Biology Reference
In-Depth Information
1.0
ww
w
w
w
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w
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vv
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v v
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v v
v v
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v v
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v v v
v v v
v v v v vv
0.9
W
W
W
W
W
W
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W
W
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W
W
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W
W
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W
VVV
V
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V
VV
VV
V
VV
VV
V
VVV
VV
V
V
VVV
VV
V
VVV
VV
VV
V
VV
0.8
w
w
0.7
w
w
W
W
W
0.6
w
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w
w
w
w
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W
0.5
W
W
W
WW
W
W
W
W
W
W
W
W
W
W
WW
0.4
w
w
w
w
w
ww
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ww
0.3
A
0.2
0.1
0
10
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40
0.05
W
W
W
W
w
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W
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WW
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W
W
V
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V
VV
VV
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VVV
VV
VV
V
V
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V
V
VVV
V
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V
VV
VV
V
V
V
W
w
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v
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v vv
v
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v v
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W
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W
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vvvv
vv
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w
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W
W
V
V
W
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v
w
v
0.0
W
W
W
W
w
w
w
W
W
w
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w
w
w
w
w
W
V
v
W
W
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V
w
w
W
W
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W
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W
w
-0.05
W
W
w
W
w
w
W
W
w
W
w
w
-0.10
W
W
B
w
-0.15
0
10
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30
40
GENERATION
Fig. 18.2
Observed heterozygosity (A) and F values (B) for four trials with identical input
conditions except as noted below. All trials took place in a preserve-corridor-preserve system.
Compared to one side of the square preserves, the centrally placed corridor was 10% its height
and 20% its length. Trials V and v had all 172 founders placed in a square in the left preserve,
while trials W and w had founders divided into two squares, one placed in each preserve.
Each individual in all trials has 30 loci, each with the same number of distinct alleles. A single
allelic array for trials with uppercase symbols (V and W) has 21 unique alleles in the source
population as described in the text. Trials v and w use the usual array of 100 distinct alleles,
each with a frequency = 0.01.
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