Study of semi-synthetic plastic objects of historic interest using non-invasive total reflectance FT-IR

A significant proportion of modern and contemporary artifacts and objects of historical interest, are composed of materials in the form of synthetic, semi-synthetic, and natural polymers. Each class of polymer and corresponding composite plastics are subject to different degradation processes. This means that conservators and curators of 20th century collections are faced with varied, nontrivial preservation issues. An unresolved problem is the identification of early plastics based on semi-synthetic polymers such as cellulose nitrate, cellulose acetate, and casein formaldehyde, which were often used to imitate the more valuable natural materials such as ivory, tortoiseshell, ebony, and bone. This exemplifies the need for non-invasive methods specifically tailored for identification of plastic materials in collections, so as to provide conservators with a means of materials classification to support preventive conservation strategies and interventive treatments. The present work is aimed at evaluating the effectiveness of non-invasive Total Reflectance (TR) FT-IR spectroscopy, coupled with a custom reference spectral TR FT-IR library, for the identification of materials comprising a series of unknown objects. A set of ten heritage objects made from early semi-synthetic materials was used as a training test set to validate the proposed methodological approach. The FT-IR data acquired on the test objects were pre-processed and finally classified using commercial software tools used for the automatic classification of spectra in FT-IR spectroscopy. The procedure was successfully applied to several cases, although residual uncertainties remained in a few examples. The results obtained are critically analyzed and discussed in the perspective of proposing a robust method for in-field prescreening of the chemical composition of plastic artistic and historical objects

Natural Diagonal Riemannian Almost Product and Para-Hermitian Cotangent Bundles

We obtain the natural diagonal almost product and locally product structures on the total space of the cotangent bundle of a Riemannian manifold. We find the Riemannian almost product (locally product) and the (almost) para-Hermitian cotangent bundles of natural diagonal lift type. We prove the characterization theorem for the natural diagonal (almost) para-K\"ahlerian structures on the total spaces of the cotangent bundle.Comment: 10 pages, will appear in Czechoslovak Mathematical Journa

Superconformal N=2, D=5 matter with and without actions

We investigate N=2, D=5 supersymmetry and matter-coupled supergravity theories in a superconformal context. In a first stage we do not require the existence of a Lagrangian. Under this assumption, we already find at the level of rigid supersymmetry, i.e. before coupling to conformal supergravity, more general matter couplings than have been considered in the literature. For instance, we construct new vector-tensor multiplet couplings, theories with an odd number of tensor multiplets, and hypermultiplets whose scalar manifold geometry is not hyperkaehler. Next, we construct rigid superconformal Lagrangians. This requires some extra ingredients that are not available for all dynamical systems. However, for the generalizations with tensor multiplets mentioned above, we find corresponding new actions and scalar potentials. Finally, we extend the supersymmetry to local superconformal symmetry, making use of the Weyl multiplet. Throughout the paper, we will indicate the various geometrical concepts that arise, and as an application we compute the non-vanishing components of the Ricci tensor of hypercomplex group manifolds. Our results can be used as a starting point to obtain more general matter-couplings to Poincare supergravity.Comment: 67 pages; v2: title of reference changed and small editing corrections; v3: small typing errors corrected, version published in JHEP; v4: typos corrected; v5: additional term in (2.109) and (4.11); v6: change of order of indices in (2.89

Polymorphisms in the RNASE3 Gene Are Associated with Susceptibility to Cerebral Malaria in Ghanaian Children

BACKGROUND: Cerebral malaria (CM) is the most severe outcome of Plasmodium falciparum infection and a major cause of death in children from 2 to 4 years of age. A hospital based study in Ghana showed that P. falciparum induces eosinophilia and found a significantly higher serum level of eosinophil cationic protein (ECP) in CM patients than in uncomplicated malaria (UM) and severe malaria anemia (SA) patients. Single nucleotide polymorphisms (SNPs) have been described in the ECP encoding-gene (RNASE3) of which the c.371G>C polymorphism (rs2073342) results in an arginine to threonine amino acid substitution p.R124T in the polypeptide and abolishes the cytotoxicity of ECP. The present study aimed to investigate the potential association between polymorphisms in RNASE3 and CM. METHODOLOGY/PRINCIPAL FINDINGS: The RNASE3 gene and flanking regions were sequenced in 206 Ghanaian children enrolled in a hospital based malaria study. An association study was carried out to assess the significance of five SNPs in CM (n=45) and SA (n=56) cases, respectively. The two severe case groups (CM and SA) were compared with the non-severe control group comprising children suffering from UM (n=105). The 371G allele was significantly associated with CM (p=0.00945, OR=2.29, 95% CI=1.22-4.32) but not with SA. Linkage disequilibrium analysis demonstrated significant linkage between three SNPs and the haplotype combination 371G/*16G/*94A was strongly associated with susceptibility to CM (p=0.000913, OR=4.14, 95% CI=1.79-9.56), thus, defining a risk haplotype. The RNASE3 371GG genotype was found to be under frequency-dependent selection. CONCLUSIONS/SIGNIFICANCE: The 371G allele of RNASE3 is associated with susceptibility to CM and forms part of a risk associated haplotype GGA defined by the markers: rs2073342 (G-allele), rs2233860 (G-allele) and rs8019343 (A-allele) respectively. Collectively, these results suggest a hitherto unrecognized role for eosinophils in CM pathogenesis

Eculizumab treatment: stochastic occurrence of C3 binding to individual PNH erythrocytes

C5 blockade by eculizumab prevents complement-mediated intravascular hemolysis in paroxysmal nocturnal hemoglobinuria (PNH). However, C3-bound PNH red blood cells (RBCs), arising in almost all treated patients, may undergo extravascular hemolysis reducing clinical benefits. Despite the uniform deficiency of CD55 and of CD59, there are always two distinct populations of PNH RBCs, with (C3+) and without (C3-) C3 binding

Human malarial disease: a consequence of inflammatory cytokine release

Malaria causes an acute systemic human disease that bears many similarities, both clinically and mechanistically, to those caused by bacteria, rickettsia, and viruses. Over the past few decades, a literature has emerged that argues for most of the pathology seen in all of these infectious diseases being explained by activation of the inflammatory system, with the balance between the pro and anti-inflammatory cytokines being tipped towards the onset of systemic inflammation. Although not often expressed in energy terms, there is, when reduced to biochemical essentials, wide agreement that infection with falciparum malaria is often fatal because mitochondria are unable to generate enough ATP to maintain normal cellular function. Most, however, would contend that this largely occurs because sequestered parasitized red cells prevent sufficient oxygen getting to where it is needed. This review considers the evidence that an equally or more important way ATP deficency arises in malaria, as well as these other infectious diseases, is an inability of mitochondria, through the effects of inflammatory cytokines on their function, to utilise available oxygen. This activity of these cytokines, plus their capacity to control the pathways through which oxygen supply to mitochondria are restricted (particularly through directing sequestration and driving anaemia), combine to make falciparum malaria primarily an inflammatory cytokine-driven disease