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<dpdpoint x=“0.1” y=“6”/><dpdpoint x=“0.1” y=“7”/><dpdpoint x=“0.1”
y=“8”/>
<dpdpoint x=“0.1” y=“9”/>
</locus>
<locus>
<dpdpoint x=“0.1” y=“0”/><dpdpoint x=“0.1” y=“1”/><dpdpoint x=“0.1”
y=“2”/>
<dpdpoint x=“0.1” y=“3”/><dpdpoint x=“0.1” y=“4”/><dpdpoint x=“0.1”
y=“5”/>
<dpdpoint x=“0.1” y=“6”/><dpdpoint x=“0.1” y=“7”/><dpdpoint x=“0.1”
y=“8”/>
<dpdpoint x=“0.1” y=“9”/>
</locus>
0.5
B
0.4
B
B
B
0.3
B
B
B
B
B
0.2
B
B
B
B
0.1
B
B
B
B
B
B
B
B
B
0.0
B
B
1
10 100
FOUNDERS
Fig. 7.8
Variation in standard deviation for the average heterozygosity values of founding
populations of different sizes shown in Fig. 7.7. In the source population from which founders
are randomly drawn, there is only one locus with 10 alleles of equal frequency (all 0.1).
Each letter represents the standard deviation value for one trial (25 replicate runs per trial).
Overlapping values are shown as one letter. As the number of founders increases, standard
deviation for average heterozygosity values converges on 0.
The above are two loci with 10 unique alleles each, so append nine copies
of the above code to the above code, and then insert the resulting total code
into the NEWGARDEN input fi le where loci information is requested. Note
that, in the previous two examples, the opening statement of the input fi le
was as follows:
<LOCI number_loci=“1”>
whereas when entering the 20 replicate loci, the statement must be changed
to the following:
<LOCI number_loci=“20”>
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