Xiong JING,Yongxia BAI,Man SHEN*,Pingsheng LENG 1.Plant Science and Technology College,Beijing University of Agriculture,Beijing 102206,China;2.Key Laboratory of New Technology in Agricultural Application of Beijing,Beijing University of Agriculture,Beijing 102206,China;.Landscape Architecture College,Beijing University of Agriculture,Beijing 102206,China
Chrysanthemum is a perennial flower ofDendranthema,Asteraceae,and ground-cover chrysanthemum (Dendranthema×grandiflorumKitamura)is a new variety group in chrysanthemum family,which was bred by Professor Chen Junyu from Beijing Forestry University in the 1980s[1].It has dwarf plant,long florescence,close flower shape and strong stress resistance,and is able to bear extensive cultivation,So this mum variety group is used well as groundcover plant.In recent years,the researches about ground-cover chrysanthemum mainly focus on introduction,breeding,cultivation[2-4],drought resistance[5-6]and saline alkali resistance[7],and there are few reports about cold resistance.The ground-cover chrysanthemum ‘Zixunzhang’was used as the experimental material in this study.By determining physiological and biochemical indexes of leaves,emergent rhizomesand rootsfrom ‘Zixunzhang’which grew in the open field during overwintering period,we tried to analyze correlation between cold tolerance of ground-cover chrysanthemum and these physiological and bio-chemical indexes,which could provide test proof for correctly identifying cold tolerance of different varieties.
The ground-cover chrysanthemum ‘Zixunzhang’ was used as the experimental material in this study,which was planted in open field of nursery of Science and Technology Park,Beijing University of Agriculture in spring of 2011.From September of 2011 to May of 2012,leaves and emergent rhizomes of ground-cover chrysanthemum were sampled every 15 days,while roots were sampled every 30 days.Relative water content,water content,root activity,soluble protein content and activities of three protection enzymes(POD,SOD and CAT)from the fresh materials were measured,and samples used for measuring other related indexes were conserved at-80℃.
Referring to the methods of Li Hesheng et al.[8-9],the below indexes were determined.Relative water content and water content were determined by drying method;SOD enzyme activity measurement used NBT photo reduction method;POD enzyme activity measurementused guaiacol method;CAT enzyme activity measurement used ultraviolet absorption method;soluble sugar content was determined by anthrone method;soluble protein content was determined by Kaumas blue staining method;proline content measurement used acid three indene keton colorimetric method;root activity was determined by TTC method.Variance analysis and correlation analysis of test data were conducted by Microsoft Excel and SPSS 17.0 software.
According to atmosphere temperature every day from September of 2011 to May of 2012 recorded by weather forecast,monthly average maximum,minimum and average atmosphere temperature were obtained(Fig.1).Right angle thermometer inserting into underground 20 cm was used to record surface temperature,and monthly average minimum,maximum and average temperature at underground 20 cm were obtained(Fig.2).Seen from Fig.1,atmosphere temperature continuously declined in winter.Average minimum atmosphere temperature in December was-5.4℃,and daily minimum atmosphere temperature reached-10℃.To January,atmosphere temperature reached the minimum.Monthly average minimum atmosphere temperature in January reached-8.3℃,and daily minimum atmosphere temperature was-13℃,which then gradually rose.Seen from Fig.2, surface temperature also reached the minimum in January,and monthlyaverageminimum surface temperature in January was-3.4℃,which then gradually rose.
During overwintering period,morphological changes of leaves,emergent rhizomes and roots from‘Zixunzhang’were shown as Fig.3.Leaves of‘Zixunzhang’ still maintained green in the end of October,but basically withered after early frost in middle dekad of November.Emergent rhizomes sprouting tillers still grew in middle dekad of November,and some emergentrhizomesstillmaintained green after snowfall in December.But as low temperature below zero celsius continued to middle dekad of December,emergent rhizomes at rhizosphere basically died,which germinated again until next April.Roots always maintained activity during whole overwintering period.Although lateral roots had black and dead phenomenon during January-February,most of principal roots still maintained white or light brown.Seen from morphological observation results,it seems that cold tolerance of ground-cover chrysanthemum mainly depended on the vitality of root system.
Perennial flower mainly depends on roots activity to overwinter in open field.Thence,vitality state of plant roots can reflect cold tolerance of plant in certain degree[10].Seen from Fig.4,as temperature slowly declined,vitality value of roots slowly declined before December 23.But vitality value of roots fell after significantly rose in January when temperature was the minimum and on March 18 when temperature abruptly declined,and increase magnitudes were 19.21% and 81.18% respectively.It was suggested that maybe prior slow temperature reduction made roots obtain certain lowtemperature domestication,thereby causing that low temperature in short time stimulated root vitality rising.
Water content of plant tissue declines in late autumn and early winter,which is conducive to accumulation of dry matter and improvement of cold resistance[11].Seen from Table 1,as winter temperature declined,relative water contents of aboveground part and water content of underground part from ‘Zixunzhang’ all presented declining tendency,and gradually rose again after next spring.Relative water contents of leaves and emergent rhizomes reached the minimum before withered.Water content of root started to slowly rise after reaching the minimum on January 15,in which water content of root abruptly rose on December 23.It was speculated that maybe snowfall on December 2 increased soil water content,causing water content of root rose in short time.
Table 1 Changes in water contents of leaves,emergent rhizomes and roots of‘Zixunzhang’mum during the overwintering %
Table 2 Changes in SOD activities of leaves,emergent rhizomes and roots of‘Zixunzhang’mum during the overwintering U/g
As temperature declined,SOD and CAT enzyme activities of leaves presented rise-decline tendency(Table 2,Table 3),while POD enzyme presented decline-rise tendency(Table 4).SOD enzyme activity significantly rose on October 15,and increase magnitude reached 309.81%,while POD enzyme activity significantly declined at this time,and decline magnitude was 32.28%.Both SOD and CAT enzyme activities declined after rising to the maximum on October 30,while POD rose after declining to the minimum on October 15.As temperature declined,enzyme activity of leaves had significant difference.
Both SOD and CAT enzyme activities of emergent rhizomes overall presented rise-decline-rise tendency,while POD presented decline-rise tendency.SOD enzyme activity significantly declined on December 2,and decline magnitude reached 39.90%.CAT enzyme activity significantly rose on October 30,with increase magnitude of 46.77%,then gradually declined,and reached the minimum on December 2.POD significantly declined on October 30,with decline magnitude of 58.92%,then gradually rose,and reached the maximum on December 2.After next spring,each enzyme activity gradually rose and recovered normal.Seen from the above analysis,abrupt temperature reduction on December 2 had larger impact on enzyme activity change of emergent rhizomes.
SOD and CAT enzyme activities of leaves and emergent rhizomes had consistent change rule,while POD had contrary rule.It was speculated that maybe the three protective enzymes alternately played role under low temperature,to commonly resist the impact of low temperature on plant metabolism.
SOD enzyme activity of root significantly declined on December 2,and decline magnitude reached 71.39%.CAT enzyme activity significantly rose on January 3,with increase magnitude of 454%,and significantly declined on March 30.POD activity reached the maximum on March 30,and increase magnitude was 150.94%.It was clear thatenzyme activity ofrootonly changed greatly in January and when temperature abruptly declined,and total change tendency during whole overwintering period was not very significant.
Seen from Table 5 to Table 7,as variation of winter outdoor temperature,soluble sugar of leaves accumulated,while soluble protein and proline content presented declining tendency.Before leaves withered,its soluble protein and soluble sugar reached the minimum and maximum respectively.Proline content significantly declined on October 15,with decline magnitude of 77.55%.
Soluble protein and proline content of emergent rhizomes overall presented decline-rise-decline-rise tendency,and soluble protein reached the maximum on November 29.Proline content significantly declined on October 30,with decline magnitude of 66.53%,and reached the maximum on December 2.Soluble sugar content presented rise-decline-rise-decline tendency,and significantly rose on October 30,with increase magnitude of 280.96%,and reached the maximum on December 2.After next spring,content of each osmotic adjustment substance of emergent rhizomes gradually recovered to the October level.
Seen from the above analysis,soluble protein and proline of leaves and emergent rhizomes had consistent variation,and they had contrary change tendency with that of soluble sugar content.The common point was that osmotic adjustment substances reached the extreme value before plant withered and temperature was the lowest.
Soluble protein content of root changed stably,and overall presented rise-decline tendency.Soluble protein content of root reached the maximum(31.61 mg/g)on December 2,and had transient increase on March 30.It was speculated that it was caused by abrupt temperature reduction on March 18.Soluble sugarcontent reached the maximum (71.79 mg/g)on January 3,and then gradually declined,in which it significantly rose on November 20,with increase magnitude of 389.51%.Change of proline was not stable,and it significantly rose on November 20,December 23 and February 22.As temperature declined,osmotic adjustment substances from root all increased somewhat.
Table 8 showed correlation coefficients among the measured indexes in natural temperature reduction process.Seen from Table 8,water content and relative water content presented significantly positive correlation,while POD and SOD presented extremely significant positive correlation.Soluble protein presented extremely significant positive correlation with water content,and extremely significant negative correlation with SOD and POD.Soluble sugar presented extremely significant negative correlation with relative water content and water content,and extremely significant positive correlation with SOD.Proline presented significantly negative correlation with relative water content,and extremely significant positive correlation with SOD.Root activity presented extremely significant positive correlation with relative water content and CAT,and significantly negative correlation with soluble sugar and soluble protein.Seen from the above analysis,correlation among relative water content,SOD,soluble protein,soluble sugar and root activity was higher,followed by that among water content,proline,POD and CAT.
Change of the plant root function is bound to affect physiological characteristics of aboveground leaves[12].Root activity can change under temperature.In the research,it was found that root activity slowly declined inslow temperature reduction process during September-October.But in January when the temperature was the lowest and latter period of winter when temperature abruptly declined after rise,root activity had falling phenomenon after transient rise.It illustrated that certain low temperature could cause decline of root activity,but slow temperature reduction might make roots obtain low temperature domestication at certain degree.When encountering low temperature with larger reduction magnitude,protective enzyme activity in plant roots was activated because of low temperature domestication within certain low temperature range,thereby causing that root activity rose.
Table 3 Changes in CAT activities of leaves,emergent rhizomes and roots of‘Zixunzhang’ mum during the overwintering U/(g﹒min)
Table 4 Changes in POD activities of leaves,emergent rhizomes and roots of‘Zixunzhang’ mum during the overwintering U/(g﹒min)
Table 5 The changes in soluble protein contents of leaves,emergent rhizomes and roots of‘Zixunzhang’ mum during the overwintering mg/g
Table 6 The changes in soluble sugar contents of leaves,emergent rhizomes and roots of‘Zixunzhang’mum during the overwintering mg/g
When water content of plant declines,the amount of intracellular osmotic matter relatively increases,which can increase cell concentration,decline osmotic potential,make freezing possibility decline,and enhance the ability of resisting coldness and preventing freeze[13].In the research,it was found that relative water content of aboveground part and water content of underground part overall presented declining tendency in overwintering process,which may be conducive to plant resisting the injury of low temperature.The conclusion was consistent with research results of Bao Siweiet al[14-15].
When plant suffers cold injury,some enzymes andnonenzymes cleaning free radicals and reactive oxygen in plant can regulate membrane permeability and increase structure and function stability of membrane,to protect plant cell from injury[16].Under low temperature,SOD,CAT and POD enzyme activities in plant are directly related to plant’s ability resisting low temperature injury[17].In the research,it was found that SOD and CAT enzyme activities of leaves and emergent rhizomes overall presented the tendency of first rising and then declining,while POD presented the tendency of first declining and then rising.It was suggestedthatthese three enzymes maybe alternately play role.Enzyme activity of root had small difference during whole overwintering period except at several points with larger temperature reduction magnitude.It was speculated that low temperature had smaller impact on these protective enzymes in the root.
In plant metabolism process,plant can ease the injury of low temperature and regulate cell osmotic equilibrium by accumulating or decomposing osmotic adjustment substances[16].The test result found that leaves could accumulate a lot of soluble sugar,while soluble protein and proline content overall presented declining tendency.It was speculated that when leaves entered into the aging stage,decomposing velocity was larger than synthesis velocity.Maybe it was caused by these matters transferring from aboveground part to underground part.Total tendency displayed that contents of osmotic adjustment substances of emergent rhizomes and roots overall presented rise-decline tendency,showing that winter low temperature induced emergent rhizomes and roots synthesizing a lot of osmotic adjustment substances to improve their own cold resistance.
For ground-cover chrysanthemum,its physiological and biochemical indexes changed at the amountduring overwintering period,which was related to low temperature.According to the result of correlation analysis method,it was initially judged that relative water content,SOD,soluble protein,soluble sugar,root system activity of ground-cover chrysanthemum were closely related to its cold resistance,followed by water content,proline,POD and CAT.
Table 7 The changes in proline contents of leaves,emergent rhizomes and roots of‘Zixunzhang’mum during the overwintering mg/g
Cold tolerance of ground-cover chrysanthemum is affected by integrated effect of its physiological and biochemicalcharacteristics,and its cold resistant mechanism is complicated[18].It is not accurate to judge cold resistance of ground-cover chrysanthemum only by single cold resistance index.Therefore,it has important actual significance for identifying cold resistance of ground-cover chrysanthemum by multiple physiological and biochemical indexes.
Table 8 Relative coefficient between each pair of indexes of‘Zixunzhang’ mum during the overwintering
[1]WANG PW(王彭伟),CHEN JY(陈俊愉).Breeding study on new variety of ground-cover chrysanthemum(地被菊新品种选育研究)[J].Acta Horticulturae Sinica(园艺学报),1990,17(8):223-228.
[2]ZHANG XB(张玄兵),YAO S(姚胜),LIANG DN(梁冬霓).Study on introduction of six species of ground-cover chrysanthemum(地被菊六个品种的引种研究)[J].Journal of Hainan Normal University(海南师范学院学报),2001,14(2):69.
[3]LI JJ(李进进).Suitability observation report of ground-cover chrysanthemum introduction(地被菊引种适应性观察初报)[J].Journal of Guangdong Industry Technical College(广东轻工职业技术学院学报),2003,2(3):17-18.
[4]WANG T(王涛).Study on hybrid breeding technology of ground-cover chrysanthemum(地被菊杂交育种技术的研究)[D].Urumqi:Xinjiang Agricultural University(乌鲁木齐:新疆农业大学),2010.
[5]CUI JP(崔娇鹏).Initial study on drought resistance and water saving of groundcover chrysanthemum(地被菊抗旱节水性初步研究)[D].Beijing:Beijing Forestry University(北京:北京林业大学),2005.
[6]SHI LR(时丽冉),CHEN HY(陈红艳),CUI XG(崔兴国).The impact of drought stress on peroxide and antioxidant enzyme activities of membrane lipid of ground-cover chrysanthemum(干旱胁迫对地被菊膜脂过氧化和抗氧化酶活性的影响)[J].Northern Horticulture(北方园艺),2010(9):96-98.
[7]SHI LR(时丽冉),ZHAO BC(赵炳春),BAI LR(白丽荣).The study on salt tolerance of ground-cover chrysanthemum(地被菊抗盐性研究)[J].Chinese Agricultural Science Bulletin(中国农学通报),2010,26(12):139-142.
[8]LI HS(李合生).Physiological and biochemicalexperiment principle and technology of plant(植物生理生化实验原理和技术)[M].Beijing:Higher Education Press(北京:高等教育出版社),2000.
[9]ZHANG ZL(张志良).Experimental guide of plant physiology(植物生理学实验指导)[M].Beijing:Higher Education Press(北京:高等教育出版社),1990.
[10]LIU ZY(刘志洋),GONG S(宫书),CHEN X(陈曦).The impact of low temperature on root activities of six kinds of perennial flowers(低温处理对六种宿根花卉根系活力的影响)[J].Northern Horticulture(北方园艺),2009(7):201-203.
[11]WU N(吴娜),ZHOU HJ(周怀军),XIAO F(肖芳).Changes of water content and soluble sugar in the leaves of three evergreen broad-leaf plants of Celastraceae during overwintering(3种常绿阔叶植物越冬期间叶片水分及可溶性糖的动态变化)[J].Journal of Northwest Forestry University(西北林学院学报),2006,21(4):36-38.
[12]FELDMAN LJ.Regulation of root development[J].Ann Rev Plant Physiol,1984,35:223-242.
[13]PAN RZ(潘瑞帜),DONG YD(董愚得).Plant physiology(植物生理学)[M].Beijing:Higher Education Press(北京:高等教育出版社),1985.to industry and food security in China(中国马铃薯产业发展与食物安全)[J].Scientia Agricultura Sinica(中国农业科学),2005,(2):258-262.
[5]TIAN F(田芳).Occurrence and control of diseases of potato in cellars in Northern China(北方地区马铃薯窖藏病害的发生及防治)[J].Guide of Sci-tech Magazine(科技致富向导),2012,(27):378-402.
[6]CARNEGIE SF,RUTHVEN AD,LINDSAY DA,et al.Effects of fungicides applied to seed potato at harvest or after grading on fungal storage diseases and plant development[J].Ann Appl Biol,1990,116:61-72.
[7]ZHAO SS(赵生山),NIU LH(牛乐华).Survey on potato disease and chemical control during storage(马铃薯贮藏期病害调查及药剂防治研究)[J].Information of Agricultural Science and Technology(农业科技与信息),2008,(11):44-46.
[8]PENG XW(彭学文),ZHU WH(朱杰华).Fungal diseases and distribution of in potato in Hebei Province(河北省马铃薯真菌病害种类及分布)[J].Chinese Potato Journal(中国马铃薯),2008,22(1):31-33.
[9]LIU CH(刘程惠),HU WZ(胡文忠).Physio-biochemical changes of freshcut potato at different storage temperatures(不同贮藏温度下鲜切马铃薯的生理生化变化)[J].Food&Machinery(食品与机械),2008,24(2):38-42.
[10]LI GL(李国龙),WU HX(吴海霞),WEN L(温丽).Progress in physiological and molecular mechanism of drought resistant in crop(作物抗旱生理与分子作用机制研究进展)[J].Chinese Agricultural Science Bulletin(中国农学通报),2010,40(23):185-191.
[11]CHEN Q,SUN HS,YANG JL,et al.Inheritance and molecular mapping of new genes conferring late blight and CPB resistance in Mexican wild potato speciesSolanum pinnatisectum[J].Agricultural Science & Technology,2009(5):257-261.
[12]ZHANG RJ,CHEN YJ,MENG Ml,et al.Regulation of nitrogen on potato under NaCl stress[J].Agricultural Science&Technology,2010,11(11-12):65-67.
[13]BI Y,LI YC,GE YH.Induced resistance in postharvest fruits and vegetables by chemicals and its mechanism[J].Stewart Postharvest Review,2007,(6):1-7.
[14]WU B(吴斌),WANG FL(王建富),SUN RL(孙瑞林),et al.Potato pest occurrence and control in Taixing City(泰兴市马铃薯病虫害发生特点与防治技术)[J].Modern Agricultural Sciences and Technology(现代农业科技),2011,(14):179-180.
[15]THEV DJ,LIAO XL(廖晓兰).Effects of temperature on dry occurrence in potatoes inoculated with differentFusariumspecies(温度对接种不同镰刀菌的马铃薯干腐病发展的影响)[J].Rain Fed Crops(国外农学:杂粮作物),1991(6):30-33.
[16]HOU ZY(侯忠艳).Occurrence and control of Fusarium dry rot in potato(马铃薯干腐病的发生与防治)[J].Modern Agricultural Sciences and Technology(现代农业科技),2012,(10):173-179.
[17]MIN FX(闵凡祥),WANG XD(王晓丹),HU LS(胡林双),et al.Identification of species and pathogenicity ofthe Fusarium on potato in Heilongjiang Province(黑龙江省马铃薯干腐病菌种类鉴定及致病性)[J].Plant Protection(植物保护),2010,(4):112-115.
[18]LI FL(李凤兰),JIANG XF(蒋先锋),SHI LJ(史丽娟),et al.Isolation and identification of two pathogenic stains associated with potato dry rot(两株马铃薯干腐病病原菌的分离和鉴定)[J].Crops(作物杂志),2013,4:125-127.
[19]WANG QM(汪俏梅),GUO DP(郭得平),KYIKYI WIN.Effect of 1-MCP on storage life,quality and antioxidant enzyme activities of broccoli(1-MCP对青花菜贮藏寿命、品质和抗氧化酶活性的影响)[J].Journal of Zhejiang University(Agriculture&Life Sciences)(园艺学报:农业与生命科学版),2004,31(2):205-209.
[20]BRISSON LF,TENHAKEN R,LAMB CJ.Function of oxidative cross-linking of cell wall structural proteins in plant disease resistance[J].Plant Cell,1994,6:1703-1712.
[21]HU JJ(胡景江),LIU ST(刘树滔),PAN JR(潘剑茹).Research progress on technologies of SOD propertyimprovement(SOD特性改善技术研究进展)[J].Strait Pharmaceutical Journal(海峡药学),2009,21(2):11-14.
[22]LI JH(李金华),WANG F(王丰),LIAO YL(廖亦龙).Advance on seed vigor physiological-biochemical and genetic mechanisms in rice(水稻种子活力的生理生化及遗传研究)[J].Molecular Plant Breeding(分子植物育种),2009,7(4):772-777.
[23]WANG JY(王晶英),ZHAO YS(赵雨森),WANG Z(王臻),et al.Effect of drought stress on physiologic and biochemical characteristic of Populus alba×Populus berolinensis(干旱胁迫对银中杨生理生化特性的影响)[J].Journal of Soil and Water Conservation(水土保持学报),2006,20(1):197-200.
[24]JIAO LL(缴丽莉),NI ZY(倪志云),LU BS(路丙社),et al.Effects of low temperature on cold-resistance of David maple(低温胁迫对青榨槭幼树抗寒指标的影响)[J].Journal of Agricultural University of Hebei(河北农业大学学报),2006,29(4):44-47.
[25]ZHANG SN(张蜀宁),ZHANG ZC(张振超),ZHANG HL(张红亮),et al.Growth,physiological and biochemical characteristics of non-heading Chinese cabbage under low temperature stress(低温胁迫对不同倍性不结球白菜生长及生理生化特征的影响)[J].Acta Botanica Boreali-Occidentalia Sinica(西北植物学报),2008,28(1):109-112.
[26]ZHAO SJ(赵世杰),XU ZC(许长成),ZOU Q(邹琦),et al.Improved method for determining malondialdehyde content in plant tissues(植物组织中丙二醛测定方法的改进)[J].Plant Physiology Communications(植物生理学通讯),1994,(3):207-210.
Agricultural Science & Technology2015年11期