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Permafrost, Phillips, Springman & Arenson (eds)<br />
© 2003 Swets & Zeitlinger, Lisse, ISBN 90 5809 582 7<br />
<strong>Late</strong>-<strong>Quaternary</strong> <strong>paleoenvironmental</strong> <strong>record</strong> <strong>from</strong> a palsa-scale frost mound in<br />
northern Alaska<br />
W.R. Eisner & K.M. Hinkel<br />
Department of Geography, University of Cincinnati, Cincinnati, OH, USA<br />
F.E. Nelson<br />
Department of Geography, University of Delaware, Newark, DE, USA<br />
J.G. Bockheim<br />
Department of Soil Science, University of Wisconsin, Madison, WI, USA<br />
ABSTRACT: A peat-covered, palsa-scale frost mound was discovered near the White Hills on the North Slope of<br />
Alaska, in the continuous permafrost zone. The palsa is situated within a partially drained lake basin and currently<br />
supports willow-birch shrub vegetation very dissimilar to that of the surrounding bog. In 1997 and 1998, the palsa<br />
was cored to a depth of 1.83 m; the upper 1.78 m contains undisturbed (non-cryoturbated) layers of frozen peat while<br />
the lower 5 cm is lacustrine silt containing thin ice lenses. The organic sediments were analyzed for pollen, fungi,<br />
algae, and other microfossils. Combined with sediment textural analysis, the <strong>record</strong> demonstrates local changes<br />
in hydrology, mound formation, and vegetation succession in response to landscape processes. In situ wood <strong>from</strong> the<br />
core <strong>from</strong> a depth of 123 cm yielded an age of 9610 60 14 C yr BP, indicating that the palsa contains organic<br />
sediments encompassing the entire Holocene.<br />
1 INTRODUCTION<br />
“Palsa-scale frost mound” is a generic term used to<br />
describe a variety of morphologically similar aggradational<br />
features developed within the active layer above<br />
permafrost. Although several formative processes have<br />
been identified, the positive relief of all frost mounds<br />
is ascribable to accumulation of ice in the substrate<br />
(Nelson et al. 1992, Gurney 2001).<br />
The periglacial literature contains a great deal of<br />
controversy about the term palsa. At its root lies<br />
disagreement about whether classification schemes<br />
should be based on morphology, genesis, constituent<br />
materials, or combinations of these parameters. In this<br />
paper we follow conventions established by Washburn<br />
(1983a, b) and Nelson et al. (1992), using “palsa” in a<br />
strictly morphological sense with reference to mediumscale<br />
frost mounds, independent of genesis, constituent<br />
material, or location in the hierarchy of permafrost<br />
continuity.<br />
Terminological issues aside, palsa-scale frost<br />
mounds can be important sources of <strong>paleoenvironmental</strong><br />
information (e.g., Vorren 1972, Vorren & Vorren<br />
1975, Lavoie & Payette 1995). Once a palsa is formed,<br />
its microclimate changes and new plant associations,<br />
very different than those of surrounding low areas,<br />
occupy palsa summits (Sjörs 1961, Railton & Sparling<br />
1973, Seppälä 1990). Vegetation differences atop and<br />
around frost mounds can play a useful role in applying<br />
14 C techniques to date the inception of mound growth.<br />
Vorren (1972, 1979a, 1979b) and Vorren & Vorren<br />
(1975) first demonstrated that radiocarbon dating, in<br />
combination with pollen analysis, could be used to estimate<br />
timing of the onset of frost mound growth.<br />
This paper reports results of a palsa coring program.<br />
Patterns of pollen, soil organic carbon, and soil<br />
texture <strong>from</strong> a core collected <strong>from</strong> a palsa summit are<br />
analysed. The palsa is located in an area that has undergone<br />
significant landscape evolution, with consequent<br />
impact on local hydrology and vegetation. These local<br />
patterns are superimposed on a long-term signal reflecting<br />
regional climate and vegetation changes in the late<br />
<strong>Quaternary</strong>. Our primary goal is to use pollen and soil<br />
analysis to test the feasibility of separating the signals<br />
and reconstruct local landscape processes.<br />
2 SITE DESCRIPTION AND FIELD METHODS<br />
During the summer of 1997 we investigated a frost<br />
mound located west of the White Hills on Alaska’s<br />
North Slope (N 69°29.34, W 150°05.27). The site is<br />
near the boundary between the Arctic Coastal Plain and<br />
Arctic Foothills physiographic provinces and lies within<br />
the zone of continuous permafrost. The mound meets<br />
Washburn’s (1983b) morphological definition of a<br />
palsa: 6 m in height, it has a basal diameter of 12 m and<br />
contains abundant peat. It is developed near the edge<br />
of a series of nested, partially drained lake basins<br />
(Fig. 1). A prominent outer beach scarp is associated<br />
with an older lake basin. A less pronounced beach<br />
scarp, formed by a younger lake, lies basinward and is<br />
highlighted in Figure 1. The younger basin has been<br />
partially infilled by sediments and vegetation. The palsa<br />
229
Figure 1. Aerial view of palsa, bog, and pond; inner beach<br />
scarp is noted with dotted line.<br />
is located near the outlet of the remnant lake, where it<br />
drains into an adjacent basin through a narrow strait.<br />
The climate of the site is cold and semi-continental,<br />
with estimated mean annual temperature of 10.7°C<br />
and annual monthly range of 41.4°C (Willmott &<br />
Matsuura 2001). Although the thickness of the permafrost<br />
is unknown, it is estimated to exceed 300 m<br />
based on an assumed geothermal gradient of 3°C/<br />
100 m. Average snowcover depth has not been measured,<br />
but snowdrifts on the palsa’s flanks are likely to<br />
be substantial. Vegetation atop the palsa and flanking<br />
slopes is a shrub assemblage consisting of Betula<br />
nana (dwarf birch), Salix glauca (willow), and Ericad<br />
(heath), with some mosses and grasses. Thaw depth,<br />
measured in mid-August in two years, averaged 45 cm.<br />
By contrast, vegetation in the bog surrounding the<br />
palsa is dominated by Carex aquatilis (sedge), and the<br />
thaw depth averaged 28 cm.<br />
A sediment core was obtained <strong>from</strong> the bog surrounding<br />
the palsa, at a distance of 15 m <strong>from</strong> it, using<br />
a 7.62 cm (3 inch) diameter coring barrel designed by<br />
USA CRREL, driven by a Little Beaver © power auger.<br />
A second core, 128 cm in length, was obtained <strong>from</strong> a<br />
position atop the palsa. Peat was present throughout<br />
the core, indicating that we had not penetrated into the<br />
massive ice core. Although equipment limitations prevented<br />
drilling deeper in the palsa in 1997, we returned<br />
to the site the following year and exactly re-occupied<br />
the borehole. We used extension rods and core extractors<br />
to penetrate an additional 54 cm, to a total depth<br />
of 182 cm. The palsa core can therefore be considered<br />
continuous. The extended section of the core showed<br />
that peat continues downward another 50 cm, and is<br />
derived <strong>from</strong> aquatic plants. The peat is underlain by<br />
ice-rich lacustrine silts typical of thaw lake bottom<br />
sediments. Thin (3 mm) ice lenses grade into massive<br />
segregation ice in the palsa core.<br />
Cores were sampled at 10–15 cm intervals for soil<br />
bulk density and texture, pollen, and microfossil content.<br />
The organic carbon content was discontinuously<br />
sampled in the upper 40 cm, but regularly sampled at a<br />
5-cm interval <strong>from</strong> 40 to 130 cm depth. Oven-dried soils<br />
(dried at 65°C for 48 hr) were passed through a 2-mm<br />
230<br />
Figure 2.<br />
analysis.<br />
White Hill core textural and compositional<br />
sieve and characterized using methods established by<br />
the Soil Survey Staff (1996). These analyses included<br />
easily oxidizable organic C by dichromate digestion<br />
(6A1a) and particle-size distribution with sand and silt<br />
fractionation by sieving and pipette, respectively (3A,<br />
3A1). The results are summarised in Figure 2.<br />
Subsamples were prepared for pollen analysis<br />
by standard procedures including treatment with<br />
hydrofluoric acid and acetolysis (Berglund & Ralska-<br />
Jasiewiczowa 1986). A known amount of Lycopodium<br />
clavatum spores was added in tablet form to each<br />
sample to determine pollen concentrations and as a<br />
processing control. Samples were mounted in silicon<br />
oil and identified at 400 magnification. Pollen<br />
accumulation rates were not calculated. Identification<br />
of algal, fungal, and zoological remains was carried<br />
out using an extensive collection of photographs and<br />
reference material (Van Geel 1978, 1986, Eisner &<br />
Peterson 1998a, b). Photographs of the microfossil<br />
types mentioned in the text, as well as further<br />
information on type ecological significance, can be<br />
found online (Eisner 2000).<br />
3 STRATIGRAPHY AND DATING<br />
Cored sediment <strong>from</strong> the palsa showed little evidence of<br />
mixing or deformation, except near the base where<br />
some cryoturbation was apparent. Discreet macrofossils<br />
included twigs <strong>from</strong> willow shrubs and complete leaf<br />
and seed remains. These were found throughout the<br />
palsa core, and are ideal for identification and dating.
Carbon stored in the palsa amounts to 135 kg C m 3 ,<br />
greater than that reported <strong>from</strong> other sites on Alaska’s<br />
North Slope (Michaelson et al. 1996).<br />
Results <strong>from</strong> AMS dating are reported in Table 1,<br />
and confirm that the palsa contains organic sediments<br />
encompassing at least the entire Holocene. The consistency<br />
of the dates demonstrates stratigraphic integrity<br />
throughout the 9,000 yr <strong>record</strong>.<br />
We also obtained dates <strong>from</strong> plant material in the<br />
lower core (128–183 cm), as indicated in Table 1.<br />
Although marginally younger than the sediments immediately<br />
above, this unit was interspersed with plant<br />
roots, making precise dating problematic. The dates,<br />
and the composition of the material, indicate that these<br />
sediments represent a basal detrital unit composed of<br />
eroded, reworked, and redeposited peat, organic silts,<br />
and roots of aquatic plants (Hopkins & Kidd 1988). This<br />
unit was deposited in a lacustrine environment, and has<br />
little stratigraphic integrity. The pollen and microfossils<br />
were derived <strong>from</strong> older reworked materials, or could<br />
have been transported <strong>from</strong> elsewhere in the watershed.<br />
Because the pollen and microfossils represent a variety<br />
of environments, we concluded that this layer<br />
(128–183 cm) was unsuitable for detailed analysis.<br />
Initially we hypothesized that a comparison of pollen<br />
stratigraphy <strong>from</strong> the palsa summit and the adjacent<br />
bog sediment, combined with dating at the point of<br />
divergence between the two pollen signals, should<br />
Table 1. Radiocarbon and calibrated 14 C ages 1<br />
CAMS Lab nr. Depth (cm) 14 C age Cal age ranges<br />
43556 3–8 modern 1954 AD<br />
43557 40–45 1420 60 596–665 AD<br />
42609 65–70 4720 100 3633–3556;<br />
3540–3496;<br />
3465–3375*<br />
42610 120–123 9610 60 9175–9111;<br />
9008–8888;<br />
8883–8821*<br />
53255 156–161 9190 50 uncalibrated**<br />
53256 176–182 9440 50 uncalibrated**<br />
1 CALIB rev. 4.3 (Stuiver & Reimer 1993); * BCE.; ** second (lower) core.<br />
0<br />
10<br />
20<br />
30<br />
40<br />
50<br />
60<br />
70<br />
80<br />
90<br />
100<br />
110<br />
120<br />
130<br />
Depth (cm)<br />
Picea/Pinus<br />
Alnus<br />
Betula<br />
Ericaceae<br />
Salix<br />
Populus<br />
Juniperus<br />
Artemisia<br />
Cyperaceae<br />
Gramineae<br />
Equisitum<br />
indicate the timing of frost mound incipience. However,<br />
the core collected <strong>from</strong> the adjacent lake margin bog<br />
was found to contain modern aquatic plant roots in the<br />
upper 26 cm, and this was immediately underlain by<br />
lacustrine silts. Lacking a thick sequence of peat to<br />
date, we chose to discontinue further analysis of the bog<br />
core and focus exclusively on the palsa.<br />
The pollen and microfossil percentage diagram (Fig.<br />
3) has been divided into local Zones A (base at 128 cm)<br />
to D (near-surface). Zone discrimination is based on<br />
qualitative analysis of pollen, microfossils, radiocarbon<br />
dates, and sediment texture. Fungi, algae and other<br />
microfossils are presented as percentages of the pollen<br />
sum. Fossils are represented as percentages of the total<br />
pollen sum, although they are not part of the total fossil<br />
pollen. More than 30 fungal, algal, and rhizopod types<br />
were identified during the analysis, although only those<br />
discussed here are depicted in the diagram.<br />
Zone A (128–98 cm) comprises most of the early and<br />
middle Holocene, beginning around 9600 14 C yr BP.<br />
This zone represents a period of several thousand years,<br />
and the pollen reflects a series of major vegetation fluctuations.<br />
The local environment of Zone A is characterized<br />
by birch (Betula), fluctuating between 3 and 28%,<br />
heaths (Ericaceae) and willow (Salix). Dominant herbs<br />
are sedge (Cyperaceae) and grass (Gramineae), which<br />
also fluctuate within the zone, becoming dominant during<br />
the period in which shrub pollen decreases. The<br />
major non-pollen microfossil, type 55A, is a fungal<br />
spore that favors mesotrophic (moderately nutrient-rich)<br />
conditions and peaks concurrently with grass pollen.<br />
Most of the pollen and microfossil fluctuations represent<br />
the influence of local vegetation and landscape<br />
processes. However, alder (Alnus) and spruce (Picea)<br />
pollen are present through most of the core in small<br />
amounts (5–10%), suggesting that these are products<br />
of long-distance transport. The poplar (Populus) peak<br />
(12%) at 107 cm may indicate climate change. The<br />
poplar rise occurred in northern Alaska and northwestern<br />
Canada between ca. 11,000 and ca. 8000 14 C yr BP<br />
and is generally described as a period of increased solar<br />
insolation (Ritchie 1984, Anderson & Brubaker 1994,<br />
Sphagnum<br />
Nuphar<br />
Forbs<br />
Unidentifiable<br />
type 3<br />
type 16<br />
type 20<br />
Type 46<br />
type 55A<br />
Type 79-hyphae<br />
Type 332<br />
352 Arcella<br />
353<br />
Testate amoeba<br />
Algae<br />
Rhizopods<br />
Fungal remains<br />
20 20 40 60 80 20 20 20 20 40 60 20 20 20 20 20 20 40 60 20 20 20 20 40 60 20 20 40 60 80<br />
Zone D<br />
Zone C<br />
Zone B<br />
Zone A<br />
Figure 3.<br />
White Hills pollen and microfossil percentage diagram.<br />
231
Bartlein et al. 1995). Poplar pollen does not have a wide<br />
dispersal range (Edwards & Dunwiddie 1985), and the<br />
percentages found at this level may indicate establishment<br />
of a localized poplar grove some time after 9600<br />
14 C yr BP and before 4720 14 C yr BP.<br />
Sediments in Zone A (Fig. 2) contain a large component<br />
of organic material (25–35%) and silt (35–45%),<br />
with 15–25% sand and clay sized particles. These proportions<br />
are similar to those near the surface (Zone D),<br />
and the mineral fraction may be of aeolian origin.<br />
The pollen, microfossils, and sediment texture/composition<br />
evidence <strong>from</strong> Zone A indicate that a terrestrial,<br />
mesotrophic shrub/graminoid tundra, consisting<br />
mainly of low willow, birch, sedges and grasses, existed<br />
during this entire period.<br />
The transition <strong>from</strong> Zone A to Zone B (98–65 cm) is<br />
marked by a sharp increase in horsetail (Equisitum) to<br />
23%, which may be indicative of surface disturbance. An<br />
abrupt rise in birch pollen occurs at 98 cm (87%), followed<br />
by an abrupt return to moderate levels. The birch<br />
spike probably reflects the expansion of local birch, or<br />
possibly even birch catkins incorporated into the sediment,<br />
since much of the sample was composed of birch<br />
pollen clusters. The remainder of Zone B (98–65 cm) is<br />
marked by high frequencies of Cosmarium turpini (Type<br />
332B), a pioneering species of green algae preferring<br />
low-nutrient aquatic environments and typically flourishing<br />
in shallow, sandy pools. Rapid growth of this<br />
algae could have been encouraged when the supply of<br />
nutrients <strong>from</strong> groundwater was cut off and the primary<br />
nutrient source was meteoric water. Several fungal<br />
remains and rhizopods (or Thecamoebe) are notable:<br />
Centropyxis aculeata Ehrenberg (Type WH8) is an<br />
invertebrate adapted to living in highly acidic environments<br />
of wet mosses and Sphagnum. Sphagnum percentages<br />
rise concurrently with Type WH8 in Zone B. An<br />
abundant fossil in this zone is Type 353B, eggs of aquatic<br />
flatworm Microdalyellia armigera, typical of eutrophic<br />
environments. Conversely, Type 352 (Arcella), which<br />
shows up in the early part of the zone, is typical of nutrient-poor<br />
environments. Despite their conflicting signals<br />
in terms of nutrient levels, both rhizopods are indicative<br />
of an aquatic environment. The vascular plants also<br />
reflect this change, with sedges dominant throughout the<br />
period and dry-ground vegetation such as birch, willow,<br />
and grass at relatively low levels.<br />
Textural and compositional analysis (Fig. 2) demonstrate<br />
an increase in the coarse (sand) and very fine<br />
(clay) mineral fraction, with a concurrent reduction in<br />
the silt component. The increased presence of sand<br />
indicates that Zone B formed in a higher energy environment<br />
than Zone A. The organic component remains<br />
high, but decreases steadily upsection. Based on the<br />
various lines of evidence, there appears to have been<br />
a shift to an aquatic environment. We interpret this<br />
period as one of inundation <strong>from</strong> rising lake levels and<br />
increased peat accumulation along the Sphagnum/<br />
sedge bogs of the lake margin.<br />
Zone C (65–20 cm) shows a long period of increasingly<br />
terrestrial conditions, indicated by the prevalence<br />
of birch (15–22%), heath (1–10%), and willow<br />
(2–5%). Sage (Artemisia) pollen increases for the first<br />
time (to 10%). The zone is again introduced by a rise,<br />
although smaller, of Equisitum. Zone C also contains<br />
large amounts of fungal hyphae (Type 79) which is<br />
typically an indication of increased biotic activity and<br />
soil formation. Most of the aquatic species (C. turpin,<br />
C. aculeate E., and M. armigera) that were present in<br />
Zone B decline dramatically.<br />
Zone C shows a pronounced decline in organic matter.<br />
The coarse mineral component virtually disappears,<br />
silt dominates (70%), and the clay fraction increases<br />
to around 25%. These trends indicate a period of partial<br />
lake drainage around 4700 14 C yr BP, with a consequent<br />
lowering of the lake’s water level. The site, located near<br />
the margins of the smaller basin, was at least partially<br />
drained. Soil formation was initiated at this time. The<br />
fine mineral fraction was delivered by aeolian processes<br />
or during episodic inundation events.<br />
Zone D (20 cm to surface) is problematic for the<br />
analysis of discreet intervals due to rooting by shrubs<br />
and herbs, which can cause penetration of older<br />
deposits by younger material. Although one water lily<br />
pollen grain (Nuphar) was found at a depth of 16 cm,<br />
it is highly unlikely that the site was under water;<br />
animal importation or bioturbation is more likely. In<br />
general, the pollen closely reflects present-day vegetation<br />
at the crest of the palsa, with very high birch<br />
percentages (68%), some heath, willow, and sage, and<br />
a sharp decline in sedge and grass. Fungal hyphae rise<br />
again in this zone, as does fungal type 55A. The<br />
organic matter component increases <strong>from</strong> 10% to<br />
40% across the Zone C-D transition, and the proportion<br />
of silt and clay decreases.<br />
It is very likely that the transition between Zones C<br />
and D reflects palsa formation, followed by birch<br />
shrub growth and the initiation of soil formation. The<br />
dates indicate that this event took place at some time<br />
between 1420 14 C yr BP and the present.<br />
4 DISCUSSION<br />
Interpretation of the core data, which varies in<br />
response to local landscape changes, is summarized in<br />
Table 2. The lowermost layer (pre-A) is interpreted as<br />
a basal detrital unit deposited above lacustrine silts.<br />
The environmental setting is typical of shallow lake<br />
margins vegetated with Carex. Over time organics accumulate<br />
and water shallows, and eventually the surface<br />
is at or near the lake water level. A similar setting<br />
is present today along the lake margin, and the core<br />
collected <strong>from</strong> the bog adjacent to the palsa has a<br />
232
Table 2.<br />
Pollen zonation and landscape processes.<br />
Zone Landscape process Biotic response Sediments OM mineral<br />
D Palsa formation Birch, willow shrubs, OM and silt dominates<br />
20 cm<br />
soil development<br />
C Partial lake drainage/infilling of lake margin Grasses, shrubs, herbs OM and sand much<br />
65–20 cm by sediments and aquatic plants appear; aquatics disappear reduced, silt dominates<br />
B Rising lake level and inundation; Aquatic indicators (vegetation, OM persists, silt much reduced,<br />
98–65 cm inner beach scarp forms algae, zoological remains) increase sand and clay %<br />
A Terrestrial; lake level lowered by drainage or Shrub/graminoid tundra OM and silt dominates<br />
128–98 cm reduced input/drought elements<br />
Pre-A Infilling of lake margin by Aquatic plant remains, OM to 180 cm, lacustrine silt<br />
183–128 cm sediments and aquatic plants; reworked detritus below with ice lenses, grading<br />
outer beach scarp active<br />
into ice<br />
similar composition. Given the thickness of the pre-A<br />
unit (50 cm), it is likely that the existing lake occupied<br />
the larger basin and, during this time, the outermost<br />
beach scarp formed.<br />
The transition to Zone A is interpreted as representing<br />
a lowering of the lake water level, and subsequent<br />
replacement of aquatic with terrestrial vegetation. This<br />
could be triggered by partial lake drainage, by a reduction<br />
in precipitation, or an increase in evapotranspiration.<br />
A mesotrophic shrub/graminoid tundra developed,<br />
similar to that existing today. Local peat accumulation<br />
began at the same time (approximately 9340 14 C yr BP)<br />
as at the Meade River bluffs near Atqasuk (Eisner &<br />
Peterson 1998a), located approximately 200 km west<br />
of this site.<br />
Our findings at the White Hills site indicate relatively<br />
warm, dry conditions accompanied by peat<br />
accumulation, and are consistent with those <strong>from</strong> other<br />
parts of the Arctic Coastal Plain. Despite dry conditions,<br />
high peat accumulation rates are typical throughout<br />
northern Alaska in the early part of the Holocene,<br />
owing to the accompanying warmer temperatures.<br />
Eisner (1999) suggested that initiation of peat accumulation<br />
in Arctic Alaska was fostered by melting of<br />
ice-rich sediments and increased availability of ground<br />
water. The appearance of poplar at the White Hills site<br />
during this period also indicates that warmer and drier<br />
conditions prevailed.<br />
In Zone B, aquatic microfossil indicators and<br />
increased sand content indicate that standing water<br />
existed at the site. This reflects the effect of rising lake<br />
levels, possibly induced by regional climatic changes.<br />
Although we do not have a date at the beginning of<br />
Zone B, other studies show that the middle Holocene<br />
(8000 to 5000 14 C yr BP) was a period of rapid peat<br />
accumulation on the Arctic Coastal Plain (Marion &<br />
Oechel 1993, Eisner 1999), and also of higher precipitation<br />
and lake levels in northern Alaska (Edwards<br />
et al. 2000). We conclude that lake water level rose<br />
in response to increased precipitation around 8000<br />
14 C yr BP, which is consistent with our core dates.<br />
At this time, a new basin developed and formed the<br />
inner beach scarp apparent in Figure 1.<br />
In time, sedimentation and accumulation of organic<br />
remains infilled the lake margin, and the lake bottom<br />
aggraded toward the surface. Terrestrial vegetation<br />
replaced aquatics around 4700 14 C yr BP, as reflected<br />
in Layer C. Along the lake margin, this condition still<br />
exists. At the palsa site, however, palsa formation did<br />
not occur until after 1420 14 C yr BP, but before 1954<br />
cal A.D. This caused topographic uplift and vegetation<br />
succession on the drier palsa crest. It is likely<br />
that the growth of shrubs helped to limit sediment deflation<br />
and augment peat accumulation. Northern Alaska<br />
experienced cooler conditions around 5000 14 C yr BP.<br />
Ice-wedge formation and a decrease in peat accumulation<br />
occurred at this time (Ritchie 1984, Mackay<br />
1992, Marion & Oechel 1993, Eisner 1999).<br />
5 CONCLUSION<br />
The pollen and microfossil stratigraphy <strong>from</strong> the White<br />
Hills palsa core should be interpreted primarily as a<br />
<strong>record</strong> of local changes in the area delineated by the<br />
outer beach scarp of the ancient lake. The major<br />
changes in hydrology, palsa formation, and vegetation<br />
development are all responses to landscape processes<br />
that could occur independently of climate variation.<br />
The climatic interpretations we have made for the timing<br />
of basin flooding and for fluctuations in peat accumulation<br />
should be further corroborated with evidence<br />
<strong>from</strong> other regional basins of similar age. One climatic<br />
event is clearly <strong>record</strong>ed – the poplar rise – and indicates<br />
a widespread expansion of poplar in this part of<br />
northern Alaska during the early Holocene.<br />
ACKNOWLEDGEMENTS<br />
This material is based upon work supported by the<br />
National Science Foundation under grants OPP-<br />
9911122, ATM 9416858, and GER 99550382 to<br />
Eisner, OPP-0094769 to Hinkel and OPP-0095088 to<br />
233
Nelson. Any opinions, findings, conclusions, or recommendations<br />
expressed in the material are those of<br />
the authors and do not necessarily reflect the views<br />
of the National Science Foundation. The authors would<br />
like to thank Kim Peterson and Lynn Everett for their<br />
invaluable assistance.<br />
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