Encyclopedia of Environmental Microbiology 2003
DOI: 10.1002/0471263397.env042
|View full text |Cite
|
Sign up to set email alerts
|

Image Analysis of Microorganisms

Abstract: Obtaining an Image Fluorescent Labels for Epifluorescence, CLSM and 2‐PLSM Video/Digital Camera Selection Image Analysis/Processing Systems The Basics of Image Acquisition Presegmentation Processing Steps Segmentation/Thresholding … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

1
7
0

Year Published

2006
2006
2020
2020

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 8 publications
(8 citation statements)
references
References 61 publications
1
7
0
Order By: Relevance
“…The preponderance of empirical D e values that are available in the scientific literature are only 0- or 1-dimensional (that is, volume-averaged or surface-averaged). The primary techniques used to measure D e are fluorescence recovery after photobleaching with scanning confocal laser microscopy 48-50 ; porosity determination using microtomed slices 51 ; injected dyes or tagged molecules 52 ; and microelectrodes 53 . Regardless of the specific technique used, researchers generally measure D e in distinct cell clusters (0-dimensional) or as depth profiles through the biofilm layers (1-dimensional), without monitoring how the values change with biofilm age.…”
Section: Introductionmentioning
confidence: 99%
“…The preponderance of empirical D e values that are available in the scientific literature are only 0- or 1-dimensional (that is, volume-averaged or surface-averaged). The primary techniques used to measure D e are fluorescence recovery after photobleaching with scanning confocal laser microscopy 48-50 ; porosity determination using microtomed slices 51 ; injected dyes or tagged molecules 52 ; and microelectrodes 53 . Regardless of the specific technique used, researchers generally measure D e in distinct cell clusters (0-dimensional) or as depth profiles through the biofilm layers (1-dimensional), without monitoring how the values change with biofilm age.…”
Section: Introductionmentioning
confidence: 99%
“…The individual particles of the chemical populations are then allowed to undergo unbiased random walks by jumping from one compartment to the next, i.e., each particle has an equal probability per unit time, or transition rate, of jumping to one of the neighboring boxes. We are interested in diffusion as it is a fundamental mechanism of transport that underpins a large number of biological processes [31][32][33]. We approach the biological system through a chemical master-equation formalism and use white-noise expansions to derive Fokker-Planck equations that allow us to characterize the properties of the noise [6].…”
Section: Introductionmentioning
confidence: 99%
“…A plethora of researchers have investigated diffusion phenomena within biofilms using various experimental techniques such as microelectrodes [7,8], fiberoptic microsensors [9], nuclear magnetic resonance spectroscopy [10,11], infrared spectroscopy combined with Raman microscopy [12], and confocal laser scanning microscopy [13][14][15]. Although some of the experimental results were well explained using the hindered diffusion concept, effects of physical and chemical hindrances are somewhat ambiguously combined into a single quantity, i.e., diffusive tortuosity factor.…”
Section: Introductionmentioning
confidence: 99%