A Novel Hybrid Wind-Wave Energy Converter for Jacket-Frame Substructures

The research dataset supporting this publication can be accessed at http://hdl.handle.net/10026.1/11045.The growth of the offshore wind industry in the last couple of decades has made this technology a key player in the maritime sector. The sustainable development of the offshore wind sector is crucial for this to consolidate within a global scenario of climate change and increasing threats to the marine environment. In this context, multipurpose platforms have been proposed as a sustainable approach to harnessing different marine resources and combining their use under the same platform. Hybrid wind-wave systems are a type of multipurpose platform where a single platform combines the exploitation of offshore wind and wave energy. In particular, this paper deals with a novel hybrid wind-wave system that integrates an oscillating water column wave energy converter with an offshore wind turbine on a jacket-frame substructure. The main objective of this paper is to characterise the hydrodynamic response of the WEC sub-system of this hybrid energy converter. A 1:50 scale model was tested under regular and irregular waves to characterise the hydrodynamic response of the WEC sub-system. The results from this analysis lead to the proof of concept of this novel hybrid system; but additionally, to characterising its behaviour and interaction with the wave field, which is a requirement for fully understanding the benefits of hybrid systems

Pensar el cine blockbuster : el rol de la educación y el conocimiento en Indiana Jones y el Reino de la Calavera de Cristal

The Indiana Jones series is on the foundation of the so called «blockbuster» phenomenon, a cinema that represents huge financial investments for the studios every year but is usually disregarded by scholars as empty. Despite that, it would be fair to ask if blockbuster movies can transmit a given «ethos» beyond entertainment. The movie «Indiana Jones and the Kingdom of the Crystal Skull» is analyzed here to show that, along with the pursuit of economic profits, it is possible to find more complex intentions. In this specific case, education is fostered as an essential human value that must be cultivated

SÍNTESIS Y CARACTERIZACIÓN DE COMPUESTOS DE COORDINACIÓN: UNA

El presente trabajo muestra los resultados exitosos en el desarrollo de un curso de laboratorio de química inorgánica mediante la implementación del modelo de Aprendizaje por Investigación, como una estrategia integradora de conocimientos que permite a los estudiantes el desarrollo de competencias de reconocimiento, interpretación y producción relacionadas con los procesos de síntesis de compuestos de coordinación de interés en el área de la química inorgánica. El desarrollo riguroso de la metodología científica condujo a la comprensión y aplicación de las teorías de enlace de valencia y orbital molecular, la teoría de coordinación de Werner y la teoría de campo cristalino; como también principios de simetría, teoría de grupos y espectroscopía infrarroja, IR

The impact of resolution on ship plume simulations with NOx chemistry

A high resolution chemical transport model of the marine boundary layer is designed in order to investigate the detailed chemical evolution of a ship plume in a tropical location. To estimate systematic errors due to finite model resolution, otherwise identical simulations are run at a range of model resolutions. Notably, to obtain comparable plumes in the different simulations, it is found necessary to use an advection scheme consistent with the Large Eddy Model representation of sub-grid winds for those simulations with degraded resolution. Our simulations show that OH concentration, NOx lifetime and ozone production efficiency of the model change by 8%, 32% and 31% respectively between the highest (200 m x 200 m x 40 m) and lowest resolution (9600 m x 9600 m x 1920 m) simulations. Interpolating to the resolution of a typical global composition transport model (CTM, 5 degrees x 5 degrees), suggests that a CTM overestimates OH, NOx lifetime and ozone production efficiency by approximately 15%, 55% and 59% respectively. For the first time, by explicitly degrading the model spatial resolution we show that there is a significant reduction in model skill in accurately simulating the aforementioned quantities due to the coarse resolution of these CTMs and the non-linear nature of atmospheric chemistry. These results are significant for the assessment and forecasting of the climate impact of ship NOx and indicate that for realistic representation of ship plume emissions in CTMs, some suitable parametrisation is necessary at current global model resolutions

The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy

Background: Hypertrophic (HCM) and dilated (DCM) cardiomyopathies results from sarcomeric protein mutations, including cardiac troponin T (cTnT, TNNT2). We determined whether TNNT2 mutations cause cardiomyopathies by altering cTnT function or quantity; whether the severity of DCM is related to the ratio of mutant to wildtype cTnT; whether Ca2+ desensitization occurs in DCM; and whether absence of cTnT impairs early embryonic cardiogenesis. Methods and Findings: We ablated Tnnt2 to produce heterozygous Tnnt2+/ mice, and crossbreeding produced homozygous null Tnnt2-/-embryos. We also generated transgenic mice overexpressing wildtype (TGWT) or DCM mutant (TGK210Δ) Tnnt2. Crossbreeding produced mice lacking one allele of Tnnt2, but carrying wildtype (Tnnt2+/-/TGWT) or mutant (Tnnt2+/-/TGK210Δ) transgenes. Tnnt2+/-mice relative to wildtype had significantly reduced transcript (0.82 ± 0.06 [SD] vs. 1.00 ± 0.12 arbitrary units; p = 0.025), but not protein (1.01 ± 0.20 vs. 1.00 ± 0.13 arbitrary units; p = 0.44). Tnnt2+/-mice had normal hearts (histology, mass, left ventricular end diastolic diameter [LVEDD], fractional shortening [FS]). Moreover, whereas Tnnt2+/-/ TGK210Δ mice had severe DCM, TGK210Δ mice had only mild DCM (FS 18 ± 4 vs. 29 ± 7%; p < 0.01). The difference in severity of DCM may be attributable to a greater ratio of mutant to wildtype Tnnt2 transcript in Tnnt2+/-/TGK210Δ relative to TGK210Δ mice (2.42±0.08, p = 0.03). Tnnt2+/-/TGK210Δ muscle showed Ca2+ desensitization (pCa50 = 5.34 ± 0.08 vs. 5.58 ± 0.03 at sarcomere length 1.9 μm. p<0.01), but no difference in maximum force generation. Day 9.5 Tnnt2-/-embryos had normally looped hearts, but thin ventricular walls, large pericardial effusions, noncontractile hearts, and severely disorganized sarcomeres. Conclusions: Absence of one Tnnt2 allele leads to a mild deficit in transcript but not protein, leading to a normal cardiac phenotype. DCM results from abnormal function of a mutant protein, which is associated with myocyte Ca2+ desensitization. The severity of DCM depends on the ratio of mutant to wildtype Tnnt2 transcript. cTnT is essential for sarcomere formation, but normal embryonic heart looping occurs without contractile activity. © 2008 Ahmad et al

Dengue fever in pregnancy: a case report

<p>Abstract</p> <p>Background</p> <p>Dengue, a mosquito-borne flavivirus infection, is endemic in Southeast Asia. Currently, the incidence has been increasing among adults.</p> <p>Case presentation</p> <p>A 26-year-old Thai woman, G₁P₀ 31 weeks pregnancy, presented with epigastric pain for 1 day. She also had a high-grade fever for 4 days. The physical examination, complete blood counts as well as serology confirmed dengue fever. The patient was under conservative treatment despite severe thrombocytopenia. She was well at the 3^rd day of discharge and 1-week follow-up. The pregnancy continued until term without any complication and she delivered vaginally a healthy female baby.</p> <p>Conclusions</p> <p>More cases of dengue infection in pregnancy can be found due to the increasing incidence during adulthood. It should be suspected when a pregnant woman presents with symptoms and signs like in a non-pregnant. Conservative treatment should be conducted unless there are any complications.</p

Dengue Deaths in Puerto Rico: Lessons Learned from the 2007 Epidemic

Dengue is a major public health problem in the tropics and subtropics; an estimated 50 million cases occur annually and 40 percent of the world's population lives in areas with dengue virus (DENV) transmission. Dengue has a wide range of clinical presentations from an undifferentiated acute febrile illness, classic dengue fever, to severe dengue (i.e., dengue hemorrhagic fever or dengue shock syndrome). About 5% of patients develop severe dengue, which is more common with second or subsequent infections. No vaccines are available to prevent dengue, and there are no specific antiviral treatments for patients with dengue. However, early recognition of shock and intensive supportive therapy can reduce risk of death from ∼10% to less than 1% among severe dengue cases. Reviewing dengue deaths is one means to identify issues in clinical management. These findings can be used to develop healthcare provider education to minimize dengue morbidity and mortality

Tightening slip knots in raw and degummed silk to increase toughness without losing strength

NMP is supported by the European Research Council (ERC StG Ideas 2011 BIHSNAM n. 279985 on “Bio-Inspired hierarchical super-nanomaterials”, ERC PoC 2013-1 REPLICA2 n. 619448 on “Large-area replication of biological anti-adhesive nanosurfaces”, ERC PoC 2013-2 KNOTOUGH n. 632277 on “Super-tough knotted fibres”), by the European Commission under the Graphene Flagship (WP10 “Nanocomposites”, n. 604391) and by the Provincia Autonoma di Trento (“Graphene Nanocomposites”, n. S116/2012-242637 and reg.delib. n. 2266)

Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene

<p>Abstract</p> <p>Background</p> <p>Ellis-van Creveld (EvC) syndrome is characterized by short limbs, short ribs, postaxial polydactyly, dysplastic nails and teeth and is inherited in an autosomal recessive pattern. We report a family with complex septal cardiac defects, rhizomelic limb shortening, and polydactyly, without the typical lip, dental, and nail abnormalities of EvC. The phenotype was inherited in an autosomal recessive pattern, with one instance of pseudodominant inheritance.</p> <p>Methods</p> <p>Because of the phenotypic overlap with EvC, microsatellite markers were used to test for linkage to the <it>EVC/EVC2 </it>locus. The results did not exclude linkage, so samples were sequenced for mutations.</p> <p>Results</p> <p>We identified a c.1868T>C mutation in <it>EVC</it>, which predicts p.L623P, and was homozygous in affected individuals.</p> <p>Conclusion</p> <p>We conclude that this <it>EVC </it>mutation is hypomorphic and that such mutations can cause a phenotype of cardiac and limb defects that is less severe than typical EvC. <it>EVC </it>mutation analysis should be considered in patients with cardiac and limb malformations, even if they do not manifest typical EvC syndrome.</p

Extending the spectrum of Ellis van Creveld syndrome: a large family with a mild mutation in the EVC gene

<p>Abstract</p> <p>Background</p> <p>Ellis-van Creveld (EvC) syndrome is characterized by short limbs, short ribs, postaxial polydactyly, dysplastic nails and teeth and is inherited in an autosomal recessive pattern. We report a family with complex septal cardiac defects, rhizomelic limb shortening, and polydactyly, without the typical lip, dental, and nail abnormalities of EvC. The phenotype was inherited in an autosomal recessive pattern, with one instance of pseudodominant inheritance.</p> <p>Methods</p> <p>Because of the phenotypic overlap with EvC, microsatellite markers were used to test for linkage to the <it>EVC/EVC2 </it>locus. The results did not exclude linkage, so samples were sequenced for mutations.</p> <p>Results</p> <p>We identified a c.1868T>C mutation in <it>EVC</it>, which predicts p.L623P, and was homozygous in affected individuals.</p> <p>Conclusion</p> <p>We conclude that this <it>EVC </it>mutation is hypomorphic and that such mutations can cause a phenotype of cardiac and limb defects that is less severe than typical EvC. <it>EVC </it>mutation analysis should be considered in patients with cardiac and limb malformations, even if they do not manifest typical EvC syndrome.</p