Only positive m is allowed (here mutation introduces a bias towards m=0.5)
L=4
Sexual selection
32_600_0.0025_0.1
32_600_0.01_0.1
32_600_0.0025_0.2
L=8
Assortative mating (almost no
variation)
32_600_0.0025_0.1
32_600_0.0025_0.2
32_600_0.01_0.1
32_600_0.01_0.2
Sexual selection (divergence with
sigma_a=0.1, variation with sigma_a=0.2)
32_600_0.0025_0.1
32_600_0.0025_0.2
32_600_0.01_0.1
32_600_0.01_0.2
Symmetric preference function (-1<=m<=1,
m=0.0 is random mating)
L=8
Assortative mating (no variation)
32_600_0.0025_0.1
Sexual selection
24_500_0.0025_0.1
24_600_0.0025_0.1
32_500_0.0025_0.1
32_600_0.0025_0.1
(23/30 cases with |m|>0.5)
32_600_0.0025_0.15
(3/15 cases with |m|>0.5)
24_500_0.0025_0.2
24_600_0.0025_0.2
32_500_0.0025_02
32_600_0.0025_0.2
(0/15 cases with |m|>0.5)
32_600_0.01_0.1
(15/15 cases with |m|>0.5; only
once 4 species)
32_600_0.01_0.15
(5/15 cases with |m|>0.5)
32_600_0.01_0.2
(3/15 cases with |m|>0.5)
not much speciation in 24_500
max 2 species in 24_600; divergence in sigma_a=0.1, variation in
sigma_a=0.2
variation, no divergence in 32 with sigma_a=0.2
Linear gradient in
the frequency of theta_2=1 in 32_600_0.0025_0.1
30
runs _slope=0.0
(same as 32_600_0.0025_0.1
above; 12 cases with 2 "ecological" species; 18 cases with 4
eco-species) T=68435 (+/-28600)
15
runs _slope=0.25
(always 4 eco-species) average time to m=0.5 is T=75107
(+/-28088)
15 runs _slope=0.5
T=56800 (+/-23198)
15 runs _slope_0.75
T=57000 (+/-13996)
15 runs _slope=1.0
T=72733 (+/-23327)
Linear gradient in
the frequency of theta_2=1 in 32_600_0.0025_0.15
15
runs _slope=0.0
(same as 32_600_0.0025_0.15
above) 3/15 cases with |m|>0.5;
15
runs _slope=0.25
5/15 cases with |m|>0.5
15 runs _slope=0.5
4/15 cases with |m|>0.5
15 runs _slope_0.75
1/15 cases with |m|>0.5
15 runs _slope=1.0
6/15 cases with |m|>0.5