New Product Development in Small Food Enterprises

Purpose – The purpose of this paper is to demonstrate how small businesses may deploy a formalised Stage-Gate approach to new product development (NPD). The original Stage-Gate framework was modified to better suit a small business B2B environment in the seafood industry, and was subsequently applied to a small vertically-integrated crab catching, processing and marketing business.Design/methodology/approach – This paper uses a case study methodology. The method used at each stage of the Stage-Gate framework, as well as the time and location details, the people and skills involved, and the evaluative criteria applied for NPD are outlined and discussed; and subsequently synthesized in a modified framework.Findings – The modified Stage-Gate approach was shown to be an effective NPD method, allowing for 92 initial product concepts to be narrowed down to three commercially viable and acceptable products, over a period of less than 11 months. Cost and time were minimised by the four-day ideation process. Furthermore, repeated evaluation of the sensory and market acceptability resulted in strengthened confidence in market attractiveness, while ensuring that appearance, portion size and packaging were based on expert market opinion. Moreover, this approach was successfully completed at less than 25% of the cost of the previous unsuccessful NPD undertaken by the firm.Originality/value – This study advances our understanding of how small businesses may use a formal NPD process to increase the success rate of new products, through development of a modified Stage-Gate approach

A cultural challenge for the Western Australian legal profession: a lack of diversity at the WA Bar?

At the request of the Western Australian Bar Association, the authors undertook a study into issues of diversity at the Western Australian Bar. Members of the Association had noticed, but not specifically studied, various demographic imbalances in the Bar’s constitution. A review of the literature revealed that there was a paucity of statistical analysis of the makeup of Australian barrister associations generally, let alone into any specific reasons as to how and why a demographic imbalance might exist. Recognising that a clearer picture of the breakdown of the demographics of the Western Australian legal profession and of the specific cultures that might exist at the Bar was needed, the authors undertook a study that examined whether there was an existing legal monoculture at the Bar, and if so what some of the reasons for this might be

Complete Genome Sequence of Mesorhizobium ciceri Strain CC1192, an Efficient Nitrogen-Fixing Microsymbiont of Cicer arietinum.

We report the complete genome sequence of Mesorhizobium ciceri strain CC1192, an efficient nitrogen-fixing microsymbiont of Cicer arietinum (chickpea). The genome consists of 6.94 Mb distributed between a single chromosome (6.29 Mb) and a plasmid (0.65 Mb)

Complete Genome Sequence of Mesorhizobium ciceri bv. biserrulae Strain WSM1284, an Efficient Nitrogen-Fixing Microsymbiont of the Pasture Legume Biserrula pelecinus.

We report the complete genome sequence of Mesorhizobium ciceri bv. biserrulae strain WSM1284, a nitrogen-fixing microsymbiont of the pasture legume Biserrula pelecinus The genome consists of 6.88 Mb distributed between a single chromosome (6.33 Mb) and a single plasmid (0.55 Mb)

Improving Grassland Quality in Communal Arable Lands in the Eastern Cape Province, South Africa

Overgrazing and shifting cultivation practise have severely degraded communal lands in the Eastern Cape of South Africa. Methods need to be developed to improve forage quality of grazing land, especially previously cultivated lands. The aim of the study was to investigate legume species to rehabilitate arable lands abandoned from cropping, to enhance their forage quality, productivity and ecological integrity. The study was conducted in seven communities within the Eastern Cape Province. This study showed that within the communal lands studied extensive areas have been cultivated and the majority of this land is now poorly utilised. Natural grasslands ploughed for cropping did not recover its original composition and therefore lost its primary ecological condition. New improved legume cultivars can significantly enhance forage quality on cultivated lands but individual species may not have the resilience to survive nutrient poor lands and variable winter rainfall. This study shows that using a mixture of annual and perennial legume species with different life traits contributed to enhanced forage quality, especially during winter when the nutritional value of grasses was low. Because of management constraints, pasture legumes cannot be seen as stand-alone pastures, but provide a mechanism to extend the forage potential of communal grazing lands

Mining the sequence data of Rhizobium Leguminosarum BV Trifolii WSM1325 and WM2304

Most clover rhizobial inoculants form effective nitrogen-fixing symbioses with either annual or perennial species (and very few with both). This constraint provides a considerable barrier to agricultural productivity since background populations of R. trifolii may nodulate with an incompatible host but ineffectively fix nitrogen (Yates et al 2008)

Structural phase transitions in the geometric ferroelectric LaTa O4

Funding: School of Chemistry, University of St Andrews for funding of a studentship to GWH through the EPSRC doctoral training grant (Grant No. EP/N509759/1). This work was also facilitated by funding provided by the EPSRC (Grant No. EP/P024637/1). K.K.M. and R.S.K. acknowledge financial support from the Department of Defense, USA (DoD Grant No. FA9550-20-1-0064). The RUS component of this work was funded by EPSRC Grant No. EP/P024904/1.The recent report of an intermediate incommensurately modulated orthorhombic phase in LaTaO4 has prompted a re-examination of the phase transition sequence in LaTaO4 as a function of temperature. With falling temperature, the sequence of phases examined is (orthorhombic) Cmc21(C)↔Cmc21(IC)↔(monoclinic)P21/c, with C and IC denoting commensurate and incommensurate phases, respectively. The orthorhombic to monoclinic transition, Tm-o, is a first order reconstructive transition occurring at 440 K and TIC-C is a first-order displacive transition occurring at 500-530 K. Strain and elasticity data confirm a first-order transition between the basic and modulated Cmc21 phases, with similarities to the isostructural fluoride BaMnF4. A Raman spectroscopic study of the LaTaO4 phase transition indicates that the IC-C phase transition is driven by a soft zone-boundary phonon (unstable) of the commensurate orthorhombic (Cmc21) phase. The soft phonon is found to appear (underdamped) above 443 K and vanishes (overdamped) around 528 K. A large supercell of the monoclinic phase below Tm-o is proposed based on the Raman spectroscopic results.Publisher PDFPeer reviewe

High-quality permanent draft genome sequence of the Parapiptadenia rigida-nodulating Burkholderia sp. strain UYPR1.413

Burkholderia sp. strain UYPR1.413 is an aerobic, motile, Gram-negative, non-spore-forming rod that was isolated from a root nodule of Parapiptadenia rigida collected at the Angico plantation, Mandiyu, Uruguay, in December 2006. A survey of symbionts of P. rigida in Uruguay demonstrated that this species is nodulated predominantly by Burkholderia microsymbionts. Moreover, Burkholderia sp. strain UYPR1.413 is a highly efficient nitrogen fixing symbiont with this host. Currently, the only other sequenced isolate to fix with this host is Cupriavidus sp. UYPR2.512. Therefore, Burkholderia sp. strain UYPR1.413 was selected for sequencing on the basis of its environmental and agricultural relevance to issues in global carbon cycling, alternative energy production, and biogeochemical importance, and is part of the GEBA-RNB project. Here we describe the features of Burkholderia sp. strain UYPR1.413, together with sequence and annotation. The 10,373,764 bp high-quality permanent draft genome is arranged in 336 scaffolds of 342 contigs, contains 9759 protein-coding genes and 77 RNA-only encoding genes