From: Demographic history, genetic structure and gene flow in a steppe-associated raptor species
Country | Region | Abrev. | n | nH | Hd (± SD) | π (± SD) | D | F S |
---|---|---|---|---|---|---|---|---|
Breeding range | ||||||||
Spain | Extremadura | SpW | 38 | 8 | 0.3798 ± 0.100 | 0.000469 ± 0.00038 | -2.26* | -3.28* |
Spain | Toledo, Ciudad Real | SpC | 12 | 4 | 0.5606 ± 0.150 | 0.000639 ± 0.00050 | -1.53* | 0.62 |
Spain | Castellón | SpE | 22 | 6 | 0.6797 ± 0.095 | 0.000672 ± 0.00041 | -1.19 | -0.96 |
Spain | Galicia | SpNW | 20 | 8 | 0.7421 ± 0.096 | 0.000758 ± 0.00055 | -1.82* | -3.71* |
France | Provence-Alps-Cote Azur | PACA | 19 | 7 | 0.8246 ± 0.064 | 0.000987 ± 0.00067 | -0.92 | -0.24 |
France | Pays Loire | PLO | 6 | 4 | 0.8667 ± 0.125 | 0.001651 ± 0.00116 | -0.49 | 1.36 |
France | Poitou-Charente | PCH | 51 | 13 | 0.6894 ± 0.070 | 0.000954 ± 0.00063 | -1.55* | -3.17 |
France | Champagne-Ardenne | CHAR | 21 | 8 | 0.6762 ± 0.111 | 0.000820 ± 0.00058 | -1.84* | -0.36 |
France | Aquitaine-Pyrenees | AQPY | 10 | 5 | 0.7556 ± 0.129 | 0.000538 ± 0.00045 | -1.11 | -0.33 |
The Netherlands | Oldenzaal | NED | 12 | 4 | 0.4545 ± 0.170 | 0.000963 ± 0.00068 | -0.84 | 0.32 |
Germany | Lower Saxony | GER | 6 | 2 | 0.3333 ± 0.215 | 0.000188 ± 0.00025 | -0.93 | -0.00 |
Czech Republic | Vysočyna | CZE | 13 | 4 | 0.6026 ± 0.130 | 0.000909 ± 0.00065 | 0.45 | 0.32 |
Kazakhstan | Naurzum, Kostanay | KZ | 32 | 8 | 0.6875 ± 0.077 | 0.000845 ± 0.00058 | -0.60 | -0.61 |
Wintering areasWintering areas | ||||||||
Senegal | Nianing | SEN | 10 | 2 | 0.3556 ± 0.155 | 0.000200 ± 0.00024 | ||
Pakistan | Hyderabad | PAK | 12 | 8 | 0.9242 ± 0.057 | 0.001808 ± 0.00113 | ||
Geographic originGeographic origin | ||||||||
SW | -2.27* | -28.5* | ||||||
NE | -1.18 | -10.2* | ||||||
Pooled | 284 | 51 | 0.663 ± 0.032 | 0.000826 ± 0.00007 |