Genotypic variation within Zea mays for susceptibility to and rate of recovery from chill-induced photoinhibition of photosynthesis

被引:39
作者
Aguilera, C
Stirling, CM [1 ]
Long, SP
机构
[1] Univ Coll N Wales, Sch Agr & Forest Sci, Bangor LL57 2UW, Gwynedd, Wales
[2] Univ Almeria, Escuela Super Argon, Dept Biol Vegetal, E-04120 Almeria, Spain
[3] Univ Essex, John Tabor Labs, Dept Biol Sci, Colchester CO4 3SQ, Essex, England
关键词
D O I
10.1034/j.1399-3054.1999.106411.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Six genotypes of Zea mays L. were grown in pots inside a glasshouse at a mean temperature of 22 +/- 2 degrees C and a minimum photosynthetic photon flux density (Q) during the daylight period of 400 mu mol m(-2) s(-1). Chilling-dependent photoinhibition was induced by exposing plants to a temperature of 7 degrees C and a Q of 1000 mu mol m(-2) s(-1) for 6 h, Recovery from photoinhibition was then followed at a temperature of 25 degrees C and a Q of 200 mu mol m(-2) s(-1). Leaf gas exchange and chlorophyll fluorescence were measured on attached leaves at room temperature prior to the photoinhibitory treatments and at 6 sampling intervals from 0 to 24 h during the recovery period. The relative water content (RWC) was also measured during the recovery period. The results showed a significant genotypic variation in the susceptibility to and rate of recovery from chilling-dependent photoinhibition of photosynthesis in Zea mays seedlings. The Highland Pool la from highland sites in Mexico was the least susceptible to chill-induced photoinhibition, but had the slowest rate of recovery. The hybrid variety LG11 showed the highest rate of recovery, whilst the inbred line ZPF307 was the most susceptible to chill-induced photoinhibition, Susceptibility to photoinhibition and subsequent recovery were at least partially independent, suggesting that selection for improved genotypes will require independent selection for both tolerance and capacity for recovery. Although chlorophyll fluorescence provided a more rapid method of assessing the occurrence of photoinhibition, it was not as effective as direct gas-exchange measurements of the maximum quantum yield of photosynthesis (Phi) in separating genotypes with respect to their susceptibility to photoinhibition, especially in the most vulnerable genotypes such as ZPF307, Water stress induced by chilling and high Q treatments appeared to impair the recovery processes. Decreases in stomatal conductance (g(s)) produce a significant decrease in intercellular CO(2) concentration (C(i)), although this decrease was never so extreme that it limited photosynthetic rates at the light intensities used to determine Phi. Nevertheless, closure of stomata in patches, producing local restriction of CO(2) supply, would explain the poor correlation between chlorophyll fluorescence and quantum yield measurements in some genotypes immediately after photoinhibitory treatments.
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页码:429 / 436
页数:8
相关论文
共 38 条
[1]   CHARACTERIZATION OF CHILLING EFFECTS ON PHOTOSYNTHETIC PERFORMANCE OF MAIZE CROPS DURING EARLY-SEASON GROWTH USING CHLOROPHYLL FLUORESCENCE [J].
ANDREWS, JR ;
FRYER, MJ ;
BAKER, NR .
JOURNAL OF EXPERIMENTAL BOTANY, 1995, 46 (290) :1195-1203
[2]  
[Anonymous], 1983, Statistical methods
[3]  
Arnon DI, 1940, SOIL SCI, V50, P463
[4]  
Baker N.R., 1994, PHOTOINHIBITION PHOT, P349
[5]   MEASUREMENTS OF THE QUANTUM YIELD OF CARBON ASSIMILATION AND CHLOROPHYLL FLUORESCENCE FOR ASSESSMENT OF PHOTOSYNTHETIC PERFORMANCE OF CROPS IN THE FIELD [J].
BAKER, NR ;
BRADBURY, M ;
FARAGE, PK ;
IRELAND, CR ;
LONG, SP .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1989, 323 (1216) :295-308
[6]   CHILLING DAMAGE TO PHOTOSYNTHESIS IN YOUNG ZEA-MAYS .2. PHOTOCHEMICAL FUNCTION OF THYLAKOIDS INVIVO [J].
BAKER, NR ;
EAST, TM ;
LONG, SP .
JOURNAL OF EXPERIMENTAL BOTANY, 1983, 34 (139) :189-197
[7]  
BAKER NR, 1988, SYM SOC EXP BIOL, V42, P347
[8]   PHOTOSYNTHESIS - IS IT LIMITING TO BIOMASS PRODUCTION [J].
BEADLE, CL ;
LONG, SP .
BIOMASS, 1985, 8 (02) :119-168
[9]  
BONGI G, 1987, PLANT CELL ENVIRON, V10, P241
[10]  
CORNIC G, 1992, PHOTOSYNTHETICA, V27, P295