245 research outputs found
Agricultural expansion in Uruguayan grasslands and priority areas for vertebrate and woody plant conservation
Habitat loss due to land-use change is the greatest threat to biodiversity on a global scale, and agriculture has been the principal driver of change. In Uruguay, the conversion of native grasslands to croplands (e.g., soybean) and exotic forest plantations (Eucalyptus and Pinus) has accelerated during the last two decades. We studied the vulnerability of vertebrate and woody plant diversity to the loss of grassland areas, driven by agricultural and forestry expansion, to identify priority areas for conservation. We assessed the spatial variability of biodiversity vulnerability in function of species richness and number of focal species (i.e., prioritized species) of woody plants and terrestrial vertebrates that use grassland ecosystem as habitat. The top 17% of vulnerable sites (51 of 302 cells) were selected as priority conservation areas for Uruguay, following Aichi Target number 11. Approximately 36 % of the original continental territory of Uruguay, mainly grasslands, was converted to cropland (28%) and exotic forest plantations (8%) in 2015. Approximately 27% of the priority cells for conservation of vertebrates and woody plant diversity have been transformed, especially in three ecoregions in which habitat loss was between 35-45%. We simulated a land-use scenario for 2030, based on national production goals of soybean and exotic forest plantations, projecting that: (1) the overall loss of original habitat (mainly grasslands) would reach 48% of the country’s land area, and (2) 45% of the priority cells would be converted to agricultural lands, especially in four ecoregions, with habitat losses greater than 50%. Our results suggest an urgent need to develop strategies to reduce the rate of natural grassland loss in Uruguay, as well as to conserve biodiversity and ecosystem services associated with these systems. Conservation efforts should focus on prioritized cells, especially those with no protection status and a high likelihood of agricultural conversion in 2030, through expanding public and private protected areas and promoting wildlife-friendly agricultural alternatives, such as beef production in natural grasslands
de Sitter symmetry of Neveu-Schwarz spinors
We study the relations between Dirac fields living on the 2-dimensional
Lorentzian cylinder and the ones living on the double-covering of the
2-dimensional de Sitter manifold, here identified as a certain coset space of
the group . We show that there is an extended notion of de Sitter
covariance only for Dirac fields having the Neveu-Schwarz anti-periodicity and
construct the relevant cocycle. Finally, we show that the de Sitter symmetry is
naturally inherited by the Neveu-Schwarz massless Dirac field on the cylinder.Comment: 24 page
Polarized Dirac fermions in de Sitter spacetime
The tetrad gauge invariant theory of the free Dirac field in two special
moving charts of the de Sitter spacetime is investigated pointing out the
operators that commute with the Dirac one. These are the generators of the
symmetry transformations corresponding to isometries that give rise to
conserved quantities according to the Noether theorem. With their help the
plane wave spinor solutions of the Dirac equation with given momentum and
helicity are derived and the final form of the quantum Dirac field is
established. It is shown that the canonical quantization leads to a correct
physical interpretation of the massive or massless fermion quantum fields.Comment: 19 pages, LaTeX w AMS sym
Calcium-dependent dephosphorylation of the histone chaperone DAXX regulates H3.3 loading and transcription upon neuronal activation.
Activity-dependent modifications of chromatin are believed to contribute to dramatic changes in neuronal circuitry. The mechanisms underlying these modifications are not fully understood. The histone variant H3.3 is incorporated in a replication-independent manner into different regions of the genome, including gene regulatory elements. It is presently unknown whether H3.3 deposition is involved in neuronal activity-dependent events. Here, we analyze the role of the histone chaperone DAXX in the regulation of H3.3 incorporation at activity-dependent gene loci. DAXX is found to be associated with regulatory regions of selected activity-regulated genes, where it promotes H3.3 loading upon membrane depolarization. DAXX loss not only affects H3.3 deposition but also impairs transcriptional induction of these genes. Calcineurin-mediated dephosphorylation of DAXX is a key molecular switch controlling its function upon neuronal activation. Overall, these findings implicate the H3.3 chaperone DAXX in the regulation of activity-dependent events, thus revealing a new mechanism underlying epigenetic modifications in neurons
THGEM operation in Ne and Ne/CH4
The operation of Thick Gaseous Electron Multipliers (THGEM) in Ne and Ne/CH4
mixtures, features high multiplication factors at relatively low operation
potentials, in both single- and double-THGEM configurations. We present some
systematic data measured with UV-photons and soft x-rays, in various Ne
mixtures. It includes gain dependence on hole diameter and gas purity,
photoelectron extraction efficiency from CsI photocathodes into the gas,
long-term gain stability and pulse rise-time. Position resolution of a 100x100
mm^2 X-rays imaging detector is presented. Possible applications are discussed.Comment: Submitted to JINST, 25 pages, 33 figure
Molecular Architectures of Trimeric SIV and HIV-1 Envelope Glycoproteins on Intact Viruses: Strain-Dependent Variation in Quaternary Structure
The initial step in target cell infection by human, and the closely related simian immunodeficiency viruses (HIV and SIV, respectively) occurs with the binding of trimeric envelope glycoproteins (Env), composed of heterodimers of the viral transmembrane glycoprotein (gp41) and surface glycoprotein (gp120) to target T-cells. Knowledge of the molecular structure of trimeric Env on intact viruses is important both for understanding the molecular mechanisms underlying virus-cell interactions and for the design of effective immunogen-based vaccines to combat HIV/AIDS. Previous analyses of intact HIV-1 BaL virions have already resulted in structures of trimeric Env in unliganded and CD4-liganded states at ∼20 Å resolution. Here, we show that the molecular architectures of trimeric Env from SIVmneE11S, SIVmac239 and HIV-1 R3A strains are closely comparable to that previously determined for HIV-1 BaL, with the V1 and V2 variable loops located at the apex of the spike, close to the contact zone between virus and cell. The location of the V1/V2 loops in trimeric Env was definitively confirmed by structural analysis of HIV-1 R3A virions engineered to express Env with deletion of these loops. Strikingly, in SIV CP-MAC, a CD4-independent strain, trimeric Env is in a constitutively “open” conformation with gp120 trimers splayed out in a conformation similar to that seen for HIV-1 BaL Env when it is complexed with sCD4 and the CD4i antibody 17b. Our findings suggest a structural explanation for the molecular mechanism of CD4-independent viral entry and further establish that cryo-electron tomography can be used to discover distinct, functionally relevant quaternary structures of Env displayed on intact viruses
The physical meaning of the de Sitter invariants
We study the Lie algebras of the covariant representations transforming the
matter fields under the de Sitter isometries. We point out that the Casimir
operators of these representations can be written in closed forms and we deduce
how their eigenvalues depend on the field's rest energy and spin. For the
scalar, vector and Dirac fields, which have well-defined field equations, we
express these eigenvalues in terms of mass and spin obtaining thus the
principal invariants of the theory of free fields on the de Sitter spacetime.
We show that in the flat limit we recover the corresponding invariants of the
Wigner irreducible representations of the Poincare group.Comment: 22 pages no figure
Cross-Conjugated n-Dopable Aromatic Polyketone
This paper describes the synthesis and characterization of a high molecular weight cross-conjugated polyketone synthesized via scalable Friedel Crafts chemistry. Cross-conjugated polyketones are precursors to conjugated polyions; they become orders of magnitude more conductive after a two-electron reduction and demonstrate reversible spinless doping upon protonation with acids. Cross-conjugated polyketones are a new polymer platform that possess the same optoelectronic tunability as conventional polymers but with excellent thermal and oxidative stability. We constructed a proof-of-concept organic light-emitting diode device and demonstrate that a cross-conjugated polyketone can be successfully used as an n-dopable semiconducting material
Quantification of nitrotyrosine in nitrated proteins
For kinetic studies of protein nitration reactions, we have developed a method for the quantification of nitrotyrosine residues in protein molecules by liquid chromatography coupled to a diode array detector of ultraviolet-visible absorption. Nitrated bovine serum albumin (BSA) and nitrated ovalbumin (OVA) were synthesized and used as standards for the determination of the protein nitration degree (ND), which is defined as the average number of nitrotyrosine residues divided by the total number of tyrosine residues in a protein molecule. The obtained calibration curves of the ratio of chromatographic peak areas of absorbance at 357 and at 280 nm vs. nitration degree are nearly the same for BSA and OVA (relative deviations <5%). They are near-linear at low ND (< 0.1) and can be described by a second-order polynomial fit up to \documentclass[12pt]{minimal}
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\begin{document}\end{document}. A change of chromatographic column led to changes in absolute peak areas but not in the peak area ratios and related calibration functions, which confirms the robustness of the analytical method. First results of laboratory experiments confirm that the method is applicable for the investigation of the reaction kinetics of protein nitration. The main advantage over alternative methods is that nitration degrees can be efficiently determined without hydrolysis or digestion of the investigated protein molecules
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