This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Warkentin, M.
Right arrow Articles by Schumann, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Warkentin, M.
Right arrow Articles by Schumann, R.
Agricola
Right arrow Articles by Warkentin, M.
Right arrow Articles by Schumann, R.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, November 2007, p. 6722-6729, Vol. 73, No. 21
0099-2240/07/$08.00+0     doi:10.1128/AEM.00405-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

New and Fast Method To Quantify Respiration Rates of Bacterial and Plankton Communities in Freshwater Ecosystems by Using Optical Oxygen Sensor Spots{triangledown}

Mareike Warkentin,* Heike M. Freese, Ulf Karsten, and Rhena Schumann

Institute of Biological Sciences, Applied Ecology, University of Rostock, 18059 Rostock, Germany

Received 21 February 2007/ Accepted 23 August 2007

A new method of respiration rate measurement based on oxygen luminescence quenching in sensor spots was evaluated for the first time for aquatic bacterial communities. The commonly used Winkler and Clark electrode methods to quantify oxygen concentration both require long incubation times, and the latter additionally causes signal drift due to oxygen consumption at the cathode. The sensor spots proved to be advantageous over those methods in terms of precise and quick oxygen measurements in natural bacterial communities, guaranteeing a respiration rate estimate during a time interval short enough to neglect variations in organism composition, abundance, and activity. Furthermore, no signal drift occurs during measurements, and respiration rate measurements are reliable even at low temperatures and low oxygen consumption rates. Both a natural bacterioplankton sample and a bacterial isolate from a eutrophic river were evaluated in order to optimize the new method for aquatic microorganisms. A minimum abundance of 2.2 x 106 respiring cells ml–1 of a bacterial isolate was sufficient to obtain a distinct oxygen depletion signal within 20 min at 20°C with the new oxygen sensor spot method. Thus, a culture of a bacterial isolate from a eutrophic river (OW 144; 20 x 106 respiring bacteria ml–1) decreased the oxygen saturation about 8% within 20 min. The natural bacterioplankton sample respired 2.8% from initially 94% oxygen-saturated water in 30 min. During the growth season in 2005, the planktonic community of a eutrophic river consumed between 0.7 and 15.6 µmol O2 liter–1 h–1. The contribution of bacterial respiration to the total plankton community oxygen consumption varied seasonally between 11 and 100%.


* Corresponding author. Mailing address: Institute of Biological Sciences, Applied Ecology, University of Rostock, Albert-Einstein-Strasse 3, 18059 Rostock, Germany. Phone: 49-3814986095. Fax: 49-3814986072. E-mail: mareike.warkentin{at}uni-rostock.de

{triangledown} Published ahead of print on 31 August 2007.


Applied and Environmental Microbiology, November 2007, p. 6722-6729, Vol. 73, No. 21
0099-2240/07/$08.00+0     doi:10.1128/AEM.00405-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.