Plant Macrofossils
- ISBN: 9780444527479
- DOI: 10.1111/j.1469-8137.1974.tb01329.x
Abstract
Since the early 1990s, chronological frameworks of late Pleistocene and Holocene terrestrial records are mostly based on AMS radiocarbon dating of plant macrofossils. In contrast to the previous use of bulk organic matter, plant macrofossils are inherently more reliable since the source of their carbon is known and should not be composed of heterogeneous material that could be of different ages. Nevertheless, even within the plant macrofossils chronologies, inconsistencies are still common. This article reviews the most common plant macrofossils and considers their suitability and reliability for 14C-AMS dating. Due to their specificity, volcanic areas and modern environments are independently examined.
Plant Macrofossils
Hopkins, M. S., Graham, A. W., Hewett, R., Ash, J., and Head, J.
Masiello, C. A., and Druffel, E. R. M. (1998). Black carbon in
deep-sea sediments. Science 280, 1911–1913.
then, the preferred strategy has been to date plant
2958 RADIOCARBON DATING/Plant MacrofossilsReferences
Alon, D., Mintz, G., Cohen, I., Weiner, S., and Boaretto, E. (2002).
The use of Raman spectroscopy to monitor the removal of
humic substances from charcoal: Quality control for 14C dating
of charcoal. Radiocarbon 44, 1–11.
Arnold, J. R., and Libby, W. F. (1949). Age determinations by
radiocarbon content: Checks with samples of known age.
Science 110, 678–680.
Bird, M. I., and Gro¨cke, D. (1997). Determination of the abun-
dance and carbon-isotope composition of elemental carbon in
sediments. Geochimica et Cosmochimica Acta 61, 3413–3423.
Bird, M. I., Moyo, E., Veenendaal, E., Lloyd, J. J., and Frost, P.
(1999a). Stability of elemental carbon in a savanna soil. Global
Biogeochemical Cycles 13, 923–932.
Bird, M. I., Ayliffe, L. K., Fifield, K., et al. (1999b). Radiocarbon
dating of ‘old’ charcoal using a wet oxidation–stepped combus-
tion procedure. Radiocarbon 41, 127–140.
Bird, M. I., Turney, C. S. M., Fifield, L. K., et al. (2002).
Radiocarbon analysis of the early archaeological site of
Nauwalabila I Arnhemland Australia: Implications for sample
suitability and stratigraphic integrity. Quaternary Science
Reviews 21, 1061–1075.
Bird, M. I., Fifield, L. K., Santos, G. M., et al. (2003). Radiocarbon
dating from 40–60ka BP at Border Cave South Africa.
Quaternary Science Reviews (Quaternary Geochronology) 22,
943–947.
Cachier, H. P., Bremond, M. P., and Buat-Me´nard, P. (1989).
Determination of atmospheric soot carbon by a simple thermal
method. Tellus 41B, 379–390.
Chughtai, A. R., Jassim, J. A., Peterson, J. H., Stedman, D. H., and
Smith, D. M. (1991). Spectroscopic and solubility characteristics
of oxidized soots. Aerosol Science and Technology 15, 112–126.
Cohen-Ofri, I., Weiner, L., Boaretto, E., Mintz, G., and Weiner, S.
(2006). Modern and fossil charcoal: Aspects of structure and
diagenesis. Journal of Archaeological Science 33, 428–439.
Cope,M. J., and Chaloner,W.G. (1980). Fossil charcoal as evidence
of past atmospheric composition. Nature 283, 647–649.
Czimczik, C. I., Preston, C. M., Schmidt, M. W. I., and Schulze,
E.-D. (2003). How surface fire in Siberian Scots pine forests
affects soil organic carbon in the forest floor: Stocks molecular
structure and conversion to black carbon (charcoal). Global
Biogeochemical Cycles 17, 1024.
Demeyer, A., Voundi Nkana, J. C., and Verloo, M. G. (2001).
Characteristics of wood ash and influence on soil properties
and nutrient uptake: An overview. Bioresource Technology 77,
287–295.
De Vries, H. L., and Barendsen, G. W. (1954). Measurements of
age by the carbon-14 technique. Nature 174, 1138.
Dickens, A. F., Gelinas, Y., Masiello, C. A., Wakeham, S., and
Hedges, J. I. (2004). Reburial of fossil organic carbon in marine
sediments. Nature 427, 336–339.
Elias, V. O., Simoneit, B. R. T., Cordeiro, R. C., and Turcq, B.
(2001). Evaluating levoglucosan as an indicator of biomass
burning in Carajas Amazonia: A comparison to the charcoal
record. Geochimica et Cosmochimica Acta 65, 267–272.
Franklin, R. E. (1951). Crystallite growth in graphitizing and non-
graphitizing carbons. Proceedings of the Royal Society Series A
209, 196–218.
Gavin, D. G. (2001). Estimation of inbuilt age of soil charcoal
from fire history studies. Radiocarbon 43, 27–44.
Gillespie, R. (1997). Burnt and unburnt carbon: Dating charcoal
and burnt bone from the Willandra Lakes, Australia.
Radiocarbon 39, 225–236.
Gillespie, R., Hammond, A. P., Goh, K. M., et al. (1992). AMS
radiocarbon dating of a late Quaternary tephra site at
Graham’s Terrace, New Zealand. Radiocarbon 34, 21–28.Pessenda, L. C. R., Gouveia, S. E. M., and Aravena, R. (2001).
Radiocarbon dating of total soil organic matter and humin
fraction and its comparison with 14C ages of charcoal.
Radiocarbon 43, 595–601.
Pietika¨inen, J., Kiikkila¨, O., and Fritze, H. (2000). Charcoal as a
habitat for microbes and its effect on the microbial community
of the underlying humus. Oikos 89, 231–242.
Reddy, C. M., Pearson, A., Xu, L., et al. (2002). Radiocarbon as a
tool to apportion sources of polycyclic aromatic hydrocarbons
and black carbon in environmental samples. Environmental
Science and Technology 36, 1774–1782.
Schmidt, M. W. I., Skjemstad, J. O., Czimczik, C. I., et al. (2001).
Comparative analysis of black carbon in soils. Global
Biogeochemical Cycles 15, 163–168.
Skjemstad, J. O., Clarke, P., Taylor, J. A., Oades, J. M., and
McClure, S. G. (1996). The chemistry and nature of protected
carbon in soil. Australian Journal of Soil Research 34, 251–271.
Turney, C. S. M., Bird, M. I., Fifield, L. K., et al. (2001). Breaking
the radiocarbon barrier and early human occupation at Devil’s
Lair, southwestern Australia. Quaternary Research 55, 3–13.
Wolbach, W. S., and Anders, E. (1989). Elemental carbon in sedi-
ments: Determination and isotopic analysis in the presence of
kerogen. Geochimica et Cosmochimica Acta 53, 1637–1647.
Zackrisson, O., Nilsson, M.-C., and Wardle, D. A. (1996). Key
ecological function of charcoal from wildfire in the boreal
forest. Oikos 77, 10–19.
Plant Macrofossils
C Hatte´, University of Arizona, Arizona, USA
A J T Jull, University of Arizona, AZ, USA
ª 2007 Elsevier B.V. All rights reserved.
Introduction
Until the late 1980s, the majority of radiocarbon
dates for lacustrine or palustrine paleoclimatic stu-
dies from the late Pleistocene and Holocene were
obtained by beta-counting of samples of organic
lake muds or bulk peat sediment. However, since(1990). Evidence of late Pleistocene fires and eucalypt forest
from a north Queensland humid tropical rainforest site.
Australian Journal of Ecology 15, 345–347.
Libby, W. F. (1955). Radiocarbon Dating. University of Chicago
Press, Chicago.
Masiello, C. A. (2004). New directions in black carbon organic
geochemistry. Marine Chemistry 92, 201–203.Glaser, B., Haumaier, L., Guggenberger, G., and Zech, W. (1998).
Black carbon in soils: The use of benzenecarboxylic acids as
specific markers. Organic Geochemistry 29, 811–819.
Gustafsson, O¨, Bucheli, T. D., Kukulska, Z., et al. (2001).
Evaluation of a protocol for the quantification of black carbon
in sediments. Global Biogeochemical Cycles 15, 881–890.
Hatte´, C., Morvan, J., Noury, C., and Paterne, M. (2001). Is
classical acid–alkali–acid treatment responsible for contamina-
metry (AMS) (see AMS Method). This is partly
because AMS offers the possibility of dating a
much higher level of stratigraphic resolution,
since it is possible to obtain dates on very small
samples of material. It is also because of the
widely-held view that AMS dates on plant macro-
fossils are inherently more reliable than those
obtained from the sediment matrix. In such cases,
the source of the carbon is known and therefore
should not be composed of heterogeneous material
that could be of different ages. In general, it has
not been taken into account that plant macrofossils
may be species-dependent or that the plant macro-
fossils themselves may be redeposited. Consequently,
even within the plant macrofossils chronologies,
inconsistencies are still common. This suggests that
the choice of appropriate material is not trivial and
requires serious investigation.
It is evident that all warnings for paleoclimatic
studies can be extended to archeological investiga-
tions that make increasing use of plant macrofossils
for 14C dating.
Lacustrine and Palustrine Records
Algae and aquatic moss macrofossils
Aquatic cells photosynthesize subaquaticly and hence
build carbon from dissolved inorganic carbon (DIC)
into their cellular material, so they reflect the 14C : 12C
ratios of the water. The DIC is influenced by:
(1) exchange with the atmospheric CO2 reservoir;
(2) decomposition of organic matter;
(3) dissolved carbonate from surrounding limestone
catchments; and
(4) residence time of lake or peat-bog water.
Depth (cm)
eed
30 40 50 60
ulk
of r
lix l
RADIOCARBON DATING/Plant Macrofossils 2959Large numbers of terrestrial paleoclimatic stu-
dies aim to address the Last Glacial Holocene
transition. The characterization of this transition
is mostly based on lacustrine or palustrine (marsh)
records. Establishment of a reliable and accurate
chronology remains one of the major challenges in
these late glacial environments. Indeed, due to the
variations in the amount of 14C in atmospheric
CO2, this means that the measured amount of
14C is not linearly related to age, and the aging
is highly critical. This article focuses first on plant
macrofossils from these humid environments, from
algae to higher plant macrofossils. Other environ-
ments will then be considered. Finally, there will
be some reminders about sampling, storage and
pretreatments of samples and inherent possible
contaminants.
9,000
10,000
11,000
12,000
Salix leaves Carex s
14
C
yr
B
P
0 10 20
Figure 1 Radiocarbon ages obtained from macrofossil and b
(modified from Turney et al., 2000). Notice the systematic aging
Salix leaves and the age difference between Carex seeds and Sas bulk organic material
organic matter samples from Finglas River, southwest Ireland
adiocarbon ages obtained on bulk organic material compared to
eaves.This means that the 14C activity of DIC does not
reflect the 14C activity of the atmosphere, but is 14C-
depleted. This results in an artificial age, the so-
called ‘hard water effect’ inherited by algae cells,
which can show wide variation (Fontana, 2005;
Macdonald et al., 1991). See Figure 1 on bulk
organic matter.
Consequently, the AMS dating of algae macrofossils
should be avoided if possible. If there is no other
choice, an evaluation of the reservoir age should be
associated with the measurements. This could be done
by the collection, at a ‘reference’ level, of algae macro-
fossils and subaerial plant or beetle remains. Once
again, attention should be given to the choice of refer-
ence level and to the beetle species. Indeed, the level
chosen to determine the reservoir age should corre-
spond to a climatic context matching to the one for
Sign up today - FREE
Mendeley saves you time finding and organizing research. Learn more
- All your research in one place
- Add and import papers easily
- Access it anywhere, anytime


