摘要
采用藻类生长抑制试验和光合活性抑制试验两种方法对蛋白核小球藻受不同浓度Cd2+胁迫作用下叶绿素浓度及藻活性荧光参数进行测量,依据Sigmoidal曲线拟合及单因素方差分析(one-way ANOVA)的方法对Cd2+不同胁迫时间下藻活性抑制率和96 h比生长率抑制率的相关性进行研究.结果表明,48、53、72、77和96 h的藻活性抑制率和96 h比生长率抑制率间具有较好的S函数关系(R2>0.95),因此可采用藻活性抑制率48 h-EC10和53 h-EC10来代替96 h的藻类半数比生长率抑制率EC50进行Cd2+藻类毒性实验评价.进一步分析了蛋白核小球藻受Cd2+胁迫48 h和53 h藻活性抑制率和Cd2+毒性当量的剂量-效应关系.该方法为实验室内单一Cd2+毒性的监测提供了一种快速有效的新方法,为水环境综合毒性预警提供了一种切实可行的方法依据.
Chlorophyll concentration and photosynthesis activity fluorescence parameters of Chlorella pyrenoidosa stressed by different concentrations of Cd2 +were measured based on algal growth inhibition tests and photosynthetic activity inhibition tests. The relationship between the algal photosynthetic activity inhibition rate and 96 h inhibition rate of specific growth rate at different Cd2 +stress times was studied by sigmoidal curve fitting and one-way ANOVA analysis. The result shows that S function relevance exists between the algal photosynthetic activity inhibition rates for 48 h,53 h,72 h,77 h and 96 h respectively and 96 h inhibition rate of specific growth rate( R2> 0. 95). Consequently,EC10( 10% effective concentration) after 48 h and 53 h inhibition in photosynthetic activity inhibition tests could be used to represented EC50( 50% effective concentration) in 96 h algal growth inhibition tests for evaluating the Cd2 +toxicity. Dose-response relationships between the algal photosynthetic activity inhibition rates after 48 h and 53 h inhibition and Cd2 +toxic equivalency quantity were further analyzed. The method provided a rapid and viable new thought to monitoring single Cd2 +toxicity in lab and early warn integrated toxicity of pollution in water.
出处
《环境科学》
EI
CAS
CSCD
北大核心
2014年第4期1555-1560,共6页
Environmental Science
基金
国家自然科学基金项目(61378041)
国家高技术研究发展计划(863)项目(2009AA063005
2013AA065502)
安徽省杰出青年科学基金项目(1108085J19)
安徽光学精密机械研究所所长基金项目(Y03AG31144)
中国科学院仪器设备功能开发技术创新项目(yg2012071)
关键词
蛋白核小球藻
藻类生长抑制试验
光合活性抑制试验
叶绿素荧光技术
Cd2+毒性监测
Chlorella pyrenoidosa
algal growth inhibition test
photosynthetic activity inhibition test
chlorophyll fluorescence measurements
Cd2 +toxicity monitoring