Ice Age
Ice Age
Ice Age
Contents
1
Ice age
1.1
1.2
1.3
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.4
1.5
1.5.1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.5.2
1.6.1
1.6.2
1.6.3
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.6.4
Uplift of the Tibetan plateau and surrounding mountain areas above the snowline . . . . . .
1.6.5
1.6.6
1.6.7
Volcanism
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.7.1
1.7.2
Last Glacial Period in the semiarid Andes around Aconcagua and Tupungato . . . . . . . .
1.8
Eects of glaciation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
1.9
See also . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
10
1.6
1.7
1.10 References
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
10
13
Megafauna
14
2.1
Ecological strategy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
14
2.2
14
2.2.1
In terrestrial mammals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
15
2.2.2
In marine mammals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
15
2.2.3
In ightless birds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
15
16
2.3.1
16
2.3.2
17
2.3
ii
CONTENTS
2.4
Examples . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
17
2.5
Gallery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
21
2.5.1
Extinct . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
21
2.5.2
Living . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
22
2.6
See also . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
23
2.7
Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
23
2.8
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
23
2.9
External links . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
26
Pleistocene
27
3.1
Dating . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
27
3.2
28
3.2.1
Glacial features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
28
3.2.2
Major events . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
28
3.2.3
Palaeocycles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
29
3.3
Fauna . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
30
3.4
Humans . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
30
3.5
Deposits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
31
3.6
See also . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
31
3.7
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
31
3.8
External links . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
32
Prehistoric mammal
33
4.1
33
4.2
See also . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
33
Stone Age
34
5.1
Historical signicance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
34
5.2
34
5.2.1
34
5.2.2
35
5.2.3
35
5.2.4
36
5.2.5
37
Chronology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
37
5.3.1
Three-age chronology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
37
5.3.2
Three-stage chronology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
43
Material culture . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
43
5.4.1
Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
43
5.4.2
43
5.4.3
44
5.4.4
Art . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
44
5.3
5.4
CONTENTS
5.4.5
45
5.5
45
5.6
See also . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
45
5.7
Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
46
5.8
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
47
5.9
Further reading . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
47
47
Woolly mammoth
49
6.1
Taxonomy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
49
6.1.1
Etymology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
50
6.1.2
Evolution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
50
Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
51
6.2.1
Coat . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
52
6.2.2
Dentition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
53
Palaeobiology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
54
6.3.1
Diet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
54
6.3.2
55
6.4
56
6.5
57
6.5.1
Exploitation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
57
6.6
Extinction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
58
6.7
Frozen specimens . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
59
6.7.1
61
Cultural signicance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
62
6.8.1
Cryptozoology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
62
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
63
6.10 Bibliography . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
67
Woolly rhinoceros
68
7.1
Evolution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
68
7.2
Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
68
7.3
68
7.3.1
Diet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
69
7.4
Extinction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
69
7.5
See also . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
70
7.6
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
70
7.7
External links . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
70
7.8
71
7.8.1
Text . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
71
7.8.2
Images . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
74
7.8.3
Content license . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
78
6.2
6.3
6.8
6.9
iii
Chapter 1
Ice age
4
This article is about a generic geological period of temperature reduction. For the most recent glacial period
commonly referred to as the Ice Age, see Last glacial period. For other uses, see Ice age (disambiguation).
An ice age is a period of long-term reduction in the
0
2
4
6
8
10
400
350
300
250
200
150
100
300
50
Carbon Dioxide
280
ppmv
260
240
220
200
ppm
180
1.8
1.6
1.4
1.2
1
0.8
0.6
0.4
0.2
0
400
350
300
250
200
150
100
50
Dust concentration
400
350
300
250
200
150
100
50
Variations in temperature, CO
2, and dust from the Vostok ice core over the last 400,000 years
The Antarctic ice sheet. Ice sheets expand during an ice age.
2
ously extending further.[7] An unknown woodcutter from
Meiringen in the Bernese Oberland advocated a similar idea in a discussion with the Swiss-German geologist
Jean de Charpentier (17861855) in 1834.[8] Comparable explanations are also known from the Val de Ferret
in the Valais and the Seeland in western Switzerland[9]
and in Goethe's Scientic Work.[10] Such explanations
could also be found in other parts of the world. When the
Bavarian naturalist Ernst von Bibra (18061878) visited
the Chilean Andes in 18491850 the natives attributed
fossil moraines to the former action of glaciers.[11]
Meanwhile, European scholars had begun to wonder what
had caused the dispersal of erratic material. From the
middle of the 18th century some discussed ice as a means
of transport. The Swedish mining expert Daniel Tilas
(17121772) was, in 1742, the rst person to suggest
drifting sea ice in order to explain the presence of erratic
boulders in the Scandinavian and Baltic regions.[12] In
1795, the Scottish philosopher and gentleman naturalist,
James Hutton (17261797), explained erratic boulders in
the Alps with the action of glaciers.[13] Two decades later,
in 1818, the Swedish botanist Gran Wahlenberg (1780
1851) published his theory of a glaciation of the Scandinavian peninsula. He regarded glaciation as a regional
phenomenon.[14] Only a few years later, the DanishNorwegian Geologist Jens Esmark (17621839) argued
a sequence of worldwide ice ages. In a paper published in
1824, Esmark proposed changes in climate as the cause
of those glaciations. He attempted to show that they originated from changes in Earths orbit.[15] During the following years, Esmarks ideas were discussed and taken
over in parts by Swedish, Scottish and German scientists. At the University of Edinburgh Robert Jameson
(17741854) seemed to be relatively open to Esmarks
ideas, as reviewed by Norwegian professor of glaciology Bjrn G. Andersen (1992).[16] Jamesons remarks
about ancient glaciers in Scotland were most probably
prompted by Esmark.[17] In Germany, Albrecht Reinhard Bernhardi (17971849), a geologist and professor
of forestry at an academy in Dreissigacker, since incorporated in the southern Thuringian city of Meiningen,
adopted Esmarks theory. In a paper published in 1832,
Bernhardi speculated about former polar ice caps reaching as far as the temperate zones of the globe.[18]
tending from near Sault Ste. Marie to Sudbury, northeast of Lake Huron, with giant layers of now-lithied till
beds, dropstones, varves, outwash, and scoured basement
rocks. Correlative Huronian deposits have been found
near Marquette, Michigan, and correlation has been made
with Paleoproterozoic glacial deposits from Western Australia.
The next well-documented ice age, and probably the most
severe of the last billion years, occurred from 850 to 630
million years ago (the Cryogenian period) and may have
produced a Snowball Earth in which glacial ice sheets
reached the equator,[33] possibly being ended by the accumulation of greenhouse gases such as CO
2 produced by volcanoes. The presence of ice on the
continents and pack ice on the oceans would inhibit both
silicate weathering and photosynthesis, which are the two
major sinks for CO
2 at present.[34] It has been suggested that the end of this
ice age was responsible for the subsequent Ediacaran and
Cambrian Explosion, though this model is recent and controversial.
The Andean-Saharan occurred from 460 to 420 million
years ago, during the Late Ordovician and the Silurian
period.
The evolution of land plants at the onset of the Devonian
period caused a long term increase in planetary oxygen
levels and reduction of CO
2 levels, which resulted in the Karoo Ice Age. It is named
after the glacial tills found in the Karoo region of South
Africa, where evidence for this ice age was rst clearly
identied. There were extensive polar ice caps at intervals
2.5
-2
-4
-6
-8
3
3.5
4
18
41 kyr cycle
O Benthic
Carbonate (per mil)
Equivalent
Vostok T (C)
4.5
Millions of Years Ago
Shows the pattern of temperature and ice volume changes associated with recent glacials and interglacials
The current ice age, the Pliocene-Quaternary glaciation, started about 2.58 million years ago during the late
Pliocene, when the spread of ice sheets in the Northern
Hemisphere began. Since then, the world has seen cycles of glaciation with ice sheets advancing and retreating
on 40,000- and 100,000-year time scales called glacial
periods, glacials or glacial advances, and interglacial periods, interglacials or glacial retreats. The earth is currently in an interglacial, and the last glacial period ended
about 10,000 years ago. All that remains of the continental ice sheets are the Greenland and Antarctic ice sheets
and smaller glaciers such as on Ban Island.
Ice ages can be further divided by location and time;
for example, the names Riss (180,000130,000 years bp)
and Wrm (70,00010,000 years bp) refer specically to
glaciation in the Alpine region. The maximum extent of
the ice is not maintained for the full interval. The scouring action of each glaciation tends to remove most of the
evidence of prior ice sheets almost completely, except in
regions where the later sheet does not achieve full coverage.
Minimum (interglacial, black) and maximum (glacial, grey)
glaciation of the northern hemisphere
5
rent projected consequences of global warming include
a largely ice-free Arctic Ocean within 520 years, see
Arctic shrinkage.) Additional fresh water owing into
the North Atlantic during a warming cycle may also reduce the global ocean water circulation (see Shutdown of
thermohaline circulation). Such a reduction (by reducing the eects of the Gulf Stream) would have a cooling
eect on northern Europe, which in turn would lead to
increased low-latitude snow retention during the summer.
It has also been suggested that during an extensive glacial,
glaciers may move through the Gulf of Saint Lawrence,
extending into the North Atlantic ocean far enough to
block the Gulf Stream.
ple, changes in Earths atmospheric composition (especially the concentrations of greenhouse gases) may alter
the climate, while climate change itself can change the
atmospheric composition (for example by changing the
rate at which weathering removes CO
2).
1.6.3
1.6.4
Uplift of the Tibetan plateau and surrounding mountain areas above the
snowline
Matthias Kuhles geological theory of Ice Age development was suggested by the existence of an ice sheet covering the Tibetan plateau during the Ice Ages (Last Glacial
Maximum?). According to Kuhle, the plate-tectonic uplift of Tibet past the snow-line has led to a surface of c.
2,400,000 square kilometres (930,000 sq mi) changing
from bare land to ice with a 70% greater albedo. The reection of energy into space resulted in a global cooling,
triggering the Pleistocene Ice Age. Because this highland
is at a subtropical latitude, with 4 to 5 times the insolation
of high-latitude areas, what would be Earths strongest
heating surface has turned into a cooling surface.
Kuhle explains the interglacial periods by the 100,000-
7
year cycle of radiation changes due to variations in Earths
orbit. This comparatively insignicant warming, when
combined with the lowering of the Nordic inland ice areas
and Tibet due to the weight of the superimposed ice-load,
has led to the repeated complete thawing of the inland ice
areas.[49][50][51][52]
Past and future of daily average insolation at top of the atmosphere on the day of the summer solstice, at 65 N latitude.
1.6.7 Volcanism
Volcanic eruptions may have contributed to the inception and/or the end of ice age periods. At times during the paleoclimate, carbon dioxide levels were two or
three times greater than today. Volcanoes and movements in continental plates contributed to high amounts
of CO2 in the atmosphere. Carbon dioxide from volcanoes probably contributed to periods with highest overall temperatures.[60] One suggested explanation of the
Paleocene-Eocene Thermal Maximum is that undersea
volcanoes released methane from clathrates and thus
caused a large and rapid increase in the greenhouse effect. There appears to be no geological evidence for such
eruptions at the right time, but this does not prove they
Another worker, William Ruddiman, has suggested did not happen.
a model that explains the 100,000-year cycle by the
modulating eect of eccentricity (weak 100,000-year cycle) on precession (26,000-year cycle) combined with 1.7 Recent glacial and interglacial
greenhouse gas feedbacks in the 41,000- and 26,000phases
year cycles. Yet another theory has been advanced by
Peter Huybers who argued that the 41,000-year cycle has
always been dominant, but that the Earth has entered
a mode of climate behavior where only the second or
third cycle triggers an ice age. This would imply that
the 100,000-year periodicity is really an illusion created
by averaging together cycles lasting 80,000 and 120,000
years.[57] This theory is consistent with a simple empirical
multi-state model proposed by Didier Paillard.[58] Paillard suggests that the late Pleistocene glacial cycles can be
seen as jumps between three quasi-stable climate states.
The jumps are induced by the orbital forcing, while in
the early Pleistocene the 41,000-year glacial cycles resulted from jumps between only two climate states. A
dynamical model explaining this behavior was proposed
by Peter Ditlevsen.[59] This is in support of the suggestion
that the late Pleistocene glacial cycles are not due to the Northern hemisphere glaciation during the last ice ages. The set
weak 100,000-year eccentricity cycle, but a non-linear re- up of 3 to 4 km thick ice sheets caused a sea level lowering of
sponse to mainly the 41,000-year obliquity cycle.
about 120 m.
1.6.6
In the very long term, astrophysicists believe that the The major glacial stages of the current ice age in North
Suns output increases by about 7% every one billion America are the Illinoian, Sangamonian and Wisconsin
stages. The use of the Nebraskan, Afton, Kansan,
(109 ) years.
and Yarmouthian (Yarmouth) stages to subdivide the ice
Shorter-term variations such as sunspot cycles, and age in North America have been discontinued by Qualonger episodes such as the Maunder minimum, ternary geologists and geomorphologists. These stages
have all been merged into the Pre-Illinoian Stage in the 8.4C here was an increase in precipitation. Accord1980s.[61][62][63]
ingly, at glacial times the humid climatic belt that today
further to the S, was
During the most recent North American glaciation, dur- is situated several latitude degrees
[67][68]
shifted
much
further
to
the
N.
ing the latter part of the Wisconsin Stage (26,000 to
13,300 years ago), ice sheets extended to about 45 degrees north latitude. These sheets were 3 to 4 km
thick.[62]
1.7.2
10
hydration systems resulting in newly submerged lands,
emerging lands, collapsed ice dams resulting in salination
of lakes, new ice dams creating vast areas of freshwater,
and a general alteration in regional weather patterns on
a large but temporary scale. It can even cause temporary reglaciation. This type of chaotic pattern of rapidly
changing land, ice, saltwater and freshwater has been proposed as the likely model for the Baltic and Scandinavian
regions, as well as much of central North America at the
end of the last glacial maximum, with the present-day
coastlines only being achieved in the last few millennia
of prehistory. Also, the eect of elevation on Scandinavia submerged a vast continental plain that had existed
under much of what is now the North Sea, connecting the
British Isles to Continental Europe.[70]
The redistribution of ice-water on the surface of the
Earth and the ow of mantle rocks causes changes in the
gravitational eld as well as changes to the distribution
of the moment of inertia of the Earth. These changes to
the moment of inertia result in a change in the angular
velocity, axis, and wobble of the Earths rotation.
[2] Gribbin, J.R. (1982). Future Weather: Carbon Dioxide, Climate and the Greenhouse Eect. Penguin. ISBN
0140224599.
[3] Rmis, F.; Testus, L.; Testut (2006). Mais comment scoule donc un glacier ?
Aperu historique (PDF). C. R. Geoscience (in French) 338
(5):
368385.
Bibcode:2006CRGeo.338..368R.
doi:10.1016/j.crte.2006.02.004. Note: p. 374
[4] Montgomery 2010
[5] Martel, Pierre (1898). Appendix: Martel, P. (1744) An
account of the glacieres or ice alps in Savoy, in two letters,
one from an English gentleman to his friend at Geneva ;
the other from Pierre Martel , engineer, to the said English
gentleman. In Mathews, C.E. The annals of Mont Blanc.
London: Unwin. p. 327. See (Montgomery 2010) for a
full bibliography
[6] Krger, Tobias (2013). Discovering the Ice Ages. International Reception and Consequences for a Historical Understanding of Climate (German editon: Basel 2008). Leiden.
p. 47. ISBN 978-90-04-24169-5.
The weight of the redistributed surface mass loaded the [7] Krger 2013, pp. 78-83
lithosphere, caused it to ex and also induced stress within
the Earth. The presence of the glaciers generally sup- [8] Krger 2013, p. 150
pressed the movement of faults below.[71][72][73] How- [9] Krger 2013, pp. 83, 151
ever, during deglaciation, the faults experience accelerated slip triggering earthquakes. Earthquakes triggered [10] Goethe, Johann Wolfgang von: Geologische Probleme
und Versuch ihrer Ausung, Mineralogie und Geologie
near the ice margin may in turn accelerate ice calving and
in Goethes Werke, Weimar 1892, ISBN 3-423-05946-X,
[74]
may account for the Heinrich events. As more ice is rebook 73 (WA II,9), p. 253, 254.
moved near the ice margin, more intraplate earthquakes
are induced and this positive feedback may explain the [11] Krger 2013, p. 83
fast collapse of ice sheets.
In Europe, glacial erosion and isostatic sinking from
weight of ice made the Baltic Sea, which before the Ice
Age was all land drained by the Eridanos River.
1.10 References
[1] Imbrie, J.; Imbrie, K.P (1979). Ice ages: solving the mystery. Short Hills NJ: Enslow Publishers. ISBN 978-089490-015-0.
1.10. REFERENCES
11
12
[64] Kuhle, M. (1984). Spuren hocheiszeitlicher Gletscherbedeckung in der Aconcagua-Gruppe (3233 S)". Zentralblatt fr Geologie und Palontologie Teil I, Geologie.
11/12: 163546. ISSN 0340-5109. Verhandlungsblatt
des Sdamerika-Symposiums 1984 in Bamberg.
[65] Kuhle, M. (1986). Die Vergletscherung Tibets und die
Entstehung von Eiszeiten. Spektrum der Wissenschaft
(9/86): 4254. ISSN 0170-2971.
[66] Kuhle, Matthias (June 1987). Subtropical Mountain- and
Highland-Glaciation as Ice Age Triggers and the Waning of the Glacial Periods in the Pleistocene. GeoJournal 14 (4): 393421. doi:10.1007/BF02602717. JSTOR
41144132.
[67] Kuhle, M. (2004). The Last Glacial Maximum (LGM)
glacier cover of the Aconcagua group and adjacent massifs in the Mendoza Andes (South America)". In Ehlers,
J.; Gibbard, P.L. Quaternary Glaciations: South America, Asia, Africa, Australasia, Antarctica. Development in
Quaternary Science. Amsterdam: Elsevier. pp. 7581.
ISBN 978-0-444-51593-3.
[68] Kuhle, M. (2011). Ch 53: The High-Glacial (Last
Glacial Maximum) Glacier Cover of the Aconcagua
Group and Adjacent Massifs in the Mendoza Andes
(South America) with a Closer Look at Further Empirical Evidence. In Ehlers, J.; Gibbard, P.L.; Hughes, P.D.
Quaternary Glaciations Extent and Chronology: A Closer
Look. Development in Quaternary Science. Amsterdam:
Elsevier. pp. 7358. ISBN 978-0-444-53447-7.
[69] Brggen, J. (1929). Zur Glazialgeologie der chilenischen Anden.
Geol.
Rundsch.
20 (1): 135.
doi:10.1007/BF01805072.
[70] Andersen, Bjrn G.; Borns, Harold W. Jr. (1997).
The Ice Age World: an introduction to quaternary history and research with emphasis on North America and
Northern Europe during the last 2.5 million years. Oslo:
Universitetsforlaget. ISBN 97-88200376-83-5. Retrieved 2013-10-14.
[71] Johnston, A. (1989). The eect of large ice sheets on
earthquake genesis. In Gregersen, S.; Basham, P. Earthquakes at North-Atlantic passive margins: Neotectonics
and postglacial rebound. Dordrecht: Kluwer. pp. 581
599. ISBN 0792301501.
[72] Wu, P.; Hasegawa, H.S.; Hasegawa (October 1996).
Induced stresses and fault potential in eastern Canada
due to a realistic load: a preliminary analysis.
Geophysical Journal International 127 (1): 215229.
Bibcode:1996GeoJI.127..215W.
doi:10.1111/j.1365246X.1996.tb01546.x.
[73] Turpeinen, H.; Hampel, A.; Karow, T.; Maniatis, G.
(2008). Eect of ice sheet growth and melting on the slip
evolution of thrust faults. Earth and Planetary Science
Letters 269: 230241. Bibcode:2008E&PSL.269..230T.
doi:10.1016/j.epsl.2008.02.017.
[74] Hunt, A.G.; Malin, P.E.; Malin (14 May 1998).
Possible triggering of Heinrich events by ice-loadinduced earthquakes. Nature 393 (6681): 1558.
Bibcode:1998Natur.393..155H. doi:10.1038/30218.
13
Chapter 2
Megafauna
This article is about large land animals. For naked-eye
visible bottom-dwelling animals, see Macrobenthos. For
giant animals in mythology, see Megafauna (mythology).
In terrestrial zoology, megafauna (Ancient Greek megas
14
2.2.1
In terrestrial mammals
15
been predicted based on the metabolic rate of mammals,
the energetic cost of obtaining prey, and the maximum estimated rate coecient of prey intake.[9] It has also been
suggested that maximum size for mammalian carnivores
is constrained by the stress the humerus can withstand at
top running speed.[8]
Analysis of the variation of maximum body size over the
last 40 Ma suggests that decreasing temperature and increasing continental land area are associated with increasing maximum body size. The former correlation would
be consistent with Bergmanns rule,[10] and might be related to the thermoregulatory advantage of large body
mass in cool climates,[6] better ability of larger organisms to cope with seasonality in food supply,[10] or other
factors;[10] the latter correlation could be explainable in
terms of range and resource limitations.[6] However, the
two parameters are interrelated (due to sea level drops accompanying increased glaciation), making the driver of
the trends in maximum size more dicult to identify.[6]
16
CHAPTER 2. MEGAFAUNA
of megafaunal extinction pulses that have occurred during the last 50,000 years over much of the Earths surface,
with Africa and southern Asia being largely spared. The
latter areas did suer a gradual attrition of megafauna,
particularly of the slower-moving species (a class of vulnerable megafauna epitomized by giant tortoises), over
the last several million years.[20][21]
Outside the mainland of Afro-Eurasia, these megafaunal extinctions followed a highly distinctive landmass-bylandmass pattern that closely parallels the spread of humans into previously uninhabited regions of the world,
and which shows no correlation with climatic history
(which can be visualized with plots over recent geological time periods of climate markers such as marine oxygen isotopes or atmospheric carbon dioxide levels).[22][23]
Australia was struck rst around 45,000 years ago,[24]
followed by Tasmania about 41,000 years ago (after
formation of a land bridge to Australia about 43,000
years ago),[25][26][27] Japan apparently about 30,000 years
ago,[28] North America 13,000 years ago, South America about 500 years later,[29][30] Cyprus 10,000 years
ago,[31][32] the Antilles 6000 years ago,[33] New Caledonia[34] and nearby islands[35] 3000 years ago, Madagascar
2000 years ago,[36] New Zealand 700 years ago,[37] the
Mascarenes 400 years ago,[38] and the Commander Islands 250 years ago.[39] Nearly all of the worlds isolated islands could furnish similar examples of extinctions occurring shortly after the arrival of Homo sapiens, though most of these islands, such as the Hawaiian
Islands, never had terrestrial megafauna, so their extinct
fauna were smaller.[22][23]
An analysis of Sporormiella fungal spores (which derive mainly from the dung of megaherbivores) in swamp
sediment cores spanning the last 130,000 years from
Lynchs Crater in Queensland, Australia showed that
the megafauna of that region virtually disappeared about
41,000 years ago, at a time when climate changes were
minimal; the change was accompanied by an increase
in charcoal, and was followed by a transition from rainforest to re-tolerant sclerophyll vegetation. The highresolution chronology of the changes supports the hypothesis that human hunting alone eliminated the megafauna,
and that the subsequent change in ora was most likely
a consequence of the elimination of browsers and an increase in re.[40][41][42] The increase in re lagged the disappearance of megafauna by about a century, and most
likely resulted from accumulation of fuel once browsing stopped. Over the next several centuries grass increased; sclerophyll vegetation increased with a lag of
another century, and a sclerophyll forest developed after about another thousand years.[42] During two periods
of climate change about 120 and 75 thousand years ago,
sclerophyll vegetation had also increased at the site in response to a shift to cooler, drier conditions; neither of
these episodes had a signicant impact on megafaunal
abundance.[42] Similar conclusions regarding the culpability of human hunters in the disappearance of Pleis-
2.4. EXAMPLES
17
Continuing human hunting and environmental disturbance has led to additional megafaunal extinctions in the
recent past, and has created a serious danger of further
extinctions in the near future (see examples below).
2.3.2
Consequences
megafauna
of
depletion
of
2.4 Examples
The following are some notable examples of animals often considered as megafauna (in the sense of the large
animal denition). This list is not intended to be exhaustive:
Clade Synapsida
Class Mammalia (phylogenetically, a clade
within Therapsida; see below)
Infraclass Metatheria
Order Diprotodontia
The red kangaroo (Macropus rufus) is the largest living Australian
mammal and marsupial at a weight
of up to 85 kg (187 lb). However, its extinct relative, the giant
short-faced kangaroo Procoptodon
goliah reached 230 kg (510 lb),
while extinct diprotodonts attained
the largest size of any marsupial in
history, up to an estimated 2,750 kg
(6,060 lb). The extinct marsupial
lion (Thylacleo carnifex), at up to
160 kg (350 lb) was much larger
than any extant carnivorous marsupial.
18
CHAPTER 2. MEGAFAUNA
Infraclass Eutheria
Superorder Afrotheria
Order Proboscidea
Elephants are the largest living
land animals. They and their relatives arose in Africa, but until
recently had a nearly worldwide
distribution. The African bush
elephant (Loxodonta africana) has
a shoulder height of up to 4.3
m (14 ft) and weighs up to 13
tons.
Among recently extinct
proboscideans, mammoths (Mammuthus) were close relatives of elephants, while mastodons (Mammut) were much more distantly
related. The steppe mammoth
(M. trogontherii) is estimated to
have commonly weighed around
10 tonnes, making it possibly the
largest proboscid, which would
make it the second largest land
mammal after indricotherines.
Order Sirenia
The largest sirenian at up to 1500
kg is the West Indian manatee
(Trichechus manatus). Stellers
sea cow (Hydrodamalis gigas) was
probably around ve times as massive, but was exterminated by humans within 27 years of its discovery o the remote Commander
Islands in 1741. In prehistoric
times this sea cow also lived along
the coasts of northeastern Asia
and northwestern North America;
it was apparently eliminated from
these more accessible locations by
aboriginal hunters.
Superorder Xenarthra
Order Cingulata
The glyptodonts were a group of
large, heavily armored ankylosaurlike xenarthrans related to living armadillos. They originated
in South America, invaded North
America during the Great American Interchange, and went extinct at the end of the Pleistocene
epoch.[54]
Order Pilosa
Ground sloths were another group
of slow, terrestrial xenarthrans,
related to modern tree sloths.
They had a similar history, although they reached North America earlier, and spread farther
2.4. EXAMPLES
19
of Panthera are distinguished by
morphological features which enable them to roar. Larger extinct felids include the American
lion (Panthera leo atrox) and the
South American saber-toothed cat
Smilodon populator.
Bears are large carnivorans of the
caniform suborder. The largest
living forms are the polar bear (Ursus maritimus), with a body weight
of up to 680 kg (1,500 lb), and
the similarly sized Kodiak bear
(Ursus arctos middendor), again
consistent with Bergmanns rule.
Arctotherium augustans, an extinct short-faced bear from South
America, was the largest predatory
land mammal ever with an estimated average weight of 1,600 kg
(3,500 lb).[59]
Seals, sea lions, and walruses
are amphibious marine carnivorans that evolved from bearlike
ancestors.
The southern elephant seal (Mirounga leonina) of
Antarctic and subantarctic waters
is the largest carnivoran of all time,
with bull males reaching a maximum length of 67 m (2023 ft)
and maximum weight of 5,000 kg
(11,000 lb).
Order Perissodactyla
Tapirs are browsing animals, with
a short prehensile snout and piglike form that appears to have
changed little in 20 million years.
They inhabit tropical forests of
Southeast Asia and South and
Central America, and include the
largest surviving land animals of
the latter two regions. There are
four species.
20
CHAPTER 2. MEGAFAUNA
North America, reaching 6 m (20 ft) and
2 tonnes.
Order Therapsida
Anteosaurus was a headbutting, semiaquatic, carnivorous dinocephalian of
Middle Permian South Africa. It reached
56 m (1620 ft) long, and weighed about
500600 kg (1,1001,300 lb).[63]
Clade Sauropsida
Class Aves (phylogenetically, a clade within
Coelurosauria, a taxon within the order
Saurischia; see below)
Order Struthioniformes
The ratites are an ancient and
diverse group of ightless birds
that are found on fragments of the
former supercontinent Gondwana.
The largest living bird, the ostrich
(Struthio camelus) was surpassed by
the extinct Aepyornis of Madagascar,
the heaviest of the group (400 kg
(880 lb)), and the extinct giant moa
(Dinornis) of New Zealand, the
tallest, growing to heights of 3.4 m
(11 ft). The latter two are examples
of island gigantism.
Order Anseriformes
Extinct dromornithids of Australia
such as Dromornis may have exceeded the largest ratites in size.
(Due to its small size for a continent
and its isolation, Australia is sometimes viewed as the worlds largest island; thus, these species could also be
considered insular giants.)
Class Reptilia (traditional; paraphyletic)
Order Crocodilia
Alligators and crocodiles are large
semiaquatic reptiles, the largest
of which, the saltwater crocodile
(Crocodylus porosus), can grow to
a weight of 1,360 kg (3,000 lb).
Crocodilians distant ancestors and
their kin, the crurotarsans, dominated the world in the late Triassic,
until the TriassicJurassic extinction
event allowed dinosaurs to overtake them. They remained diverse
during the later Mesozoic, when
crocodyliforms such as Deinosuchus
and Sarcosuchus reached lengths
of 12 m. Similarly large crocodilians, such as Mourasuchus and
Purussaurus, were present as recently as the Miocene in South
America.
Order Saurischia
Saurischian dinosaurs of the Jurassic
and Cretaceous include sauropods,
the longest (at up to 40 m or 130 ft)
and most massive terrestrial animals
known (Argentinosaurus reached 80
100 metric tonnes, or 90110 tons),
as well as theropods, the largest terrestrial carnivores (Spinosaurus grew
to 79 tonnes; the more famous
Tyrannosaurus, to 6.8 tonnes).
Order Squamata
While the largest extant lizard, the
Komodo dragon (Varanus komodoensis), another island giant, can
reach 3 m (10 ft) in length, its extinct
Australian relative Megalania may
have reached more than twice that
size. These monitor lizards' marine
relatives, the mosasaurs, were apex
predators in late Cretaceous seas.
The heaviest extant snake is considered to be the green anaconda (Eunectes murinus), while the reticulated
python (Python reticulatus), at up
to 8.7 m or more, is considered
the longest. An extinct Australian
Pliocene species of Liasis, the Blu
Downs giant python, reached 10 m,
while the Paleocene Titanoboa of
South America reached lengths of
1215 m and an estimated weight of
about 1135 kilograms (2500 lb).
Order Testudines
The largest turtle is the critically endangered marine leatherback turtle
(Dermochelys coriacea), weighing
up to 900 kg (2,000 lb). It is distinguished from other sea turtles by
its lack of a bony shell. The most
massive terrestrial chelonians are
the giant tortoises of the Galpagos
Islands (Chelonoidis nigra) and
Aldabra Atoll (Aldabrachelys gigantea), at up to 300 kg (660 lb). These
tortoises are the biggest survivors
of an assortment of giant tortoise
species that were widely present
on continental landmasses[64][65]
and additional islands[64] during the
Pleistocene.
Class Amphibia (in the wide, probably paraphyletic,
sense)
Order Temnospondyli (relationship to extant
amphibians is unclear)
2.5. GALLERY
The
Permian
temnospondyl
Prionosuchus, the largest amphibian
known, reached 9 m in length and
was an aquatic predator resembling a
crocodilian. After the appearance of
real crocodilians, temnospondyls such as
Koolasuchus (5 m long) had retreated to
the Antarctic region by the Cretaceous,
before going extinct.
Class Actinopterygii
Order Tetraodontiformes
The largest extant bony sh is the ocean
sunsh (Mola mola), whose average adult
weight is 1,000 kg (2,200 lb). While phylogenetically a bony sh, its skeleton is
primarily cartilage (which is lighter than
bone). It has a disk-shaped body, and propels itself with its long, thin dorsal and
anal ns; it feeds primarily on jellysh.
In these three respects (as well as in its
size and diving habits), it resembles a
leatherback turtle.
Order Acipenseriformes
The critically endangered beluga (European sturgeon, Huso huso) at up to
1,476 kg (3,254 lb) is the largest sturgeon
(which are also mostly cartilaginous) and
is considered the largest anadromous sh.
Order Siluriformes
The critically endangered Mekong giant
catsh (Pangasianodon gigas), at up to
293 kg (646 lb), is often viewed as the
largest freshwater sh.
Class Chondrichthyes
Order Lamniformes
The largest living predatory sh, the great
white shark (Carcharodon carcharias),
reaches weights up to 2,240 kg (4,940
lb). Its extinct relative C. megalodon (the
disputed genus being either Carcharodon
or Carcharocles) was more than an order
of magnitude larger, and is the largest
predatory shark or sh of all time (and
possibly the largest predator in vertebrate
history); it preyed on whales and other
marine mammals.
Order Orectolobiformes
21
Order Rajiformes
The manta ray (Manta birostris) is another
lter feeder and the largest ray, growing
to up to 2300 kg.
Class Placodermi
Order Arthrodira
The largest armored sh, Dunkleosteus,
arose during the late Devonian. At up
to 10 metres (33 ft) in length[66] and 3.6
tonnes (4.0 short tons) in mass,[67] it was a
hypercarnivorous apex predator that employed suction feeding.[68][69] Its contemporary, Titanichthys, apparently an early
lter feeder, rivaled it in size. The anthrodires were eliminated by the environmental upheavals of the Late Devonian
extinction, after existing for only about 50
million years.
Class Cephalopoda
Order Teuthida
A number of deep ocean creatures exhibit abyssal gigantism. These include
the giant squid (Architeuthis) and colossal
squid (Mesonychoteuthis hamiltoni); both
(although rarely seen) are believed to attain lengths of 12 m (39 ft) or more. The
latter is the worlds largest invertebrate,
and has the largest eyes of any animal.
Both are preyed upon by sperm whales.
Subphylum Chelicerata
Order Eurypterida
Eurypterids (sea scorpions) were a diverse group of aquatic and possibly amphibious predators that included the most
massive arthropods to have existed. They
survived over 200 million years, but nally died out in the PermianTriassic extinction event along with trilobites and
most other forms of life present at the
time, including most of the dominant terrestrial therapsids. The Early Devonian
Jaekelopterus reached an estimated length
of 2.5 m (8.2 ft), not including its
raptorial chelicerae, and is thought to
have been a freshwater species.
22
CHAPTER 2. MEGAFAUNA
Polar bears, the largest bears and semiaquatic carnivores, are vulnerable to global warming.
2.8. REFERENCES
3. ^ Cite error: The named reference Stewart2006 was
invoked but never dened (see the help page).
4. ^ Penny, M. (2002). The Secret World of Kangaroos. Austin TX: Raintree Steck-Vaughn. ISBN 07398-4986-7.
Cite error: There are <ref group=note> tags on this
page, but the references will not show without a {{reist|group=note}} template (see the help page).
2.7 Notes
[1] Nonavian dinosaur size was not similarly constrained because they had a dierent relationship between body mass
and egg size than birds. The 400 kg Aepyornis had larger
eggs than nearly all dinosaurs.[17][18]
23
2.8 References
[1] Stuart, A. J. (November 1991). Mammalian extinctions
in the Late Pleistocene of northern Eurasia and North
America. Biological Reviews (Wiley) 66 (4): 453562.
doi:10.1111/j.1469-185X.1991.tb01149.x.
[2] Johnson, C. N. (2002-09-23). Determinants of Loss of
Mammal Species during the Late Quaternary 'Megafauna'
Extinctions: Life History and Ecology, but Not Body
Size. Proceedings of the Royal Society of London B (The
Royal Society) 269 (1506): 22212227 (see p. 2225).
doi:10.1098/rspb.2002.2130. JSTOR 3558643.
[3] Martin, P. S.; Steadman, D. W. (1999-06-30).
Prehistoric extinctions on islands and continents.
In MacPhee, R. D. E. Extinctions in near time: causes,
contexts and consequences. Advances in Vertebrate
Paleontology 2. New York: Kluwer/Plenum. pp. 1756.
ISBN 978-0-306-46092-0. OCLC 41368299. Retrieved
2011-08-23.
[4] Ice Age Animals. Illinois State Museum
[5] Evans, A. R.; et al. (2012-01-30). The maximum rate of mammal evolution.
PNAS 109.
doi:10.1073/pnas.1120774109.
Retrieved 2011-0211.
[6] Smith, F. A.; Boyer, A. G.; Brown, J. H.; Costa, D. P.;
Dayan, T.; Ernest, S. K. M.; Evans, A. R.; Fortelius,
M.; Gittleman, J. L.; Hamilton, M. J.; Harding, L.
E.; Lintulaakso, K.; Lyons, S. K.; McCain, C.; Okie,
J. G.; Saarinen, J. J.; Sibly, R. M.; Stephens, P. R.;
Theodor, J.; Uhen, M. D. (2010-11-26). The Evolution
of Maximum Body Size of Terrestrial Mammals. Science
330 (6008): 12161219. Bibcode:2010Sci...330.1216S.
doi:10.1126/science.1194830. Retrieved 2012-01-07.
[7] Clauss, M.; Frey, R.; Kiefer, B.; Lechner-Doll, M.;
Loehlein, W.; Polster, C.; Roessner, G. E.; Streich, W.
J. (2003-04-24). The maximum attainable body size of
herbivorous mammals: morphophysiological constraints
on foregut, and adaptations of hindgut fermenters.
Oecologia 136 (1): 1427. doi:10.1007/s00442-0031254-z. PMID 12712314. Retrieved 2012-01-08.
[8] Sorkin, B. (2008-04-10).
A biomechanical constraint on body mass in terrestrial mammalian predators. Lethaia 41 (4): 333347. doi:10.1111/j.15023931.2007.00091.x. Retrieved 2011-08-02.
[9] Carbone, C.; Teacher, A; Rowclie, J. M. (2007-01-16).
The Costs of Carnivory. PLoS Biology 5 (2, e22): 363
368. doi:10.1371/journal.pbio.0050022. PMC 1769424.
PMID 17227145. Retrieved 2012-01-08.
[10] Ashton, K. G.; Tracy, M. C.; de Queiroz, A. (October 2000). Is Bergmanns Rule Valid for Mammals?". The American Naturalist 156 (4): 390415.
doi:10.1086/303400. Retrieved 2012-01-07.
[11] Thewissen, J. G. M.; Bajpai, S. (1 January 2001).
Whale Origins as a Poster Child for Macroevolution.
BioScience 51 (12): 10371049. doi:10.1641/00063568(2001)051[1037:WOAAPC]2.0.CO;2. ISSN 00063568.
24
CHAPTER 2. MEGAFAUNA
2.8. REFERENCES
25
[35] White, A. W.; Worthy, T. H.; Hawkins, S.; Bedford, S.; Spriggs, M. (2010-08-16).
Megafaunal
meiolaniid horned turtles survived until early
human settlement in Vanuatu, Southwest Pacic. Proc. Natl. Acad. Sci. USA 107 (35):
1551215516.
Bibcode:2010PNAS..10715512W.
doi:10.1073/pnas.1005780107. PMC 2932593. PMID
20713711.
26
CHAPTER 2. MEGAFAUNA
Chapter 3
Pleistocene
before the present, as opposed to the currently accepted
2.588 million years BP: publications from the preceding
years may use either denition of the period.
3.1 Dating
Earth during the Pleistocene epoch.
The Pleistocene /plastsin/ (symbol PS[1] ) is the geological epoch which lasted from about 2,588,000 to
11,700 years ago, spanning the worlds recent period of
repeated glaciations.
Charles Lyell introduced this term in 1839 to describe
strata in Sicily that had at least 70% of their molluscan fauna still living today. This distinguished it
from the older Pliocene Epoch, which Lyell had originally thought to be the youngest fossil rock layer. He
constructed the name Pleistocene (Most New or
Newest) from the Greek , plestos, most,
and , kains (latinized as cnus), new";[2] this
contrasting with the immediately preceding Pleiocene
(More New or Newer, from , plen, more,
and kains; usual spelling: Pliocene), and the immediately subsequent Holocene (wholly new or entirely
new, from , hlos, whole, and kains) epoch,
which extends to the present time.
28
CHAPTER 3. PLEISTOCENE
mean annual temperature at the edge of the ice was 6
C (21 F); at the edge of the permafrost, 0 C (32 F).
Each glacial advance tied up huge volumes of water in
continental ice sheets 1,500 to 3,000 metres (4,900
9,800 ft) thick, resulting in temporary sea-level drops of
100 metres (300 ft) or more over the entire surface of
the Earth. During interglacial times, such as at present,
drowned coastlines were common, mitigated by isostatic
or other emergent motion of some regions.
The eects of glaciation were global. Antarctica was icebound throughout the Pleistocene as well as the preceding
Pliocene. The Andes were covered in the south by the
Patagonian ice cap. There were glaciers in New Zealand
and Tasmania. The current decaying glaciers of Mount
Kenya, Mount Kilimanjaro, and the Ruwenzori Range in
east and central Africa were larger. Glaciers existed in
the mountains of Ethiopia and to the west in the Atlas
mountains.
In the northern hemisphere, many glaciers fused into one.
The Cordilleran ice sheet covered the North American
northwest; the east was covered by the Laurentide. The
Fenno-Scandian ice sheet rested on northern Europe, including Great Britain; the Alpine ice sheet on the Alps.
Scattered domes stretched across Siberia and the Arctic
shelf. The northern seas were ice-covered.
The maximum extent of glacial ice in the north polar area during
the Pleistocene period.
29
comes from the underlying cyclical motions of the planet,
which eventually drag all the transients into harmony with
them. The repeated glaciations of the Pleistocene were
caused by the same factors.
Milankovitch cycles
Main article: Milankovitch cycles
30
CHAPTER 3. PLEISTOCENE
3.3 Fauna
Both marine and continental faunas were essentially modern and many animals, specically, mammals were much
larger in body form than their modern relatives .
North American land mammal ages (NALMA) include Blancan (4.751.8), Irvingtonian (1.80.24)
and Rancholabrean (0.240.01) in millions of years.
The Blancan extends signicantly back into the
Pliocene.
South American land mammal ages (SALMA) include Uquian (2.51.5), Ensenadan (1.50.3) and
Lujanian (0.30.01) in millions of years. The
Uquian previously extended signicantly back into
the Pliocene, although the new denition places it
entirely within the Pleistocene.
The severe climatic changes during the ice age had major impacts on the fauna and ora. With each advance of
the ice, large areas of the continents became totally depopulated, and plants and animals retreating southward
in front of the advancing glacier faced tremendous stress.
The most severe stress resulted from drastic climatic
changes, reduced living space, and curtailed food supply.
A major extinction event of large mammals (megafauna),
which included mammoths, mastodons, saber-toothed
cats, glyptodons, ground sloths, Irish elk, cave bears, and
short-faced bears, began late in the Pleistocene and continued into the Holocene. Neanderthals also became extinct during this period. At the end of the last ice age,
cold-blooded animals, smaller mammals like wood mice,
migratory birds, and swifter animals like whitetail deer
3.4 Humans
Main articles: Human evolution, Paleolithic and Models
of migration to the New World
Scientic evidence[14] indicates that humans evolved into
their present form during the Pleistocene.[15] In the beginning of the Pleistocene Paranthropus species are still
present, as well as early human ancestors, but during the
lower Palaeolithic they disappeared, and the only hominid
species found in fossilic records is Homo erectus for much
of the Pleistocene. The Middle and late Palaeolithic saw
the appearance of new types of humans, as well as the
development of more elaborate tools than found in previous eras. According to mitochondrial timing techniques,
modern humans migrated from Africa after the Riss
glaciation in the middle Palaeolithic during the Eemian
3.7. REFERENCES
Stage, spreading all over the ice-free world during the late
Pleistocene.[16][17][18] A 2005 study posits that humans
in this migration interbred with archaic human forms already outside of Africa by the late Pleistocene, incorporating archaic human genetic material into the modern
human gene pool.[19]
3.5 Deposits
31
3.7 References
[1] Geologic Age Symbol Font (StratagemAge)". USGS.
99-430. Retrieved 2011-06-22.
[2] Pleistocene. Online Etymology Dictionary.
[3] Gibbard, P. and van Kolfschoten, T. (2004) The Pleistocene and Holocene Epochs Chapter 22 PDF (3.1 MB)
In Gradstein, F. M., Ogg, James G., and Smith, A. Gilbert
(eds.), A Geologic Time Scale 2004 Cambridge University
Press, Cambridge, ISBN 0-521-78142-6
[4] For the top of the series, see: Lourens, L., Hilgen, F.,
Shackleton, N.J., Laskar, J., Wilson, D., (2004) The
Neogene Period. In: Gradstein, F., Ogg, J., Smith, A.G.
(Eds.), A Geologic Time Scale 2004. Cambridge: Cambridge University Press.
[5] Moore, Mark; Brumm (2007). Stone artifacts and hominins in island Southeast Asia: New insights from Flores, eastern Indonesia. Journal of Human Evolution 52:
88. Retrieved 10 April 2014.
32
CHAPTER 3. PLEISTOCENE
50+
images
of
Chapter 4
Prehistoric mammal
4.2 See also
Cynodont
List of extinct mammals
Mammaliaformes
Megamammals
Pleistocene extinctions
Pleistocene megafauna
Synapsid
Therapsid
An early drawing depicting prehistoric mammals
Prehistoric mammals are groups of mammals that became extinct before humans developed writing. 164
million years ago, in the Jurassic period, Castorocauda
lutrasimilis, a mammaliaform (mammal-shaped) animal
weighing about 500 grams (1.1 lb), had a full mammalian
pelt, with guard hairs and underfur, webbed feet, and
scales on the tail like a modern beaver, as well as teeth
specialized for catching sh.
Later, about 130 million years ago in the Cretaceous,
there existed larger mammals; a fossil of Repenomamus
giganticus indicates that the animal was about 1 meter (3 ft) long. In the stomach of a smaller cousin,
Repenomamus robustus at 52 cm (20 in), the remains
of a juvenile dinosaur have been preserved.
The lineages of many varieties continued through the
Cenozoic era where some reached very large sizes. Most
of the very large mammals became extinct in the last ice
age, but have smaller descendants.
Chapter 5
Stone Age
For other uses, see Stone Age (disambiguation).
The Stone Age is a broad prehistoric period during
Modern Awash River, Ethiopia, descendant of the PalaeoAwash, source of the sediments in which the oldest Stone Age
tools have been found
35
the initial period of the Bronze Age and is unquestionably
part of the Age of Metals. The Bronze Age was followed
by the Iron Age. During this entire time stone remained
in use in parallel with the metals for some objects, including those also used in the Neolithic, such as stone pottery.
The transition out of the Stone Age occurred between
6000 BCE and 2500 BCE for much of humanity living in
North Africa and Eurasia. The rst evidence of human
metallurgy dates to between the 5th and 6th millennium
BCE in the archaeological sites of Majdanpek, Yarmovac
and Plonik (a copper axe from 5500 BCE belonging to
the Vinca culture), though not conventionally considered
part of the Chalcolithic or Copper Age, this provides
the earliest known example of copper metallurgy.[8] and
the Rudna Glava mine in Serbia. tzi the Iceman, a
mummy from about 3300 BCE carried with him a copper
axe and a int knife.
36
The archaeologists of the late 19th and early 20th centuries CE, who adapted the three-age system to their
ideas, hoped to combine cultural anthropology and archaeology in such a way that a specic contemporaneous
tribe can be used to illustrate the way of life and beliefs
of the people exercising a specic Stone-Age technology.
As a description of people living today, the term stone age The duo thus reinvented the Stone Age. In Sub-Saharan
is controversial. The Association of Social Anthropolo- Africa, however, it was ended by the intrusion of the Iron
gists discourages this use, asserting:[9]
Age from the north. The Neolithic and the Bronze Age
never occurred. Moreover, the technologies included in
To describe any living group as 'primitive'
those 'stages, as Goodwin called them, were not exactly
or 'Stone Age' inevitably implies that they are
the same. Since then, the original relative terms have beliving representatives of some earlier stage of
come identied with the technologies of the Paleolithic
human development that the majority of huand Mesolithic, so that they are no longer relative. Moremankind has left behind. For some, this could
over, there has been a tendency to drop the comparative
be a positive description, implying, for examdegree in favor of the positive: resulting in two sets of
ple, that such groups live in greater harmony
Early, Middle and Late Stone Ages of quite dierent conwith nature .... For others, ... 'primitive' is
tent and chronologies.
5.3. CHRONOLOGY
By voluntary agreement, archaeologists respect the decisions of the Pan-African Congress of Prehistory, which
meets every four years to resolve archaeological business
brought before it. Delegates are actually international; the
organization takes its name from the topic. Louis Leakey
hosted the rst one in Nairobi in 1947. It adopted Goodwin and Lowes 3-stage system at that time, the stages to
be called Early, Middle and Later.
5.2.5
37
but were ocially rejected in 1965 (again on an advisory basis) by Burg Wartenstein Conference #29, Systematic Investigation of the African Later Tertiary and
Quaternary,[15] a conference in anthropology held by the
Wenner-Gren Foundation, at Burg Wartenstein Castle,
which it then owned in Austria, attended by the same
scholars that attended the Pan African Congress, including Louis Leakey and Mary Leakey, who was delivering
a pilot presentation of her typological analysis of Early
Stone Age tools, to be included in her 1971 contribution
to Olduvai Gorge, Excavations in Beds I and II, 1960
1963.[16]
18
Equivalent
Vostok T (C)
O Benthic
Carbonate (per mil)
The problem of the transitions in archaeology is a branch However, although the intermediate periods were gone,
of the general philosophic continuity problem, which the search for the transitions continued.
examines how discrete objects of any sort that are
contiguous in any way can be presumed to have a relationship of any sort. In archaeology, the relationship is
5.3 Chronology
one of causality. If Period B can be presumed to descend
from Period A, there must be a boundary between A and
B, the AB boundary. The problem is in the nature of
2
2
41 kyr cycle
100 kyr cycle
this boundary. If there is no distinct boundary, then the
2.5
0
-2
population of A suddenly stopped using the customs char3
Five Million Years of
-4
acteristic of A and suddenly started using those of B, an
3.5
Climate Change
-6
unlikely scenario in the process of evolution. More real4
-8 From Sediment Cores
istically, a distinct border period, the A/B transition, ex4.5
Millions of Years Ago
isted, in which the customs of A were gradually dropped
and those of B acquired. If transitions do not exist, then
Time series plot of temperature over the previous 5 million years
there is no proof of any continuity between A and B.
The Stone Age of Europe is characteristically in decit
of known transitions. The 19th and early 20th-century
innovators of the modern three-age system recognized
the problem of the initial transition, the gap between
the Paleolithic and the Neolithic. Louis Leakey provided
something of an answer by proving that man evolved in
Africa. The Stone Age must have begun there to be carried repeatedly to Europe by migrant populations. The
dierent phases of the Stone Age thus could appear there
without transitions. The burden on African archaeologists became all the greater, because now they must nd
the missing transitions in Africa. The problem is dicult
and ongoing.
boundary
Main articles: Paleolithic, Human evolution and ThreeOnce seriously questioned, the intermediates did not wait age system
for the next Pan African Congress two years hence,
38
nal stone is called a core; the resultant pieces, akes. Typically, but not necessarily, small pieces are detached from
a larger piece, in which case the larger piece may be called
the core and the smaller pieces the akes. The prevalent
usage, however, is to call all the results akes, which can
be confusing. A split in half is called bipolar aking.
Consequently the method is often called core-andake. More recently, the tradition has been called small
ake since the akes were small compared to subsequent
Acheulean tools.[20]
The essence of the Oldowan is the making
and often immediate use of small akes.
Another naming scheme is Pebble Core Technology
(PBC)":[21]
Pebble cores are ... artifacts that have
been shaped by varying amounts of hardhammer percussion.
Various renements in the shape have been called choppers, discoids, polyhedrons, subspheroid, etc. To date no
reasons for the variants have been ascertained:[22]
From a functional standpoint, pebble
cores seem designed for no specic purpose.
However, they would not have been manufactured for no
purpose:[22]
Pebble cores can be useful in many cutting, scraping or chopping tasks, but ... they
are not particularly more ecient in such tasks
than a sharp-edged rock ....
The tools were formed by knocking pieces o a river peb- The whole point of their utility is that each is a sharpble, or stones like it, with a hammerstone to obtain large edged rock in locations where nature has not provided
and small pieces with one or more sharp edges. The origi- any. There is additional evidence that Oldowan, or Mode
5.3. CHRONOLOGY
1, tools were utilized in percussion technology"; that is,
they were designed to be gripped at the blunt end and
strike something with the edge, from which use they were
given the name of choppers. Modern science has been
able to detect mammalian blood cells on Mode 1 tools
at Sterkfontein, Member 5 East, in South Africa. As the
blood must have come from a fresh kill, the tool users
are likely to have done the killing and used the tools for
butchering. Plant residues bonded to the silicon of some
tools conrm the use to chop plants.[23]
Although the exact species authoring the tools remains
unknown, Mode 1 tools in Africa were manufactured and
used predominantly by Homo habilis. They cannot be said
to have developed these tools or to have contributed the
tradition to technology. They continued a tradition of yet
unknown origin. As chimpanzees sometimes naturally
use percussion to extract or prepare food in the wild, and
may use either unmodied stones or stones that they have
split, creating an Oldowan tool, the tradition may well be
far older than its current record.
39
temporaneously in the same regions H. habilis inherited
the tools around 2.3 mya. At about 1.9 mya H. erectus
came on stage and lived contemporaneously with the others. Mode 1 was now being shared by a number of Hominans over the same ranges, presumably subsisting in different niches, but the archaeology is not precise enough
to say which.
Oldowan out of Africa Tools of the Oldowan tradition rst came to archaeological attention in Europe,
where, being intrusive and not well dened, compared
to the Acheulean, they were puzzling to archaeologists.
The mystery would be elucidated by African archaeology at Olduvai, but meanwhile, in the early 20th century,
the term Pre-Acheulean came into use in climatology.
C.E.P, Brooks, a British climatologist working in the
United States, used the term to describe a chalky boulder
clay underlying a layer of gravel at Hoxne, central England, where Acheulean tools had been found.[31] Whether
any tools would be found in it and what type was not
known. Hugo Obermaier, a contemporary German archaeologist working in Spain, quipped:
Towards the end of Oldowan in Africa a new species appeared over the range of Homo habilis: Homo erectus.
The earliest unambiguous evidence is a whole cranium,
KNM-ER 3733 (a nd identier) from Koobi Fora in
Unfortunately, the stage of human indusKenya, dated to 1.78 mya.[24] An early skull fragment,
try which corresponds to these deposits cannot
KNM-ER 2598, dated to 1.9 mya, is considered a good
be positively identied. All we can say is that
candidate also.[25] Transitions in paleoanthropology are
it is pre-Acheulean....
always hard to nd, if not impossible, but based on the
long-legged limb morphology shared by H. habilis and
H. rudolfensis in East Africa, an evolution from one of This uncertainty was claried by the subsequent excavations at Olduvai; nevertheless, the term is still in use for
those two has been suggested.[26]
pre-Acheulean contexts, mainly across Eurasia, that are
The most immediate cause of the new adjustments apyet unspecied or uncertain but with the understanding
pears to have been an increasing aridity in the region and
that they are or will turn out to be pebble-tool.[32]
consequent contraction of parkland savanna, interspersed
with trees and groves, in favor of open grassland, dated There are ample associations of Mode 2 with H. erectus in
1.81.7 mya. During that transitional period the percent- Eurasia. H. erectus Mode 1 associations are scantier but
age of grazers among the fossil species increased from they do exist, especially in the Far East. One strong piece
1525% to 45%, dispersing the food supply and requir- of evidence prevents the conclusion that only H. erectus
ing a facility among the hunters to travel longer distances reached Eurasia: at Yiron, Israel, Mode 1 tools have been
[33]
comfortably, which H. erectus obviously had.[27] The ul- found dating to 2.4 mya, about 0.5 my earlier than the
timate proof is the dispersal of H. erectus across much known H. erectus nds. If the date is correct, either anof Africa and Asia, substantially before the development other Hominan preceded H. erectus out of Africa or the
of the Mode 2 technology and use of re ....[26] H. erectus earliest H. erectus has yet to be found.
carried Mode 1 tools over Eurasia.
After the initial appearance at Gona in Ethiopia at 2.7
According to the current evidence (which may change at
any time) Mode 1 tools are documented from about 2.6
mya to about 1.5 mya in Africa,[28] and to 0.5 mya outside
of it.[29] The genus Homo is known from H. habilis and
H. rudolfensis from 2.3 to 2.0 mya, with the latest habilis
being an upper jaw from Koobi Fora, Kenya, from 1.4
mya. H. erectus is dated 1.80.6 mya.[30]
According to this chronology Mode 1 was inherited by Homo from unknown Hominans, probably
Australopithecus and Paranthropus, who must have continued on with Mode 1 and then with Mode 2 until their
extinction no later than 1.1 mya. Meanwhile living con-
40
Pebble tools are found the latest rst in southern Europe
and then in northern. They begin in the open areas of Italy
and Spain, the earliest dated to 1.6 mya at Pirro Nord,
Italy. The mountains of Italy are rising at a rapid rate
in the framework of geologic time; at 1.6 mya they were
lower and covered with grassland (as much of the highlands still are). Europe was otherwise mountainous and
covered over with dense forest, a formidable terrain for
warm-weather savanna dwellers. Similarly there is no evidence that the Mediterranean was passable at Gibraltar
or anywhere else to H. erectus or earlier hominans. They
might have reached Italy and Spain along the coasts.
In northern Europe pebble tools are found earliest at
Happisburgh, United Kingdom, from 0.8 mya. The
last traces are from Kents Cavern, dated 0.5 mya. By
that time H. erectus is regarded as having been extinct; however, a more modern version apparently had
evolved, Homo heidelbergensis, who must have inherited
the tools.[35] He also explains the last of the Acheulean in
Germany at 0.4 mya.
In the late 19th and early 20th centuries archaeologists
worked on the assumptions that a succession of Hominans and cultures prevailed, that one replaced another.
Today the presence of multiple hominans living contemporaneously near each other for long periods is accepted
as proved true; moreover, by the time the previously assumed earliest culture arrived in northern Europe, the
rest of Africa and Eurasia had progressed to the Middle and Upper Palaeolithic, so that across the earth all
three were for a time contemporaneous. In any given region there was a progression from Oldowan to Acheulean,
Lower to Upper, no doubt.
In North Africa, the presence of Mode 2 remains a mysAcheulean in Africa Main article: Acheulean
The end of Oldowan in Africa was brought on by the tery, as the oldest nds are from Thomas Quarry in
Morocco at 0.9 mya.[34] Archaeological attention, however, shifts to the Jordan Rift Valley, an extension of
the East African Rift Valley (the east bank of the Jordan is slowly sliding northward as East Africa is thrust
away from Africa). Evidence of use of the Nile Valley
is in decit, but Hominans could easily have reached the
palaeo-Jordan river from Ethiopia along the shores of the
Red Sea, one side or the other. A crossing would not have
been necessary, but it is more likely there than over a theoretical but unproven land bridge through either Gibraltar
or Sicily.
Meanwhile Acheulean went on in Africa past the 1.0 mya
mark and also past the extinction of H. erectus there. The
last Acheulean in East Africa is at Olorgesailie, Kenya,
dated to about 0.9 mya. Its owner was still H. erectus,[34]
but in South Africa, Acheulean at Elandsfontein, 1.0
0.6 mya, is associated with Saldanha man, classied as
H. heidelbergensis, a more advanced, but not yet modAn Acheulean tool, not worked over the entire surface
ern, descendant most likely of H. erectus. The Thoman
Quarry Hominans in Morocco similarly are most likely
appearance of Acheulean, or Mode 2, stone tools. The Homo rhodesiensis,[37] in the same evolutionary status as
earliest known instances are in the 1.71.6 mya layer
5.3. CHRONOLOGY
41
H. heidelbergensis.
itation of archeology, but after 1 mya evidence not available to Movius indicates the prevalence of Acheulean.
For example, the Acheulean site at Bose, China, is dated
Acheulean out of Africa Mode 2 is rst known out 0.8033K mya.[46] The authors of this chronologically
of Africa at 'Ubeidiya, Israel, a site now on the Jordan later East Asian Acheulean remain unknown, as does
River, then frequented over the long term (hundreds of whether it evolved in the region or was brought in.
thousands of years) by Homo on the shore of a variableThere is no named boundary line between Mode 1 and
level palaeo-lake, long since vanished. The geology was
Mode 2 on the west; nevertheless, Mode 2 is equally late
created by successive transgression and regression of
in Europe as it is in the Far East. The earliest comes
the lake[38] resulting in four cycles of layers. The tools
from a rock shelter at Estrecho de Qupar in Spain, dated
are located in the rst two, Cycles Li (Limnic Inferior)
to greater than 0.9 mya. Teeth from an undetermined
and Fi (Fluviatile Inferior), but mostly in Fi. The cyHominan were found there also.[47] The last Mode 2 in
cles represent dierent ecologies and therefore dierent
Southern Europe is from a deposit at Fontana Ranuccio
cross-sections of fauna, which makes it possible to date
near Anagni in Italy dated to 0.45 mya, which is generally
them. They appear to be the same faunal assemblages as
linked to Homo cepranensis, a late variant of H. erectus,
the Ferenta Faunal Unit in Italy, known from excavations
a fragment of whose skull was found at Ceprano nearby,
at Selvella and Pietertta, dated to 1.61.2 mya.[39]
dated 0.46 mya.[48]
At 'Ubeidiya the marks on the bones of the animal species
found there indicate that the manufacturers of the tools
butchered the kills of large predators, an activity that has Middle Paleolithic
been termed scavenging.[40] There are no living oors,
nor did they process bones to obtain the marrow. These Main article: Middle Paleolithic
activities cannot be understood therefore as the only or
even the typical economic activity of Hominans. Their
This period is best known as the era during which the
interests were selective: they were primarily harvesting
Neanderthals lived in Europe and the Near East (c.
the meat of Cervids,[41] which is estimated to have been
300,00028,000 years ago). Their technology is mainly
available without spoiling for up to four days after the kill.
the Mousterian, but Neanderthal physical characterisThe majority of the animals at the site were of tics have been found also in ambiguous association with
Palaearctic biogeographic origin.[42] However, these the more recent Chtelperronian archeological culture
overlapped in range on 3060% of African biogeo- in Western Europe and several local industries like the
graphic origin.[43] The biome was Mediterranean, not Szeletian in Eastern Europe/Eurasia. There is no evisavanna. The animals were not passing through; there dence for Neanderthals in Africa, Australia or the Amerwas simply an overlap of normal ranges. Of the Homi- icas.
nans, H. erectus left several cranial fragments. Teeth of
Neanderthals nursed their elderly and practised ritual
undetermined species may have been H. ergaster.[44] The
burial indicating an organised society. The earliest evitools are classied as Lower Acheulean and Developed
dence (Mungo Man) of settlement in Australia dates to
Oldowan. The latter is a disputed classication created
around 40,000 years ago when modern humans likely
by Mary Leakey to describe an Acheulean-like tradition
crossed from Asia by island-hopping. Evidence for symin Bed II at Olduvai. It is dated 1.531.27 mya. The date
bolic behavior such as body ornamentation and burial is
of the tools therefore probably does not exceed 1.5 mya;
ambiguous for the Middle Paleolithic and still subject to
1.4 is often given as a date. This chronology, which is
debate. The Bhimbetka rock shelters exhibit the earliest
denitely later than in Kenya, supports the out of Africa
traces of human life in India, some of which are approxhypothesis for Acheulean, if not for the Hominans.
imately 30,000 years old.
From Southwest Asia, as the Levant is now called, the
Acheulean extended itself more slowly eastward, arriving
at Isampur, India, about 1.2 mya. It does not appear in Upper Paleolithic
China and Korea until after 1mya and not at all in Indonesia. There is a discernible boundary marking the furthest Main article: Upper Paleolithic
extent of the Acheulean eastward before 1 mya, called the
Movius Line, after its proposer, Hallam L. Movius. On From 50,000 to 10,000 years ago in Europe, the Upthe east side of the line the small ake tradition contin- per Paleolithic ends with the end of the Pleistocene and
ues, but the tools are additionally worked Mode 1, with onset of the Holocene era (the end of the last ice age).
aking down the sides. In Athirampakkam at Chennai in Modern humans spread out further across the Earth durTamil Nadu the Acheulean age started at 1.51 mya and it ing the period known as the Upper Paleolithic. The Upis also prior than North India and Europe.[45]
per Paleolithic is marked by a relatively rapid succession
The cause of the Movius Line remains speculative, of often complex stone artifact technologies and a large
whether it represents a real change in technology or a lim- increase in the creation of art and personal ornaments.
42
43
were noticeably more hierarchical than the Paleolithic years ago.[53] It is considered as an equivalent of Eurocultures that preceded them.[51]
pean Middle Paleolithic.[54] It is associated with anatomically modern or almost modern Homo sapiens. Early
physical evidence comes from Omo [55] and Herto,[56]
both in Ethiopia and dated respectively at c. 195 ka and
5.3.2 Three-stage chronology
at c. 160 ka.
The Earlier or Early Stone Age (ESA)
The Later Stone Age (LSA)
Main articles: Paleolithic and Lower Paleolithic
This period is not to be identied with Old Stone Age,
Main article: Later Stone Age
The Later Stone Age (LSA, sometimes also called the
Late Stone Age) refers to a period in African prehistory.
Its beginnings are roughly contemporaneous with the European Upper Paleolithic. It lasts until historical times
and this includes cultures corresponding to Mesolithic
and Neolithic in other regions.
Stone tools were made from a variety of stone. For example, int and chert were shaped (or chipped) for use
as cutting tools and weapons, while basalt and sandstone
were used for ground stone tools, such as quern-stones.
Wood, bone, shell, antler (deer) and other materials were
widely used, as well. During the most recent part of
the period, sediments (such as clay) were used to make
pottery. Agriculture was developed and certain animals
were domesticated.
Some species of non-Primates are able to use stone tools,
such as the Sea Otter, which breaks Abalone shells with
them. Primates can both use and manufacture stone tools.
This combination of abilities is more marked in apes and
men, but only men, or more generally Hominans, depend
on tool use for survival.[57] The key anatomical and behavioral features required for tool manufacture, which are
possessed only by Hominans, are the larger thumb and the
ability to hold by means of an assortment of grips.[58]
44
5.4.3
A structure with a roof supported with timber, disIn paleolithic times, mostly animals were painted, in thecovered in Dolni Vestonice, The Czech Republic,
ory ones that were used as food or represented strength,
dates to around 23,000 BCE. The walls were made
such as the rhinoceros or large cats (as in the Chauvet
of packed clay blocks and stones.
Cave). Signs such as dots were sometimes drawn.
Rare human representations include handprints and half Many huts made of mammoth bones were found in human/half-animal gures. The Cave of Chauvet in the
Eastern Europe and Siberia. The people who made Ardche dpartement, France, contains the most importhese huts were expert mammoth hunters. Exam- tant cave paintings of the paleolithic era, dating from
ples have been found along the Dniepr river valley about 31,000 BCE. The Altamira cave paintings in Spain
of Ukraine, including near Chernihiv, in Moravia, were done 14,000 to 12,000 BCE and show, among othCzech Republic and in southern Poland.
ers, bisons. The hall of bulls in Lascaux, Dordogne,
France, dates from about 15,000 to 10,000 BCE.
An animal hide tent dated to around 15000 to 10000 The meaning of many of these paintings remains unBCE, in the Magdalenian, was discovered at Plateau known. They may have been used for seasonal rituParain, France.
als. The animals are accompanied by signs that suggest
5.4.4
Art
5.4.5
45
46
Homo
5.7 Notes
[1] http://www.nhm.ac.uk/about-us/news/2010/august/
oldest-tool-use-and-meat-eating-revealed75831.html
5.8. REFERENCES
47
5.8 References
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First Africans: African Archaeology from the Earliest Toolmakers to Most Recent Foragers. Cambridge
World Archaeology. Oxford: Oxford University
Press.
Belmaker, Miriam (March 2006). Community
Structure through Time: 'Ubeidiya, a Lower Pleistocene Site as a Case Study (Thesis). Paleoanthropology Society.
Deacon, Hilary John; Deacon, Janette (1999). Human beginnings in South Africa: uncovering the secrets of the Stone Age. Walnut Creek, Calif. [u.a.]:
Altamira Press.
Piccolo, Salvatore (2013). Ancient Stones: The Prehistoric Dolmens of Sicily. Abingdon (UK): Brazen
Head Publishing.
Rogers, Michael J.; Semaw, Sileshi (2009). From
Nothing to Something: The Appearance and Context of the Earliest Archaeological Record. In
Camps i Calbet, Marta; Chauhan, Parth R. Sourcebook of paleolithic transitions: methods, theories,
and interpretations. New York: Springer.
Schick, Kathy D.; Nicholas Toth (1993). Making Silent Stones Speak: Human Evolution and the
Dawn of Technology. New York: Simon & Schuster. ISBN 0-671-69371-9.
Shea, John J. (2010). Stone Age Visiting Cards Revisited: a Strategic Perspective on the Lithic Technology of Early Hominin Dispersal. In Fleagle,
John G.; Shea, John J.; Grine, Frederick E.; Boden,
Andrea L.; Leakey, Richard E,. Out of Africa I: the
First Hominin Colonization of Eurasia. Dordrecht;
Heidelberg; London; New York: Springer. pp. 47
64.
48
Re-
Chapter 6
Woolly mammoth
The woolly mammoth (Mammuthus primigenius) was a
species of mammoth, the common name for the extinct
elephant genus Mammuthus. The woolly mammoth was
one of the last in a line of mammoth species, beginning
with Mammuthus subplanifrons in the early Pliocene. M.
primigenius diverged from the steppe mammoth, M. trogontherii, about 200,000 years ago in eastern Asia. Its
closest extant relative is the Asian elephant.
49
50
paper was based on travellers descriptions and a few scattered bones collected in Siberia and Britain. He discussed
the question of whether or not the remains were from elephants, but drew no conclusions.[5]
In 1738, Johann Philipp Breyne argued that mammoth
fossils represented some kind of elephant. He could not
explain why a tropical animal would be found in such a
cold area as Siberia, and suggested that they might have
been transported there by the Great Flood.[6] In 1796,
French anatomist Georges Cuvier was the rst to identify
the woolly mammoth remains not as modern elephants
transported to the Arctic, but as an entirely new species.
He argued this species had gone extinct and no longer
existed, a concept that was not widely accepted at the
time.[2][7]
6.1.1
Etymology
6.1.2 Evolution
The earliest known proboscideans, the clade which contains elephants, existed about 55 million years ago around
the Tethys Sea. The closest known relatives of the Proboscidea are the sirenians and the hyraxes. The family Elephantidae existed six million years ago in Africa
and includes the modern elephants and the mammoths.
Among many now extinct clades, the mastodon is only a
distant relative of the mammoths, and part of the separate
Mammutidae family, which diverged 25 million years before the mammoths evolved.[13] The following cladogram
shows the placement of the genus Mammuthus among
other proboscideans, based on hyoid characteristics:[14]
Following Cuviers identication, Johann Friedrich Blumenbach gave the woolly mammoth its scientic name,
Elephas primigenius, in 1799, placing it in the same genus
as the Asian elephant. This name means the rstborn
elephant. Henry Faireld Osborn chose a molar from
Blumenbachs collection as the lectotype specimen for
6.2. DESCRIPTION
51
Individuals and populations showing transitional morphologies between each of the mammoth species are
known, and primitive and derived species coexisted as
well until the former disappeared. The dierent species
and their intermediate forms therefore can be termed
"chronospecies". Many intermediate subspecies have
also been proposed, but their validity is uncertain; depending on author, they are either considered primitive forms of an advanced species or advanced forms of
a primitive species.[21] Regional and intermediate subspecies such as M. p. primigenius, M. p. jatzkovi, M.
p. sibiricus, and M. p. fraasi have been proposed.[24]
The St. Paul Island and Wrangel Island populations
were described as dwarf varieties, much smaller than the
mainland woolly mammoth; the Wrangel Island population was also proposed to be a new subspecies, M. p.
vrangeliensis.[25][26] The Wrangel mammoths were isolated for 5000 years, but experienced only a slight loss
of genetic variation.[27]
6.2 Description
The appearance of the woolly mammoth is probably the
best known of any prehistoric animal due to the many
frozen specimens with preserved soft tissue and depictions by contemporary humans in their art. Fully grown
males reached shoulder heights between 2.7 and 3.4 m (9
and 11 ft) and weighed up to 6 tonnes (6.6 short tons).
This is almost as large as extant male African elephants,
52
dle Kolyma mammoth, which was preserved with a complete trunk tip. Unlike the trunk lobes of modern elephants, the upper nger at the tip of the trunk had a long
pointed lobe and was 10 cm (3.9 in) long, while the lower
thumb was 5 cm (2.0 in) and was broader. The trunk
of Dima was 76 cm (2.49 ft) long, whereas the trunk
of the adult Liakhov mammoth was 2 metres (6.6 ft)
long.[31] Few frozen specimens have preserved genitals,
so the gender is usually determined through examination
of the skeleton. Males were generally larger and had more
robust skeletons and tusks. The best indication of sex is
the size of the pelvic girdle, as the birth canal is always
wider in females than in males.[33]
Coat
6.2. DESCRIPTION
53
6.2.2
Dentition
54
replacement.[41]
Distortion in the molars is the most common health problem found in woolly mammoth fossils. Sometimes the
replacement was disrupted, and the molars were pushed
into abnormal positions, but some animals are known
to have survived this. Teeth from Britain showed that
2% of specimens had periodontal disease, with half of
these containing caries. The teeth also sometimes had
cancerous growths.[42]
6.3 Palaeobiology
Adult woolly mammoths could eectively defend themselves from predators with their tusks, trunks and size, but
juveniles and weakened adults were vulnerable to pack
hunters such as wolves, cave hyenas and large felines. The
tusks may also have been used in intra-species ghting,
such as territorial ghts or ghts over mates. Because
of their curvature, the tusks were not suitable for stabbing, but may have been used for hitting, as indicated
by injuries to some fossil shoulder blades. As in modern elephants, the sensitive and muscular trunk worked
as a limb-like organ with many functions. It was used
for manipulating objects, and in social interactions. The
very long hairs on the tail probably compensated for the
shortness of the tail, enabling its use as a yswatter, similar to the tail on modern elephants.[43] As in reindeer and
musk oxen, the haemoglobin of the woolly mammoth was
adapted to the cold, with three mutations to improve oxygen delivery around the body and prevent freezing. This
feature may have helped the mammoths to live in high
latitudes.[44]
6.3.1 Diet
Food at various stages of digestion has been found in the
intestines of several woolly mammoths, giving a good picture of their diet. Woolly mammoths sustained themLike modern elephants, woolly mammoths were likely selves on plant food, mainly grass and sedges, which were
very social and lived in matriarchal family groups. This is supplemented with herbaceous plants, owering plants,
Mounted family group
6.3. PALAEOBIOLOGY
55
56
At this age, the second set of molars would be in the process of erupting, and the rst set would be worn out at
18 months of age. The third set of molars lasted for ten
years, and this process was repeated until the nal, sixth
set emerged when the animal was 30 years old. A woolly
mammoth could probably reach the age of 60, like modern elephants of the same size. By then the last set of
molars would be worn out, the animal would be unable to
chew and feed, and it would die of starvation.[55]
Possible distribution during the last glacial period, based on locations of fossil nds
57
eas during times when Columbian mammoth populations day, more than ve hundred depictions of woolly mamwere absent.[68]
moths are known, in media ranging from cave paintings
and engravings on the walls of 46 caves in Russia, France
and Spain to engravings and sculptures (termed "portable
art") made from ivory, antler, stone and bone. Cave paint6.5 Relationship with humans
ings of woolly mammoths exist in several styles and sizes.
The French Rougnac cave has most depictions, 159,
and some of the drawings are more than 2 metres (6.5
ft) in length. Other notable caves with mammoth depictions are the Chauvet Cave, Les Combarelles Cave,
and Font-de-Gaume.[70] A depiction in the Cave of El
Castillo may instead show Palaeoloxodon, the straighttusked elephant.[71]
Modern humans coexisted with woolly mammoths during the Upper Palaeolithic period when they entered Europe from Africa between 30,000 and 40,000 years ago.
Prior to this, Neanderthals had coexisted with mammoths
during the Middle Palaeolithic. Woolly mammoths were
very important to ice age humans, and human survival
may have depended on the mammoth in some areas. Evidence for such coexistence was not recognised until the
19th century. William Buckland published his discovery of the Red Lady of Paviland skeleton in 1823, which
was found in a cave alongside woolly mammoth bones, 6.5.1
but he mistakenly denied that these were contemporaries.
In 1864, douard Lartet found an engraving of a woolly
mammoth on a piece of mammoth ivory in the Abri de
la Madeleine cave in Dordogne, France. This was the
rst widely accepted evidence for the coexistence of humans with prehistoric extinct animals and is the rst contemporary depiction of such a creature known to modern
science.[69]
Exploitation
Woolly mammoth bones were used as construction material for dwellings by both Neanderthals and modern humans during the ice age. More than 70 such dwellings
are known, mainly from the Russian Plain. The bases of
the huts were circular, and ranged from 8 to 24 square
metres (86 to 258 sq ft). The arrangement of dwellings
varied, and ranged from 1 m (3.3 ft) to 20 m (66 ft) apart,
depending on location. Large bones were used as foundations for the huts, tusks for the entrances, and the roofs
were probably skins held in place by bones or tusks. Some
huts had oors that extended 40 cm (16 in) below ground.
Some huts included replaces, which used bones as fuel,
probably because wood was scarce. It is possible that
58
some of the bones used for materials came from mam- hunted intensively, but perhaps mainly when ivory was
moths killed by humans, but the state of the bones, and needed.[77]
the fact that bones used to build a single dwelling varied
by several thousands of years in age, suggests that they
were collected remains of long-dead animals. Woolly 6.6 Extinction
mammoth bones were also made into various tools, furniture, and musical instruments. Large bones, such as
shoulder blades, were also used to cover dead human bodies during burial.[72]
that humans hunted the remaining populations to extinction at the end of the last glacial period.[89][90] Studies
of an 11,30011,000 year old trackway in southwestern
Canada showed that M. primigenius was in decline while
coexisting with humans, since far fewer tracks of juveniles were identied than would be expected in a normal
herd.[46]
59
fewer nds in the latter. Such remains are mostly found
above the Arctic Circle, in permafrost. It appears that
soft tissue was less likely to be preserved between 30,000
and 15,000 years ago, perhaps because the climate was
milder during that period. Most specimens have partially
degraded prior to discovery, due to exposure or to being scavenged. This "natural mummication" required
the animal to have been buried rapidly in liquid or semisolids such as silt, mud and icy water, which then froze.[92]
The presence of undigested food in the stomach and seed
pods still in the mouth of many of the specimens suggests neither starvation nor exposure are likely. The maturity of this ingested vegetation places the time of death
in autumn rather than in spring, when owers would be
expected.[93] The animals may have fallen through ice
into small ponds or potholes, entombing them. Many
are certainly known to have been killed in rivers, perhaps
through being swept away by oods. In one location, by
the Berelekh River in Yakutia in Siberia, more than 8,000
bones from at least 140 mammoths have been found in
a single spot, apparently having been swept there by the
current.[94]
Early 19th century interpretation of the "Adams mammoth" carcass prior to excavation
Woolly mammoth fossils have been found in many dierent types of deposits, including former rivers and lakes,
and also in "Doggerland" in the North Sea, which was
dry at times during the ice age. Such fossils are usually fragmentary and contain no soft tissue. Apart from
frozen remains, the only soft tissue known is from a specimen that was preserved in a petroleum seep in Starunia,
Poland. Frozen remains of woolly mammoths have been
found in the northern parts of Siberia and Alaska, with far
60
the Kolyma River in northeastern Siberia. This specimen weighed approximately 100 kg (220 lb) at death
and was 104 cm (41 in) high and 115 cm (45 in) long.
Radiocarbon dating determined that Dima died about
40,000 years ago. Its internal organs are similar to those
of modern elephants, but its ears are only one-tenth the
size of those of an African elephant of similar age. A less
complete juvenile, nicknamed Mascha, was found on
the Yamal Peninsula in 1988. It was 34 months old, and
a laceration on its right foot may have been the cause of
death. It is the westernmost frozen mammoth found.[102]
In 1997, a piece of mammoth tusk was discovered protruding from the tundra of the Taymyr Peninsula in
Siberia, Russia. In 1999, this 20,380 year old carcass and
25 tons of surrounding sediment were transported by an
Mi-26 heavy lift helicopter to an ice cave in Khatanga.
The specimen was nicknamed the Jarkov mammoth.
In October 2000, the careful defrosting operations in this
cave began with the use of hairdryers to keep the hair and
other soft tissues intact.[103][104]
61
preserved.[108] Lyuba is believed to have been suocated by mud in a river that its herd was crossing.[52][109]
After death, its body may have been colonised by bacteria that produce lactic acid, which pickled it, preserving
the mammoth in a nearly pristine state.[52]
In 2012, a juvenile was found in Siberia, which had manmade cut marks. Scientists estimated its age at death to
be 2.5 years, and nicknamed it Yuka. Its skull and
pelvis had been removed prior to discovery, but were
found nearby.[110][76] Another mammoth discovery was
reported in October 2012, when it was excavated on the
Taymyr Peninsula. It was dated to 30,000 years old. It
was named Zhenya after the boy who found it.[111]
62
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[126] Strong, W. D. (1934).
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6.10 Bibliography
Chapter 7
Woolly rhinoceros
The woolly rhinoceros (Coelodonta antiquitatis) is an
extinct species of rhinoceros that was common throughout Europe and northern Asia[1] during the Pleistocene
epoch and survived the last glacial period. The genus
name Coelodonta means cavity tooth. The woolly
rhinoceros was a member of the Pleistocene megafauna.
7.1 Evolution
7.2 Description
The external appearance of woolly rhinos is known from
mummied individuals from Siberia as well as cave
paintings.[3] An adult woolly rhinoceros was typically
around 3 to 3.8 metres (10 to 12.5 feet) in length, with
The woolly rhinoceros used its horns for defensive purposes and to attract mates. During Greenland Stadial 2
(the Last Glacial Maximum[8] ) the North Sea retreated
northward, as sea levels were up to 125 metres (410 ft)
lower than today. The woolly rhinoceros roamed the ex-
68
7.4. EXTINCTION
69
constructed using several lines of evidence. Climatic reconstructions indicate the preferred environment to have
been cold and arid steppe-tundra, with large herbivores
forming an important part of the feedback cycle. Pollen
analysis shows a prevalence of grasses and sedges within
a more complicated vegetation mosaic.
7.3.1
Diet
7.4 Extinction
70
diocarbon plateaus exist around this time. The extinction
does not coincide with the end of the last ice age but does
coincide with a minor yet severe climatic reversal that
lasted for about 1,0001,250 years, the Younger Dryas
(GS1 - Greenland Stadial 1), characterized by glacial
readvances and severe cooling globally, a brief interlude
in the continuing warming subsequent to the termination
of the last major ice age (GS2), thought to have been due
to a shutdown of the thermohaline circulation in the ocean
due to huge inuxes of cold fresh water from the preceding sustained glacial melting during the warmer Interstadial (GI1 - Greenland Interstadial 1 - ca. 16,00011,450
14
C years B.P.).
The Pinhole Cave Man is a late Paleolithic gure of a man
engraved on a rib bone of the Woolly rhinoceros, found
at Creswell Crags in England.[16]
[6] Fortelius, Mikael (1983). The morphology and paleobiological signicance of the horns ofCoelodonta
antiquitatis(Mammalia:
Rhinocerotidae)".
Journal of Vertebrate Paleontology 3 (2):
125135.
doi:10.1080/02724634.1983.10011964.
ISSN 02724634.
71
Text
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7.8.2
Images
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File:Hebior_Mammoth_Clean.png Source: http://upload.wikimedia.org/wikipedia/commons/7/7a/Hebior_Mammoth_Clean.png License: CC-BY-SA-3.0 Contributors: Own work Original artist: MCDinosaurhunter
File:IceAgeEarth.jpg Source: http://upload.wikimedia.org/wikipedia/commons/b/b4/IceAgeEarth.jpg License: CC-BY-SA-3.0 Contributors: Own work Original artist: Ittiz
File:Ice_Age_Temperature.png Source: http://upload.wikimedia.org/wikipedia/commons/f/f8/Ice_Age_Temperature.png License: CCBY-SA-3.0 Contributors: ? Original artist: ?
File:Ice_age_fauna_of_northern_Spain_-_Mauricio_Antn.jpg Source: http://upload.wikimedia.org/wikipedia/commons/e/e6/Ice_
age_fauna_of_northern_Spain_-_Mauricio_Ant%C3%B3n.jpg License: CC-BY-2.5 Contributors: http://www.plosbiology.org/article/
slideshow.action?uri=info:doi/10.1371/journal.pbio.0060099&imageURI=info:doi/10.1371/journal.pbio.0060099.g001, from C. Sedwick (1 April 2008). What Killed the Woolly Mammoth?". PLoS Biology 6 (4): e99. DOI:10.1371/journal.pbio.0060099. Original
artist: Mauricio Antn
File:Iceage_north-glacial_hg.png Source: http://upload.wikimedia.org/wikipedia/commons/2/26/Iceage_north-glacial_hg.png License:
CC-BY-3.0 Contributors: Own work Original artist: Hannes Grobe/AWI
File:Iceage_north-intergl_glac_hg.png Source: http://upload.wikimedia.org/wikipedia/commons/e/ef/Iceage_north-intergl_glac_hg.
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