From: Evolutionary relationships and divergence times among the native rats of Australia
 | Tree topologies | -lnL | Pvalues | |
---|---|---|---|---|
 |  |  | AU | KH |
1 | (Out,(AR,((((((Rsor,Rvil),Rlut),Rtun),Rfus),Rleu),Rpraet))) | <41273.6> | -- | -- |
2 | (Out,(AR,((((((Rsor,Rvil),Rlut),Rtun),Rfus),Rpraet),Rleu))) | 2.6 | 0.556 | 0.351 |
3 | (Out,(AR,(((((Rsor,Rvil),Rlut),Rtun),Rfus),(Rleu,Rpraet)))) | 4.1 | 0.393 | 0.254 |
4 | (Out,(AR,(((((Rsor,Rvil),(Rlut,Rtun)),Rfus),Rpraet),Rleu))) | 9.3 | 0.208 | 0.170 |
5 | (Out,(AR,((((Rsor,Rvil),(Rtun,Rlut)),Rfus),(Rleu,Rpraet)))) | 11.2 | 0.144 | 0.126 |
6 | (Out,(AR,(((((Rsor,Rvil),Rlut),Rtun),(Rleu,Rfus)),Rpraet))) | 16.3 | 0.082 | 0.054 |
7 | (Out,(AR,((((((Rsor,Rvil),Rlut),Rtun),Rleu),Rpraet),Rfus))) | 25.8 | 0.020* | 0.018* |
8 | (Out,(AR,(((((Rsor,Rvil),Rtun),Rlut),(Rfus,Rpraet)),Rleu))) | 30.9 | 0.019* | 0.018* |
9 | (Out,(AR,((((Rsor,Rvil),Rtun),Rlut),((Rleu,Rfus),Rpraet)))) | 31.2 | 0.028* | 0.021* |
10 | (Out,(AR,(((Rsor,Rvil),(Rtun,Rlut)),((Rfus,Rpraet),Rleu)))) | 34.0 | 0.025* | 0.013* |
11 | (Out,(AR,((((Rsor,Rvil),Rtun),Rlut),((Rleu,Rfus),Rpraet)))) | 101.9 | >0.001* | >0.001* |
12 | (Out,(AR,((Rsor,Rvil),((Rlut,Rtun),(Rfus,(Rleu,Rpraet)))))) | 133.8 | >0.001* | >0.001* |
13 | (Out,(AR,((((Rsor,Rtun),Rvil),(Rlut,Rfus)),(Rleu,Rpraet)))) | 199.0 | >0.001* | >0.001* |
14 | (Out,(AR,(((((Rsor,Rvil),Rleu),Rfus),(Rtun,Rlut)),Rpraet))) | 208.6 | >0.001* | >0.001* |
15 | (Out,(AR,((((Rsor,Rvil),Rlut),Rtun),(Rfus,(Rleu,Rpraet))))) | 274.2 | >0.001* | >0.001* |
16 | (Out,(AR,(((((Rsor,Rvil),Rlut),Rtun),(Rpraet,Rfus)),Rleu))) | 277.7 | >0.001* | >0.001* |
17 | (Out,(AR,((((Rsor,Rlut),Rtun),((Rvil,Rfus),Rpraet)),Rleu))) | 343.5 | >0.001* | >0.001* |
18 | (Out,(AR,((Rsor,Rvil),((Rlut,Rtun),((Rfus,Rpraet),Rleu))))) | 409.9 | >0.001* | >0.001* |