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25th International Meeting on Organic Geochemistry IMOG 2011

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P-291<br />

Geochemical parameters for unravelling mixtures. Examples<br />

from the South Atlantic c<strong>on</strong>tinental margins and the giant northcentral<br />

West Siberian gas fields<br />

John Moldowan 1,2 , David Zinniker 1 , Zhaoqian Liu 1 , Alla Rovenskaya-Nemchenko 3 ,<br />

Jeremy Dahl 1 , Tatyana Nemchenko 4<br />

1 Geological & Envir<strong>on</strong>mental Science, Stanford University, Stanford, United States of America, 2 Biomarker<br />

Technology, Sebastopol, United States of America, 3 The Foundati<strong>on</strong> for East-West Cooperati<strong>on</strong>, Moscow,<br />

Russian Federati<strong>on</strong>, 4 Vernadsky Institute of <strong>Geochemistry</strong> and Analytical Chemistry (GEOKHI), Moscow,<br />

Russian Federati<strong>on</strong> (corresp<strong>on</strong>ding author:moldowan@yahoo.com)<br />

The recogniti<strong>on</strong>, correlati<strong>on</strong> and quantificati<strong>on</strong> of oil<br />

mixtures remain challenging in many petroleum<br />

system studies. Most prolifically productive basins or<br />

regi<strong>on</strong>s have multiple source rocks generating at wide<br />

ranges of maturity. Mixtures present themselves in<br />

many forms, including any proporti<strong>on</strong>s of black oil,<br />

light oil and c<strong>on</strong>densate, which can be single-sourced<br />

or co-sourced. Knowledge of all active sources and<br />

the maturities of their generated hydrocarb<strong>on</strong>s is the<br />

critical starting point to develop correct basin models.<br />

Selecti<strong>on</strong> of the best parameters to de-c<strong>on</strong>volute oilsource<br />

mixtures can best be determined from singly<br />

sourced end-member oil and source rock samples.<br />

The ideal parameters show very large differences in<br />

magnitude between the candidate sources and are<br />

independent of maturity difference. In parallel,<br />

maturity differences can be taken into account and<br />

also provide useful informati<strong>on</strong> about the mixtures.<br />

In the absence of data from end-member samples<br />

such parameters can be c<strong>on</strong>strued by inference<br />

based <strong>on</strong> informati<strong>on</strong> about source rock depositi<strong>on</strong>al<br />

envir<strong>on</strong>ment and burial depth or history (maturity)<br />

where different source types often have widely<br />

c<strong>on</strong>trasting characteristics.<br />

In the south atlantic margins, we are faced with oil<br />

mixtures that may include oil generated in the<br />

lacustrine rift secti<strong>on</strong>s of Barremian-Aptian age,<br />

transiti<strong>on</strong>al to marine post-rift sources of late Aptian<br />

into the late Cretaceous and Tertiary marine-deltaic<br />

oil from the latest Cretaceous through the Tertiary.<br />

Parameter value ranges depend <strong>on</strong> the specific basin<br />

in questi<strong>on</strong> and analysis of some end-member<br />

samples from the area of interest can more precisely<br />

define those values. However, we find that purely<br />

lacustrine sourced oil samples from Angola show C29hopane<br />

C-isotope ratios of < -35 ‰, near absence of<br />

C30 (desmethyl) steranes (C30/C29 ≤ 0.01%), and<br />

c<strong>on</strong>centrati<strong>on</strong> ratio differences from other sources for<br />

diam<strong>on</strong>doid pseudohomologues (e.g., adamantanes /<br />

diamantanes).<br />

Post-rift marine sources generally show C29-hopane<br />

C-isotope ratios > -24‰, C30/C29 sterane ratios ~10%.<br />

Younger marine-deltaic oil often shows geochemical<br />

parameter values intermediate between the marine<br />

and lacustrine end-members. TPP ratios and certain<br />

plant biomarkers (diterpanes, oleanane, bicadinane<br />

and their C-isotope ratios) differentiate those sources.<br />

The source(s) of gas in the giant gas fields (e.g.,<br />

Urengoi, Yamburg) of north central Western Siberia<br />

has been a subject of studies that have reached<br />

different c<strong>on</strong>clusi<strong>on</strong>s. The possibilities include<br />

thermogenic origins of various source ages and facies<br />

versus biogenic. Our recent studies show that at<br />

least some of the gas is thermogenic in origin. This is<br />

indicated by elevated diam<strong>on</strong>doid c<strong>on</strong>centrati<strong>on</strong>s in<br />

light oil samples obtained from those fields. Further,<br />

the C-isotope ratios of diam<strong>on</strong>doids correlate them to<br />

end-member Early – Middle Jurassic Tyumensourced<br />

oil (Figure 1). This correlati<strong>on</strong> str<strong>on</strong>gly infers<br />

a Tyumen source for the gas, which is probably,<br />

therefore, the major source. Some samples in the<br />

basin also show mixtures of Late Jurassic Bashenov<br />

oil with Tyumen c<strong>on</strong>densate that can be unravelled by<br />

compound specific isotope analysis of biomarkers<br />

(CSIA-B) and diam<strong>on</strong>doids (CSIA-D).<br />

� 13 C PDB (‰)<br />

Urengoi & Yamburg<br />

cracked -19 oil samples<br />

-20<br />

-21<br />

-22<br />

-23<br />

-24<br />

-25<br />

-26<br />

-27<br />

-28<br />

-29<br />

-30<br />

-31<br />

-32<br />

-33<br />

-34<br />

-35<br />

-36<br />

All cracked oil & Tyumen<br />

end-members<br />

(heavy isotope group)<br />

Only n<strong>on</strong>-cracked oil and<br />

Bashenov end-members<br />

(lighter isotopes group)<br />

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17<br />

Diam<strong>on</strong>doids (adamantane & alkyladamantanes)<br />

Figure 1. CSIA-D distinguishes Bashenov and Tyumen oil. In every<br />

case the deep source correlates with the Tyumen<br />

424

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