34 research outputs found
On the symmetries of BF models and their relation with gravity
The perturbative finiteness of various topological models (e.g. BF models)
has its origin in an extra symmetry of the gauge-fixed action, the so-called
vector supersymmetry. Since an invariance of this type also exists for gravity
and since gravity is closely related to certain BF models, vector supersymmetry
should also be useful for tackling various aspects of quantum gravity. With
this motivation and goal in mind, we first extend vector supersymmetry of BF
models to generic manifolds by incorporating it into the BRST symmetry within
the Batalin-Vilkovisky framework. Thereafter, we address the relationship
between gravity and BF models, in particular for three-dimensional space-time.Comment: 29 page
Symmetries of topological field theories in the BV-framework
Topological field theories of Schwarz-type generally admit symmetries whose
algebra does not close off-shell, e.g. the basic symmetries of BF models or
vector supersymmetry of the gauge-fixed action for Chern-Simons theory (this
symmetry being at the origin of the perturbative finiteness of the theory). We
present a detailed discussion of all these symmetries within the algebraic
approach to the Batalin-Vilkovisky formalism. Moreover, we discuss the general
algebraic construction of topological models of both Schwarz- and Witten-type.Comment: 30 page
A classmate in distress: schoolchildren as bystanders and their reasons for how they act
Observation of the lateral displacement of surface acoustic beams reflected at boundaries of layered substrates
Christmas Disease (Haemophilia B) in a Girl with Deletion of the Short Arm of One X-Chromosome (Functional Turner Syndrome)
A I-year-old girl with severe Christmas disease and a factor IX content less than 1% of normal is described. The family history was negative and coagulation studies on her relatives were normal. Genetic investigation showed an XXp-karyotype with deletion of the short arm of one X-chromosome, a cytogenetic variant of Turner syndrome. The transmission pathway of the haemophilia gene is discussed