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25th International Meeting on Organic Geochemistry IMOG 2011

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P-239<br />

Differentiati<strong>on</strong> of organic matter in soil, loess and rhizoliths at<br />

the Nussloch sedimentary sequence via n-alkane molecular<br />

proxies<br />

Martina Gocke, Guido Wiesenberg<br />

Department for Agroecosystem Research, University of Bayreuth, Bayreuth, Germany (corresp<strong>on</strong>ding<br />

author:martina.gocke@uni-bayreuth.de)<br />

Loess-paleosol sequences are important terrestrial<br />

archives to study Quaternary climate, based <strong>on</strong><br />

proxies like pollen, stable carb<strong>on</strong> isotope compositi<strong>on</strong><br />

(δ 13 C) of organic matter (OM) and many others.<br />

Comm<strong>on</strong>ly, loess OM is thought to represent the<br />

signal of the vegetati<strong>on</strong> prevailing during depositi<strong>on</strong>,<br />

i.e. mainly grass vegetati<strong>on</strong> without large abundances<br />

of trees or shrubs.<br />

However, the presence of large calcified roots<br />

(rhizoliths) in the loess profile of Nussloch (SW<br />

Germany) gives an example, how loess-paleosol<br />

sequences have been penetrated postsedimentary by<br />

deep-rooting plants. These plants could have a<br />

different size and shape compared to synsedimentary<br />

grass vegetati<strong>on</strong> and likely modified the initial loess<br />

OM via release of root exudates and fine root hairs.<br />

This can entail uncertainties for paleoenvir<strong>on</strong>mental<br />

studies based <strong>on</strong> loess OM. Therefore, identificati<strong>on</strong><br />

and source apporti<strong>on</strong>ment of OM of different origin in<br />

loess is required to reduce related uncertainties.<br />

However, this remains difficult due of low organic<br />

carb<strong>on</strong> (Corg) c<strong>on</strong>tents in loess (usually < 0.5%). Lipid<br />

molecular proxies, e.g. from n-alkanes and fatty acids,<br />

enable the required source apporti<strong>on</strong>ment of OM in<br />

recent and ancient soils and sediments [1].<br />

The aim of this study was to identify different sources<br />

of OM in the loess sequence of Nussloch, SW<br />

Germany, and to dem<strong>on</strong>strate the relevance of<br />

postsedimentary incorporati<strong>on</strong> of root-derived OM for<br />

an overprint of the original Corg signal in terrestrial<br />

sediments. Therefore, pairs of rhizoliths and reference<br />

loess without visible root remains were sampled from<br />

the profile in depths between 0.8 and 6.9 m. For<br />

comparis<strong>on</strong>, the modern soil and recent vegetati<strong>on</strong>,<br />

c<strong>on</strong>sisting of grasses, herbaceous plants and robinia,<br />

were sampled. Further, loess in direct vicinity to the<br />

rhizoliths up to a distance of 5 cm (rhizoloess), was<br />

sampled. The samples were compared for their<br />

alkane compositi<strong>on</strong>, lipid and Corg c<strong>on</strong>tents.<br />

Alkane compositi<strong>on</strong> with C31 as most abundant l<strong>on</strong>g<br />

chain homologue revealed that both, loess and soil<br />

organic matter (OM), were derived from grass<br />

vegetati<strong>on</strong>. While arable crops mainly c<strong>on</strong>tributed to<br />

the recent soil OM, these were natural grasses for<br />

loess. The recent vegetati<strong>on</strong> did not c<strong>on</strong>tribute to OM<br />

in rhizoliths and rhizoloess. Rhizoliths were formed<br />

under tree and/or shrub vegetati<strong>on</strong> more than 3000<br />

years BP and reflect the natural former vegetati<strong>on</strong>,<br />

which likely was dominated by beech, oak, alder and<br />

hazelnut. Low values for the carb<strong>on</strong> preference index<br />

(CPI) in rhizoliths and rhizoloess revealed the<br />

presence of former root tissue and associated<br />

rhizomicrobial remains [2]. The overprint of loess<br />

organic matter even distant to former roots cannot be<br />

excluded as revealed by molecular proxies like<br />

average chain length (ACL) or CPI. Therefore,<br />

paleoenvir<strong>on</strong>mental investigati<strong>on</strong>s of terrestrial<br />

sediments based <strong>on</strong>ly <strong>on</strong> bulk carb<strong>on</strong> analyses should<br />

be regarded with cauti<strong>on</strong>.<br />

Besides further investigati<strong>on</strong>s <strong>on</strong> recent root biomass<br />

and rhizoliths, rhizoloess must be investigated in<br />

more detail to assess the postsedimentary<br />

modificati<strong>on</strong> of loess OM near to the former roots and<br />

to determine the extensi<strong>on</strong> of the former rhizosphere.<br />

Fig. 1: CPI and ACL of rhizoliths, loess, soil and<br />

modern vegetati<strong>on</strong> at the Nussloch site.<br />

References<br />

[1] Harwood J.L., Russel N.J. 1984. Lipids in plants<br />

and microbes. Allen & Unwin, L<strong>on</strong>d<strong>on</strong>.<br />

[2] Cranwell P.A. 1981. <strong>Organic</strong> <strong>Geochemistry</strong>.<br />

376

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