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Diversidad y control biológico de insectos - CyberTesis UACh ...

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The pairwise genetic distance matrixes were calculated using the Arlequin 3.01 software<br />

package (Schnei<strong>de</strong>r et al., 2000) to additionally compare the putative populations.<br />

Results.<br />

Phylogenetic analyses.<br />

The neighbour-joining (NJ), maximum parsimony (MP) and minimum evolution (ME)<br />

trees showed no major differences on the inferred phylogenies and consequently only the<br />

NJ tree is shown in Figure 1. The only relevant difference between trees was the sister<br />

position of the isolate B900 (haplotype 11). The branching pattern suggests a <strong>de</strong>ep division<br />

for the B. bassiana s.l. in Chile. The two large clusters inclu<strong>de</strong> some smaller but well<br />

supported clusters. When the phylogenetic and geographic data were crossed (Figure 1), the<br />

phylogenetic relatedness between isolates did not agree with their geographic relatedness,<br />

except for a small cluster which exclusively comprised isolates collected at Eastern Island.<br />

As expected, the haplotype tree shows a con<strong>de</strong>nsed sight of the findings (Figure 2).<br />

The Figure 3 shows the haplotype network constructed from the most parsimonous trees<br />

supported by the dataset. Remarkly, the network grouped the haplotypes into two large<br />

clusters, with the haplotype 11 in a intermediate position. The most exten<strong>de</strong>d haplotype<br />

(H1) has not a interior position in the network as expected if this haplotype was the<br />

ancestral state.<br />

The segment had a nucleoti<strong>de</strong> composition of A=0.24, C=0.28, G=0.27 and T=0.21, with<br />

G+C content = 55%. The 97 sequences gave 20 different haplotypes, which inclu<strong>de</strong>d 282<br />

variable (19%) and 218 parsimony informative (15%) sites. The overall nucleoti<strong>de</strong><br />

diversity was 0.035.<br />

Demographic analyses.<br />

The mismatch distributions for all pairwise combinations of the individuals for each<br />

population are shown in the Figure 4, except for Tarapacá, which was revealed fixed for the<br />

haplotype 1 and consequently the mismatch distribution can not be calculated. All the six<br />

populations had bimodal or multimodal distributions which did not conformed to the<br />

expected distribution from a mo<strong>de</strong>l of constant growth population expansion.<br />

25

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