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Physiological Response of Different Croftonweed (Eupatorium adenophorum) Populations to Low Temperature

Published online by Cambridge University Press:  20 January 2017

Hui Li ,
Sheng Qiang  and
Yaling Qian
Hui Li
Affiliation:
Weed Research Laboratory, Nanjing Agricultural University, Nanjing 210095, China
Sheng Qiang*
Affiliation:
Weed Research Laboratory, Nanjing Agricultural University, Nanjing 210095, China
Yaling Qian
Affiliation:
Department of Horticulture and Landscape Architecture, Colorado State University, Fort Collins, CO 80523, USA
*
Corresponding author's E-mail: qiangs@njau.edu.cn; wrl@njau.edu.cn
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Abstract

Croftonweed is a major invasive weed in China and, although of subtropical origin, has invaded into regions with colder climates. Freezing tolerances of nine croftonweed populations from different geographies were studied using a freezing injury index. Physiological responses to freezing temperature were determined to elucidate mechanisms of freezing tolerance. Plants from Baise, Guangxi (BSG), and Qujing, Yunnan (QJY), China, showed the most freezing injury symptoms, whereas plants from Huangguoshu, Guizhou (HGG), China, displayed the least. Under freezing stress, physiological changes, including increases in malondialdehyde (MDA) and total soluble protein contents; reductions in total soluble sugar, chlorophyll contents, and ratios of variable chlorophyll fluorescence to maximum chlorophyll fluorescence (Fv : Fm); and fluctuation of superoxide dismutase (SOD) activity, were observed among all nine populations. However, different degrees of physiological responses were found among populations with diverse low-temperature sensitivities. After 4 d of treatment at −5 C, MDA content increased 25-fold in leaves of the sensitive BSG population compared with untreated leaves, whereas a range of 0.8-fold to ∼5.3-fold increase was found in other populations. Total soluble protein content in leaves of the tolerant HGG population increased to the highest value among the nine populations. SOD activity of the freezing-sensitive BSG population decreased 36% of the control, whereas the tolerant HGG population reduced to 70%. Moreover, soluble sugar of the tolerant HGG population decreased 29%, less than the sensitive BSG population (87%). There were fewer declines in the percentages of chlorophyll content and Fv : Fm value in HGG than in BSG (less 44% and 32%). Freezing injury index had significant negative correlations with Fv : Fm values and chlorophyll contents (−0.619 and −0.622, respectively). These results suggest that croftonweed has evolved into different ecotypes with regard to freezing tolerance through physiological adaptation during their invasion of southwest regions of China. The freezing-tolerant croftonweed population would have more chances to invade distant northeastern areas in the future.

Keywords

Croftonweed, Eupatorium adenophorum Spreng EUPADLow temperature stressphysiological responseinvasive plant
Type
Physiology, Chemistry, and Biochemistry
Information
Weed Science , Volume 56 , Issue 2 , April 2008 , pp. 196 - 202
Copyright
Copyright © Weed Science Society of America 

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References

Literature Cited

Arnon, D. I. 1949. Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris . Plant Physiol. 24:1–15.Google Scholar
Bailly, C., Benamar, A., Corbineau, F., and Come, D. 1996. Changes in malondialdehyde content and in superoxide dismutase, catalase and glutathione reductase activities in sunflower seed as related to deterioration during accelerated aging. Physiol. Plant. 97:104–110.CrossRefGoogle Scholar
Bowler, C., Montagu, M. V., and Inze, D. 1992. Superoxide dismutase and stress tolerance. Ann. Rev. Plant Physiol. Plant Mol. Biol. 43:83–116.Google Scholar
Bradford, M. M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principal of protein-dye binding. Anal. Biochem. 72:248–254.Google Scholar
Bravo, L. A., Zuniga, G. E., Alberdi, M., and Corcuera, L. J. 1998. The role of ABA in freezing tolerance and cold acclimation in barley. Physiol. Plant. 103:17–23.Google Scholar
Giannopolitis, C. N. and Ries, S. K. 1977. Superoxide dismutases, I: occurrence in higher plants. Plant Physiol. 59:309–314.CrossRefGoogle ScholarPubMed
Gray, G. R., Savitch, L. V., Ivanov, A. G., and Huner, N. P. A. 1996. Photosystem II excitation pressure and development of resistance to photoinhibition II. Adjustment of photosynthetic capacity in winter wheat and winter rye. Plant Physiol. 110:61–71.Google Scholar
Griffith, M. and McIntyre, H. C. H. 1993. The interrelationship of growth and frost tolerance in winter rye. Physiol. Plant. 87:335–344.Google Scholar
Guy, C. L. 2003. Freezing tolerance of plant: current understanding and selected emerging concepts. Can. J. Bot. 81:1216–1223.CrossRefGoogle Scholar
Hakam, N., Khanizadeh, S., DeEll, J. R., and Richer, C. 2000. Assessing chilling tolerance in roses using chlorophyll fluorescence. Hortscience. 35:184–186.Google Scholar
Hodges, D. M., DeLong, J. M., Forney, C. F., and Prange, R. K. 1999. Improving the thiobarbituric acid-reactive-substances assay for estimating lipid peroxidation in plant tissues containing anthocyanin and other interfering compounds. Planta. 207:604–611.CrossRefGoogle Scholar
Huner, P. A. N., Öquist, G., Hurry, V. M., Krol, M., Falk, S., and Griffith, M. 1993. Photosynthesis, photoinhibition and low-temperature acclimation in cold tolerant plants. Photosynth. Res. 37:19–39.Google Scholar
Hurry, V. M., Malmberg, G., Gardeström, P., and Öquist, G. 1994. Effects of a short-stem shift to low temperature and of long-stem cold hardening on photosynthesis and ribulose 1,5-bisphosphate carboxylase/oxygenase and sucrose phosphate synthase activity in leaves of winter rye (Secale cereale L.). Plant Physiol. 106:983–990.Google Scholar
Hurry, V. M., Strand, Å, Tobiæson, M., Gardestrom, P., and Oquist, G. 1995. Cold hardening of spring and winter wheat and rape results in differential effects on growth, carbon metabolism, and carbohydrate content. Plant Physiol. 109:697–706.Google Scholar
Irigoyen, J. J., Emerich, D. W., and Sanchez-Diaz, M. 1992. Water stress induced changes in concentrations of proline and total soluble sugars in nodulated alfalfa (Medicago sativa) plants. Physiol. Plant. 84:55–60.Google Scholar
Jiang, M. Y. and Zhang, J. H. 2001. Effect of abscisic acid on active oxygen species, antioxidative defense system and oxidative damage in leaves of maize seedlings. Plant Cell Physiol. 42:1265–1273.Google Scholar
Lee, C. E. 2002. Evolutionary genetics of invasive species. Trends Ecol. Evol. 17:386–391.Google Scholar
Li, H., Qiang, S., and Cui, J. 2005. Eupatorium adenophorum micro-propagation by bud and callus culture. Acta Bot. Boreali Occident. Sin. 25:1458–1462.Google Scholar
Mooney, H. H. and Hobbs, R. J. 2000. Invasive Species in a Changing World. 1st ed. Washington, DC Island. 115–138.Google Scholar
Öncel, I., Yurdakulol, E., Keles, Y., Kurt, L., and Yildiz, A. 2004. Role of antioxidant defense system and biochemical adaptation on stress tolerance of high mountain and steppe plants. Acta Oecol. 26:211–218.Google Scholar
Papes, M. and Peterson, A. T. 2003. Predicting the potential invasive distribution for Eupatorium adenophorum Spreng. in China. J Wuhan Bot. Res. 21:137–142. [in Chinese].Google Scholar
Posmyk, M. M., Bailly, C., Szafrańskaa, K., Janas, K. M., and Corbineau, F. 2005. Antioxidant enzymes and isoflavonoids in chilled soybean (Glycine max (L.) Merr.) seedlings. J. Plant Physiol. 162:403–412.Google Scholar
Price, A. H. and Hendry, G. A. R. 1991. Iron-catalyzed oxygen radical formation and its possible contribution to drought damage in nine native grasses and three cereals. Plant Cell Environ. 14:451–477.CrossRefGoogle Scholar
Qiang, S. 1998. The history and status of the study croftonweed (Eupatorium adenophorum Spreng.) a worst worldwide weed. J. Wuhan Bot. Res. 16:366–372. [in Chinese].Google Scholar
Savitch, L. V., Gray, G. R., and Huner, N. P. A. 1997. Feedback-limited photosynthesis and regulation of sucrose-starch accumulation during cold acclimation and low-temperature stress in a spring and winter wheat. Planta (Berl.) 201:18–26.Google Scholar
Schlichting, C. D. and Pigliucci, M. 1998. Phenotypic Evolution: A Reaction Norm Perspective. 1st ed. Sunderland, MA Sinauer. 152–160.Google Scholar
Semeniuk, P. and Moline, H. K. 1986. A comparison of effect of ABA and antitranspirant on freezing injury of coleus, cucumber and dieffenbachia. J. Am. Soc. Hortic. Sci. 11:866–868.CrossRefGoogle Scholar
Shahba, M. A., Qian, Y. L., Hughes, H. G., Christensen, D., and Koski, A. J. 2003. Cold hardiness of saltgrass accessions. Crop Sci. 43:2142–2147.Google Scholar
Stitt, M. and Hurry, V. 2002. A plant for all seasons: alterations in photosynthetic carbon metabolism during cold acclimation in Arabidopsis . Curr. Opin. Plant Biol. 5:199–206.Google Scholar
Strand, Å, Foyer, C. H., Gustafsson, P., Gardeström, P., and Hurry, V. 2003. Altering flux through the sucrose biosynthesis pathway in transgenic Arabidopsis thaliana modifies photosynthetic acclimation at low temperatures and the development of freezing tolerance. Plant Cell Environ. 26:523–535.Google Scholar
Strand, A., Hurry, V., Henkes, S., Huner, N., Gustafsson, P., Gardeström, P., and Stitt, M. 1999. Acclimation of Arabidopsis leaves developing at low temperatures. Increasing cytoplasmic volume accompanies increased activities of enzymes in the Calvin cycle and in the sucrose-biosynthesis pathway. Plant Physiol. 119:1387–1397.Google Scholar
Su, X., Qiang, S., and Song, X. 2005. Comparison of Eupatorium adenophorum heat tolerances of different geographical populations. Acta Bot. Boreali Occident. Sin. 25:1766–1771.Google Scholar
Takagi, T., Nakamura, M., Hayashi, H., Inatsugi, R., Yano, R., and Nishida, I. 2003. The leaf-order-dependent enhancement of freezing tolerance in cold-acclimated Arabidopsis rosettes is not correlated with the transcript levels of the cold-inducible transcription factors of CBF/DREB1 . Plant Cell Physiol. 44:922–931.Google Scholar
Thomashow, M. E. 1999. Plant cold acclimation: freezing tolerance gene and regulatory mechanisms. Ann. Rev. Plant Physiol. Plant Mol. Biol. 50:571–599.Google Scholar
Waldhoff, D., Furch, B., and Junk, W. J. 2002. Fluorescence parameters, chlorophyll concentration, and anatomical features as indicators for flood adaptation of an abundant tree species in central Amazonia: Symmeria paniculata. Environ. Exp. Bot. 48:225–235.Google Scholar
Wang, M., Feng, Y., and Li, X. 2006. Effects of soil phosphorus level on morphological and photosynthetic characteristics of Ageratina adenophora and Chromolaena odorata . J. Appl. Ecol. 17:602–606. [in Chinese].Google ScholarPubMed
Wanner, L. A. and Junttila, O. 1999. Cold-induced freezing tolerance in Arabidopsis . Plant Physiol. 120:391–399.Google Scholar
Watanabe, S., Kojima, K., Ide, Y. J., and Sasaki, S. 2000. Effects of saline and osmotic stress on proline and sugar accumulation in Populus euphratica in vitro. Plant Cell Tissue Organ Cult. 63:199–206.Google Scholar
Yu, J. Q., Zhou, Y. H., Huang, L. F., and Allen, D. J. 2002. Chill-induced inhibition of photosynthesis: genotypic variation within Cucumis sativus . Plant Cell Physiol. 43:1182–1188.Google Scholar