Morphogenesis describes the various processes that result in the development of form in cellular biological systems. A study of morphogenesis gives us insight into some of the spatial outcomes of self-organisation. We are able to see aspects of different morphogenetic processes on the urban scale.
Unsupervised network formation through cell-tip growth is evident in inter-urban linkages, particularly where policies of containment or
Fig. 1 Epithelial cell networking video.
Mitosis creates very dense but essentially decentralised morphologies. We can say they’re decentralised because a centrality analysis of the network representation will show us that no cell in the system is especially important from the point of view of the global connectivity of the system. Cellular systems provide us with a good demonstration of this fact, that high-density form is not the same as centralised form. We do not see this kind of decentralisation very often in metropolitan form.
Fig. 2 Mitotic processes in a one-hour old fruit fly embryo imaged via confocal microscopy. A Histone protein is tagged with a substance that allows us to track cell nuclei.
The movie below depicts branching morphogenesis in a fragment of epithelium growing in a 3D gel of extracellular matrix proteins. New ducts initiate, elongate, bifurcate, and stop. This morphogenetic process underpins the fractal cardiovascular structures in our own bodies. It creates self-similar, dendritic structures, a tree topology.
Branching morphogenesis is evident in the arterial nature of street networks throughout the Western world. It is the mechanism behind some of the fractal geometries of the modern post-metropolis.
Fig. 3 Branching Morphogenesis in epithelial cells.
Reaction-diffusion dynamics proposed by Alan Turing in the 50s arose out of an attempt to produce a mathematical model to explain pattern formation in organisms, from butterfly wing patterns to zebra stripes.
He proposed the diffusion of an activator and inhibitor through an evolving cellular system over a period of time, the concentration gradients dictating cell differentiation, ie a zebra skin cell can be black or white according to the concentration of a white-cell activator at the point when it forms. Biologists would call these activators morphogens, as these are the proteins that regulate gene expression.
Fig. 4 Alan Turing’s reaction-diffusion model for pattern formation has successfully been applied to the wing patterns of Papilio Dardanus.
[ source ]
I’ve used reaction-diffusion dynamics to explore some morphological outcomes of morphogenetic activation using generative models. They constitute a means of visual thinking on the topic.
Fig. 5 Generative model showing how reaction-diffusion dynamics can produce pattern formation in a matrix of lines.
Fig. 6 Generative model showing how reaction-diffusion dynamics can produce gradients in a matrix of lines.
In my models I’ve used a growing matrix of straight lines, one added at each time step, to investigate what kind of formations this kind of dynamics can produce. My morphogens, an activator and inhibitor, hidden from view, are placed randomly on the canvas. They react, diffuse and deplete over time. In this graphic you can see a gradient operating from left-to-right, deforming lines and affecting line growth. No two vertical slices of this image are the same as a result. Gradients in morphogenesis are capable of creating this kind of heterogenous space, with no two spatial elements alike.
Fig. 7 Generative model showing how an uninhibited attractor can produce intensities in a matrix of lines.
Reaction-diffusion models can be useful in modeling land-use patterns in response to policy mechanisms, in the form of morphogens, that activate or inhibit certain land-uses, exerting forces on the surrounding urban landscape in the form of gradients.
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Morphogenesis describes the various processes that result in the development of form in cellular biological systems. A study of morphogenesis gives us insight into some of the spatial outcomes of self-organisation. We are able to see aspects of different morphogenetic processes on the urban scale.
Unsupervised network formation through cell-tip growth is evident in inter-urban linkages, particularly where policies of containment or
Fig. 1 Epithelial cell networking video.
Mitosis creates very dense but essentially decentralised morphologies. We can say they’re decentralised because a centrality analysis of the network representation will show us that no cell in the system is especially important from the point of view of the global connectivity of the system. Cellular systems provide us with a good demonstration of this fact, that high-density form is not the same as centralised form. We do not see this kind of decentralisation very often in metropolitan form.
Fig. 2 Mitotic processes in a one-hour old fruit fly embryo imaged via confocal microscopy. A Histone protein is tagged with a substance that allows us to track cell nuclei.
The movie below depicts branching morphogenesis in a fragment of epithelium growing in a 3D gel of extracellular matrix proteins. New ducts initiate, elongate, bifurcate, and stop. This morphogenetic process underpins the fractal cardiovascular structures in our own bodies. It creates self-similar, dendritic structures, a tree topology.
Branching morphogenesis is evident in the arterial nature of street networks throughout the Western world. It is the mechanism behind some of the fractal geometries of the modern post-metropolis.
Fig. 3 Branching Morphogenesis in epithelial cells.
Reaction-diffusion dynamics proposed by Alan Turing in the 50s arose out of an attempt to produce a mathematical model to explain pattern formation in organisms, from butterfly wing patterns to zebra stripes.
He proposed the diffusion of an activator and inhibitor through an evolving cellular system over a period of time, the concentration gradients dictating cell differentiation, ie a zebra skin cell can be black or white according to the concentration of a white-cell activator at the point when it forms. Biologists would call these activators morphogens, as these are the proteins that regulate gene expression.
Fig. 4 Alan Turing’s reaction-diffusion model for pattern formation has successfully been applied to the wing patterns of Papilio Dardanus.
[ source ]
I’ve used reaction-diffusion dynamics to explore some morphological outcomes of morphogenetic activation using generative models. They constitute a means of visual thinking on the topic.
Fig. 5 Generative model showing how reaction-diffusion dynamics can produce pattern formation in a matrix of lines.
Fig. 6 Generative model showing how reaction-diffusion dynamics can produce gradients in a matrix of lines.
In my models I’ve used a growing matrix of straight lines, one added at each time step, to investigate what kind of formations this kind of dynamics can produce. My morphogens, an activator and inhibitor, hidden from view, are placed randomly on the canvas. They react, diffuse and deplete over time. In this graphic you can see a gradient operating from left-to-right, deforming lines and affecting line growth. No two vertical slices of this image are the same as a result. Gradients in morphogenesis are capable of creating this kind of heterogenous space, with no two spatial elements alike.
Fig. 7 Generative model showing how an uninhibited attractor can produce intensities in a matrix of lines.
Reaction-diffusion models can be useful in modeling land-use patterns in response to policy mechanisms, in the form of morphogens, that activate or inhibit certain land-uses, exerting forces on the surrounding urban landscape in the form of gradients.
Revision from April 23, 2010 11:07 by Anil Bawa-Cavia
