Stable carbon, nitrogen, and oxygen isotope analysis as a potential tool for verifying geographical origin of beef

Stable isotope analysis of organic elements such as carbon and nitrogen has been employed as a powerful tool for provenance determination of food materials, because isotopic compositions of the materials reflect many factors in natural environment. In this study, we examined carbon, nitrogen, and oxygen isotope signatures of beef from Australia, Japan, and USA, in order to confirm the method as a potential tool for verifying geographical origin of beef commercially distributed in Japan. Defatted dry matter of beef from USA was characterized by higher carbon isotopic composition (-13.6 per thousand to -11.1 per thousand) than that from Japan (-19.6 per thousand to -17.0 per thousand) and Australia (-23.6 per thousand to -18.7 per thousand). That from Australia was characterized by higher oxygen isotopic composition (+15.0 per thousand to +19.4 per thousand) than that from Japan (+7.3 per thousand to +13.6 per thousand) and USA (+9.5 per thousand to +11.7 per thousand). The oxygen isotopic composition in Japanese beef showed a positive correlation with the isotopic composition of cattle drinking water, the difference in which is clearly latitude dependent. These results suggest that a comparison of carbon, nitrogen, and oxygen isotopic compositions is applicable as a potential tool to discriminate the provenance of beef not only between different countries (i.e. Australia, Japan, and USA) but also among different regions within Japan.     

Characterization and differentiation of iron ores using X-ray diffractometry,k0 instrumental neutron activation analysis and inductively coupled plasma optical emission spectrometry

This study was aimed at developing methodology for the characterization and differentiation of iron ores from different ore deposits. X-ray diffractometry (XRD) was used for the determination of major and minor chemical phases in the ores, k₀-instrumental neutron activation analysis (k₀-INAA) and inductively coupled plasma optical emission spectrometry (ICP-OES) were employed for the determination of elemental profiles of iron ores. The quality of the ores was evaluated to establish their suitability to serve as a raw material for iron production. Principal component analysis was performed on the elemental data for the classification of ores. It was also shown that ores can be differentiated on the basis of rare earth elemental profiles. In this paper a new indicator, based on four elements (Ca, S, Sb, Yb), was proposed for the classification.

     

Evaluation of relative comparator and <Emphasis Type="Italic">k</Emphasis><Subscript>0</Subscript>-NAA for characterization of Aboriginal Australian ochre

Ochre is a significant material in Aboriginal Australian cultural expression from ceremonial uses to its application on many types of artifacts. However, ochre is a complex material, with associated surrounding minerals potentially challenging the overall analysis. In recent literature several studies have attempted to characterize ochre by a variety of techniques to understand procurement and trade. However, ochre is difficult to differentiate on major elemental or mineralogical composition and requires a detailed analysis of its geochemical “fingerprint”. Neutron activation analysis (NAA) provides the high sensitivity (sub-ppm), precision and accuracy in multi-elemental analysis required for ochre. The elements of interest for ochre generally include rare earth elements (REEs) and certain transition metal elements as well as arsenic and antimony. Data from relative comparator NAA (MURR, University of Missouri, USA) is compared with data from k ₀-NAA OPAL (ANSTO, Lucas Heights, Australia). A discussion of the two methods will be examined for their utility in “fingerprinting” the provenance of ochre. The continuing importance of NAA to archaeometry will also be discussed.     

Element profiles of onion producing districts in Japan, as determined using INAA and PGA

We carried out instrumental neutron activation analysis (INAA) as well as k ₀-based prompt gamma-ray analysis (k ₀-PGA) to measure the amount of the elements in onions and studied whether the onions collected from different sites can be categorized based on the elemental concentration profile. Six elements (Na, Mg, Cl, K, Ca, Mn) and 3 elements (B, S, Cl) were measured by INAA and PGA in the onions grown in two districts, Hokkaido and Saga, in Japan, respectively. After principal component analysis, it was found that Cl was an important element to feature the producing districts of onions.     

The use of the <Emphasis Type="Italic">k</Emphasis><Subscript>0</Subscript>-IAEA program in NIRR-1 NAA laboratory

The k ₀-IAEA program developed for implementation of the single comparator instrumental neutron activation analysis method (k ₀-INAA) has been used for elemental analysis with NIRR-1 irradiation and counting facilities. The existing experimental protocols for routine analysis based on the relative method were used to test the capability and reliability of the program for the analyses of geological and biological samples. The Synthetic Multi-element Standards (SMELS) types I, II and III recommended by the international k ₀ user community for the validation of k ₀-NAA method in NAA laboratories, furthermore, the following standard reference materials: NIST-1633b (Coal Fly Ash) and IAEA-336 (Lichen) were analyzed. Results obtained with the version 3.12 of the k ₀-IAEA program were found to be in good agreement with the data obtained with the established relative method using WINSPAN-2004 software. Detection limits for elemental analysis of geological and biological samples with NIRR-1 facilities are provided.     

Some irregularities observed in the analysis results of k0-NAA

Since 1996, two new cases were detected in our laboratory for which the elemental concentrations derived from k ₀ neutron activation analysis seem questionable. These cases concern the inconsistencies observed (1) in the concentration of Ca obtained via ⁴⁷Ca and ⁴⁷Sc, and (2) in the concentration of Yb obtained via the 228.5 and 396.3 keV lines of ¹⁷⁵Yb. A recommendation is made to re-evaluate the corresponding k ₀-values or true-coincidence correction factors.     

Application of the INAA methods for KRISS infant formula CRM analysis: standardization of INAA at KRISS

We have established an instrumental neutron activation analysis (INAA) method, including k₀-based INAA, at the Korea Research Institute of Standards and Science (KRISS) for the certification of reference materials. As part of establishing INAA measurements, KRISS infant formula certified reference material was analysed for multiple elements at three different metrological institutes: KRISS and NIST for the standard comparator method, and JSI for the k₀-INAA method. The mass fraction of most elements was consistent within expanded uncertainty (k?=?2). In addition, the results were used to verify the validity of elemental analysis of Zn using the standard comparator INAA at KRISS, and spreadsheet-based INAA calculations were evaluated.

     

Establishing a basis for nuclear archaeometry in Australia using the 20 MW OPAL research reactor

The k ₀-method of standardisation for instrumental neutron activation analysis (INAA) has been used at the OPAL research reactor to determine the elemental composition of three certified reference materials: coal fly ash (SRM 1633b), brick clay (SRM 679) and Montana soil (SRM 2711). Of the 41 certified elements in the three materials, 88 percent were within five percent of the certified values and all determinations were within 15 percent of the certified values. The average difference between the measured and certified values was 0.1 percent, with a standard deviation of 4.1 percent. Since these reference materials are widely used as standards in the analysis of archaeological ceramics by INAA, it has been concluded that the INAA facility in Australia is particularly well-suited for nuclear archaeometry.     

Progress of prompt gamma activation analysis in Korea

Summary The new PGAA facility using diffracted neutron beam was developed in Korea. The basic characteristics of the facility were studied in detail. A general formalism of the k₀ factor as extended to non-1/v absorber and arbitrary neutron spectrum was discussed and the actual data for Cd, Sm, Eu, Gd have been measured and determined successfully owing to the simple nature of the diffracted neutron spectrum. The k₀ factors for B, N, Si, P, S and Cl were also determined and showed consistent results with previously reported ones. At an early stage, feasibility of boron concentration analysis and measurement of thermal neutron capture cross sections has been studied. The PGAA facility is now open to users. A considerable amount of beam time is already dedicated to studies on the elemental analysis.     

GammaLab: a suite of programs for k0-NAA and gamma-ray spectrum analysis

The GammaLab is a collection of computer codes, written in MATLAB, for performing calculations involved in k ₀ neutron activation analysis. The main features of the program include calibrations including energy-channel, energy-FWHM and energy-efficiency for different geometries, background subtraction, nuclide identification, spectral interference correction, elemental concentration and limit of detection determination. The data input is taken from two files one is the spectrum file stored in IAEA ASCII format and other is report file containing peak energy and peak area data. The information about sample, irradiation and counting conditions, background spectra are retrieved from QAQCData database. GammaLab takes nuclear data such as gamma lines, emission probabilities, half-lives, and k ₀ factors from NucData database. The sample results which contain elemental concentrations with uncertainties are stored in the QAQCData database. The program has been evaluated by analyzing several hundred spectra and results were found satisfactory.     

Utilization ofk o-factors for quality assurance in neutron activation analysis

Multielement certification analysis by instrumental neutron activation analysis requires simultaneous irradiation of several elemental comparator standards in order to ascertain traceability. Internal consistency of different comparators may be checked by calculation ofk _o-ratios, which show large deviations from unity in case of stoichiometric or other gross errors. Quality assurance based on the Analysis of Precision ofk _o-ratios from replicate analyses detects unexpected variability associated with inaccurate comparator standards. In two actual cases of cerification lack of statistical control amongk _o-ratios led to biased analytical results.     

Elemental bioaccumulators in air pollution studies

k₀-Based instrumental neutron activation analysis (k₀ INAA) was used to determine the concentrations of Cr, Fe, Co, Zn, Se, Sb and Hg in the vascular plantsCistus salvifolius andInula viscosa and in the lichenParmelia sulcata. The samples were collected in the neighbourhood of industrial complexes. The elemental accumulation in the vascular plants and the lichen are compared to optimize the choice of the bioaccumulator. It is concluded thatP. sulcata seems to be the best accumulator of the three species for the elements studied;Cistus salvifolius is sensitive to the contents of Zn, Fe, Cr and Sb in the air;Inula viscosa seems to accumulate Fe, Sb, Co, Cr and Zn. Nevertheless, it is concluded that lichen is a good air pollution indicator, while the vascular plants are not due to the large seasonal variations found in the elemental concentrations.     

Metal concentrations in Japanese medaka,mosquitofish and insect larvae living in uncontaminated rivers in Kumamoto,Japan

Elemental concentrations in Japanese medaka and mosquitofish collected from uncontaminated rivers in Kumamoto, Japan were analyzed by instrumental neutron activation analysis with k ₀ standardization method to know the background levels. A statistical analysis indicated the difference in metal concentrations among rivers and species. Background levels of elemental concentrations in some aquatic insect larvae were analyzed and metal concentrations were different among species, though they were collected at the same point. Enrichment factors of heavy metals in insect larvae were in the order of 10³−10⁴ suggesting effectiveness of insect larvae as bioindicator.     

Moment theory for the analytical determination of rate constants for solute permeation at the interface of spherical molecular aggregates

Moment equations were developed on the basis of the Einstein equation for diffusion and the random walk model to analytically determine the rate constant for the interfacial solute permeation from a bulk solvent into molecular aggregates (k_in) and the inverse rate constant from the molecular aggregates to the bulk solvent (k_out). The moment equations were in good agreement with those derived in a different manner. To demonstrate their effectiveness in one concrete example, the moment equations were used to analytically determine the values of k_in and k_out of three electrically neutral solutes, i.e. resorcinol, phenol, and nitrobenzene, from the first absolute (μ_1A) and second central (μ_2C) moments of their elution peaks, as measured by electrokinetic chromatography (EKC), in which the sodium dodecyl sulfate (SDS) micelles were used as a pseudostationary phase. The values of k_in and k_out should be determined with no chemical modifications and no physical action with the molecular aggregates because they are dynamic systems formed through weak interactions between the components. The moment analysis of the elution peak profiles measured by EKC is effective to unambiguously determine k_in, k_out, and the partition equilibrium constant (k_in/k_out) under appropriate experimental conditions.     

Multi-element analysis of soil from the north-western region of India by neutron activation analysis using the single comparator method with special reference to selenium toxicity

The single comparator (k₀) instrumental neutron activation analysis (INAA) was employed to determine the elemental composition of soil from the north-western region of India. The radiometric assay was carried out using high resolution gamma-ray spectrometry. Seventeen elements were detected including selenium whose concentration was found to be in the range of 1.02 to 6.79 mg/g.     

Prompt-gamma activation analysis using thek 0 approach

Applying thek ₀ standardization method to prompt-gamma activation analysis (PGAA) offers similar benefits as in instrumental neutron activation analysis. It has been demonstrated that under constant flux conditionsk ₀-factors obtained by normalizing to a titanium comparator, measured separately, yield consistent analytical sensitivity ratios. The ratio method has been generalized by using stoichiometric compounds for the determination ofk ₀-factors. Since chlorine forms compounds with essentially everyelement and it also serves as a detector efficiency standard,k ₀ values have been determined relative to chlorine as an internal standard for several analytically important elements in two reactor facilities: the thermal guided beam at the BRR in Budapest and the cold-neutron beams at the NBSR at NIST.     

The application and development of k0-standardization method of neutron activation analysis at Dalat research reactor

In recent years the k ₀-NAA method has been applied and developed at the 500 kW Dalat research reactor, which includes (1) the establishment of a PC database of k ₀-NAA-related nuclear parameters, e.g., radionuclide produced, half-lives, k ₀-factors, Q ₀, _r, E _g, etc; the access to the database is able by a k ₀-NAA software or by manual; (2) the detection efficiency calibration of gamma spectrometers used in k ₀-NAA, (3) the determination of reactor neutron spectrum parameters such as a and f factors and neutron fluxes in the irradiation channels, and (4) the validation of the developed k ₀-NAA procedure by analysing some SRMs, namely Coal Fly Ash (NIST-1633b), Bovine Liver (NIST-1577b) and IAEA-Soil7. The analytical results showed the deviations between experimental and certified values were mostly less than 15% with most Z-scores lower than 2. The k ₀-NAA procedure established at the Dalat research reactor has been regarded as a reliable standardization method of NAA and as available for practical applications, in particularly for airborne particulate and crude oil samples.     

Measurement and evaluation of k0 factors for PGA at JAERI

In order to determine multiple elements by k ₀ standardization-based neutron induced prompt gamma-ray analysis (PGA), measurements and evaluation of k ₀ factors for the elements have been performed. The k ₀ factors using Cl as a comparator for 27 elements, which are effective for the analysis by PGA, were measured with precision almost less than 3% using the cold and thermal guided neutron beams at JRR-3M. The accuracy of the k ₀ factors were better than 10% except for the non-1/v elements of Cd and Sm. Neutron spectrum correction is necessary for common use of k ₀ factors of the non-1/v elements.     

Brazilian Experience on k0 Standardized Neutron Activation Analysis

After more than ten years working with multicomparator instrumental neutron activation analysis, mainly applied to the characterization of environmental samples, the Radioisotopes Laboratory (CENA/USP) started changing gradually to the k ₀-method in 1997. The main activities developed, as well as some of the results obtained, are presented here. Even though there is much more work to be done, the good quality of the results and the possibility of elemental determinations without the co-irradiation of standards may lead to the definitive adoption of the k ₀-method in a near future.     

Air-quality assessment of Pico-mountain environment (Azores) by using chemometric and trajectory analyses

This article illustrates the use of chemometrics in the interpretation of aerosol data collected by a seven-wavelength aethalometer at the PICO-NARE observatory, in Pico island, Azores, Portugal. Samples were assessed through k ₀-standardized, instrumental neutron activation analysis (k ₀-INAA), and concentrations of up to 20 airborne elements were determined. The chemometric analysis by self-organizing maps (SOM) tried to identify groups of similarity for sampling events and chemical tracers, discriminating in this way each group of similarity thus obtained. Additionally, synoptic back trajectories for each of the sampling days distributed into four clusters were calculated, in order to associate the classified groups with possible pollution sources.