Many of the physical and biological processes that characterize arctic ecosystems are unique to high latitudes, and their sensitivities to climate change are poorly understood. Stratigraphic records of land-surface processes and vegetation change in the Arctic Foothills of northern Alaska reveal how tundra landscapes responded to climatic changes between 13,000 and 8000 14 C yr BP. Peat deposition began and shrub vegetation became widespread ca. 12,500 14 C yr BP, probably in response to the advent of warmer and wetter climate. Increased slope erosion caused rapid alluviation in valleys, and Populus trees spread northward along braided floodplains before 11,000 14 C yr BP. Lake levels fell and streams incised their floodplains during the Younger Dryas (YD) (11,000-10,000 14 C yr BP). A hiatus in records of Populus suggest that its geographic range contracted, and pollen records of other species suggest a cooler and drier climate during this interval. Basal peats dating to the YD are rare, suggesting that rates of paludification slowed. Immediately after 10,000 14 C yr BP, lake levels rose, streams aggraded rapidly again, intense solifluction occurred, and Populus re-invaded the area. Moist acidic tundra vegetation was widespread by 8500 14 C yr BP along with wet, organic-rich soils. Most of these landscape-scale effects of climatic change involved changes in moisture. Although low temperature is the most conspicuous feature of arctic climate, shifts in effective moisture may be the proximate cause for many of the impacts that climate change has in arctic regions. r

Stratigraphic records from lake sediment cores and slope deposits on Rapa Nui document prehistoric human impacts and natural environmental changes. A hiatus in sedimentation in Rano Raraku suggests that this lake basin dried out sometime after 4090–4410 cal yr BP and refilled only decades to centuries before AD 1180–1290. Widespread ecosystem changes caused by forest clearance by Polynesian farmers began shortly after the end of this drought. Terrestrial sections show a chronology of burning and soil erosion similar to the lake cores. Although changing sediment types and shifts in the pollen rain suggest that droughts occurred earlier in the Holocene, as yet there is no evidence for droughts occurring after AD 1180–1290. The timing of the agricultural colonization of Rapa Nui now seems well established at ca. AD 1200 and it was accompanied by rapid deforestation that was probably exacerbated by the island's small size, its droughty climate, and the rarity of primeval fires. Detailed records of a large interval of Rapa Nui's ecological history remain elusive due to the drought hiatus in the Rano Raraku sediment record. We find no evidence for a "rat outbreak impact" on Rapa Nui's vegetation preceding anthropogenic forest clearance.

Groves, Pamela; Kunz, Michael L.; Reanier, Richard E.; and Gaglioti, Benjamin V., "Ice-age megafauna in Arctic Alaska: extinction, invasion, survival" (2013 a b s t r a c tRadical restructuring of the terrestrial, large mammal fauna living in arctic Alaska occurred between 14,000 and 10,000 years ago at the end of the last ice age. Steppe bison, horse, and woolly mammoth became extinct, moose and humans invaded, while muskox and caribou persisted. The ice age megafauna was more diverse in species and possibly contained 6Â more individual animals than live in the region today. Megafaunal biomass during the last ice age may have been 30Â greater than present. Horse was the dominant species in terms of number of individuals. Lions, short-faced bears, wolves, and possibly grizzly bears comprised the predator/scavenger guild. The youngest mammoth so far discovered lived ca 13,800 years ago, while horses and bison persisted on the North Slope until at least 12,500 years ago during the Younger Dryas cold interval. The first people arrived on the North Slope ca 13,500 years ago. Bone-isotope measurements and foot-loading characteristics suggest megafaunal niches were segregated along a moisture gradient, with the surviving species (muskox and caribou) utilizing the warmer and moister portions of the vegetation mosaic. As the ice age ended, the moisture gradient shifted and eliminated habitats utilized by the dryland, grazing species (bison, horse, mammoth). The proximate cause for this change was regional paludification, the spread of organic soil horizons and peat. End-Pleistocene extinctions in arctic Alaska represent local, not global extinctions since the megafaunal species lost there persisted to later times elsewhere. Hunting seems unlikely as the cause of these extinctions, but it cannot be ruled out as the final blow to megafaunal populations that were already functionally extinct by the time humans arrived in the region.

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Understanding the population dynamics of megafauna that inhabited the mammoth steppe provides insights into the causes of extinctions during both the terminal Pleistocene and today. Our study area is Alaska's North Slope, a place where humans were rare when these extinctions occurred. After developing a statistical approach to remove the age artifacts caused by radiocarbon calibration from a large series of dated megafaunal bones, we compare the temporal patterns of bone abundance with climate records. Megafaunal abundance tracked ice age climate, peaking during transitions from cold to warm periods. These results suggest that a defining characteristic of the mammoth steppe was its temporal instability and imply that regional extinctions followed by population reestablishment from distant refugia were characteristic features of ice-age biogeography at high latitudes. It follows that long-distance dispersal was crucial for the long-term persistence of megafaunal species living in the Arctic. Such dispersal was only possible when their rapidly shifting range lands were geographically interconnected. The end of the last ice age was fatally unique because the geographic ranges of arctic megafauna became permanently fragmented after stable, interglacial climate engendered the spread of peatlands at the same time that rising sea level severed former dispersal routes. (10,000-45,000 calendar y ago) when some 65% of terrestrial megafauna genera (animals weighing >45 kg) became globally extinct (1). Based on what we know about recent species extinctions, the causes of extinction are usually synergistic, often species-specific, and therefore, complex, which implies that there is no universal explanation for end-Pleistocene extinctions (2, 3). Globally and specifically in the Arctic (3-10), megafaunal extinctions have been variously blamed on overhunting, rapid climate change, habitat loss, and introduced diseases (3-10). Further complicating a clear understanding of the causes of ice-age extinctions is that the magnitude and tempo of environmental change during the last 100,000 y of the Pleistocene were fundamentally different than during the Holocene (11), and these differences had far-reaching implications for community structure, evolution, and extinction causes (12).A recent survey comparing the extinction dates of circumboreal megafauna with ice-age climate suggests that extinctions and genetic turnover were most frequent during warm, interstadial events (13). However, the mechanisms for these extinctions remain unclear, partly because this previous study considered multiple taxa living in many different ecosystems. Here, we focus on five megafaunal species that coinhabited a region of the Arctic with an ecological setting that is relatively well-understood. To avoid the methodological problems involved in pinpointing extinction dates (13), we infer population dynamics from changes in the relative abundance of megafauna over time. Using a uniquely large dataset of dated megafaunal bones from one particular area, we t...

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Excavations at the Mesa site in arctic Alaska provide evidence for a Paleoindian occupation of Beringia, the region adjacent to the Bering Strait. Eleven carbon-14 dates on hearths associated with Paleoindian projectile points place humans at the site between 9,730 and 11,660 radiocarbon years before present (years B.P.). The presence of Paleoindians in Beringia at these times challenges the notion that Paleoindian cultures arose exclusively in mid-continental North America. The age span of Paleoindians at the Mesa site overlaps with dates from two other cultural complexes in interior Alaska. A hiatus in the record of human occupation occurs between 10,300 and 11,000 years B.P. Late Glacial climatic fluctuations may have made northern Alaska temporarily unfavorable for humans and spurred their southward dispersal.