Hui Wang

Dr. Hui Wang


Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
14 April 2023 in Forests
Verified
Journal Article
Open access
PDF file
ZYZhenya Yang
Zhenya Yang
JZJiancheng Zhao
Jiancheng Zhao
HNHuijing Ni
Huijing Ni
HWHui Wang
Hui Wang
BZBenzhi Zhou
Benzhi Zhou
The drought tolerance of plants is significantly influenced by their root architecture traits and root adaptive strategies, but the key root architecture traits that affect drought tolerance and the differences in drought adaptative strategies of species with varying root architectures are not yet clear. This study aimed to investigate the response of three species’ roots to drought and evaluate the key root architecture traits affecting the drought tolerance of the three species. One-year-old potted seedlings of three species [Chinese fir (Cunninghamia lanceolata (Lamb.) Hook.), masson pine (Pinus massoniana (Lamb.)), and moso bamboo (Phyllostachys edulis (Carr.) H. de Lehaie f. edulis)] were planted in a greenhouse under three drought conditions (sufficient water supply, moderate drought, and severe drought) for 90 days. Biomass, root morphology [root surface area (RSA), root length (RL), root diameter (RD)], root architecture [root topological index (TI), fractal dimension (FD), and root branching angle (RBA)] of seedlings were measured monthly. The drought tolerance of species was quantified by studying the response ratio (RR) of root length and biomass in response to drought. We found that: (i) different levels of drought inhibited the biomass accumulation and root growth of the three species, and drought tolerance showed a decreasing order as pine > Chinese fir > bamboo; (ii) drought decreased the RD in bamboo but increased it in pine. Both bamboo and Chinese fir reduced their FD and RBA under drought stress, while pine was relatively stable. All the three species’ roots tended to develop a herringbone branching architecture (increase their TI) under drought stress; (iii) both TI and FD were negatively correlated with the drought tolerance of the seedlings. Our results indicated that plants could adapt to drought by different strategies such as adjusting biomass allocation and root morphology, reducing root branch strength, and branching angles. Roots with narrower branching angles, greater branching complexity, larger TI, and consuming higher cost are more drought-tolerant.

2 August 2025 in Forests
Verified
Journal Article
Open access
PDF file
ZYZhenya Yang
Zhenya Yang
HWHui Wang
Hui Wang
Soil phosphorus (P) availability is an important determinant of productivity in Pinus massoniana (Masson pine) forests. The mechanistic bases governing the physiological and growth responses of Masson pine to varying soil P conditions remain insufficiently characterized. This study aims to decipher the adaptive strategies of Masson pine to different soil P levels, focusing on root morphological–architectural plasticity and the allocation dynamics of nutrient elements and photosynthetic assimilates. One-year-old potted Masson pine seedlings were exposed to four P addition treatments for one year: P0 (0 mg kg−1), P1 (25 mg kg−1), P2 (50 mg·kg−1), and P3 (100 mg kg−1). In July and December, measurements were conducted on seedling organ biomass, root morphological indices [root length (RL), root surface area (RSA), root diameter (RD), specific root length (SRL), and root length ratio (RLR) for each diameter grade], root architectural indices [number of root tips (RTs), fractal dimension (FD), root branching angle (RBA), and root topological index (TI)], as well as the content of nitrogen (N), phosphorus (P), carbon (C), and non-structural carbohydrates (NSCs) in roots, stems, and leaves. Compared with the P0 treatment, P2 and P3 significantly increased root biomass, root–shoot ratio, RL, RSA, RTs, RLR of finer roots (diameter ≤ 0.4 mm), nutrient accumulation ratio in roots, and starch (ST) content in roots, stems and leaves. Meanwhile, they decreased soluble sugar (SS) content, SS/ST ratio, C and N content, and N/P and C/P ratios in stems and leaves, as well as nutrient accumulation ratio in leaves. The P3 treatment significantly reduced RBA and increased FD and SRL. Our results indicated that Masson pine adapts to low P by developing shallower roots with a reduced branching intensity and promoting the conversion of ST to SS. P’s addition effectively alleviates growth limitations imposed by low P, stimulating root growth, branching, and gravitropism. Although a sole P addition promotes short-term growth and P uptake, it triggers a substantial consumption of N, C, and SS, leading to significant decreases in N/P and C/P ratios and exacerbating N’s limitation, which is detrimental to long-term growth. Under high-P conditions, Masson pine strategically prioritizes allocating limited N and SS to roots, facilitating the formation of thinner roots with low C costs.