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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.

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).

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).