A CRL–IRMM joint proficiency test for trace elements in fish tissue

The Community Reference Laboratory (CRL) for residues and contaminants in food of animal origin at the Istituto Superiore di Sanità (ISS) plans and undertakes on a regular basis Proficiency Tests Schemes (PTSs) focused on the residues under its responsibility, as prescribed by the Council Directive 96/23/EC of April 29, 1996. In consideration of the benefits ensuing from a constant monitoring of the daily activities of the National Reference Laboratories (NRLs) for residues in the Member States, the ISS–CRL frequently prepares test materials to promote comparability of data and support harmonisation of routine analytical procedures. When target values for the analytes are set, the PTSs also provide objective assessment and improvement of the analytical trueness in the daily work.In this context, an interlaboratory comparison for trace elements in tuna fish matrix was organised in cooperation with the Institute for Reference Materials and Measurements (IRMM), Joint Research Centre, European Commission. Freeze-dried tuna fish samples were sent out to the NRLs for chemical elements in the Member States. Participants were requested to carry out at least three independent measurements of the elements As, Cd, Cr, Cu, Fe, Hg, Pb and Zn. The assessment of the proficiency was based on the z-score approach and a relative bias better than or equal to 10% of the target value was deemed to be an acceptable performance for this kind of measurements. On this basis, more than 50% of the laboratories returned accurate results for As, Cu, Fe, Hg and Zn, whereas the analysis of Cd, Cr and Pb appeared to be more problematic.     

Determination of arsenic, cadmium, mercury, and lead by inductively coupled plasma/mass spectrometry in foods after pressure digestion: NMKL interlaboratory study

Thirteen laboratories participated in an interlaboratory method performance (collaborative) study on a method for the determination of arsenic, cadmium, mercury, and lead by inductively coupled plasma/mass spectrometry (ICP/MS) after pressure digestion including the microwave heating technique. Prior to the study, the laboratories were able to practice on samples with defined element levels (pretrial test). The method was tested on a total of 7 foodstuffs: carrot puree, fish muscle, mushroom, graham flour, simulated diet, scampi, and mussel powder. The elemental concentrations in mg/kg dry matter (dm) ranged from 0.06-21.4 for As, 0.03-28.3 for Cd, 0.04-0.6 for Hg, and 0.01-2.4 for Pb. The materials used in the study were presented to the participants as blind duplicates, and the participants were asked to perform single determinations on each sample. The repeatability relative standard deviations (RSDr) for As ranged from 3.8 to 24%, for Cd from 2.6 to 6.9%, for Hg from 4.8 to 8.3%, and for Pb from 2.9 to 27%. The reproducibility relative standard deviations (RSDR) for As ranged from 9.0 to 28%, for Cd from 2.8 to 18%, for Hg from 9.9 to 24%, and for Pb from 8.0 to 50%. The HorRat values were less than 1.5 for all test samples, except for the determination of Pb in wheat flour at a level close to the limit of quantitation (0.01 mg/kg dm). The study showed that the ICP/MS method is satisfactory as a standard method for elemental determinations in foodstuffs.     

Establishment of SI-traceable reference values for the content of various elements in the IMEP-14 sediment sample

For the first time in the International Measurement Evaluation Programme (IMEP)-14, a sediment sample was offered to analytical laboratories to perform measurements of As, Cd, Cr, Cu, Fe, Pb, Hg, Ni, U and Zn. In line with IMEP policy, the results were presented according to the certified / assigned reference values established by several reference laboratories around the world. The certification campaign is described in detail. Isotope dilution mass spectrometry was applied as a primary method of measurement, whenever possible, to achieve SI-traceable results. For reference measurements of As, Fe, Hg and Zn, k₀-neutron activation analysis and Zeeman atomic absorption spectrometry were applied. The reference values (ranges) were characterised as ”certified” (for Cd, Cr, Pb, Ni and U) or ”assigned” (for As, Cu, Fe, Hg and Zn) according to IMEP policy. The measurement uncertainty of the certified / assured reference values was calculated according to the ISO/BIPM Guide. Received: 7 June 2001-10-27 Accepted: 19 August 2001     

An intercomparison exercise for trace metal monitoring in oxygen-rich and anoxic Baltic waters

Seawater samples for a laboratory intercomparison of trace metal concentrations (Mn, Fe, Ni, Cu, Cd, Pb) in the dissolved (<0.4 μm filtered) and particle-bound phases as well as total and reactive Hg were collected in the Gotland Basin, a region in the Baltic Sea with trace metal gradients in the halocline and the redox boundary. Two laboratories took part in this exercise, each laboratory analysing samples from two vertical profiles collected using ”clean” sampling techniques. The hydrographic and hydrochemical situation was determined to characterise the water column and help interpret the results. An estimation of the conformity of the two laboratories was performed by comparing the results with international intercalibration exercises and certified reference materials. For all metals the characteristic vertical distribution and the concentration range of the data were comparable to other results published for the region. The concentration differences in the amount contents of Mn, Fe, Ni, Cu, Cd, Pb and Hg determined between both laboratories were better than the confidence intervals given by an ICES (International Council for the Exploration of the Sea) international comparison exercise for Baltic waters. Differences for Ni in the anoxic water body are attributed to the sulphidic matrix and their influence on the different methods used by the laboratories. For Pb and Hg the concentrations were near the detection limit of our methods, low level contamination was possibly responsible for the concentration differences. Small differences for dissolved Mn were attributed to different sampling techniques. We conclude that sampling and sample handling are still weak links in the trace metal analysis of anoxic seawater and that the analytical methods we used for this exercise are satisfactory for the accurate determination of Cd, Cu, Pb, Mn, Fe, and also for studying biogeochemical cycling of these trace metals in oxygen-rich and anoxic water bodies. Received: 8 February 2001 Accepted: 8 August 2001     

Graphite furnace atomic absorption spectrometric determination of lead and cadmium extracted from ceramic foodware: Collaborative Study

A modification of the official flame atomic absorption spectrometric (FAAS) method for determining lead and cadmium extracted from ceramic foodware was collaboratively studied. In the modified method, graphite furnace atomic absorption spectrometry (GFAAS) is substituted for FAAS. The modified method also includes mandatory quality control procedures to improve method performance. The extraction procedure of the official method (leaching with 4% acetic acid for 24 h at room temperature) remains unchanged. Seven laboratories analyzed blind duplicate portions of 3 ceramicware leach solutions containing Pb at concentrations of 0.0196, 0.403, and 3.73 microg/mL and Cd at concentrations of 0.00236, 0.0456, and 0.544 microg/mL. Performance of the modified method compared well with that of the official method. The repeatability relative standard deviation (RSDr) ranged from 0.87 to 6.7% for Pb and from 3.7 to 11% for Cd. The reproducibility relative standard deviation (RSDR) ranged from 4.5 to 12% for Pb and from 7.0 to 11% for Cd. Accuracy of collaborator results was 97-98% for Pb and 93-101% for Cd. Quality control results and quantitation limits were excellent. Method quantitation limits varied among laboratories from 0.005 to 0.019 microg/mL for Pb and from 0.0004 to 0.0019 microg/mL for Cd. The modified method was adopted First Action by AOAC INTERNATIONAL.     

Different approaches to legal requirements on validation of test methods for official control of foodstuffs and of veterinary drug residues and element contaminants in the EC

 In order to ensure food consumer protection as well as to avoid barriers to trade and unnecessary duplications of laboratory tests and to gain mutual recognition of results of analyses, the quality of laboratories and test results has to be guaranteed. For this purpose, the EC Council and the Commission have introducedprovisions – on measures for quality assurance for official laboratories concerning the analyses of foodstuffs on the one hand and animals and fresh meat on the other, – on the validation of test methods to obtain results of sufficient accuracy. This article deals with legal requirements in the European Union on basic principles of laboratory quality assurance for official notification to the EC Commission and on method validation concerning official laboratories. Widespread discussions and activities on measurement uncertainty are in progress, and the European validation standards for official purposes may serve as a basis for world-wide efforts on quality harmonization of analytical results. Although much time has already been spent, definitions and requirements have to be revised and further additions have to be made.     

Zur Anwendung statistischer Methoden bei der Auswertung von Ringversuchen

Zusammenfassung Um die Kennzahlen (Vergleichbarkeit und Wiederholbarkeit) eines Ringversuchs abzuleiten, sind statistische Verfahren anzuwenden, die die Überprüfung von Ausreißern ermöglichen (Grubbs u. Dixon), den Vergleich der intralaboriellen Streuungen durchführen (Bartlett u. Cochran) und die systematischen Fehler/Mittelwertunterschiede feststellen (Varianzanalyse/Kruskal-Wallis).Diese Verfahren, die in der amtlichen Sammlung des § 35 LMBG und im DIN ISO 5725 vorgeschlagen werden, wurden bei der Auswertung eines Ringversuches über Pb, Cd und Hg in biologischem Material angewandt.Als Ergebnis dieses Ringversuches, an dem sich 63 Laboratorien beteiligten, kann festgestellt werden, daß die Verfahren für Cd im Bereich von 1,5 mg/kg akzeptable, dagegen für Pb im Bereich von 1,2 mg/kg sowie für Hg im Bereich von 0,030 mg/kg keine zufriedenstellenden Ergebnisse liefern.

---

Application of statistical methods in the evaluation of interlaboratory tests

Summary Statistical tests are necessary for deducing the parameters (reproducibility and repeatability) of a interlaboratory test. They enable a check of outliers (Grubbs and Dixon), the comparison of the intralaboratory variations (Bartlett and Cochran) and the detection of systematic errors/differences of the mean (analysis of variance/Kruskal-Wallis).These methods, which are proposed in the official collection of § 35 LMBG and in DIN ISO 5725, were used in the evaluation of an interlaboratory test for lead, cadmium and mercury in biological material. As a result of this interlaboratory test with 63 laboratories it can be concluded that the analytical methods for the detection of Cd in the concentration range of 1.5 mg/kg give acceptable values; for Pb (1.2 mg/kg) and Hg (0.030 mg/kg) the results were not satisfactory.

---

---

Herrn Prof. Dr. W. Fresenius zum 70. Geburtstag gewidmet     

Determination of trace Pb(Ⅱ), Cd(Ⅱ) and Zn(Ⅱ) using differential pulse stripping voltammetry without Hg modification

In this work,we reported a simultaneous determination approach for Pb(II),Cd(II)and Zn(II)atμg L 1concentration levels using differential pulse stripping voltammetry on a bismuth film electrode(BiFE).The BiFE could be prepared in situ when the sample solution contained a suitable amount of Bi(NO)3,and its analytical performance was evaluated for the simultaneous determination of Pb(II),Cd(II)and Zn(II)in solutions.The determination limits were found to be 0.19μg L 1for Zn(II),and0.28μg L 1for Pb(II)and Cd(II),with a preconcentration time of 300 s.The BiFE approach was successfully applied to determine Pb(II),Cd(II)and Zn(II)in tea leaf and infusion samples,and the results were in agreement with those obtained using an atomic absorption spectrometry approach.Without Hg usage,the in situ preparation for BiFE supplied a green and acceptability sensitive method for the determination of the heavy metal ions.     

Instrumental Neutron Activation Analysis (INAA) and Inductively Coupled Plasma/Mass Spectrometry (ICP-MS) for Trace Element Biomonitoring using Mosses

Two analytical methods - instrumental neutron activation analysis (INAA) and inductively coupled plasma mass spectrometry (ICP-MS) - were used for the trace element analysis of naturally growing mosses for a heavy metal biomonitoring survey. The techniques were applied to reference mosses to evaluate the feasibility, analytical variability, detection limits and accuracy. These parameters were evaluated using 563 mosses sampled in the 1996 French survey. All the elements of interest in the European program "Atmospheric Heavy Metal Deposition in Europe - estimation based on moss analysis" (As, Cd, Cr, Cu, Fe, Hg, Pb, Ni, V, Zn) were able to be determined by ICP-MS. INAA appeared suitable for the determination of As, Cr, Fe, Hg, V and Zn. The Cd, Cu, Ni and Pb concentrations determined by ICP-MS were preferred to the INAA results, because of increased feasibility or accuracy. The results provided by both methods on the French mosses were statistically compared for 14 elements. Significant linear correlation appeared for: Ba, Ce, Cs, La, Rb, Sm, Th and V. Among these eight elements, Ba, Cs, La and Sm concentrations determined by both methods exhibited a strong statistical similarity. The correlations obtained for As, Eu, Fe and Sb were not as strong and no correlation at all was observed for Co and Cr. These differences were attributed to instrumental factors (e.g. spectral interference occurred for both methods) or due to the sample preparation prior to ICP-MS. The consequences of such results on the regional trend evaluation of atmospheric heavy metal deposition were discussed.     

SI-traceable certification of the IMEP-12 water sample combining contributions from different reference laboratories

In the International Measurement Evaluation Programme (IMEP-12) comparison, a synthetically prepared water sample was offered to the analytical laboratories to perform measurements of As, B, Cd, Cr, Cu, Fe, Mg, Mn, Ni and Pb. The choice of elements to be measured was based on EU legislation, which the comparison was aiming to support. As to the IMEP policy, the laboratories’ results were presented according to the certified/assigned reference values established by several reference laboratories all around the world. The performed certification campaign is described in detail in this paper. Isotope dilution mass spectrometry (IDMS) was applied as a primary method of measurement (PMM), whenever possible, to achieve SI-traceable results. Apart from IDMS for reference measurements of some elements, k _o-neutron activation analysis (k _o-NAA) and external calibration (Ext-Calib) using inductively coupled plasma-mass spectrometry (ICP-MS) were applied. The reference values were characterised as “certified” (for B, Cd, Cr, Cu, Fe, Mg, Ni and Pb) or “assigned” (for As and Mn) according to the IMEP policy. Measurement uncertainty of the certified/assigned reference values was calculated according to the ISO/BIPM guide using the specialised software GUM Workbench.     

Elektrophorese der halogenokomplexe von Hg(II), Bi(III), Cd(II), Pb(II) und -Cu(II) : Chlorokomplexe in chlorwasserstoffsäure

An apparatus for heavy-current and high-tension electrophoresis on filter paper is described This apparatus enables one to avoid the difficulties that occur in electrophoresis in base electrolytes that are highly concentrated or show greater electric conductivity The zones migrate along the paper strips with constant speed and, consequently, it is possible to measure the mobility The effective length of the filter paper strips is 660 mm Correction of the apparent mobility in the porous adsorbent is treated thoroughly.Diagrams of the electrophoretic mobility of the chloro-complexes of Hg(II), Bi(III), Cd(II), Pb(II), and Cu(II) in hydrochloric acid, are given in the experimental part The concentration of the hydrochloric acid varied between 0.1N and 6N In 6N HCl all the metals investigated are present asani onic complexes. Hg, Bi.Cd, and Pb chloro-complexes show a pronounced maximum of mobility in the anionic range. The sequence of the zones in the direction anode to cathode is Hg, B1, Cd, Pb, Lu al 0.1–2.3N HCl and B1, Hg, Cd, Pb.Cu at2.3–6N HCl.Finally, the electrophoretic separation of a mixture of Hg, Bi, Cd, Pb, Cu in 1N, 2N and 4N HCl is illustrated Complete separation of the zones was achieved in each experiment     

Effect of Anions on the Development of Color Reactions of Cadmium, Lead, and Mercury with Dithizone and 4-(2-Pyridylazo)resorcinol on a Fibrous Material Filled with the Anion Exchanger AV-17

The effect of nitrates, chlorides, iodides, sulfates, thiosulfates, thiocyanates, acetates, tartrates, nitrilotriacetates, and ethylenediaminetetraacetates in the sorption of Cd(II), Pb(II), and Hg(II) and their subsequent determination with dithizone and 4-(2-pyridylazo)resorcinol (PAR) on the solid phase of a fibrous anion-exchange sorbent filled with AV-17 was studied. The dependences of the analytical signals of complexes adsorbed on the solid phase on the concentration of anions in the solution and on the stability of anionic complexes were revealed. The analytical signals in the sorption and determination of Cd, Pb, and Hg with dithizone and PAR on the solid phase were maximum for iodide and thiosulfate complexes. Conditions of the sorption of Cd(II), Pb(II), and Hg(II) were found for their subsequent total and separate determination with PAR and dithizone.     

Simultaneous analysis of cadmium, lead, mercury, and arsenic content in foodstuffs of animal origin by inductively coupled plasma/mass spectrometry after closed vessel microwave digestion: method validation

A method validation of the total analysis of cadmium (Cd), lead (Pb), arsenic (As), and mercury (Hg) in foodstuffs by inductively coupled plasma/mass spectrometry (ICP/MS) after closed vessel microwave digestion is presented. Due to the lack of reference method for ICP/MS techniques in food and, based on the project of the European Committee of Normalization (CEN/TC 275/WG 10), the Agence Fran?aise de Normalisation (AFNOR) guidelines NF V03-110 were used for the evaluation of this method based on 2 steps, sample preparation and multielement detection. Several criteria considered as compulsory (linearity, specificity, precision under repeatability conditions, and trueness) have been estimated and discussed, in addition to intermediate precision reproducibility, the limit of detection, and the limit of quantification. Furthermore, a comparison with in-house methods using electrothermal atomic absorption was performed using an external proficiency testing scheme and food samples. The results indicated that this method could be used in the laboratory for the routine determination of these 4 cumulative toxic metals in foodstuffs with acceptable analytical performance.     

Natural sources and heavy metals

PTS, PM10 and PM2.5 samples have been collected at a rural site of south-east Italy (40 degrees 20' 13" N; 18 degrees 6' 47" E) from June to October, 2004 to investigate natural and anthropogenic contributions on particulate matter and heavy metal mass concentrations. It is shown that sharp-peak particulate-matter concentrations have been recorded during most African dust outbreaks occurred over south-east Italy. In particular, PM10 concentrations exceeding the 24-hour limit value of 50 microg/m3 have been monitored during dust events. Al, Cd, Cr, Cu, Fe, Mn, V, Ni, Pb, and Zn metal concentrations have been evaluated by an inductively coupled plasma atomic emission spectrometer and Al mass concentrations >500 ng/m3 have been observed in PTS and PM10 samples during the advection of African dust particles. Accordingly to geochemical calculations Al, Fe, and Mn, have a significant crustal origin while, Cd, Cu, Pb, and Zn are of anthropogenic origin. Moreover, Fe resulted predominant in the coarse particle fraction, while Ni, Pb, V, and Zn were predominant in the fine particle fraction. It is also shown that Cd, Mn, Ni, Pb, and V concentrations never exceeded guide and/or limit values recommended by the World Health Organization and the European Council Directives.     

Determination of Hg,As, Pb,and Cd in Orchard Soils by Sequential Injection Vapor Generation Atomic Fluorescence Spectrometry

An analytical procedure was developed for determination of Hg, As, Pb, and Cd in soil samples using sequential injection vapor generation atomic fluorescence spectrometry (SI-VG-AFS) with sample preparation by microwave digestion system. The effects of analytical conditions on the fluorescence intensity were investigated and optimized. Under the optimized condition, the detection limits of the method were 5, 68, 40, and 3 ng L^?1 for Hg, As, Pb, and Cd, respectively. The accuracy of method was verified by the determination of the certified reference soil, and the recoveries for Hg, As, Pb, and Cd were in the range of 98.7–106.1%. The proposed method has been successfully applied to determine the heavy metals in navel orange orchard soils in Ganzhou, and the environmental quality of the orchard soils was assessed based on the content of the heavy metals. According to the second criterion of environmental quality standard for soils, Pb content in all soil samples collected from the orchards of 18 districts were within safe limits, but a few orchards were slightly contaminated with Hg, As, and Cd. Comparison of heavy metal mean concentrations with the safe limits of environmental quality standard for soils, the quality of Ganzhou navel orange orchard soils were in line with the request of the green food production base.     

The handbook of analytical methods for trace elements as adopted by the national reference laboratories for residues

The instrumental approaches, quality assurance schemes and management of chemical laboratories should in general be harmonized at the highest possible level. This is all the more so for the national reference laboratories (NRLs) for residues in live animals and their products which have to implement quality assurance systems inspired to the principles of good laboratory practice as well as to the general norms for the operation of testing laboratories (EN 45000 criteria). Directive 23/96/EC of 29 April 1996 prescribes that NRLs are assisted in this process by the four community reference laboratories (CRLs) for residues. To this end, the Rome CRL systematically collects in a handbook all the analytical methods in use at NRLs for the determination of As, Cd, Cu, Hg and Pb, as well as other chemical elements, in animal matrices. One major goal of this action is to foster the harmonization of analytical approaches by the NRLs and their ability to provide comparable results of similar quality. The Rome CRL is committed to revise this handbook twice a year. The role of the handbook is also to encourage the exchange of information among the NRLs as regards the possibility of improving existing methods.     

Interlaboratory study of trace and other elements in the iaea powdered human hair reference material,HH-1

A powdered intercomparison material for trace element studies was prepared from human scalp hair and distributed to more than 100 laboratories of which 66 reported results for altogether more than 40 elements. By statistical evaluation of these data certified concentration values were derived for 20 elements, namely As, Au, Br, Ca, Cd, Cl, Co, Cr, Cu, Fe, Hg, Mg, Mn, Na, Pb, S, Sb, Se, Sr and Zn. The data also made it possible to compare different methods of analysis and to judge the value of different levels of experience on the part of the analyst concerned; these comparisons are presented here with special reference to the elements As, Cd, Hg, Pb and Sb.     

Characterization of ARC/CL wheat flour, pork meat and skim milk powder reference materials for contents of toxic elements

Summary Wheat flour, pork meat and skim milk powder reference materials (RM) prepared and employed for the activities of the Sub-network on Trace Element Status in Food of the FAO European Cooperative Research Network on Trace Elements were subjected to an interlaboratory comparison study on the contents of Pb, Cd and Hg. The homogeneity of the above materials had earlier been shown to be within 2% for several essential elements and within 5 to 10% for Pb and Cd. An interlaboratory comparison study was conducted involving 17 reference laboratories recognized for their reliability and specialized in heavy metal determinations in biological materials. A total of seven methods based on four different analytical principles were employed to determine the contents of the above heavy metals. After the exclusion of outliers, the recommended concentration values expressed as the medians ±95% confidence limits were established. All of the recommended values reported here fell into category A, i.e. values recommended with a high degree of confidence according to the certification criteria established by Pszonicki. The present materials contain very low naturally occurring levels of all the heavy metals studied and have been successfully employed in the analytical quality control program of the above FAO study during the past five years.     

典型表面活性物质在汞、镉汞齐和铅汞齐电极上的吸附行为

本文采用DD-1型电镀参数测试仪,测定了汞、镉汞齐和铅汞齐电极在1MKCl的基底溶液中,四下基碘化铵等十二种典型有机表面活性物质在三种电极上的脱附电位。由于镉汞齐和铅汞齐电极的阳极溶解电位比较负,未观测到F^-、Cl^-、Br^-离子的吸附现象。I^-离子及同一有机表面活性物质在三种电极上的吸附活性顺序为:Hg>Pb(Hg)>Cd(Hg)。测试结果表明:同浓度的同一种表面活性物质,在三种电极上的脱附峰电位值之差小于10mV。反映了镉汞齐和铅汞齐电极在脱附峰电位时的表面性质接近于纯汞。     

Determination of cadmium,mercury and lead in seawater by electrothermal vaporization isotope dilution inductively coupled plasma mass spectrometry

Electrothermal vaporization isotope dilution inductively coupled plasma mass spectrometry (ETV-ID-ICP-MS) has been applied to the determination of Cd, Hg and Pb in seawater samples. The isotope ratios of the elements studied in each analytical run were calculated from the peak areas of each isotope. Various modifiers were tested for the best signal of these elements. After preliminary studies, 0.15% m/v TAC and 4% v/v HCl were added to the sample solution to work as the modifier. The ETV-ID-ICP-MS method has been applied to the determination of Cd, Hg and Pb in NASS-4 and CASS-3 reference seawater samples and seawater samples collected from Kaohsiung area. The results for reference sample NASS-4 and CASS-3 agreed satisfactorily with the reference values. Results for other samples determined by isotope dilution and method of standard additions agreed satisfactorily. Detection limits were approximately 0.002, 0.005 and 0.001 ng ml⁻¹ for Cd, Hg and Pb in seawater, respectively, with the ETV-ICP-MS method. Precision between sample replicates was better than 20% for most of the determinations.