A maturity sequence
from the Keluke Formation of the Upper Carboniferous
marine–continental transitional depositional environment in
the Qaidam basin, NW China has been geochemically characterized by
bulk and molecular compositions, especially the behavior of polyaromatic
hydrocarbons and organosulfur compounds. Some commonly used maturity
parameters such as the methylnaphthalene ratio (MNR), the dimethylnaphthalene
ratio (DNR), the methylphenanthrene ratio (MPR), methylphenanthrene
index-3 (MPI-3), dimethylphenanthrene index-2 (DMPI-2), the methyldibenzothiophene
ratio (MDR) and dimethyldibenzothiophene (DMDBT) ratios (4,6-/1,6-
+ 1,8- + l,4-DMDBT and 2,4-/1,6- + 1,8- + l,4-DMDBT),
Rock-Eval T
max, and measured vitrinite
reflectance (%R
o) increase gradually with
burial depth, whereas others such as the trimethylnaphthalene ratio
(TMNr), the tetramethylnaphthalene ratio (TeMNr), MPI-1, and DMPI-1
show no correlation with these maturity indicators. The calculated
equivalent R
o values from MPR and MDR
based on empirical correlation reported in the literature overestimate
the maturity level. The degree of alkylation plays a dominant role
in molecular compositional variation and maturity parameter validity,
which is in turn controlled by the nature of organic input, depositional
environment, and lithology rather than solely controlled by maturation.
Dealkylation of alkylnaphthalenes at R
o ∼ 1.0% removes most thermally unstable isomers from C3- and
C4 homologues, which makes parameters based on them lose sensitivity.
The proportion of phenanthrene varies greatly in the marine–continental
transitional depositional system and the involvement of phenanthrene
in the formulation makes MPI-1 and DMPI-1 fail to reflect the maturity
level. Overestimation of the maturity level based on the degree of
isomerization is caused by a high catalytic effect in the marine–continental
transitional depositional system, which facilitates isomerization
and dealkylation processes.