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25th International Meeting on Organic Geochemistry IMOG 2011

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O-32<br />

The role of light intensity in c<strong>on</strong>trolling the �D and � 13 C values of<br />

organic compounds in leaf waxes: Should we worry about it?<br />

Nikolai Pedentchouk 1 , Kirill Peskov 2 , Tracy Laws<strong>on</strong> 3 , Yvette Eley 1<br />

1 The University of East Anglia, Norwich, United Kingdom, 2 Institute for Systems Biology SPb, Moscow,<br />

Russian Federati<strong>on</strong>, 3 The University of Essex, Colchester, United Kingdom (corresp<strong>on</strong>ding<br />

author:n.pedentchouk@uea.ac.uk)<br />

Several recent studies have suggested that a<br />

simultaneous analysis of � 13 C and �D of n-alkyl<br />

biomarkers in leaf waxes may help identify the type of<br />

vegetati<strong>on</strong> c<strong>on</strong>tributing to the sedimentary record. The<br />

rati<strong>on</strong>ale behind this approach is that in C3 plants the<br />

� 13 C and �D are linked because of their dependence<br />

<strong>on</strong> water use efficiency (WUE) [1]. Here we show that<br />

the assumpti<strong>on</strong> about this link might not necessarily<br />

be correct, because during biosynthesis �D of lipids<br />

could also be influenced by other factors that are<br />

decoupled from those c<strong>on</strong>trolling the � 13 C values.<br />

We measured � 13 C and �D of leaf wax n-alkanes<br />

from 4 lines of Arabidopsis thaliana grown indoors.<br />

The plants were subjected to 3 light treatments, while<br />

the rest of parameters (durati<strong>on</strong> of illuminati<strong>on</strong>,<br />

temperature, relative humidity, and water) were kept<br />

c<strong>on</strong>stant. In additi<strong>on</strong>, we measured leaf water �D,<br />

transpirati<strong>on</strong>, CO2 c<strong>on</strong>ductance, net photosynthesis,<br />

as well as chlorophyll c<strong>on</strong>centrati<strong>on</strong> and fluorescence.<br />

The isotope and gas flux data were then used to<br />

develop a kinetic model to estimate �D of NADPH.<br />

As expected, the plants differed in their<br />

physiological resp<strong>on</strong>se to various light treatments.<br />

WUE was c<strong>on</strong>siderably greater in high (HL) than in<br />

middle (ML) and in low (LL) lights. We found that � 13 C<br />

of n-C31 alkane are c<strong>on</strong>sistent with the differences in<br />

WUE am<strong>on</strong>g the plants at 3 light levels. However, our<br />

data also showed that �D of n-C31 in HL are more<br />

negative than in ML and LL, which, unlike � 13 C in ML<br />

and LL, almost totally overlap (Fig.1). Furthermore,<br />

the pattern am<strong>on</strong>g �D of n-C31 at 3 light levels is<br />

different from that shown by the transpirati<strong>on</strong> data.<br />

Our kinetic model, which includes the effects of<br />

light sensitive enzyme-driven processes, allowed us<br />

to estimate��D of NADPH at 3 light levels. We found<br />

that the pattern am<strong>on</strong>g �D of NADPH is similar to nalkane<br />

�D and dissimilar to transpirati<strong>on</strong>.<br />

The results of this work suggest that light intensity<br />

is an important envir<strong>on</strong>mental parameter that<br />

significantly influences both � 13 C and �D of leaf<br />

waxes. However, �D is decoupled from � 13 C because<br />

of the different biochemical mechanisms affecting D/H<br />

and 13 C/ 12 C fracti<strong>on</strong>ati<strong>on</strong>s during photosynthesis.<br />

Fig. 1. �D values of n-C31 alkane (measured) and NADPH<br />

(modelled), and transpirati<strong>on</strong> measured for 4 different lines<br />

of Arabidopsis thaliana at 3 light levels. D/H fracti<strong>on</strong>ati<strong>on</strong><br />

between H2O and NADPH equal to � = 0.40 [2] was used<br />

during model simulati<strong>on</strong>s for calculating the resultant �D of<br />

NADPH at each of 3 light levels.<br />

References<br />

[1] Hou, J. et al. (2007) Org. Geochem. 38, 1251-1255.<br />

[2] Luo, Y.-H. et al. (1991) Plant Cell Physiol. 32, 897-900.<br />

91

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