原子荧光光谱法测定天然水体中的Se(IV)

采用氢化物—原子荧光光谱法(HG-AFS)，在1mol/L HCl介质中用KBH4作还原剂测定天然水体中痕量Se(IV)。利用正交实验对实验条件进行了优化选择，在确定的条件下，方法的检出限为0．06nmol／L，对Se(IV)含量为0．51nmol／L和1．14nmol／L的样品分析精密度为3．9％和3．5％，方法的回收率为96％-105％，线性范围为0．06—250nmol/L。在不同介质中工作曲线的变动范围小于5％。     

长江口及其邻近海域溶解硒的地球化学控制过程研究

Dissolved selenium in the Changjiang(Yangtze) Estuary and its adjacent waters was determined by hydride generation atomic fluorescence spectrometry to elucidate the source, behavior in estuary, adsorption-desorption process and biological role. In surface water, Se(IV) concentration ranged 0.05–1.14 nmol/L and Se(VI) concentration varied 0.01–1.20 nmol/L, with the means of 0.76 and 0.49 nmol/L, respectively. In bottom water, Se(IV) content varied 0.03–0.27 nmol/L and Se(VI) content ranged 0.04–0.85 nmol/L, with the averages of 0.10 and 0.40 nmol/L, respectively. High level of Se(IV) was observed near the shore with a significant decrease towards the open sea, suggesting the continental input from the adjacent rivers. Large value of Se(VI) was found in bottom water, reflecting the release from suspended sediment. Besides, high value appeared in the same latitude of the Changjiang Estuary and Hangzhou Bay illustrated the effect of lateral mixing and the long-distance transport of selenium. Se(VI), more soluble, occupied higher percentage in aqueous environment. The presence of Se(IV) resulted from the degradation of residue and the reduction of Se(VI) under anaerobic condition. The positive relationship to suspended particulate material(SPM) and negative correlation to depth indicated that Se(IV) tended to be released from the high density particulate matter. Instead, Se(VI) content did not significantly relate to SPM since it generally formed inner-sphere complex to iron hydroxide. Se(IV) content negatively varied to salinity and largely depended on the freshwater dilution and physical mixing. While, Se(VI) level deviated from the dilution line due to the in situ biogeochemical process such as removal via phytoplankton uptake and inputs via organic matter regeneration. As the essential element, Se(IV) was confirmed more bioavailable to phytoplankton growth than Se(VI), and moreover, seemed to be more related to phosphorus than to nitrogen.     

Spatial distribution and behavior of dissolved selenium speciation in the South China Sea and Malacca Straits during spring inter-monsoon period

Selenium(Se) has been recognized as a key trace element that is associated with growth of primary producers in oceans. During March and May 2018, surface water(67 samples) was collected and measured by HG-ICP-MS to investigate the distribution and behavior of selenite [Se(IV)], selenate [Se(VI)] and dissolved organic selenides(DOSe) concentrations in the Zhujiang River Estuary(ZRE), South China Sea(SCS) and Malacca Straits(MS). It showed that Se(IV)(0.14–3.44 nmol/L) was the dominant chemical species in the ZRE, related to intensive manufacture in the watershed; while the major species shifted to DOSe(0.05–0.79 nmol/L) in the MS, associated with the wide coverage of peatland and intensive agriculture activities in the Malaysian Peninsula. The SCS was identified as the northern and southern sections(NSCS and SSCS) based on the variations of surface circulation.The insignificant variation of Se(IV) in the NSCS and SSCS was obtained in March, potentially resulting from the high chemical activity and related preferential assimilation by phytoplankton communities. Contrastively, the lower DOSe concentrations in the SSCS likely resulted from higher primary production and utilization during March. During May, the concentration of Se(IV) remained low in the NSCS and SSCS, while DOSe concentrations increased notably in the SSCS, likely due to the impact of terrestrial inputs from surface current reversal and subsequent accumulation. On a global scale, DOSe is the dominant Se species in tropical oceans, while Se(IV) and Se(VI) are major fractions in high-latitude oceans, resulting from changes in predominated phytoplankton and related biological assimilation.     

Se(Ⅳ)和Te(Ⅳ)对钝顶螺旋藻的急性毒性和联合毒性

用化学品对藻类毒性测试的标准试验方法,分别研究了硫属元素Se(Ⅳ)和Te(Ⅳ)单组分对钝顶螺旋藻(Spirulina platensis)的毒性效应,用相加指数法评价了Se(Ⅳ)和Te(Ⅳ)双组分对螺旋藻的联合毒性效应.结果表明,Te(Ⅳ)对螺旋藻的毒性大于Se(Ⅳ),其EC50,96h分别为125.2 mg/L和36.1 mg/L;Se(IV)和Te(Ⅳ)的联合毒性效应为拮抗作用, 其EC50,96h为103.1 mg/L.     

Se(IV)和Te(IV)对钝顶螺旋藻的急性毒性和联合毒性

用化学品对藻类毒性测试的标准试验方法,分别研究了硫属元素Se(IV)和Te(IV)单组分对钝顶螺旋藻(Spirulina platensis)的毒性效应,用相加指数法评价了Se(IV)和Te(IV)双组分对螺旋藻的联合毒性效应。结果表明,Te(IV)对螺旋藻的毒性大于Se(IV),其EC50,96h分别为125.2mg/L和36.1mg/L;Se(IV)和Te(IV)的联合毒性效应为拮抗作用,其EC50,96h为103.1mg/L。     

对虾养殖生态系中有机碳的初步研究本研究由

对于围隔养殖对虾生态系中有机碳的变动进行了研究 ,结果表明 :溶解有机碳 (DOC)含量波动在 5 .2 99～ 13.39mg/ L之间 ,平均为 8.5 3mg/ L± 2 .2 5 mg/ L;颗粒有机碳 (POC)含量波动在0 .6 5～ 6 .6 3mg/ L之间 ,平均为 3.2 5 mg/ L± 1.76 mg/ L;总有机碳 (TOC)含量波动在 6 .92～ 2 0 .0 2mg/ L之间 ,平均为 11.78mg/ L± 3.82 mg/ L ;其中 DOC∶ POC∶ TOC为 0 .72∶ 0 .2 8∶ 1。各种有机碳组分的含量明显高于自然海水中各种有机碳的含量 ;各种有机碳组分的含量在养殖期间总体上呈上升的趋势 ;其变化与 DCOD的变化呈显著线性正相关的关系。     

长江口及其邻近海域2012年3月和7月溶解态铝的分布特征分析

分别于2012年3月和7月对长江口及其邻近海域水体中溶解态铝的分布及其影响因素进行了研究,并在2012年3月至2013年11月期间对长江徐六泾进行了连续观测。结果表明,徐六泾溶解态铝在夏季出现最高值,在冬季呈现最低值,平均值分别为(313±130)nmol/L和(140±43)nmol/L,表现出与径流量相似的季节变化规律。受陆源输入变化的影响,长江口溶解态铝的浓度由近岸向外海逐渐降低,且呈现出明显的季节性差异,即7月明显高于3月。3月表、底层海水中溶解态铝的浓度范围分别为21~129 nmol/L和27~146 nmol/L,平均值分别为(49±21)nmol/L和(59±27)nmol/L;7月表、底层溶解态铝的浓度范围分别为6~332 nmol/L和9~252 nmol/L,平均值分别为(66±69)nmol/L和(83±74)nmol/L。在7月,表、底层溶解态铝呈现显著性差异,底层沉积物的再悬浮可能是造成差异的主要原因。调查结果表明,溶解态铝在长江口呈现出清除型行为,清除主要发生在咸淡水混合初期,初步计算出7月份溶解态铝的清除率约为55%。     

闭合循环水产养殖系统中生物过滤器的水处理效果研究

对闭合循环水产养殖系统中生物过滤器生物膜的培养、处理能力等方面进行了研究。试验结果表明 ,在生产性试验阶段 :(1 )系统中添加培养液培养生物膜 ,水温在 2 0～ 2 2℃时需要 1 1 d,生物膜成熟后生物过滤器具有较强的转化能力 ;(2 )系统稳定后放养暗纹东方豚 ,连续运行 5个月 ,系统中 NH4- N浓度平均值为 0 .6 8mg/L ,NO2 - N平均值为 0 .5 8mg/L。在规模化生产阶段 :(1 )不预先培养生物膜 ,而直接放养饲养对象 ,这种情况下系统中的水质波动比较明显 ,NH4- N,NO2 - N浓度最高值分别为 2 .2 2 mg/L ,1 .1 2 mg/L ,经过 2个月的运行 ,分别降为 0 .4 7mg/L ,0 .1 4 mg/L ;(2 )在系统中加入 2 .5 mg/L的五倍子和 2 0～ 30 mg/L的生石灰均不影响生物过滤器的处理能力。加入 5 0 mg/L的福尔马林和 2 mg/L的土霉素对生物过滤器的处理能力影响比较明显 ;(3)生物过滤器对流经水体的NH4- N,NO2 - N,COD1次性去除率分别为 4 4.79%,2 0 .31 %,2 0 .1 0 %。     

春季东海溶存氧化亚氮的分布和海气交换通量

于2011年5至6月在东海采集不同深度海水样品,研究了其中溶存氧化亚氮(N2O)的分布并估算其海-气交换通量。结果表明,春季东海表层海水中溶存N2O浓度范围为6.31~11.88 nmol/L,平均值为(9.13±1.45)nmol/L;底层海水中N2O浓度范围为7.53~39.75 nmol/L,平均值为(13.71±7.76)nmol/L。随着深度的增加,N2O浓度逐渐升高。温度是影响春季东海N2O分布的主要因素,N2O浓度与温度呈负相关关系。长江冲淡水和黑潮水是东海N2O的重要来源。东海表层海水中N2O的饱和度范围为92.5%~139.3%,平均值为118.5%±10.3%,绝大多数站位都处于过饱和状态,因此,春季东海是大气N2O的净源。利用LM86公式和W92公式求得东海的海-气交换通量分别为(4.96±6.12)μmol/(m2·d)和(10.25±17.18)μmol/(m2·d),初步估算出东海年释放N2O通量约为0.061~0.127 Tg/a,占全球海洋释放总量的2.0%,远高于其所占的面积比0.2%。     

国产河鲀毒素的生物效应

采用电压箝和膜片箝技术,观测河北河鲀毒素对神经和肌肉细胞的电生理效应,并与日本河鲀毒素进行比较.结果表明阻断钠电流的ED50的河北河鲀毒素浓度是3.68 nmol/L,对钠电流阻断的回复率为75%～92%;阻断钠电ED50的日本河鲀毒素浓度是4.1 nmol/L,对钠电流阻断的回复率为70%～80%.河北河鲀毒素比日本河鲀毒素的有效性和可逆性约高10%.