Sex‐specific phosphorus acquisition strategies and cycling in dioecious Populus euphratica forests along a natural water availability gradient

Author:

Liu Miao12ORCID,Ye Liyun1,Chen Liangliang1,Korpelainen Helena3ORCID,Niinemets Ülo4ORCID,Li Chunyang2ORCID

Affiliation:

1. Department of Ecology, College of Life and Environmental Sciences Hangzhou Normal University Hangzhou China

2. Department of Landscape Architecture, College of Agriculture and Biotechnology Zhejiang University Hangzhou China

3. Department of Agricultural Sciences, Viikki Plant Science Centre University of Helsinki Helsinki Finland

4. Department of Crop Science and Plant Biology, Institute of Agricultural and Environmental Sciences Estonian University of Life Sciences Tartu Estonia

Abstract

AbstractSoil phosphorus (P) availability affects plant growth and distribution. However, it is still unknown how sex‐specific variation in functional traits affects plants’ P acquisition and soil P transformation. On wet sites, female poplars had a greater specific root length (SRL), and a higher diversity of arbuscular mycorrhizal fungi (AMF) and phosphate‐solubilizing bacteria (PSB). Male poplars living on wet sites increased the abundance of AMF and PSB communities and enhanced moderately labile and highly resistant organic P mineralisation via increased phosphatase activity. In contrast, on the dry site, the abundance and diversity of AMF and PSB communities increased in females, enhancing moderately labile and highly resistant organic P mineralisation via elevating phosphatase activities. Males maintained greater SRL and promoted Ca‐P mobilisation via the release of root carboxylic acids and rhizosphere acidification on the dry site. The AMF community diversity followed a similar pattern as that of the PSB community when altering the P availability of different‐sex plants. Our results indicated that organic P and Ca‐P are the major sources of plant‐available P in natural P. euphratica forests. Seasonal shifts and geographic locations affected the share of organic and inorganic P pools, and AMF and PSB diversities, ultimately altering sex‐specific P acquisition strategies of plants.

Publisher

Wiley

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3