190 research outputs found
Approximation of conformal mappings using conformally equivalent triangular lattices
Consider discrete conformal maps defined on the basis of two conformally
equivalent triangle meshes, that is edge lengths are related by scale factors
associated to the vertices. Given a smooth conformal map , we show that it
can be approximated by such discrete conformal maps . In
particular, let be an infinite regular triangulation of the plane with
congruent triangles and only acute angles (i.e.\ ). We scale this
tiling by and approximate a compact subset of the domain of
with a portion of it. For small enough we prove that there exists a
conformally equivalent triangle mesh whose scale factors are given by
on the boundary. Furthermore we show that the corresponding discrete
conformal maps converge to uniformly in with error of
order .Comment: 14 pages, 3 figures; v2 typos corrected, revised introduction, some
proofs extende
Discrete complex analysis on planar quad-graphs
We develop a linear theory of discrete complex analysis on general
quad-graphs, continuing and extending previous work of Duffin, Mercat, Kenyon,
Chelkak and Smirnov on discrete complex analysis on rhombic quad-graphs. Our
approach based on the medial graph yields more instructive proofs of discrete
analogs of several classical theorems and even new results. We provide discrete
counterparts of fundamental concepts in complex analysis such as holomorphic
functions, derivatives, the Laplacian, and exterior calculus. Also, we discuss
discrete versions of important basic theorems such as Green's identities and
Cauchy's integral formulae. For the first time, we discretize Green's first
identity and Cauchy's integral formula for the derivative of a holomorphic
function. In this paper, we focus on planar quad-graphs, but we would like to
mention that many notions and theorems can be adapted to discrete Riemann
surfaces in a straightforward way.
In the case of planar parallelogram-graphs with bounded interior angles and
bounded ratio of side lengths, we construct a discrete Green's function and
discrete Cauchy's kernels with asymptotics comparable to the smooth case.
Further restricting to the integer lattice of a two-dimensional skew coordinate
system yields appropriate discrete Cauchy's integral formulae for higher order
derivatives.Comment: 49 pages, 8 figure
Approximation of conformal mappings by circle patterns
A circle pattern is a configuration of circles in the plane whose
combinatorics is given by a planar graph G such that to each vertex of G
corresponds a circle. If two vertices are connected by an edge in G, the
corresponding circles intersect with an intersection angle in .
Two sequences of circle patterns are employed to approximate a given
conformal map and its first derivative. For the domain of we use
embedded circle patterns where all circles have the same radius decreasing to 0
and which have uniformly bounded intersection angles. The image circle patterns
have the same combinatorics and intersection angles and are determined from
boundary conditions (radii or angles) according to the values of (
or ). For quasicrystallic circle patterns the convergence result is
strengthened to -convergence on compact subsets.Comment: 36 pages, 7 figure
Terbium to Quantum Dot FRET Bioconjugates for Clinical Diagnostics: Influence of Human Plasma on Optical and Assembly Properties
Förster resonance energy transfer (FRET) from luminescent terbium complexes (LTC) as donors to semiconductor quantum dots (QDs) as acceptors allows extraordinary large FRET efficiencies due to the long Förster distances afforded. Moreover, time-gated detection permits an efficient suppression of autofluorescent background leading to sub-picomolar detection limits even within multiplexed detection formats. These characteristics make FRET-systems with LTC and QDs excellent candidates for clinical diagnostics. So far, such proofs of principle for highly sensitive multiplexed biosensing have only been performed under optimized buffer conditions and interactions between real-life clinical media such as human serum or plasma and LTC-QD-FRET-systems have not yet been taken into account. Here we present an extensive spectroscopic analysis of absorption, excitation and emission spectra along with the luminescence decay times of both the single components as well as the assembled FRET-systems in TRIS-buffer, TRIS-buffer with 2% bovine serum albumin, and fresh human plasma. Moreover, we evaluated homogeneous LTC-QD FRET assays in QD conjugates assembled with either the well-known, specific biotin-streptavidin biological interaction or, alternatively, the metal-affinity coordination of histidine to zinc. In the case of conjugates assembled with biotin-streptavidin no significant interference with the optical and binding properties occurs whereas the histidine-zinc system appears to be affected by human plasma
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