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25th International Meeting on Organic Geochemistry IMOG 2011

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P-439<br />

Origin of alkane hydrocarb<strong>on</strong>s in the hydrothermal deposits of<br />

the Mid-Atlantic Ridge and East Pacific Rise<br />

Natalia Shulga 1 , Valerij Peresypkin 2<br />

1 P.P. Shirshov Institute of Oceanology, Moscow, Russian Federati<strong>on</strong>, 2 P.P. Shirshov Institute of Oceanology,<br />

Moscow, Russian Federati<strong>on</strong> (corresp<strong>on</strong>ding author:nash.ocean@gmail.com)<br />

The purpose of this abstract is to present results of<br />

initial investigati<strong>on</strong> related to n-alkanes distributi<strong>on</strong> in<br />

various regi<strong>on</strong>s of the oceanic rift systems. Alkane<br />

hydrocarb<strong>on</strong>s are type of biomarkers show little or no<br />

change in structure from their parent organic<br />

molecules in living organisms, bacteria or plants.<br />

They are chemically stable and, hence, retain primary<br />

biological and geological informati<strong>on</strong>.<br />

The samples for research were collected from<br />

numerous expediti<strong>on</strong>s by using deep manned<br />

submersibles Mir-1 and Mir-2.<br />

Molecular and group compositi<strong>on</strong> of n-alkanes were<br />

analyzed in sulphide and carb<strong>on</strong>ate deposits of<br />

hydrothermal fields from the Mid-Atlantic Ridge and<br />

East Pacific Rise, related to the process of<br />

serpentinizati<strong>on</strong> of ultrabasic rocks in the oceanic<br />

core (Rainbow, Lost City); basaltic volcanism (Broken<br />

Spur, Lucky Strike, TAG, Snake Pit, 9°50‘N) and oilsaturated<br />

ores from Guaymas Basin. All solvent<br />

extracts from samples have been studied by gas<br />

chromatography/ mass-spectrometry method.<br />

Total n-alkanes c<strong>on</strong>centrati<strong>on</strong>s in the samples are low<br />

and vary widely from 0,01 to 1,82 µg/g of dry weight<br />

of ore deposits, but this values incommensurable low<br />

in comparis<strong>on</strong> with c<strong>on</strong>centrati<strong>on</strong>s of hydrothermal<br />

sediments. These differences can be explained by<br />

organic matter formati<strong>on</strong> features of both in<br />

hydrothermal deposits and sediments (pressure,<br />

temperature, different mineralogical compositi<strong>on</strong> etc.).<br />

It was shown a presence of n-alkanes C12-C35 in most<br />

explored samples of hydrothermal deposits. The<br />

major amount of n-alkanes from hydrothermal<br />

deposits has a biologic origin (transformati<strong>on</strong> of<br />

chemoautotrophic organisms), except samples from<br />

Guaymas Basin, where instant thermolytic generati<strong>on</strong><br />

of hydrocarb<strong>on</strong>s (so-called ‘‘hydrothermal petroleum‘‘)<br />

has been observed [1].<br />

The n-alkane distributi<strong>on</strong>s in the hydrothermal<br />

formati<strong>on</strong>s from Rainbow, 9°50‘N East Pacific Rise<br />

and Guaymas Basin has comparable c<strong>on</strong>centrati<strong>on</strong>s<br />

of even/odd homologies (CPI=0,90÷1) while the<br />

values of C23-C35 range from 11,7 to 29,6 (% relat.).<br />

This distributi<strong>on</strong> can be interpreted as abiogenic<br />

thermocatalitic oil, since it difficult to supply highmolecule<br />

weight odd n-alkanes derived from<br />

terrestrial plants to these sediment-free hydrothermal<br />

systems of the ocean. Al<strong>on</strong>g with this, <strong>on</strong>e may<br />

assume that in the hydrothermal systems with no<br />

sedimentary layer, oil hydrocarb<strong>on</strong>s are also formed<br />

owing to the Fisher-Tropsch type reacti<strong>on</strong>s [2].<br />

Fig.1. Relative distributi<strong>on</strong> of n-alkanes in the<br />

samples from the A) Rainbow (4396-1), B) 9°50‘N<br />

East Pacific Rise (4658-3), C) Guaymas Basin (4713-<br />

3).<br />

References<br />

[1] Sim<strong>on</strong>eit, B.R.T. Appl. Geochem., No. 6, 49-56<br />

(1985).<br />

[2] McCollom, T.M., Seewald, J.S. Chem. Rev.<br />

107(2), 382-401 (2007).<br />

565

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