screen (BS), ChromatiNet® screen (CS), red screen (RS) and full sun (FS). TR—transmittance, Infrared radiation (IR), ultraviolet radiation (UV) and photosynthetically active radiation (PAR).
Horticulturae 07 00553 g002
Table
Table 1. Summary of analysis of variance for reducing sugar content (RS); total soluble sugar content (TSS); the activity of the enzymes superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD); and commercial fresh matter (FCP) of iceberg lettuce cultivars under different shade screens.
Table 1. Summary of analysis of variance for reducing sugar content (RS); total soluble sugar content (TSS); the activity of the enzymes superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD); and commercial fresh matter (FCP) of iceberg lettuce cultivars under different shade screens.
SVRSTSSSODCATPODFCP
Environment (Env.)17.07 *83.58 *95.80 *117.29 *59.00 *47.78 *
Cultivar (Cv)16.49 *106.63 *44.74 *55.12 *29.51 *266.53 *
Env. * Cv8.17 *137.86 *10.41 *28.88 *15.99 *12.58 *
Coefficient of variation (%)21.809.3022.3018.948.6416.76
SV, source of variation. * Significant at 5% probability (p ≤ 0.05).
Table
Table 2. Total soluble sugar content (TSS) and reducing sugar content (RS) of iceberg lettuce cultivars under different shade screens.
Table 2. Total soluble sugar content (TSS) and reducing sugar content (RS) of iceberg lettuce cultivars under different shade screens.
Total Soluble Sugar Content—TSS Reducing Sugar Content—RS
µmol·g−1 FM
BSCSRSFSMean BSCSRSFSMean
GL2.52 Bc2.35 Ac6.14 Aa3.82 Ab3.71GL30.88 Cb27.88 Ab28.52 Bb73.15 Aa40.11
WLW2.15 Ba2.25 Aa2.98 Ba2.14 Ba2.38WLW37.99 Ba13.43 Cc32.89 Ab13.44 Cc24.44
DEL1.84 Ba2.28 Aa2.43 Ba3.08 Ba2.41DEL25.73 Db19.20 Bc25.97 Bb34.04 Ba26.24
BAL3.36 Aa2.41 Aa2.52 Ba2.87 Ba2.79BAL48.74 Aa24.43 Ab27.68 Bb10.08 Cc27.73
Mean2.472.323.522.98 Mean35.8421.2428.7732.68
Averages followed by different letters, upper case in columns, differ between cultivars; lowercase in lines, between environments; by the Scott and Knott test, at 5% probability. FS, full sun; RS, red screen; CS, ChromatiNet® screen; BS, black screen. Cultivars: GL, Great Lakes; WLW, Winslow; DEL, Delícia; BAL, Balsamo.
Table
Table 3. Activity of enzymes superoxide dismutase (SOD) and catalase (CAT) of iceberg lettuce cultivars under different shade screens.
Table 3. Activity of enzymes superoxide dismutase (SOD) and catalase (CAT) of iceberg lettuce cultivars under different shade screens.
Superoxide Dismutase—SOD Catalase—CAT
UE min−1 mgTP−1 μmolH2O2·min−1·μgTP−1
BSCSRSFSMean BSCSRSFSMean
GL5701.6 Ca4190.9 Bb4549.2 Ba5343.2 Ba5095.2GL6.33 Ac8.44 Ad12.05 Aa2.76 Bd7.39
WLW6875.1 Ba4441.1 Bc4549.2 Bc5781.7 Bb5411.7WLW2.86 Ca2.07 Ca3.56 Ca3.48 Aa2.99
DEL7832.5 Aa7179.5 Aa5288.2 Ab4771.6 Cb6267.9DEL4.68 Bb4.28 Bb6.86 Ba4.05 Ab4.97
BAL8348.4 Aa4560.1 Bd5763.7 Ac7466.7 Ab6534.6BAL0.93 Dc4.68 Bb13.06 Aa1.74 Bc5.1
Mean7189.45092.95186.55840.7 Mean3.714.878.883.01
Averages followed by different letters, upper case in columns, differ between cultivars; lowercase in lines, between environments; by the Scott and Knott test, at 5% probability. FS, full sun; RS, red screen; CS, ChromatiNet® screen; BS, black screen. Cultivars: GL, Great Lakes; WLW, Winslow; DEL, Delícia; BAL, Balsamo.
Table
Table 4. Activity of enzyme peroxidase (POD) and fresh consumable part (FCP) of iceberg lettuce cultivars under different shade screens.
Table 4. Activity of enzyme peroxidase (POD) and fresh consumable part (FCP) of iceberg lettuce cultivars under different shade screens.
Peroxidase—POD Fresh Consumable Part—FCP
UE·min−1·g−1g·plant−1
BSCSRSFSMean BSCSRSFSMean
GL10.41 Ab10.44 Ab19.35 Ba19.67 Aa14.97GL0.0 Ca0.0 Ca0.0 Ca0.0 Ba0
WLW6.81 Bc5.46 Bc23.97 Aa10.95 Cb11.81WLW144.2 Ba107.2 Bb148.6 Aa75.1 Ac118.8
DEL1.12 Cb2.52 Cb16.14 Ca14.37 Ba8.54DEL137.0 Bb195.0 Aa121.5 Bb80.7 Ac133.5
BAL2.85 Cb6.62 Bb10.77 Da3.78 Db6.01BAL168.2 Ab210.0 Aa168.0 Ab82.5 Ac157.1
Mean5.316.2617.5612.19 Mean112.62128.31109.7959.85
Averages followed by different letters, upper case in columns, differ between cultivars; lowercase in lines, between environments; by the Scott and Knott test, at 5% probability. FS, full sun; RS, red screen; CS, ChromatiNet® screen; BS, black screen. Cultivars: GL, Great Lakes; WLW, Winslow; DEL, Delícia; BAL, Balsamo.
Table
Table 5. Simple correlation matrix between reducing sugar content (RS); total soluble sugar content (TSS); the activity of superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD); and commercial fresh matter (FCP) of iceberg lettuce cultivars under different shade screens.
Table 5. Simple correlation matrix between reducing sugar content (RS); total soluble sugar content (TSS); the activity of superoxide dismutase (SOD), catalase (CAT), and peroxidase (POD); and commercial fresh matter (FCP) of iceberg lettuce cultivars under different shade screens.
VariablesRSTSSSODCATPOD FCP
RS1
TSS0.34 **1
SODnsns1
CAT0.40 **ns−0.32 **1
POD 0.51 **0.39 **−0.63 **0.32 **1
FCP−0.37 **ns0.32 **ns−0.40 **1
** Significant by the t-test at the 1% probability p ≤ 0.01; ns not significant.
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Aires, E.S.; Aragão, C.A.; Dantas, B.F.; Rodrigues, J.D.; Ono, E.O. Light Intensity Modulates the Accumulation of Carbohydrates, Antioxidant Enzymes and Production of Iceberg Lettuce under Tropical Conditions. Horticulturae 2021, 7, 553. https://doi.org/10.3390/horticulturae7120553

AMA Style

Aires ES, Aragão CA, Dantas BF, Rodrigues JD, Ono EO. Light Intensity Modulates the Accumulation of Carbohydrates, Antioxidant Enzymes and Production of Iceberg Lettuce under Tropical Conditions. Horticulturae. 2021; 7(12):553. https://doi.org/10.3390/horticulturae7120553

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Aires, Eduardo Santana, Carlos Alberto Aragão, Bárbara França Dantas, João Domingos Rodrigues, and Elizabeth Orika Ono. 2021. "Light Intensity Modulates the Accumulation of Carbohydrates, Antioxidant Enzymes and Production of Iceberg Lettuce under Tropical Conditions" Horticulturae 7, no. 12: 553. https://doi.org/10.3390/horticulturae7120553

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