72 research outputs found

    Information-theoretic assessment of on-board near-lossless compression of hyperspectral data

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    A rate-distortion model to measure the impact of near-lossless compression of raw data, that is, compression with user-defined maximum absolute error, on the information avail- able once the compressed data have been received and decompressed is proposed. Such a model requires the original uncompressed raw data and their measured noise variances. Advanced near- lossless methods are exploited only to measure the entropy of the datasets but are not required for on-board compression. In substance, the acquired raw data are regarded as a noisy realization of a noise-free spectral information source. The useful spectral information at the decoder is the mutual information between the unknown ideal source and the decoded source, which is affected by both instrument noise and compression-induced distortion. Experiments on simulated noisy images, in which the noise-free source and the noise realization are exactly known, show the trend of spectral information versus compression distortion, which in turn is related to the coded bit rate or equivalently to the compression ratio through the rate-distortion characteristic of the encoder used on satellite. Preliminary experiments on airborne visible infrared imaging spec- trometer (AVIRIS) 2006 Yellowstone sequences match the trends of the simulations. The main conclusion that can be drawn is that the noisier the dataset, the lower the CR that can be tolerated, in order to save a prefixed amount of spectral information. © The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. (DOI: 10.1117/1.JRS.

    Decarboxylation of Dialkyl Carbonates to Dialkyl Ethers over Alkali Metal-exchanged Faujasites

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    Non-toxic DAlCs, especially lighter dimethyl- and diethyl-carbonate, are regarded as very green alkylating reagents, particularly when coupled with metal-exchanged Y- and X-faujasites as catalysts. These reactions are selective, free from wastes or byproducts, and often require no additional solvent other than the carbonate. Nonetheless, this paper demonstrates that the operating temperature and the nature of the faujasite must be carefully chosen in order to avoid DAlC decomposition. In fact, at temperatures ranging from 150 to 240 ◦ C, faujasites can promote decarboxylation of light DAlCs to the corresponding ethers CH3OCH3 and CH3CH2OCH2CH3 plus CO2. Heavier DAlCs (dipropyl- and dioctyl-carbonate) undergo a similar decomposition pathway, followed by further reactions to the corresponding alcohols (n-propanol and n-octanol) and alkenes [propylene and octene(s)]. These transformations not only consume DAlCs, but also give rise to dangerously flammable ethers, as well as undesirable alcohols, alkenes and CO2.The present work reports an original investigation of the decarboxylation of DAlCs on faujasites with the aim of providing operative boundaries to the experimental conditions to minimise unwanted decomposition. The reaction is strongly affected by the nature of the catalyst: the more basic zeolites, NaX and CsY, are by far more active systems than NaY and LiY. However, solid K2CO3 proves to be rather inefficient. The temperature also plays a crucial role: for example, the onset of the decarboxylation of DMC requires a temperature of ~30 ◦ C lower than that for DEC and DPrC. Overall, awareness that certain zeolites cause decomposition of DAlCs under conditions similar to the ones used for DAlC-promoted alkylations allows determination of the correct experimental boundaries for a safer and more productive use of DAlCs as alkylating agent

    Genome-wide classification of MYB-regulatory genes in the perennial grass Eragrostis curvula and identification of the ZmFDL1 orthologue

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    Eragrostis curvula is a perennial grass native to Southern Africa that was introduced into semiarid regions of Australia, USA, and Argentina as forage grass. In the recent years, E. curvula has been considered one of the model organisms for the study of the molecular mechanisms underlying apomixis in plants. However, this species has also received much interest for its ability to adapt to marginal environments. Ecotypes with different drought stress response are characterized by changes in cuticle wax deposition, a trait that may influence plants capability to maintain a high-water content. Aim of this work is to isolate key regulatory genes of wax biosynthesis and deposition in E. curvula and investigate their involvement in drought stress response. The recent availability of E curvula genome sequence allowed us to identify the whole family of MYB transcription factors. The construction of a phylogenetic tree allowed to establish the relationships among MYB genes of E. curvula and closely related grasses. This analysis highlighted the presence, among different candidates, of the Eragrostis curvula orthologue of the ZmMYB94/fused leaves1 (fdl1) gene. This MYB factor is required in maize for a proper cuticle deposition in the juvenile phase of plant development, and its expression, which is confined to seedling tissues, is modulated by drought stress. Ecfdl1 is also expressed in the aerial parts of the plant, however, differently from what observed in maize, it is specifically expressed in adult tissues. The Ecfdl1 transcript level was measured in Eragrostis ecotypes characterized by different drought stress tolerance and wax content. Variations of Ecfdl1 gene expression observed in four ecotypes nicely correlated with differences in the amount of waxes. Our results indicate that the two MYB orthologs are characterized by distinct spatial-temporal expression patterns in the perennial E. curvula and the annual Zea mays plants. They may contribute to a general understanding of the cuticle role in stress adaptation mechanisms.Fil: Castorina, Giulia. Università degli Studi di Milano; ItaliaFil: Carballo, José. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Centro de Recursos Naturales Renovables de la Zona Semiárida. Universidad Nacional del Sur. Centro de Recursos Naturales Renovables de la Zona Semiárida; Argentina. Universidad Nacional del Sur. Departamento de Agronomía; ArgentinaFil: Selva, Juan Pablo. Universidad Nacional del Sur. Departamento de Agronomía; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Centro de Recursos Naturales Renovables de la Zona Semiárida. Universidad Nacional del Sur. Centro de Recursos Naturales Renovables de la Zona Semiárida; ArgentinaFil: Zilio, Massimo. Università degli Studi di Milano; ItaliaFil: Echenique, Daniela Rosalia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Centro de Recursos Naturales Renovables de la Zona Semiárida. Universidad Nacional del Sur. Centro de Recursos Naturales Renovables de la Zona Semiárida; Argentina. Universidad Nacional del Sur. Departamento de Agronomía; ArgentinaFil: Consonni, Gabriella. Università degli Studi di Milano; Italia63rd Italian Society of Agricultural Genetics Annual Congress: Science and innovation for sustainable agriculture intensification. The contribution of plant genetics and breedingNapolesItaliaUniversità degli Studi di Napoli Federico IIDipartimento di AgrariaConsiglio Nazionale dele RicercheIstituto di Bioscienze e Biorisors

    Sequential Coupling of The Transesterification of Cyclic Carbonates with The Selective N-Methylation of Anilines Catalysed by Faujasites

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    Anilines (R¢C6H4NH2: R¢ = H, p-MeO, p-Me; p-Cl, and p-NO2) react with a mixture of ethylene carbonate and methanol at 180 ◦C in the presence of alkali metal exchanged faujasites—preferably of the X-type—to give the corresponding N,N-dimethyl derivatives (R¢C6H4NMe2) in isolated yields up to 98%. Evidence proves that methanol is not the methylating agent. The reaction instead takes place through two sequential transformations, both catalyzed by faujasites: first transesterification of ethylene carbonate with MeOH to yield dimethyl carbonate, followed by the selective N-methylation of anilines by dimethyl carbonate. Propylene carbonate, is less reactive than ethylene carbonate, but it can be used under the same conditions. The overall process is highly chemoselective since the competitive reactions between the anilines and the cyclic carbonates is efficiently ruled out. Ethanol and propanol form the corresponding diethyl- and dipropyl- carbonates in the first step, but these compounds are not successful for the domino alkylation of anilines

    The Reaction of Glycerol Carbonate with Primary Aromatic Amines in the Presence of Y- and X-Faujasites: the Synthesis of N-(2,3-dihydroxy)propyl anilines and the Reaction Mechanism

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    At 140 ◦C, in the presence of alkali metal exchanged faujasites, preferably NaY, as catalysts, glycerine carbonate (GlyC) is an efficient and green alkylating agent of primary aromatic amines (p-XC6H4NH2, X = H, OMe, OH, Cl): the reaction takes place with a high conversion (~90%) and a good selectivity (80–90%) for the formation of N-(2,3-dihydroxy)propyl anilines (p-XC6H4NHCH2CH(OH)CH2OH). The alkylation process does not proceed through an exclusive nucleophilic substitution of anilines at the C5 position of GlyC. Evidence proves that a dehydrative condensation of anilines with GlyC produces intermediate species, and both transesterification and hydrolysis reactions are involved to obtain the final N-alkyl derivatives. A mechanism is proposed accordingly. Experiments show that faujasites are recyclable catalysts on condition that they are exposed to a mild thermal activation (70 ◦C, 18 mbar) prior to their re-use. Otherwise, if zeolites are calcined (400 ◦C, air), both the catalyst activity and the reaction selectivity drop. Isolated yields (60–65%) of N-(2,3-dihydroxy)propyl anilines are somewhat limited by the difficult separation of the unreacted GlyC and of the by-product glycerine. Nonetheless, the overall efficiency of the method is comparable to that of alternative routes based on highly toxic reagents (glycidol and aryl halides)

    Selective Catalytic Etherification of Glycerol Formal and Solketal with Dialkyl Carbonates and K2CO3

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    At T ≥ 200 ◦ C,in the presence of K2CO3 as a catalyst, an original etherification procedure of non-toxic acetals such as glycerol formal (GlyF) and solketal has been investigated by using dialkyl carbonates as safe alkylating agents. The effects of parameters including the temperature, the reaction time, and the loading of both the catalyst and the dialkyl carbonate have been detailed for the model case of dimethyl carbonate (DMC). Both GlyF and solketal were efficiently alkylated by DMC to produce the corresponding O-methyl ethers with selectivity up to 99% and excellent yields (86–99%, by GC). The high selectivity could be accounted for by a mechanistic study involving a combined sequence of methylation, carboxymethylation, decarboxylation and hydrolysis processes. The O-methylation of GlyF and solketal could be successfully scaled up for multigram synthesis even operating with a moderate excess (5 molar equiv.) of DMC and in the absence of additional solvent. Notwithstanding the advantageous reduction of the process mass index, scale up experiments provided evidence that prolonged reaction times may induce the decomposition of DMC mainly by the loss of CO2.TheK2CO3-catalyzed etherification of solketal with other carbonates such as dibenzyl and diethyl carbonate (DBnC and DEC, respectively), proceeded with the same good selectivity observed for DMC. However, at 220 ◦ C, the solketal conversion did not exceed 81% since both DBnC and DEC were extensively consumed in competitive decarboxylation and hydrolysis reactions

    N-Doped Carbon Dot Hydrogels from Brewing Waste for Photocatalytic Wastewater Treatment

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    The brewery industry annually produces huge amounts of byproducts that represent an underutilized, yet valuable, source of biobased compounds. In this contribution, the two major beer wastes, that is, spent grains and spent yeasts, have been transformed into carbon dots (CDs) by a simple, scalable, and ecofriendly hydrothermal approach. The prepared CDs have been characterized from the chemical, morphological, and optical points of view, highlighting a high level of N-doping, because of the chemical composition of the starting material rich in proteins, photo-luminescence emission centered at 420 nm, and lifetime in the range of 5.5-7.5 ns. With the aim of producing a reusable catalytic system for wastewater treatment, CDs have been entrapped into a polyvinyl alcohol matrix and tested for their dye removal ability. The results demonstrate that methylene blue can be efficiently adsorbed from water solutions into the composite hydrogel and subsequently fully degraded by UV irradiation

    The Italian Earthquakes and Tsunami Monitoring and Surveillance Systems

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    The Osservatorio Nazionale Terremoti (ONT) is the Italian seismic operational centre for monitoring earthquake, it is part of Istituto Nazionale di Geofisica e Vulcanologia (INGV) the largest Italian research institution, with focus in Earth Sciences. INGV runs the Italian National Seismic Network (network code IV) and other networks at national scale for monitoring earthquakes and tsunami. INGV is a primary node of European Integrated Data Archive (EIDA) for archiving and distributing, continuous, quality checked seismic waveforms (strong motion and weak motion recordings). ONT designed the data acquisition system to accomplish, in near-real-time, automatic earthquake detection, hypocentre and magnitude determination and evaluation of moment tensors, shake maps and other products. Database archiving of all parametric results are closely linked to the existing procedures of the INGV seismic monitoring environment and surveillance procedures. ONT organize the Italian earthquake surveillance service and the tsunami alert service (INGV is Tsunami Service Provider of the ICG/NEAM for the entire Mediterranean basin). We provide information to the Dipartimento di Protezione Civile (DPC) and to several Mediterranean countries. Earthquakes information are revised routinely by the analysts of the Italian Seismic Bulletin. The results are published on the web and are available to the scientific community and the general public.PublishedMontreal1SR TERREMOTI - Sorveglianza Sismica e Allerta Tsunam

    Overview of DISCOVER22 experiment in the framework of INFN-LNGS Cosmic Silence activity: challenges and improvements in underground radiobiology

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    One of the most intriguing and still pending questions in radiobiology is to understand whether and how natural environmental background radiation has shaped Life over millions of years of evolution on Earth. Deep Underground Laboratories (DULs) represent the ideal below-background exposure facilities where to address such a question. Among the few worldwide DULs, INFN-Laboratorio Nazionale del Gran Sasso (LNGS) is one of the largest in terms of size and infrastructure. Designed and built to host neutrino and dark matter experiments, since the 1990 s the LNGS has been one of the first DULs to systematically host radiobiology experiments. Here we present the DISCOVER22 (DNA Damage and Immune System Cooperation in VEry low Radiation environment 2022) experiment recently started at LNGS. DISCOVER22 aims at investigating how the low radiation background modulates the Immune System (IS) response in in vitro and in vivo models. Underground radiobiology experiments are particularly complex and tricky to design and perform. In these studies, the accurate characterization of exposure scenarios is mandatory, but a challenging aspect is to understand how the very few ionizing tracks in the ultra-Low Radiation Environment (LRE) interact with the living matter in space and time in order to trigger different biological responses. In this Perspective, we describe these challenges and how we address them through a microdosimetric and a radiobiological approaches. We aim at linking physical microdosimetric measurements and the corresponding biological radiation responses by using radiation biophysical models that could shed light on many as yet unresolved questions
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