The study site was located in Banqiao town, Lin’an city (30°10’ N, 119°45’ E), Zhejiang Province (Figure 1), China. The mean annual precipitation at the study site is 1,420 mm, and the monthly precipitation is 118 mm, ranging from 47 mm in December to 231 mm in June. The mean annual temperature is 17.49°C, with monthly mean temperatures reaching a maximum of 24°C in July and a minimum of 3°C in January. The area receives an average of 1,774 h of sunshine per year and 236 h of sunshine per month, ranging from 108 h per month in February to 216 h per month in August. The soil is a slightly acidic red soil derived from siltstone (Li et al., 2018). The original Chinese fir plantation at the study site was all logged approximately 15 years ago, but Chinese fir trees have continued to grow on the plantation. Thus, all Chinese fir plantation trees were 15 years old in the study site. Furthermore, a plantation of moso bamboo was established adjacent to the Chinese fir plantation at approximately the same time as the Chinese fir plantation was logged. The transition zone between the Chinese fir and moso bamboo plantations is approximately 30–50 m in width. In this zone, the moso bamboos reach the same height as the canopy formed by the Chinese fir. Moso bamboos more than 4 years old are usually harvested in November during even-numbered years to maximize the economic benefits. Thus, the moso bamboo plantations are uneven-aged forests with a 2-year difference in the age of the trees (Song et al., 2016).

In February 2019, three experimental sites were established, including a monoculture moso bamboo plantation site (PMB), a monoculture Chinese fir plantation site (PCF) and a mixed forest site with both species (MCM). There were three replicate plots in each site, meaning that a total of 9 plots (20 m × 20 m) were established (Figure 1). The plots were separated by buffer zones of at least 20 m to keep them independent of each other. The stand characteristics are summarized in Table 1.

A 20 m tall observation tower with a walkway was built to reach the crown of the trees in each plot of the PCF, PMB, and MCM sites (9 observation towers in total). Around each tower, three Chinese fir trees were selected in the PCF site, six moso bamboo plants (three 1-year-old and three 2-year-old moso bamboo plants) were selected in the PMB site, and a total of nine plants (three Chinese fir trees, three 1-year-old and three 2-year-old moso bamboo plants) were selected in the MCM site. Then, several mature and healthy leaves of both Chinese fir and moso bamboo trees on the southern side from the middle layer canopy of the selected sample plants in each plot were chosen randomly for measurement. These leaves were similar in size and were all taken from the middle of each twig (Van Goethem et al., 2013; Zhang et al., 2017a; Wang et al., 2019; Figure 1). The leaf gas exchange and fluorescence parameters were measured, chlorophyll contents were determined and samples were collected in the tower in Spring (May) 2019.

The net photosynthesis rate (Amax), stomatal conductance (gsw), intracellular CO₂ concentration (Ci), and transpiration rate (Tr) were measured with an open gas-exchange system connected to a leaf fluorometer chamber (2 cm²; Li-6800; Li-Cor, Inc., United States). Measurements from the selected leaves were taken on sunny days between 8:00 and 16:00. The CO₂ concentration was maintained at 400 μmol mol^–1 at a leaf temperature of 25°C, and the vapor pressure deficit was maintained as close to 1 kPa as possible. Several leaves (two moso bamboo or six to eight Chinese fir leaves) were flat into the leaf chamber and with full covered, when measuring photosynthesis. Once a steady state was reached (usually 10 min after clamping the leaf), data were recorded every 5 s for a total of 10 data points for every single leaf. The WUE was calculated as WUE = Amax/Tr, and the instantaneous carboxylation efficiency (CUE) was calculated as CUE = Amax/Ci.

The fluorescence parameters were measured with a PAM-2500 instrument (WALZ Inc., Germany). The leaves (one moso bamboo of three to four Chinese fir leaves) were fully dark adapted with leaf clips for approximately 20 min and then exposed to weak actinic light (0.05 μmol m^–2 s^–1) to detect the initial minimal fluorescence (Fo). Then, a saturating light pulse (6,000 μmol m^–2 s^–1) was applied for 2 s to detect the maximal fluorescence (Fm). The maximal potential quantum yield of photosystem PSII was calculated as Fv/Fm = (Fm-Fo)/Fm. Leaves were exposed to the saturating light pulse repeatedly to determine the non-photochemical quenching (NPQ), photochemical quenching coefficient (qP) (Genty et al., 1989) and effective quantum yield of PSII [Y(II)] (Murchie and Lawson, 2013). A detailed documentation of the measurement of the fluorescence parameters is given by Murchie and Lawson (2013). The chlorophyll content was measured with a SPAD-502 portable chlorophyll meter (Minolta Camera Co., Ltd., Osaka, Japan). Ten mature and healthy leaves per selected sample plants from the middle layer canopy in each plot were chosen randomly for chlorophyll content measurement. For each leaf, the mean of three readings was used to represent the chlorophyll content.

After the in situ parameters were measured, the measured leaves were collected in plastic bags and immediately transported to the laboratory for further measurements. Fresh leaf samples (0.5 g) were collected for extraction. The enzymes were extracted at 4°C with 5 mL of 50 mM potassium phosphate buffer (pH 7.8). The extracting solutions were centrifuged at 8,000 × g at 4°C for 15 min, and the homogenate was stored at 4°C for the analysis of superoxide dismutase (SOD), peroxidase (POD), catalase (CAT), and Rubisco activity.

SOD activity was measured according to the method of Giannopolitis and Ries (1977), where the activity was determined by inhibiting the effect of β-nitro blue tetrazolium chloride (NBT) on photoreduction. POD and CAT activity was determined by the method of Chance and Maehly (1955). The reaction was conducted at 470 and 240 nm, and extinction coefficients of 2.47 and 36 Mm cm^–1 were used to determine the activity of POD and CAT, respectively. Rubisco was quantified by capillary electrophoresis using a method modified from Warren et al. (2000).

The malondialdehyde (MDA) content was determined with the thiobarbituric acid method (TBA) (Li and Wang, 2003). Leaf tissue samples of 0.5 g were homogenized in 2 mL supernatant and a 2-mL mixture of TBA (0.6%, v/v) and trichloroacetic acid (TCA, 10%, v/v). The mixture was heated for 25 min at 100°C. Then, the mixture was centrifuged at 5,000 × g for 20 min after cooling. The supernatant was analyzed at 532, 600, and 450 nm with a spectrophotometer. The MDA content was calculated using the following formula: C (μM) = 6.45 (OD₅₃₂ - OD₆₀₀) - 0.56OD₄₅₀.

Nutrient contents were determined in leaf samples oven dried at 105°C during the first 30 min, then at 65°C until reaching a constant weight and then ground with a grinder (DFT-50A, Wenling LINDA Machinery Co., Ltd., China). Total leaf nitrogen content was determined using a Sumigraph NC-80 high-sensitivity CN analyser (Sumitomo Chemical Industry Co., Ltd., Japan).

To determine the effects of mixture, species (Chinese fir and two ages of moso bamboo) and their interaction on the photosynthetic, chlorophyll a parameters, enzyme activity and leaf chemistry parameters, data were subjected to a two-way ANOVA. Similarly, to determine the effects of mixture, age and their interaction effects on the photosynthetic, chlorophyll a parameters, enzyme activity and leaf chemistry parameters in moso bamboo, data were subjected to a two-way ANOVA. One-way ANOVA was used to analyze the effect of mixture on each parameter. Before the ANOVAs, the data were checked for normality and homogeneity of variances and log-transformed to correct deviations from these assumptions as needed. Post hoc comparisons were tested using the least significant difference (LSD) test at a significance level of P < 0.05. The changes in on photosynthetic performance parameters (Amax, WUE, CUE, Fv/Fm, NPQ, and chlorophyll content) was conducted with a fixed-effects model (Forrester and Albrecht, 2014; Andrés et al., 2017). We included as fixed factors “mixture,” “age,” and “species” to detect the differences in the rates of change of 1-year-old moso bamboo, 2-year-old moso bamboo and Chinese fir of photosynthetic performance parameters. All of the data were analyzed using SPSS statistical software (version 19.0, Armonk, NY, United States). Raincloud plots were used to evaluate the distributions of the average of various photosynthetic parameters for both species in the monoculture plantation and mixed stand. In addition, radar charts were drawn using Origin 2021 to estimate the average fluorescence parameters of the leaves of both species in the monocultures and mixed stand. The radial column chart was drawn using the ggplot2 package in R statistical software to estimate the average antioxidant enzyme activities of the leaves of both species in the monocultures and mixed stand (R v3.6.1).

The carbon assimilation of both Chinese fir and moso bamboo in MCM was significantly higher than that in PMB and PCF (Figure 2A). The photosynthetic parameters Amax, WUE, and CUE measured in Chinese fir trees grown in mixed stands (MCM) were 9.3, 82.6, and 70.7% higher, respectively, than those measured in Chinese fir monoculture plots (PCF) (P < 0.01; Figures 2A,E,F), whereas Ci, gsw, and Tr were 35.5, 34.4, and 44.7% lower, respectively, in MCM than in PCF (P < 0.001; Figures 2B,C,D). Compared with PMB, 1-year-old moso bamboo in MCM exhibited significantly higher Amax, gsw, Tr and CUE, by 20.5, 18.2, 88.4, and 35.2%, respectively (P < 0.001; Figures 2A,C,D,F). Similarly, compared with PMB, 2-year-old moso bamboo in MCM exhibited significantly higher Amax, gsw, Tr and CUE, by 23.3, 19.5, 61.6, and 15.5%, respectively (P < 0.001; Figures 2A,C,D,F). However, 1-year-old moso bamboo exhibited significantly lower Ci and WUE, by 9.1 and 29.8%, respectively, in MCM than in PMB (P < 0.001; Figures 2B,E). There was no significant differences in the Ci and WUE of 2-year-old moso bamboos grown in MCM and PMB (P > 0.05; Figures 2B,E).

The values of all fluorescence parameters (Fv/Fm, qP, and Y(II), with the exception of NPQ) of Chinese fir and two-year-old moso bamboo in MCM were slightly higher than those in PCF and PMB (P > 0.05; Figures 3A,B). NPQ was 19.8 and 24.1% lower, respectively, for Chinese fir and 2-year-old moso bamboo in MCM than in PCF and PMB (P < 0.05; Figures 3A,B), while NPQ was 40.4% higher in the 1-year-old moso bamboo in MCM than in PMB (P < 0.05; Figure 3C).

Growing in MCM had significant effects on antioxidant enzyme activity and MDA content in Chinese fir and moso bamboo of both ages (Figure 4). Compared with PCF, MCM significantly increased SOD and CAT activity and MDA content in Chinese fir by 53.2, 55.4, and 17.6%, respectively (P < 0.001; Figure 4). Similarly, for 1-year-old moso bamboo, the POD, CAT and Rubisco activities and MDA content were 8.7, 121.4, 50.4, and 9.2% higher, respectively, in MCM than in PMB (P < 0.001; Figure 4). For 2-year-old moso bamboo, the SOD, POD, CAT and Rubisco activities and MDA content were 24.4, 19.9, 48.2, 149.8, and 11.4% higher, respectively, in MCM than in PMB (P < 0.001; Figure 4).

The chlorophyll contents of Chinese fir and 1-year-old moso bamboo in MCM were 7.5 and 3.7% higher, respectively, than those in PMB and PCF (P < 0.05; Figure 5). Similarly, the N content was 30.3, 15.3, and 4.6% higher among Chinese fir, 1-year-old and 2-year-old moso bamboo plants, respectively, in MCM than in PCF and PMB (P < 0.001; Figure 5).

Photosynthesis is an indispensable component of plant activity, and it is the only process on earth that converts inorganic matter into organic matter and light energy into chemical energy (Wu et al., 2018b). The photosynthetic capability of plants reflects their productivity to a certain extent. We aimed to evaluate the effects of growing in a mixed stand on the physiological activity of Chinese fir and moso bamboo plantation trees under subtropical conditions. This information is relevant both for understanding how growing in mixed stands may affect the performance of moso bamboo and Chinese fir and for assessing the potential benefits of mixed stands in subtropical forests. Our results showed that growing in MCM significantly affected all photosynthetic parameters in both Chinese fir and moso bamboo, including Amax, Ci, gsw, Tr, WUE, and CUE. The increase in Amax supported our first hypothesis, according to which the plants growing in mixed stands would exhibit greater photosynthetic capacity than those growing in monocultures. Moreover, we observed that the reasons for the increase in Amax differed between moso bamboo and Chinese fir.

The increase in photosynthesis in Chinese fir in MCM was driven by its optimization of CO₂ and water uptake when it was grown with moso bamboo. This explanation is supported by the observed increases in the WUE and CUE, which were higher in MCM than in PCF (Figures 2E,F and Supplementary Table 1). On the one hand, the increase in WUE and the reduction in transpiration may have also increased the competitive advantage of Chinese fir growing in environments where water is a limiting resource (Figures 2D,E; Andrés et al., 2017). On the other hand, a shadier environment proportioned by the taller moso bamboo may reduce incoming radiation in Chinese fir so that the damaging effects of excessive light energy on the photosynthetic complex was reduced. Meanwhile, transpiration rate was reduced, although lower stomatal conductance rates were keeping stable, thereby supporting higher WUE and photosynthesis (Liu et al., 2016). The higher CUE of the Chinese fir in MCM suggests that these trees maximized their use of carbon resources; this strategy may have increased their energy production and minimized the harmful effects of excessive light energy on the photosynthetic complex (He et al., 2011).

However, the Tr, gsw, and Ci were lower in Chinese fir growing in MCM than in Chinese fir growing in PCF. This result can be explained by the fact that Chinese fir exhibits strong physiological self-regulation abilities when adapting to water resource competition (Annicchiarico et al., 2015; Li et al., 2015). First, the decrease in the Tr and the increase in the WUE of Chinese fir in MCM may indicate that water stress in Chinese fir might occur due to interspecific competition under these conditions (Zhang et al., 2017a). Because of the shallow rooting depths (0–40 cm) of both moso bamboo (Chen et al., 2013; Shinohara et al., 2019) and Chinese fir (Fan, 2019; Liao et al., 2019), competition for soil water may induce water stress when the plants are taking up water from shallow soil layers (Schwendenmann et al., 2014). To tolerate water stress, complex physiological responses in Chinese fir that regulate photosynthetic productivity and promote survival are triggered (Xu, 2013). Stomatal closure is one of the first responses to water stress (Van Goethem et al., 2014; Nadal and Flexas, 2018); it allows plants to maintain an adequate water status by reducing transpiration to sustain critical physiological and biochemical processes (Han et al., 2019). In general, stomatal closure induced by water stress can reduce the photosynthetic capacity of plants (Xu, 2013), though our results indicated that moderate stomatal closure may benefit water preservation and promote WUE. To some extent, the high photosynthetic capacity of Chinese fir in the mixed stand (Amax = 3.7 μmol m^–2 s^–1 in the mixture; Figure 2A) may have contributed to its strong resistance to water stress (Annicchiarico et al., 2015; Li et al., 2015).

Second, a decrease in gsw usually leads to a decrease in the Ci and photosynthesis due to the limited CO₂ diffusion from the atmosphere to the intercellular airspace. Fortunately, the decrease in photosynthesis caused by decreased gsw under drought conditions can be alleviated by maintaining the mesophyll conductance (gm) (Aranda et al., 2007; Han et al., 2016). Because the variability of gm has little or no effect on leaf water transpiration, it can affect CO₂ diffusion from substomatal cavities to the carboxylation sites within chloroplasts (Flexas et al., 2012; Cano et al., 2014; Flexas, 2016; Han et al., 2016). It is possible that maintaining the gm can indirectly balance CO₂ uptake and water loss, thereby achieving optimization between CO₂ and water at the carboxylation sites in the chloroplast and contributing to improved photosynthesis and drought tolerance.

Since not all tree species utilize resources in the same manner, growth in mixed stands is more active than that in monocultures. The strategy of moso bamboo differs from those observed in Chinese firs for increasing its photosynthetic capacity. The Amax was much higher in both 1-year-old and 2-year-old moso bamboo growing in MCM than those growing in PMB. Because moso bamboo growing in MCM has a higher competitive advantage than Chinese fir for obtaining soil water from shallow soil layers due to its complex belowground rhizomatous clonal growth system (Song et al., 2017; Shinohara et al., 2019), moso bamboo in the MCM can more readily access soil water resources than that growing in the PMB, suggesting a release from intraspecific competition in the MCM. It is generally recognized that increasing soil water competition ability can help increase CO₂ diffusion from the atmosphere to the carboxylation site due to stomatal opening and increased gm, which, in turn, contribute to an increase in Amax (Chaves and Oliveira, 2004; Ashraf and Harris, 2013). In addition, due to the tightly coupled relationship between leaf photosynthesis and Tr, the higher Tr of moso bamboo was expected to result in higher photosynthesis (Zhang et al., 2017a; Gu et al., 2019). The physiological integration of moso bamboo through the belowground rhizome system may promote its advantages in competing for soil moisture in mixed stands and thus higher productivity. Similarly, increased photosynthetic capacity and WUE were found in grass-legume mixtures (Liu et al., 2016) and in mixed conifer-hardwood forests (Fernández-de-Uña et al., 2016). Forrester et al. (2010, 2012) also found that the Amax and WUE of Eucalyptus globulus Labill increased in mixtures with Acacia mearnsii de Wildeman; several different processes can contribute to this response (Forrester et al., 2010; Forrester, 2015; Pretzsch et al., 2016). These findings are consistent with our results that the photosynthetic capacity and water stress responses of moso bamboo and Chinese fir in MCM were different from those in PMB and PCF. Hence, mixed stands may result in species interactions and increased interspecies competition. The fierce interspecies competition in mixed stands drives trees to achieve a competitive advantage in obtaining soil water resources through physiological self-regulation or interspecific morphological differences, which ultimately enhances their net photosynthetic capacity (Forrester, 2015; Forrester and Bauhus, 2016). Different strategies bring different benefits to plants as well as different risks. The risk of the photosynthesis improvement strategy in moso bamboo is that opening the stomata to increase Tr will be accompanied by a decrease in WUE (Figures 2C–E). As a result, moso bamboo may lose more water through transpiration, making it more difficult for Chinese fir to obtain soil water. For Chinese fir, the disadvantage of this lower stomatal conductance and lower transpiration water is its weakened capacity to compete for soil water resources under drought stress when growing in mixed stands with moso bamboo.

Previous studies have shown that mixed plantations have a higher carbon sequestration capacity and stand-level productivity than monocultures (Liang et al., 2016; Pretzsch et al., 2016; Huang et al., 2018) consistent with our results. However, mixed stands do not always promote the productivity of each component species in comparison to their performance in monocultures, perhaps due to changes in species proportions and inter-specific differences in biomass allocation patterns (Lee et al., 2003). In a pot trial with mixtures of Norway spruce (P. abies L.) and European beech, the former suffered a competitive disadvantage in mixtures, which had lower crown volumes, above-ground biomass and Amax compared to monocultures (Kozovits et al., 2005). Similarly, in another pot trial with mixtures of Pinus taeda and Acer rubrum, the Acer rubrum of biomass, height, Amax and biomass allocation to leaves were significantly lower in mixtures than in monocultures (Groninger et al., 1996). The reason for the difference photosynthesis capacity of the mixed plantation may be depended on the competitive ability of the admixed species and their influence on the availability and uptake of resources (Forrester et al., 2012). In addition, the stand density may be a critical factor affecting forest growth photosynthesis capacity (Forrester and Bauhus, 2016), and the changes in soil microorganism diversity and soil microbial activities in the mixed plantation may also contribute to the different photosynthetic capacity by improving soil nutrition conditions for plants (Wu et al., 2018a). In addition, these results may only represent the performance of plants in May. Long-term seasonal changes will be examined in the future study.

Our results showed that the interaction of mixture and species had significant effect on WUE and CUE, which may indicate that growing in mixed stands exacerbated the competitive for nutrition (such as water and nitrogen) between species. The previous study also confirmed that N addition alleviates the competitive effect between the introduced invasive plant Robinia pseudoacacia L. and the native tree Quercus acutissima Carr. (Luo et al., 2014).

Chlorophyll fluorescence, as an important component of plant photosynthesis, is widely used to study photosynthetic performance in leaves, and it can provide useful information about physical changes in pigment-protein complexes and the electron transport rate through PSII (Baker and Rosenqvist, 2004). Chlorophyll fluorescence parameters [Fv/Fm, Y(II), NPQ, and qN] are sensitive to water stress (Pan et al., 2012; Van Goethem et al., 2013; Yuan et al., 2016; Wu et al., 2018b) and photosynthetic status (Man et al., 2017; Rudzani et al., 2017). Thus, we further investigated whether the photochemical response can detect the potential stresses and changes in photosynthetic status induced in mixed stands.

In our study, all fluorescence parameters of moso bamboo and Chinese fir were slightly higher in MCM than in PCF and PMB, and only the NPQ of Chinese fir and 2-year-old moso bamboo was significantly lower in MCM. Among the fluorescence parameters, the value of Fv/Fm can be used to detect damage to PSII and to the photosynthetic efficiency of leaves resulting from environmental stress (Yuan et al., 2016; Wu et al., 2018b). Numerous studies have confirmed that when the Fv/Fm decreases due to water stress, it may destroy the PSII oxygen-evolving complex and the PSII reaction centers and in turn degrade the D1 protein (Van Goethem et al., 2013; Man et al., 2017; Rudzani et al., 2017). Our photosynthetic data may indicate that Chinese fir suffered from water stress in MCM, but this was not reflected in its Fv/Fm, which was slightly higher in MCM than PCF. The reason for this discrepancy may be that a decrease in Fv/Fm can be detected only when structural damage occurs in the photosystem II primary photochemistry, resulting in a decrease in the photosynthetic rate (Wu et al., 2018b).

The parameter qP represents the photochemical capacity and the number of QA oxidation states in PSII under light adaptation. A higher qP value is advantageous for the separation of electric charges in the reaction center and is beneficial to electron transport and PSII yield (Rudzani et al., 2017). The slight increases in Fv/Fm, qP, and Y(II) in both Chinese fir and moso bamboos of both ages in MCM were consistent with the increased photosynthetic rate, which may indicate that mixed plantations can protect plant photochemical efficiency from the damage caused by environmental stresses, such as water stress (Wu et al., 2018b). The reason for the slightly higher fluorescence parameters of each species may attribute to higher leaf nitrogen concentrations in moso bamboo and Chinese fir growing in the mixed stand (Figure 5) which is mainly involved in light energy capture, electron transfer and carboxylation processes in photosynthesis (Forrester et al., 2012).

The lower NPQ in Chinese fir and 2-year-old moso bamboo in MCM indicates that the light energy captured by leaves was fully used for photosynthesis (Liu et al., 2016), increasing photoprotection for the plants and reducing the risk of light damage (Zhang et al., 2017a; Demmig-Adams et al., 1996). However, the significantly higher NPQ of the 1-year-old moso bamboo in the MCM suggested that thermal energy dissipation was activated to dissipate the excess light energy, thereby preventing ROS generation and maintaining the balance between the absorption and consumption of light energy under a moderate water deficit (Yi et al., 2018). The above results suggested that MCM improved the light use efficiency of each component compared to that of PCF and PMB. In addition, these results also suggest that Chinese fir and 2-year-old moso bamboo have a higher light use efficiency compared to 1-year-old moso bamboo. The different responses of Chinese fir and 2-year-old moso bamboo and 1-year-old moso bamboo can be explained by the differences in growth stage and environmental adaptation mechanism (Wen et al., 2011).

While Fv/Fm has served as an indicator of water stress in previous studies (Van Goethem et al., 2013; Yuan et al., 2016; Zhang et al., 2017b; Wu et al., 2018b), our study also further supported previous results showing that NPQ is very sensitive to light use efficiency and could be a useful indicator of the impacts of mixed plantations (Mathobo et al., 2017; Zhang et al., 2017a).

ROS are often produced in chloroplasts during photosynthesis. Under normal circumstances, a balance exists between ROS production and elimination in plants (Wu et al., 2020). However, water stress can change the electron transport chain and exacerbate the production of ROS such as O₂ and H₂O₂ (Man et al., 2017), which ultimately results in the disruption of this balance. This effect is harmful to organelles, including chloroplasts, mitochondria and peroxisomes, and may damage the photosynthetic apparatus through the oxidation of lipids, proteins, carbohydrates and nucleic acids (Mittler, 2002; Wu et al., 2018b). To minimize the occurrence of oxidative damage, plants have developed an array of protective and repair systems; these systems include the antioxidative system, which involves enzymes such as SOD, POD, and CAT that react with ROS and keep ROS levels low (Imlay, 2003; Reddy et al., 2004).

Cell membrane lipid peroxidation is an important index of plant damage caused by water deficit. It occurs due to the accumulation of ROS when the balance between ROS generation and removal is disturbed. Thus, the content of MDA (a product of lipid peroxidation) is often used to assess the extent of oxidative damage in plant tissue (Noctor and Foyer, 1998; Mittler, 2002). An increase in MDA content suggests that lipid peroxidation caused by ROS accumulation has resulted in cellular damage. Our results showed an increase in the MDA concentration of both species in MCM, which may indicate that oxidative stress caused cellular damage and therefore metabolic disorders in these plants (Wu et al., 2020). However, an effective antioxidative system in plants can minimize oxidative stress levels and protect their tissues. The activity of SOD catalyses the disproportionation of O₂^– to molecular oxygen and H₂O₂, which is further reduced to water by CAT; these processes maintain a very low steady-state concentration of O₂^– and H₂O₂ and minimize the production of hydroxyl radicals (Yi et al., 2018). Similarly, POD activity plays an important role in antioxidative protection. We observed that the activities of SOD, CAT, and POD were higher in MCM than in PCF and PMB, suggesting that antioxidative enzymes were mobilized to protect the plant tissue from oxidative damage, which showed that mixed plantations may induce water stress conditions (Wu et al., 2020). In addition, future studies should focus on sap flux density to quantify the water stress of both species in the different mixture conditions. Our results indicate that growing in mixed plantations can hone the ability of plant antioxidant systems, stimulate cells to enter a sensitized state, induce plants to effectively control excessive ROS concentrations and increase the ability of plants to resist stress.

Rubisco activity has been considered a useful indicator for breeding programmes aiming to enhance plant WUE as well as yield (Hirel et al., 2007). In our study, an increase in Rubisco activity in MCM was considered beneficial for plant survival under water stress conditions because a positive relationship between leaf Rubisco content and Amax has been reported in most C₃ plants (Taub, 2010; Makino, 2011). An increase in the rate of the Rubisco-catalyzed reaction has been reported to occur due to changes in CO₂ availability at the chloroplast level or in the availability of the Rubisco substrate or due to the activation of Rubisco (Han et al., 2019).

The results also showed that Chinese fir and moso bamboo of both ages had significantly higher chlorophyll and leaf nitrogen contents in MCM than PMB and PCF, which corresponds to the high photosynthesis rate in MCM (Liu et al., 2016). Because the majority of leaf nitrogen is used in the photosynthetic apparatus, a high leaf nitrogen content results in an increase in the number of thylakoids and an increase in thylakoid proteins in chloroplasts (Evans, 1989). A strong, positive, causal correlation between the photosynthetic rate of the leaf and the leaf nitrogen content has been reported (Xu, 2013). In other words, the increase in leaf nitrogen content in mixed plantations can increase the maximum photosynthetic rates of the trees. In addition, the chlorophyll content per unit of leaf area, the specific activity of RuBP carboxylase and the electron transport capacity increase with increasing nitrogen content, which improves the plant photosynthetic capacity (Sugiharto et al., 1990; Nakaji et al., 2001; Xu, 2013). Küppers (1996) found that E. delegatensis R. T. Bak. saplings growing with Acacia dealbata Link. had higher leaf N levels in a native forest. Similarly, Forrester et al. (2012) observed that the leaf nitrogen content of Eucalyptus globulus was greater in mixed plantations than in monocultures. These results are consistent with our results, in which the leaf nitrogen content of Chinese fir and both ages of moso bamboo in MCM was significantly higher than that in PMB and PCF. The researchers found that the possible cause of this increase was that higher N availability in the mixed stands resulted from increased rates of N₂-fixation and accelerated rates of nutrient cycling (Forrester et al., 2005; Forrester et al., 2012). However, Amax did not increase with increasing leaf nitrogen in Acacia mearnsii in a mixed stand as it did in a monoculture (Forrester et al., 2012), and others found no relationships, suggesting that leaf nitrogen content was in excess of photosynthetic requirements and that Amax was limited by other factors (Warren et al., 2000; Close et al., 2004). The difference of the facilitative influence of mixed planting was caused by species specific (Küppers, 1996; Forrester et al., 2012).