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Article

Chitosan Reduces Damages of Strawberry Seedlings under High-Temperature and High-Light Stress

by
Erting Fu
1,2,
Yuzheng Zhang
1,2,
Huiling Li
1,2,
Xiaozhe Wang
1,2,
Hanxiao Zhang
1,2,
Wei Xiao
1,2,
Xiude Chen
1,2,* and
Ling Li
1,2,*
1
College of Horticulture Science and Engineering, Shandong Agricultural University, Taian 271018, China
2
State Key Laboratory of Crop Biology, Taian 271018, China
*
Authors to whom correspondence should be addressed.
Agronomy 2023, 13(2), 517; https://doi.org/10.3390/agronomy13020517
Submission received: 11 December 2022 / Revised: 3 February 2023 / Accepted: 8 February 2023 / Published: 10 February 2023
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Abstract

:
High-temperature and high-light are the main adversity stresses faced by strawberry seedlings and open-field cultivation in summer. Chitosan (CTS) is widely used in agriculture as a soil amendment, plant growth regulator, and promoter of cold resistance. However, the effects of CTS on strawberry seedlings under the combined stress of high-temperature and high-light are unclear. This study aimed to determine the effect of CTS on strawberry seedlings under the combined stress of high-temperature and high-light. In this study, Xuelixiang strawberry was used as the experimental plant material. The leaves were sprayed with 100 mg/Kg CTS or deionized aqueous solution and placed under high-temperature and high-light (38 °C, 1800 μ mol·m−2·s−1, respectively) for 8 h. In addition, a suitable temperature and light (23 °C, 400 μ mol·m−2·s−1, respectively) was sprayed with deionized water as a control. The results showed that compared with non-CTS treatment, the chlorophyll (Chl) content in strawberry plants increased by 16.9% after CTS treatment; the net CO2 exchange (Pn) increased by 74.9%; and the maximum photochemical efficiency increased by 20.1%. In addition, CTS treatment increased the content of antioxidants; increased osmotic adjustment substances; improved the activity of reduced glutathione with reduced ascorbic acid (AsA-GSH) circulating antioxidant enzymes; removed reactive oxygen species in plants in time; and reduced the damage of reactive oxygen species to photosynthetic organs and cell membranes, thereby reducing high-temperature and high-light injury to strawberry seedlings. This study shows that CTS can improve the negative effects of high-temperature and high-light stress on strawberry seedlings.

1. Introduction

Strawberry (Fragaria × ananassa Duch.) is a perennial herbaceous fruit tree species belonging to the Rosaceae family, and it is an economically important crop species that is widely cultivated worldwide [1]. According to the statistics of the Chinese Horticultural Society, the total planting area of strawberry plants in China is approximately 133,400 hectares; the total output is 2 million tons, which ranks first in the world in both total area and total output [2]. High-quality strawberry seedlings are the basis for high yield, and the quality of seedlings directly affects the yield [3]. At present, domestic strawberry seedlings are generally grown in the open field, and seedlings are generally grown in May–July and transplanted in mid-July to August. When growing strawberry seedlings and cultivating them in open fields, the light intensity often exceeds 1800 μmol·m−2·s−1, far exceeding the saturation light intensity of strawberry plants (approximately 600 μ mol·m−2·s−1), which is likely to cause photoinhibition because of excess light energy [4]. Under natural conditions, high light is often accompanied by high-temperature, and high-temperature can aggravate the degree of photoinhibition induced by high-light [5].
Photoinhibition is a phenomenon in which the photosynthesis rate and photosynthesis efficiency are reduced when the light energy captured by the light-harvesting pigment proteins of green plants exceeds the amount used by the photosynthetic mechanism; this phenomenon is manifested mainly in a reduction of the net photosynthesis rate (Pn), photochemical efficiency, and quantum efficiency. The main site of photoinhibition is photosystem II (PSII) [6,7]. Both P+680 and 1O2 produced by PSII after being inhibited by light are strong oxidants that can oxidize and disrupt nearby chlorophyll (Chl) and D1 proteins, causing permanent damage to photosynthetic organs and a decrease in photosynthesis, eventually leading to plant death [8]. To resist high-temperature and high-light stress, plants have evolved a protective defense mechanism to avoid the effects of photoinhibition and reduce photooxidative damage, such as increasing the photosynthesis rate and the activity of the reactive-oxygen-species-scavenging system [9].
The chemical name of chitosan (CTS) is poly-N-acetylglucosamine, and it is generally referred to as polyglucosamine. CTS is the product of the deacetylation of the natural polysaccharide chitin, which is quite abundant and ranks second in terms of the Earth’s renewable resources [10]. Owing to its nontoxicity, biocompatibility, broad-spectrum antibacterial properties, and permeability-enhancing properties, CTS has been widely used in agriculture as a soil amendment, plant growth regulator, and promoter of cold resistance [11]. Studies have shown that CTS can improve the cold resistance of rice seedlings [12] and promote rice seed germination and seedling growth under salt-stress conditions [13]. Wang et al. [14] pointed out that exogenous CTS can reduce the malondialdehyde (MDA) content; increase the contents of Chl, proline and soluble protein; enhance the activity of antioxidant enzymes; and alleviate the damage to cucumber seedlings under high-temperature stress. However, the role of CTS in the response to high-temperature stress and high-light stress combined has not been reported, and its effect on strawberry under high-temperature stress and high-light stress combined is still unclear.
In this study, Xuelixiang strawberry was used as the experimental plant material, and 100 mg·kg−1 CTS solution was sprayed onto the leaves. Relevant indicators such as strawberry Chl content, membrane peroxidation, reactive oxygen species content, antioxidant enzyme content, and AsA-GSH cycle activity were determined under the combined stress of high-temperature and high-light, and the role of exogenous CTS in the process of strawberry resistance to high-temperature and high-light stress was studied. The mechanism associated with the resulting physiological and biochemical effects provides a theoretical basis for reducing the damage caused by high-temperature and high-light stress in the production of strawberry seedlings. To our knowledge, this is the first study of the effect of CTS on strawberry seedlings under high-temperature and high-light compound stress.

2. Materials and Methods

2.1. Materials and Design

In this study, Xuelixiang strawberry was used as the experimental plant variety and cultivated in the Innovation Park of Shandong Agricultural University. Three-leaf, one-hearted seedlings were selected for the study. The CTS treatment involved foliar spraying of a CTS (the concentration was 100 mg·kg−1; preliminary tests were conducted to select the optimum spraying concentration) solution, and leaf sprayed with deionized water as the control treatment. Each treatment included 28 strawberry seedlings, and the treatments were replicated three times. The plants were sprayed once a day at 5:00 p.m. for three consecutive days, spraying 50 mL of each plant; placed in an incubator (23 °C and 400 μmol·m−2·s−1) for 12 h; and then subjected to a high-temperature and high-light stress treatment (through preliminary experimental screenings, it was determined that the high-temperature stress and high-light stress consisted of 38 °C + 1800 μmol·m−2·s−1, respectively). Serving as controls, plants were sprayed deionized water and grown under a suitable temperature and light (23 °C + 400 μmol·m−2·s−1). Fresh leaves of strawberry seedlings were taken at six time periods, namely, 0 h, 0.5 h, 1 h, 2 h, 4 h, and 8 h after treatment; frozen in liquid nitrogen; and stored at −80 °C.

2.2. Determination Indicators and Methods

2.2.1. Chl Content Determination

Using the ethanol extraction method [15], we extracted 0.2 g of strawberry leaves in 20 mL of 95% ethanol for 24 h. The absorbance at 665 and 649 nm was subsequently measured using a UV-2600 spectrophotometer (Daojin, Suzhou, China) and substituted into formulas to calculate the Chl content.

2.2.2. Determination of Gas Exchange Parameters and Chl Fluorescence Parameters

Using a CIRAS-3 portable photosynthetic system (PP-Systems, Amesbury, MA, USA), we selected five similarly growing leaves to measure the Pn, intercellular carbon dioxide concentration (Ci), stomatal conductance (gs), and transpiration rate (E). In addition, using an FMS-2 portable pulse-modulated fluorometer (Hansatech, UK), we selected five similarly growing leaves, and the initial fluorescence (Fo), maximum fluorescence (Fm), and maximum photochemical efficiency (Fv/Fm) were measured; the leaves were sufficiently allowed to adapt to the dark for 30 min prior to the measurements.

2.2.3. Tissue Staining and Determination of the Contents of H2O2 and O2−

Tissues were stained for H2O2 and O2− using 1% 3,3′-diaminobenzidine (DAB) and 0.5% nitro blue tetrazolium (NBT), respectively, according to the methods of Tao et al. [16]. The H2O2 content was determined according to the methods of Lin et al. [17]. We extracted 0.5 g of fresh leaves of strawberry, to which acetone was added. The material was then ground into a slurry and centrifuged at 3000 r/min for 10 min. Afterward, 1 mL of supernatant was removed, and 0.1 mL of 5% titanium sulfate and 0.2 mL of concentrated ammonia in H2O were added. The material was subsequently centrifuged at 3000 r/min for 10 min. After the precipitate formed, the supernatant was discarded. The plant pigments were then removed with acetone, after which, 5 mL of 2 mol/L sulfuric acid and 10 mL of deionized H2O were added. The absorption value of the reaction solution at a wavelength of 415 nm was then measured, and the corresponding H2O2 content was calculated according to a known H2O2 curve. A kit (Geruisi, Suzhou, China) was used to measure the O2− content.

2.2.4. Determination of the Proline Content

The proline content was determined by the acid ninhydrin method [18]. We extracted 0.5 g together with 5 mL of 3% sulfosalicylic acid, which were ground into a slurry. After extraction in boiling water for 10 min, 2 mL of the supernatant was collected. Afterward, 2 mL of glacial acetic acid and 3 mL of 5% ninhydrin chromogenic solution were added, and 5 mL of toluene was added after the material was incubated in a 100 °C water bath for 40 min. The supernatant was collected after layering, and the absorption value of the reaction solution was measured at a wavelength of 520 nm according to proline standards. The corresponding proline concentration was calculated according to the curve.

2.2.5. Determination of the Relative Conductivity

The relative conductivity was determined according to the methods of Zhang [19]. We extracted 0.5 g of fresh leaves were obtained and then immersed in deionized water for 12 h. R1 was subsequently measured with a conductivity meter, and R2 was measured after 30 min in boiling water. The relative conductivity was calculated as R1/R2·100%

2.2.6. Determination of the Malondialdehyde (MDA) Content

The MDA content was determined by the thiobarbituric acid method [20]. After plant material was added to 10 mL of 50 mol/L phosphate buffer solution (pH = 8; including 1% polyvinylpyrrolidone (PVP), 0.1 mM EDTA, and 1% Triton X-100), the mixture was ground to a slurry in an ice bath and then centrifuged at 12,000 rpm at 4 °C for 10 min, after which the supernatant was collected. Then, 1.5 mL of enzyme solution was added to 2.5 mL of TCA-TBA reaction solution, which was then boiled in water for 15 min and centrifuged at 4800 rpm for 10 min after cooling. The absorbance was measured at wavelengths of 532 nm and 600 nm, after which the values were substituted into the formula to calculate the MDA content.

2.2.7. AsA and GSH Contents and Determination of the AsA/DHA GSH/GSSG Ratios

The contents of AsA, GSH, oxidized ascorbic acid (DHA), and oxidized glutathione (GSSG) were determined using kits (Geruisi, Suzhou, China).

2.2.8. Determination of AsA-GSH Cycle-Related Enzyme Activities

The activities of ascorbate peroxidase (APX), glutathione reductase (GR), monodehydroascorbate reductase (MDHAR), and dechlorascorbate reductase (DHAR) were determined using kits (Geruisi, Suzhou, China).

2.3. Statistics and Data Analysis

The means of three replications of the above indicators were determined and collated using Excel. SPSS 24 was used to perform univariate significant ANOVA (p < 0.05), and Prism was used to construct the charts.

3. Results

3.1. Effect of CTS on Chl Content

As shown in Figure 1, high-temperature and high-light stress significantly affected the Chl content of strawberry leaves, and the Chl content increased sharply after 0.5 h of stress treatment but decreased slowly after 1–8 h. However, CTS-treated plants showed significant mitigation under stress. At 8 h of treatment, the Chl content was increased by 16.9% in CTS treatment compared with non-CTS treatment.

3.2. Effect of CTS Treatment on Gas Exchange Parameters

After high-temperature and high-light stress, the Pn of each treatment first increased and then decreased. At 8 h, the CTS treatment increased the Pn value by 74.9% compared to the non-CTS treatment (Figure 2a). After stress, Ci in the CTS treatment first decreased and then increased, and the rise was significantly slower than that in the non-CTS treatment (Figure 2b); gs was similar to the change trend of E, showing a downward trend with the prolongation of stress time, and the downward trend of CTS treatment was significantly slower than that of non-CTS treatment (Figure 2c,d).

3.3. Effect of CTS on PSII Photoinhibition

After high-temperature and high-light treatment for 0–2 h, the Fo under each treatment was not significantly different; during 2–8 h stress, the Fo under the non-CTS treatment and CTS treatment increased significantly, and the rising trend under the non-CTS treatment was greater than that under the CTS treatment (Figure 3a). The values of Fm and Fv/Fm decreased with increasing stress duration; when the stress was imposed for 8 h, the CTS treatment increased the Fv/Fm value by 20.1% compared to the non-CTS treatment, in comparison with that of the control (Figure 3b,c).

3.4. Effect of CTS on Membrane Peroxidation Level

Figure 4 shows that the MDA content in the strawberry leaves showed a significant upward trend after high-temperature and high-light treatment for 0–8 h, and the rate of upward trend under the CTS treatment was slower than that under the non-CTS treatment. Compared with that under the control treatment, the electrical conductivity of the strawberry leaves under the CTS and non-CTS treatments increased significantly (by 79.7% and 105.7%, respectively) when the plants were subjected to high-temperature and high-light stress for 8 h (Figure 4a).

3.5. Effect of CTS on the H2O2 and O2− Contents

With increased stress duration, the H2O2 and O2− contents in the strawberry leaves showed a significant upward trend, and the increasing trend of the H2O2 and O2− contents under the non-CTS treatment was significantly greater than that under the CTS treatment (Figure 5a,b). The H2O2 and O2− contents were consistent with the results of the DAB and NBT staining (Figure 5c).

3.6. Effect of CTS on the Proline Content

High-temperature and high-light stress significantly led to an increase in proline content in the strawberry leaves. After 8 h of stress, the CTS treatment increased the proline content by 9.9% compared to the non-CTS treatment (Figure 6).

3.7. Effect of CTS on the AsA and GSH Contents and the AsA/DHA and GSH/GSSG Ratios

The AsA content under the non-CTS treatment showed an upward trend within 2 h of high-temperature and high-light stress and a downward trend from 2 h to 8 h. The AsA content under the CTS treatment increased with prolonged stress time (Figure 7a), and the GSH content under each treatment increased with prolonged stress time. According to the results, the GSH content under the CTS treatment was significantly higher than that under the non-CTS treatment. After 8 h of stress, the AsA and GSH contents increased by 15.3% and 12.1%, respectively, in CTS compared with non-CTS treatment (Figure 7c).
The AsA/DHA and GSH/GSSG ratios can be used as scales to judge the level of plant stress. As shown in Figure 7b,d, within 2 h of stress, there was no significant difference in the AsA/DHA ratio between the CTS treatment and non-CTS treatment. However, during 2 h to 8 h of stress, the AsA/DHA ratio under the CTS treatment was significantly higher than that under the non-CTS treatment. Compared with the non-CTS treatment, it increased by 25.6% (Figure 7b). The GSH/GSSG ratio under the CTS treatment was significantly higher than that under the non-CTS treatment (Figure 7d).

3.8. Effect of CTS on the Activities of Key Enzymes of the AsA-GSH Cycle

As shown in Figure 8, under the stress of high temperature and high light combined, the activities of GR, APX, DHAR, and MDHAR under each treatment tended to increase with prolonged stress time. The GR, DHAR, and MDHAR activities in plants treated with CTS were significantly higher than those treated with non-CTS, whereas the difference in APX activity was not significant (Figure 8).

4. Discussion

In complex and dynamic natural environments, plants usually face a variety of stresses. The simultaneous occurrence of different stresses can lead to overlapping, potentiating, or antagonistic effects [21]. High temperature and high light are most common during the hot summer, and previous studies have shown that the simultaneous occurrence of high temperature and high light can lead to the destruction of Chl, resulting in a decrease in Chl content [22]. At the same time, too much light energy cannot be used quickly enough, and photosynthetic organs in turn can experience oxidative damage [23]. The AsA-GSH cycle plays a very important role in maintaining redox balance [24].

4.1. Effect of CTS on the Photosynthesis of Strawberry Seedlings under High-Temperature and High-Light Stress

The Chl content is an important indicator of plant adaptations to environmental factors [25]. Studies by Wei Xiaoling, Ma Peifang, and others have shown that high-temperature and high-light stress can inhibit the synthesis of Chl in tobacco, wheat, and other crops species and promote Chl degradation, thereby reducing the Chl content [26,27]. In addition, a decrease in Chl content can lead to decreased photosynthesis capacity and efficiency of plants [28]. In this study, after 0–0.5 h of high-temperature and high-light stress, the Chl content under each treatment increased sharply. This sudden increase in Chl content may be due to the sudden increase in light intensity and a sharp increase in plants to adapt to high amounts of photons. In addition, the Chl content decreased from 1 to 8 h after stress, and compared with with non-CTS treatment, the CTS treatment significantly delayed the decline in Chl content (Figure 1). Studies have shown that both high temperature and high light can reduce the photosynthesis rate [29,30]. In this study, the Ci under the non-CTS treatment decreased significantly at 0–2 h of stress and increased sharply after 2 h; the Ci under the CTS treatment increased after 4 h, and but this increase was significantly less than that under the non-CTS treatment (Figure 2b). The reason for the increase in Ci was the destruction of cell structure and excess carbon dioxide, which led to an increase in the Ci [23], and CTS can protect the cell structure to a certain extent. The Pn, gs, and E of the plants in each treatment under high-temperature and high-light stress were lower than those under suitable temperature and light, although the CTS treatment delayed the decline in each index (Figure 2a,c,d). This showed that CTS can alleviate the degradation of Chl caused by high-temperature and high-light stress, promote the synthesis of Chl, increase the content of Chl, and thus increase the photosynthesis rate of strawberry seedlings.

4.2. Effects of CTS on PSII Photoinhibition of Strawberry Seedlings under High-Temperature and High-Light Stress

Studies have shown that photoinhibition occurs when plants are stressed by both high temperature and high light [5], and the main location of photoinhibition is PSII [31]. Fo and Fm represent fluorescence yields when the PSII reaction centers are fully open and closed, respectively. The difference in the Fo under each treatment was statistically insignificant from 0–2 h after the high-temperature and high-light stress, and the Fo increased significantly during 2–8 h of the stress (Figure 3a); deactivation of the PSII reaction center is the reason for the increase in Fo [32]. CTS treated Fo increased the least, indicating that CTS can reduce the damage but cannot prevent it (Figure 3a). The values of Fm and Fv/Fm decreased significantly with prolonged stress (Figure 3b,c). However, spraying CTS maintained a certain level of Fv/Fm and reduced the degree of injury (Figure 3c). This showed that spraying CTS can effectively alleviate the damage induced by high-temperature and high-light to PSII in strawberry leaves.

4.3. Effects of CTS on Reactive Oxygen Species Metabolism in Strawberry Seedlings under High-Temperature and High-Light Stress

Stress can induce the production of reactive oxygen species in plants, and excessive reactive oxygen species have a strong toxic effect on cells [33]. Studies have shown that CTS can reduce the H2O2 content in soybean under NaCl stress [34] and the H2O2 and O2− contents in corn under cadmium stress [35]. Proline is an important osmotic adjustment substance in plants under stress. Plants can improve their stress resistance through increasing their proline content [36]. In this study, with increasing high-temperature and high-light stress duration, the H2O2 and O2− contents under each treatment showed an upward trend, and the H2O2 and O2− contents under the CTS treatment were significantly lower than those under the non-CTS treatment (Figure 5a,b); however, the proline content was higher than that in the non-CTS treatment (Figure 6). These findings indicated that when strawberry plants are under stress, exogenous CTS can reduce the accumulation of reactive oxygen species, increase the content of osmotic adjustment substances, and thus improve the stress resistance.

4.4. Effects of CTS on Membrane Peroxidation of Strawberry Seedlings under High-Temperature and High-Light Stress

The integrity of the cell membrane system is crucial for plant growth and development. Stress resistance tests performed on various plant species have shown that the stability of the membrane system is closely related to the stress resistance of plants [37,38]. MDA is the final product of plasma membrane peroxidation, and changes in MDA content can reflect the degree of temperature stress on cell membrane damage [39]. Tao et al. [16] found that high-temperature and high-light stress can cause the MDA content in tomato plants to increase. It has also been shown that CTS can reduce the MDA content in walnut under cold stress [40]. In this study, the MDA content in strawberry seedlings showed an increasing trend after the seedlings were subjected to high-temperature and high-light stress (Figure 4b), which occurred because high-temperature and high-light disrupted the metabolic balance of reactive oxygen species, resulting in the accumulation of MDA; moreover, the relative electroconductivity increased with increasing stress duration (Figure 4a). This showed that high temperature and high light disrupted the integrity of the membrane system of the strawberry seedlings, resulting in a large amount of electrolyte leakage. As the stress duration of the strawberry seedlings increased, the damage to the membrane system became more severe (Figure 4a). After spraying CTS, we found that the increases in MDA and relative electroconductivity in the leaves of the stressed strawberry seedlings decreased (Figure 4a,b), which indicated that CTS had a protective effect on the cell membrane system.

4.5. Effects of CTS on the AsA-GSH Cycle in Strawberry Seedlings under High-Temperature High-Light Stress

The AsA-GSH cycle plays an important role in the process of removing reactive oxygen species [41]. This cycle can effectively remove the H2O2 produced during metabolism, and the substances and enzymes participating in the cycle interact and coregulate [42]. As an important antioxidant enzyme in the AsA-GSH cycle, APX catalyzes the oxidation of AsA to scavenge reactive oxygen components such as O2− and H2O2 [43]; the regeneration reaction provides the reaction substrate for APX [44]. AsA and GSH are important antioxidants in plant cells. The ratio of oxidative and reducing components (AsA/DHA, GSH/GSSG) is an important indicator of the redox state of cells. The content of AsA and GSH in cells and the AsA/DHA and GSH/GSSG ratios can accurately reflect the redox state of cells. In this study, under the combined stress of high temperature and high light, the AsA and GSH contents under the CTS treatment were significantly higher than those under the H2O treatment (Figure 7a,c), and the activities of the four key enzymes of the AsA-GSH cycle, namely, APX, GR, DHAR, and MDHAR, increased after CTS was sprayed onto the plants (Figure 8). The AsA and GSH contents and the AsA/DHA and GSH/GSSG ratio under the CTS treatment were also significantly higher than those under the H2O treatment (Figure 7), which showed that CTS can increase the contents of antioxidants in strawberry plants and the activity of key enzymes in the AsA-GSH cycle, thereby improving the stress resistance of strawberry.

5. Conclusions

In summary, the results of this study showed that CTS could effectively alleviate the damage of strawberry seedlings under high-temperature and high-light stress. There are three reasons for reducing stress damage: (1) CTS relieves chlorophyll degradation caused by high temperature and high light and also reduces the damage to photosynthetic organs and cell membranes caused by high temperature and high light, thereby improving photosynthetic efficiency; (2) CTS increases proline content in plants, so as to improve the stress resistance of plants; (3) CTS increases the antioxidant content and antioxidant enzyme activity in strawberry seedlings, as well as removing active oxygen in time. This study clarified the effect of CTS on strawberry seedlings under high-temperature and high-light stress and provided a theoretical basis for actual production.

Author Contributions

Conceptualization, E.F., L.L. and X.C.; methodology, E.F., H.L., X.W., W.X. and H.Z.; data curation, E.F.; writing—original draft preparation, E.F.; writing—review and editing, L.L. and Y.Z.; funding acquisition, L.L. All authors have read and agreed to the published version of the manuscript.

Funding

Shandong Provincial Fruit Industry Technology System (No. SDAIT-06-04).

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Effect of CTS on the Chl content of leaves of strawberry seedlings under high-temperature and high-light stress. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. The different lowercase letters indicate significant differences between the treatments (Duncan’s multiple range test; p < 0.05).
Figure 1. Effect of CTS on the Chl content of leaves of strawberry seedlings under high-temperature and high-light stress. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. The different lowercase letters indicate significant differences between the treatments (Duncan’s multiple range test; p < 0.05).
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Figure 2. Effect of CTS on leaf gas exchange parameters of strawberry seedlings under high-temperature and high-light stress.(a) net CO2 exchange, Pn; (b) intercellular carbon dioxide concentration, Ci; (c) stomatal conductance, gs; (d) transpiration rate, E. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * indicates that there is a significant difference between treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
Figure 2. Effect of CTS on leaf gas exchange parameters of strawberry seedlings under high-temperature and high-light stress.(a) net CO2 exchange, Pn; (b) intercellular carbon dioxide concentration, Ci; (c) stomatal conductance, gs; (d) transpiration rate, E. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * indicates that there is a significant difference between treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
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Figure 3. Effect of CTS on the PSII photoinhibition of strawberry seedlings under high-temperature and high-light stress. (a) initial fluorescence, Fo; (b) maximum fluorescence, Fm; (c) maximum photochemical efficiency, Fv/Fm. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * indicates that there is a significant difference between treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
Figure 3. Effect of CTS on the PSII photoinhibition of strawberry seedlings under high-temperature and high-light stress. (a) initial fluorescence, Fo; (b) maximum fluorescence, Fm; (c) maximum photochemical efficiency, Fv/Fm. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * indicates that there is a significant difference between treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
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Figure 4. Effects of CTS on the degree of membrane peroxidation of strawberry seedlings under high-temperature and high-light stress. (a) electrical conductivity; (b) malondialdehyde content, MDA content. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * and the different lowercase letters indicate that there are significant differences between treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
Figure 4. Effects of CTS on the degree of membrane peroxidation of strawberry seedlings under high-temperature and high-light stress. (a) electrical conductivity; (b) malondialdehyde content, MDA content. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * and the different lowercase letters indicate that there are significant differences between treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
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Figure 5. Effect of CTS on the H2O2 and O2− contents of strawberry seedlings under high-temperature and high-light stress. (a) O2− content; (b) H2O2 content; (c) tissues were stained for H2O2 and O2− using 3,3′-diaminobenzidine (DAB) and nitro blue tetrazolium (NBT). CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. The different lowercase letters indicate significant differences between the treatments (Duncan’s multiple range test; p < 0.05).
Figure 5. Effect of CTS on the H2O2 and O2− contents of strawberry seedlings under high-temperature and high-light stress. (a) O2− content; (b) H2O2 content; (c) tissues were stained for H2O2 and O2− using 3,3′-diaminobenzidine (DAB) and nitro blue tetrazolium (NBT). CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. The different lowercase letters indicate significant differences between the treatments (Duncan’s multiple range test; p < 0.05).
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Figure 6. Effects of CTS on the proline content of strawberry seedlings under high-temperature and high-light stress. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. The different lowercase letters indicate significant differences between the treatments (Duncan’s multiple range test; p < 0.05).
Figure 6. Effects of CTS on the proline content of strawberry seedlings under high-temperature and high-light stress. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. The different lowercase letters indicate significant differences between the treatments (Duncan’s multiple range test; p < 0.05).
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Figure 7. Effect of CTS on the AsA and GSH contents and the AsA/DHA and GSH/GSSG ratios in strawberry seedlings under high-temperature and high-light stress. (a) ascorbic acid content, AsA content; (b) the ratio of ascorbic acid to oxidized ascorbic acid, AsA/DHA; (c) glutathione content, GSH content; (d) ratio of glutathione to oxidized glutathione. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * indicates a significant difference between the treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
Figure 7. Effect of CTS on the AsA and GSH contents and the AsA/DHA and GSH/GSSG ratios in strawberry seedlings under high-temperature and high-light stress. (a) ascorbic acid content, AsA content; (b) the ratio of ascorbic acid to oxidized ascorbic acid, AsA/DHA; (c) glutathione content, GSH content; (d) ratio of glutathione to oxidized glutathione. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * indicates a significant difference between the treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
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Figure 8. Effects of CTS on the activities of key enzymes of the AsA-GSH cycle of strawberry seedlings under high-temperature and high-light stress. (a) activities of glutathione reductase, GR; (b) activities of ascorbate peroxidase, APX; (c) activities of dechlorascorbate reductase, DHAR; (d) activities of monodehydroascorbate reductase, MDHAR. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * indicates a significant difference between the treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
Figure 8. Effects of CTS on the activities of key enzymes of the AsA-GSH cycle of strawberry seedlings under high-temperature and high-light stress. (a) activities of glutathione reductase, GR; (b) activities of ascorbate peroxidase, APX; (c) activities of dechlorascorbate reductase, DHAR; (d) activities of monodehydroascorbate reductase, MDHAR. CK: H2O + 23 °C + 400 μmol·m−2·s−1; H2O + HH: H2O + 38 °C + 1800 μmol·m−2·s−1; CTS + HH: CTS + 38 °C + 1800 μmol·m−2·s−1. * indicates a significant difference between the treatments (Duncan’s multiple range test; p < 0.05); and **, a very significant difference (Duncan’s multiple range test; p < 0.01).
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Fu, E.; Zhang, Y.; Li, H.; Wang, X.; Zhang, H.; Xiao, W.; Chen, X.; Li, L. Chitosan Reduces Damages of Strawberry Seedlings under High-Temperature and High-Light Stress. Agronomy 2023, 13, 517. https://doi.org/10.3390/agronomy13020517

AMA Style

Fu E, Zhang Y, Li H, Wang X, Zhang H, Xiao W, Chen X, Li L. Chitosan Reduces Damages of Strawberry Seedlings under High-Temperature and High-Light Stress. Agronomy. 2023; 13(2):517. https://doi.org/10.3390/agronomy13020517

Chicago/Turabian Style

Fu, Erting, Yuzheng Zhang, Huiling Li, Xiaozhe Wang, Hanxiao Zhang, Wei Xiao, Xiude Chen, and Ling Li. 2023. "Chitosan Reduces Damages of Strawberry Seedlings under High-Temperature and High-Light Stress" Agronomy 13, no. 2: 517. https://doi.org/10.3390/agronomy13020517

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