2011
DOI: 10.1080/09593330.2011.588401
|View full text |Cite
|
Sign up to set email alerts
|

Fluorescence spectroscopy as a tool for determining microbial quality in potable water applications

Abstract: Building on previous work where fluorescence spectroscopy has been used to detect sewage in rivers, a portable LED spectrophotometer was used for the first time to establish bacterial numbers in a range of water samples. A mixed-method approach was used with standard bacteria enumeration techniques on diluted river water and sewage works final effluent using a number of diluents (Ringer's solution, tap water and potable spring water). Fluorescence from uncultured dilutions was detected at a 280 nm excitation/3… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

3
64
0

Year Published

2014
2014
2023
2023

Publication Types

Select...
4
4

Relationship

1
7

Authors

Journals

citations
Cited by 63 publications
(67 citation statements)
references
References 30 publications
3
64
0
Order By: Relevance
“…This suggests that Peak T fluorescence intensity can be attributed to an increase in E. coli population size, in accordance with previous studies Cumberland et al, 2012;Dartnell et al, 2013;Deepa and Ganesh, 2017;Sohn et al, 2009). However, as tryptophan is an essential amino acid, necessary for protein formation during growth and other metabolic pathways, it will be produced as a result of cell multiplication and metabolic processing (Coble et al, 2014;Hogg, 2005).…”
Section: Resultssupporting
confidence: 79%
See 1 more Smart Citation
“…This suggests that Peak T fluorescence intensity can be attributed to an increase in E. coli population size, in accordance with previous studies Cumberland et al, 2012;Dartnell et al, 2013;Deepa and Ganesh, 2017;Sohn et al, 2009). However, as tryptophan is an essential amino acid, necessary for protein formation during growth and other metabolic pathways, it will be produced as a result of cell multiplication and metabolic processing (Coble et al, 2014;Hogg, 2005).…”
Section: Resultssupporting
confidence: 79%
“…Recent literature suggests that Peak T fluorescence may act as a surrogate for microbial and bacterial activity Cumberland et al, 2012), as first highlighted by Hudson et al (2008). Recent surface freshwater research has also attempted to use Peak T fluorescence to determine enumeration of specific species.…”
Section: Introductionmentioning
confidence: 99%
“…Standard methods used to test for the presence of heterotrophic bacteria (HB), total coliforms (TC), faecal coliforms (FC) and E. coli include, inter alia, the multiple tube method (presence of gas and acid at 44°C), membrane filtration (MF), and colony-forming units (cfu) on agar media (Great Britain Department of Environment, 1983;Cumberland et al, 2011). The genera enumerated by any of these methods are highly variable since the cultivation medium of choice, incubation temperature and time, origin (river, surface water reservoir, treated and disinfected drinking water, etc.…”
Section: Current Methods Of Organic and Microbial Determinationmentioning
confidence: 99%
“…In particular, the development of short-wave ultra-violet light emitting diodes (LEDs) has permitted the excitation of dissolved organic matter at~280 nm using portable instrumentation (Cumberland et al, 2012). At this wavelength, the intensity of fluorescence emitted at~350 nm (often referred to as peak T or peak T2) has been shown to relate to the water quality in sewage-impacted rivers (Baker, 2001).…”
Section: Introductionmentioning
confidence: 99%
“…Cumberland et al (2012) tested a portable fluorescence spectrometer to measure fluorescence intensity at these excitation and emission wavelengths and sought to determine whether there was a relationship with bacterial numbers. Their pilot-study, of 24 samples from four urban river and sewerage sites in the UK, demonstrated a linear correlation between fluorescence intensity and microbial water quality as determined by bacterial enumerations, over a three-log range of bacterial counts.…”
Section: Introductionmentioning
confidence: 99%