Rice rhizodeposition and its utilization by microbial groups depends on N fertilization

被引:141
作者
Ge, Tida [1 ,2 ]
Li, Baozhen [1 ,2 ]
Zhu, Zhenke [1 ,2 ]
Hu, Yajun [1 ,2 ]
Yuan, Hongzhao [1 ]
Dorodnikov, Maxim [3 ]
Jones, Davey L. [1 ,4 ]
Wu, Jinshui [1 ,2 ]
Kuzyakov, Yakov [1 ,3 ]
机构
[1] Chinese Acad Sci, Inst Subtrop Agr, Key Lab Agroecol Proc Subtrop Reg, Changsha 410125, Hunan, Peoples R China
[2] Chinese Acad Sci, Inst Subtrop Agr, Changsha Res Stn Agr & Environm Monitoring, Changsha 410125, Hunan, Peoples R China
[3] Univ Gottingen, Dept Soil Sci Temperate Ecosyst, Dept Agr Soil Sci, D-37077 Gottingen, Germany
[4] Bangor Univ, Sch Environm Nat Resources & Geog, Bangor LL57 2UW, Gwynedd, Wales
基金
中国国家自然科学基金;
关键词
Nutrient cycling; N fertilization; Stable isotope labeling; Root exudation; Microbial community structure; ARBUSCULAR MYCORRHIZAL FUNGI; DISSOLVED ORGANIC-CARBON; NITROGEN-USE EFFICIENCY; COMMUNITY STRUCTURE; LITTER CHEMISTRY; SOIL; BACTERIAL; GROWTH; BIOMASS; DYNAMICS;
D O I
10.1007/s00374-016-1155-z
中图分类号
S15 [土壤学];
学科分类号
0903 ; 090301 ;
摘要
Rhizodeposits have received considerable attention, as they play an important role in the regulation of soil carbon (C) sequestration and global C cycling and represent an important C and energy source for soil microorganisms. However, the utilization of rhizodeposits by microbial groups, their role in the turnover of soil organic matter (SOM) pools in rice paddies, and the effects of nitrogen (N) fertilization on rhizodeposition are nearly unknown. Rice (Oryza sativa L.) plants were grown in soil at five N fertilization rates (0, 10, 20, 40, or 60 mg N kg(-1) soil) and continuously labeled in a (CO2)-C-13 atmosphere for 18 days during tillering. The utilization of root-derived C by microbial groups was assessed by C-13 incorporation into phospholipid fatty acids. Rice shoot and root biomass strongly increased with N fertilization. Rhizodeposition increased with N fertilization, whereas the total C-13 incorporation into microorganisms, as indicated by the percentage of C-13 recovered in microbial biomass, decreased. The contribution of root-derived C-13 to SOM formation increased with root biomass. The ratio of C-13 in soil pools (SOM and microbial biomass) to C-13 in roots decreased with N fertilization showing less incorporation and faster turnover with N. The C-13 incorporation into fungi (18:2 omega 6,9c and 18:1 omega 9c), arbuscular mycorrhizal fungi (16:1 omega 5c), and actinomycetes (10Me 16:0 and 10Me 18:0) increased with N fertilization, whereas the C-13 incorporation into gram-positive (i14:0, i15:0, a15:0, i16:0, i17:0, and a17:0) and gram-negative (16:1 omega 7c, 18:1 omega 7c, cy17:0, and cy19:0) bacteria decreased with N fertilization. Thus, the uptake and microbial processing of root-derived C was affected by N availability in soil. Compared with the unfertilized soil, the contribution of rhizodeposits to SOM and microorganisms increased at low to intermediate N fertilization rates but decreased at the maximum N input. We conclude that belowground C allocation and rhizodeposition by rice, microbial utilization of rhizodeposited C, and its stabilization within SOM pools are strongly affected by N availability: N fertilization adequate to the plant demand increases C incorporation in all these polls, but excessive N fertilization has negative effects not only on environmental pollution but also on C sequestration in soil.
引用
收藏
页码:37 / 48
页数:12
相关论文
共 72 条
[1]   Plant genotype strongly modifies the structure and growth of maize rhizosphere microbial communities [J].
Aira, Manuel ;
Gomez-Brandon, Maria ;
Lazcano, Cristina ;
Baath, Erland ;
Dominguez, Jorge .
SOIL BIOLOGY & BIOCHEMISTRY, 2010, 42 (12) :2276-2281
[2]   Arbuscular mycorrhizal fungi and organic fertilizer influence photosynthesis, root phosphatase activity, nutrition, and growth of Ipomoea carnea ssp fistulosa [J].
Amaya-Carpio, L. ;
Davies, F. T., Jr. ;
Fox, T. ;
He, C. .
PHOTOSYNTHETICA, 2009, 47 (01) :1-10
[3]   Chronic nitrogen additions reduce total soil respiration and microbial respiration in temperate forest soils at the Harvard Forest [J].
Bowden, RD ;
Davidson, E ;
Savage, K ;
Arabia, C ;
Steudler, P .
FOREST ECOLOGY AND MANAGEMENT, 2004, 196 (01) :43-56
[4]   Coevolution of roots and mycorrhizas of land plants [J].
Brundrett, MC .
NEW PHYTOLOGIST, 2002, 154 (02) :275-304
[5]   Opportunities for increased nitrogen-use efficiency from improved resource management in irrigated rice systems [J].
Cassman, KG ;
Peng, S ;
Olk, DC ;
Ladha, JK ;
Reichardt, W ;
Dobermann, A ;
Singh, U .
FIELD CROPS RESEARCH, 1998, 56 (1-2) :7-39
[6]   Genomic regions involved in response to grain yield selection at high and low nitrogen fertilization in maize [J].
Coque, M ;
Gallais, A .
THEORETICAL AND APPLIED GENETICS, 2006, 112 (07) :1205-1220
[7]   Living in a fungal world: impact of fungi on soil bacterial niche development [J].
de Boer, W ;
Folman, LB ;
Summerbell, RC ;
Boddy, L .
FEMS MICROBIOLOGY REVIEWS, 2005, 29 (04) :795-811
[8]   Microbial community composition and rhizodeposit-carbon assimilation in differently managed temperate grassland soils [J].
Denef, Karolien ;
Roobroeck, Dries ;
Manimel Wadu, Mihiri C. W. ;
Lootens, Peter ;
Boeckx, Pascal .
SOIL BIOLOGY & BIOCHEMISTRY, 2009, 41 (01) :144-153
[9]   Kinetics and relative significance of remobilized and current C and N incorporation in leaf and root growth zones of Lolium perenne after defoliation: Assessment by C-13 and N-15 steady-state labelling [J].
deVisser, R ;
Vianden, H ;
Schnyder, H .
PLANT CELL AND ENVIRONMENT, 1997, 20 (01) :37-46
[10]   Management-induced structural dynamics in paddy soils of south east China simulated in microcosms [J].
Eickhorst, Thilo ;
Tippkoetter, Rolf .
SOIL & TILLAGE RESEARCH, 2009, 102 (02) :168-178