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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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