|
TABLE 3. Local species diversity by region. Mean abundances per grid cell
(10,000 km) for alpha, beta, habitat type, source pool diversity, and
connectivity are given for each sampling interval. Values in parentheses
indicate rarefied alpha diversity, which is not given for the Holocene due to
sparseness of the data. Asterisks indicate peak values, except for early Eocene
European beta diversity, which was a local peak. Europe and Japan represent
convergent tectonic settings, and eastern North America represents passive.3
Local species diversity by region. Mean abundances per grid cell (10,000 km) for
alpha, beta, habitat type, source pool diversity, and connectivity are given for
each sampling interval. Values in parthenthases indicate rarefied alpha
diversity, which is not given for the Holocene due to sparseness of the data.
Asterisks indicate peak values, except for early Eocene European beta diversity,
which was a local peak. Europe and Japan represent convergent tectonic settings,
and eastern North America represents passive.
|
Interval
|
Region
|
Alpha-Div.
|
Beta-Div.
|
Habitat Types
|
Source Pool Div.
|
Connectivity
|
|
Holocene
|
E. N.Am.
|
44.3
|
0.00
|
2.2
|
1
|
0.00
|
|
|
Europe
|
61.6
|
0.00
|
6.3
|
1.2
|
0.00
|
|
|
Japan
|
4.5
|
0.67
|
1.3
|
1.9
|
0.08
|
|
Pleistocene
|
E. N.Am.
|
95.5 (12.5)
|
0.87
|
5
|
281.6
|
0.40
|
|
|
Europe
|
22.4 (12.2)
|
0.52
|
2.3
|
32.3
|
0.16
|
|
|
Japan
|
17.7 (9.7)
|
0.75
|
2.2
|
18.4
|
0.14
|
|
Pliocene
|
E. N.Am.
|
89.4 (13.2)
|
0.82
|
4.5
|
268.5
|
0.35
|
|
|
Europe
|
24.5 (11.9)
|
0.74
|
3.1
|
33.9
|
0.14
|
|
|
Japan
|
27.9 (11.7)
|
0.73
|
3.3
|
28.4
|
0.12
|
|
Late Miocene
|
E. N.Am.
|
60.7 (13.2)
|
0.90
|
5.1
|
104.4
|
0.21
|
|
|
Europe
|
29.6 (12.3)
|
0.75
|
2.8
|
57.9
|
0.19
|
|
|
Japan
|
58.5 (12.6)
|
0.73
|
4.7
|
114.8
|
0.21
|
|
Middle Miocene
|
E. N.Am.
|
90.7 (11.7)
|
0.57
|
4.7
|
122.3
|
0.11
|
|
|
Europe
|
65.0 (12.1)
|
0.69
|
4.5
|
141.9
|
0.23
|
|
|
Japan
|
29.8 (12.2)
|
0.86
|
2.8
|
47.3
|
0.20
|
|
Early Miocene
|
E. N.Am.
|
107.2 (12.5)
|
0.93
|
5.8
|
207.4
|
0.30
|
|
|
Europe
|
57.4 (12.2)
|
0.49
|
3.7
|
37.7
|
0.10
|
|
|
Japan
|
15.1 (11.2)
|
0.60
|
2.7
|
12.8
|
0.11
|
|
Late Oligocene
|
E. N.Am.
|
13.1 (12.0)
|
0.22
|
2.9
|
1.9
|
0.03
|
|
|
Europe
|
48.2 (13.6)
|
0.26
|
5.1
|
9.7
|
0.04
|
|
|
Japan
|
31.0 (12.0)
|
0.65
|
4.9
|
27.1
|
0.12
|
|
Early Oligocene
|
E. N.Am.
|
98.3 (13.1)
|
0.77
|
4.7
|
192.4
|
0.30
|
|
|
Europe
|
58.7 (11.8)
|
0.47
|
4
|
5
|
0.09
|
|
|
Japan
|
40.9 (11.8)
|
0.13
|
2.5
|
9.9
|
0.02
|
|
Late Eocene
|
E. N.Am.
|
75.3 (13.0)
|
0.83
|
4.7
|
170.5
|
0.21
|
|
|
Europe
|
87.9 (13.1)
|
0.57
|
7
|
123
|
0.12
|
|
|
Japan
|
19.8 (9.8)
|
0.57
|
3.4
|
23.1
|
0.10
|
|
Middle Eocene
|
E. N.Am.
|
68.3 (13.1)
|
0.88
|
5.2
|
110.7
|
0.23
|
|
|
Europe
|
76.6 (11.0)
|
0.58
|
4.5
|
177
|
0.16
|
|
|
Japan
|
39.7 (9.5)
|
0.69
|
4
|
52
|
0.22
|
|
Early Eocene
|
E. N.Am.
|
36.4 (12.7)
|
0.82
|
6.6
|
53
|
0.22
|
|
|
Europe
|
49.2 (13.0)
|
0.68
|
4
|
127.9
|
0.26
|
|
|
Japan
|
23.2 (12.0)
|
0.00
|
1.1
|
1.1
|
0.00
|
|