1. Introduction
Ascorbic acid (AsA), also known as vitamin C, is an organic compound that plays a vital role in plant growth and development [
1]. It is essential for both plants and animals as a vital enzymatic cofactor, as well as an antioxidant believed to be important in preventing oxidative stress-related conditions [
2,
3,
4]. Its antioxidant properties and metabolic functions protect plants against oxidative stress caused by various environmental factors, such as high light intensity, pollutants, and pathogens [
5]. Moreover, the antioxidant capabilities of AsA contribute to the neutralization of reactive oxygen species (ROS), which are undesirable byproducts of oxygen generated during photosynthesis [
6]. As cofactor in plants, AsA participates in the regulation of photosynthesis, hormone biosynthesis, and senescence [
7]. It is required for cell division, expansion, and differentiation [
1], contributing to plants’ immune responses by enhancing the production of defense-related compounds, such as phytoalexins and pathogenesis-related proteins [
5]. Finally, AsA helps plants cope with various stress conditions, including drought, salinity, and extreme temperatures [
8]. Humans, along with several other animal species, are unable to synthesize AsA; therefore, they are dependent on the inclusion of plants in their diets to ensure adequate ascorbate levels [
9]. Plants, especially leaves and fruits, are excellent sources of ascorbate, making it important to incorporate sufficient amounts of fruits and vegetables into one’s diet [
10].
The primary biosynthesis pathway for L-ascorbic acid is the Smirnoff–Wheeler pathway. In addition to this pathway, three alternative biosynthesis pathways have also been proposed in plants, involving synthesizing AsA through either D-galacturonate, L-gulose, or myo-inositol [
11]. Due to its antioxidant function, AsA can be rapidly oxidized once synthesized. Therefore, there is also a recycling pathway for AsA, which plays a crucial role in maintaining AsA levels and the redox state in plant cells [
12]. The oxidized form of AsA, monodehydroascorbate, can be recycled back into AsA through catalysis from monodehydroascorbate reductase [
13]. If this does not occur, monodehydroascorbate undergoes disproportionation, forming dehydroascorbate, which can also be recycled back into AsA, except this is catalyzed by a dehydroascorbate reductase utilizing glutathione [
14]. If neither of these reactions occur to recycle these oxidized compounds back into AsA, dehydroascorbate is irreversibly hydrolyzed to 2,3-diketogulonic acid [
14]. This recycling pathway ensures that AsA is more consistently readily available, while maintaining a good redox state.
The production of AsA in plants is influenced by both endogenous and exogenous factors, which alter the enzymatic activity of key AsA biosynthesis enzymes. Indeed, different plant species, organs, and growth stages can exhibit different AsA levels [
15]. Moreover, exogenous factors, such as light intensity, temperature, and water availability, can also regulate AsA levels [
11]. The impact of temperature is pivotal in the accumulation of ascorbic acid (AsA) in citrus fruits [
16] and tomatoes [
12]. Research indicates that treating tomatoes with a post-harvest temperature of around 12 °C results in a higher accumulation of AsA compared to the use of post-harvest treatment at 31 °C [
12]. Light exposure is also important; a meta-analysis by Appolloni et al., 2021, showed that supplemental LED lighting can enhance AsA content in tomatoes. During postharvest, exposure to light can also increase AsA levels in tomato fruit [
17]. Depending on the intensity of the light, it can double the AsA content compared that resulting from exposure to darkness. Moreover, it was found that blue light treatment during postharvest resulted in the highest levels of AsA in tomato fruits, while red and green light exhibited no significant difference compared to the results for white light treatment [
18]. The red–far-red light ratio is another critical factor in regulating antioxidant production, including AsA and glutathione, in common beans [
19]. In contrast, adding green light to various combinations of red and blue LED lighting did not significantly affect the contents of ascorbic acid and mineral nutrients in lettuce [
20]. Drought can also impact AsA levels, as gradually reduced water availability was found to decrease AsA levels in soybean leaves and stems [
8]. Finally, the nutrients made available to crops can influence AsA production. Ref. [
21] found that a combination of rich fertilization of soil and growth in the late season resulted in higher amounts of AsA in broccoli cultivars. Additionally, Ref. [
22] studied the response of lettuce cultivars to different iron concentrations in nutrient solutions and reported significant variations across different treatments and types of cultivars. Indeed, in the red Salanova, there was a variation in the amount of AsA obtained by raising the iron concentration, while the green-pigmented lettuce showed a positive correlation between the increase in AsA and iron concentration in the nutrient solution.
Despite numerous studies on AsA production, there is still an incomplete understanding of the specific effects of environmental variables on the growth of ascorbic acid in crops. This is partly because measuring AsA can be challenging, as the accuracy of the measurement depends on the technique and the instruments used for analysis [
23]. As a result, extraction processes can lead to high measurement variability, making it difficult to compare different studies. Therefore, to best compare multiple studies, it is important to develop a methodology that can overcome this variability. This work aims to present a model in which a specific methodology is applied to merge the findings of previous studies to investigate the development of AsA in lettuce under different light treatments.
The adoption of advanced modeling techniques can significantly contribute to the increased need for sustainable and resource-efficient agriculture [
24]. The model for AsA development presented in this work allows for optimizing resource use, particularly light radiation, by predicting how different light combinations will affect AsA levels in lettuce. Thus, this approach not only enhances product quality but also promotes more efficient resource utilization, aiming towards a more sustainable agricultural practice.
This paper first introduces the methodology and dataset (
Section 2), then presents the model and the results obtained (
Section 3), and finally, discusses similar results found in the literature, along with further developments of the methodology (
Section 4).
2. Materials and Methods
The methodology aims to merge various studies to investigate the effect of different light treatments on AsA production in lettuce, overcoming the measurement variability.
First, is important to choose a reliable method to reduce the measurement variability as much as possible. HPLC analysis is widely considered the most reliable and accurate method for precisely measuring the AsA content in crops. Moreover, spectrophotometric methods and fluorimetric methods utilizing o-phenylenediamine can also be utilized. Fresh lettuce typically contains AsA within the concentration range of 5 to 30 milligrams per 100 g.
Moreover, to be able to best compare different light treatments, certain conditions must be met. First, the experiments must be carried out in a controlled system that allows for precise control over the environmental variables during the experimental phase. Secondly, to compare different studies, each must employ one or more treatments compared to a set of parameters intentionally kept constant in an experiment (the control). The control serves as a reference point or baseline against which the effects of other treatments can be measured. On the other hand, the treatments are specific experimental conditions applied to a set of crops, corresponding to the factors of interest that are to be studied. The control is often either a full experiment with standard growing conditions or an acclimatization period at the beginning of the growing period. Similarly, treatments can be either stand-alone experiments or treatments applied after the acclimatization period or postharvest treatments. Usually, the experimental designs include a germination period of a few days during which the same environmental conditions are used for both the control and the treatment groups.
The choice between using a single control group throughout the experiment and using an acclimatization period as a control depends on the specific goals of the study and the nature of the plant response being investigated. A single control group is typically used when investigating short-term changes in plants or assessing the immediate impact of different treatments [
25]. However, if the studies involve long-term plant adaptation, an acclimatization period used as a control can be beneficial. This allows plants to acclimate to their environment before treatments are applied [
26]. Furthermore, in experiments where treatments may be stressful or harmful to the plants, an acclimatization period can help ensure that all plants start from a healthy and similar initial state.
The methodology first calculates the relative change of each independent variable expressing the light treatments (
Section 2.1). The relative changes are made between the treatment and control values of each case study. Secondly, three independent variables are added to differentiate each case study (
Section 2.2). Then, the mean of each response is calculated using bootstrapping, and the relative change in the response is calculated using the mean value (
Section 2.3). Finally, a linear regression model is applied, with the relative changes in the light treatments as independent variables in each case study and the relative change in the ascorbic acid between the treatments and controls as the response.
2.1. Independent Variables
To compare different light treatments, the following independent variables regarding the spectrum and the daily light integral (DLI) are considered.
The relative change in the DLI,
x1, between the control and the treatment is given as follows:
In this formula, x1 is the relative change in DLI, Ic is the light intensity (in µmol m−2 s−1) during the control phase, It is the light intensity (in µmol m−2 s−1) during the treatment phase, is the photoperiod (in hours) during the control phase, and is the photoperiod (in hours) during the treatment phase. By employing this variable, it is assumed that the increase in photoperiod or light intensity has a similar influence when they both undergo an equivalent relative change.
The relative change in the blue light spectrum,
, (400–500 nm) between the control and the treatment is obtained as follows:
where
Bc corresponds to the percentage of light that falls into the blue spectrum multiplied by the light intensity (in µmol m
−2 s
−1) during the control phase.
Bt corresponds to the percentage of light that falls into the blue spectrum multiplied by the light intensity (in µmol m
−2 s
−1) during the treatment phase.
The relative change in the green light spectrum,
, (500–600 nm) between the control and the treatment is obtained as follows:
where
Gc corresponds to the percentage of light that falls into the green spectrum multiplied by the light intensity (in µmol m
−2 s
−1) during the control phase.
Gt corresponds to the percentage of light that falls into the green spectrum multiplied by the light intensity (in µmol m
−2 s
−1) during the treatment phase.
The relative change in the red light spectrum,
, (600–700 nm) between the control and the treatment is given as follows:
where
Rc corresponds to the percentage of light that falls into the red spectrum multiplied by the light intensity (in µmol m
−2 s
−1) during the control phase.
Rt corresponds to the percentage of light that falls into the red spectrum multiplied by the light intensity (in µmol m
−2 s
−1) during the treatment phase.
The relative change in the far-red light spectrum,
, (700–800 nm) between the control and the treatment:
where
FRc corresponds to the percentage of light that falls into the far-red spectrum multiplied by the light intensity (in µmol m
−2 s
−1) during the control phase.
FRt corresponds to the percentage of light that falls into the blue spectrum multiplied by the light intensity (in µmol m
−2 s
−1) during the treatment phase.
Some studies may only use specific wavelengths, excluding certain variables on the spectrum.
If the light conditions during the control phase vary between studies, then it is necessary to consider the following hypothesis: within the range of light conditions observed in the case studies, crops will respond in the same way to the same relative changes.
2.2. Additional Variables
Three other independent variables are used in this methodology. (1) Case study (A, B, C, etc.) is a categorical variable used to specify the study to which the treatments belong. (2) Control time (tc) is a continuous variable that expresses the number of days of the control period. (3) Treatment time (tt) is a continuous variable that expresses the number of days in the treatment period. The last two variables, tc, and tt, are used only when the studies have different control and treatment periods to verify whether different experiment times influence the plant response.
2.3. Bootstrapping and Dependent Variable
In experimental studies concerning plant responses to various light treatments, it is common practice to evaluate the average values derived from a minimum of four samples for each treatment group. However, when dealing with unreliable measurements due to equipment or sample processing issues, a method known as bootstrapping can prove to be a valuable solution. Bootstrapping is a resampling technique that involves generating multiple resamples, known as bootstrap samples, from the original dataset. This technique is employed to estimate the properties of a statistic or make inferences about a population. Bootstrapping enhances the representativeness of the population mean.
Once the mean values for both the control and treatment groups are obtained through the bootstrapping method, the relative change in the ascorbic acid (AsA) is calculated with the following formula:
where
AsAt is the total amount of ascorbic acid at the end of the treatment, and
AsAc is the total amount of ascorbic acid at the end of the control period.
2.4. Analysis
To understand and quantify the impact of light treatments on the variable being studied, an analysis is conducted. Depending on the size and quality of the dataset, various types of analysis are performed, ranging from multiple linear regression to implementing machine learning algorithms [
27].
Figure 1 provides a summary of all the instances and steps involved in the methodology. In this study, only certain steps of the methodology were tested due to the limitations of the dataset, which was created by merging different case studies described in the next section.
2.5. Dataset on Ascorbic Acid
To analyze the AsA production with respect to different light treatments, a dataset was created by grouping three studies that analyzed AsA content. The methodology was then applied to the dataset (
Figure 2), consisting of experiments from these three studies, which investigated the effect of different light treatments on the development of AsA in lettuce (Lactuca sativa L. cv. ‘Yidali’) [
28,
29,
30]. A total of eight treatments were tested, and 34 experiments were analyzed. Although some experiments employed the same light treatments, they differed in the duration of cultivation. Each case study involved germinating seeds to the seedling stage over 15 days, followed by a control period of 7 to 10 days. After that, in each case study, one or more light treatments were applied to the cultivar. This resulted in one or more variables in regards to photoperiod, light intensity, and spectrum, with variations also noted in the length of the treatment period. Each treatment continued for either 12 or 15 days, and the amount of AsA in each sample was measured every 3 days. Therefore, the total growth period from germination to the end of treatment ranged from 34 to 40 days. The mean AsA value reported in the studies was calculated for each measurement day, corresponding to a single experiment within the dataset.
The green and far-red spectrum independent variables are not used in the analysis because these two wavelengths are not tested in the case studies considered (
Figure 2). Moreover, the bootstrapping step was skipped in this analysis since only the AsA mean values of the treatment and control were reported.
A summary of the experimental design of each case study is reported in
Table 1. Two case studies used a spectrophotometric method to measure the amount of AsA in lettuce, while Ref. [
30] used UPLC, a higher-pressure version of HPLC. The UPLC procedure was conducted as follows. Frozen leaf tissue (0.1 g) was homogenized in 1 mL of precooled extraction solution, comprised of 1.5% (
w/
v) metaphosphoric acid, 4% (
v/
v) acetic acid, and 0.5 mM EDTA. Following centrifugation (15,000×
g, 4 °C, 15 min), the supernatant was filtered through PTFE filters with a pore size of 0.22 μm and collected for the assay of AsA concentration. To prepare for analysis, 50 μL of the supernatant was mixed with 10 μL of filtered dithiothreitol (750 mM), 190 μL of Tris (275 mM), and 50 μL of sulfuric acid (0.4 M) and then incubated at 25 °C for 30 min. The resulting reaction mixture was analyzed using an Acquity UPLC system (Waters Corp, Milford, MA, USA) equipped with an Acquity UPLC HSS T3 column (2.1 × 100 mm, 1.8 μm, Waters). The column was eluted with 0.1% (
v/
v) formic acid at a flow rate of 0.25 mL⋅min
−1, and absorbance was monitored at 245 nm using a Waters Acquity UPLC photodiode array (PDA) detection system (Waters Corp, Milford, MA, USA).
3. Results
As indicated in
Section 2.1, the light treatment effects were estimated using the relative change in DLI, with the blue and red spectrum as independent variables (Formulas (1), (2), and (4), respectively). These variables were calculated from the starting values of 200 micromoles of light intensity (µmol m
−2 s
−1), a 16 h photoperiod, and a red–blue ratio of 3:1 during the acclimatization period. As is shown in
Table 2, the relative change in light intensity varies from −25% to +125%, with the blue spectrum (400–500 nm) ranging from −25% to +350% and the red spectrum (600–700 nm) from −50% to +125%.
First (shown in
Figure 3), a descriptive analysis was conducted, plotting the AsA response, calculated through Formula (6), to the relative change in DLI (
Figure 3A) and the blue light spectrum (
Figure 3B).
In study A,
x1 did not vary (
Figure 3A), so for that study, only the effect of
xb on AsA could be analyzed. For the other two studies, if
x1 increased, then
xb also simultaneously increased, due to the dataset limitations, as shown in
Figure 3A,B. For both case studies B and C,
x1 and
xb were tested, and the increase in both leads to an increase in the mean AsA. As shown in
Figure 3B, the slopes of the regression lines corresponding to case studies B and C differ substantially from the line corresponding to Case Study A due to the implicit effect of increasing
x1 in the two case studies. Assuming an identical effect of increasing
xb for the three case studies yields an estimate of the separate effects of
x1 and
xb, as given in the regression results shown below (
Table 3).
If we use a model that combines the effects of, or the relative changes in, the two variables
x1 and
xb on the relative change in AsA, we obtain a multiple linear regression model in which we allow for different intercepts for the three cases. Interactions were excluded from the model because there are not enough tested levels of the independent variables
x1,
xb, and
xr in the dataset. The resulting equations for the three case studies are given in
Table 3.
In the regression model for each of the case studies, a linear relationship is assumed between AsA increment, as the dependent variable, and x1 and xb, as independent variables. Variable xr was not included in the model because it is highly correlated with xb. Indeed, due to limitations in the dataset, xr decreases as xb increases.
As can be seen from
Table 3, intercepts can differ for the case studies, but the slopes are the same. For Case Study A,
xb is the only variable that changes. Thus, the A-data only influence the
xb slope. On the other hand, the changes in mean for B and C can be attributed partly to the change in
xb (and we assume this effect to be the same as for A) and partly to the changes in
x1. The changes in
x1 in Case Studies B and C determine the
x1 slope.
The model assumes that the effects of x
1 and
xb are equal across all case studies. However, upon analyzing the three equations, it is evident that Case Study B shows an intercept close to 0, while Case Studies A and C differ from B. This means that there are variations among case studies in the increment of AsA which cannot be solely explained by the light treatments. We hypothesized that this difference could be due to varying environmental conditions (apart from DLI and light spectrum) among the case studies, such as temperature and nutrient solution, as shown in
Table 4. The different environmental conditions may have a direct impact on the development of AsA in lettuce, or they may interact significantly with
x1 and
xb to increase the light effect on the AsA content in lettuce.
Thus, from this analysis, we hypothesize that illumination alone may not be the sole significant factor influencing the development of AsA in lettuce. But it is possible that other factors and interactions, not accounted for in the model, could also influence AsA levels.
Furthermore, it can be concluded from this analysis that the effect of DLI and blue spectrum light influence AsA production in lettuce. A statistically significant positive relationship (p-value < 0.05) was observed between DLI and blue light content in the spectrum, with an increase in AsA in lettuce. Specifically, doubling the DLI (from 200 µmol m−2 s−1 to 400 µmol m−2 s−1) results in an approximately 30% increase in AsA, while doubling the blue radiation (from 50 µmol m−2 s−1 to 100 µmol m−2 s−1) leads to an 8% rise in AsA content in lettuce. Generally, combining the effect of increased DLI with a greater portion of the blue spectrum enhanced AsA production.
4. Discussion
In this study, we determined that increasing both the DLI and the blue light spectrum has a positive effect on the development of AsA in lettuce. Indeed, doubling the DLI (from 200 µmol m−2 s−1 to 400 µmol m−2 s−1) will increase AsA by 30%, while doubling the blue (from 50 µmol m−2 s−1 to 100 µmol m−2 s−1) light spectrum will increase AsA by 8%. This model can assist farmers in enhancing the development of ascorbic acid in lettuce by suggesting adjustments to the spectrum and DLI. Moreover, this model can assist farmers in achieving more sustainable cultivation practices by identifying the optimal light spectrum and DLI for AsA production. By optimizing these parameters, farmers can utilize light more efficiently, thus promoting sustainable agriculture. Through the precise control of light conditions, light wastage is minimized, ensuring that the energy input is directly proportional to the desired output in terms of AsA content. This contributes to a more sustainable and resource-efficient agricultural system, aligning with the goals of sustainable agriculture by reducing environmental impact and enhancing crop quality.
However, it is important to note that the results from this model are reliable only within the tested ranges shown in
Table 2, and the dataset used was small (n = 34). In our analysis, only three case studies were considered, as it was essential for the control light conditions to be consistent, or at least within a comparable range, across all studies to ensure that lettuce would respond similarly to the same relative changes. To our knowledge, no other studies have analyzed the same cultivar (Lactuca sativa L. cv. ‘Yidali’) under these control light conditions. Moreover, green and far-red light were not considered in the regression model because these two spectra were not included in the treatments of the case studies. The red spectrum was used in the treatments of the case studies, but due to the high correlation with the blue spectrum, it was not included in the regression model.
Similar findings to those obtained from the regression analysis in this study have been observed in previous research. The studies included in the dataset described in
Section 2.5 align with our model, which highlights the positive effects of the daily light integral (DLI) and the blue light spectrum on ascorbic acid (AsA) accumulation in lettuce. For example, Ref. [
28] reported a positive correlation between photoperiod and the ascorbate pool, while Ref. [
29] identified a positive correlation with light intensity alone. Moreover, Ref. [
30] demonstrated that a higher ratio of blue light (25:75 R) enhanced the ascorbate pool at the same total light intensity. Furthermore, AsA production was found to positively correlate with a combination of high light intensity and longer photoperiods in lettuce [
26]. Moreover, high light treatments during end-of-production can increase AsA contents at harvest [
31], and these increased levels of AsA at harvest can lengthen postharvest shelf life [
32].
Additionally, several works studied the effect of light quality on lettuce. First, higher portions of blue light spectrum during light treatments enhanced the development of AsA in lettuce [
33,
34,
35]. This aligns with previous research that has indicated that long-wavelength light (such as red light) promotes plant growth, whereas short-wavelength light (such as blue light and UV A) enhances the accumulation of ascorbate and flavonoids [
36,
37]. Finally, Ref. [
20] concluded that additional green light does not affect the development of AsA in lettuce, while Ref. [
38] affirmed that the AsA content of the lettuce leaves was increased by about 23% with the addition of purple light, with a total proportion of 60% Red, 20% Blue, and 20% Purple.
In this study, we developed and employed a methodology to compare various research studies that investigated AsA development in lettuce crops under different light treatments. Our methodology is versatile, enabling not only the analysis of AsA development in response to light treatments but also the comparison of studies exploring diverse environmental factors. These factors include temperature, humidity, CO2 concentration, and other environmental parameters that can influence crop growth. Consequently, in experiments wherein a control and treatment group are consistently employed, our methodology can assess the relative changes in these variables. This approach could facilitate the comparison of different studies examining not only light but also other environmental factors that could influence AsA development, ultimately contributing to the development of a unified model that incorporates the effects of all relevant environmental variables on AsA development.
As previously mentioned, when applying our methodology (
Figure 1), the bootstrapping step was not applied because the dataset was built from the results of existing literature studies where only the means of AsA content were described. However, the utilization of the bootstrapping method is an innovative solution to measurement variability. By repeatedly resampling the available data with replacement data, bootstrapping not only acknowledges the inherent variability of measurements but also permits the extraction of robust, unbiased estimates of the means. Therefore, we suggest that the bootstrapping method should also be implemented in future studies that present data without using the means of the analyzed variable.
Furthermore, future studies should consider expanding the model by including additional treatments with the same control light conditions as those employed in the three case studies tested (3R:1B, 16/8 h, 200 µmol m−2 s−1) to make it more robust and applicable to a broader range of light treatments. Additionally, it would be beneficial to integrate new case studies with longer treatment durations into the model to evaluate whether an extended period affects the light treatment of the crop.
In future studies, it would be valuable to expand the investigation to a wider range of lettuce varieties to determine whether the light treatments produce consistent effects across different cultivars. Additionally, incorporating various environmental conditions and exploring the interactions between light and other environmental factors could significantly enhance the model’s generalizability. By including these variables, we can better understand how diverse conditions affect ascorbic acid levels and improve the applicability of the model to broader agricultural practices.