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Henrik Ronellenfitsch

Publications and source records attributed to Henrik Ronellenfitsch.

24 records · Page 2Linked to original sources

Global Optimization, Local Adaptation, and the Role of Growth in Distribution Networks

Highly-optimized complex transport networks serve crucial functions in many man-made and natural systems such as power grids and plant or animal vasculature. Often, the relevant optimization functional is non-convex and characterized by many local extrema. In general, finding the global, or nearly global optimum is difficult. In biological systems, it is believed that natural selection slowly guides the network towards an optimized state. However, general coarse grained models for flow networks with local positive feedback rules for the vessel conductivity typically get trapped in low efficiency, local minima. In this work we show how the growth of the underlying tissue, coupled to the dynamical equations for network development, can drive the system to a dramatically improved optimal state. This general model provides a surprisingly simple explanation for the appearance of highly optimized transport networks in biology such as leaf and animal vasculature.

physics.bio-ph↗

Network susceptibilities: theory and applications

We introduce the concept of network susceptibilities quantifying the response of the collective dy- namics of a network to small parameter changes. We distinguish two types of susceptibilities: vertex susceptibilities and edge susceptibilities, measuring the responses due to changes in the properties of units and their interactions, respectively. We derive explicit forms of network susceptibilities for oscillator networks close to steady states and offer example applications for Kuramoto-type phase- oscillator models, power grid models and generic flow models. Focusing on the role of the network topology implies that these ideas can be easily generalized to other types of networks, in particular those characterizing flow, transport, or spreading phenomena. The concept of network susceptibil- ities is broadly applicable and may straightforwardly be transferred to all settings where networks responses of the collective dynamics to topological changes are essential.

nlin.AO↗

A Dual Method for Computing Power Transfer Distribution Factors

Power Transfer Distribution Factors (PTDFs) play a crucial role in power grid security analysis, planning, and redispatch. Fast calculation of the PTDFs is therefore of great importance. In this paper, we present a non-approximative dual method of computing PTDFs. It uses power flows along topological cycles of the network but still relies on simple matrix algebra. At the core, our method changes the size of the matrix that needs to be inverted to calculate the PTDFs from $N\times N$, where $N$ is the number of buses, to $(L-N+1)\times (L-N+1)$, where $L$ is the number of lines and $L-N+1$ is the number of independent cycles (closed loops) in the network while remaining mathematically fully equivalent. For power grids containing a relatively small number of cycles, the method can offer a speedup of numerical calculations.

eess.SY↗

Topological phenotypes constitute a new dimension in the phenotypic space of leaf venation networks

The leaves of angiosperms contain highly complex venation networks consisting of recursively nested, hierarchically organized loops. We describe a new phenotypic trait of reticulate vascular networks based on the topology of the nested loops. This phenotypic trait encodes information orthogonal to widely used geometric phenotypic traits, and thus constitutes a new dimension in the leaf venation phenotypic space. We apply our metric to a database of 186 leaves and leaflets representing 137 species, predominantly from the Burseraceae family, revealing diverse topological network traits even within this single family. We show that topological information significantly improves identification of leaves from fragments by calculating a "leaf venation fingerprint" from topology and geometry. Further, we present a phenomenological model suggesting that the topological traits can be explained by noise effects unique to specimen during development of each leaf which leave their imprint on the final network. This work opens the path to new quantitative identification techniques for leaves which go beyond simple geometric traits such as vein density and is directly applicable to other planar or sub-planar networks such as blood vessels in the brain.

q-bio.QM↗

Scaling of phloem structure and optimality of photoassimilate transport in conifer needles

The phloem vascular system facilitates transport of energy-rich sugar and signaling molecules in plants, thus permitting long range communication within the organism and growth of non-photosynthesizing organs such as roots and fruits. The flow is driven by osmotic pressure, generated by differences in sugar concentration between distal parts of the plant. The phloem is an intricate distribution system, and many questions about its regulation and structural diversity remain unanswered. Here, we investigate the phloem structure in the simplest possible geometry: a linear leaf, found, for example, in the needles of conifer trees. We measure the phloem structure in four tree species representing a diverse set of habitats and needle sizes, from 1 cm (\textit{Picea omorika}) to 35 cm (\textit{Pinus palustris}). We show that the phloem shares common traits across these four species and find that the size of its conductive elements obeys a power law. We present a minimal model that accounts for these common traits and takes into account the transport strategy and natural constraints. This minimal model predicts a power law phloem distribution consistent with transport energy minimization, suggesting that energetics are more important than translocation speed at the leaf level.

physics.bio-ph↗

Generalised Mathieu Moonshine

The Mathieu twisted twining genera, i.e. the analogues of Norton's generalised Moonshine functions, are constructed for the elliptic genus of K3. It is shown that they satisfy the expected consistency conditions, and that their behaviour under modular transformations is controlled by a 3-cocycle in H^3(M_24,U(1)), just as for the case of holomorphic orbifolds. This suggests that a holomorphic VOA may be underlying Mathieu Moonshine.

hep-th↗