A simple optode based imaging technique to measure O2 distribution and dynamics in tap water biofilms

Research output: Contribution to journal › Journal article › Research › peer-review

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A simple optode based imaging technique to measure O2 distribution and dynamics in tap water biofilms. / Staal, Marc Jaap; Prest, E.; Vrouwenvelder, H.; Rickelt, Lars F; Kühl, Michael.

In: Water Research, Vol. 45, No. 16, 2011, p. 5027-5037.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Staal, MJ, Prest, E, Vrouwenvelder, H, Rickelt, LF & Kühl, M 2011, 'A simple optode based imaging technique to measure O2 distribution and dynamics in tap water biofilms', Water Research, vol. 45, no. 16, pp. 5027-5037. https://doi.org/10.1016/j.watres.2011.07.007

APA

Staal, M. J., Prest, E., Vrouwenvelder, H., Rickelt, L. F., & Kühl, M. (2011). A simple optode based imaging technique to measure O2 distribution and dynamics in tap water biofilms. Water Research, 45(16), 5027-5037. https://doi.org/10.1016/j.watres.2011.07.007

Vancouver

Staal MJ, Prest E, Vrouwenvelder H, Rickelt LF, Kühl M. A simple optode based imaging technique to measure O2 distribution and dynamics in tap water biofilms. Water Research. 2011;45(16):5027-5037. https://doi.org/10.1016/j.watres.2011.07.007

Author

Staal, Marc Jaap ; Prest, E. ; Vrouwenvelder, H. ; Rickelt, Lars F ; Kühl, Michael. / A simple optode based imaging technique to measure O2 distribution and dynamics in tap water biofilms. In: Water Research. 2011 ; Vol. 45, No. 16. pp. 5027-5037.

Bibtex

@article{c2a418a8e773424987173cf52f6c48d9,
title = "A simple optode based imaging technique to measure O2 distribution and dynamics in tap water biofilms",
abstract = "A ratiometric luminescence intensity imaging approach is presented, which enables spatial O2 measurements in biofilm reactors with transparent planar O2 optodes. Optodes consist of an O2 sensitive luminescent dye immobilized in a 1–10 µm thick polymeric layer on a transparent carrier, e.g. a glass window. The method is based on sequential imaging of the O2 dependent luminescence intensity, which are subsequently normalized with luminescent intensity images recorded under anoxic conditions. We present 2-dimensional O2 distribution images at the base of a tap water biofilm measured with the new ratiometric method and compare the results with O2 distribution images obtained in the same biofilm reactor with luminescence lifetime imaging. Using conventional digital cameras, such simple normalized luminescence intensity imaging can yield images of 2-dimensional O2 distributions with a high signal-to-noise ratio and spatial resolution comparable or even surpassing those obtained with expensive and complex luminescence lifetime imaging systems. The method can be applied to biofilm growth incubators allowing intermittent experimental shifts to anoxic conditions or in systems, in which the O2 concentration is depleted during incubation.",
author = "Staal, {Marc Jaap} and E. Prest and H. Vrouwenvelder and Rickelt, {Lars F} and Michael K{\"u}hl",
year = "2011",
doi = "10.1016/j.watres.2011.07.007",
language = "English",
volume = "45",
pages = "5027--5037",
journal = "Water Research",
issn = "0043-1354",
publisher = "I W A Publishing",
number = "16",

}

RIS

TY - JOUR

T1 - A simple optode based imaging technique to measure O2 distribution and dynamics in tap water biofilms

AU - Staal, Marc Jaap

AU - Prest, E.

AU - Vrouwenvelder, H.

AU - Rickelt, Lars F

AU - Kühl, Michael

PY - 2011

Y1 - 2011

N2 - A ratiometric luminescence intensity imaging approach is presented, which enables spatial O2 measurements in biofilm reactors with transparent planar O2 optodes. Optodes consist of an O2 sensitive luminescent dye immobilized in a 1–10 µm thick polymeric layer on a transparent carrier, e.g. a glass window. The method is based on sequential imaging of the O2 dependent luminescence intensity, which are subsequently normalized with luminescent intensity images recorded under anoxic conditions. We present 2-dimensional O2 distribution images at the base of a tap water biofilm measured with the new ratiometric method and compare the results with O2 distribution images obtained in the same biofilm reactor with luminescence lifetime imaging. Using conventional digital cameras, such simple normalized luminescence intensity imaging can yield images of 2-dimensional O2 distributions with a high signal-to-noise ratio and spatial resolution comparable or even surpassing those obtained with expensive and complex luminescence lifetime imaging systems. The method can be applied to biofilm growth incubators allowing intermittent experimental shifts to anoxic conditions or in systems, in which the O2 concentration is depleted during incubation.

AB - A ratiometric luminescence intensity imaging approach is presented, which enables spatial O2 measurements in biofilm reactors with transparent planar O2 optodes. Optodes consist of an O2 sensitive luminescent dye immobilized in a 1–10 µm thick polymeric layer on a transparent carrier, e.g. a glass window. The method is based on sequential imaging of the O2 dependent luminescence intensity, which are subsequently normalized with luminescent intensity images recorded under anoxic conditions. We present 2-dimensional O2 distribution images at the base of a tap water biofilm measured with the new ratiometric method and compare the results with O2 distribution images obtained in the same biofilm reactor with luminescence lifetime imaging. Using conventional digital cameras, such simple normalized luminescence intensity imaging can yield images of 2-dimensional O2 distributions with a high signal-to-noise ratio and spatial resolution comparable or even surpassing those obtained with expensive and complex luminescence lifetime imaging systems. The method can be applied to biofilm growth incubators allowing intermittent experimental shifts to anoxic conditions or in systems, in which the O2 concentration is depleted during incubation.

U2 - 10.1016/j.watres.2011.07.007

DO - 10.1016/j.watres.2011.07.007

M3 - Journal article

C2 - 21803395

VL - 45

SP - 5027

EP - 5037

JO - Water Research

JF - Water Research

SN - 0043-1354

IS - 16

ER -

ID: 33728093