Picture of a black hole

Strathclyde Open Access research that creates ripples...

The Strathprints institutional repository is a digital archive of University of Strathclyde's Open Access research outputs. Strathprints provides access to thousands of research papers by University of Strathclyde researchers, including by Strathclyde physicists involved in observing gravitational waves and black hole mergers as part of the Laser Interferometer Gravitational-Wave Observatory (LIGO) - but also other internationally significant research from the Department of Physics. Discover why Strathclyde's physics research is making ripples...

Strathprints also exposes world leading research from the Faculties of Science, Engineering, Humanities & Social Sciences, and from the Strathclyde Business School.

Discover more...

Cell identification and sizing using digital image analysis for estimation of cell biomass in High Rate Algal Ponds

Gray, A.J. and Young, D. and Martin, N.J. and Glasbey, C.A. (2002) Cell identification and sizing using digital image analysis for estimation of cell biomass in High Rate Algal Ponds. Journal of Applied Phycology, 14 (3). pp. 193-204. ISSN 0921-8971

Full text not available in this repository. (Request a copy from the Strathclyde author)

Abstract

Current environmental concerns make estimation of microbial biomass apriority for monitoring purposes and to advance scientific understanding. Thispaper considers problems associated with algal cell imaging and measurement forcell biomass estimation in samples from high rate algal ponds. In a complexsystem, the only way of measuring microbial activity is to measure theindividual cells and estimate biovolumes. Accurate biomass determinationsdemanddirect microscopic counting and measurement of the sizes of individualmicrobialcells taken from known volumes of water. The system used for routinemeasurementat the laboratory where the images were generated, based on standard microscopeequipment, is only suitable for treatment of well dispersed specimens.Differential interference contrast (DIC) microscopy, on the other hand, offersthe best solution for optical enhancement of cell contrast, and produces animage with well defined edges, yet presents a great challenge to routine cellidentification by digital image analysis, owing to the bas-relief type imageproduced. The paper outlines several image analysis methods developedspecifically for this purpose, and presents illustrative results.