Xin Zhang

Dr. Xin Zhang

College of Forestry, Northwest A&F University, Yangling, China
orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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8 February 2019 in BMC Plant Biology
Verified
Journal Article
Open access
PDF file
JSJunyu Song
Junyu Song
YWYang Wang
Yang Wang
YPYuehan Pan
Yuehan Pan
JPJiayin Pang
Jiayin Pang
Xin ZhangXin Zhang
Xin Zhang
YZYi Zhang
Yi Zhang
Drought and nitrogen (N) deficiency are two major limiting factors for forest productivity in many ecosystems. Elucidating the mechanisms underlying the influence of soil N availability on drought responses of tree species is crucial to improve tree growth under drought. The root proliferation under drought was enhanced by adequate N application. Vessel frequency in xylem increased upon drought, with more significant increase under adequate N conditions compared with that under low N conditions, possibly leading to increased hydraulic safety. Nitrogen application under drought increased indole acetic acid (IAA), which contributed to the adaptive changes of xylem. Nitrogen application increased leaf abscisic acid (ABA) concentration, therefore regulated stomata adjustment, and promoted intrinsic water use efficiency (WUEi). Moreover, N application promoted antioxidant defense in leaves by showing increased level of free proline and carotenoid, which improved drought tolerance and growth performance of poplars. Anatomical and physiological responses of Populus to drought were suppressed by N deficiency. Adequate N application promoted adaptive changes of root and xylem under drought and increased hydraulic safety. Nitrogen addition under drought also increased leaf ABA level which may regulate stomata adjustment and promote WUEi. Moreover, nitrogen application improved antioxidant defense in leaves with increased levels of antioxidants. These positive regulations improved drought tolerance and growth performance of poplars.

1 June 2017 in Environmental and Experimental Botany
Verified
Journal Article
Closed access
HZHuifang Zheng
Huifang Zheng
Xin ZhangXin Zhang
Xin Zhang
WMWenjun Ma
Wenjun Ma
JSJunyu Song
Junyu Song
SRSiddiq Ur Rahman
Siddiq Ur Rahman
YZYi Zhang
Yi Zhang

1 August 2019 in Environmental and Experimental Botany
Verified
Journal Article
Closed access
JWJunchen Wang
Junchen Wang
HWHao Wang
Hao Wang
JCJuan Chen
Juan Chen
SZSenmao Zhang
Senmao Zhang
JXJiuting Xu
Jiuting Xu
YZYi Zhang
Yi Zhang

21 April 2017 in PLOS ONE
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Journal Article
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Xin ZhangXin Zhang
Xin Zhang
WLWenzhe Liu
Wenzhe Liu
Xin WangXin Wang
Xin Wang
Angiosperms distinguish themselves from gymnosperms by their ovules that are enclosed before pollination. However, how the ovules get enclosed in angiosperms remains a mystery, especially for Magnoliaceae. The only key to this mystery is finding a series of carpels transitional from fully closed with enclosed ovules to open with naked ovules. We use routine paraffin section technology, LM, SEM to document the morphology and anatomy of carpel variation in Michelia figo (Magnoliaceae). A series of carpel variations within a single flower of Michelia figo (Magnoliaceae) are documented, in which the ovules are exposed in atypical carpels. These atypical and typical carpels for the first time demonstrate clearly how the naked ovule get enclosed. Each atypical carpel, with naked ovules, clearly comprises two parts, namely, subtending foliar part and branches bearing ovules, suggesting that a typical carpel is actually an end-product of the fusion between the ovuliferous branches and subtending foliar parts. The only difference among these carpels is the extent of fusion between these two parts. This generalization is in full agreement with the molecular genetic studies on angiosperm flowers.

22 April 2024 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
QGQiong Gao
Qiong Gao
GLGang Li
Gang Li
HRHailin Ran
Hailin Ran
YHYiru Hou
Yiru Hou
YJYongmei Jiang
Yongmei Jiang
WWWanggang Wanggang
Wanggang Wanggang

11 April 2019 in PeerJ
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Journal Article
Open access
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QZQianyi Zhou
Qianyi Zhou
ZJZhaohong Jiang
Zhaohong Jiang
Xin ZhangXin Zhang
Xin Zhang
TZTian Zhang
Tian Zhang
HZHailan Zhu
Hailan Zhu
ZZZhong Zhao
Zhong Zhao
Platycladus orientalis L. (Cupressaceae) has a lifespan of thousands of years. Ancient trees have very high scientific, economic and cultural values. The senescence of ancient trees is a new research area but is poorly understood. Leaves are the primary and the most sensitive organ of a tree. To understand leaf structural response to tree senescence in ancient trees, experiments investigating the morphology, anatomy and ultrastructure were conducted with one-year leaves of ancient P. orientalis (ancient tree >2,000 years) at three different tree senescent levels (healthy, sub-healthy and senescent) at the world’s largest planted pure forest in the Mausoleum of Yellow Emperor, Shaanxi Province, China. Observations showed that leaf structure significantly changed with the senescence of trees. The chloroplast, mitochondria, vacuole and cell wall of mesophyll cells were the most significant markers of cellular ultrastructure during tree senescence. Leaf ultrastructure clearly reflected the senescence degree of ancient trees, confirming the visual evaluation from above-ground parts of trees. Understanding the relationships between leaf structure and tree senescence can support decision makers in planning the protection of ancient trees more promptly and effectively by adopting the timely rejuvenation techniques before the whole tree irreversibly recesses.