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1.
An ion chromatographic method with a valve switching facility was developed to determine trace nitrate concentrations in seawater using two pumps, two different suppressors, and two columns. A carbohydrate membrane desalter was used to reduce the high concentrations of sodium salts in samples. In this method, trace nitrate was eluted from the concentrator column to the analytical columns, while the matrix flowed to waste. Neither chemical pre-treatment nor sample dilution was required. In the optimized separation conditions, the method showed good linearity （R〉0,99） in the 0.05 and 50 mg/L concentration range, and satisfactory repeatability （RSD〈5%, n=6）. The limit of detection for nitrate was 0.02 mg/L. Results showed that the valve switching system was suitable and practical for the determination of trace nitrate in seawater.  相似文献   

2.
In the current study, we determined concentrations and transfer rates of Ag, Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, P, Rb, Sr and Zn to Brown Birch Scaber Stalks (Leccinum scabrum) mushrooms emerged in the area of Sudety Mountains (Sudetes) in Poland. Fruiting bodies and topsoil samples beneath L. scabrum were collected form the K odzka Dale. The trace elements were determined using validated method and inductively coupled plasma - atomic emission spectroscopy (ICP-AES) for final measurement. Mushrooms contained Ag, Cr, Hg, Co, Ni and Sr at < 1.0 μg/g dry weight; Ba and Pb at ~1.0 μg/g dw; Cd at < 5 μg/g dw; Cu and Mn at > 10 μg/g dw; Al and Ca at ~100 μg/g dw; Fe, Na, Rb and Zn at 100 to 500 μg/g dw, Mg at ~1,000 μg/g dw; P at ~5,000 μg/g dw and K at ~30,000 μg/g dw. Ca, Mn and Ni were nearly equally distributed between stipes and caps; stipes compared to caps were enriched in Ba, Na and Sr, while caps were enriched in Ag, Al, Cd, Co, Cr, Cu, Fe, K, P, Pb, Rb and Zn. The values of bioconcentration factor (BCF) varied highly depending on chemical element and were >1 for Ag, Cd, Cu, K, Mg, Na, P, Rb and Zn, while <1 for Al, Ba, Ca, Co, Cr, Fe, Mn, Ni, Pb and Sr. Topsoil showed elevated content of lead and mean concentration was 99 ± 32 μg/g dw, while cadmium was at 0.41 ± 0.15 and those two highly toxic to human elements occurred in edible caps of L. scabrum at 4.5 ± 2.2 and 2.9 ± 2.0 μg/g dw, respectively.  相似文献   

3.
A method for determining calcium(Ca),potassium(K),magnesium(Mg) and iron(Fe) in four fish species was optimized and validated.It included microwave mineralization of the samples and subsequent quantification by flame atomic absorption spectroscopy(FAAS) with Zeeman-effect background correction.Using HNO3(65%) and H2O2(33%) as extraction solutions,the optimal conditions of extraction were established as follows:0.5 g of sample mass;microwave time program of 300 W/5 min and 600 W/5 min.The method was free of matrix interferences.The linear correlation coefficients were ≥0.9991,the recovery percentage of analytes was from 99.31% to 103.70% and the RSD(relative standard deviation) was lower than 2.06%.The detection limits obtained were 32.3,43.2,14.0 and 68.6 ng mL-1 for Ca,K,Mg and Fe in FAAS respectively.It is shown that the method is rapid,simple,sensitive and accurate.The method was applied to the studies of digestibility and measurement of these nutrients in samples of fish collected from Norway,Japan and China.  相似文献   

4.
The concentration of Fe(Ⅱ) is high in some groundwater supplies used in turbot culture,and the toxicity of waterborne Fe(Ⅱ) is unknown.We investigated the stress responses of juvenile turbot,Scophthalmus maximus,exposed to Fe(Ⅱ) of different concentrations (0.01,0.05,0.1,0.5,1,and 2 mg/L) for 1,7,14,and 28 d,under the same ambient conditions of other parameters.Changes in respiratory rate,hematological parameters,and gill structure were determined.The results show that waterborne Fe(Ⅱ) did not cause severe hematological perturbation to turbot.A low-medium Fe(Ⅱ) concentration (lower than 0.1 mg/L) could boost the respiratory rate,and caused no or very limited damage to fish.A high Fe(Ⅱ) concentration (0.1 mg/L or higher),however,caused gill damage,such as vacuoles in branchial lamellae,epithelial necrosis,and hypertrophy of epithelial cells,and even death after extended exposure time.Therefore,excess waterborne Fe(Ⅱ) and long-term exposure to Fe(Ⅱ) could be responsible for poor growth and high mortality of turbot in culture.The concentration of waterborne Fe(Ⅱ) in turbot culture should be kept below 0.1 mg/L.  相似文献   

5.
1INTRODUCTIONInrecentyearsglobalclimatechangehasbeenanissueofbothpublicandscientificconcern.Oceanscover71 %ofearthandplayamajorroleinglobalclimatechange.Phosphorus,asacriticalelement,regulatespri maryproductioninaquaticecosystems.Therefore,thefunctionofphosphorusinoceansystemhasreceivedin creasingscientificinterest(Songetal.,2 0 0 3 ) .PP (particulatephosphorus)isanimportantforminphosphorustransferinseawater(Song,2 0 0 1 ) .Pro portionofPPintotalphosphorus(TP)inseawatervar iesfrom 1 0 …  相似文献   

6.
长江中游平原区面临着一系列严重的地质环境问题，其中地下水铵氮和磷的问题十分突出，但目前对于二者共存规律的认识还十分薄弱。以长江中游沿岸故道区为典型研究区，对采集的地下水样品进行了水文地球化学分析，并综合运用因子分析和随机森林模型探讨了铵氮和磷的赋存规律。结果表明:地下水整体处于还原环境中，NH4-N的质量浓度为0.03~71.0 mg/L（均值9.92 mg/L），P的质量浓度为0.02~3.38 mg/L（均值0.51 mg/L）。地下水中高浓度的铵氮与磷均主要为天然成因，但铵氮与磷的迁移富集过程存在差异:铵氮的迁移富集与含氮有机质矿化过程密切相关；磷的迁移富集与铁氧化物或氢氧化物的还原性溶解密切相关，而含磷有机质矿化是磷富集的次要过程。Eh很低的地下水环境易产生高浓度铵氮的地下水，相对中等的还原环境会产生高浓度的磷但通常不会伴生高浓度的铵氮；当地下水中S2-，DOC，I均处于相对较高的浓度水平时会伴生大量的铵氮，而磷的浓度在很大程度上受控于Fe2+浓度；当DOC，I和Fe2+浓度都高时，通常会出现铵氮和磷浓度都较高的现象。   相似文献   

7.
A new kinetic spectrophotometric method has been developed for the determination of iron (Ⅲ). The method is based on the catalytic effect of iron (Ⅲ) on the oxidation of weak acid brilliant blue dye (RAWL) by KIO4 in acid medium. The advantages of the proposed method are that it is sensitive, accurate, rapid, inexpensive, can be operated under room temperature and has a large determination concentration range compared to other techniques. The obtained optimum conditions are pH 3.15, RAWL (200 mgL-1) 5.00mL, Potassium periodate solution (0.01 molL-1) 0.30mL, phenanthroline (0.02molL-1) 1.00mL, reaction temperature 25℃ and reaction time 7 miu. With this method iron could quantitively be determined in the range 0.00-0.02 mgL-1, the detection limit being 4.10×10-10mL-1. The relative standard deviations (RSD) in five replicate determinations for 3 μgL-1 and 5μgL-1 iron (Ⅲ) are 3.1% and 1.9%, respectively. The method has been applied to the determination of iron (Ⅲ) in tap water samples and seawater samples (from the South China Sea), the recovery rates being 98.0% and 100.5%, respectively.  相似文献   

8.
To increase the cell concentration and the accumulation of astaxanthin in the cultivation of Haematococcus pluvialis, effects of different iron eleetrovalencies (Fe2+-EDTA and Fe3+-EDTA) and species (Fe-EDTA, Fe(OH)32x and FeC6H5O7) addition on cell growth and accumulation of astaxanthin were studied. Results show that different iron electrovalencies have various effects on cell growth and astaxanthin accumulation of H. pluvialis. Compared with Fe3+-EDTA, Fe2+-EDTA stimulate more effectively the formation of astaxanthin. The maximum astaxanthin content (30.70 mg/g biomass cell)was obtained under conditions of 18 μmol/L Fe2+-EDTA, despite the lower cell density (2.3x105 cell/ml)in such condition. Fe3+-EDTA is more effective than Fe2+-EDTA in improving the cell growth. Especially,the maximal steady-state cell density, 2.9x105 cell/ml was obtained at 18 μmol/L Fe3+-EDTA addition. On the other hand, all the various species of iron (EDTA-Fe, Fe(OH)32x, FeC6H5O7) are capable to improve the growth of the algae and astaxanthin production. Among the three iron species, FeC6H5O7 performed the best. Under the condition of a higher concentration (36 μmol/L) of FEC6H5O7, the cell density and astaxanthin production is 2 and 7 times higher than those of iron-limited group, respectively. The present study demonstrates that the effects of the stimulation with different iron species increased in the order of FeC6H5O7, Fe(OH)32x/x and EDTA-Fe.  相似文献   

9.
rmDUCnONInthecultUreofbenthicdiatomsasfeedforabalone,itisnecesoptoaddsomnu-trientssuchasnitIngen,Phosphorus,ironandsilicontotheSeawatermwhum.Thecom-monraioofthenutrientswas(lO-25):(l-2.5):o.l:l(mg/L)(Chenetal.,1977).Anstinetal-(l99o)rePOrtedthatheratioofnibogenandphosphorusinfluencedthebio-massdensityofthePeriphyton,whichInainlyconsistedOfbenthicdiatomPOPulations.However,theirrestiltswerenotbasedonmonoalgalwwh,andtherewerenodetallsonthereasonableratioofthesenutrientsintheirreports-Ther…  相似文献   

10.
合成了新型席夫碱试剂3，5-二溴水杨醛缩甘氨酸（DBSAGLY），建立该试剂荧光度法测定微量Zn（Ⅱ）的新体系，在pH＝7.0～8.0时Zn(Ⅱ)与DBSAGLY形成1∶1的络合物，络合物最大激发和发射波长分别为λ  相似文献   

11.
Effects of iron and silicon nutrients and of orthogonal combinations of nitrogen, phosphorus, iron and silicon on the growth rate of three benthic diatoms were studied by using an in situ OD measurement method. The results of monofactor tests of iron and silicon showed that Fe-EDTA was better than ferric citrate in the culture of these diatoms; that the favourable concentration of Fe-EDTA was about 0.5 mg/L of Fe and that of silicate was 2.5 mg/L of Si or more. The orthogonal test showed that the optimal concentration ratios (mg/L) of nitrogen, phosphorus, iron and silicon were: 5.0: 0.25: 0.5: 2.0 forCocconeis scutellum var.parva; 2.5: 1.0: 1.0: 2.0 forAmphora coffeaeformis; and 5.0: 0.15: 0.5: 2.0 forN. mollis. Project 39470065 supported by NSFC.  相似文献   

12.
洞庭湖平原西部地区浅层承压含水层是当地主要的地下水开采层,却面临严重的水质型缺水问题,其中以铵氮异常最为典型,但目前对于其来源和富集机制的认识十分薄弱。以洞庭湖平原西部为研究区,沿区域地下水流方向对地下水样品进行水文地球化学分析,旨在查明地下水中铵氮的来源,揭示地下水流动对铵氮富集的控制机理。结果表明:NH4-N质量浓度为0.05~16.75 mg/L,且与DOC、HCO3-、As、Fe2+、Mn、P质量浓度呈现较好正相关性;而高质量浓度的NH4-N对应着很低质量浓度的Cl-、SO42-、NO3-和很低的Cl/Br比值,可以推测浅层承压水中的铵氮主要由天然有机质矿化作用产生,而非人为输入。沿着地下水流向,NH4-N和As、Fe2+、Mn质量浓度均显著升高,说明由于水流越来越滞缓,含水介质颗粒越来越细,沉积物有机质越来越富集,含氮有机质矿化作用逐渐增强,使得NH4-N质量浓度逐渐升高,并形成了还原性逐渐增强的地下水环境,相关地球化学过程产生的还原性组分（砷、铁、锰等）也逐渐富集。本研究进一步丰富了地下水原生铵氮的成因理论,可为当地的供水安全保障提供理论基础。   相似文献   

13.
土壤有效硫检测的常规方法是利用硫酸钡比浊法,鉴于规范推荐的测试步骤在批量土壤样品测试时效率较低,因此对常规方法进行了改进。加入2.0g氯化钡晶粒改为加入浓度为200g/L氯化钡溶液10mL;加稳固剂阿拉伯胶水溶液4mL改为加入浓度为6%甘油-乙醇(1+2)溶液5mL。通过对比实验,改进后检测方法比常规方法操作简便快捷,省时、省力、数据准确可靠,标准曲线线性相关系数达到0.9982。对土壤有效态成分分析标准物质土样GBW07459(ASA-8)、GBW07460(ASA-9) GBW07461(ASA-10)进行多次平行测试,测试结果全部在标准值范围内,且平行相对相差≤10%,证明改进后的检测方法可用于土壤有效硫的检测。  相似文献   

14.
A new kinetic-spectrophotometric method is proposed for the determination of copper （ Ⅱ ）. The method is based on the catalytic effect of copper （ Ⅱ ） on the oxidation of weak acid brilliant blue dye （RAWL） by hydrogen peroxide. The copper （ Ⅱ ） can be determined spectrophotometrically by measuring the decrease of absorbance of RAWL at λ = 626 nm using the fix-time method. The optimum reaction conditions are as follows： pH 7.20, buffer solution NaOH-KH2PO4, RAWL （200 mgL-1） 5.00 mL, H2O2 （30%） 0.50 mL, reaction temperature 80 ？？ and reaction time 20 min. The linear range of this method is between 0 μg L^-1 and 12 μg L^-1 and the limit of detection is 0.011 μg L-1, the relative standard deviation （RSD） in five replicate determinations for 2 and 8 μg L-1 copper （ Ⅱ ） are 3.2% and 2.3%, respectively. Twenty ions do not interfere in the determination of copper （ Ⅱ ）. The method has been applied satisfactorily to the determination of copper （ Ⅱ ） in freshwater samples （tap water and Yellow River water from Lijin, Shandong, China） and seawater samples （from the South China Sea）, the recovery rates are 98.0%, 102.5% and 96.0%, respectively.  相似文献   

15.
A new kinetic spectrophotometric method has been developed for the determination of iron (Ⅲ). The method is based on the catalytic effect of iron (Ⅲ) on the oxidation of weak acid brilliant blue dye (RAWL) by KIO4 in acid medium. The advantages of the proposed method are that it is sensitive, accurate, rapid, inexpensive, can be operated under room temperature and has a large determination concentration range compared to other techniques. The obtained optimum conditions are: pH 3.15, RAWL (200 mgL-1) 5.00mL, Potassium periodate solution (0.01 molL-1) 0.30mL, phenanthroline (0.02molL-1) 1.00mL, reaction temperature 25℃ and reaction time 7 miu. With this method iron could quantitively be determined in the range 0.00-0.02 mgL-1, the detection limit being 4.10×10-10mL-1. The relative standard deviations (RSD) in five replicate determinations for 3 μgL-1 and 5μgL-1 iron (Ⅲ) are 3.1% and 1.9%, respectively. The method has been applied to the determination of iron (Ⅲ) in tap water samples and seawater samples (from the South China Sea), the recovery rates being 98.0% and 100.5%, respectively.  相似文献   

16.
A 12-month program of monitoring potentially toxic microalgae(that produce lipophilic shellfi sh toxins; LSTs) and their toxins in bivalves was conducted from April 2006 to March 2007 in the Nanji Islands, East China Sea. Two Dinophysis species, D. caudata and D. acuminata, were identifi ed, and D. caudat a was found to be the dominant species. D. caudata was detected in water samples between April and June 2006, and between February and March 2007. It reached its highest abundances in May, with a mean abundance of 1.38×10 2 cells/L in surface water and 1.25×10 2 cells/L in bottom water(10 m deep). The temporal distribution of D. caudata was associated with the occurrence of LSTs in bivalve samples, which mostly occurred at the same time as D. caudata blooms, between April and July 2006. All of the cultured bivalves sampled between April and June were contaminated with LSTs, with an average toxicity of 85 μg okadaic acid(OA) eq./100 g meat, which was four times higher than the Chinese regulatory limit(20 μg OA eq./100 g meat). Ten out of fi fteen wild samples(66.7%) collected during the same period were positive for LSTs, and contained an average LST toxicity of 45 μg OA eq./100 g meat(more than twice the regulatory value). Cultured Patinopecten yessoensis collected on 15 May 2006 had the highest toxicity, 320 μg OA eq./100 g meat, and relatively high toxicities(80 to 160 μg OA eq./100 g meat) were found in bivalves until the end of July.  相似文献   

17.
This study showed lethal concentrations (LC) of copper forPeneaus penicillatus at various stages of its life cycle were 1000 μg/L for nauplii, 1000 μg/L for Zoea I, 2000 vg/L for Zoea II, 2500 μg/L for Zoea III, 3000 μg/L for Mysis I, II and III and that for almost 100% mortality for postlarvae was 3000 μg/L. For cadmium LC were 100 μg/L for nauplii, 500 μg/L for Zoea I, 1000 μg/L for Zoea II, 2000 μg/L for Zoea III, 2500 μg/L for Mysis I and 3500 μg/L for Mysis II, III and postlarvae. For mixture of both metals, LC were 400 μg/L for nauplii, 1000 μg/L for Zoea I, 2000 μg/L for Zoea II and 3000 μg/L for Mysis I, II, III and post larvae.  相似文献   

18.
金属元素活动态是我国5种深穿透地球化学技术中应用最广的方法之一。此方法是通过提取地表土壤一定深度介质中元素活动态的微弱隐伏矿信息而找寻隐伏矿,属于通过直接信息找矿,目前该方法的标准化程度不高。为将铜元素活动态应用于地质找矿,该文对铜元素4个活动态的相态(水浸出态、粘土吸附态、有机链合态、铁锰氧化物态)循序提取的条件及ICP-AES测定技术进行了研究,包括采样深度、分析样品粒度、样品存放时间、提取条件、测定干扰等,通过对铜活动态提取液处理方法的改进,提高了分析速度和分析数据的精度。由实验数据计算出各相态方法的检出限和精密度RSD(n=10),水浸出态为0.079mg/L,13.90%~22.49%;粘土吸附态为0.275mg/L,11.99%~23.29%;有机链合态为0.362mg/L,10.70%~57.27%;铁锰氧化物态为0.230mg/L,17.83%~38.61%。该方法操作方便,精密度较好,应用于碑楼隐伏铜矿的野外探测实验,探测结果所圈定的综合异常与实际矿体的水平投影相符,取得了较满意的试验效果,该方法可应用于不同地质景观区。  相似文献   

19.
Batch culture experiments were conducted with a red tide dinoflagellateScrippsiella trochoidea (Stein) Loeblch III collected from Jiaozhou Bay, Shangdong, China. Growth rates and oellular Chl—a were measured in media with iron and manganese ion concentrations controlled at different levels using EdTA-trace metal buffer systems. Cell density increased 3.2 times to 6.5 times over the range of lowest (0 mol/L) to highest (10−5 mol/L) iron and manganese ion concentrations. The range of cell density response was much lower than the range of total available iron and manganese, which was >100—fold that of Fe. This nonlinear relationship indicates that the cells adapt to make more efficient use of iron and manganese under limiting conditions. The cellular Chl—a content maximized after 3 days incubation and then decreased gradually under either iron or manganese limitation conditions. It indicated that the algae gained higher photosynthesis ability when transferred to a new environment. Growth responses to iron and manganese limitation can be both modeled according to the equation of Monod. The half—saturation constant for growth,k, is 4.6×10−8 mol/L for Fe and 5.1×10−8 mol/L for Mn. Our results showed that the iron availability in Jiaozhou Bay does not limit the growth ofS. trochoidea. Contribution No. 2831 from the Institute of Oceanology, Chinese Academy of Sciences. Project 9389008 supported by NSFC; Study supported by PDB6.  相似文献   

20.
The influence of alkali on astaxanthin and the optimal working wave length for measurement of astaxanthin from Haematococcus crude extract were investigated, and a spectrophotometric method for precise quantification of the astaxanthin based on the method of Boussiba et al. was established. According to Boussiba's method, alkali treatment destroys chlorophyll. However, we found that: 1) carotenoid content declined for about 25% in Haematococcus fresh cysts and up to 30% in dry powder of Haematococcus broken cysts after alkali treatment; and 2) dimethyl sulfoxide (DMSO)-extracted chlorophyll of green Haematococcus bares little absorption at 520-550 nm. Interestingly, a good linear relationship existed between absorbance at 530 nm and astaxanthin content, while an unknown interference at 540-550 nm was detected in our study. Therefore, with 530 nm as working wavelength, the alkali treatment to destroy chlorophyll was not necessary and the influence of chlorophyll, other carotenoids, and the unknown interference could be avoided. The astaxanthin contents of two samples were measured at 492 nm and 530 nm; the measured values at 530 nm were 2.617 g/100 g and 1.811 g/100 g. When compared with the measured values at 492 nm, the measured values at 530 nm decreased by 6.93% and 11.96%, respectively. The measured values at 530 nm are closer to the true astaxanthin contents in the samples. The data show that 530 nm is the most suitable wave length for spectrophotometric determination to the astaxanthin in Haematococcus crude extract.  相似文献   

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