108 research outputs found

    wall to wall spatial prediction of growing stock volume based on italian national forest inventory plots and remotely sensed data

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    Abstract Spatial predictions of forest variables are required for supporting modern national and sub-national forest planning strategies, especially in the framework of a climate change scenario. Nowadays methods for constructing wall-to-wall maps and calculating small-area estimates of forest parameters are becoming essential components of most advanced National Forest Inventory (NFI) programs. Such methods are based on the assumption of a relationship between the forest variables and predictor variables that are available for the entire forest area. Many commonly used predictors are based on data obtained from active or passive remote sensing technologies. Italy has almost 40% of its land area covered by forests. Because of the great diversity of Italian forests with respect to composition, structure and management and underlying climatic, morphological and soil conditions, a relevant question is whether methods successfully used in less complex temperate and boreal forests may be applied successfully at country level in Italy. For a study area of more than 48,657 km2 in central Italy of which 43% is covered by forest, the study presents the results of a test regarding wall-to-wall, spatially explicit estimation of forest growing stock volume (GSV) based on field measurement of 1350 plots during the last Italian NFI. For the same area, we used potential predictor variables that are available across the whole of Italy: cloud-free mosaics of multispectral optical satellite imagery (Landsat 5 TM), microwave sensor data (JAXA PALSAR), a canopy height model (CHM) from satellite LiDAR, and auxiliary variables from climate, temperature and precipitation maps, soil maps, and a digital terrain model. Two non-parametric (random forests and k-NN) and two parametric (multiple linear regression and geographically weighted regression) prediction methods were tested to produce wall-to-wall map of growing stock volume at 23-m resolution. Pixel level predictions were used to produce small-area, province-level model-assisted estimates. The performances of all the methods were compared in terms of percent root mean-square error using a leave-one-out procedure and an independent dataset was used for validation. Results were comparable to those available for other ecological regions using similar predictors, but random forests produced the most accurate results with a pixel level R2 = 0.69 and RMSE% = 37.2% against the independent validation dataset. Model-assisted estimates were more precise than the original design-based estimates provided by the NFI

    A compact Time-Of-Flight detector for space applications: The LIDAL system

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    Abstract LIDAL (Light Ion Detector for ALTEA system) is a compact detector designed to upgrade ALTEA (Anomalous Long Term Effects on Astronauts) silicon detector apparatus, in order to study in detail the low-Z part of ions spectrum inside the International Space Station (ISS) and to enhance the Particle Identification (PID) capability of the system. The new detector is designed to trigger ALTEA and to perform Time-Of-Flight measurements. It is based on plastic scintillators for fast timing applications read by Photo-Multiplier-Tubes (PMTs). A custom Front End Electronics (FEE) has been designed to reach time resolutions less than 100 ps ( σ ) for protons. A LIDAL prototype has been developed at the University of Rome Tor Vergata to test the timing performance of the scintillators, the PMTs and of the custom FEE using the proton beam line at the TIFPA (Trento Institute for Fundamentals Physics Applications) center in Trento, Italy. The results of these tests are reported and discussed. They have also been used for a preliminary evaluation of the Particle Identification (PID) capability of the final LIDAL-ALTEA detector system in response to the ions spectra expected on-board the ISS

    Structural and morphological alterations induced by cobalt substitution in LaMnO3 perovskites

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    [EN] The chemical composition of a LaMnO3 perovskite was modified sequentially by an improved sol-gel method to include cobalt centers in some B sites formerly occupied by Mn. In this way, a representative set of materials of general formula LaMn1-xCoxO3 was obtained whose composition extends from LaMnO3 to LaCoO3. These perovskites, as promising materials for oxygen reduction or oxygen evolution reactions, were characterized by several imaging (SEM), spectroscopic (XPS, EDX) and diffraction (XRD) techniques to elucidate their structure and to demonstrate the existence of composition differences between the catalytic surface and the bulk material. Specifically, it was found that lanthanum ions prevail at the surface of the catalyst but high cobalt-substitution levels stimulate the surface enrichment in B cations in their respective higher oxidation states (Mn4+ and Co3+ against Mn3+ and Co2+). This phenomenon opens the possibility of tuning their electrocatalytic properties and to synthesize suitable materials for electrochemical reactions involving molecular oxygen. (C) 2019 Elsevier Inc. All rights reserved.The authors thank MINECO and FEDER (MAT2016-76595-R) for the financial support. J.X.F.-L. gratefully acknowledges MINECO for the financial support through FPI contract (BES-2017-081598).Flores-Lasluisa, JX.; Huerta, F.; Cazorla-Amoros, D.; Morallón, E. (2019). Structural and morphological alterations induced by cobalt substitution in LaMnO3 perovskites. Journal of Colloid and Interface Science. 556:658-666. https://doi.org/10.1016/j.jcis.2019.08.112S65866655

    Breast cancer screening in women at increased risk according to different family histories: an update of the Modena Study Group experience

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    BACKGROUND: Breast cancer (BC) detection in women with a genetic susceptibility or strong family history is considered mandatory compared with BC screening in the general population. However, screening modalities depend on the level of risk. Here we present an update of our screening programs based on risk classification. METHODS: We defined different risk categories and surveillance strategies to identify early BC in 1325 healthy women recruited by the Modena Study Group for familial breast and ovarian cancer. Four BC risk categories included BRCA1/2 carriers, increased, intermediate, and slightly increased risk. Women who developed BC from January 1, 1994, through December 31, 2005 (N = 44) were compared with the number of expected cases matched for age and period. BRCA1/2 carriers were identified by mutational analysis. Other risk groups were defined by different levels of family history for breast or ovarian cancer (OC). The standardized incidence ratio (SIR) was used to evaluate the observed and expected ratio among groups. All statistical tests were two-sided. RESULTS: After a median follow-up of 55 months, there was a statistically significant difference between observed and expected incidence [SIR = 4.9; 95% confidence interval (CI) = 1.6 to 7.6; p < 0.001]. The incidence observed among BRCA carriers (SIR = 20.3; 95% CI = 3.1 to 83.9; P < 0.001), women at increased (SIR = 4.5; 95% CI = 1.5 to 8.3; P < 0.001) or intermediate risk (SIR = 7.0, 95% CI = 2.0 to 17.1; P = 0.0018) was higher than expected, while the difference between observed and expected among women at slightly increased risk was not statistically significant (SIR = 2.4, 95% CI = 0.9 to 8.3; P = .74). CONCLUSION: The rate of cancers detected in women at high risk according to BRCA status or strong family history, as defined according to our operational criteria, was significantly higher than expected in an age-matched general population. However, we failed to identify a greater incidence of BC in the slightly increased risk group. These results support the effectiveness of the proposed program to identify and monitor individuals at high risk, whereas prospective trials are needed for women belonging to families with sporadic BC or OC

    The potential role of mitochondrial ATP synthase inhibitory factor 1 (IF1) in coronary heart disease: a literature review

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    Cardiovascular disease (CVD) is the leading cause of death worldwide, and so the search for innovative and accurate biomarkers for guiding prevention, diagnosis, and treatment is a valuable clinical and economic endeavor. Due to a recent findings that the serum concentration of mitochondrial ATP synthase inhibitory factor 1 (IF1) is an independent prognostic factor in patients with coronary heart disease (CHD), we reviewed the role of this protein in myocardial ischemic preconditioning, its correlation to plasma high density lipoprotein (HDL), the predictive potential in patients with CHD, and its interplay with angiogenesis. IF1 has been positively correlated with plasma HDL-cholesterol, and is independently negatively associated with all-cause and CV mortality in patients with CHD. However, this conclusion is prevalently based on limited data, and more research is needed to draw definitive conclusions. IF1 seems to play an additional role in increasing cell vulnerability in oncologic diseases but may also function as modest inhibitor of angiogenesis in physiological conditions. It has been also explored that IF1 may rather act as a modulator of other molecules more significantly involved in angiogenesis, especially apolipoprotein A1 on which the largest effect could be observed. In conclusion, more research is needed to characterize the role of IF1 in patients with CHD

    Ambiti e limiti delle prescrizioni farmaceutiche nell'esercizio dell'odontoiatria e protesi dentaria

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    L'articolo esamine le problematiche legate alla introduzione della nuova laurea in Odontoiatria e Protesi dentaria in relazione alla possibilità di prescfrizione dei farmaci da parte dei nuovi laureati. In conclusione l'articolo propone di formulare un prontuario ad ho per questi laureati che però non abbia valore vincolante

    mPGES-1 knock-out mice are resistant to cancer-induced anorexia despite the absence of central mPGES-1 up-regulation in wild-type anorexic mice.

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    International audienceAnorexia-cachexia syndrome is a very common symptom observed in individuals affected by chronic inflammatory diseases. The present study was designed to address the possible involvement of the inducible microsomal prostaglandin E synthase-1 (mPGES-1) in the hypopaghia observed during these pathological states. To this end, we used a model of cancer-induced anorexia and we report here that despite the absence of up-regulation of the mPGES-1 enzyme within the brain during anorexia-cachexia syndrome, mPGES-1 knock-out mice exhibit resistance to tumor-induced anorexia and maintain their body mass
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