394 research outputs found

    Relativistic approaches to structure functions of nuclei

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    We employ a propagator technique to derive a new relativistic 1/\qq expansion of the structure function of a nucleus, composed of point-nucleons. We exploit non-relativistic features of low-momentum nucleons in the target and only treat relativistically the nucleon after absorption of a high-momentum virtual photon. The new series permits a 3-dimensional reduction of each term and a formal summation of all Final State Interaction terms. We then show that a relativistic structure function can be obtained from its non-relativistic analog by a mere change of a scaling variable and an addition of an energy shift. We compare the obtained result with an ad hoc generalized Gersch-Rodriguez-Smith theory, previously used in computations of nuclear structure functions.Comment: Comparison with data is included, to be published in PRC, Feb. 200

    Growth hormone inhibits hepatic de novo lipogenesis in adult mice

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    Patients with nonalcoholic fatty liver disease (NAFLD) are reported to have low growth hormone (GH) production and/or hepatic GH resistance. GH replacement can resolve the fatty liver condition in diet-induced obese rodents and in GH-deficient patients. However, it remains to be determined whether this inhibitory action of GH is due to direct regulation of hepatic lipid metabolism. Therefore, an adult-onset, hepatocyte-specific, GH receptor (GHR) knockdown (aLivGHRkd) mouse was developed to model hepatic GH resistance in humans that may occur after sexual maturation. Just 7 days after aLivGHRkd, hepatic de novo lipogenesis (DNL) was increased in male and female chow-fed mice, compared with GHR-intact littermate controls. However, hepatosteatosis developed only in male and ovariectomized female aLivGHRkd mice. The increase in DNL observed in aLivGHRkd mice was not associated with hyperactivation of the pathway by which insulin is classically considered to regulate DNL. However, glucokinase mRNA and protein levels as well as fructose-2,6-bisphosphate levels were increased in aLivGHRkd mice, suggesting that enhanced glycolysis drives DNL in the GH-resistant liver. These results demonstrate that hepatic GH actions normally serve to inhibit DNL, where loss of this inhibitory signal may explain, in part, the inappropriate increase in hepatic DNL observed in NAFLD patients

    Theoretical aspects of the CEBAF 89-009 experiment on inclusive scattering of 4.05 GeV electrons from nuclei

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    We compare recent CEBAF data on inclusive electron scattering on nuclei with predictions, based on a relation between structure functions (SF) of a nucleus, a nucleon and a nucleus of point-nucleons. The latter contains nuclear dynamics, e.g. binary collision contributions in addition to the asymptotic limit. The agreement with the data is good, except in low-intensity regions. Computed ternary collsion contributions appear too small for an explanation. We perform scaling analyses in Gurvitz's scaling variable and found that for yG0y_G\gtrless 0, ratios of scaling functions for pairs of nuclei differ by less than 15-20% from 1. Scaling functions for 00 are, for increasing Q2Q^2, shown to approach a plateau from above. We observe only weak Q2Q^2-dependence in FSI, which in the relevant kinematic region is ascribed to the diffractive nature of the NN amplitudes appearing in FSI. This renders it difficult to separate asymptotic from FSI parts and seriously hampers the extraction of n(p)n(p) from scaling analyses in a model-independnent fashion.Comment: 11 p. Latex file, 2 ps fig

    GRS computation of deep inelastic electron scattering on 4He

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    We compute cross sections for inclusive scattering of high energy electrons on 4He, based on the two lowest orders of the Gersch-Rodriguez-Smith (GRS) series. The required one- and two-particle density matrices are obtained from non-relativistic 4He wave functions using realistic models for the nucleon-nucleon and three-nucleon interaction. Predictions for E=3.6 GeV agree well with the NE3 SLAC-Virginia data.Comment: 18 pages, 7 figures, submitted to PR

    Damping mechanisms of the Delta resonance in nuclei

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    The damping mechanisms of the Delta(1232) resonance in nuclei are studied by analyzing the quasi-free decay reactions 12C(pi+,pi+ p)11B and 12C(3He,t pi+ p)11B and the 2p emission reactions 12C(pi+,pp)10B and 12C(3He,t pp)10B. The coincidence cross sections are calculated within the framework of the isobar-hole model. It is found that the 2p emission process induced by the decay of the Delta resonance in the nucleus can be consistently described by a pi+rho+g' model for the Delta+N -> N+N decay interaction.Comment: 9 pages, 5 Postscript figures, uses RevTex, psfig.sty. Accepted by Physical Review

    Artificial intelligence-based software (AID-FOREST) for tree detection: A new framework for fast and accurate forest inventorying using LiDAR point clouds

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    Forest inventories are essential to accurately estimate different dendrometric and forest stand parameters. However, classical forest inventories are time consuming, slow to conduct, sometimes inaccurate and costly. To address this problem, an efficient alternative approach has been sought and designed that will make this type of field work cheaper, faster, more accurate, and easier to complete. The implementation of this concept has required the development of a specifically designed software called "Artificial Intelligence for Digital Forest (AID-FOREST)", which is able to process point clouds obtained via mobile terrestrial laser scanning (MTLS) and then, to provide an array of multiple useful and accurate dendrometric and forest stand parameters. Singular characteristics of this approach are: No data pre-processing is required either pre-treatment of forest stand; fully automatic process once launched; no limitations by the size of the point cloud file and fast computations.To validate AID-FOREST, results provided by this software were compared against the obtained from in-situ classical forest inventories. To guaranty the soundness and generality of the comparison, different tree spe-cies, plot sizes, and tree densities were measured and analysed. A total of 76 plots (10,887 trees) were selected to conduct both a classic forest inventory reference method and a MTLS (ZEB-HORIZON, Geoslam, ltd.) scanning to obtain point clouds for AID-FOREST processing, known as the MTLS-AIDFOREST method. Thus, we compared the data collected by both methods estimating the average number of trees and diameter at breast height (DBH) for each plot. Moreover, 71 additional individual trees were scanned with MTLS and processed by AID-FOREST and were then felled and divided into logs measuring 1 m in length. This allowed us to accurately measure the DBH, total height, and total volume of the stems.When we compared the results obtained with each methodology, the mean detectability was 97% and ranged from 81.3 to 100%, with a bias (underestimation by MTLS-AIDFOREST method) in the number of trees per plot of 2.8% and a relative root-mean-square error (RMSE) of 9.2%. Species, plot size, and tree density did not significantly affect detectability. However, this parameter was significantly affected by the ecosystem visual complexity index (EVCI). The average DBH per plot was underestimated (but was not significantly different from 0) by the MTLS-AIDFOREST, with the average bias for pooled data being 1.8% with a RMSE of 7.5%. Similarly, there was no statistically significant differences between the two distribution functions of the DBH at the 95.0% confidence level.Regarding the individual tree parameters, MTLS-AIDFOREST underestimated DBH by 0.16 % (RMSE = 5.2 %) and overestimated the stem volume (Vt) by 1.37 % (RMSE = 14.3 %, although the BIAS was not statistically significantly different from 0). However, the MTLS-AIDFOREST method overestimated the total height (Ht) of the trees by a mean 1.33 m (5.1 %; relative RMSE = 11.5 %), because of the different height concepts measured by both methodological approaches. Finally, AID-FOREST required 30 to 66 min per ha-1 to fully automatically process the point cloud data from the *.las file corresponding to a given hectare plot. Thus, applying our MTLS-AIDFOREST methodology to make full forest inventories, required a 57.3 % of the time required to perform classical plot forest inventories (excluding the data postprocessing time in the latter case). A free trial of AID -FOREST can be requested at [email protected]

    Turning defence into offence? Intrusion of cladoceran brood chambers by a green alga leads to reproductive failure

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    We observed a novel anti-grazer strategy in the green alga Chlorella vulgaris, where the cells entered the brood chambers of two grazers, Daphnia magna and Simocephalus sp, densely colonized the eggs, and significantly reduced the grazers' reproductive success

    Matched sizes of activating and inhibitory receptor/ligand pairs are required for optimal signal integration by human Natural Killer cells

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    It has been suggested that receptor-ligand complexes segregate or co-localise within immune synapses according to their size, and this is important for receptor signaling. Here, we set out to test the importance of receptor-ligand complex dimensions for immune surveillance of target cells by human Natural Killer (NK) cells. NK cell activation is regulated by integrating signals from activating receptors, such as NKG2D, and inhibitory receptors, such as KIR2DL1. Elongating the NKG2D ligand MICA reduced its ability to trigger NK cell activation. Conversely, elongation of KIR2DL1 ligand HLA-C reduced its ability to inhibit NK cells. Whereas normal-sized HLA-C was most effective at inhibiting activation by normal-length MICA, only elongated HLA-C could inhibit activation by elongated MICA. Moreover, HLA-C and MICA that were matched in size co-localised, whereas HLA-C and MICA that were different in size were segregated. These results demonstrate that receptor-ligand dimensions are important in NK cell recognition, and suggest that optimal integration of activating and inhibitory receptor signals requires the receptor-ligand complexes to have similar dimensions
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