Search

Peas (Pisum sativum) are the fourth most cultivated pulses worldwide and a critical source of protein in animal feed and human food. Developing pea core collections improves our understanding of pea evolution and may ease the exploitation of their genetic diversity in breeding programs. We carefully selected a highly diverse pea core collection of 325 accessions and established their genetic diversity and population structure. DArTSeq genotyping provided 35,790 polymorphic DArTseq markers, of which 24,279 were SilicoDArT and 11,511 SNP markers. More than 90% of these markers mapped onto the pea reference genome, with an average of 2787 SilicoDArT and 1644 SNP markers per chromosome, and an average LD50 distance of 0.48 and 1.38 Mbp, respectively. The pea core collection clustered in three or six subpopulations depending on the pea subspecies. Many admixed accessions were also detected, confirming the frequent genetic exchange between populations. Our results support the classification of Pisum genus into two species, P. fulvum and P. sativum (including subsp. sativum, arvense, elatius, humile, jomardii and abyssinicum). In addition, the study showed that wild alleles were incorporated into the cultivated pea through the intermediate P. sativum subsp. jomardii and P. sativum subsp. arvense during pea domestication, which have important implications for breeding programs. The high genetic diversity found in the collection and the high marker coverage are also expected to improve trait discovery and the efficient implementation of advanced breeding approaches.

Software has become one of the most critical parts of a measuring instrument. Despite the sophistication and complexity of measuring instruments, legal metrology framework on the software are still poor. Several legal cases related to manipulation and modification of software used in measuring instrument have been discovered in ASEAN countries particularly in Malaysia. A survey has been conducted and shows that most ASEAN countries have yet to implement and enforce legal metrology control on the software in their metrological system. This paper discussed an approach to legalizing software for measuring instrument in the Malaysian context.

A fast, simple and easily automated method was developed for the simultaneous determination of pesticide residues in tea using accelerated solvent extraction (ASE) with in-cell cleanup and gas chromatography-tandem mass spectrometry (GC-MS/MS). This method integrates extraction and cleanup processes into a single step, by adding a clean-up sorbent along with the sample into the extraction cell. The efficiency of this method was characterized in terms of its recovery (with values ranging from 90 to 98%), repeatability along with intermediate precision (showing relative standard deviations less than 15%), and sensitivity (providing detection limits between 0.001 and 0.007 μg g−1). The concentration range of the pesticide residues found in the sample is from 0.008 to 0.161 μg g−1. The relative expanded uncertainty achieved for this method ranged from 24% to 34%. The results indicate that the proposed method is easy and reliable for the determination of pesticide residues in tea, and it is suitable for use in routine analysis.

Comparative studies of two multi-walled carbon nanotubes (MWCNT) from different manufacturers were reported. The purification and functionalization of commercial multiwall carbon nanotubes were investigated. MWCNTs were treated with boiling concentrated HNO3 under a reflux condenser for 2 hours at 100 °C in order to purify and oxidize the raw material. The oxidized MWCNTs were rinsed with deionized water until stabilization of the filtrate pH. The measurement technique was by thermogravimetric analysis (TGA) for thermal analysis decomposition products. Meanwhile, the chemical shifted in MWCNTs can be determined by using Raman Spectroscopy.

A reliable method for measurement of the nonlinear refractive index through application of multi wavelength phenomenon. Multi wavelength realisation based on Erbium doped fibre laser (EDFL) is proposed and experimentally demonstrated. A combination of 15 m high efficiency Erbium doped fibre (EDF) and a 20 m Photonic Crystal Fibre (PCF) as main catalyst to suppress the homogenous broadening of EDF and to obtain highly stability of multi wavelength through insertion of a set of fibre Bragg gratings (FBGs) in the cavity. This PCF has zero dispersion of 1040 nm which mismatch from transmission window of 1550 nm. A reliable repeatability of multi wavelength based on multiple configuration of FBGs less than 0.2% obtained. This consistent results influence in determination of nonlinear refractive index by relation of four wave mixing (FWM).

This paper proposes a measurement of nonlinear refractive index in the course of multi wavelength technique. We have generated a multi wavelengths formation by utilising a photonic crystal fibre (PCF) which mismatches zero dispersion wavelength from transmission wavelength at 1550 nm. We provide an experimental set-up in generating the multi wavelength phenomenon. A fibre ring laser configuration consists of erbium doped fibre amplifier (EDFA) set up and arrangement of FBGs is described. Encouraging results obtained from the set up proves the relations of signals generated through FBGs and new wavelengths. These findings shows, multi wavelengths able to present valuable inputs in determination of nonlinear refractive index parameter.

This study investigates the written performance of the Sudanese EFL students at tertiary level. The study aims to assess the written texts produced by the students in order to find out how successful they are in their use of writing as a mechanism through which meaning is communicated. To achieve this aim, the researchers employed the analytic descriptive method. The subjects of the study consist of 65 Sudanese EFL teachers working at some Sudanese universities and 240 fourth level students who are taking English as a major course in five universities. Three tools were used for data collection: writing test, two questionnaires (one for the teachers and the other for the students) and an interview with the students. Analysis shows that Sudanese EFL students did cope with the different modes of writing. They were unable to make use of writing strategies such as pre-activities and organization. Furthermore, the study suggests that the students made no use of teachers and peers feedback while writing. Findings also revealed a total lack of awareness of cohesive devices on the part of the students. That is, they produced disconnected sentences and incoherent paragraphs. The study concludes that the students’ language problems, lack of organizational skills, and inability to meet the audience expectations were among the factors that would make them produce less informative written texts.

The APMP.QM-K19 was organised by TCQM of APMP to test the abilities of the national metrology institutes in the APMP region to measure a pH value of a borate buffer. This APMP comparison on pH measurement was proposed by the National Metrology Institute of Japan (NMIJ) and the National Institute of Metrology (Thailand) (NIMT) at the APMP-TCQM meeting held 26?27 November 2012. After approval by TCQM, the comparison has been conducted by NMIJ and NIMT. The comparison is a key comparison following CCQM-K19 and CCQM-K19.1. The comparison material was a borate buffer of pH around 9.2 and the measurement temperatures were 15 ?C, 25 ?C and 37 ?C. This is the second APMP key comparison on pH measurement and the fourth APMP comparison on pH measurement following APMP.QM-P06 (two phosphate buffers) in 2004, APMP.QM-P09 (a phthalate buffer) in 2006 and APMP.QM-K9/APMP.QM-P16 (a phosphate buffer) in 2010?2011. The results can be used further by any participant to support its CMC claim at least for a borate buffer. That claim will concern the pH method employed by the participant during this comparison and will cover the used temperature(s) or the full temperature range between 15?C and 37 ?C for the participant which measured pH values at the three temperatures. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

Under the auspices of the Organic Analysis Working Group (OAWG) of the Comit? Consultatif pour la Quantit? de Mati?re (CCQM) a key comparison, CCQM K55.c, was coordinated by the Bureau International des Poids et Mesures (BIPM) in 2012. Twenty National Measurement Institutes or Designated Institutes and the BIPM participated. Participants were required to assign the mass fraction of valine present as the main component in the comparison sample for CCQM-K55.c. The comparison samples were prepared from analytical grade L-valine purchased from a commercial supplier and used as provided without further treatment or purification. Valine was selected to be representative of the performance of a laboratory's measurement capability for the purity assignment of organic compounds of low structural complexity [molecular weight range 100?300] and high polarity (pKOW > ?2). The KCRV for the valine content of the material was 992.0 mg/g with a combined standard uncertainty of 0.3 mg/g. The key comparison reference value (KCRV) was assigned by combination of KCRVs assigned from participant results for each orthogonal impurity class. The relative expanded uncertainties reported by laboratories having results consistent with the KCRV ranged from 1 mg/g to 6 mg/g when using mass balance based approaches alone, 2 mg/g to 7 mg/g using quantitative 1H NMR (qNMR) based approaches and from 1 mg/g to 2.5 mg/g when a result obtained by a mass balance method was combined with a separate qNMR result. The material provided several analytical challenges. In addition to the need to identify and quantify various related amino acid impurities including leucine, isoleucine, alanine and ?-amino butyrate, care was required to select appropriate conditions for performing Karl Fischer titration assay for water content to avoid bias due to in situ formation of water by self-condensation under the assay conditions. It also proved to be a challenging compound for purity assignment by qNMR techniques. There was overall excellent agreement between participants in the identification and the quantification of the total and individual related structure impurities, water content, residual solvent and total non-volatile content of the sample. Appropriate technical justifications were developed to rationalise observed discrepancies in the limited cases where methodology differences led to inconsistent results. The comparison demonstrated that to perform a qNMR purity assignment the selection of appropriate parameters and an understanding of their potential influence on the assigned value is critical for reliable implementation of the method, particularly when one or more of the peaks to be quantified consist of complex multiplet signals. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

The supplementary comparison APMP.QM-S5 was undertaken to demonstrate the capability of participating national metrology institutes (NMIs) and designated institutes (DIs) in measuring the contents of the incurred essential elements (iron and zinc) and toxic elements (total arsenic and cadmium) at ?g/g levels in a test sample of dried shrimp by various analytical techniques. At the APMP TCQM Meeting held in Pattaya, Thailand in November 2010, Government Laboratory of the Government of the Hong Kong Special Administrative Region (GLHK) proposed this APMP supplementary comparison. The proposal was further discussed and agreed upon at the CCQM Inorganic Analysis Working Group Meeting held in Paris in April 2011. GLHK was the coordinating laboratory for the supplementary comparison. For enhancing the collaboration amongst specialized regional bodies in Asia-Pacific and to help build the laboratory capacity of NMIs/DIs from developing economies, the reference values of the supplementary comparison are used for evaluation of performance of participants of an APMP proficiency testing programme (APMP PT 11-01), an Asia-Pacific Laboratory Accreditation Cooperation proficiency testing programme (APLAC T082) and an Asia-Pacific Economic Co-operation proficiency testing programme (APEC PT), which were concurrently run using the same testing material as in APMP.QM-S5. The supplementary comparison serves to facilitate claims by participants on the Calibration and Measurement Capabilities (CMCs) as listed in Appendix C of the Key Comparison Database (KCDB) under the Mutual Recognition Arrangement of the International Committee for Weights and Measures (CIPM MRA). A total of 18 institutes registered for the supplementary comparison and all of them submitted their results. Most of the participants used microwave acid digestion methods for sample dissolution. For the instrumental determination, a variety of techniques like ICP-MS, ICP-OES, INAA and AAS were employed by the participants. For this supplementary comparison, inorganic core capabilities have been demonstrated by concerned participants with respect to methods including ICP-MS (without isotope dilution), ID-ICP-MS, ICP-OES, INAA and AAS on the determination of total arsenic, cadmium, iron and zinc in a matrix of seafood. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the APMP, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

From within AFRIMETS, the Regional Metrology Organization (RMO) for Africa, the RMO Key Comparison AFRIMETS.QM-K27 was coordinated by the National Metrology Institute of South Africa (NMISA) in 2011. Ten Metrology Institutes participated, comprising three AFRIMETS, two APMP, four EURAMET and one SIM participant. Participants were required to determine the forensic level concentration of two aqueous ethanol solutions that were gravimetrically prepared by the NMISA. Concentrations were expected to lie in the range of 0.1 mg/g to 5.0 mg/g. The accurate determination of ethanol content in aqueous medium is critical for regulatory forensic and trade purposes. The CCQM Organic Analysis Working Group has carried out several key comparisons (CCQM-K27 series) on the determination of ethanol in wine and aqueous matrices. Developing NMIs now had the opportunity to link to the earlier CCQM-K27 studies through the AFRIMETS.QM-K27 study. Gas chromatography coupled to flame ionisation or mass spectrometric detection was applied by eight of the participants, while three participants (including NMISA) applied titrimetry for the ethanol assay. The assigned reference value of the aqueous ethanol solutions was used to link AFRIMETS.QM-K27 to the CCQM-K27 key comparison reference value. The assigned reference values for AFRIMETS.QM-K27 Level 1 and Level 2 were (0.3249 ± 0.0021) mg/g (k = 2) and (4.6649 ± 0.0152) mg/g (k = 2), respectively. The reference values were determined using the purity-corrected gravimetric preparation values, while the standard uncertainty incorporated the gravimetric preparation and titrimetric homogeneity uncertainties. From previous CCQM-K27 studies, the expected spread (%CV) of higher order measurements of ethanol in aqueous medium is about 0.85% relative. In this study the CV for Level 1 is about 12% (10% with two outliers removed) and for Level 2 about 4%. Three of the ten laboratories submitted results within 1.5% of the gravimetric reference value for Level 1; four of the ten participating laboratories submitted mean results within 1.5% of the gravimetric reference value for Level 2. Two of the participating laboratories achieved mean results within 1.5% of the gravimetric reference value for both levels. Participants in the AFRIMETS-K27 study would therefore have benefited from a pilot study in which to test their measurement capability prior to participation in the key comparison. Several NMIs, however, will still be able to make new CMC claims based on their performance in this comparison. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCQM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

Traceability in analytical measurements is a key issue to ensure all measurement results are accurate, comparable and the products are safe for consumption. Therefore, validity of measurements can be assured when reference materials (RMs) are used to calibrate the equipments before the test report can be published. The role of reference materials in analytical process is outlined with specific example on high purity substances and validation process involved in quality assurance (QA). The main tasks of National Metrology Laboratory, SIRIM Berhad (NML-SIRIM) are reviewed including to ensure all measurement results are traceable to the international system of unit (SI), setting up the national primary standards and participating in international comparison organized by International Bureau of Weight and Measures (BIPM). Several advantages and crucial aspects for the validation of high purity organic RMs using quantitative nuclear magnetic resonance (qNMR) are discussed and illustrated by recent example for detection of lard in animal fats.