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Imaging complex nutrient dynamics in mycelial networks

Fricker, M. D., Lee, J. A., Bebber, D. P., Tlalka, M., Hynes, Juliet, Darrah, P. R., Watkinson, S. C. and Boddy, Lynne 2008. Imaging complex nutrient dynamics in mycelial networks. Journal of Microscopy 231 (2) , pp. 317-331. 10.1111/j.1365-2818.2008.02043.x

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Abstract

Transport networks are vital components of multi-cellular organisms, distributing nutrients and removing waste products. Animal cardiovascular and respiratory systems, and plant vasculature, are branching trees whose architecture is thought to determine universal scaling laws in these organisms. In contrast, the transport systems of many multi-cellular fungi do not fit into this conceptual framework, as they have evolved to explore a patchy environment in search of new resources, rather than ramify through a three-dimensional organism. These fungi grow as a foraging mycelium, formed by the branching and fusion of threadlike hyphae, that gives rise to a complex network. To function efficiently, the mycelial network must both transport nutrients between spatially separated source and sink regions and also maintain its integrity in the face of continuous attack by mycophagous insects or random damage. Here we review the development of novel imaging approaches and software tools that we have used to characterise nutrient transport and network formation in foraging mycelia over a range of spatial scales. On a millimetre scale, we have used a combination of time-lapse confocal imaging and fluorescence recovery after photobleaching to quantify the rate of diffusive transport through the unique vacuole system in individual hyphae. These data then form the basis of a simulation model to predict the impact of such diffusion-based movement on a scale of several millimetres. On a centimetre scale, we have used novel photon-counting scintillation imaging techniques to visualize radiolabel movement in small microcosms. This approach has revealed novel N-transport phenomena, including rapid, preferential N-resource allocation to C-rich sinks, induction of simultaneous bi-directional transport, abrupt switching between different pre-existing transport routes, and a strong pulsatile component to transport in some species. Analysis of the pulsatile transport component using Fourier techniques shows that as the colony forms, it self-organizes into well demarcated domains that are identifiable by differences in the phase relationship of the pulses. On the centimetre to metre scale, we have begun to use techniques borrowed from graph theory to characterize the development and dynamics of the network, and used these abstracted network models to predict the transport characteristics, resilience, and cost of the network.

Item Type: Article
Date Type: Published Online
Status: Published
Schools: Biosciences
Uncontrolled Keywords: Amino acid transport; biological network; confocal microscopy; fluorescence recovery after photobleaching; metabolic oscillation; network resilience; Oregon Green; phase mapping; Phanerochaete velutina; photon-counting scintillation imaging; transport network; vacuole
Publisher: Wiley
ISSN: 0022-2720
Date of Acceptance: 5 December 2007
Last Modified: 31 Jan 2020 03:50
URI: http://orca-mwe.cf.ac.uk/id/eprint/8924

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