Observations on soil-atmosphere interactions after long-term monitoring at two sample sites subjected to shallow landslides

Soil-atmosphere interaction has implications in different scientific research contexts and is increasingly investigated through field measurements. This paper reports a detailed description of interaction between shallow soil and atmosphere at two test sites in Oltrepò Pavese area (Northern Italy). The two test sites are in the same climatic area but are characterised by different geological features. In fact, the first objective is to compare the behaviour of two different soils, namely a clayey-sandy silt (CL) and a silty clay (CH), under similar meteorological events. Soil-atmosphere interaction is studied on the basis of long-term (about 87 and 42 months for the two test sites, respectively) monitoring data of both volumetric water content and soil water potential, recorded at different depths along two vertical soil profiles in the first two metres from ground level. Field measurements, together with meteorological data such as precipitation and air temperature, allow for clear identification of the seasonal fluctuations of unsaturated soil hydraulic properties. To infer detailed information, the recorded data were processed and relationships between soil water potential and water content were investigated. Different time spans, from several months to a few days, even including single rainy events, are considered to show the hydraulic soil behaviour. The hysteretic cycles of water content with respect to soil water potential and non-equilibrium flow are highlighted. In particular, the measured soil water potential is in the range of 0–800 kPa and of 0–1500 kPa for the CL and CH soil, respectively. At both sites, the observed hysteretic cycles are more frequent in the hot season (summer) than in the cold season (winter) and tend to reduce with depth. The experimental results are compared with the soil water characteristic curves (SWCCs) to assess whether and to what extent the SWCCs are reliable in modelling the hydraulic behaviour of partially saturated soils, under atmospheric forcing, at least in the considered climatic contexts

Seeking an alliance between farmers and genebanks

In Bolivia and Malaysia, farmers are increasingly affected by drought, water logging and unpredictable weather patterns. To cope, they plant an array of traditional crops and varieties to spread the risk of crop loss, whether from pests, diseases or the weather. However for these farmers, agrobiodiversity is not just a way to insure against crop losses; it's an important source of cultural pride and value. Seventy three year old Don Victor, who farms at 4,100 metres above sea level in Colomi, Bolivia, maintains 39 varieties of native potato. ”These are like my family,” he says, sharing his planting material only with those he trusts

Quantum limit in resonant vacuum tunneling transducers

We propose an electromechanical transducer based on a resonant-tunneling configuration that, with respect to the standard tunneling transducers, allows larger tunneling currents while using the same bias voltage. The increased current leads to an increase of the shot noise and an increase of the momentum noise which determine the quantum limit in the system under monitoring. Experiments with micromachined masses at 4.2 K could show dominance of the momentum noise over the Brownian noise, allowing observation of the quantum-mechanical noise at the mesoscopic scale

C-N coupling between µ-aminocarbyne and nitrile ligands promoted by tolylacetylide addition to [Fe2CN(Me)(Xyl)}(CO)(CO)(NCCMe3)(Cp)2][SO3CF3]: formation of a novel bridging allene-diaminocarbene ligand

The reaction of the mu-aminocarbyne complex [Fe-2{mu-CN(Me)(Xyl)}(mu-CO)(CO)(NCCMe3)(CP)(2)][SO3CF3] (2) (Xyl = 2,6-Me2C6H3) with tolylacetylide, followed by treatment with HSO3CF3 affords the complex [Fe-2{mu-eta(1):eta(3)C(Tol)double bondCdouble bondC(CMe3)N(H)CN(Me)(Xyl)}(mu-CO)(CO)(Cp-2)][SO3CF3] (3) (Tol = 4-MeC6H4). The X-ray molecular structure of 3 reveals the peculiar character of the bridging ligand, which exhibits both eta(1):eta(2) allene and aminocarbene nature. The formation of 3 proceeds through several intermediate species, which have been detected by IR spectroscopy. Addition of HSO3CF3 at an early stage of the reaction between 2 and LiCdropCTol leads to the formation of the imine complex [Fe-2{mu-CN(Me)Xyl}(mu-CO)(CO){NHC(CdropCTol)CMe3}(Cp)(2)][SO3CF3] (6) indicating that the first step of the reaction consists in the acetylide addition at the coordinated NCCMe3. The molecular structure of 6 has been elucidated by an X-ray diffraction study

A data-driven method for the temporal estimation of soil water potential and its application for shallow landslides prediction

Soil water potential is a key factor to study water dynamics in soil and for estimating the occurrence of natural hazards, as landslides. This parameter can be measured in field or estimated through physically-based models, limited by the availability of effective input soil properties and pre-liminary calibrations. Data-driven models, based on machine learning techniques, could overcome these gaps. The aim of this paper is then to develop an innovative machine learning methodology to assess soil water potential trends and to implement them in models to predict shallow landslides. Monitoring data since 2012 from test-sites slopes in Oltrepò Pavese (northern Italy) were used to build the models. Within the tested techniques, Random Forest models allowed an outstanding recon-struction of measured soil water potential temporal trends. Each model is sensitive to meteorological and hydrological characteristics according to soil depths and features. Reliability of the proposed models was confirmed by correct estimation of days when shallow landslides were triggered in the study areas in December 2020, after implementing the modeled trends on a slope stability model, and by the correct choice of physically-based rainfall thresholds. These results confirm the potential application of the developed methodology to estimate hydrological scenarios that could be used for decision-making purposes

Remarkable effect of [Li(G4)]TFSI solvate ionic liquid (SIL) on the regio- And stereoselective ring opening of α-gluco carbasugar 1,2-epoxides

Carba analogues of biologically relevant natural carbohydrates are promising structures for the development of future drugs endowed with enhanced hydrolytic stability. An open synthetic challenge in this field is the optimization of new methodologies for the stereo- and regioselective opening of α-gluco carbasugar 1,2-epoxides that allow for the preparation of pseudo mono- and disaccharides of great interest. Therefore, we investigated the effect of Lewis acids and solvate ionic liquids (SILs) on the epoxide ring opening of a model substrate. Of particular interest was the complete stereo- and regioselectivity, albeit limited to simple nucleophiles, toward the desired C(1) isomer that was observed using LiClO4. The results obtained with SILs were also remarkable. In particular, Li[NTf2]/tetraglyme ([Li(G4)]TFSI) was able to function as a Lewis acid and to direct the attack of the nucleophile preferentially at the pseudo anomeric position, even with a more complex and synthetically interesting nucleophile. The regioselectivity observed for LiClO4 and [Li(G4)]TFSI was tentatively ascribed to the formation of a bidentate chelating system, which changed the conformational equilibrium and ultimately permitted a trans-diaxial attack on C(1). To the best of our knowledge, we report here the first case in which SILs were successfully employed in a ring-opening process of epoxides

(Poly)phenolic content and profile and antioxidant capacity of whole-grain cookies are better estimated by simulated digestion than chemical extraction

It is widely recognized that the biological effects of phytochemicals cannot be attributed to the native compounds present in foods but rather to their metabolites endogenously released after intake. Bioavailability depends on bioaccessibility, which is the amount of the food constituent that is released from the matrix in the gastrointestinal tract. The use of chemical extraction to evaluate the content and profile of phytochemicals does not mirror the physiological situation in vivo, and their bioaccessibility should be considered while assessing their nutritional significance in human health. The current study was designed to compare the (poly)phenolic profile and content and antioxidant capacity of whole-grain (WG) cookies using chemical extraction and a more physiological approach based on simulated digestion. Three types of organic WG cookies (made with durum, Italian khorasan, or KAMUT\uae khorasan wheat) were considered, either fermented by Saccharomyces Cerevisiae or sourdough. Although the flour type and the fermentation process influenced the release of phytochemicals from the cookie matrix, in almost all samples, the simulated digestion appeared the most efficient procedure. Our results indicate that the use of chemical extraction for evaluation of the phytochemicals content and antioxidant capacity of food could lead to underestimation and underline the need for more physiological extraction methods

Malonic acid: A potential reagent in decontamination processes for Ni-rich alloy surfaces

The ability of malonic acid as a dissolution agent toward synthetic Ni ferrite and Alloy 600 and 800 corrosion products was explored. Its performance in the dissolution kinetics of Ni ferrite powders was compared with the one of oxalic acid. Kinetic parameters were obtained and the dependency on external Fe(II) was modelled. Oxidized samples used in descaling tests were prepared by exposure of coupons of both alloys to lithiated aqueous solutions, under hydrothermal conditions and hydrogen overpressure, simulating PHWR conditions. Oxide layer morphology, the influence of exposure time to corrosive medium and LiOH concentration on its thickness were characterized. Descaling tests consisting on a two-stage method (a first oxidizing step with alkaline permanganate followed by a reducing step with oxalic or malonic acid were carried out). Results were compared to those obtained with a well known chemical cleaning formulation (APAC: Alkaline Permanganate Ammonium Citrate) used in decontamination of several reactors and loops and the competitiveness of malonic acid was demonstrated.Fil: García, D.. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Universidad Nacional de San Martín. Instituto Sabato; ArgentinaFil: Bruyre, V. I. E.. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Universidad Nacional de San Martín. Instituto Sabato; ArgentinaFil: Bordoni, R.. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; ArgentinaFil: Olmedo, A. M.. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; ArgentinaFil: Morando, Pedro Juan. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Universidad Nacional de San Martín. Instituto Sabato; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentin

Carba-D,L-allal- and -D,L-galactal-derived vinyl N-nosyl aziridines as useful tools for the synthesis of 4-deoxy-4-(N-nosylamino)-2,3-unsaturated-5a-carbasugars

The novel carba-D,L-allal- and carba-D,L-galactal-derived vinyl N-nosyl aziridines were prepared and the regio- and stereoselective behavior in opening reactions with O- and N-nucleophiles examined. The carbaglycosylating ability of the novel aziridines, as deduced by the amount of 1,4-addition products (1,4-regioselectivity) obtained in the acid-catalyzed methanolysis taken as a model reaction, is similar or superior to that observed with the corresponding carba-D,L-allal- and -D,L-galactal-derived vinyl epoxides, respectively. In all 1,2- and 1,4-addition products obtained, a –(N-nosylamino) group is regio- and stereoselectively introduced at the C(4) carbon of a 1,2- or 2,3-unsaturated carbasugar, susceptible to further elaborations toward aminocyclitol derivatives. The stereoselective synthesis of the corresponding, enantiomerically pure carba-D,L-allal- and -D,L-galactal-derived vinyl N-acetyl aziridines is also described

Algebraic-matrix calculation of vibrational levels of triatomic molecules

We introduce an accurate and efficient algebraic technique for the computation of the vibrational spectra of triatomic molecules, of both linear and bent equilibrium geometry. The full three-dimensional potential energy surface (PES), which can be based on entirely {\it ab initio} data, is parameterized as a product Morse-cosine expansion, expressed in bond-angle internal coordinates, and includes explicit interactions among the local modes. We describe the stretching degrees of freedom in the framework of a Morse-type expansion on a suitable algebraic basis, which provides exact analytical expressions for the elements of a sparse Hamiltonian matrix. Likewise, we use a cosine power expansion on a spherical harmonics basis for the bending degree of freedom. The resulting matrix representation in the product space is very sparse and vibrational levels and eigenfunctions can be obtained by efficient diagonalization techniques. We apply this method to carbonyl sulfide OCS, hydrogen cyanide HCN, water H$_2$O, and nitrogen dioxide NO$_2$. When we base our calculations on high-quality PESs tuned to the experimental data, the computed spectra are in very good agreement with the observed band origins.Comment: 11 pages, 2 figures, containg additional supporting information in epaps.ps (results in tables, which are useful but not too important for the paper