Hi everyone.

I have developed a R package named eemR (https://github.com/PMassicotte/eemR and https://cran.r-project.org/web/packages/eemR/index.html) which aims at providing an easy way to manipulate fluorescence matrix.

One of the function in the package is used to extract peak values at different regions in the fluorescence matrix (Coble's peaks for instance). I have noticed that the reported locations of these peaks are not consistent in the literature.

In Coble's 1996 paper, peaks are reported as follow (these are the values I am using in the R package):

Coble, P. G. (1996). Characterization of marine and terrestrial DOM in seawater using excitation-emission matrix spectroscopy. Mar. Chem. 51, 325–346. doi:10.1016/0304-4203(95)00062-3.

Peak B: ex = 275 nm, em = 310 nm

Peak T: ex = 275 nm, em = 340 nm

Peak A: ex = 260 nm, em = 380:460 nm

Peak M: ex = 312 nm, em = 380:420 nm

peak C: ex = 350 nm, em = 420:480 nm

In Coble's 2007 paper, peaks are reported as follow:

Coble, P. G. (2007). Marine optical biogeochemistry: The chemistry of ocean color. Chem. Rev. 107, 402–418. doi:10.1021/cr050350+.

Peak B: ex = 275 nm, em = 305 nm

Peak T: ex = 275 nm, em = 340 nm

Peak A: ex = 260 nm, em = 260/400 - 460 nm

Peak M: ex = 290 nm, em = 310/370 - 410 nm

peak C: ex = 320 nm, em = 420:460 nm

On the USGS website (http://or.water.usgs.gov/proj/carbon/EEMS.html):

Peak B: ex = 270 nm, em = 306 nm

Peak T: ex = 270 nm, em = 340 nm

Peak A: ex = 260 nm, em = 450 nm

Peak M: ex = 300 nm, em = 390 nm

peak C: ex = 340 nm, em = 440 nm

At first, these differences seem to be minors but I was wondering what were your thoughts about that. Should I review my code to change or adjust peak positions?

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