eemR (version 1.0.1)

eem_raman_normalisation: Fluorescence Intensity Calibration Using the Raman Scatter Peak of Water

Description

Normalize fluorescence intensities to the standard scale of Raman Units (R.U).

Usage

eem_raman_normalisation(eem, blank = NA)

Arguments

eem

An object of class eemlist.

blank

An object of class eemlist.

Value

An object of class eemlist.

An object of class eem containing:

• sample The file name of the eem.

• x A matrix with fluorescence values.

• em Emission vector of wavelengths.

• ex Excitation vector of wavelengths.

Details

The function will first try to use the provided blank. If the blank is omitted, the function will then try to extract the blank from the eemlist object. This is done by looking for sample names containing one of these complete or partial strings (ignoring case):

1. nano

2. miliq

3. milliq

4. mq

5. blank

Note that if blank is omitted, the function will group the eemlist based on file location and will assumes that there is a blank sample in each folder. In that context, the blank will be used on each sample in the same folder. If more than one blank is found they will be averaged (a message will be printed if this appends).

Consider the following example where there are two folders that could represent scans performed on two different days `scans_day_1` and `scans_day_2`.

scans_day_1
	nano.csv
	sample1.csv
	sample2.csv
	sample3.csv
scans_day_2
	blank.csv
	s1.csv
	s2.csv
	s3.csv

In each folder there are three samples and one blank files. In that context, `eem_remove_blank()` will use the blank `nano.csv` from `sample1.csv`, `sample2.csv` and `sample3.csv`. The same strategy will be used for files in folder `scans_day_2` but with blank named `blank.csv`.

Note that the blanks eem are not returned by the function.

The normalization procedure consists in dividing all fluorescence intensities by the area (integral) of the Raman peak. The peak is located at excitation of 350 nm. (ex = 370) between 371 nm. and 428 nm in emission (371 <= em <= 428). Note that the data is interpolated to make sure that fluorescence at em 350 exist.

References

Lawaetz, A. J., & Stedmon, C. A. (2009). Fluorescence Intensity Calibration Using the Raman Scatter Peak of Water. Applied Spectroscopy, 63(8), 936-940.

https://journals.sagepub.com/doi/10.1366/000370209788964548

Murphy, K. R., Stedmon, C. a., Graeber, D., & Bro, R. (2013). Fluorescence spectroscopy and multi-way techniques. PARAFAC. Analytical Methods, 5(23), 6557.

http://xlink.rsc.org/?DOI=c3ay41160e

Examples

# NOT RUN {
# Open the fluorescence eem
file <- system.file("extdata/cary/scans_day_1", "sample1.csv", package = "eemR")
eem <- eem_read(file, import_function = "cary")

plot(eem)

# Open the blank eem
file <- system.file("extdata/cary/scans_day_1", "nano.csv", package = "eemR")
blank <- eem_read(file, import_function = "cary")

# Do the normalisation
eem <- eem_raman_normalisation(eem, blank)

plot(eem)
# }