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1.
Phys Rev E ; 96(6-1): 062146, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29347450

ABSTRACT

In this work we study an effective three-mode model describing interacting bosons. These bosons can be considered as exciton-polaritons in a semiconductor microcavity at the magic angle. This model exhibits quantum phase transition (QPT) when the parameters of the corresponding Hamiltonian are continuously varied. The properties of the Hamiltonian spectrum (e.g., the distance between two adjacent energy levels) and the phase space structure of the thermodynamic limit of the model are used to indicate QPT. The relation between spectral properties of the Hamiltonian and the corresponding classical frame of the thermodynamic limit of the model is established as indicative of QPT. The average number of bosons in a specific mode and the entanglement properties of the ground state as functions of the parameters are used to characterize the order of the transition and also to construct a phase diagram. Finally, we verify our results for experimental data obtained for a setting of exciton-polaritons in a semiconductor microcavity.

2.
FEMS Microbiol Lett ; 191(2): 249-54, 2000 Oct 15.
Article in English | MEDLINE | ID: mdl-11024271

ABSTRACT

Metarhizium anisopliae var. acridum (syn. M. flavoviride) is recognized as a highly specific and virulent mycopathogen of locusts and grasshoppers and is currently being developed as a biological control agent for this group of insects in Brazil. Intact conidia of M. anisopliae var. acridum strain CG423 were transformed using microparticle bombardment. Plasmids used were: (1) pBARKS1 carrying the bar gene of Streptomyces hygroscopicus fused to the Aspergillus nidulans trpC promoter, encoding resistance to glufosinate ammonium (or phosphinothricin) and modified by addition of the telomeric repeat (TTAGGG)(18) of Fusarium oxysporum and 2.pEGFP/gpd/tel carrying a red-shifted variant gene for Aequorea victoria green fluorescent protein (EGFP) which we have fused to the A. nidulans gpd promoter and trpC terminator. Highly fluorescent co-transformants were selected on solid minimal medium containing 100 microg ml(-1) glufosinate ammonium using an inverted microscope with 450-490 nm excitation/510 nm emission filter set. Southern blot analysis of co-transformants revealed varying multiple chromosomal integrations of both bar and egfp genes at both telomeric and non-telomeric loci. Transformants retained pathogenicity in bioassays against Rhammatocerus schistocercoides and showed unaltered lack of pathogenicity against larvae of the non-target insect Anticarsia gemmatalis. One co-transformant from four tested, however, showed a significant, but non-dose-dependent, elevation in virulence against Tenebrio molitor.


Subject(s)
Aminobutyrates/pharmacology , Biolistics , Fungi/genetics , Herbicides/pharmacology , Luminescent Proteins/genetics , Transformation, Genetic , Animals , Drug Resistance, Microbial , Fungi/drug effects , Fungi/pathogenicity , Grasshoppers/microbiology , Green Fluorescent Proteins , Luminescent Proteins/metabolism , Organophosphorus Compounds/pharmacology , Pest Control, Biological , Virulence
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