Photosynthesis, N2 fixation and taproot reserves during the cutting regrowth cycle of alfalfa under elevated CO2 and temperature

被引:32
作者
Erice, G. [1 ,4 ,5 ]
Sanz-Saez, A. [1 ,4 ,5 ]
Aranjuelo, I. [2 ]
Irigoyen, J. J. [1 ,4 ,5 ]
Aguirreolea, J. [1 ,4 ,5 ]
Avice, J. -C. [3 ]
Sanchez-Diaz, M. [1 ,4 ,5 ]
机构
[1] Univ Navarra, Dept Biol Vegetal, Secc Biol Vegetal, Fac Ciencias & Farm, E-31080 Pamplona, Spain
[2] Univ Publ Navarra, CSIC Gobierno Navarra, Inst Agrobiotecnol, E-31192 Mutilva Baja, Spain
[3] Univ Caen Basse Normandie, Inst Biol Fondamentale & Appl, INRA, UMR INRA,UCBN 950,EVA Ecophysiol Vegetale & Agron, F-14032 Caen, France
[4] EEAD, Unidad Asociada CSIC, Zaragoza, Spain
[5] ICVV, Logrono, Spain
关键词
Alfalfa; Biological nitrogen fixation; Photosynthesis down-regulation; Regrowth; Isotopes; MEDICAGO-SATIVA L; VEGETATIVE STORAGE PROTEINS; LOLIUM-PERENNE L; WHITE CLOVER; NITROGEN-FIXATION; ATMOSPHERIC CO2; NODULATED ALFALFA; CARBON-DIOXIDE; N FERTILIZATION; DOWN-REGULATION;
D O I
10.1016/j.jplph.2011.07.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Future climatic conditions, including rising atmospheric CO2 and temperature may increase photosynthesis and, consequently, plant production. A larger knowledge of legume performance under the predicted growth conditions will be crucial for safeguarding crop management and extending the area under cultivation with these plants in the near future. N-2 fixation is a key process conditioning plant responsiveness to varying growth conditions. Moreover, it is likely to increase under future environments, due to the higher photosynthate availability, as a consequence of the higher growth rate under elevated CO2. However, as described in the literature, photosynthesis performance is frequently down-regulated (acclimated) under long-term exposure to CO2, especially when affected by stressful temperature and water availability conditions. As growth responses to elevated CO2 are dependent on sink-source status, it is generally accepted that down-regulation occurs in situations with insufficient plant C sink capacity. Alfalfa management involves the cutting of shoots, which alters the source-sink relationship and thus the photosynthetic behaviour. As the growth rate decreases at the end of the pre-cut vegetative growth period, nodulated alfalfa plants show photosynthetic down-regulation, but during regrowth following defoliation, acclimation to elevated CO2 disappears. The shoot harvest also leads to a drop in mineral N uptake and C translocation to the roots, resulting in a reduction in N-2 fixation due to the dependence on photosynthate supply to support nodule function. Therefore, the production of new shoots during the first days following cutting requires the utilization of reduced C and N compounds that have been stored previously in reserve organs. The stored reserves are mediated by phytohormones such as methyl jasmonate and abscisic acid and in situations where water stress reduces shoot production this potentially enables the enhancement of taproot protein levels in nodulated alfalfa, which may lead to these plants being in better condition in the following cut/regrowth cycle. Furthering our knowledge of legume performance under predicted climate change conditions will be crucial for the development of varieties with better adaptation that will achieve greater and more efficient production values. Furthermore, for this purpose it will be necessary to improve existing methodologies and create new ones for phenotype characterization. Such knowledge will provide key information for future plant breeding programs. (C) 2011 Elsevier GmbH. All rights reserved.
引用
收藏
页码:2007 / 2014
页数:8
相关论文
共 101 条
[11]  
Avice JC, 2003, CAN J BOT, V81, P1198, DOI [10.1139/B03-122, 10.1139/b03-122]
[12]  
Avice JC, 1996, PLANT PHYSIOL BIOCH, V34, P561
[13]   Root protein and vegetative storage protein are key organic nutrients for alfalfa shoot regrowth [J].
Avice, JC ;
Ourry, A ;
Lemaire, G ;
Volenec, JJ ;
Boucaud, J .
CROP SCIENCE, 1997, 37 (04) :1187-1193
[14]   Nitrogen and carbon flows estimated by N-15 and C-13 pulse-chase labeling during regrowth of alfalfa [J].
Avice, JC ;
Ourry, A ;
Lemaire, G ;
Boucaud, J .
PLANT PHYSIOLOGY, 1996, 112 (01) :281-290
[15]   Supplemental nitrogen effects on alfalfa regrowth and nitrogen mobilization from roots [J].
Barber, LD ;
Joern, BC ;
Volenec, JJ ;
Cunningham, SM .
CROP SCIENCE, 1996, 36 (05) :1217-1223
[16]   Climate change and winter survival of perennial forage crops in eastern Canada [J].
Bélanger, G ;
Rochette, P ;
Castonguay, Y ;
Bootsma, A ;
Mongrain, D ;
Ryan, DAJ .
AGRONOMY JOURNAL, 2002, 94 (05) :1120-1130
[17]  
Belanger G., 2005, CAN J PLANT SCI, V86, P33
[18]   Elevated atmospheric CO2 and strain of rhizobium alter freezing tolerance and cold-induced molecular changes in alfalfa (Medicago sativa) [J].
Bertrand, Annick ;
Prevost, Danielle ;
Bigras, Francine J. ;
Castonguay, Yves .
ANNALS OF BOTANY, 2007, 99 (02) :275-284
[19]  
Bewley JD, 2002, CAN J BOT, V80, P321, DOI [10.1139/B02-025, 10.1139/b02-025]
[20]   CHANGES IN THE ACTIVITIES OF NITROGEN ASSIMILATION ENZYMES OF LOLIUM-PERENNE L DURING REGROWTH AFTER CUTTING [J].
BOUCAUD, J ;
BIGOT, J .
PLANT AND SOIL, 1989, 114 (01) :121-125