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25th International Meeting on Organic Geochemistry IMOG 2011

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P-454<br />

Tracing of palaeofloristic changes in the Paris basin (France)<br />

during Jurassic: c<strong>on</strong>tributi<strong>on</strong> of the retene/cadalene ratio<br />

Yueming Lu, Yann Hautevelle, Raym<strong>on</strong>d Michels<br />

UMR7566 G2R, CNRS, Nancy Université Faculté des Sciences Boulevard des Aiguillettes BP 70239,<br />

Vandoeuvre-lès-Nancy, France (corresp<strong>on</strong>ding author:yueming.lu@g2r.uhp-nancy.fr)<br />

Vascular plants synthesize a large diversity<br />

of low molecular weight compounds and more<br />

particularly bioterpenoids. Many biochemical studies<br />

<strong>on</strong> extant plants have pointed out that certain<br />

bioterpenoids are specific and <strong>on</strong>ly occur in precise<br />

taxa while others are generic and are widely<br />

distributed in plant kingdom. Because these<br />

bioterpenoids can be preserved within sediments,<br />

their diagenetic counterparts (also called<br />

geoterpenoids) are useful proxies of ancient<br />

vegetati<strong>on</strong>. Therefore, vascular plant biomarkers can<br />

be used as a chemostratigraphic tool for tracing<br />

palaeovegetati<strong>on</strong> changes <strong>on</strong> hinterlands. Because<br />

these changes are under climatic c<strong>on</strong>trol, they can<br />

also be used for tracing climatic evoluti<strong>on</strong>s through<br />

geological times.<br />

Am<strong>on</strong>g all these plant biomarkers, cadalene<br />

and retene are certainly the most well-known.<br />

Cadalene is a sesquiterpenoid c<strong>on</strong>sidered as a<br />

generic plant biomarker because it comes from the<br />

diagenesis of cadinenes and cadinols. Indeed, these<br />

biological compounds are synthesized by many plant<br />

taxa. At the opposite, retene is a more specific<br />

diterpenoid since it comes from the diagenesis of<br />

biological abietanoids (abietic acid, ferruginol, etc.)<br />

mainly produced by c<strong>on</strong>ifers.<br />

This is why, the ratio retene/cadalene<br />

(Re/Ca) can be used, in a first approach, to trace<br />

paleofloristic changes through geological times (van<br />

Aarssen et al., 2000). Then, a careful study of plant<br />

biomarkers can allow to assess more precise<br />

informati<strong>on</strong> <strong>on</strong> palaeofloras.<br />

Hautevelle et al., (2006) pointed out a<br />

significant increase of the Re/Ca ratio at the end of<br />

the Lower Oxfordian in the eastern part of the Paris<br />

basin. This evoluti<strong>on</strong> is also remarkably synchr<strong>on</strong>ous<br />

with the progressive installati<strong>on</strong> of the Oxfordian<br />

carb<strong>on</strong>ate platform. A careful study of the<br />

diterpenoids associated to retene shows that their<br />

distributi<strong>on</strong> is very typical of those of fossil Pinaceae.<br />

This increase in the Re/Ca ratio were thus interpreted<br />

as an increase of the proporti<strong>on</strong> of Pinaceae <strong>on</strong> the<br />

L<strong>on</strong>d<strong>on</strong>-Brabant massif at the end of the Lower<br />

Oxfordian which can be linked to an increase of<br />

aridity.<br />

Then, this same approach was extended to<br />

the study of the whole Jurassic of the Paris basin. For<br />

this, we calculated the Re/Ca ratio for nearly 60<br />

samples coming from the A901 core. It is located in<br />

the Northern part of the Paris basin and the studied<br />

sedimentary series are dated from Hettangian to<br />

Middle Oxfordian. Calculated ratios show significant<br />

evoluti<strong>on</strong>s through the Jurassic indicating<br />

palaeofloristic and palaeoclimatic changes.<br />

Furthermore, these evoluti<strong>on</strong>s seem to be correlated<br />

to the 2 nd order alternati<strong>on</strong>s of carb<strong>on</strong>ate platforms<br />

and argillaceous deposits. Unfortunately, it is not<br />

possible to determine more precisely these floristic<br />

and climatic changes as it was the case for the Lower<br />

Oxfordian.<br />

More recently, we studied two another cores<br />

(EST 432 & EST 433) drilled in the eastern part of the<br />

Paris basin and allowing the study of the whole<br />

Jurassic. More than 50 samples were studied in order<br />

to calculate the Re/Ca ratio. The preliminary study<br />

shows that we found the same evoluti<strong>on</strong>ary trend as<br />

that obtained in the northern part of the Paris basin.<br />

Furthermore, the evoluti<strong>on</strong> of the Re/Ca ratio<br />

through Jurassic in the Paris basin appears to be<br />

quite similar to that published by van Aarssen et al.<br />

(2000) c<strong>on</strong>cerning the Jurassic of the Carnarv<strong>on</strong><br />

Basin (Australia). Such similarities in places very<br />

remote lead us to believe that these evoluti<strong>on</strong>s are<br />

linked to global palaeofloristic and palaeoclimatic<br />

changes.<br />

References:<br />

Hautevelle, Y., R. Michels, F. Malartre, and A.<br />

Trouiller (2006), Vascular plant biomarkers as proxies<br />

for palaeoflora and palaeoclimatic changes at the<br />

Dogger/Malm transiti<strong>on</strong> of the Paris Basin (France),<br />

<strong>Organic</strong> <strong>Geochemistry</strong>, 37(5), 610-625.<br />

van Aarssen, B. G. K., R. Alexander, and R. I. Kagi<br />

(2000), Higher plant biomarkers reflect<br />

palaeovegetati<strong>on</strong> changes during Jurassic times,<br />

Geochimica et Cosmochimica Acta, 64(8), 1417-<br />

1424.<br />

579

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