
Shrinking of the Bering land bridge
The
Bering land bridge was a
land bridge roughly 1,000 miles (1,600 km) north to south at its greatest extent, which joined present-day
Alaska and eastern
Siberia at various times during the
Pleistocene ice ages. It was not
glaciated because
snowfall was
extremely light due to the southwesterly winds from the
Pacific Ocean having lost their moisture over the fully glaciated
Alaska Range. The grassland
steppe, including the land bridge, that stretched for several hundred miles into the continents on either side has been called
Beringia. It is believed that a small human population of at most a few thousand survived the
Last Glacial Maximum in Beringia, isolated from its ancestor populations in Asia for at least 5,000 years, before expanding to
populate the Americas sometime after 16,500 years ago, during the
Late Glacial Maximum as the American glaciers blocking the way southward melted.
Geography
thumb|right|140px|Berengia -Wisconsin glaciationthumb|right|140px|Berengia - deglaciation periodthumb|right|140px|Berengia - present dayThe
Bering Strait, the
Chukchi Sea to the north and the
Bering Sea to the south, are all shallow seas (
maps, right). During cycles of global cooling, such as the most recent
ice age, enough sea water became concentrated in the ice caps of the
Arctic and
Antarctic that the subsequent drop in
eustatic sea levels exposed shallow sea floors that have subsequently re-flooded. Other land bridges around the world have been created and re-flooded in the same way: approximately 14,000 years ago, mainland
Australia was linked to both
New Guinea and
Tasmania; the
British Isles were an extension of continental
Europe via the dry bed of the
English Channel; and the dry basin of the
South China Sea linked
Sumatra,
Java and
Borneo to the
Asian mainland.
The rise and fall of global sea levels has exposed and submerged the bridging land mass called "Beringia" in several periods of the
Pleistocene. The Beringian land bridge is believed to have existed both in the
glaciation that occurred before 35,000
BP and during the more recent period 22,000-7,000 years Before Present. The
strait reopened about 15,500 BP and by c. 6000 BP the coastlines had assumed approximately their present configurations.
The ice-free heartland of Beringia served as a giant
ecological refugium during maximal glaciation for those
tundra plants that could survive its windswept Arctic desert conditions. But Beringia constantly transformed its
ecosystem as the changing climate affected the environment, determining which plants and animals were able to survive. The land mass could be a barrier as well as a bridge: during colder periods, glaciers advanced and precipitation levels dropped. During warmer intervals clouds, rain and
snow altered
soils and drainage patterns.
Fossil remains show that
spruce,
birch and
poplars once grew beyond their northernmost modern range today, indicating there were periods when the climate was warmer and wetter.
Mastodons, which depended on shrubs for food, were uncommon in the open dry
tundra landscape characteristic of Beringia during the colder periods; in this tundra,
mammoths flourished instead.
Human habitation
The Bering land bridge is significant for several reasons, not least because it is believed to have enabled
human migration to the Americas from Asia about 25,000 years ago. A study by Hey (2005) has indicated that of the people migrating across this land bridge during that time period, only 70 left their genetic print in modern descendants, a minute
effective founder population—easily misread as though implying that only 70 people crossed to North America. Seagoing coastal settlers may also have crossed much earlier, but
scientific opinion remains divided on this point, and the coastal sites that would offer further information now lie submerged in up to a hundred metres of water offshore. Land animals were able to migrate through Beringia as well, bringing
mammals that evolved in Asia to
North America, mammals such as
proboscideans and
lions, which
evolved into now-extinct
endemic North American species, and allowing
equids and
camelids that evolved in North America (and later became extinct there) to migrate to Asia.
A study published in 2007 in
PLoS Genetics, led by University of Michigan and University College London researchers, suggests that the Bering land bridge migration occurred 12,000 years ago, that every human who migrated across the land bridge came from Eastern Siberia, and that every Native American is directly descended from that same group of Eastern Siberian migrants. The authors note a "unique genetic variant widespread in natives across both continents — suggesting that the first humans in the Americas came in a single migration or multiple waves from a single source, not in waves of migrations from different sources".
Previous connections
thumb|left|140px|Beringia area coverageBiogeographical evidence demonstrates previous connections between North America and Asia. Similar
dinosaur fossils have been found between
Asia and
North America. For instance the dinosaur
Saurolophus was found in both Mongolia and western North America. Relatives of
Troodon,
Triceratops, and even
Tyrannosaurus rex all came from Asia.
While there is considerable evidence for faunal interchange of dinosaurs in the Campanian and Maastrichtian phases of the
Late Cretaceous, mammals, however, seem not to have dispersed so easily, perhaps because of their relatively small size; at any rate, there is no direct evidence supporting mammalian faunal exchange in the
Cretaceous. Fossils in
China demonstrate a migration of Asian mammals into North America around 55 million years ago. By 20 million years ago, evidence in North America shows a further interchange of mammalian species. Some, like the ancient
saber-toothed cats, have a recurring geographical range: Europe, Africa, Asia, and North America. The only way they could reach the
New World is through the Bering land bridge. Had this bridge not existed at that time, the
fauna of the world would be very different.
Molecular
phylogenetics is now being used to trace the history of faunal exchange and diversification, through the genetic history of parasites and pathogens of North American
ungulates. An international Beringian Coevolution Project is collaborating to provide material to assess the pattern and timing of faunal exchange and the potential impact of past climatic events on differentiation.
See also