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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/(
yþ
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.
y¼
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