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Historical CO2 records from the Law Dome DE08, DE08-2, and DSS ice cores
Source

Period of Record
1006 A.D.-1978
A.D.
[Karl Note:
The information presented here is VERY carefully dry and
politically correct. Normally this type of data is presented
in a context of the disaster awaiting the planet if "something"
isn't done yesterday. Many people have used the data on this
page to "prove" many things. I, Karl Loren, wish to draw
only the simple undeniable conclusion that the percentage of
carbon dioxide in the atmosphere has increased dramatically over
time, with the largest rate of increase from 1830 to present time.
What you might want to conclude from this is somewhat up to you,
but I suggest that the very air we breathe, despite its relatively
constant percentage of oxygen, contains other components
(including carbon dioxide) that could well be a major factor in
health.
The actual
amount of carbon dioxide shown with these very, very precise
studies varies from a very stable range of about 175 PPM over a
period of some 1800 years from the year 1000 to 1830.
After 1830 the
amount of carbon dioxide in the atmosphere increased dramatically
to where it is now, at about 320, or so, PPM. This
virtual doubling in 150 years, compared to almost no change for
1800 years may have dramatic consequences on health]
Methods
The CO2 records
presented here are derived from three ice cores obtained at Law
Dome, East Antarctica from 1987 to 1993. The Law Dome site
satisfies many of the desirable characteristics of an ideal ice
core site for atmospheric CO2 reconstructions including
negligible melting of the ice sheet surface, low concentrations of
impurities, regular stratigraphic layering undisturbed at the
surface by wind or at depth by ice flow, and high snow
accumulation rate. Further details on the site, drilling, and
cores are provided in Etheridge et al. (1996), Etheridge and
Wookey (1989), and Morgan et al (1997).
Air bubbles were extracted using
the "cheese grater" technique. Ice core samples weighing 500-1500
g were prepared by selecting crack-free ice and trimming away the
outer 5-20 mm. Each sample was sealed in a polyethylene bag and
cooled to -80°C before being placed in the extraction flask where
it was evacuated and then ground to fine chips. The released air
was dried cryogenically at -100°C and collected cryogenically in
electropolished stainless steel "traps", cooled to about -255°C.
Further details on the extraction technique can be found in
Etheridge et al. (1988 and 1992) and additional information on the
ice and air sample handling are provided in Etheridge et al.
(1996).
The ice core air samples,
ranging from about 50 to 150 ml standard temperature and pressure
(STP), were measured for CO2 mixing ratio with a Carle
400 Series analytical gas chromatograph (GC). After separation on
the GC columns, the CO2 was catalytically converted to
methane before flame ionization detection. As many as three
separate analysis were made on each ice core sample. Each sample
injection to the GC was bracketed by calibration gas injections.
CO2 mixing ratios were then found for each aliquot by
multiplying the ratio of the sample peak area to calibration gas
peak area (interpolated to the time of sample analysis) by the CO2
mixing ratio assigned to the calibration gas. The precision of
analysis of the Law Dome ice core air samples was 0.2 ppm. For
greater details on the experimental techniques used on the DE08,
DE08-2, and DSS ice cores, please refer to Etheridge et al.
(1996).
The ice cores were dated by
counting the annual layers in oxygen isotope ratio ( 18O
in H2O), ice electroconductivity measurements (ECM),
and hydrogen peroxide (H2O2) concentrations.
For these three parameters, each core displayed clear,
well-preserved seasonal cycles allowing a dating accuracy of ±2
years at 1805 A.D. for the three cores and ±10 years at 1350 A.D.
for DSS.
The enclosed air at any depth in
the ice has a mean age, (aa), that is younger than the
age of the host ice layer (ai), from which the air is
extracted. The difference ( a)
equals the time (Ts) for the ice layer to reach a depth
(ds), where air becomes sealed in the pore space, minus
the mean time (Td) for air to mix down the depth. The
mean air age is thus
aa = ai +
a = ai + Ts
- Td
where ages are dates A.D.
Mixing of air from the ice sheet
surface to the sealing depth is primarily by molecular diffusion.
The rate of air mixing by diffusion in the firn decreases as the
density increases and the open porosity decreases with depth.
Etheridge et al. (1996) determined the sealing depth at DE08 to be
72 m where the age of the ice is 40±1 years; at DE08-2 to be 72 m
depth and 40 years; and at DSS to be 66 m depth and 68 years. For
more details on dating the Law Dome ice cores and sealing
densities, please refer to Etheridge et al. (1996).
Law Dome, Antarctica
66°44' S, 112°50' E, 1390 mean annual sea level (M.A.S.L.)
Graphical Representations

[Karl Note:
The image above, somewhat indistinct, shows a range of dates from
the year 1830 to 1980! During that period of time the amount
of CO2 increased on at a dramatic rate.]

[Karl Note:
The image above, somewhat indistinct, shows a range of dates from
the year 1000 to 2000! During that period of time the amount
of CO2 stayed fairly level until about 1830 when it started to rise,
dramatically.]
Trends
The atmospheric CO2
reconstructions presented here offer records of atmospheric CO2
mixing ratios from 1006 A.D. to 1978 A.D. The air enclosed in the
three ice cores from Law Dome, Antarctica has unparalled age
resolution and extends into recent decades, because of the high rate
of snow accumulation at the Law Dome drill sites (Etheridge et al.
1996). Etheridge et al. (1996) reported the uncertainty of the ice
core CO2 mixing ratios is 1.2 ppm. Preindustrial CO2
mixing ratios were in the range 275-284 ppm, with the lower levels
during 1550-1800 A.D., probably as a result of colder global climate
(Etheridge et al. 1996). The Law Dome ice core CO2
records show major growth in atmospheric CO2 levels over
the industrial period, except during 1935-1945 A.D. when levels
stabilized or decreased slightly.
References
Etheridge, D.M., and C.W. Wookey. 1989.
Ice core drilling at a high
accumulation area of Law Dome, Antarctica. 1987. In Ice Core
Drilling, edited by C. Rado and D. Beaudoing, pp. 86-96.
Proceedings of the Third International Workshop on Ice Core Drilling
Technology, Grenoble, France, October 10-14, 1988, CNRS,
Grenoble.
Etheridge, D.M., G.I. Pearman, and F. de
Silva. 1988.
Atmospheric trace-gas variations
as revealed by air trapped in an ice core from Law Dome, Antarctica.
Ann. Glaciol. 10:28-33.
Etheridge, D.M., G.I. Pearman, and P.J.
Fraser. 1992.
Changes in tropospheric methane
between 1841 and 1978 from a high accumulation rate Antarctic ice
core. Tellus 44B:282-294.
Etheridge, D.M., L.P. Steele, R.L.
Langenfelds, R.J. Francey, J.-M. Barnola, and V.I. Morgan. 1996.
Natural and anthropogenic changes
in atmospheric CO2 over the last 1000 years from air in
Antarctic ice and firn. Journal of Geophysical Research
101:4115-4128.
Hamley, T.C., V.I. Morgan, R.J. Thwaites,
and X.Q. Gao. 1986.
An ice-core drilling site at Law
Dome summit, Wilkes Land, Antarctica, Res. Note 37, Aust. Natl.
Antarc. Res. Exped., Tasmania.
Morgan, V.I., C.W. Wookey, J. Li, T.D. van
Ommen, W. Skinner, and M.F. Fitzpatrick. 1997.
Site information and initial
results from deep ice drilling on Law Dome. J. Glaciol.
43:3-10.
CITE AS: D.M. Etheridge,
L.P. Steele, R.L. Langenfelds, R.J. Francey, J.-M. Barnola and V.I.
Morgan. 1998. Historical CO2 records from the Law Dome
DE08, DE08-2, and DSS ice cores. In Trends: A Compendium of Data on
Global Change. Carbon Dioxide Information Analysis Center, Oak Ridge
National Laboratory, U.S. Department of Energy, Oak Ridge, Tenn.,
U.S.A
Graphics
Digital Data
D.M. Etheridge, L.P. Steele, R.L. Langenfelds and R.J. Francey
Division of Atmospheric Research, CSIRO, Aspendale,
Victoria, Australia
J.-M. Barnola
Laboratoire de Glaciologie et Géophysique de
l'Environnement, Saint Martin d'Hères-Cedex, France
V.I. Morgan
Antarctic CRC and Australian
Antarctic Division, Hobart, Tasmania, Australia
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