• Scopus
  • Chinese Science Citation Database (CSCD)
  • A Guide to the Core Journal of China
  • CSTPCD
  • F5000 Frontrunner
  • RCCSE
Advanced search
WANG Cong-peng, JIA Fu-li, LIU Sha, LIU Chao, XIA Xin-li, YIN Wei-lun. Drought induces alterations in stomatal development in Populus deltoides×P. nigra[J]. Journal of Beijing Forestry University, 2016, 38(6): 28-34. DOI: 10.13332/j.1000-1522.20160050
Citation: WANG Cong-peng, JIA Fu-li, LIU Sha, LIU Chao, XIA Xin-li, YIN Wei-lun. Drought induces alterations in stomatal development in Populus deltoides×P. nigra[J]. Journal of Beijing Forestry University, 2016, 38(6): 28-34. DOI: 10.13332/j.1000-1522.20160050

Drought induces alterations in stomatal development in Populus deltoides×P. nigra

More Information
  • Received Date: February 17, 2016
  • Revised Date: February 17, 2016
  • Published Date: June 29, 2016
  • To explore the effect of drought to stomatal development in woody plants, five Populus deltoides× P. nigra clones, i.e., R270 (P. deltoides× P. nigra), NE-19 [P. nigra× (P. deltoides× P. nigra)], 107 (P.× euramericana ‘74/76'), 109 (P. deltoides× P. alba ‘Mincio') and 111 (P. deltoides× euramericana ‘Bellotto') were selected to undergo 14 days of drought and 7 days of re-watering treatment. The results showed that photosynthesis of NE-19, R270 and 107 returned to the normal level at the fifth day after re-watered, with stomatal conductance back to normal level after 3 days. However, 109 and 111 recovered slowly. As for the growth rate after re-watered, the order from high to low was NE-19 (64.96%), R270 (55.73%), 107(49.87%), 109(35.08%), and 111(23.62%). According the results of photosynthesis, stomatal conductance and growth rate, the drought tolerance was ranked as NE-19 > R270 > 107 > 109 > 111. For all five clones, the stomatal development slowed down when subjected to the drought, indicated by the stomatal index (SI) in young leaves. The SI of NE-19 and R270 had the most remarkable change during the drought, being 30.75% and 29.24%, respectively. The clones with better drought tolerance may be more positively responsive to ambient water content change through stomatal development. Using qRT-PCR we tested the difference of transcript abundance of five genes associated with stomatal development between control and drought treatment groups. EPFL9 and FAMA, which positively control stomatal development, were down-regulated during drought, but ERECTA and EPF1 which negatively regulate the process were up-regulated during drought, and SDD1 had no change during the whole treatment. Our findings highlight that poplar inhibits stomatal development through adjusting expression of ERECTA, EPF1, EPFL9 and FAMA in immature leaves to reduce water loss so as to withstand drought stress.
  • [1]
    COWAN I R, FARQUHAR G D. Stomatal function in relation to leaf metabolism and environment[J]. Symposia of the Society for Experimental Biology, 1977, 31(31):471-505.
    [2]
    CHAVES M M, MAROCO O P, PEREIRA O S. Understanding plant responses to drought: from genes to the whole plant[J]. Functional Plant Biology, 2003, 30(3):239-264.
    [3]
    PILLITTERI L J, DONG J. Stomatal development in Arabidopsis [J]. Arabidopsis Book, 2012, 11(1):e0066.
    [4]
    BERGMANN D, SACK F. Stomatal development[J]. Annual Review of Plant Biology, 2007, 58(4):163-181.
    [5]
    CASSON S A, HETHERINGTON A M. Environmental regulation of stomatal development[J]. Current Opinion in Plant Biology, 2009, 13(1):90-95.
    [6]
    KENTA H, RYOKO K, TORII K U, et al. The secretory peptide gene EPF1 enforces the stomatal one-cell-spacing rule[J]. Genes & Development, 2007, 21(14):1720-1725.
    [7]
    HARA K, YOKOO T, KAJITA R, et al. Epidermal cell density is autoregulated via a secretory peptide, EPIDERMAL PATTERNING FACTOR 2 in Arabidopsis leaves[J]. Plant & Cell Physiology, 2009, 50(6):1019-1031.
    [8]
    TATSUHIKO K, RYOKO K, AYA M, et al. Stomatal density is controlled by a mesophyll-derived signaling molecule[J]. Plant & Cell Physiology, 2010, 51(1):1-8.
    [9]
    SUGANO S S, TOMOO S, YU I, et al. Stomagen positively regulates stomatal density in Arabidopsis [J]. Nature, 2010, 463:241-244.
    [10]
    NADEAU J A, SACK F D. Control of stomatal distribution on the Arabidopsis leaf surface[J]. Science, 2002, 296:1697-1700.
    [11]
    SHPAK E D, JESSICA M M, LYNN J P, et al. Stomatal patterning and differentiation by synergistic interactions of receptor kinases[J]. Pediatrics, 2005, 115(Suppl.4):1160-1164.
    [12]
    LEE J S, KUROHA T, HNILOVA M, et al. Direct interaction of ligand-receptor pairs specifying stomatal patterning[J]. Genes & Development, 2012, 26(2):126-136.
    [13]
    BERGER D, ALTMANN T. A subtilisin-like serine protease involved in the regulation of stomatal density and distribution in Arabidopsis thaliana [J]. Genes & Development, 2000, 14(9):1119-1131.
    [14]
    URITZA V G, DIETER B, THOMAS A. The subtilisin-like serine protease SDD1 mediates cell-to-cell signaling during Arabidopsis stomatal development[J]. Plant Cell, 2002, 14(7):1527-1539.
    [15]
    BERGMANN D C, WOLFGANG L, SOMERVILLE C R. Stomatal development and pattern controlled by a MAPKK kinase[J]. Science, 2004, 304:1494-1497.
    [16]
    PILLITTERI L, TORII K. Breaking the silence: three bHLH proteins direct cell-fate decisions during stomatal development[J]. Bioessays, 2007, 29(9):861-70.
    [17]
    WANG H, NGWENYAMA N, LIU Y, et al. Stomatal development and patterning are regulated by environmentally responsive mitogen-activated protein kinases in Arabidopsis [J]. Plant Cell, 2007, 19(1):63-73.
    [18]
    MIYAZAWA S I, TURPIN D H. Stomatal development in new leaves is related to the stomatal conductance of mature leaves in poplar ( Populus trichocarpa×P. deltoides )[J]. Journal of Experimental Botany, 2006, 57(2):373-380.
    [19]
    SAKURAI N, AKIYAMA M, KURAISHI S. Irreversible effects of water stress on growth and stomatal development in cotyledons of etiolated squash seedlings[J]. Plant & Cell Physiology, 1986, 27(6):1177-1185.
    [20]
    QUARRIE S A, JONES H G. Effects of abscisic acid and water stress on development and morphology of wheat [J]. Journal of Experimental Botany, 1977, 28(1): 192-203.
    [21]
    XU Z, ZHOU G. Responses of leaf stomatal density to water status and its relationship with photosynthesis in a grass[J]. Journal of Experimental Botany, 2008, 59(12): 3317-3325.
    [22]
    CLIFFORD S C, BLACK C R, ROBERTS J A, et al. The effect of elevated atmospheric CO 2 and drought on stomatal frequency in groundnut ( Arachis hypogaea (L.))[J]. Journal of Experimental Botany, 1995, 46(288): 847-852.
    [23]
    CASSON S, GRAY J E. Influence of environmental factors on stomatal development[J]. New Phytologist, 2008, 178(1): 9-23.
    [24]
    SHIMADA T, SUGANO S S, HARA-NISHIMURA I. Positive and negative peptide signals control stomatal density[J]. Cellular and Molecular Life Sciences, 2011, 68(12): 2081-2088.
  • Related Articles

    [1]Wang Xuerui, Yue Qingmin, Hao Minhui, He Huaijiang, Zhang Chunyu, Zhao Xiuhai. Modeling and parameter optimization of net primary productivity in the Korean pine-broadleaved forests of northeast China[J]. Journal of Beijing Forestry University. DOI: 10.12171/j.1000-1522.20250026
    [2]Xu Jianwei, Luo Haifeng, Kan Jiangming, Li Wenbin, Tong Siyuan. Underground self-sealing pressure injection equipment for forest and fruit trees[J]. Journal of Beijing Forestry University, 2023, 45(6): 137-144. DOI: 10.12171/j.1000-1522.20220514
    [3]Ye Qi, Guan Cheng, Zhang Houjiang, Gong Yingchun, Sui Yongfeng, Liu Lige. Optimization of finger joint parameters and nondestructive testing of bending properties of radiata pine laminates[J]. Journal of Beijing Forestry University, 2022, 44(3): 148-160. DOI: 10.12171/j.1000-1522.20210351
    [4]Li Yun, Zhang Wangfei, Cui Junbo, Li Chunmei, Ji Yongjie. Inversion exploration on forest aboveground biomass of optical and SAR data supported by parameter optimization method[J]. Journal of Beijing Forestry University, 2020, 42(10): 11-19. DOI: 10.12171/j.1000-1522.20190389
    [5]LI Ning, CHEN Li-hua, YANG Yuan-jun.. Factors influencing root tensile properties of Pinus tabuliformis and Larix principis-rupprechtii.[J]. Journal of Beijing Forestry University, 2015, 37(12): 77-84. DOI: 10.13332/j.1000-1522.20150131
    [6]XU Mei-jun, LI Li, LUO Bin. Factors affecting sanding force and optimal sanding parameters of Populus.[J]. Journal of Beijing Forestry University, 2015, 37(1): 122-133. DOI: 10.13332/j.cnki.jbfu.2015.01.002
    [7]CAO Lin, DAI Jin-song, XU Jian-xin, XU Zi-qian, SHE Guang-hui. Optimized extraction of forest parameters in subtropical forests based on airborne small footprint LiDAR technology[J]. Journal of Beijing Forestry University, 2014, 36(5): 13-21. DOI: 10.13332/j.cnki.jbfu.2014.05.009
    [8]ZHANG Shuang-yan, FEI Ben-hua, YU Yan, CHENG Hai-tao, WANG Chuan-gui. Influence of lignin content on tensile properties of single wood fiber.[J]. Journal of Beijing Forestry University, 2012, 34(1): 131-134.
    [9]WANG Ping-hua, CHEN Li-hua, JI Xiao-dong, SONG Heng-chuan, GAI Xiao-gang, JIANG Kun-yun, Lv Chun-juan. Establishing an integrated mechanical model of root tensile strength—taking four common arbor species in North China for example[J]. Journal of Beijing Forestry University, 2012, 34(1): 39-45.
    [10]LUO Bin, YIN Ya-fang, JIANG Xiao-mei, LUO Xiu-qin, LIU Bo, GUO Qi-rong. Evaluating bending and compressive strength properties of Eucalyptus grandia×E. urophylla plantation wood with three nondestructive methods[J]. Journal of Beijing Forestry University, 2008, 30(6): 137-140.
  • Cited by

    Periodical cited type(3)

    1. 赵尧,付伟莲,关惠元. T型圆竹家具构件力学性能研究. 林产工业. 2024(10): 42-46 .
    2. 刘燕,唐斌,万川,何叶,胡文刚. 实木家具斜角接合结构的可拆装设计与评估. 林产工业. 2023(04): 38-42+50 .
    3. 陈炳睿,胡文刚. 一种可拆装式椭圆榫节点的设计与性能分析. 木材科学与技术. 2022(02): 65-70+86 .

    Other cited types(0)

Catalog

    Article views (1696) PDF downloads (23) Cited by(3)

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return