Nations' water footprints and virtual water trade of wood products

[EN] Several studies addressed the water footprint (WF) of countries and virtual water (VW) trade in agricultural and industrial products, but freshwater use associated with wood products has received little attention. Yet, international trade in wood products has been growing, and forestry competes with other forest ecosystem services over limited freshwater resources. Therefore, the objective of this paper is to assess nations' WFs of consumption of wood products, the sustainability of these WFs, and the VW flows associated with international trade in wood products. We account nations' WFs of and VW trade in wood products with a Multi-regional Input-Output model (MRIO-forest) that tracks wood flows along global supply chains (production, processing, trade, and final uses) for the period 1997-2017 and assess the sustainability of the green and blue WF of wood products in 2017. The WF of wood production increased from 8.37 x 1011 m(3)/y in 1997 to 9.87 x 1011 m(3)/y in 2017. About 38% (3.76 x 1011 m3/y) of this WF relates to wood products for export (in 2017), which means that VW trade associated with wood products ranks in between agricultural and industrial products in absolute volumes. About 10% (9.9 x 1010 m3/y) of the green WF and 11% (3.4 x 109 m3/y) of the blue WF of wood products in 2017 are unsustainable, meaning that they are located in areas where the total green/blue WF exceeds the maximum sustainable green/blue WF. The unsustainable green WF occurs mainly in Germany, Indonesia, the Czech Republic and the UK, and mainly relates to coniferous sawnwood, paper and paperboard other than newsprint, fibreboard and non-coniferous sawnwood. The unsustainable blue WF, which is much smaller, occurs in the USA, Russia. Nigeria, Canada and India, and mainly relates to fuelwood, paper and paperboard other than newsprint, sawnwood and fibreboard. This study increases our understanding of how forest evaporation flows link to the final consumption of wood products and contributes to the wider debate on the allocation of freshwater resources in the global economy.BC3 authors thank the support of the Spanish Ministry of Science, Innovation and Universities through the project Modeling and analysis of low carbon transitions (MALCON, RTI2018-099858-A-I00), and the Spanish State Research Agency through María de Maeztu Excellence Unit accreditation 2018-2022 (Ref. MDM-2017-0714, funded by MCIN/AEI/10.13039/501100011033/) and Basque Government BERC 2022-2025 Programme. I. Cazcarro thanks the support of the Spanish Ministry of Science, Innovation and Universities (State Research Agency. 2019 Call for R+D+i) PID2019-106822RB-I0 “Multisectoral and multiregional models, innovation and dynamics, for economic, social and environmental sustainability. J.F. Schyns was supported by funding from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (Earth@lternatives project, grant agreement No 834716). This article has been also a parallel study to one developed on land footprints under Letter of Agreement between the Food and Agriculture Organization of the United Nations (FAO, UN-REDD Programme) and the Basque Centre for Climate Change (BC3). BC3 authors thank the staff of the FAO and BC3 for their comments, discussions and suggestions related to forest data and policy. We are especially grateful to Malgorzata Buszko-Briggs and Tina Vahanen (FAO Forestry Department) for their contribution to frame and coordinate the research, and to Salar Tayyib, Daniela Di Filippo, Tomasz Filipczuk (FAO Statistics Division) and Arvydas Lebedys (FAO Forestry Department) for providing datasets and for their discussions and comments on data and methodological issues

Desarrollo de una placa de osteosíntesis personalizada como técnica de fijación y posicionamiento simultáneo del maxilar superior en osteotomías tipo Lefort I en cirugía ortognática

En este estudio se desarrolla una técnica de posicionamiento y fijación para osteotomías tipo Lefort I en cirugía ortognática. En concreto, se lleva a cabo una prueba de concepto de diseño de una placa de osteosíntesis multifunción customizada. Inicialmente se han analizado parámetros influyentes en la morfología y situación de la placa, según lo cual se ha diseñado la placa. Este diseño se ha validado mediante la impresión 3D de prototipos plásticos y ha sido validado por un cirujano maxilofacial especialista en cirugía ortognática. El resultado del diseño CAD (Computer-Aided Design) de la placa de osteosíntesis ha sido exitoso y se ha completado en un tiempo aceptable para una cirugía electiva. Gracias a las características de la placa se prevé que aumente la precisión del procedimiento y que, por tanto, se obtengan mejores resultados clínicos

Desarrollo de una placa de osteosíntesis personalizada como técnica de fijación y posicionamiento simultáneo del maxilar superior en osteotomías tipo Lefort I en cirugía ortognática

En este estudio se desarrolla una técnica de posicionamiento y fijación para osteotomías tipo Lefort I en cirugía ortognática. En concreto, se lleva a cabo una prueba de concepto de diseño de una placa de osteosíntesis multifunción customizada. Inicialmente se han analizado parámetros influyentes en la morfología y situación de la placa, según lo cual se ha diseñado la placa. Este diseño se ha validado mediante la impresión 3D de prototipos plásticos y ha sido validado por un cirujano maxilofacial especialista en cirugía ortognática. El resultado del diseño CAD (Computer-Aided Design) de la placa de osteosíntesis ha sido exitoso y se ha completado en un tiempo aceptable para una cirugía electiva. Gracias a las características de la placa se prevé que aumente la precisión del procedimiento y que, por tanto, se obtengan mejores resultados clínicos

Self-Assembly of CsPbBr3Perovskites in Micropatterned Polymeric Surfaces: Toward Luminescent Materials with Self-Cleaning Properties

In this work, we present a series of porous, honeycomb-patterned polymer films containing CsPbBr3 perovskite nanocrystals as light emitters prepared by the breath figure approach. Microscopy analysis of the topography and composition of the material evidence that the CsPbBr3 nanocrystals are homogeneously distributed within the polymer matrix but preferably confined inside the pores due to the fabrication process. The optical properties of the CsPbBr3 nanocrystals remain unaltered after the film formation, proving that they are stable inside the polystyrene matrix, which protects them from degradation by environmental factors. Moreover, these surfaces present highly hydrophobic behavior due to their high porosity and defined micropatterning, which is in agreement with the Cassie-Baxter model. This is evidenced by performing a proof-of-concept coating on top of 3D-printed LED lenses, conferring the material with self-cleaning properties, while the CsPbBr3 nanocrystals embedded inside the polymeric matrix maintain their luminescent behavior.This work was funded by the Ministry of Science, Innovation and Universities (project TEC2017-86102-C2-2-R) and Junta de Andalucía (Research group INNANOMAT, ref. TEP-946) and co-financed by the 2014-2020 ERDF Operational Programme and by the Department of Economy, Knowledge, Business and University of the Regional Government of Andalusia (ref: FEDER-UCA18-106586). Co-funding from UE is also acknowledged. A.S.d.L. acknowledges the Ministry of Science, Innovation and Universities for his Juan de la Cierva Incorporación postdoctoral fellowship (IJC2019-041128-I). R.A. also acknowledges the support of the Spanish MINECO through projects: Retos-Colaboración 2016 Project Safetag (no. RTC-2016-5197-2) and Retos de la Sociedad Project Nirvana (no. PID2020-119628RB-C31) by MCIN/AEI/10.13039/ 501100011033 and the “Agencia Valenciana de la Innovació” for the Valorització 2018 Project Hidronio (no. INNVAL10/ 18/032) and Valorització 2021 Project CATIOX (no. INNVA1/2021/56). R.A. also thanks the Spanish MINECO for their Ramón y Cajal Fellowship (no. RYC-2015-18349). SEM and TEM measurements were carried out at the DME-SCICyT- ELECMI-UCA

Urinary cyclophilin A as marker of tubular cell death and kidney injury

Background: Despite the term acute kidney injury (AKI), clinical biomarkers for AKI re-flect function rather than injury and independent markers of injury are needed. Tubular cell death, including necroptotic cell death, is a key feature of AKI. Cyclophilin A (CypA) is an intracellular protein that has been reported to be released during necroptosis. We have now explored CypA as a potential marker for kidney injury in cultured tubular cells and in clinical settings of ischemia-reperfusion injury (IRI), characterized by limitations of current diagnostic criteria for AKI. Meth-ods: CypA was analyzed in cultured human and murine proximal tubular epithelial cells exposed to chemical hypoxia, hypoxia/reoxygenation (H/R) or other cell death (apoptosis, necroptosis, fer-roptosis) inducers. Urinary levels of CypA (uCypA) were analyzed in patients after nephron sparing surgery (NSS) in which the contralateral kidney is not disturbed and kidney grafts with initial function. Results: Intracellular CypA remained unchanged while supernatant CypA increased in parallel to cell death induction. uCypA levels were higher in NSS patients with renal artery clamping (that is, with NSS-IRI) than in no clamping (NSS-no IRI), and in kidney transplantation (KT) recipients (KT-IRI) even in the presence of preserved or improving kidney function, while this was not the case for urinary Neutrophil gelatinase-associated lipocalin (NGAL). Furthermore, higher uCypA levels in NSS patients were associated with longer surgery duration and the incidence of AKI increased from 10% when using serum creatinine (sCr) or urinary output criteria to 36% when using high uCypA levels in NNS clamping patients. Conclusions: CypA is released by kidney tubular cells during different forms of cell death, and uCypA increased during IRI-induced clinical kidney injury independently from kidney function parameters. Thus, uCypA is a potential bi-omarker of kidney injury, which is independent from decreased kidney functionResearch by the authors was funded by FIS/ FEDER funds (PI17/00257, PI18/01386, PI19/00588, PI19/00815, DTS18/00032, ERA-PerMed-JTC2018 (KIDNEY ATTACK AC18/00064 and PERSTIGAN AC18/00071, ISCIII-RETIC REDinREN RD016/0009), Sociedad Española de Nefrología, FRIAT, Comunidad de Madrid en Biomedicina B2017/BMD-3686 CIFRA2-CM. Salary support: ISCIII Miguel Servet to A.B.S., MICIN Ramon y Cajal to M.D.S.-N., REDinREN RD016/0009 to M.F.-B.,SENEFRO to D.M.-S. and Consejería de Educación, Juventud y Deporte (Comunidad de Madrid/FSE) to A.M.L.-

Relevant domains, core outcome sets and measurements for implant dentistry clinical trials: The Implant Dentistry Core Outcome Set and Measurement (ID-COSM) international consensus report

AIM: Lack of consistently reported outcomes limits progress in evidence-based implant dentistry and quality of care. The objective of this initiative was to develop a core outcome set (COS) and measurements for implant dentistry clinical trials (ID-COSM). MATERIALS AND METHODS: This Core Outcome Measures in Effectiveness Trials (COMET)-registered international initiative comprised six steps over 24 months: (i) systematic reviews of outcomes reported in the last 10 years; (ii) international patient focus groups; (iii) a Delphi project with a broad range of stakeholders (care providers, clinical researchers, methodologists, patients and industry representatives); (iv) expert group discussions organizing the outcomes in domains using a theoretical framework and identifying the COSs; (v) identification of valid measurement systems to capture the different domains and (vi) final consensus and formal approval involving experts and patients. The methods were modified from the best practice approach following the Outcome Measures in Rheumatoid Arthritis Clinical Trial and COMET manuals. RESULTS: The systematic reviews and patient focus groups identified 754 (665 + 89, respectively) relevant outcome measures. After elimination of redundancies and duplicates, 111 were formally assessed in the Delphi project. By applying pre-specified filters, the Delphi process identified 22 essential outcomes. These were reduced to 13 after aggregating alternative assessments of the same features. The expert committee organized them into four core outcome areas: (i) pathophysiology, (ii) implant/prosthesis lifespan, (iii) life impact and (iv) access to care. In each area, core outcomes were identified to capture both the benefits and harms of therapy. Mandatory outcome domains included assessment of surgical morbidity and complications, peri-implant tissue health status, intervention-related adverse events, complication-free survival and overall patient satisfaction and comfort. Outcomes deemed mandatory in specific circumstances comprised function (mastication, speech, aesthetics and denture retention), quality of life, effort for treatment and maintenance and cost effectiveness. Specialized COSs were identified for bone and soft-tissue augmentation procedures. The validity of measurement instruments ranged from international consensus (peri-implant tissue health status) to early identification of important outcomes (patient-reported outcomes identified by the focus groups). CONCLUSIONS: The ID-COSM initiative reached a consensus on a core set of mandatory outcomes for clinical trials in implant dentistry and/or soft tissue/bone augmentation. Adoption in future protocols and reporting on the respective domain areas by currently ongoing trials will contribute to improving evidence-informed implant dentistry and quality of care

Relevant domains, core outcome sets and measurements for implant dentistry clinical trials: The Implant Dentistry Core Outcome Set and Measurement (ID-COSM) international consensus report

AimLack of consistently reported outcomes limits progress in evidence‐based implant dentistry and quality of care. The objective of this initiative was to develop a core outcome set (COS) and measurements for implant dentistry clinical trials (ID‐COSM).Materials and MethodsThis Core Outcome Measures in Effectiveness Trials (COMET)‐registered international initiative comprised six steps over 24 months: (i) systematic reviews of outcomes reported in the last 10 years; (ii) international patient focus groups; (iii) a Delphi project with a broad range of stakeholders (care providers, clinical researchers, methodologists, patients and industry representatives); (iv) expert group discussions organizing the outcomes in domains using a theoretical framework and identifying the COSs; (v) identification of valid measurement systems to capture the different domains and (vi) final consensus and formal approval involving experts and patients. The methods were modified from the best practice approach following the Outcome Measures in Rheumatoid Arthritis Clinical Trial and COMET manuals.ResultsThe systematic reviews and patient focus groups identified 754 (665 + 89, respectively) relevant outcome measures. After elimination of redundancies and duplicates, 111 were formally assessed in the Delphi project. By applying pre‐specified filters, the Delphi process identified 22 essential outcomes. These were reduced to 13 after aggregating alternative assessments of the same features. The expert committee organized them into four core outcome areas: (i) pathophysiology, (ii) implant/prosthesis lifespan, (iii) life impact and (iv) access to care. In each area, core outcomes were identified to capture both the benefits and harms of therapy. Mandatory outcome domains included assessment of surgical morbidity and complications, peri‐implant tissue health status, intervention‐related adverse events, complication‐free survival and overall patient satisfaction and comfort. Outcomes deemed mandatory in specific circumstances comprised function (mastication, speech, aesthetics and denture retention), quality of life, effort for treatment and maintenance and cost effectiveness. Specialized COSs were identified for bone and soft‐tissue augmentation procedures. The validity of measurement instruments ranged from international consensus (peri‐implant tissue health status) to early identification of important outcomes (patient‐reported outcomes identified by the focus groups).ConclusionsThe ID‐COSM initiative reached a consensus on a core set of mandatory outcomes for clinical trials in implant dentistry and/or soft tissue/bone augmentation. Adoption in future protocols and reporting on the respective domain areas by currently ongoing trials will contribute to improving evidence‐informed implant dentistry and quality of care

Effect of peri-implant mucosal thickness on esthetic outcomes and the efficacy of soft tissue augmentation procedures: Consensus report of group 2 of the SEPA/DGI/OF workshop

OBJECTIVES The aim of this study was to comprehensively assess the literature in terms of the effect of peri-implant mucosal thickness on esthetic outcomes and the efficacy of soft tissue augmentation procedures to increase the mucosal thickness with autogenous grafts or soft tissue substitutes. MATERIAL AND METHODS Two systematic reviews (SR) were performed prior to the consensus meeting to assess the following questions. Review 1, focused question: In systemically healthy patients with an implant-supported fixed prosthesis, what is the influence of thin as compared to thick peri-implant mucosa on esthetic outcomes? Review 2, focused question 1: In systemically healthy humans with at least one dental implant (immediate or staged implant), what is the efficacy of connective tissue graft (CTG), as compared to absence of a soft tissue grafting procedure, in terms of gain in peri-implant soft tissue thickness (STT) reported by randomized controlled clinical trials (RCTs) or controlled clinical trials (CCTs)? Review 2, focused question 2: In systemically healthy humans with at least one dental implant (immediate or staged implant), what is the efficacy of CTG, as compared to soft tissue substitutes, in terms of gain in peri-implant STT reported by RCTs or CCTs? The outcomes of the two SRs, the consensus statements, the clinical implications, and the research recommendations were discussed and subsequently approved at the consensus meeting during the group and plenary sessions. CONCLUSIONS There was a tendency of superior esthetic outcomes in the presence of a thick mucosa. The connective tissue graft remains the standard of care in terms of increasing mucosa thickness

Los Olmos empiezan a recuperar sus territorios

El artículo describe la problemática de la grafiosis y el papel del proyecto LIFE+"Olmos Vivos" (LIFE13 BIO/ES/000556)en la recuperación de los olmos

Performance of Magnetic-Superconductor Non-Contact Harmonic Drive for Cryogenic Space Applications

Harmonic drives are profusely used in aerospace mainly because of their compactness and large reduction ratio. However, their use in cryogenic environments is still a challenge. Lubrication and fatigue are non-trivial issues under these conditions. The objective of the Magnetic-Superconductor Cryogenic Non-contact Harmonic Drive (MAGDRIVE) project, funded by the EU Space FP7, is to design, build, and test a new concept of MAGDRIVE. Non-contact interactions among magnets, soft magnetic materials, and superconductors are efficiently used to provide a high reduction ratio gear that smoothly and naturally operates at cryogenic environments. The limiting elements of conventional harmonic drives (teeth, flexspline, and ball bearings) are substituted by contactless mechanical components (magnetic gear and superconducting magnetic bearings). The absence of contact between moving parts prevents wear, lubricants are no longer required, and the operational lifetime is greatly increased. This is the first mechanical reducer in mechanical engineering history without any contact between moving parts. In this paper, the test results of a −1:20 inverse reduction ratio MAGDRIVE prototype are reported. In these tests, successful operation at 40 K and 10−3 Pa was demonstrated for more than 1.5 million input cycles. A maximum torque of 3 N·m and an efficiency of 80% were demonstrated. The maximum tested input speed was 3000 rpm, six times the previous existing record for harmonic drives at cryogenic temperature