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1.
赵树兰  多立安 《广西植物》2008,28(1):100-106
采用砂培法,研究了匍茎翦股颖对Cu2+、Zn2+、Cd2+与Pb2+胁迫的生长响应及阈限浓度,结果表明:种子萌发率随着4种重金属浓度的增加而下降。对株高的影响是当重金属浓度小于100mg/L时会促进株高生长,高于100mg/L则产生抑制作用。Cu2+显著抑制根系生长,并随浓度的增加抑制效应愈加显著;在Cu2+浓度为600mg/L时匍茎翦股颖的根长比对照下降了93.75%。Cu2+、Zn2+、Pb2+浓度小于200mg/L时会促进地上生物量的增加,但高于200mg/L时,地上生物量会随着3种重金属的增加而减少。Cu2+、Zn2+浓度小于100mg/L或Cd2+、Pb2+浓度小于200mg/L会增加叶绿素的含量,高浓度会降低叶绿素的含量;Cd2+在浓度为600mg/L时显著降低叶绿素含量,与对照相比,下降了43.55%。匍茎翦股颖生长的综合效应分析表明,匍茎翦股颖对Cu2+胁迫最敏感,具有较低的阈限浓度,而Zn2+胁迫对匍茎翦股颖的生长影响最小,阈限浓度相对较高。  相似文献   

2.
采用原子吸收、原子荧光等分析检测技术,探讨了Cd2+、Hg2+在可口革囊星虫中的富集规律及其对生长与主要营养成分的影响.结果表明: 在试验设定的胁迫浓度内,可口革囊星虫体壁肌肉对Cd2+、Hg2+的富集均随胁迫时间的延长而增加,最终达到饱和浓度;环境中Cd2+、Hg2+浓度越高,富集速度越快,达到饱和的时间越短,饱和浓度也越高.可口革囊星虫体质量增长随着重金属胁迫浓度的升高而减慢,且联合胁迫的影响程度大于单一胁迫.体壁肌肉蛋白质含量随重金属胁迫浓度的增加而升高,Cd2+、Hg2+分别在0.05和0.02 mg·L-1胁迫浓度下达到最高,然后开始降低.联合胁迫也呈同样的规律,且影响程度更大.体壁肌肉脂肪含量随重金属胁迫浓度的增加而降低,联合胁迫下降低程度更大.  相似文献   

3.
Fe2+、Cu2+、Zn2+对植物生理特性影响的比较分析   总被引:1,自引:0,他引:1       下载免费PDF全文
雷桅  王双明  孙敏 《广西植物》2007,27(5):770-774
以浸水处理为对照系统分析了Fe2+、Cu2+、Zn2+等金属离子对植物胁迫损伤相关的7个生理指标,并应用数理统计学和生物化学的相关原理和方法从氧自由基伤害的角度比较分析了这三种离子处理对植物生理特性的影响。结果表明:不同离子处理由于对植物造成的胁迫损伤不同,因而它们对植物生理特性的影响效应也有明显差异,并且这种差异与其所处理的离子胁迫性质间存在显著的关联性。  相似文献   

4.
Cu2+胁迫对2种速生柳幼苗生长及生理特性的影响   总被引:2,自引:0,他引:2  
以营养溶液中培养的‘苏柳172’(Salix jiangsuensis CL J-172)和垂柳(Salix babylonica Linn)幼苗为材料,分析它们在不同浓度Cu2+溶液(0、20、40、80、100、200、300μmol.L-1)下的生长以及部分生理指标的变化,以明确2种速生柳树用于植物修复的潜力。结果显示:2种柳树幼苗的生物量、叶片色素含量、根系活力以及根系形态的各指标都随Cu2+浓度的增加而显著降低。它们叶片SOD和POD活性以及脯氨酸含量随Cu2+浓度的增加呈先上升后下降的趋势,‘苏柳172’和垂柳中SOD活性在Cu2+浓度为20μmol.L-1时最大,其POD活性分别在Cu2+浓度为100和40μmol.L-1时达到最大,而其脯氨酸含量在Cu2+浓度为200μmol.L-1时达到最大。可见,2种柳树生长均受到Cu2+胁迫的抑制,它们能够在一定程度上通过增加保护酶活性和脯氨酸含量来提高对Cu2+的耐受性,且‘苏柳172’对Cu2+的忍耐力强于垂柳。  相似文献   

5.
以黑藻(Hydrilla verticillata)为供试材料,采用Cd2+和Cu2+等两种重金属分别在5个浓度梯度水平下的河砂水培方法,研究Cd2+或Cu2+不同浓度胁迫对黑藻株高、生物量、成活率和叶绿素含量的影响,以及对黑藻叶片最小荧光(Fo)、最大荧光(Fm),PSⅡ最大量子产率(QYmax,)、稳态下的PSⅡ反应中心关闭程度(1-Qp_Lss)、稳态下的非光化学淬灭(NPQ_Lss)等光合荧光参数及其荧光成像的影响,探讨各个参数分别随镉、铜浓度递增的变化规律。研究结果表明,Cd2+胁迫下黑藻的株高显著下降,说明Cd2+可能对黑藻叶片的维管束结构产生伤害作用;Cd2+和Cu2+胁迫对黑藻鲜重均无显著影响,说明与水生植物自由水含量存在一定关系;Cd2+和Cu2+胁迫均使黑藻干重显著下降,其中Cu2+胁迫对黑藻干重的影响更显著,说明Cu2+胁迫对黑藻累积生物量的影响远大于Cd2+;Cd2+和Cu2+胁迫下叶绿素各值均呈下降趋势,而Cu2+胁迫对叶绿素的影响更大,说明Cu2+对黑藻叶绿体的毒害比Cd2+更大。随着Cd2+或Cu2+胁迫浓度梯度的增加,黑藻的叶绿素荧光参数(Fo、Fm、QYmax)呈显著下降趋势,(1-Qp_Lss)呈上升趋势,而NPQ_Lss先上升后下降。黑藻在不同重金属胁迫下的生理指标、荧光参数及成像特征等方面所表现出的变化差异性,反映出同等浓度下黑藻受重金属胁迫的影响程度为:Cd2+胁迫Cu2+胁迫;黑藻可以在Cu2+浓度低于1 mg/L的环境下具有正常的光合活性,可推测将黑藻用于低浓度Cu污染水域的修复;在Cu2+浓度达3 mg/L以上环境下黑藻即无法长时间生存,可推测黑藻可以作为Cd污染水环境的指示种。  相似文献   

6.
采用原子吸收、原子荧光等分析检测技术,探讨了Cd2+、Hg2+在可口革囊星虫中的富集规律及其对生长与主要营养成分的影响.结果表明:在试验设定的胁迫浓度内,可口革囊星虫体壁肌肉对Cd2+、Hg2+的富集均随胁迫时间的延长而增加,最终达到饱和浓度;环境中Cd2+、Hg2+浓度越高,富集速度越快,达到饱和的时间越短,饱和浓度也越高.可口革囊星虫体质量增长随着重金属胁迫浓度的升高而减慢,且联合胁迫的影响程度大于单一胁迫.体壁肌肉蛋白质含量随重金属胁迫浓度的增加而升高,Cd2+、Hg2+分别在0.05和0.02 mg·L-1胁迫浓度下达到最高,然后开始降低.联合胁迫也呈同样的规律,且影响程度更大.体壁肌肉脂肪含量随重金属胁迫浓度的增加而降低,联合胁迫下降低程度更大.  相似文献   

7.
[目的] 为探究重金属对淡水绿藻生长的影响。[方法] 选取对水质检测具有明显指示作用的普通小球藻(Chlorella vulgaris)为实验材料,CdCl2·2H2O和CrCl3·7H2O提供重金属离子,探究不同浓度Cr3+和Cd2+在单一和复合胁迫下对藻细胞浓度、叶绿素a及相关抗氧化酶活性的影响。[结果] 随着Cr3+和Cd2+浓度不断增加,藻细胞浓度呈先增长后下降趋势;叶绿素a含量呈现先下降后升高再下降的现象,浓度为1 mg/L的单一和复合胁迫下有最大值,且毒性作用表现为Cr3+ < Cd2+ < Cr3++Cd2+;与藻细胞膜相关的丙二醛(MDA)和过氧化氢(H2O2)含量随着重金属离子浓度的增大而增长;重金属离子浓度低于10 mg/L时对藻细胞内抗氧化酶系统中的超氧化物歧化酶(SOD)、过氧化氢酶(CAT)和过氧化物酶(POD)表现为促进作用,而大于10 mg/L时具有抑制作用。[结论] 结果表明在单一或复合重金属胁迫下,普通小球藻会充分调动与抗逆性相关的酶来维持自身的正常生长。  相似文献   

8.
河流、湖泊等水生环境中普遍存在的重金属污染破坏水生生态系统并间接威胁人类健康。为探究重金属胁迫下水生昆虫花翅摇蚊(Chironomus kiiensis)生态毒理,测定了重金属Cd2+和Pb2+胁迫对花翅摇蚊化蛹率和羽化率的影响,检测了摇蚊的口器致畸与富集效应。研究结果表明,Cd2+和Pb2+影响摇蚊幼虫化蛹和羽化过程,单一重金属离子处理14 d Pb2+处理组的化蛹率和羽化率分别为22.22%和8.89%,低于Cd2+的化蛹率(25.56%)和羽化率(11.11%),表现出更强的抑制效应。混合离子1:2和2:1配比处理组化蛹率和羽化率均为11.11%和4.44%,显著低于单一重金属离子胁迫下的化蛹率和羽化率。单一重金属离子及混合离子处理均能导致花翅摇蚊幼虫口器致畸,表现为上颚前齿断裂,中齿和基齿磨损、缺失,下唇板齿部不规则,下唇板边缘齿与中央齿磨损、断裂、增生、缺失。不同重金属离子处理下幼虫口器致畸率不同,并与暴露时间呈正相关,其中1:2配比处理14 d致畸率达到40.61%。重金属离子在摇蚊幼虫体内产生生物富集效应,单一重金属离子处理下的Pb2+富集含量7 d至14 d由11.46 mg/kg上升至31.32 mg/kg,不同配比混合离子处理下Pb2+富集含量均呈增加趋势,其中1:2配比处理组由15.48 mg/kg上升至42.50 mg/kg,而Cd2+在单一重金属与1:1混合离子处理组7 d至14 d的富集含量无显著性变化,2:1配比处理组由14.20 mg/kg下降至9.52 mg/kg,1:2配比由5.85 mg/kg上升至20.99 mg/kg。这些研究结果表明Cd2+和Pb2+胁迫影响花翅摇蚊幼虫生长发育且口器出现畸型,与重金属在幼虫体内的富集密切相关,为研究重金属对水生生态系统多重效应提供了理论依据。  相似文献   

9.
为了探讨同一菌根真菌不同菌株对重金属的耐受性,选用采集于内蒙古阴山山脉不同地区的粘盖牛肝菌(Suillus bovinus)的不同菌株进行研究。首先,在不同浓度Zn^2 、Cd^2 液体培养基中培养菌丝体,以了解各菌株菌丝体对重金属的耐受性及吸附能力,采用烘干法和原予吸收法分别测定菌丝体的生物量和菌丝体、培养液中Zn^2 、Cd^2 含量,结果表明:劈柴沟粘盖牛肝菌在Zn^2 、Cd^2 胁迫条件下,生物量、吸附能力约为其余各菌株的1.5~2倍。其次,为了探明油松(Pinus tabulaeformis)形成菌根后对Zn^2 、Cd^2 胁迫的耐受性及其耐受机理,采用一次性定量浇灌不同浓度Zn^2 、Cd^2 溶液的方法,测定了菌根化油松苗地上、地下生物量及Zn^2 、Cd^2 含量的分配,结果表明:菌根形成后能显著促进油松的生长及对Zn^2 、Cd^2 胁迫的耐受性,并且菌根能够帮助油松吸收基质中大量的Zn^2 、Cd^2 ,根中重金属的含量是茎叶中的2~3倍以上,非菌根苗在重金属浓度稍高(Zn^2 400mg/kg;Cd^2 40mg/kg)时就会死亡。经方差分析及多重比较证实,劈柴沟粘盖牛肝菌对Zn^2 、Cd^2 的耐受性及对油松的促生效果与其它各菌株存在显著的差异,这可能是它通过把吸收的Zn^2 、Cd^2 最大限度地输送到根中的同时,也输送到了茎叶中,使重金属在体内得到一定程度的稀释,使自身免受毒害。  相似文献   

10.
研究了在培养基中分别添加不同浓度的重金属离子Hg2+、Pd2+、Cd2+和Cu2+作为人工配制的污水对光合细菌沼泽红假单胞菌生长与净化PO4-P和NH4-N能力的影响.实验结果表明当培养基中Hg2+的浓度达到2×10-6mol@L-1,该菌生长趋势开始减慢;当增至4×10-6mol@L-1时,生长完全被抑制.Cu2+的浓度达到1×10-6mol@L-1,该菌生长趋势也开始减慢;当增至8×10-6mol@L-1时生长完全被抑制.Cd2+的浓度达4×10-5mol@L-1时,其延缓期大大延长;增至16×10-5mol@L-4时生长完全被抑制.培养基中Pd2+的浓度达到8×10-4mol@L-1时,对该菌生长并未产生影响.当培养基中重金属离子浓度未达到完全抑制其生长时,对其净化PO4-P和NH4-N能力的影响不显著.  相似文献   

11.
研究了外源一氧化氮对Pb2+1000mg/L胁迫下高羊茅生长及无机离子含量变化的影响。结果表明,与对照相比,单用Pb2+胁迫使高羊茅鲜重、干重、含水量、根系活力和无机离子如NO-3、K+、Na+、Ca2+、Mg2+和Mn2+含量均下降,而其根的丙二醛含量和质膜透性、Pb2+含量均上升;与单用Pb2+胁迫相比,用SNP(Sodium Nitroprusside,NO供体)0.01~1mmol/L处理Pb2+胁迫下高羊茅,其鲜重、干重、含水量、根系活力、无机离子如NO3-、K+、Na+、Ca2+、Mg2+和Mn2+含量呈先上升后下降的变化趋势,而根的丙二醛含量和质膜透性、Pb2+含量呈相反的变化趋势。综合结果表明,外源NO对Pb2+胁迫下高羊茅生长影响具有剂量效应,适宜浓度能缓解铅毒害,提高耐铅性。  相似文献   

12.
孟令博  赵曼  亢燕  祁智 《西北植物学报》2021,41(10):1681-1690
以羊草幼苗为研究对象,通过调整全营养培养基(CK,0.05 mmol/L Fe2+、0.015 mmol/L Zn2+)中铁或者锌含量设置0、10倍、20倍Fe2+(Zn2+)浓度处理Fe0(Zn0)、Fe10(Zn10)、Fe20(Zn20),以及在高铁培养基中单独添加0.15 mmol/L Zn2+或同时添加10 mmol/L Ca2+、5 mmol/L Mg2+、20 mmol/L K+处理,测定培养6 d后幼苗生长指标和矿质元素含量、以及高铁(Fe20)处理下幼苗根中抗氧化指标和相关基因表达量,探究不同浓度Fe2+、Zn2+对羊草幼苗生长、矿质元素吸收积累及抗氧化指标、基因表达的影响。结果表明:(1)缺锌(Zn0)显著抑制羊草幼苗鲜重的增加和Zn元素的积累,但促进Fe、Mg元素的积累;高浓度锌(Zn10、Zn20)显著促进幼苗叶片生长和Zn元素的积累;缺铁(Fe0)显著抑制幼苗的根长、鲜重和Fe元素的积累,促进Mg、Zn元素的积累;高浓度铁(Fe10、Fe20)显著抑制羊草幼苗根叶生长、根毛发育和Ca、Zn、Mg、K元素的积累。(2)增加Zn2+和Ca2+、Mg2+、K+浓度无法恢复高铁胁迫对幼苗生长的抑制作用。(3)高浓度铁(Fe20)处理羊草幼苗48 h后,根部过氧化物酶、超氧化物歧化酶、过氧化氢酶、抗坏血酸过氧化物酶、谷胱甘肽还原酶活性和丙二醛、抗坏血酸、还原型谷胱甘肽含量显著升高;烟酰胺合成酶基因、过氧化物酶基因表达量显著下调,植物类萌发素蛋白基因表达量显著上调。研究发现,羊草幼苗生长发育和矿质元素积累对环境中Zn2+浓度变化不敏感,却受到环境中高浓度Fe2+的显著抑制,并造成严重的氧化胁迫伤害,这种伤害无法在添加Zn2+或同时添加Ca2+、Mg2+、K+的条件下恢复。  相似文献   

13.
Mg2+- and Ca2+-uptake was measured in dark-grown oat seedlings ( Avena sativa L. cv. Brighton) cultivated at two levels of mineral nutrition. In addition the stimulation of the ATPase activity of the microsomal fraction of the roots by Mg2+ was measured. Ca2+-uptake by the roots was mainly passive. Mg2+-uptake mainly active; the passive component of Mg2+-uptake was accompanied by Ca2+-efflux up to 60% of the Ca2+ present in the roots.
In general Mg2+ -uptake of oat roots was biphasic. The affinity of the second phase correspond well with that of the Mg2+-stimulation of the ATPase activity, in low-salt roots as well as in high-salt roots and in roots of plants switched to the other nutritional condition. Linear relationships were observed when [phase 2] Mg2+-uptake was plotted against Mg2+-stimulation of the ATPase activity of the microsomal fraction of the roots. In 5 days old high-salt plants 1 ATP (hydrolysed in the presence of Mg2+ J corresponded with active uptake of a single Mg2+ ion, but in older high-salt roots and in low-salt roots more ATP was hydrolysed per net uptake of a Mg2+ ion. The results are discussed against the background of regulation of the Mg2+-level of the cytoplasm of root cells by transport of Mg2+ by a Mg2+-ATPase to the vacuole, to the xylem vessels, and possibly outwards.  相似文献   

14.
The effects of external K+, H+ and Ca2+ concentrations on the intracellular K+ concentration, [K+]i, and the K+-ATPase activity in 2-day-old mung bean roots [ Vigna mungo (L.) Hepper] were investigated. [K+]i, in mung bean roots was markedly decreased by external K+ or H+ stress and did not recover the initial value even after the stress was removed. This decrease in [K+]i, gradually disappeared with the addition of (Ca2+. Ca2+ may offset the harmful effects of ion stress. Ca2+ seems to have two effects on K+ transport; control of K+ permeability and activation of K+ uptake, although K+-ATPase activity was inhibited by Ca2+ concentrations higher than 10–4 M. We suggest that Ca2+ activates K+ uptake indirectly through the acidification of the cytoplasm.  相似文献   

15.
在温度(150.5)C,盐度15.50.5的条件下,研究了Cu2+和Zn2+对西藏拟溞(DaphniopsistibetanaSars)存活、生长和生殖的影响。结果表明,西藏拟溞在各Cu2+活度组中的存活率差异不显著,而在10-8.60mol/L组中的体长增长率显著高于其他各组。当水环境中Cu2+活度为10-8.30和10-8.13mol/L时,西藏拟溞的内禀增长率(rm)为0.2211和0.2171/d,显著高于对照组,而西藏拟溞在不同Cu2+活度组中的产卵率均高于对照组,为0.9705-1.1742。西藏拟溞在各Cu2+活度组中的存活率和生长率差异均不显著。当Zn2+活度为10-7.04-10-6.82mol/L时,西藏拟溞的rm为0.2249-0.2296/d,显著高于对照组。西藏拟溞在Zn2+活度为10-7.04mol/L组中的产卵率最大,为1.0178,10-6.82mol/L组次之,为0.867。当Zn2+活度为10-7.04-10-6.82mol/L时,西藏拟溞一生生殖次数显著高于对照组(1.58),为1.92-2.17次。因此,综合来看,当水环境中的Cu2+活度为10-8.60-10-8.13mol/L、Zn2+活度为10-7.04-10-6.82mol/L时能明显的促进西藏拟溞的种群增长、发育和生殖。论文讨论了Cu2+和Zn2+对西藏拟溞的促长机理。    相似文献   

16.
Six cultivars of spring barley ( Hordeum vulgare L. cvs Salve, Nümberg II, Bomi, Risø 1508, Mona and Sv 73 608) were grown in water culture for three weeks with various combinations of mineral supply and differential roots/shoot temperatures during the growth period. Most important for growth and accumulation of N, K+, Ca2+ and Mg2+ was the mineral supply, followed by the root temperature and the choice of cultivar. Treatments with low mineral supply or low root temperature induced a uniform reduction in growth and accumulation of the ions studied. The effects of low mineral supply and low root temperature on growth and N accumulation was additive, which indicates that these factors exert their influence independently of each other.
Roots grown at 10°C were smaller and Rb+(86Rb) influx was higher than in roots grown at 20°C. It is suggested that the control of Rb+(86Rb) influx is affected by the root temperature and the age of the plants. The higher 86Rb+ (86Rb) influx into the low temperature roots could not compensate for the smaller root size. However, the lower total mineral accumulation made up for the needs of the smaller plants and cannot explain the reduction in growth.  相似文献   

17.
The binding of [3H]nimodipine to purified synaptic plasma membranes (SPM) isolated from sheep brain cortex was characterized, and the effects of nimodipine, nifedipine, and (+)-verapamil on the [3H]nimodipine binding were compared to the effects on 45Ca2+ translocation under conditions that separate 45Ca2+ fluxes through Ca2+ channels from 45Ca2+ uptake via Na+/Ca2+ exchange. [3H]Nimodipine labels a single class of sites in SPM, with a KD of 0.64 +/- 0.1 nM, a Bmax of 161 +/- 27 fmol X mg-1 protein, and a Hill slope of 1.07, at 25 degrees C. Competition of [3H]nimodipine binding to purified SPM with unlabelled Ca2+ channel blockers shows that: nifedipine and nimodipine are potent competitors, with IC50 values of 4.7 nM and 5.9 nM, respectively; verapamil and (-)-D 600 are partial competitors, with biphasic competition behavior. Thus, (+)-verapamil shows an IC50 of 708 nM for the higher affinity component and the maximal inhibition is 50% of the specific binding, whereas for (-)-verapamil the IC50 is 120 nM, and the maximal inhibition is 30%; (-)-D 600 is even less potent than verapamil in inhibiting [3H]nimodipine binding (IC50 = 430 nM). However, (+)-verapamil, nifedipine, and nimodipine are less potent in inhibiting depolarization-induced 45Ca2+ influx into synaptosomes in the absence of Na+/Ca2+ exchange than in competing for [3H]nimodipine binding. Thus, (+)-verapamil inhibits Ca2+ influx by 50% at about 500 microM, whereas it inhibits 50% of the binding at concentrations 200-fold lower, and the discrepancy is even larger for the dihydropyridines. The Na+/Ca2+ exchange and the ATP-dependent Ca2+ uptake by SPM vesicles are also inhibited by the Ca2+ channel blockers verapamil, nifedipine, and d-cis-diltiazem, with similar IC50 values and in the same concentration range (10(-5)-10(-3) M) at which they inhibit Ca2+ influx through Ca2+ channels. We conclude that high-affinity binding of the Ca2+ blockers by SPM is not correlated with inhibition of the Ca2+ fluxes through channels in synaptosomes under conditions of minimal Na+/Ca2+ exchange. Furthermore, the relatively high concentrations of blockers required to block the channels also inhibit Ca2+ translocation through the Ca2+-ATPase and the Na+/Ca2+ exchanger. In this study, clear differentiation is made of the effects of the Ca2+ channel blockers on these three mechanisms of moving Ca2+ across the synaptosomal membrane, and particular care is taken to separate the contribution of the Na+/Ca2+ exchange from that of the Ca2+ channels under conditions of K+ depolarization.  相似文献   

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