Growth and production of basil under different luminosity and water replacement levels

Basil is used as spice and for medicinal purposes. Its growth is influenced by environmental factors, mainly soil moisture and air temperature. Thus, this study was installed to evaluate growth and production of basil under different levels of luminosity and water replacement. The experimental design was completely randomized, with six replicates, arranged in split plot scheme, with three luminosity levels in the plots (full sun, 50% and 70% shading) and four water replacement levels in the subplots (25, 50, 75 and 100% ETc). We evaluated plant height, stalk diameter, number of leaves and branches, root system volume, the largest root length, fresh and dry mass of roots and leaves. Data were submitted to variance analysis to observe significant differences between treatments and interactions. Luminosity effects were evaluated using Tukey test (p≤0.05%) and the effects of water regime, with the aid of regression analysis. According to data, 50% shading and 100% water replacement, lost through crop evapotranspiration, resulted in higher values of plant height, stalk diameter, branch growth, fresh and dry mass of leaves, and number of leaves. Full sun environment and 100% water replacement provided an increase in root dry mass and volume.

According to Taiz et al. (2017), light influences metabolism and plant developing. In addition to photosynthesis, radiation interferes with germination processes, cotyledon expansion, leaf formation, stem and root growth, flowering, among other morphological responses. These processes are complex and occur due to interaction among several photoreceptors.
Some of the effects observed in plants under water deficit are stomatal closure, inhibition of photosynthetic activity, reduction in cellular and metabolic activities, reduction in cell and leaf expansion, change in carbon partition, reduction in the relationship between root biomass and shoot, leaf abscission, destabilization of membranes and proteins and, finally, cell death (Taiz & Zeiger, 2013;Taiz et al., 2017).
Hormonal dysfunction, mainly linked to the increased concentration of ethylene in leaves, induces chlorophyll loss and senescence (Taiz et al., 2017).
Since basil leaves are supposed to be eaten in natura, they should be very attractive for commercialization and show high biomass yield (Abreu et al., 2013).
This study was installed to evaluate the development and production of basil under different luminosity levels and water replacements.
The experimental design was completely randomized. Plant height (cm), stalk diameter (mm) and number of leaves and branches were evaluated every 15 days. A split-split plot scheme was adopted to perform statistical analysis of data, with five evaluations (15, 30, 45, 60 and 75 days) in plots, three environments (full sun, 50 and 70% shading), in the subplots and four water replacements according to crop evapotranspiration (25, 50, 75 and 100% ETc) in the subplots and six replicates.
Root system volume, the largest root length, fresh and dry mass of roots and leaves were evaluated at 75 days after the beginning of the research. For these variables, the authors adopted the statistical analysis of data, 3x4 factorial scheme, being three environments, four water replacements according to the crop evapotranspiration and six replicates, totalizing 72 plants.
In transplant, substrate moisture was increased to the pot capacity (CV) based on the methodology used by Casaroli & Van Lier (2008). The substrate was kept in this moisture level during eight days and, 9 days after transplant (DAT), we started to apply water replacement treatments, according to Etc (equation 1) measured in each environment.

ETc = ETo x kc
(1) where, ETc= crop evapotranspiration ( m m d a y -1 ) ; E To = r e f e r e n c e evapotranspiration (mm day -1 ) and kc= crop coefficient (dimensionless). ETo was obtained from daily reading in an evaporimetric mini tank installed in the three evaluated environments, using the coefficient of the tank (kp)= 1, according to Salomão (2012) recommendation. For phases I, II, III and IV, the authors adopted respectively kc 0.23; 0.27; 0.38 and 1.02 (Marques et al., 2015).
Water replacement was carried out using a localized irrigation system, button-type drippers and selfcompensating flow, at 2.0 L h -1 flow and 2 kgf cm -2 pressure.
Obtained data were submitted to variance analysis and, when significant differences, considering interaction between treatments, were noticed, luminosity effects were evaluated with the aid of Tukey test (p≤0.05) and effects of water regime, using regression analysis.

RESULTS AND DISCUSSION
Under full sun, temperatures ranged from 9.8 to 40.0ºC; humidity, from 10 to 99%; and evapotranspiration from 0 to 7 mm. In 50% shading experiment, temperatures ranged from 9.8 to 37.6ºC; humidity was from 10 to 99% and evapotranspiration from 0 to 5 mm. In 70% shading experiment, temperature ranged from 10.1 to 36.5ºC; humidity ranged from 10 to 99% and evapotranspiration from 0 to 5 mm.
Higher temperatures and radiation under full sun, resulted in greater evapotranspiration, especially in plants kept without water deficit, due to greater water flow and consequently more active energy balance in this environment.
L o w l u m i n o s i t y a n d h i g h temperatures are associated with an increase in endogenous level of gibberellins, which influences directly on plant growth. Oh & Kim (2014) verified that low light intensity and higher temperatures potentiated the effect of gibberellic acid on the petiole elongation of Cyclamen persicum.
Plant height, stalk diameter and number of branches per plant were influenced by interactions between plant age and the crop environment, between plant age and water replacement, and between the crop environment and water replacement.
Over time, plants grown under shading conditions tended to be higher than plants grown under full sun. In the relationship between plant age and water replacement, the authors noticed an increase in height in plants at all ages, however, under water deficit, shorter height was noticed in relation to 100% water replacement. Reduction in water replacement limited the height of basil plants in all growing environments. The plants grown under shading conditions (50 or 70%) were higher in relation to plants grown under full sun (Figure 1).
These responses of plant height can be associated with hormonal changes in plants, as well as to the relationship among phytochromes, cryptochromes and phototropins in plants. Considering that phyB is the dominant phytochorome species in full-sun-grown plants and phyA is the most abundant in plants which grow in shade, possibly, 50% shading was already enough to alter phyA and phyB in basil and provide higher plants, stimulating etiolation conditions. Plants grown under full sun were kept under high radiation, typical under the conditions where the experiment was carried out. Luminosity reduces stem elongation, which can compromise photosynthesis and, consequently, plant growth.
Growth and development of plants are directly related to growing environment. Generally, plants exposed to greater solar radiation show greater need for water replacement, due to an increase in transpiration and photoassimilate translocation. According to Taiz et al. (2017), water deficit can limit plant growth due to restrictions in division, differentiation and cell stretching. Low water availability causes a reduction in opening of stomata, transpiration, photoassimilate production, nutrient uptake and accumulation of molecules, and changes hormonal balance in tissues. Vargas (2007) studied basil cultivars Maria Bonita, Mara and Genovese at different water levels, in Sergipe State, and observed partial stomatal closure, decrease in photosynthesis rate and transpiration rate, showing that basil created mechanisms for adaptation to water-deficit stress.
The 70% shading environment provided less need for water replacement and fewer leaves in relation to other treatments (full sun and 50% shading).
Basil plants showed positive response to 100% evapotranspiration replacement in relation to stem diameter. The 70% shading environment provided smaller stem diameter.  ); DLW= leaf dry mass (g/plant); DRW= root dry mass (g/ plant); RSV= root system volume (cm 3 /plant); RL= root length (cm).  Plants grown in a 70% shading environment showed fewer branches in relation to plants grown in 50% shading and full sun. Luminosity influences on sprouting and inhibition of vegetative bud development in petunia and it is associated with low light intensity (Drummond et al., 2015). Gelderen et al. (2018) verified that long red wavelength increased auxin signaling in Arabidopsis thaliana shoots, despite not being associated with reduction or increase in auxin signaling in the root. These authors also reported that long red light wavelength reduces auxin signaling in the cortex cells and, consequently, lateral root growth.
Sprout formation still depends on the action of cytokinins, auxin and gibberellin and, probably, shading has altered the balance between auxin and cytokinins, reducing the action of cytokinins. Mutant plants, with low level of cytokinin, showed reduced sprout growth and an increase in root growth. Whereas luminosity favors cytokinins, low luminosity intensity, as well as long days, increased the synthesis of gibberellins, which are associated with auxin. Thus, crop environments directly influence endogenous hormonal balance, providing different morphological responses in plants.
Growing environments influenced leaf fresh mass, root system volume, root length, leaf dry mass and root dry mass (Table 1). Leaf dry and fresh masses of plants grown under full sun and 50% shading were greater than the ones obtained under 70% shading.
An increase in water replacement favored the number of branches. Leaf fresh mass, root fresh mass (Figure 2), root system volume, root length, leaf dry mass and root dry mass were influenced by water replacement levels, whereas only the root length was influenced by interaction.
Root growth in response to an increase in water replacement was more significant in shading environments (Figure 3). The water replacement increased the root volume ( Figure 4).
Under maximum luminosity conditions (900 μmol m −2 s −1 ), luminosity increased up to 90% of total light increased biomass of stem and roots, number of branches, and provided higher allocation of biomass in roots in relation to shoot (Scanga, 2011). The highest levels of radiation provided increases in length, volume and fresh and dry root masses of Raphanus sativus (Zha & Liu, 2018).
Studying Lamium species, under high luminosity, similar results were found by Barisic et al. (2006).
Finally, we noticed that luminosity and water replacement influenced basil growth. The 50 and 70% solar radiation environments and 100% water replacement provided an increase in plant height, stem diameter, branch growth, fresh and dry masses of leaves, and number of leaves. However, full sun environment and water replacement increase in 100% level favored an increase in root dry mass and root volume.