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Table 2 δD values obtained from FI-1 and FI-2, and calculated δ18O and/or δ13C values of the aqueous fluid at the equilibrium with the quartz and calcite minerals at 175 and 310 °C (see Fig. 8 for the reconstructed isochores)

From: Sediment provenance during Alpine orogeny: fluid inclusions and stable isotopes on quartz–calcite veins from detritic pebbles

Whole rocks

Vein

Fluid inclusion

Sample

Pebble petrology

Host mineral

δD (‰ relative to SMOW)

δ18O (‰ relative to SMOW)

δ13C (‰ relative to PDB)

SL1a

Basalt

Qtz

−26.6

 

9.3

17.3

  
  

Cal

  

9.6

15.3

−2.61

−0.09

SL2b

Sandy limestone

Cal

  

16.2

21.9

−1.74

0.96

SL2c

Dolomitic sandstone

Qtz

−44.3

 

9.8

17.8

  

SL2g

Dolomitic sandstone

Qtz

−60.2

 

10.0

18.0

  

SL2h

Dolomitic sandy limestone

Cal

−73.3

−44.6

14.6

20.3

1.45

4.15

SL2i

Sandy limestone

Qtz

  

12.8

20.8

  
  

Cal

−35.9

−28.7

13.4

19.1

0.75

3.45

SL3b

Dolomitic sandstone

Qtz

−47.2

−24

11.2

19.2

  

SL5a

Micaceous sandstone

Cal

−50.4

 

14.2

19.9

1.09

3.79

   

FI-1

FI-2

H2O-175

H2O-310

CO2-175

CO2-310

  1. The oxygen compositions are mean values after using different fractionation factors from Zheng (1993) and Méheut et al. (2007) for the H2O–Qz equilibrium and from O’Neil et al. (1969), Zheng (1999) and Horita (2014) for the H2O–Ca equilibrium. The carbon compositions are values calculated using the fractionation factor from Ohmoto and Rye (1979) for the CO2–Ca equilibrium