Magnetic properties of HgTe quantum wells

Using analytical formulas as well as a finite-difference scheme, we investigate the magnetic field dependence of the energy spectra and magnetic edge states of HgTe/CdTe-based quantum wells in the presence of perpendicular magnetic fields and hard walls, for the band-structure parameters corresponding to the normal and inverted regimes. Whereas one cannot find counterpropagating, spin-polarized states in the normal regime, below the crossover point between the uppermost (electron-like) valence and lowest (hole-like) conduction Landau levels, one can still observe such states at finite magnetic fields in the inverted regime, although these states are no longer protected by time-reversal symmetry. Furthermore, the bulk magnetization and susceptibility in HgTe quantum wells are studied, in particular their dependence on the magnetic field, chemical potential, and carrier densities. We find that for fixed chemical potentials as well as for fixed carrier densities, the magnetization and magnetic susceptibility in both the normal and the inverted regimes exhibit de Haas-van Alphen oscillations, whose amplitude decreases with increasing temperature. Moreover, if the band structure is inverted, the ground-state magnetization (and consequently also the ground-state susceptibility) is discontinuous at the crossover point between the uppermost valence and lowest conduction Landau levels. At finite temperatures and/or doping, this discontinuity is canceled by the contribution from the electrons and holes and the total magnetization and susceptibility are continuous. In the normal regime, this discontinuity of the ground-state magnetization does not arise and the magnetization is continuous for zero as well as finite temperatures.Comment: 19 pages, 26 figure

Co-infection with different subtypes of feline immunodeficiency virus can complicate subtype assignment of phylogenetic analysis

Phylogenetic analyses of the V3-V5 region of the env gene are used to determine Feline immunodeficiency virus (FIV) subtypes but can be complicated by co-infection with different subtypes or the presence of recombinant subtypes. FIV in blood samples from 30 domestic cats in New Zealand was subtyped by sequencing three overlapping fragments of the V3-V5 region of the env gene and 467 bp of the gag gene. Phylogenetic analyses revealed that the isolates clustered with subtype A and C viruses. Seven samples showed discrepancies in subtype assignment from analyses of their env gene sequences. Nucleotide differences of 19.6% and 20.9% in overlapping regions in two cats suggest co-infection with subtypes A and C