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  • Author or Editor: Liang Tao x
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Xin Zhao, Qianqian Dong, Shubang Ni, Xiyong He, Hai Yue, Liang Tao, Yanli Nie, Caixian Tang, Fusuo Zhang and Jianbo Shen

Macadamia (Macadamia spp.) has been widely planted in southern China and has been now developed into an important industry. China has the largest area of macadamia plantation in the world but provides only 3% production of the world. Current farming systems have a fertilizer surplus of about 73 g of nitrogen (N), 103 g of phosphorus (P), and 24 g of potassium (K) per macadamia plant per year in southern China. Optimizing fertilization recommended for macadamia improves production by about 5 kg per plant. Macadamia develops cluster roots (i.e., proteoid roots) in a P-starvation environment. Overuse of P fertilizers restrains the development of cluster roots as well as rhizosphere processes, thus decreasing the P-use efficiency. Excessive fertilization, especially P fertilization, is one of the major limiting factors in China macadamia production. This study is the first to analyze current management practices and then discuss approaches of improving nutrient management based on the specific root biology of macadamia. For a sustainable macadamia industry, it is imperative to develop appropriate nutrient management by integrating root-zone soil nutrient supply, fertilizer application, and rhizosphere processes.

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Zhuang-Zhuang Liu, Tao Chen, Fang-Ren Peng, You-Wang Liang, Peng-Peng Tan, Zheng-Hai Mo, Fan Cao, Yang-Juan Shang, Rui Zhang and Yong-Rong Li

Cytosine methylation plays important roles in regulating gene expression and modulating agronomic traits. In this study, the fluorescence-labeled methylation-sensitive amplified polymorphism (F-MSAP) technique was used to study variation in cytosine methylation among seven pecan (Carya illinoinensis) cultivars at four developmental stages. In addition, phenotypic variations in the leaves of these seven cultivars were investigated. Using eight primer sets, 22,796 bands and 950 sites were detected in the pecan cultivars at four stages. Variation in cytosine methylation was observed among the pecan cultivars, with total methylation levels ranging from 51.18% to 56.58% and polymorphism rates of 82.29%, 81.73%, 78.64%, and 79.09% being recorded at the four stages. Sufficiently accompanying the polymorphism data, significant differences in phenotypic traits were also observed among the pecan cultivars, suggesting that cytosine methylation may be an important factor underlying phenotypic variation. Hypermethylation was the dominant type of methylation among the four types observed, and full methylation occurred at higher levels than did hemimethylation in the pecan genomes. Cluster analysis and principal coordinate analysis (PCoA) identified Dice coefficients ranging from 0.698 to 0.778, with an average coefficient of 0.735, and the variance contribution rates of the previous three principal coordinates were 19.6%, 19.0%, and 18.2%, respectively. Among the seven pecan cultivars, four groups were clearly classified based on a Dice coefficient of 0.75 and the previous three principal coordinates. Tracing dynamic changes in methylation status across stages revealed that methylation patterns changed at a larger proportion of CCGG sites from the 30% of final fruit-size (30%-FFS) stage to the 70%-FFS stage, with general decreases in the total methylation level, the rate of polymorphism, and specific sites being observed in each cultivar. These results demonstrated that the F-MSAP technique is a powerful tool for quantitatively detecting cytosine methylation in pecan genomes and provide a new perspective for studying many important life processes in pecan.