Analysis of Circular Economy Research and Innovation (R&I) intensity for critical products in the supply chains of strategic technologies.

To develop renewable energy, digital, space and defence technologies, the European Union (EU) needs access to critical raw materials of which a large share is currently imported from third countries. To mitigate the risk of supply disruptions, the Critical Raw Materials Act proposes to diversify sources of imports, while increasing domestic extraction, processing, and recycling. The circular economy is therefore positioned as a key element of the EU strategy to deploy strategic technologies for navigating the sustainability transition in a complex geopolitical landscape. In line with this position, the present study analyses the intensity of circular economy research and innovation (R&I) in the supply chains of strategic technologies. The focus is placed on four critical products containing raw materials having high supply risks: lithium-ion battery cells; neodymium-iron-boron permanent magnets; photovoltaic cells; hydrogen electrolysers and fuel-cells. The R&I analysis is based on the identification of scientific articles, patents, and innovation projects on the subject, with a global scope, in the period between 2014 and 2022. The analysis is enriched by connecting to parallel work on the subject, conducted by Joint Research Centre (JRC) as well as academic institutions, industry, and policy stakeholders. This is functional to provide insight into: where circularity efforts R&I have been placed in terms of different products and supply chains; which countries are undertaking these efforts; how the EU is positioned and how much funding was deployed so far; what are the current gaps and trends going forward. Main insights include the following: 1) circularity R&I for critical products is not balanced, with a prominent focus placed on Li-ion cells on a global level 2) the EU has followed this trend in terms of number of innovation projects and public spending; 3) Next to EU efforts, China and the USA focus intensely on circular economy R&I as well. This study contributes with evidence to advance scientific research and policymaking on the role of a circular economy to achieve open strategic autonomy and climate neutrality in the EU

Efecto de las características psicográficas en la intención de compra de marcas privadas en Chile

Private Labels are steadily but slowly included in Chileans´ consumption baskets. However, they have not reached the market share and penetration levels of European countries. The main objective of this article is to study how customers` psychographics affect private labels buying intentions. A shopping center intercept study was conducted, interviewing 300 female shoppers, regarding 14 psychographic variables and private labels purchase intentions. Nine product categories were used, in order to improve the generalizability of findings. Using discriminant analysis, the relative importance of each psychographic variable to explain private labels´ purchasing intentions was assessed, in order to help retailers and manufacturers optimize their marketing efforts of private labels.Las marcas privadas se han incorporado estable, pero lentamente en las canastas de compra de los chilenos. Sin embargo, ellas no han alcanzado los niveles de participación de mercado y penetración que se observan en países europeos. El principal objetivo de este artículo es estudiar cómo las características psicográficas de los consumidores pueden afectar la intención de compra de las marcas privadas. Para ello, se realizó una encuesta de intercepción de mall a 300 compradoras, en relación a 14 variables psicográficas y a la intención de compra de marcas privadas. Se usaron nueve categorías de productos como una manera de aumentar la posibilidad de generalización de los resultados. Utilizando la técnica de análisis discriminante, se estableció la importancia de cada variable para explicar las intenciones de compra de marcas privadas y así orientar de mejor forma los esfuerzos de marketing de marcas privadas por parte de detallistas y fabricantes

Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane

Tecta is a modular, non-collagenous protein of the tectorial membrane, an extracellular matrix of the cochlea essential for normal hearing. Missense mutations in Tecta cause dominant forms of nonsyndromic deafness and a genotype-phenotype correlation has been reported in humans, with mutations in different Tecta domains causing mid- or high-frequency hearing impairments that are either stable or progressive. Three mutant mice were created as models for human Tecta mutations; the TectaL1820F, G1824D/+ mouse for zona pellucida (ZP) domain mutations causing stable mid-frequency hearing loss in a Belgian family, the TectaC1837G/+ mouse for a ZP-domain mutation underlying progressive mid-frequency hearing loss in a Spanish family, and the TectaC1619S/+ mouse for a zonadhesin-like (ZA) domain mutation responsible for progressive, high-frequency hearing loss in a French family. Mutations in the ZP and ZA domains generate distinctly different changes in the structure of the tectorial membrane. ABR thresholds in the 8-40 kHz range are elevated by 30-40 dB in the ZP-domain mutants, whilst those in the ZA-domain mutant are elevated by 20-30 dB. The phenotypes are stable and no evidence has been found for a progressive deterioration in tectorial membrane structure or auditory function. Despite elevated auditory thresholds, the Tecta mutant mice all exhibit an enhanced tendency to have audiogenic seizures in response to white noise stimuli at low sound pressure levels (≤84 dB SPL), revealing a previously unrecognised consequence of Tecta mutations. These results, together with those from previous studies, establish an allelic series for Tecta unequivocally demonstrating an association between genotype and phenotype

Co-directional replication-transcription conflicts lead to replication restart

August 24, 2011Head-on encounters between the replication and transcription machineries on the lagging DNA strand can lead to replication fork arrest and genomic instability1, 2. To avoid head-on encounters, most genes, especially essential and highly transcribed genes, are encoded on the leading strand such that transcription and replication are co-directional. Virtually all bacteria have the highly expressed ribosomal RNA genes co-directional with replication3. In bacteria, co-directional encounters seem inevitable because the rate of replication is about 10–20-fold greater than the rate of transcription. However, these encounters are generally thought to be benign2, 4, 5, 6, 7, 8, 9. Biochemical analyses indicate that head-on encounters10 are more deleterious than co-directional encounters8 and that in both situations, replication resumes without the need for any auxiliary restart proteins, at least in vitro. Here we show that in vivo, co-directional transcription can disrupt replication, leading to the involvement of replication restart proteins. We found that highly transcribed rRNA genes are hotspots for co-directional conflicts between replication and transcription in rapidly growing Bacillus subtilis cells. We observed a transcription-dependent increase in association of the replicative helicase and replication restart proteins where head-on and co-directional conflicts occur. Our results indicate that there are co-directional conflicts between replication and transcription in vivo. Furthermore, in contrast to the findings in vitro, the replication restart machinery is involved in vivo in resolving potentially deleterious encounters due to head-on and co-directional conflicts. These conflicts probably occur in many organisms and at many chromosomal locations and help to explain the presence of important auxiliary proteins involved in replication restart and in helping to clear a path along the DNA for the replisome.Biotechnology and Biological Sciences Research Council (Great Britain) (Grant BB/E006450/1)Wellcome Trust (London, England) (Grant 091968/Z/10/Z)National Institutes of Health (U.S.) (Grant GM41934)National Institutes of Health (U.S.) (Postdoctoral Fellowship GM093408)Biotechnology and Biological Sciences Research Council (Great Britain) (Sabbatical Visit

Co-Orientation of Replication and Transcription Preserves Genome Integrity

In many bacteria, there is a genome-wide bias towards co-orientation of replication and transcription, with essential and/or highly-expressed genes further enriched co-directionally. We previously found that reversing this bias in the bacterium Bacillus subtilis slows replication elongation, and we proposed that this effect contributes to the evolutionary pressure selecting the transcription-replication co-orientation bias. This selection might have been based purely on selection for speedy replication; alternatively, the slowed replication might actually represent an average of individual replication-disruption events, each of which is counter-selected independently because genome integrity is selected. To differentiate these possibilities and define the precise forces driving this aspect of genome organization, we generated new strains with inversions either over ∼1/4 of the chromosome or at ribosomal RNA (rRNA) operons. Applying mathematical analysis to genomic microarray snapshots, we found that replication rates vary dramatically within the inverted genome. Replication is moderately impeded throughout the inverted region, which results in a small but significant competitive disadvantage in minimal medium. Importantly, replication is strongly obstructed at inverted rRNA loci in rich medium. This obstruction results in disruption of DNA replication, activation of DNA damage responses, loss of genome integrity, and cell death. Our results strongly suggest that preservation of genome integrity drives the evolution of co-orientation of replication and transcription, a conserved feature of genome organization

Partner notification for sexually transmitted infections in developing countries: a systematic review

<p>Abstract</p> <p>Background</p> <p>The feasibility and acceptability of partner notification (PN) for sexually transmitted infections (STIs) in developing countries was assessed through a comprehensive literature review, to help identify future intervention needs.</p> <p>Methods</p> <p>The Medline, Embase, and Google Scholar databases were searched to identify studies published between January 1995 and December 2007 on STI PN in developing countries. A systematic review of the research extracted information on: (1) willingness of index patients to notify partners; (2) the proportion of partners notified or referred; (3) client-reported barriers in notifying partners; (4) infrastructure barriers in notifying partners; and (5) PN approaches that were evaluated in developing countries.</p> <p>Results</p> <p>Out of 609 screened articles, 39 met our criteria. PN outcome varied widely and was implemented more often for spousal partners than for casual or commercial partners. Reported barriers included sociocultural factors such as stigma, fear of abuse for having an STI, and infrastructural factors related to the limited number of STD clinics, and trained providers and reliable diagnostic methods. Client-oriented counselling was found to be effective in improving partner referral outcomes.</p> <p>Conclusions</p> <p>STD clinics can improve PN with client-oriented counselling, which should help clients to overcome perceived barriers. The authors speculate that well-designed PN interventions to evaluate the impact on STI prevalence and incidence along with cost-effectiveness components will motivate policy makers in developing countries to allocate more resources towards STI management.</p

MicroMotility: State of the art, recent accomplishments and perspectives on the mathematical modeling of bio-motility at microscopic scales

Mathematical modeling and quantitative study of biological motility (in particular, of motility at microscopic scales) is producing new biophysical insight and is offering opportunities for new discoveries at the level of both fundamental science and technology. These range from the explanation of how complex behavior at the level of a single organism emerges from body architecture, to the understanding of collective phenomena in groups of organisms and tissues, and of how these forms of swarm intelligence can be controlled and harnessed in engineering applications, to the elucidation of processes of fundamental biological relevance at the cellular and sub-cellular level. In this paper, some of the most exciting new developments in the fields of locomotion of unicellular organisms, of soft adhesive locomotion across scales, of the study of pore translocation properties of knotted DNA, of the development of synthetic active solid sheets, of the mechanics of the unjamming transition in dense cell collectives, of the mechanics of cell sheet folding in volvocalean algae, and of the self-propulsion of topological defects in active matter are discussed. For each of these topics, we provide a brief state of the art, an example of recent achievements, and some directions for future research