Next Article in Journal
NaCl Modifies Biochemical Traits in Bacterial Endophytes Isolated from Halophytes: Towards Salinity Stress Mitigation Using Consortia
Previous Article in Journal
Ecology of Elodea canadensis Michx. and Elodea nuttallii (Planch.) H. St. John—Insights from National Water Monitoring in Croatia
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Phenotypic Variation in Moso Bamboo and the Selection of Key Traits

1
International Centre for Bamboo and Rattan, Key Laboratory of National Forestry and Grassland Administration, Beijing 100102, China
2
Yunnan Diannan Bamboo Forest Ecosystem Research Station, Cangyuan County, Lincang 677400, China
*
Author to whom correspondence should be addressed.
Plants 2024, 13(12), 1625; https://doi.org/10.3390/plants13121625
Submission received: 29 April 2024 / Revised: 6 June 2024 / Accepted: 8 June 2024 / Published: 12 June 2024
(This article belongs to the Special Issue Biodiversity Informatics and Plant Conservation)

Abstract

:
This research aimed to explore the diverse phenotypic characteristics of moso bamboo in China and pinpoint essential characteristics of moso bamboo. In this study, 63 grids were selected using the grid method to investigate 28 phenotypic traits of moso bamboo across the entire distribution area of China. The results suggest that the phenotypic traits of moso bamboo exhibit rich diversity, with coefficients of variation ranging from 5.87% to 36.57%. The phenotypic traits of moso bamboo showed varying degrees of correlation. A principal component analysis was used to identify seven main phenotypic trait indicators: diameter at breast height (DBH), leaf area (LA), leaf weight (LW), branch-to-leaf ratio (BLr), leaf moisture content (Lmc), wall-to-cavity ratio (WCr), and node length at breast height (LN), which accounted for 81.64% of the total information. A random forest model was used, which gave good results to validate the results. The average combined phenotypic trait value (D-value) of most germplasm was 0.563. The highest D-value was found in Wuyi 1 moso in Fujian (0.803), while the lowest D-value was observed in Pingle 2 moso in Guangxi (0.317). The clustering analysis of phenotypic traits classified China’s moso bamboo germplasm into four groups. Group I had the highest D-value and is an important candidate germplasm for excellent germplasm screening.

1. Introduction

Moso bamboo (Phyllostachys edulis) is a member of the Phyllostachys genus of the Gramineae family and is mainly found in subtropical regions. The Ninth National Forest Resources Inventory Report reveals that China’s abundant moso bamboo forest spans 4.67 million hectares, making up 72.96% of the nation’s overall bamboo forest expanse [1]. Phenotypic traits are easily observed, as are measured characteristics produced by the adaptation of plants to different environments during the evolutionary process [2]. The study of phenotypic trait characteristics can reveal the degree of phenotypic variation in plants [3], divide plant germplasm taxa, screen representative traits [4], and is an important basis for the selection of excellent seed sources.
The growth characteristics of moso bamboo resources exhibit notable variations in different geographical areas due to artificial introduction and natural variation over time [5]. For instance, a study identified distinct geographical variability among 17 natural moso bamboo populations in Jiangxi Province, leading to the selection of several dominant moso bamboo germplasm based on four utilization indicators: diameter at breast height, bamboo wall thickness at breast height, height under branches, and culm length [6]. Moreover, the phenotypic characteristics of moso bamboo seeds displayed significant variation across different seed sources, with culm nodes and crown length playing a pivotal role in seed yield [7]. Notably, researchers found that the nutrient characteristics of moso bamboo fine roots varied considerably at different altitudes in the Wuyi Mountain area, suggesting adaptive strategies to the environment [8]. Additionally, a study investigating moso bamboo in six sites within China’s range revealed varying leaf traits across geographical regions [9]. Furthermore, the growth and phenotypic traits of moso bamboo populations in different latitudinal regions (Anhui, Guangxi, and Zhejiang) showed significant differences, with the average length nodes under branches and leaf traits emerging as the most dominant phenotypic traits based on a principal component analysis [10]. Overall, these findings underscore the presence of geographic variation in different moso bamboo populations.
The moso bamboo is widely distributed in 14 provinces across China, from the Qinling Mountains and the Han River Basin to the southern part of the Yangtze River Basin. However, current research on the phenotypic traits of moso bamboo is primarily focused on specific provinces and regions or areas where the distribution of moso bamboo is concentrated. This has led to a relatively narrow focus on phenotypic traits. Therefore, there is a need to expand research on the phenotypic diversity of moso bamboo across the entire range of China. In this study, we used a grid method to systematically examine the phenotypic traits of moso bamboo, aiming to uncover the phenotypic diversity of moso bamboo germplasm in China. Our goal is to explore the relationship between different phenotypic traits of moso bamboo, identify the most important ones, and provide a theoretical basis for selecting excellent moso bamboo germplasm.

2. Materials and Methods

2.1. Bamboo Germplasm for Testing

The distribution of moso bamboo in China was determined based on the literature, China Digital Herbarium, and a field survey, and 63 grids of 150 km × 150 km were established. Based on the distribution of moso bamboo, two sample points were selected in each grid to investigate the phenotypic characteristics of moso bamboo. Three 20 m × 20 m sample plots were established for each sample point (the interval between sample plots was more than 50 m), and a total of 338 sample plots were established. The survey was conducted to investigate the diameter at breast height (DBH), age, and management history of the moso bamboo in the sample plots. According to the average diameter at breast height of the moso bamboo in the sample plot, five standard plants were selected to study the growth characteristics of the moso bamboo, and one second-degree moso bamboo (2–3 years old) was felled for further determination of culm characteristics, leaf blade morphology, and other traits.

2.2. Measurement of Phenotypic Traits

2.2.1. Measurement of Phenotypic Character

Phenotypic traits were determined concerning the Specification for the Description of Forest Germplasm Resources [11] and growth traits (plant height, diameter at breast height, plant crown, branch-to-leaf ratio, water content, and biomass), culm shape traits (diameter at ground level, taper grade, number of nodes of the whole culm, length of node at breast diameter, height under the branch, number of nodes under the branch, thickness at base of pole, thickness at breast height, and wall-to-cavity ratio) and leaf traits (leaf area, leaf shape, leaf dry matter content, leaf thickness, and specific leaf area) were measured in a total of 28 traits.
We used a 0.1 cm diameter tape to measure diameter at breast height, diameter at ground level, and section length at breast height. The SENSSUM EP170 portable electronic scale was used to measure biomass. We used vernier calipers with a precision of 0.01 mm to measure the bamboo wall thickness of the diameter at breast height and the wall thickness at the base of the culm in the four directions of east, south, west, and north to obtain the mean value; we randomly selected 60 leaves from the upper, middle, and lower parts of the culm, and 10 leaves were used as a group to measure the leaf thickness with vernier calipers (0.01 mm) and leaf thickness with a camera (0.01 mm). Leaf thickness was measured with calipers (0.01 mm), photographs were taken with a camera, and leaf length, width, and area were calculated with Image J (2.3.0/1.54d). The leaves, some culms, and branches were taken back to the laboratory, and the weights were determined with an electronic balance with an accuracy of 0.01 g. The leaves were dried in an oven at 105 °C for 30 min; then, the temperature was adjusted to 60 °C to dry to a constant mass, and the corresponding dry mass was measured. The calculation of astringency was carried out using the absolute astringency calculation method.
Wall-to-cavity ratio WCr (mm/mm) = 2 × thorax wall thickness/cavity diameter × 100%
Knot-to-leaf ratio BLr (g/g) = Knot fresh weight/leaf fresh weight × 100%
Specific leaf area SLA (cm2/kg) = Leaf area/leaf dry weight

2.2.2. Statistical Analysis

The maximum, minimum, mean, standard deviation, and coefficient of variation in each trait were statistically calculated using Excel 2019 [12]. R 4.3.2 was used to perform a cluster analysis [13], principal component analysis [14], and correlation heat map; random forest modeling of phenotypic trait data was achieved using the R extension package random Forest [15,16]; ArcGis 10.7 was used to draw distribution maps; and the affiliation function was used to generate a comprehensive index score D to evaluate moso bamboo germplasm resources [17,18].
The value of the affiliation function is as follows:
μ   ( X i ) = ( X i X m i n ) / ( X m a x X m i n ) ,   i = 1 , 2 , , n .
where Xi is the ith composite indicator, Xmin is the minimum value of the ith composite indicator, and Xmax is the maximum value of the ith composite indicator.
The composite indicator weights are as follows:
W i = P i P i , i = 1 , 2 , , n .
where Wi is the weight of the ith composite indicator among all composite indicators and Pi represents the contribution of the ith principal component factor.
The composite indicator superiority is as follows:
D j = μ X i × W i , j = 1 , 2 , , n .
where n is the number of samples and D is the composite indicator assessment value.

3. Results

3.1. Phenotypic Traits

The coefficients of variation in the phenotypic traits of moso bamboo ranged from 5.87% to 36.57% (Table 1), indicating that the numerical traits of moso bamboo were rich in variation. The coefficient of variation for branch moisture content was the highest at 36.57%, and the coefficient of variation for leaf length to width was the lowest at 5.87%. The degree of variation in traits related to the weight and water content of moso bamboo were larger, both exceeding 20%, indicating that the variation in biomass of moso bamboo was larger, and the morphological indices of moso bamboo were rich in variation in growth, with a high diversity of phenotypic traits; the coefficients of variation in leaf blade traits ranged from 5.87% to 14.69%; and the range of variation in height under branches was from 4.36 to 10.87 m, with a coefficient of variation of 18.56%, which was the most obvious variation in the traits of moso bamboo culms. The coefficients of variation for whole culm node number and breast diameter node length were 7.51% and 7.53%, respectively, which were smaller.

3.2. Characterisation of Correlations between Phenotypic Traits

The results of the correlation analysis indicate varying degrees of associations among phenotypic traits (Figure 1). Apart from length of node at breast diameter (LN), branch moisture content, and leaf traits, diameter at breast height (DBH) exhibits significant or highly significant correlations with other traits. The correlation coefficients between DBH and diameter at ground, weight of branches, total weight, and cavity diameter exceed 0.9, while negative correlations are observed with wall-to-cavity ratio and Bmc, with coefficients of −0.50 and −0.11, respectively. Taper grade is highly negatively correlated with LN, leaf thickness, leaf area, leaf width, and leaf length–width ratio. LN shows highly significant positive correlations with leaf thickness, leaf area, leaf length, and leaf width and highly significant negative correlations with branch moisture content, leaf moisture content, leaf length–width ratio, and specific leaf area. Leaf thickness, leaf area, leaf length, and leaf width are highly negatively correlated with culm moisture content and leaf moisture content but are unrelated to branch moisture content. Specific leaf area is significantly positively correlated with branch moisture content, branch moisture content, and leaf moisture content, while exhibiting a highly significant negative correlation with under-branch height; plant crown is highly positively correlated with leaf length–width ratio.

3.3. Screening for Key Phenotypic Characteristics

Since there are varying degrees of correlation between phenotypic traits, direct evaluation of the germplasm based on this information will affect its authenticity. The use of a principal component analysis for comprehensive evaluation of the participating germplasm can explain the variation in moso bamboo phenotypic traits with fewer traits. Using an eigenvalue greater than 1.0 as the basis for principal component screening, the first eight principal components were extracted with a cumulative contribution rate of 81.64%, which can better summarize most of the information of the 28 phenotypic traits of the participating germplasm (Table 2). The eigenvalues of the principal components were 9.241, 3.985, 2.335, 1.967, 1.83, 1.29, 1.185, and 1.026, respectively, among which the contribution rate of the first principal component was 33.002%, and the eigenvectors of breast diameter, total weight of moso bamboo, ground diameter, and cavity diameter were larger; the contribution rate of the second principal component was 14.231%, and the eigenvectors of leaf area, leaf width, leaf length, node length at breast diameter, and specific leaf area were larger leaf area; the contribution rate of the third principal component was 8.338%, the eigenvectors of leaf weight, branch and leaf weight, height under branch, leaf length, and leaf aspect ratio were larger. The first and third principal components reflected the biomass of moso bamboo. The contribution rate of the fourth principal component was 7.026%, and the eigenvectors of branch and leaf ratio and sharpness were larger, which reflected the plant type of moso bamboo; the contribution of the fifth principal component was 6.536%, the eigenvectors of leaf water content and specific leaf area were larger, and the second and fifth principal components reflected the phenotypic characteristics of moso bamboo leaf blades; the contribution rate of the sixth principal component was 4.608%, the eigenvectors of wall to cavity ratio, wall thickness at breast diameter and culm water content were larger, reflecting the situation of the morphological characteristics of the wall of the culm of moso bamboo. The largest eigenvectors of the seventh and eighth principal components were branch-to-leaf ratio and node length at breast diameter, respectively. Seven phenotypic traits, namely breast diameter, leaf area, leaf weight, branch-to-leaf ratio, leaf water content, wall-to-cavity ratio, and node length, were extracted from the 28 traits, which were the main factors leading to the differences in phenotypic traits of moso bamboo and were used as important indices for evaluating the germplasm resources of moso bamboo.

3.4. Comprehensive Evaluation of Phenotypic Characteristics

By standardizing the 28 trait values of the moso bamboo germplasm and substituting them into the above eight principal components, the eight principal component scores of each germplasm were obtained, the eight principal component scores were normalized using the fuzzy affiliation function method, and the weight coefficients of the eight principal components were calculated (0.404, 0.174, 0.102, 0.086, 0.08, 0.056, 0.052, and 0.045), and then, the composite scores (D-value) of each type of germplasm were calculated (Table 3), and all the germplasm were comprehensively evaluated by D-value. The results showed that the average composite score (D-value) of phenotypic characteristics of moso bamboo germplasm was 0.563, with the highest D-value of Wuyi 1 moso bamboo in Fujian Province (0.803) and the lowest D-value of Pingle 2 moso bamboo in the Guangxi Zhuang Autonomous Region (0.317), indicating that Wuyi 1 moso bamboo had the best comprehensive characteristics and Pingle 2 moso bamboo had the worst comprehensive characteristics.
Correlation analyses were conducted based on 28 phenotypic traits and D-values (Table 4). The results showed that the D-value was positively correlated with 13 trait indices, including diameter at breast height, diameter at ground level, plant height, and number of whole culm nodes, and the correlation reached a highly significant level (p < 0.001), was negatively correlated with the wall-to-cavity ratio and reached a highly significant level (p < 0.001), whereas diameter at node length, branch-to-leaf ratio, culm water content, leaf water content, leaf thickness, leaf area, leaf length, leaf width, and the composite value of D were not correlated with the composite value of D.

3.5. Comprehensive Evaluation of Phenotypic Traits

Based on the above 28 characters, when the Euclidean distance was 62, all the moso bamboo germplasm could be divided into four clusters using the full maximum distance method (Figure 2a), and there were differences in moso bamboo phenotypic traits among the clusters (Table 5). The clustering of germplasm from different provinces was not strictly based on geographical location (Figure 2b).
Group I includes 54 germplasm with a large diameter at breast height, large diameter at ground level, large total biomass, high plant height, high under branching, thick culm wall, high number of nodes in the whole culm, large leaf blade area, small specific leaf area, and low water content in the culm and branches. Overall, the germplasm is excellent, containing all the germplasm from Yunnan, more than 70% of the germplasm from Anhui and Fujian, and more than 38% of the germplasm from Hubei, Sichuan, Chongqing, Zhejiang, Jiangxi, and Hunan.
Group II includes 26 germplasm with a small diameter at breast height, small diameter at ground level, low sharpness, small biomass, low plant height, low height under branches, small branch-to-leaf ratio, and thin culm walls, but long nodes at breast height. The germplasm was poor overall, containing all the germplasm from Henan and 75% of the germplasm from Jiangsu.
Group III includes 25 germplasm with a larger diameter at breast height, large diameter at ground level, large biomass, large sharpness, short node length at breast height, high culm water content, thin leaf thickness, and large leaf aspect ratio and contains all the germplasm from Guizhou and 56% of the germplasm from Jiangxi.
Group IV includes eight germplasm with a large branch-to-leaf ratio, high branch water content, high leaf water content, small leaf area, and larger than leaf area, and contains 50% of the germplasm from Guangxi.

3.6. Identification of Different Taxa of Moso Bamboo Germplasm

A random forest discriminant model was constructed to classify and predict the four taxa using seven phenotypic characters, namely, breast diameter, leaf area, leaf weight, branch-to-leaf ratio, leaf water content, wall-to-cavity ratio, and node length. From 113 germplasm, 70% of the samples were selected as the training set, and 30% were made as the independent test set. The random forest algorithm was used to train the training set to construct the prediction model, and the number in the random forest was 500, and when the number of model node variables was 6, the mean of the model misclassification rate was the lowest at 26.58%, and the prediction accuracy of its cross-validation was 70.59% (Table 6). The importance of the phenotypic traits of moso bamboo based on the random forest classification output is shown in Figure 3. The significance of the average reduction in accuracy is in the following order: diameter of breast > leaf water content > leaf area > diameter of breast node length > leaf weight > branch-to-leaf ratio > wall cavity ratio. The established random forest discriminant model can effectively discriminate different types of germplasm and verifies that these seven phenotypic traits can be used as indicators to evaluate the germplasm resources of moso bamboo.

4. Discussion

4.1. Phenotypic Diversity of Moso Bamboo Germplasm Resources

Plant germplasm resources have been selected naturally and artificially to form the diversity of plant phenotypic traits, and the study of plant phenotypic trait diversity is the basis for the effective organization, conservation, and use of crop improvement [19]. In this study, the mean coefficient of variation in phenotypic traits of moso bamboo was 16.65%. The variation ranged from 5.87% (leaf aspect ratio) to 36.57% (branch moisture content). The coefficients of variation in the traits varied, which were lower than those of Dendrocalamus lactiferous Munro (30.84%), Salix psammophila (22.53%), and Ziziphus jujuba var. spinosa (Bunge) Hu ex H.F.Chow. (19. 80%) [20,21,22], indicating that the moso bamboo germplasm has smaller variations than other species, which is similar to previous research [10], but is different in terms of variation in traits. The results of previous studies have shown that in the coefficient of variation in traits, the following order is observed: Thoracic diameter < Thoracic node length < Thoracic wall thickness, whereas with the results of the present study, the following order is observed: Thoracic node length < Thoracic diameter < Thoracic wall thickness, which may be due to the difference in the study area and scale of this study. Among leaf traits, there is a close correlation between specific leaf area and biomass allocation, leaf morphology, and phenotypic plasticity in physiology [23], and the coefficient of variation in specific leaf area of moso bamboo was the largest in leaf morphological traits in this study (14.69%), suggesting that adaptive changes in functional traits of leaf blades of moso bamboo in China are an important strategy to adapt to different growth environments.

4.2. Key Phenotypic Traits of Moso Bamboo Germplasm Resources

There were obvious correlations among the traits in this study that reached significant or highly significant levels, and the correlation coefficients between breast diameter, ground diameter, and total biomass exceeded 0.9, which was consistent with the results of studies on conifers [24] and horsetail pine [25]. The correlation coefficient between sharpness and breast pitch length was −0.83, having the largest absolute value of the negative correlation coefficient. Phenotypic traits are not independent of one another [26]; there are varying degrees of correlation among the phenotypic traits of bamboo. Evaluating germplasm solely based on this information may compromise its authenticity. Therefore, we conducted a principal component analysis on all phenotypic traits to identify which traits best represent the overall variation in the data [27]. In this study, seven phenotypic traits, namely, breast diameter, leaf area, leaf weight, branch–leaf ratio, leaf water content, wall-to-cavity ratio, and node length, were screened as the main phenotypic indices in evaluating the germplasm resources of moso bamboo, with cumulative contribution rates of 81% and 64%; at the same time, the seven main phenotypic indices were validated by applying the Random Forest Discriminant Model, which could better reflect the characteristics of moso bamboo germplasm resources from different regions. They can be taken as the key for the next round of research on the phenotypic characteristics of moso bamboo germplasm resources [28].

4.3. Evaluation of Moso Bamboo Germplasm Resources

Comprehensive evaluation of moso bamboo germplasm resources through the combination of the affiliation function method and principal component analysis has high reliability and feasibility and has been widely used in studies such as ginkgo [29] and soybean [30]. In this study, the average comprehensive value (D-value) of phenotypic traits of China’s moso bamboo germplasm was 0.563, with the highest D-value (0.803) and the best comprehensive traits for Wuyi 1 moso bamboo germplasm in Fujian Province and the lowest D-value (0.317) and the worst comprehensive traits for Pingle 2 moso bamboo germplasm in the Guangxi Zhuang Autonomous Region. By clustering the phenotypic traits, China’s moso bamboo was divided into four groups, and the evaluation of the D-value of the four groups could also better respond to the status of different types of germplasm, with Group I having the highest D-value, optimal in diameter at breast height, biomass, and wall thickness and greater application value. The lowest D-value was found in Group II, and the growth of moso bamboo germplasm was poor. The range of species distribution area is determined by climatic conditions [31]; in the same climatic environment, moso bamboo obtains similar hydrothermal conditions, and phenotypic traits are similar [32]; the distribution of taxon II in the higher latitude area belongs to the edge of the distribution of moso bamboo germplasm; the hydrothermal conditions are poorer, resulting in the lowest value of D of taxa from Group II, which is similar to the results of cluster analysis by Liu Jiping [33] on the ten climatic factors of the key bamboo-producing areas of China’s moso bamboo. This is similar to the results of Liu Jiping’s cluster analysis of ten climatic factors in key bamboo-producing areas in China. The quality of moso bamboo in taxa from Group III was superior, and the diameter at breast height was similar to that of taxa from Group I, but the length of the node at breast height was shorter. Increasing the specific leaf area and keeping the nutrients in the body can allow the plant to better adapt to the rich environment [34]. In the present study, taxa from Group IV had a smaller leaf area and leaf length and a larger specific leaf area, reflecting that taxon IV may have better environmental adaptation.

5. Conclusions

The phenotypic traits of China’s moso bamboo germplasm resources have a certain degree of variation and differentiation, and in general, the diversity of phenotypic traits is low. Seven key phenotypic indices, namely diameter at breast height (DBH), leaf area (LA), leaf weight (LW), branch-to-leaf ratio (BLr), leaf water content (LWC), wall-to-cavity ratio (WCR) and node length (NL), were selected to evaluate the moso bamboo germplasm resources. Based on the 28 phenotypic traits, China’s moso bamboo germplasm was divided into four groups, each with its characteristics, and important candidate germplasm could be screened out based on the characteristics of each group and the D-value, which could provide a reference for the development and utilization of moso bamboo resources.

Author Contributions

S.Z. and S.W.: investigation, formal analysis, methodology, and writing—review and editing; J.L.: investigation, methodology, and writing—original draft; J.W.: methodology and investigation; Z.D.: methodology and investigation; R.G.: investigation and software; S.F.: investigation and supervision; G.L.: supervision, investigation, and funding acquisition. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported by the National Key R&D Program of China (2021YFD2200501) and the Fundamental Research Funds for the International Centre for Bamboo and Rattan (1632021021).

Data Availability Statement

The original contributions presented in the study are included in the article, further inquiries can be directed to the corresponding author.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Li, Y.M.; Feng, P.F. Analysis of bamboo resources in China based on the ninth national forest resources inventory. World Bamboo Ratt. Newsl. 2019, 17, 45–48. (In Chinese) [Google Scholar]
  2. Wang, X.M.; Qiu, L.J.; Jing, R.L.; Ren, G.; Li, Y.; Li, C.; Qin, P.; Gu, Y.; Li, L. Phenotypic trait identification and evaluation of crop germplasm resources: Current status and trends. J. Plant Genet. Resour. 2022, 23, 12–20. [Google Scholar] [CrossRef]
  3. Khadivi-Khub, A.; Sarooghi, F.; Abbasi, F. Phenotypic variation of Prunus scoparia germplasm: Implications for breeding. Sci. Hortic. 2016, 207, 193–202. [Google Scholar] [CrossRef]
  4. Wang, Y.L.; Li, Y. Genetic diversity analysis of phenotypic traits among 37 Xanthoceras sorbifolium elite germplasms. J. For. Res. 2022, 27, 140–147. [Google Scholar] [CrossRef]
  5. Xia, X.W.; Huang, Y.F.; Zhou, M.P. Biodiversity of moso bamboo. Bamboo Res. Repos. 2014, 33, 6–15. (In Chinese) [Google Scholar]
  6. Shi, J.M.; Yang, G.Y.; Guo, Q.R.; Fan, G.; Zhong, A.; Zhang, W.; Wu, L.; He, G.; Xia, F. Geographic variation of phenotypic traits of moso bamboo in Jiangxi. J. Jiangxi Agric. Univ. 2008, 5, 824–828. (In Chinese) [Google Scholar]
  7. Jia, D.D.; Xu, Z.G.; Huang, R.; Zheng, Y.; Li, Z. Correlation analysis between phenotypic traits and seed yield of flowering moso bamboo. Guangxi For. Sci. 2022, 51, 331–336. [Google Scholar] [CrossRef]
  8. Huang, A.M.; Fang, Y.; Sun, J.; Li, J.; Hu, D.; Zhong, Q.; Cheng, D. Functional traits of fine roots of moso bamboo at different elevations in Wuyi Mountain. J. Ecol. 2023, 43, 398–407. [Google Scholar]
  9. Guo, W.; Paolo, C.; Zhang, J.; Hu, X.; Li, M.; Qi, L. Soil physicochemical properties determine leaf traits but not size traits of moso bamboo. Environ. Res. Lett. 2022, 17, 114061. [Google Scholar] [CrossRef]
  10. Zhang, W.B.; Fei, B.H.; Tian, G.L.; Yue, X.H.; Jiang, Z.H. Comparison of growth and phenotypic traits of moso bamboo in different regions. J. Northeast. For. Univ. 2019, 47, 1–5. [Google Scholar] [CrossRef]
  11. Zheng, Y.Q.; Lin, F.R.; Li, B.; Zong, Y.C.; Guo, W.Y.; Yu, X.D.; Li, W.Y. General Descriptors for Forest Germplasm Resources; China Standard Publishing House: Beijing, China, 2013; pp. 3–6. (In Chinese) [Google Scholar]
  12. Li, Y.L.; Zhang, Y.S.; Dong, A.H.; Liu, C.; Dong, Y.; Fu, Y.; Mao, X. Survey of germplasm resources and analysis of phenotypic trait diversity of Hepatica. South. For. Sci. 2022, 50, 17–23. [Google Scholar] [CrossRef]
  13. Liu, D.; Wang, X.; Li, W.; Li, J.; Tan, W.; Xing, W. Genetic Diversity Analysis of the Phenotypic Traits of 215 Sugar Beet Germplasm Resources. Sugar Technol. 2022, 24, 1790–1800. [Google Scholar] [CrossRef]
  14. Vaughan, P.I.; Ormerod, J.S. Increasing the Value of Principal Components Analysis for Simplifying Ecological Data: A Case Study with Rivers and River Birds. J. Appl. Ecol. 2005, 42, 487–497. [Google Scholar] [CrossRef]
  15. Li, X.H. Application of random forest model in classification and regression analysis. J. Appl. Entomol. 2013, 50, 1190–1197. (In Chinese) [Google Scholar]
  16. Meng, Y.D.; Du, H.Y.; Wang, L.; Lv, G.; Qing, J.; He, F.; Huang, H.; Du, Q. Diversity analysis of leaf phenotypic traits in Cortex Eucommia germplasm resources. For. Sci. Res. 2022, 35, 103–112. [Google Scholar] [CrossRef]
  17. Xu, X.; Yang, M.Y.; Man, Q.C.; Li, W.; Su, R.; Wang, L.; Zhang, Z.; Cui, J. A comprehensive evaluation of 195 potato germplasm resources for phenotypic traits. J. Nucl. Agric. 2023, 37, 1710–1722. (In Chinese) [Google Scholar]
  18. Zhang, C.B. Analysis of the Diversity of Leaf and Fruit Saponin Content of Sapindus and Screening of High Quality Germplasm Resources; Central South University of Forestry and Technology: Changsha, China, 2023; pp. 8–12. (In Chinese) [Google Scholar]
  19. Chikh-Rouhou, H.; Mezghani, N.; Mnasri, S.; Mezghani, N.; Garcés-Claver, A. Assessing the Genetic Diversity and Population Structure of a Tunisian Melon (Cucumis melo L.) Collection Using Phenotypic Traits and SSR Molecular Markers. Agronomy 2021, 11, 1121. [Google Scholar] [CrossRef]
  20. Hao, L.; Zhang, G.S.; Mu, X.Y.; Han, S.; Wang, Y.; Ning, R.; Bai, Y.; Zhang, L. Phenotypic Diversity of Resident Populations of Northern Salix Germplasm Resources. Northwest J. Bot. 2017, 37, 1012–1021. (In Chinese) [Google Scholar]
  21. Li, D.B.; Wu, M.; Yu, R.; He, T.; Rong, J.; Zheng, Y.; Chen, L. Phenotypic diversity of moso bamboo from different seed sources and its correlation with environmental factors. J. Plant Resour. Environ. 2023, 32, 39–50. (In Chinese) [Google Scholar]
  22. Qu, K.L.; Zhang, Y.C.; Wang, H.Q.; Li, B.; Kang, Y.; Dong, S. Phenotypic diversity analysis of sour jujube from different seed sources. J. Plant Resour. Environ. 2024, 33, 58–70. (In Chinese) [Google Scholar]
  23. Stotz, G.C.; Salgado-Luarte, C.; Escobedo, V.M.; Valladares, F.; Gianoli, E. Phenotypic plasticity and the leaf economics spectrum: Plasticity is positively associated with specific leaf area. Oikos 2022, 2022, e09342. [Google Scholar] [CrossRef]
  24. Sun, X.L.; Zhang, Z.P.; Jiang, L.C. Construction of a prediction model of breast diameter and wood volume of major conifer species in Xiaoxinganling by applying ground diameter. J. Northeast. For. Univ. 2023, 51, 60–65+73. [Google Scholar] [CrossRef]
  25. Li, H. Comparison and selection of models for the relationship between ground diameter and diameter at breast height in Pinus sylvestris. Zhejiang For. Sci. Technol. 2020, 40, 71–76. (In Chinese) [Google Scholar]
  26. Wei, S.W.; Yang, H.; Zhang, Q.R.; Chen, S.; Luo, L.; Long, P. Diversity analysis of leaf lettuce resources based on phenotypic traits. J. Plant Genet. Resour. 2016, 17, 871–876. [Google Scholar] [CrossRef]
  27. Rui, W.J.; Wang, X.M.; Zhang, Q.N.; Hu, X.; Hu, X.; Fu, J.; Gao, Y.; Li, J. Analysis of genetic diversity of phenotypic traits in 353 germplasm resources of tomato. J. Hortic. 2018, 45, 561–570. [Google Scholar] [CrossRef]
  28. Jan, C. A new membership function approach to uncertain functions. Fuzzy Sets Syst. 2019, 387, 68–80. [Google Scholar] [CrossRef]
  29. Li, J.; Su, X.; Guo, J.; Xu, W.; Feng, L.; Wang, T.; Fu, F.; Wang, G. Sex-Related Differences of Ginkgo biloba in Growth Traits and Wood Properties. Forests 2023, 14, 1809. [Google Scholar] [CrossRef]
  30. Le, X.; Zhang, W.; Sun, G.; Fan, J.; Zhu, M. Research on the Differences in Phenotypic Traits and Nutritional Composition of Acer Truncatum Bunge Seeds from Various Regions. Foods 2023, 12, 2444. [Google Scholar] [CrossRef] [PubMed]
  31. Ingmar, R.S.; Alexandra, W.; Christian, W. Biodiversity change in light of succession theory. Oikos 2023, 2023, e09883. [Google Scholar] [CrossRef]
  32. de Oliveira Buzatti, R.S.; Pfeilsticker, T.R.; Carneiro, M.A.; Ellis, V.A.; de Souza, R.P.; Lemos-Filho, J.P.; Lovato, M.B. Disentangling the Environmental Factors That Shape Genetic and Phenotypic Leaf Trait Variation in the Tree Qualea grandiflora across the Brazilian Savanna. Front. Plant Sci. 2019, 10, 1580. [Google Scholar] [CrossRef]
  33. Liu, J.P. Research on climatic zoning of moso bamboo production areas. Bamboo Res. Repos. 1987, 3, 1–12. (In Chinese) [Google Scholar]
  34. Tayir, M.; Dai, Y.; Shi, Q.; Abdureyim, A.; Erkin, F. Distinct leaf functional traits of Tamarix chinensis at different habitats in the hinterland of the Taklimakan desert. Front. Plant Sci. 2023, 13, 1094049. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Correlation between phenotypic traits of moso bamboo. *: p < 0.05; **: p < 0.01; ***: p < 0.001.
Figure 1. Correlation between phenotypic traits of moso bamboo. *: p < 0.05; **: p < 0.01; ***: p < 0.001.
Plants 13 01625 g001
Figure 2. 113 moso bamboo germplasm resource clusters: (a) cluster map of 113 moso bamboo germplasm resources; (b) distribution of different taxa of moso bamboo in China.
Figure 2. 113 moso bamboo germplasm resource clusters: (a) cluster map of 113 moso bamboo germplasm resources; (b) distribution of different taxa of moso bamboo in China.
Plants 13 01625 g002
Figure 3. Degree of importance of phenotypic traits in moso bamboo.
Figure 3. Degree of importance of phenotypic traits in moso bamboo.
Plants 13 01625 g003
Table 1. Diversity analysis of phenotypic traits of moso bamboo.
Table 1. Diversity analysis of phenotypic traits of moso bamboo.
TraitMinimum ValueMaximum ValueMean ValueStandard DeviationCoefficient of Variation/%
DBH/cm6.4512.7310.281.2311.97
DG/cm7.1315.2711.821.5212.84
TG/cm * m−10.521.140.750.0911.84
H/m12.0819.6715.71.549.84
TNN/node507263.274.757.51
HuB/m4.3610.877.211.3418.56
NNuB/node183527.223.1711.65
LN/cm20.833024.351.837.53
PC/m1.583.022.270.2511.06
WC/kg9.7344.4526.446.9126.14
BLr/g * g−10.723.561.720.5733.33
WBL/kg2.3611.036.491.7526.9
WB/kg1.656.93.851.1429.65
WL/kg0.534.992.640.933.96
W/kg13.6252.8232.917.9724.23
Cwr/g * g−10.511.630.880.1921.84
Bmc/g * g−10.421.660.610.1321.15
Lmc/g * g−10.494.541.10.436.57
TABP/mm9.8521.7116.541.9912.03
TABH/mm6.6616.0410.221.312.68
CD/mm49.21104.3280.4810.3812.89
WCr/mm * mm−10.20.390.260.0310.78
LT/mm0.090.160.130.0111.13
LA/cm26.815.1410.451.4914.24
LL/cm7.2912.0810.050.757.49
LW/cm1.211.811.480.127.81
LAr/cm * cm−15.247.916.820.45.87
SLA/cm2 * g−1129.26271.07182.5926.8314.69
Mean 16.65
Note: DBH. Diameter at breast height; DG. Diameter at ground; TG. Taper grade; H. Height; TNN. Total number of nodes; HuB. Height under branch; NNuB. Number of nodes under branch; LN. Length of node at breast diameter; PC. Plant crown; WC. Weight of culms WN; BLr. Branch-to-leaf ratio; WBL. Weight of branches and leaves; WB. Weight of branches; WL. Weight leaves; W. Total weight; Cwr. Culm moisture content; Lmc. Leaf moisture content; Bmc. Branch moisture content; TABP. Thickness at base of pole; TABH. Thickness at breast height; CD. Cavity diameter; WCr. Wall-to-cavity ratio; LT. Leaf thickness; LA. Leaf area; LL. Leaf length; LW. Leaf width; LAr. Leaf aspect ratio; SLA. Specific leaf area.
Table 2. Principal component analysis of 28 phenotypic traits.
Table 2. Principal component analysis of 28 phenotypic traits.
Comp. 1Comp. 2Comp. 3Comp. 4Comp. 5Comp. 6Comp. 7Comp. 8
DBH0.1050.006−0.0220.053−0.008−0.003−0.0360.009
DG0.103−0.001−0.0120.093−0.0770.0010−0.045
TG0.038−0.1020.0850.235−0.2470.0760.071−0.215
H0.0880.095−0.066−0.0630.0660.045−0.1540.124
TNN0.083−0.059−0.0080.02−0.0550.025−0.03−0.21
HuB0.0690.111−0.209−0.1160.022−0.011−0.1690.014
NNBB0.0830.033−0.189−0.023−0.074−0.042−0.039−0.174
LN−0.0140.15−0.037−0.1270.244−0.027−0.1860.371
PC0.0310.0380.1880.0910.0790.1170.0860.292
WC0.1020.057−0.053−0.0340.007−0.0140.0290.019
BLr0.0120.072−0.1580.30.016−0.1050.3970.279
WBL0.071−0.0550.215−0.1070.2040.0440.16−0.053
WB0.074−0.0230.1430.0170.1760.0070.3430.108
WL0.043−0.0770.237−0.230.1720.077−0.125−0.24
W0.1040.0370.001−0.0540.053−0.0030.0590.004
Cwr0−0.108−0.0840.1970.1050.284−0.3490.113
Bmc−0.016−0.056−0.1320.1220.220.1750.024−0.169
Lmc0.002−0.027−0.1090.1570.2690.121−0.008−0.228
TABP0.0630.0280.1030.065−0.084−0.1760.057−0.053
TABH0.076−0.011−0.074−0.126−0.1520.3750.1520.168
CD0.1030.001−0.0350.0670.01−0.016−0.0890.005
WCr−0.038−0.012−0.048−0.223−0.1840.4520.2870.174
LT−0.0140.1190.120.1030.099−0.1770.1430.042
LA−0.0210.210.0920.097−0.0160.242−0.036−0.227
LL−0.0080.1910.1610.153−0.060.245−0.136−0.076
LW−0.0290.2090.0040.020.0460.1650.114−0.333
LAr0.026−0.0320.2010.174−0.1360.081−0.3450.366
SLA−0.007−0.122−0.0620.1180.2550.2140.0950.071
Eigenvalue9.2413.9852.3351.9671.831.291.1851.026
Contribution rate33.00214.2318.3387.0266.5364.6084.2323.663
Cumulative contribution rate33.00247.23455.57262.59869.13473.74277.97481.637
Table 3. Comprehensive score and ranking of 113 moso bamboo germplasm.
Table 3. Comprehensive score and ranking of 113 moso bamboo germplasm.
NumberDRankNumberDRank
Huangshan 10.5562Jiujiang 10.445100
Huangshan 20.55661Jiujiang 20.6929
Guangde 10.6958Yifeng 10.55759
Guangde 20.46697Yifeng 20.582
Ningguo 10.59944Anfu 10.59348
Ningguo 20.58451Anfu 20.63825
Huoshan 10.7852Shangrao 10.5179
Huoshan 20.63428Shangrao 20.5755
Dehua 10.64423Yihuang 10.53169
Dehua 20.68910Yihuang 20.51577
Yongan 10.427105Ruijin 10.50481
Yongan 20.61239Ruijin 20.427105
Wuyi 10.8031Chongyi 10.59447
Wuyi 20.7035Chongyi 20.56956
Jianou 10.7163Fenghua 10.66715
Jianou 20.66814Fenghua 20.49384
Jiaocheng 10.66417Huangyan 10.68612
Jiaocheng 20.64721Huangyan 20.49983
Nanzhao 10.405108Jinyun 10.64820
Shihe 10.49384Jinyun 20.62134
Xinxian 10.61438Longyou 10.52273
Xinxian 20.48790Longyou 20.51774
Yiliang 10.53368Anji 10.58352
Yiliang 20.68413Anji 20.46796
Changning 10.53567Zhuji 10.62333
Changning 20.63825Zhuji 20.47891
Muchuan 10.63129Chun’an 10.61636
Muchuan 20.61735Chun’an 20.56358
Tianquan 10.62432Jurong 10.445100
Tianquan 20.49187Yixing 10.426107
Zizhong 10.64324Yixing 20.48988
Pingle 10.375111Liyang 10.58352
Pingle 20.317113Chibi 10.54863
Xing’an 10.51774Chibi 20.59944
Xing’an 20.4698Yangxin 10.405108
Sanjiang 10.5466Yangxin 20.59150
Sanjiang 20.52870Huangmei 10.7016
Rong’an 10.49286Lutian 10.66516
Rong’an 20.64721Jingshan 10.47294
Pingjiang 10.60840Shishou 10.48988
Pingjiang 20.441103Enshi 10.6997
Taojiang 10.62931Enshi 20.445100
Taojiang 20.54465Yidu 10.59646
Taoyuan 10.54863Nanzhang 10.382110
Taoyuan 20.60741Zhushan 10.374112
Xiangtan 10.51676Changshou 10.47692
Xiangtan 20.47493Changshou 20.52671
Hengyang 10.52671Liangping 10.65918
Hengyang 20.50680Fengdu 10.429104
Suining 10.63825Fengdu 20.7084
Suining 20.60542Xiushan 10.63129
Shuangpai 10.55759Xiushan 20.68910
Shuangpai 20.59249Jiangjin 10.51478
Yanling 10.57654Jiangjin 20.46895
Yanling 20.56557Chishui 10.61537
Wanli 10.45199Chishui 20.643
Wanli 20.64919
Table 4. Correlation coefficients between composite scores (D-value) and phenotypic traits.
Table 4. Correlation coefficients between composite scores (D-value) and phenotypic traits.
TraitDTraitD
DBH0.851 ***W0.863 ***
DG0.815 ***Cwr−0.105
TG0.184 *Bmc−0.144 **
H0.767 ***Lmc−0.062
TNN0.538 ***TABP0.548 ***
HuB0.500 ***TABH0.572 ***
NNBB0.539 ***CD0.816 ***
LN0.107WCr−0.395 ***
PC0.501 **LT0.219
WC0.826 ***LA0.250
BLr0.372LL0.333
WBL0.611 ***LW0.171
WB0.748 ***LAr0.217 *
WL0.262 **SLA−0.032 *
Note: *: p < 0.05; **: p < 0.01; ***: p < 0.001.
Table 5. Comparison of phenotypic traits of different groups of moso bamboo germplasm resources.
Table 5. Comparison of phenotypic traits of different groups of moso bamboo germplasm resources.
TraitItemsGroup
IIIIIIIV
DBHM ± SD11.05 ± 0.8 a8.88 ± 1.03 d10.28 ± 0.55 b9.7 ± 1.48 c
DGM ± SD12.77 ± 1.03 a10.1 ± 1.25 d11.79 ± 0.62 b11.03 ± 1.81 c
TGM ± SD0.76 ± 0.07 a0.7 ± 0.08 b0.78 ± 0.07 a0.76 ± 0.17 a
HM ± SD16.66 ± 1.39 a14.37 ± 0.91 b15.3 ± 0.91 bc14.81 ± 1.62 c
TNNM ± SD65.37 ± 3.55 a58.92 ± 5.01 b64.12 ± 3 a60.63 ± 5.55 b
HuBM ± SD7.98 ± 1.29 a6.34 ± 0.9 b6.61 ± 1.01 b6.68 ± 0.88 b
NNBBM ± SD29.17 ± 2.59 a24.31 ± 2.69 c26.4 ± 2.18 b26.13 ± 1.81 b
LNM ± SD24.32 ± 1.79 ab25.05 ± 2.17 a23.72 ± 1.36 b24.28 ± 1.82 ab
PCM ± SD2.31 ± 0.27 a2.2 ± 0.2 a2.25 ± 0.27 a2.22 ± 0.21 a
WCM ± SD31.07 ± 5.47 a19.56 ± 4.82 c24.91 ± 3.59 b22.24 ± 6.4 bc
BLrM ± SD1.81 ± 0.51 a1.51 ± 0.57 a1.7 ± 0.65 a1.86 ± 0.65 a
WBLM ± SD6.84 ± 1.52 ab5.27 ± 1.45 c7.2 ± 1.8 a5.93 ± 1.99 bc
WBM ± SD4.19 ± 1.04 a2.93 ± 0.67 b4.19 ± 1.24 a3.56 ± 1.14 ab
WLM ± SD2.66 ± 0.77 ab2.34 ± 0.92 b3.01 ± 1 a2.37 ± 0.96 b
WM ± SD37.88 ± 6.28 a24.83 ± 5.85 c32.11 ± 4.54 b28.17 ± 8.09 bc
CwrM ± SD0.83 ± 0.19 a0.88 ± 0.21 a0.96 ± 0.15 a0.93 ± 0.22 a
BmcM ± SD0.58 ± 0.07 c0.6 ± 0.08 bc0.67 ± 0.21 ab0.71 ± 0.16 a
LmcM ± SD1.08 ± 0.54 a1.06 ± 0.19 a1.13 ± 0.14 a1.31 ± 0.32 a
TABPM ± SD17.37 ± 1.86 a15.31 ± 1.63 b16.21 ± 1.79 ab15.88 ± 2.18 b
TABHM ± SD86.69 ± 7.36 a69.17 ± 9.08 c80.23 ± 4.85 ab76.18 ± 11.98 bc
CDM ± SD10.77 ± 1.08 a9.14 ± 1.2 c10.34 ± 1.07 b9.72 ± 1.42 b
WCrM ± SD0.25 ± 0.03 a0.27 ± 0.03 a0.26 ± 0.03 a0.26 ± 0.02 a
LTM ± SD0.13 ± 0.01 a0.13 ± 0.02 a0.12 ± 0.01 a0.13 ± 0.01 a
LAM ± SD10.66 ± 1.18 a10.61 ± 2.04 a10.26 ± 1.13 a9.15 ± 1.77 b
LLM ± SD10.2 ± 0.55 a10 ± 0.97 a10.06 ± 0.55 a9.07 ± 1.06 b
LWM ± SD1.49 ± 0.1 a1.5 ± 0.16 a1.44 ± 0.09 a1.44 ± 0.14 a
LArM ± SD6.87 ± 0.31 ab6.69 ± 0.33 b7.01 ± 0.29 a6.35 ± 0.83 c
SLAM ± SD166.91 ± 16.42 c176.21 ± 13.32 c202.19 ± 9.89 b247.93 ± 14.37 a
DM0.620.470.560.5
Note: Different letters in indicate significant difference at p < 0.05.
Table 6. Classification prediction results of moso bamboo germplasm in different taxa.
Table 6. Classification prediction results of moso bamboo germplasm in different taxa.
Sample TypeTraining SetTest Set
IIIIIIIVIIIIIIIV
Number of samples41181371211101
Accurate prediction number3414739690
Prediction accuracy/%82.93%77.78%53.85%42.86%75.00%54.55%90.00%0.00%
Average accuracy/%73.42%70.59%
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Zheng, S.; Wei, S.; Li, J.; Wang, J.; Deng, Z.; Gu, R.; Fan, S.; Liu, G. The Phenotypic Variation in Moso Bamboo and the Selection of Key Traits. Plants 2024, 13, 1625. https://doi.org/10.3390/plants13121625

AMA Style

Zheng S, Wei S, Li J, Wang J, Deng Z, Gu R, Fan S, Liu G. The Phenotypic Variation in Moso Bamboo and the Selection of Key Traits. Plants. 2024; 13(12):1625. https://doi.org/10.3390/plants13121625

Chicago/Turabian Style

Zheng, Shihui, Songpo Wei, Jiarui Li, Jingsheng Wang, Ziyun Deng, Rui Gu, Shaohui Fan, and Guanglu Liu. 2024. "The Phenotypic Variation in Moso Bamboo and the Selection of Key Traits" Plants 13, no. 12: 1625. https://doi.org/10.3390/plants13121625

APA Style

Zheng, S., Wei, S., Li, J., Wang, J., Deng, Z., Gu, R., Fan, S., & Liu, G. (2024). The Phenotypic Variation in Moso Bamboo and the Selection of Key Traits. Plants, 13(12), 1625. https://doi.org/10.3390/plants13121625

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

Article Metrics

Back to TopTop