Temporal dynamics of carbon partitioning and rhizodeposition in wheat

被引:117
作者
Dilkes, NB
Jones, DL [1 ]
Farrar, J
机构
[1] Univ Coll N Wales, Sch Agr & Forest Sci, Bangor LL57 2UW, Gwynedd, Wales
[2] Univ Coll N Wales, Sch Biol Sci, Bangor LL57 2UW, Gwynedd, Wales
关键词
D O I
10.1104/pp.103.032045
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The temporal dynamics of partitioning and rhizodeposition of recent photosynthate in wheat (Triticum aestivum) roots were quantified in situ in solution culture. After a 30-min pulse of "CO2 to a single intact leaf, C-14 activities of individual carbon fluxes in the root, including exudation, respiration, and root content, were measured continuously over the next 20 h concurrently with C-14 efflux from the leaf. Immediately after the end of the "CO2 pulse, C-14 activity was detected in the root, the hydroponic solution, and in root respiration. The rate of (14)(C) exudation from the root was maximal after 2 to 3 h, and declined to one-third of maximum after a further 5 h. Completion of the rapid phase of C-14 efflux from the leaf coincided with peak C-14 exudation rate. Thus, exudation flux is much more rapidly and dynamically coupled to current photosynthesis than has been appreciated. Careful cross-calibration of C-14 counting methods allowed a dynamic C-14 budget to be constructed for the root. Cumulative C-14 exudation after 20 h was around 3% of C-14 fixed in photosynthesis. Partitioning of photosynthate between shoot and root was manipulated by partial defoliation before applying the (CO2)-C-14 pulse to the remaining intact leaf. Although the rate of photosynthesis was largely unaffected by partial defoliation, the proportion of new photosynthate subsequently partitioned to and exuded from the root was substantially reduced. This clearly indicates that exudation depends more on the rate of carbon import into the root than on the rate of photosynthesis.
引用
收藏
页码:706 / 715
页数:10
相关论文
共 32 条
[1]   Export of carbon from leaf blades of Poa alpina L-at elevated CO2 and two nutrient regimes [J].
Baxter, R ;
Farrar, JF .
JOURNAL OF EXPERIMENTAL BOTANY, 1999, 50 (336) :1215-1221
[2]   REGULATION OF RESPIRATION IN ROOTS OF BARLEY [J].
BINGHAM, IJ ;
FARRAR, JF .
PHYSIOLOGIA PLANTARUM, 1988, 73 (02) :278-285
[3]   Natural abundance of 13C in CO2 respired from forest soils reveals speed of link between tree photosynthesis and root respiration [J].
Ekblad, A ;
Högberg, P .
OECOLOGIA, 2001, 127 (03) :305-308
[4]   FLUXES OF CARBON IN ROOTS OF BARLEY PLANTS [J].
FARRAR, JF .
NEW PHYTOLOGIST, 1985, 99 (01) :57-69
[5]   CARBON FLUXES IN LEAF BLADES OF BARLEY [J].
FARRAR, SC ;
FARRAR, JF .
NEW PHYTOLOGIST, 1985, 100 (03) :271-283
[6]   Ozone inhibits phloem loading from a transport pool: compartmental efflux analysis in Pima cotton [J].
Grantz, DA ;
Farrar, JF .
AUSTRALIAN JOURNAL OF PLANT PHYSIOLOGY, 2000, 27 (8-9) :859-868
[7]  
HEWITT E. J., 1966, SAND WATER CULTURE M
[8]   Characterisation and microbial utilisation of exudate material from the rhizosphere of Lolium perenne grown under CO2 enrichment [J].
Hodge, A ;
Paterson, E ;
Grayston, SJ ;
Campbell, CD ;
Ord, BG ;
Killham, K .
SOIL BIOLOGY & BIOCHEMISTRY, 1998, 30 (8-9) :1033-1043
[9]   A novel method for characterisation and quantification of plant root exudates [J].
Hodge, A ;
Grayston, SJ ;
Ord, BG .
PLANT AND SOIL, 1996, 184 (01) :97-104
[10]   Large-scale forest girdling shows that current photosynthesis drives soil respiration [J].
Högberg, P ;
Nordgren, A ;
Buchmann, N ;
Taylor, AFS ;
Ekblad, A ;
Högberg, MN ;
Nyberg, G ;
Ottosson-Löfvenius, M ;
Read, DJ .
NATURE, 2001, 411 (6839) :789-792