Use of paleochemotaxonomy for tracing paleoflora and paleoclimatic changes during Jurassic...

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Use of paleochemotaxonomy for

tracing

paleoflora and paleoclimatic

changes

during JurassicHAUTEVELLE Yann

MICHELS Raymond, MALARTRE Fabrice, TROUILLER Alain

22nd IMOG, Seville - Spain September 12-16, 2005

Desertic climate

Temperate climate

Tropical climate

Polar climate

flora ↔ climate

Paleoflora as paleoclimatic recorder

INTRODUCTION

INTRODUCTION

PALEOBOTANY(fossil plants assemblages)

PALYNOLOGY(spore & pollens assemblages)

classically used for the

reconstruction of paleofloras

and paleoclimates

Paleoflora and paleoclimatic proxies

Vascular plant biomarkers have a paleochemotaxonomic value and are specific of a restricted number of plant taxa

PALEOCHEMOTAXONOMY (plant biomarkers assemblages)

Extant & fossil plants classification

Plantae kingdom

INTRODUCTION

Phytocenose or floraat the time

of the deposition

angiospermspines pines

cypress

sequoia

Land plant biomarkers

distribution in sediment

ferns

paleoflora reconstruction

Vascular plant biomarkers distribution in sediments & rocks is a « picture » of the terrestrial paleophytocenose at the time of

the deposition

Stratigraphicrecord

paleobiodiversity

paleoflora

paleoclimate

T°, humidity

desertic climate

Geolo

gic

al ti

mes

tropical climate

temperate climate

Molecularfacies

Use of paleochemotaxonomy in stratigraphy

INTRODUCTION

Aims

INTRODUCTION

Aims of this work :

1) study the evolution of vascular plant biomarkers on a stratigraphic series of paleoclimatic interest ;

2) interpret this evolution in terms of paleoflora then in terms of paleoclimatic changes ;

Cadinane class biomarkers (sesquiterpenoids)

cadalene

diagenetic evolution

I) Paleochemotaxonomic data used in this study

Cadalene Generic plant biomarker

Molecularbiomarkers

Biologicalprecursors

O/ Gingkoales

O/ Coniferales

P/ Bryophytaand others…

Biologicalproducers Reactional intermediates

cadinenes

cadinols

I) Paleochemotaxonomic data used in this study

Abietane class biomarkers (diterpenoids)

(keto)phenolic

abietanes

abietanoicacids

diageneticevolution

Molecularbiomarkers

Biologicalprecursors

retene

Reactional intermediates

O/ Coniferales

Biologicalproducers

O/ Coniferales

F/ Pinaceae

O/ Coniferales

F/ all families except

Pinaceae

I) Paleochemotaxonomic data used in this study

Saturated bi-, tri & tetracyclic diterpanes (diterpenoids)

bi-, tricyclic diterpanes (labdanes, norabietanes, pimaranes, …)

bi-, tricyclic diterpanes ½ specific conifers biomarkers

tetracyclic diterpanesAll conifer familiesexcept Pinaceae

O/ Coniferales

F/ all families

tetracyclic diterpanes (phyllocladanes, kauranes, beyeranes, …)

O/ Coniferales

F/ all families except

Pinaceae

Geological background of studied series

II) Geological and paleobotanical background

Jurassic stratigraphy of Paris basin (France)Type-section of the Paris

basin

Paleoenvironments

Deep ←→ Shallow

Terrigenous deposits & flooding events

Pliensbachian

Sinemurian

Toarcian

AalenianBajocian

Bathonian

Callovian

Oxfordian

Kimmeridgian

Tithonian

Paleoclimatic interest

Eustatic regression cooling

event (glaciation ?)

(Dromart et al., 2003, Cecca et al., 2005)

Upper Callovian

Global warming(Cecca et al., 2005)

Oxfordian & Kim-meridgian

Climatic control of the alternance

carbonate / terrigenous deposits ?

Geological background of studied series

East ofParisBasin

(4 wells)

London-BrabantMassif

marine environment

Paleogeography 5 studied wells (Callovo-Oxfordian)

A 901well

II) Geological and paleobotanical background

Paleobotanical background of studied sedimentary series

O/ Filicales(Ferns)

Some paleobotanical studies indicate the presence of many plant taxa on emerged lands boundering the Paris basin (London-Brabant Massif).

East ofParisBasin

(4 wells)

London-BrabantMassif

marine environment

A 901well

II) Geological and paleobotanical background

Paleobotanical background of studied sedimentary series

Some paleobotanical studies indicate the presence of many plant taxa on emerged lands boundering the Paris basin (London-Brabant Massif).

East ofParisBasin

(4 wells)

London-BrabantMassif

marine environment

A 901well

O/ Cycadales

II) Geological and paleobotanical background

Paleobotanical background of studied sedimentary series

Some paleobotanical studies indicate the presence of many plant taxa on emerged lands boundering the Paris basin (London-Brabant Massif).

East ofParisBasin

(4 wells)

London-BrabantMassif

marine environment

A 901well

Ferns(Filicales)

O/ Ginkgoales

II) Geological and paleobotanical background

Paleobotanical background of studied sedimentary series

Some paleobotanical studies indicate the presence of many plant taxa on emerged lands boundering the Paris basin (London-Brabant Massif).

East ofParisBasin

(4 wells)

London-BrabantMassif

marine environment

Bennettitalesand

Caytoniales(presently

extinct orders)

A 901well

II) Geological and paleobotanical background

Paleobotanical background of studied sedimentary series

Some paleobotanical studies indicate the presence of many plant taxa on emerged lands boundering the Paris basin (London-Brabant Massif).

East ofParisBasin

(4 wells)

London-BrabantMassif

marine environment

Ferns(Filicales)

O/ ConiferalesF/ AraucariaceaeF/ PodocarpaceaeF/ CupressaceaeF/ TaxodiaceaeF/ Pinaceae

F/ CheirolepidiaceaeA 901well

II) Geological and paleobotanical background

Retene/cadalene ratio

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

MSE 101-649 m m/z=183+219+237+223+241+233

m/z=183+219+ 237+223+241+233MSE 101-493.3 m

Other vascular plant biomarkers

Retene-rich extract (Oxfordian platform)

Retene-poor extract (Callovo-Oxfordian claystones)

aromatic fraction

cadalene

cadalene

retene

retene

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

MSE 101-649 m

hopanes

hopanes

MSE 101-493.3 m High content ofsaturated diterpanes

m/z=123+109+ 163+191

m/z=123+109+ 163+191

Other vascular plant biomarkers

Retene-rich extract (Oxfordian platform)

Retene-poor extract (Callovo-Oxfordian claystones)

aliphatic fraction

Very low contentor absence of

saturated diterpanes

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

hopanes

MSE 101-493.3 m m/z=123+109+ 163+191High content ofsaturated diterpanes

Other vascular plant biomarkers

Retene-rich extract (Oxfordian platform)aliphatic fraction

isomers

Retene-poor extract (Callovo-Oxfordian claystones)

Tetracyclic diterpanes

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

MSE 101-649 m

m/z=239+253MSE 101-493.3 m

m/z=239+253

Dehydroabieticacid

Abietic acid

Other vascular plant biomarkers

Retene-rich extract (Oxfordian platform)

Retene-poor extract (Callovo-Oxfordian claystones)

Polar fraction

Dehydroabieticacid

Abietic acid

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

Cause of the increase of the retene/cadalene ratio

Hypothesis 1 :A better preservation of the retene precursors

by clay minerals

Hypothesis 2 :

Formation of saturated abietanes instead of

retene in the claystones

Hypothesis 3 :Increase of the abietane-class diterpenoids

input into the depositional environment

paleoflora change on emerged lands (London-

Brabant Massif)

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

In Callovo-Oxfordian claystones, the absence

— of abietanoic acids

— their reactional intermediates

— of saturated abietanes

}Hypothesis 1

Hypothesis 2

Hypothesis 1 : a better preservation of retene precursors by clay minerals

Hypothesis 2 : formation of saturated abietanes in claystones instead of aromatic abietanes

The increase of retene/cadalene ratio reflects a paleoflora

change from the Cordatum zone (top of the Lower Oxfordian)

on the London-Brabant Massif

Hypothesis 3 : increase of the abietane-type diterpenoids input in the depositional environment

Cause of the increase of the retene/cadalene ratio

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

Nature of the paleoflora change

(keto)phenolic

abietanes

O/ Coniferales

F/ all families except

Pinaceae

Biologicalproducers

O/ Coniferales

F/ Pinaceae

abietanoicacids

diageneticevolution

retene

All conifer families All conifer families except Pinaceae

di-, tricyclic diterpanes

tetracyclic diterpanes

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

What is its meaning in terms of paleoclimatic

change ?

Nature of the paleoflora change

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

This evolution indicates an

increase of the proportion of

Pinaceae since the end of

the Lower Oxfordian

(Cordatum zone).

Pinaceae have acquired many xeromorphic adaptations :

+ more or less flat niddle-like leaves+ leaves covered by a thick layer of epicuticular waxes

Cheirolepidia-, Podocarpa-, Cupressa- & Taxodiaceae frequently colonize peat and swamps, not the Pinaceae.

Paleoclimatic interpretation

+ stomata sunken in wells and furrows+ stomata mostly closed by gardian cells

Others conifers families :

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

Pinaceae have acquired many xeromorphic adaptations :

+ more or less flat niddle-like leaves+ leaves covered by a thick layer of epicuticular waxes

+ stomata sunken in wells and furrows

Ferns, Cycadales, Bennettitales preferably occur under wet climates.

+ stomata mostly closed by gardian cells

Paleoclimatic interpretation

Plants other than conifers :

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

Extant Cycadaleslocalisation

The increase of the

Pinaceae proportion indicates

an increase of aridity since

the end of the Lower

Oxfordian (Cordatum zone).

Paleoclimatic interpretation

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

Information brought by other paleoclimatic proxies

Isotopic paleothermometry δO18 & Paleobiogeography of marine invertebrates : increase of the oceanic water temperature at the western european scale (Riboulleau et al., 1998; Cecca et al., 2005; Martin Garin et al., 2005)

Clay mineralogy : disapearance & decrease of the kaolinite content around the Lower / Middle Oxfordian increase of aridity (Pellenard et al., 2005)

Palynology : increase of temperature and aridity in England (Abbink et al., 2001)

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

Paleophytogeography :Upper JurassicLondon-Brabant Massif is within the Winterwet paleo- climatic zone.

Dry climate with one humid season.

Middle JurassicLondon-Brabant Massif is within the tropical paleo- climatic zone.

Wet and warm climate.

(Rees et al., 2000)

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

Information brought by other paleoclimatic proxies

A similar increase of the relative proportion of retene compared to cadalene in the Oxfordian sedimentary series of Australia

Comparison with Callovo-Oxfordian sedimentary series of Australia(van Aarssen et al., 2000)

This increase is also interpreted as a global paleoclimatic change (van Aarssen et al., 2000).

retene

(van Aarssen et al., 2000)

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

Comparison with Jurassic sedimentary series of Australia(van Aarssen et al., 2000)

III) Chemostratigraphic evidence of a paleofloral and paleoclimatic change

400

500

600

800

900

1000

0 5 10 15 20

Stratigraphic time line

Retene/cadalene

Cycle 2

Cycle 1

700Cycle 1Cycle 3

Cycle 2 ?

Cycle 1 ?

Cycle 3 ?

Stratigraphic time line

Carnavaron Basin, Australia(van Aarssen et al., 2000)

Paris Basin, France(preliminary results)

CONCLUSIONS

— vascular plant biomarkers constitute an efficient tool

for tracing paleoflora and paleoclimatic changes during

geological times.

— Vascular plant biomarker chemostratigraphy indicates an

increase of the proportion of Pinaceae on the London-Brabant

Massif at the end of the Lower Oxfordian which is related to

an increase of aridity.

— Because a similar evolution is reported in the Oxfordian

sedimentary series of Australia, this climatic change could be

recorded at the global scale.

Poster session

POSTER II. PC2-4.

POSTER II. PC2-5.

Thank you for your attention