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Geology; May 2002; v. 30; no. 5; p. 427–430; 4 figures; 1 table. 427
Anomalously mild Younger Dryas summer conditions in southern
Greenland
Svante Bjo¨rck* Department of Geology, Quaternary Geology, Lund University, Tornavagen 13, SE-223 63 Lund, Sweden
Ole Bennike Geological Survey of Denmark and Greenland, Thoravej 8, DK-2400 Copenhagen, Denmark
Peter Rose´n Department of Ecology and Environmental Science, Umea˚ University, SE-901 87 Umea˚, Sweden
Camilla S. Andresen Geological Institute, University of Copenhagen, Øster Voldgade 10, DK-1350 Copenhagen K, Denmark
Sjoerd Bohncke Department of Quaternary Geology and Geomorphology, Vrije University, De Boelelaan 1085, 1081 HV
Amsterdam, Netherlands
Eigil Kaas Danish Meteorological Institute, Lyngbyvej 100, DK-2100 Copenhagen, Denmark
Daniel Conley Department of Marine Ecology, Danish National Environmental Research Institute (DMU), P.O. Box 358, DK-
4000 Roskilde, Denmark
ABSTRACT
The first late-glacial lake sediments found in Greenland were analyzed with respect to
a variety of environmental variables. The analyzed sequence covers the time span between
14400 and 10 500 calendar yr B.P., and the data imply that the conditions in southernmost
Greenland during the Younger Dryas stadial, 12800–11 550 calendar yr B.P., were char-
acterized by an arid climate with cold winters and mild summers, preceded by humid
conditions with cooler summers. Climate models imply that such an anomaly may be
explained by local climatic phenomenon caused by high insolation and Fo¨hn effects. It
shows that regional and local variations of Younger Dryas summer conditions in the North
Atlantic region may have been larger than previously found from proxy data and mod-
eling experiments.
Keywords: Southern Greenland, lake sediments, paleoclimatic proxy records, Younger Dryas.
Figure 1. Location map. A: Greenland’scen-
tral position within North Atlantic region. B:
Nanortalik–Kap Farvel area in southern-
most Greenland with N14 site indicated.
INTRODUCTION
The interest in the so-called Younger Dryas
stadial—which terminates the last glacial
stage and precedes the present interglacial, the
Holocene—has grown strong during the last
few decades of the twentieth century, and the
general implications of this climatic event
have also been avidly discussed (e.g., Alley
and Clark, 1999).
Although originally discovered and de-
scribed in detail for a century from Scandi-
navian lacustrine sediments (Hartz and Milth-
ers, 1901), the records from the deep
Greenland Summit ice cores have become a
template of this cool event, defined as the
Greenland stadial 1 (GS-1) event (Bjo¨rck et
al., 1998) and dated to 12 650–11500 calen-
dar (cal.) yr B.P. in the GRIP (Greenland Ice
Core Project) ice core. The d
18
O values of the
ice as well as other techniques imply that cen-
tral Greenland was subject to mean annual
temperature drops and rises at the beginning
and end of the GS-1 event on the order of 10–
20 8C (Cuffey et al., 1995; Severinghaus et
al., 1998).
LATE-GLACIAL LACUSTRINE
RECORD FROM SOUTHERN
GREENLAND
Five lakes with pre-Holocene records were
cored on islands south and southeast of Na-
nortalik, southwesternmost Greenland. The
oldest of these records was found on the island
*E-mail: svante.bjorck@geol.lu.se.
of Angissoq (Fig. 1), and was retrieved with
a Russian corer (chamber 1 m long, 7.5 cm
diameter) from a lake named N14
(59858.999N, 44810.819W, 33 m above sea lev-
el, 3.3 m water depth). Because of glacial un-
loading, crustal rebound exceeded the global
sea-level rise following the deglaciation, and
the island rose above sea level. This process
turned former marine basins into lakes, and
the
14
C age of the isolation of N14 from the
sea was calibrated to 13 800 cal. yr B.P. (Ben-
nike and Bjo¨rck, 2000). At the Younger Dryas
onset, the lake had thus been a proper lake for
;1000 yr, but the seashore was only a few
hundred meters away and the Greenland ice-
sheet margin was possibly situated ,20 km
from the site.
The sediments were analyzed with a mul-
tistratigraphic-data approach (organic and
mineral matter; biogenic silica [bioSi], sulfur
content; magnetic susceptibility; diatom, pol-
len, and macrofossil content; and annual dry-
mass accumulation rate [DMAR] of organic
and mineral matter and of bioSi), including
high-resolution
14
C dating. Here we report
from the lower part of the sequence, which
begins at 780 cm below the lake surface with
a marine silty clay and gyttja clay (Fig. 2). At
771 cm, the sediments become lacustrine, ow-
ing to the isolation from the sea. Clay gyttjas
alternating with moss gyttjas thereafter dom-
inate the sequence (Fig. 2).
The 18
14
C dates of this soft-water lake
were calibrated (Table 1) to create a calendar
year–based time scale. Apart from the well-
known
14
C plateau at 9900–10 100
14
Cyr
B.P., where calibration is almost meaningless,
the calibrated ages display two main sedimen-
tation rates, one below and one above the pla-
teau. If the two sedimentation rates are ex-
trapolated over the plateau, the two curves
meet at 742 cm. Because accumulation rates
usually alter in connection with sedimentary
changes and the only such change during the
time of the plateau occurs at 741.5 cm, this is
most likely the point at which the sedimen-
tation rate changed markedly. This results in
an age of 11 550 cal. yr B.P. for the 741.5 cm
level and produces the proper time span, 700
yr, for the plateau (Stuiver et al., 1998). Be-
cause of the well-established chronology, all
data presented here are related to time (Figs.
2–4).
The boundary between the Allerød intersta-
dial (GI-1a) and the onset of the Younger
Dryas stadial (GS-1) is characterized by a dis-
tinct shift in
14
C ages (e.g., Bjo¨rck et al.,
1996; Hughen et al., 1998); ages of 11 000–
428 GEOLOGY, May 2002
Figure 2. Left diagram shows dry weight percentage of three main sediment components.
Sediment lithology is displayed in center; abbreviations: cl—clay, si—silt, sa (mo)—sand
and mosses. Gyttja is organic sediment consisting of plant and animal remains (detritus)
and with .30% organic material by dry weight. Clay gyttja contains 6%–30% and gyttja clay
contains 3%–6% organic material. Right diagram shows annual influx of three components
per square centimeter. Note that age scale to right is linear, whereas depth scale to left
changes as consequence of changing sedimentation rate at 741.5 cm (see text).
TABLE 1. THE RADIOCARBON DATING SERIES FROM N14
Depth (cm) Dated
material*
d
13
C
(‰)
14
C age
(
14
C yr B.P.)
Calibrated age
(cal. yr B.P.)
Lab no.
708.75–708.25 Aqm 220.4 9335 6 60 10 600–10 420 AAR-5805
712.75–712.25 Aqm 219.6 9445 6 55 10 750–10 560 AAR-5804
719.25–718.75 Aqm 218.9 9690 6 70 11 200–10 860 AAR-5803
727.25–726.75 Aqm 217.5 9810 6 60 11 235–11 170 AAR-5801
730.2–729.8 Aqm 220.2 10 025 6 80 11 650–11 290 Ua-15411
736.2–735.8 Aqm 221.1 10 005 6 95 11 640–11 250 Ua-15410
738.1–737.9 Aqm 222.3 9955 6 85 11 450–11 220 Ua-15409
740.1–739.9 Aqm 222.7 10 100 6 100 11 950–11 300 Ua-14925
747.1–746.9 Aqm 222.0 10 040 6 95 11 700–11 290 Ua-15407
748.9–748.7 Aqm 222.6 10 330 6 90 12 350–11 900 Ua-15406
751.2–750.8 Aqm 223.5 10 430 6 85 12 650–12 100 Ua-15405
754.1–753.9 Aqm 223.9 10 585 6 85 12 860–12 350 Ua-15404
757.25–756.75 Bulk 219.9 10 780 6 95 12 980–12 800 Ua-15883
759.75–759.25 Bulk 222.0 11 030 6 95 13 150–12 940 Ua-15884
761.25–760.75 Bulk 220.7 11 355 6 95 13 430–13 170 Ua-15885
762.75–762.25 Bulk 220.7 11 510 6 100 13 550–13 150 Ua-15886
764.25–763.75 Bulk 218.3 11 600 6 95 13 700–13 430 Ua-15887
771–765 Tem 222.3 11 665 6 125 13 830–13 450 Ua-14844
Note
: Calibrated ages are shown with age ranges of more than 50% probability according to Oxcal 3.5 (Bronk
Ramsey, 1998), based on the INTCAL98 calibration data set (Stuiver et al., 1998). Datings were performed at
the AMS laboratories in A
˚
rhus and Uppsala.
*Abbreviations: Aqm 5 aquatic mosses, Bulk 5 bulk sediment, Tem 5 terrestrial mosses.
10 900
14
C yr B.P. below the boundary sud-
denly shift to ages of 10 700
14
C yr B.P. This
shift is situated at 758 cm (Table 1), corre-
sponding to 12800 cal. yr B.P. in our age
model, and is between the two established
Greenland Summit ice-core ages (Johnsen et
al., 1992; Alley et al., 1993) for the onset of
the Younger Dryas cooling.
Apart from the lithologic change at the iso-
lation of the lake from the sea, the clearest
sedimentary change occurs at 11 550 cal. yr
B.P. (Fig. 2), which possibly constitutes a re-
sponse to altered limnic conditions at the on-
set of the Holocene. The sedimentary changes
between the isolation at 13 800 cal. yr B.P. and
11 550 cal. yr B.P. are, however, very subtle,
and the clear lithologic shift at the start of the
Younger Dryas cooling, usually seen in north-
west European lake records, is clearly lacking.
By plotting the main sediment components
as a percentage of dry weight (Fig. 2), a de-
creasing trend in mineral matter is seen be-
tween 14 400 and 11550 cal. yr B.P (Fig. 2).
This trend is partly balanced by increasing or-
ganic matter, especially from 12 600 cal. yr
B.P. onward, and by bioSi percentages, es-
pecially between 12 700 and 11 600 cal. yr
B.P. If, however, these components are ex-
pressed as annual DMAR (expressed as
mg·yr
2
1
·cm
2
2
), a somewhat different picture
emerges. The DMAR of organic matter is sta-
ble after isolation, followed by an abrupt rise
at 11550 cal. yr B.P., whereas the DMAR of
mineral matter shows a decreasing trend, but
with no distinct change in connection with the
lithologic shift at 11 550 cal. yr B.P. The
DMAR of bioSi reaches a peak during the iso-
lation phase, followed by fairly stable values
until 13 000 cal. yr B.P. Between 13 000 and
12 200 cal. yr B.P., higher values are attained,
followed by slightly lower but varying values.
It is noteworthy that higher bioSi values are
usually found in connection with the moss-
barren sediments (Fig. 2), i.e., the clay gyttjas,
and that these sediments after 13 000 cal. yr
B.P. have considerably higher contents and
DMARs of bioSi than corresponding sedi-
ments before 13 000 cal. yr B.P.
We conclude that pre-Holocene lake pro-
ductivity was fairly constant, but with possi-
bly higher productivity and less surface runoff
(decreased DMAR of mineral matter), after
13 000 cal. yr B.P., i.e., during Younger Dryas
time. The increase in DMAR of organic mat-
ter at 11 550 cal. yr B.P. is explained by the
sudden moss dominance. This implies better
light conditions at the lake bottom due to, e.g.,
decreased phytoplankton biomass in the upper
water column, but possibly not because of a
decreased amount of suspended mineral mat-
ter; the previously decreasing trend of DMAR
of mineral matter is interrupted by slightly in-
creasing values after 11600 cal. yr B.P. (Fig.
2). Instead, the latter implies increased surface
runoff.
The sediments are extremely poor in pollen
grains. With the exception of the 13 150 cal.
yr B.P. level, pollen concentrations vary be-
tween 0 and 5700 grains per cubic centimeter.
Because of the low pollen sums, we only pre-
sent concentration and influx curves (Fig. 3).
Apart from the 13 150 cal. yr B.P. level, pollen
concentrations and influx values are very low
until 11 400 cal. yr B.P., followed by a gradual
rise. This occurs a few hundred years into the
Holocene, beginning at 11 550 cal. yr B.P., im-
plying a gradual establishment of higher veg-
etation. The appearance of, e.g., Empetrum ni-
grum and Vaccinum pollen types in the core
at 11 500 cal. yr B.P. suggests that these plants
were present on the island already during the
Younger Dryas. Other types present between
12 900 and 11 500 cal. yr B.P. are, e.g., Po-
aceae, Caryophyllaceae of Sagina type, Chen-
opodiaceae, and Saxifraga caespitosa type.
The latter may suggest arid conditions, partly
in contrast to the more wet-demanding Saxi-
GEOLOGY, May 2002 429
Figure 3. Magnetic susceptibility and sulfur content of sediments, as well as
total pollen concentrations, pollen influx values, and flux of
Pediastrum
(green
algae) colonies related to calendar years before present.
Figure 4. Most abundant diatom species, related to calendar years B.P., as well as diatom-inferred pH and
diatom diversity. Between 330 and 400 diatom valves per sample were counted; methods followed Rose´net
al. (2000). For pH reconstruction, weighted-average model was employed with inverse deshrinking (Birks et
al., 1990) used on 50-lake training set from northern Sweden (Rose´n et al., 2000), where 5 0.61 and root-
2
R
jack
mean-squared error of prediction (RMSEP) 5 0.30 units.
R
2
and RMSEP are based on jackknifing. Diatom
diversity was calculated as Shannon index (Zar, 1996). To right is shown July insolation curve for 608N (Berger,
1978) and inferred local climatic development and correlations to North Atlantic climatic events, with both
traditional terminology and new event stratigraphy (Bjo¨rck et al., 1998; Walker et al., 1999).
fraga stellaris found before 12 800 and after
11 550 cal. yr B.P. More than half of the pol-
len grains at 13 150 cal. yr B.P. are of the Car-
yophyllaceae Sagina type, which indicates
that the plant must have grown close to the
lake. The only macroscopic remains of vas-
cular plants were a few seeds of Minuartia sp.
(Caryophyllaceae) and Saxifraga cf. opposi-
tifolia in a sample between 13 800 and 13 400
cal. yr B.P., and the former was also found
between 12 800 and 12 600 cal. yr B.P.
The sediments are rich in colonies of green
alga Pediastrum. The Pediastrum flux curve
shows a maximum between 12 900 and 12500
cal. yr B.P., followed by lower, but still high
values (Fig. 3). The lower frequencies after
11 500 cal. yr B.P., causing better light con-
ditions at the bottom of the lake, can partly
explain the abundance of aquatic mosses dur-
ing the early Holocene.
The diatom flora, with 53 different species,
is dominated by a few pioneer species (Fig.
4). The lower part of the sequence is domi-
nated by Achnanthes conspicua and Fragilar-
ia virescens var. exigua. The former is a
brackish-water–tolerant species, indicating,
e.g., influence from sea spray, whereas the lat-
ter often occurs early in lake successions. At
12 800 cal. yr B.P., the flora became dominat-
ed by Achnanthes [minutissima agg.] and Ach-
nanthes pusilla, but F. virescens var. exigua
was still common. The two former taxa are
cosmopolitan, and especially A. [minutissima
agg.] is common in early Holocene profiles
(Bradshaw et al., 2000; Rose´n et al., 2001),
following disturbances of different types. The
lake was thus dominated by three pioneer spe-
cies during the Younger Dryas stadial, but the
increasing dominance of the two Achnanthes
taxa is best explained by increased pH; A.
[minutissima agg.] often occurs after liming
(Rhodes, 1991). The pH reached a maximum
between 12 500 and 11 500 cal. yr B.P. (Fig.
4), indicating increased weathering and leak-
age of base cations from the drainage area or
430 GEOLOGY, May 2002
increased concentration of nutrients. The si-
multaneous decreasing flux of mineral matter
(Fig. 2) implies that the latter explanation is
the most likely one. This is also supported by
high Pediastrum fluxes (Fig. 3), the maximum
in diatom diversity (Fig. 4), and the fairly high
content and fluxes of bioSi (Fig. 2).
LATE-GLACIAL PALEOCLIMATIC
SCENARIO
Our data suggest that the time period for
the Younger Dryas stadial was preceded and
followed by more unstable and humid condi-
tions. They also imply that lake productivity
during the Younger Dryas was high and that
the pH of the lake water increased, possibly
because of an increased nutrient load during
the growing seasons. This suggests that Youn-
ger Dryas summers, with high insolation,
were fairly warm and dry, causing lake levels
to drop, concentrating the nutrients, and in-
creasing lake-water temperatures. The pres-
ence of the diatom Synedra tenera, with an
abundance optimum at temperatures of 14 8C
(Rose´n et al., 2000), during the Younger
Dryas and after 11 000 cal. yr B.P. (Fig. 4)
also implies fairly warm lake temperatures.
The seemingly stable conditions and the lack
of vegetation succession imply that winters
were cold and dry. A thin snow cover reduced
spring melt effects and the possibility for most
plants to survive harsh winter conditions.
Our data therefore suggest that the Younger
Dryas climate in southernmost Greenland was
characterized by fairly arid conditions. Fur-
thermore, the Younger Dryas minimum of the
sea-spray–indicating diatom Achnanthes con-
spicua (Fig. 4), together with the sulfur min-
imum (Fig. 3), suggests that the surrounding
ocean was ice covered during most of the year,
preventing a wind- and wave-induced sea-
spray influence.
At 11 550 cal. yr B.P., the conditions rap-
idly changed into a humid climate with sig-
nificantly warmer winters, and the previously
ice-covered sea opened. However, a period of
less favorable conditions occurred a few hun-
dred years into the Holocene (Figs. 3 and 4),
which may correspond to the Preboreal oscil-
lation (Bjo¨rck et al., 1996) or the GH-11.2
event (Walker et al., 1999).
DISCUSSION
A reduction of the Atlantic thermohaline
circulation, triggered by increased freshwater
fluxes, is an important hypothesis to explain
the Younger Dryas cooling. We therefore
compare our results with the output from
global coupled atmosphere ocean models
forced to simulate the consequences of such a
process. Schiller et al. (1997) forced the
ECHAM3/LSG coupled general circulation
model (GCM) with increased meltwater dis-
charge into the North Atlantic to directly sim-
ulate the isolated effect of a reduction in the
North Atlantic deepwater formation. Aiming
at simulating the rapid warming terminating
the Younger Dryas, Fawcett et al. (1997) used
the GENESIS model—an atmospheric GCM
coupled to a mixed-layer ocean model with
specified meridional heat transport—and in-
directly specified a change in the deep-water
formation by varying the heat convergence in
the Nordic Seas. The simulation responses are
consistent with our reconstruction: a south-
eastward extension of the North Atlantic sea-
ice margin with an associated winter cooling
spreading over most of the northern North At-
lantic region, resulting in winter temperature
drops between 20 8C (Schiller et al., 1997) and
15 8C (Fawcett et al., 1997) in southern
Greenland. Both models show reduced Youn-
ger Dryas precipitation as compared to the sit-
uation with nonreduced deep-water formation.
Regarding seasonality, both models (although
not shown in Schiller et al., 1997) show by
far the largest anomalies in winter, in contrast
to small or even close to zero temperature and
precipitation anomalies in summer. None of
the simulations, however, indicate anomalous-
ly warm summers as suggested by our data
set. This discrepancy could be attributed to lo-
cal weather conditions, which cannot be cap-
tured at the coarse horizontal resolution of the
two models. In particular, this may relate to
locally very dry lee conditions with high in-
solation, i.e., a so-called Fo¨hn effect, devel-
oping in southernmost Greenland if the anom-
alous wind has a northerly direction. It is
likely that such local phenomena could offset
larger scale patterns and lead to anomalous lo-
cal energy inputs during summer—an effect
that, compared to present day, could be en-
hanced by the high summer insolation during
the Younger Dryas.
The study demonstrates the necessity of a
dense network of paleoclimatic sites in com-
bination with fine-resolution modeling, to ad-
vance our knowledge about the complexities
of seemingly stable climatic scenarios, e.g.,
the Younger Dryas cooling in the North At-
lantic region.
ACKNOWLEDGMENTS
Supported by the Commission for Scientific Research in
Greenland, the Danish Research Council, and the Carlsberg
Foundation.
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Printed in USA