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Ef kj ¼
m
þ
m
1
2
1
2
f G 1 ðÞ j 1
f G 1 ðÞ j
f G 2 ðÞ j 1
f G 2 ðÞ j
ð
m
Þþ
ð
m
Þþ
1
1
ð
6
Þ
Substituting f G 1 ðÞ j
¼
ð
1
þ
q G 1 ðÞ j
=
2
Þ
and f G 2 ðÞ j
¼
ð
1
þ
q G 2 ðÞ j
=
2
Þ
from Eq. (3)
gives:
Ef kj
q G 1 ðÞ j
2
q G 1 ðÞ j
2
q G 1 ðÞ j
2
1
2
1
þ
1
þ
1
¼
þ m
þ m m
1
2
1
þ
q G 2 ðÞ j
2
1
þ
q G 2 ðÞ j
2
1
q G 2 ðÞ j
2
þ
þ m
þ m m
;
ð
7
Þ
and after simplification, we obtain:
Ef kj ¼
þ
þ
q G 1 ðÞ j
2
q G 2 ðÞ j
2
1
2
1
2 m
1
2
1
2 m
q G 1 ðÞ j
q G 2 ðÞ j
þ
;
ð
8
Þ
Ef kj ¼
m
þ
1
2
q G 1 ðÞ j
2 þ
q G 2 ðÞ j
2
q G 1 ðÞ j
q G 2 ðÞ j
1
m
;
ð
9
Þ
and substituting in Eq. (2) :
Eq kj ¼
2Ef kj
m
þ
q G 1 ðÞ j
2
q G 2 ðÞ j
2
q G 1 ðÞ j
q G 2 ðÞ j
¼
m
þ
;
1
1
1
ð
10
Þ
and after simplification, we obtain:
<
0
1
1
2 m
@
A q G 1 ðÞ j
Eq kj
½
¼
ð
þ
q G 2 ðÞ j
Þ;
ð
Þ
11
:
Eq kk
½
¼
1
;
and the expected mean genetic similarity at equilibrium is Q*
¼
1/(
1),
where
( Higgs and Derrida, 1992; Meli´n et al., 2010 ). In summary,
each new offspring has a genome inherited from its two parents with repro-
duction producing similar individuals and mutation acting so that offspring
differ from their parents and from all the individuals in the population.
4J
m
2. Integrating Population Genetics in the Neutral Metacommunity
Model
In the previous section, we derived the expected genetic similarity among all
the individuals in the initial population of size J starting from all individuals
with an extremely large and similar genome. The dynamics in the original
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