3,520 research outputs found
Unstable and elusive superconductors
We briefly review earlier and report original experimental results in the
context of metastable or possible superconducting materials. We show that
applied electric field induces conducting state in Copper Chloride (CuCl) whose
characteristics resemble behavior of sliding charge-density-wave(s) (CDW). We
discuss whether the sliding CDW or collective transport of similar ordered
charge phase(s) may account for the problem of "high-temperature
superconductivity" observed in this and other materials, including Cadmium
Sulfide (CdS), metal-ammonia solutions, polymers, amorphous carbon and tungsten
oxides. We also discuss a local superconductivity that occurs at the surface of
graphite and amorphous carbon under deposition of foreign atoms/molecules.Comment: Invited review article published in a special edition on
Superconducting Materials in honor of the 95th birthday year of Ted Geballe,
edited by M. B. Maple, J. Hirsch, and F. Marsigli
Local and Global Superconductivity in Bismuth
We performed magnetization M(H,T) and magnetoresistance R(T,H) measurements
on powdered (grain size ~ 149 micrometers) as well as highly oriented
rhombohedral (A7) bismuth (Bi) samples consisting of single crystalline blocks
of size ~ 1x1 mm2 in the plane perpendicular to the trigonal c-axis. The
obtained results revealed the occurrence of (1) local superconductivity in
powdered samples with Tc(0) = 8.75 \pm 0.05 K, and (2) global superconductivity
at Tc(0) = 7.3 \pm 0.1 K in polycrystalline Bi triggered by low-resistance
Ohmic contacts with silver (Ag) normal metal. The results provide evidence that
the superconductivity in Bi is localized in a tiny volume fraction, probably at
intergrain or Ag/Bi interfaces. On the other hand, the occurrence of global
superconductivity observed for polycrystalline Bi can be accounted for by
enhancement of the superconducting order parameter phase stiffness induced by
the normal metal contacts, the scenario proposed in the context of "pseudogap
regime" in cuprates [E. Berg et al., PRB 78, 094509 (2008)].Comment: 12 pages including 9 figures and 1 table, Special Issue to the 80th
birthday anniversary of V. G. Peschansky, Electronic Properties of Conducting
System
Charge Ordering in Amorphous WO Films
We report on the observation of highly anisotropic viscous electronic
conducting phase in amorphous WO films that occurs below a current
(I)- and frequency (f)- dependent temperature T*(I, f). At T < T*(I, f) the
rotational symmetry of randomly disordered electronic background is broken
leading to the appearance of mutually perpendicular metallic- and
insulating-like states. A rich dynamic behavior of the electronic matter
occurring at T < T*(I, f) provides evidence for an interplay between pinning
effects and electron-electron interactions. The results strongly suggest a
dynamic crystallization of the disordered electronic matter, viz. formation of
sliding Wigner crystal, as well as the occurrence of quantum smectic or stripe
phase in the pinning-dominated regime.Comment: 17 pages including 5 figure
Orange Pectin Mediated Growth and Stability of Aqueous Gold and Silver Nanocolloids
International audienceThe role of orange based pectin in the nucleation and growth of silver and gold nanoparticles is addressed. Pectin is a complex polysaccharide found in fruits such as oranges, lemons, passion fruits or apples. It displays smooth and hairy chain regions contg. hydroxyl-, ester-, carboxylate- and eventually amine groups that can act as surface ligands interacting under various pH conditions more or less efficiently with growing nanometals. Here, a high methoxy pectin (>50% esterified) was used as a stabilizer/reducing agent in the prepn. of gold, silver and silver-gold nanoparticles. Com. pectin (CP) and pectin extd. from orange bagasse (OP) were used. Optionally, trisodium citrate or oxalic acid we used to reduce AgNO3 and HAuCl4 in aq. environment. Characterization methods included UV-vis absorption spectroscopy, transmission electron microscopy, electron diffraction and energy-dispersive X-ray spectroscopy. The results show that under different pH conditions, pectin and reducing agents allow producing various nanostructures shapes (triangles, spheres, rods, octahedrons and decahedrons) often with high polydispersity and sizes ranging between 5 nm and 30 nm. In addn., depending on Ag/Au-ratio and pH, the surface plasmon bands can be continuously shifted between 410 nm and 600 nm. Finally, pectin seems to be a highly efficient stabilizer of the colloidal systems that show a remarkable stability and unchanged optical spectral response even after five years
ACE2-angiotensin-(1-7)-Mas axis in renal ischaemia/reperfusion injury in rats
AngII (angiotensin II), ACE (angiotensin I-converting enzyme) and the AT(1) receptor (AngII type I receptor) are associated with the inflammatory process and microvascular dysfunction of AKI (acute kidney injury) induced by renal I/R (ischaemia/reperfusion). However, Ang-(1-7) [angiotensin-(1-7)], ACE2 (angiotensin I-converting enzyme 2) and the Mas receptor also play a role in renal disease models. Therefore, in the present study, we have examined the renal profile of Ang-(1-7), ACE2 and the Mas receptor in renal I/R and compared them with that of AngII, ACE and the AT(1) receptor. Male Wistar rats were submitted to left nephrectomy and ischaemia (45 min) followed by reperfusion (2 or 4 h) in the right kidney. At 4 h of reperfusion, renal AngII was increased (P < 0.01) and renal Ang-(1-7) was decreased substantially (P < 0.05), although plasma levels of both angiotensins were unchanged. in addition, renal I/R decreased the renal mRNA expression of renin (P < 0.05), AT(1) receptors (P < 0.001) and ACE2 (P < 0.05). At 2 and 4 h of reperfusion, renal ACE activity was reduced (P < 0.05). On the other hand, renal expression of the Mas receptor was greatly increased at 4 h of reperfusion (P < 0.01), which was confirmed by immunohistochemical and Western blot analysis. in conclusion, increased renal expression of the Mas receptor associated with changes in the RAS (renin-angiotensin-system)-related peptidases support an important role for the ACE2 Ang-(1-7) Mas axis in AKI.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)Univ Fed Minas Gerais, Inst Biol Sci, Dept Physiol & Biophys, BR-31270901 Belo Horizonte, MG, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Dept Biophys, BR-04044020 São Paulo, SP, BrazilUniv Fed Minas Gerais, Dept Pathol, BR-31270901 Belo Horizonte, MG, BrazilUniv Fed Minas Gerais, Dept Microbiol, BR-31270901 Belo Horizonte, MG, BrazilUniv Fed Minas Gerais, Clin Pathol Unit COLTEC, BR-31270901 Belo Horizonte, MG, BrazilUniv Fed Minas Gerais, Dept Biochem, Inst Biol Sci, BR-31270901 Belo Horizonte, MG, BrazilUniv Fed Minas Gerais, Dept Pediat, Fac Med, BR-31270901 Belo Horizonte, MG, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, Dept Biophys, BR-04044020 São Paulo, SP, BrazilCAPES: PRDEX2009CNPq: 8701480/1997-4FAPEMIG: CBS 2044/96Web of Scienc
The role of P2 receptors in controlling infections by intracellular pathogens
A growing number of studies have demonstrated the importance of ATPe-signalling via P2 receptors as an important component of the inflammatory response to infection. More recent studies have shown that ATPe can also have a direct effect on infection by intracellular pathogens, by modulating membrane trafficking in cells that contain vacuoles that harbour intracellular pathogens, such as mycobacteria and chlamydiae. A conserved mechanism appears to be involved in controlling infection by both of these pathogens, as a role for phospholipase D in inducing fusion between lysosomes and the vacuoles has been demonstrated. Other P2-dependent mechanisms are most likely operative in the cases of pathogens, such as Leishmania, which survive in an acidic phagolysosomal-like compartment. ATPe may function as a ‘danger signal–that alerts the immune system to the presence of intracellular pathogens that damage the host cell, while different intracellular pathogens have evolved enzymes or other mechanisms to inhibit ATPe-mediated signalling, which should, thus, be viewed as virulence factors for these pathogens
Different pathways in the larval development of the crab Ucides cordatus (Decapoda, Ocypodidae) and their relation with high mortality rates by the end of massive larvicultures
One of the most limiting factors affecting the larval rearing of Ucides cordatus in the laboratory is a period of high mortality, which usually occurs late in the course of the larviculture during the metamorphosis from the zoeal to the megalopal phase. The objective of the present research was to analyze the post-embryonic development of U. cordatus on an individual basis and, in particular, to search for patterns linking disturbances in the molting process to the high larval death rates observed in massive larvicultures. A total of 50 larvae were individually reared from hatching to metamorphosis into the megalopal phase under controlled conditions, fed a combination of microalgae and rotifers. The survivorship rate was 70% until zoea V. The 35 surviving zoea V larvae followed two different pathways. Eleven underwent metamorphosis directly to megalopa, eighteen molted to zoea VI and six died as zoea V. In the last molting event, only two zoea VI larvae reached the megalopal stage, while the remaining sixteen died. In further observation under microscope, 13 of the dead zoea VI showed characteristics of the pre-molt stage and pereiopods disproportionably large in relation to the carapace. The observed pattern resembles the Molt Death Syndrome (MDS) described for other decapod species, in which larvae die in the late pre-molt phase of the molting cycle. We suggest that U. cordatus larvae develop disturbances in the molting process similar to the MDS described for other species and that these disturbances are related to a more complex pathway involving the emergence of larval stage zoea VI
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