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

We examine the role of complexity on arterial tree structures, determining globally optimal vessel arrangements using the Simulated AnneaLing Vascular Optimization (SALVO) algorithm, which we have previously used to reproduce features of cardiac and cerebral vasculatures. Fundamental biophysical understanding of complex vascular structure has applications to modelling of cardiovascular diseases, and for improved representations of vasculatures in large artificial tissues. In ...

We introduce a mesoscopic model for natural network formation processes, acting as a bridge between the discrete and continuous network approach proposed by Hu and Cai. The models are based on a common approach where the dynamics of the conductance network is subject to pressure force effects. We first study topological properties of the discrete model and we prove that if the metabolic energy consumption term is concave with respect to the conductivities, the optimal network...

The model by Hu and Cai [Phys. Rev. Lett., Vol. 111(13) (2013)1 ] describes the self-organization of vascular networks for transport of fluids from source to sinks. Diameters, and thereby conductances, of vessel segments evolve so as to minimize a cost functional E. The cost is the trade-off between the power required for pumping the fluid and the energy consumption for vessel maintenance. The model has been used to show emergence of cyclic structures in the presence of local...

Following up on a previous work we examine a model of transportation network in some source-sink flow paradigm subjected to growth and resource allocation. The model is inspired from plants, and we add rules and factors that are analogous to what plants are subjected to. We study how different resource allocation schemes affect the tree and how the schemes interact with additional factors such as embedding the network into a 3D space and applying gravity or shading. The diffe...

Vascular networks are used across the kingdoms of life to transport fluids, nutrients and cellular material. A popular unifying idea for understanding the diversity and constraints of these networks is that the conduits making up the network are organized to optimize dissipation or other functions within the network. However the general principles governing the optimal networks remain unknown. In particular Durand showed that under Neumann boundary conditions networks, that m...

Reinforced elastic sheets surround us in daily life, from concrete shell buildings to biological structures such as the arthropod exoskeleton or the venation network of dicotyledonous plant leaves. Natural structures are often highly optimized through evolution and natural selection, leading to the biologically and practically relevant problem of understanding and applying the principles of their design. Inspired by the hierarchically organized scaffolding networks found in p...

The dynamics of flow within a material transport network is dependent upon the dynamics of its power source. Responding to a change of these dynamics is critical for the fitness of living flow networks, e.g. the animal vasculature, which are subject to frequent and sudden shifts when the pump (the heart) transitions between different steady states. The combination of flow resistance, fluid inertia, and elasticity of the vessel walls causes the flow and pressure of the fluid t...

Transport networks play a key role across four realms of eukaryotic life: slime molds, fungi, plants, and animals. In addition to the developmental algorithms that build them, many also employ adaptive strategies to respond to stimuli, damage, and other environmental changes. We model these adapting network architectures using a generic dynamical system on weighted graphs and find in simulation that these networks ultimately develop a hierarchical organization of the final we...

We provide new results on the structure of optimal transportation networks obtained as minimizers of an energy cost functional consisting of a kinetic (pumping) and material (metabolic) cost terms, constrained by a local mass conservation law. In particular, we prove that every tree (i.e., graph without loops) represents a local minimizer of the energy with concave metabolic cost. For the linear metabolic cost, we prove that the set of minimizers contains a loop-free structur...

Leaf venation is a pervasive example of a complex biological network, endowing leaves with a transport system and mechanical resilience. Transport networks optimized for efficiency have been shown to be trees, i.e. loopless. However, dicotyledon leaf venation has a large number of closed loops, which are functional and able to transport fluid in the event of damage to any vein, including the primary veins. Inspired by leaf venation, we study two possible reasons for the exist...