Table 1. Probability of clonal identity in alpine (HTM and Pyr) and lowland (LLaP) populations where identical microsatellite genotypes (MLMGs) were encountered.
Region | Population | Repeated MLMGs | n | Psex | Psex (Fis) |
HTM | ZelKriv | 1 | 36 | 0.000 | 0.000 |
ZelKriv | 2 | 23 | 0.000 | 0.000 | |
CzarStaw | 1 | 31 | 0.000 | 0.000 | |
CzarStaw | 2 | 29 | 0.000 | 0.000 | |
VTSM | 1 | 29 | 0.000 | 0.000 | |
VTSM | 2 | 33 | 0.000 | 0.000 | |
MHinc | 1 | 60 | 0.000 | 0.000 | |
ZelJ | 1 | 30 | 0.000 | 0.000 | |
Pyr | Estats | 1 | 2 | 0.357 | 0.688 |
Estats | 2 | 3 | 0.154 | 0.623 | |
Sotllo | 1 | 2 | 0.114 | 0.158 | |
Sotllo | 2 | 2 | 0.477 | 0.707 | |
Redon | 1 | 21 | 0.000 | 0.000 | |
Redon | 2 | 2 | 0.002 | 0.037 | |
EG1 | 1 | 3 | 0.349 | 0.511 | |
EG1 | 2 | 2 | 0.549 | 0.638 | |
EG1 | 3 | 2 | 0.065 | 0.152 | |
EG3 | 1 | 2 | 0.276 | 0.261 | |
EG3 | 2 | 4 | 0.051 | 0.189 | |
EG3 | 3 | 1 | 0.321 | 0.305 | |
ENS | 1 | 4 | 0.026 | 0.260 | |
ENS | 2 | 3 | 0.072 | 0.422 | |
ENS | 3 | 2 | 0.815 | 0.799 | |
ENS | 4 | 2 | 0.283 | 0.469 | |
EPS | 1 | 2 | 0.139 | 0.244 | |
ENG | 1 | 5 | 0.928 | 0.836 | |
ENG | 2 | 5 | 0.467 | 0.657 | |
ENG | 3 | 2 | 0.697 | 0.776 | |
ENG | 4 | 5 | 0.467 | 0.657 | |
LLaP | KGeorge | 1 | 11 | 0.000 | 0.000 |
KGeorge | 2 | 2 | 0.003 | 0.023 | |
KGeorge | 3 | 3 | 0.000 | 0.000 | |
KGeorge | 4 | 2 | 0.008 | 0.023 | |
KGeorge | 5 | 5 | 0.000 | 0.000 | |
Chabarovice | 1 | 2 | 0.053 | 0.219 | |
Chabarovice | 2 | 3 | 0.000 | 0.012 | |
Chabarovice | 3 | 15 | 0.000 | 0.000 | |
Ohrid | 1 | 2 | 0.073 | 0.885 | |
Ohrid | 2 | 9 | 2.153 | 0.002 | |
Ohrid | 3 | 12 | 0.000 | 0.000 |
n, number of replicates; Psex, probability of clonal identity; Psex (Fis), corrected probability to consider possible departure from Hardy-Weinberg expectations.