The retention times are calculated from the moment the sample is injected
in the chromatographic column (IT FLASH or GC INJECTION). In the chromatogram, this
corresponds to the first peak observed in time, which is generated by the
flash heating of the injection trap of SAM-GC. This time is 
564697487 s (sclk) for GC 1 chromatogram and 
564701685 s (sclk) for GC 4 chromatogram . The retention times are 
calculated by subtracting this time, to the times of the peaks maxima.
The original TCD chromatograms are available in the file noise.csv.

GC column 1 run

peak 0 ;  GC1 INJECTION ; 0
peak 1 ;   ; 336
peak 2 ;   ; 751
peak 3 ;  ; 889
peak 4 ;  ; 982
#peak 5 ; ; 1721
#peak 6 ;  ; 981
#peak 7 ;  ; 1839

GC column 4 run

peak 6 ; GC4 IT FLASH 1 ; 0
peak 7 ;  ; 192
peak 8 ;  ; 196
peak 9 ; ; 260
peak 10 ; ; 318
peak 11 ;  ; 442
peak 12 ;  ; 614
peak 13 ; ; 633
peak 14 ; BENZENE ; 702
peak 15 ;  ; 753
peak 16 ; TOLUENE ; 791
peak 17 ;  ; 941
peak 18 ;  ; 1041
peak 19 ; GC4 IT FLASH 2 ; 1102
peak 20 ;  ; 1335

The abundance given in the table (species.csv) corresponds to the area of the 
most abundant mass peak which are measurable for each peak. The unit is 
counts/sec/sec. There is no baseline correction for this fit.
These surfaces are proportional to the amount of the species
detected when a peak is eluted. When peaks are co-eluted (over of different
peaks), the peaks are fitted using a gaussian function. If the fit does not work, 
only one surface value is given, corresponding to the sum of the
abundances of the species contributing to the peak.