3.1. Water Analysis
The suitability of water for a specific purpose depends on the types and amounts of dissolved salts. Some of the dissolved salts or other constituents may be useful for crops, such as NO
3 [
26]. The most important characteristics that determine the quality of irrigation water are the pH; the total concentration of soluble salts, assessed through the EC; the sodium adsorption ratio (SAR), described as the relative proportion of Na to other cations such as Ca and Mg; the concentration of B and other elements that may be toxic to plants; the residual sodium carbonate (RSC), described as the difference between the sum of the carbonates and bicarbonates concentrations and the sum of the Ca and Mg concentrations; and the content of anions such as chloride, sulfate, and nitrate [
27].
The trends of the ionic concentrations, specifically cations (Ca, Mg, Na, K, Na + K) and anions (SO
4, NO
3 HCO
3 + CO
3) in the soil circulating solution for the treatment N100, at a depth of 15 cm, are shown in
Figure 1A. From the second week of March toward April and May, it is possible to find a light increase in the ionic concentrations due to fertigation. The more evident trend is for calcium and nitrate: the calcium ranges from 5.1 meq/L to 13.2 meq/L, with a monthly average of 7.4 meq/L in March, 11.5 meq/L in April, and 12.16 meq/L in May. The nitrates range from 1.94 meq/L to 12.04 meq/L, with a monthly average of 1.94 meq/L in March, 9.88 meq/L in April, and 9.46 meq/L in May. These trends may be related to the phases of plant development: a stronger uptake of these elements from the plants occurs in March, while this is stable in the following months. The sharp peaks appearing in the graphic are due to a long lag time between treatments. This is clear in the nitrate levels on the 10th and 20th of April of 11.96 and 7.10 meq/L, respectively. The same trend was registered between the 26th of April and the 5th of May, with 13.29 and 6.88 meq/L of nitrates, respectively. The concentrations of the other elements appear to be quite linear during the trial. The trends in ionic concentrations of the soil-circulating solution for the same trial, but at a depth of 35 cm, showed results like those obtained at 15 cm, but with lower amplitudes (results not shown).
Considering the ion concentration in the soil-circulating solution for the N80 treatment at a depth of 15 cm (
Figure 1B), a decrease in overall concentration values compared to N100 is evident. In particular, the lower amounts start from March. The values of the calcium and nitrate concentrations remain the most relevant. Ca ranges from 5.41 to 11.71 meq/L, with a monthly average of 5.94 meq/L in March, 9.54 meq/L in April, and 8.68 meq/L in May. Nitrates range from 0.95 to 7.74 meq/L, with a monthly average of 1.87 meq/L in March, 6.08 meq/L in April, and 4.16 meq/L in May. There are also similar sharp peaks, but of a smaller entity, with those obtained at N100, corresponding to the 10th and 20th of April (6.28 and 5.86 meq/L) and the 26th of April and 5th of May (7.74 and 4.16 meq/L). The concentrations of the other elements appear to be quite linear during the trial, with fewer variations in comparison to trial N100.
The analyzed soil-circulating solution for the N60 (at 15 cm of depth) thesis shows slightly lower ionic concentrations and a more linear trend in comparison to N80 (
Figure 1C). Calcium ranges from 5.62 to 9.38 meq/L, with a monthly average of 5.82 meq/L in March, 7.53 meq/L in April, and 9.30 meq/L in May. Nitrates range from 1.09 to 4.85 meq/L, with a monthly average of 1.49 meq/L in March, 4.54 meq/L in April, and 6.83 meq/L in May. The range in concentrations of the remaining elements is almost linear.
The NO
3 concentrations available in trials N100, N80, and N60 at different soil depths (15 cm/35 cm) are reported in
Figure 2.
Figure 2A shows that the NO
3 concentration in the soil solution analyzed at 15 cm of depth is higher than that at 35 cm in the N100 trial; there is a generally positive trend for the NO
3 concentrations at both depths during the months of the trial. The inflection points related to the 20th of April and the 5th of May should be due to a wide timing interval that separates two successive fertigations.
At the same depth (15 cm), the N80 and N100 theses show a halving of the nitrogen concentration (
Figure 1B); the reason can be attributed to the lower nitrogen supply at N80, according to the trial; moreover, the maximum reduction in NO
3 availability can be detected in N60 (
Figure 1C). Comparing the three theses, a reduction can be noticed in the NO
3 availability from thesis N100 to N60 for both depths. Furthermore, a drop of −31% can be observed for the nitrate value (mg/L NO
3) from N100 to N80 (15 cm), and a decrease of 44% from N100 to N60 (15 cm) (
Table 2). The same trend is observed between N100 and N60, but to a smaller extent, in the 35 cm experiment.
Strawberries negatively respond to salt stress in terms of growth and yield, so it is a salinity-sensitive species [
28]. The hydric stress, due to the electrical conductivity (ECs) of the saturated soil extract, is a factor that contributes to reducing the number of leaves, the leaf area, the shoot dry weight, the number of crowns, the yield, and the fresh weight of the fruit [
29,
30]. In the study of Barroso and Alvarez [
31], the leaves of strawberry cultivars did not develop symptoms of toxicity for EC values lower than 2000 μS/cm. In the study of HA-Joon et al. [
32], the optimal EC value was detected at 1000 μS/cm instead of 2000 μS/cm; the compared parameters were fruit length, diameter, weight, and plant yield. Moreover, the dry branch crowns and dry roots in the 1000 μS/cm experiment were heavier than those in the 2000 μS/cm experiment.
In our study, the electrical conductivity of the water during April and May 2017 at 15 cm of depth showed higher values for the three nitrogen trials. These results agree with the nutrient concentration explained above. In N100 and N80, the maximum registered value is 1400 μS/cm (
Figure 3A,B), while in N60 this value is lower, slightly exceeding 1000 μS/cm (
Figure 3C). The trends are similar, but to a lesser extent, for the water sampled at 35 cm of soil depth.
3.2. Vegetative Parameters
The vegetative crops’ growth is dependent on the organic matter, which enhances both the soil’s microbiological and biochemical activities [
33]. Nevertheless, the soil organic matter content hides the effect of mineral nitrogen intake, the principal macro-element for the growth of plants [
34]. This study took place in soil that was poor in both nitrogen concentration (0.90 g/kg) and organic matter (11.9 g/kg) so that the fertilization practices were not masked by the soil properties. Given an overview of the studied vegetative parameters (
Table 3), it is evident that that year of cultivation (a) resulted as an impacting factor influencing the branch crowns, plant height, and leaf number. Cultivar (b) was decisive for the branch crowns and plant height. Treatment (c) seemed to have a single key role in the branch crown number. Furthermore, it is remarkable that the interaction (a) × (b) impacted all of the vegetative features. The interaction (a) × (c) showed a significant incidence for the branch crowns. The interaction (a) × (b) × (c) seemed to have an insignificant impact on the studied parameters, as well as interaction (b) × (c). Considering the majority of the studied parameters, each cultivar responded similarly to every treatment.
The plant height, branch crown number, and inflorescence number did not exhibit statistically significant differences among the treatments (
Table 4 and
Table 5). A possible reason could be that all of the plants followed a standard fertilization plan from September until March and reduced nitrogen treatments during spring when the plants had already a developed vegetative structure. It is conceivable that a reduction in the fertilizer administered in September may have resulted in different vegetative features between cultivars managed under different treatments. A previous study [
17] demonstrated the crucial importance of fertilization timing for short-day (SD) strawberry plants. It is demonstrated that, under controlled photoperiod conditions conducted in a phytotron, feeding SD strawberry plants one week from the beginning of the SD period could double the number of flowers compared to plants treated two weeks before the start of SD conditions [
17].
Among the vegetative parameters, the only significant result seemed to be the “Sibilla”’s leaf number (
Table 4). The “Sibilla” cultivar treated with 60% nitrogen administration showed a significant foliage decrease (26.2 ± 5.6 leaves at N100 and 23.6 ± 4.3 leaves at N60) in contrast with the other two tested plant cultivars, which did not show any significant differences among the treatments. Medeiros et al. [
35] observed the same feature of the “Sibilla” cultivar in the “Oso Grande” cultivar, namely a great increase in terms of the leaves number with increasing nitrogen intake.
3.3. Productive Parameters
In considering the productive parameters (
Table 6) year (a), cultivar (b), treatment (c), and interaction (a) × (b) generally exhibited a great impact on the average fruit weight (AFW) and commercial production. The interaction (a) × (c) seemed to influence the AFW, as well as the interaction (a) × (b) × (c). Interaction (b) × (c) did not manifest any correlation with any of the productive parameters. The evaluation of the productive parameters did not highlight any great change among the different treatments.
More specifically, the average fruit weight values did not show significant differences among the three nitrogen treatments (
Table 7). Similar results but at lower nitrogen doses (60, 40, 20 kg N/ha) were obtained in the trial conducted by Cvelbar Weber et al. [
13]. Regardless of the nitrogen supplied to the plants, “Cristina” exhibited a higher average fruit weight than “Romina” (of about 13–15 g) and “Sibilla” (about 10–13 g).
The statistical analysis confirmed an insignificant difference in the commercial production among the different nitrogen supplies (
Table 7). Similar findings were already observed in the studies from Darnell and Stutte, Cantliffe et al., and D’Anna et al. [
36,
37,
38], which indicated that plant growth and yield may not be reduced by the volume of the administrated NO
3−, but by the capacity to reduce and assimilate the NO
3. This capacity could be inhibited by the lack of reductants, like NADH and NADPH, or the deficiency of skeleton carbohydrates needed for the assimilation. In our study, the commercial production originating from plants with the lowest dose of nitrogen showed a slight downward trend of −7% compared to N100. In the N100 trial, “Cristina” appeared to be commercially more productive, followed by “Sibilla”, and then “Romina”. This tendency was maintained for all of the nitrogen trials, although the reduction in this element provided no significant decrease in production for all three cultivars. In other studies, the effect of higher rates of N fertilization on marketable yield was clear, with a significant increase with respect to the lower doses [
12,
39,
40].
In general, from the productive point of view, the results of our study showed that there was not a negative effect of nitrogen reduction on plant yield, and this outcome could be read as an indication of the need to better test the nitrogen requirements of the different cultivars in different conditions, in order to reduce the environmental impact that can be derived from the excessive use of nitrogen.
3.4. Qualitative Parameters
In evaluating all of the studied qualitative parameters, year (a) seemed to affect the sugar content, firmness, brightness, and redness of the fruit of the three tested cultivars. Among the factors, cultivar (b) showed the greatest influence in terms of the fruit sugar content, titratable acidity, firmness, brightness *L, redness *a, yellowness *b, and the Chroma index. The combination of (a) × (b) greatly influenced the fruit sugar content, firmness, brightness *L, redness *a, yellowness *b, and the Chroma index. The impacts of treatment (c) and the interactions (a) × (c), (b) × (c), and (a) × (b) × (c) were not relevant to the studied parameters (
Table S1).
According to our results, genotype was the principal factor affecting the sugar content and titratable acidity of strawberry fruit (
Table 8), and this outcome is in line with those other previous studies [
41,
42,
43,
44]. In particular, the fruits of “Romina” and “Sibilla” revealed the highest sugar content in all of the nitrogen trials (
Table 8). The fruit sugar content and titratable acidity did not show significant differences among treatments for these cultivars, as registered by Sedri and Farami [
45]. However, these results contrast with other studies [
38,
39,
40,
46], which pointed out the correlation between lower doses of nitrogen supply and higher fruit soluble solids content.
The fruits’ firmness did not seem to be influenced by the administration of nitrogen (
Table 9). The “Sibilla” fruits showed the hardest texture, followed by “Romina” and “Cristina” in all the nitrogen trials. These results were in contrast with the studies conducted by D’Anna et al., Asghari et al., and Cardenosa et al. [
38,
40,
47], which found a higher fruit consistency when reducing the administration of nitrogen. According to Van der Boon [
48], the excess nitrogen could cause an irregular ripening of fruits, resulting in soft consistency and poor taste. An excessive nitrogen presence in the fruits corresponds to a calcium reduction, which decreases the texture and consequently, the shelf life of the product, considering that calcium is an intermolecular binding agent that is responsible for the pectin–protein complexes of the middle lamella [
13]. Therefore, a decrease in nitrogen administration should determine a better quality of fruit firmness.
In the present study, changing the nitrogen doses in all of the treatments did not sway the Chroma index (
Table 9). The only difference was found in comparing the studied cultivars: “Sibilla” had the darkest fruits, followed by “Romina”, and then “Cristina”. On the contrary, the study conducted by Yoshida et al. [
49] exhibited a correlation between anthocyanin synthesis and nitrogen fertilization. Lack of nitrogen during the fertilization treatment seemed to lower the anthocyanins accumulation in fruit. Anthocyanins accumulate in the inner strawberry flesh over the course of the late stage of fruit development, and improper fertilization may reduce the biosynthesis of these molecules.