Effect of light regime and provenance on leaf characteristics, growth and flavonoid accumulation in Cyclocarya paliurus (Batal) Iljinskaja coppices
© The Author(s) 2016
Received: 2 June 2016
Accepted: 11 October 2016
Published: 17 October 2016
As a highly valued and multiple function tree species, Cyclocarya paliurus is planted and managed for timber production and medical use. However, limited information is available on its genotype selection and cultivation for growth and phytochemicals. Responses of growth and secondary metabolites to light regimes and genotypes are useful information to determine suitable habitat conditions for the cultivation of medicinal plants.
Both light regime and provenance significantly affected the leaf characteristics, leaf flavonoid contents, biomass production and flavonoid accumulation per plant. Leaf thickness, length of palisade cells and chlorophyll a/b decreased significantly under shading conditions, while leaf areas and total chlorophyll content increased obviously. In the full light condition, leaf flavonoid contents showed a bimodal temporal variation pattern with the maximum observed in August and the second peak in October, while shading treatment not only reduced the leaf content of flavonoids but also delayed the peak appearing of the flavonoid contents in the leaves of C. paliurus. Strong correlations were found between leaf thickness, palisade length, monthly light intensity and measured flavonoid contents in the leaves of C. paliurus. Muchuan provenance with full light achieved the highest leaf biomass and flavonoid accumulation per plant.
Cyclocarya paliurus genotypes show diverse responses to different light regimes in leaf characteristics, biomass production and flavonoid accumulation, highlighting the opportunity for extensive selection in the leaf flavonoid production.
Cyclocarya paliurus (Batal) Iljinskaja, commonly called “sweet tea tree” because of the flavor of its leaves, is a sole species from Cyclocarya genus and is widely distributed in sub-tropical regions of China (Fang et al. 2006). Leaves of this plant are traditionally used in China as a medicine or nutraceutical tea (Birari and Bhutani 2007; Fang et al. 2011). Many studies have demonstrated that C. paliurus possesses a variety of bioactivities, including antihypertensive activity, hypoglycemic activity, enhancement of mental efficiency, anticancer, anti-HIV-1, and antioxidant activity (Kurihara et al. 2003; Xie et al. 2010, 2013; Zhang et al. 2010). These beneficial effects have been partly attributed to its content of several chemical components, including proteins, polysaccharides, triterpenoids, flavonoids, steroids, saponins, phenolic compounds, and minerals (Xie et al. 2010, 2013; Li et al. 2011; Fang et al. 2011). Owing to its multiple beneficial effects on human health, a huge production of leaves is required for C. paliurus tea production and for medical use. However, most studies on C. paliurus were focused on extraction procedures and low molecular weight substances, such as triterpenoids, flavonoids, steroids, saponins, and other compounds present in this plant, whereas less attention was paid to the silvics of the species (Deng et al. 2012, 2015).
Flavonoids are a large group of phenolic constituents of plants, and the bioavailability of flavonoids varies greatly among different subgroups and compounds (Erlund 2004). Some beneficial bioactivities of flavonoids have been proved, such as antibacterial, anticarcinogenic, antioxidant, antimutagenic, anti-inflammatory, antiallergic, antiobesity, and antidiabetic activities (Peterson and Dwyer 1998; Erlund 2004; Zhang et al. 2010). Quercetin and its glycoside derivatives, such as isoquercitrin, have been found to promote human health through cytoprotective effects, including reducing lipid peroxidation, protein carbonylation and radical oxygen species (ROS) production (Ciancolini et al. 2013; Palazzolo et al. 2012), while kaempferol was found to have remarkable antioxidant potential and has the capacity to lower the risks of coronary heart disease (Schmidt et al. 2010). According to Iwashina (2000), biosynthesis of flavonoids is mostly carried out by plant, with a few exceptions of animals and fungi.
The content of phytochemicals in plants is affected by numerous internal and external factors that occur during the growing period (Graham 1998; Björkman et al. 2011; Cui et al. 2013; Liu et al. 2015). Thus, factors influencing the phytochemical content and profile in the production of plants are worth considering for improved cultivation. Recently, attempts have been made to develop plantations of C. paliurus as a functional food or ingredient to be used in traditional Chinese medicine. Fang et al. (2011) investigated the genetic and temporal variations in the flavonoid (quercetin, kaempferol, and isoquercitrin) content in leaves of C. paliurus, while Deng et al. (2012) explored the effects of environment and fertilization on growth and flavonoid content of C. paliurus. Xie et al. (2015) had examined the effects of plant growth regulating substances on growth and phytochemical content of C. paliurus leaves. Björkman et al. (2011) indicated that factors that influence plant growth and phytochemical content may interact, and it is now possible to design multifactorial experiments that simulate their combined effects. However, very little is known about the influences of interaction between genetic and environmental factors on plant growth and phytochemical contents of C. paliurus leaves, especially the mechanism of flavonoid accumulation in C. paliurus plants.
For these reasons, it is necessary to investigate the integrated influences of provenance and light intensity on plant growth, leaf characteristics, accumulation of total flavonoid and key health promoting flavonoids (quercetin, kaempferol, and isoquercitrin) in the leaves of C. paliurus. The information provided by this study would be of great value for understanding the light-regulating mechanism for different provenances of C. paliurus, and contribute to establishing optimal cropping strategies for C. paliurus plants.
Plant material and growth conditions
The experiment was carried out during the 2011 growing season in Zhenjiang Nursery, Jiangsu Province, China, and the site conditions were the same as described by Fang et al. (2011). For each provenance, seed trees (generally dominant or co-dominant tree in the stand) were selected based on tree age, stem form and growth vigor. Number of trees for collecting seeds for each provenance was determined according to stand area and quantity of C. paliurus naturally distributed on the area (about 10 % of the total). Seeds of C. paliurus were collected in late October 2009 and were subjected to chemical scarification, exogenous gibberellin A3 (GA3) treatments, and stratification treatments in early January 2010, according to the method proposed by Fang et al. (2006). After a 3 month stratification treatment, the germinated seeds were sown in containers, and then transplanted into the experimental site at a spacing of 40 × 50 cm in early June 2010. After 1-year growth, the seedlings of C. paliurus were cut from the bottom in March 2011 for coppice management.
A split-plot randomized design was used to establish nine treatments with three shading levels and three provenances. Three shading treatments were subjected to three light intensity regimes: 100 % sunlight (A1, without shading net), about 50 % of solar radiation (A2, covered with one layer of shading net at 2 m height), and around 15 % of solar radiation (A3, covered with two layers of shading net at 2 m height). Three provenances were Wufeng (30° 19′ N, 110° 89′ E) from Hubei Province (B1), Yuanling (28° 46′ N, 110° 39′ E) from Hunan Province (B2) and Muchuan (28° 96′ N, 103° 78′ E) from Sichuan Province (B3), respectively. With three replications, the trial gave a total of 27 subplots, and each subplot consisted of 20 plants.
Shading treatments were conducted from June 2011. To monitor environmental factors automatically, a hand-held Agricultural Weather Station (TNHY series model, Zhejiang Top Instrument Co. Ltd., Hangzhou, China) was set up in different shading treatments. Photosynthetic photon flux density (PPFD) was recorded at full sunlight and under shade conditions at intervals of 30 min, whereas air temperature (T) and relative humidity (RH) were measured at intervals of 10 min during the experimental periods by the set hand-held Agricultural Weather Station.
Growth and biomass assessment
Growth and biomass assessments of the plants were conducted on October 20, 2011. Based on the measurements of base diameter and height, three intact C. paliurus plants with most close to mean base diameter and height in each treatment were selected and harvested for biomass analysis. After excavating, the sample plants were washed with tap water. Then leaf, stem, and root components of each sample tree were separated, weighed, and dried at 70 °C. The total dry mass of each was calculated as the sum of leaf, stem, and root dry weights.
Measurement of leaf characteristics and chlorophyll concentration
Leaf area (LA) per plant (cm2) of fully expanded leaves was measured by an area meter (Li-Cor, Model 3100 area meter, USA). Leaves of similar size were used for anatomical measurements. Cross sections were cut into about 4 mm × 6 mm by hand from the same levels of leaves (1 cm below the leaf tip) in all materials. The sections were fixed in a FAA (formalin/glacial acetic/70 % ethanol in the ratio of 0.5:0.5:9.0) and dehydrated through the gradual ethanol series and t-butanol. Samples were then sectioned with a microtome (Leica CM1850, Leica Instruments, Nussloch, Germany) into slices of 30 μm thickness. The section tissues were stained 10 min with a 1 % aluminium chloride-ethanol solution. Microphotographs were taken with a Nikon YS100 microscope (Nikon Co. Tokyo, Jena, Japan), while leaf thickness and palisade length were examined using a FW4000 software.
For the analysis of chlorophyll concentrations, 0.1 g of finely cut and well-mixed sample was extracted with 8 mL 95 % acetone for 24 h at 4 °C in darkness and shaken 3 or 4 times until they were bleached, according to the method of Tang et al. (2015). The absorbance was measured with a spectrophotometer Shimadzu UV-2550 (Kyoto, Japan) at 646.6, 663.6 and 450 nm respectively, after centrifugation of the mixture on standing. Chlorophyll concentrations were calculated by the standard method of Porra et al. (1989) and expressed in mg g−1 fresh weight (FW).
Determination of flavonoid concentration
Approximately 50 g of fresh fully developed leaves of each provenance and shading treatment was sampled at about 1 month intervals (20 July, 20 August, 20 September, 20 October and 15 November in 2011). All samples were dried, sliced and ground into fine powder before extraction. Samples were stored at room temperature prior to analysis.
For flavonoid extraction, flavonoids were extracted using an ultrasonic-assisted method with minor modifications (Huang et al. 2009). Briefly, 50 mL of 75 % ethanol was added to each sample and the extraction was conducted for 45 min at 65 °C.
The total flavonoid concentration was determined by using a colorimetric method with minor modification (Bao et al. 2005). About 2.0 g sample was placed in a soxhlet extractor and refluxed with petroleum ether for 4 h at 80 °C to remove fat soluble impurities. The extract was discarded, and the retained residues were dried at room temperature. The extract was evaporated to dryness in a rotary vacuum evaporator at <40 °C and then dissolved with methanol. Exactly 0.3 mL of 5 % NaNO2 was added to a 1 mL extract in a 10 mL volumetric flask, and the mixture was kept for 5 min at room temperature. The residue was extracted two times and the obtained extract was combined and condensed to 10 mL. Addition of 0.3 mL of 10 % AlCl3·6H2O to the mixture, which was incubated for another 5 min, was followed by the addition of 2 mL of 1 M NaOH. After 15 min of incubation at room temperature for color development, the absorbance at 415 nm was measured. Total flavonoid concentration was calculated using the standard rutin curve and expressed as milligrams rutin equivalent per gram of dry mass (mg/g dm).
Analysis of selected flavonoids (kaempferol, quercetin and isoquercitrin) was performed using high-performance liquid chromatography. All obtained extracts were filtered through a 0.45 um polytetrafluoroethylene (PTFE) filter prior to HPLC analysis. An Agilent 1200 series HPLC system (Waldbronn, Germany), which consists of an online degasser, a quaternary pump solvent management system, an autosampler, a column heater, an UV/VIS diode array detector (DAD), and a data processing system, was used for the flavonoid separation. Quercetin and kaempferol were quantified as aglycones after acid hydrolysis. The hydrolyzed extracts were separated on an Eclipse Plus C18 column (250 mm × 4.6 mm, 5 um) at 30 °C. The mobile phases were methanol (A) and 0.3 % phosphoric acid (B) at 55: 45 (VA/VB). The flow rate was 1.0 mL min−1and the wavelength of detection was 365 nm. For isoquercitrin determination, the mobile phases were methanol (A) and 0.5 % phosphoric acid (B). The gradient elution included 0–25 min, 15 % A; 15–26 min, 15–90 % A; 26–36 min, 90 % A; 36–37 min, 90–15 % A; and 37–45 min, 25 % A. The detection wavelength was 350 nm. The column temperature and flow rate were similar to the conditions described for the detection of quercetin and kaempferol. The standards of quercetin, kaempferol (Sigma–AldrichInc., St. Louis, USA), and isoquercitrin (National Institute for the Control of Pharmaceutical and Biological Products, Beijing, China) were used to obtain an external calibration curve.
Data are reported as the mean ± standard deviation (SD), and all tests were performed using the SPSS 16.0 statistical software program (SPSS, Chicago, IL, USA). A two-way ANOVA model with shading and provenance as the main fixed factors plus a shading × provenance interaction term, followed by Tukey’s multiple-range test, was performed for each leaf characteristic, flavonoid concentration, plant growth, and flavonoid accumulation per plant. Relationships be-tween leaf characteristics, individual environmental factors (solar radiation, air temperature, and RH values) and leaf flavonoid concentration were evaluated using the Pearson’s correlation analysis. The data were tested for normality (Shapiro–Wilk normality test) before analysis of variance. All statistical analyses were performed at a 95 % confidence level.
Variation in environmental factors
The microclimatic parameters varied in different shading conditions. From June 20 to October 20, values of daily mean air temperature in the three shading treatments were 31.04 ± 4.92 °C for A1, 29.39 ± 4.99 °C for A2, and 27.41 ± 4.11 °C for A3, whereas the daily mean RH values were 63.2 ± 16.25, 69.82 ± 4.99, and 74 ± 16.08 % for A1, A2, and A3, respectively. Also, a great difference in the range of PPFD was observed at the same time. The distribution of PPFD in treatment A1 was 29.2 % in 0–200 μmol/m2/s, 25.3 % in 201–400 μmol/m2/s, 14.5 % in 401–600 μmol/m2/s, 10.2 % in 601–800 μmol/m2/s, 6.6 % in 801–1000 μmol/m2/s, and 14.2 % in >1000 μmol/m2/s during the 4 months. The PPFD in treatment A2 ranged from 0 to 600 μmol/m2/s, and the distribution was 73.3 % in 0–200 μmol/m2/s, 20.3 % in 201–400 μmol/m2/s, and 5.4 % in 401–600 μmol/m2/s, whereas the greatest PPFD distribution in treatment A3 was in 0–200 μmol/m2/s (accounting for 98.2 %) in the same periods.
Variation in leaf characteristics
Leaf characteristics and chlorophyll concentration of Cyclocarya paliurus leaves under different treatments
Leaf area per plant (cm2)
Leaf thickness (μm)
Palisade length (μm)
Total chlorophyll concentration (mg g−1)
Chlorophyll ratio a/b
846 ± 25.8a
244.1 ± 19.5d
110.1 ± 4.5c
1.69 ± 0.28abc
4.00 ± 0.02e
793 ± 15.8a
301.0 ± 20.6e
134.7 ± 2.2d
1.43 ± 0.16a
3.54 ± 0.04c
1158 ± 23.2abc
257.2 ± 9.1d
123.1 ± 8.2cd
1.35 ± 0.24a
3.96 ± 0.20e
1299 ± 177.3abc
135.5 ± 24.4ab
79.0 ± 6.3b
2.19 ± 0.22d
3.78 ± 0.06d
867 ± 79.5a
170.2 ± 1.5c
78.2 ± 4.3b
1.63 ± 0.08ab
3.43 ± 0.03bc
1610 ± 115.6c
126.0 ± 14.2ab
60.8 ± 3.2a
1.94 ± 0.29bcd
3.56 ± 0.06c
959 ± 16.0ab
105.0 ± 19.7a
55.8 ± 6.3a
2.15 ± 0.21cd
3.55 ± 0.03c
1156 ± 48.1abc
147.8 ± 17.2ab
76.1 ± 7.5b
1.79 ± 0.24abcd
3.25 ± 0.04a
1384 ± 43.3bc
116.3 ± 1.1a
50.0 ± 6.5a
2.08 ± 0.11cd
3.38 ± 0.06b
Summary of significance levels (Two-way ANOVA) for the effects of shading, provenance and their interaction on leaf characteristics and chlorophyll concentration of Cyclocarya paliurus leaves
Leaf area (cm2)
Leaf thickness (μm)
Palisade length (μm)
Total chlorophyll concentration (mg g−1)
Interaction (A × B)
Tukey’s multiple-range test of leaf characteristics and chlorophyll concentration of Cyclocarya paliurus leaves after a Two-way ANOVA
Leaf area (cm2)
Leaf thickness (μm)
Palisade length (μm)
Total chlorophyll concentration (mg g−1)
Variation in leaf flavonoid concentration and seasonal dynamics
Summary of significance levels (Two-way ANOVA) for the effects of shading, provenance and their interaction on biomass accumulation, flavonoid concentrations and flavonoid yield in leaves of Cyclocarya paliurus
Biomass accumulation (g plant−1 dm)
Flavonoid concentrations (mg g−1 dm)
Flavonoid yield (mg plant−1 dm)
Flavonoid concentrations in leaves of Cyclocarya paliurus under various treatments of shading and provenance (mean ± SD, samples collected in October 20, 2011)
Flavonoid concentrations (mg g−1)
40.9 ± 4.6b
2.11 ± 0.19c
2.37 ± 0.32b
2.12 ± 0.79b
42.6 ± 2.8b
2.13 ± 0.03c
4.35 ± 0.53d
2.10 ± 0.01b
45.8 ± 9.3b
1.28 ± 0.31b
3.67 ± 0.64c
2.97 ± 0.35c
24.8 ± 3.4a
0.62 ± 0.05a
0.53 ± 0.07a
0.87 ± 0.08a
23.3 ± 2.2a
0.40 ± 0.04a
0.76 ± 0.07a
0.59 ± 0.06a
28.0 ± 6.1a
0.41 ± 0.08a
0.77 ± 0.20a
0.91 ± 0.17a
27.6 ± 1.8a
0.54 ± 0.05a
0.49 ± 0.06a
0.71 ± 0.07a
28.8 ± 6.4a
0.50 ± 0.13a
1.06 ± 0.16a
0.44 ± 0.01a
30.7 ± 0.6a
0.25 ± 0.03a
0.50 ± 0.05a
0.35 ± 0.03a
Variation in biomass production and allocation
Variation in biomass production of Cyclocarya paliurus under different treatments of shading and provenance (mean ± SD, samples collected in October 20, 2011)
Biomass production (g)
57.9 ± 4.00cd
62.9 ± 7.08cd
21.6 ± 2.72a
142.5 ± 13.8bc
47.8 ± 5.42cd
46.4 ± 4.70bc
21.9 ± 2.48a
112.6 ± 12.6b
104.5 ± 9.50d
129.3 ± 13.76d
82.7 ± 8.75b
316.5 ± 32.02d
20.1 ± 2.08bc
30.8 ± 2.36b
11.5 ± 1.73a
62.5 ± 6.18ab
36.9 ± 3.22bcd
40.4 ± 3.25bc
25.8 ± 2.05a
103.1 ± 8.53ab
59.8 ± 5.50 cd
106.0 ± 10.27d
71.3 ± 6.67b
237.2 ± 22.46cd
9.4 ± 1.48a
11.3 ± 0.82a
5.6 ± 0.47a
26.4 ± 2.77a
17.2 ± 1.92b
12.6 ± 0.77a
10.3 ± 0.74a
40.3 ± 3.44ab
12.6 ± 2.18b
10.7 ± 0.98a
8.8 ± 0.46a
32.2 ± 2.59a
Variation in flavonoid accumulation
Effects of light regime and provenance on leaf characteristics
Photosynthetic light acclimation involves a variety of responses, including changes in leaf anatomy (Weston et al. 2000). The palisade parenchyma and spongy parenchyma in the leaf mesophyll are important photosynthetic tissues. Palisade tissue enables a better light penetration to the chloroplasts, while spongy tissue enhances the light capture by scattering light (Evans 1989). In the current study, higher light intensity seemed to positively affect the leaf growth and structure of the palisade parenchyma of C. paliurus, as the maximum length of palisade cells was observed under full light conditions (Table 1; Fig. 1). This indicated that the adjustment of palisade lengths under different light conditions is part of photosynthetic acclimation. Plants under full light conditions had a significantly higher biomass accumulation, while insufficient light under shading treatments resulted in reduced net carbon gain and plant growth (Table 6). Larger leaves and increased pigments concentrations in shading treatments may be a response to low photosynthetic photon flux density (PPFD), as larger leaves and more pigments would improve light interception and absorption for photosynthesis when light levels are low (Delagrange et al. 2006; Peri et al. 2007; Valladares and Niinemets 2008). In addition, the reduction in the Chla/b ratio was observed under shade treatments mainly due to the increase in Chlb concentration (Tables 1, 3), which contributes to the light capture for photosynthesis (Murchie and Horton 1997). These findings are similar to the results reported in other species (Zhao et al. 2012; Ma et al. 2015; Tang et al. 2015).
A two-way ANOVA showed that both light intensity and provenance significantly affected the morphology and leaf growth index of C. paliurus (Table 2). However, no significant interaction of light intensity and provenance was observed in LA, leaf thickness and total chlorophyll concentration of C. paliurus. The results from this study also showed that C. paliurus of Muchuan provenance presented a better adjustment to shading conditions compared with Wufeng provenance and Yuanling provenance, as the largest value of LA was observed in shading treatments of Wufeng provenance (Tables 1, 3), which indicated that provenance selection is important for planting C. paliurus under different environments.
Effects of light regime and provenance on growth and flavonoid concentration
It is generally recognized that light intensity plays an important role in plant growth and photosynthetic capacity (Gottschalk 1994). Insufficient light may stress plant growth by limiting photosynthesis, while high light levels may damage the photosynthetic apparatus (Tang et al. 2015). The present study demonstrated that shading had significant negative effects on leaf and total biomass production of C. paliurus coppices, while full light condition resulted in the highest growth for all the components, indicating that C. paliurus is a heliophyte. The observed growth response of C. paliurus to light intensity was similar to that of many tree species growing under various light intensities (Poorter 1999; Cai et al. 2009; Ma et al. 2015; Tang et al. 2015). The present study also indicated that leaf biomass ratio of C. paliurus increased at lower light intensity, whereas full sunlight increased the root and stem biomass ratios, respectively (Table 6). The reason might be that higher transpiration rate leads to increasing root biomass allocation in order to improve water uptake ability under full sunlight conditions, in agreement with that reported on Rauvolfia species, Anoectochilus formosanus Hayata, and freshwater macrophytes (Cai et al. 2009; Ma et al. 2010; Cronin and Lodge 2003).
Light intensity is known to affect not only plant growth and development but also the biosynthesis of both primary and secondary metabolites (Hemm et al. 2004). Fang et al. (2011) reported that genotypes play a significant role in flavonoid accumulation of C. paliurus grown under the same environment. In the present study, a two-way ANOVA showed that shading significantly affected concentrations of total and selected flavonoids in C. paliurus leaves, and meanwhile provenance and the interaction between shading and provenance also significantly affected the concentrations of quercetin and isoquercitrin. However, provenance and the interaction had no significant effects on concentrations of total flavonoid and kaempferol (Table 4). Differences in flavonoid concentration were significant among the five sampling times, showing that flavonoid accumulation was strongly affected by seasonal progression. This finding suggests that shading treatments not only reduced the leaf concentrations of flavonoids but also delayed the appearance of the highest flavonoid concentrations in C. paliurus leaf of different provenances during the growing season. Seasonal changes of flavonoid concentrations under different light conditions also indicated that the contents of flavonoids were highly positively correlated with total solar radiation in the period from planting to the sampling time, in agreement with the results from previous study (Gliszczyńska-Świgło et al. 2007). Overall, shading had a significantly negative effect on the accumulation of total flavonoids and the studied flavonoids (Table 5), supporting that high photosynthetic active radiation (PAR) triggers biosynthesis of flavonoids (Xu et al. 2014).
Pearson correlation coefficients between environmental parameters and leaf flavonoid concentrations (n = 27)
Flavonoid concentrations (mg g−1)
Monthly light intensity (μmol m−2 s−1)
Monthly air temperature (°C)
Monthly relative humidity (%)
Pearson correlation coefficients between leaf characteristics and leaf flavonoid concentrations (n = 27)
Flavonoid concentrations (mg g−1)
Leaf area per plant (cm2)
Leaf thickness (μm)
Palisade length (μm)
Total chlorophyll concentration (mg g−1)
Chlorophyll ratio a/b
Effects of light regime and provenance on flavonoid production
Plant growth and content of phytochemicals are affected by genetic, management practice, harvesting and environment factors that occur during the growing period (Graham 1998; Björkman et al. 2011; Deng et al. 2012). Two-way analysis of variance indicated that biomass accumulation of C. paliurus coppices was not only significantly influenced by light intensity, but also significantly by genotype and interactions between these two variables (Table 4). The present study indicated that B3 treatment (Muchuan provenance) achieved the highest total biomass, and the highest leaf biomass in all shading conditions, compared with other provenances. Thus, provenance selection is crucial to optimize higher flavonoids yield of C. paliurus coppices, as leaf biomass has a great contribution to the accumulation of total flavonoid and key health promoting flavonoids (quercetin, kaempferol, and isoquercitrin) per plant.
In leaf-harvest plantations of C. paliurus coppice, the goal is to obtain not only higher quality (higher flavonoid concentrations) but also higher yield (equal to flavonoid concentrations multiplied by leaf biomass), thus both provenance selection and the optimal silvicultral measures are important for production practices aimed at obtaining higher flavonoids yields (Poutaraud and Girardin 2005). However, the response may be quite different and also vary for different crops and secondary metabolites. For example, fertilizer application did not promote polyphenolic formation in apples (Morales-Sillero et al. 2008) and leaf flavonoid content in C. paliurus (Deng et al. 2012), whereas leaf phenolics concentrations were 31 % higher in fertilized than in unfertilized plants of freshwater macrophytes (Cronin and Lodge 2003). In the present study, the A1B3 treatment (full light and Muchuan provenance) was the most effective way to improve the accumulations of total and selected flavonoids because it resulted in the highest leaf biomass production. Overall, in order to achieve the highest flavonoid yield per area for food and medicinal utilization, it is important to manipulate field-growing conditions such as light intensity and select genotypes in C. paliurus coppices. However, more provenance trials are required to clarify the genotype effects of this species at different sites.
In conclusion, significant variations in leaf morphology, growth and accumulations of total and selected flavonoids were found in C. paliurus growing under light intensity and genotype treatments. Both light regime and provenance significantly affected the morphology and growth index of C. paliurus leaves. In the full light condition, leaf flavonoid concentrations showed a bimodal variation pattern. However, shading treatments not only reduced the leaf concentrations of flavonoids but also delayed the peak appearing of the flavonoid concentrations in C. paliurus leaf of different provenances. Muchuan provenance with full light achieved the highest leaf biomass and flavonoid accumulation. Moreover, documentation of genotypic variation among different light environments provides a basis for extensive selection and breeding programs in improving the leaf concentrations of flavonoids compounds of C. paliurus.
SF and XS conceived and designed the experiments. YL did data analysis and prepared the manuscript. CQ and SD carried out field work and the chemical analysis. WY and XS contributed to field work and data collection. SF also supervised the study, reviewed and edited the work. All authors read and approved the final manuscript.
We acknowledge financial support from the National Natural Science Foundation of China (No. 31270673), a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD) and the Doctorate Fellowship Foundation of Nanjing Forestry University.
The authors declare that they have no competing interests.
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