Bar formation and evolution in disc galaxies with gas and a triaxial halo: Morphology, bar strength and halo properties

We follow the formation and evolution of bars in N-body simulations of disc galaxies with gas and/or a triaxial halo. We find that both the relative gas fraction and the halo shape play a major role in the formation and evolution of the bar. In gas-rich simulations, the disc stays near-axisymmetric much longer than in gas-poor ones, and, when the bar starts growing, it does so at a much slower rate. Due to these two effects combined, large-scale bars form much later in gas-rich than in gas-poor discs. This can explain the observation that bars are in place earlier in massive red disc galaxies than in blue spirals. We also find that the morphological characteristics in the bar region are strongly influenced by the gas fraction. In particular, the bar at the end of the simulation is much weaker in gas-rich cases. In no case did we witness bar destruction. Halo triaxiality has a dual influence on bar strength. In the very early stages of the simulation it induces bar formation to start earlier. On the other hand, during the later, secular evolution phase, triaxial haloes lead to considerably less increase of the bar strength than spherical ones. The shape of the halo evolves considerably with time. The inner halo parts may become more elongated, or more spherical, depending on the bar strength. The main body of initially triaxial haloes evolves towards sphericity, but in initially strongly triaxial cases it stops well short of becoming spherical. Part of the angular momentum absorbed by the halo generates considerable rotation of the halo particles that stay located relatively near the disc for long periods of time. Another part generates halo bulk rotation, which, contrary to that of the bar, increases with time but stays small.Comment: 21 pages, 16 figures, accepted for publication in MNRAS. A high resolution version is at http://195.221.212.246:4780/dynam/paper/amr12/rm_3axhalo_gas.pd

The graphene sheet versus the 2DEG: a relativistic Fano spin-filter via STM and AFM tips

We explore theoretically the density of states (LDOS) probed by an STM tip of 2D systems hosting an adatom and a subsurface impurity,both capacitively coupled to AFM tips and traversed by antiparallel magnetic fields. Two kinds of setups are analyzed, a monolayer of graphene and a two-dimensional electron gas (2DEG). The AFM tips set the impurity levels at the Fermi energy, where two contrasting behaviors emerge: the Fano factor for the graphene diverges, while in the 2DEG it approaches zero. As result, the spin-degeneracy of the LDOS is lifted exclusively in the graphene system, in particular for the asymmetric regime of Fano interference. The aftermath of this limit is a counterintuitive phenomenon, which consists of a dominant Fano factor due to the subsurface impurity even with a stronger STM-adatom coupling. Thus we find a full polarized conductance, achievable just by displacing vertically the position of the STM tip. To the best knowledge, our work is the first to propose the Fano effect as the mechanism to filter spins in graphene. This feature arises from the massless Dirac electrons within the band structure and allows us to employ the graphene host as a relativistic Fano spin-filter

CCM pilot study overview: geometrical measurement of the Rockwell diamond indenter

This paper describes an overview of the capability of the NMIs that participated on the CCM Pilot Study measurement systems, conducted by the CIPM/CCM/Working Group on Hardness, to characterize the Rockwell hardness diamond indenter geometry, by measuring the included cone angle, the straightness of the generatrix, the spherical tip radius, the deviation of the local radius and the tilt angle. Nine NMIs took part in this study: INMETRO (Brazil); INRiM (Italy); KRISS (South Korea); NIM/PR (China); NIMT (Thailand); NIST (USA); PTB (Germany); TUBITAK UME (Turkey); VNIIFTRI (Russia), where INMETRO (Brazil) served as pilot laboratory

GORLIN-GOLTZ SYNDROME: A CASE REPORT

Introdução: O Síndrome de Gorlin-Goltz é uma condição hereditária autossómica dominante rara caracterizada por: carcinomas basocelulares, queratoquistos odontogénicos, depressões palmo-plantares, calcificações da foice cerebral e malformações esqueléticas. Associa-se também a meduloblastoma e outras neoplasias. Caso Clínico: Adolescente de 11 anos, com antecedentes de macrocefalia. Referenciada à consulta de estomatologia por quistos mandibulares recidivantes. O exame anátomo-patológico revelou tratarem-se de queratoquistos odontogénicos, pelo que é encaminhada para a consulta de pediatria. Objetivamente, apresentava macrocefalia e facies “gros seiro” com bossas frontais e hipertelorismo. Efetuou estudo genético, que detetou mutação do gene PTCH1, confirmando a suspeita clínica. Discussão: Os queratoquistos odontogénicos são o achado mais representativo do síndrome de Gorlin-Goltz nas duas primeiras décadas de vida, sendo de extrema importância um elevado índice de suspeição por parte do pediatra, com especial relevância para as alterações minor. Após o estabelecimento do diagnóstico, é necessária uma equipa multidisciplinar para um adequado seguimento e tratamento atempado.Introduction: The Gorlin-Goltz syndrome is a rare autosomal dominant inherited condition characterized by: basal cell carcinomas, odontogenic keratocysts, palmar or plantar pits, calcification of the falx cerebri and skeletal malformations. Medulloblastoma and other tumors are also associated with it. Case report: An 11-year-old female, with a history of macrocephaly, was referred to the Stomatology Department for recurrent mandibular cyst. Histopathological exam revealed odontogenic keratocysts, so the patient was referred to the Pediatric Department. Physical examination revealed macrocephaly and coarse face, with frontal bossing and hy pertelorism. The genetic study performed detected a mutation in PTCH1 gene, confirming the clinical suspicion. Discussion: Odontogenic keratocysts are the most representative finding in Gorlin-Goltz Syndrome in the first two decades of life, therefore a high suspicion level is mandatory among pediatricians concerning detection of minor changes. After the diagnosis, a multidisciplinary team is required for adequate follow-up and timely treatment