Next Article in Journal
The Effect of Antibiotic Treatment on the Bacterial Community of the Brown Planthopper and Its Correlation with Rice Virulence
Next Article in Special Issue
The Effect of Titanium Organic Complex on Pollination Process and Fruit Development of Apple cv. Topaz
Previous Article in Journal
Regulation of Phosphorus and Zinc Uptake in Relation to Arbuscular Mycorrhizal Fungi for Better Maize Growth
Previous Article in Special Issue
Exogenous Application of Biostimulants and Synthetic Growth Promoters Improved the Productivity and Grain Quality of Quinoa Linked with Enhanced Photosynthetic Pigments and Metabolomics
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Agronomy
Volume 11
Issue 11
10.3390/agronomy11112326
agronomy-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effects of Nitrogen, Azoxystrobin and a Biostimulant Based on Brown Algae and Yeast on Wild Rocket Features at Harvest and During Storage

by
Maria Immacolata Schiattone
1,
Francesca Boari
2,*,
Vito Cantore
2,
Donato Castronuovo
1,
Michele Denora
3,
Donato Di Venere
2,
Michele Perniola
3,
Massimiliano Renna
2,4,
Lucrezia Sergio
2,* and
Vincenzo Candido
3
1
School of Agriculture, Forest, Food and Environmental Sciences, University of Basilicata, Viale dell’Ateneo Lucano, 10, 85100 Potenza, Italy
2
Institute of Sciences of Food Production, National Research Council (CNR-ISPA), Via Amendola, 122/O, 70125 Bari, Italy
3
Department of European and Mediterranean Cultures, University of Basilicata, Via Lanera, 10, 75100 Matera, Italy
4
Department of Agricultural and Environmental Science, University of Bari Aldo Moro, Via Amendola, 165/a, 70126 Bari, Italy
*
Authors to whom correspondence should be addressed.
Agronomy 2021, 11(11), 2326; https://doi.org/10.3390/agronomy11112326
Submission received: 14 October 2021 / Revised: 11 November 2021 / Accepted: 15 November 2021 / Published: 17 November 2021
(This article belongs to the Special Issue Biostimulants as Physiological Modulators of Crop Performance and Product Quality)
Browse Figures
Versions Notes

Abstract

:
Recently, the use of biostimulant substances of different origins has been affirmed. They act differently on the physiological processes of the plant, helping to improve its productive response and resistance to biotic and abiotic stress. Therefore, the response of the wild rocket to two substances known to have biostimulating activity (Azoxystrobin, and a fluid extract of brown algae and yeast), was evaluated. Two experimental trials (Exp 1 and Exp 2) were carried out in the greenhouse. The collected product, in addition to being evaluated from a qualitative point of view, was used for evaluation of shelf life. Exp 1 involved the comparison of two N levels with two Azoxystrobin levels (treated–Azo+, and untreated control). Exp 2 involved the comparison of two N levels, and two biostimulating substances based on Azoxystrobin (Azo+) and on fluid extracts of yeast and brown algae (YBA+), in addition to untreated control. A split-plot experimental design with three replications was used. Azo+ increased marketable yield of wild rocket by 16.8% and enhanced some qualitative features at harvest as the increase in chlorophyll (+17.8%) and carotenoids (+13.5%), and decrease in nitrates (−10.6%), regardless of the nitrogen level. Furthermore, Azo+ increased the shelf life (+2.5 days) of wild rocket stored at 3.5 °C. In particular, Azo+ slowed the loss of chlorophyll (yellowing) and the worsening of odor and visual appearance. As Azoxystrobin is a fungicide effective for the control of some diseases of wild rocket, its use should be promoted as it would offer not only the benefit of disease control but also improved production and shelf life. YBA+ caused an increase in the chlorophyll content (+12.5%) at harvest of wild rocket, but reduced its antioxidant activity (−40%). YBA+ did not cause substantial variations in shelf life with the exception of a slowdown in the degradation of carotenoids. Further research is desirable to evaluate other variables such as the dose and time of application.

1. Introduction

Wild rocket (Diplotaxis tenuifolia L. DC) represents a worldwide species of the Brassicaceae family that is well known for its spicy flavor and has a continuously increasing demand [1,2]. This is mainly because it represents a basic ingredient of ready-to-eat salads in combination with other leafy vegetables, such as lettuce, lamb’s lettuce and spinach. Moreover, in recent years, the use of this species as baby leaf has become widespread [3].
Wild rocket is sold washed or unwashed packaged in plastic trays wrapped in polypropylene film or in pouches to create modified atmosphere packages. Sanitizing and drying is a stressful process for such delicate leaves [4,5], and avoiding these processes may result in higher product quality and longer shelf-life. For this, often wild rocket is sold unwashed, packaged in trays wrapped in film to keep physical damage of leaves to a minimum and to prevent wilting of leaves from loss of water [6].
The ready-to-use market requires a product of high quality and long shelf life which, on the one hand, has a low content of compounds harmful to health such as nitrates and on the other a high content of beneficial compounds such as antioxidants.
The quality of the produce is the result of the interaction of numerous factors (i.e., genetic, environmental, agronomic). The agronomic factors that can significantly influence the quality of leafy vegetables include the availability of nutrients and the application of substances with a biostimulating action [7]. Nitrogen is the fertilizing element that can influence mostly some quality parameters of leafy vegetables (i.e., content of nitrates, chlorophyll, tenderness, chromatic characteristics, etc.). For wild rocket, considered a nitrate hyperaccumulating species, particular attention must be paid to the nitrogen fertilization management to avoid the risk of exceeding the nitrate limits imposed by the Regulations of the European Commission (EU No 1258/2011) [8].
On the other hand, the literature reports examples concerning the improvement of yield and quality performances following the application of substances with a vigor effect or biostimulating action. These include strobilurins, substances of natural origin whose structural variants (i.e., Pyraclostrobin, Azoxystrobin, Kresoxim-methyl) are marketed as broad-spectrum fungicides, with no harmful effects on humans and the environment, and whose complementary positive effects on plant physiology, yield and quality are emphasized [9,10,11].
Based on the previous statement, agronomic techniques that can reduce the nitrate content in the product are certainly welcome. These include the use of products with a biostimulating action which, by promoting nitrogen metabolism, could limit its accumulation in nitric form into plant organs. Positive results in this sense concern, for example, the application of strobilurins which, by increasing the nitrate reductase activity, limit the accumulation of nitrates in wild rocket leaves [7] as well as in lettuce and spinach [12,13].
Among the biostimulating substances used in agriculture, there is a growing spread of products based on algae and yeast extracts, which have been found to have a biostimulating effect on various species. Algae extracts, even at low concentrations, are able to induce a series of physiological responses of the plant, such as increasing growth, flowering, yield, polyphenol content, shelf life, tolerance to abiotic stress of different origins (salinity, water stress, heat and frost) [14,15,16]. Considering the need of having high quality plant material for fresh-cut products and the high perishability of wild rocket, it is important to implement all the agronomic strategies that improve yield and qualitative characteristics together with an adequately long shelf life.
According to the literature, some agronomic practices such as the availability of nitrogen and the application of biostimulating substances can improve the quality of the product at harvest and the shelf life of some vegetables [15,17]. It has been speculated that this could also be the case of the wild rocket. To the best of our knowledge, while there is some information on the effects of nitrogen and Azoxystrobin on the harvest quality of this species [7], information regarding the effects on shelf life and evolution of some nutrients during storage is lacking. To demonstrate our hypothesis, two trials were carried out to evaluate the shelf life of the wild rocket collected in two experimental field trials in which were studied the effects on yield and some qualitative characteristics (i) of N and Azoxystrobin level, (ii) of N level and the application of Azoxystrobin or an yeast and brown algae extract based biostimulant.

2. Materials and Methods

2.1. Description of the Experimental Field Trial

2.1.1. Characteristics of the Experimental Site

The field trials were carried out in the period November 2014–February 2015 (Exp 1) and November 2015–March 2016 (Exp 2) at the Troyli company’s farm in the countryside of Policoro (MT) (40°22′ N, 16°62′ E; 150 m asl), in an unheated greenhouse, covered with ethylene vinyl acetate (EVA) film with a thickness of 200 µm. The soil type, according to USDA, is ‘Typic Haploxeralfs fine loamy, mixed, superactive, thermic’ [18], very fertile and over 1 m deep. The climate, according to De Martonne’s classification, is subhumid [19].

2.1.2. Treatments, Experimental Design and Crop Management

Exp 1 involved the comparison of two N levels (24 and 84 kg ha−1, indicated respectively NL and NH) with two Azoxystrobin levels (Ortiva®, Syngenta, Milan, Italy) (treated and untreated control, indicated Azo+ and C respectively). A split-plot experimental design with three replications was used, in which the N level occupied the plot and Azoxystrobin levels the subplot (experimental unit, EU). Where expected, two foliar applications of Ortiva® (1.0 L ha−1) were carried out, twenty and ten days before harvesting.
Exp 2 involved the comparison of two N levels (32 and 112 kg ha−1, indicated respectively with NL and NH), and the application of two biostimulating substances (BS) based on Azoxystrobin (Ortiva®, Syngenta) and a biostimulant based on fluid extracts of yeast and brown algae (Bioproject SM23 Foliar-BioKimia® International Srl, Castel San Pietro Terme, Bologna, Italy), indicated respectively Azo+ and YBA+, in addition to untreated control (C). A split-plot experimental design with three replications was used by arranging N levels in the plots and BS in the sub-plots (EU). Where foreseen by the experimental plan, foliar applications of BS (Ortiva®, 1.0 L ha−1; Bio Project SM 23 Foliar, 1.5 L ha−1), considering also that Ortiva® has a withdrawal period of 7 days, were performed twenty and ten days before harvest.
In both experiments, soil P-K fertilizations were carried out with 100 kg ha−1 of P2O5 (superphosphate) and 100 kg ha−1 of K2O (potassium sulfate). Nitrogen, as ammonium nitrate, was applied following the experimental plan. Disease and pest were controlled by applying the IPM disciplinary of Basilicata Region (Regione Basilicata, 2014). Weeds were controlled both by the false sowing method and hand removal. The water supply of the crop was optimal throughout the crop cycles, irrigating by sprinkler. In order to exclude the fungicidal effect, compared to the ‘growth promoting’ one, the observations that excluded the presence of fungal diseases in all the treatments compared were appropriately performed.

2.2. Yield Assessment

The collections were made by machine in a sampling area of 2 m2 for each subplot, on 27 February 2015 and 7 March 2016, cutting the plants at a height of about 3 cm above the collar. Leaves and stems of the sampling area were used to determine the marketable yield.

2.3. Shelf Life Assessment

The shelf life was assessed on the marketable product, setting up two experimental trials as described below.
About thirty minutes after harvesting, unwashed wild rocket samples of about 100 g were packaged on a commercial packaging line (at the Troyli company, Tursi – MT, Italy) in polyethylene terephthalate (PET) trays (185 mm × 145 mm × 70 mm) and wrapped with laser perforated, oriented polypropylene film (OPP) with an O2 transmission rate (OTR) of 17.8 pmol s−1m−2 kPa−1, at 23 °C and 50% relative humidity. The packages were immediately (about 1 h) transported to the laboratories by means of a refrigerated van at 4 °C.
Just after arriving at the laboratory, for each EU, 18 packs were tagged and stored in a dark controlled temperature chamber, set at constant temperature of 3.5 °C. On the film of three trays for each EU, small (ϕ10 mm) rubber caps were applied, through which, every 2–3 days, the concentrations of O2 and CO2 were monitored by means of a small needle inserted into the package headspace, connected to a gas analyzer (Check-Point, MPIM Srl, San Giovanni Teatino-CH, Italy).
The trials lasted 14 (Exp 1) and 16 (Exp 2) days, and for each trial, surveys were carried out every 2–3 days. At the beginning of the conservation trial on the fresh unpackaged wild rocket and at each survey date for the packaged stored wild rocket, the following qualitative parameters were assessed: dry matter (DM), total phenols (TP), total antioxidant activity (TAA), nitrates (Ni), total chlorophyll (TCh), total carotenoids (TC), odor (Od), visual appearance (VA), color characteristics of the leaves (L*, a*, b*, yellow index).

2.4. Quality Features Measurement

Dry matter. For the determination of the DM, a marketable product sample of approximately 150 g was used. The plant material, after weighing, was placed in a thermoventilated oven at a temperature of 60 °C until reaching the constant weight (about 48 h). The DM was expressed as a percentage of fresh.
Total phenols, total antioxidant activity. For each EU, about 20 g of fresh marketable product were homogenized and subjected to reflux extraction on a water bath (two times in one hour), with methanol (1:5 w/v). After filtration through a Whatmann filter paper, the methanolic extract was concentrated under vacuum and, therefore, used for the determination of TP and TAA. The TP were determined by spectrophotometry with the Folin–Ciocalteu method, as reported by Sergio et al. [20], and expressed as mg CAE (caffeic acid equivalent) g−1 DM. This method exploits the redox reaction in a basic environment between phenolic compounds and the Folin–Ciocalteau reagent. From this reaction, blue complexes of oxides of W8O23 and Mo8O23 are formed. They have a maximum absorption in the visible at about 750 nm. The TAA was determined by means of the analysis of the radical cations ABTS (2,2’-azino-bis-3-ethylbenzothiazolin-6-sulfonic) [21] and expressed as g Trolox 100 g−1 DM.
Nitrates. To carry out the analysis of the Ni (NO3-), a sample of about 10 g of dry biomass was used which was finely ground by means of a mill (IKA, Labortechnik, Staufen, Germany) equipped with a sieve 1 mm. Analyses were performed on a 0.5 g sub-sample, with ion chromatography (Dionex DX120; Dionex Corporation, Sunnyvale, CA, USA), with a conductivity detector, using an IonPack AG14 pre-column and an IonPack separation column AS14 [22]. The Ni concentration was determined based on standards prepared with sodium nitrate (NaNO3).
Total chlorophyll, total carotenoids. For each EU, a sample of about 30 g of leaf blades was finely chopped in a mortar after the addition of liquid nitrogen and, then, stored at −20 °C until use. To carry out the extraction, this material was homogenized with 80% acetone (0.2 g mL−1), kept in a dark cold chamber at 4 °C for 24 h and then centrifuged for 10 min at 14,000 rpm. Three spectrophotometric readings (at 662, 646 and 470 nm) were performed on the recovered supernatant. The method is based on the property of chlorophyll to absorb light in the red zone of the visible spectrum. The absorbance values obtained were then used to calculate TCh and TC concentrations according to Wellburn [23]. All extraction procedures were performed in low light conditions.
Odor and visual appearance. Odor (Od) and visual appearance (VA) were determined by a panel of six judges (three female and three male), aged between 30 and 60, and adequately trained. The judges were selected among 10 potential panelists based on their interest in vegetables and their experience in sensory evaluation. The intensity of the evaluated attributes were quantified on a scale of 1 to 5 [24] where 5 = excellent, without defects; 4 = very good, slight defects; 3 = medium, moderate defects; 2 = poor, serious defects; 1 = not edible. The value of 3 was considered as the marketability limit while 2 was considered as the edibility limit. The assessment was performed in a room with individual booths under normal lighting conditions (ISO/DIS 8589). The samples of each EU and each repetition were subjected to panel analysis in a randomized order.
Chromatic characteristics. On 10 leaves randomly selected for each EU, the chromatic parameters L*, a*, b*, and yellow index (YI) were measured. L* represents the brightness, and the values are in the range 0–100 where 0 = black and 100 = white. a* and b* represents the chromaticity coordinates indicating, respectively, the red-green and yellow-blue components [25]. The YI was obtained by the following equation:
YI = (142.86 b*)/L*
The measurements were carried out with a colorimeter (CR-400, Konica Minolta, Osaka, Japan; using the Spectra Magic NX software), in the apical part of the upper surface of the leaf blade, avoiding the midbird.

2.5. Statistical Analysis

The data collected at each sampling date were subjected to the analysis of variance (ANOVA) according to the split-plot experimental design, using the SPSS 17 software. The comparative analysis between means were based on the F test. Mean values were separated with the Student–Newman–Keuls (SNK) test (P = 0.05).

3. Results

3.1. Effect of Preharvest Treatments on Rocket’s Yield and Quality at Harvest

In Exp 1, a positive effect of the higher N amount on the marketable yield was obtained. In fact, this parameter in NH was on average 11.6% higher than in NL. The application of Azoxystrobin increased marketable yield by 10.1%.
No effect of N and Azo+ treatments on DM and Ni content were observed. The higher N input increased TCh content by 12.8%; on the other hand, TC, TP and TAA decreased on average by 15.4, 11.0 and 18.2%, respectively. With the application of Azo+, TCh and TC, increased by 22.3 and 15.6%, respectively. Azo+ did not affect the phenolic content and antioxidant activity, parameters related to each other, since the latter is predominantly determined by phenols (Table 1).
In Exp 2, as in Exp 1, the highest marketable yield was obtained in the highest N level (+25.7%). Also in this case, Azo+ improved the yield (+ 23.4%), while no effects of YBA+ were manifested.
No effect of N, Azo+ and YBA+ treatments on DM content was observed. The higher N input increased Ni and TCh content by 37.5 and 15.4%, respectively; on the other hand, TC and TAA decreased on average by 7.8 and 26.4%, respectively, as observed in Exp 1. In respect to the control, Azo+ reduced Ni by 17.1% and improved TCh and TC by 15.6 and 10.9%, respectively. On the other hand YBA+ improved TCh by 11.7%, but reduced TAA by about 35.3% (Table 2).

3.2. Effect of Preharvest Treatments on Rocket’s Characteristics during the Shelf-Life

In Exp 1, during the storage period, no significant differences between the nitrogen levels for all the parameters examined were observed. Therefore, the effects of preharvest application of Azoxystrobin will be described below, considering the average values of the two nitrogen levels.
The concentration of oxygen (O2) inside the packages during the storage of the wild rocket was always higher in the samples treated with Azoxystrobin than in the control (Figure 1a) and, correspondingly, the carbon dioxide (CO2) was always lower (Figure 1b).
From the analysis of the qualitative attributes, a positive effect of Azoxystrobin on freshness indicators (VA, Od, YI) is generally highlighted. The VA and Od progressively worsen during storage in both treatments, but with less intensity in Azo+ (Figure 2a,b).
The nonmarketable values of these two indicators are reached 10 days after storage (DAS) in C and 12 DAS in Azo+. The YI also increased more rapidly in the control (Figure 2c). This parameter, in fact, from the beginning of storage to the end, was reduced by 11.0 and 24.1%, respectively for Azo+ and C. TC decreased during storage by 19.1 and 23.3%, respectively for Azo+ and C (Figure 3b).
No significant effects of Azoxystrobin were observed on TP, TAA (Figure 4a,b) and Ni (Figure 5a) during storage. Ni remained unchanged while TP and TAA tended to a slight reduction and a slight increase during storage, respectively.
In Exp 2, similarly to the results of Exp 1, no significant differences were observed in all the parameters examined between the two nitrogen levels during storage. Therefore, the effects of the preharvest application of biostimulants based on Azoxystrobin and the fluid extracts of yeast and brown algae, will be described below, considering the average values of the two nitrogen levels.
From Figure 1c,d, which shows the trend of the O2 and CO2 concentration inside the packages during the wild rocket storage, it can be observed that, as observed in Exp 1, in the Azo+ samples O2 is always maintained higher than in C and, correspondingly, the CO2 is always lower. The biostimulant based on yeast and brown algae extract, on the other hand, did not have any significant effects on the concentration of the two gases (Figure 1c,d).
From the analysis of the qualitative attributes, as in Exp 1, a positive effect of Azoxystrobin on freshness indicators (VA, Od, YI) occurred. The VA and Od progressively worsen during storage in the three treatments. However, the rate of deterioration is lower in Azo+ and higher in YBA+ (Figure 2d,e).
The nonmarketable values of these two indicators reached 13 DAS in C and YBA+ and 16 DAS in Azo+. The YI also increased more rapidly in C and YBA+ (Figure 2f), probably due to the more rapid degradation of chlorophyll. In fact, between the start of storage and the end, the chlorophyll content decreased by 15.7, 27.9 and 36.4% respectively for Azo+, YBA+ and C (Figure 3c). TC also decreased between the beginning and the end of storage period of 14.9, 13.0 and 25.7%, respectively, for Azo+, YBA+ and C (Figure 3d).
During storage, the Ni remained unchanged (Figure 5b) while TP and TAA showed a trend to decrease and increase, respectively (Figure 4c,d). Furthermore, during storage, no significant effects of Azo+ and YBA+ were observed on TP, TAA (Figure 4c,d) and Ni (Figure 5b).

4. Discussion

4.1. Effect of Preharvest Treatments on Wild Rocket’s Yield and Quality at Harvest

For both trials, for all evaluated features the interaction between N levels and use of biostimulating substances was not significant. Regarding the main effects of treatments on rocket’s quality at harvest the results show that total chlorophylls content was higher by using the higher N level as well as by using the biostimulants (Table 1 and Table 2). The yield rose with the increase in the nitrogen dose. These results agree with those obtained on wild rocket [26] and other leafy vegetables [27,28,29]. Azo+ has made a significant contribution to increasing the marketable yield. In addition to the normal fungicidal activity, a biostimulating action of this substance has also been observed in the literature. In support of this, a positive effect of strobilurins on cell proliferation was observed which would favor plant growth, probably linked to the transport of nitrates, iron and sugar [30]. Other authors, on the other hand, have attributed improvement in yield to the increase in chlorophyll [10,31].
The increase in chlorophyll in relation to the rise in the nitrogen level is consistent with the results obtained on wild rocket [7,26], lettuce [12] and spinach [13], as one would expect, since nitrogen is one of the main constituents of the pigment [32].
The application of Azoxystrobin and fluid extracts of yeast and brown algae improved TCh in agreement with others authors who attribute the biostimulating action of strobilurins to the rise in chlorophyll [12,13,31,33], whose biosynthesis is favored by the higher content of cytokinins [34], and by the lower synthesis of ethylene. In fact, the latter hormone is involved in the degradation of pigments and of senescence processes [35]. The application of Azoxystrobin and fluid extracts of yeast and brown algae improved TCh according to numerous authors who attribute the biostimulating action of these substances to the increase in chlorophyll [12,13,31,33], in turn determined by the increase of cytokinins, involved in its biosynthesis [34], and by the reduction of the synthesis of ethylene, a hormone known to be involved in the processes of senescence and degradation of pigments [35].
The phenol content and antioxidant activity decreased with the increase in the amount of N as also observed by others [7,26,36,37].
The increase in the nitrogen level has favored a greater accumulation of nitrates in wild rocket (Exp 2), consistent with the literature data according to which the higher soil N availability it increases the removal by the plant and, therefore, the accumulation of nitrates in the various organs [38,39,40]. This result partially contrasts with the data obtained in Exp 1 which show no effects of the N level on the Ni. This can be explained by the different climatic conditions that occurred before harvesting: during the 3 days prior to the harvest, the weather had been sunny in Exp 1 and cloudy in Exp 2. In fact, the accumulation of nitrates in vegetables can be influenced by various factors including the availability of the nitrogen in the soil, climatic variables, genotype, etc. [2]. The application of Azoxystrobin reduced nitrates in wild rocket plants, consistent with the experimental evidence that Azoxystrobin has a stimulating action on the activity of nitrate reductase, an enzyme involved in nitrogen metabolism [12,13,41]. The results of our study highlight that, although the agronomic management of fertilization has made it possible to obtain a product with a much lower nitrate content than the limits set by the EU regulation (7000 mg/kg FW) [8], Azo+ has made it possible to further reduce the presence of this anion, allowing to have a qualitatively better product, considering that the intake of high levels of nitrate can have negative effects on human health. Azo+ had no effect on phenol content, as also observed on lettuce [12]. Instead, Conversa et al. [13] observed an increase in these compounds in baby leaf spinach.
The increase in chlorophyll determined by YBA+ confirms the findings of other authors, according to which these compounds favor the biosynthesis of chlorophyll and delay its degradation [42,43]. On the contrary, the reduction of TAA and no variation of phenols, due to the effect of YBA+, contrasts with the literature [14].

4.2. Effect of Preharvest Treatments on Rocket’s Characteristics during the Shelf-Life

In both experiments the nitrogen level did not significantly affect the shelf life of the rocket stored in polyethylene packages at 3.5 °C. Bonasia et al. [12] and Conversa et al. [13] instead observed a positive effect of a higher amount of nitrogen on the shelf life of lettuce and spinach. In particular, these authors report that the positive effects caused by the increased availability of N on the chlorophyll content and on the general appearance of the product affect the maintenance of these parameters at satisfactory levels during storage. The preharvest application of Azoxystrobin, in addition to improving the quality characteristics of the wild rocket at the time of harvest, favored a significant extension of the shelf life of the packaged and stored product at 3.5 °C. In particular, during storage, a higher O2 content was found in the Azo+ packages than in C, which corresponded to a lower CO2 content. This suggests that the wild rocket treated with Azoxystrobin had less respiratory activity. The parameter that best highlights the positive effect of Azoxystrobin on the slowing of the senescence process is represented by the chlorophyll, which underwent a slower degradation than the control. This is attributable to the inhibitory effect of ethylene biosynthesis by Azoxystrobin [35], a hormone known to promote the degradation of chlorophyll and the senescence process. The nitrate content did not change during storage in accordance with the results obtained on lettuce [12,44,45]. Although the phenols did not undergo significant changes, the antioxidant activity showed a slight increasing trend. Other authors, on the other hand, report an increase in phenols especially in the last phase of the conservation period [13,21,46]. This increase could be related to the stress caused by storage and wound-like response, thus indicating as such bioactives are the main responsible for antioxidant properties.
As regards the use of biostimulants, our study shows that the use of Azoxystrobin allowed to obtain highest and lowest scores respectively of visual appearance and yellowness index during the shelf life in both experiments (Figure 2a,c,d,f). This, could be due to higher chlorophyll content in samples treated with Azoxystrobin with respect to the control during the shelf life (Figure 3a–c). In this context it is important to highlight that chlorophyll in vegetables is important for the visual appearance of the products [47] if considering that its decrease is associated with cellular degradation and/or senescence, and it is often used to estimate quality loss of green vegetables [48,49]. Indeed, strong relation of chlorophyll content with overall visual quality of vegetables has been reported [50]. Moreover, from a nutritional point of view, it could be considered that chlorophyll is important for its health benefits, since its dietary naturally occurring derivatives showed antioxidant and antimutagenic activity [51,52,53]. Therefore, results of our study suggest that the preharvest application of Azoxystrobin is effective to enhance the quality of wild rocket during storage.

5. Conclusions

The effect of preharvest application of N levels and biostimulating substances based on Azoxystrobin or yeast and algae extract was evaluated in two trials carried out in Southern Italy on wild rocket. The main results showed that rising N availability increased yield and chlorophyll content, while it reduced TC, TP and TAA. Furthermore, the increase in N level led to a greater accumulation of nitrates in the leaves of the wild rocket only when the harvest was preceded by cloudy days. The N level did not affect quality characteristics of the wild rocket during storage.
Azoxystrobin increases yield and improves some qualitative characteristics, such as the increase in chlorophyll and carotenoids, and decrease in nitrates content of wild rocket at harvest, regardless of nitrogen level. In addition, Azoxystrobin increases the shelf life of unwashed wild rocket, packaged in PET trays and wrapped with OPP film, and stored at 3.5 °C. In particular, Azoxystrobin slowed the loss of chlorophyll (yellowing) and the worsening of odor and visual appearance. Therefore, although Azoxystrobin is not included among biostimulants, but is thought of as a fungicide effective for the control of some diseases of wild rocket, its introduction in the phytosanitary defense plan should be promoted, not only for effective disease control but also for the positive complementary physiological, productive, qualitative and shelf life effects.
The biostimulant based on yeast and algae extracts did not affect marketable yield, improved the chlorophyll content at harvest of wild rocket, but reduced its antioxidant activity. It also caused no substantial changes in shelf life except for a slowdown in carotenoids degradation. In consideration of the numerous positive effects of this type of biostimulant on various crops, reported in the literature, further research is desirable to evaluate other variables such as dose and time of application.

Author Contributions

V.C. (Vito Cantore), V.C. (Vincenzo Candido), M.R. and M.P.; methodology, V.C. (Vito Cantore), V.C. (Vincenzo Candido), D.D.V., M.R. and L.S.; software, F.B., D.C. and M.I.S.; validation, V.C. (Vito Cantore) and D.C.; formal analysis F.B., D.C. and M.I.S.; investigation, D.C., M.D., M.R. and M.I.S.; data collection, V.C. (Vincenzo Candido), M.D., D.D.V., M.R., M.I.S. and L.S.; data curation, F.B., V.C. (Vito Cantore), D.C. and M.I.S.; writing—original draft preparation, M.I.S., L.S.; writing—review and editing, F.B., V.C. (Vincenzo Candido), V.C. (Vito Cantore), D.D.V., M.R. and L.S.; supervision, V.C. (Vincenzo Candido); project administration, V.C. (Vincenzo Candido) and M.P.; funding acquisition, V.C. (Vincenzo Candido) and M.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by Research Project PIFOL—Production Chain Integrated Project (PIF)—territorial productive fruit and vegetable sector, Basilicata. PSR Basilicata Region 2007–2013. Misura 124, founded by Basilicata Region.

Data Availability Statement

The data presented in this study are available on request from the corresponding authors.

Acknowledgments

The authors wish to thank Paolo Putignano for technical support, Domenico Genchi for informatic support and Rocco De Ruggieri, owner of the ‘Troyli’ farm, who made available the experimental field, the staff and the equipment for the management of the field trials and the packing of the wild rocket.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Fallovo, C.; Rouphael, Y.; Rea, E.; Battistelli, A.; Colla, G. Nutrient solution concentration and growing season affect yield and quality of Lactuca sativa L. var. acephala in floating raft culture. J. Sci. Food Agric. 2009, 89, 1682–1689. [Google Scholar] [CrossRef]
  2. Bonasia, A.; Lazzizera, C.; Elia, A.; Conversa, G. Nutritional, biophysical and physiological characteristics of wild rocket genotypes as affected by soilless cultivation system, salinity level of nutrient solution and growing period. Front. Plant Sci. 2017, 8, 300. [Google Scholar] [CrossRef] [Green Version]
  3. Hall, M.K.D.; Joblling, J.J.; Rogers, G.S. Influence of storage temperature on the seasonal shelf life of perennial wall rocket and annual garden rocket. Int. J. Veg. Sci. 2013, 19, 83–95. [Google Scholar] [CrossRef]
  4. Martínez-Sánchez, A.; Allende, A.; Cortes-Galera, I.; Gil, M.I. Respiration rate response of four baby leaf Brassica species to cutting at harvest and fresh cut washing. Postharvest Biol. Technol. 2008, 47, 382–388. [Google Scholar] [CrossRef]
  5. Martínez-Sánchez, A.; Luna, M.C.; Selma, M.V.; Tudela, J.A.; Abad, J.; Gil, M.I. Baby-leaf and multi-leaf of green and red lettuces are suitable raw materials for the fresh-cut industry. Postharvest Biol. Technol. 2012, 63, 1–10. [Google Scholar] [CrossRef]
  6. Cantwell, M.; Rovelo, J.; Nie, X.; Rubatzky, V. Specialty salad greens: Postharvest physiology and shelf-life. Acta Hortic. 1998, 467, 371–377. [Google Scholar] [CrossRef]
  7. Candido, V.; Boari, F.; Cantore, V.; Castronuovo, D.; Di Venere, D.; Perniola, M.; Sergio, L.; Viggiani, R.; Schiattone, M.I. In-teractive effect of nitrogen and Azoxystrobin on yield, quality, nitrogen and water use efficiency of wild rocket in Southern Italy. Agronomy 2020, 10, 849. [Google Scholar] [CrossRef]
  8. EC. Regulation (EU) December 2011 amending Regulation (EC) No. 1881/as regards maximum levels for nitrates in foodstuffs. Off. J. Eur. Union L. 2011, 320, 15–17. [Google Scholar]
  9. Amaro, A.C.E.; Baron, D.; Ono, E.O.; Rodrigues, J.D. Physiological effects of strobilurin and carboxamides on plants: An overview. Acta Physiol. Plant. 2020, 42, 4. [Google Scholar] [CrossRef]
  10. Boari, F.; Cantore, V.; Di Venere, D.; Sergio, L.; Candido, V.; Schiattone, M.I. Pyraclostrobin can mitigate salinity stress in tomato crop. Agric. Water Manag. 2019, 222, 254–264. [Google Scholar] [CrossRef]
  11. Venancio, W.S.; Rodrigues, M.A.T.; Begliomini, E.; de Souza, N.L. Physiological effects of strobilurin fungicides on plants. UEPG Ciência Exatas Terra Ciênc. Agrar. Eng. Ponta Grossa 2003, 9, 59–68. [Google Scholar]
  12. Bonasia, A.; Conversa, G.; Lazzizzera, C.; Elia, A. Pre-harvest nitrogen and Azoxystrobin application enhances postharvest shelf-life in Butterhead lettuce. Postharvest Biol. Technol. 2013, 85, 67–76. [Google Scholar] [CrossRef]
  13. Conversa, G.; Bonasia, A.; Lazzizzera, C.; Elia, A. Pre-harvest nitrogen and Azoxystrobin application enhances raw product quality and post-harvest shelf-life of baby spinach (Spinacia oleracea L.). J. Sci. Food Agric. 2014, 94, 3263–6272. [Google Scholar] [CrossRef] [PubMed]
  14. Battacharyya, D.; Babgohari, M.Z.; Rathor, P.; Prithiviraj, B. Seaweed extracts as biostimulants in horticulture. Sci. Hortic. 2015, 196, 39–48. [Google Scholar] [CrossRef]
  15. Ronga, D.; Biazzi, E.; Parati, K.; Carminati, D.; Carminati, E.; Tava, A. Microalgal biostimulants and biofertilisers in crop productions. Agronomy 2019, 9, 192. [Google Scholar] [CrossRef] [Green Version]
  16. Campobenedetto, C.; Agliassa, C.; Mannino, G.; Vigliante, I.; Contartese, V.; Secchi, F.; Bertea, C.M. A biostimulant based on seaweed (Ascophyllum nodosum and Laminaria digitata) and yeast extracts mitigates water stress effects on tomato (Solanum lycopersicum L.). Agriculture 2021, 11, 557. [Google Scholar] [CrossRef]
  17. Drobek, M.; Fraç, M.; Cybulska, J. Plant Biostimulants: Importance of the Quality and Yield of Horticultural Crops and the Improvement of Plant Tolerance to Abiotic Stress—A Review. Agronomy 2019, 9, 335. [Google Scholar] [CrossRef] [Green Version]
  18. Cassi, F.; Viviano, L. I Suoli della Basilicata-Carta pedologica della Regione Basilicata in scala 1:250.000. In The Soils of Basilica-ta-Soil Map of the Basilicata Region in Scale 1:250,000; Reg. Basilicata-Dip. Agric. Svilup. Rurale. Dir. Gen.: Potenza, Italy, 2006; 343p. [Google Scholar]
  19. Cantore, V.; Iovino, F.; Pontecorvo, G. Aspetti climatici e zone fitoclimatiche della Basilicata. In Climatic Aspects and Phytoclimatic Zones of Basilicata; CNR-IEIF: Cosenza, Italy, 1987; Volume 2, 49p. [Google Scholar]
  20. Sergio, L.; Boari, F.; Pieralice, M.; Linsalata, V.; Cantore, V.; Di Venere, D. Bioactive phenolics and antioxidant capacity of some wild edible greens as affected by different cooking treatments. Foods 2020, 9, 1320. [Google Scholar] [CrossRef]
  21. Sergio, L.; Gonnella, M.; Renna, M.; Linsalata, V.; Gatto, M.A.; Boari, F.; Di Venere, D. Biochemical traits of asparagus cultivars and quality changes in two differently coloured genotypes during cold storage. LWT 2019, 101, 427–434. [Google Scholar] [CrossRef]
  22. Bonasia, A.; Conversa, G.; Gonnella, M.; Serio, F.; Santamaria, P. Effects of ammonium and nitrate nutrition on yield and quality in endive. J. Hortic. Sci. Biotechnol. 2008, 83, 64–70. [Google Scholar] [CrossRef]
  23. Wellburn, A.R. The spectral determination of chlorophyll a and chlorophyll b, as well as total carotenoids, using various solvents with spectrophotometers of different resolution. J. Plant Physiol. 1994, 144, 307–313. [Google Scholar] [CrossRef]
  24. Amodio, M.L.; Derossi, A.; Mastrandrea, L.; Colelli, G. A study of the estimated shelf life of fresh rocket using a non-linear model. J. Food Eng. 2015, 150, 19–28. [Google Scholar] [CrossRef]
  25. CIE. Colorimetry, 2nd ed.; Central Bureau of the Commission Internationale the L’Eclairage: Vienne, France, 1986. [Google Scholar]
  26. Schiattone, M.I.; Viggiani, R.; Di Venere, D.; Sergio, L.; Cantore, V.; Todorovic, M.; Perniola, M.; Candido, V. Impact of irrigation regime and nitrogen rate on yield, quality and water use efficiency of wild rocket under greenhouse conditions. Sci. Hortic. 2018, 229, 182–192. [Google Scholar] [CrossRef]
  27. Sharma, L.K.; Bali, S.K. A review of methods to improve nitrogen use efficiency in agriculture. Sustainability 2018, 10, 51. [Google Scholar] [CrossRef] [Green Version]
  28. Wang, Z.; Li, S. Effects of nitrogen and phosphorus fertilization on plant growth and nitrate accumulation in vegetables. J. Plant Nutr. 2004, 27, 539–556. [Google Scholar] [CrossRef]
  29. Zhang, J.; Sha, Z.; Zhang, Y.; Bei, Z.; Cao, L. The effects of di_erent water and nitrogen levels on yield, water and nitrogen utilization effciencies of spinach (Spinacia oleracea L.). Can. J. Plant Sci. 2015, 95, 671–679. [Google Scholar] [CrossRef]
  30. van Dingenen, J.; Antoniou, C.; Filippou, P.; Pollier, J.; Gonzalez, N.; Dhondt, S.; Goossens, A.; Fotopoulos, V.; Inzé, D. Strobilurins as growth-promoting compounds: How Stroby regulates Arabidopsis leaf growth. Plant Cell Environ. 2017, 40, 1748–1760. [Google Scholar] [CrossRef]
  31. Liang, S.; Xu, X.; Lu, Z. Effect of Azoxystrobin fungicide on the physiological and biochemical indices and ginsenoside contents of ginseng leaves. J. Ginseng Res. 2018, 42, 175–182. [Google Scholar] [CrossRef] [PubMed]
  32. Taiz, L.; Zeiger, E. Plant Physiology; The Benjamin/Cummings Publishing Company, Inc.: Redwood City, CA, USA; Berlin, Germany, 2002; 675p. [Google Scholar]
  33. Chbani, A.; Majed, S.; Mawlawi, H.; Kammoun, M. The use of seaweed as a bio-fertilizer: Does it influence Proline and Chlorophyll concentration in plants treated? Arab. J. Med. Aromat. Plants 2015, 1, 67–77. [Google Scholar]
  34. Sundqvist, C.; Bjorn, L.O.; Virgin, H.I. Factors in chloroplast differentiation. In Results and Problems in Cell Differentiation—Chloroplast; Reinert, J., Heidelberg, D.E., Eds.; Springer: Berlin/Heidelberg, Germany, 1980; pp. 202–224. [Google Scholar]
  35. Abeles, G.B.; Morgan, P.W.; Saltveit, M.E. Ethylene in Plant Biology; Academic Press: San Diego, CA, USA, 1982. [Google Scholar]
  36. Koyama, R.; Itoh, H.; Kimura, S.; Morioka, A.; Uno, Y. Augmentation of antioxidant constituents by drought stress to roots in leafy vegetables. HortTecnology 2012, 22, 121–125. [Google Scholar] [CrossRef] [Green Version]
  37. Luoh, J.W.; Begg, C.B.; Symonds, R.C.; Ledesma, D.; Yang, R.-Y. Nutritional yield of african indigenous vegetables in wa-ter-deficient and water-sufficient conditions. Food Nutr. Sci. 2014, 5, 812–822. [Google Scholar]
  38. Devienne-Barret, F.; Justes, E.; Machet, J.M.; Mary, B. Integrated control of nitrate uptake by crop growth rate and soil nitrate availability under field conditions. Ann. Bot. 2000, 86, 995–1005. [Google Scholar] [CrossRef] [Green Version]
  39. Chen, B.-M.; Wang, Z.-H.; Li, S.-X.; Wang, G.-X.; Song, H.-X.; Wang, X.-N. Effects of nitrate supply on plant growth, nitrate accumulation, metabolic nitrate concentration and nitrate reductase activity in three leafy vegetables. Plant Sci. 2004, 167, 635–643. [Google Scholar] [CrossRef]
  40. Weightman, R.M.; Huckle, A.J.; Roques, S.E.; Ginsburg, D.; Dyer, C.J. Factors influencing tissue nitrate concentration in field-grown wild rocket (Diplotaxis tenuifolia) in southern England. Food Addit. Contam. Part A 2012, 29, 1425–1435. [Google Scholar] [CrossRef]
  41. Joshi, J.; Sharma, S.; Guruprasad, K.N. Foliar application of Pyraclostrobin fungicide enhances the growth, rhizobial-nodule formation and nitrogenase activity in soybean (var. JS-335). Pestic. Biochem. Physiol. 2014, 114, 61–66. [Google Scholar] [CrossRef]
  42. Abd El-Baky, H.H.; Hussein, M.M.; El-Baroty, G.S. Algal extracts improve antioxidant defense abilities and salt tolerance of wheat plant irrigated with sea water. Afr. J. Biochem. Res. 2008, 2, 151–164. [Google Scholar]
  43. Jannin, L.; Arkoun, M.; Etienne, P.; Laîné, P.; Goux, D.; Garnica, M.; Fuentes, M.; Francisco, S.S.; Baigorri, R.; Cruz, F.; et al. Brassica napus growth is promoted by Ascophyllum nodosum (L.) Le Jol. seaweed extract: Microarray analysis and physiological characterization of N, C, and S me-tabolisms. J. Plant Growth Regul. 2013, 32, 31–52. [Google Scholar] [CrossRef]
  44. Siomos, A.S.; Papadopoulou, P.P.; Dogras, C.C.; Vasiliadis, E.; Dosas, A.; Georgiou, N. Lettuce composition as affected by genotype and leaf position. Acta Hortic. 2002, 579, 635–639. [Google Scholar] [CrossRef]
  45. Konstantopoulou, E.; Kapotis, G.; Salachas, G.; Petropoulos, S.A.; Karapanos, I.C.; Passam, H.C. Nutritional quality of greenhouse lettuce at harvest and after storage in relation to N application and cultivation season. Sci. Hortic. 2010, 125, 93–94. [Google Scholar] [CrossRef]
  46. Fukumoto, L.R.; Toivonen, P.M.A.; Delaquis, P.J. Effect of wash water temperature and chlorination on phenolic metabolism and browning of stored iceberg lettuce photosynthetic vascular tissues. J. Agric. Food Chem. 2002, 50, 4503–4511. [Google Scholar] [CrossRef]
  47. Bulgari, R.; Baldi, A.; Ferrante, A.; Lenzi, A. Yield and quality of basil, Swiss chard, and rocket microgreens grown in a hy-droponic system. New Zeal. J. Crop. Hortic. Sci. 2017, 45, 119–129. [Google Scholar] [CrossRef]
  48. Hodges, D.M.; Forney, C.F.; Wismer, W. Processing Line Effects on Storage Attributes of Fresh-cut Spinach Leaves. HortScience 2000, 35, 1308–1311. [Google Scholar] [CrossRef] [Green Version]
  49. Toivonen, P.M.A.; Sweeney, M. Differences in Chlorophyll Loss at 13 °C for Two Broccoli (Brassica oleracea L.) Cultivars As-sociated with Antioxidant Enzyme Activities. J. Agric. Food Chem. 1998, 46, 20–24. [Google Scholar] [CrossRef]
  50. Aguero, M.V.; Barg, M.V.; Yommi, A.; Camelo, A.; Roura, S.I. Postharvest changes in water status and chlorophyll content of lettuce (Lactuca sativa L.) and their relationship with overall visual quality. J. Food Sci. 2008, 73, S47–S55. [Google Scholar] [CrossRef] [PubMed]
  51. Hsu, C.Y.; Chen, Y.H.; Chao, P.Y.; Chen, C.M.; Hsiehm, L.L.; Hu, S.P. Naturally occurring chlorophyll derivatives inhibit aflatoxin B1-DNA adduct formation in hepatoma cells. Mutat Res.—Genet. Toxicol. Environ. Mutagen. 2008, 657, 98–104. [Google Scholar] [CrossRef]
  52. Ferruzzi, M.G.; Bohm, V.; Courtney, P.D.; Schwartz, S.J. Antioxidant and antimutagenic activity of dietary chlorophyll deri-vates determined by radical scavenging and bacterial reverse mutagenesis assays. J. Food Sci. 2002, 67, 2589–2595. [Google Scholar] [CrossRef]
  53. Ferruzzi, M.G.; Blakeslee, J. Digestion, absorption, and cancer preventative activity of dietary chlorophyll derivatives. Nutr. Res. 2007, 27, 1–12. [Google Scholar] [CrossRef]
Agronomy 11 02326 g001 550
Figure 1. And carbon dioxide (CO2) concentration trend inside the packages during the storage of the wild rocket treated with Azoxystrobin (Azo+) at preharvest in Exp 1 (a,b), and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (c,d), and of that relating to the untreated control (C). Vertical bars indicate SD (n = 3). ns, * and ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (P = 0.05). Different lower case letter denotes significant differences.
Figure 1. And carbon dioxide (CO2) concentration trend inside the packages during the storage of the wild rocket treated with Azoxystrobin (Azo+) at preharvest in Exp 1 (a,b), and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (c,d), and of that relating to the untreated control (C). Vertical bars indicate SD (n = 3). ns, * and ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (P = 0.05). Different lower case letter denotes significant differences.
Agronomy 11 02326 g001
Agronomy 11 02326 g002 550
Figure 2. Trend of the visual appearance, odor and yellow index during the storage of the wild rocket treated with Azoxystrobin (Azo +) at preharvest in Exp 1 (a–c), and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (d–f), and of that relating to the untreated control (C). Vertical bars indicate SD (n = 3). ns, * and ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (P = 0.05). Different lower case letter denotes significant differences.
Figure 2. Trend of the visual appearance, odor and yellow index during the storage of the wild rocket treated with Azoxystrobin (Azo +) at preharvest in Exp 1 (a–c), and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (d–f), and of that relating to the untreated control (C). Vertical bars indicate SD (n = 3). ns, * and ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (P = 0.05). Different lower case letter denotes significant differences.
Agronomy 11 02326 g002
Agronomy 11 02326 g003 550
Figure 3. Trend of total chlorophyll (TCh) and total carotenoid (TC) content during the storage of the wild rocket treated with Azoxystrobin (Azo +) at preharvest in Exp 1 (a,b), and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (c,d), and of that relating to the untreated control (C). DM = dry matter. Vertical bars indicate SD (n = 3). ns, * and ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (P = 0.05). Different lower case letter denotes significant differences.
Figure 3. Trend of total chlorophyll (TCh) and total carotenoid (TC) content during the storage of the wild rocket treated with Azoxystrobin (Azo +) at preharvest in Exp 1 (a,b), and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (c,d), and of that relating to the untreated control (C). DM = dry matter. Vertical bars indicate SD (n = 3). ns, * and ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (P = 0.05). Different lower case letter denotes significant differences.
Agronomy 11 02326 g003
Agronomy 11 02326 g004 550
Figure 4. Trend of the nitrate content (Ni), total phenols (TP) and antioxidant activity (TAA) during the storage of the wild rocket (a,b) and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (c,d), and of that relating to the untreated control (C). DM = dry matter. Vertical bars indicate SD (n = 3). ns, ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (P = 0.05). Different lower case letter denotes significant differences.
Figure 4. Trend of the nitrate content (Ni), total phenols (TP) and antioxidant activity (TAA) during the storage of the wild rocket (a,b) and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (c,d), and of that relating to the untreated control (C). DM = dry matter. Vertical bars indicate SD (n = 3). ns, ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (P = 0.05). Different lower case letter denotes significant differences.
Agronomy 11 02326 g004
Agronomy 11 02326 g005 550
Figure 5. Trend of the nitrate content during the storage of the wild rocket treated with Azoxystrobin (Azo +) at preharvest in Exp 1 (a), and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (b), and of that relating to the untreated control (C). FW = fresh weight. Vertical bars indicate SD (n = 3). ns, * indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (Taiz, L.; Zeiger, E. Plant Physiology; The Benjamin/Cummings Publishing Company, Inc., 2002; 675p = 0.05). Different lower case letter denotes significant differences.
Figure 5. Trend of the nitrate content during the storage of the wild rocket treated with Azoxystrobin (Azo +) at preharvest in Exp 1 (a), and with Azoxystrobin or an algae-based biostimulant (YBA+) in Exp 2 (b), and of that relating to the untreated control (C). FW = fresh weight. Vertical bars indicate SD (n = 3). ns, * indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Separation of mean within the days from the start of storage by SNK test (Taiz, L.; Zeiger, E. Plant Physiology; The Benjamin/Cummings Publishing Company, Inc., 2002; 675p = 0.05). Different lower case letter denotes significant differences.
Agronomy 11 02326 g005
Table
Table 1. Effects of N level (NL) and Azoxystrobin (Azo) application on marketable yield (MY), leaf dry matter (DM), nitrate (Ni), total phenols (TP), total antioxidant activity (TAA), total chlorophyll (TCh) and total carotenoids (TC) of wild rocked at harvest time. C = control without Azoxystrobin, Azo+ = with Azoxystrobin; NL = 24 kg ha−1 of N, NH = 84 kg ha−1 of N; FW = fresh weight.
Table 1. Effects of N level (NL) and Azoxystrobin (Azo) application on marketable yield (MY), leaf dry matter (DM), nitrate (Ni), total phenols (TP), total antioxidant activity (TAA), total chlorophyll (TCh) and total carotenoids (TC) of wild rocked at harvest time. C = control without Azoxystrobin, Azo+ = with Azoxystrobin; NL = 24 kg ha−1 of N, NH = 84 kg ha−1 of N; FW = fresh weight.
TreatmentsMYDMNiTPTAATChTC
(kg m−2)(g 100 g−1 FW)(mg kg−1 FW)(mg CAE g−1 DM)(g Trolox 100 g−1 DM)(μg g−1 DM)(μg g−1 DM)
N level (NL)*nsns*****
NL1.478.64398.014.50.43825.6175.2
NH1.648.64374.412.90.35931.8147.7
Azoxystrobin (Azo)*nsnsnsns***
C1.488.54438.113.60.40790.7149.8
Azo+1.638.74334.713.80.38966.7173.1
NL x Azonsnsnsnsnsnsns
ns, * and ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively.
Table
Table 2. Effects of N level (NL) and biostimulant (BS) (Azoxystrobin, Azo+; extracts of yeast and brown algae, YBA+) application on marketable yield (MY), leaf dry matter (DM), nitrate (Ni), total phenols (TP), total antioxidant activity (TAA), total chlorophyll (TCh) and total carotenoids (TC) of wild rocket at harvest time. C = control without biostimulant, Azo+ = with Azoxystrobin; YBA+ = with extracts of yeast and brown algae; NL = 32 kg ha−1 of N, NH = 112 kg ha−1 of N; FW = fresh weight.
Table 2. Effects of N level (NL) and biostimulant (BS) (Azoxystrobin, Azo+; extracts of yeast and brown algae, YBA+) application on marketable yield (MY), leaf dry matter (DM), nitrate (Ni), total phenols (TP), total antioxidant activity (TAA), total chlorophyll (TCh) and total carotenoids (TC) of wild rocket at harvest time. C = control without biostimulant, Azo+ = with Azoxystrobin; YBA+ = with extracts of yeast and brown algae; NL = 32 kg ha−1 of N, NH = 112 kg ha−1 of N; FW = fresh weight.
TreatmentsMYDMNiTPTAATChTC
(kg m−2)(g 100 g−1 FW)(mg kg−1 FW)(mg CAE g−1 DM)(g Trolox 100 g−1 DM)(μg g−1 DM)(μg g−1 DM)
N level (NL)*ns**ns***
NL1.368.73200.114.80.53779.8192.3
NH1.718.24399.913.90.39900.2176.7
Biostimulants (BS)**ns*ns***
C1.41 b8.74100.0 a14.20.51 a771.2 b175.4 b
Azo+1.74 a8.43400.5 b14.90.54 a889.4 a194.0 a
YBA+1.46 b8.53899.5 a14.00.33 b859.2 a184.6 ab
NL x BSnsnsnsnsnsnsns
ns, * and ** indicate F test not significant, significant at P ≤ 0.05 and significant at P ≤ 0.01, respectively. Mean separation within columns by SNK test (P = 0.05).
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Schiattone, M.I.; Boari, F.; Cantore, V.; Castronuovo, D.; Denora, M.; Di Venere, D.; Perniola, M.; Renna, M.; Sergio, L.; Candido, V. Effects of Nitrogen, Azoxystrobin and a Biostimulant Based on Brown Algae and Yeast on Wild Rocket Features at Harvest and During Storage. Agronomy 2021, 11, 2326. https://doi.org/10.3390/agronomy11112326

AMA Style

Schiattone MI, Boari F, Cantore V, Castronuovo D, Denora M, Di Venere D, Perniola M, Renna M, Sergio L, Candido V. Effects of Nitrogen, Azoxystrobin and a Biostimulant Based on Brown Algae and Yeast on Wild Rocket Features at Harvest and During Storage. Agronomy. 2021; 11(11):2326. https://doi.org/10.3390/agronomy11112326

Chicago/Turabian Style

Schiattone, Maria Immacolata, Francesca Boari, Vito Cantore, Donato Castronuovo, Michele Denora, Donato Di Venere, Michele Perniola, Massimiliano Renna, Lucrezia Sergio, and Vincenzo Candido. 2021. "Effects of Nitrogen, Azoxystrobin and a Biostimulant Based on Brown Algae and Yeast on Wild Rocket Features at Harvest and During Storage" Agronomy 11, no. 11: 2326. https://doi.org/10.3390/agronomy11112326

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop