Solar Energy in Space Applications: Review and Technology Perspectives

Solar cells (SCs) are the most ubiquitous and reliable energy generation systems for aerospace applications. Nowadays, III-V multijunction solar cells (MJSCs) represent the standard commercial technology for powering spacecraft, thanks to their high-power conversion efficiency and certified reliability/stability while operating in orbit. Nevertheless, spacecraft companies are still using cheaper Si-based SCs to amortize the launching costs of satellites. Moreover, in recent years, new SCs technologies based on Cu(In,Ga)Se-2 (CIGS) and perovskite solar cells (PSCs) have emerged as promising candidates for aerospace power systems, because of their appealing properties such as lightweightness, flexibility, cost-effective manufacturing, and exceptional radiation resistance. In this review the current advancements and future challenges of SCs for aerospace applications are critically discussed. In particular, for each type of SC, a description of the device's architecture, a summary of its performance, and a quantitative assessment of the radiation resistance are presented. Finally, considering the high potential that 2D-materials (such as graphene, transition metal dichalcogenides, and transition metal carbides, nitrides, and carbonitrides) have in improving both performance and stability of SCs, a brief overview of some important results concerning the influence of radiation on both 2D materials-based devices and monolayer of 2D materials is also included

Haemoglobin S and haemoglobin C: 'quick but costly' versus 'slow but gratis' genetic adaptations to Plasmodium falciparum malaria

Haemoglobin S (HbS; beta 6Glu -> Val) and HbC (beta 6Glu -> Lys) strongly protect against clinical Plasmodium falciparum malaria. HbS, which is lethal in homozygosity, has a multi-foci origin and a widespread geographic distribution in sub-Saharan Africa and Asia whereas HbC, which has no obvious CC segregational load, occurs only in a small area of central West-Africa. To address this apparent paradox, we adopted two partially independent haplotypic approaches in the Mossi population of Burkina Faso where both the local S (S-Benin) and the C alleles are common (0.05 and 0.13). Here we show that: both C and S-Benin are monophyletic; C has accumulated a 4-fold higher recombinational and DNA slippage haplotypic variability than the S-Benin allele (P = 0.003) implying higher antiquity; for a long initial lag period, the C alleles did apparently remain very few. These results, consistent with epidemiological evidences, imply that the C allele has been accumulated mainly through a recessive rather than a semidominant mechanism of selection. This evidence explains the apparent paradox of the uni-epicentric geographic distribution of HbC, representing a 'slow but gratis' genetic adaptation to malaria through a transient polymorphism, compared to the polycentric 'quick but costly' adaptation through balanced polymorphism of HbS

Volcanic Risk Management: the Case of Mt. Etna 2006 Eruption

Mt. Etna volcano is located in a very populated area of eastern Sicily (Italy). Its permanent degassing activity from summit craters and frequent eruptions impact significantly on town habitations and cultivated areas. In the latest years Etna has produced copious ash emission causing great losses to local economy and causing serious hazards to national and international air traffic over Mediterranean area and the often closure of Catania airport. In July 2006 eruptive vents opened on the East and South flanks of the summit craters showing irregular explosive and effusive activity lasting 6 months. This eruption represented the opportunity to perform the pre-operative test of FP6 Eurorisk-Preview (Prevention, Information and Early Warning) project aimed to develop tools for monitoring volcanoes. The test was performed during two temporal phases: the first one of early-warning was aimed to measure ground deformation and the second one during the crisis to survey volcanic ash produced during the explosions. The ground deformations were measured through the elaboration of SAR data. Beside the geophysical objectives, the test was also important to check data availability and efficiency of European Space Agency procedures. The pre-operative test has been peculiar to understand and quantify the delivering time of the final satellite products expected from the Volcanological Observatory in operative case. The analysis of July 2005 - July 2006 SAR data showed a pre-eruptive inflation trend in agreement with the ground network of GPS data. The magmatic source, that produced the September - October activity, has been located about 2.7 km below the summit craters. During the crisis phase characterized by paroxysmal activity, the Italian Civil Protection (DPC) in charge of airport closure in case of volcanic hazard, requested the satellite volcanic ash product retrieved from the NASA-MODIS data. An agreement between the industry Telespazio as direct broadcast of satellite data at Matera station and INGV was signed in order to elaborate the data in near-real time. The volcanic ash product provided information about: the presence of volcanic ash in the air; the affected area; the volcanic plume dispersal direction, dimensions and altitude and the volcanic ash loading. The satellite products and the observations report have been successively inserted in a web-interface. At the same time the observations report has been linked to the DPC dedicated Web-GIS interface that allows in a short time the availability of volcanic ash information to DPC in support to their decisions.Published77-811.10. TTC - Telerilevamentoope

Volcanic Risk Management: the Case of Mt. Etna 2006 Eruption

Mt. Etna volcano is located in a very populated area of eastern Sicily (Italy). Its permanent degassing activity from summit craters and frequent eruptions impact significantly on town habitations and cultivated areas. In the latest years Etna has produced copious ash emission causing great losses to local economy and causing serious hazards to national and international air traffic over Mediterranean area and the often closure of Catania airport. In July 2006 eruptive vents opened on the East and South flanks of the summit craters showing irregular explosive and effusive activity lasting 6 months. This eruption represented the opportunity to perform the pre-operative test of FP6 Eurorisk-Preview (Prevention, Information and Early Warning) project aimed to develop tools for monitoring volcanoes. The test was performed during two temporal phases: the first one of early-warning was aimed to measure ground deformation and the second one during the crisis to survey volcanic ash produced during the explosions. The ground deformations were measured through the elaboration of SAR data. Beside the geophysical objectives, the test was also important to check data availability and efficiency of European Space Agency procedures. The pre-operative test has been peculiar to understand and quantify the delivering time of the final satellite products expected from the Volcanological Observatory in operative case. The analysis of July 2005 - July 2006 SAR data showed a pre-eruptive inflation trend in agreement with the ground network of GPS data. The magmatic source, that produced the September - October activity, has been located about 2.7 km below the summit craters. During the crisis phase characterized by paroxysmal activity, the Italian Civil Protection (DPC) in charge of airport closure in case of volcanic hazard, requested the satellite volcanic ash product retrieved from the NASA-MODIS data. An agreement between the industry Telespazio as direct broadcast of satellite data at Matera station and INGV was signed in order to elaborate the data in near-real time. The volcanic ash product provided information about: the presence of volcanic ash in the air; the affected area; the volcanic plume dispersal direction, dimensions and altitude and the volcanic ash loading. The satellite products and the observations report have been successively inserted in a web-interface. At the same time the observations report has been linked to the DPC dedicated Web-GIS interface that allows in a short time the availability of volcanic ash information to DPC in support to their decisions

A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals

Given q as the global frequency of the alleles causing a disease, any allele with a frequency higher than q minus the cumulative frequency of the previously known disease-causing mutations (threshold) cannot be the cause of that disease. This principle was applied to the analysis of cystic fibrosis transmembrane conductance regulator (CFTR) mutations in order to decide whether they are the cause of cystic fibrosis. A total of 191 DNA samples fl-om random individuals from Italy, France, and Spain were investigated by DGGE (denaturing gradient gel electrophoresis) analysis of all the coding and proximal non-coding regions of the gene. The mutations detected by DGGE were identified by sequencing. The sample size was sufficient to select essentially all mutations with a frequency of at least 0.01. A total of 46 mutations was detected, 20 of which were missense mutations. Four new mutations were identified: 1341+28 C/T, 2082 C/T, L1096R, and I1131V. Thirteen mutations (125 G/C, 875+40 A/G, TTGAn, IVS8-6 5T, IVS8-6 9T, 1525-61 A/G, M470V, 2693 T/G, 3061-65 C/A, 4002 A/G, 4521 G/A, IVS8 TG10, IVS8 TG12) were classified as non-CF-causing alleles on the basis of their frequency. The remaining mutations have a cumulative frequency far exceeding q; therefore, most of them cannot be CF-causing mutations. This is the first random survey capable of detecting all the polymorphisms of the coding sequence of a gene

Highly preferential association of NonF508del CF mutations with the M470 allele

AbstractBackgroundOn the basis of previous findings on random individuals, we hypothesized a preferential association of CF causing mutations with the M allele of the M470V polymorphic site of the CFTR gene.MethodsWe have determined the M/V-CF mutation haplotype in a series of 201 North East Italian and 73 Czech CF patients who were not F508del homozygotes, as F508del was already known to be fully associated with the M allele.ResultsOut of 358 not F508del CF genes, 84 carried the V allele and 274 the less common M allele. In the N-E Italian population, MM subjects have a risk of carrying a CF causing mutation 6.9× greater than VV subjects when F508del is excluded and 15.4× when F508del is included. In the Czech population a similar, although less pronounced, association is observed.ConclusionsBesides the possible biological significance of this association, the possibility of exploiting it for a pilot screening program has been explored in a local North East Italian population for which CF patients were characterized for their CF mutation. General M470V genotyping followed by common CF mutation screening limited to couples in which each partner carries at least one M allele would need testing only 39% of the couples, which contribute 89% of the total risk, with a cost benefit

A large-scale study of the random variability of a coding sequence: a study on the CFTR gene

Coding single nucleotide substitutions (cSNSs) have been studied on hundreds of genes using small samples (ngapproximate to100-150 genes). In the present investigation, a large random European population sample (average ngapproximate to1500) was studied for a single gene, the CFTR ( Cystic Fibrosis Transmembrane conductance Regulator). The nonsynonymous (NS) substitutions exhibited, in accordance with previous reports, a mean probability of being polymorphic (q>0.005), much lower than that of the synonymous ( S) substitutions, but they showed a similar rate of subpolymorphic (q<0.005) variability. This indicates that, in autosomal genes that may have harmful recessive alleles (nonduplicated genes with important functions), genetic drift overwhelms selection in the subpolymorphic range of variability, making disadvantageous alleles behave as neutral. These results imply that the majority of the subpolymorphic nonsynonymous alleles of these genes are selectively negative or even pathogenic