Application of the Worldline Path Integral Method to the Calculation of Inverse Mass Expansions

Higher order coefficients of the inverse mass expansion of one-loop effective actions are obtained from a one-dimensional path integral representation. For the case of a massive scalar loop in the background of both a scalar potential and a (non Abelian) gauge field explicit results to $O(T^5)$ in the proper time parameter are presented.Comment: 6 pages, LaTeX. Talk given at 5th International Workshop on Software Engineering and Artificial Intelligence for High Energy and Nuclear Physics (AIHENP96), Lausanne (Switzerland), 2-6 September 199

Determinant Calculations Using Random Walk Worldline Loops

We use statistical ensembles of worldline loops generated by random walk on hypercubic lattices to calculate matter determinants in background Yang-Mills fields.Comment: 3 pages, 3 ps figures, Lattice2002 (algor

Resummed effective action in the world-line formalism

Using the world-line method we resum the scalar one-loop effective action. This is based on an exact expression for the one-loop action obtained for a background potential and a Taylor expansion of the potential up to quadratic order in x-space. We thus reproduce results of Masso and Rota very economically. An alternative resummation scheme is suggested using ``center of mass'' based loops which is equivalent under the assumption of vanishing third and higher derivatives in the Taylor expansion but leads to simplified expressions. In an appendix some general issues concerning the relation between world-line integrals with fixed end points versus integrals with fixed center are clarified. We finally note that this method is also very valuable for gauge field effective actions where it is based on the Euler--Heisenberg type resummation.Comment: 15 page

Effective Action in a General Chiral Model: Next to Leading Order Derivative Expansion in the Worldline Method

We present a formalism to determine the imaginary part of a general chiral model in the derivative expansion. Our formalism is based on the worldline path integral for the covariant current that can be given in an explicit chiral and gauge covariant form. The effective action is then obtained by integrating the covariant current, taking account of the anomaly.Comment: 33 pages, minor changes, published versio

An Improved Heat Kernel Expansion from Worldline Path Integrals

The one--loop effective action for the case of a massive scalar loop in the background of both a scalar potential and an abelian or non--abelian gauge field is written in a one--dimensional path integral representation. From this the inverse mass expansion is obtained by Wick contractions using a suitable Green function, which allows the computation of higher order coefficients. For the scalar case, explicit results are presented up to order O(T**8) in the proper time expansion. The relation to previous work is clarified.Comment: 13 pages, Plain TEX, no figure

Ingestive behaviour and physiology of the medicinal leech

Ingestion lasts 25 min in Hirudo medicinalis and is characterized by pharyngeal peristalsis which fills the crop. This peristalsis has an initial rate of 2.4 Hz which decays smoothly to 1.2 Hz at termination of ingestion. During ingestion, the leech body wall undergoes peristalsis which appears to aid in filling the crop diverticula. Body peristalsis begins at a rate of 10 min^(-1) and decreases linearly to 2 min^(-1) at termination. The body also undergoes dorsoventral flexions when blood flow is occluded. Blood meal size increases slightly with leech size: 8.4 g for 1-g leeches and 9.7 g for 2-g leeches. However, relative meal size decreases markedly with increasing animal size; from 8.15 times body mass for 1-g to 4.80 times for 2-g leeches. When intact leeches were exposed to micromolar concentrations of serotonin, there was an increase in the rate of pharyngeal peristalsis and the size of the blood meals. Leeches excrete the plasma from their ingested blood meals. Excretion is activated during ingestion, which increases feeding efficiency by increasing the proportion of blood cells in the ingestate. Excretion continues for 4–6 days following ingestion, removing all the remaining plasma from the ingestate. Leech ingestion comprises stereotyped muscular movements, secretion of saliva and excretion of plasma. A strikingly similar feeding physiology is seen in the blood-sucking insect Rhodnius, and we suggest that efficient sanguivory may require the convergent evolution of similar ingestive mechanisms