Environmental Effects on Spatial and Temporal Patterns of Leaf and Root Growth

被引:175
作者
Walter, Achim [1 ]
Silk, Wendy K. [2 ]
Schurr, Ulrich [1 ]
机构
[1] Forschungszentrum Julich, Inst Chem & Dynam Geosphere Phytosphere ICG 3, D-52425 Julich, Germany
[2] Univ Calif Davis, Dept Land Air & Water Resources, Davis, CA 95616 USA
基金
美国国家科学基金会;
关键词
growth analysis; image processing; carbohydrate metabolism; environmental control; plant-environment interactions; TIME-LAPSE ANALYSIS; MAIZE PRIMARY ROOT; ARABIDOPSIS-THALIANA; CELL-DIVISION; PLANT-GROWTH; ZEA-MAYS; WATER-DEFICIT; BIOMASS ALLOCATION; LIGHT CONDITIONS; ELONGATION ZONE;
D O I
10.1146/annurev.arplant.59.032607.092819
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Leaves and roots live in dramatically different habitats, but are parts of the same organism. Automated image processing of time-lapse records of these organs has led to understanding of spatial and temporal patterns of growth on time scales from minutes to weeks. Growth zones in roots and leaves show distinct patterns during a diel cycle (24 h period). In dicot leaves under nonstressful conditions these patterns are characterized by endogenous rhythms, sometimes superimposed upon morphogenesis driven by environmental variation. In roots and monocot leaves the growth patterns depend more strongly on environmental fluctuations. Because the impact of spatial variations and temporal fluctuations of above- and belowground environmental parameters must be processed by the plant body as an entire system whose individual modules interact on different levels, growth reactions of individual modules are often highly nonlinear. A mechanistic understanding of plant resource use efficiency and performance in a dynamically fluctuating environment therefore requires an accurate analysis of leaf and root growth patterns in conjunction with knowledge of major intriplant communication systems and metabolic pathways.
引用
收藏
页码:279 / 304
页数:26
相关论文
共 157 条
[1]   Ethylene regulates Arabidopsis development via the modulation of DELLA protein growth repressor function [J].
Achard, P ;
Vriezen, WH ;
Van Der Straeten, D ;
Harberd, NP .
PLANT CELL, 2003, 15 (12) :2816-2825
[2]   DELLAs contribute to plant photomorphogenesis [J].
Achard, Patrick ;
Liao, Lili ;
Jiang, Caifu ;
Desnos, Thierry ;
Bartlett, Joanne ;
Fu, Xiangdong ;
Harberd, Nicholas P. .
PLANT PHYSIOLOGY, 2007, 143 (03) :1163-1172
[3]   ROOT ELONGATION RATE IS ACCOUNTED FOR BY INTERCEPTED PPFD AND SOURCE-SINK RELATIONS IN-FIELD AND LABORATORY-GROWN SUNFLOWER [J].
AGUIRREZABAL, LAN ;
DELEENS, E ;
TARDIEU, F .
PLANT CELL AND ENVIRONMENT, 1994, 17 (04) :443-450
[4]   Glycine max leaflets lack a base-tip gradient in growth rate [J].
Ainsworth, EA ;
Walter, A ;
Schurr, U .
JOURNAL OF PLANT RESEARCH, 2005, 118 (05) :343-346
[5]   Using L-systems for modeling source-sink interactions, architecture and physiology of growing trees: the L-PEACH model [J].
Allen, MT ;
Prusinkiewicz, P ;
DeJong, TM .
NEW PHYTOLOGIST, 2005, 166 (03) :869-880
[6]   DELLA proteins: integrators of multiple plant growth regulatory inputs? [J].
Alvey, L ;
Harberd, NP .
PHYSIOLOGIA PLANTARUM, 2005, 123 (02) :153-160
[7]  
[Anonymous], 1995, SOIL NUTR BIOAVAILAB
[8]  
[Anonymous], 1998, ENV SOIL PHYS FUNDAM
[9]   The role of root exudates in rhizosphere interations with plants and other organisms [J].
Bais, Harsh P. ;
Weir, Tiffany L. ;
Perry, Laura G. ;
Gilroy, Simon ;
Vivanco, Jorge M. .
ANNUAL REVIEW OF PLANT BIOLOGY, 2006, 57 :233-266
[10]   Cytoskeleton-plasma membrane-cell wall continuum in plants. Emerging links revisited [J].
Baluska, F ;
Samaj, J ;
Wojtaszek, P ;
Volkmann, D ;
Menzel, D .
PLANT PHYSIOLOGY, 2003, 133 (02) :482-491