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Table 2 Carbon isotope analyses by ion microprobe of possible synthetic standards

From: A synthetic standard for the analysis of carbon isotopes of carbon in silicates, and the observation of a significant water-associated matrix effect

Sample material

Primary Cs+ intensity

Pre sputter (s)

C2 intensity (cps)

Observed δ13C ± σ

PPRG #215-1 Instrument mass fractionation factor α

Corrected δ13C

True δ13C

Observed matrix effect

905

6.7E−10

15

1.7E+05

−33.1 ± 1.1

1.0006 (0.6 ‰)

−33.7

−27.9

−6.0

905

6.7E−10

15

3.4E+05

−34.5 ± 0.7

1.0006 (0.6 ‰)

−35.1

−27.9

−7.4

905

2.2E−10

15

3.7E+05

−35.9 ± 0.7

1.0006 (0.6 ‰)

−36.5

−27.9

−8.9

905

2.2E−10

45

2.6E+05

−35.5 ± 0.7

1.0006 (0.6 ‰)

−36.1

−27.9

−8.4

905

2.2E−10

45

2.3E+05

−35.4 ± 1.1

1.0006 (0.6 ‰)

−36.0

−27.9

−8.4

     

Weighted mean

−35.7

 

−8.0

     

Weighted standard deviation

1.0

  

526N

8.30E−11

45

1.3E+05

−41.9 ± 0.7

1.0006 (0.6 ‰)

−41.9

−27.7

−14.7

526N

8.40E−11

45

7.6E+05

−40.0 ± 1.1

1.0006 (0.6 ‰)

−40.0

−27.7

−12.7

     

Weighted mean

−40.4

 

−13.1

     

Weighted standard deviation

1.4

  

Sample material

Primary Cs+ intensity

PrE−sputter (s)

C2 intensity (cps)

Observed δ13C ± σ

PPRG #215-1 Instrument mass fractionation factor α

Corrected δ13C

True δ13C

Observed matrix effect

905

7.5E−11

60

1.2E+05

−24.9 ± 1.4

1.0046 (4.6 ‰)

−29.4

−27.9

−1.6

905

1.1E−10

60

2.6E+05

−22.9 ± 0.8

1.0046 (4.6 ‰)

−27.4

−27.9

0.5

905

5E−11

60

1.4E+05

−24.0 ± 1.2

1.0046 (4.6 ‰)

−28.5

−27.9

−0.7

905

5.2E−11

60

1.6E+05

−24.4 ± 1.0

1.0046 (4.6 ‰)

−29.0

−27.9

−1.1

905

4.1E−11

60

1.4E+05

−22.5 ± 1.4

1.0046 (4.6 ‰)

−27.0

−27.9

0.9

905

5E−11

60

1.6E+05

−22.9 ± 0.8

1.0046 (4.6 ‰)

−27.4

−27.9

0.5

905

1E−10

60

2.1 E+05

−26.0 ± 0.8

1.0046 (4.6 ‰)

−30.5

−27.9

−2.7

905

1E−10

60

2.0E+05

−24.1 ± 1.1

1.0046 (4.6 ‰)

−28.6

−27.9

−0.7

905

1.6E−10

60

2.4E+05

−24.4 ± 1.1

1.0046 (4.6 ‰)

−28.9

−27.9

−1.0

905

1.6E−10

60

3.0E+05

−22.9 ± 0.8

1.0046 (4.6 ‰)

−27.4

−27.9

0.5

     

Weighted mean

−28.4

 

−0.5

     

Weighted standard deviation

1.1

  

526N

9.5E−10

60

1.2E+05

−32.8 ± 2.0

1.0046 (4.6 ‰)

−37.2

−27.7

−9.8

526N

3.6E−10

60

3.9E+04

−35.2 ± 3.5

1.0046 (4.6 ‰)

−39.7

−27.7

−12.4

526N

9.4E−10

60+

2.7E+05

−25.4 ± 1.2

1.0046 (4.6 ‰)

−29.9

−27.7

−2.3

526N

3.6E−10

60+

6.2E+04

−28.4 ± 2.1

1.0046 (4.6 ‰)

−32.9

−27.7

−5.4

     

Weighted mean

−32.5

 

−4.9

     

Weighted standard deviation

4.5

  

CN703

3.1E−11

60

4.5E+05

−17.5 ± 1.1

1.0046 (4.6 ‰)

−22.1

0.0

6.7

CN703

3.1E−11

60

2.5E+05

−15.9 ± 1.2

1.0046 (4.6 ‰)

−20.5

0.0

8.3

     

Weighted mean

−21.3

 

7.4

     

Weighted standard deviation

1.1

  
  1. Instrument mass factionation (IMF) factor α = (δ13Cobs + 1000)/(δ13CExp + 1000)
  2. IMF in ‰ = 1000 * Ln (α). Corrected δ13C = ((δ13Cobs + 1000/α) − 1000
  3. True δ13C is that measured by conventional elemental analyzer-isotope ratio mass spectrometry (EA-IRMS). apparent matrix effect (AS) = Corrected δ13C − True δ13C
  4. The last two 526N samples add the following additional pre-sputter respectively: 20 seconds of an ~2 nA beam and 60 s of an ~0.4 nA beam; 20 s of an ~2 nA beam