Relative humidity is a key factor in the acclimation of the stomatal response to CO2

被引:76
作者
Talbott, LD [1 ]
Rahveh, E [1 ]
Zeiger, E [1 ]
机构
[1] Univ Calif Los Angeles, Dept Ecol Evolut & Organismal Biol, Los Angeles, CA 90024 USA
基金
美国国家科学基金会;
关键词
acclimatization; carbon dioxide; relative humidity; stomata; Vicia faba;
D O I
10.1093/jxb/erg215
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Previous work has shown that stomata of growth chamber-grown Vicia faba leaves have an enhanced CO2 response when compared with stomata of greenhouse-grown plants. This guard cell response to CO2 acclimatizes to the environmental conditions on the transfer of plants between the two environments. In the present study, air relative humidity is identified as a key environmental factor mediating the changes in stomatal sensitivity to CO2. In the greenhouse environment, elevation of relative humidity to growth chamber levels resulted in an enhanced CO2 response, whereas a reduction in the light level to that comparable to growth chamber conditions had no effect on stomatal CO2 sensitivity. The transfer of plants between humidified and normal greenhouse conditions resulted in an acclimation response with a time-course matching that previously obtained in transfers of plants between greenhouse and growth chamber environments. The high stomatal sensitivity to CO2 Of growth chamber-grown plants could be reduced by lowering growth chamber relative humidity and then restored with its characteristic acclimation time-course by an elevation of relative humidity. Leaf temperature was unchanged during this restoration, eliminating it as a primary factor in the acclimation response. Humidity regulation of stomatal CO2 sensitivity could function as a signal for leaves inside dense foliage canopies, promoting stomatal opening under low light, low CO2 conditions.
引用
收藏
页码:2141 / 2147
页数:7
相关论文
共 33 条
[1]   SIGNAL-TRANSDUCTION IN GUARD-CELLS [J].
ASSMANN, SM .
ANNUAL REVIEW OF CELL BIOLOGY, 1993, 9 :345-375
[2]   The cellular basis of guard cell sensing of rising CO2 [J].
Assmann, SM .
PLANT CELL AND ENVIRONMENT, 1999, 22 (06) :629-637
[3]   ABA-deficient (aba1) and ABA-insensitive (abi1-1, abi2-1) mutants of Arabidopsis have a wild-type stomatal response to humidity [J].
Assmann, SM ;
Snyder, JA ;
Lee, YRJ .
PLANT CELL AND ENVIRONMENT, 2000, 23 (04) :387-395
[4]   The multisensory guard cell. Stomatal responses to blue light and abscisic acid [J].
Assmann, SM ;
Shimazaki, K .
PLANT PHYSIOLOGY, 1999, 119 (03) :809-815
[5]  
Bunce J. A., 1996, PLANT CELL ENVIRON, V19, P131, DOI DOI 10.1046/J.1365-3040.1997.D01-3.X
[6]   Control of stomatal conductance by leaf water potential in Hymenoclea salsola (T&G), a desert subshrub [J].
Comstock, J ;
Mencuccini, M .
PLANT CELL AND ENVIRONMENT, 1998, 21 (10) :1029-1038
[7]   Analysis of the sensing and transducing processes implicated in the stomatal responses to carbon dioxide in Commelina communis L. [J].
Cousson, A .
PLANT CELL AND ENVIRONMENT, 2000, 23 (05) :487-495
[8]   GAIN OF FEEDBACK LOOP INVOLVING CARBON-DIOXIDE AND STOMATA - THEORY AND MEASUREMENT [J].
FARQUHAR, GD ;
DUBBE, DR ;
RASCHKE, K .
PLANT PHYSIOLOGY, 1978, 62 (03) :406-412
[9]  
FLETCHER A, 1988, LANCET, V2, P4
[10]   CANOPY CARBON-DIOXIDE PROFILE IN RELATION TO ROW SPACING OF ESSEX SOYBEAN [J].
FRANCIS, PB ;
PARKS, WL .
AGRONOMY JOURNAL, 1988, 80 (03) :425-430