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Jian Xin Shi, Joseph Riov, Raphael Goren, Eliezer E. Goldschmidt, and Ron Porat

[ Pyrus persica (L.) Batsch] ( Bonghi et al., 1999 ), sweet pepper ( Capsicum annuum L.) ( Imahori et al., 2000 ), and tomato ( Chen and Chase, 1993 ) upon postharvest exposure to hypoxia or anoxia. However, the expression profile of PDC in grape

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Junqin Zong, Yanzhi Gao, Jingbo Chen, Hailin Guo, Yi Wang, Fan Meng, Yiwei Jiang, and Jianxiu Liu

with more coleoptile elongation ( Kato-Noguchi and Morokuma, 2007 ). The results of that study suggest that the ability to increase ethanolic fermentation may be one of the determinants in anoxia tolerance of rice coleoptiles under short-term stress. In

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Vicente Gimeno, James P. Syvertsen, Inma Simon, Vicente Martinez, Jose M. Camara-Zapata, Manuel Nieves, and Francisco Garcia-Sanchez

, an energy shortage can occur so remobilization of stored carbohydrates can play a vital role in providing energy needed for cell and organ maintenance as well as for stress responses ( Greenway and Gibbs, 2003 ). For example, anoxia-tolerant plants

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Roberto López-Pozos, Gabino Alberto Martínez-Gutiérrez, Rafael Pérez-Pacheco, and Miguel Urrestarazu

aeration and plant root metabolism Soil Sci. 154 259 268 Drew, M.C. 1997 Oxygen deficiency and root metabolism: Injury and acclimation under hypoxia and anoxia Annu. Rev. Plant Physiol. Plant Mol. Biol. 48 223 250 Gislerød, H.R. Adams, P. 1983 Diurnal

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Lisa G. Neven

this study, the pattern of diminishing differential stage thermotolerance was similar to our results. The influence of anoxia on insect physiological response to temperature was documented in flesh fly ( Sacrophaga crassipalpis ) cold hardiness response

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En-chao Liu, Li-fang Niu, Yang Yi, Li-mei Wang, You-wei Ai, Yun Zhao, Hong-xun Wang, and Ting Min

characteristics and volatile composition of mulberry wine J. Inst. Brewing 124 45 56 Min, T. Fang, F. Ge, H. Shi, Y.N. Luo, Z.R. Yao, Y.C. Grierson, D. Yin, X.R. Chen, K.S. 2014 Two novel anoxia-induced ethylene response factors that interact with promoters of

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Fang Yu, Zhiming Ni, Xingfeng Shao, Lina Yu, Hongxing Liu, Feng Xu, and Hongfei Wang

-glucose (UDPG). Sucrose also modulates the response in field and model plants to cold ( Uemura et al., 2003 ), heat ( Zhao et al., 2013 ), drought ( Hoffmann, 2010 ), and anoxia ( Lara et al., 2011 ). Sucrose may protect the cytomembrane by acting as a

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S. Shukla, B.J. Boman, R.C. Ebel, P.D. Roberts, and E.A. Hanlon

production ( Else et al., 1995 ; Else and Jackson, 1998 ) and reactive oxygen species ( Bailey-Serres and Chang, 2005 ), serve as secondary messengers for the aerial portion of the plant. Root anoxia causes changes in ultrastructure ( Vartapetian et al

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Guodong Liu, D. Marshall Porterfield, Yuncong Li, and Waldemar Klassen

uptake by anoxia and linked them to cytosol acidosis. They proved that one early response of plants to oxygen deficiency is the downregulation of water uptake of roots. The present study indirectly showed that corn seeds downregulated imbibition in

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Ling Ma, Xingquan Rao, and Xiaoyang Chen

waterlogging have not been fully revealed, and further exploration is needed. Under waterlogging conditions, additional stress can arise because hypoxia or anoxia in the rhizosphere can induce the accumulation of large quantities of reactive oxygen species in